VAERS Reports #EW0186

VAERS 2719998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 01.12.2023
Impfdatum: 24.11.2021
Beginn: 25.11.2023
Tage bis Beginn: 731,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Hypoxia Pneumonia Positive airway pressure therapy Respiratory distress SARS-CoV-2 test positive

Symptomtext

Admit date: 11/25/2023 Discharge date: 11/30/2023 Admitting Physician: MD Attending Physician at the Time of Discharge: DO Reason for Admission: Acute Respiratory Failure Brief Summary of Hospital Stay: Pateint is a 80 YO year old female with a history of hypertension, TIA, hypothyroidism, brain aneurysm, OSA on CPAP, home 1-2 L, asthma, was admitted on 11/25/2023 with acute respiratory distress with hypoxia. She was recently treated for community-acquired pneumonia (with ceftriaxone and doxycycline and prednisone for 5 days) in a previous admission on 11/17/23 and returns with new positive COVID test . Differential Diagnoses are possible worsening community-acquired pneumonia or COVID pneumonia. On this admission she was given 1 day of Ceftriaxone-Doxy, followed by COVID therapies of Decadron and remdesivir for 5 days. She showed continuous improvement from BIPAP to now 1L oxygen therapy prior to discharge. Discharged to home.

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

VAERS 2641099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: FL
Alter: 77,0
Geschlecht: M
Eingang: 05.06.2023
Impfdatum: 03.12.2021
Beginn: 02.05.2023
Tage bis Beginn: 515,0
Dosis: 2
Route/Site: IM / -

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

Acute respiratory failure COVID-19 SARS-CoV-2 test positive

Symptomtext

Hospitalization: 5/2/2023 - 5/7/2023 (5 days) Presentation to the ED: acute respiratory failure with hypoxia COVID + date: 5/2/23 Treatment: Remdesivir Discharge to: home. EL9267 2/15/2021 EW0186 5/24/2021 FJ1620 12/3/2021

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: BPH, HLD, LUNG CA, RA, AAA, CKDii
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2558544

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 12.01.2023
Impfdatum: 17.11.2021
Beginn: 16.12.2022
Tage bis Beginn: 394,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary normal Asthenia Atelectasis COVID-19 Chest X-ray abnormal Computerised tomogram head normal Computerised tomogram spine Confusional state Dehydration Diarrhoea Fall Hyponatraemia Hypoxia Magnetic resonance imaging head normal Mental status changes Metabolic encephalopathy Pneumonia viral

Symptomtext

Patient is a 74 y.o. male patient of CNP with history of hypertension, hyperlipidemia, BPH s/p prostate cancer, hypothyroidism, Lewy body dementia presented with severe confusion found to be COVID-positive and febrile. Confusion likely metabolic encephalopathy due to acute viral infection. Completed course of remdesivir and received a course of Decadron with improvement of respiratory symptoms. To be discharged to SNF. Acute metabolic encephalopathy suspect due to COVID-19 Virus Infection with viral pneumonia Febrile 102.1 on admission Date of onset of symptoms: unclear though believed to be about a week ago Symptoms present on admission: severe confusion and mental decline, severe weakness, and frequent falls Initially on room air however became hypoxic shortly after admission Date of covid positive test: 12/16/2022 Vaccination status: vaccinated Imaging: Chest x-ray mild right basilar atelectasis CT head - no acute intracranial abnormality; CT cervical spine - no injury Oxygen requirements on admission: None Current oxygen requirements: RA with sats 93-94%. 96% on 2 L. Requires oxygen at night Medical therapy: completed remdesivir, IV Lasix 20 mg daily x3 for dry lung strategy. Patient received 7 days of decadron. He has been having progressive worsening confusion. Will discontinue steroids, should that be contributing to his confusion. Consultants following: infectious disease Completed 5 days of abx Anticipated special isolation end date:12/26/2022 CT angiogram of the lungs was done which ruled out any pulmonary embolism Acute hypoxic respiratory failure - secondary to covid - improving with decreased oxygen requirements Lewy body dementia with anxiety Hard of hearing Patient uses hearing aids Rns informed of communication barrier Per daughter, patient's memory is usually sharp and his dementia Continue Zoloft and Exelon Worsened due to underlying COVID infection. Frequent falls S/p scalp trauma Patient with fall 12/14 prompting ER eval and again with repeat fall earlier today Usually ambulates with use of a walker and able to participate with PT Currently at assisted living for ST and PT which he usually is able to participate with PT/OT, speech consulted Hyponatremia due to dehydration and possibly due to Diarrhea: Resolved Anemia, chronic OSA not on CPAP HTN, essential Hyperlipidemia Hypothyroidism:Continue atorvastatin, levothyroxine, metoprolol BPH s/p prostate cancer Continue tamsulosin PSA screening MRI brain given sudden onset confusion which is normal

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

VAERS 2531018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 14.12.2022
Impfdatum: 20.10.2021
Beginn: 05.12.2022
Tage bis Beginn: 411,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Anticoagulant therapy Blood creatinine increased Blood lactic acid increased COVID-19 Chest X-ray abnormal Chest tube insertion Cough Drain placement Dyspnoea Empyema Hypotension Hypoxia Lactic acidosis Leukocytosis Lung abscess Lung consolidation Pleural effusion

Symptomtext

Discharge Provider: MD Primary Care Provider: DNP, A-GNP Admission Date: 12/5/2022 Discharge Date: Dec 5, 2022 PRESENTING PROBLEM: Hypoxia Community acquired bacterial pneumonia Severe sepsis (HCC) Elevated lactic acid level Pneumonia of right lung due to infectious organism, unspecified part of lung Leukocytosis, unspecified type HOSPITAL COURSE: Patient is a 84 y.o. male who presented today with 3 days of worsening dyspnea and cough. He was severely hypoxic when EMS found him at home he was given 10 L of supplemental oxygen nebulizer treatments and steroids EN route to the emergency department on arrival at the emergency department he was breathing better but still requiring 10 L. Aggressive nebulizer therapy in the emergency department and supportive care allow them to reduce his oxygen to 2 L and still maintain sats in the 90s. Workup demonstrated a pneumonia picture with a large right pleural effusion elevated white count elevated procalcitonin and lactic acidosis. He was diagnosed with severe sepsis due to pneumonia and the hospitalist service was contacted for admission. He had been started on Rocephin and azithromycin which was continued. He was also found to be COVID-19 positive remdesivir therapy was ordered as well as Decadron. Interventional Radiology was consulted for right thoracentesis. He has AFib on Eliquis so we are holding the Eliquis until after his thoracentesis. Unfortunately, Interventional Radiology was unable to complete the thoracentesis until Wednesday, due to the anticoagulation. Lovenox was ordered to the unit. Throughout the evening shift, the patient had increasing supplemental oxygen requirements. A repeat CXR was performed, which showed much worsening right sided pleural effusion to the point where the right lung was collapsed. Patient was placed on BiPAP for greater oxygen support. Dr. from the hospital was contacted, who agreed to accept the patient for higher level of care. Patient will be transferred by EMS to the Hospital. Discharge Provider: MD Primary Care Provider: A-GNP, DNP Admission Date: 12/6/2022 Discharge Date: 12/12/22 COVID positive date: 12/5/2022 PRESENTING PROBLEM: Acute respiratory failure with hypoxia (HCC) HOSPITAL COURSE: 84 y.o. male with a past medical history of chronic obstructive pulmonary disease, atrial fibrillation on Eliquis, hyperlipidemia, tobacco use who presents with acute hypoxic and hypercapnic respiratory failure, very large right pleural effusion, developing lung abscess with sepsis, and COVID-19 infection. Patient reports that he has been feeling short of breath for the past several days and denies any other associated symptoms. He presented to an outside emergency department for further evaluation where he was found to require up to 10 L of oxygen and received steroids by EMS. He was given to DuoNebs in the emergency department with improvement of his oxygen requirements to 2 L. Other vitals notable for tachycardia, tachypnea, hypoxia to 74%, and was transiently hypotensive. Imaging revealed a very large right-sided pleural effusion with near complete collapse of the right lung, right posterior lobe irregular area concerning for developing parenchymal abscess, consolidative focus in the left lower lobe concerning for atelectasis or pneumonia. Labs revealed creatinine 1.25, procalcitonin 0.26, lactic acid 3.2, WBC 29.5, positive COVID-19. Patient was admitted to the Hospital. Initially required BiPAP support for hypoxia. Patient had successful image guided right-sided pleural drain placement by Interventional Radiology. Fluid analysis revealed consistency with empyema. Patient's respiratory status significantly improved with IV antibiotics and drainage. Patient was weaned off of BiPAP support and off nasal cannula. Patient was treated with IV Unasyn and transition to Augmentin to complete a further 4 week course. Will need follow-up imaging post discharge. IR to schedule for outpatient follow-up for chest tube removal and further imaging. Home health care arranged for continued outpatient monitoring/indication with chest tube, nutrition, ongoing antibiotic therapy for empyema. Patient getting discharged with chest tube supplies for daily care.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: GOLD stage A COPD Pleural effusion on right Acute respiratory failure with hypoxia (HCC) Longstanding persistent atrial fibrillation (HCC) Heart murmur Dysphagia Acute right hip pain Hearing loss due to cerumen impaction, bilateral Mixed hyperlipidemia Severe sepsis with acute organ dysfunction (HCC) Tobacco use disorder History of duodenal ulcer History of carotid artery disease Encounter for screening for lung cancer
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amoxicillin-clavulanate (AUGMENTIN) 875-125 MG per tablet apixaban (ELIQUIS) 2.5 MG tablet atorvastatin (LIPITOR) 20 MG tablet cholecalciferol (VITAMIN D3
Allergien: NKA
Vorherige Impfungen: -

VAERS 2490113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 29.04.2021
Beginn: 25.10.2022
Tage bis Beginn: 544,0
Dosis: 2
Route/Site: - / -

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

Asymptomatic COVID-19 Cerebrovascular accident SARS-CoV-2 test positive

Symptomtext

Pt was admitted on 10/19 for CVA. She was due to be transferred to 3W for inpatient rehab and required a COVID test which was positive on 10/25. She is asymptomatic at this time.

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

VAERS 2482073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: TX
Alter: 82,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 13.06.2021
Beginn: 14.10.2022
Tage bis Beginn: 488,0
Dosis: 1
Route/Site: IM / LA

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

Blood gases abnormal COVID-19 COVID-19 pneumonia Cardio-respiratory arrest Death Hypophagia Hypoxia Nausea Positive airway pressure therapy Productive cough Respiratory failure Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. Rec'd Pfizer BioNTech vaccine on 5/22/2021 and 6/13/2021. Admitted 10/10/22 for COVID PNA and respiratory failure. Pt had c/o of productive cough and congestion for one week with increased use of NC O2. Pt also experienced nausea and poor PO intake. During stay pt had worsening of respiratory status and ABG showed severe hypoxemia. Pt was placed on Airvo then progressed to BiPAP. Code blue was called without ROSC and pt expired on 10/14/22. Tx'd with Decadron, solumedrol, remdesivir, doxycycline, and azithromycin.

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Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: 4,0
Labordaten: Covid + 10/10/22 - This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
Aktuelle Erkrankungen: AKI
Vorgeschichte: CKD3, HTN, Affib, PAD s.p bilateral LE amputations
Andere Medikamente: HC/APAP, albuterol, xanax, apixaban, bisacodyl, vitamin d3, colchicine, diclofenac, docusate, febuxostat, fluticasone, hydrocortisone, hydroxyzine, ipratropium, lidocaine, loperamide, lovastatin, multivitamin, omeprazole, ondansetron, PEG 3
Allergien: Penicillin V, Sulfa, Avocado, Levofloxacin
Vorherige Impfungen: -

VAERS 2460667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 26.08.2021
Beginn: 20.09.2022
Tage bis Beginn: 390,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure COVID-19 Chest pain Death Dyspnoea Fatigue Metabolic encephalopathy Pyrexia SARS-CoV-2 test positive

Symptomtext

"Patient with 3 COVID vaccines who admitted to hospital with COVID detected PCR and complications of COVID who subsequently died of COVID complications. Hospice provider consult note (patient died prior to admission to hospice): ""86 YO female with a past medical history of mild chronic obstructive pulmonary disease, prior lung cancer status post LUL resection, scleroderma, Sjogren's syndrome. Followed with Dr. outpatient. Presented with fever, dyspnea and chest pain and admitted with diagnosis of COVID-19 and acute hypoxic respiratory failure. She continued worsening inpatient with increased oxygen requirement. Care service is now asked to see the patient for goals of care. At time of initial consult she is on high-flow nasal cannula oxygen 40 liters/minute at 90%. Per family report she is much more greatly fatigued today than previously. She has asked several family members to just let me go and I do not want to do this anymore. IMPRESSIONS / PLAN: Care Issues: Conversion to comfort directed end of life care 1. Medical decision making capacity: At the time of our consult the patient has limited ability for participation and medical decision making due to being in extremis. Recent history of encephalopathy over past few days. Neurology had evaluated as multifactorial metabolic encephalopathy. There are documents. Medical power of attorney 1. Is husband 2. Is daughter 2. Goals of Care: medical team had several meetings with family members today. First meeting today involved daughter, with myself and medical care chaplain. We shared some of the prognostic information from consultants and primary medical team. Shared likely end of life trajectory given her acute on chronic respiratory failure. Shared the ethics of decision making involving the patient's previously expressed personal wishes, including stating that she wanted to stop with aggressive care. Discussed a reasonable plan for symptom management and the burdens and benefits of symptom management at end of life, including down and off titration of high-flow nasal cannula oxygen. Another meeting was held this afternoon with myself, again daughter, and brothers. The patient's husband, is present however he prefers to stay at the wife's bedside. Comfort-directed End of Life care 3. Code Status: No CPR/DNI/comfort 4. Psychosocial and Spiritual Support: Chaplain was present at family meeting today and religious priest was called by hospital chaplain this afternoon 5. medical care follow up : medical Care will help to place comfort care orders. Also placed hospice referral order and asking liaison to get hospice consent signed. We can begin the process of admitting. Family has already agreed to that plan.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: COIVD Detected PCR on 9/15/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular; HTN (hypertension); Carotid artery plaque; Digestive; Gastroesophageal reflux disease without esophagitis; Endocrine; Hypothyroidism; Integumentary; Skin cancer; basal cell; Respiratory; Primary cancer of left upper lobe of lung (*); Moderate COPD (chronic obstructive pulmonary disease) (*); Acute respiratory failure with hypoxia (*); Urinary; Chronic renal failure, stage 3a (*); Other Sjogren's disease (*) Personal history of malignant; neoplasm of bronchus and lung; History of nonmelanoma skin cancer; History of lymphoma Chronic insomnia; Generalized OA; Osteoporosis; Anxiety; MGUS (monoclonal gammopathy of unknown significance); History of malignant neoplasm of head and neck; Invasive ductal carcinoma of breast, left (*); Postmenopausal; Immunocompromised (*); Metabolic encephalopathy.
Andere Medikamente: -
Allergien: Latex; Adhesive
Vorherige Impfungen: -

VAERS 2402977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 06.05.2021
Beginn: 02.08.2022
Tage bis Beginn: 453,0
Dosis: 2
Route/Site: - / -

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

Acute myocardial infarction Angiogram pulmonary abnormal Arthralgia Back pain Blood creatinine normal Blood electrolytes normal Brain natriuretic peptide normal COVID-19 Chest pain Echocardiogram abnormal Cardiac stress test normal Coronary artery disease Ejection fraction Haemoglobin normal Pain Pericardial effusion Ejection fraction normal Platelet count normal

Symptomtext

78 yo female w/ hx of recent COVID, HTN, HLP, PVD, Carotid artery dz, GERD, H pylori, asthma,hypothyroidism who presented to ED secondary to CP. Recent hospitalization for COVID and NSTEMI. 2D echo w/ EF 60%, no WMA, small pericardial effusion w/o compromise. Completed hep gtt x 48h. Recommended OP ischemic work up. Pt overall did well and was discharged home. Pt w/ intermittent L sided burning chest pain w/ radiation to her back and shoulder over the past 1.5 weeks. Chest pain did get worse therefore she came to ED for further evaluation. Upon arrival to ED, 159/95, HR 93, afebrile, no hypoxia. No leukocytosis, Hgb 12.4, plts 157k. Lytes/renal function WNL. Cr 0.95. Trops WNL, BNP 43.COVID remains positive. CTA PE w/o thrombus , 3-vessel dz noted. Noted Extensive vascular calcifications and complete occlusion of the proximal left subclavian artery with a patent shunt through left carotid artery. Pt admitted for further care with cardio consult. Stress MPI done - no ischemia. Pt feeling well and agreeable for DC on 8/4. Pt notes she cannot tolerate statin. Pt was feeling well on day of discharge and medically stable for discharge. Pt was present during discharge planning and agreeable to plan.

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Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 2,0
Labordaten: 8/2 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2402948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 30,0
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 24.04.2021
Beginn: 13.07.2022
Tage bis Beginn: 445,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Aspiration COVID-19 Computerised tomogram thorax abnormal Condition aggravated Dysphagia Hyporesponsive to stimuli Hypoxia Lung infiltration Patient uncooperative SARS-CoV-2 test positive Seizure Somnolence Swallow study abnormal

Symptomtext

7/13-7/17 31 y/o M with medical history significant for autism(non-verbal at baseline), intractable epilepsy, status epilepticus, aggressive behavior who was brought into the ED via EMS 12 hours ago due to hypoxia and decreased responsiveness. Mother reports patient used to have seizures weekly prior to medication changes 1 month ago, since that time he had been seizure free until two days ago, at which time he had 3 seizures in a 24 hour period. Patient did not receive his antiepileptic medication prior to the onset of seizures. He was started on remdesivir and decadron. A CT of chest was done and was remarkable for bilateral infiltrates. He was initially on HFNC oxygen but improved drastically within 24 hrs and was weaned to RA. Because of the rapid recovery, COVID was deemed less likely the cause of his ARF and aspiration as the more likely culprit and a bedside swallow study was done which was not very revealing because patient was not cooperative and somnolent, thus he was made NPO. He continued to improve. A bedside swallow was repeated on day of discharge and he was allowed to have pureed and honey thick liquids. Because of his severe autism and being in soft restraints in the hospital, his mother was anxious to take him home to his own environment with the plan to follow up with PCP for further evaluation of dysphagia with a MBS. He was discharged home on 5 more doses of Augmentin to complete a 5 day course of Unasyn.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: 7/13 -- SARS-CoV-2 by NAA, detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2400444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 16,0
Geschlecht: M
Eingang: 03.08.2022
Impfdatum: 15.09.2021
Beginn: 16.07.2022
Tage bis Beginn: 304,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Adenovirus test Alkalosis hypochloraemic Anaemia Anaemia macrocytic Anaemia of chronic disease Anal fissure Angiogram pulmonary abnormal Anticoagulant therapy Blood creatinine Blood folate normal Blood osmolarity Blood sodium increased COVID-19 Chest X-ray abnormal Colitis Computerised tomogram abdomen abnormal

Symptomtext

Discharge Provider: MD Primary Care Physician at Discharge: MD Admission Date: 7/16/2022 Discharge Date: 7/30/2022 DETAILS OF HOSPITAL STAY: Shortness of breath [R06.02] Diarrhea, unspecified type [R19.7] Intractable vomiting with nausea, unspecified vomiting type [R11.2] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 17-year-old male with history of epilepsy, cerebral palsy, VP shunt, chronic lung disease who presented on 7/16 with vomiting, diarrhea, and hypoxia. Initial workup included EKG, chest x-ray, complete blood count, CMP, D-dimer, and fluids, found to be COVID-19 positive. Initially there was concern for aspiration pneumonia, so he received one dose of Unasyn. On admission he met criteria for severe sepsis secondary to acute COVID-19 infection with associated lethargy/AMS, acute hypoxic respiratory failure, decreased oral intake with AKI, and gastroenteritis. Shunt studies and quick brain MRI were stable. He met criteria for VTE prophylaxis with lovenox. Treatment for COVID-19, including remdesivir and steroids, offered to parents on admission. Decided to defer remdesivir due to concerns for liver injury, completed 10 day steroid course. Restarted outpatient azithromycin in shared decision making with family. They would like to continue on discharge. Hospital course complicated by many factors. Near the beginning of his admission, KUB was obtained due to diarrhea. Radiologist remarked on possible bowel obstruction. CT ab/pelvis was obtained, significant for pancolitis, no bowel obstruction. Patient with diarrhea throughout hospital stay. ID consulted and many stool studies were obtained, including enteric stool pathogens, basic O&P, adenovirus stool antigen, CMV IgG, IgM and quant. Studies were all negative. Diarrhea likely due to COVID-19 colitis. Started low-dose loperamide on 7/27 with improvement in quantity of diarrhea. Given patient's continued tachycardia, increasing oxygen requirement, and hypercoagulable state, there was large concern for pulmonary embolism. Given patient's long history of radiation from CT scans, parents were understandably hesitant to proceed with further imaging. Duplex ultrasound of bilateral lower extremities was obtained, negative for DVT. V/Q scan could not be performed due to hospital protocol against performing scan on COVID + patients. His D-dimer continued to rise and risk of not imaging outweighed risk of further radiation, and CTA of the chest was obtained, which was negative for PE, but did show moderate-sized bilateral pleural effusions. Obtained Echo on 7/21 to rule out heart failure as cause for pleural effusions, was within normal limits. Physical exam notable for bilateral periorbital edema and pitting edema in the hands and feet. Pleural effusions thought to be due to fluid overload with low intravascular volume. Administered albumin and lasix on 7/22 with improvement on physical exam and pleural effusion size on x-ray. Unfortunately, patient experienced contraction alkalosis following lasix administration, limiting further diuresis. Nephrology was consulted and recommended administration of albumin without lasix. He received second albumin administration of 7/27 with resulting improvement in oxygen requirements. Intervention Radiology was consulted for drainage of pleural effusions, but size was not great enough for intervention. NG was placed on 7/20 due to decreased oral intake and inability of patient to take oral anti-epileptic drugs. Enteral nutrition was also given via NG. Nutrition was consulted to recommend management of PO vs NG feeds. Patient began taking enough PO to meet daily nutritional needs at time of discharge. Additionally, he was able to tolerate administration of AEDs and Xarelto via PO. CBC on presentation was notable for thrombocytopenia which continued throughout admission. This is likely due to COVID-19 suppression of bone marrow as well as adverse effects of his AEDs. Platelet count returned to normal on day of discharge. He had three episodes of hematochezia on 7/21, etiology of which thought to be due to visible anal fissure compounded by lovenox use and thrombocytopenia. He had two episodes of severe hypernatremia, as high as 156. The first episode was treated with IVF and frequent sodium checks. The second episode resolved without intervention. There was concern for diabetes insipidus given patient's central CNS defects. Urine and serum osmolality, sodium, and creatinine were obtained. Studies negative for DI. Sodium levels returned to normal prior to discharge. Patient with macrocytic anemia on presentation. Monitored with daily CBCs. B12 and folate were normal. This is thought to be anemia of chronic disease exacerbated by COVID. He received one unit of PRBCs on 7/26. No infusion reactions. Hemoglobin increased from 6.7 prior to transfusion to 10.7 on day of discharge. Patient was safe for discharge when he maintained his oxygen saturation above 94% on room air. Per pulmonary, he was safe for discharge with home oxygen up to 0.5L at night, though that was not necessary for over 36 hours prior to discharge. He was able to take all medications by mouth and maintain his nutritional status with PO intake.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 14,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Dysphagia, pharyngeal phase VP (ventriculoperitoneal) shunt status Lennox-Gastaut syndrome UTI (urinary tract infection) Status epilepticus Upper respiratory infection, viral Parapneumonic effusion History of recurrent pneumonia Ineffective airway clearance Snoring Acute on chronic anemia Neuromuscular scoliosis of thoracic region Neuromuscular scoliosis Postoperative anemia due to acute blood loss Constipation Cognitive dysfunction Chronic lung disease of prematurity Dandy Walker malformation Epilepsy, Lennox Gastaut Low serum prealbumin Spastic quadriplegia Hypercoagulable state associated with COVID-19
Andere Medikamente: acetaminophen (TYLENOL) 32 MG/ML suspension albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization azithromycin (ZITHROMAX) 200 MG/5ML suspension BANZEL 40 MG/ML SUSP budesonide (PULMICORT) 0.5 MG/2ML nebulizer solution cloBAZam (ONFI)
Allergien: LatexOther
Vorherige Impfungen: -

VAERS 2367437

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 13.07.2022
Impfdatum: 16.11.2021
Beginn: 01.07.2022
Tage bis Beginn: 227,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Blood pressure decreased COVID-19 Cardiac failure acute Cardiac failure congestive Condition aggravated Death Hypokalaemia Left ventricular failure Positive airway pressure therapy Respiratory failure

Symptomtext

Admission Date: 7/1/2022 Discharge Date: Jul 5, 2022 PRESENTING PROBLEM: Acute on chronic diastolic heart failure (HCC) [I50.33] Hypokalemia [E87.6] Respiratory insufficiency [R06.89] Increased oxygen demand [R68.89] Acute on chronic congestive heart failure, unspecified heart failure type (HCC) [I50.9] COVID-19 virus infection [U07.1] HOSPITAL COURSE: Acute on chronic hypoxic hypercapnic respiratory failure on admission not resolved prior to discharge patient is still on BiPAP however patient's family had decided on comfort measures, there was an attempt to take patient home on comfort measures yesterday but this was postponed to today. I discussed with the patient's son by the bedside this morning and he confirmed the patient is do not resuscitate and family wants comfort measures, he understands the patient is dying actively, but he wants us to be able to arrange patient to go home on BiPAP with ambulance today so that patient can pass it with quietly at home amongst his family. On discharge I prescribed a comfort measure medications like morphine, Ativan and scopolamine. Medical social worker will arrange for hospice at home to continue adjusting his meds however I would doubt if patient with being home long enough for hospice to visit, patient seems to be actively passing away. Blood pressures have dropped, patient's son is aware of these and he understands the patient might pass away today, but he would prefer patient passed away at home Patient passed on 7/5/22 at his residence.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Anemia of chronic disease Lab test positive for detection of COVID-19 virus BPH without obstruction/lower urinary tract symptoms Permanent atrial fibrillation (HCC) Essential hypertension, benign Cervical spinal mass (HCC) Chronic systolic congestive heart failure (HCC) Pulmonary hypertension (HCC) Severe obstructive sleep apnea Obesity due to excess calories Hyperlipidemia Aortic insufficiency Long term (current) use of anticoagulants Choledocholithiasis with obstruction Left bundle branch block (LBBB) on electrocardiogram Parotid mass Severe aortic stenosis Thrombocytopenia (HCC) Sensorineural hearing loss, bilateral Tinnitus, bilateral Complete heart block (HCC) Cardiac pacemaker in situ Anasarca Acute respiratory failure with hypoxemia (HCC) Acute on chronic respiratory failure with hypoxia and hypercapnia (HCC) Acute heart failure (HCC) Bacteremia due to Enterococcus History of pulmonary embolism AKI (acute kidney injury) (HCC) Bilateral pleural effusion Pressure injury of sacral region, stage 2 (HCC) Stage 1 skin ulcer of sacral region (HCC) Acute on chronic diastolic heart failure (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet apixaban (ELIQUIS) 2.5 MG tablet bumetanide (BUMEX) 1 MG tablet Carboxymethylcellulose Sodium (ARTIFICIAL TEARS OPTH) dilTIAZem (CARDIZEM) 90 MG tablet docusate (COLACE) 100 MG capsule latanoprost
Allergien: Definity [Perflutren Lipid Microsphere
Vorherige Impfungen: -

VAERS 2273189

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 14.05.2022
Impfdatum: 05.10.2021
Beginn: 18.04.2022
Tage bis Beginn: 195,0
Dosis: 3
Route/Site: - / LA

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

Cardiac arrest Myocardial infarction SARS-CoV-2 test COVID-19 Vaccination failure

Symptomtext

Heart attack; Cardiac arrest; This is a spontaneous report received from contactable reporter(s) (Physician). The reporter is the patient. A 57-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Oct2021 at 14:30 as dose 3 (booster) , single (Lot number: EW0186) at the age of 57 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "hypertension" (unspecified if ongoing), notes: Well controlled hypertension. Concomitant medication(s) included: NORVASC. Vaccination history included: BNT162b2 (Dose:1, Vaccine lot number= EL3248,, Vaccine lot unknown=False, Vaccine dose number unknown=False, Vaccine location=Left arm), administration date: 12Jan2021, when the patient was 57-year-old, for COVID-19 Immunization; BNT162b2 (Dose:2, Vaccine lot number=EN5318,, Vaccine lot unknown=False, Vaccine dose number unknown=False, Vaccine location=Left arm), administration date: 12Feb2021, when the patient was 57-year-old, for COVID-19 Immunization. The following information was reported: CARDIAC ARREST (hospitalization, medically significant, life threatening) with onset 18Apr2022 at 07:45, outcome "recovered with sequelae" (01May2022); MYOCARDIAL INFARCTION (hospitalization, medically significant, life threatening) with onset 18Apr2022 at 07:45, outcome "recovered with sequelae" (01May2022), described as "Heart attack". The patient was hospitalized for myocardial infarction, cardiac arrest (hospitalization duration: 5 day(s)). The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (08Apr2022) positive. Therapeutic measures were taken as a result of myocardial infarction, cardiac arrest. Clinical course: Antiviral details was reported as for product COVID 19 treatment Paxlovid and treatment start date 28Apr2022 and stop date 03May2022 for the indication of treatment of COVID-19. Patient reported that Adverse event COVID related heart attack on 18Apr2022 after testing positive for COVID on 08Apr2022 with cardiac arrest x2 stent occlusion 2 hours after placement CCU stay with intubation, defribillation and temporary pacemaker. AE resulted in Hospitalization, Life threatening illness (immediate risk of death from the event) and patient was hospitalized for 5 days. AE treatment was received as catherization, stent, defibrillation, intubation. No known allergies was reported.; Sender's Comments: Based on possible temporal association the causal role of BNT162B2 Vaccine cannot be excluded for reported events .Case will be reviewed further on receipt of FU information The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 5,0
Labordaten: Test Date: 20220408; Test Name: COVID; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension (Well controlled hypertension)
Andere Medikamente: NORVASC
Allergien: -
Vorherige Impfungen: -

VAERS 2258988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 19.11.2021
Beginn: 17.01.2022
Tage bis Beginn: 59,0
Dosis: 3
Route/Site: IM / -

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

Agitation Animal scratch Anticoagulant therapy Atrial fibrillation Bacteraemia Behaviour disorder COVID-19 Cerebral ischaemia Computerised tomogram head abnormal Depressed level of consciousness Endotracheal intubation Extubation Faeces discoloured Haemoglobin decreased Hypotension Hypoxia Infusion Intensive care

Symptomtext

Patient was recently hospitalized for a septic shock secondary to UTI with Klebsiella and myroides bacteremia likely cat scratch and discharged home on ciprofloxacin. Patient return to the ER on 01/17 for altered mental status and found to be hypoxic. CT head revealed small area of ischemia and internal capsule could be artifactual. COVID test was positive. Patient admitted and continued to be obtunded and hypotensive and was intubated and started on with active support. Patient was admitted to ICU and started on bicarb infusion and broad-spectrum antimicrobials. On 01/19 patient self extubated and tolerated it well. Patient was transferred out of ICU on 01/20/2022 and continued to have behavioral issues, psych was consulted with no intervention, likely it acute metabolic encephalopathy due to medical conditions. Patient also developed RVR with AFib and cardiology was consulted and started patient on amio drip and warfarin and was rate controlled. Patient had acute drop of hemoglobin and given 1 unit PRBC, due to episodes of black stools GI consulted and warfarin was held. Patient underwent EGD on 01/23/2022, which did not show any active bleed. Pt discharged on Levaquin for two more days to complete 5 days course. Pt also discharged with seven day course of dexamethasone 1mg and amiodarone 400po bid X7 days followed by 200mg po daily along with warfarin. Psych was on consult, d/ced Zyprexa and Cymbalta, agitation much improved but somnolent. Pt discharged home with HHC in stable condition.

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Praegender Schweregrund: Septic shock
Hospital-Tage: 8,0
Labordaten: Positive COVID 19 test on 01/17/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety and depression, Bilateral thumb pain (12/6/2016), Calculus of ureter (9/2015), CPAP (continuous positive airway pressure) dependence, Diabetes mellitus (HCC), Fatty liver (8/18/15), HTN (hypertension), Hyperlipidemia, Hyperuricemia (12/6/2016), Kidney infection (8/18/15), Left knee pain (3/1/2016), Lymphedema, Mental disorder, Migraine without aura and without status migrainosus, not intractable (3/8/2016), Migraines, Obstructive sleep apnea, Osteoarthritis, Primary osteoarthritis involving multiple joints (3/1/2016), Right knee pain (3/1/2016), Skin disease, Sleep disorder, and Tendinitis
Andere Medikamente: acidophillus/lactobacillus (FLORANEX) chew tablet albuterol (VENTOLIN HFA) 108 (90 BASE) MCG/ACT HFA inhaler alendronate (FOSAMAX) 70 MG tablet amiodarone (CORDARONE) 200 MG tablet Ascorbic Acid (VITAMIN C) 500 MG CAPS atorvastatin (LI
Allergien: Amlodipine, bee, mobic
Vorherige Impfungen: -

VAERS 2134495

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 27.08.2021
Beginn: 02.12.2021
Tage bis Beginn: 97,0
Dosis: 2
Route/Site: UN / UN

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

Acute respiratory failure Affective disorder COVID-19 COVID-19 pneumonia Condition aggravated Decreased appetite Failure to thrive Grief reaction Illness Pneumonia SARS-CoV-2 test positive

Symptomtext

Provider hospital summary "Patient is a 67 YO female with h/o DM2, HTN, PVD, COPD, depression/anxiety/FM, admitted with pneumonia and acute hypoxic respiratory failure due to COVID-19 pneumonia. She was treated with supplemental oxygen, decadron, remdesivir and supportive care. She was slow to improve and noted to have failure to thrive due to her current illness, grief with recent death of a loved one, and chronic health conditions (GPA). Nutrition was consulted and she was started on remeron with significant improvement in appetite and mood. She improved slowly with treatment. Oxygen was weaned to 4L NC for >24 hours prior to discharge. Discharged home in stable condition. Has 2 more days of decadron. Will participate with home care on discharge. Follow-up with PCP and pulmonary. "

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: Positive COVID test 12/2/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes mellitus type 2, uncomplicated (*) Mixed hyperlipidemia HTN (hypertension) COPD (chronic obstructive pulmonary disease) (*) Granulomatosis with polyangiitis (*) PVD (peripheral vascular disease) (*) Fibromyalgia BMI less than 19,adult Failure to thrive in adult Lung nodules COVID-19 virus infection
Andere Medikamente: albuterol sulfate 90 mcg/actuation 2 puffs Inhalation every 4 hours PRN aspirin 81 mg Oral Daily atorvastatin calcium 10 mg Oral NIGHTLY benzonatate 100 mg Oral 3 TIMES DAILY PRN budesonide/formoterol fumarate 160-4.5 mcg/actuation 2 pu
Allergien: Amoxicillin High Shortness Of Breath Eggs High Rash Sulfa (sulfonamide Antibiotics) High Anaphylaxis Ampicillin Not Specified Nausea And Vomiting, Other Blackouts Aspirin Not Specified Other Peptic ulcers Keflex [cephalexin] Not Specified Hives, Nausea And Vomiting Methotrexate Analogues Not Specified Other Alopecia and GI upset -N and vomiting Nasonex [mometasone] Not Specified Other Migraines, nose bleeds Penicillins Not Specified Hives Strawberry Not Specified Hives Asthma attacks Wellbutrin [bupropion Hcl] Not Specified Other Increased heart rate and weakness Gabapentin Rash
Vorherige Impfungen: -

VAERS 2110212

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge EW0186

kritisch

Staat: MD
Alter: 21,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 18.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: SYR / RA

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

Anticoagulant therapy Cough Dizziness Dyspnoea Intensive care Pulmonary embolism Pulmonary thrombosis Thrombectomy

Symptomtext

Suffered an acute massive pulmonary embolism. Two-weeks prior to returning to campus, I immediately start with symptoms of shortage of breathe, dry coughing, and dizziness. Hospitalized for six(6) days of which, I spent three days in ICU. Dr. had to perform an emergency caterization to remove the massive blood clot from my lungs. Additionally, they found other smallers clots that they used Heparin and other blood thinners to resolve the clots. Currently I am on Eliquis twice a day and plan to be seen as a follow up with Hemologist. Lot number - First Vaccination was EW0186 Second Vaccination lot number is EW0191

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 6,0
Labordaten: PE with massive blood clots
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vestura 3 mg (to control acne) Spironolazton - E 50 mg
Allergien: Fruit allergies
Vorherige Impfungen: -

VAERS 2079412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: TX
Alter: 76,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 24.05.2021
Beginn: 12.01.2022
Tage bis Beginn: 233,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Angiogram COVID-19 COVID-19 pneumonia Death Dyspnoea Fibrin D dimer increased General physical health deterioration Renal impairment SARS-CoV-2 test positive Ventilation/perfusion scan

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 5/3/2021 and 5/24/2021. Presented to ED on 1/12/2022 with complaint of shortness of breath, Covid+ on 1/10/22. Admitted for acute hypoxemic respiratoratory failure due to Covid PNA. On arrival O2 sat was 70% requiring Oxymask at 11 L. Treated w/decadron, did not qualified for further covid therapies. Kidney function deteriorated and started on HD. Required higher level of O2 with HFNC. He completed steroid course however his conditions continued to deteriorate. Concern for possible PE as d-dimer was elevated critical condition complicated assessment with V/Q scan and CTA. Family updated, code status changed to DNAR. Patient expired 1/28/2022.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 16,0
Labordaten: COVID-19 Positive on 1/10/2022 using the Hologic Panther System platform using PCR or equivalent Nucleic Acid Amplification(NAA)technology
Aktuelle Erkrankungen: -
Vorgeschichte: Anemia, PVD, Basal cell carcinoma, BPH, Vertigo, Metastatic Prostate Cancer, H/O Cerebral infarction, Ischemic heart disease, CKD stage 3, CAD, Hypertension, Hyperlipidemia, Plantar fascial fibromatosis, Sialoadenitis, DM type 2.
Andere Medikamente: Tylenol #3, Amlodipine, Calcitriol, Cilostazol, Clindamycin, Enzalutamide, Ergocalciferol, Hydralazine, Losartan, Metoprolol, Oxybutynin, Pravastatin, Sodium bicarbonate.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2070099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: WA
Alter: 83,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 01.10.2021
Beginn: 26.01.2022
Tage bis Beginn: 117,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia SARS-CoV-2 test positive Viral sepsis

Symptomtext

Patient received Pfizer COVID vaccine on 1/23/21 (lot # EL3302), 2/12/21 (lot # EL3302), and 10/1/21 (lot # EW0186). On 1/26/22, patient admitted to our inpatient facility with acute hypoxic respiratory failure and viral sepsis secondary to COVID19 pneumonia. As of today (1/27/22), patient is still admitted in the med/surg unit.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: COVID status positive 1/26/22.
Aktuelle Erkrankungen: -
Vorgeschichte: ulcerative colitis, oropharyngeal dysphagia 2/2 zenker diverticulum/PD s/p PEG (1/2021), parkinson's disorder, and HLD
Andere Medikamente: acetaminophen PRN, albuterol inh, Sinemet, vitamin d3, cholestyramine, Lomotil, famotidine, fluticasone/salmeterol inh, fluticasone nasal sp, Duoneb, Culturelle, loperamide, melatonin, perdnisone, tiotropium inh
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2063078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 23.11.2021
Beginn: 14.01.2022
Tage bis Beginn: 52,0
Dosis: 3
Route/Site: IM / AR

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

Acute kidney injury Acute left ventricular failure Acute respiratory failure Angiogram abnormal Angiogram pulmonary abnormal Anticoagulant therapy Asthenia Atrial fibrillation Bacteraemia Biopsy adrenal gland Blood bilirubin increased Blood creatinine normal Blood glucose normal Blood pH decreased Blood test Breast cancer female Breast cancer stage I CHA2DS2-VASc-score

Symptomtext

Hospitalized (1.17.22 - present); COVID-19 positive (1.14.22); fully vaccinated (3 doses) ASSESSMENT / PLAN: Patient is a 64 y.o. female with a past medical history of left breast cancer on chemotherapy presented with fatigue found to be in shock, undifferentiated requiring norepinephrine, covid-19 pna, pancytopenia, new onset afib with RVR Brief History and Medical Decision-Making: This is a 64 year old female patient with past medical hx significant for left breast cancer (stage 1A) s/p left partial mastectomy and SLNB performed on 10/4/21. She is currently receiving adjuvant chemotherapy. She recently underwent CT guided left adrenal biopsy which was complicated by hemothorax and pseudoaneurysm of left T1 intercostal artery, s/p IR embolization of T10, T11 and T12 and pleural drain placement. She was diagnosed with COVID-19 Pneumonia on 1/14/2022, she presented to ED today with feeling of generalized weakness and not feeling well. Noted to be in acute hypoxemic respiratory failure and shock requiring pressors to maintain MAP more than 65. She was also noted to be in acute kidney injury ( suspect pre-renal in etiology). In regards to the shock, the main differential currently is septic shock given neutropenia and findings on CT chest of With increasing left sided pleural effusion that is mostly likely related to recent hemothorax and differential include empyema, She also has nodule opacities in left upper lobe. We will contine broad spectrum Abx ( cefepime and vancomycin) pending blood culture results and consult ID. We will add stress dose steroids. Obtain echo to assess for LV function and presence of pericardial effusion. Consult IR for potential drain placement in the left chest and send diagnostic samples to rule out empyema ( her platelets are low and given recent bleeding, we need to transfuse before any intervention, She might also require thoracic surgery consult). No active signs of bleeding but we will continue to follow serial Hemoglobin, anticipate the drop in hemoglobin is related to chemotherapy given findings of neutropenia and thrombocytopenia. Start Amiodarone given Atrial fibrillation with RVR on presentation. For the COVID-19 pneumonia, we will hold off on remedisivr given AKI and she is currently on stress dose steroids. Check D--dimer and obtain DVT US of both lower extremities. Progress Note from 1.25.22: ASSESSMENT / PLAN: 64-year-old female with past medical history of left breast cancer stage IA, status post left partial mastectomy and sentinel lymph node biopsy on 10/04/2021, currently receiving adjuvant chemo with curative intent, who recently underwent CT-guided left adrenal biopsy was complicated by hemothorax and pseudoaneurysm of left T1 intercostal artery, status post IR embolization of T10, T11, and T12, with pleural drain placement. Patient also recently diagnosed with COVID on 1/14. Patient presented with generalized weakness and not feeling well. Admitted to intensive care unit with shock, acute hypoxic respiratory failure. 1. Acute hypoxic respiratory failure Multifactorial in setting COVID-19 PCR, left empyema, Staph aureus pneumonia and bacteremia. Had acute tachypneic and hypoxic event on 1/24 requiring increased vent settings and further sedation. Plan: - Wean vent settings as tolerated - Lasix 40 IV qd, goal net negative - goal O2 sat 88% and above 2. Shock - resolved - multifactorial in setting of left empyema, multifocal bilateral pneumonia, Staph aureus pneumonia and bacteremia. Plan: - Off Pressors - Solumedrol taper - 40, 30, 20, 10 per day 3. Left empyema IR placed left chest tube on 01/18. Pleural fluid exudative with pH 6.72, glucose less than 2. IR recommended tPA / dornase. However, initially held off on tPA / dornase given recent hemothorax requiring emoblization and also pancytopenia. CT scan of the chest 1/19 showed improving left-sided empyema, however, with minimal drainage on 1/20. Drainage likely will be limited due to loculated infection. - 1/20: s/p trial tPA / dornase at 1/2 dose (5 mg) x 1 on 1/20. - 1/21: started on tPA / dornase at normal dose, plan for 5 total doses - 1/23: receiving final doses/ CXR appears well improved, no further drainage from chest tube, no signs of bleeding - 1/24: Completed tPA / dornase therapy, no immediate complications, stable and improved left lower consolidation on CXR - 1/25: significant drainage from L chest tube 355cc over last 24 hours 4. Febrile Patient became febrile during the night of 1/24-1/25. This was in the setting of recently starting Precedex and following return from IR procedure. This is likely 2/2 medication effects however superimposed new bacterial infection cannot be ruled out on exam alone. Plan: - Follow-up culturers - Discontinued Precedex - Continue to monitor temperature 5. Multifocal bilateral pneumonia Left lower lobe Staph aureus pneumonia Staph aureus bacteremia 1/18 respiratory cultures positive for MSSA, with left pleural fluid cultures positive for Staph aureus, and blood cultures positive for GPC in clusters. CT chest 1/19 (obtained for re-evaluation of left empyema) showed new multifocal pneumonia in right side, suspected to be a progression of left-sided Staph aureus pneumonia. Plan: - Escalated current abx based on repeat fever with CXR and clinical course concerning for HAP/VAP, continue Zosyn + Vanc for empiric coverage pending cultures and ID recommendations - Obtain sputum culture, if unable patient will need bronchoscopy w/ BAL - Given Staph aureus bacteremia, will need to consider future TEE for rule out infective endocarditis when stabilized - IR successfully removed R portacath evening of 1/24, will need replaced once discharged for continued chemotherapy 6. Acute systolic heart failure / heart failure with reduced ejection fraction 22% New reduced EF 22%, compared to EF 65% in 12/14/2021. Cardiology consulted, and discussed case with Cardiology Oncology, who thinks that overall less likely due to anthracycline therapy, but possible. Patient's new reduced systolic function likely due to stress-induced cardiomyopathy in setting of shock. Plan: - could consider future repeat echo 7. Loose Stools - prolonged illness with tube feeds, unlikely to be infectious at this time, will continue to monitor temperature and for other signs of infection. Plan: - remove rectal tube as soon as possible, high risk for adverse sequela including pressure ulcers - monitor rectal tube output - follow-up C. Diff and enteric pathogens - bowel regiment changed from standing to PRN 8. Atrial fibrillation with RVR - resolved No history of atrial fibrillation, likely 2/2 shock in the setting of stress cardiomyopathy. Converted to sinus rhythm while on amiodarone drip on 1/20, has remained in sinus rhythm since. Plan: - On PO amiodarone 400mg BID, decrease dosing once received entire 10g loading dose - Patient is high risk for thromboembolic event based on CHADS-VASC2 > 3, for that reason we are starting therapeutic heparin drip - Patient also plans on receiving chemotherapy on discharge causing transient thrombocytopenia, this puts her at high risk for bleeding sequela, this issue will have to be addressed on discharge for further anticoagulation planning - plan to resume BB as able now that shock resolved 9. Pancytopenia - stable In the setting of active chemotherapy for breast cancer. On arrival had significant neutropenia, now improved but is on stress dose steroids for shock. Hb and Plt stable. Plan: - transfuse if platelets less than 10 or less than 50 if active bleeding - transfuse if hemoglobin less than 7 10. AKI - resolved Likely prerenal in setting of shock on presentation. Based on chart review, patient has a baseline creatinine of 0.5-0.7. Plan: - patient continues to be at baseline following resuscitation - continue to trend on daily CMP 11. Elevated liver enzymes - resolved RUQ US 1/19 obtained due to gradually rising bilirubin. Negative for biliary obstruction, cholelithiasis, cholecystitis. Showed heterogeneous liver which may be due to hepatic steatosis. Consider dedicated liver screening with patient more stable. 12. Metastatic breast cancer Stage IA, status post left partial mastectomy and sentinel lymph node biopsy on 10/04/2021, currently receiving adjuvant chemo with curative intent, who recently underwent CT-guided left adrenal biopsy was complicated by hemothorax and pseudoaneurysm of left T1 intercostal artery, status post IR embolization of T10, T11, and T12, with pleural drain placement. Plan: - holding chemotherapy pending clinical course - palliative care consult, for supportive care for husband who is patient's sole caregiver and management of chronic conditions

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: 12.20.21-12.24.21 - hospital admission - Hemothorax on left - HOSPITAL COURSE: Patient is a 64 year old female with PMH significant for invasive ductal breast carcinoma, HTN, rosacea, who presented to the ED following a CT guided adrenal bx due to acute bleeding. After procedure pt c/o pain and shortness of breath, BP was found to be 74/38, pt received fluid bolus and a CT was obtained with findings of hemothorax, Pseudoaneurysm of left T11 intercostal artery with extravasation into left pleural space. Pt was taken to IR and underwent intercostal angios (T 10, 11, and 12) with microcoil embolizations. Left internal mammary angio; left pleural drain placement. Her blood counts where closely monitored throughout hospitalization. She received 1 unit PRBC in ED but did not require any further transfusions. Cardiothoracic team was consulted for evaluation and recommended continuing current conservative managment with drain. The patient did have one episode of near-syncopal episode which resolved after fluid bolus. Her antihypertensive medications where briefly held and all restarted before discharge.
Vorgeschichte: Family history of coronary artery disease Essential hypertension Class 2 obesity due to excess calories without serious comorbidity with body mass index (BMI) of 39.0 to 39.9 in adult Psoriasis Family history of leukemia Pain in joint, multiple sites Family history stroke in brother and father in early 60s Leukocytosis Chronic pain of left knee Rosacea, acne Encounter for consultation Carcinoma of upper-outer quadrant of left breast in female, estrogen receptor positive (HCC) Hemothorax on left
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 5 MG tablet atenolol-chlorthalidone (TENORETIC) 100-25 MG per tablet B Complex Vitamins (VITAMIN B COMPLEX) tablet Cholecalciferol 2000 units CAPS diphenhydrAMINE (BENADRYL) 25 MG t
Allergien: Contrast Dye [Ivp Dye, Iodine Containing]Itching TramadolDizziness CephalexinRash Ciprofloxacin CyclobenzaprineRash EtodolacOther, Palpitations Fish Flu Virus VaccineSwelling Lisinopril MacrolidesRash, Swelling Neomycin-bacitracin-polymyxinRash Nickel Nitrofuran DerivativesRash Nitrous Oxide PenicillinsRash Sulfa DrugsRash Taxotere [Docetaxel]Rash
Vorherige Impfungen: -

VAERS 2042963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 21.07.2020
Beginn: 16.01.2022
Tage bis Beginn: 544,0
Dosis: 2
Route/Site: - / -

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

Asthenia Cough Death Dyspnoea General physical health deterioration Myalgia Pyrexia

Symptomtext

Pt had a medical history of diabetes and presented with shortness of breath. He also has cough, fevers, weakness and muscle aches. Pt deteriorated quickly and passed on 1/17/2022.

Weitere VAERSDATA-Felder

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

VAERS 1974744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

kritisch

Staat: MN
Alter: 15,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 17.06.2021
Beginn: 11.12.2021
Tage bis Beginn: 177,0
Dosis: 1
Route/Site: - / UN

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

Air embolism Autopsy Death Toxicologic test

Symptomtext

Patient passed away on 12/11/21 at 12:11pm from bilateral pulmonary emboli (air bubbles not DVT). Final autopsy results pending toxicology results.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Autopsy conducted through the Medical Examiner, pending final toxicology results.
Aktuelle Erkrankungen: None.
Vorgeschichte: Bipolar
Andere Medikamente: Latuda, Wellbutrin, Topiramate, Gabapentin, Metformin
Allergien: None.
Vorherige Impfungen: -

VAERS 1955764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MA
Alter: 46,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 24.05.2021
Beginn: 04.12.2021
Tage bis Beginn: 194,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Computerised tomogram thorax abnormal Exposure to SARS-CoV-2 Exposure via direct contact Hypoxia Lung opacity Oxygen saturation decreased Procalcitonin SARS-CoV-2 test positive

Symptomtext

#COVID-19 pneumonia #Acute Hypoxemic Respiratory Failure Patient (vaccinated x2, no booster) with multiple comorbidities that make him high risk including DCM, obesity, and OSA with pHTN. Hypoxic at home ot 88, and on admission as well to 88-89%. Patient has recent COVID contact or recent travel. Bacterial pneumonia was considered given procalcitonin of 0.20, but felt unlikely given chest CT findings showing bilateral ground glass opacities, predominantly in the lingula and left lower lobe. He was started on oral dexamethasone with plan for 10 day total course. He was also started on remdesivir and rapidly improved on 2-4L of O2 by nasal cannula. On the day of discharge, he was satting >94% on room air. With ambulation, he desaturated to 88% but quickly recovered, which the patient attests is his baseline. He was discharged on 12/6 without supplemental home O2. On discharge, remdesivir was stopped and dexamethasone was continued for a full 10 day course.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: covid positive 12/4/21.
Aktuelle Erkrankungen: unk
Vorgeschichte: Morbid obesity due to excess calories Hypertension Asthma Low back pain Nonischemic cardiomyopathy COPD, pulm hypertension, infertility, hyperuricemia, heart failure.
Andere Medikamente: FLUTICASONE/SALMETEROL (ADVAIR HFA INHL) Sig: Inhale into the lungs. Patient not taking: Reported on 8/29/2021 PROAIR HFA 90 mcg/actuation inhaler Sig: Inhale 2 puffs into the lungs every 4 (four) hours as needed for wheezing. albuterol (VE
Allergien: nkda
Vorherige Impfungen: -

VAERS 1955579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 39,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 13.05.2021
Beginn: 11.12.2021
Tage bis Beginn: 212,0
Dosis: 2
Route/Site: UN / UN

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

Acute kidney injury Acute respiratory failure Asthenia Blood culture negative COVID-19 COVID-19 pneumonia Chest X-ray abnormal Clostridium test negative Cough Dehydration Diarrhoea Hyperglycaemia Hypomagnesaemia Hyponatraemia Hypoxia Lung disorder Lung opacity Nausea

Symptomtext

Patient currently inpatient at (5) days admission. H & P: PT is a 40 y.o. female who presents today with cough, fever, diarrhea weakness Pt is a 40 yo female s/p renal transplant for AGA nephropathy. Pt has been faithful with her anti-rejection regimen. Pt states started with fever 3 weeks ago. Cough 2 weeks ago and tested positive for COVID. She is fully vaccinated but has not had Booster for COVID. She saw her PCP last week and was started on doxycycline and Augmentin. Nausea and Diarrhea started next day. Today she felt much worse and presented to ED ASSESSMENT / PLAN: Elevated procalcitonin Assessment & Plan 0.54 - treat with broad spectrum antibiotics Diarrhea Assessment & Plan Possible secondary to Augmentin as started day after this medication was started. Will watch to see if continues on zosyn - gentle hydration - supportive care Renal osteodystrophy Assessment & Plan Continue home Ca and Mag Hypomagnesemia Assessment & Plan 1.4 pt normally takes BID - will increase to TID for 2 days then return to BID - monitor daily Hypertension Assessment & Plan Monitor -hold ACE with current AKI, may restart with improvement in renal function Hyperglycemia Assessment & Plan Over 200 for first time today - a1c in am Hyperkalemia Assessment & Plan 5.1 today -gentle hydration - follow closely, repeat at 1am today and daily Hyponatremia Assessment & Plan 130 today --gentle hydration - follow closely, repeat at 1am today and daily AKI (acute kidney injury) (HCC) Assessment & Plan Nephrology felt to be prerenal secondary to dehydration secondary to diarrhea, baseline Cr. 1.5-1.8 over last 2 years. Today 2.66, baseline GFR low 30's last 2 years. Today 20 -gentle hydration - follow closely, repeat at 1am today and daily S/p cadaver renal transplant Assessment & Plan ED provider contacted on call Nephrology. Comfortable with keeping pt here gentle hydration. - US renal transplant protocol in am -treat with broad spectrum antibiotic -continue anti rejection regimen * Acute hypoxemic respiratory failure due to COVID-19 (HCC) Assessment & Plan Admit to HCF. Pt positive for COVID per patient at outpt facility will repeat as pt has had symptoms for 3 weeks. If negative could take out of isolation -O2, -dexamethasone -renal function precludes use of remdismivir - supportive care

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: DR CHEST SINGLE VIEW [358351446] Resulted: 12/14/21 0935 Order Status: Completed Updated: 12/14/21 0938 Narrative: EXAMINATION: Single View Chest EXAM DATE: 12/14/2021 8:56 AM TECHNIQUE: Single view chest INDICATION: COVID-19 COMPARISON: 12/11/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: The heart is within normal limits. There is no pulmonary vasculature congestion. Subtle bilateral lower lobe opacities, overall improved from the prior examination. No significant pleural effusion. No definite pneumothorax. _________________________ Impression: Improved bilateral opacities. US RENAL TRANSPLANT EXAM [357958379] Resulted: 12/12/21 0112 Order Status: Completed Updated: 12/12/21 0114 Narrative: EXAMINATION: Renal Transplant Ultrasound EXAM DATE: 12/12/2021 12:49 AM TECHNIQUE: Gray scale imaging of the transplant kidney was performed. Color Doppler and spectral Doppler imaging of the transplant kidney was utilized. INDICATION: Acute kidney injury. History of renal transplant. COMPARISON: None ____________________ FINDINGS: Ultrasound of the transplant kidney: 1. Transplant Kidney Size: 15.6 x 6.2 x 7.6 cm (length x AP x width). 2. Hydronephrosis: No hydronephrosis. 3. Renal parenchyma: The renal parenchyma has a normal echogenicity. 4. Renal masses: No mass is present. 5. Perirenal fluid collections: None. Duplex Doppler imaging of the renal artery and vein: 1. External Iliac Artery Peak Systolic Velocity: 132 cm/sec. 2. Transplant Renal/Iliac Artery Anastomosis Peak Systolic Velocity: 117 cm/sec. 3. Transplant Renal Artery Peak Systolic Velocity: 103 cm/sec. 4. Cortical and Interlobar Arteries: The interlobar and segmental renal arteries demonstrate a low resistive waveform. The waveforms shows no sharp peaks, diminished diastolic flow or loss of diastolic flow to suggest allograft rejection. 5. Transplant Renal Vein: Blood flow is antegrade within the renal veins with color and spectral Doppler imaging. 6. Transplant Renal Cortical Artery Resistive Index: 0.56-0.71. ADDITIONAL FINDINGS: None. _____________________ Impression: 1. Unremarkable sonographic appearance of the right lower quadrant renal transplant. ** USV Venous Lower Extremity Duplex Bilateral [357965364] Resulted: 12/12/21 0106 Order Status: Completed Updated: 12/12/21 0108 Narrative: EXAMINATION: Complete Right and Left Lower Extremity Venous Duplex Doppler Ultrasound EXAM DATE: 12/12/2021 12:50 AM TECHNIQUE: Real-time B-mode imaging with and without compression was used to evaluate the right and left lower extremity for deep venous thrombosis (DVT). Duplex Doppler with color and spectral Doppler was used. INDICATION: covid pneumonia, pain in bilateral legs COMPARISON: None _____________________ Right Lower Extremity Findings: Right Common Femoral Vein: No DVT. Right Femoral Vein: No DVT. Right Popliteal Vein: No DVT. Right Posterior Tibial Veins: No DVT. Right Peroneal Veins: No DVT. Right proximal Greater Saphenous Vein: No thrombus. Left Lower Extremity Findings: Left Common Femoral Vein: No DVT. Left Femoral Vein: No DVT. Left Popliteal Vein: No DVT. Left Posterior Tibial Veins: No DVT. Left Peroneal Veins: No DVT. Left proximal Greater Saphenous Vein: No thrombus. Duplex Doppler: Spectral Doppler demonstrates bilateral normal respirophasic waveforms in the common femoral veins. Additional Findings: None. _____________________ Impression: There is no deep venous thrombosis in the visualized deep veins of the right or left lower extremity. * DR CHEST SINGLE VIEW [356603544] Resulted: 12/11/21 2214 Order Status: Completed Updated: 12/11/21 2217 Narrative: EXAMINATION: Single View Chest EXAM DATE: 12/11/2021 9:54 PM TECHNIQUE: Single view chest INDICATION: covid+, hypoxia COMPARISON: 12/4/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: Bilateral, multifocal, patchy airspace disease, relative apical sparing. No effusion or pneumothorax. Normal heart size. _________________________ Impression: Bilateral airspace disease, correlate for Covid 19 pneumonia. Orange result. MRSA Screen Culture12/13/21 0035- Abnormal -This screen determines MRSA carrier status. When negative, it predicts the absence of MRSA lower respiratory tract infection. When positive, infection due to MRSA is possible, yet cultures from the site of infection must be used to guide diagnosis and therapy Peripheral Blood Culture12/11/21 2027No growth at 4 days. Peripheral Blood Culture12/11/21Collected: 12/11/21 2119No Growth 4 Days Ova and Parasites, Complete 12/11/2021-2100 Negative Enteric Pathogens by PCR 12/11/21-2100 Negative COVID-19 PCR - Rapid 12/12/21 0049 Detected Abnormal Clostridioides difficile Toxin 12/11/21- 2100 Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Hospital Acute hypoxemic respiratory failure due to COVID-19 (HCC) S/p cadaver renal transplant Acute kidney injury superimposed on chronic kidney disease III (HCC) Hyperkalemia Type 2 diabetes mellitus with hyperglycemia (HCC) Hypertension Renal osteodystrophy Diarrhea Elevated procalcitonin Pneumonia due to COVID-19 virus Non-Hospital IgA nephropathy determined by renal biopsy CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amoxicillin-clavulanate (AUGMENTIN) 875-125 MG per tablet benzonatate (TESSALON) 200 MG capsule CALCIUM PO carvedilo
Allergien: NSAIDS
Vorherige Impfungen: -

VAERS 1924572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MN
Alter: 61,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 02.06.2021
Beginn: 04.12.2021
Tage bis Beginn: 185,0
Dosis: 2
Route/Site: - / -

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

Death Lung neoplasm malignant Respiratory failure

Symptomtext

Dose 1 given 4/24/2021 Lot # EW0173 Patient was hospitalized and died of respiratory failure- lung cancer in the hospital, family initiated comfort care. Patient did not have Covid 19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Metastatic lung cancer, COPD, brain aneurysm
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1897883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 17.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Angiogram pulmonary abnormal Blood creatinine normal Blood glucose normal C-reactive protein increased COVID-19 Chest X-ray abnormal Culture stool Dyspnoea exertional Fibrin D dimer Full blood count Laboratory test abnormal Lung opacity Metabolic function test SARS-CoV-2 test positive White blood cell count decreased

Symptomtext

Hospitalized 11/23/2021-still admitted currently; COVID-19 positive 11/23/2021; fully vaccinated plus booster CHIEF COMPLAINT: COVID ASSESSMENT / PLAN: Acute Respiratory Failure, secondary to COVID-19 o COVID-19 Infection - confirmed on 11/23/2021. o Vaccine Status: Fully vaccinated (Pfizer). Booster: Yes, dose on 11/17/2021 o Outpatient CXR (11/8/2021) suspicious for CAP - treated with Augmentin and Azithromycin o CTA Thorax (11/23/2021) - bilateral ground glass opacities, negative for PE o Abnormal Labs: ? Glucose - 61 ? Corrected in ER ? Cr - 1.10 ? WBC - 3.94 o Plan for Admission to Blodgett ? Hold Decadron as patient is not requiring O2. Did desaturate with ambulation but otherwise normal. Start if hypoxia occurs. ? Hold ABX, secondary to questionable Cdiff. ? Procalitonin ordered ? Not eligible for Remdesivir ? Trend CBC, CMP, D-Dimer, CRP ? Follow stool cultures ? Acapella, mucinex BID and Albuterol BID ? Encourage prone positioning, tessalon perles PRN, albuterol PRN ? Continuous O2 monitoring - not currently on O2. ? Respiratory Isolation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Bipolar 2 disorder DM (diabetes mellitus), type 2 with renal complications Chronic kidney disease (CKD), stage III (moderate) HTN (hypertension) Restless leg syndrome IBS (irritable bowel syndrome) Hyperlipidemia PAD (peripheral artery disease) Gastroparesis Coronary artery disease due to lipid rich plaque History of pulmonary embolism Osteoporosis Morbid obesity with BMI of 40.0-44.9, adult S/P total knee arthroplasty Binswanger's encephalopathy Back pain Carotid artery disease Thyroid nodule Colonoscopy refused Urge incontinence of urine Impaired mobility Dyspnea on exertion Chronic diastolic heart failure
Andere Medikamente: amoxicillin-clavulanate (AUGMENTIN) 875-125 MG per tablet Ascorbic Acid (VITAMIN C PO) aspirin 81 MG tablet benzonatate (TESSALON) 200 MG capsule betamethasone dipropionate 0.05 % cream clonazePAM (KLONOPIN) 0.5 MG tablet clotrimazole (LOTR
Allergien: Statins Clonidine Dyazide Norvasc Prilosec
Vorherige Impfungen: -

VAERS 1872888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 17.05.2021
Beginn: 15.11.2021
Tage bis Beginn: 182,0
Dosis: 2
Route/Site: UN / UN

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

Acute respiratory failure COVID-19 Hypokalaemia Microcytic anaemia

Symptomtext

Acute hypoxemic respiratory failure due to COVID-19; microcytic anemia; hypokalemia

Weitere VAERSDATA-Felder

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

VAERS 1865597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MN
Alter: 54,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 16.06.2021
Beginn: 22.10.2021
Tage bis Beginn: 128,0
Dosis: 2
Route/Site: - / -

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

Death

Symptomtext

Patient passed away on 10/22/2021

Weitere VAERSDATA-Felder

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

VAERS 1851818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 22.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / AR

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

Acute respiratory failure Atrial fibrillation COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram thorax abnormal Condition aggravated Cough Critical illness Diarrhoea Dyspnoea Electrocardiogram abnormal Endotracheal intubation Fatigue Fibrin D dimer Full blood count Gait disturbance Leukocytosis

Symptomtext

Hospitalized (10.28.21 - still admitted); COVID-19 positive (10.28.21); fully vaccinated PLUS booster CHIEF COMPLAINT: Pneumonia due to COVID-19 virus HISTORY OF PRESENT ILLNESS: Patient is a 70 y.o. female who presents today with past medical history of obesity, AF on eliquis, OSA, HTN, venous stasis who presents with shortness of breath. She had developed a cough that started approximately 6 days ago after receiving her booster Pfizer COVID vaccine. She developed diarrhea 2 days later. She has not had any fevers or chils. She lives with her husband and states that she started feeling more short of breath today. She began having difficulty with ambulating around her home to just use the restroom. She has no history of CHF, COPD but does have a history of atrial fibrillation. In the ED, she received 1 dose of Rocephin for presumed UTI. She also received 125 mg Solumedrol and 500 ml of normal saline. EKG showed atrial fibrillation with RVR at 112 beats per minute. She also received Lasix 20 mg IV. Acute hypoxic respiratory failure Sepsis COVID-19 pneumonia Obesity, BMI 52 Patient presented with tachycardia, leukocytosis tachypnea, hypoxia. Upon arrival, she was placed on high-flow nasal cannula 50 L. Patient is significant respiratory distress, she is short of breath with short sentences. Notably, she is fully vaccinated and received her booster shot 6 days ago. Tested Positive: 10/28 Day of Illness #6 Oxygen Requirements: HFNC 50 L, 65% FiO2 - Decadron: s/p Solumedrol x 1, - Remdesivir: start loading dose - Daily CBC, CMP, D-dimer. - DVT Prophylaxis: Eliquis - Oxygen PRN - Immodium for diarrhea - monitor I/o with goal of net negative - consider Foley Daily renal and liver function monitoring for kidney and liver toxicity due to Remdesvir is required. Progress Note from 11/8/21: Plan of the day: -Continue lung protective ventilation, we will attempt decreasing the PEEP to 12 -Repeat CXR if she develop any decompensation to assess for development of PTX -Keep paralyzed for now given worsening hypoxia and pneumomediastinum This patient is critically ill and is requiring active support and intensive surveillance to prevent life threatening clinical deterioration. -Worsening hypoxia overnight, CT chest showed pneumomediastinum and small apical PTX. ETT was pulled up, -CXR this morning with satisfactory position of ETT tube, I could not visualize PTX on left side. dexamethasone changed to solumedrol and Started on Zosyn and vancomycin overnight,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 12,0
Labordaten: Assessment and Plan Acute respiratory failure with hypoxia Assessment & Plan Due to COVID-19 pneumonia. CXR 10/29 with diffuse bilateral infiltrates but there is a more distinct lobar pattern in the RUL. Cannot rule out a secondary bacterial pneumonia. She was not able to maintain her O2 sats on HFNC and a nonrebreather and was placed on BIPAP. This is not an ideal situation because she is not expected to improve quickly and cannot tolerate any oral intake/nutrition while on continuous BIPAP. However, she is currently maintaining acceptable O2 sats on BIPAP and work of breathing also appears to be acceptable. Her body habitus places her at higher risk for difficult intubation as does her oxygen requirements. It is reasonable to keep her on BIPAP overnight as long as her work of breathing is stable and oxygenation can be maintained but she will likely need intubation in the morning unless FiO2 requirements have improved to the point she can transition back to HFNC + nonrebreather. - continue ceftriaxone empirically for possible bacterial pneumonia - Ok to continue BIPAP 12/6, FiO2 95% for now. Low threshold to intubate if work of breathing or oxygen requirements worsen any further. - Agree with continued diuresis for goal net fluid balance negative - Steroids and remdesivir as noted under COVID-19 pneumonia.
Aktuelle Erkrankungen: 10.28.21: Went to ED: COUGH (since Saturday , had booster shot for pfizer on Friday ( flu shot 2 weeks prior)), SHORTNESS OF BREATH, and FATIGUE
Vorgeschichte: OSA on CPAP Atrial fibrillation Lung nodule < 6cm on CT Obesity Lower extremity venous stasis Normocytic anemia Morbid obesity Venous stasis dermatitis of right lower extremity Essential hypertension IFG (impaired fasting glucose) Gross hematuria
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet apixaban (ELIQUIS) 5 MG tablet bismuth subsalicylate (PEPTO-BISMOL) 262 MG/15ML suspension digoxin (LANOXIN) 125 MCG tablet ferrous sulfate 325 (65 Fe) MG tablet furosemide (LASIX) 20 MG tablet guaiFENe
Allergien: PenicillinsDizziness
Vorherige Impfungen: -

VAERS 1846679

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: ID
Alter: 31,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 24.05.2021
Beginn: 25.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / AR

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

Basophil percentage increased Blood glucose normal Chest pain Dizziness Fibrin D dimer increased Pulmonary embolism Pyrexia

Symptomtext

Extreme chest pain, fever, dizziness, pulmonary embolism, hospitalization. No treatment was given at the hospital due to staff negligence. I left the hospital to take my own pain medicine since staff had me waiting for two hours and could not produce pain treatment during my time of need.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: D-Dimer Quant: 562 ng/mL Date: 5/25/21 Basophils: 1.3 Date: 5/25/21 Glucose: 113 Date: 5/25/21 D-Dimer Quant: 1.57 Date: 5/27/21 (standard range <0.50 mcg/mL)
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1846663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 91,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 25.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / AR

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

Acute respiratory failure Agitation COVID-19 Chest X-ray normal Choking Condition aggravated Cough Dysphagia Dyspnoea Fatigue General physical health deterioration Hypoxia Laboratory test Pyrexia SARS-CoV-2 test positive Unresponsive to stimuli

Symptomtext

Hospitalized (10.31.21 - still hospitalized / admitted); COVID-19 positive (10.31.21); fully vaccinated CHIEF COMPLAINT: Acute respiratory failure due to COVID-19 (HCC) HISTORY OF PRESENT ILLNESS: Patient is a 91 y.o. male who presents today with shortness of breath, fatigue, fever and cough for the past few days. PMH of mod-severe COPD (not on O2), venous insufficiency with chronic left ankle ulcer, dysphagia, s/p RLL resection d/t aspirating gold crown, anemia of CKD. He received a Covid booster and flu vaccine 4 days ago, s/s s/s started the next couple days. In the ED, he was initially afebrile, then temp 100F, non tachycardic (on Lopressor), BP normal. CXR without acute airspace disease; however hypoxic to 88% at rest on multiple trials with ED provider. He did test (+) for Covid. He requires admission for treatment of acute respiratory failure in setting of COPD. At time of my exam, he is resting in bed, appears tired with mild increased work of breathing, but alert and oriented. Daughter, who is a nutritionist, is at bedside and assists with hx. He's not having other concerns besides the fatigue and SHOB. At baseline, he is independent at an independent living facility. He does have chronic anemia of CKD, gets somewhat regular Fe infusions as well as Retacrit. He had a stroke in the past, has residual dysphagia and often coughs/chokes while eating. He's had venous insufficiency since he was a teen, and has wraps on his legs all the time; follows with general surgery for OP management of an ulcer on left ankle. He is a beloved member of the volunteer team at this hospital. * Acute respiratory failure due to COVID-19 (HCC) Assessment & Plan -S/P vaccine x2, received booster and influenza vaccine 4 days ago -Fever/cough and fatigue/SHOB for the past 2-3 days, tested (+) today -CXR no acute disease -Needing 2L O2 to maintain sats -Daily inflammatory labs, check viral film array -Remdesivir, decadron, BID lovenox, guaifenesin, duonebs q4 -Treat for CAP, check blood cultures Progress Note from 11.4.21: SUBJECTIVE: Patient is on unresponsive. Family made a decision yesterday they want to convert him to comfort care only. I discontinued all medicines. Discontinue the IVs. Apparently he has not been doing well for the past 6 months or so also and their minds he has been declining dramatically. Progress Note from 11.5.21: SUBJECTIVE: Patient is unresponsive. He is having still lot of agitation discontinue the Haldol switch him over to Ativan. He is a do not resuscitate comfort care

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: 9.30.21: fever 10.4.21, 10.19.21, 10.26.21: Unna Boot Application for chronic cutaneous venous stasis ulcer 10.6.21; Appt. follow-up chronic conditions - Anemia of Chronic Renal Failure; B12 deficiency; zinc deficiency, iron deficiency anemia due to chronic blood loss 10.11.21: daughter reported some low BPs - patient seen in office
Vorgeschichte: Malignant neoplasm of urinary bladder, unspecified site (HCC) Intracerebral hemorrhage (HCC) OSA (obstructive sleep apnea) Gastroesophageal reflux disease Foreign body in lung Lung nodules History of bladder cancer Obesity Former tobacco use Rheumatoid arthritis (HCC) Venous stasis dermatitis of left lower extremity Blood loss anemia Fecal occult blood test positive Cognitive deficit as late effect of cerebral aneurysm BPPV (benign paroxysmal positional vertigo), unspecified laterality Pleural thickening Atelectasis, right Abnormality of gait Frequent falls Muscular deconditioning Macrocytic anemia Iron deficiency anemia due to chronic blood loss Gastritis Zinc deficiency Anemia of chronic renal failure Cataract Hearing loss, sensory Hypertension B12 deficiency
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet ammonium lactate (LAC-HYDRIN) 12 % lotion Bioflavonoid Products (ESTER-C) 500-550 MG TABS budesonide (PULMICORT) 0.5 MG/2ML nebulizer solution Carbamide Peroxide (EAR DROPS OTIC) chlorhexidine (PERIDEX)
Allergien: ClindamycinRash MitomycinRash
Vorherige Impfungen: -

VAERS 1842856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Death

Symptomtext

Patient passed away hours after receiving vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Awaiting autopsy.
Aktuelle Erkrankungen: None.
Vorgeschichte: High blood pressure, hypertension.
Andere Medikamente: -
Allergien: None.
Vorherige Impfungen: -

VAERS 1829398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: WI
Alter: 53,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 19.05.2021
Beginn: 25.10.2021
Tage bis Beginn: 159,0
Dosis: 1
Route/Site: IM / LA

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

Brain injury COVID-19 Cardiac arrest Hypoxic-ischaemic encephalopathy Magnetic resonance imaging head abnormal Pneumonia Respiratory failure SARS-CoV-2 test positive

Symptomtext

hospitalized from 9/17-10/20 for acute anoxic encephalopathy after unknown total downtime / cardiac arrest, respiratory failure, pneumonia, found to have MRI brain on 9/18 showing diffuse global anoxic injury, off all sedation since 9/21. On hospice, then transferred on 10/25 for aggressive medical treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: Negative Covid Test 10/19. Positive Test 10/25
Aktuelle Erkrankungen: -
Vorgeschichte: COVID-19 08/22/2020
Andere Medikamente: LORazepam (ATIVAN) 2 mg/mL oral concentrate LORazepam (ATIVAN) 2 mg/mL oral concentrate MORphine sulfate 100 mg/5 mL (20 mg/mL) oral solution . atropine 1% (ISOPTO ATROPINE) 1 % Opht ophthalmic (EYE) solution bisacodyl (DULCOLAX) 10 mg R
Allergien: -
Vorherige Impfungen: -

VAERS 1505250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MD
Alter: 13,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 11.07.2021
Beginn: 26.07.2021
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: IM / AR

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

Alanine aminotransferase normal Anion gap increased Aspartate aminotransferase increased Blood albumin decreased Blood alkaline phosphatase normal Autopsy Death Myocarditis Blood bilirubin normal Blood chloride normal Blood creatinine normal Blood glucose increased Blood potassium decreased Full blood count Metabolic function test normal Pulseless electrical activity Blood sodium normal Blood urea normal

Symptomtext

Patient received first COVID vaccine on 7/11/21. She was well until 7/26/21 when she developed nausea, vomiting, shortness of breath and dizziness. At approximately 04:00 on 7/27/21, she woke up feeling poorly, went into the bathroom and then lost consciousness. EMS was called, she was in a tachycardia at 180 bpm, BP 88/64, unresponsive. EMS report states she was "in SVT and cardioverted at 30J then 70 J. Still in SVT but becoming more alert. HR 165 bpm, sats 98%." In ED, she was felt to be in ventricular tachycardia, She received attempted resuscitation with multiple rounds of CPR including chest compressions, defibrillation for reported ventricular fibrillation, and medications. She was unable to be resuscitated and death was pronounced in the ED. Autopsy is pending.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Initial CBC with WBC 6.59, Hg 12.2, HCT 35.3, platelets 278. CMP with CO2 18, anion gap 22, glucose 270, Na 139, K 2.8, Cl 103, BUN 16, Creatinine 0.77, Albumin 3.4, ALK 97, AST 152, ALT 32, bilirubin 0.3. COVID PCR not detected.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: -
Allergien: None known
Vorherige Impfungen: -

VAERS 1505250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MD
Alter: 13,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 11.07.2021
Beginn: 26.07.2021
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: SYR / UN

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

Alanine aminotransferase normal Anion gap increased Aspartate aminotransferase increased Blood albumin decreased Blood alkaline phosphatase normal Autopsy Death Myocarditis Blood bilirubin normal Blood chloride normal Blood creatinine normal Blood glucose increased Blood potassium decreased Full blood count Metabolic function test normal Pulseless electrical activity Blood sodium normal Blood urea normal

Symptomtext

Patient received first COVID vaccine on 7/11/21. She was well until 7/26/21 when she developed nausea, vomiting, shortness of breath and dizziness. At approximately 04:00 on 7/27/21, she woke up feeling poorly, went into the bathroom and then lost consciousness. EMS was called, she was in a tachycardia at 180 bpm, BP 88/64, unresponsive. EMS report states she was "in SVT and cardioverted at 30J then 70 J. Still in SVT but becoming more alert. HR 165 bpm, sats 98%." In ED, she was felt to be in ventricular tachycardia, She received attempted resuscitation with multiple rounds of CPR including chest compressions, defibrillation for reported ventricular fibrillation, and medications. She was unable to be resuscitated and death was pronounced in the ED. Autopsy is pending.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Initial CBC with WBC 6.59, Hg 12.2, HCT 35.3, platelets 278. CMP with CO2 18, anion gap 22, glucose 270, Na 139, K 2.8, Cl 103, BUN 16, Creatinine 0.77, Albumin 3.4, ALK 97, AST 152, ALT 32, bilirubin 0.3. COVID PCR not detected.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: -
Allergien: None known
Vorherige Impfungen: -

VAERS 1804251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: VA
Alter: 77,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / -

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

Acute myocardial infarction Angiogram pulmonary abnormal Atrial fibrillation Blood electrolytes Chest discomfort Dyspnoea Fatigue Full blood count normal Malaise Pneumothorax

Symptomtext

77y/o male with h/o of HTN , HLD, Carotid artery stenosis, osteoarthritis, prostate cancer s/p, lung cancer s/p recent lobectomy on 9/27 who presents with 1 day hstory of fatigue, shortness of breath, chest tightness and general malaise. He was just discharged home yesterday 10/1 from a LLL lobectomy in stable condition. In the ED he was found to be in new onset afib with RVR, with CTPA negative for PE , but positive for postsurgical changes including small apical hydropneumothorax. Doctor saw the patient in the ED. He was given 3 dose of 5 mg of IV Metoprolol for Atrial Fib with RVR with rates into the low 100s. He will be admitted with new onset afib with RVR and NSTEMI likely type 2 in the setting of recent Left Lower Lobectomy. 10/4/2021 Afib with RVR resolved on discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 3,0
Labordaten: 10/1/2021 09:25 Basic electrolytes, CBC within normal limits
Aktuelle Erkrankungen: On the day of admission [9/27/2021] patient underwent left lower lobectomy using minimally invasive approach. He tolerated the operation well and was admitted to postanesthesia care unit and then to the intermediate care unit. He did well overnight and the following day he was transferred to MedSurg. Foley catheter was removed on postoperative day #1. He had a moderate amount of drainage and small air leak so his chest tube was left in until postoperative day #3. He was up ambulating and tolerating his diet. When chest tube was removed on postoperative day #3 follow-up chest x-ray demonstrated no pneumothorax. He was discharged home in stable condition.
Vorgeschichte: Prostate cancer, COPD, hypertension, myalgia, hearing loss, cardiac murmur, carotid artery stenosis, peripheral vascular disease, rosacea, history of tobacco use, cataracts, impotence, tinnitus, prediabetes, hyperlipidemia, malignant neoplasm of lower lobe of left lung
Andere Medikamente: Albuterol MDI, Anoro Ellipta MHD, Ascorbic Acid, Aspirin, Cholecalciferol, Flonase MDI, Multivitamin, gabapentin, ibuprofen, Atrovent spray, metoprolol XL, oxycodone, rosuvastatin
Allergien: Atorvastatin, cilostazol, baclofen, varenicline
Vorherige Impfungen: -

VAERS 1750163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MI
Alter: 41,0
Geschlecht: F
Eingang: 30.09.2021
Impfdatum: 10.06.2021
Beginn: 27.09.2021
Tage bis Beginn: 109,0
Dosis: 1
Route/Site: - / -

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

Acidosis Anaphylactic shock Asthenia Bronchospasm COVID-19 COVID-19 pneumonia Cardiac arrest Cardio-respiratory arrest Chronic obstructive pulmonary disease Hepatic failure Hyperkalaemia Hypotension Infusion Intensive care Ischaemic hepatitis Loss of personal independence in daily activities Mechanical ventilation Multiple organ dysfunction syndrome

Symptomtext

"Fully vaccinated patient who admitted to the hospital on 09/25/21 with positive COVID test. Patient had recently discharged from facility on 09/23/21 after a repeat pneumothorax and returned on 09/25/21 due to weakness and inability to care for self and upon admission testing was positive for COVID. Discharge summary from provider below: "42/F with long-standing history of COPD and recurrent pneumothorax for which she L partial lobectomy in 2015 and VATS/pleurodesis recently 9/2021. Pt had just been in our ICU August 2021 for respiratory failure due to COPD Exacerbation and was on the vent for 12 days. Unfortunately, she contracted COVID-19 PNA despite being fully vaccinated and was admitted to the hospital for that reason. We believe she had an anaphylactic shock and acute respiratory failure/bronchospasm due to Regeneron that caused her cardiac arrest with prolonged resuscitation 9/26/21. She developed multi-organ failure -- shock liver and aneuric renal failure thereafter. She was profoundly hypotensive, acidotic and hyperkalemic despite HD/CRRT and bicarb infusion. She had limited ventilatory compensation /difficult to ventilate because of underlying COPD with possible bronchospasm from anaphylaxis. She had coded multiple times in the ICU this am and family decided to stop CPR during the last code" Pharmacy has submitted a report to the FDA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic shock
Hospital-Tage: -
Labordaten: COVID detected swab on 09/23/21.
Aktuelle Erkrankungen: Recent history of pneumothorax.
Vorgeschichte: Pulmonary emphysema, hypertension, dyslipidemia, CHF, CAD, pneumothorax, COPD, hyperlipidemia, history of lobectomy of lung.
Andere Medikamente: Albuterol, aspirin, atorovastatin, QVAR inhaler, pulmicort, coreg, catapres, plavix, colace, drisdol, norco, duonebs, mag-ox, depo-provera, prednisone, zoloft.
Allergien: Penicillin, clindamycin, and tomatoes (all which patient reported caused anaphylaxis).
Vorherige Impfungen: -

VAERS 1746198

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

kritisch

Staat: CA
Alter: 45,0
Geschlecht: M
Eingang: 29.09.2021
Impfdatum: 01.08.2021
Beginn: 01.09.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: SYR / LA

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

Arteriosclerosis coronary artery Chest pain Condition aggravated Coronary artery disease Dyspnoea Myocardial infarction Pain

Symptomtext

Short of breath. Chest pain, body ache resulting heart attack Cad of native artery

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: Heart attack
Vorgeschichte: Cad of native artery
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1715357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: CT
Alter: 30,0
Geschlecht: F
Eingang: 20.09.2021
Impfdatum: 05.06.2021
Beginn: 14.08.2021
Tage bis Beginn: 70,0
Dosis: 2
Route/Site: IM / RA

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

Blood test normal Exposure during pregnancy Foetal death Pathology test Stillbirth

Symptomtext

Estimated delivery Nov. 10, 2021. Intrauterine fetal death was diagnosed August 13, stillbirth delivered August 14th. As of now there is no known cause despite the tests that have been run.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Foetal death
Hospital-Tage: 3,0
Labordaten: Autopsy (fetal), Placenta pathology, Various blood work for different viruses, etc. All results of tests were normal, unremarkable.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Prenatal
Allergien: No
Vorherige Impfungen: -

VAERS 1688955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: TX
Alter: 66,0
Geschlecht: U
Eingang: 10.09.2021
Impfdatum: 03.06.2021
Beginn: 06.08.2021
Tage bis Beginn: 64,0
Dosis: 2
Route/Site: IM / UN

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chest pain Chills Death Dyspnoea Hypoxia Intensive care Oxygen saturation decreased Pyrexia SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccine on 05/06/2021 and 06/03/2021. Patient presents to ER on 8/6/2021 referred directly from outpatient clinic with chief complaint of fever, chills, chest pain and dyspnea times 3 days. He was admitted to medical floor 08/06/2021 for acute hypoxemic respiratory failure secondary to COVID pneumonia requiring 2 L supplemental oxygen via nasal cannula. Patient received remdesivir, ceftriaxone, Bactrim and Baricitinib. On 08/10, oxygen demand increased from 7 L nasal cannula to high-flow nasal cannula 40 L 40% FiO2. Oxygen demand slowly increased requiring 60 L 100% FiO2. Patient was transferred to ICU for worsening hypoxia. 8/14-8/15 patient remained on HFNC and desaturated in the 50s. 8/15 patient left the hospital against medical advice. Patient expired on 8/26/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: COVID-19 Positive 8/6/2021: This assay was performed on the RP2.1 platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology
Aktuelle Erkrankungen: -
Vorgeschichte: Kidney Transplant 11/11/2020, HTN, T2DM with diabetic foot ulcer, ESRD, elevated EBV antibody titer positivie CMV antibody
Andere Medikamente: Calcium carbonate 600mg/Vitamin D3 daily, Vitamin D2 1250mcg weekly, famotidine 20mg BID, Myfortic 360mg 1 tab BID, Nifedipine 60mg daily, prednisone 5mg 2 tab daily, sirolimus 1mg 3 tab daily, Bactrim 400-80mg daily, aspirin 81mg daily, s
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1632254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 27.08.2021
Impfdatum: 24.08.2021
Beginn: 25.08.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac arrest Death Resuscitation

Symptomtext

Patient was found down, CPR initiated, TOD called at 0723.

Weitere VAERSDATA-Felder

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

VAERS 1637252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: WI
Alter: 27,0
Geschlecht: M
Eingang: 26.08.2021
Impfdatum: 05.08.2021
Beginn: 05.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Cardio-respiratory arrest Dizziness Fall

Symptomtext

Patient has a history of fear of needles. Pharmacist administered the vaccine and asked the patient to wait in the pharmacy waiting area for 15 minutes. After about 5 minutes of waiting in the pharmacy, patient felt anxious and dizzy. He fell out of chair and was on the ground. Pharmacy called a first response code for the ER staff to help the patient.

Weitere VAERSDATA-Felder

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

VAERS 2670691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: LA
Alter: 63,0
Geschlecht: F
Eingang: 19.08.2021
Impfdatum: 17.08.2021
Beginn: 18.08.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / -

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

Chest discomfort Chest pain Limb discomfort Myocardial infarction Pain in extremity

Symptomtext

I took the shot yesterday morning at 930 am. This evening 08/18/21, my left arm started a dull ache and felt like dead weight, tightening in my chest and pain in my chest. I immediately took a nitrate pill, the didn't subside after 15 minutes I took a second one at that point the pain and my have started to subside. I was having the beginning of a heart attack. I haven't had one of these in over 10 years, since they placed 4 stints in. I will notify and follow up with my doctor in the morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: 4 stints May 2011
Andere Medikamente: Amplodine 2.5; Vit C; Tumeric; Biotin; Vit D3
Allergien: Pollen
Vorherige Impfungen: -

VAERS 1500622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: NV
Alter: 16,0
Geschlecht: M
Eingang: 24.07.2021
Impfdatum: 20.05.2021
Beginn: 06.07.2021
Tage bis Beginn: 47,0
Dosis: 2
Route/Site: - / LA

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

Cerebral haemorrhage Cerebral thrombosis Cerebrovascular accident SARS-CoV-2 test

Symptomtext

Clot and bleed in brain causing stroke; Clot and bleed in brain causing stroke; Clot and bleed in brain causing stroke; This is a spontaneous report from a contactable consumer (patient's parent). A 16-year-old male patient received BNT162B2 (Lot Number: EW0186), dose 2 via an unspecified route of administration, administered in arm left on 20May2021 11:30 as single dose for covid-19 immunisation. Medical history included attention deficit hyperactivity disorder (ADHD). No known allergies. Concomitant medication included paracetamol (TYLENOL). The patient previously received first dose of BNT162B2 (lot number: ER8735) in left arm on 29Apr2021 17:15 for covid-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced clot and bleed in brain causing stroke on 06Jul2021 17:00. The events were reported as serious due to hospitalization. Events resulted in: doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care, hospitalization. Treatment received for the adverse events: Current hospitalization in PICU, rehabilitation, and pending further follow up actions. Prior to vaccination, was the patient diagnosed with COVID-19. The patient underwent lab tests and procedures which included nasal swab for Covid-19: negative on 06Jul2021. The outcome of events was recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: Test Date: 20210706; Test Name: Nasal Swab for COVID-19; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADHD
Andere Medikamente: TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 1478618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: WA
Alter: 52,0
Geschlecht: M
Eingang: 16.07.2021
Impfdatum: 25.06.2021
Beginn: 15.07.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Death Resuscitation Seizure like phenomena Unresponsive to stimuli

Symptomtext

Patient reported deceased to public health today. Date of death: 7/15/2021. Sister of patient reports that case reported chest pain while at home walking on his treadmill, he then had to lie down and sister asked him if he was having pain and wanted ambulance called. Reports that patient declined 911 call. Sister then reports that patient had what looked like a seizure, but then went completely unresponsive, so she initiated CPR and called 911. Reports that CPR and 911 response was not successful and patient passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: homebound client for vaccine outreach, this RN not precisely sure of circumstances leading up to "homebound" status.
Andere Medikamente: unknown
Allergien: none reported
Vorherige Impfungen: -

VAERS 1470249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: TX
Alter: 26,0
Geschlecht: F
Eingang: 14.07.2021
Impfdatum: 27.05.2021
Beginn: 27.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Chills Death Feeding disorder Feeling abnormal Feeling of body temperature change Headache Illness Vomiting

Symptomtext

The first dose of vaccine (lot number EW0176) was taken on 05/06/2021, and the second dose of vaccine (lot number EW0186) was taken on 05/27/2021. within 12 hours of second does she had gotten severe headache, she couldn't eat for severe vomiting, she said she felt like she was hit by a truck, and had the chills. she would go from really cold to really hot. She couldn't keep anything down even water. On the third day after the vaccine she was very sick and we ( the family) thought she was sleeping but when we went to try and wake her up we discovered her dead.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, Hypoglycemia
Andere Medikamente: Zoloft
Allergien: None
Vorherige Impfungen: -

VAERS 1446849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: FL
Alter: 18,0
Geschlecht: M
Eingang: 14.07.2021
Impfdatum: 29.06.2021
Beginn: 04.07.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / LA

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

Cardiac arrest Death Syncope Sudden death

Symptomtext

Patient received 1st dose of Pfizer vaccine on 6/29/21. On 7/4/21, he collapsed suddenly while playing football. Arrived to the emergency department in cardiac arrest and expired. He had been recently diagnosed with hypertrophic obstructive cardiomyopathy, and I suspect this was the cause of death and that the vaccine was unrelated.

Weitere VAERSDATA-Felder

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

VAERS 1427880

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: MN
Alter: 69,0
Geschlecht: M
Eingang: 25.06.2021
Impfdatum: 13.05.2021
Beginn: 06.06.2021
Tage bis Beginn: 24,0
Dosis: 2
Route/Site: - / -

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

Death

Symptomtext

Patient was hospitalized and died within 60 days of receiving a COVID vaccine series

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1382202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: CT
Alter: 78,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: 04.06.2021
Beginn: 05.06.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac assistance device user Death Resuscitation Unresponsive to stimuli

Symptomtext

During rounds at 10pm, CNA observed resident unresponsive. Nurse was immediately called, who in turn call the code. Nursing staff responded and started CPR. A total of 16 rounds of compressions and shocked x 2, prior to Paramedics taking over 10 minutes later. They continued CPR for another 10 minutes before resident was pronounced dead.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO ACUTE ILLNESS AT TIME OF VACCINATION - RESIDENT WITH CHRONIC HEALTH CONDITIONS.
Vorgeschichte: 1. CARDIOMYOPATHY WITH SUSPECTED CARDIAC AMYLOISDOSIS 2. SEVERE STENOSIS 3. ADVANCED LIVER CIRRHOSIS 4. ATRIAL FIBRILLATION 5. TYPE 2 DIABETES MELLITUS WITH DIABETIC NEPHROPATHY 6. BENIGN PROSTATIC HYPERPLASIA WITH LOWER URINARY TRACT SYMPTOMS 7. CHRONIC SYSTOLIC (CONGESTIVE) HEART FAILURE 8. WEAKNESS 9. GERD 10. HYPOTHYROIDISM 11. DEPRESSION
Andere Medikamente: Sertraline HCl Tablet 50 MG Give 1 tablet by mouth one time a day for Depression Rosuvastatin Calcium Tablet 10 MG Give 1 tablet by mouth one time a day for lipid control OXcarbazepine Tablet 300 MG Give 1 tablet by mouth two times a d
Allergien: NO KNOWN ALLERGIES
Vorherige Impfungen: -

VAERS 1317744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

kritisch

Staat: WI
Alter: 55,0
Geschlecht: M
Eingang: 14.05.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

Death

Weitere VAERSDATA-Felder

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

VAERS 2724157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: ME
Alter: 15,0
Geschlecht: M
Eingang: 14.12.2023
Impfdatum: 02.06.2021
Beginn: 03.06.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Fatigue Loss of consciousness Malaise Syncope

Symptomtext

Patient fainted in bathroom after getting out of bed the morning after the vaccination. She lost consciousness for 30 seconds. When she regained consciousness, she was extremely tired and felt sick. She went back to bed to sleep. She did not want to eat or drink, but she did with assistance. This continued for 48 hours. Primary care physician's office was notified. They advised that patient be monitored and to update them if condition worsened.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Cetirizine, multi-vitamin , epi-pen prn
Allergien: Allergies to furred animals, dogs in particular. Secondary allergy to amoxicillin.
Vorherige Impfungen: -

VAERS 2683881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NY
Alter: 16,0
Geschlecht: F
Eingang: 20.09.2023
Impfdatum: 07.05.2021
Beginn: 07.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / AR

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

Asthenia Complex regional pain syndrome Dizziness Drug hypersensitivity Ehlers-Danlos syndrome Food allergy Hypermobility syndrome Hypoaesthesia Immediate post-injection reaction Impaired gastric emptying Mast cell activation syndrome Nausea Pain Postural orthostatic tachycardia syndrome Syncope Vomiting

Symptomtext

-Episode of syncope + Dizziness immediately after vaccine -Onset of new chronic health conditions (hEDS,CRPS,MCAS,POTS,and gastroparesis) -Pain, nausea, vomiting, weakness, numbness, dizziness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Pre vaccine: None known Post vaccine: Ehlers-Danlos syndrome, MCAS, CRPS, POTS, gastroparesis
Vorgeschichte: Ehlers-Danlos Syndrome / gastroparesis, Mast Cell Activation Syndrome Postural Orthostatic Tachycardia/Complex Regional Pain Syndrome
Andere Medikamente: PRE VACCINE NONE POST VACCINE: Zyrtec, Pepcid, Aprepitant, Zofran, Benadryl
Allergien: PRE Vaccine: Peanuts, Penicillin POST Vaccine: Several antibiotics, many food allergies
Vorherige Impfungen: -

VAERS 2651319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 37,0
Geschlecht: M
Eingang: 30.06.2023
Impfdatum: 03.07.2021
Beginn: 01.07.2023
Tage bis Beginn: 728,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Embolic stroke Obstructive sleep apnoea syndrome

Symptomtext

OBSTRUCTIVE SLEEP APNEA 3/27/2023 DIZZINESS ACUTE STROKE DUE TO EMBOLISM OF UNSPECIFIED ARTERY 4/1/2023 DIZZINESS

Weitere VAERSDATA-Felder

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

VAERS 2575640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 04.02.2023
Impfdatum: 01.03.2021
Beginn: 20.11.2021
Tage bis Beginn: 264,0
Dosis: 2
Route/Site: - / -

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

COVID-19 immunisation Chest X-ray Echocardiogram Laboratory test Myocarditis Scan myocardial perfusion Suspected COVID-19

Symptomtext

SUSPECTED COVID-19 INFECTION; MYOCARDITIS; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient via another pharmaceutical company (Pfizer) concerned a 65 year old female of an unspecified ethnicity. The patient's weight was 58.06 kilograms, and height was 163 centimeters. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin, and batch number were not reported, expiry: unknown) dose was not reported, 1 total, administered on MAR-2021 for covid-19 prophylaxis. The batch number was not reported and has been requested. Age at the time of vaccination 64 year old. No concomitant medications were reported. It was unknown whether patient had any adverse event following vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 1). Patient reported that she had a good night's sleep and was fine after Janssen vaccine. The patient additionally received non-company suspect vaccine Pfizer Biontech covid-19 vaccine (tozinameran) (dose number in series 2) (form of admin and route of admin were not reported, batch number: EW0186 expiry: unknown) dose was not reported, administered on 20-NOV-2021 for covid-19 prophylaxis which was revaccination with different covid-19 vaccine (dose number in series 2). On 25-NOV-2021, 5 days after Pfizer booster vaccine the patient experienced myocarditis (dose number in series 2). She went to the doctor, had a number of tests then went to the cardiologist and had a number of tests. Patient had some chest pain. She mentioned that after 5 weeks she was fine. Cardiologist read all the results and told her even though she did not fit in the demographic that he believed she had myocarditis and it passed. Patient did not receive any treatment for myocarditis. On an unspecified date, patient had a chest X-ray, echocardiogram and a lunar nuclear stress test for which results were not reported. On 31-DEC-2022, the patient experienced covid-19 (suspected covid-19 infection, dose number in series 2). Patient still had some effect and had not received any treatment for covid-19. On the day of reporting, the patient said that she will be tested tomorrow for covid. The action taken with covid-19 vaccine ad26.cov2.s, and tozinameran was not applicable. The patient recovered from myocarditis on JAN-2022, had not recovered from suspected covid-19 infection, and the outcome of revaccination with different covid-19 vaccine was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0- 20230203582- Myocarditis. The event has an compatible/suggestive temporal relationship, is unlabeled, and is scientifically plausible. There is no information on any other factors potentially associated with the event. Therefore, the WHO Causality is considered indeterminate. The company causality is considered related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Test Date: 20211125; Test Name: LABORATORY TEST; Result Unstructured Data: Not reported; Test Name: ECHOCARDIOGRAM; Result Unstructured Data: Not reported; Test Name: LUNAR NUCLEAR STRESS TEST; Result Unstructured Data: Not reported; Test Name: CHEST X-RAY; Result Unstructured Data: Not reported
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2568943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 31.01.2023
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Cardiac stress test Chest X-ray Echocardiogram Investigation Myocarditis COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

Got Covid on 31Dec2022.; got Covid on 31Dec2022.; she got the J and J as dose 1/Pfizer COVID booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 65-year-old female patient received BNT162b2 (BNT162B2), on 20Nov2021 as dose 2 (booster), single (Lot number: EW0186) at the age of 65 years, in arm for covid-19 immunisation; coviD-19 vaccine nrvv ad26 (jnj 78436735) (JANSSEN COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 20Nov2021, outcome "unknown", described as "she got the J and J as dose 1/Pfizer COVID booster"; DRUG INEFFECTIVE (medically significant) with onset 31Dec2022, outcome "unknown", described as "Got Covid on 31Dec2022."; COVID-19 (medically significant) with onset 31Dec2022, outcome "unknown", described as "got Covid on 31Dec2022.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (31Dec2022) Positive, notes: got COVID virus on 31Dec2022. Therapeutic measures were not taken as a result of drug ineffective, covid-19, interchange of vaccine products.The patient had no other medical conditions. Indication for the Pfizer booster was also mentioned as general health guidelines as a good citizen. Reporter stated that she wanted to alert that she had an adverse reaction to the booster shot. In 2021, when she was 64 as soon as she was eligible in Mar2021, she got the J and J and had a good night's sleep and was fine. In Nov2021, 7-8 months later the J and J was not available so she got the Pfizer booster vaccine. Patient mentioned that she would like to get another booster but does not know if there has been any research done on individuals who suffered from myocarditis after the Pfizer shot and asked if ther was a vaccine recommended for that demographic. There may be clinical research done and they may share that with her. She mentioned that she did get Covid three weeks ago because she did not know which vaccine to take. She did not go to a physician. She did not know if she still has it and she will be tested for Covid tomorrow. She still has some effects. It was further specified that patient received Pfizer COVID booster on 20Nov2021 and got COVID virus on 31Dec2022.; Sender's Comments: Linked Report(s) : PFIZER INC-202300036615 same reporter, product and patient, different event.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Test Date: 20221231; Test Name: COVID Test; Test Result: Positive ; Comments: got COVID virus on 31Dec2022.
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 2568943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 31.01.2023
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Cardiac stress test Chest X-ray Echocardiogram Investigation Myocarditis COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

Got Covid on 31Dec2022.; got Covid on 31Dec2022.; she got the J and J as dose 1/Pfizer COVID booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 65-year-old female patient received BNT162b2 (BNT162B2), on 20Nov2021 as dose 2 (booster), single (Lot number: EW0186) at the age of 65 years, in arm for covid-19 immunisation; coviD-19 vaccine nrvv ad26 (jnj 78436735) (JANSSEN COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 20Nov2021, outcome "unknown", described as "she got the J and J as dose 1/Pfizer COVID booster"; DRUG INEFFECTIVE (medically significant) with onset 31Dec2022, outcome "unknown", described as "Got Covid on 31Dec2022."; COVID-19 (medically significant) with onset 31Dec2022, outcome "unknown", described as "got Covid on 31Dec2022.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (31Dec2022) Positive, notes: got COVID virus on 31Dec2022. Therapeutic measures were not taken as a result of drug ineffective, covid-19, interchange of vaccine products.The patient had no other medical conditions. Indication for the Pfizer booster was also mentioned as general health guidelines as a good citizen. Reporter stated that she wanted to alert that she had an adverse reaction to the booster shot. In 2021, when she was 64 as soon as she was eligible in Mar2021, she got the J and J and had a good night's sleep and was fine. In Nov2021, 7-8 months later the J and J was not available so she got the Pfizer booster vaccine. Patient mentioned that she would like to get another booster but does not know if there has been any research done on individuals who suffered from myocarditis after the Pfizer shot and asked if ther was a vaccine recommended for that demographic. There may be clinical research done and they may share that with her. She mentioned that she did get Covid three weeks ago because she did not know which vaccine to take. She did not go to a physician. She did not know if she still has it and she will be tested for Covid tomorrow. She still has some effects. It was further specified that patient received Pfizer COVID booster on 20Nov2021 and got COVID virus on 31Dec2022.; Sender's Comments: Linked Report(s) : PFIZER INC-202300036615 same reporter, product and patient, different event.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Test Date: 20221231; Test Name: COVID Test; Test Result: Positive ; Comments: got COVID virus on 31Dec2022.
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 2475897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 95,0
Geschlecht: F
Eingang: 12.10.2022
Impfdatum: 28.06.2022
Beginn: 24.09.2022
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: - / -

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

Asthenia COVID-19 Condition aggravated Dementia Glomerular filtration rate normal Hypertension Hypoxia Presyncope SARS-CoV-2 test positive Urinary tract infection

Symptomtext

"Provider d/c note: ""Patient brought to hospital with weakness, presyncope. Found to be COVID positive on 9/24, with mild hypoxia requiring small amount of supplemental O2. Also noted to have debility, dementia at baseline likely worsened by COVID. She was noted to be high fall risk, and PT/OT was ordered. CKD noted on chart, GFR improved during stay to be 80 by calculation. Also found to have UTI, patient treated with five days of antibiotics. History of complete heart block with pacemaker placement, as well as afib. Continued home beta blocker, aspirin, Plavix. Hypertension controlled with lisinopril and beta blocker. Very hard of hearing at baseline, does well with hearing aids in. Patient continued to recover from COVID, and worked with PT and OT, also with SLP evaluation. Therapy teams agreed patient likely to benefit from rehab. After ten days COVID isolation discontinued, as patient was no longer requiring oxygen and remained afebrile with minimal to no symptoms. Patient accepted for rehab, and discharged in stable and improved condition."""

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 11,0
Labordaten: COIVD Detected PCR on 9/24/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular HTN (hypertension) Hypercholesteremia Essential hypertension Complete heart block (*) NSTEMI (non-ST elevated myocardial infarction) (*) Longstanding persistent atrial fibrillation (*) Coronary artery disease involving native coronary artery of native heart without angina pectoris Digestive GERD (gastroesophageal reflux disease) Endocrine Other specified hypothyroidism Integumentary Dermatitis Rash of perineum Skin lesion Generalized skin lesions Sebaceous cyst Psychological Generalized anxiety disorder Dementia (*) Depression Dementia with behavioral disturbance (*) Respiratory Bilateral pulmonary infiltrates on chest x-ray Urinary Acute cystitis without hematuria Stage 3a chronic kidney disease (*) Other Patellar fracture Normocytic normochromic anemia Ear problems Knee pain Environmental allergies Symptomatic bradycardia At high risk for falls Insomnia Edema of both legs Left displaced femoral neck fracture (*) History of left hip hemiarthroplasty Personal history of COVID-19 History of complete heart block Pacemaker Bilateral hearing loss Hx of recurrent urinary tract infection Generalized muscle weakness
Andere Medikamente: -
Allergien: Azithromycin, Donepezil Hcl, Erythromycin Base, Norco, Pcn, Sulfa
Vorherige Impfungen: -

VAERS 2433410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 59,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 31.08.2021
Beginn: 11.08.2022
Tage bis Beginn: 345,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Endotracheal intubation Fall Intensive care Mental status changes SARS-CoV-2 test positive Subarachnoid haemorrhage Subdural haematoma

Symptomtext

60y.o. female patient, presented to the EC yesterday with altered mental status, the patient sustained a fall at home. On evaluation the hospital she was found to have traumatic frontal and parietal occipital subarachnoid hemorrhage and left acute subdural hematoma. She is currently in the ICU setting, she is intubated. She has a past medical history for metastatic breast cancer with involvement in the brain, suboccipital craniotomy tumor resection in 2003. History of hyperlipidemia, type 2 diabetes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: 8/12 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC-- detected
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2398022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TX
Alter: 49,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 31.08.2021
Beginn: 14.09.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: - / LA

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

Alopecia Antinuclear antibody Arthralgia Atonic seizures Autoimmune arthritis Autoimmune disorder Blood pressure increased Blue toe syndrome Bone pain Burning sensation Autonomic seizure Axonal neuropathy Cerebellar infarction Cerebral ischaemia Chest discomfort Chest pain Chronic fatigue syndrome Confusional state

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49-year-old male patient received BNT162b2 (BNT162B2), on 31Aug2021 at 13:15 as dose 1, single (Lot number: EW0186) at the age of 49 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. No known allergies were reported. Patient had not taken other vaccines in four weeks. Patient did not have Covid prior to vaccination and was not tested for Covid post vaccination. Concomitant medication(s) included: IBUPROFEN; ACETAMINOPHEN. The following information was reported: BLUE TOE SYNDROME (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; MULTIFOCAL MOTOR NEUROPATHY (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "Multifocal motor neuropathy (MMN)"; ATONIC SEIZURES (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; AUTOIMMUNE ARTHRITIS (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered"; AUTOIMMUNE DISORDER (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered"; AUTONOMIC SEIZURE (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "autonomic seizures"; AXONAL NEUROPATHY (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "axonal loss"; VISION BLURRED (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "blurred vision"; BONE PAIN (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; CEREBELLAR INFARCTION (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered"; CEREBRAL ISCHAEMIA (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "cerebral vessel ischemic disease (cerebral ischaemia)"; CHRONIC FATIGUE SYNDROME (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; DISORIENTATION (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; MALAISE (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "feeling unwell"; GAIT DISTURBANCE (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; GENERALISED ONSET NON-MOTOR SEIZURE (hospitalization, disability, medically significant), PETIT MAL EPILEPSY (hospitalization, disability, medically significant) all with onset 14Sep2021 at 18:00, outcome "not recovered" and all described as "generalised onset non-motor seizures (staring spells, absences seizures)"; GROIN PAIN (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; ALOPECIA (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "hair loss"; ARTHRALGIA (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "joint pain"; LOSS OF CONSCIOUSNESS (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "loss of consciousness and awareness"; MEMORY IMPAIRMENT (hospitalization, disability), FEELING ABNORMAL (hospitalization, disability) all with onset 14Sep2021 at 18:00, outcome "not recovered" and all described as "memory impairment (brain/ fibro fog) loss"; NAUSEA (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; POLYARTHRITIS (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered"; DEMYELINATION (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "punctuated in the frontoparietal demyelination/chronic inflammatory demyelination"; DYSPNOEA (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "shortness of breath"; CONFUSIONAL STATE (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "temporary confusion"; TONIC CLONIC MOVEMENTS (hospitalization, disability, medically significant), GENERALISED TONIC-CLONIC SEIZURE (hospitalization, disability, medically significant) all with onset 14Sep2021 at 18:00, outcome "not recovered" and all described as "tonic clonic movements/seizures, anticonvulsants"; DYSKINESIA (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "uncontrollable jerking movements of the arms and legs"; CONTUSION (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "unusual skin bruising"; URINE ABNORMALITY (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "urine disorders". The patient was hospitalized for autonomic seizure, autoimmune arthritis, polyarthritis, autoimmune disorder, cerebellar infarction, cerebral ischaemia, demyelination, loss of consciousness, multifocal motor neuropathy, generalised onset non-motor seizure, petit mal epilepsy, tonic clonic movements, generalised tonic-clonic seizure, atonic seizures, dyskinesia, arthralgia, bone pain, axonal neuropathy, confusional state, disorientation, memory impairment, feeling abnormal, alopecia, malaise, nausea, groin pain, urine abnormality, gait disturbance, chronic fatigue syndrome, dyspnoea, contusion, blue toe syndrome (hospitalization duration: 4 day(s)). The events "autonomic seizures", "autoimmune arthritis", "polyarthritis", "autoimmune disorder", "cerebellar infarction", "cerebral vessel ischemic disease (cerebral ischaemia)", "punctuated in the frontoparietal demyelination/chronic inflammatory demyelination", "loss of consciousness and awareness", "multifocal motor neuropathy (MMN)", "generalised onset non-motor seizures (staring spells, absences seizures)", "tonic clonic movements/seizures, anticonvulsants", "atonic seizures", "uncontrollable jerking movements of the arms and legs", "joint pain", "bone pain", "axonal loss", "temporary confusion", "disorientation", "memory impairment (brain/ fibro fog) loss", "hair loss", "feeling unwell", "nausea", "groin pain", "urine disorders", "gait disturbance", "chronic fatigue syndrome", "blurred vision", "shortness of breath", "unusual skin bruising" and "blue toe syndrome" required physician office visit and emergency room visit. Therapeutic measures were taken as a result of autonomic seizure, autoimmune arthritis, polyarthritis, autoimmune disorder, cerebellar infarction, cerebral ischaemia, demyelination, loss of consciousness, multifocal motor neuropathy, generalised onset non-motor seizure, petit mal epilepsy, tonic clonic movements, generalised tonic-clonic seizure, atonic seizures, dyskinesia, arthralgia, bone pain, axonal neuropathy, confusional state, disorientation, memory impairment, feeling abnormal, alopecia, malaise, nausea, groin pain, urine abnormality, gait disturbance, chronic fatigue syndrome, vision blurred, dyspnoea, contusion, blue toe syndrome with Methylprednisolone and anticonvulsants.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atonic seizures
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: IBUPROFEN; ACETAMINOPHEN
Allergien: -
Vorherige Impfungen: -

VAERS 2398022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TX
Alter: 49,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 31.08.2021
Beginn: 14.09.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: SYR / LA

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

Alopecia Antinuclear antibody Arthralgia Atonic seizures Autoimmune arthritis Autoimmune disorder Blood pressure increased Blue toe syndrome Bone pain Burning sensation Autonomic seizure Axonal neuropathy Cerebellar infarction Cerebral ischaemia Chest discomfort Chest pain Chronic fatigue syndrome Confusional state

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49-year-old male patient received BNT162b2 (BNT162B2), on 31Aug2021 at 13:15 as dose 1, single (Lot number: EW0186) at the age of 49 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. No known allergies were reported. Patient had not taken other vaccines in four weeks. Patient did not have Covid prior to vaccination and was not tested for Covid post vaccination. Concomitant medication(s) included: IBUPROFEN; ACETAMINOPHEN. The following information was reported: BLUE TOE SYNDROME (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; MULTIFOCAL MOTOR NEUROPATHY (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "Multifocal motor neuropathy (MMN)"; ATONIC SEIZURES (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; AUTOIMMUNE ARTHRITIS (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered"; AUTOIMMUNE DISORDER (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered"; AUTONOMIC SEIZURE (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "autonomic seizures"; AXONAL NEUROPATHY (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "axonal loss"; VISION BLURRED (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "blurred vision"; BONE PAIN (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; CEREBELLAR INFARCTION (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered"; CEREBRAL ISCHAEMIA (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "cerebral vessel ischemic disease (cerebral ischaemia)"; CHRONIC FATIGUE SYNDROME (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; DISORIENTATION (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; MALAISE (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "feeling unwell"; GAIT DISTURBANCE (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; GENERALISED ONSET NON-MOTOR SEIZURE (hospitalization, disability, medically significant), PETIT MAL EPILEPSY (hospitalization, disability, medically significant) all with onset 14Sep2021 at 18:00, outcome "not recovered" and all described as "generalised onset non-motor seizures (staring spells, absences seizures)"; GROIN PAIN (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; ALOPECIA (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "hair loss"; ARTHRALGIA (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "joint pain"; LOSS OF CONSCIOUSNESS (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "loss of consciousness and awareness"; MEMORY IMPAIRMENT (hospitalization, disability), FEELING ABNORMAL (hospitalization, disability) all with onset 14Sep2021 at 18:00, outcome "not recovered" and all described as "memory impairment (brain/ fibro fog) loss"; NAUSEA (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered"; POLYARTHRITIS (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered"; DEMYELINATION (hospitalization, disability, medically significant) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "punctuated in the frontoparietal demyelination/chronic inflammatory demyelination"; DYSPNOEA (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "shortness of breath"; CONFUSIONAL STATE (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "temporary confusion"; TONIC CLONIC MOVEMENTS (hospitalization, disability, medically significant), GENERALISED TONIC-CLONIC SEIZURE (hospitalization, disability, medically significant) all with onset 14Sep2021 at 18:00, outcome "not recovered" and all described as "tonic clonic movements/seizures, anticonvulsants"; DYSKINESIA (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "uncontrollable jerking movements of the arms and legs"; CONTUSION (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "unusual skin bruising"; URINE ABNORMALITY (hospitalization, disability) with onset 14Sep2021 at 18:00, outcome "not recovered", described as "urine disorders". The patient was hospitalized for autonomic seizure, autoimmune arthritis, polyarthritis, autoimmune disorder, cerebellar infarction, cerebral ischaemia, demyelination, loss of consciousness, multifocal motor neuropathy, generalised onset non-motor seizure, petit mal epilepsy, tonic clonic movements, generalised tonic-clonic seizure, atonic seizures, dyskinesia, arthralgia, bone pain, axonal neuropathy, confusional state, disorientation, memory impairment, feeling abnormal, alopecia, malaise, nausea, groin pain, urine abnormality, gait disturbance, chronic fatigue syndrome, dyspnoea, contusion, blue toe syndrome (hospitalization duration: 4 day(s)). The events "autonomic seizures", "autoimmune arthritis", "polyarthritis", "autoimmune disorder", "cerebellar infarction", "cerebral vessel ischemic disease (cerebral ischaemia)", "punctuated in the frontoparietal demyelination/chronic inflammatory demyelination", "loss of consciousness and awareness", "multifocal motor neuropathy (MMN)", "generalised onset non-motor seizures (staring spells, absences seizures)", "tonic clonic movements/seizures, anticonvulsants", "atonic seizures", "uncontrollable jerking movements of the arms and legs", "joint pain", "bone pain", "axonal loss", "temporary confusion", "disorientation", "memory impairment (brain/ fibro fog) loss", "hair loss", "feeling unwell", "nausea", "groin pain", "urine disorders", "gait disturbance", "chronic fatigue syndrome", "blurred vision", "shortness of breath", "unusual skin bruising" and "blue toe syndrome" required physician office visit and emergency room visit. Therapeutic measures were taken as a result of autonomic seizure, autoimmune arthritis, polyarthritis, autoimmune disorder, cerebellar infarction, cerebral ischaemia, demyelination, loss of consciousness, multifocal motor neuropathy, generalised onset non-motor seizure, petit mal epilepsy, tonic clonic movements, generalised tonic-clonic seizure, atonic seizures, dyskinesia, arthralgia, bone pain, axonal neuropathy, confusional state, disorientation, memory impairment, feeling abnormal, alopecia, malaise, nausea, groin pain, urine abnormality, gait disturbance, chronic fatigue syndrome, vision blurred, dyspnoea, contusion, blue toe syndrome with Methylprednisolone and anticonvulsants.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atonic seizures
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: IBUPROFEN; ACETAMINOPHEN
Allergien: -
Vorherige Impfungen: -

VAERS 2366535

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NC
Alter: 32,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 29.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Acne cystic Biopsy Biopsy skin Ear disorder Echocardiogram Electrocardiogram abnormal Eye oedema Eye swelling Face oedema Fatigue Feeling abnormal Headache Malaise Palpitations Fear General physical health deterioration Inflammation Laboratory test

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 32-year-old male patient received BNT162b2 (BNT162B2), on 29Apr2021 as dose 1, single (Lot number: EW0171) at the age of 32 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: MALAISE (non-serious) with onset 2021, outcome "unknown", described as "did not feel well."; FATIGUE (non-serious) with onset 2021, outcome "unknown"; FEELING ABNORMAL (non-serious) with onset 2021, outcome "unknown", described as "felt like something was wrong"; HEADACHE (non-serious) with onset 2021, outcome "unknown"; PALPITATIONS (non-serious) with onset 2021, outcome "unknown", described as "heart palpitations"; WEIGHT DECREASED (non-serious) with onset 2021, outcome "unknown", described as "his weight used to be 160 pounds and now is 134 pounds/ weight loss occurred after the vaccine". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: It was reported that everything started with heart palpitations, fatigue and headache; kept telling everyone that right after he got the vaccine he felt like something was wrong and made sure he was eating and sleeping enough and did not feel well, was so fatigued and it did not make sense but got a headache at the same time every afternoon and it was uncanny. Height was 5'10'' or 5'11'' and his weight used to be 160 pounds and was then 134 pounds and he was always a solid 160 pounds and the weight loss occurred after the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Name: body weight; Result Unstructured Data: Test Result:134 lbs; Comments: weight used to be 160 pounds and now is 134 pounds.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2400436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 49,0
Geschlecht: F
Eingang: 03.08.2022
Impfdatum: 18.11.2021
Beginn: 19.07.2022
Tage bis Beginn: 243,0
Dosis: 3
Route/Site: - / -

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

Angiogram pulmonary normal Anxiety disorder Blindness COVID-19 Chest X-ray normal Computerised tomogram head normal Electrocardiogram abnormal Electroencephalogram normal Impaired driving ability Magnetic resonance imaging head normal Respiratory tract congestion SARS-CoV-2 test positive Seizure Seizure like phenomena Sinus tachycardia Tremor Troponin normal Urinary incontinence

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 7/19/2022 Discharge Date: Jul 21, 2022 PRESENTING PROBLEM: Seizure (HCC) Seizure-like activity (HCC) Anxiety disorder, unspecified type COVID-19 HOSPITAL COURSE: 50-year-old female history of type 2 diabetes, hypertension, psychiatric illness bipolar/schizophrenia came to local ER were seizure-like event. She had noted around 16:00 and 7/19 showed episode of involuntary shaking in her hands bilaterally with symmetric vision loss and urinary incontinence. Patient did say she had seizure-like event in the past secondary to Wellbutrin medication but this was in remote history. Upon arrival to ER, patient afebrile, normotensive. Had troponins which were negative and flat. COVID screen came back positive. Urinalysis bland. EKG with sinus tachycardia. She had CT head negative for any acute intracranial process. Chest x-ray and CTA thorax negative for acute intrathoracic process. Patient was satting above 90% on room air. She was admitted to the hospital observation status for EEG and MRI per neuro request. Patient's EEG came back showing no evidence of epilepsy. MRI brain came back showing no evidence of any acute abnormality. Patient said she was still having some upper chest congestion she thinks related to COVID diagnosis. Repeat chest x-ray day of discharge was negative for any acute abnormalities. For duration of stay patient was not hypoxic. Did prescribe patient albuterol inhaler and Tessalon Perles. Patient inquired about Paxlovid medications for COVID. Discussed with inpatient pharmacy and we do offer Paxlovid inpatient. Patient can follow-up with her PCP to get this medication at discharge as outpatient for COVID. Neurology discussed with patient seizure precautions for discharge including: "no showering/bathing alone, operation of heavy machinery, use of ladders and driving for 6 months seizure free. Patient agreed with plan and verbalized understanding."Did reach out to Neurology and per Neurology no need for neuro follow-up at this time. Discharge stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Bipolar disorder (HCC) Pure hypercholesterolemia Anemia, unspecified Abnormal Pap smear Subglottic stenosis Thyroid nodule Non-toxic multinodular goiter Schizophrenia (HCC) Shortness of breath Hypertension, benign Type 2 diabetes mellitus without complication (HCC) Abnormal involuntary movement Tardive syndrome Hashimoto's thyroiditis Admission for sterilization Seizure-like activity (HCC)
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler atorvastatin (LIPITOR) 20 MG tablet benzonatate (TESSALON) 100 MG capsule citalopram (CELEXA) 40 MG tablet cyclobenzaprine (FLEXERIL) 10 MG tablet du
Allergien: BupropionSeizure Clozaril [Phenothiazines]Palpitations FluoxetinePalpitations GlimepirideNausea and Vomiting GlipizideNausea Only
Vorherige Impfungen: -

VAERS 2328818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 45,0
Geschlecht: M
Eingang: 23.06.2022
Impfdatum: 25.08.2021
Beginn: 12.06.2022
Tage bis Beginn: 291,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Condition aggravated SARS-CoV-2 test positive Seizure

Symptomtext

6/12 45 y/o male with medical history significant for seizures post TBI from MVA, HTN, who presented to the hospital for 3 episodes of break through seizures.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: 6/12 Sars-Cov-2 by NAA, detected 6/22 Sars-Cov-2 by NAA, not detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2271081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 17,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 28.05.2021
Beginn: 04.02.2022
Tage bis Beginn: 252,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Syncope

Symptomtext

02/04/22 presented to ED for "syncope ". PMHx of "ADHD, depression, anxiety, and asthma"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 02/04/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2177161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CO
Alter: 56,0
Geschlecht: M
Eingang: 12.03.2022
Impfdatum: 02.07.2021
Beginn: 02.03.2022
Tage bis Beginn: 243,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Cardiac ventricular thrombosis Fibrin D dimer increased Inappropriate schedule of product administration Mechanical ventilation SARS-CoV-2 test positive

Symptomtext

COVID Positive Patient (s/p 2 Pfizer doses 5/5/21 & 7/2/21) - admit 3/2/22 w/ covid & has been on a vent ever since; found to have LV thrombus (ddimer 8223)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac ventricular thrombosis
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2147290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: PA
Alter: 13,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 21.05.2021
Beginn: 01.06.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: - / LA

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

Blood oestrogen Blood test Menstrual disorder Syncope

Symptomtext

Daughter fainted as a result of having blood drawn; her daughter has not had a menstrual cycle since receiving both primary doses in June2021/Her daughter has not had her menstrual cycle since JUN 2021.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 14 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 21May2021 11:00 (Lot number: EW0186) at the age of 13 years as dose 1, single and administered in arm left, administration date 17Jun2021 13:00 (Lot number: EW0171) as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: SYNCOPE (medically significant), outcome "unknown", described as "Daughter fainted as a result of having blood drawn"; MENSTRUAL DISORDER (non-serious) with onset Jun2021, outcome "not recovered", described as "her daughter has not had a menstrual cycle since receiving both primary doses in June2021/Her daughter has not had her menstrual cycle since JUN 2021.". The event "her daughter has not had a menstrual cycle since receiving both primary doses in june2021/her daughter has not had her menstrual cycle since jun 2021." was evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood oestrogen: unknown result, notes: had all the hormones checked, nothing adverse or hormonal going on that would trigger why she isn't getting her period patient thinks its the vaccine; blood test: unknown result, notes: Her daughter had blood work done. Caller is patient's mother. She states her daughter has not had a menstrual cycle since receiving both primary doses in Jun2021. Her PCP has checked her Hormone levels and they were normal. Is there any more information available. Will there be any special studies of prepubescent children and the vaccine? There really needs to be more studies done. Her daughter has not had her menstrual cycle since Jun2021. Her last vaccine was on 06Jun2021. Her daughter had blood work done, had all the hormones checked nothing adverse or hormonal going on that would trigger why she isn't getting her period, patient thinks it's the vaccine. Prescribing HCP: When querying HCP name, caller states the last time the were there it was a different one than they usually see. Caller provided Practice Information. No HCP email address to provide. Indication: immunity, caller states it's the best thing to do. Caller states daughter had blood work, a series of hormones. Daughter fainted as a result of having blood drawn. They were trying to see if there everything was working as it should, making sure everything in the brain that is responsible for the hormones. Caller states she is looking at the description on the bill, not sure what it all means. There is a synopsis listed, the doctor said it was all normal. Caller states she is at least, glad, not sure who to reach out to, since it has been abnormal ever since getting the vaccine. The doctor pushed it off like how can it be an adverse reaction. Time the Vaccination Was Given: First dose: unknown, roughly 11:00. Second dose: may have been 13:00. Anatomical Location of Administration of Pfizer vaccine considered as suspect: Both doses received in the Left Arm. Caller confirms both vaccines received at same location. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available): none. Additional Vaccines Administered on Same Date of the Pfizer Suspect: no. Adverse Event (AE) Details: Provide the time of onset of AE(s): Her daughter has not had her menstrual cycle since JUN 2021. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): none. Caller states her daughter started her menstrual cycle at age 10 and it was fairly regular. The blood tests would have shown diabetes or cholesterol, everything was fine. Relevant Tests: None or Unknown, List other relevant diagnostic and confirmatory test results for event(s), for example, from blood tests, cerebro-spinal fluid culture, pleural fluid culture, urine culture, diagnostic imaging, (e.g., chest X-ray, MRI) Test: Date: Result: Units: Normal Range: Low: High: Caller states not that she knows of. They tried to take 7 vials of blood.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: Hormone test; Result Unstructured Data: Test Result:Unknown result; Comments: had all the hormones checked, nothing adverse or hormonal going on that would trigger why she isn't getting her period patient thinks its the vaccine.; Test Name: Blood work; Result Unstructured Data: Test Result:Unknown result; Comments: Her daughter had blood work done.
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2079626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MA
Alter: 21,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 01.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: UN / UN

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

C-reactive protein increased Cardiac imaging procedure abnormal Electrocardiogram abnormal Electrocardiogram normal Fibrosis Myocarditis Pleuritic pain SARS-CoV-2 test negative Scar Troponin

Symptomtext

Patient received pfizer vaccine on 4/21/21 and 5/19/21 and the booster dose with moderna vaccine on 12/1/21. patient presented to hospital with pleuritic chest pain, troponin leak and EKG changes most c/f myopericarditis secondary to covid booster. troponin: 686-> 791 -> 880, initial EKG: diffuse STE, not seeing any PR depressions, repeat ECG improved. Covid negative. CRP 24.3. Cardiac MRI revealed myopericarditis and patient was treated with ibuprofen and colchicine and symptoms completely resolved within 2 days.

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Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: Impression on mri cardiac imaging done on 12/6/21: Overall, the LGE pattern is consistent with myocarditis. There is no definitive edema on T2 weighted images; thus, findings may represent fibrosis/scar. However, 6 months follow-up CMR is recommended to assess the evolution.
Aktuelle Erkrankungen: N/A
Vorgeschichte: ADHD, MDD, PCOS
Andere Medikamente: bupropion, adderall, melatonin, omega3, multivitamin
Allergien: hydrocodone
Vorherige Impfungen: -

VAERS 2059012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: AZ
Alter: 47,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 20.08.2021
Beginn: 21.10.2021
Tage bis Beginn: 62,0
Dosis: 3
Route/Site: SYR / LA

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

Bundle branch block left Cardiac stress test Catheterisation cardiac normal Echocardiogram Ejection fraction decreased Electrocardiogram ambulatory Glycosylated haemoglobin increased Hemiparesis Laboratory test Liver function test increased Magnetic resonance imaging heart Renal impairment Syncope

Symptomtext

Syncope followed by ER visit determined Left Bundle Branch Block Cardiology follow up - Holter Monitor, Stress Test and Echo - Low Normal EF 50% Cath Lab visit - Clean Cardiac MRI - Low EF Left side weakness

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 10/21 - ER visit ECK and Labs 11/3 - Labs , poor renal function, high LFT and high A1C 11/18 - 5 Day holder monitor 12/21 - Echo and Stress Test 12/23 - Cardiac Cath 12/25 - More labs drawn 1/11/2022 - Cardiac MRI
Aktuelle Erkrankungen: cold, not COVID
Vorgeschichte: High BP
Andere Medikamente: Losartin 100 Proscar 1.25 Nexium Loratadine Iron Multi vitamin B complex Vitamin c, d
Allergien: None
Vorherige Impfungen: -

VAERS 2028849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: AZ
Alter: 36,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 30.08.2021
Beginn: 01.09.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Computerised tomogram Dyspnoea Hypoaesthesia Pain in extremity Pyrexia Respiration abnormal Thrombosis Ultrasound scan

Symptomtext

Shortness of breath, sore arm, fever, numbness of arm. Symptoms went away except the shortness of breath. After second shot symptoms got worse. Arm and face went numb. Went to ER and they found two blood clots. Lungs aren?t filling with oxygen and now on inhalers. Symptoms are still going on since shots.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultrasound, CT scan, bloodwork
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1946712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 20,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Dyspnoea Electrocardiogram Myocarditis Ultrasound scan X-ray

Symptomtext

Myocarditis, chest pain, shortness of breath. Chest pain starting 15 hours after vaccination. Diagnosis 2 days later in hospital.

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Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: EKG (11/22/2021) (11/23/2021) (12/10/2021) Ultrasound (11/22/2022) XRay (11/22/2021)
Aktuelle Erkrankungen: -
Vorgeschichte: None
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1936352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: AZ
Alter: 49,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 01.09.2021
Beginn: 01.11.2021
Tage bis Beginn: 61,0
Dosis: 1
Route/Site: SYR / RA

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

Blood pressure increased Chest discomfort Dyspnoea Electrocardiogram normal Heart rate abnormal Lethargy Myalgia Myocarditis Pain Palpitations Sleep disorder

Symptomtext

9/1/2021 - post vaccine ~ 7 hours: lethargy, muscle and body aches - extremely painful, hurt to sleep, chest pressure, shortness of breath, heart palpitations. 48 hours post vaccine - all symptoms except SOB, chest pressure and heart palps resolved. Sought Cardiovascular work up - EKG normal, resting heart rate 100 (completely abnormal for myself), elevated BP. Per Cardiologist - presentation appeared to be in line with myocarditis. Recommended f/u if symptoms do not resolve.

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Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: EKG
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Sertraline daily, 100mg
Allergien: None
Vorherige Impfungen: -

VAERS 1916774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 35,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 04.06.2021
Beginn: 06.06.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Adverse reaction Bell's palsy Chills Condition aggravated Eyelid function disorder Hypoaesthesia Illness Paraesthesia Paralysis Pyrexia Sensory loss Taste disorder

Symptomtext

Within 36 hours of receiving the 2nd dose of vaccine, in addition to the usual side effects of fever, chills, and illness I also developed an adverse reaction which triggered me to have a full-blown episode of Bell's palsy on the entire right side of my body. This was concentrated particularly on my face and affected my eyelid (opening/shutting), tongue (sense of taste) and included paralysis, loss of sensation, tingling, and numbness. This lasted for approximately 3 weeks and has not since fully recovered to 100% from before the vaccine. I do have a history of Bell's palsy but the last time I had an episode was over 15 years ago.

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Went to an Urgent Care and was diagnosed and prescribed steroids on 6/6/21.
Aktuelle Erkrankungen: n/a
Vorgeschichte: Bell's palsy
Andere Medikamente: n/a
Allergien: penecillin
Vorherige Impfungen: -

VAERS 1915822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: AZ
Alter: 43,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 27.08.2021
Beginn: 05.11.2021
Tage bis Beginn: 70,0
Dosis: UNK
Route/Site: - / -

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

Hypoaesthesia Pain in extremity Paraesthesia Peripheral coldness Peripheral swelling Skin discolouration Superficial vein thrombosis Ultrasound Doppler abnormal

Symptomtext

numbness and tingling in hands, hands also turned purple and cold. lasted about 6 hours. Later leg pain and swelling, superficial thrombophlebitis

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Praegender Schweregrund: Superficial vein thrombosis
Hospital-Tage: -
Labordaten: bilateral ultrasound of the leg veins
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: raw onions
Vorherige Impfungen: -

VAERS 1879590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 08.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Bone swelling Diarrhoea Fatigue Loss of consciousness Pain Vaccination site pain Vomiting

Symptomtext

Vomiting; Diarrhea; She passed out; Woke up all achy; Tired; sore at the injection site; Felt like they hit a bone/ swollen; This is a spontaneous report from a contactable consumer (patient). A 67-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 3 via an unspecified route of administration, administered in Deltoid Right (reported as right shoulder/right arm) on 08Oct2021 between 10am to noon (Batch/Lot Number: EW0186; Expiration Date: Nov2021) at age of 67-years-old as DOSE 3 (BOOSTER), SINGLE for COVID-19 immunisation. Medical history was none. Concomitant medication included influenza vaccine (FLU SHOT) taken for immunization within 4 weeks. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 on 19Dec2020 (Batch/Lot Number: EJ1685; Expiration Date: 31Mar2021) and dose 2 on 09Jan2021 (Batch/Lot Number: EL0142; Expiration Date: 31Mar2021) for COVID-19 immunisation. Vaccination facility type was hospital. No additional vaccines administered on same date of the Pfizer suspect. No AE following prior vaccinations. No family medical history relevant to AE. The patient experienced passed out on 09Oct2021 with outcome of unknown, woke up all achy on 09Oct2021 with outcome of recovered in Oct2021, tired on 09Oct2021 with outcome of recovered in Oct2021, vomiting on 09Oct2021 17:00 with outcome of recovered in Oct2021, diarrhea on 09Oct2021 17:00 with outcome of recovered in Oct2021, felt like they hit a bone/swollen on 2021 with outcome of unknown. AE require a visit to emergency room and not admitted to the hospital. Clinical course reported as follow: Patient had the Pfizer COVID booster shot on 08Oct2021 and the following morning she woke up all achy and tired, sore at the injection site. Then it went to vomiting and diarrhea and she went to the ER. First two shots went very smoothly. Felt like they hit a bone when she was given the booster injection, it was hurting, it was swollen and sore for a week. She passed out on 09Oct2021 and her husband called an ambulance and she went to ER and was kept till the morning. Confirmed she was not admitted, they kept her in the ER. 1700 was when vomiting and diarrhea started on 09Oct2021, it only lasted for a day or two. Put patient on iv something for the vomiting. No relevant tests. Follow-up attempts are completed. No further information is expected.

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

VAERS 1872700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 16.11.2021
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: ja Erholt: ja

Anxiety Feeling of body temperature change Presyncope

Symptomtext

Vaso/vagal response with anxiety, hot/cold Encouraged laying on the floor with feet on chair but anxiety prevented a prolonged laying time Hydrated with water, spoke calmly and tried to engage patient in conversation Gave 25mg diphenhydramine at 15 minute intervals twice. Decided to call the ambulance

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Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Unknown Done in ER patient was discharged 4 hours later
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1861310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 28.09.2021
Beginn: 04.11.2021
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: SYR / LA

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

Bone densitometry Pain in extremity Sleep disorder Thrombosis

Symptomtext

I have the blood clot in my left leg, and I've been off blood thinners since April 28, 2021. In the last couple of weeks, I started having greater pain in my left calf. And the pain was going up my leg and it would wake me up. I kept thinking that it would get better, but it gradually got worse. So, I called my doctor and she ordered me to get an ultrasound to see if I had another blood clot in the same leg.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Bone density week or so ago no results back yet.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension Chronic migraines. Asthma Thalassemia Environmental allergies DVT in the left calf Bilateral occipital neuralgia Heart failure
Andere Medikamente: Bayer Aspirin Amlodipine Cetirizine Breo Ellipta Sumatriptan Methocarbamol Ondansetron EPIPEN Albuterol sulfate Furosemide Prednisone
Allergien: Shrimp Fish Any seafoods Peanuts Sensitivities to food Iodine contrast dye Codeine Divalproex Fish containing products Influenza virus vaccines Penicillin Phenergan Singular Topamax
Vorherige Impfungen: Influenza vaccinations - weakness and numbness on the whole right side of the body.

VAERS 1829194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: AZ
Alter: 41,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 17.09.2021
Beginn: 18.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain lower Alopecia Blood test Cardiac monitoring Dermatitis Dry skin Echocardiogram Electrocardiogram Fatigue Feeling abnormal Memory impairment Nocturia Pain Pain of skin Pollakiuria Pruritus Seizure Sleep disorder

Symptomtext

Severe Fatigue as of 09/18/2021- Continuing to increase daily 09/20/2021- increased fatigue and tachycardia with PVC?s 10/04/2021- Syncope incident with seizure to follow. Overnight hospital monitoring. EKG, echocardiograph, blood tests, 21 day heart monitoring. Continuing symptoms of- Foggy brain Forgetfulness Body Achy when I lay down or sit. PVC?s Continuing Weight gain Skin itchy/ dry Lower/ left side abdomen cramping Hair loss Fatigue Wake up in the middle of the night having to urinate. Having to urinate more often than normal. Inflammation/ painful skin

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Praegender Schweregrund: Seizure
Hospital-Tage: 1,0
Labordaten: EKG Echocardiogram Blood tests
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic headaches Raynaud?s Phenomenon
Andere Medikamente: Topiramate 50 mg Escitalopram 5 mg Vitamin D Zinc CoQ10 Biotin Magnesium 250 mg
Allergien: Epinephrine Lactose intolerant Eggs- intestinal issues
Vorherige Impfungen: -

VAERS 1359307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 23.05.2021
Beginn: 24.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Abnormal faeces Asthenia Blood pressure decreased Malaise Nausea Fall Head discomfort Presyncope SARS-CoV-2 test Vision blurred Vomiting Visual impairment

Symptomtext

About 24 hours after my second dose of Covid vaccine, I felt strong nausea and was very close to fainting: my head felt heavy, sudden weakness, losing control of the environment, my vision blackened,; About 24 hours after my second dose of Covid vaccine, I felt strong nausea and was very close to fainting: my head felt heavy, sudden weakness, losing control of the environment, my vision blackened,; About 24 hours after my second dose of Covid vaccine, I felt strong nausea and was very close to fainting: my head felt heavy, sudden weakness, losing control of the environment, my vision blackened,; About 24 hours after my second dose of Covid vaccine, I felt strong nausea and was very close to fainting: my head felt heavy, sudden weakness, losing control of the environment, my vision blackened,; About 24 hours after my second dose of Covid vaccine, I felt strong nausea and was very close to fainting: my head felt heavy, sudden weakness, losing control of the environment, my vision blackened,; collapsed in bed before hitting the floor; Blood pressure Drop; Few minutes later urge to vomit (spasm); This is a spontaneous report from a contactable consumer (patient). A 50-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EW0186; Expiration Date: 31Aug2021), via intramuscular route of administration in right arm on 23May2021 at 09:15 (at the age of 50 years old, not pregnant at the time of vaccination) as dose 2, single for covid-19 immunisation. Medical history included hypothyroidism and family medical history included hypertension, stroke, heart attack, diabetes mellitus. The patient had known allergies penicillin, cantaloupe. Concomitant medications the patient received within 2 weeks of vaccination included levothyroxine sodium (SYNTHROID), 75mg for thyroid disorder; ascorbic acid, betacarotene, biotin, calcium, chlorine, chromium, copper, cyanocobalamin, dl-alpha tocopheryl acetate, folic acid, iodine, magnesium, manganese, molybdenum, nickel, nicotinamide, pantothenic acid, phosphorus, phytomenadione, potassium, pyridoxine hydrochloride, retinol, riboflavin, selenium, silicon, thiamine, vanadium, vitamin d nos, xantofyl, zinc (multivitamin +50); biotin; ascorbic acid (VITAMIIN C); colecalciferol (VITAMIN D 3). Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EN5318), via intramuscular route of administration in left arm on 02May2021 at 10:00 AM (at the age of 50 years old) for covid-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. On 24May2021 at 09:00 AM, about 24 hours after second dose of Covid vaccine, she felt strong nausea and was very close to fainting: her head felt heavy, sudden weakness, losing control of the environment, her vision blackened, she collapsed in bed before hitting the floor, but remained conscious. A minute or so later she had the urge to throw up but nothing came out, then she had a normal bowl movement, took 1 tylenol 500 mg, and went to bed to rest. Strong nausea followed by vison darkness, loss of environment control, her head felt heavy, blood pressure drop on 24May2021, almost collapsed on the floor. Few minutes later urge to vomit (spasm). The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 23Jun2020 Other. no relevant tests were performed. Autopsy not performed. The patient did not received treatment due to the events. The outcome of blood pressure drop, few minutes later urge to vomit (spasm) was unknown, presyncope was recovered on an unspecified date in 2021, while with other events was recovering. Follow-Up (29Jul2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 20200623; Test Name: Saliva COVID Test; Result Unstructured Data: Test Result:Negative; Comments: Other
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes; Fruit allergy; Heart attack; Hypertension; Hypothyroidism; Penicillin allergy; Stroke
Andere Medikamente: SYNTHROID; multivitamin +50; BIOTIN; VITAMIIN C; VITAMIN D 3
Allergien: -
Vorherige Impfungen: -

VAERS 1359307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 23.05.2021
Beginn: 24.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: OT / RA

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

Abnormal faeces Asthenia Blood pressure decreased Malaise Nausea Fall Head discomfort Presyncope SARS-CoV-2 test Vision blurred Vomiting Visual impairment

Symptomtext

About 24 hours after my second dose of Covid vaccine, I felt strong nausea and was very close to fainting: my head felt heavy, sudden weakness, losing control of the environment, my vision blackened,; About 24 hours after my second dose of Covid vaccine, I felt strong nausea and was very close to fainting: my head felt heavy, sudden weakness, losing control of the environment, my vision blackened,; About 24 hours after my second dose of Covid vaccine, I felt strong nausea and was very close to fainting: my head felt heavy, sudden weakness, losing control of the environment, my vision blackened,; About 24 hours after my second dose of Covid vaccine, I felt strong nausea and was very close to fainting: my head felt heavy, sudden weakness, losing control of the environment, my vision blackened,; About 24 hours after my second dose of Covid vaccine, I felt strong nausea and was very close to fainting: my head felt heavy, sudden weakness, losing control of the environment, my vision blackened,; collapsed in bed before hitting the floor; Blood pressure Drop; Few minutes later urge to vomit (spasm); This is a spontaneous report from a contactable consumer (patient). A 50-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EW0186; Expiration Date: 31Aug2021), via intramuscular route of administration in right arm on 23May2021 at 09:15 (at the age of 50 years old, not pregnant at the time of vaccination) as dose 2, single for covid-19 immunisation. Medical history included hypothyroidism and family medical history included hypertension, stroke, heart attack, diabetes mellitus. The patient had known allergies penicillin, cantaloupe. Concomitant medications the patient received within 2 weeks of vaccination included levothyroxine sodium (SYNTHROID), 75mg for thyroid disorder; ascorbic acid, betacarotene, biotin, calcium, chlorine, chromium, copper, cyanocobalamin, dl-alpha tocopheryl acetate, folic acid, iodine, magnesium, manganese, molybdenum, nickel, nicotinamide, pantothenic acid, phosphorus, phytomenadione, potassium, pyridoxine hydrochloride, retinol, riboflavin, selenium, silicon, thiamine, vanadium, vitamin d nos, xantofyl, zinc (multivitamin +50); biotin; ascorbic acid (VITAMIIN C); colecalciferol (VITAMIN D 3). Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EN5318), via intramuscular route of administration in left arm on 02May2021 at 10:00 AM (at the age of 50 years old) for covid-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. On 24May2021 at 09:00 AM, about 24 hours after second dose of Covid vaccine, she felt strong nausea and was very close to fainting: her head felt heavy, sudden weakness, losing control of the environment, her vision blackened, she collapsed in bed before hitting the floor, but remained conscious. A minute or so later she had the urge to throw up but nothing came out, then she had a normal bowl movement, took 1 tylenol 500 mg, and went to bed to rest. Strong nausea followed by vison darkness, loss of environment control, her head felt heavy, blood pressure drop on 24May2021, almost collapsed on the floor. Few minutes later urge to vomit (spasm). The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 23Jun2020 Other. no relevant tests were performed. Autopsy not performed. The patient did not received treatment due to the events. The outcome of blood pressure drop, few minutes later urge to vomit (spasm) was unknown, presyncope was recovered on an unspecified date in 2021, while with other events was recovering. Follow-Up (29Jul2021): Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 20200623; Test Name: Saliva COVID Test; Result Unstructured Data: Test Result:Negative; Comments: Other
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes; Fruit allergy; Heart attack; Hypertension; Hypothyroidism; Penicillin allergy; Stroke
Andere Medikamente: SYNTHROID; multivitamin +50; BIOTIN; VITAMIIN C; VITAMIN D 3
Allergien: -
Vorherige Impfungen: -

VAERS 1808216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Anaphylactic reaction Chest discomfort Dyspnoea Palpitations

Symptomtext

Patient had palpitations while driving following vaccine. She reported chest tightness and shortness of breath similar to that of an anaphylactic reaction she had previously with a blood transfusion. Reports not feeling well for a few hours following the event.

Weitere VAERSDATA-Felder

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

VAERS 1381819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 15,0
Geschlecht: M
Eingang: 13.10.2021
Impfdatum: 04.06.2021
Beginn: 07.06.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: - / LA

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

Brain natriuretic peptide normal Chest pain Immunoglobulin therapy Inflammatory marker increased Magnetic resonance imaging heart Chills Echocardiogram Electrocardiogram Headache Electrocardiogram abnormal Laboratory test Myocarditis Pericarditis Pain Troponin I increased Myocardial oedema N-terminal prohormone brain natriuretic peptide increased Nausea

Symptomtext

3 days after vaccine presented with acute chest pain, nausea, vomiting, elevated inflammatory markers, extremely elevated Troponin. MRI and clinical picture dx myocarditis treated with IVIG and prednisone.

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Praegender Schweregrund: Myocarditis
Hospital-Tage: 4,0
Labordaten: Trop I: 6/7/21: 33, 31 TRop T: 6/8/21" 2208 2266 6/9 3557 4455 6/19 1174 6/11 751 6/13 138 Trop I: 6/18 0.1, 8/25 0.04 NT-BNP 6/8 664.7 BNP 6/18 38 6/13 cMRI: VENTRICLES: On T2 weighted imaging, there is abnormal increased signal intensity of the left ventricular myocardium, greater than 2 times the signal intensity of the skeletal muscle, representing edema. This involves the mid wall and the sub epicardial wall of the myocardium in the septal wall, inferior septal wall, between the mid ventricle and the apex and also slightly involve the septal wall and the septal inferior wall near the base. There is slight enhancement on the immediate post-contrast imaging but there is too much motion and flow artifacts. On the viability sequence, there is evidence of late gadolinium enhancement in the sub epicardial and mid wall in the same distribution as the edema seen on T2 weighted imaging. These findings together meets the criteria for the diagnosis of myocarditis.
Aktuelle Erkrankungen: none
Vorgeschichte: BMI 27
Andere Medikamente: none
Allergien: none- had prior reaction to mussels but neg mollusk IgE
Vorherige Impfungen: -

VAERS 1381819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 15,0
Geschlecht: M
Eingang: 13.10.2021
Impfdatum: 04.06.2021
Beginn: 07.06.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Brain natriuretic peptide normal Chest pain Immunoglobulin therapy Inflammatory marker increased Magnetic resonance imaging heart Chills Echocardiogram Electrocardiogram Headache Electrocardiogram abnormal Laboratory test Myocarditis Pericarditis Pain Troponin I increased Myocardial oedema N-terminal prohormone brain natriuretic peptide increased Nausea

Symptomtext

3 days after vaccine presented with acute chest pain, nausea, vomiting, elevated inflammatory markers, extremely elevated Troponin. MRI and clinical picture dx myocarditis treated with IVIG and prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 4,0
Labordaten: Trop I: 6/7/21: 33, 31 TRop T: 6/8/21" 2208 2266 6/9 3557 4455 6/19 1174 6/11 751 6/13 138 Trop I: 6/18 0.1, 8/25 0.04 NT-BNP 6/8 664.7 BNP 6/18 38 6/13 cMRI: VENTRICLES: On T2 weighted imaging, there is abnormal increased signal intensity of the left ventricular myocardium, greater than 2 times the signal intensity of the skeletal muscle, representing edema. This involves the mid wall and the sub epicardial wall of the myocardium in the septal wall, inferior septal wall, between the mid ventricle and the apex and also slightly involve the septal wall and the septal inferior wall near the base. There is slight enhancement on the immediate post-contrast imaging but there is too much motion and flow artifacts. On the viability sequence, there is evidence of late gadolinium enhancement in the sub epicardial and mid wall in the same distribution as the edema seen on T2 weighted imaging. These findings together meets the criteria for the diagnosis of myocarditis.
Aktuelle Erkrankungen: none
Vorgeschichte: BMI 27
Andere Medikamente: none
Allergien: none- had prior reaction to mussels but neg mollusk IgE
Vorherige Impfungen: -

VAERS 1776614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: IL
Alter: 60,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 08.07.2021
Beginn: 28.07.2021
Tage bis Beginn: 20,0
Dosis: UNK
Route/Site: SYR / LA

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

Amnesia Asthenia Computerised tomogram head normal Dizziness Electroencephalogram normal Laboratory test Loss of consciousness Lumbar puncture normal Syncope Viral test negative West Nile virus test negative

Symptomtext

Jul 29, 2021 Felt weak & fainted twice at night, had to call an ambulance. Jul 29, 2021 Went into the emergency room at Hospital feeling weak and dizzy. Jul 29- October 1, 2021 Constant dizziness October 1, 2021 Loss of consciousness & memory. October 1-7, 2021 Hostpital, multiple tests run was. Discharged from the hospital without a diagnosis.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 7,0
Labordaten: Underwent two different lumbar punctures on 10/2 and 10/5 and both did not reveal bacterial meningitis. Studies for a virus did not reveal any findings at the time of discharge. West Nile results are negative. CT head was negative. CTA head was negative. Electroencephalogram was negative for seizure-like activity. Neurology and infectious disease were following my case. Received intravenous antibiotics during your hospital stay. Were deemed stable for discharge per both neuro and infectious disease.
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 1770573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NH
Alter: 17,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 16.05.2021
Beginn: 16.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Breast enlargement Chills Fatigue Heart rate Loss of consciousness Lymphadenopathy Migraine Postural orthostatic tachycardia syndrome

Symptomtext

passing out; fatigue; Migraine; postural orthostatic tachycardia syndrome/symptoms of headache, tachycardia, dizziness and felt horrible; Breast enlargement; chills; Lymphnode swelling in armpit; This is a spontaneous report from a contactable consumer (mother). A 17-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 16May2021 12:00 at 17-year-old (Batch/Lot number EW0186) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included ongoing Cholinergic urticaria. The patient's concomitant medications were not reported. The patient previously took first dose of bnt162b2, on right arm on 18Apr2021 09:00 at 17-year-old for covid-19 immunisation and experienced overtired (18Apr2021 to 20Apr2021). 2 months after they reported to as 2 in half weeks after getting the vaccine got symptoms of headache, tachycardia, dizziness and felt horrible. She was diagnosed with POTS(postural orthostatic tachycardia syndrome). Her symptoms have been debilitating at times. Asking if Pfizer has any reports on this in younger people after getting the vaccine. Stated that no medication is working very well as they are trying to treat these symptoms. Asking if symptoms will worsen if she gets covid because she responded this way to the vaccine. Also information on booster shot for people with POTS. Asking where she could see more information about clinical trial. Stated that non information has Pfizer has provided from the life changing event that her daughter is experiencing is appalling. Caller states she is calling about the Pfizer vaccine, reclarified as the Pfizer Covid vaccine. Caller states she is calling about her daughter, who got the second dose of vaccine. Caller states 4 weeks, her daughter woke up on 11Jun2021 with a severe headache, and ended up in the emergency room. Caller states she also was passing out and felt like a light switch went off. Caller states her daughter has no prior medical history. Caller states her daughter has seen a series of doctors and she, herself, is feeling desperate. Caller states she was later diagnosed with POTS(postural orthostatic tachycardia syndrome). Caller states her daughter also had dizziness and tachycardia. Caller states her daughter is now followed by a cardiologist and a neurologist. Caller states she was calling various institutions, and at the PRIVACY, she cannot get an appointment for 14 months, because she was told they are inundated with post vaccine injury cases and post Covid cases of POTS. Caller states her daughter is a national level swimmer, and she got her daughter in to see a doctor, who assumed she had a Migraine, and started her on medication, which had no effect. Specifics identified later in report. Caller states her daughter had dizziness, and the room was spinning, and she had an MRI (Magnetic resonance imaging), which was normal. Caller states her daughter was referred to a neurologist. Caller states her daughter was diagnosed with POTS by a neurologist at PRIVACY on 21Jul2021. Caller states her daughter did see a cardiologist, who did various tests, and she was ruled out for myocarditis, and all the tests came back normal. Caller states her daughter still has tachycardia, and she is constantly dizzy and her heart rate will go from 50 to 100 without warning and she feels like she is going to pass out. Caller states her daughter feels horrible and can't really function. Caller states that her husband is in the medical field and she does understand that reactions and POTS can occur. Caller states she is looking for any studies that can provide information. Caller states she is looking for information, to find out how she can understand any data on POTS and the vaccines, what the findings are, or if she can be directed to any studies that are being done. Caller states her daughter's life has changed overnight. Caller states she is just trying to get information. Caller states her daughter was on medications to treat some of the symptoms but they did not work. Caller states another reason for reaching out today to Pfizer, is she understands the recent FDA decision to provide boosters to certain population. Caller states no one truly knows the data well enough to know how the vaccines, affect children. Caller states that before they put another vaccine into her daughter's arm, her daughter has gotten a medical exemption, because of the way she responded to the Covid vaccine. Caller asks now, because of her reactions, will her daughter have worsened symptoms if she contracts Covid? Caller states that her daughter did not have any issues prior to the vaccination. Caller clarifies from earlier in call that the doctors tried her daughter on a two medication trial for her headache. First medication: Caller states it was a migraine medication that did not work. Caller states the medication should have worked quickly if her daughter truly had a migraine. Caller states she does not know the name of the medication. Caller states the doctor determined quickly that her daughter did not have a traditional migraine. Second medication: Gabapentin, titrating dose: 100mg for 3 days, 200mg for 3 days, 300mg for 3 days. Caller states this medication did not work. Caller states her daughter had a reaction and it actually made her headaches worse. Caller states her daughter felt more dizzy. Caller states she just went through all the medications that they are not using and disposed of any medications not used. Caller states later that after the second vaccine, her daughter had chills, lymph node swelling in caller thinks left armpit, and she thinks, left breast enlargement (probably in the morning). Caller states it was on the same side as vaccine, but cannot remember if it was on the left or right side. The caller understood the risks and common side effects. The development of POTS triggers in her system. She said when it is in the percentage it's lifechanging. She developed tachycardia; debilitating dizziness; headaches that are excruciating. She even had an MRI (Magnetic resonance imaging) done and she didn't have a brain tumor. There are severe symptoms. She said they are a drug company they are collecting data all the time. They are compiling information; someone she spoke with before said they are seeing clusters of symptoms but they are not calling it POTS. She has tachycardia, fatigue and headaches. They are not getting diagnosed. She know they have this. She wanted to know the ideology of this going forward. She wanted to know if her daughter gets a booster; both cardiologist and neurologist said not to. They are looking for medications. She's on 2 cardiac meds that are not helping. What are they seeing in POTS diagnosis; if there is a study for her. They are being followed by people are taking the information. She didn't know if it's going to be compiled. It's frustrating. The drug company have got studies and investigators. They are acting like nothing is going on. Other have a POTS clinic and it's inundated with post covid POTS and vaccine related POTS. It's incredibly frustrating. Where can she be followed? She was frantically looking for help. Agency as been more helpful. They gave her specific information on places that are studying this and who to contact. The CDC does nothing: they say report an adverse event and look for studies. The website: pfizer vaccine/research: that website doesn't give you contact person. She and her husband are not antivaxxers. They are grateful for the company, but there has to be moral responsibility. It's not being talked about. When it's presented you are sent through these dead end holes. If it was the precedents child experiencing this they would be doing everything to help. She wanted useful information. She knew that's not their fault. Caller was upset there wasn't more information Pfizer MI could present. She was upset that they are collecting this information but it isn't available and it's not being talked about. The patient experienced passing out (hospitalization) on an unspecified date with outcome of unknown, postural orthostatic tachycardia syndrome/symptoms of headache, tachycardia, dizziness and felt horrible on 11Jun2021 with outcome of not recovered, chills on 16May2021 20:00 with outcome of recovered on 17May2021, breast enlargement on 17May2021 with outcome of recovering, lymphnode swelling in armpit on 16May2021 with outcome of recovered, fatigue on an unspecified date with outcome of unknown, migraine on an unspecified date with outcome of unknown. No follow-up attempts are needed. No further information is expected.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Name: heart rate; Result Unstructured Data: Test Result:50; Comments: will go from 50 to 100 without warning; Test Name: heart rate; Result Unstructured Data: Test Result:100; Comments: will go from 50 to 100 without warning; Test Name: MRI; Result Unstructured Data: Test Result:normal; Test Name: MRI; Result Unstructured Data: Test Result:she didn't have a brain tumor
Aktuelle Erkrankungen: Cholinergic urticaria
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1765040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CO
Alter: 50,0
Geschlecht: M
Eingang: 06.10.2021
Impfdatum: 28.08.2021
Beginn: 22.09.2021
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: IM / RA

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

Bell's palsy Facial paralysis Tooth abscess

Symptomtext

Patient developed sudden onset of left sided facial nerve paralysis, consistent with Bell's Palsy on 9/22/2021. He was treated with oral steroids through Urgent Department on 9/22/2021. He saw me in our clinic on 9/27/2021 and was also started on antibiotics for left upper molar abscess. He continues to have facial nerve paralysis.

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: No medical tests or lab results.
Aktuelle Erkrankungen: None known
Vorgeschichte: Tobacco Dependence
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1761262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: VA
Alter: 38,0
Geschlecht: M
Eingang: 05.10.2021
Impfdatum: 04.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Fatigue Pyrexia Seizure

Symptomtext

First Shot: Mild fatigue Second Shot: Mild fatigue and approximately 10 hours later convulsions with fever reaching over 100 degrees per oral testing.

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Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Seasonal Allergies
Vorgeschichte: Bad back and bad kidneys, genetic. Several other undiagnosed afflictions as well.
Andere Medikamente: Zyrtec, Fish Oil, and Ambien. Monthly Allergy shots
Allergien: NASIDS
Vorherige Impfungen: Nasal Flu shot in 2015, unknow type or maker.

VAERS 1745256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0186

schwer

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 29.09.2021
Impfdatum: 02.07.2021
Beginn: 02.07.2021
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 Blood gases Blood magnesium Chest X-ray Dyspnoea Full blood count Heart rate increased Hypoaesthesia Hypoaesthesia oral Metabolic function test Urine analysis

Symptomtext

After got the vaccine in 20 minutes I felt numbness of my face and lips, I took epi pen X 2 by myself and my heart rate was high with breathing difficulty. I was rushed to emergency department and treated there for anaphylactic reaction. They gave me benadryl 50 mg IV,Famotidine, solu-medrol IV, solu-cortef IV, oxygen mask and IV fluid

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: X ray chest, CBC, CHEM7,Blood gas, UA,Magnesium serum
Aktuelle Erkrankungen: Breast cancer
Vorgeschichte: Lymphedema
Andere Medikamente: none
Allergien: flu vaccine, Levofloxin, Lobster
Vorherige Impfungen: flu vaccine on 2014

VAERS 1745247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: WI
Alter: 46,0
Geschlecht: M
Eingang: 29.09.2021
Impfdatum: 05.08.2021
Beginn: 13.08.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram Deep vein thrombosis Ultrasound Doppler Venogram

Symptomtext

DVT with PE with no hx of thrombosis or history significant risk factors for dvt

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 3,0
Labordaten: leg ultrasound venogram and CTA
Aktuelle Erkrankungen: right knee arthritis
Vorgeschichte: cyclic vomiting syndrome
Andere Medikamente: pantoprazole
Allergien: none
Vorherige Impfungen: -

VAERS 1735609

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

schwer

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 26.09.2021
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Arthralgia Electric shock sensation Eructation Feeling abnormal Hypoaesthesia Musculoskeletal discomfort Nausea Paraesthesia

Symptomtext

I was Injected @ 2:30pm and about 2:35 i started to feel my right hand and arm tingling and going numb. Next my back started to tense up. About 2:38pm i started ti feel extremely nauseous and felt as if i had to constantly burp. About 2:40pm i started to get electric shock on the right side of my upper back. I would get a shock about every 3min. I continued to feel this way while waiting the required 15min. Driving home i felt very spacey and as if i was incapable of driving. This continued the entire day and the following day 9/23/21. Now it?s 9/25 and I?m experiencing terrible joint pain on the right side of my bad. My fingers on the right hand and right knee are the worst. I have not had any issues with joint pain in either places until i received the covid vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Will be following up with my PCP ASAP
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1682701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: WV
Alter: 19,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 31.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Asthma Chest pain Dehydration Diarrhoea Dyspnoea Blood test Chest X-ray Computerised tomogram Electrocardiogram Headache Loss of consciousness Menstrual disorder SARS-CoV-2 test Vaccination site rash Rash Vomiting

Symptomtext

blacked out; throwing up to point of severe dehydration; Shortness of breathe caused asthma to flare up; Shortness of breathe caused asthma to flare up; throwing up to point of severe dehydration; chest pain; rash on arm of injection; diarrhea; affected menstrual cycle; Severe headache; This is a spontaneous report from a contactable consumer (patient). A 19-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 at the age of 19-years-old via an unspecified route of administration, administered in Arm Left on 31Aug2021 11:15 (Batch/Lot Number: EW0186) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included gastrointestinal issues and bronchial asthma from unknown dates. The patient has no known allergies. Concomitant medication included ethinylestradiol, norgestrel (LOW-OGESTREL-28) taken for an unspecified indication, start and stop date were not reported. On 31Aug2021 12:45, the patient experienced Shortness of breathe caused asthma to flare up, blacked out, throwing up to point of severe dehydration, chest pain, rash on arm of injection, diarrhea, affected menstrual cycle and severe headache. The events resulted in Emergency room/department or urgent care. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 31Aug2021. Therapeutic measures were taken as a result of the events which included IV fluid for dehydration and rescue inhaler. The patient recovered with sequel from the events on an unspecified date. The lot number for the vaccine, [BNT162B2] was not provided and will be requested during follow-up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210831; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bronchial asthma; Gastrointestinal disorder
Andere Medikamente: LOW-OGESTREL-28
Allergien: -
Vorherige Impfungen: -

VAERS 1682701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: WV
Alter: 19,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 31.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthma Chest pain Dehydration Diarrhoea Dyspnoea Blood test Chest X-ray Computerised tomogram Electrocardiogram Headache Loss of consciousness Menstrual disorder SARS-CoV-2 test Vaccination site rash Rash Vomiting

Symptomtext

blacked out; throwing up to point of severe dehydration; Shortness of breathe caused asthma to flare up; Shortness of breathe caused asthma to flare up; throwing up to point of severe dehydration; chest pain; rash on arm of injection; diarrhea; affected menstrual cycle; Severe headache; This is a spontaneous report from a contactable consumer (patient). A 19-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 at the age of 19-years-old via an unspecified route of administration, administered in Arm Left on 31Aug2021 11:15 (Batch/Lot Number: EW0186) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included gastrointestinal issues and bronchial asthma from unknown dates. The patient has no known allergies. Concomitant medication included ethinylestradiol, norgestrel (LOW-OGESTREL-28) taken for an unspecified indication, start and stop date were not reported. On 31Aug2021 12:45, the patient experienced Shortness of breathe caused asthma to flare up, blacked out, throwing up to point of severe dehydration, chest pain, rash on arm of injection, diarrhea, affected menstrual cycle and severe headache. The events resulted in Emergency room/department or urgent care. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 31Aug2021. Therapeutic measures were taken as a result of the events which included IV fluid for dehydration and rescue inhaler. The patient recovered with sequel from the events on an unspecified date. The lot number for the vaccine, [BNT162B2] was not provided and will be requested during follow-up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210831; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bronchial asthma; Gastrointestinal disorder
Andere Medikamente: LOW-OGESTREL-28
Allergien: -
Vorherige Impfungen: -

VAERS 1723624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NY
Alter: 12,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 20.09.2021
Beginn: 21.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Partial seizures

Symptomtext

Aprox 12:30pm, teh day following vaccination, patient was at school with friends and just started to stare off and not answer her friends when they addressed her. The kids said this last a few minutes and then patient answered and someone walked her to the nurse. Sounds like a focal aware seizure that she has experienced 2x during summer when her medication needed to be increased. She has not had one since July, 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Partial seizures
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diagnosed with benign childhood seizure disorder in 2016
Andere Medikamente: Oxcarbazepine 7.5mL/2xday 15 mg Lexapro
Allergien: None aware of
Vorherige Impfungen: -

VAERS 1656080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 21.09.2021
Impfdatum: 12.08.2021
Beginn: 12.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Aphasia Blood test Chills Cough Endoscopy abnormal Dizziness Dysarthria Feeling abnormal Illness Inappropriate schedule of product administration Intracranial aneurysm Paraesthesia oral Pharyngeal paraesthesia Speech disorder Vocal cord paralysis Vocal cord paresis

Symptomtext

Brain aneurysm; Can't speak, speech problems; Diagnosed with bilateral paresis of the vocal cord; Diagnosed with dysarthria/Very slurred; First Dose: 17Feb2021/Second dose: 12Aug2021; Felt a rush to the brain, wanted to cough; Tingly in the mouth; Tingly in the mouth, throat area; Problems with the head, dizziness; She is very sick; This is a spontaneous report from a contactable consumer (Patients mother) A 46-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EW0186) on 12Aug2021 at single dose via an unspecified route of administration on arm for COVID-19 immunization. Relevant medical history included kidney problems that occurred after infection in 2020. Concomitant medications were not reported. The patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: ENG200, age of vaccination 45 years) on 17Feb2021 and experienced throat irritation, oral pruritus, chest pain, oropharyngeal discomfort, aphonia, speech disorder, secretion discharge, cough, upper-airway cough syndrome, hypersensitivity, skin discoloration, white blood cell count increased, red blood cell count decreased, haemoglobin decreased, blood potassium decreased, blood chloride decreased, blood creatinine increased, blood glucose increased, alanine aminotransferase increased, dysphonia, gerd. On 12Aug2021 about 2 or 3 minutes, right after the second dose the patient a rush to the brain, then she wanted to cough. She started getting very tingly. She clarified that her mouth was tingly in the throat area. It lasted until now. She had it at the allergist office. They had told her because of the first incident that happened, she should take the vaccine in the presence of the allergist. She can't speak, and is sorry to say but, it is like someone who is mentally challenged and verbally challenged. It has stayed the same and she is not able to speak. Her diagnosis was bilateral paresis of the vocal cord, dysarthria, brain aneurysm. This diagnosis was because the patient cannot verbalize clearly. The patient's verbal language right now is very slurred and very, like a person who is mentally disabled with speech problems. The allergist gave her some prednisone and allergy medication to take. It was not very much medication. Then, they sent her home. It wasn't getting much better. Then, she started getting sicker and had problems with the head. Reporter informed that the problems with the head started on the same day, 12Aug2021 and never went away. It just stayed the same and did not bring the speech back. At the time of the reporting outcome for the event ?Felt a rush to the brain, wanted to cough' and Brain aneurysm, Problems with the head, dizziness and inappropriate schedule of vaccine administered was unknown, while outcome of other reported evens was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vocal cord paralysis
Hospital-Tage: 3,0
Labordaten: Test Name: Blood work; Result Unstructured Data: Test Result:Brain aneurysm; Test Name: MRI; Result Unstructured Data: Test Result:Brain aneurysm
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Kidney failure (kidney problems that occurred after infection in 2020.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1656080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 21.09.2021
Impfdatum: 12.08.2021
Beginn: 12.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Aphasia Blood test Chills Cough Endoscopy abnormal Dizziness Dysarthria Feeling abnormal Illness Inappropriate schedule of product administration Intracranial aneurysm Paraesthesia oral Pharyngeal paraesthesia Speech disorder Vocal cord paralysis Vocal cord paresis

Symptomtext

Brain aneurysm; Can't speak, speech problems; Diagnosed with bilateral paresis of the vocal cord; Diagnosed with dysarthria/Very slurred; First Dose: 17Feb2021/Second dose: 12Aug2021; Felt a rush to the brain, wanted to cough; Tingly in the mouth; Tingly in the mouth, throat area; Problems with the head, dizziness; She is very sick; This is a spontaneous report from a contactable consumer (Patients mother) A 46-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EW0186) on 12Aug2021 at single dose via an unspecified route of administration on arm for COVID-19 immunization. Relevant medical history included kidney problems that occurred after infection in 2020. Concomitant medications were not reported. The patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: ENG200, age of vaccination 45 years) on 17Feb2021 and experienced throat irritation, oral pruritus, chest pain, oropharyngeal discomfort, aphonia, speech disorder, secretion discharge, cough, upper-airway cough syndrome, hypersensitivity, skin discoloration, white blood cell count increased, red blood cell count decreased, haemoglobin decreased, blood potassium decreased, blood chloride decreased, blood creatinine increased, blood glucose increased, alanine aminotransferase increased, dysphonia, gerd. On 12Aug2021 about 2 or 3 minutes, right after the second dose the patient a rush to the brain, then she wanted to cough. She started getting very tingly. She clarified that her mouth was tingly in the throat area. It lasted until now. She had it at the allergist office. They had told her because of the first incident that happened, she should take the vaccine in the presence of the allergist. She can't speak, and is sorry to say but, it is like someone who is mentally challenged and verbally challenged. It has stayed the same and she is not able to speak. Her diagnosis was bilateral paresis of the vocal cord, dysarthria, brain aneurysm. This diagnosis was because the patient cannot verbalize clearly. The patient's verbal language right now is very slurred and very, like a person who is mentally disabled with speech problems. The allergist gave her some prednisone and allergy medication to take. It was not very much medication. Then, they sent her home. It wasn't getting much better. Then, she started getting sicker and had problems with the head. Reporter informed that the problems with the head started on the same day, 12Aug2021 and never went away. It just stayed the same and did not bring the speech back. At the time of the reporting outcome for the event ?Felt a rush to the brain, wanted to cough' and Brain aneurysm, Problems with the head, dizziness and inappropriate schedule of vaccine administered was unknown, while outcome of other reported evens was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vocal cord paralysis
Hospital-Tage: 3,0
Labordaten: Test Name: Blood work; Result Unstructured Data: Test Result:Brain aneurysm; Test Name: MRI; Result Unstructured Data: Test Result:Brain aneurysm
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Kidney failure (kidney problems that occurred after infection in 2020.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1682616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: IL
Alter: 52,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 14.08.2021
Beginn: 27.08.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: IM / RA

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

Anticoagulant therapy Deep vein thrombosis Fibrin D dimer increased Ultrasound Doppler abnormal

Symptomtext

DVT symptoms developed on right leg on Aug 27. Went to urgent care on Sept 1. Had d-dimer which was elevated. Was sent to the ER. Had ultrasound which determined DVT present. Started on Xarelto 15mg BID for 3 weeks then Xarelto 20 mg daily for life. Consult with Hematology made.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: D-Dimer and Bilateral lower extremity ultrasound
Aktuelle Erkrankungen: none
Vorgeschichte: Tachycardia Factor V leiden
Andere Medikamente: Metoprolol 150mg daily
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1678862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: FL
Alter: 45,0
Geschlecht: M
Eingang: 07.09.2021
Impfdatum: 18.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Asthenia Blood test normal Disorientation Electrocardiogram normal Headache Inflammation Influenza like illness Loss of consciousness Seizure Syncope Vomiting X-ray normal

Symptomtext

About 5 minutes after getting the shot I fainted. I am not sure for how long I was out since I was seated in a corner of the pharmacy, away from others. I woke up having some sort of seizure, vomiting on myself, and disoriented. I was noticed by another customer who yelled for help. The pharmacy staff came over and assisted me towels and water, and began asking me questions. I remained at the pharmacy for about 30 min before I felt strong enough to walk out and leave. The only thing they offered was to call paramedics which I refused since I have always been a very healthy individual and I was assuming this was just part of the side effects. I had flu-like symptoms, headaches, and body weakness for 4 weeks, and inflammation on the right side of my chest for 2 months. The reason why I did not report this event sooner was because I thought that the pharmacy was going to do so. Once I was able to get seen by my primary physician, she advised me to go back to pharmacy and request the VAERS report. When I realized that they had not done it, my doctor advised me to report it myself. She also concluded that I might have gotten rid of the inflammation myself after I began taking garlic pills. Currently I no longer suffer any symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: All tests came back normal since they were conducted 3 months after the shot when I was able to see my doctor. (EKG, X-Rays, Blood Work)
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Multivitamins, D3, Zinc, C Vitamin.
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1675862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: NY
Alter: 21,0
Geschlecht: M
Eingang: 06.09.2021
Impfdatum: 01.09.2021
Beginn: 06.09.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Presyncope Unresponsive to stimuli

Symptomtext

Patient developed vasovagal reaction and was unresponsive a brief moment

Weitere VAERSDATA-Felder

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

VAERS 1656602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 15,0
Geschlecht: M
Eingang: 30.08.2021
Impfdatum: 18.08.2021
Beginn: 20.08.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

C-reactive protein Cardiac monitoring Chest pain Echocardiogram Electrocardiogram Full blood count Heart rate increased Immunoglobulin therapy Intensive care Laboratory test Loss of personal independence in daily activities Myocarditis Pericarditis Red blood cell sedimentation rate Troponin increased Ventricular arrhythmia

Symptomtext

Pt recieved vaccine on 8/18/21 then on 08/20/21 had chest pain we then went to the ER. his Troponin levels kept climbing he was then admitted to hospital his chest pain was severe his troponins kept climbing he was not responding to typical treatment for pericarditis and started to have some ventricular beats that sent him to ICU he then was diagnosed with MYOPERICARDITIS and recieved Immunoglobulin.l He was in Hospital for 5 days. He has to wear a heart monitor for 1 month and can not have activity for 3 months. his troponins are still not at normal level as of 8/20/21 but he does not have chest pain. He just was able to return to school on 8/30/21 with no activity. he is on Motrin 600mg tid. when he walks his heart rate is still elevated in the 110-120's just brisk walking. but he is not in pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 5,0
Labordaten: Multiple inpatient and outpatient Labs and tests, Echos and Ekgs, many many Troponin levels, cbc chem 7 Crp Esr.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1656139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NJ
Alter: 17,0
Geschlecht: F
Eingang: 30.08.2021
Impfdatum: 27.08.2021
Beginn: 27.08.2021
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 saw down in the chair and was very nervous to get vaccinated. Father was present. Vaccine was given and nurse had patient stay in the chair for a few minutes. School cafeteria where the clinic was held was very hot; did not have air condition but fans were blowing. Cold water was given to patient. After approx 3 minutes patient stated she was feeling better and wanted to go to the waiting area. Nurse walked patient to seating area and on the way she stated she was going to vomit and then she dropped slowly to the floor and asked to lay down. Cold compress and ice pack provided. Patient never lost consciousness. EMS was called due to both siblings incident/ After approx 10 minutes school principal came with wheelchair and patient was moved to nurse office that had air conditioning. EMS checked patient and cleared to go home. Patient walked out with father and 2 siblings. Father and patient stated that she passed out after flu shot last fall as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None noted
Vorgeschichte: None noted
Andere Medikamente: None noted
Allergien: None noted on consent form
Vorherige Impfungen: Similar incident after flu shot last year

VAERS 1655830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 13,0
Geschlecht: M
Eingang: 30.08.2021
Impfdatum: 08.06.2021
Beginn: 08.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Asthma Bronchitis Chest X-ray abnormal Chills Cough Dyspnoea Enuresis Lethargy Myalgia Pyrexia Seizure Vomiting

Symptomtext

First day started with 103 degree fever, shivering and muscle pain. Getting worse with cough and lethargy continues for 5 days, on 5th day severe asthma attack, seen in urgent care and transported to ER where he received iv steroids to stabilize and x-ray found bronchitis, he also had a seizure at home and wet the bed. During this I did stay in touch with pediatrician almost daily. On day 5, my son was coughing so bad that he was vomiting and could not catch a breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Chest x-ray 06/13/2021
Aktuelle Erkrankungen: Anxiety, adhd,
Vorgeschichte: -
Andere Medikamente: Wellbutrin
Allergien: -
Vorherige Impfungen: -

VAERS 1651214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

schwer

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 17.06.2021
Beginn: 25.07.2021
Tage bis Beginn: 38,0
Dosis: 2
Route/Site: IM / LA

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

Cellulitis Electric shock sensation Herpes zoster Lymph node pain Lymphadenopathy Pruritus Swelling

Symptomtext

Shingles (trigeminal, V1) with local swelling and painful swollen lymphnodes. First diagnosed as cellulitis, given antibiotics (Cefalexon). Did not improve after several days. Suspected shingles when electrical sensations and itching in the area developed . Prescribed Valtrex, which resolved symptoms. Skin is still healing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine
Andere Medikamente: Ubrelvy (25mg) as needed
Allergien: None
Vorherige Impfungen: -

VAERS 1646846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 06.08.2021
Beginn: 01.08.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Haemorrhage SARS-CoV-2 test Thrombosis

Symptomtext

when she got her second dose on that Friday, within 2 hours, she was back to heavy bleeding.; In the last 48 hours, she started passing blood clots again; This is a spontaneous report from a contactable consumer (patient). A 48-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number EW0186) via an unspecified route of administration in right arm on 06Aug2021 (at 48 years)as single dose for covid-19 immunisation. Medical history included Covid 19 virus from Oct2020 and did have a change to her menstrual cycles after having the Covid 19 virus. She would have a period then she would skip a period, she has had 3 vaginal births (her children are 27, 21, and 13 years old). She doesn't have a history of bleeding disorders; she had big blood clots after her daughters were born especially the last one 13 years ago. Concomitant medication included cyanocobalamin (VITAMIN B12) taken for an unspecified indication, start and stop date were not reported.On 10Jul2021 (at the age of 48 years) patient took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number EW0181) in right arm for covid-19 immunisation and 9 days later she was passing large golf ball sized clots, experienced abnormal vaginal bleeding that got heavier and heavier, HCPs think maybe the type of vaccine (mRNA) led her to possibly have early diagnosis of uterine cancer, she lost so much blood had to have transfusion, she had her period a week previously so knew it wasn't time for one( It was heavy for the first 7 days, wouldn't stop, then got heavier), thickened endometrium, complex hyperplasia, was frustrated, had hemoglobin at 8/ 5.Patient got a Rubella shot when she was 18 years old (30 years ago, as reported) and she got encephalitis after the Rubella vaccine. She had severe headaches for 3 weeks. The doctor thought it was related to the Rubella vaccine.On 06Aug2021, she got her second Covid 19 vaccine and in the night (within 2 hours) she was back to heavy bleeding, she started bleeding heavily even though she took medroxyprogesterone 10 mg. She's still bleeding now after the second Covid 19 vaccine. The caller thought her bleeding was related to the Covid 19 vaccine but her doctor thinks she's crazy. In the last 48 hours (Aug2021), she started passing blood clots again. Medroxyprogesterone wasn't stopping it this time .The outcome of bleeding was not recovered; outcome of blood clots was unknown.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101023313 Same patient/Vaccine, different event, different vaccine dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 202010; Test Name: Covid-19; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Clot blood (after her daughters were born especially the last one 13 years ago); COVID-19; Irregular menstruation; Vaginal delivery (3 births (her children are 27, 21, and 13 years old))
Andere Medikamente: VITAMIN B12 [CYANOCOBALAMIN]
Allergien: -
Vorherige Impfungen: -

VAERS 1645810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: VA
Alter: 43,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 19.06.2021
Beginn: 04.07.2021
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: - / LA

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

Asphyxia Asthenia Chest pain Chills Claustrophobia Crying Depression Dizziness Dysgraphia Dyspnoea Electric shock sensation Fatigue Fear Insomnia Malaise Palpitations Tachyphrenia Tremor

Symptomtext

Shocks in her hands and feet; Like suffocating; When I get up I can't breath/Having hard time breathing; Dizziness; Trouble sleeping/Insomnia; Trouble focusing; Heart palpitations; Racing thoughts; Claustrophobia; Chest pain weakness and chills; Chest pain weakness and chills; Chest pain weakness and chills; Crying all the time; Face blue and insomnia/ she wasn't breathing, she was blue in the face; Shaking; I want relief. I am not doing well/ not feeling well; Making her more mentally depressed; scared for her life; having trouble just writing emails; This is a spontaneous report from a contactable consumer (patient). A 43-year-old female patient received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in left arm (left upper arm) on 19Jun2021 15:30 (Batch/Lot Number: EW0186) as DOSE 2, SINGLE so she could be granted immunity towards the corona virus (COVID-19 immunization). Medical history was reported none. Concomitant medications included unspecified antacids. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in left arm (left upper arm) on 26May2021 15:30 (Batch/Lot Number: EW0171) as DOSE 1, SINGLE for COVID-19 immunization; and other historical vaccines like Flu, Tetanus and measles/ mumps vaccines taken for immunization on unspecified dates. Patient had no prior vaccinations (within 4 weeks) prior to the first administration date of the suspect vaccine. Vaccine was not administered at Facility. On 04Jul2021, since early morning, the patient experienced dizziness, trouble sleeping/insomnia, having hard time breathing, trouble focusing, heart palpitations, racing thoughts, claustrophobia, chest pain weakness and chills, shocks in her hands and feet, having trouble writing emails, and crying all the time, shocks in her hands and feet, like suffocating, face blue and insomnia, shaking, not doing well/ not feeling well, making her more mentally depressed, scared for her life. The events caused hospitalization overnight from 04Jul2021 to 05Jul2021 then went to urgent care. All of them started that day and persisting, worsened and not getting better. The hospital just said they did not know and patient can leave, they did not think it was myocarditis, they checked her heart. Patient reported side effects from Pfizer covid 19 vaccine and asked if anyone having symptoms and wanted help, not sure if it will pass. Patient stated that she wished she never took it, her life has been turned upside down, she can barely function day to day and was scared. She wished to find relief. It's been a month like this. She was wondering what was going on with her body. She's been dealing with a tremendous amount of symptoms. She's barely making it from day to day. She wanted to get to the bottom of what's going on with her body since she took a experimental drug and since she has had extra side effects not in the pamphlet. She felt like she can't function, she can't work, she can barely write an email, she can barely sleep for the past 3.5 to 1 month. This experimental drug, she did not know what's in it and she would like to know when it is going to wear off. She was scared for her life. She is going to all the doctors she can go to. She stated she has been hospitalized 2 times because of this. She has read that these cause more things like vertigo and anxiety attacks, heavy breathing; all the things she's been experiencing and doctor's did not know where it was coming. She went to the hospital, she wasn't breathing, she was blue in the face, all of these things, and had to be taken by the ambulance to the hospital. She had a couple episodes there and they wouldn't let her get off the stretcher. She reported she was hospitalized the morning of 04Jul2021 and was discharged 05Jul2021 early in the morning maybe like 10:00AM. She clarified she wasn't admitted into the hospital, she was in the outpatient area, but she stayed overnight. They sent her a $5,000 bill for that night. She also had to go to (name redacted) on 14Jul2021, it was in the middle of the night so she couldn't go back there the same day. Patient confirmed she wasn't hospitalized when she visited urgent care. She confirmed all of her symptoms have been persistent ever since 04Jul2021 and the longer it went, it felt like it was getting worse. She actually has worsened and was not improving all all. She confirmed all of her symptoms have worsened. It was also making her mentally more depressed, just kind of like a vegetable. She gets up, she can't sleep, she has to go out for air, she felt like she's losing air, it was really affecting her life. The patient did not go to physician office. She reported they are so backed up at her medical group. She will be going- she did speak to some people at time of report and will be going to the neurologist on unspecified date. She also mentioned she will be going to urgent care again. There were no relevant tests. The events were reported as ongoing, worsening. The outcome of the events was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1523369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NY
Alter: 16,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 03.07.2021
Beginn: 07.07.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: - / LA

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

Chest pain Echocardiogram Electrocardiogram Laboratory test Magnetic resonance imaging Myocarditis

Symptomtext

Four days after receiving vaccine started having chest pain; This is a spontaneous report from a contactable consumer (patient). A 16 years old male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) dose 2 via an unspecified route of administration, administered in arm left at age of 16 years on 03Jul2021 (Lot Number: EW0186) as single dose for covid-19 immunisation. Medical history was none. There were no concomitant medications, patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine, no other medications the patient received within 2 weeks of vaccination. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) dose 1 via an unspecified route of administration, administered in arm left at age of 15 years on 12Jun2021 (lot number: EW0177) for covid-19 immunisation. Four days after receiving vaccine patient started having chest pain on 07Jul2021 10:00 and hospitalized for 4 days, unspecified medication was received as treatment. The event resulted in Doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care (as reported). Prior to vaccination, was the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the event was unknown. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1523369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NY
Alter: 16,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 03.07.2021
Beginn: 07.07.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Echocardiogram Electrocardiogram Laboratory test Magnetic resonance imaging Myocarditis

Symptomtext

Four days after receiving vaccine started having chest pain; This is a spontaneous report from a contactable consumer (patient). A 16 years old male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) dose 2 via an unspecified route of administration, administered in arm left at age of 16 years on 03Jul2021 (Lot Number: EW0186) as single dose for covid-19 immunisation. Medical history was none. There were no concomitant medications, patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine, no other medications the patient received within 2 weeks of vaccination. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) dose 1 via an unspecified route of administration, administered in arm left at age of 15 years on 12Jun2021 (lot number: EW0177) for covid-19 immunisation. Four days after receiving vaccine patient started having chest pain on 07Jul2021 10:00 and hospitalized for 4 days, unspecified medication was received as treatment. The event resulted in Doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care (as reported). Prior to vaccination, was the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the event was unknown. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1916099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: IL
Alter: 21,0
Geschlecht: F
Eingang: 26.08.2021
Impfdatum: 26.08.2021
Beginn: 26.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anxiety Dizziness Fear of injection Haemophobia Syncope Vision blurred

Symptomtext

Blurry vision > Resolved right away lightheady faint Customer said she was anxious, drove in, didn't eat. and had a cup of coffee. She doesn't do well with blood, needles, etc. Her parent's picked her up but were not worried.

Weitere VAERSDATA-Felder

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

VAERS 1602677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: TX
Alter: 13,0
Geschlecht: M
Eingang: 24.08.2021
Impfdatum: 18.08.2021
Beginn: 20.08.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / -

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

Blood creatine phosphokinase increased Brain natriuretic peptide increased C-reactive protein increased Chest pain Echocardiogram normal Brain natriuretic peptide normal Chest X-ray normal Electrocardiogram ST segment elevation Headache Intensive care SARS-CoV-2 test negative Troponin increased Electrocardiogram ST-T change Full blood count normal Metabolic function test normal Myocarditis Pericarditis Red blood cell sedimentation rate normal

Symptomtext

First dose Pfizer vaccine: 7/28/21 and second dose 8/18/21. On 8/20 PM he developed headache and chest pain. He returned to Medical Center and was tested for COVID and was negative. He had evaluation for chest pain which revealed elevated troponin (9.5), elevated CRP (5.2) and EKG with ST elevation. He was transferred to MC PICU.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: Troponin high: 7.90 ng/mL on admission 8/21 @ 15:23- has been down trending to 1.64 ng/mL at time of report (8/24 @06:09) BNP: 51 pg/mL (8/21 @ 15:23) CK 981 units/L (8/21 @ 15:23) ECG 8/21: mild ST elevation in lateral precordial leads ECHO: 8/21 GLS -14.1%, Normal right ventricular contractility; Left ventricle: Systolic function is low normal to mildly depressed. ECHO 8/23 : no structural abnormalities, coronary artery abnormalities, or pericardial effusion identified. Normal L ventricular dimensions and systolic function. ECG 8/24: normal sinus rhythm, nonspecific T wave abnormality
Aktuelle Erkrankungen: n/a
Vorgeschichte: Anxiety, depression
Andere Medikamente: trazodone, duloxetine, bupropion
Allergien: n/a
Vorherige Impfungen: -

VAERS 1417721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: WI
Alter: 57,0
Geschlecht: M
Eingang: 22.08.2021
Impfdatum: 20.04.2021
Beginn: 07.05.2021
Tage bis Beginn: 17,0
Dosis: 2
Route/Site: IM / LA

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

Blood magnesium Blood potassium Blood test Blood thyroid stimulating hormone C-reactive protein Electrocardiogram Heart rate increased Echocardiogram Electrocardiogram ambulatory Full blood count Metabolic function test Myocarditis Palpitations Supraventricular extrasystoles Supraventricular tachycardia Troponin

Symptomtext

Palpitations which were found to be a very high amount of supraventricular ectopy. This happened occasionally before the vaccine but became much worse on the date indicated after first vaccine. It became even worse after the second dose. Cardiologist believes that it could have been vaccine induced myocarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: EKG 5/10/21, 24 hour holter monitor 5/10/21, echocardiogram 6/8/21, potassium, magnesium, TSH on 5/10/21. CMP and CBC on 5/18/21. CRP and troponin 6/16/21. EKG 5/18/21 and 6/3/21. 24 hour holter again on 6/23/21. 48 hour holter on 6/28/21. Blood work and echocardiogram normal. Holter monitors with PSVT.
Aktuelle Erkrankungen: none
Vorgeschichte: hypercholesterolemia, loss of sense of smell, anxiety, heterozygous MTHFR mutation C677T.
Andere Medikamente: Adderall XR 15 mg daily, atorvastatin, Tums, Co-Q10, famotidine, vitamin, Vitamin D, clonazepam 1 mg QHS PRN, propranolol 40 mg daily PRN., topical clindamycin lotion and topical terbinafine cream.
Allergien: amoxicillin causing rash.
Vorherige Impfungen: -

VAERS 1591536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: OR
Alter: 13,0
Geschlecht: M
Eingang: 20.08.2021
Impfdatum: 18.08.2021
Beginn: 19.08.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Blood alkaline phosphatase increased Blood creatinine decreased Blood glucose increased Computerised tomogram head normal Drug screen negative Electrocardiogram normal Full blood count normal Mean platelet volume normal Metabolic function test Red cell distribution width normal Seizure Urine analysis

Symptomtext

8/19/21 @ 1654 in the afternoon, call received from parent that child was at the emergency department of Hospital. Had a reaction to vaccine or medication prior to arrival. Reported patient had a bad seizure. Pt advised to discontinue guanfacine, see primary care provider, and neurology follow up. Discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Urine drug screen-negative; UA normal; CMP glucose 117, creatinine 0.46, alkaline phosphatase 404, all other results in panel normal; CBC RDW-CV 12.0, RDW-SD 35.1, MPV 9.5, all other results normal; CT cranial-no acute intracranial findings; EKG Normal.
Aktuelle Erkrankungen: No illnesses
Vorgeschichte: Behavior concerns, Conduct disorder, Encopresis with constipation and overflow incontinence, Fecal impaction of rectum, Slow transit constipation.
Andere Medikamente: Guanfacine 1 Mg nightly, Lactulose 10 gm/15 mL BID, Polyethylene glycol powder q 12 days.
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1591187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0186

schwer

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 20.08.2021
Impfdatum: 25.06.2021
Beginn: 27.06.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Blood test Confusional state Dizziness Echocardiogram Electrocardiogram Fatigue Headache Hypoaesthesia Influenza like illness Loss of consciousness Presyncope Pruritus Syncope

Symptomtext

Following dose 1, bad flu like symptoms, headache and fatigue for approximately 10 days. Also experienced very itchy skin, but no rash, dizziness and numbness in face/jaw. Following dose 2, on day 2 after injection, have severe flu like symptoms including confusion and extreme dizziness. on day 3 after dose 2, at approximately 7:30 AM, fainted and out cold for approximately 20 minutes. Experienced 4 additional near fainting incidents throughout the day. Episodes continued (near fainting) for approximately one month.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: ECHO cardiogram, EKG, blood test. Doctor indicated may do MRI if symptoms continue.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Citalopram; trazodone
Allergien: amoxicillian ampicillian meperidine sulfamethoxazole-trimethoprim
Vorherige Impfungen: -

VAERS 1574069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TN
Alter: 25,0
Geschlecht: M
Eingang: 16.08.2021
Impfdatum: 21.06.2021
Beginn: 25.07.2021
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: IM / LA

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

Computerised tomogram Electroencephalogram Magnetic resonance imaging Seizure

Symptomtext

Experienced 2 Seizures. Landed in hospital via an ambulance. After an EEG, CT scan, & MRI there is no explanation for the seizures.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 6,0
Labordaten: EEG, CT scan, & MRI
Aktuelle Erkrankungen: None
Vorgeschichte: Good
Andere Medikamente: THC
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1573951

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TX
Alter: 39,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Impaired work ability Migraine Nausea SARS-CoV-2 test negative Syncope

Symptomtext

Nausea, dizziness, syncope, and migraine headache. Treatment included ibuprofen, acetaminophen, and loratadine. Unable to work for first week, symptoms slowly abated over the course of eight weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Covid 19 test completed on May 25 2021 (negative result).
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic pain
Andere Medikamente: Magnesium citrate (dietary supplement)
Allergien: None known
Vorherige Impfungen: -

VAERS 1573638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 16.08.2021
Impfdatum: 17.06.2021
Beginn: 10.08.2021
Tage bis Beginn: 54,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Hyponatraemia Seizure like phenomena

Symptomtext

E87.1 - Hyponatremia N17.9 - AKI (acute kidney injury) R56.9 - Seizure-like activity

Weitere VAERSDATA-Felder

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

VAERS 1554581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 15,0
Geschlecht: M
Eingang: 13.08.2021
Impfdatum: 12.08.2021
Beginn: 12.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Blood pressure decreased Headache Hypotension Lethargy Loss of consciousness Pallor Presyncope

Symptomtext

Pt had a vasovagal response to first dose Pfizer ~3pm, about 8 minutes after receiving the vaccine with father present. Patient passed out, but remained in chair with no injuries and woke up quickly. Patient appeared pale and lethargic, but responsive and oriented to name/age. Ice pack applied to neck, feet propped up on chair, and juice given. BP was hypotensive at 55/34 and HR 44. Patient was transferred to the gurney with legs elevated and he expressed immediate relief of headache that he was experiencing. BP improved at 104/61 and HR 77. Patient drank more juice and water over the hour that he spent with us here in the COVID vaccine clinic. BP's and HR remained stable with last check BP 101/65 and HR 74. Patient and father instructed to inform staff that he needs to receive second dose lying down when he comes for his next appointment. They verbalized understanding. Pt stated he felt back to normal before leaving our clinic and vitals remained stable.

Weitere VAERSDATA-Felder

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

VAERS 1549789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CO
Alter: 13,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 07.08.2021
Beginn: 07.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Cyanosis Emotional distress Fall Hyperhidrosis Loss of consciousness Pallor

Symptomtext

11:05/Vaccine administered, 1120 patient became pale, diaphoretic, fell back in her chair. According to Patient's mum, Pt lost consciousness 15 minutes after receiving vaccine. One unit lead notified and witnessed Pt sitting in her chair alert and in distress. Medical lead and an EMT on the bus arrived to the scene. Upon assessment, Pt. AOX4, cyanotic and pale looking. Pt placed on the floor, supine position, 911 called. V/S checked, BP 101/51, HR 44, O2 80%, RR 16. Pt able to followed commands and answer questions. Pt remained calm, reassessed after 5-minute, V/S: BP 104/60 HR 66, O2 90%, RR. 16, still cyanotic. EMS Personnel onsite arrived. Care transferred. Pt transported to the ER via ambulance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No Medications
Allergien: NKA
Vorherige Impfungen: -

VAERS 1549313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 12.08.2021
Beginn: 12.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Hypotension Syncope

Symptomtext

Patient experienced dizziness, lightheadedness and brief (30-60 seconds) syncopal episode. Patient was visibly diaphoretic and hypotensive. Patient placed in recumbent position and blood pressure recovered within 5 minutes. Patient observed for 35 minutes total and left in stable condition.

Weitere VAERSDATA-Felder

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

VAERS 1541128

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: UT
Alter: 14,0
Geschlecht: F
Eingang: 10.08.2021
Impfdatum: 09.08.2021
Beginn: 09.08.2021
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

syncope event lasting less than 4 seconds. Patient recovered immediately and was monitored and released

Weitere VAERSDATA-Felder

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

VAERS 1540469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NY
Alter: 41,0
Geschlecht: M
Eingang: 10.08.2021
Impfdatum: 30.07.2021
Beginn: 30.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain upper Arthralgia Asthenia Bell's palsy Chest discomfort Cough Dysgeusia Dysstasia Energy increased Erythema Facial paresis Flatulence Gait disturbance Headache Hypersensitivity Hypoaesthesia Injection site pain Insomnia

Symptomtext

Day 1: Within a few minutes of left arm injection of Pfizer vaccine my fingers go numb on left hand. Several minutes later my right leg gets a slight numb feeling. A few minutes later while I'm still at the vaccination site, the right side of my face starts to go numb and I experience muscle tightness like my jaw is clenching. During this the nurse who injected me apologizes repeatedly saying she only wanted to help people. Nurses observe me for Bell's and discuss the possible use of a steroid. I am told that I may have a sensitive nervous system and a strong immune system as this is happening. The nurses suggest I go to my doctor, then urgent care, and finally the ER in an ambulance. My mom who was also vaccinated starts crying. I decline. The head nurse/researcher from hospital says instead she will call me every 30 minutes. My shoulder where I was injected gets increasingly sore through the night. Day 2: The feeling comes back to my fingers about 24 hours later and the pain went away at the injection site by 36 hours. On the second night, I got severe abdominal gas pain like a stabbing sensation. I was nauseated and pain was so severe I couldn't even move. Briefly had a strange metallic taste in mouth. My right side leg and face remain numb. Day 3: Stomach pain is gone. My calf and the back of quad began to get occasional shooting pain if I walked quickly or went up/down stairs. By the end of the night sensation and muscle strength suddenly came back to my face and my right leg. I feel a strange sensation in my sinsues and chest like the last days of a cold. Day 4: My knees became red and very painful. I had trouble sleeping as a result of the pain. My calf and quad continue to experience pain when walking fast, driving (calf muscle is used to press the gas and brake pedals), and using stairs. By end of day noticed left knee was much more red and red line going from knee to ankle. Day 5: Woke up and immediately felt some numbness and weakness on right side of face, covering a larger area than originally. This time from the eyelid to chin and nose to ear instead of just over the cheekbone. Numbness is less than previously, but covering a much larger area of the face. Similar feeling to sleeping on a part of your body, but the numbness does not pass. Mild pain was also observed in a lower section of left calf muscle for first time. Knees feel better than previous day, but knees remain red with a red line going down to ankle. Doctor prescribed high-dose prednisone. Doctor indicates that delaying steroid treatment puts me at risk of permanent damage, recurrent Bell's Palsy and potentially even Guillain-Barre. He says these conditions are known to be caused by vaccines. Pharmacist agrees with doctor and advises to take prednisone immediately. The nerve pain in my legs is increasing and the feeling of Bell's Palsy is getting more intense in my face. After discussing side effects with friends and family, I decide to take prednisone. Day 6: I am taking 50mg prednisone for 5 days. I make a big breakfast with milk and take my first pill before 6 am. I haven't gotten much sleep, but I feel a lot of energy. My face feels much better with none of the numb paresthesia sensation right now. My legs are still painful from the ankles to the knees. My mood feels good, but otherwise don't feel any side effects. Day 7: Having trouble sleeping from severe pain in legs and knees. Prednisone is making it hard to get sleepy. I am experiencing extreme anxiety, racing heart and am unable to sleep at all. By the afternoon my leg pain is much less than the night before, but still present. The nerves on the side of the knee going to the back are very sensitive. My right and left hands have a strange almost carpal tunnel sensation going down the pinky side. My appointment with the neurologist does not produce many answers and she seems confused by the transcience of my symptoms. Symptoms become noticeably more severe at night with pain shooting up from my shins to lower thighs with every step I take. I am concerned that nerve pain is gradually going up higher on my legs. I try desperately to sleep all day. I am able to finally dose off late at night in a recliner. Day 8: I wake up feeling great after finally getting some sleep. I don't notice any pain at first and am relieved, but then as I walk to the bathroom and kitchen, the initial numb feeling I had a week ago starts to return to my right cheek and right calf muscle. Vine-like nerve pain is starting to return to my shins and calves with every step I take. I quickly make a big breakfast and take 50mg prednisone knowing I will probably struggle to sleep again. I put on classical music to try to lower my anxiety. It's been a week now and I just want to get back to my life. By afternoon my face begins to feel better and the pain in my legs is more manageable, but still noticeable and present. Initially going down stairs I have to hold a railing and when doing my laundry I choose to sit instead of stand, but as afternoon approaches I feel less pain. At night I notice occassional shooting pains across sides of head. I decide to drink water and try to relax by watching a movie. At night I notice a cough and tickle in chest. Throughout the week I have noticed that some paresthesia/neuralgia occurs almost like an echo after I've been griping/pressing against something tightly (steering wheel/doorknob) or leaning against something. It happens on both my hands and legs. Day 9: Wake up with mild numbness all over right side of face again, observe mild but greatly reduced nerve pain in legs. Some nerve pain remains around the back of the knee and the shins. This is my 4th day on prednisone. I've noticed an occaional cough starting last night. The tickle in the chest is gradually becoming more irritating. The echo pain continues in my hands like when I grab a doorknob tightly or hold my smartphone. Sensation it reminds me of is carpal tunnel or arthritis. Driving at night I notice that bright headlights are hurting my eyes. Day 10: Wake up with similar mild facial numbness and mild nerve pain around knees. I take a 5th prednisone pill. Chest tickles a little but not too bad. The past two days the pain has been much more manageable. I'm not sure how big of a role prednisone is playing in alleviating the paresthesia, but I will find out in the coming days without it. After my shower I notice that the left leg has a lot of redness and stinging pain. Knee and top of foot is very red with red line running from foot to knee. Right leg has some redness but it is much less pronounced, becoming more painful toward the evening. Mild numbness of the face is felt throughout the day and into night. My eyelid feels more paresthesia. When I laugh I notice that my jaw hurts around the lower part of my ear. I'm still noticing that bright lights are unbearable at night. I don't know if this is related to prednisone or something else. Day 11: Relieved to wake up with full feeling in my face in the morning and no more pain in jaw/under ear. My legs start hurting while I am standing on them to make breakfast or take a shower. I try to take a colder shower as the warm water hitting my legs hurts. The left leg is much worse than the right. As the afternoon goes on my hands start going numb. The knuckle joints might be swollen. I wonder if my joints are swelling and cutting off circulation? Appointment with allergist is very good, she says she has seen many patients with similar adverse effects after covid vaccination. She does not believe it is an allergic reaction and usually sends patients to a neurologist, but admits there may not be anyone within Northwell Health specializing on this reaction to the vaccine. Allergist says she will try to find me a neurologist and schedule blood work. At night the pain and swelling in my hands is intense and I am repeatedly losing sensation in my hands. I drink lots of water as I believe it helps a little.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Swab test of face indicated a partial loss of sensation. Upcoming: MRI, EMG nerve tests, blood work
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Finasteride, minoxidil, vitamin D, vitamin K2, zinc, horse chestnut, rutin, ashwagandha, whey protein.
Allergien: None
Vorherige Impfungen: -

VAERS 1531995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 16,0
Geschlecht: F
Eingang: 06.08.2021
Impfdatum: 06.08.2021
Beginn: 06.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Crying Dizziness Dyspnoea Loss of consciousness

Symptomtext

Patient received in RN observation area, post-COVID vaccination administration. Observed for 30 minutes as recommended per CDC guidelines and policy on post-vaccination RN monitoring. Reports Hx of anaphylactic reaction to penicillins, nuts, avocado. Patient and parents of patient reports similar reactions to vaccinations in past. At 10:36 parents reported that patient was passing out. Patient on sitting on floor awake and crying when I arrived to her side promptly. Patient reporting feeling dizzy. Patient instructed to lie down, Patient stating she can't breath and she needs epi. No drooling, facial, tongue or throat swelling noted. Patient speaking in full sentences, no shortness of breath noted. Vitals as documented in flowsheet, O2 sats 100%. Rapid response called. Patient placed on gurney. 10:40: RRT arrived. Per Dr orders, patient will be monitored in observation. COVID vaccination fact sheet and discharge information provided to patient and parents on D/c from clinic, patient advised to review. Verbalized understanding. Appointment for second COVID vaccination provided to patient. All questions and concerns addressed. Advised to follow up as needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: denies
Vorgeschichte: FOOD ALLERGY MODERATE PERSISTENT ASTHMA ALLERGIC RHINITIS DUE TO ANIMAL HAIR OR DANDER ALLERGIC URTICARIA DUE TO FOOD ALLERGIC RHINITIS BILAT ALLERGIC CONJUNCTIVITIS LACTOSE INTOLERANCE ADVERSE REACTION TO FOOD TREE NUT ANAPHYLAXIS
Andere Medikamente: Albuterol (PROAIR/PROVENTIL/VENTOLIN) 90 mcg/actuation Inhl HFAA Inhale 2 puffs by mouth every 4 hours as needed for shortness of breath , wheezing or cough . 100 days supply for use at school is 1 canister. Use with spacer device if prescr
Allergien: Allergies Penicillins Class Shock and/or Unconsciousness High Allergy 11/23/2020 Avocado - Dietary Skin Rash and/or Hives Not Specified 6/11/2016 Cat Dander Skin Rash and/or Hives Not Specified 6/11/2016 Dog Dander Skin Rash and/or Hives Not Specified 6/11/2016 Pineapple Skin Rash and/or Hives Not Specified 6/11/2016 Tree Nut
Vorherige Impfungen: TDAP

VAERS 1531886

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: AR
Alter: 20,0
Geschlecht: M
Eingang: 06.08.2021
Impfdatum: 06.08.2021
Beginn: 06.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Contusion Fall Flushing Headache Hyperhidrosis Loss of consciousness Syncope Unresponsive to stimuli Visual impairment

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Mild, Systemic: Headache-Medium, Systemic: Visual Changes/Disturbances-Mild, Additional Details: Conciousness regained immediately upon lower extremity elevation. Fell from seated, left temporal contusion. Applied ice, notified EMT/firefighter father. No PCP, directed to nearby Urgent Care, notified urgent care of his arrival. Will follow up further

Weitere VAERSDATA-Felder

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

VAERS 1529756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CO
Alter: 12,0
Geschlecht: M
Eingang: 05.08.2021
Impfdatum: 05.08.2021
Beginn: 05.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Hyperhidrosis Pallor Syncope

Symptomtext

17:45/Vaccine administered , 17:50 patient became pale, diaphoretic, collapsed to ground, while being Assisted by medical staff. Vitals Stable: HR99, O2 94%, BP 130/77. Able to follow commands and answer questions. 18:05 Vitals Stable: HR83, O2 98%, BP 100/60 18:15 patient able to stand unassisted, vitals remained stable Walked independently to personal vehicle accompanied by mother.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None (FEAR of Needles)
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1529112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NY
Alter: 28,0
Geschlecht: F
Eingang: 05.08.2021
Impfdatum: 04.06.2021
Beginn: 08.06.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Dyspnoea Myocarditis Palpitations Pericarditis

Symptomtext

Myocarditis/pericarditis (chest pain, palpitation, shortness of breath)

Weitere VAERSDATA-Felder

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

VAERS 1525790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: IA
Alter: 12,0
Geschlecht: M
Eingang: 04.08.2021
Impfdatum: 03.08.2021
Beginn: 03.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chills Flushing Hyperhidrosis Nausea Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Chills-Severe, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Severe, Systemic: Nausea-Medium, Systemic: Shakiness-Medium

Weitere VAERSDATA-Felder

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

VAERS 1520763

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 02.08.2021
Impfdatum: 02.08.2021
Beginn: 02.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anaphylactic reaction Anxiety Blood pressure increased Pruritus Throat clearing

Symptomtext

Pt states history of two anaphylactic episodes requiring epi-pen use in the past, most recent January of 2021. Does not know what the allergen is. Pt received first dose Pfizer and stated top of head "itch" within 2 minutes followed by resolution of these symptoms several minutes later. Pt's vitals: 138/92, HR 82, lungs clear, unlabored breathing, no acute distress, no s/s shock, no notable oral swelling. Repeat vitals appx 5 minutes later 150/90 HR 96, states feeling anxious. EMS arrival at 2:37 pt not in distress states feeling well but anxious (states history of anxiety) EMS vitals 150's/90's and SpO2 97%. Pt clearing throat but states this is "normal" for her when nervous, daughter confirms this. Pt also states clears throat frequently because it's always "raw". EMS assessment no airway swelling/redness/compromise at this time. No visible hives/rash. Lungs clear bilateral on repeat auscultation. Pt educated safety of ride to hospital via EMS, states would like to take self to hospital with daughter instead of EMS, has epi-pen with her, declines EMS ride. Pt leaves after 30+ minute observation period, ambulating freely, speaking in clear/coherent sentences and able to swallow water freely, state going to the hospital down the street. States itching at top of head resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: pt states history cervical disk herniation
Andere Medikamente: ibuprofen
Allergien: allergies to unknown substances, pt states thinks it's to shellfish but can't confirm
Vorherige Impfungen: -

VAERS 1519736

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: KS
Alter: 16,0
Geschlecht: M
Eingang: 02.08.2021
Impfdatum: 13.07.2021
Beginn: 18.07.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / LA

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

Alanine aminotransferase increased Aspartate aminotransferase increased Seizure

Symptomtext

7/18/21 3 pm Seizure 7/18/21 Elevated AST and ALT

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: 7/18/21 Elevated AST and ALT
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Seasonal allergies & cats
Vorherige Impfungen: -

VAERS 1505691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 20,0
Geschlecht: M
Eingang: 27.07.2021
Impfdatum: 27.07.2021
Beginn: 27.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Head injury Hyperhidrosis Loss of consciousness

Symptomtext

Patient sitting in chair and lost full consciousness. Patient fell over out of chair, hitting head on floor. Patient face mask removed, patient noted breathing but remained unconscious for a about 30 seconds. Upon regaining consciousness patient is alert and oriented x4, and diaphoretic. Denies any pain or discomfort at this time. Denies any other signs and symptoms. Denies Hx of anaphylactic reaction to medications, food, or vaccines. Patient denies adverse reactions to vaccinations in past. Vitals: 11:07: BP 123/55. Pulse 55, SpO2: 97%. Pain: 0; Rapid response called by staff. Rapid response team arrived and updated on patient's status. Patient transported to ER with rapid team per physicians recommendation at 11:10.

Weitere VAERSDATA-Felder

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

VAERS 1408253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 18,0
Geschlecht: M
Eingang: 26.07.2021
Impfdatum: 02.06.2021
Beginn: 03.06.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: UN / UN

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

Back pain C-reactive protein increased Chest X-ray normal Chest pain Computerised tomogram thorax abnormal Chest X-ray Chest scan Chills Dyspnoea Echocardiogram normal Electrocardiogram ST segment elevation Full blood count normal Fungal test negative Fatigue Immediate post-injection reaction Lymph node pain Myalgia Laboratory test normal

Symptomtext

One day after second COVID-19 vaccine, Jack developed sudden shortness of breath, fever, palpitations, chest pain and back pain and a fever of 100.4. Fever resolved, but other symptoms persisted and one week after vaccination he presented to the ED where he was diagnosed with pericarditis by EKG (new J-point elevations in leads I, V5 and V6). He received NSAIDs and colchicine. He was discharged later that same day with instructions to take colchicine and ibuprofen for one week. He was supposed to follow up with Pediatric Cardiology as an outpatient but this does not appear to have been done. Given his history of disseminated histoplasmosis, Fungitell and Histoplasma urine antigen were sent to rule out continued disease and both later returned negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 1,0
Labordaten: CBCPD - WNL Troponin - WNL CRP - 4.2 mg/dL ESR - 27 EKG - new J-point elevations in leads I, V5 and V6 CXR - WNL Chest CT - L axillary LAD, new groundglass nodular opacities in R lung, trace pericardial fluid Echocardiogram - WNL Fungitell - negative Histoplasma urine antigen - negative
Aktuelle Erkrankungen: None
Vorgeschichte: Carcinoid tumor (2019) s/p resection Disseminated histoplasmosis (2019) - resolved
Andere Medikamente: Flexeril (unsure if taking prior to vaccination or just after)
Allergien: None
Vorherige Impfungen: -

VAERS 1500909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MN
Alter: 31,0
Geschlecht: F
Eingang: 24.07.2021
Impfdatum: 21.05.2021
Beginn: 02.07.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: IM / OT

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

Acute hepatic failure Alanine aminotransferase increased Aspartate aminotransferase increased Autoimmune hepatitis Biopsy liver abnormal Blood albumin decreased Blood bilirubin increased Hepatitis Hepatitis acute Jaundice Syncope

Symptomtext

On 7/2/2021, the patient presented to clinic in the system with complaints of jaundice. Symptoms had been present for several days prior to this. She was found to have acute liver failure (AST 933, ALT 816, Bilirubin 12.8, Albumin 3.0) and was hospitalized at hospital. She had a liver biopsy on 7/6 which was consistent with severe acute hepatitis with hepatocyte loss (see more below). She was treated with steroids and discharged home. She was readmitted to Hospital on 7/21 after a syncopal event and with continued worsening liver failure. She was transferred to the medical center on 7/23 for evaluation by transplant hepatology.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 10,0
Labordaten: Specialty pathology read of previous 7/6 biopsy by doctor, MD at clinic: severe lymphoplasmacytic inflammation affecting protal, interface and lobules, and resulting in broad areas of confluent and bridging necrosis/parenchymal collapse. The surviving islands of hepatocytes appear regenerative and give the appearance of "multiple nodules" which could possibly explain radiologic findings. The trichrome stain however highlights the absence of fibrosis while iron stain is negative for stainable parenchymal or Kupffer iron. The bile ducts experience focal injury but overall appear secondary to hepatic process rather than an overlapping true cholangitis. No duct loss is seen. We observed the absence of drug history, viral infections from clinical and serologic data, as well preceding vaccination. Although a more comprehensive history for potential drug (or herbal, or supplement) induced immune-mediated hepatitis needs to be fully ascertained if possible, it seems very likely that this is an example of vaccine-induced autoimmune hepatitis (AIH).
Aktuelle Erkrankungen: -
Vorgeschichte: Recently post-partum (delivered in January 2021). She had a period of mildly elevated transaminitis during the first and second trimester (AST 67, ALT 82) with normal bilirubin and alk phos, which resolved during the third trimester.
Andere Medikamente: -
Allergien: Penicillin allergy
Vorherige Impfungen: -

VAERS 1484278

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: IL
Alter: 32,0
Geschlecht: M
Eingang: 19.07.2021
Impfdatum: 17.07.2021
Beginn: 17.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Fear of injection Hypotension Loss of consciousness Refusal of treatment by patient Syncope

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Systemic: Hypotension-Severe, Additional Details: PATIENT PASSED OUT AFTER ABOUT 5-10 MINUTES OF THE VACCINE, HISTORY OF FAINTING. MAY HAVE BEEN DEHYDRATED DUE TO YARD WORK. FEAR OF NEEDLES AS PER PATIENT. PATIENT CAME BACK BY HIMSELF, CALLED 911 FIRE DEPT MONITORED BP AND DID CHECKS BEFORE LETTING HIM GO. PATIENT REFUSED TO GO TO THE HOSPITAL AND WALKED OUT WITHOUT HELP.

Weitere VAERSDATA-Felder

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

VAERS 1446463

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NJ
Alter: -
Geschlecht: F
Eingang: 18.07.2021
Impfdatum: 02.07.2021
Beginn: 02.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Arrhythmia Dyspnoea Feeling abnormal Heart rate increased Inflammation Burning sensation Cardiac flutter Condition aggravated Dizziness Dysgeusia Flushing Feeling hot Tachycardia Taste disorder Limb discomfort Loss of consciousness Paraesthesia Pulmonary congestion

Symptomtext

I got up my heart was racing like 125, it was fluttering it was almost as if it was arrhythmia definitely tachycardia obviously; felt like I was going to passed out; I have congestion too; getting rapid heartbeat/heart rate was like 109-108; tachycardia and along with tachycardia; getting my limbs started getting really hard and heavy they felt as if somebody put menthol on them; I was getting tingling; getting my limbs started getting really hard and heavy they felt as if somebody put menthol on them; I was getting tingling; could not catch my breath and I still can't catch my breath today/have trouble in breathing; If I could take this vaccine out of my body I would because it's just very scary; I am nothing feeling and I have still some of it threatened of it today; I have trouble in breathing so, I don't know if it is called inflammatory reaction; This is a spontaneous report from a contactable consumer (patient). A female patient of unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EW0186, Expiration date: unknown), via an unspecified route, administered on 02Jul2021 16:00 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On 02Jul2021 at 10:00 pm, after the vaccination, the patient experienced rapid heartbeat, tachycardia, limbs started getting hard and heavy they felt as if somebody put menthol on them, patient experienced tingling and patient got up and her heart rate was like 109-108 and patient said she was experiencing the tachycardia and having the adverse reaction. later back night she went to bed and then about 4 O'clock or 3 O'clock she got up, and her heart was racing like 125, it was fluttering and was almost as if it was arrhythmia. she thinks there was arrhythmia because there was fluttering and skipping, and she felt like she was going to passed out and she could not catch breath and still can't catch breath today. She has congestion and she had trouble in breathing, she doesn't know if it is called inflammatory reaction, or it is making her asthma worse. Patient said she experienced some of those side effects on 03July. She said if she could take the vaccine out of her body she would because it's just very scary and she is feeling nothing, and she still have some of it threatened of it today and she don't know why they are using vaccines that haven't 100% prevent. The outcome of all events was unknown. Follow-Up (06Jul2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1481347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 15,0
Geschlecht: M
Eingang: 17.07.2021
Impfdatum: 03.07.2021
Beginn: 06.07.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / -

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

Chest pain Magnetic resonance imaging abnormal Myocarditis Troponin increased

Symptomtext

Chest pain, received motrin, MRI with myocarditis, elevated troponin le els

Weitere VAERSDATA-Felder

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

VAERS 1478362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NC
Alter: 46,0
Geschlecht: F
Eingang: 16.07.2021
Impfdatum: 20.05.2021
Beginn: 29.06.2021
Tage bis Beginn: 40,0
Dosis: 2
Route/Site: SYR / RA

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

Dysmenorrhoea Heavy menstrual bleeding Thrombosis

Symptomtext

Period lasted longer than 8 days, then restarted and was very heavy and super painful for 5 more days, lots of clotts.

Weitere VAERSDATA-Felder

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

VAERS 1478268

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MN
Alter: 22,0
Geschlecht: F
Eingang: 16.07.2021
Impfdatum: 23.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Head injury Loss of consciousness Syncope

Symptomtext

Pt fainted hitting R/frontal side of head. Loss of consciousness for 1-3 seconds. Ice applied to head, but no swelling or discoloration noted. BP 116/86 P80 R16 3:08 Moved to observation area to cot with legs elevated. Color improving 3:15 Pt alert & talking w/mother 3:30 Eating crackers & drinking juice. left w/o assistance with mother.

Weitere VAERSDATA-Felder

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

VAERS 1471280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 14.07.2021
Impfdatum: 10.07.2021
Beginn: 12.07.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Blood chloride normal Blood glucose normal Blood potassium normal Blood sodium decreased Blood urea normal C-reactive protein increased Carbon dioxide increased Chest discomfort Chest pain Eosinophil percentage Full blood count Haematocrit normal Haemoglobin normal Lymphocyte percentage increased Malaise Mean cell volume normal Monocyte percentage increased Myocarditis

Symptomtext

12 Y 4 M old male with a history of chest pain that started two days ago on Monday. On 7/11 night, he didn't feel well felt nauseous. He was able to sleep but had chest pain the following morning that improved after he vomited. The chest pain is midsternal and feels pressure-like. It lasted a few hours. He swam on 7/12 without problems (at a swim club) for an hour. He had his second dose of COVID-19 vaccine on Saturday 7/10/21. There has not been any fevers. Elevated troponin and CRP with recent COVID-19 vaccine, suspicious for post-vaccine myocarditis. He is hemodynamically stable with normal vitals and no evidence of ventricular ectopy or depressed left ventricular function. His troponin peaked at 11.05 and trended down, but his most recent value is slightly up at 8.2 from 7.6. Recommended continuing to trend the troponins for now (if they show a downward trend then twice daily is adequate, unless he develops chest pain). At this time, IVIG is held unless he becomes unstable or the troponins trend upward .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: 07/13/21 2313 NA 135 K 3.5 CO2 30 CL 97* BUN 11 CR 0.46 RBS 106 CBC Recent Labs 07/13/21 1554 WBC 5.8 HGB 14.8 HCT 41.2 PLT 273 MCV 81 NEUT 46 LYMPH 41 MONO 11 EOS 1 Cardiac Recent Labs 07/14/21 1130 07/14/21 0543 07/13/21 2313 TROP 8.20* 7.57* 11.05* Results as of 7/14/2021 17:40 7/13/2021 15:54 CRP, SER QL: 1.0 (H) 7/13/2021 23:13 CRP, SER QL: 0.9 7/14/2021 11:30 CRP, SER QL: 0.6
Aktuelle Erkrankungen: None
Vorgeschichte: Autism Spectrum disorder and Speech delay
Andere Medikamente: -
Allergien: nka
Vorherige Impfungen: -

VAERS 1470624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NC
Alter: 19,0
Geschlecht: F
Eingang: 14.07.2021
Impfdatum: 14.07.2021
Beginn: 14.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Dizziness Dyspnoea Heat therapy Hyperhidrosis Lung disorder Presyncope Pruritus

Symptomtext

Pt is a 19 y/o F who suddenly endorsed feeling dizzy, hot, short of breathe, and peri-oral itchiness ~ 10min after receiving first dose of Pfizer vaccine (done at 1357). PMHx pertinent for hx of anaphylaxis to bee stings, currently being treated with allergy shots, last injections given 12JUL21. Pt was immediately evaluated, with initial VS done at 1415 with BP 110/70, SPO2 99%, HR of 94, RR >20. Endorse chest tightness. Lungs CTA B/L, pt noted to be diaphoretic. Patient had a near syncopal episode and was placed in supine position and given an epi-pen 0.3mg at 1418. EMS was called. Repeat VS at 1420 found BP of 115/60, SpO2 100%, HR 100, RR >20. Lungs still CTA b/l. Patient endorsed improved SOB and less peri-oral itching. Chest tightness improved, Pt was AOX3. EMS arrived at 1435, pt stable. Transferred pt to EMS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Pt given 0.3mg of Epinephrine at 1418 on 14JUL21in R thigh via epi-pen.
Aktuelle Erkrankungen: Hx of CoVID-19 (symptomatic 23JUN21, + PCR 27JUN21)
Vorgeschichte: Currently receiving Venom Immunotherapy (VIT) vaccine for allergic reaction to bee venom, last doses given 12JUL21.***Venom Immunotherapy (VIT) vaccine given 12JUL21**** Administered 1ml SQ RX 02204609 honey bee 100mcg vial per schedule maint in Right arm Administered 1ml SQ RX02204611 mixed vespid 300mcg vial per schedule maint in Left arm Administered 1ml SQ RX 02204612 wasp 100mcg vial per schedule maint in Right Upper arm
Andere Medikamente: Ibuprofen 400mg po q8 prn pain. Zyrtec 10mg po daily.
Allergien: Anaphylaxis to Bee stings
Vorherige Impfungen: -

VAERS 1454907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 30,0
Geschlecht: M
Eingang: 07.07.2021
Impfdatum: 06.07.2021
Beginn: 06.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Immediate post-injection reaction Pallor Skin warm Syncope

Symptomtext

Pt received first dose of Pfizer at 0856 to left deltoid and felt immediately lightheaded and had syncopal episode. Pt was able to regain consciousness 5-10 seconds after syncopal episodes but still complaint about feeling lightheaded. Pt felt warm to touch and had was pale. An ice pack was applied to back of neck, vital signs were checked immediately. Pt was asked if he has anything to eat prior to vaccine and he stated he did not have anything to eat. Ice water and granola bar was offered. Around 0858 pt stated he started to feel better, 0859 vital signs indicated the following BP 111/45, HR 47, SpO2 97% RA. Pt denied going to treatment room for further observation or laying down on gurney. Pt kept insisting he felt a lot better and "none of that was necessary". Pt's skin color came back to normal state and stopped feeling lightheaded after eating and drinking a cup of water. Vital Signs were taken again as the following: BP 104/57, HR 62, SpO2 98% RA. Pt felt safe to go home with significant other. Pt doing well, speaking in full sentences, laughing, alert and oriented x 4.

Weitere VAERSDATA-Felder

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

VAERS 1454819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: TX
Alter: 15,0
Geschlecht: M
Eingang: 07.07.2021
Impfdatum: 07.07.2021
Beginn: 07.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope

Symptomtext

Patient experienced light headedness and fainting after receiving vaccine. Patient was give soda to drink and issue resolved. He had not eaten all day before vaccine and had swim practice for several hours

Weitere VAERSDATA-Felder

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

VAERS 1453914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MO
Alter: 15,0
Geschlecht: F
Eingang: 07.07.2021
Impfdatum: 06.07.2021
Beginn: 06.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Eye movement disorder Hypotension Listless Pallor Syncope Unresponsive to stimuli Vision blurred Visual impairment

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Hypotension-Severe, Systemic: Visual Changes/Disturbances-Severe, Additional Details: I gave the patient the vaccine and within 5 minutes she reported to her mother her vision was blurry and she did not feel right. Shortly after reporting this she fainted and her eyes went back into her head. I ran to her and helped her mother lower her to the ground. I noticed her eyes were now open but she was pale and listless. I called to a tech to call 911. I asked her if she could speak and she nodded. I asked if she had eaten and she shook her head no and her mother said she had not.

Weitere VAERSDATA-Felder

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

VAERS 1450586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 13,0
Geschlecht: F
Eingang: 06.07.2021
Impfdatum: 14.06.2021
Beginn: 19.06.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / LA

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

Dizziness Feeling abnormal Syncope

Symptomtext

Fainted for the first time ever. Light-headed, fuzzy and woozy, and fainted while standing outside on the grass, viewing a performance.

Weitere VAERSDATA-Felder

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

VAERS 1449751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: MO
Alter: 16,0
Geschlecht: M
Eingang: 06.07.2021
Impfdatum: 05.07.2021
Beginn: 05.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Nausea Skin discolouration Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Mild, Systemic: Nausea-Mild, Additional Details: pt became very white, started to look like he was going to faint, got wet towels and applied to face, neck, arms. kept him conscious be talking to him, called ems but by the time they arrived, he had color and was ok

Weitere VAERSDATA-Felder

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

VAERS 1442650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 39,0
Geschlecht: F
Eingang: 02.07.2021
Impfdatum: 08.06.2021
Beginn: 08.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Abdominal pain upper Asthenia Body temperature COVID-19 Decreased appetite Dizziness postural Dyspnoea Fatigue Feeding disorder Gastrointestinal tract irritation Headache Nausea Oral discomfort Pain Pyrexia Shock Syncope Vomiting

Symptomtext

Fell on the floor and could not get herself up; Felt a shock; Puking and throwing up; Headache; Dizziness and could not get self up; Feeling like throwing up; Tightening of the lips; stomach was so painful; Unable to eat; Feeling so weak; Fever; Feeling so tired; Lost a lot of weight; She could not do anything; GI issues like feeling like things in her stomach and not feeling comfortable at all.; She was out of breath from the puking.; Not constipation but a sharp pain.; She does fasting and does not have an appetite; This is a spontaneous report from Other HCP (Nurse assistant; patient herself). A 39-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: EW0186; Expiration Date: 31Aug2021) via an unspecified route of administration, administered in Arm Left on 08Jun2021 as single dose for COVID-19 immunization. Medical history included vitamin D from an unknown date and unknown if ongoing she used to take Vitamin D, accident from 2020 to an unknown date She states there was one time she had an accident and took a baby aspirin. History: Caller used to take supplement but not she did not, she used to take Vitamin D which was a supplement she takes every day like a Vitamin D and a women's pill and she used to take a fish pill but since this time she was not taking anything because she did not want anything that would be contraindication. Caller did not clarify statement or provide any additional details. She states there was one time she had an accident and took a baby aspirin but she did not take it anymore. Caller confirmed she was not taking these at time of vaccination and that her accident occurred prior to the vaccine. Caller added she was not allergic to anything, she had never reported an allergic reaction, and any medication she did not have anything she feels she was allergic to. She was good. Her health was good. Patient had not any other history and products. The patient's concomitant medications were not reported. It was reported that, she received her first injection on 08Jun2021 and she felt like that night and the whole day she threw up, had some puking and stomach, heavy headache, and a lot of dizziness. She called back her husband and her husband called back because she could not do anything. She had a headache, dizziness, fell on the floor and could not get herself up. Caller added that she started feeling like throwing up and her lips would tighten up and her stomach was so painful she has not been able to eat and has been throwing up which is a problem. Right now, she had one week without eating well. She feels like she have to go to the bathroom or like her stomach was upset and she has to throw up instead of having a BM. She had a headache and was feeling so tired and like a headache. She decided to call to see if Pfizer had experienced something like this because of how her stomach was acting. Caller was asked for clarification as she was speaking fast and states she was having GI issues like feeling like things in her stomach and not feeling comfortable at all. Caller stated that night they called 911 because it was serious and was told to take tylenol and she just had been taking tylenol and drinking water for her headache. Caller stated that she was continuing that thing - she was feeling fever and wanted to know. They were taking her temperature and it was 98 points and she was concerned about her fever. Caller stated that they told her husband to give her water and rest which did not work. She did not call because she was so weak and she usually has a good appetite but she did not have an appetite. Caller got her injection at this hospital and this was where she has her primary. Caller did not provide any additional details. Her stomach was hurting, she could not eat anything it was so terrible. Puking and throwing up: first of all, that day, when she went for her vaccine she went to come from work in the morning at 9:45 and went for the injection and they said it was horrible, she felt dizziness, she was sleepy the whole night so she thought she was sleeping like she felt the need to sleep and fell asleep immediately at 11 so that night she was feeling dizzy and weak. She was weak and dizzy and because she was sleepy she woke up around 7 in the evening to get ready for work and that was when she woke up. She fell on the floor, felt a shock and a fall. She started throwing up and her husband came and picked her up because he did not want her to choke because she was sleeping down on the floor. That is when she started throwing up and he gave her a container to throw up. He gave her one to do it, but she was feeling like she could not hold anything and was puking and felt a headache pounding up and felt like everything was going around like she was feeling dizzy. Caller clarifies she does not know what it is called, everything is going around and at that time she was out of breath from the puking. She did not eat because she slept there and there was nothing to puke so she was forcing something to come out so it was just she did not have anything in her stomach to come up. She woke up, and was asleep, she did not know what happened when she went to sleep and when she woke up too. Caller did not provide clear timeline and was asked regarding if events are still occurring and she states for now, the dizziness is not now and was not coming. The headache she takes tylenol now and she takes tylenol when she feels feverish. Caller stated what led her to call Pfizer was about the stomach problems and not eating. Also, the pain that was sharp and was going and it was not constipation but a sharp pain. She did not know how she can describe it a lot, she was having troubles like a stomachache. When she ate something, like the more she eats, like a little pancake one week, he said do not eat because she did fasting and did not have an appetite. When she ate and drinks it was like drinking a lot of water, she could not even drink things she likes. Caller added she was sure she did not have Covid because of every week they get a test. The reporter seriousness for all the events was unspecified. Patient was taking tylenol for headache and fever. The patient underwent lab tests and procedures which included body temperature: 98 points on 08Jun2021, and COVID-19: negative on an unspecified date. The outcome of event dizziness and could not get self up was recovered on an unspecified date while unknown for all other events.; Sender's Comments: Based on plausible temporal relationsip the causal role of the suspect vaccine bnt162b2 cannot be excluded for reported adverse events 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: Shock
Hospital-Tage: -
Labordaten: Test Date: 20210608; Test Name: Temperature; Result Unstructured Data: Test Result:98; Comments: 98 points; Test Name: Covid-19; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Accident (She states there was one time she had an accident and took a baby aspirin.); Vitamin D (she used to take Vitamin D.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1432298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 12,0
Geschlecht: F
Eingang: 02.07.2021
Impfdatum: 26.06.2021
Beginn: 27.06.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

C-reactive protein increased Chest pain Echocardiogram Electrocardiogram T wave amplitude decreased Electrocardiogram abnormal C-reactive protein normal Cough Electrocardiogram T wave abnormal Enterovirus infection Enterovirus test positive Human rhinovirus test positive Pericarditis Pleuritic pain Red blood cell sedimentation rate increased Inflammatory marker increased Influenza virus test Respiratory symptom Respiratory tract congestion

Symptomtext

Pericarditis. Patient was admitted on Monday night 6/28/21 with chest pain for 2 days- constant, pleuritic chest pain that was worse when supine, better when sitting up. EKG with T-wave abnormality. She was admitted for suspected pericarditis by EKG and history of chest pain. Her troponin was negative x2, no evidence of myocarditis by ultrasound. No pericardial effusion. Started on colchicine and ibuprofen. She improved and discharged the next morning 6/29/21. Of note, she also developed congestion, runny nose and mild cough since Sunday night 6/27/21. No fever. Her 2 younger siblings who are in daycare were sick first with colds. Patient RV panel was +enterovirus/rhinovirus on 6/29/21. Therefore the differential diagnosis of her acute pericarditis was upper respiratory viral infection associated pericarditis Vs. COVID-19 Vaccine associated pericarditis given the timing of onset.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 1,0
Labordaten: EKG with T-wave abnormality. Troponin was negative. ESR 59, CRP 26.8 mg/L. Respiratory viral panel resulted positive on 6/29/21 +enterovirus/rhinovirus. COVID serology was negative
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1441131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: ID
Alter: 15,0
Geschlecht: F
Eingang: 01.07.2021
Impfdatum: 17.06.2021
Beginn: 27.06.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Facial paralysis Muscular weakness

Symptomtext

Bells Palsy - Paralysis of left facial muscles - difficulty smiling & blinking with left side. No treatment. Spontaneous recovery started 12 day after onset. Muscle weakness continues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: A week prior, had a minor cold - stuffy nose.
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1440231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: PA
Alter: 13,0
Geschlecht: M
Eingang: 01.07.2021
Impfdatum: 28.06.2021
Beginn: 28.06.2021
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: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Additional Details: pt passed out for less than 1 min after administration. mother was advised to report to md office for follow up and to recieve 2nd dose

Weitere VAERSDATA-Felder

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

VAERS 1439875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 01.07.2021
Impfdatum: 26.05.2021
Beginn: 28.05.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Synovitis Thrombosis

Symptomtext

blood clotted; had persistent synovitis in all knuckles; This is a spontaneous report from a non-contactable consumer (patient). A 57-year-old male patient received first dose of bnt162b2 (BNT162B2, Formulation: Solution for injection, Lot number: ew0186 and Expiration date: unknown), via an unspecified route of administration, in arm left on 26May2021 (at the age of 57-years-old) as dose 1, single for covid-19 immunisation. The patient medical history was not reported. Concomitant medications included amitriptyline hydrochloride (ELAVIL [AMITRIPTYLINE HYDROCHLORIDE]) (MANUFACTURER UNKNOWN), via an unspecified route of administration on an unspecified date at 10 mg and frequency for unknown indication; cetirizine hydrochloride (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) (MANUFACTURER UNKNOWN), via an unspecified route of administration on an unspecified date at unknown dose and frequency for unknown indication; fluticasone propionate (FLONASE [FLUTICASONE PROPIONATE]) (MANUFACTURER UNKNOWN), via an unspecified route of administration on an unspecified date at unknown dose and frequency for unknown indication. The patient previously took flu shot on an unspecified date in 2017 and experienced synovitis. Patient did not receive any other vaccine within 4 weeks prior to the covid vaccine. Prior to vaccination, the patient was not diagnosed with covid-19 and not tested for covid-19 since the vaccination. On 28May2021, since his first Pfizer shot have had persistent synovitis in all knuckles. On an unspecified date in Jun2021, 12 days after first Pfizer shot donated blood and blood clotted in tubes before completion. He had donated about 40 times and that was the first time his blood has clotted. The case was assessed as non-serious. No treatment was received for events. The clinical outcome of had persistent synovitis in all knuckles, blood clotted were not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ELAVIL [AMITRIPTYLINE HYDROCHLORIDE]; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; FLONASE [FLUTICASONE PROPIONATE]
Allergien: -
Vorherige Impfungen: -

VAERS 1437958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 16,0
Geschlecht: F
Eingang: 30.06.2021
Impfdatum: 16.06.2021
Beginn: 16.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood glucose normal Loss of consciousness Pallor Unresponsive to stimuli

Symptomtext

Attendee became pale and momentarily lost consciousness - did not initially respond to verbal of tactile stimuli - required sternal rub, awakened after 1 minute. Vital signs normal. EMS were called. Glucose 86. No transport - mother of Attendee refused this.

Weitere VAERSDATA-Felder

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

VAERS 1437818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 14,0
Geschlecht: M
Eingang: 30.06.2021
Impfdatum: 24.06.2021
Beginn: 27.06.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Echocardiogram Electrocardiogram ST segment elevation Pericarditis Troponin normal

Symptomtext

14 year old male with autism who has chest pain and ECG showing diffuse ST elevation (normal troponin) consistent with pericarditis. He also received his second dose of the Pfizer vaccine 5 days prior to onset of chest pain. Although it is difficult to know for sure if this is vaccine mediated, the timing makes it suspicious. Now hospitalized with observation and pending ECHO results. Symptomatic management with NSAIDS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 3,0
Labordaten: troponin <0.02 on 6/30/21. ECHO results pending 6/30/21 EKG Order: 1378499770 Status: Final result 0 Result Notes Ref Range & Units 6/30/21 0923 Ventricular Rate BPM 80 Atrial Rate BPM 80 P-R Interval ms 158 QRS Duration ms 86 Q-T Interval ms 356 QTC Calculation(Bezet) ms 410 P Axis degrees 63 R Axis degrees 46 T Axis degrees 19 Diagnosis ** ** ** ** * Pediatric ECG Analysis * ** ** ** ** Diagnosis Normal sinus rhythm Diagnosis Diffuse ST elevation consistent with pericarditis. Diagnosis When compared with ECG of 29-JUN-2021 15:44,no significant change was found. Diagnosis Diagnosis Confirmed by MD (605) on 6/30/2021 12:14:48 PM Resulting Agency Specimen Collected: 06/30/21 09:23 Last Resulted: 06/30/21 12:14
Aktuelle Erkrankungen: none
Vorgeschichte: Autism
Andere Medikamente: Aripiprazole 10mg daily Dymista 1 spray to each nostril twice daily Guafacine 1mg twice daily at 1145 and 1630, 2mg daily at 2200 Hydroxyzine 75mg every bedtime melatonin 3mg every bedtime
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1431525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 15,0
Geschlecht: M
Eingang: 28.06.2021
Impfdatum: 28.06.2021
Beginn: 28.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Eye movement disorder Loss of consciousness Malaise Pallor Seizure

Symptomtext

1435, pt received 1st dose of covid vaccine (Pfizer) while sitting in a chair in covid vaccine clinic. NKDA. No known history of seizure per pt's mother. Mother with pt, stated pt started feeling unwell, pale, then losing consciousness. Patient's mother stating patient's eyes started to roll back. 1436, pt had seizure activity, staff lowered pt on the floor, laying on side, no n/v noted, lasted for 25 seconds. VS taken, Oxygen applied. Initial BP 77/26, 100% with 2 L NC oxygen. BP improved to 139/81, HR 74, 100% 2 L NC oxygen after sitting. Pt regained his consciousness, aao x4. 1445, 911 placed. BP 127/64, HR 66, 100% with 2 L NC Oxygen 1500, EMT arrived and transported pt to ER, accompanied by pt's mother

Weitere VAERSDATA-Felder

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

VAERS 1430529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: VA
Alter: 18,0
Geschlecht: M
Eingang: 28.06.2021
Impfdatum: 18.05.2021
Beginn: 03.06.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: IM / RA

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

Deep vein thrombosis Pain Peripheral swelling Thrombosis Ultrasound scan abnormal

Symptomtext

Blood Clot/DVT Pain and swelling in lower extremity following left elbow reconstruction with contralateral gracilis autograft.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound done in ED and patient diagnosed with DVT.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: tree nuts, cefazolin
Vorherige Impfungen: -

VAERS 1382634

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

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Staat: MA
Alter: 13,0
Geschlecht: F
Eingang: 28.06.2021
Impfdatum: 04.06.2021
Beginn: 07.06.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Blood thyroid stimulating hormone Brain natriuretic peptide normal Chest X-ray normal Chest pain Dyspnoea C-reactive protein increased Magnetic resonance imaging abnormal Magnetic resonance imaging heart Myocarditis Electrocardiogram abnormal Full blood count normal Metabolic function test Red blood cell sedimentation rate Red blood cell sedimentation rate increased Troponin T increased SARS-CoV-2 test negative Troponin increased

Symptomtext

Chest pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: Elevated Troponin T high sensitivity. Mildly elevated ESR and CRP. Cardiac MRI - mild myocarditis features.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1430470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: VA
Alter: 50,0
Geschlecht: M
Eingang: 27.06.2021
Impfdatum: 24.06.2021
Beginn: 25.06.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Altered state of consciousness Angiogram cerebral Arteriogram carotid Cardiac monitoring Chills Computerised tomogram head Computerised tomogram neck Echocardiogram Ejection fraction normal Fall Feeling abnormal Incontinence Loss of consciousness Pyrexia Scan normal Scan with contrast Seizure Somnambulism

Symptomtext

First: I had the coronavirus infection at the end of December/beginning of January. Second: I received my First dose of the Pfizer shot on May 24th. Got a fever and body aches for about 24 hours. Thursday June 24th: T-0: Received PFIZER-BIONTECH COVID-19 VACCINE (Link is to the Pfizer Factsheet) T-11.5: Began having fever of 100?F and chills. Took a dose of Nyquil. T-14: Woke up in a daze and was half sleep walking around the room. While walking around in the room I passed out and fell to the floor. Was out for about 10 seconds. My wife woke me. I then passed out a second time and experienced a mild incontinence for about 15 seconds, came out of it and then went to the bathroom. When in the bathroom I passed out on the toilet for about 30 seconds, I experienced incontinence of everything left in me, bowel and bladder, I experienced convulsions and altered state(thousand yard stare). When I came too I began vomiting and had extreme body shakes. Some of this information was relayed to me by my wife obviously. T-15.3: Arrived at hospital and during check in I had another episode. (15 seconds) T-25: In hospital bed I had another episode duration unknown, no one saw me go out but I recall regaining consciousness. T-29: In hospital bed I had another episode duration unknown, no one saw me go out but I recall regaining consciousness. I passed out a total of 6 times.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: I had a heart monitor device on my person monitoring my heart rhythm which remained between 60 to 70 bpm for the duration of my stay. 6/25/21 - 6/26/21 CT CTA HEAD, NECK - 6/26/21 CTA head and CTA neck with contrast 6/26/2021. CLINICAL INDICATION/HISTORY: Multiple syncopal episodes.. COMPARISON: CT scan of the head from 6/25/2021. TECHNIQUE: Multiple axial CT images of the neck were obtained extending from the level of the aortic arch to the skull base during the dynamic infusion 100cc of IV Omnipaque 350 utilizing a CTA protocol. Multiple axial CT images of the head were obtained extending from below the level of the skull base to the vertex after the administration of the IV contrast utilizing a CTA protocol. Multiplanar reconstructions were obtained, including MIP reconstructions as well as curved planar reformats. Multiple additional 3-D surface rendering reformations were performed at a separate workstation. Dose reduction techniques: Automated exposure control, mAs and/or kVp reductions based on patient size, and iterative reconstruction. The specific techniques utilized on this CT exam have been documented in the patient's electronic medical record. Digital imaging and communications and medicine (DICOM) format image data are available to nonaffiliated external healthcare facilities or entities on a secure, media free, reciprocally searchable basis with patient authorization for at least a 12 month period after this study. FINDINGS: GREAT VESSEL ORIGINS: The origins of the great vessels from the aortic arch and the origin of the right common carotid artery from the innominate artery are patent CERVICAL VASCULATURE: Both common carotid arteries are patent throughout their thoracic and cervical segments. The carotid bifurcations are clear with 0% stenosis by NASCET criteria The cervical portions of both internal carotid arteries are also patent.. The right internal carotid artery is asymmetrically small in comparison to the left related to an isolated configuration intracranially. Left vertebral artery dominance is noted. Mild to moderate stenosis is suggested just distal to the origin of the left vertebral artery but this may be exaggerated by beam hardening artifacts related to dense contrast material in the adjacent veins. The origin of the right vertebral artery is patent. Both vertebral arteries are otherwise patent throughout their cervical segments. INTRACRANIAL VASCULATURE: There is no evidence of hemodynamically significant stenosis or occlusion involving the main intracranial branches. The right vertebral artery predominantly ends in the posterior inferior cerebellar artery. Incidental note is made of a hypoplastic A1 segment to the right anterior cerebral artery. There is no evidence of aneurysm formation or underlying vascular malformation. ECHO LIMITED STUDY (W/O COLOR) 6/25/21 Narrative CONCLUSIONS * Limited two-dimensional transthoracic echocardiogram is performed. * No evidence of shunt at atrial level by 2D and negative bubble study X2. * Left ventricular systolic function is normal with an ejection fraction of 65 % by Simpson's biplane. * There is no increased left ventricular wall thickness. * Left ventricular chamber volume is normal. * Left ventricular diastolic function: not assess due to limited study. * Left atrial chamber is normal with a left atrial volume index of 22.66 ml/m^2 by BP MOD. * Right atrial chamber volume is normal. * Right ventricular systolic function is visually normal. * Right ventricular chamber dimension is normal. * Valves not assess due to limited study. Comparison * No prior study is available for comparison.
Aktuelle Erkrankungen: None
Vorgeschichte: Achalasia
Andere Medikamente: N/A
Allergien: Clyndamyacin
Vorherige Impfungen: -

VAERS 1375378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

schwer

Staat: IN
Alter: 26,0
Geschlecht: F
Eingang: 27.06.2021
Impfdatum: 28.05.2021
Beginn: 02.06.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: SYR / LA

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

Arteriogram coronary normal Electrocardiogram ST segment elevation Myocarditis Troponin increased Blood creatine phosphokinase Blood creatine phosphokinase MB Burning sensation C-reactive protein Cardiac discomfort Catheterisation cardiac Chest X-ray Echocardiogram Electrocardiogram Fibrin D dimer Glomerular filtration rate Lipids Myocardial necrosis marker Red blood cell sedimentation rate

Symptomtext

Woke up with burning sensation and pressure in my heart, felt like a heart attack and was treated with Myocarditis, treated with metoprolol succinate to help heal the inflammation of my heart.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: EKGs (x5), SARS antigen test, cardiac stat panel, glomerular filtration rate, CK total and CKMB, c reactive protein, sedimentation rate, d-dimer test, lipid panel, troponin tests (x4) chest X-ray, echocardiogram, heart cath procedure, all performed from June 2nd to June 4th.
Aktuelle Erkrankungen: None
Vorgeschichte: High cholesterol (hereditary)
Andere Medikamente: Rosuvastatin, Estarylla, vitafusion probiotic for digestive health
Allergien: Alcohol (beer, cider, liquor, etc)
Vorherige Impfungen: -

VAERS 1429511

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 16,0
Geschlecht: M
Eingang: 26.06.2021
Impfdatum: 12.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blepharospasm Dizziness Loss of consciousness Somnolence Unresponsive to stimuli

Symptomtext

We were sitting in the after-shot waiting area for the mandatory 15 minute wait period. Patient was getting restless and started asking to leave ~13 minutes after shot. I said ?no, we need to wait the full 15 minutes they recommend?. About on minute later, or ~14 minutes after shot, Patient said he felt like he was going to pass out. As I turned my head to look at him to began to slump towards me unconscious and I held him up by his shoulder and waved the paramedics over. He was unconscious with eyes closed for about 5 seconds and by the time the paramedics got there his eyes were fluttering, but he remained unresponsive for another ~10-15 seconds as they were calling his name, tapping his shoulder, and asking him questions. Then he finally came around and, while groggy, he was able to answer questions. He sat there a couple minutes talking to paramedics and they had wheelchair, but he said he could walk and got up slowly to walk slowly back to clinic area.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood pressure and heart rate monitoring for ~30 minutes in clinic area.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Over the counter multi-vitamin
Allergien: No history at that time
Vorherige Impfungen: -

VAERS 1427759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: UT
Alter: 14,0
Geschlecht: F
Eingang: 25.06.2021
Impfdatum: 25.06.2021
Beginn: 25.06.2021
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 Loss of consciousness

Symptomtext

Patient received vaccine. As she walked out of the consult room she felt dizzy and described that she thought she blacked out. She fell into a plastic room divider and went to the ground. Her dad was right there and hoisted her upright. Offered to call ambulance but patient's dad declined and reported that she had history of being squeamish and had passed out from needles before. Patient was breathing and quickly began responding verbally. Her dad picked her up and she sat upright in a chair. Took patient's blood pressure, provided water, and had patient sit. First blood pressure reading was low (90s over 40s). Offered to call ambulance again. Patient's dad declined. Patient drank water and juice. Retested blood pressure about 15-20 minutes later and it was 116/65 and patient reported that dizziness had subsided. Patient's dad had left message with doctor's office to report what had happened and to see if they wanted her to come in to be seen today. Encouraged him to do that and seek medical attention if anything worsened.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: No known health conditions
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1423147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

schwer

Staat: NY
Alter: 15,0
Geschlecht: M
Eingang: 24.06.2021
Impfdatum: 22.06.2021
Beginn: 23.06.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Dyspnoea Myocarditis Troponin increased

Symptomtext

Dyspnea Myocarditis, transferred to hospital for further management

Weitere VAERSDATA-Felder

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

VAERS 1396490

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NM
Alter: 13,0
Geschlecht: M
Eingang: 24.06.2021
Impfdatum: 07.06.2021
Beginn: 10.06.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: SYR / LA

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

Blood creatine phosphokinase MB increased Chest pain Echocardiogram normal Electrocardiogram ST segment elevation Influenza virus test negative Blood creatine phosphokinase MB normal Blood immunoglobulin G Blood test C-reactive protein normal COVID-19 Coxsackie virus test Cytomegalovirus test Echocardiogram Echovirus test Electrocardiogram Epstein-Barr virus test negative Headache Influenza A virus test negative

Symptomtext

Day 1 no symptoms Day 2 fever, aches Day 3 headaches Day 4 severe chest pain only - hospitalized until day 6 Diagnosed with Pericarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 3,0
Labordaten: Blood work - Triponin levels were abnormally high EKG Echocardiograms Xrays IV Blood work and negative results: C-reactive protein, CKMB, RSP Virus panel, coxsackie a ab panel, CMV AB, IGG, CMV AB IGM, PRO-BNP N-terminal, Epstein-barr, Parvovirus B19 AV, PCR, HSV, PCR, Echovirus. COVID+FLUA/B test negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1421450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: NY
Alter: 12,0
Geschlecht: F
Eingang: 23.06.2021
Impfdatum: 23.06.2021
Beginn: 23.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Electrocardiogram Loss of consciousness Malaise Syncope

Symptomtext

A few minutes after the shot, patient told her mom she didn't feel well and fainted into her mother's arms. She was put on the floor and she was conscious at that time. We put a blanket under her head. I took her BP and it was 111/67. After 5 minutes she wanted to sit up and she sat in a chair and passed out again. 911 was called at that point. We had her on the floor after that until the paramedics arrived. They retook her bp and it was 111/63. They checked her vitals and decided to take her to the ambulance just to give more privacy and have their equipment more readily available.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BP check and EKG with just shoulder and leg electrodes.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Not known
Allergien: NKA
Vorherige Impfungen: -

VAERS 1416909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: CT
Alter: 14,0
Geschlecht: F
Eingang: 22.06.2021
Impfdatum: 08.06.2021
Beginn: 11.06.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: - / -

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

Asthenia Chest X-ray normal Chest pain Chills Diarrhoea Dizziness Dyspnoea Echocardiogram normal Electrocardiogram normal Feeling hot Haemoglobin normal Hyperhidrosis Intensive care Malaise Metabolic function test normal Nausea Pallor Palpitations

Symptomtext

Patient is a 14 yo girl with PMH significant for migraines who presented with one day of chest pain and nausea that woke her from sleep in the setting of multiple days of malaise. She states that after receiving the COVID-19 vaccine three days prior to admission she has not been feeling well. She reports subjective fevers and chills the day after receiving the vaccine, and intermittent feelings of her heart racing. She also has been feeling hot and generally unwell. + shortness of breath. The night of admission, she awoke from sleep with burning central anterior chest pain and nausea. She tried to stand up and felt generally weak, and then had tunnel vision and felt she was going to faint. Per mom, she was pale and diaphoretic at that time. The pre-syncopal symptoms resolved within about 10 minutes and the chest pain persisted for approx one hour. Parents called EMS and she was brought to the ED for evaluation. Of note, she reports a history of pre-syncopal sx however has never lost consciousness before. Also reports a history of intermittent palpitations. No hx chest pain prior to this episode. + fevers/chills as mentioned after receiving COVID vaccine three days PTA but no infectious sx prior to that. No cough/URI sx, no abdominal pain, no nausea. + diarrhea night of admission. No sick contacts. She is active in dance and has good exercise tolerance for that; does not spend much time outdoors. No known insect or tick bites. + FHx of sister with heart murmur as a baby that spontaneously resolved; unclear diagnosis. In the ED BP 94/62, T 97.4, P 84, R 16, SpO2 100% on RA EKG: sinus rhythm, no ST or PR changes CMP: unremarkable CBC: WBC 11.8, Hgb 11.5 Trop T 0.33 Bedside echo w/ reported good function UA wnl COVID neg CXR PA and lat unremarkable On arrival to the PCICU she reported feeling at her baseline and denied chest pain and shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 3,0
Labordaten: see above
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: erythromycin
Vorherige Impfungen: -

VAERS 1416452

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: OR
Alter: 14,0
Geschlecht: F
Eingang: 22.06.2021
Impfdatum: 18.06.2021
Beginn: 21.06.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

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

Blood creatine phosphokinase MB increased Myocarditis Troponin increased Blood test C-reactive protein increased Chest pain Dyspnoea Echocardiogram normal Electrocardiogram normal SARS-CoV-2 test negative

Symptomtext

Pt visit ER 3 days post 2nd Covid-19 vaccine on 6/18/21. SOB started following day, CP last night. Diagnosed with Myocarditis during ER visit. Discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: 11:53 AM- Current work up is reassuring. I have paged Dr, pt's PCP, to consult. He will page me back when he is available. 12:09 PM- I have consulted Dr., pt's PCP, regarding patient. I discussed the presenting symptoms, current exam, abnormal findings, and pertinent laboratory & imaging investigations. Dr. is aware of the pt and will reach out for follow up. He has no acute concerns at this time. He recommends supervision, hydration, and treating with antiinflammatories/tylenol. 12:45 PM- Troponin is elevated. Will obtain further labs for evaluation. I have paged pediatric hospitalist on call to consult. 12:53 PM- I have consulted Dr., pediatric hospitalist, regarding patient. I discussed the presenting symptoms, current exam, abnormal findings, and pertinent laboratory & imaging investigations. Dr. recommends transfer for cardiac monitoring and telemetry. I have updated the pt and her father on our current findings and plan of care, and they are agreeable. 1:06 PM- I have paged pediatric cardiologist on call to consult. 1:31 PM- I have consulted Dr. , pediatric cardiologist, regarding patient. I discussed the presenting symptoms, current exam, abnormal findings, and pertinent laboratory & imaging investigations. Dr. recommends ECHO given normal EKG and troponin of 0.08. If ECHO shows no acute findings, she recommends discharge for follow up with her PCP tomorrow for repeat troponin. If ECHO is positive, she recommends transfer. 3:17 PM- CRP is elevated. SED rate is normal. COVID-19 test is negative. I have updated Dr., pt PCP, on our current findings and plan of care. He will see her in his office tomorrow for troponin trending if she is not transferred. 4:07 PM- The pt will be signed out to my colleague, Dr. , pending ECHO. Transthoracic ECHO: Summary Structurally normal heart Normal biventricular size and function No pericardial effusion 5:42 PM: Pt's ECHO has resulted and is reassuring. The pt is stable for discharge, we discussed plan, and they are agreeable. They will follow up with cardiology for further evaluation as needed. Strict return precautions were given prior to discharge for any worsening or concerning symptoms. Impression: 1. Myocarditis
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1415367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CO
Alter: 15,0
Geschlecht: F
Eingang: 21.06.2021
Impfdatum: 08.06.2021
Beginn: 15.06.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Pain Syncope

Symptomtext

achy- fainted when outside in the sun. We called PCP, said no reason to worry and hydrate. BUT her sister was admitted with myocarditis and her brother also passed out the same day! Feels like a HUGE coincidence.

Weitere VAERSDATA-Felder

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

VAERS 1415191

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: IL
Alter: 14,0
Geschlecht: M
Eingang: 21.06.2021
Impfdatum: 13.06.2021
Beginn: 17.06.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Conduction disorder Echocardiogram normal Electrocardiogram abnormal Myocarditis QRS axis abnormal Sinus arrhythmia Troponin increased

Symptomtext

Patient is a 14 year old male without significant past medical history presenting with chest pain and elevated troponin consistent with myocarditis after second COVID vaccine administration. His troponin level peaked at 4.0 mg/mL. Chest pain resolved prior to discharge. ECG and Echocardiogram results below, both overall unremarkable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 1,0
Labordaten: ECG demonstrated normal sinus rhythm with sinus arrhythmia, left axis deviation (mild) , and non-specific intra-ventricular conduction delay. Echocardiogram impression: 1. Normal-size right ventricle; no evidence of right ventricular hypertrophy; qualitatively normal right ventricular systolic function. 2. Normal-size left ventricle; normal left ventricular wall thickness; normal left ventricular systolic function - LV FS (2D) = 36 %, z = 0.4 - LV EF (AL) = 68 % - LV global longitudinal strain (triplane) = -20.4 %. 3. Normal cardiac valve morphology and function. 4. No pericardial effusion.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1386073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TX
Alter: 16,0
Geschlecht: M
Eingang: 21.06.2021
Impfdatum: 04.06.2021
Beginn: 06.06.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / UN

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

Adenovirus test Aspartate aminotransferase increased Asthenia Blood creatine phosphokinase increased Blood lactate dehydrogenase increased C-reactive protein increased Chest discomfort Chest pain Cold sweat Bordetella test negative Cardiac telemetry Chest X-ray normal Electrocardiogram abnormal Chlamydia test negative Cytomegalovirus test negative Drug screen positive Echocardiogram normal Electrocardiogram ST segment elevation

Symptomtext

June 4: Vaccine received June 6 (AM): felt arm pain and mild chest pain not affected by breathing or moving. Continues on and off, but was relieved by ibuprofen. June 7: 1PM- chest pain became persistent, not relieved by ibuprofen. Describes as squeezing with palpitation's. Accompanied by feeling clammy, weak, pale, subjective fever. Brought to ED and transferred to Pediatric ICU 6/7 at 18:44 for labs and imaging consistent with myopericarditis. Started treatment on scheduled Ibuprofen (600 mg q8 hours). Chest pain improving, but serial troponin continued to rise. 6/9: NSAID changed to Toradol for continued chest pain with colchicine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 4,0
Labordaten: Initial CRP-3.0; troponin-9.37; ECG with St elevation consistent with acute myopericarditis 6/7. Viral evaluation negative including respiratory PCR for adeno. 6/9 troponin 13.37 pertussis, Chlamydophila pneumoniae, Enterovirus, Human metapneumovirus, Rhinovirus, Influenza A & B, Respiratory syncytial virus, Cytomegalovirus, Mycoplasma pneumoniae, non-COVID-19 coronavirus, Parainfluenza virus. 6/7: SARS CoV-2 negative, Echocardiogram structurally normal heart, normal coronaries, no pericardial effusion noted, normal strain (-19). 6/8: troponin up to 9.91, AST 53, LDH 277, total CK 379, PT 12.7, CRP 3.0. Testing negative for adenovirus PCR, EBV panel, and toxoplasmosis serology. ECG with ST elevation (consider for acute pericarditis). Pain well controlled on scheduled Ibuprofen, stable, normal blood pressure and heart rate. on continuous pulse oximetry and telemetry for monitoring with serial troponin levels every 6 hours. 6/9/:SARS CoV-2 Spike Ab, semi Quantitative testing via clinic laboratories sent, with high positive results >250 U/ml. Troponin 13.37. ECG with ST abnormality. 6/10: Improving labs: troponin 3.10, CK 126, CRP 0.7; presumptive positive urine drug screen for cannabis. ECG normal. Echocardiogram normal, no pericardial effusion. Continued improvement clinically. 6/11: continuous CK 89, troponin 0.30. Discharged home on colchicine (0.6 Mg PO qDay x 6 weeks), famotidine (20 Mg qDay x6 weeks), hydroxizine (25 Mg PO bid as needed for anxiety; Ibuprofen (600Mg PO tid x6 weeks); and senna. Instructed to resume his SSRI until resolution of treatment for pericarditis for anxiety after consulting with psychiatry in 4-6 weeks.
Aktuelle Erkrankungen: mild congestion 2 weeks prior
Vorgeschichte: anxiety and depression (stopped Zoloft 1.5 weeks prior to vaccination)
Andere Medikamente: none
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1413225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: FL
Alter: 25,0
Geschlecht: M
Eingang: 20.06.2021
Impfdatum: 19.06.2021
Beginn: 19.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Dizziness Flushing Hyperhidrosis Hypotension Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Systemic: Weakness-Medium, Additional Details: PATIENT STARTED FEELING WEAK AFTER A FEW MINUTES OF SITTING DOWN, HE THEN FAINTED/UNRESPONSIVE SO I LAYED THE PATIENT DOWN AND RAISED HIS LEGS, PATIENT CAME CONSCIOUS IN LESS THAN A MINUTE. I STAYED BY PATIENTS SIDE UNTIL HE WAS FEELING WELL AND CONFIDENT ABOUT LEAVING THE PHARMACY. PATIENT RECOVERED PRETTY WELL.

Weitere VAERSDATA-Felder

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

VAERS 1413039

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: AZ
Alter: 49,0
Geschlecht: M
Eingang: 19.06.2021
Impfdatum: 08.06.2021
Beginn: 17.06.2021
Tage bis Beginn: 9,0
Dosis: UNK
Route/Site: IM / -

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

Facial paralysis Lacrimation increased

Symptomtext

Patient experienced facial drooping on the right side of his face starting on 6/17/21 and worsening over the next two days. He experienced tearing in his right eye. Patient denies any additional symptoms. Recommended patient be seen by provider asap to rule out potential stroke. Patient denies any additional symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: liver abscess of unknown origin
Vorgeschichte: liver abscess of unknown origin, heart failure
Andere Medikamente: entresto 49mg-51mg, amox-clav 875-125mg, spironolactone 25mg, carvedilol 12.5mg , furosemide 20mg, multivitam centrum silver, super B complex
Allergien: none known
Vorherige Impfungen: -

VAERS 1412936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: OR
Alter: 15,0
Geschlecht: M
Eingang: 19.06.2021
Impfdatum: 10.06.2021
Beginn: 12.06.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Chest X-ray normal Electrocardiogram Laboratory test normal Pericarditis Pleuritic pain

Symptomtext

Pericarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Pleuritic chest pain that is worse laying down and better sitting up. EKG with subtle changes. Chest xray and labs normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1412441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: WA
Alter: 43,0
Geschlecht: F
Eingang: 19.06.2021
Impfdatum: 02.06.2021
Beginn: 02.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Chills Head injury Nausea Pyrexia Syncope Vomiting

Symptomtext

Fainted; Bumped my head on the tiles in the bathroom; Nauseous; Fever; Chills; Vomiting; This is a spontaneous report from a contactable consumer (patient). A 43-year-old non-pregnant female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Left on 02Jun2021 10:00 (Lot Number: EW0186) as single dose for covid-19 immunisation at the age of 43-year-old. The patient was healthy, no illnesses before vaccination. Concomitant medications included calcium carbonate, colecalciferol (VITAMIN D 2000), ascorbic acid, rosa canina fruit (VITAMIN C & ROSEHIP). The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination and hasn't been tested for COVID-19 since the vaccination. The patient previously received the dose 1 administered in Arm Left on 12May2021 11:15 (Lot Number: EW0183) at the age of 43-year-old. On 02Jun2021 22:00, the patient felt nauseous, had fever, chills and vomiting. On 03Jun2021 07:00, the patient fainted and bumped the head on the tiles in the bathroom. The events resulted in visit of Emergency room/department or urgent care. Treatment received for the events. The outcome of the events was recovering. The patient reported, my symptoms began 12 hours after the second dose. I felt nauseous throughout the night and I had fever, chills and vomiting. 21 hours after vaccination I fainted and I bumped my head on the tiles in the bathroom. My husband called 911. Emergency check received from first responders. Follow up attempts are needed. Further information has been requested

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: VITAMIN D 2000; VITAMIN C & ROSEHIP
Allergien: -
Vorherige Impfungen: -

VAERS 1396023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: IL
Alter: 16,0
Geschlecht: M
Eingang: 14.06.2021
Impfdatum: 14.06.2021
Beginn: 14.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

Patient briefly passed out within 5 minutes of receiving the vaccination. He came around within 15 seconds of passing out. He was responsive. He was sitting down when he passed out. He did not fall or injure his head.

Weitere VAERSDATA-Felder

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

VAERS 1394691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: OR
Alter: 15,0
Geschlecht: M
Eingang: 13.06.2021
Impfdatum: 10.06.2021
Beginn: 13.06.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / -

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

C-reactive protein Chest pain Electrocardiogram Myocarditis Troponin I increased Pain in extremity

Symptomtext

2.5 days after dose #2 of the Pfizer COVID vaccine, Patient developed acute myocarditis with L chest/arm pain and elevated Troponin I

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: 6/13 3AM Troponin 1.89 6/13 10AM Troponin 4.01
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1392782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0186

schwer

Staat: NY
Alter: 13,0
Geschlecht: M
Eingang: 13.06.2021
Impfdatum: 06.06.2021
Beginn: 08.06.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / -

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

Cardiac monitoring Chest pain Electrocardiogram Intensive care Laboratory test Chest X-ray Echocardiogram Electrocardiogram ST segment elevation Electrocardiogram abnormal Full blood count normal Metabolic function test normal Painful respiration Pericardial effusion Troponin normal Pericarditis Tachycardia

Symptomtext

Approximately 2 days post 2nd dose of Pfizer COVID 19 vaccine, the patient developed chest pain. 3 days later the symptoms were reported to me (PCP) and I sent him to the emergency room. He was found to have troponin negative pericarditis and tachycardia and was admitted to the pediatric ICU at NY Methodist hospital for telemetry and monitoring. He was given IVF and toradol during his admission and cardiology was consulted. He was discharged < 24 hours later on indomethacin with a normal heart rate to follow up with cardiology in one week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 1,0
Labordaten: Normal troponins. EKG performed other tests drawn in ER not reported to me
Aktuelle Erkrankungen: None
Vorgeschichte: Depression
Andere Medikamente: Vitamin D, Calcium
Allergien: None
Vorherige Impfungen: -

VAERS 1391524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 11.06.2021
Impfdatum: 07.06.2021
Beginn: 07.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Flushing Loss of consciousness Nausea

Symptomtext

Patient received Pfizer dose . Son called out for assistance as patient appears "passed out". Patient was sitting in chair. Vitals 1205: 97.8, 52, 117/70, 98%. Patient states she feels "faint, dizzy and nausea". Patient looks flushed. Legs elevated, patient laying down. Last set of vitals at - 52, 102/66, 98%. No meds given. Patient nausea gone. States she feels "much better"

Weitere VAERSDATA-Felder

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

VAERS 1391514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 12,0
Geschlecht: F
Eingang: 11.06.2021
Impfdatum: 07.06.2021
Beginn: 07.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient fainted in her chair in the observation room after her first Pfizer Covid Vaccine injection. Patient was taken by wheelchair and transferred to stretcher to lay down. BP 114/76, HR 90, R 16, O2 sat 100%. Patient was awake and given some water to sip on. BP 105/72, HR 84, R 16, O2 sat 100%. She stated that she was feeling better and discharged home.

Weitere VAERSDATA-Felder

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

VAERS 1391485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 15,0
Geschlecht: F
Eingang: 11.06.2021
Impfdatum: 04.06.2021
Beginn: 04.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope

Symptomtext

Patient became lightheaded and fainted in her chair in the observation room post injection. BP 103/71, HR 66, R 16, O2 sat 100%. Patient was given water and graham crackers. Continued to monitor patient; at 1003, BP 106/70, HR 73, R 16, O2 sat 100%. Patient stated that she was feeling better and was ready to leave. Patient was discharged to mother to go home.

Weitere VAERSDATA-Felder

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

VAERS 1389568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: OR
Alter: 39,0
Geschlecht: M
Eingang: 10.06.2021
Impfdatum: 18.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Bell's palsy

Symptomtext

Bells Palsy

Weitere VAERSDATA-Felder

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

VAERS 1389037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: GA
Alter: 20,0
Geschlecht: F
Eingang: 10.06.2021
Impfdatum: 18.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Dizziness Fall Loss of consciousness Pain in jaw

Symptomtext

Adverse effects began 3 to 4 hours after vaccination. Patient reports arm soreness with pain moving down arm and into chest, back and top of jaw. Patient got up and felt dizzy. Fell over and blacked out with eyes open for a few seconds. She does not remember falling over.

Weitere VAERSDATA-Felder

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

VAERS 1387734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 10.06.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Asthma Dyspnoea Influenza like illness Musculoskeletal chest pain Oropharyngeal pain Oxygen saturation Oxygen saturation decreased Pain Seizure Sinus congestion Throat irritation Upper respiratory tract congestion

Symptomtext

Asthma; Oxygen was 89; Shortness of breath/breathing difficulties; Ribs hurt; Felt like she was coming down with the flu; Head and sinus congestion; Head and sinus congestion; Throat was on fire, it hurt so bad; Throat was on fire, it hurt so bad; Seizure; Kind of achy/achy feeling; This is a spontaneous report from a contactable consumer (patient) via medical information team. A 40-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EW0186), via an unspecified route of administration, administered in left arm on 22May2021 10:45 (at the age of 40 years old) as 1st dose, single for COVID-19 immunization, at a pharmacy. Medical history included epilepsy from an unknown date and unknown if ongoing (seizure free for two years; diagnosed in 2009 or 2010). Concomitant medications were not reported. On 23May2021, the patient was having breathing difficulties and had to go the emergency room (ER). The patient reported she went to the ER Monday, 24May2021 and was released 11 hours later. She also stated that on Sunday morning on 23May2021, she woke up at 0400 AM and her throat was on fire, it hurt so bad. This was Sunday at 0400, and her husband heard her, and they walked around the house, she had her hands over head, like when running and her ribs hurt. She raised her arms, and tried to take deep breaths, and it was working, to breathe, but it felt like she couldn't breathe, she couldn't catch her breath. She stated she went to work and in 1.5 hours came home, she called the pharmacy and said she can't breathe, then she was told this is not normal. She was told to go to the hospital, and she went and stated that her oxygen was 89 and then it shot up to 92 with standing and raising her arms up over her head, and they did 6 breathing treatments and 3 doses of steroids in her IV and oxygen and she went up to 98. She was sent home with a diagnosis of asthma with albuterol inhaler and nebulizer machine, treatments and said that she all of a sudden has asthma. She then added she had a seizure Sunday morning of 23May2021. She also felt like she was coming down with the flu. On 22May2021, Saturday night, she was kind of achy, then on Sunday, 23May2021, she felt like she was coming down with flu, she had head and sinus congestion, the achy feeling, all that was fine, it was the breathing that scares her. The patient was not hospitalized due to the events. The outcome of the event seizure was unknown and for other events was recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Test Date: 20210524; Test Name: Oxygen; Result Unstructured Data: Test Result:89; Test Date: 20210524; Test Name: Oxygen; Result Unstructured Data: Test Result:92; Test Date: 20210524; Test Name: Oxygen; Result Unstructured Data: Test Result:98
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Epilepsy (Was seizure free for two years; diagnosed in 2009 or 2010.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1381974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NC
Alter: 53,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: 07.06.2021
Beginn: 07.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Confusional state Dizziness Flushing Headache Hyperhidrosis Hypoaesthesia Hypotension Loss of consciousness Paraesthesia Syncope

Symptomtext

Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Mild, Systemic: Headache-Mild, Systemic: Hypotension-Medium, Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild

Weitere VAERSDATA-Felder

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

VAERS 1381943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: CA
Alter: 14,0
Geschlecht: F
Eingang: 08.06.2021
Impfdatum: 07.06.2021
Beginn: 07.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Asthenia Fall Injection site bruising Syncope

Symptomtext

Site: Bruising at Injection Site-Mild, Systemic: Weakness-Medium, Additional Details: pt was anxious and light headed she fainted on the floor gradualyl no bursing or hurt. pt was able to walk to car to head home and rest

Weitere VAERSDATA-Felder

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

VAERS 1381878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

schwer

Staat: NY
Alter: 53,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: 26.05.2021
Beginn: 07.06.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: SYR / LA

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

Bell's palsy Facial paralysis Headache Hypoaesthesia

Symptomtext

Headache, facial drooping, numbing sensation, 7:30am

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Bells Palsey 06/07/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1381789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 12,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: 08.06.2021
Beginn: 08.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Fall Loss of consciousness Seizure

Symptomtext

Patient collapsed to the floor and sustained a seizure <1min. patient states LOC. parent of the patient states no prior hx of seizure.

Weitere VAERSDATA-Felder

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

VAERS 1377962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NC
Alter: 27,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: 03.06.2021
Beginn: 05.06.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Blood creatine phosphokinase MB Blood creatine phosphokinase increased Dyspnoea Echocardiogram abnormal Malaise Catheterisation cardiac normal Chest pain Condition aggravated Myocarditis Pericardial effusion Pleuritic pain Pyrexia Troponin increased Painful respiration

Symptomtext

Patient received second dose of COVID vaccine on 03JUN2021 and 2 days later began having pleuritic chest pain and fever which improved with ibuprofen. Chest pain continued to worsen and presented to regional hospital. Started on Colchicine, had elevated troponins. Echocardiogram showing pericardial effusion. Left heart cath at hospital was unremarkable with no evidence of CAD. Still with mild pleuritic chest pain with deep inspiration but none at baseline. The admission diagnosis is myocarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: Tourette's
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1377138

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NY
Alter: 17,0
Geschlecht: F
Eingang: 07.06.2021
Impfdatum: 06.06.2021
Beginn: 06.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose Cold sweat Electrocardiogram Eye movement disorder Feeling abnormal Hyperhidrosis Hypoacusis Loss of consciousness Malaise Metabolic function test Pallor Seizure Urine analysis

Symptomtext

After receiving the vaccine we moved to waiting area. Within minutes she told me she was not feeling well she began sweating profusely, her skin became pale and clammy, her eyes rolled back she lost consciousness and began convulsing. She came to and said she could not hear well. She was taken to ED for observation and testing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: 6/6/2021 taken to ED urine test, glucose test, blood work up (metabolic panel), and EKG
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1341031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NC
Alter: 24,0
Geschlecht: M
Eingang: 07.06.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
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 Hyperhidrosis Loss of consciousness

Symptomtext

checked yes to having a reaction including fainting and feeling dizzy. When counseled they said they usually pass out but need a companion with them to comfort them. She was asked if she ate, and she said No. After administration, patient head tilted back, eyes closed fist clenched. Later patient recovered and said would report to doctor.

Weitere VAERSDATA-Felder

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

VAERS 1376779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: IN
Alter: 48,0
Geschlecht: F
Eingang: 06.06.2021
Impfdatum: 05.06.2021
Beginn: 05.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anaphylactic reaction Dizziness Dyspnoea Flushing Hyperhidrosis Syncope Tremor

Symptomtext

Systemic: Allergic: Anaphylaxis-Medium, Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Medium, Systemic: Shakiness-Medium, Additional Details: Patient was transported to Emergency Department, after 1 dose of epinephrine was given by EMT in store.

Weitere VAERSDATA-Felder

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

VAERS 1376739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 13,0
Geschlecht: F
Eingang: 06.06.2021
Impfdatum: 05.06.2021
Beginn: 05.06.2021
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 Syncope

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Mild, Additional Details: PATIENT PASSED OUT/FAINTED BUT DIDNT LOSE FULL CONSCIOUSNESS, WAS ABLE TO STATE HER NAME AT FIRST RECALL

Weitere VAERSDATA-Felder

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

VAERS 1376632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: AZ
Alter: 19,0
Geschlecht: F
Eingang: 06.06.2021
Impfdatum: 05.06.2021
Beginn: 05.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Hyperhidrosis Hypoaesthesia Malaise Nausea Syncope

Symptomtext

Patient experienced increased perspiration, chills, nausea, numbness in her fingertips, and syncope that lasted for about 30 seconds. This occurred about 15 minutes after receiving the vaccination. Paramedics were called per the request of the mother soon after she informed me that the patient was not feeling well. When the paramedics came, vitals were taken and she was escorted to the hospital.

Weitere VAERSDATA-Felder

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

VAERS 1376360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 06.06.2021
Impfdatum: 05.06.2021
Beginn: 05.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Dizziness Seizure Syncope Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Medium, Systemic: Seizure-Severe

Weitere VAERSDATA-Felder

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

VAERS 1376319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 12,0
Geschlecht: F
Eingang: 06.06.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
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 Syncope Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Medium

Weitere VAERSDATA-Felder

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

VAERS 1375998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NY
Alter: 25,0
Geschlecht: M
Eingang: 04.06.2021
Impfdatum: 04.06.2021
Beginn: 04.06.2021
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 decreased Dyskinesia Electrocardiogram normal Eye movement disorder Loss of consciousness Seizure Tremor

Symptomtext

25 year old Male with no significant PMH presented to the vaccination clinic for his first dose of the covid-19 vaccine. Patient recieved the dose at 6PM and around 6:10pm the nurse saw the Patients eyes roll back and began to shake all four extremities "jerky movements". Patient lost consciousness for about 15-30 seconds. Once Patient regained consciousness he began to say "What happened to me?". EMS was present and PA's. Patient reported that he had no symptoms prior to experiencing the seizure. Patient denies history of seizures, shortness of breath, chest pain, dizziness, blurry vision, abdominal pain, numbness/tingling, weakness and headache. Of note Patient has syncopized previously from blood draws. Patient was place on a 12 lead ekg: ekg unremarkable with no ST elevations, no inverted t waves, normal rate, intervals within normal intervals and no peaked t waves. Patients blood glucose was taken initially reading 54 and then Patient was given oral orange juice and the second blood glucose reading was 103. Patients initial vitals were HR: 62 RR:14, BP:117/82 with a SPO2: 100% on RA Second vital readings after 20mins there HR: 65 RR:15 BP:133/94 SPO2: 100% on RA. Patients physical exam revealed neurological exam within normal limits, Patient alert and oriented x4. Cranial nerves 2-12 intact, steady gait, ambulatory, normal finger to nose, no romberg, sensation intact in all fours extremities, all fours extremities reveal a strength of 5/5 and normal coordination. Patient was in no acute distress, alert and oriented. Cardiac exam: regular rate, rhythm, no rubs, murmurs, or gallops. Pulmonary: lungs clear bilaterally, no wheezing or rhonchi and airway patent. HEENT: Pupils equal round and reactive to light, EOM intact, airway patent, moist mucosa, no tongue lacerations, uvula mid-line. Patient was transported to the hospital via ambulance by Paramedic and EMT. Patients Mother was informed of what occurred at the vaccination site and was informed that her son was being transported to the hospital given Patients first seizure and no history of seizures.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood Glucose: 54 and second blood glucose reading was 103
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 1372786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TX
Alter: 28,0
Geschlecht: M
Eingang: 03.06.2021
Impfdatum: 03.06.2021
Beginn: 03.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Syncope

Symptomtext

Syncope and Sweating. Laying down and water. Fully recovered after 30 or so minutes.

Weitere VAERSDATA-Felder

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

VAERS 1371878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 16,0
Geschlecht: F
Eingang: 03.06.2021
Impfdatum: 03.06.2021
Beginn: 03.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Presyncope

Symptomtext

Vasovagal event. Pt fainted and immediately came to. Pt felt better after about 15 minutes and was able to walk.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NO KNOWN ALLERGIES
Vorherige Impfungen: -

VAERS 1368727

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 02.06.2021
Beginn: 02.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Confusional state Dizziness Dyspnoea Fatigue Loss of consciousness Vomiting

Symptomtext

Roughly 2 minutes after receiving her I am Pfizer vaccine, patient told mother that she was feeling slightly lightheaded. She proceeded to lose consciousness. Mother honk the horn and alerted staff to come to help. Patient was in the car on the passenger side, patient was fully sitting up. I reclined her all the way down in her passenger seat, she was slightly gasping for air, Ambulance was called for evaluation. She had loss of consciousness for approximately 30 seconds. She regained consciousness and said she was feeling confused as to what it happened. Denies any feelings of needing to vomit, Or post ictal symptoms. EMS and fire we?re on scene by then, report given to paramedics on site. Patient declined further medical treatment and Ian made with the ambulance. after this stating she was a little tired. She continue to wait for 30 minutes, she had 1 episode of emesis and felt better. At the site with no issues.

Weitere VAERSDATA-Felder

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

VAERS 1368131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: DE
Alter: 34,0
Geschlecht: M
Eingang: 02.06.2021
Impfdatum: 21.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia Disturbance in attention Dizziness Electric shock sensation Electrocardiogram normal Fall Fatigue Feeling abnormal Gait inability Heart rate increased Hyperhidrosis Influenza like illness Laboratory test normal Memory impairment Muscular weakness Nausea Speech disorder Vertigo

Symptomtext

16 hours after my second shot, I woke up with some nausea. I went to the bathroom, did not vomit, however in the middle of urinating I collapsed on the floor, couldn't walk, couldn't form full sentences, started sweating profusely, had to crawl back to my bed, and my pulse was through the roof. I almost went to the ER, but the episode subsided within 15 minutes. When I tried to fall back asleep, it felt like I was blacking out and not drifting asleep. The next day, I experienced the typical flu like symptoms. Followed by 4 days of normalcy. On the 4th day, while working, I experienced a sharp 3 second "electric shock" feeling in my left side of my chest. On the 5th day, I already had previously scheduled an appointment with my primary for a physical. I told her about my episode; she took an EKG which yielded normal results. Lab work also looked ok. On the 6th day, I started feeling some more nausea and fatigue. On the 7th day, the vertigo intensified tenfold, and the room was spinning. That's when I started experiencing the following symptoms: ? More nausea. ? Dizzy spells that come and go, especially after eating. ? Persistent periodic electric shock feeling in my left chest. It?s dull but annoying. And just when I think it?s gone for good, another 1 second shock happens. ? Left arm is weak - the entire arm. ? When I try to sleep, the left side of my head feels as though I?m blacking out when I start drifting. It almost feels like I?m getting anesthesia or something like that. But just the left side. ? Basically the left side of my body (I got the jab in my left arm) from the waist up just feels off. ? One of my arms is numb when I wake up until I shake it out. It?s not one particular arm. ? Energy levels are low. Especially when I wake up and start moving around. On the 8th day, I went to the ER thinking perhaps it was a heart attack. Nothing - EKG was again normal and lab work was normal. The doctor told me it's all in my head - anxiety. However, I'm not anxious and I'm a very level headed individual. It's now day 12 and I feel overall awful. I can't concentrate on anything. I'm not thinking clearly and forgetting simple things. The dull feeling and electric shocks on my left side continue. I've never felt this bad before. I'm a healthy 34 year old that exercises regularly, has never smoked or done drugs, rarely drinks alcohol, and eats generally very healthy. If given a second chance I would not take the covid shot. I am praying this goes away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: EKG on 5/27, 5/29 Bloodwork on 5/27, 5/29
Aktuelle Erkrankungen: None
Vorgeschichte: GERD
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1368070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 19,0
Geschlecht: M
Eingang: 02.06.2021
Impfdatum: 02.06.2021
Beginn: 02.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Syncope

Symptomtext

Faint, vaers reaction. BP: 118/72 PR: 68 SPO2:98% Room air Recorded by RN & Medic.

Weitere VAERSDATA-Felder

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

VAERS 1367756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 35,0
Geschlecht: M
Eingang: 02.06.2021
Impfdatum: 02.06.2021
Beginn: 02.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Fall Hyperhidrosis Pallor Presyncope

Symptomtext

Dizziness-Fell from chair to floor. Pale, diaphoretic-vasovagal. Moved from floor to stretcher by EMS, brought to med screening for evaluation. B.P :103/60 Rechecked 116/74. Left in stable condition at 12:53 . Recorded by RN and Medic.

Weitere VAERSDATA-Felder

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

VAERS 1362637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: OH
Alter: 16,0
Geschlecht: M
Eingang: 02.06.2021
Impfdatum: 28.05.2021
Beginn: 30.05.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / -

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

Brain natriuretic peptide increased Cardiac imaging procedure abnormal Chest X-ray normal Chest discomfort Chest pain Echocardiogram Electrocardiogram ST segment elevation Myocarditis Troponin I increased Chills Condition aggravated Echocardiogram normal Myocardial necrosis Myocardial oedema Pyrexia SARS-CoV-2 test negative

Symptomtext

Patient received second dose of Pfizer COVID-19 vaccine on 5/28/21. Within 12 hours patient experienced chills and subjective fever. The follow day patient reported developing fever. The day prior to admission (admitted 5/31/21) patient developed chest pain but worsened to 8-9 out of 10. Pain described at pressure in the center/sternal area of chest or like bricks on his chest. No pleurisy or radiation of pain, pain worsened when supine. Negative for shortness of breath, syncope, palpations. Did no improve with acetaminophen or ibuprofen at home. Patient presented to outside hospital where troponin was 0.37 and EKG showed ST abnormalities. Patient received 30 mg of ketorolac and 4 mg of ondansetron and was transferred to this facility. In our ED, pain improved to 4-5 out of 10. Diffuse ST elevations on EKG, troponin elevated to 7.38. Chest X-ray and rapid covid test were negative. Patient was started on naproxen sodium 500 mg enteral BID 5/31/21 through discharge on 6/2/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: BNP 133.3 pg/mL on admission. Troponin I peaked at 9.674 ng/mL early in admission and then down trended (last 3.884 on 6/2/21 prior to discharge). Chest x ray was negative on admission. EKG on 5/31/21 read as: normal sinus rhythm, ST elevation. Echocardiogram on 5/31 largely normal with exception was low normal left ventricular systolic function. Cardiac MRI on 6/2/21 read as "Increased T2 signal representative of myocardial edema with superimposed DME representative of myocardial necrosis, as described above. These findings are consistent with myocarditis."
Aktuelle Erkrankungen: None reported.
Vorgeschichte: None reported.
Andere Medikamente: None at the time of admission on 5/31/2021.
Allergien: None at the time of admission on 5/31/2021.
Vorherige Impfungen: -

VAERS 1365749

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: AZ
Alter: 16,0
Geschlecht: F
Eingang: 01.06.2021
Impfdatum: 31.05.2021
Beginn: 31.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypotension Loss of consciousness

Symptomtext

Pt passed out. Experienced extremely low blood pressure. Pulse couldn't be detected for a couple of seconds. Pt woke and was clear and coherence. Paramedics saw pt and provided IV fluids. Pt left under own power.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1365565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MN
Alter: 16,0
Geschlecht: F
Eingang: 01.06.2021
Impfdatum: 01.06.2021
Beginn: 01.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Syncope Vomiting

Symptomtext

After receiving the injection the patient fainted. Patient was offered juice and after taking a sip she had a small amount of emesis. A cold towel was placed on patient's forehead and then observed by EMS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: doxycycline, tretinoin cream
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1365524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0186

schwer

Staat: MN
Alter: 13,0
Geschlecht: F
Eingang: 01.06.2021
Impfdatum: 01.06.2021
Beginn: 01.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Loss of consciousness

Symptomtext

Prior to the vaccine patient and parent were given teaching about concerns for fainting. She was questioned if she had something to eat and drink prior to coming to the clinic and both indicated that she had. It was volunteered that patient has never had a fainting spell from receiving injections/vaccines. She was administered 0.3 ml of the Pfizer vaccine at 4:47 p.m. while seated securely in a chair. At about 4:50 p.m. she lost consciousness and assumed a prone position. She was held by both the R.N. and her mother and never fell or injured herself. She was unconscious for approximately 8-10 seconds and regained consciousness. She was alert and oriented. She was reassured and given some apple juice and a graham cracker which she consumed. Charge nurse and nurse manager appeared on the scene. EMT was summoned who brought a wheel chair and patient was transported to the observation area in the wheel chair. She was conversing and appeared oriented prior to going to the observation area.

Weitere VAERSDATA-Felder

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

VAERS 1365501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NV
Alter: 37,0
Geschlecht: F
Eingang: 01.06.2021
Impfdatum: 18.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: SYR / RA

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

Abdominal pain Blood test normal Exposure during pregnancy Laboratory test normal Mobility decreased Premature delivery Premature labour Pyrexia Retained placenta or membranes Thrombosis Ultrasound antenatal screen normal Vaginal haemorrhage

Symptomtext

on Tuesday 05/18/2021 i take my 2th dose of Vaccine and on 05/19/2021 at around 2100 pm i start to develop high fever at 103-104 with abdominal cramps, same way i was on the 05/20/2021 and on Friday morning 05/21/2021 i start bleeding with large clots and wasn't able to get from the bed, and around noon my waters broke following with a lot of blood and clots,i had to deliver my baby girl at home at 15 weeks, 911 was called, because the placenta didn't come out, so i was rushed to the ER Baby was Delivered at 13:30pm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 1,0
Labordaten: Genetic Testing, Ultrasound and Blood Work come up Normal/Low Risk-05/15/2021
Aktuelle Erkrankungen: NO
Vorgeschichte: NO
Andere Medikamente: NO
Allergien: NO
Vorherige Impfungen: -

VAERS 1365290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 16,0
Geschlecht: F
Eingang: 01.06.2021
Impfdatum: 25.05.2021
Beginn: 25.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blepharospasm Chills Condition aggravated Fall Gaze palsy Loss of consciousness Seizure Tremor

Symptomtext

My daughter had a mild seizure 5 minutes or less after receiving her first vaccine. She fell out of her chair, her eyes fluttered and rolled in the back of her head, her teeth were clocking and chattering and her body was shaking mildly. She lost consciousness for approximately 2 minutes. At 8:33 pm she felt a second seizure begin, her step father grabbed her before she could fall and again, her eyes fluttered and rolled in back of her head, her teeth were clicking and chattering and her whole body was shaking. The second episode lasted approximately 2 minutes as well, with her losing consciousness again. She was taken to the emergency room and stayed overnight for observation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Pt. had seizures when she was between the ages of 2 and 3. She took Neurontin daily for 2 years and had not had any seizures or ticks since.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1365067

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NH
Alter: 15,0
Geschlecht: F
Eingang: 01.06.2021
Impfdatum: 22.05.2021
Beginn: 29.05.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Alanine aminotransferase increased Angiogram normal Aspartate aminotransferase normal Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood chloride increased Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium normal Blood urea decreased C-reactive protein increased Carbon dioxide decreased Chills Computerised tomogram normal Diarrhoea Electrocardiogram normal

Symptomtext

Received vaccine 5/22/21 - had some local arm swelling & pain which resolved that night. 5/23 had fever, chills, nausea, diarrhea x2 days with complete resolution. On 5/29, developed urticarial rash on legs & arms - no improvement with OTC Benadryl. No new foods/obvious exposure to other allergens other than family had tried a new scent of their brand of fabric softener. 5/31, developed nausea, vomiting, hand/feet swelling, & had a pre-syncopal episode. Presented to ER; tachycardic with symptomatic orthostatics though vitals otherwise normal. Received IV fluids, Pepcid, Decadron with improvement in HR/symptoms. Continued to be orthostatic with some extremity swelling so received IM Epinephrine - subsequent improvement in rash, nausea. Hospitalized for monitoring. Orthostatis/nausea resolved, vitals remained stable. Some intermittent itchiness/hives present that came & went still present at the time of discharge from hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 1,0
Labordaten: Labs/tests from 5/31: CRP 44 mg/L (elevated), D-Dimer 4.5 mg/L (elevated), Troponin <3ng/L (normal), ProBNP <15pg/mL (normal), Complete metabolic panel (Normal): Na 136/K4.3/Cl 108/ CO2 22/BUN 9/Creatinine 0.89/Glucose 108, Albumin 4.5, Total Protein 6.8, ALT 44, AST 24, Bili total 0.7, Alk Phos 59 ESR <1mm/hr (normal), Pregnancy test negative, Covid Binax negative, CBC (very slightly elevated throughout): WBC 14.2, Hgb 15.2, Hct 43.9, Plt 330, 77% Neutrophils, 13% lymphocytes, 0.1% eosinophils EKG Normal, CT CTA Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Food/environmental allergies
Andere Medikamente: None
Allergien: Pineapple, Tide brand detergent, spider bites
Vorherige Impfungen: -

VAERS 1364900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 01.06.2021
Impfdatum: 01.06.2021
Beginn: 01.06.2021
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 seemed fine after dose then complained of feeling dizzy. She passed out after sitting down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: No
Vorgeschichte: Mitral valve prolapse
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1354478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: FL
Alter: 64,0
Geschlecht: M
Eingang: 01.06.2021
Impfdatum: 24.05.2021
Beginn: 25.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Aphasia Bell's palsy Facial paralysis Mobility decreased

Symptomtext

Patient noticed facial paralysis starting morning after vaccination. Had vaccination at 7:23 pm and woke ~5:30am noticing difficulty moving one side of face. Patient reports talking to medical professional and being diagnosised with Bell's palsy. Spoke with patient 06/01 and patient stated still had difficulty talking and moving on one side of body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No reported allergies
Vorherige Impfungen: -

VAERS 1354478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: FL
Alter: 64,0
Geschlecht: M
Eingang: 01.06.2021
Impfdatum: 24.05.2021
Beginn: 25.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Aphasia Bell's palsy Facial paralysis Mobility decreased

Symptomtext

Patient noticed facial paralysis starting morning after vaccination. Had vaccination at 7:23 pm and woke ~5:30am noticing difficulty moving one side of face. Patient reports talking to medical professional and being diagnosised with Bell's palsy. Spoke with patient 06/01 and patient stated still had difficulty talking and moving on one side of body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No reported allergies
Vorherige Impfungen: -

VAERS 1362161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TN
Alter: 35,0
Geschlecht: M
Eingang: 31.05.2021
Impfdatum: 28.05.2021
Beginn: 28.05.2021
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

Systemic: Fainting / Unresponsive-Mild, Additional Details: Was informed to sit after the vaccine. Waited a few minutes, then sat over by the clinic. Technician informed pharmacy staff that he fainted. Staff offered him water after he regained composure. Patient stated he had a previous history of adverse events from vaccines. Will eat and drink more fluids before coming back for second vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1361331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: AZ
Alter: 30,0
Geschlecht: M
Eingang: 29.05.2021
Impfdatum: 28.05.2021
Beginn: 28.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Loss of consciousness Unresponsive to stimuli

Symptomtext

as soon as got the shot he passed out , not responding , gave him epinephrine 0.3 mg auto injector, with in 5 minutes paramedics came and took care of him , he is fine, talking good, , feeling , after few minutes he walked away with family member

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: paramedics checked his vitals
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: unknown
Allergien: no allergies
Vorherige Impfungen: -

VAERS 1360745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: PR
Alter: 24,0
Geschlecht: M
Eingang: 29.05.2021
Impfdatum: 29.05.2021
Beginn: 29.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Dyskinesia Syncope

Symptomtext

Patient started feeling dizzy, malaise and then patient had a syncope event where he also started having uncontrollable movements.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Physical exam, vital signs
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: NeuroCore- Pre-workout Whey protein
Allergien: shellfish
Vorherige Impfungen: -

VAERS 1360119

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: NY
Alter: 24,0
Geschlecht: F
Eingang: 29.05.2021
Impfdatum: 29.05.2021
Beginn: 29.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure decreased Fall Head injury Loss of consciousness Muscle contractions involuntary Seizure Syncope

Symptomtext

A 24 y.o female fainted and appeared to have a seizure. She loss consciousness and had muscle contractions. The seizure was approximately 2 minutes. Patient did not hit her head or injury any part of her body. She was gradually dismounted from the chair and placed on the floor. 1st B/P reading was 70/40, then 108/63. Patient after waking up was alert and oriented X3. Once EMS arrived she was assessed and encouraged to go to the hospital for follow up. Patient and father refused to go to the hospital. They verbalized "She has an important exam for school". Patient stated she will follow up after her exam.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1359529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: WA
Alter: 20,0
Geschlecht: F
Eingang: 28.05.2021
Impfdatum: 26.05.2021
Beginn: 26.05.2021
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 Headache Pallor Sensory loss Syncope

Symptomtext

About 5 min after giving the vaccine, patient complained of not feeling well. Symptoms included headache, loss of sensation in arms, light headedness. Patient appeared pale, and confused. Attempted to have patient stand up and walk to counsel room opposite where she was sat. After standing, she immediately sat down, and fainted while she was seated. Pharmacist supported her head, and her boyfriend/significant other prevented her from falling off the chair. Patient was momentarily unresponsive for about 3 seconds. During this time her eyes remained open. Once patient regained consciousness, walked her to counsel room and had her lie down on her back with her legs elevated on a chair. Blood pressure was within normal limits. Patient was feeling better in about 10 minutes, and continued to monitor for another 5. Gave water to sip on, and no additional adverse effects noted.

Weitere VAERSDATA-Felder

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

VAERS 1357920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: TX
Alter: 44,0
Geschlecht: M
Eingang: 28.05.2021
Impfdatum: 28.05.2021
Beginn: 28.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood glucose normal Blood pressure normal Dizziness Dyspnoea Fall Heart rate normal Immediate post-injection reaction Loss of consciousness Tremor Unresponsive to stimuli

Symptomtext

Pt felt dizzy immediately after injection, pt had a slight tremor and labored breathing, counselled pt to take deep breaths and stay seated, pt tried to stand and fell to the floor unconscious where he remained breathing but unresponsive for over 1 minute, came to on his own.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Paramedics checked blood pressure, heart rate, and blood glucose. All were normal.
Aktuelle Erkrankungen: None
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1357666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: TX
Alter: 20,0
Geschlecht: M
Eingang: 28.05.2021
Impfdatum: 17.05.2021
Beginn: 17.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Seizure Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Systemic: Seizure-Mild, Additional Details: While sitting on the chair, patient fainted and started to have seizure for 1-2 second then recovered completely by himself. Called 911 but patient did not want to have any medical attention. After that, patient sit for more than 30 minutes before going home.

Weitere VAERSDATA-Felder

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

VAERS 1357662

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MA
Alter: 33,0
Geschlecht: F
Eingang: 28.05.2021
Impfdatum: 27.05.2021
Beginn: 27.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction

Symptomtext

Patient had a reaction to first Pfizer vaccine on 5-5-21 was treated and released with prescription for Prednisone. Patient was told by physician to receive her second dose but to pre-medicate with prednisone 50mg and Benadryl 25mg. Pt did as she was advised and received second Pfizer vaccine. She started exhibiting s/s of anaphylaxis within 5 minutes of the vaccine. Treated with 50mg benadryl and 2 epi pen injections of .3mg 5 minutes apart while awaiting EMS. Patient treated and released later in the day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: PREDNISONE 50MG TAKEN 1 HOUR PRIOR TO VACCINE AND 25MG BENADRYL TAKEN AT 1:00 pm
Allergien: Iodine, shellfish, bee venom, PCN, ampicillin, clindamycin
Vorherige Impfungen: -

VAERS 1354683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MN
Alter: 15,0
Geschlecht: F
Eingang: 27.05.2021
Impfdatum: 27.05.2021
Beginn: 27.05.2021
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 at check out desk. All necessary precautions were utilized. Patient walked to check out desk and started to fall forward. Desk staff and mom caught patient and lowered her to the floor. Patient became conscious and sent over to observation area and was monitored for 30 minutes. No injuries sustained during fall and was able to leave with mom.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: none
Vorherige Impfungen: Mom stated that she faints with most vaccines

VAERS 1354466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: OR
Alter: 13,0
Geschlecht: F
Eingang: 27.05.2021
Impfdatum: 26.05.2021
Beginn: 26.05.2021
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 experienced vasovagal syncope within a minute of her vaccination. Helped patient lie down on the floor and explained situation to her. Assisted patient to cot, and provided apple juice. Encouraged patient to call her mom and continued to monitor patient's status.

Weitere VAERSDATA-Felder

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

VAERS 1351588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: HI
Alter: 15,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 15.05.2021
Beginn: 15.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Electrocardiogram Hypotension Skin warm Syncope

Symptomtext

Prior to arrival, the patient received her first COVID vaccine at the clinic, after which she suddenly felt dizzy, described as lightheadedness, and felt warm. She was noted to be hypotensive with SBP at 67. She subsequently drank water with some improvement. No syncope, severe headache, numbness, tingling sensations, or focal weakness. Mother was concerned and brought the child to the ED for further evaluation. Currently the patient feels better. No similar symptoms in the past. The patient denies any chest pain or pressure, shortness of breath, or abdominal pain. No recent fever or cough.She is otherwise healthy and has a normal cardiopulmonary exam and reassuring EKG. The description of her symptoms and the environment which happened is very consistent with vasovagal syncope and she does not have any stigmata, and acute neurologic or cardiac emergency. I believe she is safe and stable for discharge home and she was discharged with return precautions and follow-up instructions.

Weitere VAERSDATA-Felder

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

VAERS 1350773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: PA
Alter: 12,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Pallor Syncope

Symptomtext

Patient turned pale after vaccination; fainted without injury. Completely recovered within minutes with hydration and support.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Vital Signs: BP - 86/42 with repeat 105/72 Pulse - 108 with repeat 82 RR: 14/min with repeat 17/min O2 Sat: 97% throughout exam
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1350477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TX
Alter: 17,0
Geschlecht: M
Eingang: 26.05.2021
Impfdatum: 25.05.2021
Beginn: 25.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Injection site bruising Syncope Unresponsive to stimuli

Symptomtext

Site: Bruising at Injection Site-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe

Weitere VAERSDATA-Felder

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

VAERS 1350457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 24.05.2021
Beginn: 24.05.2021
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

Systemic: Fainting / Unresponsive-Medium

Weitere VAERSDATA-Felder

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

VAERS 1350457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 24.05.2021
Beginn: 24.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Medium

Weitere VAERSDATA-Felder

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

VAERS 1350378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 13,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Pallor Syncope

Symptomtext

AE: light headed, dizzy, pale, fainted Tx: n/a, just food and drink Outcome: juice, crackers helped resolve AE. pt was discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Pulse: 49 bpm Respiration: 20 SPO2: 96% B/P 100/60
Aktuelle Erkrankungen: -
Vorgeschichte: History of similar reaction with injections and vaccine needles
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1344655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: OH
Alter: 13,0
Geschlecht: M
Eingang: 24.05.2021
Impfdatum: 24.05.2021
Beginn: 24.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Malaise Presyncope

Symptomtext

About 7 minutes after receiving vaccine, pt was out in waiting area and told mother wasn't feeling well. Slumped over and she caught him and gently brought him to the ground. Mother called out for provider who then came to patient who was laying down on the floor. Patient was able to speak coherently and had no pallor or sweating. He was able to sit up after a couple minutes but stayed sitting as directed on the floor until full 15 minutes had passed. Mother stayed with patient and they were able to leave without any residual side effects from vasovagal response.

Weitere VAERSDATA-Felder

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

VAERS 1344356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: UT
Alter: 24,0
Geschlecht: M
Eingang: 24.05.2021
Impfdatum: 24.05.2021
Beginn: 24.05.2021
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

Symptomtext

Syncopal reaction, loss of consciousness, clonic contractions, regained consciousness on own within 1 min. We lowered him to the floor, where he stayed until starting to feel better. Removed mask to increase air flow. Gave 2 bottles of water. Pt reported that he hadn't eaten or drank much water today. Recommended strongly to have a good breakfast & lunch, plus lots of water before second dose. Checked BP twice, initially 80/47, repeat reading 100/70. Pt reported feeling better & planned to take service car home.

Weitere VAERSDATA-Felder

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

VAERS 1344193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: WI
Alter: 15,0
Geschlecht: F
Eingang: 24.05.2021
Impfdatum: 24.05.2021
Beginn: 24.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Syncope

Symptomtext

patient fainted about 3 minutes after getting her vaccine injection. SHe was out for about 3 to 5 seconds and then came to. she was sweaty but her temperature was ok and pulse seemed normal. THe pharmacy called 911 as a precaution. paramedics verified her vitals and gave mom the option to take her to the ER or just let her stay and be monitored. mom decided to have her stay. Mom and patient stayed by phramcy for 30 minutes as the child drank 2 bottles of water and ate a granola bar. when she felt 100% they left the store.

Weitere VAERSDATA-Felder

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

VAERS 1343871

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TX
Alter: 15,0
Geschlecht: F
Eingang: 24.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose normal Dizziness Head injury Seizure Skin laceration Syncope Tremor

Symptomtext

Pt received vaccine and was standing outside of immunization room with her parents waiting for her brother to receive vaccine. She felt dizzy and fainted. She hit her head and collapsed. She was seizing/ shaking on the floor. She was conscious with no visible bleeding. She was able to say her name and DOB correctly. Mother reported no history of epilepsy or seizure. Called emergency services and pt was taken to Clinic for further evaluation. A 1.5cm laceration was noted behind her left ear. Pt received 2 staples in the lacerated area.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: blood glucose: 90 BP: 104/70 Pulse: 82 Resp: 20 Temp: 36.7 ?C (98 ?F) SpO2: 98%
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1343754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: TX
Alter: 60,0
Geschlecht: M
Eingang: 24.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Syncope

Symptomtext

He was administered Vaccination at 2:47pm. He stood up at about 3pm and collapsed to the floor and started to get unresponsive. I administered 1 dose of epipen 0.3mg and he started to get better. 911 arrived and patient was feeling better so he refused to go to hospital. He is in good spirits and said he was OK that day. He said he will follow up with his doctor . Tried to follow up but have not been able to reach patient but have left a couple of voice messages.

Weitere VAERSDATA-Felder

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

VAERS 1343751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: OR
Alter: 36,0
Geschlecht: M
Eingang: 24.05.2021
Impfdatum: 15.05.2021
Beginn: 16.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / -

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

Blood gases Blood lactic acid Computerised tomogram head Full blood count Hyperhidrosis Loss of consciousness Metabolic function test Seizure Troponin

Symptomtext

Diaphoresis started same day following COVID vaccine 05-15-2021. On 05-16-2021, patient lost consciousness and had a seizure. Taken to ED for evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: 05/16 = Head CT, Lactic Acid, CBC, CMP, Troponin, Venous Blood Gas. 05/21 = CMP and CBC
Aktuelle Erkrankungen: None
Vorgeschichte: N/A
Andere Medikamente: None
Allergien: Fluoxetine
Vorherige Impfungen: -

VAERS 1343575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: IA
Alter: 17,0
Geschlecht: M
Eingang: 24.05.2021
Impfdatum: 18.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Seizure Syncope Urinary incontinence

Symptomtext

Patient reported they couldnt stand the sight of blood and had fainted during draws before. Father was present in the vaccine office as well. Immediately fooling the administration of the vaccine patients eyes glazed over and he fainted. A few seconds later he began to have a spastic seizure that was short in nature, followed by a voiding of his bladder before he regained consciousness. Patient was given water, glucose tablets, and instructed to lay on the floor of the room with his feet elevated while a member of the staff stayed with him to treat and watch him. Followed up with patient and doctor soon after to learn this was the only time it has happened, patient fully recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Blood pressure was initially 92/50 following the incident, however it did raise slightly to 98/62 before the patients father took him home.
Aktuelle Erkrankungen: None
Vorgeschichte: Nurse for PCP reported a bicuspid valve issue but no other chronic conditions
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1342933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MI
Alter: 15,0
Geschlecht: F
Eingang: 24.05.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
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 Hypoaesthesia Paraesthesia Syncope Unresponsive to stimuli Visual impairment

Symptomtext

Systemic: Confusion-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Systemic: Visual Changes/Disturbances-Medium, Additional Details: TINGLING IN FEET

Weitere VAERSDATA-Felder

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

VAERS 1342015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TX
Alter: 23,0
Geschlecht: F
Eingang: 23.05.2021
Impfdatum: 23.05.2021
Beginn: 23.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Fall Head injury Presyncope

Symptomtext

Patient experienced an episode vasovagal syncope within a few minutes of receipt of vaccine while waiting the recommended 15 minutes in the waiting area. Patient was seated while episode occurred and hit their forehead on the ground as a result of falling out of chair. EMS was contacted as a result of this

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: history of syncope- no issue to CV19 dose 1

VAERS 1341776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 16,0
Geschlecht: F
Eingang: 23.05.2021
Impfdatum: 23.05.2021
Beginn: 23.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Hypotension Immediate post-injection reaction Pallor Presyncope

Symptomtext

Vasovagal response immediately after vaccination. Dizzy, pale, lightheaded, diaphoretic, hypotensive. B.P. 64/25 @10:25 and @10:35 B.P. 110/60. Laid down in medical screening with good rebound Blood pressure. Remains for 30 minutes observation. Left in stable condition at 10:53.

Weitere VAERSDATA-Felder

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

VAERS 1341757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 12,0
Geschlecht: F
Eingang: 23.05.2021
Impfdatum: 23.05.2021
Beginn: 23.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Presyncope Vomiting

Symptomtext

Reported feeling like she was about to pass out, emesis.. Seen by Medics. Left in stable condition at 10:27. Recorded by RN.

Weitere VAERSDATA-Felder

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

VAERS 1340925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 41,0
Geschlecht: F
Eingang: 22.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness Nausea Vomiting

Symptomtext

Brief loss of consciousness, nausea, Brought to med screening for evaluation, then nausea worsened, emesis x1. Vital signs: B.P =132/98 Pulse = 80 Po2=97% Declined further interventions, left in stable condition at 12:58. Recorded and Evaluated by Providers

Weitere VAERSDATA-Felder

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

VAERS 1340795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 15,0
Geschlecht: F
Eingang: 22.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fall Seizure

Symptomtext

Pt. fell to floor from chair, dizziness, possible seizure activity 12 Lead, started IV, 0 meds. Vital signs: 89/40 Pulse:60 89/41 Pulse :55 89/42 Pulse:56 Recorded by RN. Pt. transported to hospital via ambulance at 11:32 A.M. with mother.

Weitere VAERSDATA-Felder

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

VAERS 1340643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 16,0
Geschlecht: F
Eingang: 22.05.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Head injury Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Systemic: See statement below-Medium, Additional Details: Minor patient with parents in attendance. After receiving immunization, patient stood up, took a few steps and fainted, falling backward and hitting head on the floor. Pharmacy staff immediately called 911 and provided supportive first aid. Patient quickly regained consciousness, RPh had her continue to lay in the floor, provided pillow for head, elevated feet and ice pack was applied to back of head. Paramedics arrived to evaluate patient's condition, patient was released home with parents.

Weitere VAERSDATA-Felder

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

VAERS 1338149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NC
Alter: 13,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Immediate post-injection reaction Loss of consciousness Syncope

Symptomtext

Syncopal event immediately following vaccine administration. Patient was placed in a laying position with feet raised and given water for hydration. They were monitored closely and had 3 total syncopal events separated 3 to 5 minutes apart and lasting 10 to 15 seconds with loss of consciousness and no injuries. Patient declined further medical treatment and was monitored by pharmacist for 30 more minutes until they were able to walk away from pharmacy on their own.

Weitere VAERSDATA-Felder

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

VAERS 1338134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NC
Alter: 16,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Haemorrhage Head injury Loss of consciousness Syncope

Symptomtext

Syncopal episode with loss of consciousness and fall with left head injury 2 minutes after vaccine administration. First Aid was administered immediately to stop the bleeding. Patient was awake and alert and declined further medical assistance. Pharmacist monitored for 30 more minutes before patient was able to walk away on their own.

Weitere VAERSDATA-Felder

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

VAERS 1338109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MA
Alter: 17,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dry throat Loss of consciousness Palpitations Syncope

Symptomtext

17 y/o female received 1st dose of Pfizer and was sitting in the observation area. She had a witnessed syncopal episode, lasting approx. 45-60 secs. When pt. regained consciousness she was placed in a wheelchair and moved to a private area. VSS at that time. Pt. was given some water to sip on and stated she was feeling better. Pt. denied any other complaints at that time. Pt. denied any PMH/ Meds./Allergies. Pt?s grandmother is with her and states pt. appears to be back to baseline. Approx. 30mins. after syncopal episode, pt. stated ?my heart is racing and my throat feels dry?. VS reevaulated, pt?s HR was 122, BP 130/66. Pt. stated she wanted to go to the ER. She was t/p BLS to ER. See PCR for further.

Weitere VAERSDATA-Felder

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

VAERS 1337854

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 15,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Pallor Presyncope

Symptomtext

Dizziness, pale, vasovagal Discharged home at 10:40

Weitere VAERSDATA-Felder

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

VAERS 1337820

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

schwer

Staat: TN
Alter: 15,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 18.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Seizure Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Systemic: Seizure-Medium

Weitere VAERSDATA-Felder

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

VAERS 1337703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: PA
Alter: 45,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Presyncope

Symptomtext

Patient has history of fainting with needles and bloodword. Approximately 20 minutes after vaccine, patient was in observtion room and experienced a near syncopal episode. Patient accompanied by husband. Patient assisted to a laying position with legs propped-up. After several minutes patient able to sit up on her own, water given. Patient able to slowly transfer self from floor to chair without difficulty. Graham crackers given and encouraged to continue drinking water. Patient recovered and able to leave facility without difficulty. Patient exited facility approximately 45 minutes after vaccine administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Anal Fissures
Vorgeschichte: -
Andere Medikamente: None
Allergien: Hydrocodone; Soy
Vorherige Impfungen: previous fainting episodes

VAERS 1337511

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NY
Alter: 15,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Head injury Loss of consciousness Pulse abnormal Syncope

Symptomtext

Syncopal episode with Loss of Consciousness for several seconds . Radial pulse was weak Heart rate was 48 / min and BP 85/60 . Heart rate and BP improved 112/80 Struck back of head during fall

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Pulse oximetry normal
Aktuelle Erkrankungen: History of syncope following phlebotomy
Vorgeschichte: none
Andere Medikamente: None
Allergien: ? Food Allergies
Vorherige Impfungen: -

VAERS 1336880

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

schwer

Staat: TX
Alter: 13,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
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 after vaccine administration. Patient was given the vaccine and slumped in the chair ten seconds later. We were able to revive her after 20 seconds. We had her lay on her back and lift her feet. after 15 minutes she said she was feeling fine and left with her father.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: Father later said she does get nauseous after vaccines

VAERS 1335982

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MT
Alter: 14,0
Geschlecht: M
Eingang: 20.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Head injury Loss of consciousness

Symptomtext

PATIENT PASSED OUT WHILE STANDING AND HIT HEAD. ELEVATED FEET AND PARAMEDICS CAME AND CHECKED ON HIM, BUT HE FELT FINE AND WENT HOME

Weitere VAERSDATA-Felder

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

VAERS 1335977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: WA
Alter: 13,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
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 Seizure like phenomena

Symptomtext

Patient wa receiving their first Pfizer COVID vaccine. Student was well hydrated and had eaten a meal prior to vaccination. After administering vaccine, patient lost consciousness, slumped to her left side, and had seizure-like body jerk movements. She then regained consciousness, then lost consciousness again immediately after and proceeded to have whole body jerking movements. She then started sliding to the floor from her seat. Patient was lowered to ground with help from another RN. Vitals were taken, BP 102/82, HR 48 and RR 20. Dr. assessed patient and 911 was called for further assessment. Patient was not transported in ambulance and left clinic with parent recovered.

Weitere VAERSDATA-Felder

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

VAERS 1335975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NH
Alter: 30,0
Geschlecht: M
Eingang: 20.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Seizure like phenomena

Symptomtext

Patient experienced a minor seizure-like reaction that lasted for about 5 seconds. Patient was monitored for about 30 minutes. Blood pressure, heart rate and oxygen saturation were normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: Minor seizure-like reaction and fainting.

VAERS 1334890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: WI
Alter: 13,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
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 doing IM COVID injection. RN called another staff to assist lowering patient to ground and elevating feet. Patient felt better after laying down. Nursing staff took vitals (supine), which were BP - 118/84, SPO2 - 97%, pulse - 48. Patient rested for a while, taking some deep breaths and putting an ice pack on the back of her neck. After approx. five minutes staff helped patient to a seated position and re-took vitals which were 122/80, SPO2 - 99%, pulse - 57. Patient drank some water and was observed for approx. 30 minutes following injection, stating she "felt better".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Flu shot last fall

VAERS 1334739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 14,0
Geschlecht: M
Eingang: 20.05.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Fear of injection Immediate post-injection reaction Loss of consciousness Syncope

Symptomtext

Patient has a history of fainting at needles, and he lost consciousness briefly immediately after injection. When he aroused, the patient said he felt "weird." EMT evaluated patient and administered a cold compress, water, and juice. Patient's uncle drove him home. completed the following: 5/14/21: 12:43pm - TC to mom who reports her son is doing fine. No problems or concerns.

Weitere VAERSDATA-Felder

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

VAERS 1334737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: IN
Alter: 41,0
Geschlecht: M
Eingang: 20.05.2021
Impfdatum: 18.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Chills Heart rate increased Influenza like illness Pain in extremity Seizure Sleep disorder

Symptomtext

Arm soreness started on May 18 @ 3:30pm. Went to sleep with same arm soreness at 11pm. Woke up at 1:15am on May 19, walked approximately 12 feet started experiencing cold chills. At 1:20am, while standing and holding cellphone in right hand, started experience of convulsive seizure to the point of cellphone health stats saying i walked 103 steps while standing still convulsing. After calming down enough to sit, i sat on couch to sleep. Heart rate was still registering in 200 bpms for next couple hours. May 20, 2021 started experiencing sore throat at 5:30am. As day progresses am experiencing flu type symptoms.

Weitere VAERSDATA-Felder

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

VAERS 1334255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: WA
Alter: 12,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 18.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

The patient was vaccinated and then got up to walk to observation area. While waiting for her COVID vaccination card, she started leaning on mom and fainted. Mom caught her and placed her flat on the floor. A medical professional volunteering at the clinic responded to the incident and checked her O2 levels and blood pressure. Patient cam to shortly after fainting. Vitals were good and the doctor recommended she stay in observation for an additional 10 minutes. Patient left clinic with mom after waiting and without further incident.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None indicated at time of vaccination
Vorgeschichte: None indicated at time of vaccination
Andere Medikamente: Unknown
Allergien: None indicated at time of vaccination
Vorherige Impfungen: -

VAERS 1333995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TX
Alter: 15,0
Geschlecht: M
Eingang: 20.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
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

Weitere VAERSDATA-Felder

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

VAERS 1333440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

schwer

Staat: NY
Alter: 13,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope Tremor

Symptomtext

5 minutes after vaccine patient started feeling dizzy and fainted, while body was shaking for 20 seconds. Body then regained consiousness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EMT were called. Patients parents are taking patient to urgent care
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Not known
Allergien: None
Vorherige Impfungen: -

VAERS 1331268

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 15,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 19.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Hypotension Loss of consciousness

Symptomtext

Was standing passed out and fell to ground. Vital signs: @13:15 B.P=100/50 118/80 HR: 70 Pso2:100% @13:45 B.P. 97/50 Trending hypotension Recorded by staff

Weitere VAERSDATA-Felder

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

VAERS 1331256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 21,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: 19.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nausea Presyncope

Symptomtext

Lightheaded, Near Syncope Nausea Dizziness at 09:45am BP 199/80 P80 Resp: 24 O2 96 at 10:05am BP 102/80 P82 Resp: 18 O2 97

Weitere VAERSDATA-Felder

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

VAERS 1331246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 13,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: 19.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nausea Pallor Presyncope

Symptomtext

Pale, Nausea, lightheaded. B.P=84/60 history of vasovagal response after previous vaccination Vital signs returned to normal after approximately 40 minutes. Recorded by RN

Weitere VAERSDATA-Felder

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

VAERS 1331230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 12,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 19.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure decreased Blood pressure fluctuation Heart rate decreased Hyperhidrosis Loss of consciousness Pallor Syncope

Symptomtext

Pale diaphoretic, syncope witnessed loc Possible seizure Transported by ambulance with mother at11:45am BP 67/30 P 46 14 99% at 12:00am BP 84/62 P 58 12 100%

Weitere VAERSDATA-Felder

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

VAERS 1331207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 22,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: 19.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Fall Hyperhidrosis Presyncope Visual impairment

Symptomtext

Dizziness, fell out of chair Loss of vision Plae Diaphoretic Vasovagal P90 BP 137/98 O2 98%

Weitere VAERSDATA-Felder

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

VAERS 1331192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MD
Alter: 24,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: 19.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure decreased Dizziness Heart rate decreased Syncope Visual impairment

Symptomtext

Reported feeling of syncope Brief loss of vision Vasovagal BP 105/53 P55

Weitere VAERSDATA-Felder

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

VAERS 1331032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MN
Alter: 14,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 18.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

After administration of the vaccine within 1 minute, the patient had a loss of consciousness. The patient was laid supine with feet elevated. She regained consciousness after 30 seconds. Vitals remained stable throughout. BP 110/72 P64 O2 99% at the time of regaining consciousness. After 5 minutes 118/88 P 64. After 30 min 118/78 P 64. Left with mother and sibling.

Weitere VAERSDATA-Felder

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

VAERS 1330026

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: GA
Alter: 13,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: 18.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

A few minutes after receiving the vaccine, the patient fainted. The mother caught her son in her arms and we were both able to lay him on the floor safely without hitting his head. He came to within a few seconds. He remained in the pharmacy area for approximately 20 more minutes for observation. He was feeling back to normal before leaving.

Weitere VAERSDATA-Felder

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

VAERS 1327532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MN
Alter: 48,0
Geschlecht: M
Eingang: 18.05.2021
Impfdatum: 12.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness postural Fatigue Feeling abnormal Feeling cold Hyperhidrosis Loss of consciousness Paraesthesia

Symptomtext

Pt states he passed out & not feeling good. Diaphoretic. BP 102/67 Via w/c taken to Observation area to lie down. Feeling cold, tingly all over & "wiped out". 3:25PM Taking juice & crackers. Still dizzy when tried to stand up. BP 127/92 3:40PM Left w/o assistance. Feeling much better

Weitere VAERSDATA-Felder

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

VAERS 1326834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 23,0
Geschlecht: M
Eingang: 18.05.2021
Impfdatum: 18.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Hypoacusis Syncope Visual impairment

Symptomtext

Pt in waiting area and started seeing black spots and hearing became muffled. Pt had syncopal episode for less 3 sec. on floor. Pt was placed on left side v/s obtained with b/p 110/88 HR 82. A/Ox3. Pt admitted to having anxiety and stated "it was my first time having this to happen, but i do have anxiety." Pt was there with extra time placed on to his wait time. Refused EMS. Mother came in to sit with pt. No acute distress noted. A/Ox3.

Weitere VAERSDATA-Felder

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

VAERS 1324118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: MA
Alter: 14,0
Geschlecht: M
Eingang: 17.05.2021
Impfdatum: 17.05.2021
Beginn: 17.05.2021
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

Immediately after receiving vaccine, pt had a syncopal event with brief LOC. Caught by medical staff and lowered to the ground - placed supine with legs elevated. Pt quickly regained consciousness and was alert and oriented x3. Has a history of syncope with vaccines and medical procedures. Dad present. Vital signs obtained and noted to be WNL HR 84 NSR Spo2 98% on room air B/P 123/61 laying down 118/62 sitting Pt hydrated with juice and was able to sit up and ambulate freely. Stayed for an additional 15 minute of observation without incident and left for home with dad.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Vital signs
Aktuelle Erkrankungen: depression and anxiety
Vorgeschichte: -
Andere Medikamente: on medications but unknown at this time
Allergien: NKDA
Vorherige Impfungen: hx. of syncope with vaccines, do not recall which vaccine

VAERS 1323792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: TX
Alter: 14,0
Geschlecht: F
Eingang: 17.05.2021
Impfdatum: 17.05.2021
Beginn: 17.05.2021
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 HAD BEEN ON CHAIR MONITORING FOR 14 MINUTES WHEN SHE FAINTED. NOT CERTAIN IF SHE HAD A SEIZURE. HOSPITAL WAS CALLED TO THE SCENE AND SHE WAS TRANSFERRED TO HOSPITAL FOR OBSERVATION. PHARMACIST SPOKE TO PATIENT'S MOM THIRTY MINUTES LATER AND SHE WAS ENROUTE. MOM STATED SHE WAS DOING OKAY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: seizures
Andere Medikamente: Levetiracetam 500mg one tablet twice a day
Allergien: none
Vorherige Impfungen: -

VAERS 1323558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: IN
Alter: 43,0
Geschlecht: M
Eingang: 17.05.2021
Impfdatum: 15.05.2021
Beginn: 16.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Disorientation Loss of consciousness

Symptomtext

18 hours after receiving the vaccine, passed out while walking in my house. No signs of dizziness or nausea preceded the episode. Lost consciousness for about 10 seconds, then was disoriented for about 2 minutes before being able to get up with assistance and move to my bed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Viibryd - 10mg
Allergien: Percocet - Full body rash, shortness of breath
Vorherige Impfungen: -

VAERS 1322847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CA
Alter: 19,0
Geschlecht: M
Eingang: 17.05.2021
Impfdatum: 16.05.2021
Beginn: 16.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Confusional state Dizziness Flushing Hyperhidrosis Hypoacusis Hypotension Seizure Syncope Unresponsive to stimuli Visual impairment

Symptomtext

Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Systemic: Seizure-Severe, Additional Details: Difficulty seeing clearly. Difficulty hearing.

Weitere VAERSDATA-Felder

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

VAERS 1320911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 15,0
Geschlecht: M
Eingang: 15.05.2021
Impfdatum: 15.05.2021
Beginn: 15.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Loss of consciousness

Symptomtext

Patient become light headed, lost consciousness and struck head. He rest under observation, ice pack and drunk juice. He recovered and discharged home Pulse : 67 SPO2 : 99% BP: 110/58

Weitere VAERSDATA-Felder

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

VAERS 1320432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: -
Alter: 9,0
Geschlecht: F
Eingang: 15.05.2021
Impfdatum: 14.05.2012
Beginn: 14.05.2021
Tage bis Beginn: 3.287,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

Syncope, drunk water and been under observation. Looks great and let home with her father. Pulse 92 SPO2 98 BP 102/66

Weitere VAERSDATA-Felder

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

VAERS 1318033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: WA
Alter: 32,0
Geschlecht: M
Eingang: 14.05.2021
Impfdatum: 14.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Immediate post-injection reaction Loss of consciousness Vaccine positive rechallenge

Symptomtext

Pt. reported that he was feeling light headed immediately after the vaccine and passed out momentarily. EMT's arrived on scene and monitored patient for about 20-30 minutes. Pt. was OK after monitoring and was fine to leave after the EMT's did their assessment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Pt. stated that he had a similar side effect when he received first Covid-19 Pfizer dose.

VAERS 1317411

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: WI
Alter: 17,0
Geschlecht: M
Eingang: 14.05.2021
Impfdatum: 14.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Feeling abnormal Head injury Hyperhidrosis Mydriasis Syncope Unresponsive to stimuli

Symptomtext

Patient was the 4th person to receive today?s vaccine of Pfizer. This was his second dose. He did fine the first dose. Patient sat down in the chair and rolled sleeve up. Chose L deltoid for injection site. He was talking with a friend and writer gave injection. Placed band aid. Patient was quiet and looked like he was going to get up but fell forward out of the chair. He hit his L forehead on side of wall. Writer caught patient and sat him up on the ground. Eye?s were dilated, he was diaphoretic, zoned out and not responding initially to voice, but eyes were open. Eventually got patient up to a wheelchair and taken to office area to lay down and monitor. Father was notified and sat with us after he arrived at the school. Patient drank 1 full 120cc orange juice and approximately 6oz of water. Throughout monitoring patient gradually felt better. Pupils corrected to normal, wasn?t diaphoretic anymore, and vitals improved. He stated this has happened before with lab draws and shots, but not this severe. Writer and colleagues informed him to notify people that are going to give him shots or lab draws about his history. Also informed him to notify his teachers if he feels anything out the ordinary for the rest of the day. Make sure he hydrates. Patient then sat up and walked in the room. He stated he felt fine like before getting the shot. Patient left stable and under his own power.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: reports passing out but not that severe

VAERS 1315448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: CO
Alter: 14,0
Geschlecht: M
Eingang: 13.05.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
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

Near syncope. Monitored in clinic. Vitals stable. Self-resolved after 5 minutes. Monitored for 30 minutes

Weitere VAERSDATA-Felder

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

VAERS 1314822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: WI
Alter: 13,0
Geschlecht: M
Eingang: 13.05.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Dyspnoea Eye movement disorder Feeling cold Hyperhidrosis Muscle spasms Nausea Retching Syncope

Symptomtext

I administered the Pfizer COVID vaccine to the patient at about 2pm. I completed the vaccine, put the used syringe into the sharps container, grabbed the bandage, and turned back toward the patient. As I did this, he started slumping over in the chair, and his eyes rolled back into his head. I immediately put my arms around him so he wouldn't fall out of the chair. The patient's father was in the room as well and knelt down in from of him. The patient's body spasmed for a few seconds, then he came to but was breathing heavily and starting to sweat. I called to technician in the pharmacy and asked him to call 911 at 2:03pm. I brought the patient a cool cloth and asked a technician to bring some water. The patient's breathing started to slow, but he was nauseous and dizzy. He dry-heaved once, and I put the garbage can in front of him. He slumped over the garbage can for a few minutes. Then he asked to lie on the floor. He seemed to do better lying on the floor. When the EMTs arrived, they attempted to have him sit in the chair again, but his dizziness returned, and he complained of being cold. The EMTs moved the patient to the gurney and transported him to the Hospital for further medical attention.

Weitere VAERSDATA-Felder

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

VAERS 1314653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

schwer

Staat: NE
Alter: 14,0
Geschlecht: M
Eingang: 13.05.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Fainting, patient fainted after administration and was being monitored for 30 minutes sitting down in our pharmacy.

Weitere VAERSDATA-Felder

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

VAERS 2716101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: WI
Alter: 51,0
Geschlecht: F
Eingang: 20.11.2023
Impfdatum: 14.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / AR

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

Asthenia Cognitive disorder General physical health deterioration Mobility decreased

Symptomtext

I am so damaged I haven't been able to report this until now. I got this 2nd shot in the covid 19 pfizer series and my health continued to plummet (along w/the 1st shot) my energy, cognition, and state of health had, and still has me laying in bed or in a couch most days (11/12/2023)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: See family clinic
Aktuelle Erkrankungen: Type I diabetes, Hashimoto's MRN
Vorgeschichte: See above
Andere Medikamente: Insulin, Levothyroxine, Liothyronine, Lorazepam, Seroquel
Allergien: Gluten, dairy, Clonazepam Rx's need to gluten and dairy free
Vorherige Impfungen: After a hepatitis vaccine in 1993/1994, age 24, felt body overall damaged for a long time years

VAERS 2692668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 57,0
Geschlecht: M
Eingang: 09.10.2023
Impfdatum: 24.11.2021
Beginn: 02.10.2023
Tage bis Beginn: 677,0
Dosis: 3
Route/Site: IM / -

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

Asthenia Dyspnoea Fatigue Oropharyngeal pain Productive cough

Symptomtext

weakness, productive cough, sore throat, shortness of breath, fatigue.

Weitere VAERSDATA-Felder

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

VAERS 2646912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 56,0
Geschlecht: F
Eingang: 19.06.2023
Impfdatum: 13.08.2021
Beginn: 24.09.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: IM / LA

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

Arrhythmia supraventricular Blood pressure increased Cardiac monitoring Echocardiogram Electrocardiogram Fatigue Heart rate increased Injection site erythema Injection site pain Injection site swelling Palpitations Pyrexia

Symptomtext

#1 approximately 24 hours post injection, redness, swelling and pain in left deltoid area, fever 100.6 for 36 hours, severe fatigue about 5 days post injection #2 approximately 6 weeks post injection pt noticed mild to moderate fatigue and heart pounding and racing. BP 160/110. Saw PCP 9/28/21 BP & pulse still elevated started on Amlodipine 5mg, eventually upped to 10mg and referred to cardiologist, Dr. Currently diagnosed with high blood pressure and atrial arrythmia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia supraventricular
Hospital-Tage: -
Labordaten: EKG several, Echo cardiogram 1/22, Zio heart monitor latest 12/22
Aktuelle Erkrankungen: none
Vorgeschichte: Hashimoto's hypothyroidism, sleep apnea
Andere Medikamente: levothyroxine 75 mcg qd, pilocarpine 5 mg bid, biotin
Allergien: None
Vorherige Impfungen: -

VAERS 2628398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 08.05.2023
Impfdatum: 24.10.2022
Beginn: 28.02.2023
Tage bis Beginn: 127,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/28/23 presents to ED for "SOB, cough". PMHx of "HTN, HLP, AAA, bladder Ca, OA"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/28/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2592530

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge EW0186

moderat

Staat: MD
Alter: 57,0
Geschlecht: M
Eingang: 07.03.2023
Impfdatum: 01.06.2021
Beginn: 15.06.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: SYR / UN

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

Back pain Chest pain Dizziness Groin pain Nausea Rash Vomiting

Symptomtext

-5/11/21: patient received initial dose of Moderna vaccine (PFR, COVID-19, mRNA, LNP-S, PF, 0.3mL vaccination on 05/11/2021 with lot number EW0173 at (COVID Clinic). -6/01/21: patient received 2nd dose of Moderna vaccine (PFR, COVID-19, mRNA, LNP-S, PF, 0.3mL vaccination on 06/01/2021 with lot number EW0186 at (COVID Clinic). -8/23/21: patient presented to outside clinic complaining of a bilateral rash that appeared on the hands, forearms, and ankles that reportedly appeared 2 weeks after the COVID vaccine. The patient also complained of episodic dizziness, nausea, back pain, chest pain, groin pain for the past 4 weeks. Pt reported using hydrocortisone cream on rash with minimal effect. Denies new medications, detergents/soaps/other chemicals in household. At this visit, patient was diagnosed with "rash" and discharged home on a steroid taper and topical hydrocortisone cream. -3/3/23: patient had an appointment to establish care with a PCP. I reviewed the note from the encounter; however, there was not anything written regarding the COVID vaccine allergy. The allergy status in the chart was updated on 3/3/23 to say, "COVID-19 mRNA vaccine - rash, nausea, vomiting, GI bleed. Severity = not specified", however, i was not able to verify that GI bleed occurred. Therefore, I believe that was selected in error and the true allergy should read "rash, nausea, vomiting"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: mood disorder patient was told he had a "bad" heart by past provider tobacco dependence
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2587305

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge EW0186

moderat

Staat: TN
Alter: -
Geschlecht: F
Eingang: 03.03.2023
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain Amnesia Aphasia Bedridden Blindness Alopecia Aphonia Asthenia Balance disorder COVID-19 Cardiac disorder Chest pain Chills Blood test Chest X-ray Computerised tomogram Computerised tomogram head Dehydration

Symptomtext

After 1st Pfizer vaccine, I became violently ill. I tried to sleep on the toilet for 72+ hours with diarrhea & vomiting into wastebasket. When I could crawl a few feet to my bed I did & had uncontrollable tremors, sweats and chills, unable to walk, do basic hygiene, prepare food that required standing, am intolerant to light, have constant severe headache, can't think, speak correctly, remember my date of birth or SSN, make sense, lost my voice, and that's been over a year and I'm still bedridden. When I get up I'm very dizzy, have had multiple falls, and been chronically dehydrated. I've been taken by ambulance to E.R. many times for dehydration, tremors, chest pain, low oxygen levels, excessive heart rate as high as 160 when I wake. I got the 2nd Pfizer vaccine on 11/26/21 which exacerbated all the symptoms and tried to sleep on the toilet again, for 72+ hours with vomiting and diarrhea, worse tremors, weaker, could not use right arm for over two weeks. I can't hold a thought, can't figure out how to use the remote or phone, slurred speech, cannot regulate temperature, tops of lower legs and feet get icy & numb, can't spell, Can't go on like this. I then got Covid-19 1/28/22, again 12/28/22, & 1/13/2023. I live alone with no help & no family. I can't function. I now have to use inhalers to breathe. I have to take Propranolol to slow my heart rate, have groceries that I can keep in my nightstand to eat, delivered. I spray everything with Lysol, or Clorox wipes that are delivered. I only leave home to go to hospital or doctors who have no answers & suggest I see a psychiatrist. THIS WAS AN INJURY CAUSED BY THE PFIZER VACCINE & OFFERED NO PROTECTION AS I'VE TESTED POSITIVE FOR COVID TRHEE TIMES IN ONE YEAR. WHY ARE YOU ALLOWING AND TRYING TO FORCE THE PUBLIC TO TAKE THIS POISON WITH YOUR FEAR PROPAGANDA? IT DID NOTHING TO PROTECT ME IN ISOLATION!!!! THIS IS NOT A LIFE, ONLY EXISTENCE. I DO NOT WNAT TO CONTINUE EXISTING IN THIS STATE OF PERPETUAL NON-EXISTENCE. NO SUPPORT. NO HELP. JUST SLOWLY DYING. PEOPLE SHOULD BE TRIED FOR CRIMES AGAINST HUMANITY. WHY GO ON? YOU DON'T CARE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: 28-Jan-2022 RAPID ANTIGEN POSITIVE
Aktuelle Erkrankungen: -
Vorgeschichte: SINCE THE VACCINES I HAVE HEART, LUNG, NEUROLOGICAL, HORMONAL IMBALANCES, HAIR LOSS, VOICE LOSS, MEMORY LOSS, BALANCE & WALKING DIFICULTY, VISION PROBLEMS, TREMORS, LIGHT SENSITIVITY, SPEECH DIFFICULTY, SEVERE CONSTANT HEADACHE, DIZZINESS, MUTIPLE FALLS, BRAIN FOG, MY WHOLE BODY HURTS ALL THE TIME, BEDRIDDEN.
Andere Medikamente: SYMBICORT, ALBUTEROL, PROPRANOLOL, CARISOPRODOL, HRT, ARMOUR THYROID, HYDROCODONE, GABAPENTIN, D3, TOPICAL GLUTATHIONE, BIOTIN, NAC, OLIVE LEAVE EXTRACT, CALCIUM, MAGNESIUM GLYCINATE, B-12 INJECTIONS, B COMPEX, MULTIVITAMIN, COLLAGEN PROTEI
Allergien: -
Vorherige Impfungen: -

VAERS 2586253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 23.02.2023
Impfdatum: 29.11.2022
Beginn: 26.12.2022
Tage bis Beginn: 27,0
Dosis: 3
Route/Site: - / -

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

Anxiety COVID-19 COVID-19 pneumonia Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Fibrin D dimer increased Hypoxia SARS-CoV-2 test positive Treatment noncompliance

Symptomtext

Patient up to date on COVID vaccines who admitted with hypoxia and COVID detected PCR. Provider d/c note: "patient came in with increased SOB. He was found to have COVID pneumonia and COPD exacerbation. He required oxygen initially. Patient was noted to have an elevated D dimer. Patient was weaned off his oxygen quickly. He was discharged home. He was sent with his inhalers from here as he has no medication coverage. Pulmonary saw him and recommended an echo as there was some question of fluid overload. This was not done and could be ordered as an outpatient. The patient was not very compliant with care because of this. Patient was very anxious to be discharge. PFTs were also recommended after discharge and would need to be set up. Patient would benefit from a LDCT yearly. Would benefit from checking for alpha 1 antitrypsin."

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: COVID Detected PCR 12/26/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Tremor of both hands Esophagitis GERD (gastroesophageal reflux disease) COPD exacerbation (*) History of peptic ulcer disease Nocturia more than twice per night suggestive of BPH Cigarette nicotine dependence in longstanding remission - 100 pack years History of DVT (deep vein thrombosis) Stage 3 severe COPD by GOLD classification (*) Alcohol abuse Microcytic anemia Erosive esophagitis Hiatal hernia Acute superficial gastritis without hemorrhage Multiple duodenal ulcers Acute respiratory failure with hypoxia and hypercapnia (*) Borderline type 2 diabetes mellitus Hypersomnolence during day suspicious for undiagnosed OSA Chronic respiratory failure with hypoxia and hypercapnia
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2570644

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 62,0
Geschlecht: F
Eingang: 30.01.2023
Impfdatum: 17.06.2021
Beginn: 30.12.2022
Tage bis Beginn: 561,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Chest pain Cough SARS-CoV-2 test positive

Symptomtext

12/30/22 presents to ED for "cough" "chest pain". PMHx of "COPD, hypertension, GERD, DM type II, hepatitis C, hypercholesterolemia, CAD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 12/30/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2536176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 18,0
Geschlecht: F
Eingang: 18.12.2022
Impfdatum: 01.09.2021
Beginn: 07.02.2022
Tage bis Beginn: 159,0
Dosis: 2
Route/Site: IM / -

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

Anion gap increased Blood gases abnormal Blood glucose increased Blood ketone body increased Blood pH decreased COVID-19 Chest X-ray normal Condition aggravated Diabetic ketoacidosis Dyspnoea Headache Nausea SARS-CoV-2 test positive Type 1 diabetes mellitus Urine analysis normal

Symptomtext

Patient is a 18 y C/F with HO uncontrolled insulin dependent diabetes mellitus - diagnosed at age 15, likely type I with history of recurrent DKA with last admission in Sept 2021. Admitted to the hospital for 2 days with the chief complaint of elevated blood sugars. She is on Insulin Lantus and Lispro. States that she takes her insulin regularly. Her last A1c in the system is from March 2021 elevated at 15. She states that she used to follow up with pediatric endocrinologist and has now aged out and is trying to get with an adult endocrinology. Her insulin regimen is currently being managed by her PCP. She states that she has been having severe head ache, nausea, and some trouble breathing because of which she came to the ER. Based on her prior episodes she felt that she might be in DKA which made her come to the ER. At the time of admission she was noted to have blood sugar of 379, anion gap elevated, venous blood gas showed PH 6.98, Beta hydroxy butyrate elevated at 8.29. UA negative for infection. CXR negative for infiltrates. She tested positive for COVID 19 infection. Admitted to moderate care with DKA protocol

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: Positive COVID 19 test 02/17/2022
Aktuelle Erkrankungen: -
Vorgeschichte: B-D UF III MINI PEN NEEDLES 31G X 5 MM, glucose blood strip (ONETOUCH VERIO) box, HUMALOG KWIKPEN 100 UNIT/ML pen injection, insulin glargine (LANTUS SOLOSTAR) 100 UNIT/ML PEN injection, insulin lispro sliding scale (HUMALOG/ADMELOG) (see instruction)
Andere Medikamente: -
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2505890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: 08.11.2021
Beginn: 26.07.2022
Tage bis Beginn: 260,0
Dosis: 3
Route/Site: IM / AR

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

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

Symptomtext

I received my first Pfizer booster for COVID-19 on 11/8/2021. On 7/26/2022, I woke up feeling ill with a fever, body aches, and a headache. I didn't get out of bed that day, and I ended up pretty much staying in bed for three days. The fever lasted for three days and fluctuated in the 100s, with 101 being the highest temperature. After the fever went away, I developed a nagging dry cough that hung on for about six weeks. At one point, I also experienced a partial loss of taste. I took an antigen test on 7/29/2022 and got a positive result. On or about 8/2/2022, I went to the clinic and received monoclonal antibodies. I had body aches and fatigue until about 8/4/2022. During my illness, I just took TYLENOL to treat the symptoms. The cough was very persistent. I took DAYQUIL and NYQUIL to help treat the cough, though they didn't help much. However, the NYQUIL did help me get to sleep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 7/29/2022 antigen test positive result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Type II Diabetes (controlled by diet); Obesity; Hypertension; Hypercholesterolemia (controlled by medication).
Andere Medikamente: Atorvastatin; famotidine; losartan; MCT oil.
Allergien: Sulfa drugs.
Vorherige Impfungen: -

VAERS 2499108

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

moderat

Staat: IN
Alter: 50,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 24.08.2021
Beginn: 01.06.2022
Tage bis Beginn: 281,0
Dosis: 2
Route/Site: SYR / -

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

Chest pain Dyspnoea

Symptomtext

chest pain, SOB

Weitere VAERSDATA-Felder

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

VAERS 2453431

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 27.10.2021
Beginn: 09.09.2022
Tage bis Beginn: 317,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest X-ray abnormal Chills Computerised tomogram thorax abnormal Cough Diarrhoea Dyspnoea Feeding disorder Lung infiltration Malaise Obstructive airways disorder Pain Pneumonia Pulmonary cavitation Pulmonary necrosis SARS-CoV-2 test positive Vomiting Wheezing

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 9/9/2022 Discharge Date: 9/15/2022 Clinical Narrative: Patient is a 67 y.o. female who presented with malaise, body aches and chills for 10 days, with increasing SHOB as well as diarrhea/vomiting. She has PMH of rheumatoid arthritis on DMARD's, obstructive sleep apnea, former smoker, iron deficiency requiring transfusions, hypertension, GERD. She's been unable to eat x1 week and had developed a new cough the past few days. Findings on admission included consolidated right upper lobe pneumonia with some evidence of necrosis in the lower aspect of the right upper lobe, as well as concern of obstruction of the right upper lobe bronchus. COVID test was positive. She had now on lung exam, although she did a formal diagnosis of chronic obstructive pulmonary disease prior to admission. She was treated with IV Rocephin, doxycycline, IV dexamethasone, nebulizer treatments. Antibiotics were subsequently changed to Zosyn. Repeat imaging on 09/12/2022 showed no improvement in the x-ray and subsequent repeat CT imaging supported for complete obstruction of the right upper lobe with no endobronchial air, and increased changes of necrosis. Patient was felt to require transfer to a higher level of care for pulmonary specialty care to include bronchoscopy, in addition to other potential interventions. She was accepted at Hospital on Monday September 12, but a bed did not become available. Subsequently a bed did become available at different Hospital on 09/15/2022. Prior to discharge she did have a repeat chest x-ray which appears slightly worse including what appeared to me to be a small area of cavitation in the right upper lobe and some increase infiltrates evolving into the right lower lobe. Her clinical condition however remained stable with a oxygen requirement of just 2 L. Regards to chronic obstructive pulmonary disease, she had extensive wheezing throughout which improved prior to discharge with oral prednisone at 40 mg per day, combined with Symbicort, Spiriva, and albuterol inhaler 4 puffs q.i.d.. Her COVID-19 infection did not appear to meet criteria for treatment with remdesivir. Due to a concomitant explanation for her respiratory symptoms, her isolation for COVID-19 was felt to be again on the date of the positive test on September 9, 2022. The initial transfer on September 12, 2022 was discussed with Dr. who was to be the accepting physician. However, with the change to different Hospital I spoke with Dr. from the hospital service accepted the patient transfer. The case was also reviewed by Dr., a pulmonology who agreed with transfer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Pulmonary arterial hypertension Former smoker OSA (obstructive sleep apnea) Chronic obstructive pulmonary disease with acute lower respiratory infection Acute cystitis without hematuria Multiple falls Immunocompromised Elevated blood uric acid level Iron deficiency anemia secondary to blood loss (chronic)
Andere Medikamente: allopurinol (ZYLOPRIM) 300 MG tablet amLODIPine (NORVASC) 10 MG tablet amoxicillin-clavulanate (AUGMENTIN) 875-125 MG per tablet aspirin EC 81 MG enteric coated tablet buPROPion (WELLBUTRIN SR) 100 MG 12 hr tablet carvedilol (COREG) 12.5 MG
Allergien: MethotrexateNausea and Vomiting
Vorherige Impfungen: -

VAERS 2433649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 11.03.2021
Beginn: 29.08.2022
Tage bis Beginn: 536,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Coronary artery bypass Dyspnoea SARS-CoV-2 test positive

Symptomtext

08/29/22 presents to EC ED for "shortness of breath". PMHx of "CABG x3 8/13/2022, HTN, Hep C, HPL, Hepatocellular carcinoma s/p Liver transplant (2015), Chronic back pain"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 08/29/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2433601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 17.05.2021
Beginn: 24.08.2022
Tage bis Beginn: 464,0
Dosis: 2
Route/Site: - / -

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

Abdominal pain COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

08/24/22 presents to EC ED for "abdominal pain, shortness of breath". PMHx of "MS, CVA, recent fall and left rib fracture"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 08/24/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 37,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 02.09.2021
Beginn: 02.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Chest X-ray normal Cough Dyspnoea Heart rate increased Pain Paraesthesia Pyrexia SARS-CoV-2 test positive

Symptomtext

Immediately 10 minutes after the injection, my left arm got really hot. I got hot and turned red and itchy. Then the tingling started happening down the lower part of my spine. The redness and itching stopped after 4.5 hours. The tingling has lasted up until now, it's subsided but still there. My heart rate was a little fast. After the 2nd dose I contracted COVID-19 2 weeks later. With COVID-19 I had shortness of breath, fever, body aches and increased heart rate that lasted a 1.5 weeks. The cough is something the doctor can't tell if it's vaccine or COVID-19 related. The cough has not gone away and I'm seeing a Pulmonologist and taking medications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 - positive; chest x-rays- normal.
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: After 1st dose COVID-19 Moderna I had a similar reaction with the tingling, redness, pain in lower spine.

VAERS 2427535

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 60,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 30.08.2021
Beginn: 03.09.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / UN

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

Blood test Electrocardiogram Heart rate increased Heart rate irregular SARS-CoV-2 test negative Supraventricular tachycardia

Symptomtext

On 09/03/02021 around 12:00PM my heart rate went up to 220 per minutes. I called paramedics they gave me 3 shots adenosine. It brought my heart rate down. They took me to the hospital. They did blood test to make sure I wasn't haven't heart attack. They monitored me for 45 minutes to an hour. They released me and they told me to see my cardiologist. After that happened I started to irregular heart beat which continued till this day. I went to 1 and 2 electrophysiologist. I was told that the vaccine triggered birth defects which is called AVNRT. It requires an abrasion. I haven't done the abrasion yet. The irregular heart heart can not be fixed it might had come from adenosine. I have irregular heart beat ongoing. I had a first follow up in the hospital 09/10/2021, Cardiologist. I went to Electrophysiologist on 09/28/2021. Second appointment 11/15/2021 Electrophysiologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Supraventricular tachycardia
Hospital-Tage: -
Labordaten: COVID-19 test- negative; blood test; EKG
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol
Andere Medikamente: PEPCID
Allergien: Opiate
Vorherige Impfungen: Shingles- Bradycardia 2nd shot

VAERS 2421038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 39,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 30.11.2021
Beginn: 19.08.2022
Tage bis Beginn: 262,0
Dosis: 3
Route/Site: - / -

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

Angiogram pulmonary abnormal Anticoagulant therapy Asthma COVID-19 Complication of pregnancy Cough Dyspnoea Fibrin D dimer increased Condition aggravated Lung opacity Maternal exposure before pregnancy Ultrasound antenatal screen abnormal Uterine leiomyoma Laboratory test SARS-CoV-2 test positive Troponin normal

Symptomtext

Pregnant patient up to date on COVID vaccines who admitted with COVID. Provider d/c note: Patient is a 40 YO year old G9P3 (4 miscarriages), with a history patient report of cardiac problems during her last delivery, asthma, gestational diabetes, suicide attempt 23 weeks, depression with previous suicide attempt, asthma, anxiety, gestational diabetes, sleeve gastrectomy presenting to Hospital with complaint of coughing and shortness of breath. Labs show elevated ddimer, negative troponin, COVID + PCR. CTA shows ground glass opacity but not acute pulmonary embolism. She was given 1L LR, started on steroids. Started on remdesivir. Per pulmonology she is high risk. Due to her risk factors she will be transferred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: COVID detected PCR on 08/19/22
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity Anxiety Reflux History of sleeve gastrectomy Asthma Depression
Andere Medikamente: -
Allergien: Seasonal
Vorherige Impfungen: -

VAERS 2422859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 29.08.2022
Impfdatum: 27.08.2021
Beginn: 01.06.2022
Tage bis Beginn: 278,0
Dosis: 3
Route/Site: IM / LA

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

Bacterial infection Blood test abnormal COVID-19 Cough Dyspnoea Influenza virus test negative Malaise Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive White blood cell count increased

Symptomtext

I started with a sore throat and a fever. I tested myself on the 2nd of June and was positive. I was given PAXLOVID. It was the PAXLOVID gave me a Hepatitis flare up so I had to stop. I tried to get the infusion but they could not do it because I had started the PAXLOVID. The symptoms were the same for my asthma and COVID-19 symptoms. I had shortness of breath, coughing and body aches. It was almost like having the flu. I took ibuprofen, purchased an air purifiers and used a lot of nebulizer medication for breathing treatments. It took me about 5 weeks to completely recover. I went back to my doctor for a check up and ended up having a bacterial infections but the doctor did not think it related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID 19-June 02, 2022-Positive. Flu Test-June 2022-Negative. Blood Panel-WBC High-June 2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma; Autoimmune Hepatitis
Andere Medikamente: CLARITIN; IMURAN; budesonide
Allergien: Sulfa; penicillin; amoxicillin; nitrofurantoin
Vorherige Impfungen: -

VAERS 2419361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 24.08.2022
Impfdatum: 06.11.2021
Beginn: 16.08.2022
Tage bis Beginn: 283,0
Dosis: 3
Route/Site: UN / UN

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

Fatigue Myalgia Palpitations

Symptomtext

fatigue, palpitations, myalgias

Weitere VAERSDATA-Felder

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

VAERS 2400260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 03.08.2022
Impfdatum: 27.10.2021
Beginn: 27.01.2022
Tage bis Beginn: 92,0
Dosis: 3
Route/Site: IM / -

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

Angiogram pulmonary Asymptomatic COVID-19 Computerised tomogram head Computerised tomogram spine Dizziness Electrocardiogram abnormal Fall Fatigue Laboratory test normal SARS-CoV-2 test positive Sinus tachycardia Supraventricular extrasystoles

Symptomtext

Patient was admitted on 1/27/2022 with complaints of fatigue, dizziness and 3 episodes of fall. In the ER EKG showed sinus tachycardia with PACs. Workup showed unremarkable, screen for COVID-19 was positive, CTA chest, CT head, cervical spine and facial bones were unremarkable. Patient was started on oral antibiotics for possible UTI, IV fluids and was admitted to hospitalist service . Pt remained asymptomatic from COVID-19 infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sinus tachycardia
Hospital-Tage: 3,0
Labordaten: COVID 19 test positive on 01/27/22
Aktuelle Erkrankungen: -
Vorgeschichte: 11/10/16 Adnexal mass Date Unknown: HTN (hypertension) Date Unknown: Skin cancer
Andere Medikamente: carvedilol (COREG) 3.125 MG tablet multivitamin-minerals (CERTAVITE/MYADEC/CENTRUM) TABS tablet
Allergien: No know allergies.
Vorherige Impfungen: -

VAERS 2376624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: VA
Alter: 37,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 05.10.2021
Beginn: 28.12.2021
Tage bis Beginn: 84,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Fatigue Heart rate increased Joint range of motion decreased Oedema peripheral Pityriasis rosea Sinus tachycardia

Symptomtext

I got COVID-19 on 12/28/2021 but did not receive treatment, just treated at home. I had swelling in my armpit after my vaccine. I could not lift my arm. I had fatigue and fell asleep after the vaccine. I got Pityriasis rosea on 02/15/2022. I was seen by urgent care and gave me a steroid and hydroxyzine but nothing helped. It took two months but I still have a patch on my ankle. 07/07/2022 my heart rate went up high and has been that way since. I had sinus tachycardia on 7/20/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sinus tachycardia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Scoliosis; Environmental Allergies
Andere Medikamente: Calcium; vitamin D; SINGULAIR; ZYRTEC
Allergien: Latex; avocado; banana; chestnut; kiwi; apple; melons; papaya; tomato; cherry; coconut; fig; peach; pear; strawberry; pepper; spinach; paprika
Vorherige Impfungen: -

VAERS 2359500

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 01.09.2021
Beginn: 13.06.2022
Tage bis Beginn: 285,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Blood glucose increased COVID-19 pneumonia Cognitive disorder Dyspnoea Exposure to SARS-CoV-2 Hypoxia Leukocytosis Multimorbidity White blood cell count increased

Symptomtext

Provider summary "This is a 67 y/o female with a past medical history significant for advanced MS who presented to the ED on 6/9/2022 for evaluation of acute weakness and dyspnea following exposure to her daughter who had tested positive for COVID. She was found to be hypoxic in the ED. The patient was admitted to the hospitalist service for COVID pneumonia with hypoxia. She had an uneventful hospitalization and when medically stable, the patient was discharged to Lakeland Health Watervliet for acute inpatient rehabilitation of functional and cognitive deficits. Symptoms related to these abovementioned conditions and events were well-controlled, and the patient was discharged medically stable and improved. There were no significant acute episodes that affected length of stay or tolerance to therapies. Patient was noted to have elevated blood sugars and leukocytosis while on dexamethasone. Blood sugars and WBCs improved when steroid course was completed, though blood sugars did not completely return to normal despite use of home glimepiride requiring continued use of Lantus and ISS. Lantus was discontinued and patient started on Januvia in conjunction with home glimeperide. Blood sugars appear to be well controlled. The patient was also provided orthotics / durable medical equipment to ensure improved function and safety in the rehabilitation and home setting. Occupational, Physical and Speech Language Pathology therapists and a Neuropsychologist were consulted for evaluation and treatment so as to best determine the amount and extent of services required for cognitive and functional optimization. The patient received a minimum of 180 minutes of therapy per day for 5 out of 7 days, or more than 15 hours of intensive therapy over the course of a week. While in the unit, the acute rehabilitation service also held interdisciplinary team conferences on a weekly basis to establish specific short- and long-term goals during rehabilitation, and for discharge. Barriers to discharge were also noted and updated as they were addressed. Plans to assure continuity and coordination of care after discharge from the acute rehabilitation unit were also established and explained to the patient and care provider(s). While on the unit, the patient was monitored on a daily basis by a physician who evaluated and managed co-morbidities and medical conditions, as necessary. Noteworthy events related to the patient's rehabilitative stay included the below mentioned - which were treated as indicated."

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 16,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypersomnolence 9/13/2012 Hypertension 9/18/2012 Dysuria 3/29/2013 Multiple sclerosis, relapsing-remitting with secondary progression (Chronic) Unknown Dehydration 3/25/2014 Diarrhea 3/25/2014 Abnormal urinalysis 3/25/2014 Cholelithiasis 6/23/2014 OSA on CPAP 10/8/2014 Encephalopathy 11/14/2014 Falling 11/14/2014 Dysarthria 11/15/2014 Left-sided weakness 11/15/2014 Retro-orbital pain of both eyes 11/15/2014 Ataxia 11/15/2014 Neurogenic bladder and frequent UTI due to Multiple Sclerosis 11/19/2014 Urinary tract infection due to Proteus 11/20/2014 Controlled type 2 diabetes mellitus, without long-term current use of insulin (Chronic) 7/4/2017 Pelvic mass in female 9/11/2018 Polycythemia 3/12/2019 Erythrocytosis 4/11/2019 Right hip pain 5/10/2020 Weight gain 1/19/2021 Generalized weakness 4/6/2021 Falls at home 4/6/2021 Elevated liver function tests 4/6/2021 Acute respiratory insufficiency 4/6/2021 Frequent UTI (Chronic) 4/6/2021 Calculus of kidney with calculus of ureter 7/12/2021
Andere Medikamente: acetaminophen 1,000 mg Oral EVERY 8 HOURS PRN albuterol sulfate 90 mcg/actuation 2 puffs Inhalation EVERY 6 HOURS PRN alpha lipoic acid 600 mg 1 capsule Oral 2 times daily amantadine HCl 100 mg Oral 2 times daily ascorbic acid 1,000 mg
Allergien: Severity Reactions Comments Ciprofloxacin Not Specified Other (See Comments) Patient states that it affects her tendons and that she can not walk if she takes it Macrobid [nitrofurantoin Monohyd/m-cryst] Not Specified Diarrhea, Fatigue Metformin Not Specified Diarrhea
Vorherige Impfungen: -

VAERS 2327238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 60,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 25.04.2022
Beginn: 07.06.2022
Tage bis Beginn: 43,0
Dosis: 1
Route/Site: UN / UN

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

Asthenia COVID-19 Cough Diabetic ketoacidosis Dyspnoea Faeces discoloured Fall Hyperglycaemia Hypoaesthesia Loss of personal independence in daily activities Magnetic resonance imaging spinal abnormal Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

Provider summary: "Patient is a 61 YO male with a PMHx of T2 DM on insulin, diabetic neuropathy, HTN, HLD, microcytic anemia, GERD, PUD, CAD s/p CABG, depression, anxiety, and OSA who presented with hyperglycemia. Pt reports that for the past 2-3 weeks, he has been having progressively worsening weakness. It started around his groin areas and moved to his entire body. He now struggles to get his daily activities done due to weakness and reports multiple falls during this time period. He has numbness on his lower extremities at baseline. He denies recent illness. Pt states that he has been feeling nauseated for the past 2-3 weeks and did vomit about a week ago. He does admit that he does not use insulin regularly because he feels like it is not helping much (though he states that he knows that it is not true). He believes he has been using insulin every other day for the last 3 weeks. He denies sick contacts and is unsure where he may have gotten COVID-19. He does report getting dry coughs and SOB for the past 1 week. He also endorses having black stools, which started about 2 weeks ago. DKA resolved following IVF resuscitation and K+/Mg+ replacement in the ED. Diet restarted and blood glucose controlled with 50 units of glargine and lispo sliding scale insuline. Held over night due to concerns for recent falls. Neurological status remained at baseline throughout stay. It is recommended that he follow-up with neurology for lumbar spine findings on MRI dated 5/9/2022. Patient seen by gastroenterology who recommend outpatient elective endoscopy once COVID-19 has resolved. PT recommends outpatient physical therapy in the home while OT thinks that inpatient post-acute occupational therapy would be beneficial."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: Positive COVID PCR 6/7/22
Aktuelle Erkrankungen: -
Vorgeschichte: Oliguria 4/20/2021 Diabetic ketoacidosis with coma associated with type 2 diabetes mellitus 4/20/2021 Normocytic anemia 4/20/2021 Metabolic encephalopathy 4/20/2021 Gastroesophageal reflux disease without esophagitis 4/20/2021 Bilateral pleural effusion 4/20/2021 Closed fracture of transverse process of lumbar vertebra 4/20/2021 Displaced fracture of lesser trochanter of left femur, initial encounter for closed fracture 4/20/2021 Fracture of greater trochanter of left femur 4/20/2021 Critical illness myopathy 4/29/2021 Closed fracture of head of right humerus 6/8/2021 Failure to thrive in adult 6/8/2021 Closed fracture of proximal end of right humerus with routine healing 7/7/2021 Diabetic ketoacidosis without coma associated with type 2 diabetes mellitus
Andere Medikamente: dulozetine gluagon lansoprazole loperamide metformin ondastron trazodone
Allergien: -
Vorherige Impfungen: -

VAERS 2319059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

moderat

Staat: FL
Alter: 91,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 20.05.2021
Beginn: 03.06.2022
Tage bis Beginn: 379,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea Respiratory failure

Symptomtext

Presents with worsening shortness of breath and repiratory failure due to covid. Treated with oxygen, steroids, and remdesivir. Pt will discharge home with oxygen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, HLD, dementia, breast CA,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2311496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 08.07.2021
Beginn: 09.07.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Bronchiolitis Chest X-ray abnormal Chest discomfort Computerised tomogram thorax abnormal Dyspnoea Lung hyperinflation Pleural thickening Pulmonary function test abnormal Pulmonary mass

Symptomtext

After waiting to see if my breathing got better, which it did not, so on October 25th, 2021 I went to see Dr. who was my doctor at the time, for my breathing and she sent me for a chest x-ray. That evening she called me to set up an appointment for a Pulmonary Test with Dr. The x-ray showed the lungs are hyperinflated and apical pleural thickening. Now with my breathing problem, mostly when I'm bending and doing things fast is when I feel at my worst. Seems like something heavy is on my chest. Now I make an appt. on February 4, 2022 with Dr. a Pulmonologist. He sets an appt. for a CT. Scan of the chest on February 17, 2022 and a Pulmonary Test on February 24, 2022. The result of the CT Scan showed that my Lungs had clusters of small centrilobular pulmonary nodules with tree-in-bud morphology associated with thickening of the peribronchial vascular insterstitium were identified throughout the lungs bilaterally, likely related to chronic bronchiolitis. Subpleural soft tissue density pulmonary nodule in the right lower lobe measures 4 mm. Dr. no longer seemed it necessary for any other follow-ups and suggested I see a Cardiologist. I set up an appointment for Dr. from the Heart facility, on July , 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: see 18
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Calcium and Omega 3
Allergien: None
Vorherige Impfungen: -

VAERS 2303512

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: WI
Alter: 71,0
Geschlecht: M
Eingang: 31.05.2022
Impfdatum: 17.06.2021
Beginn: 24.05.2022
Tage bis Beginn: 341,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 pneumonia

Symptomtext

Patient admitted as observation on 5/24 due to pneumonia due to COVID-19 virus

Weitere VAERSDATA-Felder

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

VAERS 2283006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 53,0
Geschlecht: M
Eingang: 25.05.2022
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Injected limb mobility decreased Injection site pain X-ray normal Joint range of motion decreased Pain in extremity Vaccination site pain X-ray

Symptomtext

limited range of motion; pain at the injection site and all upper left arm pain; pain at the injection site and all upper left arm pain; This is a spontaneous report received from contactable reporter(s) (Pharmacist) from medical information team. A 53-year-old male patient received BNT162b2 (BNT162B2), on 12Nov2021 at 14:00 as dose 3 (booster), single (Lot number: EW0186) at the age of 53 years, in left arm for covid-19 immunization. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Vaccine Name: Pfizer COVID vaccine, Lot Number / Expiry Date: EN6206, expiration is unknown, Route, Anatomical Location:Injected in left arm, No. of Previous Doses: 1, Date: 03May2021), administration date: 03May2021, when the patient was 53-year-old, for Covid-19 immunization; BNT162b2 (Vaccine Name: Pfizer COVID vaccine, Lot Number / Expiry Date: EN6206, expiration is unknown, Route, Anatomical Location:Injected in left arm, No. of Previous Doses: 0, Date: 05Mar2021), administration date: 05Mar2021, when the patient was 53-year-old, for Covid-19 immunization. The following information was reported: INJECTION SITE PAIN (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 12Nov2021, outcome "not recovered" and all described as "pain at the injection site and all upper left arm pain"; JOINT RANGE OF MOTION DECREASED (non-serious), outcome "not recovered", described as "limited range of motion". The events "pain at the injection site and all upper left arm pain" and "limited range of motion" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pain in extremity, joint range of motion decreased. Additional information: Caller was a pharmacist on behalf of a 53-year-old male patient who was also on the line. The patient was administered the third dose (first booster dose) of Pfizer COVID-19 Vaccine on Nov2021. Since then, he has experienced pain at the injection site and all upper left arm pain, followed by a limited range of motion. He had tried several pain medication and treatment modalities, but nothing has helped. States that the common side effects should go away in a few days. Adverse effects that could cause a long-term health problem are extremely unusual following any vaccination, including COVID-19 vaccination. Please also note that these may not be all the possible side effects of the vaccine. Serious and unexpected side effects may occur. The possible side effects of the vaccine are still being studied in clinical trials. He has been complaining of moderate to severe pain in upper left arm which was site of injection on the day he received his 3rd booster dose of the Pfizer COVID vaccine. This has progressed to limited range of motion. He has taken multiple medications to resolve it, but the pain is still there. It has been fluctuating from moderate to severe depending on medication. Patient then came on the line and said 1st day of injection he has had severe pain. The pain was so severe that he does not know if he had limited range of motion when it first started. The severe pain lasted 10 days and that is when he started taking pain medication. Reporter told him that site reaction is common, and she said to treat with Ibuprofen and Tylenol, but now he is calling and said it has persisted. She did not think it was an adverse event and thought it was just a side effect. His physician has referred him to rehab and then said he recommended physical therapy. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): Flu vaccine a month afterwards but nothing a month prior to the Pfizer COVID vaccine. Patient would like to know if this has been reported before and is there any treatment offered by Pfizer. He has been dealing with it for 6 months and tried different courses of treatment. He may have permanent damage.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: Test Name: X-ray; Test Result: Negative; Comments: Two X-rays on left shoulder and looking to see if something wrong with bone structure and it was negative.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2283006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 53,0
Geschlecht: M
Eingang: 25.05.2022
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: nein

Injected limb mobility decreased Injection site pain X-ray normal Joint range of motion decreased Pain in extremity Vaccination site pain X-ray

Symptomtext

limited range of motion; pain at the injection site and all upper left arm pain; pain at the injection site and all upper left arm pain; This is a spontaneous report received from contactable reporter(s) (Pharmacist) from medical information team. A 53-year-old male patient received BNT162b2 (BNT162B2), on 12Nov2021 at 14:00 as dose 3 (booster), single (Lot number: EW0186) at the age of 53 years, in left arm for covid-19 immunization. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Vaccine Name: Pfizer COVID vaccine, Lot Number / Expiry Date: EN6206, expiration is unknown, Route, Anatomical Location:Injected in left arm, No. of Previous Doses: 1, Date: 03May2021), administration date: 03May2021, when the patient was 53-year-old, for Covid-19 immunization; BNT162b2 (Vaccine Name: Pfizer COVID vaccine, Lot Number / Expiry Date: EN6206, expiration is unknown, Route, Anatomical Location:Injected in left arm, No. of Previous Doses: 0, Date: 05Mar2021), administration date: 05Mar2021, when the patient was 53-year-old, for Covid-19 immunization. The following information was reported: INJECTION SITE PAIN (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 12Nov2021, outcome "not recovered" and all described as "pain at the injection site and all upper left arm pain"; JOINT RANGE OF MOTION DECREASED (non-serious), outcome "not recovered", described as "limited range of motion". The events "pain at the injection site and all upper left arm pain" and "limited range of motion" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pain in extremity, joint range of motion decreased. Additional information: Caller was a pharmacist on behalf of a 53-year-old male patient who was also on the line. The patient was administered the third dose (first booster dose) of Pfizer COVID-19 Vaccine on Nov2021. Since then, he has experienced pain at the injection site and all upper left arm pain, followed by a limited range of motion. He had tried several pain medication and treatment modalities, but nothing has helped. States that the common side effects should go away in a few days. Adverse effects that could cause a long-term health problem are extremely unusual following any vaccination, including COVID-19 vaccination. Please also note that these may not be all the possible side effects of the vaccine. Serious and unexpected side effects may occur. The possible side effects of the vaccine are still being studied in clinical trials. He has been complaining of moderate to severe pain in upper left arm which was site of injection on the day he received his 3rd booster dose of the Pfizer COVID vaccine. This has progressed to limited range of motion. He has taken multiple medications to resolve it, but the pain is still there. It has been fluctuating from moderate to severe depending on medication. Patient then came on the line and said 1st day of injection he has had severe pain. The pain was so severe that he does not know if he had limited range of motion when it first started. The severe pain lasted 10 days and that is when he started taking pain medication. Reporter told him that site reaction is common, and she said to treat with Ibuprofen and Tylenol, but now he is calling and said it has persisted. She did not think it was an adverse event and thought it was just a side effect. His physician has referred him to rehab and then said he recommended physical therapy. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): Flu vaccine a month afterwards but nothing a month prior to the Pfizer COVID vaccine. Patient would like to know if this has been reported before and is there any treatment offered by Pfizer. He has been dealing with it for 6 months and tried different courses of treatment. He may have permanent damage.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: Test Name: X-ray; Test Result: Negative; Comments: Two X-rays on left shoulder and looking to see if something wrong with bone structure and it was negative.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2284923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: WI
Alter: 43,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 18.05.2021
Beginn: 18.05.2022
Tage bis Beginn: 365,0
Dosis: 2
Route/Site: IM / RA

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

Fatigue Injected limb mobility decreased Lymph node pain Lymphadenopathy Pyrexia

Symptomtext

That night, I spiked a super high fever that lasted around 48 hours and was extremely tired. The next morning. I noticed the lymph node under my right arm was swollen. It got to about golf ball size and was really sore, I couldn't put my arm down properly. I called my doctor's office and spoke with a nurse. She stated that it was probably just from the shot and advised that I monitor it and come in if it didn't improve. The swelling lasted for a few weeks and went away on it's own.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure Diabetes
Andere Medikamente: Lisinopril Simvastatin Januvia Glipizide
Allergien: Nickel
Vorherige Impfungen: -

VAERS 2280694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 22.10.2021
Beginn: 08.05.2022
Tage bis Beginn: 198,0
Dosis: 3
Route/Site: IM / AR

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

Auscultation C-reactive protein normal COVID-19 Chest X-ray normal Chronic obstructive pulmonary disease Computerised tomogram thorax normal Condition aggravated Dyspnoea Gait disturbance Hypoxia Inflammatory marker test Laboratory test abnormal Lymphopenia Malaise SARS-CoV-2 test positive Wheezing

Symptomtext

ED for COVID (5.8.22); Hospitalized (5.10.22 - 5.13.22) with COVID-19 and COPD exacerbation; COVID-19 positive; Fully vaccinated PLUS BOOSTER ED Course: MEDICAL DECISION MAKING: Supervising Physician: DO Presents emergency department for evaluation of shortness of breath, has known emphysema. Has been sick for 6 days, is vaccinated and boost against COVID-19. She did however take a home COVID test was noted be positive. She does have significant wheezing on auscultation. She will be given 8 puffs of an albuterol inhaler, will check baseline labs get a confirmatory COVID testing per our records as she has no proof with her. Patient is not tachycardic nor hypoxic, she has no leg swelling or calf pain. She does have known emphysema, and known COVID likely contributing to her dyspnea. I see no indication for D-dimer testing this point time. However, should patient have marked infiltrates on her chest x-ray, or require admission this test may need to be ordered in order to stratify her risk from COVID-19. Patient's chest x-ray is without infiltrate, laboratory studies are reflective COVID-19, no leukocytosis, but mild lymphopenia. Are confirmatory COVID testing is positive. Patient does have chronic obstructive pulmonary disease, I am going to treat her for chronic obstructive pulmonary disease exacerbation, likely secondary to COVID. I am going to discharge her home. I did give her IM Solu-Medrol here will maintain her on prednisone for the next 3 days at home. I do not feel she requires antibiotic coverage. She was given strict return precautions and home pulse oximetry reader. Patient was given the phone number for the monoclonal antibody clinic, however I did caution her that she is on day 6, most therapies need to be started by day 5. Hospitalization information: BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: NP Admission Date: 5/10/2022 Discharge Date: May 13, 2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypoxemia [R09.02] COPD exacerbation [J44.1] COVID [U07.1] HOSPITAL COURSE: Patient is a 66 y.o. female who presents today with about a 1 week history of progressive shortness of breath. She was seen in the emergency department about 3 days ago and had a COVID-19 test which was positive. She was treated with prednisone. In spite of that her shortness of breath has progressed and today was acute and scary for her in that she had difficulty being able to walk to the bathroom because of the severity of the shortness of breath. In the emergency department her pulse oximetry at rest was in the upper 80s. She had CT a imaging of her chest which showed no evidence of pulmonary emboli or of pulmonary infiltrates. It was noted that inflammatory markers such as CRP were not elevated in spite of the positive COVID testing. Patient has a longstanding history of smoking and is currently trying to quit. Her examination showed diffuse wheezing throughout all lung fields consistent with chronic obstructive pulmonary disease exacerbation At the time of admission, although the patient did have a positive COVID-19 test, was felt that this is most likely a chronic obstructive pulmonary disease exacerbation not directly related to COVID-19. She was treated with high-dose IV Solu-Medrol, frequent nebulizer treatments, azithromycin, and IV Remdesivir. She had good improvement over the 1st couple of days with decreasing wheezing. However by the 4th hospital day she continued to have borderline hypoxemia which on room air with dip into the upper 80s with mobility. She was agreeable to home oxygen therapy at discharge. She remains committed to discontinuing smoking and recently was started on Wellbutrin, and in addition will have a nicotine patch. Medication changes at discharge: 1. Nicotine patch 21 mg daily for 6 weeks, then 14 mg daily for 2 weeks, then 7 mg daily for 2 weeks. 2. Azithromycin (antibiotic) 250 mg once in a.m. on 5/14 to complete antibiotic treatment. 3. Prednisone 20 mg twice daily for 5 days for COPD and COVID. 4. Oxygen at 1 liter per minute continuous. May remove if resting in chair. 5. Albuterol per nebulizer up to 4 times daily for the next week, then as needed as before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: 5.8.22: ED SOB COVID-19 5.10.22: Admitted COVID-19
Vorgeschichte: HTN (hypertension) Tobacco abuse COPD (chronic obstructive pulmonary disease) with emphysema Snoring Fatigue Chronic hypoxemic respiratory failure
Andere Medikamente: ALPRAZolam (XANAX) 0.25 MG tablet amLODIPine (NORVASC) 5 MG tablet atorvastatin (LIPITOR) 80 MG tablet buPROPion (WELLBUTRIN SR) 150 MG 12 hr tablet escitalopram (LEXAPRO) 20 MG tablet ibuprofen (MOTRIN) 200 MG tablet Nicotine 21-14-7 MG/24
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 2278608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 16.05.2022
Impfdatum: 13.05.2021
Beginn: 28.12.2021
Tage bis Beginn: 229,0
Dosis: 2
Route/Site: IM / AR

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

Cough Electrocardiogram normal Pain Pain in extremity Respiratory tract congestion COVID-19 Cardiac stress test normal Chest X-ray abnormal Chest discomfort Chest pain Rhinorrhoea SARS-CoV-2 test negative SARS-CoV-2 test positive Sleep disorder Vaccine breakthrough infection

Symptomtext

Breakthrough case of Covid. 12/28/2021 sx began with me waking up at 04:00AM with the worst pain in my life, I soaked in the tub for like 30 minutes and I was okay. 12/29/2021 I woke up with the same pain in my legs, I soaked in the tub for about 30 minutes and I was okay. Later in the day runny nose, congestion, cough, tightness in my chest. I knew something was not right. 12/30/2021 I went to urgent care having the same sx. They did a rapid test and a long test, lung x-ray it all came back okay. The PA thought I had an upper raspatory infection. Told to take over the counter stuff for your cough. 12/31/2021 went back to the urgent care, had another x-ray and was prescribed steroids (prednisone). I think in about 3 to 5 days I was feeling better as far as the congestion and cough, but I had a lingering chest pain that I have had ever since. I saw a cardiologist and he said everything looks good, I have a second opinion scheduled at the end of the month with another cardiologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Rapid test negative, lung X-ray negative 12/30/2021. Long test positive, lung X-ray 12/31/2021 positive. EKG, ECG, stress test negative.
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic pain; chronic neck and back pain; migraines; arthritis
Andere Medikamente: Seroquel; Lipitor; Allegra; Topamax; Valium; omeprazole; vitamin D; Cambia PRN for migraines; Emgality; Nasacort; Sudafed PRN allergies
Allergien: Aspirin sensitivity
Vorherige Impfungen: Rabies vaccine, age of 9, after being bit by a mouse. I broke out in a funky rash and they put me in quarantine because they did

VAERS 2263189

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NC
Alter: 44,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 16.06.2021
Beginn: 20.06.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia Injected limb mobility decreased Magnetic resonance imaging Pain X-ray

Symptomtext

In a few days had left severe shoulder, lost strength. Weakness persist to present. Pain with motion. Self PT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: MRI today X-ray
Aktuelle Erkrankungen: No
Vorgeschichte: Hyperthyroid
Andere Medikamente: Synthroid Cytomel Prenatal Vitamin
Allergien: No
Vorherige Impfungen: -

VAERS 2250142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MN
Alter: 64,0
Geschlecht: F
Eingang: 25.04.2022
Impfdatum: 30.07.2021
Beginn: 23.04.2022
Tage bis Beginn: 267,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia COVID-19 Decreased appetite Fatigue SARS-CoV-2 test positive Tachycardia Urinary incontinence

Symptomtext

WEAKNESS AND FATIGUE, TACHYCARDIA, DECREASE IN APPETITE, URINATY INCONTINENCE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: POSITIVE HOME COVID TEST 4/24/22 PRIOR TO ADMISSION
Aktuelle Erkrankungen: -
Vorgeschichte: Cancer Colon adenoma Coronary artery disease NSTEMI Dementia Dyslipidemia Learning disability Lung nodule Vertigo Urinary incontinence Rotator cuff tendinitis
Andere Medikamente: ARIPiprazole (ABILIFY) 5 mg oral tablet aspirin (ASPIRIN LOW DOSE) 81 mg Oral TbEC atorvastatin (LIPITOR) 80 mg oral tablet Diaper,Brief, Adult,Disposable docusate sodium (COLACE) 100 mg oral capsule losar
Allergien: Lisinopril
Vorherige Impfungen: -

VAERS 2220284

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 06.08.2021
Beginn: 06.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Alopecia Condition aggravated Decreased appetite Fatigue Hypoaesthesia Immunisation reaction Laboratory test normal Muscular weakness Pruritus Swelling

Symptomtext

Numbness on my arm, hand, feet; headache, muscle weakness, swelling, itching, hair loss, loss of appetite, fatigue. I went to the doctor, and they referred to an immunologist and this doctor said that my body is reacting to the vaccine. They told me to take Benadryl.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Lab tests were normal
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No
Vorherige Impfungen: Tetanus vaccine - 49 yrs old -swelling & bumps all over my body

VAERS 2214166

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 04.04.2022
Impfdatum: 02.02.2021
Beginn: 25.01.2022
Tage bis Beginn: 357,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Cough Dyspnoea Interchange of vaccine products

Symptomtext

01/25/22 presents to ED for "cough and shortness of breath" "diagnosed with COVID-19 5 days ago". PMHx of "AAA, diabetes mellitus, hypertension"

Weitere VAERSDATA-Felder

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

VAERS 2209277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 31.03.2022
Impfdatum: 09.09.2021
Beginn: 06.02.2022
Tage bis Beginn: 150,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

Patient with 2 doses of Pfizer COVID vaccination, last dose 09/09/2021, who admitted with complications of COVID. Provider d/c note below: "patient presented with dyspnea found to have covid pneumonia and respiratory failure. Treated with decadron/remdesivir and o2 support, weaned off to room air. Completed 10 days steroids and discharged to HCF for rehabilitation."

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 11,0
Labordaten: COVD "detected" PCR on 02/06/22.
Aktuelle Erkrankungen: -
Vorgeschichte: Depression H/O Basal cell carcinoma of multiple sites of head treated with radiation Bilateral carotid artery stenosis s/p bilateral CEA Cerebrovascular accident (CVA) due to occlusion of left anterior cerebral artery (*) Seizure (*) Dyslipidemia Hemianopia, homonymous, right Hemiparesis of right dominant side as late effect of cerebral infarction (*) Hypothyroidism (acquired) Elevated liver function tests Dysarthria Aphasia Squamous cell carcinoma in situ (SCCIS) of skin of face
Andere Medikamente: Aspirin Baclofen Plavix Depakote Colace Prozac Norco Levoxyl Multivitamin Prilosec Crestor
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2199192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

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 2176125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: PA
Alter: 44,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 06.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: OT / LA

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

Anxiety Condition aggravated Muscle contractions involuntary Muscle twitching Vaccination site pain

Symptomtext

injection site (left arm) soreness; This symptom is a daily occurrence and gets worse when patient is at rest.; anxiety; Fasciculation; muscle twitching; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from a sales representative. The reporter is the patient. A 44 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in deltoid left, administration date 06Oct2021 09:15 (Lot number: EW0186) at the age of 44 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "birth control" (unspecified if ongoing). Concomitant medication(s) included: SETLAKIN taken for contraception. Past drug history included: Amoxicillin, reaction(s): "Rash"; Compazine, reaction(s): "dystonic"; Ambien, reaction(s): "paresthesia". The following information was reported: MUSCLE TWITCHING (non-serious) with onset 13Oct2021, outcome "not recovered", described as "muscle twitching"; VACCINATION SITE PAIN (non-serious), outcome "unknown", described as "injection site (left arm) soreness"; CONDITION AGGRAVATED (non-serious), outcome "unknown", described as "This symptom is a daily occurrence and gets worse when patient is at rest."; ANXIETY (non-serious), outcome "unknown", described as "anxiety"; MUSCLE CONTRACTIONS INVOLUNTARY (non-serious) with onset 13Oct2021, outcome "not recovered", described as "Fasciculation". Therapeutic measures were taken as a result of anxiety. Additional information: On 13Oct2021, she started to have muscle twitching (Fasciculation) in her left tricep. This happens randomly throughout the day especially at rest. This has been happening every day since with the severity varying from a few minutes once or twice during the day to frequently during the day causing issues especially at night with sleep. Patient have not seen a physician yet because she was hoping this may not be related to the vaccine but rather anxiety related to receiving the vaccine and a very busy work schedule onto of other things. In an attempt to try to remedy this, she had tried to increase my water intake along with magnesium and calcium levels. So far nothing has completely resolved the issue although she do find that by targeting that muscle group through weight lifting will alleviate the symptoms for a longer period of time. Prior vaccinations (within 4 weeks): None No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Birth control
Andere Medikamente: SETLAKIN
Allergien: -
Vorherige Impfungen: -

VAERS 2175303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 15.09.2021
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Hot flush Hypoaesthesia Paraesthesia

Symptomtext

Her left knee to her hip is completely numb/ It is sending a numbness and tingling sensation and she can not pick her foot up; It is sending a numbness and tingling sensation and she can not pick her foot up; Hot flashes; 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 60 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 15Sep2021 (Lot number: EW0186) 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 no: 1), when the patient was 60 years old, for COVID-19 immunization, reaction(s): "Hot flashes", "Her left arm felt like a water balloon". The following information was reported: HYPOAESTHESIA (non-serious) with onset 18Sep2021, outcome "unknown", described as "Her left knee to her hip is completely numb/ It is sending a numbness and tingling sensation and she can not pick her foot up"; HOT FLUSH (non-serious) with onset Sep2021, outcome "unknown", described as "Hot flashes"; PARAESTHESIA (non-serious) with onset 18Sep2021, outcome "unknown", described as "It is sending a numbness and tingling sensation and she can not pick her foot up". Additional information: Patient who was in very good health, beside her left ankle that she injured that has a plate in it and she was now disabled. She considers herself a healthy girl and only takes a stupid cholesterol pill. She was not a person who does this. She received her first dose of the Pfizer Covid-19 Vaccine. She was normal, she experienced no other side effect than her left arm felt like a water balloon, but that went away after 4 days. But in turn, she began to experience hot flashes. A good amount of them during the day. They did start at night, when one would come on, she would rip her clothes off and check her temperature, but this was all coming from her inside. She added that they have subsided but do continue. She has never had a hysterectomy. She received her second dose on 15Sep2021, and she asked to receive it in her right arm because she is left-handed. She continues with her hot flashes after the second dose, but on 18Sep2021, her left knee to her hip was completely numb. It began as the size of an orange that was numb, but now the area was the size of a watermelon. It now runs into her ankle and foot. It was sending a numbness and tingling sensation and she cannot pick her foot up. She wants to nip this in the butt and not second guess herself. Caller was asking if any of the symptoms she has experienced have been reported by others. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1835571

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: WI
Alter: 60,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 14.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Angina pectoris Blood pressure increased Blood pressure measurement Burning sensation Chest pain Fatigue Hepatic enzyme Chills Diarrhoea Dyspepsia Headache Heart rate Oxygen saturation Pain Pain in extremity Vaccination site erythema

Symptomtext

the other 2 Pfizer Covid Vaccine doses she was just tired with/the first two doses of Pfizer Covid Vaccine was being tired; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. The reporter is the patient. A 60 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 14Mar2021 11:00 (Lot number: EN6206) at the age of 60 years as dose 1, single and administered in arm right, administration date 02Apr2021 11:42 (Lot number: FR8734) as dose 2, single for covid-19 immunisation. Relevant medical history included: "Thyroid issues" (ongoing), notes: initially provided as about 2012; but then clarified onset as being around 15 years ago, when she was 45 years old; "Cardiac issues", start date: 2012 (ongoing); "High blood pressure" (unspecified if ongoing), notes: She has high blood pressure that is well controlled with medication.; "non alcoholic fatty liver" (unspecified if ongoing), notes: she has high liver enzymes from non alcoholic fatty liver and takes cholesterol medication; "Cholesterol" (unspecified if ongoing), notes: she has high liver enzymes from non alcoholic fatty liver and takes cholesterol medication. The patient took concomitant medications. The following information was reported: FATIGUE (non-serious) with onset 2021, outcome "unknown", described as "the other 2 Pfizer Covid Vaccine doses she was just tired with/the first two doses of Pfizer Covid Vaccine was being tired". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Bad adverse reaction: Time of onset about 12 hours after being adminsitered booster shot/third dose of Pfizer Covid Vaccine, which would have been onset time of about 23:15, but provided by caller as around 00:00 so onset date documented as 16Oct2021 relative to time of onset clarification. When she first got the booster shot/third dose the lady did such a good job she couldn't even feel it. Patient is a cardiac patient and all of a sudden felt at the injection site on her right arm turned all red. After it turned red she started to feel like burning sensations really bad like it was on fire going down her armpit by her lymph nodes and around her heart on the right side. The burning went on for several hours. They said you can take Ibuprofen, or Tylenol. Because she has high liver enzymes from non alcoholic fatty liver and takes cholesterol medication she is not supposed to take a lot of that unless she has to. So she took 2 and event went away. About 2-4 hours event came back worse, and then was progressively getting worse for 24 hours. She ended up on emergency room night of 16Oct2021 at (Withheld). She was treated pretty shabbily by the people in there. Her blood pressure shot up to 180/80 and she had this burning pain, painful and burning. She thought well, she is a cardiac patient, so she had better go to the doctor, the emergency room. She ended up in the emergency room at midnight at (Withheld), WI-this would have been midnight of 17Oct2021-as this was night of 16Oct2021 into midnight of 17Oct2021. The emergency room doctor didn't record that she had diarrhea that day; and she had severe chest pain on the right side; this is on right side where she got the shot; it didn't say those symptoms on the card she got from the withheld; so she was starting to be concerned that she could be having a stroke. She was not admitted to the emergency room or hospital. She reported they just blow you off like a drug addict. She went in because she had extreme pain in right arm like it was burning out and then around her right side of her heart she felt burning sensations and deep pain on right side of her heart; that's why she went there. They did no testing at all. They put the oxygen thing on her and monitored her oxygen and her heart and blood pressure that's all they did. Outcome of event provided as improved, they are gradually going away. Saturday when she woke up she had diarrhea really bad but then that subsided, that stopped; and then she had the chills really bad, tired, had a headache, but that didn't happen until after 12 hours. and the other 2 Pfizer Covid Vaccine doses she was just tired with, they didn't bother her. The only thing she had with the first two doses of Pfizer Covid Vaccine was being tired, but no adverse events, that was it, no problems with the other two doses. During report caller mentioned that her husband got the shot and he had valley fever which is an infection. She clarified that her husband was not administered the Pfizer Covid Vaccine, he was adminsitered Moderna and the valley fever was ongoing prior to him being administered the Moderna. He's fine, nothing happened to him, he had no side effects, he had no problems with the Moderna and she declined to provide any further information for that patient. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 202110; Test Name: blood pressure; Result Unstructured Data: Test Result:180/180; Comments: blood pressure shot up to 180/80; Test Name: high liver enzymes; Result Unstructured Data: Test Result:High; Comments: she has high liver enzymes from non alcoholic fatty liver
Aktuelle Erkrankungen: Cardiac disorder; Thyroid disorder (initially provided as about 2012;)
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (She has high blood pressure that is well controlled with medication.); Cholesterol (she has high liver enzymes from non alcoholic fatty liver and takes cholesterol medication); Fatty liver (she has high liver enzymes from non alcoholic fatty liver and takes cholesterol medication)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2163286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 74,0
Geschlecht: M
Eingang: 07.03.2022
Impfdatum: 26.08.2021
Beginn: 27.08.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia COVID-19 Condition aggravated Dysphonia Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

The day after my vaccination I had mild symptoms. Mild fever and joint pains. I already have joint pains, but they were much worse after the vaccination. I did feel like I was hit by a truck, but I was still functional. I started to feel better after about 5 days once I started my anti-inflammatory medications. I did end up getting COVID on 01/19/2022. In the morning my voice was a bit scratchy but by the evening. I started to develop a fever and I was getting much more achy than usual. I also got a runny nose. By the time I got up the next morning I knew I needed to get tested. I called the clinic and they told me where the drive thru testing facility was. I was tested around noon on 01/20/2022. I was taking my temp readings 3x day. The highest it reached was 101 degrees. I got a prescription for Paxlovid. I started taking that 01/22/2022 in the evening. It is a 5-day course medication. I did start to feel better after about 24 hours of taking the medication. By 01/24/2022 My temperature went down to 98.6 and never went back up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: COVID, Positive 01/20/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid Arthritis; Asthma; High Blood Pressure; High Cholesterol; Acid Reflux; Ulcerative Colitis; Scoliosis
Andere Medikamente: Xeljanz 11mg 1x day; Diclofenac 100mg 1x day; Simvastatin 80mg 1x day; Losartan 50mg 2x day; Montelukast 10mg 1x day; Dexilant 60mg 1x day; Qvar RediHaler 80mcg 2x day; Testosterone Topical. 30 mg 2x day; Men's Multivitamin 1x day; Vitamin
Allergien: Sulfa drugs; Pumpkin seeds
Vorherige Impfungen: Typhoid Vaccine: I had a fever, achy joints. About 20 years.

VAERS 2154860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 03.03.2022
Impfdatum: 24.06.2021
Beginn: 13.01.2022
Tage bis Beginn: 203,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Asymptomatic COVID-19 Blood albumin decreased Blood lactate dehydrogenase increased Blood lactic acid decreased C-reactive protein increased COVID-19 Carbon dioxide decreased Chest X-ray abnormal Cough Decreased appetite Dyspnoea Exposure to SARS-CoV-2 Faeces soft Fatigue Full blood count abnormal Haematocrit decreased Haemoglobin decreased

Symptomtext

Patient presents with ? Corona Virus Concern Tested positive 1/13. Fatigue at home. "my oxygen was low at home (84%)" Pulse ox 97% in traige on room air Source of Information: Patient and Available medical record History of Present Illness: This is a 75y.o. male with a past medical history of DVT, CVA, HLD, urinary incontinence from prostate cancer s/p prostatectomy (2008) and non-Hodgkin's lymphoma presenting to the emergency department on 1-19-2022 for chief complaint of shortness of breath and weakness. Patient states that he recently tested positive for COVID on 13th of January. He previously had lunch with one of his friends who had a close contact with a covid positive individual. The patient was asymptomatic when he was tested. He has been experiencing symptoms about 2-3 days after testing COVID-positive. He noticed being short of breath and a non productive cough. He denies fever or chills during this time. Prior to coming to the into the emergency department his pulse ox that he was checking at home had dropped to 84%. He does note decreased appetite during this time, although he denies nausea or vomiting. He complains of soft stools with 1-2 bowel movements per day. He has received 2 doses of Pfizer vaccine and a booster. His last chemotherapy was in December of last year and he is not currently taking any immunosuppressant medication. ED COURSE: BP 85/51, HR 84, RR 20, SPO2 97%, temp 97.8. CHEM profile remarkable for carbon dioxide 18, albumin 3.3. CBC remarkable for WBC 2.5, hemoglobin 10.1, hematocrit 31, platelets 133. Lactate dehydrogenase 442, troponin negative. CRP 101.7, procalcitonin 0.35. Ferritin 2505. Lactic acid 0.5. Placed on 4L NC. EKG: Pending Radiology performed: CXR with bibasilar opacities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 9,0
Labordaten: NOCOVER> 1 LABORATORY Chart Review Copy (75 yrs) PT CLASS: Inpatient CSN: DEPT: PATIENT STATUS: Discharged GENDER: male BED: ORD DR: AUTH DR: Results Covid-19, Flu, RSV by NAA Contains abnormal data Covid-19, Flu, RSV by NAA Order: Status: Final result Visible to patient: Yes (not seen) Next appt: 08/02/2022 at 10:30 AM in Internal Medicine (DO) Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA) for laboratories certified under Agency to perform high complexity testing. This test has not been FDA cleared or approved. Specimen Collected: 01/19/22 11:42 PM Last Resulted: 01/20/22 12:57 AM
Aktuelle Erkrankungen: ? CVA (cerebral vascular accident) Slight left sided weakness ? DVT (deep venous thrombosis) ? Dyslipidemia ? Hyperglycemia ? Hyperlipidemia ? Nephrolithiasis 12/14 Stone analysis Dr. 12/14. Repeat US: rt & lt kidney stones 2/15 ? Neuropathy Feet ? Non Hodgkin's lymphoma ? Peripheral neuropathy ? Prostate cancer Found on bx and nodule on exam ? Urinary incontinence
Vorgeschichte: ? CVA (cerebral vascular accident) Slight left sided weakness ? DVT (deep venous thrombosis) ? Dyslipidemia ? Hyperglycemia ? Hyperlipidemia ? Nephrolithiasis 12/14 Stone analysis Dr. 12/14. Repeat US: rt & lt kidney stones 2/15 ? Neuropathy Feet ? Non Hodgkin's lymphoma ? Peripheral neuropathy ? Prostate cancer Found on bx and nodule on exam ? Urinary incontinence
Andere Medikamente: allopurinol (ZYLOPRIM) 100 MG PO Tab take 1 Tablet by mouth once daily. 1/19/2022 Unknown time apixaban (ELIQUIS) 5 MG PO Tab take 5 mg by mouth twice daily. 1/19/2022 Unknown time atorvastatin (LIPITOR) 20 MG PO Tab take 1 Tab by mouth onc
Allergien: ? Iodine Hives ? Gabapentin Other Clonus
Vorherige Impfungen: -

VAERS 2148555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: WI
Alter: 74,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 18.05.2021
Beginn: 17.02.2022
Tage bis Beginn: 275,0
Dosis: UNK
Route/Site: IM / RA

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

Blood culture negative Brain herniation COVID-19 Craniocerebral injury Dysphagia Dyspnoea Fall Pneumonia Pneumonia aspiration Sepsis Subdural haematoma Systemic candida

Symptomtext

75 y.o. Caucasian female with history of HTN, HLD, a fib not on anticoagulation, and recurrent falls at home culminating in a traumatic SDH complicated by uncal herniation and TBI in October 2021 with slow recovery in the interim, and recent candidemia who presents with shortness of breath in setting of known COVID infection. Patient was hospitalized in January 2022 for sepsis secondary to aspiration pneumonia. Hospitalization was also complicated by candidemia and dysphagia. She was treated with standard antibiotics for pneumonia and a 2 week course of micafungin for candidemia. Repeat blood cultures were negative. Although she had previously been receiving nutrition via NG tube, after working with speech path ology she was was advanced to a soft diet with nectar thickened liquids. She discharged to a nursing facility for ongoing care on 01/26/2022.

Weitere VAERSDATA-Felder

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

VAERS 2140276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 25.02.2022
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

Dizziness Feeling abnormal Flushing Nausea Pallor Palpitations

Symptomtext

After each vaccine felt flushed heart racing felt dizzy, The booster vaccine was the worst my heart rate was in 170?s for about two hours. I felt like I was going to pass out I was pale. Dizzy, nauseous. I felt horrible.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, hemifacial twitch
Andere Medikamente: Atorvastatin
Allergien: Latex, red rice yeast
Vorherige Impfungen: -

VAERS 2137145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NC
Alter: 15,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 09.06.2021
Beginn: 26.09.2021
Tage bis Beginn: 109,0
Dosis: UNK
Route/Site: IM / LA

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

Dizziness Dyspnoea Heart rate increased

Symptomtext

Patient began to notice rapid HR alerts on her smart watch HR >200 Felt SOB, dizzy sometimes with rapid HR- Events usually happen with dancing- hip hop contemporary- on a dance team per smart watch, first event HR was elevated Sept 26- 193 , Nov 28th was 200 increasing events the last few weeks, but preparing for a dance competition has not counted peripheral or central pulse

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG today 2/24/2022 normal in office setting up Holter and referring to peds cardiology
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2134392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 23.02.2022
Impfdatum: 25.05.2021
Beginn: 07.06.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Walking aid user

Symptomtext

Patient presented to ER with difficulty breathing. He received 3 days of abx and completed his azithromycin. He has worked with PT and will use a FWW to ambulate. ON day of discharge, he was no longer requiring O2. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2122579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: AZ
Alter: 74,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 20.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Asthenia Dyspnoea Fatigue Influenza like illness Malaise Pain Pain in extremity Pyrexia

Symptomtext

shortness of breath; Fatigue; felt achy the next day; flu-like symptoms (unwell, and had fever); flu-like symptoms (unwell, and had fever); flu-like symptoms (unwell, and had fever); feeling weak; sore arm, specifically on her right arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 74 year-old female patient received bnt162b2 (COMIRNATY), administered in arm right, administration date 20Oct2021 (Lot number: EW0186) at the age of 74 years as dose 3 (booster) 0.3 ml, single for covid-19 immunisation. Relevant medical history included: "Heart issue" (ongoing), notes: it started a couple of years ago.; "Heart surgery", start date: Mar2021 (unspecified if ongoing), notes: she had heart surgery in March before the vaccine. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), administration date: 2021, when the patient was 74 years old, for COVID-19 Immunization; Bnt162b2 (DOSE 2, SINGLE), administration date: 2021, when the patient was 74 years old, for COVID-19 Immunization. The following information was reported: INFLUENZA LIKE ILLNESS (non-serious), MALAISE (non-serious), PYREXIA (non-serious) all with onset 20Oct2021, outcome "recovered with sequelae" (21Oct2021) and all described as "flu-like symptoms (unwell, and had fever)"; PAIN (non-serious) with onset 21Oct2021, outcome "recovering", described as "felt achy the next day"; PAIN IN EXTREMITY (non-serious) with onset Oct2021, outcome "unknown", described as "sore arm, specifically on her right arm"; ASTHENIA (non-serious) with onset 20Oct2021, outcome "recovering", described as "feeling weak"; FATIGUE (non-serious) with onset 21Oct2021, outcome "recovering", described as "Fatigue"; DYSPNOEA (non-serious) with onset 22Oct2021, outcome "recovered" (22Oct2021), described as "shortness of breath". Therapeutic measures were taken as a result of pain, pain in extremity. Additional information: Patient received the booster dose of the Pfizer-BioNTech Covid-19 Vaccine on Wednesday, 20Oct2021. Then that night, she developed flu-like symptoms (unwell, and had fever), and felt achy the next day. She said she had sore arm, specifically on her right arm. She said she was feeling weak as if she had the flu today. She also mentioned that she was already feeling better. She took Tylenol twice for being achy. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Heart disorder (it started a couple of years ago.)
Vorgeschichte: Medical History/Concurrent Conditions: Surgery (she had heart surgery in March before the vaccine)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2116455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 35,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 29.10.2021
Beginn: 16.01.2022
Tage bis Beginn: 79,0
Dosis: 2
Route/Site: UN / UN

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

Artificial rupture of membranes COVID-19 Complication of pregnancy Delivery Drug abuse Exposure during pregnancy Hypertension Induction of cervix ripening Influenza A virus test negative Influenza B virus test Labour augmentation Obesity Pain Papilloma viral infection Perineal injury Respiratory syncytial virus test negative Rhesus antigen positive Rubella immunity confirmed

Symptomtext

Class 3 severe obesity with body mass index (BMI) of 45.0 to 49.9 in adult (CMS/HCC) Fibroid uterus Blood type, Rh positive Tetrahydrocannabinol (THC) use disorder, mild, abuse Rubella immune SVD (spontaneous vaginal delivery) High risk HPV infection Obesity affecting pregnancy in second trimester Please see the prenatal record and admission history and physical for details. Labor Analgesics: Epidural OB Complications: Pre-eclampsia Cervical Ripening Type: Misoprostol Cervical Ripening Comment: Induction: AROM;Cervical Ripening Induction Indications: Chronic Hypertension Augmentation: Oxytocin Delivery Date: 1/17/2022 Delivery Time: 7:53 AM Gestational Age(weeks days/7): 39 2/7 Method of Delivery: Vaginal, Spontaneous Birth Weight: 3.098 kg (6 lb 13.3 oz) Sex: male Apgar Score (1 min): 9 Apgar Score (5 min): 9 Laceration Episiotomy: None Laceration Type: 2nd Perineal Laceration: Quantified Blood Loss (ml): Est Blood Loss For further details of the delivery see the delivery summary. Her post partum course was complicated by: None Patient with uncomplicated post-partum recovery. On the day of discharge pain was well controlled with oral pain meds, she was ambulating and voiding without difficulty, and was tolerating diet without nausea/vomiting. Patient was requesting discharge home. Following complete examination and review of recovery course, patient was deemed stable for discharge. Patient will need a blood pressure check in 3 days. Procedures performed: SVD with repair of second degree and right periurethral Discharge All Hospital Problems (Other diagnoses): Active Hospital Problems Diagnosis ? Principal Problem: SVD (spontaneous vaginal delivery) [O80] ? Chronic hypertension with superimposed pre-eclampsia [O11.9] ? Rubella immune [Z78.9] ? Class 3 severe obesity with body mass index (BMI) of 45.0 to 49.9 in adult (CMS/HCC) [E66.01, Z68.42] ? Blood type, Rh positive [Z67.90] ? Fibroid uterus [D25.9] Resolved Hospital Problems No resolved problems to display.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: 4,0
Labordaten: Results Covid-19, Flu, RSV by NAA (Order 1281956824) Contains abnormal data Covid-19, Flu, RSV by NAA Order: 1281956824 Status: Final result Visible to patient: Yes (not seen) Next appt: None Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA) for US laboratories certified under CLIA to perform high complexity testing. This test has not been FDA cleared or approved. Specimen Collected: 01/16/22 12:30 AM Last Resulted: 01/16/22 1:32 AM
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: labetlalol ibuprofen Prenatal vit-Fe
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2091095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: UT
Alter: 15,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 09.07.2021
Beginn: 09.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Asthma Blister Blood bilirubin Blood bilirubin increased Chest X-ray Chest discomfort Confusional state Dyspnoea Fatigue Hepatic enzyme Hepatic enzyme increased Pneumothorax Pruritus Pyrexia Rash SARS-CoV-2 test

Symptomtext

sporadic lung partial collapse when on side; high fever; Difficulty breathing; weight on chest; asthma attacks; liver enzymes increase; bilirubin high; rashes to blisters; rashes to blisters; itching; fatigue; confusion; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 15 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 09Jul2021 13:30 (Lot number: EW0186) at the age of 15 years as dose 1 , single for covid-19 immunisation. Relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing). There were no concomitant medications. There was No other vaccine in four weeks and medications in two weeks. The following information was reported: PNEUMOTHORAX (medically significant) with onset 09Jul2021 15:30, outcome "recovering", described as "sporadic lung partial collapse when on side"; PYREXIA (non-serious) with onset 09Jul2021 15:30, outcome "recovering", described as "high fever"; DYSPNOEA (non-serious) with onset 09Jul2021 15:30, outcome "recovering", described as "Difficulty breathing"; CHEST DISCOMFORT (non-serious) with onset 09Jul2021 15:30, outcome "recovering", described as "weight on chest"; ASTHMA (non-serious) with onset 09Jul2021 15:30, outcome "recovering", described as "asthma attacks"; HEPATIC ENZYME INCREASED (non-serious) with onset 09Jul2021 15:30, outcome "recovering", described as "liver enzymes increase"; BLOOD BILIRUBIN INCREASED (non-serious) with onset 09Jul2021 15:30, outcome "recovering", described as "bilirubin high"; RASH (non-serious), BLISTER (non-serious) all with onset 09Jul2021 15:30, outcome "recovering" and all described as "rashes to blisters"; PRURITUS (non-serious) with onset 09Jul2021 15:30, outcome "recovering", described as "itching"; FATIGUE (non-serious) with onset 09Jul2021 15:30, outcome "recovering", described as "fatigue"; CONFUSIONAL STATE (non-serious) with onset 09Jul2021 15:30, outcome "recovering", described as "confusion". Within 2 hours, high fever, Difficulty breathing, weight on chest, sporadic lung partial collapse when on side, asthma attacks for next 10 days(no previous history), liver enzymes increase and bilirubin high, rashes to blisters, itching, fatigue, confusion. The events "sporadic lung partial collapse when on side", "high fever", "difficulty breathing", "weight on chest", "asthma attacks", "liver enzymes increase", "bilirubin high", "rashes to blisters", "rashes to blisters", "itching", "fatigue" and "confusion" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood bilirubin: (09Jul2021) high; chest x-ray: (09Jul2021) clear; hepatic enzyme: (09Jul2021) increase; pyrexia: (09Jul2021) high fever; sars-cov-2 test: (10Jul2021) negative, notes: Nasal swab. Therapeutic measures were taken as a result of pneumothorax, pyrexia, dyspnoea, chest discomfort, asthma, hepatic enzyme increased, blood bilirubin increased, rash, blister, pruritus, fatigue, confusional state. No other vaccine in four weeks. No other medications in two weeks. AE resulted in at Doctor or other healthcare professional office/clinic visit, Emergency room/department. AE treatment received with 4 Zyrtec daily, inhaler steroid, singular, Pepcid. Patient did not have covid prior vaccination and tested covid post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210709; Test Name: bilirubin; Result Unstructured Data: Test Result:high; Test Date: 20210709; Test Name: Chest X-ray; Result Unstructured Data: Test Result:clear; Test Date: 20210709; Test Name: liver enzyme; Result Unstructured Data: Test Result:increase; Test Date: 20210709; Test Name: Fever; Result Unstructured Data: Test Result:high fever; Test Date: 20210710; Test Name: covid; Test Result: Negative ; Comments: Nasal swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2090106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: PA
Alter: 34,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Bladder disorder Blood test Cardiac stress test Chest X-ray Chest pain Chills Eating disorder Electrocardiogram Erythema Fatigue Magnetic resonance imaging Migraine Myalgia Pain Pain in extremity Rhinorrhoea Ultrasound bladder Urine analysis

Symptomtext

runny nose; stabbing body aches/ She also has sporadic pains around her body; Chills; Migraines triggered after both doses; The fatigue worsened with second shot; Red stripe across right leg; Left arm pain at injection site; pain is specifically in the muscle; she cannot really eat, because it hurts her bladder; bladder issues; squeezing pain is in her left chest, left arm, and left thigh but occasionally it is in her hands fingers, toes, around her legs and arms on both sides; the stabbing, squeezing pain is in her left chest, left arm, and left thigh but occasionally it is in her hands fingers, toes, around her legs and arms on both sides; 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 34 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 21May2021 (Lot number: EW0186, Expiration Date: 31Aug2021) at the age of 34 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Seasonal allergy" (unspecified if ongoing), notes: Verbatim: Seasonal allergy. Concomitant medication(s) included: ALLEGRA taken for hypersensitivity. Vaccination history included: Bnt162b2 (1st dose, Lot#EW0176 , Anatomical site: Injected in left arm unable to confirm if given in muscle of left upper shoulder, Time the Vaccination Was Given: afternoon), administration date: 28Apr2021, when the patient was 34 years old, for COVID-19 Immunization, reaction(s): "her left arm was still hurting/ Left arm pain at injection site", "fatigue", "Migraines triggered after both doses". The following information was reported: BLADDER DISORDER (non-serious) with onset 2021, outcome "not recovered", described as "bladder issues"; CHEST PAIN (non-serious) with onset 2021, outcome "unknown", described as "squeezing pain is in her left chest, left arm, and left thigh but occasionally it is in her hands fingers, toes, around her legs and arms on both sides"; RHINORRHOEA (non-serious) with onset 22May2021, outcome "recovering", described as "runny nose"; PAIN (non-serious) with onset 22May2021, outcome "not recovered", described as "stabbing body aches/ She also has sporadic pains around her body"; EATING DISORDER (non-serious) with onset 2021, outcome "unknown", described as "she cannot really eat, because it hurts her bladder"; MIGRAINE (non-serious) with onset 21May2021, outcome "recovering", described as "Migraines triggered after both doses"; CHILLS (non-serious) with onset 22May2021, outcome "recovering", described as "Chills"; PAIN IN EXTREMITY (non-serious) with onset 2021, outcome "unknown", described as "the stabbing, squeezing pain is in her left chest, left arm, and left thigh but occasionally it is in her hands fingers, toes, around her legs and arms on both sides"; FATIGUE (non-serious) with onset 21May2021, outcome "recovering", described as "The fatigue worsened with second shot"; ERYTHEMA (non-serious) with onset 21May2021, outcome "recovering", described as "Red stripe across right leg"; VACCINATION SITE PAIN (non-serious) with onset 2021, outcome "recovering", described as "Left arm pain at injection site"; MYALGIA (non-serious) with onset 2021, outcome "unknown", described as "pain is specifically in the muscle". The events "bladder issues", "squeezing pain is in her left chest, left arm, and left thigh but occasionally it is in her hands fingers, toes, around her legs and arms on both sides", "runny nose", "stabbing body aches/ she also has sporadic pains around her body", "she cannot really eat, because it hurts her bladder", "migraines triggered after both doses", "chills", "the stabbing, squeezing pain is in her left chest, left arm, and left thigh but occasionally it is in her hands fingers, toes, around her legs and arms on both sides", "the fatigue worsened with second shot", "red stripe across right leg" and "pain is specifically in the muscle" were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient reported seeking medical care with extensive testing and doctors were unable to determine a cause. The patient was taking Allegra for her whole life or years as needed. Chills and runny nose improved within 24 hours. Her body was in constant pain and the physicians cannot figure out. She had pain all throughout the day and was not living a happy life and no one can fix her. Additional vaccines administered on same date of the Pfizer suspect were none. She had seen her GP probably 5-8 times. She has also seen a Neurologist, Rheumatologist, Cardiologist and was about to see a vascular specialist. There was another one she forgot. Prior vaccinations (within 4 weeks) prior to the first administration date of the suspect vaccine were none. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: blood clot; Result Unstructured Data: Test Result:unknown results; Test Date: 2021; Test Name: blood test; Result Unstructured Data: Test Result:Normal; Comments: Blood test for autoimmune; Test Date: 2021; Test Name: stress test; Result Unstructured Data: Test Result:Normal; Test Date: 2021; Test Name: chest xray; Result Unstructured Data: Test Result:Normal; Test Date: 2021; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Date: 2021; Test Name: MRI; Result Unstructured Data: Test Result:Normal; Comments: checked for neuropathy; Test Date: 2021; Test Name: ultrasound; Result Unstructured Data: Test Result:Normal; Test Date: 2021; Test Name: urine test; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Seasonal allergy (Verbatim: Seasonal allergy)
Andere Medikamente: ALLEGRA
Allergien: -
Vorherige Impfungen: -

VAERS 1711372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NC
Alter: 69,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 09.08.2021
Beginn: 09.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Arthralgia Condition aggravated Drug hypersensitivity Myalgia Pain in extremity

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 69 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 09Aug2021 14:00 (Lot number: EW0186) at the age of 69 years as dose 1, single for Covid-19 immunisation. Relevant medical history included: "Broke finger" (unspecified if ongoing), notes: He had the broke finger and surgeries before he got the shot; "Surgeries" (unspecified if ongoing), notes: He had the broke finger and surgeries before he got the shot; "Diagnosed allergies" (unspecified if ongoing); "Compromised immune status" (unspecified if ongoing); "Respiratory illness" (unspecified if ongoing); "Genetic/chromosomal abnormalities" (unspecified if ongoing); "Endocrine abnormalities (including diabetes)" (unspecified if ongoing); "Endocrine abnormalities (including diabetes)" (unspecified if ongoing); "Obesity" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Codeine, reaction(s): "Allergic to Codeine", notes: Illness/AE: Allergic to Codeine, Morphine and those type of things., Onset Date: It has been 20 years ago or longer.; Morphine, reaction(s): "Allergic to Morphine", notes: Illness/AE: Allergic to Codeine, Morphine and those type of things., Onset Date: It has been 20 years ago or longer. The following information was reported: ARTHRALGIA (non-serious) with onset 09Aug2021 14:30, outcome "not recovered", described as "joint pains"; ARTHRALGIA (non-serious) with onset 09Aug2021 14:30, outcome "not recovered", described as "joint pain in neck and back of shoulders"; CONDITION AGGRAVATED (non-serious) with onset 09Aug2021, outcome "unknown", described as "joint pains/Joint pain was reported as worsened". Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic reaction; Chromosomal abnormality NOS; Diabetic; Endocrine disorder; Fractured finger (He had the broken finger and surgeries before he got the shot); Immune imbalance; Obesity; Respiratory disorder; Surgery (He had the broken finger and surgeries before he got the shot).
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1346377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NC
Alter: 63,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 21.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Asthenia Bedridden Blood test Dyspnoea Exercise tolerance decreased Fatigue Feeling abnormal Gait disturbance Headache Joint noise Muscular weakness Musculoskeletal chest pain Pain Palpitations Tinnitus Vision blurred

Symptomtext

headache; heart palpitation; tinnitus in the left ear; filling not myself; excruciating pain in the upper body; weakness/ no energy to walk; cracking noise in all my joints; weakness in my left hand; bed bound with pain and weakness for 5 months; cant walk moor then 1/2 mile/ walk very slowly now; shortness of breath; constant ribs cage pain; cant exercise now because I get very tired; tired; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 63 year-old female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), administered in arm left, administration date 21May2021 (Lot number: EW0186) at the age of 63 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "High blood pressure" (unspecified if ongoing). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient's concomitant medications were not reported. Past drug history included: Novocain, reaction(s): "Allergy". The following information was reported: HEADACHE (disability) with onset 22May2021, outcome "not recovered", described as "headache"; PALPITATIONS (disability) with onset 22May2021, outcome "not recovered", described as "heart palpitation"; TINNITUS (disability) with onset 22May2021, outcome "not recovered", described as "tinnitus in the left ear"; FEELING ABNORMAL (disability) with onset 22May2021, outcome "not recovered", described as "filling not myself"; PAIN (disability) with onset 22May2021, outcome "not recovered", described as "excruciating pain in the upper body"; ASTHENIA (disability) with onset 22May2021, outcome "not recovered", described as "weakness/ no energy to walk"; JOINT NOISE (disability) with onset 22May2021, outcome "not recovered", described as "cracking noise in all my joints"; MUSCULAR WEAKNESS (disability) with onset 22May2021, outcome "not recovered", described as "weakness in my left hand"; BEDRIDDEN (disability) with onset 22May2021, outcome "not recovered", described as "bed bound with pain and weakness for 5 months"; GAIT DISTURBANCE (disability) with onset 22May2021, outcome "not recovered", described as "cant walk moor then 1/2 mile/ walk very slowly now"; DYSPNOEA (disability) with onset 22May2021, outcome "not recovered", described as "shortness of breath"; MUSCULOSKELETAL CHEST PAIN (disability) with onset 22May2021, outcome "not recovered", described as "constant ribs cage pain"; EXERCISE TOLERANCE DECREASED (disability) with onset 22May2021, outcome "not recovered", described as "cant exercise now because I get very tired"; FATIGUE (disability) with onset 22May2021, outcome "not recovered", described as "tired". The events "headache", "heart palpitation", "tinnitus in the left ear", "filling not myself", "excruciating pain in the upper body", "weakness/ no energy to walk", "cracking noise in all my joints", "weakness in my left hand", "bed bound with pain and weakness for 5 months", "cant walk moor then 1/2 mile/ walk very slowly now", "shortness of breath" and "constant ribs cage pain" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood test: unknown results. Therapeutic measures were taken as a result of palpitations. Clinical course reported as follows: The second day after injection, patient had very bad headache and heart palpitation, tinnitus in the left ear, feeling not herself. On the 22 day after injection she was not able to get out of bed because of extreme excruciating pain in the upper body, weakness, cracking noise in all her joints and weakness in her left hand. She was bed bound with pain and weakness for 5 months and couldn't go out because she had no energy to walk. Her husband took her to her doctor and he ordered blood tests. The patient stated that she used to be very healthy person, recently retired. Now she felt that she aged by 20 years. She can't walk more than 1/2 mile, she walks very slowly now and has shortness of breath, constant ribs cage pain, tinnitus, heart palpitations, especially at night and need to take metoprolol 50 mg every day. Eight months after 1 shot of Pfizer her life dramatically changed. She can't exercise now because she gets very tired. Doctors don't know how help her besides recommending ibuprofen.; Sender's Comments: Based on the information provided, the contributory of the product bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), to reported events cannot totally be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: blood tests; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2088124

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MA
Alter: 34,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 05.06.2021
Beginn: 10.06.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: SYR / -

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

Condition aggravated Sinus tachycardia

Symptomtext

Increased symptomatic episodes related to inappropriate sinus tachycardia. Experiencing much more frequent symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Inappropriate sinus tachycardia
Andere Medikamente: Adderall XR
Allergien: N/A
Vorherige Impfungen: -

VAERS 2087444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 16.08.2021
Beginn: 16.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain lower Back pain Chest pain Dyspnoea Headache Lethargy Myalgia Nasal congestion Nausea Oropharyngeal pain Peripheral coldness Photophobia Pyrexia Somnolence Swollen tongue

Symptomtext

Swollen tongue; sore throat; difficulty breathing; chest pain; nasal congestion; headache; fever; muscle pain; lethargy; nausea; lower abdominal pain; lower back pain; cold hands and feet; light sensitivity; sleepy; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 52-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 16Aug2021 13:45 (Lot number: EW0186) at the age of 52 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "chronic fatigue" (unspecified if ongoing); "hypothyroidism" (unspecified if ongoing); "allergies" (unspecified if ongoing); "allergies: gluten" (unspecified if ongoing); "allergies: diary intolerance" (unspecified if ongoing); "allergies: allergic to broccoli" (unspecified if ongoing); "allergies: allergic to mushroom" (unspecified if ongoing); "allergies: allergic to cleaning chemicals" (unspecified if ongoing). Concomitant medication(s) included: ZOLPIDEM; ARMOUR THYROID; TYLENOL; VITAMIN C ACID; VIT D [VITAMIN D NOS]. Past drug history included: Vicodin, reaction(s): "Allergies: Vicodin"; Codeine, reaction(s): "Allergies: codeine". Vaccination history included: Bnt162b2 (Product COVID 19, Brand: Pfizer, Lot number: EW0172, Lot unknown: False, Administration date:19Jul2021, Administration time: 01:45 PM, Dose number:1, Vaccine location: Right arm), administration date: 19Jul2021, when the patient was 52 years old, for COVID-19 Immunization. The following information was reported: SWOLLEN TONGUE (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "Swollen tongue"; OROPHARYNGEAL PAIN (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "sore throat"; DYSPNOEA (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "difficulty breathing"; CHEST PAIN (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "chest pain"; NASAL CONGESTION (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "nasal congestion"; HEADACHE (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "headache"; PYREXIA (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "fever"; MYALGIA (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "muscle pain"; LETHARGY (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "lethargy"; NAUSEA (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "nausea"; ABDOMINAL PAIN LOWER (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "lower abdominal pain"; BACK PAIN (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "lower back pain"; PERIPHERAL COLDNESS (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "cold hands and feet"; PHOTOPHOBIA (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "light sensitivity"; SOMNOLENCE (non-serious) with onset 16Aug2021 14:15, outcome "recovering", described as "sleepy". Therapeutic measures were not taken as a result of swollen tongue, oropharyngeal pain, dyspnoea, chest pain, nasal congestion, headache, pyrexia, myalgia, lethargy, nausea, abdominal pain lower, back pain, peripheral coldness, photophobia, somnolence. Additional Information: Report about Covid vaccine: Yes, Lot unknown: False for dose 2, Lot unknown: False for dose 1. Facility type vaccine: Doctor's office/urgent care . If other vaccine in four weeks: No. If covid prior vaccination: No. If covid tested post vaccination: No No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Allergy to chemicals; Chronic fatigue; Dairy intolerance; Gluten sensitivity; Hypothyroidism; Vegetable allergy.
Andere Medikamente: ZOLPIDEM; ARMOUR THYROID; TYLENOL; VITAMIN C ACID; VIT D [VITAMIN D NOS.]
Allergien: -
Vorherige Impfungen: -

VAERS 2071586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 25.05.2021
Beginn: 29.12.2021
Tage bis Beginn: 218,0
Dosis: 2
Route/Site: - / -

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

Back pain Chest X-ray abnormal Cough Dyspnoea Lung opacity

Symptomtext

Patient is fully vaccinated. COVID positive 12/29/2021 at ED visit. Chief complaint, cough and shortness of breath.sat is 95% Back Pain from cough. BP 157/72 | Pulse 84 | Temp 97.9 ?F (36.6 ?C) (Oral) | Resp 22 | Ht 157.5 cm (5' 2") | Wt 92.5 kg (204 lb) | SpO2 95% | BMI 37.31 kg/m? CXR: Opacities are seen in the bilateral mid to lower lungs. stable vitals, she will come back if worse. Patient discharged from ED.

Weitere VAERSDATA-Felder

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

VAERS 2065824

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 39,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 12.05.2021
Beginn: 28.12.2021
Tage bis Beginn: 230,0
Dosis: 2
Route/Site: - / -

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

Cough Headache Musculoskeletal chest pain Nausea Pain Pulmonary imaging procedure normal Vomiting

Symptomtext

Patient is fully vaccinated. COVID + at ed visit on 12/28/2021. chief complaint vomiting, headache. 40-year-old female with history of extensive coronary artery disease presents to the emergency Department with complaints of 5 days of body aches, nausea, vomiting, headache, cough. does not have any specific sick contacts. Patient states she has been taking Tylenol and ibuprofen for her symptoms. Patient states she is not on blood thinners, has no numbness, weakness, syncope, no head trauma.BP 137/90 | Pulse 96 | Temp 99 ?F (37.2 ?C) (Oral) | Resp 17 | Ht 170.2 cm (5' 7") | Wt 95.3 kg (210 lb) | LMP 12/14/2021 | SpO2 97% | BMI 32.89 kg/m? Chest wall: Tenderness> Imaging: No definite fracture or pneumothorax.we'll refer patient to infusion clinic to see if she qualifies. Recommend patient Motrin, Zofran at home. Patient to return to emergency room if shortness of breath worsens. Discharged from ED.

Weitere VAERSDATA-Felder

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

VAERS 2065727

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 40,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 26.05.2021
Beginn: 27.12.2021
Tage bis Beginn: 215,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Chest X-ray abnormal Chills Cough Dyspnoea Lung opacity Pain Pyrexia SARS-CoV-2 test positive Tachycardia

Symptomtext

Patient is fully vaccinated. COVID + on 12/27/2021 at ED visit. 41-year-old female with no significant past medical history presents to the emergency Department with complaints of cough, fever, chills, body aches and shortness of breath. Patient states she has had symptoms since she was at a party with coworkers. O2 sat 94% RA. tacycardia (121). CXR: Patchy opacities noted bilaterally mainly at the lung bases, can be seen with COVID-19. Toradol given. We'll refer patient to infusion center as she qualifies for further treatment due to her BMI. Patient discharged, recommend Motrin for body aches.

Weitere VAERSDATA-Felder

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

VAERS 2058612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 16.11.2021
Beginn: 13.01.2022
Tage bis Beginn: 58,0
Dosis: 3
Route/Site: IM / -

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

Adult failure to thrive Alanine aminotransferase normal Anion gap Aortic aneurysm Aspartate aminotransferase normal Asthenia Basophil count decreased Basophil percentage decreased Blood albumin decreased Blood alkaline phosphatase normal Blood bicarbonate normal Blood bilirubin normal Blood calcium normal Blood chloride increased Blood creatinine increased Blood glucose normal Blood magnesium normal Blood phosphorus decreased

Symptomtext

Hospitalized (1.13.22 - 1.22.22); COVID-19 positive (1.13.22); fully vaccinated PLUS Booster- pfizer x3 d/c summary:Hematology Oncology Discharge Summary BRIEF OVERVIEW: Primary Care Physician at Discharge: Medical Doctor Hematologist/Oncologist: Doctor Admission Date: 1/13/2022 Discharge Date: 01/22/2022 Problem List as of 1/22/2022 Reviewed: 2/5/2020 3:58 PM Hospital * (Principal) COVID-19 in immunocompromised patient COVID-19 Unspecified severe protein-calorie malnutrition Non-Hospital Cervical lymphadenopathy Follicular lymphoma grade IIIa of lymph nodes of multiple sites DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Fatigue, unspecified type COVID-19 DISCHARGE PROBLEM: COVID-19 pneumonia Failure to thrive; Adult Low Grade Follicular Lymphoma, stage IV Pancytopenia Infrarenal AAA CKD III COPD HTN PRESENTING COURSE: Patient is a 72 yo male with hx of COPD, HTN, and follicular lymphoma on Gazyva presented with 2 week history of significant fatigue, anorexia, nausea, and decrease urine output. In ER he was found to be febrile and positive COVID-19 with CT chest showing COVID PNA. HOSPITAL COURSE: He was admitted and started on Remdesivir, Decadron, and cefepime. Throughout hospitalization he needed low-dose supplemental oxygen twice. Further infectious work up remained negative. PT/OT evaluation showed need for home health PT and HHC. He was started on Remeron to assist in appetite. He completed 9 days of antibiotics and remained afebrile. Today, he is feeling stronger. Eating better. Denies any SOB. He was educated on when to call with questions or concerns. He will will follow up on Monday for evaluation. He is stable for discharge. CONSULTS / RECOMMENDATION: Nutrition PROCEDURES: None Discharge Physical Exam Vitals and nursing note reviewed. Constitutional: General: He is not in acute distress. Appearance: Normal appearance. He is well-developed. He is not ill-appearing. HENT: Head: Normocephalic and atraumatic. Mouth/Throat: Mouth: Mucous membranes are moist. No oral lesions. Eyes: Conjunctiva/sclera: Conjunctivae normal. Pupils: Pupils are equal, round, and reactive to light. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulses: Normal pulses. Heart sounds: Normal heart sounds, S1 normal and S2 normal. Pulmonary: Effort: Pulmonary effort is normal. No tachypnea. Breath sounds: Normal breath sounds. Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Musculoskeletal: General: Normal range of motion. Cervical back: Normal range of motion and neck supple. Right lower leg: No edema. Left lower leg: No edema. Skin: General: Skin is warm and dry. Capillary Refill: Capillary refill takes less than 2 seconds. Neurological: General: No focal deficit present. Mental Status: He is alert and oriented to person, place, and time. Psychiatric: Attention and Perception: Attention normal. Mood and Affect: Mood is depressed. Affect is blunt and flat. Speech: Speech normal. Behavior: Behavior is withdrawn. Behavior is cooperative. Thought Content: Thought content normal. Cognition and Memory: Cognition and memory normal. Judgment: Judgment normal. H&P: CHIEF COMPLAINT: COVID-19 in immunocompromised patient ASSESSMENT / PLAN: Covid 19 - Febrile in ER - Fully vaccinated - Positive Covid PCR - Pt is high risk due to follicular lymphoma on Gazyva (CD20 positive B cell targeted therapy similar to Rituxan) - CXR negative - Fatigued, nausea, poor appetite, febrile. - Regeneron not available, Sotrovimab only as outpatient - Hold on Remdesivir and Decadron unless needing supplemental oxygen. - Consider input from Pulm and ID if decompensates Febrile Illness Felt to be Covid related BC's x 2 obtained Empiric Cefepime, non neutropenic dose IVFs FTT -14 days of progressive weakness - Poor oral intake, per pt no meal since 01/11 - MN consult - IVFs - PT/OT - Daily labs Low Grade Follicular Lymphoma - Dx October 2016 following excisional biopsy of neck lymph node - Considered Stage IV high grade follicular lymphoma involving liver, muscle and bone - SP R-CHOP 2017, Achieved Complete response - Recurrence of Low Grade Follicular Lymphoma, 02/2020 - Gazyva with Bendamustine x 6 cycles. Then solo agent Gazyva. C15 D1 given 11/23/21. C16 due 01/17/22 - Surveillance CT C/A/P is due. Pending. - POC per doctor CKD III stable - Cr 1.4, baseline 1.5-1.6 - IVFs - NO ACE/ARB/NSAIDS, avoid Ct contrast and renal dose meds as able - holding home HCTZ Hypomagnesemia Mg 1.6 on admit 2 Gm Mg Mg sulfate given Am labs, PRN replacement COPD Stable Home Symbicort and rescue albuterol HTN Holding home HCTZ PRN hydralazine with parameters Prophy Heparin, hold if platelets less than 30 PPI SUBJECTIVE: This is a kind 72 yo male with hx of COPD, HTN, and follicular lymphoma. He is on Gazyva, cycle 15 11/23/21. He states he started feeling bad about 14 days ago but over the last 4 days began to have significant fatigue and no energy even to eat. He has not had a meal for 3 days. He notes decreasing urine output and nausea without emesis. He had some small loose stools yesterday, none today. He states when he gets up to ambulate he is lightheaded and is unsteady on his feet using furniture and walls to keep from falling. His wife made him go to the ER for eval. He was febrile at 38,4 in ER and Covid test returned positive. He is fully vaccinated and boosted. Subsequent CXR was negative and his vitals were otherwise stable on RA. CMP showed mildly low sodium and Cr was 1.4 but this was actually better than baseline of 1.5-1.6. He denies loss of taste or smell and denies HA. He just feels "off" and difficult to have the energy to engage. He did not think he was febrile or chilled at home. His chemo is a CD20 B cell destroyer, and he is at high risk for poor outcomes with Covid infection. He is admitted for further work up and eval. Empiric abx are initiated. BCs obtained. Review of Systems Constitutional: Positive for appetite change (severely decreased) and fatigue (profound). Negative for chills and specified pain. HENT: Negative for mouth sores, nosebleeds, trouble swallowing and voice change. Eyes: Negative for eye problems and visual disturbance. Respiratory: Negative for chest tightness, cough, dizziness on exertion, hemoptysis, shortness of breath and wheezing. Cardiovascular: Negative for chest pain, leg swelling, palpitations and edema. Gastrointestinal: Positive for nausea. Negative for abdominal distention, abdominal pain, constipation and vomiting. Genitourinary: Positive for decreased urine volume. Negative for difficulty urinating, dyspareunia and frequency. Musculoskeletal: Positive for extremity weakness (general). Negative for back pain and flank pain. Skin: Negative for rash and wound. Neurological: Positive for light-headedness and extremity weakness (general). Negative for headaches and speech difficulty. Psychiatric/Behavioral: Negative for confusion and decreased concentration. The patient is not nervous/anxious. OBJECTIVE: BP 170/83 | Pulse 87 | Temp 36.9 ?C (Oral) | Resp 24 | Wt 81.6 kg | SpO2 94% | BMI 25.83 kg/m? Body surface area is 2.01 meters squared. Physical Exam Constitutional: General: He is not in acute distress. Appearance: He is ill-appearing. HENT: Nose: No congestion. Mouth/Throat: Mouth: Mucous membranes are moist. Pharynx: Oropharynx is clear. Eyes: Extraocular Movements: Extraocular movements intact. Pupils: Pupils are equal, round, and reactive to light. Cardiovascular: Rate and Rhythm: Normal rate. Heart sounds: No murmur heard. Pulmonary: Effort: Pulmonary effort is normal. Breath sounds: Normal breath sounds. Comments: Diminished bibasilar, no wheeze, rub or rhonchi appreciated bilaterally apex to base, RRR on RA Abdominal: General: Abdomen is flat. Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. There is no guarding. Skin: General: Skin is warm and dry. Capillary Refill: Capillary refill takes less than 2 seconds. Neurological: General: No focal deficit present. Mental Status: He is alert and oriented to person, place, and time. Psychiatric: Thought Content: Thought content normal. Judgment: Judgment normal. Comments: Slow speech

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 9,0
Labordaten: Comprehensive Metabolic Panel (CMP) (Abnormal) Collected: 01/22/22 0436 Order Status: Completed Specimen: Blood, Central Line Updated: 01/22/22 0520 Sodium Level 141 134 - 146 mmol/L Potassium Level 3.6 3.4 - 5.0 mmol/L Chloride 108 98 - 112 mmol/L HCO3 23 21 - 29 mmol/L Anion Gap 10 9 - 18 mmol/L Glucose Level 108 High 70 - 99 mg/dL Blood Urea Nitrogen 45 High 8 - 20 mg/dL Creatinine 1.08 0.60 - 1.30 mg/dL MDRD eGFR >60 >=60 mL/min/1.73 m2 CG eCrCl 66 mL/min/1.73 m2 Calcium Level Total 9.0 8.6 - 10.4 mg/dL Protein Total 5.6 Low 6.0 - 8.0 g/dL Albumin Level 2.5 Low 3.5 - 5.0 g/dL Bilirubin Total 0.4 0.2 - 1.0 mg/dL Alkaline Phosphatase 59 40 - 129 IU/L Alanine Aminotransferase 27 10 - 40 IU/L Aspartate Aminotransferase 31 10 - 40 IU/L Phosphorus, Blood Level (Normal) Collected: 01/22/22 0436 Order Status: Completed Specimen: Blood, Central Line Updated: 01/22/22 0520 Phosphorus Level 2.8 2.5 - 4.5 mg/dL Magnesium, Blood Level (Normal) Collected: 01/22/22 0436 Order Status: Completed Specimen: Blood, Central Line Updated: 01/22/22 0520 Magnesium Level 1.7 1.6 - 2.5 mg/dL Complete Blood Count w/Differential (Abnormal) Collected: 01/22/22 0436 Order Status: Completed Specimen: Blood, Central Line Updated: 01/22/22 0510 White Blood Cell 3.27 Low 4.00 - 10.80 x10*3/uL Red Blood Cell 4.07 Low 4.60 - 6.00 x10*6/uL Hemoglobin 14.1 14.0 - 18.0 g/dL Comment: Not lipemic or icteric. Hematocrit 37.2 Low 42.0 - 52.0 % Mean Cell Volume 91.4 80.0 - 100.0 fL Mean Cell Hemoglobin 34.6 High 27.0 - 33.0 pg Comment: Not lipemic or icteric. Mean Cell Hemoglobin Concentration 37.9 High 32.0 - 37.0 g/dL Comment: Not lipemic or icteric. Red Cell Diameter Width 11.8 11.0 - 16.0 % NRBC Absolute Count 0.00 0.00 - 0.01 x10*3/uL NRBC Automated 0.0 0.0 - 0.1 %WBC Platelet 107 Low 140 - 400 x10*3/uL Mean Platelet Volume 11.5 High 7.4 - 11 fL Neutrophil Automated 67.3 35.0 - 80.0 % Immature Granulocyte Automated 2.4 High 0.0 - 0.6 % Lymphocyte Automated 13.5 Low 20.0 - 50.0 % Monocytes Automated 16.2 High 2.0 - 12.0 % Eosinophil Automated 0.3 0.0 - 6.0 % Basophil Automated 0.3 0.0 - 2.0 % Neutrophil Absolute Count 2.20 1.80 - 7.80 x10*3/uL Immature Granulocyte Absolute Count 0.08 High 0.00 - 0.05 x10*3/uL Lymphocyte Absolute Count 0.44 Low 1.00 - 4.00 x10*3/uL Monocyte Absolute Count 0.53 0.00 - 0.90 x10*3/uL Eosinophil Absolute Count 0.01 0.00 - 0.50 x10*3/ Basophil Absolute Count 0.01 0.00 - 0.20 x10*3/uL
Aktuelle Erkrankungen: -
Vorgeschichte: Past Medical History: Diagnosis Date ? Cancer -follicular lymphoma grade IIIa of lymph nodes of multiple sites ? High blood pressure -cervical lymphadenopathy
Andere Medikamente: Acetaminophen 1,000 mg Oral 2 times daily Albuterol Sulfate 108 (90 Base) MCG/ACT 2 puffs Inhalation Every 6 hours PRN Budesonide-Formoterol Fumarate 80-4.5 MCG/ACT 2 puffs Inhalation 2 times daily, Rinse mouth after use Dexamethasone 6 mg
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2051192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: IN
Alter: 31,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 20.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Fatigue Inflammation Injection site pain Lymphadenopathy Pain Pharyngeal paraesthesia Swelling

Symptomtext

Left arm pain at site Very swollen Lymph nodes, caused inflammation and circulation in left arm Could not hold arm up to stop pain, could not have it down at a normal position without pain Pain was more like build up pressure Took Several days to one week to go down Happened about 12 hours after injection (I did have weird tingling in my throat when I was waiting after the injection was done during my second shot) Seen by doctor, given prescription strength Aleve for swelling and pain It took almost 48-72 hours to feel back to normal and able to function without pain. I could not wear a bra or anything tight or restricting during the time. Extreme tiredness and exhaustion during that time. Booster shot I had same thing happen with arm and lymph nodes, except it did not happen for 48 hours after injection. I had tiredness for the first 24 hours after booster, then swelling kicked in.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal paraesthesia
Hospital-Tage: -
Labordaten: Physical examination was conducted
Aktuelle Erkrankungen: Allergies
Vorgeschichte: Raspatory Allergies IBS PMDD Chronic GERD
Andere Medikamente: I was also doing allergy shots at the time under the care of Dr.. I was a couple months into the 35 week treatment. I am now in the maintenance stage of the shots. I had the same reaction with my booster. ketotifen 0.025% ophthalmic solut
Allergien: Albuterol Sulfate- hives and issues bleeding Tree Nuts- itching in mouth and throat Penicillin Molds
Vorherige Impfungen: -

VAERS 2043745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: OK
Alter: 35,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 28.06.2021
Beginn: 30.06.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac stress test Chest pain Hypoaesthesia

Symptomtext

less than 48 hours post vaccine, patient experienced chest pain and arm numbness. She contacted her PCP, who directed her to a nearby Urgent Care. Once at the Urgent Care, she was sent home and advised to follow up with her PCP. She was then directed to a cardiologist but could not get in for several months. Her symptoms slowly improved over the course of 3-4 months but unknown cause. She is a healthy, 35-year old female with no chronic or known health conditions and on no medication except famotidine for stomach issues. All medical physicians refused to notify VAERS. By the time patient was able to have visit with cardiologist, symptoms had dissipated, cardiologist did stress test. Patient was unaware of any clinical findings and believes it was a result of vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Stress test in december 2021
Aktuelle Erkrankungen: no chronic or acute health conditions
Vorgeschichte: no chronic health issues
Andere Medikamente: famotidine only
Allergien: no allergies
Vorherige Impfungen: -

VAERS 2039191

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NJ
Alter: 33,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 10.09.2021
Beginn: 11.01.2022
Tage bis Beginn: 123,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Condition aggravated Hypophagia Nausea Pain SARS-CoV-2 antibody test SARS-CoV-2 test negative SARS-CoV-2 test positive Vomiting

Symptomtext

33 y/o F w/ PMH significant for metastatic breast cancer w/ diffuse osseous lesions and hypercalcemia who presented to the ED w/ nausea, vomiting, and pain. Pt stated that yesterday she started experiencing nausea and vomiting. Pt took metoclopramide for the nausea, which helped a little. Pt had 5-10 episodes of vomiting with PO intake. pt denies hematemesis or coffee ground emesis, pt endorses minimum bilious emesis, mainly food. Pt additionally states she is having severe generalized pain. This is her typical to her usual pain, however worsened given pt was not able to take PO pain medications. Pt stated her pain was 10/10 in the AM and was 8/10 on presentation. Pain was 6/10 during exam after pt received IV dilaudid. Pt denies SOB, abdominal pain, chest pain, fever, cough, chills, sick contacts

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 7,0
Labordaten: 01/12/2022 - SARS-CoV-2 Antigen (-) 01/14/2022 - SARS-COV-2 PCR (++); IgG 0.53, IgG2 QT-SPIKE >25,000
Aktuelle Erkrankungen: -
Vorgeschichte: Breast Cancer Comment ER+/PR-/HER2-, metastatic breast ca with diffuse osseous lesions- s/p 2 doses of Xygeva and Lupron, s/p 10 radiation sessions; Addt'l Med History Pancytopenia, cord compression (T9) w/ metastatic disease, Compression fx of T5, Compression fx T2, T9 Pathologic fx L2, Breast cancer, T8 & T9 decompressive surgery, bone hypertrophy w/ lesions within the skull. Significant Surg Hx As Listed Addt'l Surgical History C-section s/p T8 & T9 laminectomy for resection of tumor, decompressive surgery. Smoking Status Never Smoker.
Andere Medikamente: Last Updated: 01/12/2022 00:48 (In Progress) By: (privacy) Active baclofen 10 mg Tablet Directions: 1 tablet oral three times a day (Active) calcitonin (salmon) 200 unit/spray spray,non-aerosol Directions: 1 spray nasal daily (Active)
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2035382

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 34,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 21.05.2021
Beginn: 07.01.2022
Tage bis Beginn: 231,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Culture urine positive Maternal exposure before pregnancy Prenatal screening test Pyrexia SARS-CoV-2 test positive Tachycardia Tachypnoea Urine analysis abnormal

Symptomtext

1/7/2022 - 1/10/2022 (3 days) (Privacy)Hospital Patient is a 35 y.o. G3P2002 that presented to the hospital at 26wk0d gestation for fever. Her prenatal course had been complicated by obesity, AMA, history of Caesarean section, and a language barrier. Upon presentation she was noted to be febrile, tachycardic, and tachypneic. She subsequently tested positive for COVID as well as had a UA that was concerning for urinary tract infection/pyelonephritis. She was started on dexamethasone and remdesivir for her acute COVID as well as Rocephin for concern for pyelonephritis. She denied any respiratory symptoms throughout her stay. She clinically improved. Her urine culture was positive for E coli. Her antenatal fetal testing was reassuring. She was discharged home in good condition on hospital day 3 on the Keflex for plan for a full 14 day treatment course followed by daily suppression

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Digestive Obesity complicating pregnancy, childbirth, or puerperium, antepartum-class 1 Constipation during pregnancy in second trimester Infectious/Inflammatory COVID-19 affecting pregnancy in third trimester Urinary tract infection in mother during second trimester of pregnancy Nervous Pregnancy headache in second trimester Other MFM PLAN OF CARE History of low transverse cesarean section Language barrier History of cesarean delivery History of macrosomia in infant in prior pregnancy, currently pregnant Encounter for follow-up ultrasound of fetal anatomy Antepartum multigravida of advanced maternal age
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2024183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MN
Alter: 47,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 12.08.2021
Beginn: 12.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Abnormal dreams Arthralgia Back pain Bone pain Chills Dizziness Insomnia Myalgia Pain Pain in extremity Pyrexia Tenderness Tremor

Symptomtext

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 47 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 12Aug2021 09:00 (Lot number: EW0186) at the age of 47 years as dose 2, single for Covid-19 immunisation. Relevant medical history included: "lymphoma", start date: 1985 (unspecified if ongoing), notes: cancer survivor, he was 13 years old, diagnosed 1985-1986. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Pfizer Covid 19 Vaccine, LOT: EN0180, NDC: Unknown, Expiry Date: Unknown, Injection, unknown dosage, left shoulder), administration date: 22Jul2021, when the patient was 47 years old, for COVID-19 Immunisation, reaction(s): "shoulder hurts twice as much as the first shot". The following information was reported: CHILLS (non-serious) with onset 12Aug2021 22:30, outcome "not recovered", described as "chills"; DIZZINESS (non-serious) with onset 12Aug2021 22:30, outcome "not recovered", described as "light headed/real lightheadedness"; PYREXIA (non-serious) with onset 12Aug2021 22:30, outcome "not recovered", described as "fever"; TENDERNESS (non-serious) with onset 12Aug2021 22:30, outcome "not recovered", described as "lower back was tender"; BONE PAIN (non-serious) with onset 12Aug2021, outcome "not recovered", described as "his bones, it's not as bad as his back"; BACK PAIN (non-serious), outcome "unknown", described as "his back hurt so damn bad, he couldn't touch it"; ARTHRALGIA (non-serious) with onset 12Aug2021, outcome "not recovered", described as "His shoulder hurts twice as much as the first shot, he had it in the same arm."; ABNORMAL DREAMS (non-serious) with onset 12Aug2021, outcome "not recovered", described as "dreaming kind of funny"; TREMOR (non-serious), outcome "unknown", described as "got the shakes"; INSOMNIA (non-serious), outcome "unknown", described as "couldn't go back to sleep"; PAIN IN EXTREMITY (non-serious) with onset 12Aug2021, outcome "unknown", described as "had the second dose in the same arm, it hurt about an hour after, the muscle ache because of the needle"; MYALGIA (non-serious) with onset 12Aug2021, outcome "unknown", described as "it hurt about an hour after, the muscle ache because of the needle"; PAIN (non-serious) with onset 12Aug2021 10:30, outcome "unknown", described as "pain". Additional information: Patient confirms all symptoms are dragging on, persisting. Patient's events did not require any emergency Room and physician office visit. Patient hasn't been to a doctor. Patient did not have any other vaccinations within four weeks prior to the first administration date of the suspect vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Lymphoma (cancer survivor, he was 13 years old, diagnosed 1985-1986).
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2019472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 31.08.2021
Beginn: 01.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Abdominal pain lower Arrhythmia Back pain Burning sensation Cardiac flutter Cardiac monitoring abnormal Cardiovascular evaluation Eye pain Headache Magnetic resonance imaging abnormal Mastoiditis Ophthalmological examination abnormal Pain Pruritus Rash macular Spinal pain Ultrasound scan Uterine pain

Symptomtext

Sharp and dull re-occuring head aches behind eyes, sharp pain in the lower back/spine, sharp pains/cramp like in lower abdominal area/ uterus. Heart Flutters re-occuring on and off several times a week but by December 2021 flutters are daily occurance. The pain was speratic in nature and in times of occurances. They lasted for approximately 2 1/2 months and then went to dull headaches behind the eyes. MRI, Ultra sound, Eyes exams, Cardio work up with heart monitor were preformed. Also burning and itching began late Novemeber and progressively worsening into January 2022. - of the head hands and feat. The burning has now progressed to the neck and torso - leaving red sploches and then they go away. This happens several times a day - no particular times.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: MRI - 11/08/2021 - A moderate right mastoid cell opacification A 1.2 cm air cell in right petrous apex is partly opacified with internal air-fluid level. Finds suggest acute and chronic otomastoiditis. Perriphial Eye Exams 10/19/2021, 10/20/2021, 10/22/2021, and 11/23/2021 - Left eyes inside perriphial vision missing Heart Monitor - 12/02/2021-12/09/2021 - found heart misfire
Aktuelle Erkrankungen: none
Vorgeschichte: allergic to mold, cat hair, mites. Sudden Hearing Loss - right ear.
Andere Medikamente: zyrtec, flonaise, gaba, ashuwando, iodine, devil's claw
Allergien: no known
Vorherige Impfungen: -

VAERS 2019353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 37,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 26.08.2021
Beginn: 28.12.2021
Tage bis Beginn: 124,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

short of breath + COVID test

Weitere VAERSDATA-Felder

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

VAERS 2019351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 32,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 22.05.2021
Beginn: 28.12.2021
Tage bis Beginn: 220,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Chest pain Myalgia Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

sore throat, chest pain, myalgias + COVID test

Weitere VAERSDATA-Felder

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

VAERS 2014572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MN
Alter: 22,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 15.05.2021
Beginn: 01.01.2022
Tage bis Beginn: 231,0
Dosis: 1
Route/Site: - / -

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

Cough Diarrhoea Dyspnoea Headache Oropharyngeal pain Pain Sinus congestion

Symptomtext

cough, sore throat, sinus congestion, headache, mild shortness of breath, body aches, diarrhea. starting 1/1/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Depression. Anxiety.
Andere Medikamente: ?Venlafaxine HCl 100 MG Tablet 1 tablet with food Orally Once a day, Notes: 187.5 mg ?hydrOXYzine HCl 25 MG Tablet TAKE 1 TABLET BY MOUTH THREE TIMES DAILY AS NEEDED Oral ?Sertraline HCl 50 MG Tablet TAKE 1/2 TABLET BY MOUTH DAILY FO
Allergien: Penicillin G Sodium
Vorherige Impfungen: -

VAERS 2014172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 17.11.2021
Beginn: 02.01.2022
Tage bis Beginn: 46,0
Dosis: 3
Route/Site: IM / AR

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

Arthralgia Asthenia COVID-19 Chronic obstructive pulmonary disease Condition aggravated Cough Malaise Oxygen saturation decreased Pneumonia SARS-CoV-2 test positive Sputum discoloured

Symptomtext

Hospitalized 1/2/2022; COVID-19 positive 1/2/2022; fully vaccinated plus booster BRIEF OVERVIEW: Discharge Provider:, MD Primary Care Provider: MD Admission Date: 1/2/2022 Discharge Date: Jan 6, 2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: COPD with acute exacerbation (HCC) Community acquired pneumonia of right lower lobe of lung COVID-19 HOSPITAL COURSE: Patient is a 85 y.o. female who presented with cough, weakness. Patient has a history of COPD, chronic respiratory failure on 3L NC at baseline, Hx pseudomonas pneumonia, chronic diastolic CHF, hypothyroid. Patient's symptoms started on 12/31 with a cough and malaise. Per patient, she was having severe coughing up a greenish sputum so she called her pulmonologist who started the patient on Levaquin 2 days ago, she was able to take 2 doses, but then began having pain in both her ankles, and called her pulmonologist again who recommended she come to the emergency department for IV antibiotics. Patient took a COVID test at home which was positive. She was admitted to HCF and maintained on cefepime/azithromycin. Oxygen weaned to baseline 4L. Patient continued to improve though would desaturate to low 80's with activity. Local rehab consult was placed who recommended patient remain on 4 L nasal cannula at rest, with activity she will need to increase to 5-6 L.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD (Chronic Obstructive Pulmonary Disease), Very severe. Chronic obstructive pulmonary disease, unspecified COPD type (HCC) Bronchiectasis with acute exacerbation (HCC) Hypoxemia requiring supplemental oxygen, since 2007 Chronic sinusitis of both maxillary sinuses Pneumonia Acute on chronic respiratory failure with hypoxia (HCC) Chronic deep vein thrombosis (DVT) of femoral vein of right lower extremity (HCC) Paroxysmal atrial fibrillation (HCC) Pulmonary hypertension due to lung diseases and hypoxia (HCC) Chronic diastolic congestive heart failure (HCC) Obesity, BMI 33. Diverticulosis GERD (gastroesophageal reflux disease) COVID-19 Tobacco abuse, in remission. 30 pack years. Hyperlipidemia Hypoxemia, chronic Dyslipidemia Hypothyroidism Immunoglobulin deficiency, noted 9/2010. Osteoarthritis Osteoarthritis of lumbar spine Cyst of finger Insomnia Mild cognitive impairment
Andere Medikamente: albuterol HFA (PROAIR HFA) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 5 MG tablet B Complex Vitamins (VITAMIN B COMPLEX) tablet budesonide/formoterol (SYMBICORT) 160-4.5 MCG/ACT inhaler busPIRone (BUSPAR) 7.5 MG tablet cetirizine (ZYR
Allergien: Oxycodone
Vorherige Impfungen: -

VAERS 1996072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 41,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 01.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: SYR / RA

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

Blood test Computerised tomogram Dyspnoea Electrocardiogram Feeling hot Palpitations Pyrexia

Symptomtext

Heart palpitations Unable to breath Fever Very hot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood tests Cat scan EKG IV for fluids
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No
Vorherige Impfungen: -

VAERS 1959026

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 42,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 10.09.2021
Beginn: 16.12.2021
Tage bis Beginn: 97,0
Dosis: 2
Route/Site: - / -

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

Cough Dyspnoea Feeling cold Nasal congestion

Symptomtext

presented to the local hospital with shortness of breath, associated with mild coughing and stuffy nose and chilly feeling

Weitere VAERSDATA-Felder

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

VAERS 1947764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: OH
Alter: 51,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 20.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

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

Aphasia Blood creatine increased Confusional state Cough Dizziness Dyspnoea exertional Dysstasia Fatigue Feeling abnormal Full blood count Nasopharyngitis Palpitations Respiratory tract congestion Weight decreased

Symptomtext

About a week after the vaccine I developed extreme fatigue and a sense of dizziness causing me to have more of an awake fainting type feeling where I cant sit up or do anything when this occurs. If I am walking when this occurs I have to hurry and sit or grab onto something because I loose the ability to stand. This issue has gotten worse over time and now I have an Echocardiogram that has to be scheduled. About a month after the vaccine I begin getting heart palpations and SOB on exertion. Brain fog has gotten really bad and is getting progressively worse resulting in me forgetting words in the middle of conversations sometimes I cant even engage in conversation because I am so confused and boggled. My O2 level drops in the low 80's periodically throughout the day with no explanation and I am loosing weight for no apparent reason. My weight over the past month shows I am loosing about 6-8oz/ day. I have the feeling of a constant cold but no cold, but the mucus just wont go away and when I lay down I have a cough that comes and goes periodically. My BP has been running in the low 80/60's but CBCs has come back pretty good with the exception of my creatine level has increased a little but again with no explanation associated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: CBC-creatine level increase.
Aktuelle Erkrankungen: No
Vorgeschichte: Rheumatic Heart Disease, Hypothyroidism, History of Stroke, Asthma, Hyperlipidemia, Chronic Pain Disorder, Long term use of Anticoagulant, Fibromyalgia, UC, Thoracic Spondylosis without myelopathy; Spinal Stenosis at lumbar region at multiple levels; Post Menopausal; Pernicious Anemia; Carpal Tunnel Syndrome; Mitral Bowel Replacement with Bioprosthetic vial (PIG)
Andere Medikamente: Aspirin; Valacyclovir; Spironolactone; Vitamin D3; Levothyroxine; Bupropion; Duloxetine; Warfarin; Montelukast; Zyrtec; Lipitor; Magnesium; Trazadone; Melatonin; Gabapentin; Topamax; Baclofen; Glucosamine Chondroitin; B Vitamin w/ collagen;
Allergien: Sulfa; Adhesive; Doxycycline; Tetracycline; Niacin; Docusate sodium; Fenofibrate; Latex; Corticosteroids; Metoprolol; Mesalamine; Ferrous gluconate
Vorherige Impfungen: -

VAERS 1466465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 07.07.2021
Beginn: 07.07.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Hypoaesthesia Injection site pain Pain in extremity Paraesthesia Joint swelling Pain Peripheral swelling SARS-CoV-2 test Sensory disturbance

Symptomtext

Swelling of left wrist and hand; Swelling of left wrist and hand; Pain; Change in sensation in hand; This is a spontaneous report received from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 15 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 07Jul2021 at 13:30 (Lot number: EW0186) at the age of 15 years as dose 2, single for COVID-19 immunisation. Relevant medical history included: "Immunoglobulin G low" (unspecified if ongoing), notes: Low IgG; "Mitral regurgitation" (unspecified if ongoing), notes: Mild mitral valve regurgitation and "Pulmonic stenosis" (unspecified if ongoing), notes: Mild peripheral pulmonic stenosis. Concomitant medication(s) included: HYDROCORTISONE CREAM and ALLEGRA. Past drug history included: Codeine, reaction(s): "Drug allergy", notes: Known allergies: Codeine. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot number: EWO186, Anatomical site: left arm, Administration time: 13:30), administration date: 16Jun2021, when the patient was 15 years old, for COVID-19 immunisation. The following information was reported: JOINT SWELLING (non-serious), with onset 07Jul2021 at 14:00, outcome "not recovered", described as "Swelling of left wrist and hand", PERIPHERAL SWELLING (non-serious), with onset 07Jul2021 at 14:00, outcome "not recovered", described as "Swelling of left wrist and hand", PAIN (non-serious) with onset 07Jul2021 at 14:00, outcome "not recovered", described as ''Pain'', SENSORY DISTURBANCE (non-serious) with onset 07Jul2021 at 14:00, outcome "not recovered", described as "Change in sensation in hand". The events "Swelling of left wrist and hand, Pain and Change in sensation in hand'' were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of joint swelling, peripheral swelling, pain and sensory disturbance. Additional Information: 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-19 vaccine. Since the vaccination, the patient had been tested for COVID-19. The patient received the treatment of 9 day course of steroids

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20210715; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Immunoglobulin G low (Low IgG); Mitral regurgitation (Mild mitral valve regurgitation); Pulmonic stenosis (Mild peripheral pulmonic stenosis)
Andere Medikamente: HYDROCORTISONE; ALLEGRA
Allergien: -
Vorherige Impfungen: -

VAERS 1466465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 07.07.2021
Beginn: 07.07.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Hypoaesthesia Injection site pain Pain in extremity Paraesthesia Joint swelling Pain Peripheral swelling SARS-CoV-2 test Sensory disturbance

Symptomtext

Swelling of left wrist and hand; Swelling of left wrist and hand; Pain; Change in sensation in hand; This is a spontaneous report received from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 15 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 07Jul2021 at 13:30 (Lot number: EW0186) at the age of 15 years as dose 2, single for COVID-19 immunisation. Relevant medical history included: "Immunoglobulin G low" (unspecified if ongoing), notes: Low IgG; "Mitral regurgitation" (unspecified if ongoing), notes: Mild mitral valve regurgitation and "Pulmonic stenosis" (unspecified if ongoing), notes: Mild peripheral pulmonic stenosis. Concomitant medication(s) included: HYDROCORTISONE CREAM and ALLEGRA. Past drug history included: Codeine, reaction(s): "Drug allergy", notes: Known allergies: Codeine. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot number: EWO186, Anatomical site: left arm, Administration time: 13:30), administration date: 16Jun2021, when the patient was 15 years old, for COVID-19 immunisation. The following information was reported: JOINT SWELLING (non-serious), with onset 07Jul2021 at 14:00, outcome "not recovered", described as "Swelling of left wrist and hand", PERIPHERAL SWELLING (non-serious), with onset 07Jul2021 at 14:00, outcome "not recovered", described as "Swelling of left wrist and hand", PAIN (non-serious) with onset 07Jul2021 at 14:00, outcome "not recovered", described as ''Pain'', SENSORY DISTURBANCE (non-serious) with onset 07Jul2021 at 14:00, outcome "not recovered", described as "Change in sensation in hand". The events "Swelling of left wrist and hand, Pain and Change in sensation in hand'' were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of joint swelling, peripheral swelling, pain and sensory disturbance. Additional Information: 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-19 vaccine. Since the vaccination, the patient had been tested for COVID-19. The patient received the treatment of 9 day course of steroids

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20210715; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Immunoglobulin G low (Low IgG); Mitral regurgitation (Mild mitral valve regurgitation); Pulmonic stenosis (Mild peripheral pulmonic stenosis)
Andere Medikamente: HYDROCORTISONE; ALLEGRA
Allergien: -
Vorherige Impfungen: -

VAERS 1936321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 23,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 09.10.2021
Beginn: 08.11.2021
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: UN / UN

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

Chest discomfort Chills Dyspnoea Respiratory tract congestion

Symptomtext

This is a 23y.o. female medical history of eczema and asthma who presented to the emergency department secondary to increased dyspnea. The patient states over the past 5 days she has been getting progressively more short of breath. She admits to chills and congestion as well as chest tightness. Patient states that she use her rescue inhaler multiple times without any improvement in her dyspnea. She does admit to receiving the first part of Pfizer COVID 19 vaccine however she did not get the second part.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: Asthma ? Eczema
Vorgeschichte: -
Andere Medikamente: albuterol (2.5 MG/3ML) 0.083% INHAL Nebu Soln inhale 3 mL using breathing machine every 4 hours as needed for FOR SHORTNESS OF BREATH. 11/12/2021 Unknown time betamethasone valerate (VALISONE) 0.1 % EXTERNAL Ointment 11/12/2021 Unknown ti
Allergien: none
Vorherige Impfungen: -

VAERS 1935616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

moderat

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 14.05.2021
Beginn: 27.11.2021
Tage bis Beginn: 197,0
Dosis: UNK
Route/Site: - / -

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

Chills Cough Dyspnoea Hypoaesthesia Myalgia Nausea Paraesthesia Pyrexia Vomiting

Symptomtext

11/27/21 presents to EC ED for "cough, shortness of breath, mylagias, chills, fever, nausea, vomiting, numbness and tingling in her hands". PMHx of "asthma, MS"

Weitere VAERSDATA-Felder

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

VAERS 1919632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 69,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain upper Arthralgia Blood test Dyspnoea Hyperhidrosis Liver function test abnormal Night sweats Oxygen saturation Pain in extremity Renal function test abnormal

Symptomtext

his arm had really hurt; woke up in the middle of the night sweating; he could not stop sweating; not breathing well/ felt like he couldn't get air; his joints were hurting; his liver numbers and kidney numbers were crazy; his liver numbers and kidney numbers were crazy; had a lot of pain in his stomach/ stomach pain whenever he eats or drinks; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the patient. A 69 year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm left, administration date 30Sep2021 (Lot number: EW0186) at the age of 69 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "got a few stents" (unspecified if ongoing); "open heart surgery, quadruple bypass" (unspecified if ongoing); "Tavr" (unspecified if ongoing), notes: When they put an artificial top valve in the heart. They put it through the leg.; "esophagus removed" (unspecified if ongoing); "cancer twice" (unspecified if ongoing); "Chronic pain" (unspecified if ongoing); "cramps in his legs" (unspecified if ongoing); "Atrial fibrillation" (unspecified if ongoing). Concomitant medication(s) included: OMEPRAZOLE taken for abdominal pain upper (ongoing); ATORVASTATIN taken for blood cholesterol; LASIX [FUROSEMIDE] taken for cardiac disorder (ongoing); GABAPENTIN (ongoing); METOPROLOL taken for cardiac disorder (ongoing); PANTOPRAZOLE (ongoing); SULFAMETHOXAZOLE taken for staphylococcal infection (ongoing); TAMSULOSIN; B 12; IRON; MAGNESIUM; FOLIC ACID; TIZANIDINE HCL taken for pain, muscle spasms; CLOPIDOGREL taken for atrial fibrillation (ongoing). Vaccination history included: Bnt162b2 (LOT: EW0186), administration date: 09Sep2021, when the patient was 69 years old, for COVID-19 immunization, reaction(s): "With the first shot, there was nothing at all. he didn't feel anything"; Other flu shots (He gets them once in a blue moon), for Immunization; Pneumonia shot (He gets them once in a blue moon.), for Immunization. The following information was reported: RENAL FUNCTION TEST ABNORMAL (non-serious), LIVER FUNCTION TEST ABNORMAL (non-serious) all with onset Oct2021, outcome "unknown" and all described as "his liver numbers and kidney numbers were crazy"; PAIN IN EXTREMITY (non-serious) with onset 01Oct2021, outcome "not recovered", described as "his arm had really hurt"; NIGHT SWEATS (non-serious) with onset 01Oct2021, outcome "unknown", described as "woke up in the middle of the night sweating"; HYPERHIDROSIS (non-serious) with onset 01Oct2021, outcome "unknown", described as "he could not stop sweating"; ABDOMINAL PAIN UPPER (non-serious) with onset Oct2021, outcome "unknown", described as "had a lot of pain in his stomach/ stomach pain whenever he eats or drinks"; DYSPNOEA (non-serious) with onset 01Oct2021, outcome "unknown", described as "not breathing well/ felt like he couldn't get air"; ARTHRALGIA (non-serious) with onset 01Oct2021, outcome "not recovered", described as "his joints were hurting". The events "his liver numbers and kidney numbers were crazy", "his liver numbers and kidney numbers were crazy", "his arm had really hurt", "woke up in the middle of the night sweating", "he could not stop sweating", "had a lot of pain in his stomach/ stomach pain whenever he eats or drinks", "not breathing well/ felt like he couldn't get air" and "his joints were hurting" were evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of abdominal pain upper. Additional information: Caller states he is calling regarding the virus shot, the Corona virus shot. Clarified that the caller is referring to the Pfizer Corona virus shot. He states that he does not want to report and does not want to get involved. He states that he ended up in the hospital the day after he got the shot. He got the shot maybe on a Thursday and woke up that Friday morning saying that his arm had really hurt. He states that he has had other flu shots and other shots but they had not bothered his arm like this. At the end of that day, he could not lift his arm. He didn't think much of it but, woke up in the middle of the night sweating and not breathing well and his joints were hurting. He tried to call the doctor and ended up on the phone with the nurse answering questions. She sent for an ambulance and he really wanted to wait a little longer and call the doctor. The nurse told him that they would probably ask him the same questions and with those conditions, he should really be in the ER. Caller states that he spent the whole day in the ER and they were going to admit him but, they told him if his numbers came back down by 4, 5 or 6:00 in the morning, he would not need to be admitted. He just stayed in the ER. By 5:00am, his numbers kept coming down. They were doing blood tests every 2 hours. He is wondering, if these are similar symptoms that other people are having? Because, all of the doctors are saying that they don't know what it is. What else could it be? All of a sudden he woke up and his liver numbers and kidney numbers were crazy. His joints were going crazy and he could not stop sweating. Are these symptoms other people are having? He states that he is still experiencing symptoms but not the arm pain and being unable to lift it. Not breathing well, joints hurting: He woke up in the middle of the night soaking wet and had to change his clothes and go back to sleep. It was a little rough, he was sweating and he had a lot of pain in his stomach. He still has stomach pain. He is on meds for that now and he does not know. The medicine that he took before, they made changes to. He has stomach pain whenever he eats or drinks. He gets pain just sitting around sometimes. He believes that it has gotten a little better as time goes on, everything is a little better. Or, it may be because of the meds. Not breathing well: He felt like he couldn't get air. They said his oxygen was 97 or 98 but he couldn't get enough oxygen. Overall, he thinks that it has almost completely gone away. He states that he has some issues, any way, with breathing. He had always had shortness of breath but not when he was not doing anything. He was sleeping when this happened. He states that this all started Friday night in the middle of the night. He woke up Saturday morning and it was really full blown. It was about 3:00 am , Friday morning. He thought maybe it would pass. When clarifying that the caller went to the ER, he states that he didn't go voluntarily, they sent an ambulance that took him to the ER. Clarified that he went to the Emergency room and was not admitted to the hospital. He states that they told him that if his numbers start coming down, and stay down, he could go home and keep an eye on stuff. He states that if he did get admitted, it would have cost less. It cost twice as much going to the ER than getting admitted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Blood tests; Result Unstructured Data: Test Result:liver numbers and kidney numbers were crazy; Test Name: oxygen; Result Unstructured Data: Test Result:97 or 98
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atrial fibrillation; Bypass surgery; Cancer; Chronic pain; Cramps in legs; Esophagectomy; Stent insertion NOS; Transcatheter aortic valve implantation (When they put an artificial top valve in the heart. They put it through the leg.)
Andere Medikamente: OMEPRAZOLE; ATORVASTATIN; LASIX [FUROSEMIDE]; GABAPENTIN; METOPROLOL; PANTOPRAZOLE; SULFAMETHOXAZOLE; TAMSULOSIN; B 12; IRON; MAGNESIUM; FOLIC ACID; TIZANIDINE HCL; CLOPIDOGREL
Allergien: -
Vorherige Impfungen: -

VAERS 1916457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 35,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 30.06.2021
Beginn: 09.07.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: SYR / LA

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

Amniotic band syndrome Caesarean section Exposure during pregnancy Foetal cystic hygroma Hypertension Malaise Pre-eclampsia Protein urine absent Swelling

Symptomtext

Pregnancy history: 12 weeks cystic hygroma detected in baby and then referred to a specialist for monitoring. During the pregnancy, the remaining check-ups showed the cystic hygroma resolving itself but the doctor then detected what looked like an amniotic band. The amniotic band also seemed to disappear. Both "issues" with the baby resolved themselves. BP readings were normal and pregnancy urine was free from protein. Never any other concerns with my health (until 7/9/21 which was 1 week after my second dose). Timeline of shots and Adverse effects: 7/30/21: 2nd shot, felt really sick for 2 days 7/8/21: 33-week OBGYN appointment - everything normal, BP was 120/80 7/13/21: 34-week appointment with Specialist and BP was really high. Was sent home to take a 24-hour urine test. 7/14/21: Started urine test, admitted myself to hospital at night due to High BP at home all day. 7/15/21: Finished urine test at hospital, results came back as severe preeclampsia. Seems like the only symptoms I had were high blood pressure and swelling. No headaches, no vision impairments. Doc recommended delivery the next day. 7/16/21: Delivery at 34.5 weeks pregnant via C-Section. Baby boy weighed 5 lb, 13 oz. and was in the NICU for 10 days. The docs struggled to keep my BP down afterwards. I stayed in hospital until Tuesday 7/20.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: 7,0
Labordaten: 24 HR URINE PROTEIN TEST
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: prenatal vitamins
Allergien: shrimp
Vorherige Impfungen: -

VAERS 1909328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

moderat

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Hyperhidrosis Nausea Palpitations

Symptomtext

Heart palpitation, sweating, nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: 11/13/2020 Flu vax, throwing up, heart palpitations

VAERS 1905904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 29.07.2021
Beginn: 27.11.2021
Tage bis Beginn: 121,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Clostridium difficile infection Condition aggravated Cough Malaise Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Urinary tract infection

Symptomtext

covid symptoms including fever, sore throat, and cough started on 11/26/21 while pt was hospitalized for UTI/C diff

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: positive PCR SARS-CoV-2 (COVID-19) by NAA, Micro detected on 11/27/21
Aktuelle Erkrankungen: UTI , C difficile diarrhea, ESBL MDR infection
Vorgeschichte: breast cancer metastasized to bone, s/p radiation therapy, urinary retention, paraplegia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1896796

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 14.04.2021
Beginn: 16.11.2021
Tage bis Beginn: 216,0
Dosis: 2
Route/Site: - / -

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

COVID-19 COVID-19 pneumonia Endotracheal intubation Influenza virus test Respiratory syncytial virus test SARS-CoV-2 test positive

Symptomtext

Pt received Pfizer vaccines on 04/14/21 and 05/11/21. Pt presented to the ED on 11/16/21 due to recently testing positive for COVID while at a rehabilitation center. CXR showed COVID pneumonia. Pt required intubation

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: COVID-19, flu, RSV by NAA positive for SARS-COV-2 on 11/16/21
Aktuelle Erkrankungen: -
Vorgeschichte: DM2, dementia, HTN
Andere Medikamente: Lipitor, claritin, namenda, glucophage, toprol, bactroban, senokot, lamisil
Allergien: Heparin
Vorherige Impfungen: -

VAERS 1888042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MA
Alter: 31,0
Geschlecht: M
Eingang: 20.11.2021
Impfdatum: 28.04.2021
Beginn: 21.09.2021
Tage bis Beginn: 146,0
Dosis: 2
Route/Site: IM / AR

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

Anosmia Anxiety COVID-19 Chest X-ray Chest discomfort Cough Dyspnoea Full blood count normal Muscle tightness Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

[I'm reporting a "breakthrough" COVID-19 infection with this form after speaking with a CDC representative on the phone about my latest V-Safe submission. I'm also describing some post-acute symptoms I've experienced. To be clear, I do not associate any of these symptoms with my vaccination itself.] On September 21, I received a positive test result for COVID-19. I was experiencing a fever, loss of smell, cough, and congestion, which prompted me to get tested. During my isolation period I treated symptoms with DayQuil and ibuprofen. On the 25th, most symptoms were resolved, but I experienced some slightly difficult breathing (not wheezing, but the feeling of "incomplete" breaths) and chest/intercostal muscle tightness. This was accompanied by notable feelings of anxiety/worry. I was examined by EMTs at my home, who noted normal blood oxygen levels and blood pressure. They advised my breathing seemed within norms, and not the "shortness of breath" that would indicate a severe problem (since I was able to speak without interruption). On the 27th I spoke with a provider at my PCP's office, who agreed that I was not at high risk, but prescribed an albuterol inhaler to be used as needed. This appeared to help, although the mental/emotional symptoms were still somewhat present. Around October 30/31 I started to notice similar muscle tightness and "incomplete" breaths, provoking a significant anxiety response again. I did my best to self-manage with the albuterol, muscle stretching, and meditation. On November 1 I was seen by an urgent care center, with a follow-up chest x-ray on November 3. The x-ray was described to me as "normal, with some bronchitis" and I was advised to continue using the albuterol. I spoke with my PCP, on November 8, who recommended I switch from the albuterol to Flovent (fluticasone) since albuterol can increase heart rate and perceived anxiety. I've been on that course since November 13, and the symptoms seem to be well-managed so far.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 21 September 2021: positive result for COVID-19 (Qualitative NAAT) 3 November 2021: CBC (all results normal), chest X-ray (detailed results not available to me) I didn't see another place to provide this information: my first vaccination dose was on 04/29/2021 and my second was on 05/19/2021
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Daily: Truvada (emtricitabine-tenofovir (TDF) 200-300 mg), valacyclovir (500 mg), vitamin D supplement
Allergien: Clindamycin (mild -- rash)
Vorherige Impfungen: -

VAERS 1876415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 55,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 24.07.2021
Beginn: 15.09.2021
Tage bis Beginn: 53,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Tinnitus

Symptomtext

Tinnitus became extremely loud approximately 1 month after 2nd shot and has not quieted down since.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asymptomatic RA, mild Tinnitus, Mitral Valve Prolapse
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1872278

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: PA
Alter: 75,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 20.08.2021
Beginn: 20.08.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Back pain Chest pain Herpes zoster Immunisation Off label use Rash

Symptomtext

had his third booster shot on 20Aug2021; had his third booster shot on 20Aug2021; got shingles; had a slight pain in the chest/ pain was on the patient's left chest and back; rash; pain was on the patient's left chest and back; This is a spontaneous report from a contactable consumer. A 75-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EW0186), via an unspecified route of administration, administered in Arm Left on 20Aug2021 11:00 (At the age of 75 years) as DOSE 3 (BOOSTER), SINGLE for covid-19 immunisation at Pharmacy. Medical history included Kidney transplant (patient got his kidney transplant 11 years ago). Concomitant medications included tacrolimus (TACROLIMUS) and mycophenolate mofetil hydrochloride (CELLCEPT [MYCOPHENOLATE MOFETIL HYDROCHLORIDE]), both taken for an unspecified indication, start and stop date were not reported, high blood pressure medication, and cholesterol medication. The patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL9266), via an unspecified route of administration, on 23Feb2021 (At the age of 74 years) as DOSE 1, SINGLE for covid-19 immunization and also received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN5318), via an unspecified route of administration, on 16Mar2021 (At the age of 75 years) as DOSE 2, SINGLE for covid-19 immunization. Patient did not took other vaccination within 4 week of COVID vaccine. The patient had his third booster shot on 20aug2021 on 20aug2021, got shingles, had a slight pain in the chest/ pain was on the patient's left chest and back, rash, pain was on the patient's left chest and back on 2021. Event reported as, the patient had a slight pain in the chest area which is where the shingles started. The patient thought it was a back ache which began three days before the rash bloomed. The pain was on the patient's left chest and back. On 20Aug2021 the patient got the shot and he got the shingles medication on 26Aug2021. The patient clarified and confirmed that he had 3 doses total of the Pfizer covid vaccine. This event happened after the third dose. The patient said Aspercream helped a lot on the shingles. Adverse event resulted in physician office visit. Therapeutic measures were taken as a result of got shingles. At the time of reporting the outcome of the event shingles was recovering and for rest of the other events the outcome was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Kidney transplant (patient got his kidney transplant 11 years ago)
Andere Medikamente: TACROLIMUS; CELLCEPT [MYCOPHENOLATE MOFETIL HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 1857761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 12.07.2021
Beginn: 08.11.2021
Tage bis Beginn: 119,0
Dosis: UNK
Route/Site: IM / -

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

Arthralgia Back pain Chest discomfort Dyspnoea Dyspnoea exertional Nausea Pain Productive cough Secretion discharge

Symptomtext

hest discomfort. Patient reports that she has been experiencing left sided chest discomfort for the past couple days and it has been occurring off and on. She states that the pain radiates to her left shoulder and all the way to her back. Patient reports an associated SOB and she can no longer walk without getting out of breath. She also reports that she has been nauseous and coughing up brown mucus.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: CHF, hyperlipidemia, HTN and cardiac stents
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1851407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: AZ
Alter: 55,0
Geschlecht: F
Eingang: 08.11.2021
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: ja Erholt: nein

Aphasia Blood test Dyspnoea Electrocardiogram Feeling abnormal Headache Joint range of motion decreased Laboratory test Nausea Neck pain Pain Pain in extremity Palpitations Throat irritation

Symptomtext

An hour after taking the vaccine she started having a mental fogginess, she had difficulty forming words. About 4hrs later she had severe arm pain where she couldn't lift her arm. 8 to 10 hrs later she started to get a racing heart rate and shortness of breath. She developed severe post neck pain that radiate to the top of her head. She had nausea and a linger in her throat. She went to the ER on Nov 3rd.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: yes blood work, lab, ekg
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: codeine, sulfa drugs, augmentin , amitriptyline, ibuprofen, melatonin, nitrofurantoin, fluoxetine, trazodone,
Vorherige Impfungen: -

VAERS 1646775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 28,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 21.07.2021
Beginn: 04.08.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: - / LA

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

Anaemia Asthenia Cytogenetic analysis Gait disturbance Haemoglobin Basal ganglia infarction Hypoaesthesia Magnetic resonance imaging head abnormal Muscular weakness Hemiparesis Hypoaesthesia oral Language disorder Tachycardia Slow speech Transient ischaemic attack Vaccination complication

Symptomtext

Hospitalizaed 8/4-8/9/2021 at Hospital due to TIA. Workup showed anemia and acute right basal infarcts on brain MRI. Team suspected delayed adverse reaction to COVID vaccine. Symptoms started Aug 4th- left arm weakness and numbness, left leg weakness, facial numbness and slow speech. Symptoms occurred intermittently from 5:45am-11:00 am. Weakness immediately resolved with glucose water. Treated with lovenox (unsure of dose) x 2, plavix x 2 doses, crestor high dose initially, then switched to daily x 1 month, ASA daily x 1 month; ferrous BID x 1 month, now down to daily dosing.

Weitere VAERSDATA-Felder

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

VAERS 1837683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

moderat

Staat: WA
Alter: 44,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 01.06.2021
Beginn: 04.06.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Extrasystoles Incomplete course of vaccination Inflammation Influenza like illness Painful respiration Palpitations

Symptomtext

1. Heart inflammation for about 1 month after the 1st shot. It was occasionally quite painful to fully inhale. 2. Heart palpitations for about 3 days. Some skipped beats followed by big pumps. Both symptoms started ~3 days after the 1st shot. I did not get a 2nd shot due to these severe side effects. I also experienced flu-like symptoms about 18 hours after the vaccine, but those completely went away after another 12 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: I was told not to bother reporting side effects unless I needed to go to the hospital. Which I did not do.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1836754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 22.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / AR

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

Asthenia Balance disorder Blood culture negative Body temperature increased COVID-19 Chest X-ray normal Condition aggravated Culture urine positive Diarrhoea Dysstasia Dysuria Enterococcus test positive Escherichia test positive Fall Headache Loss of personal independence in daily activities Malaise Pollakiuria

Symptomtext

Hospitalized 10/24/2021; COVID-19 positive 10/24/2021; fully vaccinated BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider at Discharge: NP Admission Date: 10/24/2021 Discharge Date: 10/27/2021 HOSPITAL COURSE: PT is a 61 y.o. female, PMH of CAD s/p PCI in 2017, COPD o2 dependent, DM, HLD, who presented to hospital with generalized weakness. EMS received a call for lift assist at her house and found her on the ground supine. She was lost her balance with her cane and fell over and could not get up. Neighbor stated that she was not acting herself and EMS thought she felt warm and took a temperature here the temperature is 38.2?. She reported a frontal headache over the past day with no visual acuity changes. She denied any ear pain, nasal congestion, denies any loss of taste or smell. She denied any sore throat. Denied any midline neck or back pain. She denied any chest pain shortness of breath or cough. She denied any abdominal pain. She did report frequency of urine and slight dysuria. She has no changes in bowel habits including constipation and states she always has loose stool secondary to being on metformin. Patient received her 3rd COVID-19 immunization 2 days PTA and the symptoms started yesterday. She was febrile in the emergency room. She was on 3L O2 which is her baseline. CXR did not show any acute process. Her U/A was abnormal, procalcitonin elevated. She was started on Rocephin for UTI. Cultures obtained. Due to her weakness, she could not be discharged home and was admitted for further management. Patient's COVID symptoms started 10/23/21. Tested positive on 10/24/21. She required 3L o2 NC (baseline is around 2L 02), CXR did not show any acute process. There was no need for Decadron or remdesivir at that point. She was given and Lovenox daily for prophylaxis and supportive management. She remained stable and was weaned down to baseline 2L 02. She was started on Rocephin for UTI. Cultures grew E. coli and enterococcus; IV antibiotic was changed to Zosyn while awaiting culture sensitivities. PT OT evaluated patient due to her physical debility and recommended home with home health. Blood cultures were negative to date. Patient was given ampicillin secondary to urine culture sensitivities. Patient improved and she was able to be discharged home in stable condition with home health. She was given a prescription for amoxicillin 875 mg 2 times a day for 5 days and lactobacillus for new onset diarrhea the day of discharge. She was instructed to follow-up with her PCP in 5-7 days. All questions and concerns were addressed prior to discharge. 10/27/2021 H&P note (re-admission): Assessment and Plan Medical Decision Making * Physical debility Assessment & Plan Patient was admitted for 10/24-10/27 for UTI ( Ecoli and Enterococcus). She was discharged on amoxicillin after improvement in symptoms. PT/OT recommended home health which was set up. She returned within few hours of her discharge due to continued weakness and inability to care for herself at home. She has part time help with at home for cleaning and cooking, who came and was concerned about her being able to take care of herself as she lives alone. "She states that she felt somewhat weak while she was in the hospital but was having some assistance getting up and once she is standing she is able to get around and stay upright. Her biggest issue is getting into a standing position from lying down or sitting." PT/OT evaluated her in ED and now recommending SAR Care management to assist with placement 10/30/2021 note: Chief complaint Physical debility Assessment/Plan Medical Decision Making * Physical debility Assessment & Plan Patient was admitted for 10/24-10/27 for UTI ( Ecoli and Enterococcus). She was discharged on amoxicillin after improvement in symptoms. PT/OT recommended home health which was set up. She returned within few hours of her discharge due to continued weakness and inability to care for herself at home. She has part time help with at home for cleaning and cooking, who came and was concerned about her being able to take care of herself as she lives alone. "She states that she felt somewhat weak while she was in the hospital but was having some assistance getting up and once she is standing she is able to get around and stay upright. Her biggest issue is getting into a standing position from lying down or sitting." PT/OT evaluated her in ED and now recommending SAR Care management to assist with placement COVID-19 Assessment & Plan She is vaccinated and received her 3rd COVID-19 immunization 2 days PTA and the symptoms started 10/23/21. Tested positive on 10/24/21. She was requiring up to 6L NC on 10/29 ( baseline 2-3L). Now down to 3L She qualified for remdesivir, day 2/5 Continue decadron, day 2 /10 Continuous pulse ox Lovenox daily for prophylaxis CXR was not very clear due to her body habitus 11/1/2021 note: COVID-19 Assessment & Plan She is vaccinated and received her 3rd COVID-19 immunization 2 days PTA and the symptoms started 10/23/21. Tested positive on 10/24/21. SUBJECTIVE: Patient seen today without subjective complaint. She is at her baseline oxygen demand is a -9 L under fluid balance and tolerating medical therapy. Care management is pursuing placement based on physical and occupational therapy recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Dyslipidemia Coronary artery disease Type 2 diabetes mellitus (HCC) COPD (chronic obstructive pulmonary disease) (HCC) Chronic back pain Acute on chronic respiratory failure with hypoxia (HCC) UTI (urinary tract infection) Physical debility Pneumonia due to COVID-19 virus Carotid disease, bilateral (HCC) Hypertension GERD (gastroesophageal reflux disease) Varicose veins of lower extremity with edema, bilateral History of ventricular fibrillation Valvular regurgitation Dysphagia Tobacco abuse, in remission Morbid obesity with BMI of 45.0-49.9, adult (HCC) Lymphedema of both lower extremities PAD (peripheral artery disease) (HCC) Bipolar I disorder (HCC) Cervical radiculopathy Female stress incontinence
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization ALBUTEROL 108 (90 Base) MCG/ACT inhaler amoxicillin (AMOXIL) 875 MG tablet(Expired) aripiprazole (ABILIFY) 20 MG tablet Ascorbic Acid (VITAMIN C) 5
Allergien: Lyrica Diphenhydramine Fentanyl Haldol
Vorherige Impfungen: -

VAERS 1832074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Fatigue Heart rate increased Myalgia Pyrexia

Symptomtext

16 hours after dosage: Chest (heart) pain & Elevated heart rate: 100 beats per minute at complete rest (along with fever, fatigue & muscle pain) 30 hours after dosage: resting heart rate of 85-90 with chest pain & other symptoms reduced 54 hours after dosage: resting heart rate of 70 with symptoms almost gone

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: did not seek medical attention
Aktuelle Erkrankungen: no
Vorgeschichte: hypothyroidism/hashimoto
Andere Medikamente: Hormone replacement therapy (estrogen, progesterone) Synthroid
Allergien: no
Vorherige Impfungen: -

VAERS 1827311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 49,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 20.08.2021
Beginn: 20.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Paraesthesia Vaccination site discomfort Vaccination site pain

Symptomtext

Post injection site pain; Left arm feels heavy around injection site; Left arm tingling; This is a spontaneous report from a non-contactable nurse, the patient. A 49-year-old female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0186) via an unspecified route of administration in the left arm on 20Aug2021 at 12:30 (at the age of 49-years-old) as a single dose for COVID-19 immunisation. Medical history included migraines. The patient had no known allergies. 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. The patient did not receive any other medications within two weeks of vaccination. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0179) via an unspecified route of administration in the left arm on 30Jul2021 (at the age of 49-years-old) as a single dose for COVID-19 immunisation. On 20Aug2021 at 12:30, the patient experienced post injection site pain, left arm felt heavy around injection site and left arm tingling. 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 post injection site pain, left arm felt heavy around injection site and left arm tingling was not resolved at the time of this report. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Migraine (other_medical_history: Migraines)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1827271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 07.06.2021
Beginn: 07.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Arthralgia Joint range of motion decreased Joint stiffness Mobility decreased Pain in extremity

Symptomtext

Since the time of vaccination have experience increasing psin in both the left and right upper arms, across my shoulders which has affected my range of motion. Extreme pain in the mornings; increasing pain in both the left and right upper arms, across my shoulders; increasing pain in both the left and right upper arms, across my shoulders which has affected my range of motion; Extreme pain in the mornings with very limited mobility in upper body.; joint stiffness and tightness; This is a spontaneous report from a contactable consumer, the patient. A 64-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0186) via an unspecified route of administration in the left arm on 07Jun2021 at 13:45 (at the age of 64-year-old), as a single dose for COVID-19 immunisation. The patient had no medical history and had no known allergies. 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. Concomitant medications included colecalciferol (D-3) and calcium (MANUFACTURER UNKNOWN) and unspecified multivitamin; all for unspecified indication from unknown date and unknown if ongoing. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EWO183) via an unspecified route of administration in the left arm on 17May2021at 13:00 (at the age of 64-year-old), as a single dose for COVID-19 immunisation. On 07Jun2021 at 14:00, since the time of vaccination, the patient experienced increasing pain in both the left and right upper arms, across shoulders which had affected range of motion, extreme pain in the mornings with very limited mobility in upper body. Tried to treat with heat therapy and Tylenol but little relief. In pain daily to varying degrees, patient also experienced joint stiffness and tightness. Therapeutic measures were taken as a result of the events and included treatment with heat therapy and Tylenol. Since the vaccination, the patient had been tested for COVID-19. On 13Jul2021, the patient underwent lab tests and procedures which included COVID-19 virus test and the result was negative. The clinical outcome of the event increasing pain in both the left and right upper arms, across shoulders which had affected range of motion, extreme pain in the mornings with very limited mobility in upper body and joint stiffness and tightness was not resolved at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Date: 20210713; Test Name: SARS-COV2(Covid 19) Molecular Assay, NASA; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: D-3; CALCIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1827888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 33,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 27.08.2021
Beginn: 04.09.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: SYR / LA

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

Antiacetylcholine receptor antibody Dysphagia Dyspnoea Movement disorder Musculoskeletal disorder Myasthenia gravis

Symptomtext

Myasthenia Gravis. Shortness of breath, neck and arm function, lack of ability to swallow

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 28,0
Labordaten: 9/27/2021 ACHR binding
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Benadryl
Allergien: None
Vorherige Impfungen: -

VAERS 1824685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 06.07.2021
Beginn: 07.07.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Ageusia Condition aggravated

Symptomtext

can't taste anything was reported as worsened; can't taste anything was reported as worsened; This is a spontaneous report from a contactable consumer or other non hcp (patient herself). A 37-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number: EW0186), dose 2 via an unspecified route, administered in left arm on 06Jul2021 at 14:15 (at the age of 37-years-old) as dose 2, single for covid-19 immunisation. Medical history included menstruation irregular from an unknown date and unknown if ongoing. There were no concomitant medications. Previously the patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection), dose 1 via intramuscular route on 15Jun2021 (at the age of 37-years-old) (Batch/Lot number: EW0172) as dose 1, single for covid-19 immunisation. On 07Jul2021, the patient reported she she can't taste anything was reported as worsened. She took her second shot yesterday and today she can't taste anything. The patient got the shot yesterday at about 2:15 pm. Now the caller and her boyfriend were having breakfast and she can't taste the syrup on her pancakes or eggs but may be able to taste some salt in the ham. The event can't taste anything was reported as worsened. The outcome of both the events was not recovered at the time of this report. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Irregular menstrual cycle (Verbatim: Irregular menstrual cycle)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1813563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: VA
Alter: 51,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 23.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Condition aggravated Psoriasis

Symptomtext

Abrupt worsening of plaque psoriasis requiring phototherapy or oral medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Long standing very mild plaque psoriasis
Vorgeschichte: Psoriasis
Andere Medikamente: Estradiol 0.5 mg daily
Allergien: None
Vorherige Impfungen: -

VAERS 1812873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

moderat

Staat: MI
Alter: 43,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 18.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Chest discomfort Cold-stimulus headache Dizziness Feeling cold Insomnia Migraine Nausea Photophobia Rhinorrhoea

Symptomtext

Terrible Migraine headache; nausea; light sensitivity; Cold down my arm, then up my arm, & up my neck; felt like a cold blanket was wrapped around my lungs; Felt like I got a halls lozenge stuck in my lungs overnight; What felt like a cold spot in the middle of my brain; Dizziness; Nose was just pouring; Tossing and turning all night couldn't sleep; This is a spontaneous report from a contactable consumer or other non healthcare professional. A 43 year old non pregnant female patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Left on 18May2021 12:30 (Batch/Lot Number: Ew0186) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included coeliac disease from an unknown date and unknown if ongoing , drug hypersensitivity from an unknown date and unknown if ongoing known allergies to Penecillin, codeine, morphine, neosporin, gluten. Concomitant medication(s) included naproxen sodium (ALEVE) taken for an unspecified indication, start and stop date were not reported. The patient previously took codeine and experienced drug hypersensitivity, morphine and experienced drug hypersensitivity, neosporine and experienced drug hypersensitivity, gluten and experienced drug hypersensitivity. The patient experienced cold down her arm, then up her arm, & up her neck with feeling cold on 18May2021 13:00 with outcome of unknown, felt like a cold blanket was wrapped around her lungs on 18May2021 13:00 with outcome of unknown, nose was just pouring causing rhinorrhoea on 18May2021 with outcome of recovered , terrible migraine headache on 18May2021 13:00 with outcome of unknown , nausea on 18May2021 13:00 with outcome of unknown,,light sensitivity causing photophobia on 18May2021 13:00 with outcome of unknown , tossing and turning all night couldn't sleep causing insomnia on 18May2021 with outcome of unknown , felt like she got a halls lozenge stuck in her lungs overnight causing chest discomfort on 18May2021 13:00 with outcome of unknown, what felt like a cold spot in the middle of her brain causing cold-stimulus headache on 18May2021 with outcome of unknown and dizziness on 18May2021 with outcome of unknown. Follow-up (14Jul2021): Follow-up attempts are completed. No further information is expected Follow-Up (28Jul2021): Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Celiac disease; Penicillin allergy (known allergies: Penecillin, codeine, morphine, neosporin, gluten)
Andere Medikamente: ALEVE
Allergien: -
Vorherige Impfungen: -

VAERS 1791170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: KY
Alter: 41,0
Geschlecht: M
Eingang: 23.10.2021
Impfdatum: 03.05.2021
Beginn: 01.05.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Blood test Brain fog CSF oligoclonal band present Dyspepsia Hypoaesthesia Lumbar puncture Magnetic resonance imaging Myelitis transverse Neuropathy peripheral Feeling abnormal Vaccination site induration Laboratory test normal Lumbar puncture normal Magnetic resonance imaging head normal Magnetic resonance imaging spinal abnormal Mass Pain in extremity Paraesthesia

Symptomtext

Brain fog; Digestive issues; Huge knot on his left arm; This is a spontaneous report from a contactable consumer (patient). This consumer reported events for two separate vaccine doses. This is the second of two reports. This report is for the events related to the first vaccine dose. A 41-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), first dose via an unspecified route of administration, administered in the left arm on 03May2021 at 10:00am (Batch/Lot Number: EW0176, at age 41-years-old at vaccination) as a single dose for COVID-19 immunisation at a pharmacy/drug store. Medical history and concomitant medications were not reported. The patient had no prior vaccinations (within 4 weeks) of the BNT162B2 vaccine. On 03May2021, the patient received the first dose of the BNT162B2 vaccine. On an unspecified date in May2021 (after the first vaccination), the patient experienced a huge knot on his left arm and it has remained the same. It was hard as a rock. The patent has been having a lot of side effects since the vaccine and one is brain fog which began around 18May2021 at the latest after the first dose of the vaccine and was ongoing and continues to get worse. He has an appointment with a neuropsychologist to undergo testing to see what was going on. He has a lot of digestive issues and was undergoing tests. The digestive issues also began around the same time as the brain fog and was ongoing and worst. Treatment for event digestive issues included taking Linzess 150mg once per day by mouth since 24Sep2021. The outcome of events huge knot on his left arm, brain fog and digestive issues was not recovered.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101314920 Same patient/reporter; different dose/AE

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

VAERS 1367220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 70,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 17.05.2021
Beginn: 01.05.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Arthralgia COVID-19 Dyschromatopsia Eye pain Headache Feeling abnormal Joint stiffness Inappropriate schedule of product administration Pain Vaccination site pain Musculoskeletal stiffness Pain in extremity Paraesthesia Vitreous floaters

Symptomtext

Felt like someone was putting pins on her head; Eyes are hurting; Hurt when they stuck the needle in; Joints were hurting/ knees were hurting; The joints were hurting on her right side where they put it. It was stiff; All over her body it felt like pins going in; Seeing green and another color bright shells going; Joints were hurting/ knees were hurting; Pains all over the body/pain on left; I wasn't gonna take the second one, what I went through! at least I got one vaccine; This is a spontaneous report from a contactable consumer, the patient report that: A 70-years-old female patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Right on 17May2021 (Batch/Lot Number: EW0186) as dose 1, single for covid-19 immunisation (age at the vaccination 70 years old). Medical history included hospitalisation from 2020 to an unknown date She was hospitalized for pneumonia, hysterectomy, and COVID19, confirmed hospitalizations were prior to COVID shot, pneumonia from an unknown date and unknown if ongoing She was hospitalized for pneumonia, hysterectomy, and COVID19, hysterectomy from an unknown date and unknown if ongoing She was hospitalized for pneumonia, hysterectomy, and COVID19, thrombosis from an unknown date and unknown if ongoing and Pneumonia shot at pharmacy. The concomitant medication was not reported. The patient wasn't gonna take the second one, what Ishe went through at least she got one vaccine. On 17May2021, the patient experienced Felt like someone was putting pins on her head, Eyes are hurting, Hurt when they stuck the needle in and on an unspecified date in May2021, Joints were hurting/ knees were hurting, the joints were hurting on her right side where they put it. It was stiff, All over her body it felt like pins going in, Seeing green and another color bright shells going, Pains all over the body/pain on left. She took COVID shot on Monday and everything was ok. It did hurt when they stuck the needle in. She was delicate. Eight hours later she felt like someone was putting pins on her head. She rubbed it because it hurt. The joints were hurting on her right side where they put it. It was stiff. She did exercise and started moving it because she didn't want it to be stiff. It has been hurting. When she was asleep she was seeing green and another color bright shells going. She was experiencing someone poking her with a needle in her leg. The second shot was worse and she feels like that will be a danger. Could you imagine the side effects from the second shot. She said in the paper that the second one was more stronger. She doesn't plan to get the second one. Something could happen to her with the second shot. The paper said the second shot would have side effects. She went through the first one and look what happen. She doesn't want to end up in the hospital. All over her body it felt like pins going in. Her knees were hurting. She has been through so much. She has been in the hospital three times this last year. They put a lot of shots in her stomach for blood clots. She can't go through that again. She was hospitalized for pneumonia, hysterectomy, and COVID19. She had all the hospitalizations in 2020. When she got home after she had pneumonia, 2 days later she had COVID19 because one of her family members had it. She confirmed hospitalizations were prior to COVID shot. When she got up in the morning and last night she had pains all over the body. For 8 hours it was stiff but then it was fine. She also had pain on the left. She has had fever shot and pneumonia shot and not had this issue. She gets the fever shot every year. She doesn't want to get the second COVID shot. It gets stiff when she gets the fever shot and the pneumonia shot hurts because it was in the muscle. She doesn't have NDC, lot, and expiry to provide for the fever shot or the pneumonia shot. She gets them at and she throws the paper away. She has not had a fever. COVID shot vaccination card: the lot number was handwritten. It was either EW0186 or EWD186. She was supposed to go in three weeks for second dose. The patient underwent lab tests and procedures which included covid-19: positive. The outcome of the event pains all over the body/pain on left was recovered on an unspecified date in May2021 and Eyes are hurting was not recovered and rest all the events was unknown. Description of Product Complaint: Description of complaint: Caller reporting adverse event with first COVID shot. While providing information caller stated the second shot is worse and she feels like that will be a danger. They say in the paper that the second one is more stronger. She doesn't plan to get the second one. Product strength and count size dispensed: N/A as caller has not received the second shot. Follow-up (19Jul2021): Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: SARS-CoV-2; Result Unstructured Data: Test Result:Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Clot blood; Hospitalization (She was hospitalized for pneumonia, hysterectomy, and COVID19); Hysterectomy (She was hospitalized for pneumonia, hysterectomy, and COVID19); Pneumonia (She was hospitalized for pneumonia, hysterectomy, and COVID19)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1804676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 36,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Blood test Dyspnoea Heart rate increased Nausea Palpitations Wheezing

Symptomtext

About 10 minutes after receiving the vaccine, I started feeling like I had a fast heart beat. It felt like my heart was beating out of my chest. I was still waiting for my 15 minute waiting period. When I was sitting with the attendant I started feeling a shortness of breath. The attendant did an assessment for the heart and lungs. At that point the attendant asked me a few more questions. I started to feel queasy as well. The attendant suggested taking me to the emergency department. They took me to the emergency department quickly. By the time we got into the front lobby I was having even more difficulty breathing. My heart was at 130 BPM. They put me in a bed in the emergency department. Once I was in the room I was still having difficult breathing, a fast heart rate, and I felt nauseas. They gave me epi in my left leg. Then they put an iv in my right arm. They gave me 50mg of Benadryl and 1 liter of saline. My heart rate was at 120-130 BPM. They stated that I had wheezing in my lungs. An hour and a half later they had stopped hearing any wheezing, and I had no problems with my breathing. It took a little while longer for my heart rate to go down to 80-90 BPM. Within 20 minutes of that I started to feel better. They kept me for observation for 4 hours. After the 4 hours I went home. They prescribed me prednisone 50mg 1xday for 3 days. They diagnosed me with an allergic reaction. Today I feel a slight tightness when breathing. My heart rate is a little higher than normal ranging from 70-80 BPM when usually it's like 60-70 BPM. My breathing isn't back to normal still.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Bloodwork
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma Bleeding disorder
Andere Medikamente: Albuterol Tranexamic Acid 650mg 3xday for the week of my period
Allergien: sulfa drugs
Vorherige Impfungen: -

VAERS 1762155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: SC
Alter: -
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 02.09.2021
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Alopecia Arthralgia Condition aggravated Fatigue Laboratory test normal Joint swelling Peripheral swelling Systemic lupus erythematosus

Symptomtext

lupus; significant increase in hair loss; increased fatigue; joint pain; the feeling of swelling in joints and in particular hands and feet; the feeling of swelling in joints and in particular hands and feet; This is a spontaneous report from a contactable consumer. A 49-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Right on 02Sep2021 (Lot Number: EW0186) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included COVID-19, lupus, joint pain. Patient was not pregnant. Concomitant medication(s) included cetirizine hydrochloride (ZYRTEC [CETIRIZINE HYDROCHLORIDE]); omeprazole; famotidine; vitamin d nos; curcuma longa (TURMERIC [CURCUMA LONGA]) taken for an unspecified indication, start and stop date were not reported. No other vaccine in four weeks. The patient previously took antibiotics and experienced neurological reactions, and experienced allergies. The patient experienced lupus, significant increase in hair loss, increased fatigue, joint pain, the feeling of swelling in joints and in particular hands and feet in Sep2021. Clinical course reported as: In addition to the normal side effects that were fairly strong and lasted for several days for me, I also had significant increase in hair loss that began in the days after the vaccine and has continued to the present day (almost 5 weeks post injection); increased fatigue; joint pain and the feeling of swelling in joints and in particular hands and feet. Everything has gradually improved (although still present) except the hair loss. The joint pain was a problem in the past with lupus but has not been an issue for many years and it just started again after the vaccine. I have not received the second injection yet due to these lingering symptoms. No treatment received for the events. Outcome of events was recovering. AE resulted in Doctor or other healthcare professional office/clinic visit. Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Joint pain; Lupus erythematosus
Andere Medikamente: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; OMEPRAZOLE; FAMOTIDINE; VITAMIN D NOS; TURMERIC [CURCUMA LONGA]
Allergien: -
Vorherige Impfungen: -

VAERS 1762155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: SC
Alter: -
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 02.09.2021
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / RA

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

Alopecia Arthralgia Condition aggravated Fatigue Laboratory test normal Joint swelling Peripheral swelling Systemic lupus erythematosus

Symptomtext

lupus; significant increase in hair loss; increased fatigue; joint pain; the feeling of swelling in joints and in particular hands and feet; the feeling of swelling in joints and in particular hands and feet; This is a spontaneous report from a contactable consumer. A 49-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Right on 02Sep2021 (Lot Number: EW0186) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included COVID-19, lupus, joint pain. Patient was not pregnant. Concomitant medication(s) included cetirizine hydrochloride (ZYRTEC [CETIRIZINE HYDROCHLORIDE]); omeprazole; famotidine; vitamin d nos; curcuma longa (TURMERIC [CURCUMA LONGA]) taken for an unspecified indication, start and stop date were not reported. No other vaccine in four weeks. The patient previously took antibiotics and experienced neurological reactions, and experienced allergies. The patient experienced lupus, significant increase in hair loss, increased fatigue, joint pain, the feeling of swelling in joints and in particular hands and feet in Sep2021. Clinical course reported as: In addition to the normal side effects that were fairly strong and lasted for several days for me, I also had significant increase in hair loss that began in the days after the vaccine and has continued to the present day (almost 5 weeks post injection); increased fatigue; joint pain and the feeling of swelling in joints and in particular hands and feet. Everything has gradually improved (although still present) except the hair loss. The joint pain was a problem in the past with lupus but has not been an issue for many years and it just started again after the vaccine. I have not received the second injection yet due to these lingering symptoms. No treatment received for the events. Outcome of events was recovering. AE resulted in Doctor or other healthcare professional office/clinic visit. Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Joint pain; Lupus erythematosus
Andere Medikamente: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; OMEPRAZOLE; FAMOTIDINE; VITAMIN D NOS; TURMERIC [CURCUMA LONGA]
Allergien: -
Vorherige Impfungen: -

VAERS 1793864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 03.08.2021
Beginn: 07.08.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / RA

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

Asthenia Biopsy skin Blood test Burning sensation Computerised tomogram head Electromyogram Hypoaesthesia Illness Magnetic resonance imaging head Paraesthesia

Symptomtext

Numbness, tingling, burning, weakness which spread throughout my body . I?m still very sick and feel very weak for 10 weeks now . I Saw multiple drs and was in Emergency Rooms , and still have no diagnosis and no treatment. I may still need to seek emergency care and am still waiting to get another test that will be done in the hospital.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: EMG - 8/16/21, 9/9/21, 9/15/21, 10/12/21 MRI of brain and neck -8/12/21 Ct scan of brain -8/11/21 Multiple blood tests drawn- 30 vials Skin biopsies -9/30/21
Aktuelle Erkrankungen: None
Vorgeschichte: Gerd Osteoporosis High cholesterol
Andere Medikamente: Zetia Famotidine Diamox Ecotrin
Allergien: Yes
Vorherige Impfungen: -

VAERS 1793593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 30,0
Geschlecht: M
Eingang: 16.10.2021
Impfdatum: 23.09.2021
Beginn: 23.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest X-ray Chest pain Echocardiogram Electrocardiogram Inflammation Magnetic resonance imaging heart

Symptomtext

Severe chest pain, inflammation of the heart.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG 9/27/21; Vitals 9/27/21 Blood work 9/27/21 Chest x-Ray 9/27/21 Echocardiogram 10/15/21 Cardiac MRI - pending
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1782858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: SC
Alter: 71,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 02.09.2021
Beginn: 02.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Erythema Fatigue Headache Injection site reaction Mobility decreased Nausea Pain Pain in extremity Paraesthesia Peripheral swelling

Symptomtext

Pt had pain, swelling and redness in left arm that went down her arm that was size of a large apple. She also had fatigue, nausea, chills, headache, all over body aches with no fever. She felt like pins and needles were sticking her in the skin around the vaccination site. She took Tylenol 500mg. She was very tired so stayed in bed for about 4 days. Her symptoms lasted a couple of weeks but still to this day she has days that she still gets tired, nauseated, and achy.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: IVSD, Meniere's Disease, Tinnitus (left ear), Sinusitis, High Cholesterol,
Andere Medikamente: oxcarbazepine 150mg, lorazepam .5 mg, baby aspirin 81 mg, ezetimibe 10mg, Vitamin D3 2000 Units
Allergien: praluent pen, succinylcholine, metoprolol, penicillin, Augmentin, Crestor, Demerol, carbatrol, daclosen, gabapentin, HCTZ, Keflex, latex, Levaquin, Lyrica, Macrobid, Sulfa, Tamaflu, Zithromax, Zocor, Pravachol,
Vorherige Impfungen: 1st Covid Vax - pt had redness and swelling in left arm with no pain.

VAERS 1782727

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 50,0
Geschlecht: M
Eingang: 13.10.2021
Impfdatum: 25.05.2021
Beginn: 26.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Hypoaesthesia Neuralgia Paraesthesia

Symptomtext

tingling, pain, and numbness of the radial nerve from the armpit to the fingertips

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Irbesartan-HCTZ, Amlodipine Besylate, Rosuvastatin
Allergien: none
Vorherige Impfungen: -

VAERS 1782374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MA
Alter: 41,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 26.08.2021
Beginn: 03.09.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / RA

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

Blood glucose increased Blood lactic acid increased Blood magnesium decreased Blood potassium decreased Condition aggravated Diabetes mellitus Rash Sepsis Type 2 diabetes mellitus

Symptomtext

Been in and out of Hospital since 09/05/21-09/27/21 and again on 10/03/21-10/07/21 and again on 10/12/21 for a Rash from head to toe - Front and Back of Body since receiving the 3rd Booster Pfizer shot. Was absolutely fine before the 3 rd booster shot . Have run into problems with being septic and my Type 2 Diabetes sugars elevating into 500-900 and my Potassium and Magnesium being severely low that my AICD may go off

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 38,0
Labordaten: 10/05/21 Lactic Acid - 3,3mg/dl 10/12/21 Lactic Acid - 3.2mg/dl
Aktuelle Erkrankungen: Coarctation of Aorta AICD/Pacemaker Congestive Heart Failure - Category C GERD Endometriosis Scoliosis
Vorgeschichte: Coarctation of Aorta AICD/Pacemaker Congestive Heart Failure- Category C GERD Obstructive Sleep Apnea Endometriosis Scoliosis
Andere Medikamente: Lasix Cymbalta Magnesium Potassium Propranolol Valtrex Zyrtec Omeprazole Meclizine Aygestin Lipitor
Allergien: Buvipicaine Morphine Vicodin Zomig Toresmide Metformin Adhesive Tape Chicken pox live vaccine #2 Eggplant
Vorherige Impfungen: -

VAERS 1780152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Crying Dizziness Dyspnoea Inappropriate schedule of product administration Throat tightness

Symptomtext

Approximately 5 minutes after pt received her 2nd Pfizer vaccine, she came out of the room and caught the attention of vaccine staff stating she felt tightness in the chest. she was escorted to the exam room and laid down on exam table. BP 112/80. Patient stated her throat started to feel like it was tightening up, and she felt short of breath. Rapid Response was called:. 1102: RRT called and patient crying and c/o chest tightness and dizziness. Patient alert and oriented. SPO2 99% RA HR 87 BP 126/84. Patient denies chest pain, sob, lip/tongue swelling, palpitations. Dr. in room assessing patient and listening to heart and lungs. Per MD no medication needed at this time. 1105: SPO2 100% HR 85 Per MD order patient may be d/c home if feeling better and VSS. Will continue to monitor. 1116: SPO2 100% RA HR 61 BP 122/84. Patient reports feeling better and denies chest pain, sob, lip/tongue swelling, dizziness, or any other s/s distress. Patient states that husband in the parking lot. Patient offered UC appt but refuses at this time. ED and 911 precautions provided with any change or worsening in condition and patient verbalized understanding with intent to comply.She was discharged shortly after additional observation by their nurse. FYI, while I was giving her her vaccine, pt reported she ended up in the ED after her first dose back in March. She had similar symptoms almost immediately after the shot that lasted a couple hours, and then it happened again 3 days later which is when she went to the ED. They told her it was most likely a panic attack and that it was fine to get the second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Previous reaction to Pfizer Covid Vaccine Hydrocodone
Vorherige Impfungen: Pfizer dose 1, March 2021, similar response.

VAERS 1779654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MT
Alter: 41,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 24.06.2021
Beginn: 23.07.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: IM / LA

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

Electrocardiogram ambulatory abnormal Heart rate increased Palpitations Supraventricular tachycardia Ventricular extrasystoles Ventricular tachycardia

Symptomtext

heart palpitations - started near the end of July and worsened across August and September (still on-going).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: 10/4/21: Halter monitor for 48hrs- showed short runs of SVT, occasional PVC with no VTach. Increased HR at times
Aktuelle Erkrankungen: Pregnancy miscarriage
Vorgeschichte: -
Andere Medikamente: pre-natal vitamin, baby aspirin
Allergien: codine
Vorherige Impfungen: -

VAERS 1779383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: OH
Alter: 43,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 08.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Cough Dyspnoea Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Pt developed Cough, Congestion on Saturday, 10/9/2021 Developed SOB on Monday, 10/11/2021. COVID + and admitted to hospital for Oxygen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 10/11/2021 Covid +
Aktuelle Erkrankungen: URI the week prior. Resolved per patient
Vorgeschichte: None
Andere Medikamente: Unknown
Allergien: None
Vorherige Impfungen: -

VAERS 1775805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 10.10.2021
Impfdatum: 22.07.2021
Beginn: 09.08.2021
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: SYR / LA

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

Condition aggravated Malignant melanoma

Symptomtext

Melanoma went aggressively: lesions started to grow enormously, targeted therapy stoped working Alk the same had happened back in March ,2021 when i was sick with Covid -19. All the same symptoms: lesions were growing vert fast

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 10,0
Labordaten: See all health records from unspecified
Aktuelle Erkrankungen: Melanoma stage IV Diabetes
Vorgeschichte: Melanoma stage iv
Andere Medikamente: Melanoma targeted therapy
Allergien: Penicillin, amoxicillin
Vorherige Impfungen: -

VAERS 1771486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 15,0
Geschlecht: M
Eingang: 08.10.2021
Impfdatum: 05.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / -

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

Chest pain Electrocardiogram ST segment elevation Troponin T increased

Symptomtext

Chest pain 3 days after first dose of COVID-19 vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG - Diffuse ST elevation Troponin (high sensitivity troponin T) 683
Aktuelle Erkrankungen: COVID-19 virus PCR (nasal swab) positive
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1768507

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: AZ
Alter: 13,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 29.06.2021
Beginn: 29.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Condition aggravated Cough Intermenstrual bleeding SARS-CoV-2 test negative

Symptomtext

After each of the COVID injections (Dose 1 and Dose 2) : She had a breakthrough period that lasted for a couple of hours. And then it stopped. For Dose 2, it started a few hours after the injection. Sept 10, 2021 - 4 pm - took her in to her well child visit and the doctor took a look at her throat because she had been coughing. They did a COVID test and had negative results. No treatment, had missed three days of school but the doctor said just to give her OTC cough medicine. She had the cough a good three days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: COVID test - Sept 10 - Doctor visit and negative test result
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: penicillin - rash when much younger so may not be allergy
Vorherige Impfungen: At age 4 - she had charlie horses after the vaccine for a couple of hours and I'm not sure which vaccine it was after

VAERS 1764703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 13.07.2021
Beginn: 05.10.2021
Tage bis Beginn: 84,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Dehydration Troponin increased

Symptomtext

COVID-19 infection; dehydration; elevated troponin

Weitere VAERSDATA-Felder

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

VAERS 1756507

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 02.10.2021
Impfdatum: 25.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain Echocardiogram Electrocardiogram Palpitations

Symptomtext

Two days following vaccination, I started experiencing chest pain, palpitations, pressure which is still continuing. I went to see cardiologist and he believes the inflammation from the vaccine may have exacerbated my mitral valve prolapse resulting in my symptoms, which I have never experienced before the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, echocardiogram
Aktuelle Erkrankungen: -
Vorgeschichte: Mitral valve prolapse
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1753557

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 84,0
Geschlecht: F
Eingang: 01.10.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chest pain

Symptomtext

On 09/29/21 at 1330 contacted and arrived to assist patient who complained of chest pain. No signs of severe distress. A&Ox4 and verbal. Patient was transferred to urgent care via wheelchair with 2 members of urgent care staff.

Weitere VAERSDATA-Felder

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

VAERS 1741879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 18.05.2021
Beginn: 21.08.2021
Tage bis Beginn: 95,0
Dosis: 2
Route/Site: SYR / -

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

COVID-19 Chills Dyspnoea Influenza A virus test Influenza B virus test Productive cough Pyrexia SARS-CoV-2 test positive Urinary tract infection

Symptomtext

59-year-old female presented complaining of shortness of breath. Patient stated that she was recently in the hospital for urinary tract infection. She stated that the day prior to arrival she began having worsening shortness of breath and sputum production. She admitted to fever and chills. She normally wears 4 L nasal cannula at home and today was requiring 6LNC. Pt smokes 4 ppd and has not been wearing her oxygen per husband.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 22,0
Labordaten: SARS-CoV-2 (COVID-19) and Influenza AB Antigens, POC: SARS CoV 2 DETECTED (8/21/2021)
Aktuelle Erkrankungen: -
Vorgeschichte: Activity extremely limited, asthma, COPD, depression, dysphagia, GERD, hypertension, history of MI, blind in left eye, on home O2 (4L NC, 24/7), peripheral vascular disease, RLS, SOB with exertion, ulcer, uses walker, vertigo
Andere Medikamente: Acid reducer, albuterol, Lipitor, Symbicort, Sinemet, Flexeril, Cardizem, Tricor, Vistaril, Motrin, Isordil, Remeron, Ocuflox, Zofran, Protonix, Lyrica, propranolol, Seroquel, Requip, Zoloft, Carafate, Spiriva, Desyrel, Ambien
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 1740875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

moderat

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 21.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Angina pectoris Atrial fibrillation Cardiac flutter Cardiac monitoring Condition aggravated Heart rate increased Palpitations

Symptomtext

On the day of my vaccination I received it at around 4:30 pm -4:45PM on 9-21-21 - I did mention i had an episode of Afib in 2019 - I was asked if I had medical clearance not knowingly if I needed it - I was told no - After my injection - that night around 11-12am I experienced pain twinges in my heart - at least 2 times that night. The next day on 9-22-21, in the AM at work I noticed another set of twinges with pain briefly , later once i got home at at around 5-5:30 PM within 24hours of my vaccine I experienced my heart doing flips and fluttering pounding and decided to check my heart monitor which at that moment detected Atrial-Fibrillation along with heart pounding, heart palpitations fluttering and high heart rate readings up to 135-155. I am still experiencing heart palpitations and flutters.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None - i saw an electro cardio and gave me a heart monitor to wear but no other treatment i am currently going to see a new cardio dr.
Aktuelle Erkrankungen: -
Vorgeschichte: History of heart palpitations.
Andere Medikamente: Junel FE.
Allergien: Penicillin and Seratonins.
Vorherige Impfungen: -

VAERS 1553811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: IN
Alter: -
Geschlecht: F
Eingang: 25.09.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Abdominal discomfort Chest pain Chills Cough Headache Fatigue Inflammation Injection site pain Laboratory test

Symptomtext

I was having chest pain; inflammation in my chest; inflammation and stuff for my chest; I was having chest pain; inflammation in my chest; inflammation and stuff for my chest; Coughing; Headache; Fatigue; This is a spontaneous report from a contactable consumer (patient). This is the first of two reports. This 49-year-old female patient received bnt162b2 (Pfizer Covid19 vaccine), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot Number: EW0186) as dose 1, single for covid-19 immunisation. Medical history included heart medicine. Concomitant medications included hydrochlorothiazide (THIAZIDE) as heart medicine, start and stop date were not reported. Patient stated, she took the 'Thiazide'. She took the heart medicine (further not clarified) 'Thiazide' (Further not clarified). Patient stated, she was calling because she reported the first time with the adverse reaction. Her doctor told her to report, that make sure she report in, calling in about the second one. She did report the first one but she was supposed to report the 2nd one. The Pfizer (Confirmed as Pfizer Covid19 vaccine). Yeah, she had that one she had been sick, so she was getting report to second one yeah but she has told her make sure she calling in. Probed for adverse events faced by patient: patient stated, headache, she was still having them headaches daily, chest pain, and coughing and fatigues. She did let the doctors know. Patient stated, her professional was she was in automotive industry in factory. Height and Weight: patient stated, she was 5'3 and a half, 5'4 somewhat like that and she weigh 180 (pounds), but prior to this she was at personal training at the gym so you can document that since they wanna know all of the activity working out. And note that work, she was prior to all this, she was working out. Lab test: patient stated, yeah, she did have it cause she had to get to the hospital cause she was having chest pain (further not clarified). Treatment: patient stated, they gave her they say inflammation in her chest so they getting out and cough too and put that down to overall she was coughing too she didn't know after the first vaccine she ended up developing a cough so she still have the cough. Vaccination facility type: patient stated, it was at the community hospital cardiac rehabilitation center. It was (facility name). Prior vaccinations: patient stated, no, she didn't. She had been working out at the gym it was going good. Patient further stated, she was taking medications for inflammation and stuff for her chest. Yeah she did. She was like, she was asking that what are they really telling people because right she went to urgent care, urgent care sent her to, she went to urgent care last week. They sent her to the Urgent care (hospital name), she was having chest pain so they sent her to the hospital. Even in the hospital they gave her the treatment for inflammation and stuff, but she was just like and when she went to do the follow up with the doctor she told her to make sure she calling in so that's why she was asking like what you all really telling people like to these things really nobody know how to treat this. Hospitalization details: patient stated, first time, she had to go to urgent care, second time she had to go to the hospital though. 04Sep2021. Patient stated, they discharge her that day (confirmed as 04Sep2021). The outcome of event headache, coughing and fatigue was not recovered. The outcome of other event was unknown. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101205598 same reporter/patient/drug, different dose/event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: Test Name: Lab test; Result Unstructured Data: Test Result: Unknown results.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Heart disorder
Andere Medikamente: THIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 1730482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MO
Alter: 55,0
Geschlecht: M
Eingang: 24.09.2021
Impfdatum: 01.08.2021
Beginn: 01.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Condition aggravated Neuropathy peripheral Paraesthesia

Symptomtext

since the second dose the neuropathy is "three times worse"; since the second dose the neuropathy is "three times worse"; missed work because his feet and legs bother him; like standing on pins and needles; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 55-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, lot number was EW0186 and expiration date was not reported), via an unspecified route of administration, administered in Right Arm on 01Aug2021 at 16:00 hours (Age at vaccination was 55 years) as dose 2, single for covid-19 immunization. Medical history included ongoing neuropathy peripheral. The patient did not have any other adverse event within 4 weeks of vaccination and also prior to vaccination. The patient did not take any additional vaccine. There were no concomitant medications. Previously patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, lot number was EY0584 and expiration date was not reported), via an unspecified route of administration, administered in Right Arm, on 8Jul2021 (Age at vaccination was 55 years) as dose 1, single for COVID-19 immunization. In Aug2021 patient reported that he had a previous diagnosis of peripheral neuropathy in his feet and legs, related to his work in a battery factory, and since the second dose the neuropathy is three times worse like standing on pins and needles. The patient was missed work because his feet and legs bother him, like standing on pins and needles that diabetics usually get, but he was not diabetic. The patient did not perform any relevant tests. Patient was treated with Gabapentin 800mg 3 times a day, which was almost the max dose. Patient states he went to the doctor a week and a half ago and discussed it with him and he said to stick with what he was doing and if it doesn't get better to come back. Patient states it doesn't seem to be letting up, but some days are worse than others. The outcome of all the events was not recovered. No follow up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Peripheral neuropathy (Verbatim: Peripheral neuropathy)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1701921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NC
Alter: 58,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 13.08.2021
Beginn: 16.08.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: - / LA

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

Anticoagulant therapy Atrial fibrillation Blood pressure increased Blood test Cardiac disorder Cardiac septal hypertrophy Chest discomfort Dizziness Dyspnoea Echocardiogram abnormal Hypertrophic cardiomyopathy Palpitations Electrocardiogram abnormal Heart rate increased Heart rate irregular Infusion

Symptomtext

Test revealed asymmetric septal hypertrophy; thickening of heart muscle wall; palpations; chest heaviness; shortness of breath; A-Fib with RVR; This is a spontaneous report from a contactable nurse (patient). A 58-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration and administered in left arm at age of 58-years, on 13Aug2021 08:00 (Lot Number: EW0186) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included Asthma, GERD, Seasonal Allergies, Basal Cell skin cancer. Concomitant medications included montelukast; cetirizine; omeprazole and budesonide, formoterol fumarate (SYMBICORT); all taken for an unspecified indication. There was no other vaccine received in four weeks. The patient previously took NSAIDS and doxycycline and experienced allergies. The patient experienced test revealed asymmetric septal hypertrophy and thickening of heart muscle wall on 17Aug2021; and experienced palpations, chest heaviness, shortness of breath and A-Fib with RVR all on 16Aug2021 13:00. Above adverse events resulted in: Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization and Life threatening illness (immediate risk of death from the event). The patient was hospitalized for above events from 16Aug2021 to 17Aug2021 for one day. Therapeutic measures were taken included EKG, bloodwork, echocardiogram and medications as reported. There was no Covid prior vaccination or Covid tested post vaccination. The events outcome was recovered. The clinical course was reported as follows: 16Aug2021 went to ED for palpations, chest heaviness, shortness of breath. EKG revealed A-Fib with RVR. No previous history. After 5 hours in ED, converted to normal sinus rhythm with Cardizem IV drip. Cardizem drip stopped and placed on by mouth. Heparin drip started. Spent night in hospital and had echocardiogram next morning (17Aug2021). Test revealed asymmetric septal hypertrophy, thickening of heart muscle wall. Discharged on diltiazem and apixaban. PCP said was due to vaccine and after a few months with no events, will be able to discontinue medications. No follow-up attempts are needed. No further information is expected.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of events cardiac septal hypertrophy, hypertrophic cardiomyopathy, palpitations, chest discomfort, atrial fibrillation and dyspnea cannot be totally excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: Test Date: 20210817; Test Name: echocardiogram; Result Unstructured Data: Test Result:Test revealed asymmetric septal hypertrophy; Comments: and thickening of heart muscle wall; Test Date: 20210816; Test Name: EKG; Result Unstructured Data: Test Result:A-Fib with RVR
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Basal cell carcinoma; GERD; Seasonal allergy
Andere Medikamente: MONTELUKAST; CETIRIZINE; OMEPRAZOLE; SYMBICORT
Allergien: -
Vorherige Impfungen: -

VAERS 1701921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NC
Alter: 58,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 13.08.2021
Beginn: 16.08.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: IM / -

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

Anticoagulant therapy Atrial fibrillation Blood pressure increased Blood test Cardiac disorder Cardiac septal hypertrophy Chest discomfort Dizziness Dyspnoea Echocardiogram abnormal Hypertrophic cardiomyopathy Palpitations Electrocardiogram abnormal Heart rate increased Heart rate irregular Infusion

Symptomtext

Test revealed asymmetric septal hypertrophy; thickening of heart muscle wall; palpations; chest heaviness; shortness of breath; A-Fib with RVR; This is a spontaneous report from a contactable nurse (patient). A 58-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration and administered in left arm at age of 58-years, on 13Aug2021 08:00 (Lot Number: EW0186) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included Asthma, GERD, Seasonal Allergies, Basal Cell skin cancer. Concomitant medications included montelukast; cetirizine; omeprazole and budesonide, formoterol fumarate (SYMBICORT); all taken for an unspecified indication. There was no other vaccine received in four weeks. The patient previously took NSAIDS and doxycycline and experienced allergies. The patient experienced test revealed asymmetric septal hypertrophy and thickening of heart muscle wall on 17Aug2021; and experienced palpations, chest heaviness, shortness of breath and A-Fib with RVR all on 16Aug2021 13:00. Above adverse events resulted in: Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization and Life threatening illness (immediate risk of death from the event). The patient was hospitalized for above events from 16Aug2021 to 17Aug2021 for one day. Therapeutic measures were taken included EKG, bloodwork, echocardiogram and medications as reported. There was no Covid prior vaccination or Covid tested post vaccination. The events outcome was recovered. The clinical course was reported as follows: 16Aug2021 went to ED for palpations, chest heaviness, shortness of breath. EKG revealed A-Fib with RVR. No previous history. After 5 hours in ED, converted to normal sinus rhythm with Cardizem IV drip. Cardizem drip stopped and placed on by mouth. Heparin drip started. Spent night in hospital and had echocardiogram next morning (17Aug2021). Test revealed asymmetric septal hypertrophy, thickening of heart muscle wall. Discharged on diltiazem and apixaban. PCP said was due to vaccine and after a few months with no events, will be able to discontinue medications. No follow-up attempts are needed. No further information is expected.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of events cardiac septal hypertrophy, hypertrophic cardiomyopathy, palpitations, chest discomfort, atrial fibrillation and dyspnea cannot be totally excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: Test Date: 20210817; Test Name: echocardiogram; Result Unstructured Data: Test Result:Test revealed asymmetric septal hypertrophy; Comments: and thickening of heart muscle wall; Test Date: 20210816; Test Name: EKG; Result Unstructured Data: Test Result:A-Fib with RVR
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Basal cell carcinoma; GERD; Seasonal allergy
Andere Medikamente: MONTELUKAST; CETIRIZINE; OMEPRAZOLE; SYMBICORT
Allergien: -
Vorherige Impfungen: -

VAERS 1727262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: UT
Alter: 40,0
Geschlecht: F
Eingang: 23.09.2021
Impfdatum: 20.07.2021
Beginn: 21.07.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Chest pain Headache Incomplete course of vaccination

Symptomtext

Chest pains and headaches that lasted for 3 weeks after first Pfizer Covid-19 vaccination. Chose not to receive second dose due to the unusual chest pains and headaches that occurred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: I have not been to the doctor. I don't feel like my doctor would be open to discussing anything negative about the vaccination because they are pushing so hard for everyone to get it.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Armour thyroid and progesterone
Allergien: None
Vorherige Impfungen: -

VAERS 1696953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NJ
Alter: 52,0
Geschlecht: F
Eingang: 23.09.2021
Impfdatum: 13.09.2021
Beginn: 13.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Angioedema Blood pressure measurement Dyspepsia Gastrointestinal tract irritation Lip swelling Erythema Lip oedema Paraesthesia oral Pruritus Palpitations Skin swelling

Symptomtext

Stated that she did have GI symptoms when she got home; She also had indigestion while she was sitting in the waiting area after getting her shot, so she took a Pepcid for relief; Stated that she had some heart racing, but it was probably more of a fight or flight reaction, because it slowed down once she realized that it was only her lips that were swelling; angioedema; lips were tingling and started to swell; a little puffiness left on her lips; lips were tingling and started to swell; This is a spontaneous report from a contactable nurse (patient) via Pfizer sponsored program. A 52-years-old female patient received bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, solution for injection), dose 1 intramuscular, administered in Deltoid Right on 13Sep2021 08:40 AM (at the age of 52-years-old) (Batch/Lot Number: EW0186) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included ongoing Hashimoto's disease and ongoing Blood pressure high, history of anaphylaxis and irritable bowel syndrome (IBS), both from an unknown date and unknown if ongoing. Concomitant medication included levothyroxine sodium (SYNTHROID) taken for Hashimoto's disease from an unspecified start date and ongoing; lisinopril taken for Blood pressure high from an unspecified start date and ongoing; epinephrine (EPIPEN) taken for an unspecified indication, start and stop date were not reported. The patient previously took cipro [ciprofloxacin] for allergic and experienced Anaphylaxis like reaction and celebrex for allergic and experienced angioedema. The patient experienced angioedema (medically significant), lips were tingling and started to swell (medically significant), a little puffiness left on her lips (medically significant), lips were tingling and started to swell (non-serious), all events on 13Sep2021 within about 5-10 minutes after vaccination. She had a history of anaphylaxis, so they told her that she would have to wait there for 30 minutes to make sure she didn't have a reaction and she brought her EpiPen with her. Then the top right of her lips started to tingle and swell. She thought it was the mask that may have been bothering her, so she took the mask down. After 30 minutes, from the midline of her lips to the right, upper and lower, was swollen. She went back to the Pharmacist who gave her the injection for evaluation and he was going to give her a Benadryl tablet, but she asked for liquid Benadryl because she thinks the liquid works better. She took Benadryl 25mg and the swelling started to go down on the right lower side. She continued to wait there at the hospital pharmacy, but the right upper side of her lips stayed swollen and it started to spread to the upper middle, but it didn't quite go all the way over. About 20 minutes after she took the Benadryl, it started to tingle on the top and bottom left of her lips, so she talked to the Pharmacist again and asked for IM Solumedrol 125mg, which was given in her left deltoid since she got her Covid shot in her right deltoid. Stated that the swelling wasn't spreading to her tongue, and she had her EpiPen with her, but didn't need it. They let her go home, and she got home at around 10:30am she took another 25mg of liquid Benadryl. She also took another 25mg of Benadryl that afternoon. Stated that the swelling had started to go down and she just a little puffiness left on her lips, but then at 10:30pm that night her lips started to swell again, so she took 50mg of liquid Benadryl and went to bed. When she woke up this morning, there was just a little swelling on the top, but at 11:00am the swelling started to come back, and it's still there. The swelling is now on her upper and lower lips, on the front and the left side. The only part that is not swollen is the bottom right, which is where the swelling originally started. Stated that she can't take Benadryl right now because she has to work, but she will take some later. It was reported that, lips were tingling and started to swell, which started on one side and then moved around but only stayed on the lips. She has taken Benadryl several times and was given 125mg of Solu-Medrol IM injection. Caller stated she did not have anaphylaxis, just angioedema. She still has swelling on her lips. As per agent, caller has had anaphylactic reactions in the past to other medications. It was reported that caller was having an allergic reaction to the Covid 19 Vaccine, and she wants to know the ingredients in the vaccine, so she knows what she was allergic to and would like to know what were the binders in the vaccine. Stated that the swelling on her lips has gone up and down with medication. The hospital didn't want to give her a Medrol pack, so they only gave her a shot of Solumedrol, but she doesn't know if that was enough, or if it just ramped things up more. None of additional vaccines were administered on same date of the Pfizer Suspect. The patient had not received any other vaccine within 4 weeks. Patient did not receive any recent vaccines for any other conditions prior to the event being reported and did not receive any recent vaccines for SARS-CoV2 other than Pfizer-BioNTech COVID-19 Vaccine prior to the event being reported. Patient had not received any other vaccines around the time of Pfizer-BioNTech COVID-19 Vaccine vaccination, stated that it had been about 1.5-2 years since she was exposed to whooping cough and got that vaccine. When asked for seriousness, caller stated that she had Angioedema. It didn't required her to go to the ER (emergency room), but it did require extra medical attention. Stated that she did not know if she will be able to get the 2nd dose. Stated that she had some heart racing, but it was probably more of a fight or flight reaction, because it slowed down once she realized that it was only her lips that were swelling. She has had anaphylaxis in the past so once she felt the swelling she was getting worried, but then she realized it was only her lips. Angioedema- Swelling and tingling of her lips after receiving the vaccine. Stated that she did have GI symptoms when she got home, but she has IBS so she doesn't think that it was related to the vaccine. She also had indigestion while she was sitting in the waiting area after getting her shot, so she took a Pepcid for relief. The patient underwent lab tests and procedures which included blood pressure was high on an unspecified date. Therapeutic measures were taken as a result of events. Outcome of all events were not recovered.; Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal relationship between the events Angioedema, Lip swelling, Skin swelling and suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:High
Aktuelle Erkrankungen: Blood pressure high; Hashimoto's disease
Vorgeschichte: Medical History/Concurrent Conditions: Anaphylaxis; Irritable bowel syndrome
Andere Medikamente: SYNTHROID; LISINOPRIL; EPIPEN
Allergien: -
Vorherige Impfungen: -

VAERS 1696953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NJ
Alter: 52,0
Geschlecht: F
Eingang: 23.09.2021
Impfdatum: 13.09.2021
Beginn: 13.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Angioedema Blood pressure measurement Dyspepsia Gastrointestinal tract irritation Lip swelling Erythema Lip oedema Paraesthesia oral Pruritus Palpitations Skin swelling

Symptomtext

Stated that she did have GI symptoms when she got home; She also had indigestion while she was sitting in the waiting area after getting her shot, so she took a Pepcid for relief; Stated that she had some heart racing, but it was probably more of a fight or flight reaction, because it slowed down once she realized that it was only her lips that were swelling; angioedema; lips were tingling and started to swell; a little puffiness left on her lips; lips were tingling and started to swell; This is a spontaneous report from a contactable nurse (patient) via Pfizer sponsored program. A 52-years-old female patient received bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, solution for injection), dose 1 intramuscular, administered in Deltoid Right on 13Sep2021 08:40 AM (at the age of 52-years-old) (Batch/Lot Number: EW0186) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included ongoing Hashimoto's disease and ongoing Blood pressure high, history of anaphylaxis and irritable bowel syndrome (IBS), both from an unknown date and unknown if ongoing. Concomitant medication included levothyroxine sodium (SYNTHROID) taken for Hashimoto's disease from an unspecified start date and ongoing; lisinopril taken for Blood pressure high from an unspecified start date and ongoing; epinephrine (EPIPEN) taken for an unspecified indication, start and stop date were not reported. The patient previously took cipro [ciprofloxacin] for allergic and experienced Anaphylaxis like reaction and celebrex for allergic and experienced angioedema. The patient experienced angioedema (medically significant), lips were tingling and started to swell (medically significant), a little puffiness left on her lips (medically significant), lips were tingling and started to swell (non-serious), all events on 13Sep2021 within about 5-10 minutes after vaccination. She had a history of anaphylaxis, so they told her that she would have to wait there for 30 minutes to make sure she didn't have a reaction and she brought her EpiPen with her. Then the top right of her lips started to tingle and swell. She thought it was the mask that may have been bothering her, so she took the mask down. After 30 minutes, from the midline of her lips to the right, upper and lower, was swollen. She went back to the Pharmacist who gave her the injection for evaluation and he was going to give her a Benadryl tablet, but she asked for liquid Benadryl because she thinks the liquid works better. She took Benadryl 25mg and the swelling started to go down on the right lower side. She continued to wait there at the hospital pharmacy, but the right upper side of her lips stayed swollen and it started to spread to the upper middle, but it didn't quite go all the way over. About 20 minutes after she took the Benadryl, it started to tingle on the top and bottom left of her lips, so she talked to the Pharmacist again and asked for IM Solumedrol 125mg, which was given in her left deltoid since she got her Covid shot in her right deltoid. Stated that the swelling wasn't spreading to her tongue, and she had her EpiPen with her, but didn't need it. They let her go home, and she got home at around 10:30am she took another 25mg of liquid Benadryl. She also took another 25mg of Benadryl that afternoon. Stated that the swelling had started to go down and she just a little puffiness left on her lips, but then at 10:30pm that night her lips started to swell again, so she took 50mg of liquid Benadryl and went to bed. When she woke up this morning, there was just a little swelling on the top, but at 11:00am the swelling started to come back, and it's still there. The swelling is now on her upper and lower lips, on the front and the left side. The only part that is not swollen is the bottom right, which is where the swelling originally started. Stated that she can't take Benadryl right now because she has to work, but she will take some later. It was reported that, lips were tingling and started to swell, which started on one side and then moved around but only stayed on the lips. She has taken Benadryl several times and was given 125mg of Solu-Medrol IM injection. Caller stated she did not have anaphylaxis, just angioedema. She still has swelling on her lips. As per agent, caller has had anaphylactic reactions in the past to other medications. It was reported that caller was having an allergic reaction to the Covid 19 Vaccine, and she wants to know the ingredients in the vaccine, so she knows what she was allergic to and would like to know what were the binders in the vaccine. Stated that the swelling on her lips has gone up and down with medication. The hospital didn't want to give her a Medrol pack, so they only gave her a shot of Solumedrol, but she doesn't know if that was enough, or if it just ramped things up more. None of additional vaccines were administered on same date of the Pfizer Suspect. The patient had not received any other vaccine within 4 weeks. Patient did not receive any recent vaccines for any other conditions prior to the event being reported and did not receive any recent vaccines for SARS-CoV2 other than Pfizer-BioNTech COVID-19 Vaccine prior to the event being reported. Patient had not received any other vaccines around the time of Pfizer-BioNTech COVID-19 Vaccine vaccination, stated that it had been about 1.5-2 years since she was exposed to whooping cough and got that vaccine. When asked for seriousness, caller stated that she had Angioedema. It didn't required her to go to the ER (emergency room), but it did require extra medical attention. Stated that she did not know if she will be able to get the 2nd dose. Stated that she had some heart racing, but it was probably more of a fight or flight reaction, because it slowed down once she realized that it was only her lips that were swelling. She has had anaphylaxis in the past so once she felt the swelling she was getting worried, but then she realized it was only her lips. Angioedema- Swelling and tingling of her lips after receiving the vaccine. Stated that she did have GI symptoms when she got home, but she has IBS so she doesn't think that it was related to the vaccine. She also had indigestion while she was sitting in the waiting area after getting her shot, so she took a Pepcid for relief. The patient underwent lab tests and procedures which included blood pressure was high on an unspecified date. Therapeutic measures were taken as a result of events. Outcome of all events were not recovered.; Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal relationship between the events Angioedema, Lip swelling, Skin swelling and suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:High
Aktuelle Erkrankungen: Blood pressure high; Hashimoto's disease
Vorgeschichte: Medical History/Concurrent Conditions: Anaphylaxis; Irritable bowel syndrome
Andere Medikamente: SYNTHROID; LISINOPRIL; EPIPEN
Allergien: -
Vorherige Impfungen: -

VAERS 1722520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: OR
Alter: 35,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 19.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Angiogram Chest X-ray Chest pain Dyspnoea Electrocardiogram Fibrin D dimer Full blood count Gastrooesophageal reflux disease Human chorionic gonadotropin Lip discolouration Metabolic function test Nail discolouration Palpitations Pyrexia Troponin

Symptomtext

I received the 2nd dose of the pfizer vaccine in the morning. I developed a fever in the evening and by the time I was trying to fall asleep my heart began pounding for a period of time. My fever had started going away by morning and about the same time I developed chest pain and shortness of breath. My finger nail beds and lips became discolored (blueish).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: All tests were completed on 5/20/2021. CBC auto differential Comprehensive Metabolic Panel D-dimer quantitative - Tested Positive HCG Serum Qualitative Reflex Troponin CTA Chest W/IV Contrast (PE Protocol) ECG 12 lead XR Chest 2 View
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Norlyda
Allergien: None
Vorherige Impfungen: -

VAERS 1714884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 53,0
Geschlecht: F
Eingang: 20.09.2021
Impfdatum: 08.09.2021
Beginn: 10.09.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / -

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

Asthenia Back pain Chest X-ray Dizziness Dyspnoea Laboratory test Nausea

Symptomtext

Reported nausea on 2nd day post vaccine. Worked 3 twelve hour shifts in the days following vaccination. Began to get worse. On wednesday last week she was weak, dizzy, nausea, back pain, shortness of breath. All seem to be worsening. Was seen in ED with negative labs and CXR. Rested at home the next several days. Still having sx as of today. Advised to seek out COVID testing to rule this out and contact her PCP..

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 9/14/2021 ED visit with labs and CXR
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1713239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

moderat

Staat: MI
Alter: 36,0
Geschlecht: F
Eingang: 18.09.2021
Impfdatum: 14.09.2021
Beginn: 15.09.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Fatigue Headache Hot flush Nausea Pain Pain in extremity Palpitations Vomiting

Symptomtext

Dose 1 I had sore arm, fatigue 36hours. Body aches, chills, fever. Headache. Dose 2 I had sore arm, fatigue over 80hrs, body a he's. Hot flashes, head ache, nausea. Vomiting, and palpations.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: History of SVT. Resolved with surgery.
Andere Medikamente: Motrin
Allergien: None
Vorherige Impfungen: -

VAERS 1711371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 18.09.2021
Impfdatum: 26.07.2021
Beginn: 26.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Chest pain Cognitive disorder Energy increased Erythema Euphoric mood Fatigue Headache Hypoaesthesia Hypoglycaemia Lymphadenopathy Migraine Muscle spasms Oropharyngeal pain Pruritus Respiration abnormal Slow speech Swelling

Symptomtext

had the Covid arm issue; whole upper shoulder got red and swollen; getting red; spasm in left side of neck and jaw area; Breathing issues; Slight headache, what she describes as a pre-migraine on the left side; cognitive issues; slow speech; hypoglycemic; head was itching/started itching internally; tired; surges of energy, with euphoric and high feeling; surges of energy, with euphoric and high feeling; surges of energy, with euphoric and high feeling; major left elbow pain; her left palm got numb including her little finger and ring finger on her left hand; her left palm got numb including her little finger and ring finger on her left hand; shoulder starting hurting really bad, left top side of her shoulder; had an immediate pain on the right side of the breast bone straight through to the scapula; pain, to the middle suture and to the right side of the head all the way to the right jaw resulting in what she calls a classic migraine; swollen lymph nodes; sore throat; This is a spontaneous report from a contactable consumer (patient herself). A 58-years-old female patient received first dose of bnt162b2 (Solution injection; Batch/Lot Number: EW0186), via an unspecified route of administration, administered in Arm Left on 26Jul2021 at 09:00 (at the age of 58-years-old) as single dose for covid-19 immunisation. Medical history included reactivated Epstein Barr, chemical sensitivity, migraine, very low b12 and methylenetetrahydrofolate reductase gene mutation from 2012 and ongoing, this is a genetic mutation, she is C677T as there are different ones, she is the double mutation. The patient's concomitant medications were not reported. Caller reported that she got the first shot in 26Jul2021 and had lots of side effects after the first dose. After the first dose and within the first 5-10 minutes of receiving the first shot she had spasm in left side of neck and jaw area, this lasted several days, and it has resolved. Breathing issues that lasted 15-20 minutes and resolved. Slight headache, what she describes as a pre-migraine on the left side. She has a history of migraines. It then moved, the pain, to the middle suture and to the right side of the head all the way to the right jaw resulting in what she calls a classic migraine. This lasted about an hour and a half. She started having cognitive issues which was like a disconnect for her to get out what she is trying to get say, described as slow speech. Caller remarks she is hypoglycemic and has had before. This lasted about 5 minutes, she did better when drank something. She waited for 15 minutes the moved to waiting in the hall. At this time gradually her head was itching, this lasted about 10-15 minutes. She was at the facility she got the shot at for about an hour and a half just to make sure she was ok. In the evening she was tired, this lasted for a few days. It was explained during this time she also had surges of energy, with euphoric and high feeling and then she would get really tired. This lasted a couple days and went back and forth. Within 1 hour of getting the shot she started getting major left elbow pain and her left palm got numb including her little finger and ring finger on her left hand. This last 2-3 days. Her shoulder starting hurting really bad, left top side of her shoulder, not where the injection site was though. The next day her shoulder hurt more and that evening it started getting red. At the 2.5 day mark it started itching internally and the whole upper shoulder got red and swollen. She used ice and took a Tylenol. She would say at 2 days after getting the shot this got worse and was itching but she tried not to scratch. She called urgent care and on the 29th she went to the walking to make sure it was ok, confirmed she had the Covid arm issue, a mild case. even now she will get a twinge of itchiness but went away from the top but moved to the injection site. This lasted until at least 12Aug2021, so for 2.5 weeks or maybe 3 weeks. She remarks she also had swollen lymph nodes for brief time, this lasted 1.5 to 2 days. She had a sore throat at the same as swollen lymph nodes. Within the first 10 minutes, she had an immediate pain on the right side of the breastbone straight through to the scapula. This lasted awhile; it lasted about week. The events breathing issues, slight headache, what she describes as a pre-migraine on the left side, cognitive issues, hypoglycemic and head was itching/started itching internally was resolved on 26Jul2021. The outcome of the events spasm in left side of neck and jaw area, pain, to the middle suture and to the right side of the head all the way to the right jaw resulting in what she calls a classic migraine, tired, surges of energy, with euphoric and high feeling, shoulder starting hurting really bad, left top side of her shoulder, swollen lymph nodes and sore throat was resolved on unspecified date in 2021 while the outcome of major left elbow pain and her left palm got numb including her little finger and ring finger on her left hand was resolved on Jul2021. The outcome of the events had an immediate pain on the right side of the breast bone straight through to the scapula, had the Covid arm issue, getting red and whole upper shoulder got red and swollen was resolved in Aug2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: B12 deficiency anaemia (Verbatim: very low b12); Chemical sensitivity (Verbatim: Chemical sensitivity); Epstein-Barr virus infection reactivation (Verbatim: reactivated Epstein Barr); Migraine (Verbatim: Migraine); MTHFR gene mutation (this is a genetic mutation, she is C677T as there are different ones, she is the double mutation)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1709059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: UT
Alter: 37,0
Geschlecht: F
Eingang: 17.09.2021
Impfdatum: 25.08.2021
Beginn: 27.08.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Back pain Chest pain Hypoaesthesia Insomnia Neck pain Neuralgia Pain Pain in extremity

Symptomtext

All pain is located only on the right side of my body where the second shot was received. Second shot received 8/25 and on Friday 8/27 I had right side pain under my arm and chest as if I had been doing weights, but I had not. On Sunday 8/29 I had severe pain down my right side arm which included shooting nerve pain down my arm intermittently with numbness throughout the whole day. From then on through today 9/17/2021 I have had occasional shooting nerve pain down my arm and spine however I have had almost constant right side arm pain, neck pain, and upper back pain. If I do not use my arm it will not go away but I am right-handed so the more I use it the worse it gets. If I am cleaning the house it hurts but if I go rowing it hurts to the point I cannot sleep and have to take pain pills. As of 9/17/21 it has not stopped. I mentioned it at the doctor office, the nurses said it was very common and to be happy it was only one side of my body because they had a lot of patients that had problems on both sides.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None they said it is normal with the shot and wait it out.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Welbutrin
Allergien: No
Vorherige Impfungen: -

VAERS 1704984

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: OR
Alter: 14,0
Geschlecht: M
Eingang: 16.09.2021
Impfdatum: 05.06.2021
Beginn: 22.08.2021
Tage bis Beginn: 78,0
Dosis: 1
Route/Site: IM / UN

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

Alanine aminotransferase increased Bilirubin conjugated increased Blood albumin decreased Blood bilirubin increased Blood creatinine increased Blood culture negative Blood fibrinogen increased Blood glucose normal Blood sodium normal Blood urea normal Brain natriuretic peptide increased C-reactive protein increased Decreased appetite Diarrhoea Fatigue Fibrin D dimer Hypotension Immature granulocyte count increased

Symptomtext

right neck pain, fatigue, anorexia, then emesis, fever, red eyes, rash, diarrhea, tachycardia, hypotensive, cervical lymphadenopathy IVIG, pulse steroids, anakinra

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 9,0
Labordaten: sterile pyuria, lymphopenia, elevated neutrophils, elevated procalcitonin, CRP, ESR neg blood culture normal LP COVID PCR neg Spike AB positive 8/30 before ivig Nucleocapside AB positive 8/30 before IVIG W BC of 10.493% neutrophils and ALC of 400 with elevated immature granulocytes. ESR 57, ferritin of 1609, CRP of 33 procalcitonin of 13, D-dimer of 6.45, PT 15.9 INR 1.2 PTT 41, fibrinogen 774, BNP 174 troponin 63, albumin 3.3 -- >2.4, total bili 2.3 direct greater than 2, ALT 45, sodium 140, glucose 124, creatinine 1.2 with a BUN of 12.
Aktuelle Erkrankungen: None
Vorgeschichte: BMI>95% pediatric Reactive airway disease Cystic acne with scarring
Andere Medikamente: Accutane, isoretinoin 40mg PO daily since about 3 weeks prior to illness onset
Allergien: None
Vorherige Impfungen: -

VAERS 1696919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

moderat

Staat: MI
Alter: 45,0
Geschlecht: F
Eingang: 14.09.2021
Impfdatum: 27.08.2021
Beginn: 28.08.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Blood test Chest X-ray Chest pain Computerised tomogram Dyspnoea Electrocardiogram Extra dose administered Fatigue Fibrin D dimer Hypersomnia Impaired work ability Inflammation Pain Pneumonia Pyrexia SARS-CoV-2 test Urine analysis

Symptomtext

Started feeling tired, fever, severe body aches. Drank lots of fluids and took Tylenol. Was told one fever was gone I could return to work per employee health (nurse at Ortho office). I went back to work after missing 2 days (short staff as everyone) because fever had come down but still could not get over the exhaustion. Came home went to sleep till morning which is completely abnormal for me. I made it through the next two days of work feeling like I couldn't breath well but figured it was hustling with the masks on and then I woke up with the post severe pain in my chest and struggling to breath. Went to Emergency Dept. And was diagnosed with pneumonia 3 lobes and what Dr. Called what looks to be an inflammatory response in addition which may be a results of the 3rd vaccine but no data to compare. I was the first in my health system to have the 3 vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: 9/13/21 They did EKG, multiple blood tests including, d-dimer, urine, covid, chest extra x-ray, and CT
Aktuelle Erkrankungen: None
Vorgeschichte: RA, Lupus, Adult onset chronic stills disease, high BP, DDD, Spinal stenosis, thyroid
Andere Medikamente: Methotrexate, propranolol, omeprazole,levothyroxine, Lasix, gabapentin, duloxetine, Vit d3, b12, multivitamin
Allergien: Penicillin, morphine
Vorherige Impfungen: Fever, chils, GI issues, muscle and joint pain. 44, 1/9/21 covid pfizer

VAERS 1696181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: VA
Alter: 57,0
Geschlecht: F
Eingang: 14.09.2021
Impfdatum: 13.09.2021
Beginn: 14.09.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Hyperhidrosis Palpitations

Symptomtext

While getting ready for work after waking at 05:30am, my heart began racing at 120 bpm. I did not do any exercise or exertions to trigger this. I play tennis on the weekend and during the week and run for an hour twice a week. The heart rate decreased to 90 about 15 minutes later, but that is still well above my resting heart rate. At work, I usually quickly walk a 0.1 mile lap while waiting for my water to heat in the microwave (about 2 minutes). At the end of this lap, I was diaphoretic and my heart rate was 114. I never sweat while walking inside. At home at 18:35pm my heart rate is still above my resting pulse by about 20bpm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Migraineur
Andere Medikamente: Vitamin B Complex, Calcium + Vitamin D, Osteo BiFlex Triple Strength, magnesium hydroxide 250mg. Sumatriptan 50mg prn, Aspirin-acetaminophen-caffeine combo.
Allergien: Penicillin, season allergies
Vorherige Impfungen: -

VAERS 1694944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 37,0
Geschlecht: M
Eingang: 13.09.2021
Impfdatum: 21.08.2021
Beginn: 22.08.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Dyspnoea Fatigue Heart rate increased

Symptomtext

The day after Pfizer vaccine dose #1 pt c/o burning sensation to the chest, shortness of breath, fatigue and rapid heart beat. Same symptoms except for the rapid heart beat persisted until pt presented for dose #2 on 9/11/21- pt was informed he should seek medical attention to r/u cardiac involvement (myocarditis/pericarditis).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None known, pt referred for medical evaluation- when calling patient today to check on him, he stated he was not going to the doctor- once again, encouraged to seek medical attention.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1693427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

moderat

Staat: MI
Alter: 34,0
Geschlecht: F
Eingang: 12.09.2021
Impfdatum: 02.06.2021
Beginn: 05.06.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / LA

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

Barium swallow Chest X-ray Chest discomfort Computerised tomogram thorax Dyspnoea Electrocardiogram Panic reaction Pulmonary function test Stress echocardiogram

Symptomtext

Started feeling tightness in chest and hard time getting a full breath. It gets worse in the evening and makes me panic because I feel that I can't breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Chest 2 views frontal/ lateral 7/21/2021; CT chest w/ IV contrast 8/20/2021; Modified barium swallow 8/23/2021; Pulmonary function test 8/24/2021; Electrocardiogram 8/27/2021; Stress echo 8/27/2021.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Emgality 120ml
Allergien: None
Vorherige Impfungen: -

VAERS 1693235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MA
Alter: 17,0
Geschlecht: F
Eingang: 11.09.2021
Impfdatum: 19.08.2021
Beginn: 19.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Chills Electrocardiogram normal Oral pain Pain

Symptomtext

Briefly, is a 17-year-old female with no significant past medical history or family history with concerns for chest pain that began 12 hours after her second Covid 19 vaccine. She said it began last night and was upper chest pain that radiated to her mouth. She did have some mild chills at that time but no fevers. It lasted for a couple of hours and now has since resolved after eating a sandwich and taking some Tylenol. She had no shortness of breath or cough. No palpitations or syncope. No abdominal pain. Had no clear exacerbating symptoms and no relationship to exertion. No family history of cardiac concerns. My examination revealed the patient to be active, alert, and in no distress. The HEENT exam was clear, the neck was supple, the lungs clear to auscultation, no crackles or wheeze, no increased work of breathing, no abnormal cardiac sounds, no murmur or gallop, no reproducible chest pain, the abdomen was nontender throughout, no hepatomegaly. No lower extremity edema. ED course: 17-year-old female with concerns for chest pain and chills 12 hours after receiving the second COVID-19 vaccine. Now has complete resolution of her symptoms but seems primarily related to eating and Tylenol. She has no other red flag symptoms such as exertional pain, palpitations, or syncope. Has normal vital signs at this time with a normal examination. Low concerns for vaccine induced myocarditis or other cardiac etiology but will obtain EKG. More likely related to chills and possibly myalgias or could be some GERD related symptoms given it was resolved with food. EKG grossly normal however does show possible T wave change in V3 that is possibly mildly elevated although this may not fully meet criteria. Given this and her recent vaccine status will discuss with cardiology. Cardiology felt this was benign early repolarization and no other acute concerns on EKG. Will followup with PCP and aware of signs and symptoms of when to return including recurrence of CP, SOB, syncope, or other concerns. Patient safe for discharge to home. Discharged in improved condition. Written instructions reviewed with family.

Weitere VAERSDATA-Felder

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

VAERS 1689811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 24.08.2021
Beginn: 24.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Hypotension Immediate post-injection reaction Pulse abnormal Tachycardia

Symptomtext

Pfizer 2nd dose administered at 1030am and immediately patient reported feeling difficulty breathing. 911 was called at 1030am. 0.3mg of Epinephrine was administered on right vastus lateralis and patient expressed slight relief. Patient had tachycardia with weak pulses and hypotension. Second dose of 0.3mg epinephrine given at 1036am. Paramedics arrived at 1037am.

Weitere VAERSDATA-Felder

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

VAERS 1689799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 24.08.2021
Beginn: 24.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Dizziness Dyspnoea Pallor

Symptomtext

Patient complained of dizziness, slight chest pressure with pallor observed. No itching, redness or hives. Offered to rest on gurney. Ice pack on back of neck and water with some relief. Rechecked after 15min, patient complains of difficulty breath. Head elevated, no wheezing. Audible stridor. EpiPen administered at 1332 and 911 dispatched.

Weitere VAERSDATA-Felder

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

VAERS 1689603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

moderat

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 23.05.2021
Beginn: 24.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test abnormal Condition aggravated Mobility decreased Renal impairment White blood cell count increased

Symptomtext

BOTH vaccines put me in bed for 4 days straight like I had already covid but I had covid 3 months before. Since I get my blood tested every 3 months it was tested after having covid and was normal and then when I got the vaccine it was tested in all my numbers were off the chart. It made my kidneys drop down to 39, my white blood cell count went Sky High the infection numbers went up a whole bunch of numbers were off and they're never off they never change

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: June 7, 2021. Unable to print out results.
Aktuelle Erkrankungen: just the 1st pfizervaccine put me in bed for 4 days, and i had already had covid in January
Vorgeschichte: high blood pressure, AFIB, kidneys were damaged by contrast dye in 2014 with a 47 GFR, that went down to 39 adter pfizer vaccine.
Andere Medikamente: Losartan for high blood pressure , Eliquis blood thinners, and Dilthizem for AFIB, keflex to be sure my highbone infection never comes back
Allergien: no
Vorherige Impfungen: -

VAERS 1685064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: OH
Alter: 34,0
Geschlecht: F
Eingang: 09.09.2021
Impfdatum: 09.09.2021
Beginn: 09.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Injection site coldness Injection site paraesthesia Paraesthesia

Symptomtext

Cold tingling sensation around injection site that soon radiated down to forearm. Currently that problem has passed but left a constant tingling sensation in tip of left index finger for over an hour now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Topical cream for rosacea
Allergien: None
Vorherige Impfungen: -

VAERS 1682963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 23,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 27.06.2021
Beginn: 26.07.2021
Tage bis Beginn: 29,0
Dosis: 2
Route/Site: IM / RA

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

Chest pain Dyspnoea exertional Pain in extremity Paraesthesia Peripheral swelling Weight increased

Symptomtext

The patient is a 23 year old female, PMHx , presents to the ER c/o intermittent L sided chest pain and arm pain/paresthesias x 3 weeks. States to become more short of breath with exertion with gradual increased swelling of extremities, and gradual weight gain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: obesity
Andere Medikamente: Medroxyprogesterone 10mg daily for 10 days each month, pantoprazole 40mg every morning, sumatriptan nasal spray.
Allergien: None known
Vorherige Impfungen: -

VAERS 1682700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: IN
Alter: 19,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 18.08.2021
Beginn: 25.08.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / AR

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

Muscular weakness Paraesthesia

Symptomtext

Patient states that about one week after vaccination she noticed tingling / weakness in her pinky and ring finger which radiates to her arm. Today is three week out and patient state it still is bothersome. Recommended patient not take 2nd dose until reviewed with a healthcare provider.

Weitere VAERSDATA-Felder

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

VAERS 1681981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: PA
Alter: 42,0
Geschlecht: M
Eingang: 08.09.2021
Impfdatum: 02.08.2021
Beginn: 02.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Burning sensation Chest pain Dyspnoea Fatigue Poor quality sleep

Symptomtext

shortness of breath appears; I felt burning in the heart area; I have constant pain in the chest, sometimes lower, sometimes stronger; I feel constant fatigue, tiredness; I don't have enough sleep; This is a spontaneous report from a contactable consumer, the patient. A 42-years-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, solution for injection, lot number: EW0186, expiry date was not reported), via an unspecified route of administration, administered in Arm Left on 02Aug2021 (age at vaccination: 42-years-old) as dose 2, single for covid-19 immunisation. The patient did not have any other medical history or known allergies. The patient's concomitant medications were not reported. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, solution for injection, lot number: EW0181, expiry date was not reported), via an unspecified route of administration, administered in Arm Left on 23Jun2021 (age at vaccination: 42-years-old) as dose 1, single for covid-19 immunisation. On 02Aug2021, patient felt burning in the heart area which lasted for 2-3 weeks, after that he had constant pain in the chest, sometimes lower, sometimes stronger. After the second shot, he felt constant fatigue, tiredness as he did not have enough sleep. Often, when walking, shortness of breath appeared, and chest pain increased. Patient did not receive any treatment for the events. He did not have covid prior vaccination and not tested for covid post vaccination. Patient did not have other vaccine in four weeks and not received other medications in two weeks. The outcome of the event burning in the heart area was recovered and the other events was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1681910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 07.08.2021
Beginn: 01.08.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Axillary pain Cardiac flutter Chest discomfort Chest pain Erythema Hyperhidrosis Rhinorrhoea Feeling hot Insomnia Joint range of motion decreased Neck pain Pain in extremity Peripheral swelling Vaccination site erythema Vaccination site pain

Symptomtext

chest flutters / still experiencing the flutters; runny nose; sweating / sweating on her forehead; staying hot; when the flutters happen there's a little pain/ very painful, extended into neck, armpit and lower arm that kept her up at night.; a little tightening that comes and goes; arm was swollen; couldn't lift the shoulder or arm up; it was red where the needle went in; it was red where the needle went in at the injection site, very painful; it was red where the needle went in at the injection site, very painful, extended into neck, armpit and lower arm; it was red where the needle went in at the injection site, very painful, extended into neck, armpit and lower arm; it was red where the needle went in at the injection site, very painful, extended into neck, armpit and lower arm; it was red where the needle went in at the injection site, very painful, extended into neck, armpit and lower arm; kept her up at night; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 58-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 07Aug2021 (Batch/Lot number was not reported) at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient received first dose of the Pfizer BioNTech Covid 19 vaccine on 07Aug2021 and is due for her second dose on 28Aug2021. About a week after in Aug2021 she developed a runny nose and developed flutters, chest flutters. Her nose was starting to dry out but was still experiencing the flutters and has been sweating on her forehead and staying hot. She said it didn't feel like a fever and hadn't taken her temperature but she did sweat and that she got hot. She had the flutters throughout the day, not constant, it came and went. She got the shot in the left arm. Sometimes when the flutters happen there was a little pain with it, a little tightening that came and went. However, there's not always pain that's associated with it. The sweating happened first and then she got the flutters. Her husband got the vaccine and had no problems. She had a TDaP shot in her left arm back on 15Oct2012 for immunization and had a severe reaction. She had done fine with other tetanus shots in the past but she said she was told that after age 40 you receive a combination and that's the one she had this reaction with. Her arm was swollen, couldn't lift the shoulder or arm up, it was red where the needle went in at the injection site, very painful, extended into neck, armpit and lower arm that kept her up at night. The outcome of chest flutters was not resolved, the outcome of other events was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

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

VAERS 1678617

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 03.09.2021
Beginn: 04.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Abnormal dreams Arthralgia Change of bowel habit Chest discomfort Chest pain Cognitive disorder Dyspnoea Fatigue Feeling jittery Heart rate increased Hot flush Migraine Nausea Night sweats Pain in extremity

Symptomtext

Arm sore Tired Nauseous Night sweat Fast heartbeat, pulse Extremely jittery Hot flashes Ocular migraine Vivid dreams Trouble focusing and remembering what I?m doing/saying Heartburn? Not sure if that?s the right word but a pain/tightness in chest The need to do a little cough Feels like not enough breath to talk Wrist pain (feels like my blood is too thick or something. No other way to describe it)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None yet. Considering going to hospital soon
Aktuelle Erkrankungen: Slight cold a few weeks before
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: High fever after pertussis as baby

VAERS 1674394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CT
Alter: 13,0
Geschlecht: F
Eingang: 04.09.2021
Impfdatum: 06.06.2021
Beginn: 08.06.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / LA

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

Angiogram Blood test Computerised tomogram Electrocardiogram Headache Magnetic resonance imaging Migraine SARS-CoV-2 test Thinking abnormal Venogram Visual impairment

Symptomtext

Bad headaches; She complained of visual disturbance; She also said that she noticed she was thinking differently; complex migraine; This is a spontaneous report from a contactable consumer (patient). A 13-years-old female non-pregnant patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot Number: EW0186), dose 2 via an unspecified route of administration, administered in Arm Left on 06Jun2021 at 10:15 (at the age of 13-years-old) as a DOSE 2, SINGLE for covid-19 immunisation. The patient medical history was none. The patient's concomitant medications were not reported. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot Number: EW0185), dose 1 via an unspecified route of administration, administered in Arm Left on 16May2021 at 10:15 AM (at the age of 13-years-old) as a DOSE 1, SINGLE for covid-19 immunisation. No events reported after first dose. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 08Jun2021 at 15:30 the patient experienced bad headaches, she complained of visual disturbance, she also said that she noticed she was thinking differently and complex migraine. Reporter said that, my daughter got a 2nd dose of the Pfizer vaccine on 06Jun2021 and began having bad headaches that night that continued through Tuesday. On Tuesday she complained of visual disturbance. when she looked at my face she couldn't see the right side in entirety, and when she looked at her phone she couldn't see the digits on the right side of the phone. She also said that she noticed she was thinking differently: she couldn't remember how to spell the simple work "because" for example and was processing really slowly when reading very different than the norm. When I called her pediatrician to ask about this he suggested we go to the ER and not take any chances. She was immediately given catscan, bloodwork, EKG and extensive testing with MRI, MRA, MRV. All tests came back normal, and we were told to follow up with neurologist and ophthalmologist. The ER doc & neurologist we saw in the ER suggested it could have been a complex migraine. But she never complained of headaches before. Events resulted in the Emergency room/department or urgent care. Treatment was received for the events. Hospitalization was not required. The patient underwent lab tests and procedures which included angiogram which was normal on Jun2021 MRA, blood test that was normal on Jun2021, computerised tomogram that was normal on Jun2021, electrocardiogram that was normal on Jun2021, magnetic resonance imaging that was normal on Jun2021, sars-cov-2 test that was negative on 08Jun2021 and venogram which was normal on Jun2021. Outcome of all the events were recovered in 2021. Results of tests and procedures for investigation of the patient were negative for blood test on 08Jun2021. Relevant medical history and concurrent conditions were none. Device Date was reported as 09Jun2021. Case was reported as non-serious. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 202106; Test Name: MRA; Result Unstructured Data: Test Result:Normal; Comments: MRA; Test Date: 202106; Test Name: bloodwork; Result Unstructured Data: Test Result:Normal; Test Date: 202106; Test Name: Cat scan; Result Unstructured Data: Test Result:Normal; Test Date: 202106; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Date: 202106; Test Name: MRI; Result Unstructured Data: Test Result:Normal; Test Date: 20210608; Test Name: COVID-19; Result Unstructured Data: Test Result:Negative; Test Date: 202106; Test Name: MRV; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1673314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 39,0
Geschlecht: F
Eingang: 04.09.2021
Impfdatum: 24.05.2021
Beginn: 24.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Blood pressure measurement Chest discomfort Dizziness Dyspnoea Heart rate irregular Hypotension Investigation

Symptomtext

Took blood pressure noticed it was in the low range; irregular heartbeat; Tightness of chest; trouble taking deep breath; felt lightheaded and dizzy; This is a spontaneous report from a contactable consumer (patient) from Pfizer sponsored program. A 39-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Batch/Lot Number: EW0186), dose 1 via an unspecified route of administration, administered in Arm Right on 24May2021 (age at the time of vaccination was 39-year-old) as dose 1, single for COVID-19 immunization. No Medical history was reported. Concomitant medication(s) included ascorbic acid, betacarotene, calcium sulfate, colecalciferol, cyanocobalamin, ferrous fumarate, folic acid, nicotinamide, pyridoxine hydrochloride, retinol acetate, riboflavin, thiamine mononitrate, tocopheryl acetate, zinc oxide (PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS FUMARATE;FOLIC ACID;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RETINOL ACETATE;RIBOFLAVIN;THIAMINE MONONITRATE;TOCOPHERYL ACETATE;ZINC OXIDE]) taken for an unspecified indication, start and stop date were not reported; vitamin d3 (VITAMIN D3) taken for an unspecified indication, start and stop date were not reported.The patient previously took erythromycin and experienced drug hypersensitivity. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Facility where the most recent COVID-19 vaccine was administered was Hospital. The patient did not test COVID-19 positive prior to vaccination. The patient had not been tested for COVID-19 since the vaccination. It was reported that the tightness of chest and trouble taking deep breaths around 8 PM and next morning felt lightheaded and dizzy on 24May2021. The patient also experienced blood pressure noticed it was in the low range and irregular heartbeat on 25May2021. Those symptoms continued for roughly a month. The events resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures taken for events (Testing and referral for further testing). It was reported that patient saw PCP and after testing was done suggested the patient to visit a neurologist, appointment with neurologist was in Sep2021. Device Date was reported as 21Aug2021. Outcome of all the events was reported as Unknown at this time of the report. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210525; Test Name: blood pressure; Result Unstructured Data: Test Result:low range; Comments: low range; Test Date: 20210525; Test Name: heartbeat; Result Unstructured Data: Test Result:irregular; Comments: irregular
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS ; VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 1673276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 25,0
Geschlecht: F
Eingang: 04.09.2021
Impfdatum: 20.08.2021
Beginn: 20.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Paraesthesia oral Tongue pruritus

Symptomtext

tingling on her lips; Top of tongue itching; This is a spontaneous report from a contactable consumer (patient). A 25-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 vaccine, solution for injection, Batch/Lot Number: EW0186), via an unspecified route of administration, administered in Arm Left on 20Aug2021 at 09:30 Am (at the age of 25-years-old) as dose 1, single for covid-19 immunisation. Medical history included obesity, Chronic asthma from an unknown date and unknown if ongoing. The concomitant medications were none. On 20Aug2021 10:15, 45 minutes after vaccination, the patient experienced tingling on her lips, top of tongue itching. Patient stated 45 minutes post vaccination she felt itchiness on the top of her tongue and tingling on her lips. It was reported that she took Benadryl and that she is on the way to her physician. She took Benadryl and went to sleep for an hour and 30 minutes. When she woke up her lips were sill tinging, but not swollen. She can still feel her lips tingling after the COVID vaccine, but it got better because of Benadryl. Therapeutic measures taken for the events. The outcome of the event tingling on her lips was recovering while for Top of tongue itching was Recovered on Aug2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma chronic; Obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1663803

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

moderat

Staat: NY
Alter: 30,0
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 02.08.2021
Beginn: 09.08.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: SYR / LA

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

Blood pressure increased Blood test abnormal Chest X-ray Chest discomfort Computerised tomogram Dizziness Dyspnoea Echocardiogram Electrocardiogram Fibrin D dimer increased Headache Hypoaesthesia Palpitations Ultrasound Doppler

Symptomtext

Headache, tightness of chest, trouble breathing, numbness in right arm and leg, dizziness, and elevated blood pressure. Went to the ER and was given an EKG, chest X-Ray and CT scan. Blood work was drawn and came back with a high D-Dimer. No clots were found so I was sent to my PCP. More blood was drawn and D-diner was still elevated. Sent to hematologist for more test. Leg Doppler and echocardiogram was also administered. Waiting on MRI for my head. Starting on 8/31/2021, headache followed by numbness to the left side of my face surfaced. Chest is still tight and I often feel like I am having heart palpitations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Doctors said all test appear to be normal with the exception of the D-dimer. Symptoms still persist.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1662748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 20,0
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 31.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Back pain Chest pain Dyspnoea Pain Painful respiration Pyelonephritis Staphylococcus test positive

Symptomtext

20-year-old female presents to the emergency room complaining of right-sided chest pain, primarily located midclavicular approximately rib 2. Patient states pain started this evening, feels sharp. Patient states previously she has felt the same discomfort when she had COVID. She states previous workup did not find anything significant at that time in March 2021. She endorses shortness of breath, states taking deep breaths in makes it worse. She also notes pain radiating through into the back. Patient denies any fevers, chills, nausea, vomiting. Patient got her Pfizer vaccine today in the AM. Patient was seen in the emergency room recently, and diagnosed with mild pyelonephritis, treated with 1 g ceftriaxone and sent home with 5 days of ciprofloxacin. Patient just completed this course. Previous urine culture positive for staph saprophyticus ciprofloxacin susceptible."

Weitere VAERSDATA-Felder

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

VAERS 1655008

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 20,0
Geschlecht: F
Eingang: 30.08.2021
Impfdatum: 12.07.2021
Beginn: 01.07.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

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

Arrhythmia Blood count Cough Decreased appetite Electrocardiogram Headache Nausea Pyrexia SARS-CoV-2 test Vomiting

Symptomtext

EKG: Irregular heartbeat Comments: Arrythmia; severe fever/ high fever; vomiting; cough; nausea; loss of appetite; headaches; The initial safety information received was reporting only non-serious adverse drug reactions. Upon receipt of follow-up information on 20Aug2021, this case now contains serious adverse reactions. Information processed together. This is a spontaneous report from a contactable consumer (patient). A 20-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EW0186), intramuscular in left arm on 12Jul2021 at 18:15 (at the age of 20-years-old) at dose 2, single for COVID-19 immunization. Medical history included chronic migraine from Feb2013 and ongoing. She has no COVID-19 prior to vaccination. Concomitant medications were reported as none. Prior vaccines were reported as none. Family history included her brother having an autoimmune disorder and her father with NFZ and PFO (as reported). The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EW0186), intramuscular in left arm on 21Jun2021 at 18:15 (at the age of 20-years-old) at dose 1, single for COVID-19 immunization. Vaccination facility type was reported as doctor's office/urgent care. On 13Jul2021 at 06:00, the patient experienced severe high fever, vomiting, cough which were reported as causing persistent/significant disability/incapacity. She also experienced nausea, loss of appetite, and headaches on Jul2021. The events resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of all the events. Vomiting was specifically treated with omeprazole-D 40 mg and cough was specifically treated with benzonatate 100 mg, 3x day. The patient underwent lab tests and procedures on 19Jul2021 which included full blood panel: normal range, EKG: irregular heartbeat/ arrhythmia, and COVID test: negative for COVID. The outcome of the event fever and vomiting was recovered on 19Jul2021; recovered on 05Aug2021 for cough; unknown for arrhythmia; and recovered with sequel on Jul2021 for all other events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Test Date: 20210719; Test Name: Full blood pannel; Result Unstructured Data: Test Result:Normal range; Test Date: 20210719; Test Name: EKG; Result Unstructured Data: Test Result:Irregular heartbeat; Comments: Arrythmia; Test Date: 20210719; Test Name: COVID test; Result Unstructured Data: Test Result:Negative for COVID
Aktuelle Erkrankungen: Chronic migraine
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1464064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NJ
Alter: 53,0
Geschlecht: F
Eingang: 29.08.2021
Impfdatum: 07.07.2021
Beginn: 07.07.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Abdominal pain upper Chills Decreased appetite Fatigue Impaired work ability Influenza like illness Migraine Myalgia Oropharyngeal pain Pyrexia Lymphadenopathy Poor quality sleep Sleep disorder

Symptomtext

Slight stomach ache; Loss of appetite; Sore muscles; Chills; Feverish; Very tired and still tired and blah 5 days post shot; Swollen lymph nodes under left armpit; Sore throat; Bad flu like symptoms for two days post shot; Could not get a good sleep; Migraine starting about one hour post shot lasting for 2 days and on and off for up to 5 days; This is a spontaneous report from a contactable consumer, the patient. A 53-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0186) via an unspecified route of administration in the right arm on 07Jul2021 at 15:00 (at the age of 53-years-old) as a single dose for COVID-19 immunisation. Medical history included sleep apnea, high blood pressure (bp), high cholesterol, gastroesophageal reflux disease (GERD) and asthma. The patient had known allergies to eggs. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included valsartan (MANUFACTURER UNKNOWN), pantoprazole (MANUFACTURER UNKNOWN), montelukast (MANUFACTURER UNKNOWN) and rosuvastatin calcium (ROSUVASTIN); all from unknown dates for unknown indications and unknown if ongoing. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0178) via an unspecified route of administration in the left arm on 17Jun2021 at 14:30 (at the age of 53-years-old) as a single dose for COVID-19 immunisation. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 07Jul2021 at 16:00, about one hour post shot, the patient experienced migraine lasting for two days and on and off for up to five days. On 07Jul2021 at 16:30, the patient experienced very tired, sore throat, sore muscles, bad flu like symptoms for two days post shot, loss of appetite, could not get out of bed as so tired but could not get a good sleep, chills and feverish, swollen lymph nodes under left armpit. On 08Jul2021, second day post shot, the patient also had a slight stomach ache. On 12Jul2021, five days post shot, the patient still felt tired and had to take days off of work. 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 events flu like symptoms was recovered with sequelae on 09Jul2021, after the duration of 2 days; while that of the migraine was recovered with sequelae on 12Jul2021, after the duration of 5 days. The clinical outcome of the events sore throat, poor sleep, loss of appetite, sore muscles, chills, feverish, tiredness, swollen lymph nodes, stomach ache was recovered with sequelae on an unknown date in Jul2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma (Minor asthma); Blood pressure high (High bp); Egg allergy (Known allergies: Eggs); GERD; High cholesterol; Sleep apnea
Andere Medikamente: VALSARTAN; PANTOPRAZOLE; MONTELUKAST; ROSUVASTIN
Allergien: -
Vorherige Impfungen: -

VAERS 1464064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NJ
Alter: 53,0
Geschlecht: F
Eingang: 29.08.2021
Impfdatum: 07.07.2021
Beginn: 07.07.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain upper Chills Decreased appetite Fatigue Impaired work ability Influenza like illness Migraine Myalgia Oropharyngeal pain Pyrexia Lymphadenopathy Poor quality sleep Sleep disorder

Symptomtext

Slight stomach ache; Loss of appetite; Sore muscles; Chills; Feverish; Very tired and still tired and blah 5 days post shot; Swollen lymph nodes under left armpit; Sore throat; Bad flu like symptoms for two days post shot; Could not get a good sleep; Migraine starting about one hour post shot lasting for 2 days and on and off for up to 5 days; This is a spontaneous report from a contactable consumer, the patient. A 53-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0186) via an unspecified route of administration in the right arm on 07Jul2021 at 15:00 (at the age of 53-years-old) as a single dose for COVID-19 immunisation. Medical history included sleep apnea, high blood pressure (bp), high cholesterol, gastroesophageal reflux disease (GERD) and asthma. The patient had known allergies to eggs. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included valsartan (MANUFACTURER UNKNOWN), pantoprazole (MANUFACTURER UNKNOWN), montelukast (MANUFACTURER UNKNOWN) and rosuvastatin calcium (ROSUVASTIN); all from unknown dates for unknown indications and unknown if ongoing. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0178) via an unspecified route of administration in the left arm on 17Jun2021 at 14:30 (at the age of 53-years-old) as a single dose for COVID-19 immunisation. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 07Jul2021 at 16:00, about one hour post shot, the patient experienced migraine lasting for two days and on and off for up to five days. On 07Jul2021 at 16:30, the patient experienced very tired, sore throat, sore muscles, bad flu like symptoms for two days post shot, loss of appetite, could not get out of bed as so tired but could not get a good sleep, chills and feverish, swollen lymph nodes under left armpit. On 08Jul2021, second day post shot, the patient also had a slight stomach ache. On 12Jul2021, five days post shot, the patient still felt tired and had to take days off of work. 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 events flu like symptoms was recovered with sequelae on 09Jul2021, after the duration of 2 days; while that of the migraine was recovered with sequelae on 12Jul2021, after the duration of 5 days. The clinical outcome of the events sore throat, poor sleep, loss of appetite, sore muscles, chills, feverish, tiredness, swollen lymph nodes, stomach ache was recovered with sequelae on an unknown date in Jul2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma (Minor asthma); Blood pressure high (High bp); Egg allergy (Known allergies: Eggs); GERD; High cholesterol; Sleep apnea
Andere Medikamente: VALSARTAN; PANTOPRAZOLE; MONTELUKAST; ROSUVASTIN
Allergien: -
Vorherige Impfungen: -

VAERS 1647324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CT
Alter: 33,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 11.08.2021
Beginn: 11.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Cough Dyspnoea Wheezing

Symptomtext

having a hard time breathing; Started out with the need to constantly clear my throat and then became full on wheezing and coughing; Started out with the need to constantly clear my throat and then became full on wheezing and coughing; This is a spontaneous report from a contactable consumer (patient herself). A 33-years-old non-pregnant female patient received first dose of BNT162B2 (COMIRNATY, PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EW0186; Expiration Date: unknown) intramuscular, administered in Arm Left on 11Aug2021 09:00 (at age of as 33-years-old) as DOSE 1, SINGLE for COVID-19 immunization. Patient was not pregnant at the time of vaccination. Medical history and concomitant medications were not reported. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine; nor received any other medications within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. It was reported that, on 11Aug2021 09:30 (about 30mins after) receiving the shot patient started having a hard time breathing. Started out with the need to constantly clear throat and then became full on wheezing and coughing. The adverse event resulted in emergency room visit/department or urgent care. Therapeutic measures were taken as a result of adverse events as patient was checked multiple times within 2 hours. Was told to take inhaler before bed that night. Since the vaccination, patient has not been tested for COVID-19. The outcome of all events was recovered on an unspecified date in Aug2021. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

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

VAERS 1647273

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: RI
Alter: 23,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 16.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: - / LA

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

Angina pectoris Cardiac flutter Dyspnoea Electrocardiogram ambulatory Magnetic resonance imaging Palpitations SARS-CoV-2 test

Symptomtext

severe pains in my heart/squeezing pains in my heart; more heart flutters and palpitations; more heart flutters and palpitations; shortness of breath; This is a spontaneous report from a contactable consumer (patient). A 23-years-old, non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EW0186, Expiration date: Unknown), via an unspecified route of administration, administered in left arm on 16May2021 (at the age of 23-years-old) as dose 2, single for Covid-19 immunization in other facility. The patient did not receive any other vaccines within 4 weeks prior to the Covid vaccine. Since the vaccination, the patient has not been tested for Covid-19. Medical history included depression, anxiety, ptsd (Post-traumatic stress disorder), lactose intolerance, temporal lobe seizures, migraines, known allergies: lithium, Covid-19 (prior to vaccination). Concomitant medication(s) included fluoxetine hydrochloride (PROZAC); vitamin B6; cannabidiol (CBD OIL). The patient historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EW0171, Expiration date: Unknown), via an unspecified route of administration, administered in left arm on 25Apr2021 (at the age of 23-years-old) as dose 1, single for Covid-19 immunisation in other facility and experienced trouble focusing and developed a big headache, her eyes had trouble focusing, she was experiencing severe depersonalization, her legs lost function and she could hardly walk, the rest of her body felt weak but kept doing involuntary movements (like hand opening and closing), she struggled to think or talk, it felt like her body was forgetting how to work, she have been having seizures. Prior to vaccination, patient was diagnosed with Covid-19. Since the vaccination, patient has been tested for Covid-19. On 20May2021, the patient experienced severe pains in her heart/squeezing pains in her heart, more heart flutters and palpitations, shortness of breath. It was reported that, four days after her second shot, she experienced severe pains in her heart and shortness of breath, which brought her back to an ER. Since then, she still has squeezing pains in her heart, but not as frequent nor with shortness of breath as much. Yet she does have more heart flutters and palpitations. The heart pains were very regular and intense for about two weeks after the second dose, where she almost went to the ER several times. The events resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. The patient underwent lab tests and procedures which included heart monitor: results unknown and MRI: results unknown on an unspecified date in 2021, nasal Swab: negative on 06Jul2021. Therapeutic measures were taken as a result of the events with IV fluids, benadryl, Reglan. The outcome of the events was not resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Heart monitor; Result Unstructured Data: Test Result:results unknown; Test Date: 2021; Test Name: MRI; Result Unstructured Data: Test Result:results unknown; Test Date: 20210706; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to chemicals; Anxiety; COVID-19 (Prior to vaccination); Depression; Lactose intolerance; Migraine; Post-traumatic stress disorder; Temporal lobe epilepsy
Andere Medikamente: PROZAC; VITAMIN B6; CBD OIL
Allergien: -
Vorherige Impfungen: -

VAERS 1646972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: WA
Alter: 30,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 06.08.2021
Beginn: 01.08.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / LA

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

Abdominal discomfort Angina pectoris Chest discomfort Dizziness Dyspnoea Fatigue Feeling abnormal Malaise

Symptomtext

feeling off; felt very sick/don't feel too well; Out of breath; Upset stomach; uncomfortable feeling in chest; Tired; Very dizzy all the time; heart is hurting very uncomfortable; This is a spontaneous report from a contactable consumer (patient). A 30-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in left arm on 06Aug2021 (Lot Number: EW0186, unknown expiration; at the age of 30 years old) as dose number unknown, single for COVID-19 immunisation. Medical history reported as none. The patient's concomitant medications were not reported. The patient received the Pfizer COVID-19 vaccine shot on Friday, 06Aug2021. She experienced feeling off on 06Aug2021. It's been 4 days and symptoms are getting worse. She felt very sick and just don't feel too well in Aug2021. The patient also experienced out of breath, upset stomach, and her heart is hurting very uncomfortable in Aug2021. She has uncomfortable feeling in chest, was tired, and very dizzy all the time in Aug2021. The patient took one ibuprofen yesterday (on 09Aug2021). The patient asked what she should do now and if she should go to the ER. The patient had not yet recovered from feeling off, while unknown outcome for the remaining events. No follow-up attempts are possible; information about batch number was already obtained.

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Praegender Schweregrund: Dyspnoea
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 1646674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: WI
Alter: 50,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 05.08.2021
Beginn: 06.08.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Burning sensation Erythema Paraesthesia

Symptomtext

Both arms and tops of hands were burning; Both arms and tops of hands appear reddened the day after vaccine; Showering the warm water felt like pins and needles; This is a spontaneous report from a contactable consumer, the patient. A 50-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0186) via an unspecified route of administration in the left arm on 05Aug2021 at 16:30 (at the age of 50-years-old) as a single dose for COVID-19 immunisation. Medical history included fibromyalgia. The patient had known allergies to dust and shellfish. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not take any concomitant medications. The patient also took epinephrine (MANUFACTURER UNKNOWN) for unknown indication on an unknown date and experienced drug allergy. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. On 06Aug2021 at 11:00, the patient experienced both arms and tops of hands were burning and reddened the day after vaccine. When she showering the warm water felt like pins and needles on her skin. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office or clinic visit, and emergency room or department or urgent care. No therapeutic measures were taken as a result of the reported events. The clinical outcomes of events both arms and tops of hands were burning, both arms and tops of hands were reddened and showering the warm water felt like pins and needles were not resolved at the time of this report.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Dust allergy (Known_allergies: Dust); Fibromyalgia; Shellfish allergy (known_allergies: Shellfish)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1646620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 05.08.2021
Beginn: 05.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Chest discomfort Dizziness Headache Hyperhidrosis Nausea Palpitations Throat tightness Vomiting

Symptomtext

chest tightness; nauseated; vomiting; profuse sweating; Throat tightness; palpitation; Dizziness; headache; This is a spontaneous report from a contactable Nurse (patient self). A 45-year-old female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), intramuscular, administered in Arm Left on 05Aug2021 15:45 (Lot Number: EW0186) (at the age of 45-year-old, not pregnant) as dose 1, single for COVID-19 immunisation. Medical history included Bells Palsy, partial thyroidectomy, hysterectomy, asthma, known allergies: shellfish and Bactrim. Concomitant medication included orlistat. The most recent COVID-19 vaccine was administered in Hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 05Aug2021 16:15, the patient was severely nauseated and vomiting, palpitation with chest tightness and throat tightness, dizziness and headache, profuse sweating. Rapid response called she was sent to ED. The adverse event result in Emergency room/department or urgent care. Treatment received including Benadryl, zofran, Tylenol. Outcome of the events was not resolved. The reporter assessed this report as non-serious.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the events nauseated and vomiting, palpitation with chest tightness and throat tightness, dizziness and headache, profuse sweating and the suspect drug 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 regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to antibiotic; Asthma; Hysterectomy; Palsy Bells; Shellfish allergy; Thyroidectomy partial
Andere Medikamente: ORLISTAT
Allergien: -
Vorherige Impfungen: -

VAERS 1646303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 18,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 29.07.2021
Beginn: 29.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Aphasia Asthenia Asthma Dysphagia Dyspnoea Ear discomfort Ear infection Nasal congestion Oropharyngeal pain Pharyngeal swelling

Symptomtext

felt very weak and winded; felt very weak and winded; an immense amount of pressure in her ears; congestion in her nose; throat began to hurt; throat began to swell; swallowing and speaking became close to impossible; swallowing and speaking became close to impossible; asthma flare up; ear infection; This is a spontaneous report from a contactable consumer (patient). An 18-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration, administered in left arm on 29Jul2021 at 10:15 am (Batch/Lot Number: EW0186) (at the age of 18-yrs-old) as dose 1, single for COVID-19 immunisation. The patient was not pregnant at time of vaccination. Facility where the most recent COVID-19 vaccine was administered was at the Doctor office/urgent care. Medical history included bronchitis in 2011. The patient has no past drug history and concurrent conditions. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received birth control within 2 weeks of vaccination. On 29Jul2021 at 14:00 (4 hours after receiving the vaccine), the patient's throat began to hurt. As more hours passed, her throat began to swell and swallowing and speaking became close to impossible. It was like this for three days following. On the third day (on 01Aug2021) of her throat swelling, she developed an immense amount of pressure in her ears as well as congestion in her nose. The fourth day after receiving the vaccine (on 02Aug2021), she felt very weak and winded. The fifth day after (on 03Aug2021), she went to urgent care as she was still experiencing these symptoms and was informed that she had an asthma flare up. For context, she hasn't had an asthma flare up since she had bronchitis 10 years ago. She was also informed that she had an ear infection. The adverse events resulted in Doctor or other healthcare professional office/clinic visit. The patient received treatment which included Amoxicillin, Benzonatate, Inhaler, and Pseudoephedrine. The patient was not diagnosed with COVID-19 prior to vaccination and the patient has not been tested for COVID-19 Since the vaccination. The outcome of the events was recovering/resolving. 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: Bronchitis (10 years ago)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1646016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

moderat

Staat: IL
Alter: 32,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 29.06.2021
Beginn: 05.07.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: - / LA

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

Dizziness Dyspnoea

Symptomtext

shortness of breath; random light headedness; This is a spontaneous report received from a contactable consumer (patient). A 32-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number ew0186), administered in left arm on 29Jun2021 12:00 PM (at the age of 32-year-old) as dose 2, single for COVID-19 immunization. Vaccination facility type was reported as pharmacy or drug store. The patient's medical history and concomitant medications were not reported. The patient was not diagnosed with COVID-19 prior to vaccination. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number ew0180), administered in left arm on 08Jun2021 12:00 PM (at the age of 32-year-old) as dose, 1 single for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 05Jul2021 the patient experienced random light headedness and shortness of breath both reported as non-serious. No treatment was received due to the events. The patient had not been tested for COVID-19 since the vaccination. The outcome of the events was not resolved. Follow-up (04Aug2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1645995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

moderat

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 29.07.2021
Beginn: 30.07.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Palpitations

Symptomtext

heart is racing; This is a spontaneous report from a contactable consumer, the patient. A 64- year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: Ew0186) via an unspecified route of administration in the left arm on 29Jul2021 at 16:00 (at the age of 64-years-old) as a single dose for COVID-19 immunisation. Medical history included cholesterol, anxiety and menopause. 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. Concomitant medications included vitamins (MANUFACTURER UNKNOWN), escitalopram oxalate (LEXAPRO) and atorvastatin calcium (LIPITOR); all for unknown indication on unknown date, unknown if ongoing. Patient did not know of any allergies to food, medication or other products. On 30Jul2021 at 06:30, the patient experienced heart racing. 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 adverse event heart racing. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event heart racing was not recovered at the time of this report.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Cholesterol; Menopause
Andere Medikamente: LEXAPRO; LIPITOR
Allergien: -
Vorherige Impfungen: -

VAERS 1558231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

moderat

Staat: NC
Alter: 37,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 26.07.2021
Beginn: 26.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Chest discomfort Heart rate increased Pain Chest pain Dyspnoea Heart rate

Symptomtext

Increased Resting Heart rate (~+20BPM); Sharp chest Pains on 3 occasions; Difficulty Breathing; This is a spontaneous report from a contactable consumer reporting for himself. This 37-year-old male patient received on 26Jul2021 16:00 at the age of 37-years first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: ew0186) as single dose in the arm left for Covid-19 immunization. Medical history and concomitant medications were not reported. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, he has not been tested for COVID-19. On 26Jul2021 21:00, the patient had Increased Resting Heart rate (~+20BPM), Sharp chest Pains on 3 occasions, Difficulty Breathing. No treatment was provided. Outcome was recovering. The case was reported as non serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20210726; Test Name: Resting Heart Rate; Result Unstructured Data: Test Result:~+20 BPM
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1558231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NC
Alter: 37,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 26.07.2021
Beginn: 26.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Heart rate increased Pain Chest pain Dyspnoea Heart rate

Symptomtext

Increased Resting Heart rate (~+20BPM); Sharp chest Pains on 3 occasions; Difficulty Breathing; This is a spontaneous report from a contactable consumer reporting for himself. This 37-year-old male patient received on 26Jul2021 16:00 at the age of 37-years first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: ew0186) as single dose in the arm left for Covid-19 immunization. Medical history and concomitant medications were not reported. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, he has not been tested for COVID-19. On 26Jul2021 21:00, the patient had Increased Resting Heart rate (~+20BPM), Sharp chest Pains on 3 occasions, Difficulty Breathing. No treatment was provided. Outcome was recovering. The case was reported as non serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20210726; Test Name: Resting Heart Rate; Result Unstructured Data: Test Result:~+20 BPM
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1509490

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: UT
Alter: 11,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 20.07.2021
Beginn: 20.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Cardiac disorder Cardiac flutter Chest discomfort Dyspnoea Product administered to patient of inappropriate age Chest pain Palpitations

Symptomtext

heart was bugging; heart flutters; He has pressure in his chest; hard to breath; 11 years old; This is a spontaneous report from a contactable consumer (patient). An 11-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, lot number: Lot Number: EW0186), via an unspecified route of administration, administered in Arm Left on 20Jul2021 10:00 as dose 1, single for covid-19 immunization at a pharmacy. Medical history included COVID-19 from Dec2020 to an unknown date. The patient's concomitant medications were not reported. On 21Jul2021 09:00, patient reported that he has pressure in his chest and his heart flutters. At times it is hard to breath. He was at lacrosse practice last night a whole week after the shot and said his heart was bugging him on an unspecified date. He was told to take ibuprofen for the symptoms. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1509490

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

moderat

Staat: UT
Alter: 11,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 20.07.2021
Beginn: 20.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac disorder Cardiac flutter Chest discomfort Dyspnoea Product administered to patient of inappropriate age Chest pain Palpitations

Symptomtext

heart was bugging; heart flutters; He has pressure in his chest; hard to breath; 11 years old; This is a spontaneous report from a contactable consumer (patient). An 11-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, lot number: Lot Number: EW0186), via an unspecified route of administration, administered in Arm Left on 20Jul2021 10:00 as dose 1, single for covid-19 immunization at a pharmacy. Medical history included COVID-19 from Dec2020 to an unknown date. The patient's concomitant medications were not reported. On 21Jul2021 09:00, patient reported that he has pressure in his chest and his heart flutters. At times it is hard to breath. He was at lacrosse practice last night a whole week after the shot and said his heart was bugging him on an unspecified date. He was told to take ibuprofen for the symptoms. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1509490

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: UT
Alter: 11,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 20.07.2021
Beginn: 20.07.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Cardiac disorder Cardiac flutter Chest discomfort Dyspnoea Product administered to patient of inappropriate age Chest pain Palpitations

Symptomtext

heart was bugging; heart flutters; He has pressure in his chest; hard to breath; 11 years old; This is a spontaneous report from a contactable consumer (patient). An 11-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, lot number: Lot Number: EW0186), via an unspecified route of administration, administered in Arm Left on 20Jul2021 10:00 as dose 1, single for covid-19 immunization at a pharmacy. Medical history included COVID-19 from Dec2020 to an unknown date. The patient's concomitant medications were not reported. On 21Jul2021 09:00, patient reported that he has pressure in his chest and his heart flutters. At times it is hard to breath. He was at lacrosse practice last night a whole week after the shot and said his heart was bugging him on an unspecified date. He was told to take ibuprofen for the symptoms. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1505376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: UT
Alter: 44,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 19.07.2021
Beginn: 21.07.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Cardiac flutter Chest discomfort Dyspnoea Panic attack Palpitations

Symptomtext

fluttering heart; panic attack; Pressure in the chest; hard to breath; This is a spontaneous report from a contactable consumer (patient). This non-pregnant 44-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 19Jul2021 10:00 (Lot Number: EW0186) at age of 44-years-old as dose 1, single for COVID-19 immunisation. Medical history included covid-19 from Dec2020. The patient's concomitant medications were not reported. No other vaccine in four weeks. On 21Jul2021 09:00 AM, the patient experienced pressure in the chest, made her feel like it was hard to breath, fluttering heart. Made her feel like she was going to pass out, king of like a panic attack. They came and went. Worried about taking 2nd shot. Had covid back in December. Treatment included ibuprofen. No covid tested post vaccination. The outcome of the events was recovering. 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: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1505376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

moderat

Staat: UT
Alter: 44,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 19.07.2021
Beginn: 21.07.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac flutter Chest discomfort Dyspnoea Panic attack Palpitations

Symptomtext

fluttering heart; panic attack; Pressure in the chest; hard to breath; This is a spontaneous report from a contactable consumer (patient). This non-pregnant 44-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 19Jul2021 10:00 (Lot Number: EW0186) at age of 44-years-old as dose 1, single for COVID-19 immunisation. Medical history included covid-19 from Dec2020. The patient's concomitant medications were not reported. No other vaccine in four weeks. On 21Jul2021 09:00 AM, the patient experienced pressure in the chest, made her feel like it was hard to breath, fluttering heart. Made her feel like she was going to pass out, king of like a panic attack. They came and went. Worried about taking 2nd shot. Had covid back in December. Treatment included ibuprofen. No covid tested post vaccination. The outcome of the events was recovering. 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: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1362037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 15.05.2021
Beginn: 15.05.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Angina pectoris Anxiety Blood test Depression Discomfort Chest pain Cognitive disorder Feeling abnormal Hypoaesthesia Insomnia Malaise Muscle spasms Paraesthesia Muscular weakness

Symptomtext

Full body pins and needles; numb arm; malaise; chest pain; insomnia; cramped legs; brain fog/cannot feel the weight of my own body; cognitive dysfunction; This is a spontaneous report from a contactable consumer (patient). A 33-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 15May2021 (Lot Number: EW0186, expiration date not provide) at age of 33 years old as a single dose for covid-19 immunisation. The patient was not pregnancy at time of vaccination. The patient's medical history and concomitant medications were not reported. The patient experienced full body pins and needles, numb arm, malaise, chest pain, insomnia, cramped legs, brain fog/cannot feel the weight of my own body, cognitive dysfunction, all on 15May2021. The outcome of the events was not recovered. Clinical course: Full body pins and needles for a month, numb arm, malaise, cramped legs, chest pain, brain fog, cognitive dysfunction, insomnia. Currently the patient couldn't feel the weight of her own body for the last four weeks. These last two months had been hell. She couldn't convey how bad it was been. She felt lucky to be alive. All events resulted in doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. No other vaccine received in four weeks. The patient was not COVID prior vaccination. The patient was not tested post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1640734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

moderat

Staat: NJ
Alter: 58,0
Geschlecht: F
Eingang: 27.08.2021
Impfdatum: 29.05.2021
Beginn: 14.06.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / LA

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

Headache Hypertension

Symptomtext

Systemic: Headache-Severe, Systemic: Hypertension-Severe

Weitere VAERSDATA-Felder

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

VAERS 1632307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: -
Geschlecht: U
Eingang: 27.08.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Cough Dyspnoea Palpitations

Symptomtext

Patient recieved COVID 19 vaccine at 7:23AM on 8/24/2021 on 8/24/21 patient developed a cough, chest tightness with difficulty breathing. She went to Hospital. it was crowded she left & went to urgent care following city, urgent care sent patient via ambulance to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal Allergies; H/O COVID 19
Andere Medikamente: None.
Allergien: -
Vorherige Impfungen: -

VAERS 2668978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: -
Geschlecht: F
Eingang: 26.08.2021
Impfdatum: 14.08.2021
Beginn: 16.08.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / -

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

Back pain Chest pain Dyspnoea Hypoaesthesia Pain

Symptomtext

Experienced chest pain with shortness of breath, numbness in the arms and hands, and burning pain in the upper back

Weitere VAERSDATA-Felder

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

VAERS 1636356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 43,0
Geschlecht: F
Eingang: 26.08.2021
Impfdatum: 25.08.2021
Beginn: 25.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Dyspnoea

Symptomtext

Shortness of breath,. Patient, with history of allergies and asthma, said ""my PCP approved me receiving the Pfizer vaccine and I took 2 Benadryl per advise at 7:30 A.M. (Pfizer vaccine administered around 8:47) 9:13 AM Patient reported feeling some shortness of breath and chest tightness and took 2 puffs of her Albuterol inhaler. Pulse ox- 99%, Pulse-99, BP 128/74 Lungs clear. 9:20 reports ""SOB and chest tightness ""dissipating, but feels jittery."" She reports that she has been having to use her Albuterol inhaler more frequently during the past 2 weeks due to seasonal allergies. Observed, symptoms improved 9:42 discharged in stable condition and advised to speak with her MD prior to 2nd vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1633139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 25.08.2021
Impfdatum: 29.07.2021
Beginn: 29.07.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Asthmatic crisis Burning sensation Condition aggravated Dyspnoea Facial pain Lacrimation increased Lymph node pain Lymphadenopathy Lymphoedema Mast cell activation syndrome Nausea Pyrexia Retching Rhinorrhoea Swelling face Throat tightness

Symptomtext

*mast cell mediated respiratory anaphylactoid and asthmatic crisis: shortness of breath, airway constriction, watery eyes, dry heaving, mucus production, and nausea-duration approximately 4 hours critical and 3 days elevated *lymphodemia: swollen, burning, and painful lymph nodes in armpit of injection site and around face/neck-duration approximately 21 days *fever-duration approximately 3 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: see chronic conditions
Vorgeschichte: Mast Cell Activation Syndrome, asthma, endometriosis
Andere Medikamente: Zyrtec, Singulair, famotidine, cromolyn sodium oral and nebulized, Nasalcrom, Combivent inhaler
Allergien: amoxicillin, prednisone, egg, dairy, gluten, fish
Vorherige Impfungen: -

VAERS 1632865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: UT
Alter: 36,0
Geschlecht: M
Eingang: 25.08.2021
Impfdatum: 27.05.2021
Beginn: 28.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / -

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

Blood thyroid stimulating hormone normal Decreased appetite Electrocardiogram normal Full blood count normal Magnetic resonance imaging normal Metabolic function test normal Muscle disorder Muscular weakness Myalgia Thyroxine free normal Tremor Weight decreased

Symptomtext

severe uncontrolled muscle pain despite medication, loss of muscle control, muscle weakness, loss of appetite and 25 pound weight loss over 3 months, development of a pronounced essential tremor in hands, arms, head, and lower extremities

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: EKG, MRI, TSH & free T4, CMP, CBC done at the ER on 8/19 were all normal
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: cephalosporins
Vorherige Impfungen: -

VAERS 1632243

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: VT
Alter: 30,0
Geschlecht: F
Eingang: 25.08.2021
Impfdatum: 20.05.2021
Beginn: 11.07.2021
Tage bis Beginn: 52,0
Dosis: 2
Route/Site: IM / LA

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

Arrhythmia Chest discomfort Chest pain Electrocardiogram ambulatory abnormal Fatigue Injection site pain Lymphadenopathy Palpitations Supraventricular extrasystoles Ventricular extrasystoles

Symptomtext

After the 2nd dose, I developed 5 swollen lymph nodes in my neck and collar bone and 2 in my groin (I already had 2 swollen lymph nodes with the 1st dose). It took 4 weeks to resolve. I also had pain at injection site which resolved after 3-4 days. On July 11, 2021, I woke up with an achy feeling in my chest. I started having loud and hard pounding. I had about 60-70 heart palpitations episodes. I was feeling tired, fatigue, chest heaviness, chest achiness which radiated outwards when I had episode of arrhythmia. I did go see my doctor 2 weeks later on July 28 2021. By the time I saw the doctor, the intensity had decreased. I had to wear a holster monitor which showed premature ventricular contractions and atrial contractions. I was not placed on medications since my cardiac event was not hindering my quality of life or life threatening. As of now, I am still having 10-15 episodes of arrhythmias mostly in the mornings or evenings. I do l get the discomfort/achiness/soreness in my chest when I am having an episode.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: heart holster monitor
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Zyrtec; Microgestin 1/20 birth control pills
Allergien: none
Vorherige Impfungen: -

VAERS 1628703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CO
Alter: 13,0
Geschlecht: M
Eingang: 24.08.2021
Impfdatum: 29.07.2021
Beginn: 20.08.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: IM / RA

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

Brain natriuretic peptide normal C-reactive protein increased Chest pain Echocardiogram normal Electrocardiogram ST segment depression Electrocardiogram ST segment elevation Fatigue Headache Pain Pyrexia Troponin I increased Troponin increased

Symptomtext

One day after second dose, patient developed fatigue, headache and body aches. Two days after 2nd vaccine dose, patient had persistent symptoms, but developed fever to 106 and chest pain. ER evaluation showed abnormal EKG (ST elevation) and elevated troponin to 1523 ng/L. he was admitted for observation, had a normal ECHO and trended troponins. His troponin peaked at 3452, and continued to decrease. he did not require any intervention.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: Troponin 1 High Sensitivity: 8/22: 1523 ng/L, 8/23: 3452-- >2205-- >799-- >1037-- >937. B-type natriuretic peptide: 8/23/21: 59 C-reactive protein on 8/23/21: 5.1 mg/dL ECHO on 8/23/21 was normal EKG on 8/23/21: ST elevation, junctional ST depression
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillins, lactose intolerance
Vorherige Impfungen: -

VAERS 1603060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 39,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 24.05.2021
Beginn: 24.05.2021
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 Heart rate irregular Hypotension

Symptomtext

Around 8pm tightness of chest and difficulty taking deep breathes was noticed - took Benadryl and symptoms eased. Upon waking was lightheaded and took blood pressure irregular heartbeat detected. Low blood pressure, dizziness and irregular heartbeat detected for around a month then self corrected. Was able to see pcp who suggested I see neurologist. Neurologist appointment in September 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D3 and prenatal vitamins
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 1583626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NC
Alter: 42,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Blood test Confusional state Discomfort Dyspnoea Fatigue Feeling abnormal Head discomfort Headache Lethargy Ocular discomfort Urticaria

Symptomtext

Around 6 to 7 hours from the time of the vaccine I got hives on my face started feeling very tired and lethargic with a headache. The next day 5/14/21 I had lots of pressure in my face, jaw, head, neck and behind my eyes as well as shortness of breath and extreme tiredness, brain fog and confusion that has not gone away. The symptoms did not go away so I did not go for the second dose. It has been 3 months now and I still have these symptoms and have frequent headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood work was done on recent visit to the Dr to check.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Womens 1 a day multivitamin
Allergien: Shellfish and seafood allergy
Vorherige Impfungen: -

VAERS 1583625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 28,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 18.08.2021
Beginn: 18.08.2021
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 Chest pain Dizziness Electrocardiogram normal Feeling hot Hernia

Symptomtext

Chest pain from GI Hernia discomfort . Flu referred to GI specialist next wed. Warm feeling dizziness in arm , chest. EKG results wnl. Feeling OK @this and not going to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Bipolar, ADHD, Hernia
Andere Medikamente: Madform DM , Tranzodone, Inumena
Allergien: Med, Kiwi
Vorherige Impfungen: -

VAERS 1578950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: WI
Alter: 31,0
Geschlecht: M
Eingang: 17.08.2021
Impfdatum: 09.08.2021
Beginn: 09.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Atrial tachycardia Blood creatinine increased Condition aggravated Dizziness Electrocardiogram abnormal Hypoacusis Immediate post-injection reaction Palpitations Sinus bradycardia Visual impairment

Symptomtext

Patient's significant other was present throughout encounter. Patient began experiencing muffled hearing and darkened vision approximately 30 seconds after receiving vaccine. He stated he does have a history of needle phobia and fainting from previous (non-COVID) vaccinations. He did become lightheaded and dizzy but did not lose consciousness. Patient also experienced some palpitations. Requested first response to be called so he could be brought to the emergency department (ED). He stated that these symptoms are in line with anxiety attacks he has had in the past, except the muffled hearing which is a new symptom. First response arrived, spoke with the patient, and the patient agreed to go the the ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atrial tachycardia
Hospital-Tage: -
Labordaten: EKG (8/9/2021): Showed sinus bradycardia as well as paroxysmal atrial tachycardia -- These are consistent with the patient's childhood history of bradycardic arrhythmias, but the cardiologist in the ED referred the patient to follow up with an electrophysiologist in the outpatient setting. The patient was discharged from the ED the same day (8/9/2021). Heart rate: 51 (8/09/2021) Serum creatinine: 1.24 (8/09/2021)
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety, Tension headache, Vertigo, Bradycardia, BPPV (benign paroxysmal positional vertigo), Atopic dermatitis, Nocturnal cough
Andere Medikamente: -
Allergien: Amoxicillin (Hives), Nickel (dizziness)
Vorherige Impfungen: -

VAERS 1576163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 17.08.2021
Impfdatum: 03.07.2021
Beginn: 07.07.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac flutter Ear discomfort Head discomfort Heart rate increased Heavy menstrual bleeding Menstruation delayed Menstruation irregular Palpitations Tinnitus

Symptomtext

- Delayed menstrual cycle (normally about 35 days, became 58 days and slightly heavier - abnormal heart flutter/palpitations starting on July 7 (disappeared after 1 day) and then elevated heart rate for a week - pulsatile tinnitus developed 3 weeks later, feel pressure in ears and head

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: vitamin c, zinc, multi-vitamin
Allergien: keflex
Vorherige Impfungen: -

VAERS 1574271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NC
Alter: 34,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 08.06.2021
Beginn: 15.06.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Chest pain Dyspnoea Echocardiogram abnormal Ejection fraction decreased Pericardial effusion Pleural effusion Troponin normal

Symptomtext

34 yo female who received Pfizer BioNTech #1 on 08 JUN (EW0186) and a small anterior pericardial effusion and bilat pleural effusions were an incidental finding in an ER visit for abdominal pain on 15 JUN 2021 (day 7). She had also been experiencing dyspnea and intermittent positional CP, mid-chest, right of sternum estimated starting about June 09 (day 1),and symptoms have continued. Troponins were negative and echo showed normal anatomy, EF 50-55% with the effusion. Cardiology diagnosed acute nonspecific idiopathic pericarditis starting in May 2021, prior to COVID vaccine receipt.

Weitere VAERSDATA-Felder

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

VAERS 1569152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CO
Alter: 27,0
Geschlecht: M
Eingang: 15.08.2021
Impfdatum: 10.08.2021
Beginn: 15.08.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / RA

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

C-reactive protein normal Chest X-ray normal Chest discomfort Chest pain Echocardiogram Electrocardiogram normal Palpitations Troponin normal

Symptomtext

One hour after vaccine pt felt chest pressure and pain, heart pounding without racing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CXR non acute Serial EKG's on same day non ischemic. EKG 5 days later non-ischemic Trops day of and 5 days later neg CRP neg POC cardiac ultrasound neg for pericardial fluid
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, food sensitivities,
Andere Medikamente: zyrtec, singular, methyl folate
Allergien: sesame, wheat, peanuts, soy
Vorherige Impfungen: -

VAERS 1560878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 14.08.2021
Beginn: 14.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Arrhythmia Burning sensation Chest discomfort Dyspnoea Feeling abnormal Hypoaesthesia Insomnia

Symptomtext

A burning strange sensation moving to my neck. Shortness of breath, numb sensation down both right and left arms, numbness in fingers on right arm especially right first digit, fourth and fifth digit. I had strange tightness in my chest, feeling very short of breath. On the way home I kept having arrhythmia and it is 1:23AM on 6/15/21a and I still feel awful and cannot sleep.

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Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Non yet. I tried to get a rhythm report on my phone but it would not analyze my heart rhythm, it kept telling me it was inconclusive. If I continue to have this shortness of breath and tightness, arrhythmia, I will go to ED..
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroidd
Allergien: Erythromycin, Sulfa, epinephrine, Z-Pack, Augmentin, Xanax
Vorherige Impfungen: -

VAERS 1554889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: PR
Alter: 15,0
Geschlecht: M
Eingang: 13.08.2021
Impfdatum: -
Beginn: 07.07.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Clinodactyly Dyspnoea Gait inability Headache Pyrexia Speech disorder

Symptomtext

fever; headache; trouble speaking; unable to walk; unable to breath; crooked fingers/ twisted fingers; This is a spontaneous report from a contactable consumer (patient). A 15-years-old male patient received first dose of bnt162b2 (BNT162B2, BNT162B2, Pfizer-BioNTech Covid-19 mRNA Vaccine, Solution for injection, Batch/Lot number EW0178) via an unspecified route of administration, administered in arm left on 15Jun2021 09:00 as dose 1, single and dose 2 via an unspecified route of administration on an unspecified date (Batch/Lot Number: EW0186) as dose 2, single for COVID-19 immunization (Age at vaccination 15 years). Medical history included asthma; food allergy Known allergies to the shrimp, sinus disorder. There were no concomitant medications. No other vaccine in four weeks. No other medications in two weeks. No covid prior vaccination. No covid tested post vaccination. On 07Jul2021 01:00 patient experienced fever, headache, trouble speaking, unable to walk, unable to breath and crooked fingers/ twisted fingers. Therapeutic measures were taken as a result of all AE includes treatment with vein treatment solumedrol and Panadol, vendria. AE resulted in Emergency room / department or emergencies. The outcome for all events was recovered on an unspecified date in 2021 Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Seafood allergy; Sinus disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1554447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: AZ
Alter: 15,0
Geschlecht: M
Eingang: 13.08.2021
Impfdatum: 19.07.2021
Beginn: 20.07.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Back pain Chest pain Dyspnoea Pain Painful respiration

Symptomtext

Patient was seen for 2nd COVID vaccine on 8/9/21 and reported that 1 day after receiving the 1st dose he began with left sided chest pain that worsened with physical activity with radiation of pain to left side of back, back pain worsened with stretching and deep breathing, chest pain provoked some shortness of breath and lasted 7 days before symptoms subsided. No treatments were tried during that week. 8/9/21 was the first time that I heard of the incident. No current symptoms of chest pain/heart palpitation/shortness of breath reported on 8/9/21 and heart sounds were normal on exam. No history of heart problems. 2nd Pfizer dose not given until patient gets clearance from cardiologist.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Referred to specialist to be assessed and cleared prior to administration of 2nd Pfizer dose.
Aktuelle Erkrankungen: In grown toenail - keflex started on same date as vaccination
Vorgeschichte: History of anxiety
Andere Medikamente: Keflex - oral - ingrown toenail Ketonazole - topical
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1554372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 13,0
Geschlecht: M
Eingang: 13.08.2021
Impfdatum: 13.08.2021
Beginn: 13.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Auscultation Chest pain Depressed level of consciousness Dyspnoea Fatigue Pharyngeal swelling

Symptomtext

Father alerted this RN to patient development of extreme fatigue after approximately 13 minutes post administration. This RN administered Zyrtec 10mg solution p.o. and manual blood pressure via right arm was 132/90, HR=81-88, O2= 98% via pulse oximeter and respiratory rate=12. Patient became more difficult to arouse, transported via wheelchair to room with reclining chair and epinephrine on site. Father report patient with NKDA, and no known history of adverse reactions to past vaccines or injection. No known medical history, other than medication for attention deficit per father. Code called by non-clinical staff member. This RN re-assessed patient and patient reported new onset of sharp chest pain to center of chest- no abnormal heart sounds auscultated at that time. Emergency response team arrived concurrently, and Pediatric MD began assessment of patient at 14:03pm. Patient began to complain of swelling to throat and new difficulty breathing. This RN administered 0.3cc Epinephrine, at 14:04pm per protocol and Pediatric MD aware. Immediate response in patient noted. Patient alert and oriented to person and place. Patient stable and transported by pediatric emergency nurse via wheelchair to the Pediatric Emergency Department for further evaluation and monitoring after administration of Epinephrine. Patient accompanied by father.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No known per father
Vorgeschichte: No known
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1549979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 05.06.2021
Beginn: 08.06.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain Fatigue Heavy menstrual bleeding Menstruation irregular Painful respiration Pulmonary pain Ultrasound kidney Ultrasound liver

Symptomtext

After the 1st vaccine, my menstrual cycle (because I'm pre-menopausal) - about every three or four months. Before the vaccine, I get heavy bleeding for a few minutes and then it stops and then it goes to spotting. But this time, after the vaccine, it was so extremely heavy that I had to leave work. I had huge clots coming out - I had to change not even an hour later. And had to change again, not even an hour later than this. I went to change again another time and felt the blood gushing out again. I work construction and I had to tell me foreman that I had to leave. I bled heavily for about five days. I was scared but didn't go to doctor. I don't have medical insurance. I started drinking Iron due to the blood loss. After the five days, it was spotting so that was pretty normal. On the 26th of June, I had the second Pfizer of June. I felt horrible pain, on my upper left lung - that was two days after the second vaccine. It felt like a shooting pain. It hurt when I tried to take a deep breath or when I tried to move my arms. Slowly it moved to center of chest and then it disappeared. Tuesday, I started bleeding again - extreme bleeding. I told myself that I would go to ER but it seemed to calm down overnight. But I let my supervisor know and he had let me off early after I told him what was going on again. Wednesday, started bleeding again again heavily when I was at work. I went through four super tampons and four super pads and bled through my period panties and I had put a beach towel on my car seat and I had bled on that towel. I went to ER. The doctor at ER - I told her the pain I was having on my lungs. The week I had started bleeding again, I had noticed my right lung hurt on Monday and the next day is when I had gotten my period and it was just so heavy. Chest lining that was swollen. They gave me ibuprofen for the swelling and the bleeding. She told me to keep on taking Iron supplement. They won't put me on hormones because there is breast cancer history in the family. I have never bled like this or have clots like this. She did two Ultrasounds= Kidneys, liver, external and bloodwork for testing things and ovaries. I am still getting on and off chest pain and I get tired really easily. The chest pain happened one day out of the last week. I'm in shape - I swing dance and workout and workout. I work in construction and so I have a physical job. Ever since the vaccine, I feel like I get tired a lot faster - and that is still going on. I'm afraid to get my period right now because I don't know how it's going to be. And I'm afraid to be physical anymore and I have to be super cautious with wearing super pads in case it happens.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: June 21, 2021 ER - bloodwork; two ultrasounds - external and one internal Doctor confirmed I am anemic right now from loss of blood.
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Vitamin C; calcium; zinc. Albuterol - I only take that when needed.
Allergien: Food: pork and walnuts
Vorherige Impfungen: -

VAERS 1549578

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: AZ
Alter: 16,0
Geschlecht: M
Eingang: 12.08.2021
Impfdatum: 05.08.2021
Beginn: 08.08.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / -

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

C-reactive protein increased Chest X-ray Chest pain Echocardiogram Red blood cell sedimentation rate increased Troponin increased

Symptomtext

Received second dose of COVID vaccine on 8/5/21, on 8/8/21 started having chest pain no SOB. I ordered labs and the results were: ?. esr 14, crp 35.3, troponin 249. Sent to ED where he was admitted for three days. He had CXR and ECHO but I do not have these results. Saw the patient today 8/12/21, chest pain resolved with vitals normal.

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Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: 8/8/21: ESR: 14, CRP: 35.3, Troponin 249.
Aktuelle Erkrankungen: asthma
Vorgeschichte: Impetigo, asthma
Andere Medikamente: Zyprexa,
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1549180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: UT
Alter: 25,0
Geschlecht: M
Eingang: 12.08.2021
Impfdatum: 11.08.2021
Beginn: 11.08.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Dyspnoea Heart rate irregular Muscle spasms Myalgia Pyrexia

Symptomtext

Cramping on left side of chest, irregular, rapid heart beat. Muscle soreness, fever, shortness of breath. No treatment

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

VAERS 1536129

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 09.08.2021
Impfdatum: 06.08.2021
Beginn: 06.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / UN

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

Hypoaesthesia Lip swelling Paraesthesia

Symptomtext

Patient received her first dose of Pfizer vaccine, Lot number EW0186 at approximately 1021 AM. The patient reported feeling "numbness and tingling around my face for about ten minutes" at about 1100. Reported to Dr. and received a verbal order for Zyrtec 10 mg. This was administer at 1103. VS stable; 1100 139/96 100% on RA 66=Pulse 98.8 F Resp= 16 Follow up VS 1110 BP= 153/94 HR 72 O2= 100% Resp= 20 1114 Patient reported her "lips getting more swollen" She determined she would like to go to the ER to be monitored. Lung sounds remain clear, no evidence of stridor at this time. 911 called. On their way. Follow up VS= 1120 BP= 167/99 HR= 63 RA= 100% Resp= 20 Patient left with the ambulance at about 1130. VS remained stable. She indicated the swelling still persisted, however it was improving. Decided to go to the ER still because we do not have airways available and the patient reports not wanting to be injected with an epi-pen without cardiac monitoring.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Please see prior VS taken. Otherwise not further "tests or labs" were done during this time.
Aktuelle Erkrankungen: Patient denies any acute complications Chronic illnesses include;
Vorgeschichte: NEAR SYNCOPE DIZZINESS NAUSEA AND VOMITING DIARRHEA ALLERGIC RHINITIS CONTACT DERMATITIS VERTIGO LOWER ABDOMINAL PAIN URGE INCONTINENCE PNEUMATURIA HX OF SPOUSE OR PARTNER VIOLENCE, PHYSICAL NECK MUSCLE STRAIN HX OF SEXUAL ABUSE IN CHILDHOOD ADJUSTMENT DISORDER W MIXED ANXIETY AND DEPRESSED MOOD RELATIONSHIP DISTRESS W SPOUSE OR INTIMATE PARTNER ADULT ABUSE LEFT HEARING LOSS
Andere Medikamente: Patient denied taking any medications the day she received her vaccination. Chronic, as needed, medications listed in her chart include; Claritin 10 mg Flonase 16g Albuterol 90 mcg Naproxen 500 mg Tylenol 500 mg
Allergien: Iv Contrast [Ivp Dye, Iodine Containing], Keflet [Cephalexin], Nitrofurantoin Monohyd Macro, Ofloxacin, Psyllium Seed, Sulfa (Sulfonamide Antibiotics)
Vorherige Impfungen: -

VAERS 1535985

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MN
Alter: 54,0
Geschlecht: M
Eingang: 09.08.2021
Impfdatum: 06.08.2021
Beginn: 07.08.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chills Myalgia Palpitations Pyrexia

Symptomtext

Chills, Muscle aches, Heart palpitations , Fever

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: No
Vorgeschichte: COPD
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1534754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 34,0
Geschlecht: F
Eingang: 07.08.2021
Impfdatum: 05.08.2021
Beginn: 05.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia Back pain Chills Decreased appetite Headache Loss of personal independence in daily activities Mobility decreased Musculoskeletal stiffness Pain Pyrexia Sleep disorder Spinal pain

Symptomtext

The evening I received the 2nd dose of Pfizer vaccine, I began to feel feverish, with chills and body aches. This lasted throughout the night to the degree that I was unable to sleep more than a couple hours. In the morning, I felt pain and heat through my head and spine primarily, but it radiated out through the rest of my body too. I had one episode of a sudden severe headache when I turned my head, which lasted several minutes then returned to the baseline pain level. I experienced stiffness throughout my body and loss of appetite. Other symptoms included significant low back pain that was unaffected by position or movement. I am an active, fit, healthcare professional that exercises several times per week, and I was so weak that I was unable to get out of bed for nearly the whole day. I didn't have energy to read, listen to music, or do other passive activities. It was unlike anything I have ever felt before even when I have been sick in the past. By the evening of 8/6, the day after receiving the vaccine, I began to feel improvement. The morning of 8/7, I felt back to normal.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Temperature increased from normal (97.1-97.4 for me) to 101.1 degrees. SpO2 remained in normal ranges.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Daily multivitamin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1534739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CT
Alter: 45,0
Geschlecht: F
Eingang: 07.08.2021
Impfdatum: 21.07.2021
Beginn: 21.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Auscultation Flushing Hyperhidrosis Pallor Palpitations Sensory disturbance Throat tightness

Symptomtext

Vaccination given at 5:45 pm. 5:50 pm, patient reported feeling her throat tighten and heart racing. Felt the shot go through her system. Skin: pale, diaphoretic, BP with small cuff left arm was 157/101; pulse oximeter 100%; HR 71 auscultation. Reported having cream cheese and water before shot. Feet elevated; ice pack to forehead; offered water and able to swallow easily. 6 pm: BP 140/98; skin now flushed; pulse oximeter 99%; HR 71; needed reading with larger cuff; called 911. EMS arrived at 6:05 pm; BP with large cuff 145/83 taken to ER. Director notified of event and will call patient later for status.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported; overweight
Andere Medikamente: None reported
Allergien: None
Vorherige Impfungen: -

VAERS 1534656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0186

moderat

Staat: OH
Alter: 40,0
Geschlecht: F
Eingang: 07.08.2021
Impfdatum: 06.08.2021
Beginn: 06.08.2021
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 Chest pain Dyspnoea Malaise

Symptomtext

Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Chest Tightness / Heaviness / Pain-Mild, Additional Details: patient's son was with patient in waiting area. patient's son alerted pharmacist that patient was not feeling well. observed patient having difficulty breathing. son requested 911 be called. 911 called for patient.

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

VAERS 1317158

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

moderat

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 07.08.2021
Impfdatum: 12.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Dyspnoea

Symptomtext

Felt trouble breathing/ hard to breathe; This is a spontaneous report from a contactable consumer, the patient. A 26-year-old female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: Ew0186) via an unspecified route of administration in the left arm on 12May2021 at 10:00 (at the age of 26-years-old) as a single dose for COVID-19 immunisation. Medical history included allergy to mango (fruit allergy) and allergy to carbs (seafood allergy). It was unknown if the patient was pregnant at the time of reporting. Concomitant medications were not reported. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: Ew0158) via an unspecified route of administration in the left arm on 21Apr2021 at 9:00 (at the age of 26-years-old) as a single dose for COVID-19 immunisation. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccination. On 13May2021 at 14:00, after the second shot of Pfizer vaccine the patient felt trouble breathing, hard to breathe. When she stayed "chill" she felt little better, but still needed a hard hold of longer breathe, when she had a talk, she would have to breathe more to feel better. The event 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 event. The clinical outcome of the event felt trouble breathing/ hard to breathe was not resolved at the time of this report. 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: Fruit allergy (Known allergies: Mango); Seafood allergy (Known allergies: crabs)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1317158

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 07.08.2021
Impfdatum: 12.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Dyspnoea

Symptomtext

Felt trouble breathing/ hard to breathe; This is a spontaneous report from a contactable consumer, the patient. A 26-year-old female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: Ew0186) via an unspecified route of administration in the left arm on 12May2021 at 10:00 (at the age of 26-years-old) as a single dose for COVID-19 immunisation. Medical history included allergy to mango (fruit allergy) and allergy to carbs (seafood allergy). It was unknown if the patient was pregnant at the time of reporting. Concomitant medications were not reported. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: Ew0158) via an unspecified route of administration in the left arm on 21Apr2021 at 9:00 (at the age of 26-years-old) as a single dose for COVID-19 immunisation. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccination. On 13May2021 at 14:00, after the second shot of Pfizer vaccine the patient felt trouble breathing, hard to breathe. When she stayed "chill" she felt little better, but still needed a hard hold of longer breathe, when she had a talk, she would have to breathe more to feel better. The event 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 event. The clinical outcome of the event felt trouble breathing/ hard to breathe was not resolved at the time of this report. 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: Fruit allergy (Known allergies: Mango); Seafood allergy (Known allergies: crabs)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1531636

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 06.08.2021
Impfdatum: 28.07.2021
Beginn: 29.07.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Feeling abnormal Paraesthesia

Symptomtext

I had a weird throbbing sensation in right hand, it then started tingling, and went to left hand also and to my feet. The the tingling started coming up my legs and down my arms after a couple of days. Then my face started tingling. Now it is up my back and there is now a tingling sensation basically over my entire body. I tried taking Benadryl and it has not helped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: A fib
Andere Medikamente: metoprolol, flecainide, daily nutritional supplement
Allergien: penicillin, sulfur, sensitivity to gluten
Vorherige Impfungen: -

VAERS 1531283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: OH
Alter: 35,0
Geschlecht: F
Eingang: 06.08.2021
Impfdatum: 13.06.2021
Beginn: 15.06.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Heart rate increased Palpitations

Symptomtext

Systemic: heart pounding through chest and rapidly-Mild

Weitere VAERSDATA-Felder

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

VAERS 1531208

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

moderat

Staat: CO
Alter: 34,0
Geschlecht: F
Eingang: 06.08.2021
Impfdatum: 16.07.2021
Beginn: 17.07.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Blood test Chest pain Computerised tomogram thorax abnormal Dyspnoea Echocardiogram abnormal Fibrin D dimer Liver function test Lung infiltration Oxygen saturation decreased Peripheral swelling Pulmonary hypertension Pyrexia Right atrial dilatation White blood cell count increased

Symptomtext

Shortness of breath, bilateral leg swelling, chest pain, fever 103, saturation?s in low 80s lead be to the ER and ultimately admission into the hospital. Elevated WBC, d-dimer, LFTs, CT showed bilateral lung infiltrates, ECHO showed dilated right atrium and pulmonary hypertension

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Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: CT, ECHO, bloodwork
Aktuelle Erkrankungen: Postpartum Delivery 7/14/21
Vorgeschichte: N/A
Andere Medikamente: Prenatal
Allergien: Nkda
Vorherige Impfungen: -

VAERS 1528566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NC
Alter: 42,0
Geschlecht: F
Eingang: 05.08.2021
Impfdatum: 30.07.2021
Beginn: 30.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Electrocardiogram Heart rate decreased Hypotension

Symptomtext

shortness of breath with oxygen saturation of 84% low heart rate 42 low blood pressure 90/60

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: ekg
Aktuelle Erkrankungen: na
Vorgeschichte: na
Andere Medikamente: multi-vitamin
Allergien: penicillin bees
Vorherige Impfungen: shoulder injury following flu vaccine

VAERS 1526333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: IL
Alter: 46,0
Geschlecht: F
Eingang: 04.08.2021
Impfdatum: 03.08.2021
Beginn: 03.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Nausea

Symptomtext

Patient received dose 1 of the Pfizer COVID-19 vaccination at 2pm on 8/3/21. Within 5 minutes of receiving the vaccination she began feeling nauseous and experienced difficulty breathing. Staff at the facility contacted 911 while the administering pharmacist began checking vitals and advised the patient to attempt slow consistent breathing. After several minutes with no improvement in breathing the pharmacist administered 0.3mg of epinephrine intramuscularly. Shortly after administration EMT staff arrived and placed patient on to a stretcher. As patient entered the ambulance her breathing began to improve and she was transported to a local hospital ER for observation and released later in the day.

Weitere VAERSDATA-Felder

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

VAERS 1525808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NC
Alter: 38,0
Geschlecht: M
Eingang: 04.08.2021
Impfdatum: 15.07.2021
Beginn: 17.07.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / -

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

Burning sensation Condition aggravated Dyspnoea Migraine

Symptomtext

Patient complained of burning sensation of the feet and some intermittent sob not worse with exercise. burning sensation of the feet happened on the 17ths and sob of breath comes and goes starting the 17th and on. Patient also endorsed worsening migraines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Herniated disk of L5-S1
Vorgeschichte: Herniated disk of L5-S1 Chronic migraines
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Influenza

VAERS 1523439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 22,0
Geschlecht: F
Eingang: 03.08.2021
Impfdatum: 03.08.2021
Beginn: 03.08.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Tremor

Symptomtext

PATIENT STATED THAT SHE HAD SHAKING MOVEMENT; VITALS WERE TAKEN AND STABLE.

Weitere VAERSDATA-Felder

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

VAERS 1523077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: PA
Alter: 49,0
Geschlecht: F
Eingang: 03.08.2021
Impfdatum: 16.05.2021
Beginn: 24.05.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain upper Cardiac stress test normal Chest X-ray normal Chills Condition aggravated Diarrhoea Dyspnoea Electrocardiogram ambulatory normal Electrocardiogram normal Fatigue Gastrointestinal disorder Headache Hypoaesthesia Impaired work ability Injection site mass Limb discomfort Migraine Movement disorder

Symptomtext

24 hrs after the shot, 05/17/2021, I had fever, chills, headache, stomach ache, diarrhea, fatigue, migraines, lump on the arm of injection, I could not lift my arm, I could not work until Thursday, 05/20/2021. The fever and chills subsided by Wednesday., 05/19/2021. I still had trouble lifting my arm, and I still had a headache on 05/20/2021. From the elbow down to my left hand, I have a pulsing in my hand. It's a weird pulsing feeling in my left hand and that still happens till this day, daily. On 04/25/2021 I had my 1st Dose of Pfizer. On 04/27/2021- I saw Dr. for the 1st time, I went in for a wellness visit. I told her I was having minor heart palpitations, tingling in my hands, arm and my left foot was numb.. I have a family history on my maternal side, my grandfather and his brothers died before the age of 52 of coronary. She sent me to cardiology for a stress test on 05/03/2021. Then on 05/16/2021 I went for my 2nd Dose of Pfizer. Dr. on 06/18/2021 did an EKG and a halter monitor. Since 05/24 I have been short of breath and it's been getting worse. Dr. wants me to get pulmonary function test but I am not able to get an appointment until November. I have respiratory test on 08/05/2021. Dr. said my symptoms may be caused by GI, and vocal chords since my chest x-rays were normal. She is suggesting me to see an ENT because my vocal chords may be causing my symptoms. We are at a loss of what could be causing the problem. I would consider it to be a disability if I am going to be having trouble breathing for the rest of my life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: stress test EKG -normal halter monitor -results normal- did not show anything chest x-ray-normal respiratory test
Aktuelle Erkrankungen: migraines
Vorgeschichte: migraines as a kid -then they went away
Andere Medikamente: Premarin 1.25 mg od horomone replacement been taking it for 13 years simvastatin 40 mg od topiramate 50 mg bd omeprazole 40 mg od dicyclomine 20 mg 3 times a day Allergy meds- store brand Sudafed sinus and allergy, night time severe
Allergien: lactose intolerant
Vorherige Impfungen: -

VAERS 1521354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 03.08.2021
Impfdatum: 01.07.2021
Beginn: 31.07.2021
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: UN / LA

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

Injection site paraesthesia Paraesthesia

Symptomtext

Arm starting tingling at site of shot and moved down my arm, into my left hand/fingers. Right hand/fingers also started tingling. The next night, both hands were tingling, same thing the following night (Sunday). Monday morning, hands started tingling again again with my feet. Right now, Monday evening, my left foot is tingling as is my right hand. Have never had this happen before the shot, and am convinced this is all from the shot. What do you have in the shot that causes this?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: None yet. My doctor has advised me to get the 2nd shot and if this issue continues, she'll address it then. That's a BS answer for me so I'm looking for a doctor that will take this seriously as I am VERY concerned for my health and need to weigh going without the 2nd shot vs catching covid with only one shot. You want to know why people are hesitant to get this jab? It's because of this kind of crap that doesn't get talked about. This shot is a bunch that people are scared of.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Lipitor D3 Multivitamin zinc NAC Quercetin Fish Oil
Allergien: none
Vorherige Impfungen: -

VAERS 1519053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 01.08.2021
Impfdatum: 07.07.2021
Beginn: 11.07.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / AR

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

Anxiety Dyspnoea Feeling abnormal Headache Palpitations

Symptomtext

Client reported that 5 days after receiving the 1st dose COVID vaccine Pfizer she developed a headache which lasted 4 days. The client also stated she developed "trouble breathing and throbbing in her chest" 5 days after the vaccine. The client reports intermittent episodes of trouble breathing since receiving the first dose of COVID vaccine Pfizer. The last episode of shortness of breath was on 07/25/21. The client states the shortness of breath sometimes triggers an anxiety attack where she has to take deep breaths to calm down. The client stated she did seek care at a doctors office where she was prescribed some sort of pain medication that did not provide relief of her symptoms. The client did not know which specific medication she was prescribed. The client returned to the doctors where she was given some sort of medication in an injection which resulted in improvement of her symptoms. The client does not know which type of medication she was given via injection. The client reports that she "feels weird" ever since she received the first dose COVID vaccine Pfizer. The client denies any chronic conditions. She does not take any medications regularly. The client denies any known allergies. The client denies any history of shortness of breath prior to receiving the first dose COVID vaccine Pfizer. Current vitals obtained were as follows: automatic BP 122/90, HR 75 BPM.

Weitere VAERSDATA-Felder

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

VAERS 1517353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: IL
Alter: 64,0
Geschlecht: F
Eingang: 31.07.2021
Impfdatum: 18.06.2021
Beginn: 20.06.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Heart rate increased Hypotension Incomplete course of vaccination Palpitations

Symptomtext

The best way I can describe it is an amped-up heartbeat. I would put my hand on my heart and feel a strong beating. When driving I felt my heartbeat through the seatbelt pad. It lasted for at least two weeks into the third week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: I had my blood pressure taken at the school I worked for. The nurse said it was okay and on the low side. I talked with my PA who said several people reported a similar response to the vaccine, while he approved of taking it wholeheartedly. I abstained from the second shot after learning about the FDA warning that it can cause heart inflammation. That is what it felt like to me. Some degree of inflammation as a result of taking the vaccine. I also learned about the CDC reports that 1 shot is 80% coverage dated March 29th, 2021.
Aktuelle Erkrankungen: none
Vorgeschichte: h-pylori
Andere Medikamente: -
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1515606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 13,0
Geschlecht: F
Eingang: 31.07.2021
Impfdatum: 29.07.2021
Beginn: 29.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Crying Fatigue Headache Heart rate increased Oropharyngeal pain Throat tightness Injection site pain Tremor

Symptomtext

- 11:15am shot administered and went to lobby to wait - 11:20am extreme fatigue started - 11:30am pain in injection site and extreme fatigue - 11:41am extreme fatigue just wanted to eat and go home and sleep, so decided to leave as nothing severe apparent - 11:43am back of throat started hurting and indicated throat feeling tight walked back into Dr. Office - shortly after doctor gave benedryl 12.5mg per 5ml given 15ml and water - asked repeatedly if feeling any different, was able to respond indicating tightness getting worse - was also having chills/shaking - able to speak but was crying from pain in throat and tightness - Dr. Then administered 0.3 mg epi pen - within minutes she did have some relief was able to smile when asked if she wants to eat - heart beat was accelerated but expected per doctor indication of the adrenaline rush from epi pen - Mild shaking still - Ambulance arrived 12:14pm - by around 12:50pm got to er and was feeling much better - observed for several hours later and just had intense fatigue, chills, and headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma but has not taken any medications in at least two years and has not had any attacks.
Andere Medikamente: Enthromycin topical (for acne) Differin gel (topical acne)
Allergien: Cat Dander, feathers, dust, seasonal allergies ( spring and fall ), some cheeses(not identified specifically)
Vorherige Impfungen: -

VAERS 1515606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 13,0
Geschlecht: F
Eingang: 31.07.2021
Impfdatum: 29.07.2021
Beginn: 29.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Crying Fatigue Headache Heart rate increased Oropharyngeal pain Throat tightness Injection site pain Tremor

Symptomtext

- 11:15am shot administered and went to lobby to wait - 11:20am extreme fatigue started - 11:30am pain in injection site and extreme fatigue - 11:41am extreme fatigue just wanted to eat and go home and sleep, so decided to leave as nothing severe apparent - 11:43am back of throat started hurting and indicated throat feeling tight walked back into Dr. Office - shortly after doctor gave benedryl 12.5mg per 5ml given 15ml and water - asked repeatedly if feeling any different, was able to respond indicating tightness getting worse - was also having chills/shaking - able to speak but was crying from pain in throat and tightness - Dr. Then administered 0.3 mg epi pen - within minutes she did have some relief was able to smile when asked if she wants to eat - heart beat was accelerated but expected per doctor indication of the adrenaline rush from epi pen - Mild shaking still - Ambulance arrived 12:14pm - by around 12:50pm got to er and was feeling much better - observed for several hours later and just had intense fatigue, chills, and headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma but has not taken any medications in at least two years and has not had any attacks.
Andere Medikamente: Enthromycin topical (for acne) Differin gel (topical acne)
Allergien: Cat Dander, feathers, dust, seasonal allergies ( spring and fall ), some cheeses(not identified specifically)
Vorherige Impfungen: -

VAERS 1508715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: PA
Alter: 52,0
Geschlecht: F
Eingang: 28.07.2021
Impfdatum: 14.05.2021
Beginn: 01.05.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Dizziness Full blood count Headache Migraine

Symptomtext

Migraine; Dizziness; Headache; This is a spontaneous report from a contactable consumer (Patient). A 52-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EW0186), via an unspecified route of administration, administered in Arm Right on 14May2021 (at the age of 52-year-old) as dose 1, single for covid-19 immunisation. Medical history included anxiety from an unknown date and unknown if ongoing, hypothyroidism from an unknown date and unknown if ongoing, allergy to artificial sugars. Concomitant medications included celecoxib (CELEXA) taken for an unspecified indication, start and stop date were not reported; topiramate (TOPAMAX) taken for an unspecified indication, start and stop date were not reported; levothyroxine sodium (SYNTHROID) taken for an unspecified indication, start and stop date were not reported. On 16May2021, the patient experienced migraine, dizziness, headache. Patient was not informed about the vaccine containing artificial sugars and she mentioned that she is allergic to all types of artificial sugars. When asked for side effects, consumer stated, "Yes, I get migraines from the artificial sugars and I have been suffering from the migraine since I got the shot along with the dizziness but I don't know it's just a typical side effect of the shot but yeah I have been getting migraine". Consumer stated, "It's probably, I would say may be 16May, I don't think I got the headache right away but on 16 definitely it went really bad." The patient underwent lab tests and procedures which included full blood count: unknown date. Therapeutic measures were taken as a result of events included maxalt. The outcome of the events were unknown. Information on Lot/Batch number was available. Additional information has been requested

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Name: CBC; Result Unstructured Data: Test Result:unknown
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety (Verbatim: Anxiety); Food allergy (I get migraines from the artificial sugars); Thyroid function decreased (Verbatim: Low Thyroid Function)
Andere Medikamente: CELEXA [CELECOXIB]; TOPAMAX; SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 1508631

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MN
Alter: 16,0
Geschlecht: F
Eingang: 28.07.2021
Impfdatum: 12.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Chills Dizziness Fatigue Headache Heart rate Myalgia Pyrexia Tachycardia

Symptomtext

Very high heart rate over 120 for 8 hours; Fever.; Chills; Sore muscles; Headache; Dizzy; Very high heart rate over 120 for 8 hours. Fever, chills, sore muscles, headache, dizzy, and tired.; This is a spontaneous report from a contactable consumer (patient). A 16-years-old non-pregnant female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Left (at the age of 16 years old) on 12May2021 at 18:30 (Batch/Lot Number: EW0186) as DOSE 2, SINGLE for covid-19 immunization. Also reported 'Device Date:19May2021' no additional details provided. Facility where the most recent COVID-19 vaccine was administered was health facility. No other vaccines were given within 4 weeks. Prior to vaccination, was the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. Medical history included attention deficit hyperactivity disorder. Concomitant medication(s) included methylphenidate hydrochloride (CONCERTA) 54mg. Historical Vaccine includes BNT162B2 Dose 1 (at the age of 16 years old) on 21Apr2021 at 18:30 Batch/lot number ER8736, Left arm Covid-19 immunization and not events were reported. The patient previously took amoxicillin and experienced drug hypersensitivity. On 13May2021 at 02:00 The patient experienced Very high heart rate over 120 for 8 hours, Fever, chills, sore muscles, headache, dizzy, and tired. The event Very high heart rate over 120 for 8 hours was considered medically significant. The patient underwent lab tests and procedures which included heart rate: high on 13May2021 (Very high heart rate over 120 for 8 hours). No Treatment was given and No hospitalization was involved. The clinical outcome of the events was recovered May2021. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Test Date: 20210513; Test Name: Heart rate; Result Unstructured Data: Test Result:High; Comments: Very high heart rate over 120 for 8 hours.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADHD
Andere Medikamente: CONCERTA
Allergien: -
Vorherige Impfungen: -

VAERS 1459991

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NJ
Alter: -
Geschlecht: U
Eingang: 28.07.2021
Impfdatum: 06.07.2021
Beginn: 07.07.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Blood test Chest pain Dyspepsia Electrocardiogram normal Discomfort Inflammation Pain

Symptomtext

Heartburn; Inflamation; Soreness in pectoral muscles; slight pain also in pectoral muscles.; This is a spontaneous report from a contactable consumer (patient) reported in response to consumer letter sent via follow-up letter. A patient of unspecified age and gender received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EW0186) via unspecified route of administration, administered in Arm Left on 06Jul2021 at 10:30 as single dose for covid-19 immunisation. Vaccination facility type was Doctor's office/Urgent care. No prior vaccinations reported. Medical history included olfacto genital dysplasia. The patient's concomitant medications were not reported. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number EW0182) via unspecified route of administration, administered in Arm Left on 25May2021 10:30 as single dose for covid-19 immunisation. On 07Jul2021 at 10:00, the patient experienced inflammation, soreness in pectoral muscles and slight pain also in pectoral muscles. Also have heartburn started on 08Jul2021 and the patient have never had that before. Heartburn on 08Jul2021 and on 09Jul2021. The adverse event was required in a visit to Physician office. The patient had no treatment received for the adverse events. The outcome of the event Heartburn recovered on 09Jul2021 and recovering from the events inflammation, soreness in pectoral muscles and slight pain also in pectoral muscles.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Kallmann's syndrome
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1371738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 54,0
Geschlecht: F
Eingang: 28.07.2021
Impfdatum: 17.05.2021
Beginn: 17.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Anxiety Aphthous ulcer Feeling abnormal Headache Lip swelling Paraesthesia oral Rhinorrhoea Urticaria

Symptomtext

Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; This is a spontaneous report from a contactable consumer, the patient. A 54-years-old female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in the left arm on 17May2021 at 18:00 (Batch/Lot Number: EW0186) as dose 1, single (at the age of 54 years-old) for COVID-19 immunisation. Medical history included known allergy to Sulfa drugs. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not have a history of COVID-19 prior to the vaccination and was not tested for COVID-19 after the vaccination. On 17May2021 at 18:15 the patient experienced headache, feeling abnormal (just feeling generally off, almost a feeling of an adrenaline, feeling foggy), and on 17May2021 the patient also experienced tingling lips, hives, runny nose, swelling lips, canker sore lip, and anxiety. The events all resulted in a physician office visit. The clinical course is as follows: Within minutes of receiving the shot, the patient started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. The patient felt a bit antsy and foggy for 1 hr. A couple of hours later, the patient got a small hive on the bottom of their right eye, followed by small hive in their left shoulder. The patient's nose started to run a bit and the patient called their sister who brought them over some Benadryl. When the sister arrived, the patient felt the inside of bottom lip begin to tingle and mildly swell. The patient stayed awake for a bit and then took the Benadryl before going to sleep. In the morning, the inside of their bottom lip felt like it had a series of small canker sores which resolved within 24 hours. The patient had a telemedicine visit with their doctor's office, and they felt it was a local reaction, perhaps anxiety induced; they ok'd 2nd dose. The patient discussed with vaccination site coordinator, and they consulted with the County Health Department who will not administer a second dose due to CDC guidance regarding hives, etc. Therapeutic measures were taken as a result of the events tingling lips, hives, runny nose, headache, feeling abnormal (just feeling generally off, almost a feeling of an adrenaline, feeling foggy), swelling lips and included Benadryl.The patient did not receive therapeutic intervention for canker sore and anxiety. The patient recovered from the events tingling lips, hives, runny nose, headache, feeling abnormal (just feeling generally off, almost a feeling of an adrenaline, feeling foggy), swelling lips, canker sore lip, and anxiety on an unknown date in May2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1371738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 54,0
Geschlecht: F
Eingang: 28.07.2021
Impfdatum: 17.05.2021
Beginn: 17.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Anxiety Aphthous ulcer Feeling abnormal Headache Lip swelling Paraesthesia oral Rhinorrhoea Urticaria

Symptomtext

Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; Within minutes of receiving the shot, I started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. Felt a bit antsy and foggy for 1 hr. A couple of hours lat; This is a spontaneous report from a contactable consumer, the patient. A 54-years-old female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in the left arm on 17May2021 at 18:00 (Batch/Lot Number: EW0186) as dose 1, single (at the age of 54 years-old) for COVID-19 immunisation. Medical history included known allergy to Sulfa drugs. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not have a history of COVID-19 prior to the vaccination and was not tested for COVID-19 after the vaccination. On 17May2021 at 18:15 the patient experienced headache, feeling abnormal (just feeling generally off, almost a feeling of an adrenaline, feeling foggy), and on 17May2021 the patient also experienced tingling lips, hives, runny nose, swelling lips, canker sore lip, and anxiety. The events all resulted in a physician office visit. The clinical course is as follows: Within minutes of receiving the shot, the patient started getting a headache and just feeling generally off...almost a feeling of an adrenaline rush. The patient felt a bit antsy and foggy for 1 hr. A couple of hours later, the patient got a small hive on the bottom of their right eye, followed by small hive in their left shoulder. The patient's nose started to run a bit and the patient called their sister who brought them over some Benadryl. When the sister arrived, the patient felt the inside of bottom lip begin to tingle and mildly swell. The patient stayed awake for a bit and then took the Benadryl before going to sleep. In the morning, the inside of their bottom lip felt like it had a series of small canker sores which resolved within 24 hours. The patient had a telemedicine visit with their doctor's office, and they felt it was a local reaction, perhaps anxiety induced; they ok'd 2nd dose. The patient discussed with vaccination site coordinator, and they consulted with the County Health Department who will not administer a second dose due to CDC guidance regarding hives, etc. Therapeutic measures were taken as a result of the events tingling lips, hives, runny nose, headache, feeling abnormal (just feeling generally off, almost a feeling of an adrenaline, feeling foggy), swelling lips and included Benadryl.The patient did not receive therapeutic intervention for canker sore and anxiety. The patient recovered from the events tingling lips, hives, runny nose, headache, feeling abnormal (just feeling generally off, almost a feeling of an adrenaline, feeling foggy), swelling lips, canker sore lip, and anxiety on an unknown date in May2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1505432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 27.07.2021
Impfdatum: 27.07.2021
Beginn: 27.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Anxiety Headache Hypertension Injection site pain

Symptomtext

Patient indicated she had arm pain at the site of injection and a headache that started immediately after the vaccine. She indicated she felt anxious. Blood pressure was high this morning according to the patient because she knew she was going in for the vaccine. Blood pressure was 180/90 right arm. Patient indicated she had a small amount of fruit and water today. She was given some juice and we had her wait the full 30 minutes. Her blood pressure was back to her baseline of 150 /83 after sitting for the 30 minutes. She still indicated she had a slight headache but it was somewhat better. She was discharged to home with her family member and indicated she would keep an eye on her pressure at home and let someone know if the headache got worse or changed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: blood pressure checked
Aktuelle Erkrankungen: none noted
Vorgeschichte: hypertension
Andere Medikamente: calcium, vitamin, D, Iron, Multivitamin
Allergien: No known allergies to medication
Vorherige Impfungen: -

VAERS 1501959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: PA
Alter: 42,0
Geschlecht: F
Eingang: 26.07.2021
Impfdatum: 14.07.2021
Beginn: 15.07.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Arthralgia Blood test Facial pain Impaired work ability Injection site pain Injection site pustule Injection site swelling Injection site warmth Joint contracture Mobility decreased Neck pain Pain in extremity Red blood cell sedimentation rate increased

Symptomtext

Puss filled bubble at the injection area, Hot to touch and very puffy and painful. Sharp pain spreading throughout my arm and leg and where my fingers and wrist knee and ankle bend also under my chin the side of my face and back of neck all on my right side from July 14 to date. I'm still in pain to this date. I have to speak to text just to write this. I can't turn my steering wheel without my right wrist and fingers locking up in pain. I have to type for a living so this is preventing me from working and I'm right handed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Dr visit + Blood work 7/16 sed rate 32 ER visit 7/23 sed rate 47
Aktuelle Erkrankungen: -
Vorgeschichte: Neuropathy left side
Andere Medikamente: Multi vitamin
Allergien: Shellfish and iodized salt
Vorherige Impfungen: -

VAERS 1501862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 26.07.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Hypoaesthesia Paraesthesia

Symptomtext

About 40 minutes post-vaccine, patient experienced numbing sensation in both sides of face. Numbness continued and then spread to the outer right thigh and calf. Numbness in face started improving after a few days, but reoccurred several weeks post-vaccination. Numbness. tingling sensation in leg transferred to left leg, and was intermittent. Patient experienced tightness in chest 36 hours post-vaccination, but upon seeking medical attention, no heart attack or stroke was present. Numbness has continued for 8 weeks post-vaccine. Paralysis has not occurred and patient has full mobility of facial muscles and limbs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 03/22/2021 - ER visit; patient released with no conclusion as to what triggered numbness (vaccination or anxiety?)
Aktuelle Erkrankungen: no known (maybe seasonal allergies)
Vorgeschichte: none
Andere Medikamente: Wellbutrin XL 300 mg
Allergien: none
Vorherige Impfungen: -

VAERS 1500739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 28,0
Geschlecht: M
Eingang: 24.07.2021
Impfdatum: 11.07.2021
Beginn: 21.07.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Severe

Weitere VAERSDATA-Felder

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

VAERS 1499665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 23.07.2021
Impfdatum: 21.07.2021
Beginn: 21.07.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Dyspnoea Fatigue Headache Injection site pain Lymphadenopathy Myalgia

Symptomtext

generalized muscle and joint pain, extreme fatigue, shortness of breath, pain at insertion site, lymphadenopathy axillary and supraclavicular on site of infection, headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: induced hypothyroidism after total thyroidectomy due to grave's disease
Andere Medikamente: levothyroxine 100microgram daily, magnesium L-threonate200mg daily
Allergien: none
Vorherige Impfungen: fatigue and generalized muscle pain, 46, October 2020, influenza vaccine/Fluarix Quad, Left deltoid

VAERS 1497498

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: MO
Alter: 37,0
Geschlecht: F
Eingang: 23.07.2021
Impfdatum: 08.07.2021
Beginn: 10.07.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Keratosis pilaris Paraesthesia Pruritus Rash Rash papular SARS-CoV-2 test

Symptomtext

Raised rash; small bumps in large quantities spreading bilaterally from the hip, buttocks, back of the leg and down the side of the legs; tingly; itchy; whelped yup rash appeared on both arms around the elbow and wrists; This is a spontaneous report from a contactable other HCP (patient, self-reported). A 37-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EW0186 and expiry date was not reported), via an unspecified route of administration, in Arm Left, on 08Jul2021 at 15:30 PM (age at vaccination: 37 years), as a single dose for COVID-19 immunization at doctor's office/urgent care. The patient was not pregnant at the time of vaccination. The patient's medical history included Covid-19 (if covid prior vaccination: Yes). Past drug included known allergies: Sulfa, gluten, and hydrocodone. Concomitant medications included ascorbic acid, betacarotene, calcium sulfate, colecalciferol, cyanocobalamin, ferrous fumarate, folic acid, nicotinamide, pyridoxine hydrochloride, retinol acetate, riboflavin, thiamine mononitrate, tocopheryl acetate, zinc oxide (PRENATAL VITAMINS) and ibuprofen (MOTRIN). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient was not tested for COVID-19. The patient reported that on 10Jul2021 at 09:00 AM, she experienced raised rash, small bumps in large quantities spreading bilaterally from the hip, buttocks, back of the leg and down the side of the legs. It was tingly and itchy, also a whelped yup rash appeared on both arms around the elbow and wrists but cleared within the night. The patient received Benadryl and hydrocortisone cream as treatment for the events. Outcome of the events was recovering.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of events Raised rash, Keratosis pilaris, Paraesthesia, Pruritus and rash cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: Covid-19; Result Unstructured Data: Test Result:Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (if covid prior vaccination: Yes)
Andere Medikamente: PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS ; MOTRIN [IBUPROFEN]
Allergien: -
Vorherige Impfungen: -

VAERS 1494227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: OH
Alter: 45,0
Geschlecht: F
Eingang: 22.07.2021
Impfdatum: 25.05.2021
Beginn: 25.05.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Cough Dyspnoea Throat tightness

Symptomtext

started having a dry cough almost within 5 minutes of the injection. proceded to have throat tightness and some shortness of breath. while in the store i tooll 75 mg of benadryl. this caused the symptoms to stablize but not go away. took additional 50 mg benadryl 1 hour later. needed benadryl 50 mg every four hours for 24 hours. was still having throat tightness and shortness of breath. requiring albuterol about every 4-6 hours. called primary care that started me on prednisone taper. completed that and symptoms slowly resolved with prednisone over 4 days. however i have continue to have a headache since that day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: allergy induced asthma; gerd; chronic back pain
Andere Medikamente: naproxen, protonix, monteluekast, baclofen, pepcid, zyrtec
Allergien: latex; benzoine; tree nuts; coconut; kiwi
Vorherige Impfungen: -

VAERS 1487041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 20.07.2021
Impfdatum: 10.07.2021
Beginn: 10.07.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Arthralgia Back pain Fatigue Headache Joint stiffness Musculoskeletal stiffness Neck pain Pain Palpitations Swelling

Symptomtext

* Headache as well as pain in the neck, shoulders, and back * Racing heartbeat and heart palpitations * Ongoing pain, swelling, stiffness in the hands and fingers, elbows, knees, ankles, and feet * Ongoing tiredness and fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Exercise-induced asthma
Andere Medikamente: 23 MI Testosterone Progesterone DOTTI (estradiol patch) NP Thyroid B Complex Fish Oil Biotin DHEA D3 Iron Trazodone Magnesium Glycinate Melatonin Glucosamine/MSM Collagen MineralPlex supplement Zyrtec Turmeric
Allergien: Erythromycin Mangos
Vorherige Impfungen: -

VAERS 1484428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: TX
Alter: 27,0
Geschlecht: F
Eingang: 19.07.2021
Impfdatum: 17.07.2021
Beginn: 18.07.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Chest discomfort Chest pain Heart rate increased Painful respiration

Symptomtext

Chest pain, feel like blockage to chest area, worsening on deep breathing and laying down, get some relief once sit up or stand up. Had short period of fast heart beats on Sunday night, but went away after a few hours.

Weitere VAERSDATA-Felder

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

VAERS 1483931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CO
Alter: 24,0
Geschlecht: F
Eingang: 18.07.2021
Impfdatum: 01.07.2021
Beginn: 10.07.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: SYR / LA

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

Condition aggravated Pruritus Urticaria

Symptomtext

Hives from scratches, itching, jewelry. The hives are itchy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Reoccurring hives, from jewelry, and itching.
Andere Medikamente: N/A birth control: paraguard IUD
Allergien: Tetracycline Cats Dogs Hayfever
Vorherige Impfungen: -

VAERS 1483896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NE
Alter: 48,0
Geschlecht: M
Eingang: 18.07.2021
Impfdatum: 16.07.2021
Beginn: 16.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Blood urine present Chest discomfort Chills Hypertension Nausea Pain

Symptomtext

High blood pressure, blood in urine , chill, body ache,pressure on the chest, nausea,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Not yet done going to do it today
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1479066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: CA
Alter: 13,0
Geschlecht: M
Eingang: 16.07.2021
Impfdatum: 09.07.2021
Beginn: 13.07.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

C-reactive protein increased Chest pain Dyspnoea Echocardiogram normal Electrocardiogram normal Headache Myalgia Red blood cell sedimentation rate increased Troponin I increased

Symptomtext

Mid sternal chest pain on 7/13/21 after the 2nd dose of COVID vaccine ( 7/9/21), symptom last for 1 hr, spontaneous resolved. hx of shortness of breath at night on 7/10, completely resolved the next morning. headache and muscle aching after vaccination on 7/9/21, last for 3 days. no palpitation. he is seen in office on 7/13/21 due to hx of chest pain in the morning, no current chest pain/symptoms, normal CVS exam, normal EKG. Elevated troponin I/ESR/CRP and normal CBC Troponin I 1.92 ( 0.00-0.04) , ESR 20 ( <15), CRP 3.3 ( <0.9) he again seen in ER the same day for abnormal troponin I results, recheck EKG normal., troponin down to 1.73 he was seen in pediatric cardiology clinic on 7/14/21, troponin 0.68, normal EKG and normal echocardiogram. his symptoms self resolves without medical intervention.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: see in item 18
Aktuelle Erkrankungen: On 7/9. Headache, temperature at 99, muscle pain for 3 days. No cough. on 7/10 had shortness of breath at night, no chest pain. No palpitation
Vorgeschichte: hx of latent TB, complete treatment of INH in 2011
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1476561

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: UT
Alter: 30,0
Geschlecht: F
Eingang: 16.07.2021
Impfdatum: 01.06.2021
Beginn: 01.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Gait disturbance Hypoaesthesia Muscle spasms Pain in extremity Paraesthesia

Symptomtext

Tingling, numbness in limbs Hard to walk Pain in legs Hands and feet cramping for long periods of time

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 6/13/2021 went to ER 7/6/2021 went to neurologist who ruled out MS
Aktuelle Erkrankungen: No
Vorgeschichte: Headaches
Andere Medikamente: Gabapentin Klonopin Tylenol Prozac Depot-shot
Allergien: No
Vorherige Impfungen: -

VAERS 1475186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: OH
Alter: 43,0
Geschlecht: F
Eingang: 15.07.2021
Impfdatum: 04.06.2021
Beginn: 07.06.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Pain in extremity

Symptomtext

Patient said she began experiencing some leg pains after the first dose of the Pfizer COVID-19 vaccine. She said she thought it was something that was going to go away but has persisted even after getting the second dose. Rph informed patient to talk to her doctor about this issue.

Weitere VAERSDATA-Felder

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

VAERS 1470616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0186

moderat

Staat: NY
Alter: 16,0
Geschlecht: F
Eingang: 14.07.2021
Impfdatum: 02.07.2021
Beginn: 09.07.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest X-ray Chest pain Electrocardiogram Troponin

Symptomtext

Having a stabbing pain in the center of her chest, went on for a few days. Was taken to the dr whom advised them to take her to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: yes EKG, chest x-ray and run blood work for treponins
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Zyrtec
Allergien: no
Vorherige Impfungen: -

VAERS 1466045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0186

moderat

Staat: TX
Alter: 46,0
Geschlecht: F
Eingang: 13.07.2021
Impfdatum: 25.05.2021
Beginn: 25.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Feeling hot Nausea Palpitations

Symptomtext

hot; nauseous; heart was racing; This is a spontaneous report from a contactable consumer (patient). A 46-years-old female patient received first dose of BNT162b2 (COMIRNATY, solution for injection, Lot Number: EW0186), via an unspecified route of administration on 25May2021 at 12:00 (at the age of 46-years) as single dose in the left arm for covid-19 immunisation. The patient's medical history included hypothyroid and had food allergies. The patient's concomitant medications included levothyroxine sodium (SYNTHYROID), Cetrizine from an unknown date and unknown if ongoing. The patient did not receive any other vaccines within four weeks prior to the 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. On 25May2021 at 12:00 within 10 minutes of receiving vaccine the patient experienced hot, nauseous, and heart was racing. Patient stated that pharmacist gave me two doses of Benadryl and one of Tylenol. After a bit the symptoms abated. Patient scheduled an appointment with my PCP to discuss this reaction. She advised to continue and get the second dose. She had the second dose and the onset was faster and more severe. She had the shot and with 3 minutes she was dry heaving, very congested, throat felt tight. She could still breathe. This all happened even though she took Benadryl and a Tylenol 45 minutes prior to her injection. Again, the pharmacist gave a dose of Benadryl to help with the effects of the vaccine. She would like to know what is in the vaccine. Patient stated that she had food allergies and this reaction is frightening. Ae resulted in clinic visit and ER visit. The outcome of the events was resolved. Information on Lot/Batch number was available. Additional information has been requested

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Food allergy (known allergies Yes I have food allergies); Hypothyroidism
Andere Medikamente: SYNTHYROID; CETRIZINE
Allergien: -
Vorherige Impfungen: -