VAERS Reports 180 50 25

VAERS 2723125

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: TX
Alter: 69,0
Geschlecht: M
Eingang: 12.12.2023
Impfdatum: 18.03.2021
Beginn: 17.01.2022
Tage bis Beginn: 305,0
Dosis: 1
Route/Site: IM / UN

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

Asthenia COVID-19 Chest X-ray abnormal Clostridium test negative Death Diarrhoea Mental status changes Pneumonia Positive airway pressure therapy Respiratory distress SARS-CoV-2 test positive

Symptomtext

Patient presented to the hospital with reports of worsening mental status, with loss, diarrhea and generalized weakness. He reportedly has had diarrhea for the past 1 month and had been evaluated by Gastroenterology team. Clostridium difficile test was reportedly negative. On evaluation in the emergency room, he tested positive for COVID-19. Chest x-ray interpreted as follows - Faint residual densities over the lower lungs could represent mild atypical infection. Patient diagnosed with pneumonia due to covid 19. Patient received IV abx and remdesivir. Patient was weaned off oxygen by discharge. Patient was discharged to SNU but was readmitted on 1.28.22 for worsening respiratory status requiring BiPAP on admission. Family opted to transition to comfort care and patient was transferred to inpatient hospice on 2.13.22. Patient passed away on 2.16.22.

Weitere VAERSDATA-Felder

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

VAERS 2718400

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: TX
Alter: 76,0
Geschlecht: M
Eingang: 28.11.2023
Impfdatum: 08.03.2021
Beginn: 21.01.2022
Tage bis Beginn: 319,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure Asthenia COVID-19 pneumonia Cough Dyspnoea Pneumonia aspiration Pyrexia

Symptomtext

Admitted with cough, fever, SOB, weakness, acute hypoxic respiratory failure: slow improvement, Was on hfnc, now weaned to oxygen per nasal canula 2 liters, likely from COVID pna and suspected aspiration pneumonia. Little improvement, transferring to hospice

Weitere VAERSDATA-Felder

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

VAERS 2713184

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 13.11.2023
Impfdatum: 06.04.2021
Beginn: 31.08.2023
Tage bis Beginn: 877,0
Dosis: 1
Route/Site: - / -

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

Anaemia COVID-19 Chest pain Haemoglobin decreased Intensive care Red blood cell transfusion Respiratory symptom SARS-CoV-2 test positive Septic shock Staphylococcus test negative Troponin increased

Symptomtext

BRIEF OVERVIEW: Admission Date: 8/31/2023 Discharge Date: Sep 5, 2023 Discharge Disposition: home health care svc DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Septic shock [A41.9, R65.21] COVID-19 [U07.1] HOSPITAL COURSE: 78 years old woman presented with URI symptoms found to have COVID positive. She also had chest pain on admission with troponin 17 -> 17 -> 28. Discussed with on-call cardiologist, who recommended an echocardiogram on Tuesday. He also recommended daily EKG for her along with EKG if she develops chest pain. ID was consulted with recommendations for IV remdesivir for 3 days that she completed. She required vasopressor support with levophed which was weaned off gradually. She was treated with IV vanco/cefepime/flagyl with discontinuation of IV vancomycin with negative MRSA swab. Medical intensive care unit had been consulted while the patient was in the intensive care unit with recommendations for 5-7 days of empiric antibiotics. Of note, the patient had developed anemia with transfusion of 1 unit of pRBC in the setting of her history of known coronary artery disease with some earlier complaints of chest pain hemoglobin had gone down to as low as 6.9 with a baseline thought to be closer to 10. Of note, she has had similar episodes in the past, last noted in March 2022. Then, she had a hemoglobin of 6 and presented to the ER. She was transfused 2 units at that time and was advised to be admitted the hospital for further evaluation but she declined this. Since then, she is had no clinical signs of GI blood loss and her hemoglobin has overall remained stable. Her hemoglobin did improve after transfusion and went up to 8.5. There was no clinical signs of GI blood loss. Discussion was had with the patient in regards to further workup for this but she stated that she would like to follow up with her primary care provider. Patient was allowed to resume her aspirin therapy on discharge; Clopidogrel was held. Reviewing the patient's outpatient records, during a previous admission she had been diagnosed with a TIA and was recommended to be on aspirin and Plavix for 1 month, followed by aspirin monotherapy thereafter. Apparently, she is not been on monotherapy but has been taking clopidogrel and aspirin and she again was advised to remain on just aspirin. Patient was thought to be medically stable for discharge home on 09/05.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine, unspecified, without mention of intractable migraine without mention of status migrainosus Kyphosis Diabetes mellitus, type 2 Essential hypertension Gout Seizures Renal colic on left side Allergic rhinitis Hypercholesterolemia Loss of height Osteopenia Anemia Arthritis At risk for falls Coronary artery disease involving native coronary artery of native heart without angina pectoris Vertebral artery stenosis, left TIA (transient ischemic attack) Neck pain Chronic systolic (congestive) heart failure Hypophosphatemia Chronic kidney disease (CKD), stage III (moderate) Hypoalbuminemia
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet allopurinol (ZYLOPRIM) 300 MG tablet aspirin 81 MG chewable tablet BD Lancet Ultrafine 30G Lancets Blood Glucose Monitoring Suppl MISC blood glucose test strips blood glucose test strips clopidogrel (PL
Allergien: Codeine Niaspan [Niacin]Hallucinations PenicillinsSwelling Antihistamines Ivp Dye, Iodine ContainingAgitation Lipitor [Atorvastatin]Other Lipitor [Hmg-coa-r Inhibitors] MetforminOther Vicodin [Hydrocodone-acetaminophen]Other Diagnostic X-ray Materials Iodinated Contrast Media
Vorherige Impfungen: -

VAERS 2703946

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: AR
Alter: 74,0
Geschlecht: F
Eingang: 27.10.2023
Impfdatum: 19.09.2022
Beginn: 26.10.2023
Tage bis Beginn: 402,0
Dosis: 1
Route/Site: IM / LA

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

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

Symptomtext

Pt was hospitalized on 10/26 with covid and sepsis. Pt died.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Covid positive prior to hospitalization on 10/23. Tested positive at hospital 10/26.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Anxiety, congestive heart failure, chronic myeloid leukemia, depression, GERD, restless legs syndrome, chronic pain
Andere Medikamente: Unknown
Allergien: Celebrex, propoxyphene, stadol, sulfa drugs
Vorherige Impfungen: -

VAERS 2676504

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 25.08.2023
Impfdatum: 10.03.2021
Beginn: 31.12.2021
Tage bis Beginn: 296,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain upper Acute respiratory failure COVID-19 pneumonia Endotracheal intubation Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

Presented w/ epigastric pain since yesterday and n/v. Tx for acute hypoxemic resp. failure req. intubation d/t exacerbation of CHF and secondary to Covid + infection/pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 18,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2668910

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: TX
Alter: 83,0
Geschlecht: F
Eingang: 10.08.2023
Impfdatum: 10.03.2021
Beginn: 18.01.2022
Tage bis Beginn: 314,0
Dosis: 1
Route/Site: IM / UN

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

Abdominal pain lower Anticoagulant therapy Aspiration COVID-19 pneumonia Cough Death Diarrhoea Dyspnoea Encephalopathy Endotracheal intubation

Symptomtext

Presents to the ED complaining of SOB. Pt states she is vaccinated for COVID, but has not received booster. Admitted for COVID pneumonia . Associated symptoms include cough, lower abdominal pain and diarrhea. Encephalopathy due to 2019-nCoV. Aspirating after few days after hospitalization Tx. 4 L nasal cannula, intubated , Respiratory therapy treatments, Antibiotic therapy with Azithromycin, Continue with Dexamethasone , ZINC, magnesium, Pepcid, LOVENOX. Patient expired comfort care measures were initiated.

Weitere VAERSDATA-Felder

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

VAERS 2664545

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: TX
Alter: 71,0
Geschlecht: M
Eingang: 02.08.2023
Impfdatum: 11.03.2021
Beginn: 06.01.2022
Tage bis Beginn: 301,0
Dosis: 1
Route/Site: IM / UN

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

Acute myocardial infarction COVID-19 Chest pain Troponin increased

Symptomtext

Presented with left-sided chest pain consistent with elevated troponin caused by NSTEMI; incidental COVID-19 finding but asymptomatic

Weitere VAERSDATA-Felder

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

VAERS 2639247

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: FL
Alter: 96,0
Geschlecht: F
Eingang: 31.05.2023
Impfdatum: 21.03.2021
Beginn: 10.07.2022
Tage bis Beginn: 476,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Asthenia Atelectasis C-reactive protein COVID-19 Cardiomegaly Chest X-ray abnormal Chronic kidney disease Chronic obstructive pulmonary disease Computerised tomogram thorax abnormal Condition aggravated Coronary artery disease Coronavirus pneumonia Echocardiogram abnormal Ejection fraction normal Exercise tolerance decreased Fibrin D dimer increased Hiatus hernia

Symptomtext

BREAKTHROUGH COVID: FULLY VACCINATED WITH JANSSEN BOOSTER. 97 YO FEMALE WITH COVID-19 infection, COPD exacerbation , Acute on chronic hypoxic respiratory failure. Coronavirus disease 2019 pneumonia in this patient. PT On Rocephin and Zithromax procalcitonin level slightly abnormal, discontinue antibiotics at discharge. Continue dexamethasone. Pt is here for weakness, her family is at bedside and provides most of the history. Pt admitted with Pulmonary fibrosis, ELEVATED TROPONIN, CKD. Severe Pulmonary HTN on Echo ,Hyperglycemia. She was treated with antibiotics, steroids, albuterol. She has been on oxygen for several years now. She has decreased exercise tolerance. She had echo on 02/15/2022 with normal ejection fraction, there is pulmonary artery pressure was approximately 77 mmHg, mild-to-moderate MR. Moderate to severe TR. She was not able to perform lung function test in the office, invasive testing was deferred secondary to risk vs benefits. CXR here with bilateral airspace/interstitial opacity which may represent pneumonitis, pulmonary vascular congestion and/or chronic changes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: CT chest: Subpleural reticulation present with the mild associated groundglass opacities and small effusions.No large consolidation. No significant focal groundglass opacities. She had CT scan on 04/29/2022 with bilateral pleural effusion, diffuse pulmonary fibrosis, atelectasis, cardiomegaly bleed, coronary artery disease, large hiatal hernia. Troponin T HS 29, T HS Interp, SLIGHTLY ELEVATED ABN D-Dimer Quant 1.43 , Inflammatory <3.0 XR Chest 1 View, (07/10 19:16): bilateral airspace/interstitial opacity which may represent pneumonitis, pulmonary vascular congestion and/or chronic changes. large hiatal hernia. further evaluation with follow-up ct chest exam is recommended.
Aktuelle Erkrankungen: UNKNONWN
Vorgeschichte: COPD, PULMONARY FIBROSIS, 4L OXYGEN DEPENDENT, severe Pulm HTN
Andere Medikamente: UNKNOWN
Allergien: penicillins (rash) sulfADIAZINE (rash)
Vorherige Impfungen: -

VAERS 2603351

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 73,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 11.11.2021
Beginn: 21.11.2022
Tage bis Beginn: 375,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Death SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient had a breakthrough infection and passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID lab on 11/15/2023.
Aktuelle Erkrankungen: -
Vorgeschichte: CHF
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2566737

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 68,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 09.03.2021
Beginn: 29.06.2022
Tage bis Beginn: 477,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Death SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient had breakthrough infection and passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID test on 6/21/2022.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2545877

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 09.03.2021
Beginn: 30.11.2022
Tage bis Beginn: 631,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Atelectasis COVID-19 Chest X-ray abnormal Computerised tomogram thorax abnormal Hypotension Hypoxia Inflammation Injury Musculoskeletal chest pain Neoplasm Oropharyngeal pain Passive smoking Positive end-expiratory pressure Productive cough Pulmonary mass Rib fracture SARS-CoV-2 test positive

Symptomtext

Patient is a 77 y.o. female with a history of HTN, osteoporosis, idiopathic gastroparesis who presented to emergency 11/26/2022 for rib pain without a fall or injuries. Found to have multiple acute bilateral rib fractures so she was transferred to ED for trauma evaluation. Urgent Care following since admission for medical management. Hospital course complicated by diagnosis of COVID-19, acute hypoxic respiratory failure and hypotension. 1. Multiple bilateral acute rib fractures started 1 day before admission, after being hugged by a friend. In setting of known osteoporosis . CT chest 11/26/2022 found anterior to anterolateral right 3-7 and left 4-7 rib fractures, grade 2 chest wall injury. Aggressive pulmonary toilet with I-S and vibratory PEEP. Pain control. PT/OT followed. Trauma followed, f/u OP 12/15 in trauma clinic. 2. COVID-19: Vaccinated. Developed sore throat and test positive 11/29/22. CXR 11/29/22 with minimal bibasilar atelectasis, no consolidations. Initially without cough or sputum production but developed symptoms on 11/30/22 with hypoxia. Completed 6 days of dexamethasone with improvement to room air. Completed isolation. 3. Acute hypoxic respiratory failure: required 2L NC 11/30/22 AM. Secondary to COVID-19 infection, rib fracture. Resolved 4. Osteoporosis: known h/o, likely directly contributed to fx above. Continued home vitamin D, calcium and Fosamax. 5. Solitary pulmonary nodule: noted incidentally on admit imaging with new 0.5cm cavitary nodule or cystic lesions with smooth wall thickening in RUL consider traumatic vs inflammatory vs neoplastic etiologies. Extensive secondhand smoke exposure. Outpatient follow up imaging per Organization at 1 year. 6. Incidental findings: noted questionable filling defect in CBD with no intra nor extrahepatic biliary lesion. Consider MRCP if were to develop symptoms of biliary colic. Also noted unchanged distal splenic artery aneurysm measuring up to 0.8cm, repeat imaging 1 year recommended per report. 7. HTN: home meds held briefly for hypotension as above. Improved. No med changes on discharge. 8. EtOH dependence: drinks 3 beers/day. Denied any h/o EtOH withdrawal in the past. Discharged on thiamine and folate supplement. Recommended outpatient follow-up.

Weitere VAERSDATA-Felder

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

VAERS 2545574

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 29.12.2022
Impfdatum: 12.03.2021
Beginn: 08.12.2022
Tage bis Beginn: 636,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal Blood lactic acid increased COVID-19 Echocardiogram normal Electrocardiogram normal Glycosylated haemoglobin increased Hyperglycaemia Hypervolaemia Hyponatraemia Hypoxia Intensive care Lung consolidation Malaise Metabolic acidosis Pneumonia Pneumonia streptococcal Respiratory tract infection

Symptomtext

Patient is a 64 y.o. male who presented from home on 12/8/2022 with worsening hypoxia in the setting of COVID. On admission he was also found to have CAP. His oxygen requirements improved with antibiotics and steroids. Pt was discharged home on 12/10. Discharge Diagnosis and Associated Hospital Course Acute Hypoxic Respiratory Failure - In the setting of multiple respiratory infections as below. - On admission was requiring NRB/HHFNC, now weaned off and stable on RA. - cont IS Severe Sepsis without Shock - improved Community Acquired Streptococcus Pneumonia - Meeting SIRS criteria and with evidence of end organ dysfunction on presentation, improved with empiric treatment. - CTPA with LLL consolidation, concerning for CAP. Urine antigens positive for Strep Pneumoniae. - Continue empiric Levaquin therapy, end date 12/14. COVID-19 - With symptom onset reported 11/27, tested positive 12/2. - Had started Paxlovid and steroids outpatient prior to admission. - Continuing Decadron for 10 days. Metabolic Acidosis - resolved - Elevated Lactate of 4.8 in the ED in the setting of hypoxia and sepsis as above. - Normalized with resuscitation. Insulin Dependent Diabetes Mellitus Type 2 with Hyperglycemia - A1c of 8.5 noted 4/2022. - Hyperglycemia in the setting of acute illness and steroid administration. - Home regimen includes glyburide/metformin, Lantus 43 units nightly, 18 units Lispro TID AC. Mild Hyponatremia - Unclear etiology, though to be at least partially related to interval hypervolemia in the setting of volume resuscitation. - resolved. - Administered one dose of IV Lasix in ICU 12/9. Elevated Troponin - Elevated on admission and then downtrended, with apparent up-trend thereafter. - Presumed to be in the setting of sepsis and relative hypoxia. Patient denied chest pain throughout this admission. - Echocardiogram 12/9 without focal WMAs. ECG without focal ST elevations or depressions. - No further work-up inpatient. Essential Hypertension - Home regimen of Clonidine 0.2mg TID, lisinopril 40mg, and metoprolol 100mg resumed. History of Gout - Continued allopurinol. Major Depressive Disorder - Continued home Celexa. Obesity - BMI 35.83 - Continue to encourage lifestyle and dietary modification as tolerated. Possible OSA - With snoring noted in ICU, high suspicion for underlying OSA. - Referral to sleep clinic being coordinated by ICU team, appreciate assistance.

Weitere VAERSDATA-Felder

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

VAERS 2526724

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 79,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 23.04.2022
Beginn: 01.06.2022
Tage bis Beginn: 39,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Death SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient had a breakthrough infection and passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive lab test on 5/25/2022.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2525581

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: -
Alter: 48,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 25.03.2021
Beginn: 01.10.2021
Tage bis Beginn: 190,0
Dosis: 1
Route/Site: - / -

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

COVID-19 COVID-19 pneumonia Cardio-respiratory arrest Chest X-ray abnormal Death Dyspnoea Intensive care Oxygen saturation decreased SARS-CoV-2 test positive

Symptomtext

11/2/21 pt to ED with c/o SOB; states had a positive COVID test 4 days earlier; pt tested positive in ED; CXR showed COVID pneumonia; O2 supplementation; O2 sats began to drop; transferred to MICU; given Decadron, ABX, Combivent Inhaler; suffered cardiopulmonary arrest and passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, ESRD, HTN, gout, left renal cell carcinoma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2493907

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 93,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 11.03.2021
Beginn: 24.02.2022
Tage bis Beginn: 350,0
Dosis: 1
Route/Site: IM / RA

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

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

Symptomtext

PATIENT TESTED + FOR COVID 2/2022 AND PASSED 2-24-22. I HAVE NO OTHER INFORMATION OTHER THAN SHE WAS RESIDENT OF LOCAL HEALTH AND REHAB AND HAD A LAB + FOR COVID 2-19-22.

Weitere VAERSDATA-Felder

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

VAERS 2442801

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: -
Alter: 87,0
Geschlecht: M
Eingang: 13.09.2022
Impfdatum: 13.03.2021
Beginn: 27.01.2022
Tage bis Beginn: 320,0
Dosis: 1
Route/Site: - / -

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

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

Symptomtext

Patient had a positive COVID test on 1/27/22; 2/3/22 patient to ED with syncopal type episode; O2 sats 97% on RA; doctor states patient already on treatment for COVID from 1/27/22 (no specific treatment in the medical records); patient was DC'd to home where he passed away.

Weitere VAERSDATA-Felder

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

VAERS 2426658

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 41,0
Geschlecht: M
Eingang: 01.09.2022
Impfdatum: 08.03.2021
Beginn: 28.07.2022
Tage bis Beginn: 507,0
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy COVID-19 Deep vein thrombosis Diabetic ketoacidosis Pulmonary embolism Vomiting

Symptomtext

Has DVT on Eliquis. To ED and admitted with Pulmonary Embolism. Vomiting from COVID-19 infection and unable to take Eliquis for a few days. Started on Heparin drip and given Remdesivir. Also on empiric antibiotics. Initially admitted on 7/27 with DKA, but signed out AMA. Not in DKA this admission. Received third dose of Remdesivir and will be discharged home instable condition. Does not require O2. Will resume Eliquis. F/U with PCP 5-7 days.

Weitere VAERSDATA-Felder

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

VAERS 2388369

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 69,0
Geschlecht: M
Eingang: 25.07.2022
Impfdatum: 16.03.2021
Beginn: 14.07.2022
Tage bis Beginn: 485,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Patient received COVID19 vaccine on 03/16/2021; no booster doses given. Patient tested positive for covid19 on 07/07/2022, admitted to the hospital on 07/07/2022, died on 07/14/2022

Weitere VAERSDATA-Felder

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

VAERS 2367617

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: TN
Alter: 49,0
Geschlecht: M
Eingang: 13.07.2022
Impfdatum: 09.03.2021
Beginn: 15.01.2022
Tage bis Beginn: 312,0
Dosis: 1
Route/Site: - / -

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

Abdominal pain Ascites COVID-19 Colitis Computerised tomogram abdomen abnormal Death Dizziness Endotracheal intubation Gastrointestinal haemorrhage Gastrointestinal wall thickening Hepatic cirrhosis Hiatus hernia Multiple organ dysfunction syndrome Nausea Rectal haemorrhage SARS-CoV-2 test positive Sepsis Septic shock

Symptomtext

Patient presented to hospital on 01/14/2022 with rectal and GI bleeding, with abdominal pain, nausea and dizziness. In the ED tested positive for Covid-19. CT abdomen/Pelvis impression: abnormal wall thickening, hepatic cirrhosis associated with splenomegaly and small volume ascites, moderate hiatal hernia. Patient eventually needed intubation and requiring vasopressor support for sepsis. Patient expired on 01/22/2022 from sepsis d/t Covid-19 as well as colitis with septic shock and multiorgan failure.

Weitere VAERSDATA-Felder

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

VAERS 2294571

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 90,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 10.04.2021
Beginn: 02.02.2022
Tage bis Beginn: 298,0
Dosis: 1
Route/Site: - / -

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

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

Symptomtext

Patient had breakthrough infection and passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 10,0
Labordaten: Positive COVID-19 test on 1/28/2022.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Migraine Sleep Apnea Fibrotic Lung Disease HTN Atrial Fibrillation CHF Hypothyroidism
Andere Medikamente: Amlodipine apixaban carvedilol cyanocobalamin furosemide hydrocodone levothyroxine losartan Montelukast omega-3 omeprazole propafenone valsartan
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 2173269

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 63,0
Geschlecht: M
Eingang: 20.04.2022
Impfdatum: 28.10.2021
Beginn: 19.01.2022
Tage bis Beginn: 83,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal hernia Abdominal pain Abscess drainage Acidosis Anisocoria Atrial flutter Blood ketone body COVID-19 Colectomy Computerised tomogram abdomen abnormal Death Dyspnoea Electrocardiogram abnormal Endotracheal intubation Enterorrhaphy Hernia perforation Hypoxia Mental status changes

Symptomtext

pt had covid vaccines. dx with covid on 1/17/2022, passed on 01/19/2022

Weitere VAERSDATA-Felder

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

VAERS 2173269

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 63,0
Geschlecht: M
Eingang: 20.04.2022
Impfdatum: 28.10.2021
Beginn: 19.01.2022
Tage bis Beginn: 83,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal hernia Abdominal pain Abscess drainage Acidosis Anisocoria Atrial flutter Blood ketone body COVID-19 Colectomy Computerised tomogram abdomen abnormal Death Dyspnoea Electrocardiogram abnormal Endotracheal intubation Enterorrhaphy Hernia perforation Hypoxia Mental status changes

Symptomtext

pt had covid vaccines. dx with covid on 1/17/2022, passed on 01/19/2022

Weitere VAERSDATA-Felder

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

VAERS 2157696

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 65,0
Geschlecht: M
Eingang: 04.03.2022
Impfdatum: 08.03.2021
Beginn: 24.02.2022
Tage bis Beginn: 353,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure COVID-19

Symptomtext

Patient is a very pleasant 66 YO man who was admitted to hospital for acute respiratory failure 2/2 COVID. Was vaccinated J+J vaccine- no booster. While admitted was given Remdesivir and treated with steroids. Was also given antibody infusion. He was weaned down from 2L to no oxygen requirement prior to discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Aflutter, HTN, CAD, PAF, angina, IDDM, COPD, smoker
Andere Medikamente: Cymbalta, Lyrica, Colace, Synthroid, Ventolin, Humalog, Plavix, protonix, desyrel, Nitrostat, Norvasc, Flomax, Proscar, myrbetriq, Imdur, ASA,
Allergien: Bees, iodine contrast media, Xarelto, PCNS
Vorherige Impfungen: -

VAERS 2151633

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 75,0
Geschlecht: M
Eingang: 02.03.2022
Impfdatum: 11.03.2021
Beginn: 17.09.2021
Tage bis Beginn: 190,0
Dosis: 1
Route/Site: SYR / LA

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

Acute myocardial infarction Anticoagulant therapy Asthenia COVID-19 pneumonia Dyspnoea Endotracheal intubation Feeling cold General physical health deterioration Pyrexia Sepsis

Symptomtext

Presented to ED on 9-3-21 with shortness of breath, fever, chilling, and weakness. Admitting diagnosis COVID pneumonia, sepsis and NSTEMI. Treatment included IV steroids, oxygen, therapy, albuterol, vitamins, heparin drip, antibiotics-azithromycin and Rocephin and REMD. Over the next 2-3 days patient continued to decline and was intubated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 14,0
Labordaten: Patient continued to decline therefore decision was made for patient to be a DNR. He was terminally extubated on 9-17-2021.
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2150614

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: IL
Alter: 79,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 08.04.2021
Beginn: 20.12.2021
Tage bis Beginn: 256,0
Dosis: 1
Route/Site: OT / -

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

Atelectasis Blood lactic acid Blood lactic acid increased COVID-19 Cardiac arrest Chest X-ray Chest X-ray abnormal Chest tube insertion Continuous haemodiafiltration Cough Death Decreased appetite Hypertension Life support Lung opacity Oxygen saturation Oxygen saturation decreased Pain

Symptomtext

DEATH; CARDIAC ARREST; CHEST TUBE INSERTION; THROMBOSIS; ULTRASOUND DOPPLER ABNORMAL; CHEST X-RAY ABNORMAL; LIFE SUPPORT; ATELECTASIS; LUNG OPACITY; SOMNOLENCE; PAIN; COUGH; COVID-19; SARS-COV-2 TEST POSITIVE; OXYGEN SATURATION DECREASED; CONTINUOUS HAEMODIAFILTRATION; BLOOD LACTIC ACID INCREASED; HYPERTENSION; PNEUMOTHORAX; RENAL IMPAIRMENT; SEPTIC SHOCK; SEPSIS; DECREASED APPETITE; This spontaneous report received from a health care professional by a Regulatory Authority (VAERS FDA Inbound Unit 2005918) concerned a 79 year old male of unspecified race and ethnicity. Initial information was processed along with additional information received on 18-JAN-2022. The patient's height, and weight were not reported. The patient's past medical history included: cerebral vascular accident and stroke, and concurrent conditions included: coronary artery disease, gastroesophageal reflux disease, hyperlipidemia, hypertension, restless leg syndrome, and sleep apnea. The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, intramuscular, batch number: 1805025 expiry: UNKNOWN) dose was not reported, 1 total administered to left arm on 08-APR-2021 for an unspecified indication. Concomitant medications included acetylsalicylic acid, amlodipine, atorvastatin, clopidogrel, ferrous sulfate, furosemide, glyceryl trinitrate, isosorbide dinitrate, losartan, metoprolol tartrate, nifedipine, omeprazole, pramipexole, sildenafil, testosterone, tramadol, vitamin b12, and multivitamins. On Thursday (unspecified date), the patient began to develop achy pains and felt sleepy. When his symptoms did not improve he decided to call his primary care doctor. Patient thought he had a urinary tract infection. On 20-DEC-2021, the patient had SARS-CoV-2 test (NR: not provided) which resulted positive for covid-19. He states since that time he has been monitoring his oxygen saturations on his pulse oximetry at home and his oxygen saturations are dropping below 90%. On 22-DEC-2021, the patient had arrived to the emergency room at 88% on room air. He was requiring 5 Liter nasal cannula to maintain his oxygen saturations greater than 92%. On 22-DEC-2021, the chest X-ray showed areas of patchy opacification in the left mid and lower lung and right lower lung, some of this may be infectious inflammatory such as pneumonia while some of this may be atelectatic. He states that he has had decreased appetite, and non-productive cough. He reports that he took his morning medications. The patient was placed on dexamethasone, ceftriaxone, azithromycin and remdesivir. On 27-DEC-2021, Laboratory data included: Diagnostic ultrasound doppler test (NR: not provided) which was positive for nonocclusive calf vein thrombus right lower extremity posterior tibial and peroneal distributions. On 04-JAN-2021, the patient continued to be hypertensive overnight and required increased pressor therapy. He also had a small right-sided pneumothorax that was treated with a right-sided chest tube on 04-JAN-2021 with resolution of the pneumothorax. He continued to be hemodynamically unstable from the COVID sepsis, septic shock also possible pulmonary embolism with elevated lactate levels. His kidney function worsened and he needed CVVH (Continuous Venovenous Hemofiltration, coded as continuous haemodiafiltration) overnight. In the morning on 04-JAN-2021 the patient had cardiac arrest with ROSC (Return of spontaneous circulation) after 3 cycles of ACLS (Advanced cardiac life support). On 04-JAN-2021, the patient died from an unknown cause of death. The duration of hospitalization was 13 days. It was unknown whether an autopsy was performed. (Dose number in series 1). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient died from an unknown cause of death on 04-JAN-2021 and the outcome of cardiac arrest, life support, septic shock, sepsis, thrombosis, pneumothorax, oxygen saturation decreased, renal impairment, atelectasis, chest tube insertion, hypertension, lung opacity, somnolence, covid-19, decreased appetite, continuous haemodiafiltration, blood lactic acid increased, chest x-ray abnormal, ultrasound doppler abnormal, sars-cov-2 test positive, cough and pain was fatal. This report was serious (Death, and Hospitalization Caused / Prolonged). This case was associated with Product quality complaint number 90000212626. The suspected product quality complaint has been confirmed to be the reported allegation was not confirmed and the root cause was determined to be not manufacturing related based on the PQC evaluation/investigation performed. Additional information received from Central Complaint Vigilance department on 18-FEB-2022. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result.; Sender's Comments: V1: The follow up information in this version updates Patient's Product quality complaint investigation result. This updated information does not alter the causality of previously reported events. 20220126449- covid-19 vaccine ad26.cov2.s - Death, cardiac arrest, septic shock, sepsis, thrombosis, pneumothorax, renal impairment, atelectasis, life support, decreased appetite, lung opacity, somnolence, pain, cough, covid-19, sars-cov-2 test positive, chest tube insertion, oxygen saturation decreased, continuous haemodiafiltration, blood lactic acid increased, chest x-ray abnormal, ultrasound doppler abnormal. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). 20220126449-covid-19 vaccine ad26.cov2.s-hypertension. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: MEDICAL HISTORY.; Reported Cause(s) of Death: UNKNOWN CAUSE OF DEATH

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 13,0
Labordaten: Test Date: 202112; Test Name: Oxygen saturation; Result Unstructured Data: below 90%; Test Date: 20211220; Test Name: Blood lactic acid; Result Unstructured Data: increased; Test Date: 20211220; Test Name: SARS-CoV-2 test; Result Unstructured Data: positive; Test Date: 20211220; Test Name: Oxygen saturation; Result Unstructured Data: decreased; Test Date: 20211222; Test Name: Chest X-ray; Result Unstructured Data: Areas of patchy opacification; Test Date: 20211222; Test Name: Oxygen saturation; Result Unstructured Data: 88 %; Test Date: 20211227; Test Name: Diagnostic ultrasound; Result Unstructured Data: nonocclusive calf vein thrombus
Aktuelle Erkrankungen: Coronary artery disease; Gastrooesophageal reflux disease; Hyperlipidemia; Hypertension; Restless leg syndrome; Sleep apnea
Vorgeschichte: Medical History/Concurrent Conditions: Cerebrovascular accident; Stroke
Andere Medikamente: AMLODIPINE; ASPRIN; ATORVASTATIN; CLOPIDOGREL; VITAMIN B12 NOS; FERROUS SULPHATE [FERROUS SULFATE]; FUROSEMIDE; ISOSORBIDE DINITRATE; LOSARTAN; METOPROLOL TARTRATE; MULTIVITAMIN [VITAMINS NOS]; NIFEDIPINE; NITRO [GLYCERYL TRINITRATE]; OMEPR
Allergien: -
Vorherige Impfungen: -

VAERS 2141984

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 67,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 11.03.2021
Beginn: 02.10.2021
Tage bis Beginn: 205,0
Dosis: 1
Route/Site: OT / -

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

Acute kidney injury Angiogram Angiogram pulmonary abnormal C-reactive protein C-reactive protein increased COVID-19 Chronic kidney disease Computerised tomogram thorax Computerised tomogram thorax abnormal Condition aggravated Endotracheal intubation Intensive care Interstitial lung disease Leukocytosis Lung opacity Mechanical ventilation Oxygen saturation Pulmonary embolism

Symptomtext

SINUS TACHYCARDIA; LUNG OPACITY; CONDITION AGGRAVATED; ENDOTRACHEAL INTUBATION; MECHANICAL VENTILATION; INTENSIVE CARE; TROPONIN INCREASED; ANGIOGRAM PULMONARY ABNORMAL; C-REACTIVE PROTEIN INCREASED; COMPUTERISED TOMOGRAM THORAX ABNORMAL; LEUKOCYTOSIS; SARS-COV-2 TEST POSITIVE; ACUTE KIDNEY INJURY; PULMONARY EMBOLISM; CHRONIC KIDNEY DISEASE; INTERSTITIAL LUNG DISEASE; RESPIRATORY FAILURE; COVID-19; This spontaneous report received from a health care professional via a Regulatory Authority Vaccine Adverse Event Reporting System (VAERS) (VAER reference number 1909661) concerned a 67 year old male of unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's past medical history included: calculus of kidney, and myocardial infarction, and concurrent conditions included: chronic kidney disease, coronary artery disease status post stent 2016 and left carotid endarterectomy 2019, hyperlipidemia, and hypertension, and other pre-existing medical conditions included: The patient had diseases of the circulatory system. The patient had no known drug allergy. The patient was previously treated with ipratropium bromide/salbutamol sulfate. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025 expiry: unknown) dose was not reported, 1 total administered to the left arm on 11-MAR-2021 for an unspecified indication. Concomitant medications included acetylsalicylic acid, allopurinol, atorvastatin, bisoprolol, clopidogrel, lisinopril, piperacillin sodium/tazobactam sodium, prednisone and steroid tapered (60mg for 7 days, 50mg for 7 days, 40mg for 7 days, 30mg for 7 days, 20mg for 7 days, and 10mg for 7 days). On 02-OCT-2021, Laboratory data included: Computerised tomogram thorax (NR: not provided) lesser radiographically dense. Patient was diagnosed with covid-19, which was treated outpatient with supplemental oxygen over the last month patient was able to wean his oxygen to 4 liter NC (nasal cannula) until a few days ago, on admission patient on 8 on 10 liter NC at home with oxygen saturation no better than 90 percent. On 04-NOV-2021, Laboratory data included: Computerised tomogram thorax (NR: not provided) Abnormal. On arrival to Emergency department (ED) patient was alert but hypoxic with initial work up, significant for small subsegmental Pulmonary Embolism (PE), on computerised tomogram thorax abnormal (CTA), elevated troponins, leukocytosis, acute kidney injury (AKI), on chronic kidney disease (CKD) and elevated (c-reactive protein) CRP. He was admitted and started on therapeutic lovenox, levaquin and steroids. On 06-NOV-2021, the patient experienced acute kidney injury, chronic kidney disease, interstitial lung disease, pulmonary embolism, respiratory failure, angiogram pulmonary abnormal, c-reactive protein increased, computerised tomogram thorax abnormal, condition aggravated, endotracheal intubation, intensive care, leukocytosis, lung opacity, mechanical ventilation, sars-cov-2 test positive, sinus tachycardia, troponin increased and was hospitalized (date unspecified) for 24 days. During hospitalization patient was continued to have increasing oxygen requirements and was placed on HFNC (High flow nasal cannula) 100 percent 30 liter. Consulted for transfer to higher level of care per family request Upon exam patient was intubated and sedated on 100 percent on the vent. Outpatient pulm follow up encourage incentive spirometry daily 1hrs chest physiotherapy scheduled. Discontinued Duoneb since patient did not feel much significant improvement and had sinus tachycardia. Laboratory data included: C-reactive protein (NR: not provided) elevated, CT angiography (NR: not provided) Subsegmental Pulmonary Embolism, Cardiac troponin (NR: not provided) elevated, Computerised tomogram thorax (NR: not provided) Abnormal, and SARS-CoV-2 test (NR: not provided) positive. On 22-NOV-2021, Laboratory data included: Computerised tomogram thorax (NR: not provided) lesser radiographically dense. Laboratory data (dates unspecified) included: Oxygen saturation (NR: not provided) no better than 90 percent. Treatment medications (dates unspecified) included: levofloxacin. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from acute kidney injury, pulmonary embolism, chronic kidney disease, interstitial lung disease, respiratory failure, covid-19, sinus tachycardia, lung opacity, condition aggravated, endotracheal intubation, mechanical ventilation, intensive care, troponin increased, angiogram pulmonary abnormal, c-reactive protein increased, computerised tomogram thorax abnormal, leukocytosis, and sars-cov-2 test positive. This report was serious (Hospitalization Caused / Prolonged). This report was associated with product quality complaint: 90000207062. The suspected product quality complaint has been confirmed to be the reported allegation could not be confirmed. A manufacturing related root cause could not be identified based on the PQC evaluation/investigation performed. Additional information received from Central Complaint Vigilance Department on 18-FEB-2022. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result. Upon review following information was amended: dose number in series was 1 removed from narrative and confirmed clinical vaccination failure removed as event.; Sender's Comments: V1: The additional information in this version is Product quality complaint investigation result, dose number in series was 1 removed from narrative and confirmed clinical vaccination failure removed as event. This doesnot alter causality of previously reported events. 20211225843-JANSSEN COVID-19 VACCINE Ad26.COV2.S-acute kidney injury, chronic kidney disease. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: MEDICAL HISTORY, UNDERLYING DISEASE 20211225843-JANSSEN COVID-19 VACCINE Ad26.COV2.S- Pulmonary embolism, interstitial lung disease, respiratory failure,covid-19,sinus tachycardia, lung opacity, condition aggravated, endotracheal intubation, mechanical ventilation, intensive care,troponin increased, angiogram pulmonary abnormal, c-reactive protein increased, computerised tomogram thorax abnormal, leukocytosis, sars-cov-2 test positive, -This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 24,0
Labordaten: Test Date: 20211002; Test Name: Computerised tomogram thorax; Result Unstructured Data: lesser radiographically dense; Test Date: 20211104; Test Name: Computerised tomogram thorax; Result Unstructured Data: Abnormal; Test Date: 20211106; Test Name: CT angiography; Result Unstructured Data: Subsegmental Pulmonary Embolism; Test Date: 20211106; Test Name: Cardiac troponin; Result Unstructured Data: elevated; Test Date: 20211106; Test Name: C-reactive protein; Result Unstructured Data: elevated; Test Date: 20211106; Test Name: SARS-CoV-2 test; Result Unstructured Data: positive; Test Date: 20211106; Test Name: Computerised tomogram thorax; Result Unstructured Data: Abnormal; Test Date: 20211122; Test Name: Computerised tomogram thorax; Result Unstructured Data: lesser radiographically dense; Test Name: Oxygen saturation; Result Unstructured Data: no better than 90 percent
Aktuelle Erkrankungen: Chronic kidney disease; Coronary artery disease (status post stent 2016 and left carotid endarterectomy 2019); Hyperlipidemia; Hypertension
Vorgeschichte: Medical History/Concurrent Conditions: Calculus of kidney; Myocardial infarction; Comments: The patient had diseases of the circulatory system. The patient had no known drug allergy.
Andere Medikamente: ZOSYN; PREDNISONE; ALLOPURINOL; ASPIRIN [ACETYLSALICYLIC ACID]; ATORVASTATIN; BISOPROLOL; CLOPIDOGREL; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 2032598

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: IL
Alter: 70,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 18.03.2021
Beginn: 03.12.2021
Tage bis Beginn: 260,0
Dosis: 1
Route/Site: IM / -

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

Acute respiratory distress syndrome Acute respiratory failure Anticoagulant therapy Aspiration Atrial fibrillation Atrial flutter Bacteraemia COVID-19 COVID-19 pneumonia Candida test Candida test positive Cardioversion Chest X-ray Chest X-ray abnormal Deep vein thrombosis Endotracheal intubation Gastrostomy Hypotension

Symptomtext

This spontaneous report received from a health care professional by a Regulatory Authority Vaccine Adverse Event Reporting System (VAERS-US-VAERS-2032598-EHRR-20220121125256) concerned a 70 year old male of unspecified race and ethnic origin. The patient's height, and weight were not reported. The patient's concurrent conditions included chronic obstructive pulmonary disease, diabetes mellitus, and hypertension. The patient received Covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025, expiry: unknown) dose was not reported, 1 total administered on 18-MAR-2021 for an unspecified indication. Drug start period was 260 days. Concomitant medications included atorvastatin calcium, citalopram hydrobromide, dorzolamide hydrochloride and glipizide for drug used for unknown indication. On 02-DEC-2021, Laboratory data included: COVID-19 (NR: not provided) Positive. On 03-DEC-2021, patient presented to Emergency Room for COVID-19 pneumonia with acute hypoxic respiratory failure with Acute respiratory distress syndrome (ARDS) and admitted. On 03-DEC-2021, acute respiratory failure, aspiration, atrial fibrillation, bacteremia, Covid-19 pneumonia, deep vein thrombosis, intensive care unit delirium, pneumonia, septic shock, anticoagulant therapy, atrial flutter, Covid-19, candida test positive, cardioversion, chest x-ray abnormal, endotracheal intubation, gastrostomy, hypotension, intensive care unit acquired weakness, Klebsiella test positive, mechanical ventilation, sars-cov-2 test positive, superinfection, tracheal aspirate culture, tracheostomy. After that, on 23-DEC-2021, the patient was treated with Remdesivir and course of Decadron. The patient required prolonged intubation and mechanical ventilation and was subsequently trached and pegged. Hospital course was complicated by superimposed ventilator associated pneumonia with tracheal cultures growing Klebsiella species. The patient also grew Candida parapsilosis in the blood was treated with a course of cefepime and initially fluconazole subsequently switched to IV (Intravenous) micafungin from 23-DEC-2021. Patient had septic shock at some point and required pressors Bacteremia was resolved. Patient had been followed by pulmonology Critical Care. Patient also did develop bilateral upper extremity Deep vein thrombosis (DVT) and was treated with full-dose Lovenox. Later on patient developed Atrial fibrillation (AFib) with hypotension and following Cardiology evaluation was started on an amiodarone drip. On 02-JAN-2022, patient was cardioverted due to persistent hypotension and eventually converted to sinus rhythm transition to p o amiodarone and metoprolol. Patient had remained on ventilator via tracheostomy and got daily weaning trials that remained on 35% FiO2. From 10-JAN-2022, patient continued to had increased tracheal aspirate and repeat tracheal cultures again grew Klebsiella species. On 11-JAN-2021, patient was resumed on IV cefepime switched to Rocephin 1gram IV daily to 7 days and micafungin 100 mg BID to continue for 7 more days ended on 20-JAN-2021. Patient also had critical illness myopathy due to long hospitalization steroid and paralytic use and had received physical therapy. Patient had ICU delirium as well was started on Seroquel which was very helpful. Patient was hemodynamically stable. On 13-JAN-2022, patient was discharged to Long-term acute care (LTAC) to continue aggressive physical therapy and ventilator management. Patient was hospitalized from 03-DEC-2021 to 13-JAN-2022 (41 days). Laboratory data included: SARS-CoV-2 test (NR: not provided) positive. On 04-DEC-2021, Laboratory data included: Chest X-ray (NR: not provided) Diffuse bilateral pneumonias. On 23-DEC-2021, Laboratory data included: Candida test (NR: not provided) growth, and Klebsiella test (NR: not provided) positive. On 29-DEC-2021, treatment medications included: micafungin. Treatment medications included: remdesivir. Additional treatment medications (dates unspecified) included: cefepime hydrochloride, levofloxacin, dexamethasone, and fluconazole, amiodarone, metoprolol. The action taken with Covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from acute respiratory distress syndrome, acute respiratory failure, aspiration, atrial fibrillation, bacteremia, Covid-19 pneumonia, deep vein thrombosis, intensive care unit delirium, pneumonia, septic shock, anticoagulant therapy, atrial flutter, Covid-19, candida test positive, cardioversion, chest x-ray abnormal, endotracheal intubation, gastrostomy, hypotension, intensive care unit acquired weakness, Klebsiella test positive, mechanical ventilation, sars-cov-2 test positive, superinfection, tracheal aspirate culture, and tracheostomy. This report was serious (Hospitalization Caused / Prolonged). This report was associated with product quality complaint: 90000213701. The suspected product quality complaint has been confirmed to be the reported allegation could not be confirmed. A manufacturing related root cause could not be identified. Based on the PQC evaluation/investigation performed. Additional information received from central complaint vigilance department on 18-FEB-2022. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result was added. Sender's Comments: V1: Additional information received during follow up updates: Product quality complaint investigation result. This updated information does not alter the causality of previously reported events. 20220142136-COVID-19 VACCCINE AD26.COV2.S-Acute respiratory distress syndrome, Acute respiratory failure,- Aspiration, Atrial fibrillation, Bacteremia, Covid-19 pneumonia, Deep vein thrombosis, Intensive care unit delirium, Pneumonia, Septic shock, Anticoagulant therapy, Atrial flutter, Covid-19, Candida test positive, Cardioversion, Chest X-ray abnormal, Endotracheal intubation, Gastrostomy, Hypotension, Intensive care unit acquired weakness, Klebsiella test positive, Mechanical ventilation,SARS-COV2-test-positive,Superinfection,Tracheal aspirate culture, Tracheostomy. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 41,0
Labordaten: Test Date: 20211202; Test Name: COVID-19; Result Unstructured Data: Positive; Test Date: 20211203; Test Name: SARS-CoV-2 test; Result Unstructured Data: positive; Test Date: 20211204; Test Name: Chest X-ray; Result Unstructured Data: Diffuse bilateral pneumonias; Test Date: 20211223; Test Name: Candida test; Result Unstructured Data: growth; Test Date: 20211223; Test Name: Klebsiella test; Result Unstructured Data: positive.
Aktuelle Erkrankungen: Chronic obstructive pulmonary disease; Diabetes mellitus; Hypertension
Vorgeschichte: Comments: Unknown
Andere Medikamente: Lipitor; Celexa [Citalopram Hydrobromide]; Trusopt; Glipizide
Allergien: -
Vorherige Impfungen: -

VAERS 2032598

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: IL
Alter: 70,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 18.03.2021
Beginn: 03.12.2021
Tage bis Beginn: 260,0
Dosis: 1
Route/Site: OT / -

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

Acute respiratory distress syndrome Acute respiratory failure Anticoagulant therapy Aspiration Atrial fibrillation Atrial flutter Bacteraemia COVID-19 COVID-19 pneumonia Candida test Candida test positive Cardioversion Chest X-ray Chest X-ray abnormal Deep vein thrombosis Endotracheal intubation Gastrostomy Hypotension

Symptomtext

This spontaneous report received from a health care professional by a Regulatory Authority Vaccine Adverse Event Reporting System (VAERS-US-VAERS-2032598-EHRR-20220121125256) concerned a 70 year old male of unspecified race and ethnic origin. The patient's height, and weight were not reported. The patient's concurrent conditions included chronic obstructive pulmonary disease, diabetes mellitus, and hypertension. The patient received Covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025, expiry: unknown) dose was not reported, 1 total administered on 18-MAR-2021 for an unspecified indication. Drug start period was 260 days. Concomitant medications included atorvastatin calcium, citalopram hydrobromide, dorzolamide hydrochloride and glipizide for drug used for unknown indication. On 02-DEC-2021, Laboratory data included: COVID-19 (NR: not provided) Positive. On 03-DEC-2021, patient presented to Emergency Room for COVID-19 pneumonia with acute hypoxic respiratory failure with Acute respiratory distress syndrome (ARDS) and admitted. On 03-DEC-2021, acute respiratory failure, aspiration, atrial fibrillation, bacteremia, Covid-19 pneumonia, deep vein thrombosis, intensive care unit delirium, pneumonia, septic shock, anticoagulant therapy, atrial flutter, Covid-19, candida test positive, cardioversion, chest x-ray abnormal, endotracheal intubation, gastrostomy, hypotension, intensive care unit acquired weakness, Klebsiella test positive, mechanical ventilation, sars-cov-2 test positive, superinfection, tracheal aspirate culture, tracheostomy. After that, on 23-DEC-2021, the patient was treated with Remdesivir and course of Decadron. The patient required prolonged intubation and mechanical ventilation and was subsequently trached and pegged. Hospital course was complicated by superimposed ventilator associated pneumonia with tracheal cultures growing Klebsiella species. The patient also grew Candida parapsilosis in the blood was treated with a course of cefepime and initially fluconazole subsequently switched to IV (Intravenous) micafungin from 23-DEC-2021. Patient had septic shock at some point and required pressors Bacteremia was resolved. Patient had been followed by pulmonology Critical Care. Patient also did develop bilateral upper extremity Deep vein thrombosis (DVT) and was treated with full-dose Lovenox. Later on patient developed Atrial fibrillation (AFib) with hypotension and following Cardiology evaluation was started on an amiodarone drip. On 02-JAN-2022, patient was cardioverted due to persistent hypotension and eventually converted to sinus rhythm transition to p o amiodarone and metoprolol. Patient had remained on ventilator via tracheostomy and got daily weaning trials that remained on 35% FiO2. From 10-JAN-2022, patient continued to had increased tracheal aspirate and repeat tracheal cultures again grew Klebsiella species. On 11-JAN-2021, patient was resumed on IV cefepime switched to Rocephin 1gram IV daily to 7 days and micafungin 100 mg BID to continue for 7 more days ended on 20-JAN-2021. Patient also had critical illness myopathy due to long hospitalization steroid and paralytic use and had received physical therapy. Patient had ICU delirium as well was started on Seroquel which was very helpful. Patient was hemodynamically stable. On 13-JAN-2022, patient was discharged to Long-term acute care (LTAC) to continue aggressive physical therapy and ventilator management. Patient was hospitalized from 03-DEC-2021 to 13-JAN-2022 (41 days). Laboratory data included: SARS-CoV-2 test (NR: not provided) positive. On 04-DEC-2021, Laboratory data included: Chest X-ray (NR: not provided) Diffuse bilateral pneumonias. On 23-DEC-2021, Laboratory data included: Candida test (NR: not provided) growth, and Klebsiella test (NR: not provided) positive. On 29-DEC-2021, treatment medications included: micafungin. Treatment medications included: remdesivir. Additional treatment medications (dates unspecified) included: cefepime hydrochloride, levofloxacin, dexamethasone, and fluconazole, amiodarone, metoprolol. The action taken with Covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from acute respiratory distress syndrome, acute respiratory failure, aspiration, atrial fibrillation, bacteremia, Covid-19 pneumonia, deep vein thrombosis, intensive care unit delirium, pneumonia, septic shock, anticoagulant therapy, atrial flutter, Covid-19, candida test positive, cardioversion, chest x-ray abnormal, endotracheal intubation, gastrostomy, hypotension, intensive care unit acquired weakness, Klebsiella test positive, mechanical ventilation, sars-cov-2 test positive, superinfection, tracheal aspirate culture, and tracheostomy. This report was serious (Hospitalization Caused / Prolonged). This report was associated with product quality complaint: 90000213701. The suspected product quality complaint has been confirmed to be the reported allegation could not be confirmed. A manufacturing related root cause could not be identified. Based on the PQC evaluation/investigation performed. Additional information received from central complaint vigilance department on 18-FEB-2022. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result was added. Sender's Comments: V1: Additional information received during follow up updates: Product quality complaint investigation result. This updated information does not alter the causality of previously reported events. 20220142136-COVID-19 VACCCINE AD26.COV2.S-Acute respiratory distress syndrome, Acute respiratory failure,- Aspiration, Atrial fibrillation, Bacteremia, Covid-19 pneumonia, Deep vein thrombosis, Intensive care unit delirium, Pneumonia, Septic shock, Anticoagulant therapy, Atrial flutter, Covid-19, Candida test positive, Cardioversion, Chest X-ray abnormal, Endotracheal intubation, Gastrostomy, Hypotension, Intensive care unit acquired weakness, Klebsiella test positive, Mechanical ventilation,SARS-COV2-test-positive,Superinfection,Tracheal aspirate culture, Tracheostomy. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 41,0
Labordaten: Test Date: 20211202; Test Name: COVID-19; Result Unstructured Data: Positive; Test Date: 20211203; Test Name: SARS-CoV-2 test; Result Unstructured Data: positive; Test Date: 20211204; Test Name: Chest X-ray; Result Unstructured Data: Diffuse bilateral pneumonias; Test Date: 20211223; Test Name: Candida test; Result Unstructured Data: growth; Test Date: 20211223; Test Name: Klebsiella test; Result Unstructured Data: positive.
Aktuelle Erkrankungen: Chronic obstructive pulmonary disease; Diabetes mellitus; Hypertension
Vorgeschichte: Comments: Unknown
Andere Medikamente: Lipitor; Celexa [Citalopram Hydrobromide]; Trusopt; Glipizide
Allergien: -
Vorherige Impfungen: -

VAERS 1947958

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 08.04.2021
Beginn: 26.11.2021
Tage bis Beginn: 232,0
Dosis: 1
Route/Site: IM / AR

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

Acute respiratory distress syndrome Angiogram cerebral abnormal Aphasia COVID-19 pneumonia Carotid artery occlusion Angiogram cerebral Carotid artery thrombosis Cerebrovascular accident Computerised tomogram Cough Death Electrocardiogram ST segment elevation Endotracheal intubation Exposure to SARS-CoV-2 Gaze palsy Haematocrit normal Hemiparesis Haematocrit

Symptomtext

DEATH; ACUTE RESPIRATORY DISTRESS SYNDROME; COVID-19 PNEUMONIA; CAROTID ARTERY OCCLUSION; CAROTID ARTERY THROMBOSIS; ELECTROCARDIOGRAM ST SEGMENT ELEVATION; GAZE PALSY; HEMIPARESIS; HYPOXIA; ISCHAEMIC STROKE; PNEUMONIA; PULMONARY OEDEMA; UNRESPONSIVE TO STIMULI; ANGIOGRAM CEREBRAL ABNORMAL; APHASIA; COUGH; ENDOTRACHEAL INTUBATION; EXPOSURE TO SARS-COV-2; HAEMATOCRIT NORMAL; INTENSIVE CARE; MAGNETIC RESONANCE IMAGING HEAD ABNORMAL; MECHANICAL VENTILATION; NEUROLOGICAL EXAMINATION ABNORMAL; PERFUSION BRAIN SCAN ABNORMAL; PRONE POSITION; RESPIRATORY SYMPTOM; SUSPECTED CLINICAL VACCINE FAILURE; CEREBROVASCULAR ACCIDENT; This spontaneous report received from a health care professional via a Regulatory Authority VAERS (Vaccine Adverse Event Reporting System)(VAERS ID: 1947958) on 24-DEC-2021 and concerned a 66 year old male of unknown race and ethnicity. The patient's height, and weight were not reported. The patient's past medical history included: acute respiratory failure, acute systolic heart failure, and acute right middle cerebral artery stroke, and concurrent conditions included: cardiomyopathy, ischemic coronary artery disease, essential hypertension, peripheral vascular disease, carotid artery disease, anemia, chronic kidney disease, kidney disorder stage iii, renal osteodystrophy, gout, diabetes mellitus, and tobacco user, and other pre-existing medical conditions included: Patient had no known allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025 expiry: UNKNOWN) dose was not reported, 1 total, administered at right arm on 08-APR-2021 for an unspecified indication. Concomitant medications included amlodipine, amlodipine besilate, atorvastatin, atorvastatin calcium, clopidogrel, clopidogrel bisulfate, glipizide, metoprolol succinate, omeprazole, Aspirin and pantoprazole. On 26-NOV-2021, the patient experienced cerebrovascular accident, acute respiratory distress syndrome, covid-19 pneumonia, carotid artery occlusion, carotid artery thrombosis, electrocardiogram st segment elevation, gaze palsy, hemiparesis, hypoxia, ischaemic stroke, pneumonia, pulmonary oedema, unresponsive to stimuli, angiogram cerebral abnormal, aphasia, cough, endotracheal intubation, exposure to sars-cov-2, haematocrit normal, intensive care, magnetic resonance imaging head abnormal, mechanical ventilation, neurological examination abnormal, perfusion brain scan abnormal, prone position, respiratory symptom and suspected clinical vaccine failure. Patient was hospitalized on 26-NOV-2021, patient had COVID-19 exposure (unclear if test done) patient was fully vaccinated. Patient had acute right MCA stroke, Ischemic stroke. Patient had recent COVID exposure and was admitted to Medical Intensive care unit (ICU)from Emergency department (ED) for concern of stroke in the presence of COVID pneumonia. Neuro ICU was consulted for stroke to review patient was found unresponsive on 26-NOV-2021. He was last known well on the evening of 25-NOV-2021 down time is unknown. Patient has multiple family members at home who are COVID positive Per ED report patient was having some cough and respiratory symptoms while at home emergency medical services (EMS) reportedly found patient unresponsive with a right sided gaze and left sided weakness. Patient was hypoxic with O2 saturation in the 60 and a respiratory rate in the 40. On arrival to outside ED patient's exam was documented as nonverbal but following commands patient was stroke coded at 1130 on 26-NOV-2021. Initial NIH 32 Stat (hematocrit)HCT was negative for hemorrhage due to unknown down time patient was outside the window for Tissue plasminogen activator (TPA) Computed tomography angiography (CTA) shows a l eft cervical internal carotid artery (ICA) occlusion and a incompletely occlusive right cervical ICA thrombus no intracranial occlusions reported (Computed Tomography Perfusion) CTP showed a 7 ml core and 5 ml penumbra patient was showing some ST elevation in V1 V2 and lead 3 concerning for ST-elevation myocardial infarction (STEMI) He was given rectal aspirin per outside report ED physician contacted both BW cardiology and stroke neurology for recommendations per cardiology did not feel this was a STEMI, no acute need for heparin from cardiac standpoint at this time. Stroke neurology recommended STAT MRI brain there was no documented discussion regarding whether or not patient's candidacy for mechanical thrombectomy was discussed. It was assumed that patient was not a candidate. Patient was setting 90% on NRB It was ultimately decided to admit to medical ICU and patient was intubated for airway protection On 27-NOV-2021. An MRI brain was obtained and showed right MCA and watershed territory strokes Left MCA ACA watershed strokes and possible small left petechial ICH Throughout his ICU course his pulmonary status continued to decline and he developed severe ARDS pneumonia and pulmonary edema despite maximum medical efforts including high dose sedation paralytics and prone positioning the patient failed to make significant improvement from a pulmonary standpoint. Given his poor neurological exam in conjunction with his multiple bihemispheric strokes seen on brain MRI as well as failure to improve on the ventilator multiple family meetings were held to discuss goals of care. It was decided that the current level of care and anticipated poor recovery did not align with the patient's prior wishes. As such the family elected to transition him to comfort measures. After all family was able to say their goodbyes. the patient was terminally extubated on 4-DEC-2021. He passed away with family at his bedside at 3:53PM. Laboratory data (dates unspecified) included: Angiogram cerebral (NR: not provided) Abnormal, CT scan (NR: not provided) Unknown, left cervical ICA, Hematocrit (NR: not provided) Normal, Intubation (NR: not provided) Unknown, MRI brain (NR: not provided) middle cerebral artery, Neurological examination (NR: not provided) Abnormal, Oxygen saturation (NR: not provided) 60 %, Perfusion brain scan (NR: not provided) Abnormal, Respiratory rate (NR: not provided) 40 (units unspecified), and ST elevated (NR: not provided) STEMI. On 04-DEC-2021, the patient died from cerebrovascular accident. It was unknown if the autopsy was performed or not. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient died from cerebrovascular accident, acute respiratory distress syndrome, covid-19 pneumonia, carotid artery occlusion, carotid artery thrombosis, electrocardiogram st segment elevation, gaze palsy, hemiparesis, hypoxia, ischaemic stroke, pneumonia, pulmonary oedema, unresponsive to stimuli, angiogram cerebral abnormal, aphasia, cough, endotracheal intubation, exposure to sars-cov-2, haematocrit normal, intensive care, magnetic resonance imaging head abnormal, mechanical ventilation, neurological examination abnormal, perfusion brain scan abnormal, prone position, and respiratory symptom and not yet recovered from suspected clinical vaccine failure. This report was serious (Death, and Hospitalization Caused / Prolonged). This case was associated with a product quality complaint: 90000209186. The suspected product quality complaint has been confirmed to be the reported allegation was not confirmed and the root cause was determined to be not manufacturing related. based on the PQC evaluation/investigation performed. Additional information received from Complaint Department on 18-FEB-2022. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result.; Sender's Comments: V2: Additional information in this version updates: Product quality complaint investigation result. this updated information does not alter the company causality of previously reported events. 20211255568-COVID-19 VACCINE AD26.COV2.S-Cerebrovascular accident, Death, Acute respiratory distress syndrome, COVID-19 pneumonia, Carotid artery occlusion, Carotid artery thrombosis, Electrocardiogram ST segment elevation, Gaze palsy, Hemiparesis, Hypoxia, Ischaemic stroke, Pneumonia, Pulmonary oedema, Unresponsive to stimuli, Angiogram cerebral abnormal, Aphasia, Cough, Endotracheal intubation, Exposure to SARS-CoV-2, Haematocrit normal, Intensive care, Magnetic resonance imaging head abnormal, Mechanical ventilation, Neurological examination abnormal, Perfusion brain scan abnormal, Prone position, Respiratory symptom. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). 20211255568-COVID-19 VACCINE AD26.COV2.S- Suspected clinical vaccine failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS.; Reported Cause(s) of Death: CEREBROVASCULAR ACCIDENT; ACUTE RESPIRATORY DISTRESS SYNDROME; COVID-19 PNEUMONIA; CAROTID ARTERY OCCLUSION; CAROTID ARTERY THROMBOSIS; ELECTROCARDIOGRAM ST SEGMENT ELEVATION; GAZE PALSY; HEMIPARESIS; HYPOXIA; ISCHAEMIC STROKE; PNEUMONIA; PULMONARY O

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 8,0
Labordaten: Test Name: Oxygen saturation; Result Unstructured Data: 60 %; Test Name: Respiratory rate; Result Unstructured Data: 40; Test Name: Hematocrit; Result Unstructured Data: Normal; Test Name: CT scan; Result Unstructured Data: left cervical ICA; Test Name: CT scan; Result Unstructured Data: Unknown; Test Name: Perfusion brain scan; Result Unstructured Data: Abnormal; Test Name: MRI brain; Result Unstructured Data: middle cerebral artery; Test Name: Angiogram cerebral; Result Unstructured Data: Abnormal; Test Name: Intubation; Result Unstructured Data: Unknown; Test Name: Neurological examination; Result Unstructured Data: Abnormal; Test Name: ST elevated; Result Unstructured Data: STEMI
Aktuelle Erkrankungen: Anemia (in chronic kidney disease.); Cardiomyopathy; Carotid artery disease (Left-sided.); Chronic kidney disease; Diabetes mellitus; Essential hypertension; Gout; Ischemia coronary artery origin (Involving native coronary artery of native heart without angina pectoris.); Kidney disorder; Peripheral vascular disease (PVD); Renal osteodystrophy; Tobacco user
Vorgeschichte: Medical History/Concurrent Conditions: Acute respiratory failure; Acute systolic heart failure; Middle cerebral artery stroke; Comments: Patient had no known allergy.
Andere Medikamente: AMLODIPINE; NORVASC; ATORVASTATIN; LIPITOR; CLOPIDOGREL; PLAVIX; GLIPIZIDE; GLUCOTROL; METOPROLOL SUCCINATE; TOPROL XL; PANTOPRAZOLE; PROTONIX [OMEPRAZOLE]; ASPRIN
Allergien: -
Vorherige Impfungen: -

VAERS 1947958

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 08.04.2021
Beginn: 26.11.2021
Tage bis Beginn: 232,0
Dosis: 1
Route/Site: OT / -

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

Acute respiratory distress syndrome Angiogram cerebral abnormal Aphasia COVID-19 pneumonia Carotid artery occlusion Angiogram cerebral Carotid artery thrombosis Cerebrovascular accident Computerised tomogram Cough Death Electrocardiogram ST segment elevation Endotracheal intubation Exposure to SARS-CoV-2 Gaze palsy Haematocrit normal Hemiparesis Haematocrit

Symptomtext

DEATH; ACUTE RESPIRATORY DISTRESS SYNDROME; COVID-19 PNEUMONIA; CAROTID ARTERY OCCLUSION; CAROTID ARTERY THROMBOSIS; ELECTROCARDIOGRAM ST SEGMENT ELEVATION; GAZE PALSY; HEMIPARESIS; HYPOXIA; ISCHAEMIC STROKE; PNEUMONIA; PULMONARY OEDEMA; UNRESPONSIVE TO STIMULI; ANGIOGRAM CEREBRAL ABNORMAL; APHASIA; COUGH; ENDOTRACHEAL INTUBATION; EXPOSURE TO SARS-COV-2; HAEMATOCRIT NORMAL; INTENSIVE CARE; MAGNETIC RESONANCE IMAGING HEAD ABNORMAL; MECHANICAL VENTILATION; NEUROLOGICAL EXAMINATION ABNORMAL; PERFUSION BRAIN SCAN ABNORMAL; PRONE POSITION; RESPIRATORY SYMPTOM; SUSPECTED CLINICAL VACCINE FAILURE; CEREBROVASCULAR ACCIDENT; This spontaneous report received from a health care professional via a Regulatory Authority VAERS (Vaccine Adverse Event Reporting System)(VAERS ID: 1947958) on 24-DEC-2021 and concerned a 66 year old male of unknown race and ethnicity. The patient's height, and weight were not reported. The patient's past medical history included: acute respiratory failure, acute systolic heart failure, and acute right middle cerebral artery stroke, and concurrent conditions included: cardiomyopathy, ischemic coronary artery disease, essential hypertension, peripheral vascular disease, carotid artery disease, anemia, chronic kidney disease, kidney disorder stage iii, renal osteodystrophy, gout, diabetes mellitus, and tobacco user, and other pre-existing medical conditions included: Patient had no known allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025 expiry: UNKNOWN) dose was not reported, 1 total, administered at right arm on 08-APR-2021 for an unspecified indication. Concomitant medications included amlodipine, amlodipine besilate, atorvastatin, atorvastatin calcium, clopidogrel, clopidogrel bisulfate, glipizide, metoprolol succinate, omeprazole, Aspirin and pantoprazole. On 26-NOV-2021, the patient experienced cerebrovascular accident, acute respiratory distress syndrome, covid-19 pneumonia, carotid artery occlusion, carotid artery thrombosis, electrocardiogram st segment elevation, gaze palsy, hemiparesis, hypoxia, ischaemic stroke, pneumonia, pulmonary oedema, unresponsive to stimuli, angiogram cerebral abnormal, aphasia, cough, endotracheal intubation, exposure to sars-cov-2, haematocrit normal, intensive care, magnetic resonance imaging head abnormal, mechanical ventilation, neurological examination abnormal, perfusion brain scan abnormal, prone position, respiratory symptom and suspected clinical vaccine failure. Patient was hospitalized on 26-NOV-2021, patient had COVID-19 exposure (unclear if test done) patient was fully vaccinated. Patient had acute right MCA stroke, Ischemic stroke. Patient had recent COVID exposure and was admitted to Medical Intensive care unit (ICU)from Emergency department (ED) for concern of stroke in the presence of COVID pneumonia. Neuro ICU was consulted for stroke to review patient was found unresponsive on 26-NOV-2021. He was last known well on the evening of 25-NOV-2021 down time is unknown. Patient has multiple family members at home who are COVID positive Per ED report patient was having some cough and respiratory symptoms while at home emergency medical services (EMS) reportedly found patient unresponsive with a right sided gaze and left sided weakness. Patient was hypoxic with O2 saturation in the 60 and a respiratory rate in the 40. On arrival to outside ED patient's exam was documented as nonverbal but following commands patient was stroke coded at 1130 on 26-NOV-2021. Initial NIH 32 Stat (hematocrit)HCT was negative for hemorrhage due to unknown down time patient was outside the window for Tissue plasminogen activator (TPA) Computed tomography angiography (CTA) shows a l eft cervical internal carotid artery (ICA) occlusion and a incompletely occlusive right cervical ICA thrombus no intracranial occlusions reported (Computed Tomography Perfusion) CTP showed a 7 ml core and 5 ml penumbra patient was showing some ST elevation in V1 V2 and lead 3 concerning for ST-elevation myocardial infarction (STEMI) He was given rectal aspirin per outside report ED physician contacted both BW cardiology and stroke neurology for recommendations per cardiology did not feel this was a STEMI, no acute need for heparin from cardiac standpoint at this time. Stroke neurology recommended STAT MRI brain there was no documented discussion regarding whether or not patient's candidacy for mechanical thrombectomy was discussed. It was assumed that patient was not a candidate. Patient was setting 90% on NRB It was ultimately decided to admit to medical ICU and patient was intubated for airway protection On 27-NOV-2021. An MRI brain was obtained and showed right MCA and watershed territory strokes Left MCA ACA watershed strokes and possible small left petechial ICH Throughout his ICU course his pulmonary status continued to decline and he developed severe ARDS pneumonia and pulmonary edema despite maximum medical efforts including high dose sedation paralytics and prone positioning the patient failed to make significant improvement from a pulmonary standpoint. Given his poor neurological exam in conjunction with his multiple bihemispheric strokes seen on brain MRI as well as failure to improve on the ventilator multiple family meetings were held to discuss goals of care. It was decided that the current level of care and anticipated poor recovery did not align with the patient's prior wishes. As such the family elected to transition him to comfort measures. After all family was able to say their goodbyes. the patient was terminally extubated on 4-DEC-2021. He passed away with family at his bedside at 3:53PM. Laboratory data (dates unspecified) included: Angiogram cerebral (NR: not provided) Abnormal, CT scan (NR: not provided) Unknown, left cervical ICA, Hematocrit (NR: not provided) Normal, Intubation (NR: not provided) Unknown, MRI brain (NR: not provided) middle cerebral artery, Neurological examination (NR: not provided) Abnormal, Oxygen saturation (NR: not provided) 60 %, Perfusion brain scan (NR: not provided) Abnormal, Respiratory rate (NR: not provided) 40 (units unspecified), and ST elevated (NR: not provided) STEMI. On 04-DEC-2021, the patient died from cerebrovascular accident. It was unknown if the autopsy was performed or not. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient died from cerebrovascular accident, acute respiratory distress syndrome, covid-19 pneumonia, carotid artery occlusion, carotid artery thrombosis, electrocardiogram st segment elevation, gaze palsy, hemiparesis, hypoxia, ischaemic stroke, pneumonia, pulmonary oedema, unresponsive to stimuli, angiogram cerebral abnormal, aphasia, cough, endotracheal intubation, exposure to sars-cov-2, haematocrit normal, intensive care, magnetic resonance imaging head abnormal, mechanical ventilation, neurological examination abnormal, perfusion brain scan abnormal, prone position, and respiratory symptom and not yet recovered from suspected clinical vaccine failure. This report was serious (Death, and Hospitalization Caused / Prolonged). This case was associated with a product quality complaint: 90000209186. The suspected product quality complaint has been confirmed to be the reported allegation was not confirmed and the root cause was determined to be not manufacturing related. based on the PQC evaluation/investigation performed. Additional information received from Complaint Department on 18-FEB-2022. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result.; Sender's Comments: V2: Additional information in this version updates: Product quality complaint investigation result. this updated information does not alter the company causality of previously reported events. 20211255568-COVID-19 VACCINE AD26.COV2.S-Cerebrovascular accident, Death, Acute respiratory distress syndrome, COVID-19 pneumonia, Carotid artery occlusion, Carotid artery thrombosis, Electrocardiogram ST segment elevation, Gaze palsy, Hemiparesis, Hypoxia, Ischaemic stroke, Pneumonia, Pulmonary oedema, Unresponsive to stimuli, Angiogram cerebral abnormal, Aphasia, Cough, Endotracheal intubation, Exposure to SARS-CoV-2, Haematocrit normal, Intensive care, Magnetic resonance imaging head abnormal, Mechanical ventilation, Neurological examination abnormal, Perfusion brain scan abnormal, Prone position, Respiratory symptom. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). 20211255568-COVID-19 VACCINE AD26.COV2.S- Suspected clinical vaccine failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS.; Reported Cause(s) of Death: CEREBROVASCULAR ACCIDENT; ACUTE RESPIRATORY DISTRESS SYNDROME; COVID-19 PNEUMONIA; CAROTID ARTERY OCCLUSION; CAROTID ARTERY THROMBOSIS; ELECTROCARDIOGRAM ST SEGMENT ELEVATION; GAZE PALSY; HEMIPARESIS; HYPOXIA; ISCHAEMIC STROKE; PNEUMONIA; PULMONARY O

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 8,0
Labordaten: Test Name: Oxygen saturation; Result Unstructured Data: 60 %; Test Name: Respiratory rate; Result Unstructured Data: 40; Test Name: Hematocrit; Result Unstructured Data: Normal; Test Name: CT scan; Result Unstructured Data: left cervical ICA; Test Name: CT scan; Result Unstructured Data: Unknown; Test Name: Perfusion brain scan; Result Unstructured Data: Abnormal; Test Name: MRI brain; Result Unstructured Data: middle cerebral artery; Test Name: Angiogram cerebral; Result Unstructured Data: Abnormal; Test Name: Intubation; Result Unstructured Data: Unknown; Test Name: Neurological examination; Result Unstructured Data: Abnormal; Test Name: ST elevated; Result Unstructured Data: STEMI
Aktuelle Erkrankungen: Anemia (in chronic kidney disease.); Cardiomyopathy; Carotid artery disease (Left-sided.); Chronic kidney disease; Diabetes mellitus; Essential hypertension; Gout; Ischemia coronary artery origin (Involving native coronary artery of native heart without angina pectoris.); Kidney disorder; Peripheral vascular disease (PVD); Renal osteodystrophy; Tobacco user
Vorgeschichte: Medical History/Concurrent Conditions: Acute respiratory failure; Acute systolic heart failure; Middle cerebral artery stroke; Comments: Patient had no known allergy.
Andere Medikamente: AMLODIPINE; NORVASC; ATORVASTATIN; LIPITOR; CLOPIDOGREL; PLAVIX; GLIPIZIDE; GLUCOTROL; METOPROLOL SUCCINATE; TOPROL XL; PANTOPRAZOLE; PROTONIX [OMEPRAZOLE]; ASPRIN
Allergien: -
Vorherige Impfungen: -

VAERS 2130973

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 73,0
Geschlecht: M
Eingang: 22.02.2022
Impfdatum: 10.03.2021
Beginn: 22.01.2022
Tage bis Beginn: 318,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure Atrial fibrillation COVID-19 COVID-19 pneumonia Cardiac arrest Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Positive airway pressure therapy Pulseless electrical activity Resuscitation Thrombocytopenia

Symptomtext

Admitted 1/22/22 - 1/25/22 with COVID-19 causing acute hypoxic resp failure and acute COPD exacerbation. Tx w remdesivir, decadron, doxycycline. D/C w 2L o2. Readmit 2/11/22 c/o SOB on 5L o2. New afib in ED tx w metroprolol. PE ruled out. high flow heated BIPAP. Patient declined intubation. On 2/16 went to PEA cardiac arrest. CPR initiated but later discontinued after discussion with spouse. Discharge Dx: acute hypoxic resp failure d/t COVID PNA, COVID PNA, New onset paroxysmal afib, COPDE, acute on chronic thrombocytopenia.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD State 3, CAD/CABG, CKD2, BPH, HTN, DM2, Depression, HLD, RA, GERD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2129339

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 21.02.2022
Impfdatum: 15.04.2021
Beginn: 08.02.2022
Tage bis Beginn: 299,0
Dosis: 1
Route/Site: IM / UN

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

Acute respiratory distress syndrome Acute respiratory failure COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Death Dyspnoea Endotracheal intubation General physical health deterioration Hyperglycaemia Lung infiltration SARS-CoV-2 test positive Type 2 diabetes mellitus

Symptomtext

Janssen COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Received Janssen Vaccine on 3/8/21. Covid + 1/22/22. Presented to ED on 1/24/22 w/cough and SOB, admitted for acute hypoxemic resp failure 2/2 Covid PNA. Pulse ox on room air 78 %, w/Airvo nasal cannula O2 sats 94%. Noted to be hyperglymic on admission, new dx T2DM this admission. Intubated on 2/3 due to refractory ARDS. CXR revealed large chest wall ongoing severe bilateral infiltrates. Continued to declined, transitioned to DNR. Treated with tocilizumab, remdesivir, dexamethasone, zosyn and solumedrol. Expired 02/08/22.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: morbid obesity, asthma
Andere Medikamente: albuterol, cetirizine, fluticasone/salmeterol, fluticasone
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2129120

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 88,0
Geschlecht: M
Eingang: 21.02.2022
Impfdatum: 16.03.2021
Beginn: 09.02.2022
Tage bis Beginn: 330,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure Atrial fibrillation COVID-19 pneumonia Renal failure Unresponsive to stimuli

Symptomtext

89 year old vaccinated male with COPD was admitted for acute respiratory failure caused by Covid-19 pneumonia. He was in renal failure and a fib with RVR also. Despite treatments, his condition worsened and became unresponsive. He was made DNR by family and they have now accepted hospice services. He will be discharged home today with hospice.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, HLD, COPD, CKD,
Andere Medikamente: info not available
Allergien: nka
Vorherige Impfungen: -

VAERS 2119339

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: FL
Alter: 75,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 31.03.2021
Beginn: 15.01.2022
Tage bis Beginn: 290,0
Dosis: 1
Route/Site: IM / UN

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

Death

Symptomtext

ADMITTED TO HOSPITAL

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

VAERS 2110130

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 53,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 11.03.2021
Beginn: 05.02.2022
Tage bis Beginn: 331,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chills Chronic obstructive pulmonary disease Condition aggravated Cough Dyspnoea Fatigue Lung infiltration Nausea Pain SARS-CoV-2 test positive Sputum increased Wheezing

Symptomtext

As per admission H&P, "Patient is a 54 y.o. female with a history below admitted for COPD exacerbation. Pt came in with complaints of several days of chills, body aches, cough, wheezing, increased sputum production. Today tested + for covid-19. On 4l o2, home dose. Associated nausea / fatigue. Nothing makes better / worse. Discussed with er, concern for covid induced copd exacerbation. Will admit " Hospital Course: Patient, is a 54 y.o. female who presented with shortness of breath. She was managed for the following: * COPD exacerbation Acute Hypoxic Respiratory Failure - due to COVID-19 Pneumonia with acute COPD exacerbation. Patient presented with shortness of breath, wheezing, COVID-19 positive, with bilateral infiltrates on CXR. She had increased O2 requirement from her baseline 4L NC at home. She was started on IV steroids. She completed 5 day course of remdesivir. She improved and was weaned back to her home requirement of 4L O2. She was discharged home with a prednisone taper for COPD flare. To follow-up outpatient. Acute COPD Exacerbation - steroids, nebs as above. Recent PE - continue eliquis. DM2

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, Obesity, chronic constipation, Type 2 Diabetes, Asthma, COPD, Sleep apnea
Andere Medikamente: Singular, Buspar, Wellbutrin, glucophage, xyzal, ventolin, spiriva, lantus, requip, prozac
Allergien: PCN
Vorherige Impfungen: -

VAERS 2071654

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MI
Alter: 78,0
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 08.04.2021
Beginn: 27.01.2022
Tage bis Beginn: 294,0
Dosis: 1
Route/Site: UN / UN

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

Acute kidney injury Acute respiratory failure COVID-19

Symptomtext

CLINICAL IMPRESSION 1. COVID-19 2. Acute respiratory failure with hypoxia 3. AKI (acute kidney injury)

Weitere VAERSDATA-Felder

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

VAERS 2071508

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 82,0
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 12.03.2021
Beginn: 22.11.2021
Tage bis Beginn: 255,0
Dosis: 1
Route/Site: OT / -

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

COVID-19 Death General physical health deterioration Intensive care Positive airway pressure therapy Respiratory failure Thrombosis Vaccination failure

Symptomtext

DEATH; RESPIRATORY FAILURE; THROMBOSIS; COVID-19; GENERAL PHYSICAL HEALTH DETERIORATION; INTENSIVE CARE; POSITIVE AIRWAY PRESSURE THERAPY; SUSPECTED CLINICAL VACCINATION FAILURE; This spontaneous report received from a health care professional by a Regulatory Authority Vaccine Adverse Event Reporting System (VAERS) (VAERS ID 1923992) concerned an 82 year old male of unspecified race and ethnic origin. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration was not reported, batch number: 1805025 expiry: Unknown) dose was not reported, 01 total administered in left arm on 12-MAR-2021 for an unspecified (unknown) indication. No concomitant medications were reported. On 22-NOV-2021 the patient was admitted from nursing home with respiratory failure secondary to covid-19 infection (suspected clinical vaccination failure). He was admitted to the Intensive Care Unit (ICU) and placed on non-invasive ventilation (NIV). Patient continued to require more oxygen and was unable to come off bilevel positive airway pressure (BIPAP). He did expressed that he did not want to be placed on ventilator and did not want any intervention in regards to his own blood clot (thrombosis). The patient made a do-not-resuscitate (DNR) do not intubate (DNI) order. His family was contacted. Patient continued to decline over the next couple of days. Family was called in he was transitioned to comfort measures. The patient was hospitalized for 7 days discharge information was not reported. On 29-NOV-2021 at 18:46 the patient died from unknown cause of death. It was unknown if an autopsy was performed or not. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of respiratory failure, thrombosis, covid-19, general physical health deterioration, intensive care and positive airway pressure therapy were fatal, and the outcome of suspected clinical vaccination failure was unknown. This report was serious (Death, and Hospitalization Caused / Prolonged). This report was associated with product quality complaint: 90000208135. The suspected product quality complaint has been confirmed to be the reported allegation could not be determined. A manufacturing related root cause could not be identified based on the PQC evaluation/investigation performed. Additional information was received from Central Complaint Vigilance on 25-JAN-2022. The following information was updated and incorporated into the case narrative: product quality complaint investigation result was added.; Sender's Comments: V1: Follow up information in this version updated Product quality complaint investigation result. The follow up information does not change the company causality of the previously reported events. 20211240520-COVID-19 VACCINE AD26.COV2.S-Death, respiratory failure, thrombosis, covid-19, general physical health deterioration, intensive care and positive airway pressure therapy. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). 20211240520-COVID-19 VACCINE AD26.COV2.S-suspected clinical vaccination failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS.; Reported Cause(s) of Death: UNKNOWN CAUSE OF DEATH

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

VAERS 1578181

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: IL
Alter: 64,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 05.03.2021
Beginn: 09.08.2021
Tage bis Beginn: 157,0
Dosis: 1
Route/Site: IM / -

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

Acute kidney injury Acute respiratory failure Angiogram pulmonary abnormal Anxiety Atrial fibrillation Bilevel positive airway pressure COVID-19 Hypoxia Intensive care COVID-19 pneumonia Condition aggravated Dysphagia Dyspnoea Endotracheal intubation Extubation Febrile neutropenia Gastrostomy Haemofiltration

Symptomtext

COVID Vaccine Breakthrough J&J Dose 3/5/21 (1805025) COVID Positive 8/16/21 8/18/21: A 60-year-old male with history of type 2 DM, hypertension, hyperlipidemia and CAD is transferred from a local Hospital for COVID-19 pneumonia with hypoxic respiratory failure requiring endotracheal intubation mechanical ventilation. Patient is unable to provide history as he is intubated and sedated, history is obtained from the medical records from the facility. As per the medical records, patient presented to the facility on 08/16/2021 complaining of shortness of breath of about 1 week duration. He was diagnosed positive with COVID-19 infection and admitted hospital as his pulse oximetry was 83%. Patient had Johnson and Johnson vaccine in March 2021. He was requiring 10 L high-flow oxygen and then went up to 30 L oxygen to keep saturation above 90%. Initially he did not want to be intubated. Patient was also seen by cardiologist for possible congestive heart failure, he recommended to continue on Lasix 40 mg daily. CT angio chest was done on 08/17/2021 and is reported negative for pulmonary embolism, but showed extensive bilateral areas of airspace opacification with interval worsening. Patient was started on IV ceftriaxone 1 g Q 24 hours and Zithromax 500 mg IV Q 24 hours along with dexamethasone 8 mg IV Q 24 hours. Remdesivir was initiated on 08/16. Baracitinib started on 08/17. As his clinical condition worsened he was endotracheally intubated today and placed on mechanical ventilation, now on 100% FiO2. He is on propofol for sedation, also blood pressures were low was initially started on dopamine, later switched to Levophed. Patient is seen by me in ICU. He is on ventilator support with 100% FiO2. Still on Levophed support. Sedated on propofol drip. 10/5/2021: Patient is a 65-year-old male who presented on 08/18/2021. He was a transfer from a Hospital for COVID-19 with acute hypoxic respiratory failure requiring endotracheal intubation and mechanical ventilation. Patient was intubated on arrival. He remained in the ICU and was extubated on 09/03/2021. He suffered a respiratory arrest with CPR on 09/17/2021 and was reintubated. The patient was having trouble liver rating from the vent. He was also struggling with dysphagia. He therefore received a trach and PEG tube on 09/21/2021. During the patient's stay, he also struggled with MRSA bacteremia, neutropenic fever, anxiety, atrial fibrillation, AKI with fluid volume overload requiring CRRT. 10/05/2021, the patient was discharged to another Hospital to continue attempts at weaning from the ventilator on trach collar. Patient was discharged on IV doxycycline per ID recommendations.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 49,0
Labordaten: see above
Aktuelle Erkrankungen: DM type 2 HTN HLD CAD
Vorgeschichte: DM type 2 HTN HLD CAD
Andere Medikamente: acetaminophen 650 mg PO Q4h PRN albuterol 2 puffs Q4h PRN alprazolam 0.5 mg PO TID apixaban 5 mg PO BID aspirin 81 mg PO QD gauifenesin 400 mg PO TID insulin glargine 50 units SQ QD insulin lispro SSI SQ Q6h PRN lansoprazole 30 mg PO QD met
Allergien: sulfa drugs - rash
Vorherige Impfungen: -

VAERS 2050096

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: IN
Alter: 70,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: -
Beginn: 10.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Abdominal distension Biopsy bone marrow Blood test Computerised tomogram Electrocardiogram Fatigue Hypersomnia Myocardial infarction SARS-CoV-2 test Splenomegaly Urinary tract infection Viral infection

Symptomtext

VERY SEVERE UTI; FEELING OF JUST BEING FULL WHEN JUST EATING LITTLE BIT( CAN'T EAT A FULL MEAL); ENLARGED SPLEEN; COULDN'T STAY AWAKE FOR MORE THAN 2 HOURS; VIRAL INFECTION; FEELING EXHAUSTED; HEART ATTACK; This spontaneous report received from a patient concerned a 70 years old female. The patient's height and weight were not reported. The patient's concurrent conditions included muscle relaxants and penicillin allergy and other pre-existing medical conditions included that she had always been a healthy person. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration was not reported, batch number: 1805025 and expiry: unknown) dose was not reported, dose number in series was 1, 01 total administered on 11-MAR-2021 to left arm for prophylactic vaccination. No concomitant medications were reported. On 10-APR-2021, the patient got diagnosed with a Heart attack after she had severe Jaw pain and they did EKG (Electrocardiogram) decided that she needs stents placed. On 06-SEP-2021 (labor day) she went to the emergency room (ER) because she was feeling exhausted (end up taking a nap during the day) and couldn't stay awake for more than 2 hours. They said she had a viral infection. Laboratory data included: coronavirus disease (COVID-19) virus test with result negative (tested at emergency room). On 13-SEP-2021 (Monday) she went to ER again and they said that she still had the same viral infection (she doesn't know exactly the name of the viral infection). Laboratory data included: COVID-19 (Coronavirus disease) virus test with result negative (tested at emergency room) On 16-SEP-2021, she went to see her nurse practitioner who said she had a very severe urinary tract infection (UTI) and put her on an antibiotic (does not know the name of the antibiotic) and did blood test and saw some elevations in different things (blood counts) and sent her to a hematologist. On 24-SEP-2021, Laboratory data included: Computerised tomogram (CT) scan with result spleen was enlarged. On 30-SEP-2021 she saw hematologist for the first time. On 06-OCT-2021, Laboratory data included: Bone marrow biopsy with result negative. On 27-DEC-2021, Laboratory data included: COVID-19 virus test with result negative (tested at doctor's office). On an unspecified date, the patient experienced feeling of just being full when just eating little bit (can't eat a full meal), enlarged spleen (dose number in series was 1), Laboratory data (dates unspecified) included: CT scan with result normal. She had visited the physician's office. It was reported that, on 19-JAN-2021 (Wednesday) the patient had CT (computerized tomography) scan done with contrast on spleen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from feeling exhausted, feeling of just being full when just eating little bit( can't eat a full meal), very severe UTI, and viral infection, and the outcome of heart attack, enlarged spleen, severe jaw pain and couldn't stay awake for more than 2 hours was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20220126598- COVID-19 VACCINE AD26.COV2.S- Heart attack. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Test Date: 20210906; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Comments: at emergency room; Test Date: 20210913; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Comments: at emergency room; Test Date: 20210916; Test Name: Blood test; Result Unstructured Data: blood counts; Comments: elevations in different things; Test Date: 20210924; Test Name: CT scan; Result Unstructured Data: Spleen was enlarged; Test Date: 20211006; Test Name: Bone marrow biopsy; Result Unstructured Data: Negative; Test Date: 20211227; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Comments: at doctor's office.; Test Name: EKG; Result Unstructured Data: needs stents placed; Test Name: CT scan; Result Unstructured Data: Normal; Comments: on abdomen and spleen
Aktuelle Erkrankungen: Muscle relaxant; Penicillin allergy
Vorgeschichte: Comments: The patient had always been a healthy person.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028423

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MI
Alter: 87,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 03.03.2021
Beginn: 19.11.2021
Tage bis Beginn: 261,0
Dosis: 1
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Amnesia Anticoagulant therapy Blood creatinine increased C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Confusional state Death Dyspnoea Fibrin D dimer Hypoxia Lung infiltration Lung opacity Procalcitonin SARS-CoV-2 test positive

Symptomtext

Patient fully vaccinated. Patient COVID positive 11/19/2021. 88-year-old female with significant known history for atrial fibrillation/coronary artery disease, depression, who presented for shortness of breath. In the emergency department, she is alert/oriented, states she is not sure how she ended up here, cannot recall exactly who brought her and/or why she is here and is asking to be discharged home. Denies chest pain. BP 96/62. Admission dx: acute respiratory failure, SOB, Hypoxia, COVID pneumonia. CSR: multipfocal bilateral airspace opacities. Treatment: remdisivir, decadron, lovenox. On 15/15NRB. Progressive pulmonary infiltrates. broad spectrum ABX CRP 301.1-242.7; D-dimer 1021--769; procalcitonin 0.51. AKI: Cr 1.11--0.98-- 1.06--1.02--0.95--0.89--0.82-0.99--1.64-1.19. Patient expired.

Weitere VAERSDATA-Felder

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

VAERS 2014217

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 30.03.2021
Beginn: 04.01.2022
Tage bis Beginn: 280,0
Dosis: 1
Route/Site: IM / AR

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

Acute respiratory failure Atrial fibrillation Benign prostatic hyperplasia COVID-19 COVID-19 pneumonia Chest X-ray normal Condition aggravated Echocardiogram Ejection fraction normal Hypoxia Laboratory test Major depression Respiratory failure

Symptomtext

Hospitalized 1/04/2022-still currently admitted; COVID-19 positive 01/04/2022; fully vaccinated CHIEF COMPLAINT: COVID ASSESSMENT/PLAN # COVID-19 pneumonia # Acute respiratory insufficiency Symptom onset approximately 2 weeks ago Date of positive test 1/4 Current imaging: Chest x-ray which shows no significant infiltrates S/p Jansyn vaccination on 03/30/21 Out of window for monoclonal antibody infusion and remdesivir Continue to treat with dexamethasone Daily COVID labs Will monitor respiratory status closely # Chronic atrial fibrillation with RVR Exacerbated by acute illness and hypoxia Will hold BB secondary to soft BP Will monitor HR Continue cardiac monitor 01/06/2022 notes: Chief complaint COVID Assessment and Plan Principal Problem: COVID Active Problems: Atrial fibrillation with RVR Recurrent major depressive disorder, in full remission Pneumonia due to COVID-19 virus Benign prostatic hyperplasia without lower urinary tract symptoms Respiratory failure PLAN # COVID-19 # Acute respiratory insufficiency Symptom onset approximately 2 weeks ago Date of positive test 1/4 Current imaging: Chest x-ray which shows no significant infiltrates S/p J&J vaccination on 03/30/21 Out of window for monoclonal antibody infusion and remdesivir Continue to treat with dexamethasone (1/4-present) ECHO EF 69% Daily COVID labs Will monitor respiratory status closely Disposition: Continue decadron. Has been weaned to room air. Will have pulm rehab see him tomorrow to ensure no oxygen is needed at home with activity. Rates seem better controlled with metoprolol dosing. Blood pressure remains stable. Likely DC next 1-2 days

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Atrial fibrillation with RVR Recurrent major depressive disorder, in full remission Pneumonia due to COVID-19 virus Benign prostatic hyperplasia without lower urinary tract symptoms COVID Respiratory failure Closed left hip fracture Fall Pneumonia Alcohol abuse Hepatitis C Alcohol induced liver disorder
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler calcium citrate-vitamin D (CITRACAL) 315-250 MG-UNIT TABS fluticasone-salmeterol (ADVAIR DISKUS) 250-50 MCG/DOSE diskus inhaler metoprolol tartrate (LO
Allergien: NKA
Vorherige Impfungen: -

VAERS 2005918

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: IL
Alter: 79,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 08.04.2021
Beginn: 20.12.2021
Tage bis Beginn: 256,0
Dosis: 1
Route/Site: IM / LA

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

Atelectasis Blood lactic acid increased COVID-19 Cardiac arrest Chest X-ray abnormal Chest tube insertion Continuous haemodiafiltration Cough Death Decreased appetite Hypertension Life support Lung opacity Oxygen saturation decreased Pain Pneumothorax Renal impairment SARS-CoV-2 test positive

Symptomtext

Presented to ER on 12/22/21. Positive for COVID on 12/20/21. on Thursday he began to develop achy pains and feeling sleepy. When his symptoms did not improve he decided to call his primary care doctor on Monday. Patient thought he had a urinary tract infection. He was tested for COVID and was positive. He states since that time he has been monitoring his O2 saturations. On his pulse ox at home his O2 saturations are dropping below 90%. Patient arrived into the emergency room at 88% on room air. He was requiring 5 L nasal cannula to maintain his O2 saturations greater than 92%. He states that he has had decreased appetite, a nonproductive cough. He reports that he took his a.m. medications. Placed on dexamethasone, ceftriaxone, azithromycin and remdesivir. On 1/4/21, patient continued to be hypertensive overnight and required increased pressor therapy. He also had a small right-sided pneumothorax that was treated with a right-sided chest tube yesterday with resolution of the pneumothorax.He continued to be hemodynamically unstable from the COVID sepsis/septic shock also possible PE with elevated lactate. His kidney function worsened and he needed CVVH overnight. In the morning of 1/4/21 he had cardiac arrest with ROSC after 3 cycles of ACLS. Passed away on 1/4/21

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 13,0
Labordaten: 12/20/21 COVID 19: positive 12/22/21 chest xray: Areas of patchy opacification in the left mid and lower lung and right lower lung. Some of this may be infectious/inflammatory such as pneumonia. Some of this may be atelectatic. 12/27/21 US: Study positive for nonocclusive calf vein thrombus right lower extremity posterior tibial and peroneal distributions.
Aktuelle Erkrankungen: -
Vorgeschichte: Past Medical History Positives Diagnosis Date ? CAD (coronary artery disease) ? CVA (cerebral vascular accident) 9/4/2020 ? GERD (gastroesophageal reflux disease) ? Hyperlipidemia ? Hypertension ? RLS (restless legs syndrome) ? Sleep apnea ? Stroke
Andere Medikamente: Amlodipine, aspirin, atorvastatin, clopidogrel, vitamin B12, ferrous sulfate, furosemide, isosorbide dinitrate, losartan, metoprolol tartrate,l multivitamin, nifedipine, nitro PRN, omeprazole, pramipexole, sildenafil, testosterone, tramadol
Allergien: None
Vorherige Impfungen: -

VAERS 1923992

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 82,0
Geschlecht: M
Eingang: 05.12.2021
Impfdatum: 12.03.2021
Beginn: 29.11.2021
Tage bis Beginn: 262,0
Dosis: 1
Route/Site: SC / LA

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

COVID-19 Death General physical health deterioration Intensive care Positive airway pressure therapy Respiratory failure Thrombosis

Symptomtext

Pt admitted on 11/22 from nursing home with respiratory failure secondary to COVID19 infection. He was admitted to the ICU and placed on NIV. Pt continued to require more oxygen and was unable to come off BIPAP. He did express that he did not want to be placed on ventilator and did not want any intervention in regards to his own blood clot. The patient was made a DNR/DNI. His family was contacted. Pt continued to decline over the next couple of days. Family was called in. Pt was transitioned to comfort measures. He did pass away on 11/29/2021 @ 1846.

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

VAERS 1785431

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 67,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 11.03.2021
Beginn: 06.11.2021
Tage bis Beginn: 240,0
Dosis: UNK
Route/Site: IM / LA

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

Acute kidney injury Angiogram pulmonary abnormal C-reactive protein increased COVID-19 Chronic kidney disease Computerised tomogram thorax abnormal Condition aggravated Endotracheal intubation Intensive care Interstitial lung disease SARS-CoV-2 test positive Vaccine breakthrough infection Leukocytosis Lung opacity Mechanical ventilation Pulmonary embolism Respiratory failure Sinus tachycardia

Symptomtext

Patient is a 68 y.o. male with a PMH significant for COVID (10/02/21), CAD (s/p stents 2016, s/p left CEA 2019), CKD, HTN and HLD who presents to ED as a transfer for worsening hypoxic respiratory failure. Of note, contact information of providers who cared for the patient at Hospital is not available in the electronic health record. Patient was diagnosed with COVID 19 on 10/02/21 which was treated outpatient with supplemental oxygen over the last month. Patient was able to wean his O2 to 4L/NC until a few days ago. On admission patient on 8-10L NC at home with oxygen saturation no better than 90%. On arrival to ED patient was alert but hypoxic with initial work up significant for small subsegmental PE on CTA, elevated troponins, leukocytosis, AKI on CKD and elevated CRP. He was admitted and started on therapeutic lovenox, levaquin and steroids. He continued to have increasing oxygen requirements and was placed on HFNC 100% 30L. ICU was consulted for transfer to higher level of care per family request. Upon exam, patient is intubated and sedated on 100% on the vent. There is no family available so history has been taken from the chart. #Sequela of COVID 19 vs. Interstitial Pneumonitis (NSIP pattern) COVID + diagnosis 10/02/21 Home on 4L/NC at home since COVID diagnosis. -was initially admitted to ICU and required intubation. 11/22: CT chest: Extensive areas of groundglass attenuation involving both lungs. The lungs appear lesser radiographically dense than on 11/4/2021, although worse than on 10/2/2021. Completed Zosyn 11/10/21 Continue steroid taper (60mg x7 days, 50mg x7 days, 40mg x7 days, 30mg x7 days, 20mg x7 days, 10mg x7 days). Currently on prednisone 30 mg daily, Outpatient pulm follow up. encourage incentive spirometry Q 1hrs, chest physiotherapy scheduled. discontinued duoneb since pt does not feel much significant improvement and had sinus tachycardias. Discharge Disposition/Condition Disposition: (rehab facility) Condition: Stable (s/sx potential problems absent or manageable)

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 24,0
Labordaten: COVID PCR confirmed positive on 11/6/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: Past Medical History He has a past medical history of Calculus of kidney, CKD (chronic kidney disease), Coronary artery disease, HLD (hyperlipidemia), Hypertension, Old myocardial infarction, and Personal history of other diseases of the circulatory system.
Andere Medikamente: allopurinol aspirin atorvastatin bisoprolol clopidogrel lisinopril
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1749652

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MI
Alter: -
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: -
Beginn: 26.09.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / AR

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

Angiogram pulmonary abnormal Anticoagulant therapy COVID-19 COVID-19 pneumonia Chest discomfort Angiogram Angiogram pulmonary Influenza like illness Pulmonary embolism SARS-CoV-2 test SARS-CoV-2 test positive Ultrasound Doppler normal Ultrasound Doppler Ultrasound scan Vaccination failure

Symptomtext

COVID-19 pneumonia; Pulmonary embolism; COVID-19; Chest discomfort; Influenza like illness; Angiogram pulmonary abnormal; Anticoagulant therapy; Ultrasound Doppler normal; SARS-CoV-2 test positive; CONFIRMED CLINICAL VACCINATION FAILURE; This spontaneous report received from a health care professional via a Regulatory Authority Vaccine Adverse Event Reporting System (VAERS), (VAERS ID: 1749652) concerned a 56 year old male of unspecified race and ethnic origin. Initial information was processed along with the additional information received on 11-OCT-2021. The patient's height, and weight were not reported. The patient's concurrent conditions included: deep vein thrombosis (DVT), and the patient had no known drug allergies. The patient had no other acute issues. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025 and expiry: UNKNOWN) dose was not reported, 1 total, administered on 09-MAR-2021 for an unspecified indication. Concomitant medications included benzonatate. On 26-SEP-2021, the patient experienced covid-19 pneumonia, pulmonary embolism, angiogram pulmonary abnormal, anticoagulant therapy, covid-19, chest discomfort, influenza like illness, sars-cov-2 test positive, ultrasound doppler normal, confirmed clinical vaccination failure. On the same day, the patient was hospitalized. Laboratory data included: Angiogram pulmonary (NR: not provided) Abnormal, SARS-CoV-2 test (NR: not provided) COVID-19 positive, and Ultrasound Doppler (NR: not provided) Normal. On an unspecified date, laboratory data included: Computed Tomography angiography was performed and showed acute nonocclusive pulmonary emboli in the proximal basal segmental branches of the left lower lobe posterior right lower lobe and posterior right upper lobe without right heart strain. Patient was started on heparin infusion. On an unspecified date, Lower extremity ultrasound was performed and did not reveal any evidence of DVT (Deep vein thrombosis). Other acute pulmonary embolism without acute cor pulmonale Pneumonia due to COVID-19 virus. Patient was presented with flu like symptoms and chest tightness was found to be COVID positive but was not hypoxic and did not meet criteria for either Remdesivir or Decadron. The patient continued to remain hemodynamically stable and did not require any oxygen therapy. Care management did check that patient had coverage for Eliquis. The patient was transitioned off heparin drip and placed on Eliquis. The patient continued with Eliquis therapy for acute pulmonary embolism. Treatment medications (dates unspecified) included: heparin, and apixaban. The patient was discharged on 27-SEP-2021, to home in stable condition. The patient was hospitalized for 2 days. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from covid-19 pneumonia, pulmonary embolism, angiogram pulmonary abnormal, anticoagulant therapy, covid-19, chest discomfort, influenza like illness, sars-cov-2 test positive, and ultrasound doppler normal, and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Hospitalization Caused / Prolonged). This report was associated with product quality complaint: The suspected product quality complaint has been confirmed to be the reported allegation could not be confirmed. A manufacturing related root cause could not be identified based on the PQC evaluation/investigation performed. Additional information received on 19-NOV-2021. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result.; Sender's Comments: V1: This follow up adds information about Product quality complaint investigation result. This does not alter previous causality assessment of the reported events Covid-19 vaccine ad26.cov2.s -Covid-19 pneumonia, Pulmonary embolism, Covid-19, Chest discomfort, Influenza like illness, Angiogram pulmonary abnormal, Anticoagulant therapy, Ultrasound doppler normal, SARS CoV-2 test positive. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). Covid-19 vaccine ad26.cov2.s -Confirmed clinical vaccination failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: Test Date: 20210926; Test Name: SARS-CoV-2 test; Result Unstructured Data: COVID-19 positive; Test Date: 20210926; Test Name: Angiogram pulmonary; Result Unstructured Data: Abnormal; Test Date: 20210926; Test Name: Ultrasound Doppler; Result Unstructured Data: Normal; Test Name: Diagnostic ultrasound; Result Unstructured Data: No any evidence of DVT; Test Name: CT angiography; Result Unstructured Data: Reported; Comments: acute nonocclusive pulmonary emboli in the proximal basal segmental branches of the left lower lobe posterior right lower lobe and posterior right upper lobe without right heart strain
Aktuelle Erkrankungen: Deep vein thrombosis
Vorgeschichte: Comments: The patient had no known drug allergies. The patient had no other acute issues.
Andere Medikamente: TESSALON
Allergien: -
Vorherige Impfungen: -

VAERS 1884918

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: AR
Alter: 55,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 19.03.2021
Beginn: 19.11.2021
Tage bis Beginn: 245,0
Dosis: 1
Route/Site: UN / UN

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

Anticoagulant therapy Computerised tomogram thorax abnormal Dyspnoea Echocardiogram Pulmonary embolism Ultrasound Doppler X-ray

Symptomtext

Pt developed shortness of breath. Fount to have PE. Physician feels PE could be result of vaccines since pt has no known risk factors or cause for this incident. Pt started on Xarelto since other meds contraindicated due to pt allergies.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: Xray, CT (PE), venous doppler and echocardiogram performed while hospitalized
Aktuelle Erkrankungen: None
Vorgeschichte: Dislipidemia, chronic back pain, HTN
Andere Medikamente: Rosuvastatin
Allergien: Ciprofloxacin, PCN, Beef prod, pork derived prod
Vorherige Impfungen: -

VAERS 1354427

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 75,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 17.03.2021
Beginn: 24.05.2021
Tage bis Beginn: 68,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Chills Death Decreased appetite Dyspnoea COVID-19 pneumonia Computerised tomogram thorax abnormal Cough Endotracheal intubation Intensive care Myalgia Rhinorrhoea SARS-CoV-2 test positive Lung opacity

Symptomtext

Not LTCF. PCR(+) 05/24/2021. Fully vaccinated (J&J): 03/17/2021. DR survey: "NO OTHER RECORDS OBTAINED". Hospitalized, ICU, 05/23/2021. DC support covid-19 and (+)PCR is within 6 weeks of DOD. Intubated. S/S: chills, myalgia, rhinorrhea, SOA, Loss of appetite. C/M: Acid Reflux; sinus problems, former smoker.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: C/M: Acid Reflux; sinus problems, former smoker.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1354427

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 75,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 17.03.2021
Beginn: 24.05.2021
Tage bis Beginn: 68,0
Dosis: 1
Route/Site: IM / UN

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

COVID-19 Chills Death Decreased appetite Dyspnoea COVID-19 pneumonia Computerised tomogram thorax abnormal Cough Endotracheal intubation Intensive care Myalgia Rhinorrhoea SARS-CoV-2 test positive Lung opacity

Symptomtext

Not LTCF. PCR(+) 05/24/2021. Fully vaccinated (J&J): 03/17/2021. DR survey: "NO OTHER RECORDS OBTAINED". Hospitalized, ICU, 05/23/2021. DC support covid-19 and (+)PCR is within 6 weeks of DOD. Intubated. S/S: chills, myalgia, rhinorrhea, SOA, Loss of appetite. C/M: Acid Reflux; sinus problems, former smoker.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: C/M: Acid Reflux; sinus problems, former smoker.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1863357

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: CO
Alter: 58,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: -
Beginn: 20.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Angiogram Echocardiogram Malaise Myocardial infarction Stress cardiomyopathy

Symptomtext

BROKEN HEART SYNDROME TACHYCARDIA; HEART ATTACK; FEELING UNWELL; This spontaneous report received from a patient concerned a 58 year old female. The patient's height, and weight were not reported. The patient's past medical history included: sick, and covid-19 (was prescribed steroids and oxygen at home, cough medicine) and concurrent conditions included: diabetes, thyroid, fibromyalgia, chronic migraine, chronic sinusitis (was prescribed antibiotics), allergy to antibiotics, allergy to sulpha, food allergy, allergy to weed grass, allergy to dust, allergy to mould, and allergy to animal, severe anxiety, and panic attack. The patient experienced drug allergy when treated with codeine, and prednisone. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025 and expiry: 25-MAY-2021) 1 total administered on 20-MAR-2021 to left arm for prophylactic vaccination. No concomitant medications were reported. On 20-MAR-2021, the patient experienced heart attack around 11-12 pm, patient was screaming and hollering following a family incident, her son gave her some water hoping the chest pain would go away, patient's son took her to hospital and in emergency room was informed that having a heart attack. They took her for check up in an emergency room and was checked for clogged arteries [by opening up leg arteries and checking] and none was found. The doctor informed the patient that she had broken heart syndrome tachycardia. The patient was hospitalized for 1 day and was advised for complete bed rest for minimum 5 days. The patient was feeling crazy as never had anything like this before, suffered from severe anxiety and panic attack. The patient returned to emergency room on an unspecified date, as patient was feeling unwell. The doctor informed the patient, it would take months/weeks to recover from her heart attack. On JUL-2021, Laboratory data included: Echocardiogram (NR: not provided) Not reported. Laboratory data (dates unspecified) included: Angiography (NR: not provided). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from heart attack, and the outcome of feeling unwell and broken heart syndrome tachycardia was not reported. This report was serious (Hospitalization Caused / Prolonged).; Sender's Comments: V0: 20211115420 -covid-19 vaccine ad26.cov2.s- heart attack, broken heart syndrome tachycardia. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

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Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 1,0
Labordaten: Test Date: 202107; Test Name: Echocardiogram; Result Unstructured Data: Not reported; Test Name: Angiography; Result Unstructured Data: No blood clots; Test Name: Angiography; Result Unstructured Data: No clogged arteries
Aktuelle Erkrankungen: Allergy to animal; Allergy to antibiotic; Allergy to moulds; Anxiety; Chronic migraine; Chronic sinusitis (on antibiotics); Diabetes; Fibromyalgia; Food allergy; Grass allergy; House dust allergy; Panic attack; Thyroid disorder
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (The patient was treated with steroids and oxygen at home, cough medicine.); Sickness; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1857558

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 1805025

kritisch

Staat: TX
Alter: 68,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 22.03.2021
Beginn: 10.10.2021
Tage bis Beginn: 202,0
Dosis: UNK
Route/Site: IM / UN

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

COVID-19 Cerebrovascular accident

Symptomtext

dx of COVID, CVA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: breast CA, CHF, GERD
Andere Medikamente: unknown
Allergien: ace inhibitors, beta-blockers
Vorherige Impfungen: -

VAERS 1836638

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 62,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 11.03.2021
Beginn: 25.10.2021
Tage bis Beginn: 228,0
Dosis: UNK
Route/Site: IM / LA

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

Acute kidney injury Anticoagulant therapy Asthenia COVID-19 Cardio-respiratory arrest Death Decreased appetite Dyspnoea Fatigue Hypervolaemia Polyuria Productive cough Resuscitation SARS-CoV-2 test positive

Symptomtext

a 63 y.o. male has history of HFrEF due to ICM, mod-severe MR, CKD II-III, DMII, MI X2 with PCI and LV thrombus on warfarin. He is currently listed for heart transplant. Patient complaints of loss of appetite, generalized weakness, mild productive cough, and mild dyspnea since Saturday. He denies fever, chills, sore throat, nausea, vomiting, abdominal pain, diarrhea, loss of taste or smell. Patient denies any recent weight gain or weight loss. He initially went to Emergency Room where he was tested positive for COVID 19. He was given Tylenol then was transferred for higher level care. Unknown contact information for provider who cared for the patient. Review of Systems Constitutional: Positive for appetite change and fatigue. Respiratory: Positive for cough and shortness of breath. Pt remained on warfarin, was started on remdesivir and steriods. Pt was diuresed for fluid overload and developed AKI, lasix were held. Pt had worsening oxygen requirements overnight and was re-started on diuresis. Pt coded and underwent about 1 hour of CPR and was pronounced at 11:28 am.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: 5,0
Labordaten: COVID PCR confirmed positive on 10/25/21
Aktuelle Erkrankungen: N/A
Vorgeschichte: ? CHF (congestive heart failure) ? Coronary artery disease STENTS X 3 ? Hypertension ? Old myocardial infarction History of ST elevation myocardial infarction (STEMI) ? Personal history of other diseases of the circulatory system History of coronary artery disease ? Personal history of other diseases of the circulatory system History of hypertension ? Personal history of other endocrine, nutritional and metabolic disease History of type 2 diabetes mellitus ? Type 2 diabetes mellitus with diabetic chronic kidney disease CKD stage 3 secondary to diabetes
Andere Medikamente: aspirin cholecalciferol corlanor ezetimibe farxiga furosemide glipizide jantoven magnesium oxide metformin metoprolol succinate XL multivitamin nitroglycerin pantoprazole semaglutide hepatitis B (Engerix-B)
Allergien: statins - rash banana - diarrhea
Vorherige Impfungen: -

VAERS 1801421

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 77,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 06.03.2021
Beginn: 02.10.2021
Tage bis Beginn: 210,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Death Laboratory test Vaccine breakthrough infection

Symptomtext

Patient had breakthrough infection and expired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Laboratory test: 9/16/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Per death certificate- Alzheimer's dementia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1800987

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 63,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 08.03.2021
Beginn: 19.10.2021
Tage bis Beginn: 225,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Cough Dyspnoea Endotracheal intubation Fatigue Hypoxia Intensive care Malaise Mechanical ventilation Pneumonia Respiratory failure Rhinorrhoea SARS-CoV-2 test positive Septic shock Skin disorder

Symptomtext

This patient was initially seen in Emergency Department in October with a complaint of shortness of breath, cough malaise fatigue and rhinorrhea. Patient's husband did test positive for COVID-19, this patient did as well test positive during emergency department evaluation. This patient did receive COVID-19 vaccination Jansen single dose. Patient was admitted to the hospital service started on dexamethasone 10 mg q. 12 hours and 5 day course of Remdesivir. Patient also started on therapeutic Lovenox and IV antibiotic directed at acute acquired pneumonia ceftriaxone and azithromycin. 7 October pulmonary was consulted, with recommendations to continue the course of dexamethasone and Remdesivir. 10 October Pt transferred to the ICU started on noninvasive ventilation. 13 October respiratory failure with pending respiratory arrest patient was intubated placed on full mechanical ventilation. Pt then underwent proning protocol with some benefit early on. However, patient continued to be hypoxic while supine. Prone protocol was DC due to skin breakdown with persistent hypoxia as supine. Patient later developed septic shock placed on broad-spectrum antibiotics. Patient requiring pressor support to maintain map pressure above 60. Discussing patient's care with daughter, given its poor diagnosis, decision was to make patient DNR and to redirect care to comfort.

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Praegender Schweregrund: Septic shock
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1787892

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: FL
Alter: 56,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 14.03.2021
Beginn: 27.05.2021
Tage bis Beginn: 74,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac disorder Electrocardiogram Myocardial infarction

Symptomtext

according to my cardiologist I had a heart attack showing on my May 27, 2021 EKG. She states there is a heart attack showing on my September 28,2021 EKG as well. I am 57 years old and have never been told I had any reason to be concerned about heart disease. My thought is did the J&J vaccine cause the heart attack? I had the vaccine in March/April and the heart attack shows on the May EKG so I feel the timing is indicative of the vaccine being the potential cause.

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Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: EKG 5/27/21 and 9/28/21. More testing in progress
Aktuelle Erkrankungen: high blood pressure, Gilbert's disease
Vorgeschichte: hypothyroid, high blood pressure, gilbert's disease
Andere Medikamente: Synthroid .112 mcg one per day, six days per week uncertain which blood pressure med at that time
Allergien: penicillin, erythromycin, cortisone, latex
Vorherige Impfungen: -

VAERS 1785065

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 72,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 08.03.2021
Beginn: 13.10.2021
Tage bis Beginn: 219,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain upper Agitation Bacterial infection Blood sodium decreased Brain natriuretic peptide normal Constipation Death Dyspnoea Endotracheal intubation Full blood count abnormal COVID-19 COVID-19 pneumonia Cardiac arrest Cardio-respiratory arrest Chest X-ray normal Intensive care Leukocytosis Life support

Symptomtext

From H&P: "Patient is a 72 y.o. male who presented to the emergency department due to shortness of breath. According the patient symptoms started after he was diagnosed with Covid 19 on 9/29. Reports initially was mild shortness of breath but progressed to severe thus presented to the emergency department for evaluation. The patient reports symptoms were associated with mild epigastric pain and nausea. Reports constipation. Denies chest pain, fever, chills, hemoptysis, lower extremity edema, orthopnea. Evaluation emergency department included chest x-ray which was negative. CBC revealed mild leukocytosis with white count 12.7. Sodium is 131. Lipase was normal. BNP was normal in trop was negative. With ambulation the patient required 2 L nasal cannula thus admission was requested. Upon evaluation patient continues report shortness of breath. He continues to deny pertinent negatives outlined above. Does not appear to be in acute distress." Hospital Course: The patient was admitted to Hospital COVID-19 medical unit for hypoxic respiratory failure secondary to COVID-19 viral pneumonia on 10/04/2021. He reportedly received the Jansen vaccine, single dose March 2021. Upon admission he was started on dexamethasone, Remdesivir and therapeutic Lovenox. Patient was diuresed as needed throughout hospital stay and pulmonary was consulted. Unfortunately the patient continued to have increased oxygen requirements and worsening respiratory distress requiring heated high-flow nasal cannula and was transferred to the ICU on 10/12/2021 and placed on AVAPS. Patient was started on a Precedex drip for agitation also started on broad-spectrum antibiotics as superimposed bacterial infection cannot be ruled out. Morning of 10/13/2021 code blue was called, CPR was started immediately and patient was intubated. Several rounds of ACLS were performed and patient was also given bicarb, calcium and dextrose. Unfortunately patient remained asystole or PEA and the code was eventually called. Time of death 0640 October 13th, 2021. Disposition: Deceased

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

VAERS 1761883

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 05.10.2021
Impfdatum: 09.03.2021
Beginn: 26.09.2021
Tage bis Beginn: 201,0
Dosis: 1
Route/Site: SYR / UN

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

Acute respiratory failure Agitation Alanine aminotransferase increased Angiogram pulmonary abnormal Anticoagulant therapy Aspartate aminotransferase increased Asthenia Atrial fibrillation Atrial flutter Blood creatine phosphokinase increased Blood gases Blood potassium decreased Bronchogram COVID-19 COVID-19 pneumonia Computerised tomogram head normal Computerised tomogram spine Condition aggravated

Symptomtext

Patient is a 77 y.o. male that presented to the ED with hypoxia and shortness of breath. ER workup positive for COVID pneumonia and also with AFib RVR. Intensive care unit contacted by ER air in agreement with CC2 level bed and will consult on patient. Currently the patient states that he feels very short of breath and tired. Denies fevers or chills. Resting history provided by daughter at bedside given his inattentiveness and disorientation. She states that over the last few days he has become more fatigued and short of short of breath since discharge from recent hospitalization.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: CHIEF COMPLAINT Chief Complaint Patient presents with ? WEAKNESS = ASSESSMENT/ Plan Active Problems: CAD (coronary artery disease) Dyslipidemia Hypertension Atrial fibrillation and flutter Tobacco use Pneumonia due to COVID-19 virus Acute on chronic respiratory failure with hypoxia Pertinent Results: - CT angiogram thorax: 1. No evidence of acute pulmonary embolism, noting that the subsegmental branches in the lower lobes are suboptimally opacified due to artifact. 2. Right upper lobe-predominant patchy groundglass airspace disease as seen with COVID-19 infection. Volume loss in the lower lobes with small right greater than left pleural effusions. No consolidative lobar pneumonia. 3. Findings suggestive of mild positive fluid balance. Question chronic pulmonary arterial hypertension. Estimated Creatinine Clearance: 89.3 mL/min (by C-G formula based on SCr of 0.67 mg/dL). Acute hypoxic respiratory failure secondary to Severe COVID pneumonia - admit to CC2 bed for close monitoring with ICU on consult - status post IV Decadron 6 mg need E will continue Decadron 6 mg daily for 10 days - remdesivir started in the emergency department will will continue x5 days -stop IV fluids started in emergency department - will give Lasix IV Lasix 40 mg 2 times a day x2 doses for now - continue close monitoring on continuous pulse oximetry - will repeat ABG - intensive care unit consulted appreciate recommendations; spoke with intensive care unit intensivist will cover for Hospital associated bacterial pna with vancomycin/cefepime given air bronchograms on CT per intensive care unit intensivist review of CT - spoke with pharmacy given his inability to tolerate oral intake will hold Eliquis for now and start on Lovenox protocol for COVID-19; transition back to Eliquis when patient is able to tolerate oral - patient is at high risk of clinical deterioration and death due to severe COVID pneumonia requiring high amount of oxygen supplementation - Alabuterol PRN and continue home Spiriva - wean oxygen as tolerated to maintain saturations greater than 92% AFib RVR -titrate Cardizem drip - will add IV metoprolol 5 mg Q 3 as needed to help control heart rate <120 - cardiology consulted appreciate recommendations; spoke with cardiology team they agree with continuing Cardizem and p.r.n. IV metoprolol 5 mg Q 3 as needed to control heart rate as noted above - Eliquis on hold for now as noted above given inability to tolerate oral meds this time will cover with Lovenox per COVID-19 protocol for now transition back to Eliquis when able to tolerate oral meds. Agitation/delirium/disorientation - as discussed with intensive care unit will start on Precedex drip non insulin dependent DM on metformin; last hgbA1c of 5.4 - will cover with on very low dose insulin sliding scale given that he will be on steroids as above for tx of covid HTN HLD CAD - hold prior to admission meds for now given his inability to tolerate oral intake; restart home meds when he is able to tolerate orally intake Diet: NPO for now DVT prophylaxis: subcutaneous heparin Lovenox Code status: Full code per discussion with Family at bedside Plan of care above discussed with family and they expressed agreement - all questions answered. 78 minutes were spent on the unit/floor with the patient with over 50% spent counseling and coordination of care related to plan of care. History of Present Illness Patient is a 77 y.o. male that presented to the ED with hypoxia and shortness of breath. ER workup positive for COVID pneumonia and also with AFib RVR. Intensive care unit contacted by ER air in agreement with CC2 level bed and will consult on patient. Currently the patient states that he feels very short of breath and tired. Denies fevers or chills. Resting history provided by daughter at bedside given his inattentiveness and disorientation. She states that over the last few days he has become more fatigued and short of short of breath since discharge from recent hospitalization. Medical History Past Medical History: Diagnosis Date ? Arthritis ? Atrial fibrillation ? BPH (benign prostatic hyperplasia) ? CAD (coronary artery disease) 2011 NSTEMI Stent RCA ? Cancer ? COPD with emphysema ? Depression ? Diabetes ? Diabetic neuropathy ? Dyslipidemia ? HTN (hypertension) ? Pneumonia due to organism ? Type 2 diabetes mellitus Past Surgical History Past Surgical History: Procedure Laterality Date ? ENDOSCOPY, COLON, DIAGNOSTIC ? HX ADENOIDECTOMY ? HX CARPAL TUNNEL RELEASE Right R ? HX CATARACT REMOVAL Bilateral ? HX CERVICAL FUSION x2 ? HX COLONOSCOPY 3/3/14 ? HX COLONOSCOPY 06/07/2018 ? HX COLONOSCOPY N/A 6/7/2018 COLONOSCOPY POLYPECTOMY ENDO performed by MD ? HX CORONARY STENT PLACEMENT 2011 RCA DES. ? HX TONSILLECTOMY Prescriptions Prior to Admission (Not in a hospital admission) No Known Allergies Social History Socioeconomic History ? Marital status: Widowed Spouse name: Not on file ? Number of children: 4 ? Years of education: Not on file ? Highest education level: Not on file Occupational History ? Not on file Tobacco Use ? Smoking status: Current Every Day Smoker Packs/day: 0.25 Years: 46.00 Pack years: 11.50 Types: Cigarettes ? Smokeless tobacco: Never Used ? Tobacco comment: About 3 cigarettes a day Substance and Sexual Activity ? Alcohol use: No ? Drug use: No ? Sexual activity: Not on file Other Topics Concern ? Not on file Social History Narrative ? Not on file Social Determinants of Health Financial Resource Strain: Low Risk ? Difficulty of Paying Living Expenses: Not hard at all Food Insecurity: No Food Insecurity ? Worried About Running Out of Food in the Last Year: Never true ? Ran Out of Food in the Last Year: Never true Transportation Needs: No Transportation Needs ? Lack of Transportation (Medical): No ? Lack of Transportation (Non-Medical): No Physical Activity: ? Days of Exercise per Week: ? Minutes of Exercise per Session: Stress: ? Feeling of Stress : Social Connections: ? Frequency of Communication with Friends and Family: ? Frequency of Social Gatherings with Friends and Family: ? Attends Religious Services: ? Active Member of Clubs or Organizations: ? Attends Club or Organization Meetings: ? Marital Status: Family History Family History Problem Relation Age of Onset ? Cancer Mother cause of death ? Colon Polyps Brother 72 transluminal coronary angioplasty ? Heart Failure Father cause of death Review of Systems Review of Systems Unable to perform ROS: Acuity of condition (Unable to assess due to acuity and agitation/confusion.)
Aktuelle Erkrankungen: Admission Date: 9/16/2021 Discharge Date: Sep 22, 2021 Active Hospital Problems Diagnosis Date Noted POA ? Moderate protein-calorie malnutrition 09/17/2021 Unknown Resolved Hospital Problems Diagnosis Date Noted Date Resolved POA ? Rhabdomyolysis 09/16/2021 09/22/2021 Unknown Pre-Existing Active Problems Diagnosis Date Noted POA ? Tobacco use 07/22/2021 Unknown ? Atrial fibrillation and flutter 06/26/2019 Unknown ? CAD (coronary artery disease) 06/05/2014 Unknown ? Dyslipidemia 06/05/2014 Unknown ? Type II or unspecified type diabetes mellitus without mention of complication, not stated as uncontrolled 06/05/2014 Unknown ? Hypertension 06/05/2014 Unknown HOSPITAL COURSE: Patient is a 77-year-old male with a history of hypertension, atrial fibrillation on Eliquis, combined systolic and diastolic heart failure and diabetes who presented after he was found down in his apartment. He had fell in his apartment but was unable to get up and was found on the morning of admission by his apartment manager and it was estimated that he had been down on the floor for about 12 hours. In the emergency department labs were obtained that was significant for CK of 8094 with a normal renal function and mild elevation of AST and ALT. COVID-19 PCR was negative. UA did not reveal any evidence of infection. Troponins were elevated at 32 and 30. Atrial fibrillation was seen on EKG. CT of the head and CT of the cervical spine did not reveal any acute pathology. He was noted to have a small meningioma on head CT which was stable in appearance study obtained in 2019. Patient was given IV fluids and potassium was also replaced as it was found to be low. CK level had improved. He was also found to have hypomagnesemia and ongoing hypokalemia and electrolytes were replaced. Cardiology was consulted due to AFib with RVR and elevated heart rate. Echocardiogram was obtained that showed stable ejection fraction and showed inferior infarct, normal RV size and systolic function and no significant valvular dysfunction. Cardiology recommended to continue metoprolol and up titrate as needed. Amlodipine and lisinopril were held to allow further up titration of metoprolol. Heart rates did improve. He was seen by RT and felt to have moderate malnutrition. Patient's heart rate improved. Cardiology recommended that patient would need a ZIO patch at discharge and also recommended reinstituting lisinopril at 5 mg daily and to continue to hold Norvasc. He was evaluated by PT and OT and recommendation was for home health therapy. He had no other acute issues and was discharged home in stable condition 9/22/21.
Vorgeschichte: Hospital CAD (coronary artery disease) Dyslipidemia Hypertension Atrial fibrillation with RVR Acute on chronic combined systolic and diastolic heart failure Tobacco use Moderate protein-calorie malnutrition Pneumonia due to COVID-19 virus Acute on chronic respiratory failure with hypoxia Non-Hospital Type II or unspecified type diabetes mellitus without mention of complication, not stated as uncontrolled
Andere Medikamente: Hospital Medications L1 acetaminophen (TYLENOL) tablet 1,000 mg L1 acetaminophen (TYLENOL) tablet 500 mg albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 90 mcg inhaler (60 dose canister) apixaban (ELIQUIS) tablet 5 mg aspirin chewab
Allergien: Not on File
Vorherige Impfungen: -

VAERS 1731372

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: GA
Alter: 88,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 19.03.2021
Beginn: 06.05.2021
Tage bis Beginn: 48,0
Dosis: 1
Route/Site: IM / AR

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

COVID-19 Cardio-respiratory arrest Death SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough COVID-19 case with unknown symptom status. Death 6/30/2021. From Vital Records COD = ACUTE CARDIOPULMONARY ARREST, ALZHEIMER'S WITH DEMENTIA DISEASE, DIABETES MELLITUS TYPE 2. Per vital records; Other Significant Conditions include: None listed. place of death: DECEDENT'S HOME; certified by: CERTIFYING PHYSICIAN; occ/ind: HOME ECONOMICS TEACHER, EDUCATION

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Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: -
Labordaten: 05/06/2021 PCR+ COVID-19 test; 05/10/2021 PCR+ COVID-19 test
Aktuelle Erkrankungen: -
Vorgeschichte: ALZHEIMER'S WITH DEMENTIA DISEASE, DIABETES MELLITUS TYPE 2
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1722728

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 65,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 09.03.2021
Beginn: 28.08.2021
Tage bis Beginn: 172,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 pneumonia Cough Death Dyspnoea Fatigue Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Symptoms started on 8-22-21. 101 fever, runny nose, fatigue, cough, and shortness of breath. Was hospitalized on 8-28-21 with pneumonia due to COVID 19 virus and acute respiratory failure with hypoxia. Expired on 9-2-21.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: 8-23-21 tested positive on a COVID antigen test. 8-24-21 tested positive on a COVID PCR test
Aktuelle Erkrankungen: -
Vorgeschichte: multiple myeloma, history of traumatic brain injury
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1689492

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: WI
Alter: 56,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 26.03.2021
Beginn: 31.08.2021
Tage bis Beginn: 158,0
Dosis: 1
Route/Site: IM / UN

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

Acute respiratory failure Ageusia Anosmia Aortic disorder COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Lung opacity Malaise SARS-CoV-2 test positive

Symptomtext

Patient fully vaccinated for COVID-19 with Janssen on 3/26/21. Patient arrived to ER 8/31/21 with cough, shortness of breath and generalized malaise. Symptoms started 1 week prior. Patient endorses loss of taste and smell. Patient admitted to reporting hospital on 8/31 for acute hypoxic respiratory failure 2/2 COVID-19 pneumonia. Patient was discharged on 9/8/21 to home.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: COVID 19 PCR positive 8/30/21 Chest Xray 8/31/21 Cardiac silhouette is stable. Mediastinal contours are unchanged with tortuous thoracic aorta. Bilateral multifocal ill-defined hazy opacities have progressed from the prior exam, left greater than right. Possible trace left pleural effusion. There is no pneumothorax or right pleural effusion.
Aktuelle Erkrankungen: hypertension, GERD, gastric ulcer
Vorgeschichte: hypertension, GERD, gastric ulcer
Andere Medikamente: Norvasc 10mg, Ferrous sulfate, Protonix 40mg
Allergien: Ace Inhibitors
Vorherige Impfungen: -

VAERS 1689150

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: FL
Alter: 73,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 12.03.2021
Beginn: 21.08.2021
Tage bis Beginn: 162,0
Dosis: 1
Route/Site: IM / -

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

Acute respiratory failure Asthenia COVID-19 Cough Dyspnoea Fatigue SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID-19 breakthrough case. patient presents to ED with complaints of cough and SOB. She also has fatigue and generalized weakness. She received the Johnson&Johnson COVID-19 vaccine on 3/12/21. Admitted 8/21/21. tested positive for covid at outside clinic on 8/21/21. Diagnosed and treated for covid-19 related acute hypoxic respiratory failure. Improved and was discharged on 8/26/21.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, liver cirrhosis, hypertension, CHF, hypothyroidism, diabetes mellitus type 2 and GERD
Andere Medikamente: calcium acetate, carvedilol, clonazepam, cyanocobalamin, furos
Allergien: bactrim, doxycycline, apple juice, pilocarpine, sulfadiazine,
Vorherige Impfungen: -

VAERS 1655902

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 85,0
Geschlecht: M
Eingang: 30.08.2021
Impfdatum: 10.03.2021
Beginn: 07.08.2021
Tage bis Beginn: 150,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure Anxiety Aortic valve calcification Benign prostatic hyperplasia Blood creatinine increased Blood glucose increased Blood magnesium normal C-reactive protein increased COVID-19 COVID-19 pneumonia Calcium ionised decreased Cardiomegaly Chest X-ray abnormal Chest discomfort Chest pain Chills Chronic kidney disease Computerised tomogram thorax abnormal

Symptomtext

Patient vaccinated 3/10/2021, admitted 8/7/2021, tested positive for covid 8/7/2021, 8/19 and 8/21. discharged 8/22/2021 to home. admitted with COVID undergoing treatment Date of Clinic Visit or Hospitalization: 8/7/2021 Reason for clinic visit or hospitalization: COVID COVID-19 positive test result: Yes, 8/7/21 Plans to monitor (include medications if prescribed):dexamethasone and remdesivir History Of Present Illness Patient is a 85 y.o. Male with a PMH of GERD, BPH, OSA, DMII, CKD, HTN, HLD, CAD with MI s/p PCI (5/2017) who was diagnosed with COVID19 about 5 days ago presents to ED for dyspnea. Pt is alert and oriented x 3 but a very poor historian. Pt reports he was exposed to COVID19 by another family member a few weeks ago. His wife was admitted here with COVID19 about 3 days ago. Pt began having dyspnea on Monday (8/2) which has become progressively worse. Pt reports dyspnea is worse on exertion and causes anxiety and panic with chest tightness when it occurs. Pt reports fever and chills over the last few days. Pt reports nausea and diarrhea but states, "very little" Pt denies vomiting, abdominal pain, dysuria, cough, congestion, sore throat, heart palpitations, or travel. Pt with recorded SpO2 as low as 92% on room air on presentation with tachypnea 20-30's. Pt reportedly was hypoxic at home with SpO2 in the high 80's per family who is no longer at bedside. Pt on 3L nasal cannular on admission with SpO2 97%. Pt with temp 100.2. Labs significant for WBC 10.57, CRP 152, troponin 33, glucose 377, sCr 1.7, magnesium 1.4, and ical 4.4. ECG normal sinus without acute ST changes. CXR shows cardiomegaly, aortic vascular calcifications, low lung volumes, and patchy left greater than right airspace opacities consistent with atypical or viral infection, including COVID19. CT PE shows no pulmonary embolism but bilateral ground glass airspace disease consistent with viral pneumonia. IM consulted for admission. Review of Systems Constitutional: Positive for chills and fever. Negative for fatigue and unexpected weight change. HENT: Negative for congestion, hearing loss, postnasal drip, rhinorrhea, sinus pain, sore throat and trouble swallowing. Respiratory: Positive for chest tightness and shortness of breath. Negative for apnea, cough, wheezing and stridor. Cardiovascular: Positive for chest pain. Negative for palpitations and leg swelling. Gastrointestinal: Positive for diarrhea. Negative for abdominal distention, abdominal pain, constipation, nausea and vomiting. Pulmonary: Effort: Pulmonary effort is normal. Breath sounds: Rhonchi present. No wheezing. Comments: Rhonchi in the LUL and diminished throughout Hospitalization Admit Date/Time: 8/7/2021 6:20 PM Admitting Attending: Doctor M. Discharge Date: 08/22/21 Discharge Attending Physician: Doctor G. PCP name and Address: No Pcp None Referring provider name and address: No referring provider defined for this encounter. Chief Concern, Brief History of Present Illness, and Hospital Course 85 y.o. Male with a PMH of GERD, BPH, OSA, DMII, CKD, HTN, HLD, CAD with MI s/p PCI (5/2017) who was diagnosed with COVID19 about 5 days prior to admission Is admitted with acute respiratory failure with hypoxia secondary to Covid 19 viral pneumonia. Per patient he was vaccinated with Johnson & Johnson vaccine in May and pharmacy is attempting to contact family to get the vaccination card to officially document breakthrough case. The patient is currently on 3-4 L of nasal cannula and appears to be progressing well. He is on Remdesivir and dexamethasone. Patient has hyperglycemia likely secondary to steroid use in the setting of uncontrolled type 2 diabetes. His last hemoglobin A1c was 9%. He is currently on Lantus of 30 and lispro 10 units 3 times a day with meals. Adjusted insulin per FSBG. 85yo Male PMHx OSA, DMII, HTN, CAD with MI s/p PCI (5/2017) who was diagnosed with COVID19, presents with worsening dyspnea. #) Viral pneumonia secondary to SARS/CoVID-19 pneumonia #) Acute hypoxic respiratory failure requiring supplemental oxygen secondary to COVID 19 Pt began having dyspnea on 8/2 which has become progressively worse. He completed Remdesivir 200mg on day 1, then 100mg daily for 4 days (start 8/8) CRP 46.9->29.8->17.1->11.7->8.2->5.5 /Plan: - Dexamethasone 6mg PO daily x10days (started 8/10, RECOVERY Trial protocol) - Oxygen per nasal canula. Titrate O2 for 92-96%, on RA now. - Airborne precautions, including use of N95 masks, face-shields, gown, gloves - Albuterol HFA inhaler Q4h PRN - Acetaminophen 650mg PO Q6h PRN for fever - Pantoprazole while on steroids #) Diabetes Type 2, Uncontrolled, with Hyperglycemia A1c = 9.1 (8/7), Glucose was 377 on admission Pt on Glipizide and Lantus 24 units at bedtime His Glc inpatient has been labile, ranging between 80's and 300's. This is worsened by the steroids /Plan: Insulin lantus and lispro during hospital stay with ISS. - Lantus 30U at bedtime at home, decreased here, recc to continue as 15 units on discharge. #) Chronic Kidney Disease, Stage 3b sCr 1.7->1.48->1.72->1.58->1.45->1.43->1.39->(resume ACE)->1.37->1.44 Baseline unknown, but this may be his baseline. Cr is varying less than 0.3 and he has diabetes. Plan: - Continue tamsulosin - Resume home Enalapril (resumed 8/14, expect 30% Cr rise due to hemodynamics not injury) - d/c home Furosemide #) Coronary Artery Disease s/p PCI (5/2017) /Plan: - Continue home Metoprolol 12.5 BID - Continue home ASA, statin - home Enalapril #) Hypertension - Continue home Metoprolol 12.5 BID - Resume home Furosemide 20mg as needed after f/u with PCP. - home Enalapril #) OSA Patient and his son both say he uses a "mask" all night while sleeping, and provides humidified air - CPAP at night (start with 5cm pressure) #) Hyperkalemia K=4.9->4.5->5.8(hemolyzed)->4.3->4.1->4.2 - Resume home Furosemide 20 - Low K diet - Increase insulin as per Diabetes #) Thrombocytopenia - likely secondary to Covid. Monitor #) Hypomagnesemia - Monitor and replace #) Hypocalcemia - Monitor and replace #) Benign Prostatic Hyperplasia - Resume home Tamsulosin #) GERD - Resume home PPI #) Fluids/Nutrition - Low K consistent 2carb diet #) Prophylaxis - Enoxaparin 30mg subcu BID #) Discharge Planning wean off O2. Pt on RA Talked to pts son, after talking to IPAC, pt can be discharged home. Pt can stay with his wife.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: XR Chest 1 View Result Date: 8/7/2021 Narrative: Exam/Procedure: XR CHEST 1 VIEW ordered by CLINICAL INDICATION: dyspnea TECHNIQUE: XR CHEST 1 VIEW COMPARISON: Chest x-ray 5/19/2017 FINDINGS: Cardiomegaly. Aortic vascular calcifications. Low lung volumes. Patchy left greater than right airspace opacities. No large pleural effusion. No significant pneumothorax. No acute osseous finding. No subdiaphragmatic free air.
Aktuelle Erkrankungen: -
Vorgeschichte: PMH of GERD, BPH, OSA, DMII, CKD, HTN, HLD, CAD with MI s/p PCI (5/2017)
Andere Medikamente: aspirin, atorvastatin, certirizine, enalapril, fluticasone, metoprolol tartrate, nitroglycerin (PRN), pantoprazole, tamsulosin, furosemide, glipizide, insulin glargine, potassium chloride
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1627930

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 83,0
Geschlecht: M
Eingang: 25.08.2021
Impfdatum: 10.03.2021
Beginn: 22.08.2021
Tage bis Beginn: 165,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 pneumonia Sepsis COVID-19 Cough Death Dyspnoea Exposure to SARS-CoV-2 Pyrexia Respiratory viral panel SARS-CoV-2 test positive

Symptomtext

Patient admitted to the ED with SOA, cough, fever and temp to 103.1. Pt with exposure to COVID - daughter has. Pt started on O2, dexamethasone, and remdesivir on 8/23. Pt DNI; oxygenation worsened and family made plan to move to comfort care only/hospice on 8/24. Anticipate imminent death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: 8/22 Respiratory viral panel = COVID 19 +
Aktuelle Erkrankungen: Ended steroid taper for COPD exacerbation on 2/28; pt was admitted to the hospital 2/14-2/18 with chest pain; pt s/p heart cath with non-obstructive disease found during this admission
Vorgeschichte: DM2 Pulmonary HTN Hyperlipidemia HTN CAD A fib chronic diastolic heart failure COPD Sick sinus syndrome
Andere Medikamente: gabapentin 300 MG capsule 300 mg, Oral, Daily Accu-Chek Aviva Plus w/Device kit USE AS DIRECTED amLODIPine 10 MG tablet 10 mg, Oral, Daily aspirin 81 MG chewable tablet 81 mg, Oral, Daily Breo Ellipta 100-25 MCG/INH inhaler No dose,
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1361818

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 31.03.2021
Beginn: 12.05.2021
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: IM / AR

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

Ageusia Anosmia COVID-19 Chills Cough Death Diarrhoea Dyspnoea Pyrexia SARS-CoV-2 test positive

Symptomtext

A 59-year-old female without comorbidity present with complain of fever, chills, cough, dyspnea, diarrhea, loss of taste and smell since 5 days ago. Denies melena, hematochezia, dysuria, chest pain, palpitation or any other symptom. Patient was diagnosed 3 days ago with COVID 19 infection. Patient had worsening shortness of breath for which reason she presented to the ER. Patient report receiving Johnson Johnson COVID-19 vaccine on March 31, 2021. 5/12/2021 tested positive 5/30/2021 patient discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 18,0
Labordaten: 5/12/2021 tested positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1361818

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 31.03.2021
Beginn: 12.05.2021
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: IM / UN

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

Ageusia Anosmia COVID-19 Chills Cough Death Diarrhoea Dyspnoea Pyrexia SARS-CoV-2 test positive

Symptomtext

A 59-year-old female without comorbidity present with complain of fever, chills, cough, dyspnea, diarrhea, loss of taste and smell since 5 days ago. Denies melena, hematochezia, dysuria, chest pain, palpitation or any other symptom. Patient was diagnosed 3 days ago with COVID 19 infection. Patient had worsening shortness of breath for which reason she presented to the ER. Patient report receiving Johnson Johnson COVID-19 vaccine on March 31, 2021. 5/12/2021 tested positive 5/30/2021 patient discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 18,0
Labordaten: 5/12/2021 tested positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1540471

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: TN
Alter: 57,0
Geschlecht: M
Eingang: 10.08.2021
Impfdatum: 13.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy Cardiovascular evaluation Catheterisation cardiac normal Chest X-ray Chest pain Coagulation test Dyspnoea Electrocardiogram T wave inversion N-terminal prohormone brain natriuretic peptide normal Pulmonary artery occlusion Pulmonary embolism Ultrasound Doppler normal Ventilation/perfusion scan abnormal Weight increased

Symptomtext

NOTICED INCREASED SOB APPROXIMATELY 3-4 WEEKS POST VACCINATION. INITIALLY ATTRIBUTED TO RECENT WEIGHT GAIN. PROGRESSIVE SOB CONTINUED THEN ACCOMPANIED WITH CHEST PAIN. MET WITH PCP ON 6/7 WHICH RESULTED IN CARDIAC WORKUP INCLUDING A HEART CATH ON 7/9 WHICH RESULTED IN NO CORONARY OCCLUSIONS. FOLLOWED UP WITH PCP WHO RECOMMENDED FOCUS ON WEIGHT LOSS. SOB CONITNUED AND ON 8/6 I MET WITH PCP AGAIN TO COMPLAIN THAT SOB NOT GETTING ANY BETTER. HE ORDERED V-Q SCAN WHICH INDICATED PULMONARY BLOCKAGE CONSISTENT WITH PE. I WAS HOSPITALIZED SAME DAY (8/6) AND PUT ON A COURSE OF IV HEPARIN FOR DURATION OF STAY. NO DVTS WERE FOUND ON ULTRASOUND. DISCHARGED ON 8/9 WITH PO ELIQUIS PENDING RESULTS OF HYPERCOAGULABILITY STUDY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: 6/7 - CHEST XRAY; RESULT UNKNOWN BY PATIENT 6/7 - EKG: INVERTED T-WAVES 6/7 - PROBNP - NORMAL 7/9 HEART CATH: NO OCCLUSIONS 8/6- VQ SCAN: POSITIVE FOR PE 8/7 - ULTRASOUND: BILAT NEGATIVE FOR DVTS 8/8 - HYPERCOAG STUDY: RESULTS PENDING
Aktuelle Erkrankungen: -
Vorgeschichte: HYPERTENSION OBESITY HYPERLIPIDEMIA LOW VIT-D BPH OSTEOARTHRITIS
Andere Medikamente: HYZAAR CRESTOR FLOMAX VITAMIN D
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1519080

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: FL
Alter: 87,0
Geschlecht: M
Eingang: 01.08.2021
Impfdatum: 31.03.2021
Beginn: 14.04.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Aphasia Bedridden Cerebrovascular accident Feeding disorder General physical health deterioration Hemiplegia Immobile Loss of personal independence in daily activities Unresponsive to stimuli Wheelchair user

Symptomtext

Patient experienced what family and hospice home health believe to be a right sided stroke. Prior to vaccination patient was mobil with walker, able to feed himself, verbal somewhat. Post vaccination 2 weeks to the day, patient became unresponsive. Patient revived on his own but did not have use of his right side. Post vaccine +2 weeks patient became non mobil and limited to wheel chair with the help of aid. Patient no longer is able to feed himself, verbage is limited and confined to a hospital bed as of 04/17/2021. Patients health has had a rapid decline since vaccination on 03/31/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: patient is homebound and unable to transport.
Aktuelle Erkrankungen: N/A
Vorgeschichte: DEMENTIA
Andere Medikamente: MEMANTINE 10 MG TAB 1X DAILY
Allergien: N/A
Vorherige Impfungen: -

VAERS 1225926

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: -
Alter: 35,0
Geschlecht: F
Eingang: 17.07.2021
Impfdatum: -
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Activated partial thromboplastin time Blood fibrinogen Blood sodium Cerebral haemorrhage Cerebral venous sinus thrombosis Adverse event Anxiety Areflexia Blood sodium increased Brain herniation Cerebral mass effect Coma scale abnormal Computerised tomogram head abnormal Computerised tomogram head normal Condition aggravated Coma scale Computerised tomogram head Fibrin D dimer

Symptomtext

CEREBRAL HEMORRHAGE; DURAL VENOUS SINUS THROMBOSIS; THROMBOCYTOPENIA; seizure; LOSS OF CONSCIOUSNESS; SEVERE FRONTAL HEADACHE, OCULAR HEADACHE; NAUSEA, VOMITING; PHOTOPHOBIA; SODIUM LEVEL HIGH; This spontaneous report received from a health care professional via a Regulatory Authority the VAERS (Vaccine Adverse Event Reporting System) concerned a 35 year old female. Additional information was also received on 22-JUN-2021 from a literature article: The patient's height, and weight were not reported. The patient's concurrent conditions included codeine allergy, migraines, depression, and chronic thrombocytopenia. Patient had no adverse events following any previous vaccine and no recent abortive therapy. The patient had no cerebral venous sinus thrombosis risk factors. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration not reported, batch number: 1805025) dose was not reported, administered on 08-APR-2021 for prophylactic vaccination. Concomitant medications included aripiprazole, bupropion hydrochloride, butalbital/caffeine/paracetamol, fluoxetine, propranolol hydrochloride, risperidone, and topiramate. On an unspecified date in APR-2021 around 8 PM, patient presented to emergency room (ER) with a severe frontal headache since around 2 PM. She took TYLENOL and marijuana candy for relief at 4 PM with no help. Patient had computerized tomography (CT) venogram and CT head at 10:19 PM with normal results. She was given Toradol, Compazine, Decadron, and magnesium and discharged at 2 AM. Her platelet count at that time was 114 x10*3/mcL and was consistent with the patient's description of chronic thrombocytopenia. On an unspecified date in APR-2021 at 2 AM, the patient presented to ER. She again had an ocular headache that was different and clearly more severe than her typical migraines. Still had significant nausea and vomiting along with photophobia. Unspecified laboratory results and imaging were reviewed. She again received morphine, Toradol, Reglan, Benadryl, dexamethasone. She was discharged at 06:00 feeling a little bit better. On 15-APR-2021 at 22:30, the patient had an acute worsening of headache and experienced loss of consciousness. At 23:30, her husband found her unresponsive and called EMS. The patient presented to emergency room at 01:30 after sustaining a seizure in route and was subsequently intubated on arrival. She had a Glasgow coma scale of 1 with fixed pupils and no gag reflex. Platelet count was 10 x10*3/mcL and reached a nadir of 9 x10*3/mcL. The D-dimer peak value was 13.47 mcg/mL, the fibrinogen nadir was 128 mg/dL, international normalized ratio (INR) was 1.2 and the activated partial thromboplastin time (aPTT) was 24.1 seconds. The result of a SARS-CoV-2 polymerase chain reaction (PCR) test was negative, and Heparin-platelet factor (PF)4 test result was positive (value of 2.2). CT head without contrast was performed which revealed intraparenchymal and subarachnoid hemorrhage with significant sulcal and cisternal effacement and mild migration of the cerebellar tonsils below the level of the foramen magnum. Intracranial hemorrhage locations were also reported as the right temporal lobe and left cerebellar hemisphere within the literature article. Increased density within the right transverse, sigmoid and superior sagittal sinus and questionably with in the sagittal sinus may reflect underlying dural venous sinus thrombosis. The patient was also found to have sigmoid sinus thrombosis. Neurology and neurosurgery evaluated the patient around 03:00 in person. Independently, imaging and clinical presentation was deemed to be incompatible with life. Because of the sedating medications required for intubation and subsequently her sodium rising to 170, the brain death physical examination by neurology was not performed. Repeat imaging to evaluate central nervous system vasculature was under consideration by the clinical team. Action taken with vaccine was not applicable. The outcome was recovering for severe frontal headache, ocular headache, nausea, vomiting, and photophobia, and the outcome of seizure, thrombocytopenia, cerebral hemorrhage, dural venous sinus thrombosis, loss of consciousness and sodium level high was not reported. This report was serious (Hospitalization Caused / Prolonged, Life Threatening, and Disability Or Permanent Damage). This case, from Same Literature article is linked to 20210354798, 20210408478, 20210428484, 20210407314, 20210416236, 20210444498, 20210415297, 20210439653, 20210444501, 20210444497 and 20210448310. Additional information was received on 22-JUN-2021 from a literature article. The following information was updated and incorporated into the case narrative: no cerebral venous sinus thrombosis risk factors, additional late signs/symptom included loss of consciousness (added as event), additional location of sigmoid sinus thrombosis and (intra)cerebral hemorrhage locations of the right temporal lobe and left cerebellar hemisphere, timeline of events, platelet nadir, other laboratory results, and linked case numbers.; Sender's Comments: V3: Follow-up from literature confirms no CVST risk factors, symptoms, anatomic location of CVST, and lab tests. This case concerns a 35-year-old female with a history of migraines, depression, and chronic thrombocytopenia who was hospitalized for cerebral venous sinus thrombosis (CVST) and thrombocytopenia 7 days after vaccine. Concomitant medications included aripiprazole, bupropion hydrochloride, butalbital/caffeine/paracetamol, fluoxetine, propranolol, risperidone, and topiramate. On an unspecified date the patient presented to the emergency department (ED) with a severe frontal headache. A computerized tomography (CT) venogram and CT of the head were unremarkable. She was given Toradol, Compazine, Decadron, and magnesium and discharged. Her platelet count at that time was 114, thought to be consistent with the patient's description of chronic thrombocytopenia. The patient later presented again to the ED with a severe ocular headache. She was evaluated and discharged again with morphine, Toradol, Reglan, Benadryl, dexamethasone. On day 7, the patient had an acute worsening of headache and was found unresponsive that night. She was taken back to the ED by EMS, sustained a seizure in route and was intubated on arrival. She had no gag reflex. Sodium was 170, platelet nadir was 10, D dimer was 13.47 mcg/mL, Anti-PF4 ELISA was 2.2 and COVID test was negative. A CT revealed intraparenchymal and subarachnoid hemorrhage with mild migration of the cerebellar tonsils below the level of the foramen magnum as well as a suggestion of an underlying dural venous sinus thrombosis. She was determined to have brain death. Based on evolving knowledge of Thrombosis with Thrombocytopenia Syndrome (TTS, per definition from Brighton Collaboration), the low platelet count and temporal relationship to vaccination, we consider the events to have a plausible relationship with vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 2,0
Labordaten: Test Date: 202104; Test Name: Venogram; Result Unstructured Data: normal; Test Date: 202104; Test Name: CT brain scan; Result Unstructured Data: normal; Test Date: 202104; Test Name: Laboratory test; Result Unstructured Data: not reported; Test Date: 202104; Test Name: Platelet count; Result Unstructured Data: 10 10*3/uL; Test Date: 202104; Test Name: Sodium; Result Unstructured Data: 170; Test Date: 202104; Test Name: CT brain scan; Result Unstructured Data: see results; Test Date: 202104; Test Name: Glasgow coma scale; Result Unstructured Data: 1; Test Date: 202104; Test Name: Platelet count; Result Unstructured Data: 114 10*3/uL; Test Name: Heparin-induced thrombocytopenia test; Result Unstructured Data: ELISA test result was positive (2.2); Test Name: SARS-CoV-2 PCR test; Result Unstructured Data: negative; Test Name: APTT; Result Unstructured Data: 24.1 sec; Test Name: International normalized ratio; Result Unstructured Data: 1.2; Test Name: Fibrinogen; Result Unstructured Data: 128 mg/dL, nadir; Test Name: Platelet count; Result Unstructured Data: 9 10*3/uL, nadir; Test Name: Fibrin D dimer; Result Unstructured Data: 13.47 mcg/mL peak
Aktuelle Erkrankungen: Chronic thrombocytopenia; Depression; Drug allergy; Migraine
Vorgeschichte: Comments: Patient had no adverse events following any previous vaccine. no recent abortive therapy
Andere Medikamente: ARIPIPRAZOLE; WELLBUTRIN; FIORICET; FLUOXETINE; INDERAL; RISPERDAL; TOPIRAMATE
Allergien: -
Vorherige Impfungen: -

VAERS 1225926

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: -
Alter: 35,0
Geschlecht: F
Eingang: 17.07.2021
Impfdatum: -
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / UN

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

Activated partial thromboplastin time Blood fibrinogen Blood sodium Cerebral haemorrhage Cerebral venous sinus thrombosis Adverse event Anxiety Areflexia Blood sodium increased Brain herniation Cerebral mass effect Coma scale abnormal Computerised tomogram head abnormal Computerised tomogram head normal Condition aggravated Coma scale Computerised tomogram head Fibrin D dimer

Symptomtext

CEREBRAL HEMORRHAGE; DURAL VENOUS SINUS THROMBOSIS; THROMBOCYTOPENIA; seizure; LOSS OF CONSCIOUSNESS; SEVERE FRONTAL HEADACHE, OCULAR HEADACHE; NAUSEA, VOMITING; PHOTOPHOBIA; SODIUM LEVEL HIGH; This spontaneous report received from a health care professional via a Regulatory Authority the VAERS (Vaccine Adverse Event Reporting System) concerned a 35 year old female. Additional information was also received on 22-JUN-2021 from a literature article: The patient's height, and weight were not reported. The patient's concurrent conditions included codeine allergy, migraines, depression, and chronic thrombocytopenia. Patient had no adverse events following any previous vaccine and no recent abortive therapy. The patient had no cerebral venous sinus thrombosis risk factors. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration not reported, batch number: 1805025) dose was not reported, administered on 08-APR-2021 for prophylactic vaccination. Concomitant medications included aripiprazole, bupropion hydrochloride, butalbital/caffeine/paracetamol, fluoxetine, propranolol hydrochloride, risperidone, and topiramate. On an unspecified date in APR-2021 around 8 PM, patient presented to emergency room (ER) with a severe frontal headache since around 2 PM. She took TYLENOL and marijuana candy for relief at 4 PM with no help. Patient had computerized tomography (CT) venogram and CT head at 10:19 PM with normal results. She was given Toradol, Compazine, Decadron, and magnesium and discharged at 2 AM. Her platelet count at that time was 114 x10*3/mcL and was consistent with the patient's description of chronic thrombocytopenia. On an unspecified date in APR-2021 at 2 AM, the patient presented to ER. She again had an ocular headache that was different and clearly more severe than her typical migraines. Still had significant nausea and vomiting along with photophobia. Unspecified laboratory results and imaging were reviewed. She again received morphine, Toradol, Reglan, Benadryl, dexamethasone. She was discharged at 06:00 feeling a little bit better. On 15-APR-2021 at 22:30, the patient had an acute worsening of headache and experienced loss of consciousness. At 23:30, her husband found her unresponsive and called EMS. The patient presented to emergency room at 01:30 after sustaining a seizure in route and was subsequently intubated on arrival. She had a Glasgow coma scale of 1 with fixed pupils and no gag reflex. Platelet count was 10 x10*3/mcL and reached a nadir of 9 x10*3/mcL. The D-dimer peak value was 13.47 mcg/mL, the fibrinogen nadir was 128 mg/dL, international normalized ratio (INR) was 1.2 and the activated partial thromboplastin time (aPTT) was 24.1 seconds. The result of a SARS-CoV-2 polymerase chain reaction (PCR) test was negative, and Heparin-platelet factor (PF)4 test result was positive (value of 2.2). CT head without contrast was performed which revealed intraparenchymal and subarachnoid hemorrhage with significant sulcal and cisternal effacement and mild migration of the cerebellar tonsils below the level of the foramen magnum. Intracranial hemorrhage locations were also reported as the right temporal lobe and left cerebellar hemisphere within the literature article. Increased density within the right transverse, sigmoid and superior sagittal sinus and questionably with in the sagittal sinus may reflect underlying dural venous sinus thrombosis. The patient was also found to have sigmoid sinus thrombosis. Neurology and neurosurgery evaluated the patient around 03:00 in person. Independently, imaging and clinical presentation was deemed to be incompatible with life. Because of the sedating medications required for intubation and subsequently her sodium rising to 170, the brain death physical examination by neurology was not performed. Repeat imaging to evaluate central nervous system vasculature was under consideration by the clinical team. Action taken with vaccine was not applicable. The outcome was recovering for severe frontal headache, ocular headache, nausea, vomiting, and photophobia, and the outcome of seizure, thrombocytopenia, cerebral hemorrhage, dural venous sinus thrombosis, loss of consciousness and sodium level high was not reported. This report was serious (Hospitalization Caused / Prolonged, Life Threatening, and Disability Or Permanent Damage). This case, from Same Literature article is linked to 20210354798, 20210408478, 20210428484, 20210407314, 20210416236, 20210444498, 20210415297, 20210439653, 20210444501, 20210444497 and 20210448310. Additional information was received on 22-JUN-2021 from a literature article. The following information was updated and incorporated into the case narrative: no cerebral venous sinus thrombosis risk factors, additional late signs/symptom included loss of consciousness (added as event), additional location of sigmoid sinus thrombosis and (intra)cerebral hemorrhage locations of the right temporal lobe and left cerebellar hemisphere, timeline of events, platelet nadir, other laboratory results, and linked case numbers.; Sender's Comments: V3: Follow-up from literature confirms no CVST risk factors, symptoms, anatomic location of CVST, and lab tests. This case concerns a 35-year-old female with a history of migraines, depression, and chronic thrombocytopenia who was hospitalized for cerebral venous sinus thrombosis (CVST) and thrombocytopenia 7 days after vaccine. Concomitant medications included aripiprazole, bupropion hydrochloride, butalbital/caffeine/paracetamol, fluoxetine, propranolol, risperidone, and topiramate. On an unspecified date the patient presented to the emergency department (ED) with a severe frontal headache. A computerized tomography (CT) venogram and CT of the head were unremarkable. She was given Toradol, Compazine, Decadron, and magnesium and discharged. Her platelet count at that time was 114, thought to be consistent with the patient's description of chronic thrombocytopenia. The patient later presented again to the ED with a severe ocular headache. She was evaluated and discharged again with morphine, Toradol, Reglan, Benadryl, dexamethasone. On day 7, the patient had an acute worsening of headache and was found unresponsive that night. She was taken back to the ED by EMS, sustained a seizure in route and was intubated on arrival. She had no gag reflex. Sodium was 170, platelet nadir was 10, D dimer was 13.47 mcg/mL, Anti-PF4 ELISA was 2.2 and COVID test was negative. A CT revealed intraparenchymal and subarachnoid hemorrhage with mild migration of the cerebellar tonsils below the level of the foramen magnum as well as a suggestion of an underlying dural venous sinus thrombosis. She was determined to have brain death. Based on evolving knowledge of Thrombosis with Thrombocytopenia Syndrome (TTS, per definition from Brighton Collaboration), the low platelet count and temporal relationship to vaccination, we consider the events to have a plausible relationship with vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 2,0
Labordaten: Test Date: 202104; Test Name: Venogram; Result Unstructured Data: normal; Test Date: 202104; Test Name: CT brain scan; Result Unstructured Data: normal; Test Date: 202104; Test Name: Laboratory test; Result Unstructured Data: not reported; Test Date: 202104; Test Name: Platelet count; Result Unstructured Data: 10 10*3/uL; Test Date: 202104; Test Name: Sodium; Result Unstructured Data: 170; Test Date: 202104; Test Name: CT brain scan; Result Unstructured Data: see results; Test Date: 202104; Test Name: Glasgow coma scale; Result Unstructured Data: 1; Test Date: 202104; Test Name: Platelet count; Result Unstructured Data: 114 10*3/uL; Test Name: Heparin-induced thrombocytopenia test; Result Unstructured Data: ELISA test result was positive (2.2); Test Name: SARS-CoV-2 PCR test; Result Unstructured Data: negative; Test Name: APTT; Result Unstructured Data: 24.1 sec; Test Name: International normalized ratio; Result Unstructured Data: 1.2; Test Name: Fibrinogen; Result Unstructured Data: 128 mg/dL, nadir; Test Name: Platelet count; Result Unstructured Data: 9 10*3/uL, nadir; Test Name: Fibrin D dimer; Result Unstructured Data: 13.47 mcg/mL peak
Aktuelle Erkrankungen: Chronic thrombocytopenia; Depression; Drug allergy; Migraine
Vorgeschichte: Comments: Patient had no adverse events following any previous vaccine. no recent abortive therapy
Andere Medikamente: ARIPIPRAZOLE; WELLBUTRIN; FIORICET; FLUOXETINE; INDERAL; RISPERDAL; TOPIRAMATE
Allergien: -
Vorherige Impfungen: -

VAERS 1440690

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MA
Alter: 85,0
Geschlecht: F
Eingang: 01.07.2021
Impfdatum: 12.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 8,0
Dosis: N/A
Route/Site: IM / RA

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

Cerebrovascular accident Condition aggravated

Symptomtext

Pt had a stroke on 5/20/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Available from Hospital
Aktuelle Erkrankungen: Chronic illnesses: IDDM, HTN, hx stroke (2018),
Vorgeschichte: Chronic illnesses: IDDM, HTN, hx stroke (2018),
Andere Medikamente: Hydralazine, Lisinopril, Atorvastatin, amlodipine, famotidine, mirtazepine, vit B, metoprolol, chorthalidone, vitamin D , azo cranberry, Triceba insulin (diabetes)
Allergien: nka
Vorherige Impfungen: -

VAERS 1430600

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 28.06.2021
Impfdatum: 12.03.2021
Beginn: 08.04.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Abdominal pain upper Acute kidney injury Acute respiratory failure Angiogram pulmonary abnormal Anticoagulant therapy Asthenia Biopsy COVID-19 Cardiac valve vegetation Chemotherapy Cholangiocarcinoma Computerised tomogram abdomen Computerised tomogram abnormal Computerised tomogram thorax abnormal Critical illness Death Deep vein thrombosis

Symptomtext

69 YO female received one dose of J&J vaccination on 3/12/21. 4/8: Patient complaint of epigastric abdominal pain almost nightly since March 12 (coincided with her COVID vaccination) described as 10/10, crampy and without radiation. CT abdominal and pelvis with contrast showed infiltrating mass in the left hepatic lobe concerning for intrahepatic cholangiocarcinoma with reactive adenopathy. Additionally, left mid ovarian vein thrombus found. No thrombus in the renal veins or IVC. 4/28: Venous duplex demonstrated bilateral leg acute DVT. Eliquis was started. 5/7: Pt underwent laparoscopic biopsy/paracentesis. Eliquis was held 2 days prior to laparoscope...5/11: Pt presented to hospital with complaints of generalized weakness, fatigue and leg pain. CTPA showed bilateral PE. Pt received heparin drip and was switched back to Eliquis on discharge. Echocardiogram on 5/12 noted mobile round mass in RV junction, right atrial mass; presumed to be a thrombus. Pt additionally with elevated troponin, determined to likely demand ischemia related to PE; EKG without any acute changes. Discharged on 5/24. 5/27: Patient started on chemotherapy with gemcitabine/cisplatin for metastatic intrahepatic cholangiocarcinoma. 6/4: Presented to the ED again due to worsening dyspnea and home pulse ox readings in the 70s. CT chest showed moderate burden of bilateral obstructive pulmonary emboli with no overt RV strain. EKOS and clot retrieval was contraindicated d/t thrombocytopenia. Was noted to have demand ischemia, and transitioned from eliquis to heparin gtt. Vascular was consulted for eval of her ischemic right foot, and deemed that it needed amputation, but would be a high risk surgery. 6/8: Patient was transferred to this reporting institution for second opinion requested by the family. Upon arrival, patient was found to be obtunded and hypotensive requiring heated high flow nasal cannula and vasopressor with norepinephrine. Code status was deemed DNRCCA/Do not intubate per family. Bedside ultrasound was concerning for an LV mass. Cardiology and Vascular surgery were consulted and recommended that the foot be amputated as well, but requested further workup with ECHO and CTA chest/abdomen/pelvis to further evaluate the LV mass. During admission workup, she was incidentally found to be COVID PCR positive. She was started on DEXA-ARDS prednisone dosing, remdesivir, and placed in enhanced droplet isolation. Her hospital course was complicated by acute hypoxemic respiratory failure due to pulmonary emboli, COVID-19 infection, and underlying malignancy requiring heated high flow nasal cannula. Empiric cefepime was started to treat any underlying superimposed pneumonia. Due to extensive clot burden with limb ischemia, as well as + COVID, she was systemically anticoagulated with a heparin drip despite her thrombocytopenia. She was intermittently given platelet transfusions in order to keep platelet count >30. TTE was obtained on 6/11 which showed large masses in right ventricle and right atrium, vegetations on mitral valve, aortic valve, and tricuspid valve, and probable mass in IVC. She also developed AKI with oliguria related to shock and critical illness. Medical oncology was consulted and she unfortunately was not a candidate for further chemotherapy at the time due to critical illness, as well as ischemic limb. (If further treatment was pursued, she would need a left leg amputation, then would require 4-6 weeks of recovery before additional chemotherapy could be given.) She slowly became more encephalopathic and had increased oxygen requirements, requiring continuous heated high flow nasal cannula. Goals of care were discussed with her family. Given her advanced cancer, it was decided to transition to comfort-focused care. Her code status was changed to DNRCC. Symptoms were controlled with IV pain and anxiety medication. She expired on 6/13/2021 at 0225.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: No PF4 collected, admission platelets 65, lowest platelets 21 Novel Coronavirus PCR- SARS-CoV-2 detected (6/9/2021)
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1427698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 1805025

kritisch

Staat: AZ
Alter: 71,0
Geschlecht: F
Eingang: 25.06.2021
Impfdatum: 03.04.2021
Beginn: 03.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Ataxia Blindness Blood test Cerebrovascular accident Computerised tomogram Headache Hypoaesthesia Hypoaesthesia oral Seizure Tension headache X-ray

Symptomtext

As soon as getting the shot got a headache right afterwards, Getting one every day. On May 6th got numbness in lips and down arm, could not write of move arm. Same thing happened later that day, went to the hospital the night and got admitted until later the next evening having had 11 seizures. Having 6 strokes and no control over right arm and left leg. Feels like wearing a helmet everyday that is to tight on head. Lost a lot of vision in eyes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Blood work, X-Rays, CT Scans
Aktuelle Erkrankungen: Heart issues, Diabetes, Asthma
Vorgeschichte: Heart issues, Diabetes, Asthma
Andere Medikamente: Metformin, Glypizide, Alogliptin-metformin, Metoprollol, Hydralizine, Omeprazole,
Allergien: -
Vorherige Impfungen: -

VAERS 1423394

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 96,0
Geschlecht: F
Eingang: 24.06.2021
Impfdatum: 01.04.2021
Beginn: 01.06.2021
Tage bis Beginn: 61,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Resident passed away on 6/1/2021 with family at bedside.

Weitere VAERSDATA-Felder

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

VAERS 1402435

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MI
Alter: 91,0
Geschlecht: M
Eingang: 16.06.2021
Impfdatum: 11.03.2021
Beginn: 29.05.2021
Tage bis Beginn: 79,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Pt died on 5/29/2021

Weitere VAERSDATA-Felder

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

VAERS 1374219

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: IN
Alter: 64,0
Geschlecht: M
Eingang: 04.06.2021
Impfdatum: 12.03.2021
Beginn: 20.04.2021
Tage bis Beginn: 39,0
Dosis: UNK
Route/Site: SYR / LA

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

Arteriogram carotid Balance disorder Blindness unilateral Cerebrovascular accident Chest X-ray Computerised tomogram head Hemiparesis Impaired driving ability Laboratory test Magnetic resonance imaging head abnormal Mobility decreased Quality of life decreased Spinal X-ray Walking aid user

Symptomtext

April 20, 2021. PT needed to use the restroom. We stopped, he walked to the restroom, I went to the gift shop. Upon returning, I saw PT sitting on a bench. He was leaning to his left, could not see out of his left eye, very unstable when sitting. We missed lunch, so we thought it was his sugar dropping. I started to feed him jam and a chocolate bar. After 2 hours, his vision returned & he seemed better. He drove us back to the rental cabin. He rested the next 2 days. Then on Friday, we packed up our vehicle and Pt drove us back home. After arriving home, Pt's condition got worse. We went to the Dr, explained the events of the previous week & she came to the same conclusion, Diabetes spell. His condition continued to worsen, we went back to Dr several times, the ER 2 times and finally we got into see a Neurologist. That appointment, the doctor said he thought stroke. Dr scheduled a MRI for June 1, 2021. Results of that MRI was a definite stroke. Now he has started outpatient rehab with no promise he will ever regain full mobility. He can no longer drive, mow grass, walk without a cane and help, etc. Life has changed dramatically for both of us.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: CT head scan, Ct scan of Carotid arteries, Xray of back and chest, MRI Many Lab tests
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes
Andere Medikamente: Metforma 1000 mg twice daily Jardiance 10mg 1 day
Allergien: None
Vorherige Impfungen: -

VAERS 1365268

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MI
Alter: 45,0
Geschlecht: M
Eingang: 01.06.2021
Impfdatum: 13.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 8,0
Dosis: UNK
Route/Site: IM / LA

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

Angiogram pulmonary abnormal Deep vein thrombosis Dyspnoea Laboratory test Pain in extremity Peripheral swelling Pulmonary embolism Ultrasound Doppler abnormal

Symptomtext

Complained of right lower leg pain and swelling, shortness of breath, sent to hospital for Ultrasound of right lower leg, Ultra sound was positive for a DVT. Was then sent to the Emergency room for evaluation and treat for DVT. Complained of Shortness of breath. CT Scan Angiogram completed and found to have bilateral Pulmonary Embolism

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: Ultrasound, CT Scan Angiogram, labs
Aktuelle Erkrankungen: Gastritis
Vorgeschichte: Chronic Kidney Disease
Andere Medikamente: Omeprazole 20 mg
Allergien: No Allergies
Vorherige Impfungen: -

VAERS 1343784

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: AL
Alter: 84,0
Geschlecht: F
Eingang: 24.05.2021
Impfdatum: 18.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain Cerebrovascular accident Cognitive disorder Computerised tomogram head abnormal Gastric haemorrhage Gastrooesophageal reflux disease Hemiplegia Imaging procedure Laboratory test Magnetic resonance imaging head abnormal Palpitations

Symptomtext

Severe reflux within two days of vaccine; Severe abdominal pain and probable gastric bleed within 6 days of vaccine; Daily heart palpitations within two weeks of vaccine; Two acute strokes within a month of vaccine and a third stroke event after the first two acute strokes causing paralysis on right side and noticeable cognitive dysfunction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 36,0
Labordaten: Two ER visits - One visit for the gastric bleed and one for the initial two acute strokes which included CT's and later MRI's and countless other tests and scans. Still hospitalized complications of the strokes.
Aktuelle Erkrankungen: None
Vorgeschichte: Mild Pulmonary Fibrosis; Intermittent Cardiac Arrhythmias; Thyroid Removal; Osteoarthritis; Two Compound Fractures in Back
Andere Medikamente: Omeprazole; Eliquis; Lunesta; Synthroid
Allergien: Glycopyrrolate; Sulfa; Penicillin
Vorherige Impfungen: -

VAERS 1337924

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: IL
Alter: 32,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 18.03.2021
Beginn: 14.05.2021
Tage bis Beginn: 57,0
Dosis: UNK
Route/Site: IM / -

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

Anticoagulant therapy Computerised tomogram thorax abnormal Deep vein thrombosis Echocardiogram abnormal Ejection fraction normal Pain in extremity Peripheral swelling Pulmonary embolism Right ventricular dysfunction Ultrasound Doppler abnormal

Symptomtext

Patient transferred from outlying hospital for higher level of care. Patient had previously presented to ED with complaint of localized pain in the right calf for 4-5 days. Patient also noticed swelling in R calf. CT chest showed acute pulmonary embolism within distal right pulmonary artery extending into the segmental arteries to both right upper and right lower lobes. Patient was treated with heparin drip. Echo showed EF 68% and hypokinetic free right ventricular wall and apex. Echo also showed reduced right ventricular function. Patient underwent bilateral lower extremity duplex ultrasound which showed acute right femoral, popliteal, posterior tibial and peroneal vein thrombosis. Patient was transitioned and discharged to home. Patient received J&J COVID-19 vaccine in March 2021. Patient denies cigarette smoking/vaping, illicit drug use, ETOH use. Denies recent travels or long distance travels. Denies use of oral contraceptives.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: anxiety, depression
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1337780

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 72,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 08.03.2021
Beginn: 07.05.2021
Tage bis Beginn: 60,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Death Hypoxia Respiratory failure SARS-CoV-2 test positive Thrombocytopenia

Symptomtext

Person died on 5/7/2021 with death note stating acute respiratory failure with hypoxia, thrombocytopenia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 31,0
Labordaten: Received COVID-19 Janssen vaccine on 3/8/2021; tested positive for COVID-19 on 3/26/2021 by rapid antigen and PCR; was seen in ER on 3/29/2021 but not admitted to hospital; then admitted to hospital on 4/6/2021 with increased/worsening symptoms; died on 5/7/2021.
Aktuelle Erkrankungen: unknown
Vorgeschichte: type 2 diabetes; hypertension; GERD
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1319781

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MD
Alter: 70,0
Geschlecht: M
Eingang: 15.05.2021
Impfdatum: -
Beginn: 02.04.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Atrial fibrillation Cardiac arrest Cardiac stress test Catheterisation cardiac Computerised tomogram

Symptomtext

CARDIAC ARREST DURING ANESTHESIA FOR A SCHEDULED HEART SURGERY; ATRIAL FIBRILLATION; This spontaneous report received from a patient concerned a 70 year old White and Hispanic or Latino male. The patient's height, and weight were not reported. The patient's past medical history included general anesthesia. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, expiry: not reported) dose 1 total, administered on 06-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 2021, the patient experienced atrial fibrillation. On 02-APR-2021,the patient went to the hospital for ablation of atrial fibrillation and experienced cardiac arrest during anesthesia for a scheduled heart surgery. Patient heart was stopped suddenly but cardiologist were able to revive patient .Patient had tested for Catheterization of heart ,CAT scan and stress test for heart prior 2-3 weeks before heart surgery. All the test were normal .On 02-APR-2021,After an event ,Patient was hospitalized for 5 days. The surgery for heart was pending. On MAR-2021, Laboratory data included: CAT scan (NR: not provided) normal, Cardiac catheterization (NR: not provided) normal, and Stress test (NR: not provided) normal. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from cardiac arrest during anesthesia for a scheduled heart surgery on APR-2021, and the outcome of atrial fibrillation was not reported. This report was serious (Hospitalization Caused / Prolonged).; Sender's Comments: V0. 20210512607-COVID-19 VACCINE AD26.COV2.S-Cardiac arrest, Atrial fibrillation. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 5,0
Labordaten: Test Date: 202103; Test Name: Cardiac catheterisation; Result Unstructured Data: normal; Test Date: 202103; Test Name: Stress test; Result Unstructured Data: normal; Test Date: 202103; Test Name: CAT scan; Result Unstructured Data: normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: General anesthesia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1282510

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MD
Alter: 71,0
Geschlecht: F
Eingang: 03.05.2021
Impfdatum: 08.03.2021
Beginn: 28.03.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / LA

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

Cerebrovascular accident Computerised tomogram head abnormal Confusional state Dizziness Electrocardiogram Facial paralysis Headache Hypoaesthesia Laboratory test Magnetic resonance imaging head abnormal Nausea X-ray

Symptomtext

pt says she had a few episodes of feeling dizzy before having a stroke. Pts right hand became numb, she had some confusion, she was nauseated and had a severe headache several days prior to going to the emergency room. On 3/28/21 her face was dropping on the right side so was brought ER. She was admitted and given CT and multiple test. She was treated for a Stroke and stayed for about 3 days. She was discharged to FU w/ Neurologist next week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: CT MRI Lab work X-ray EKG
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: levothyroxine, amlodipine,
Allergien: nka
Vorherige Impfungen: -

VAERS 1280064

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: FL
Alter: 80,0
Geschlecht: F
Eingang: 02.05.2021
Impfdatum: 01.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: SYR / UN

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

Coronary angioplasty Death Dyspepsia Intracardiac thrombus

Symptomtext

4/13/2021 heartburn like symptoms started. 4/20/2021 admitted to emergency room, received diagnosis of 3 blood clots in the heart, 4/27/2021 died as a result of blood clots in heart

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: 4/21/2021 angioplasty confirms number, size and location of blood clots
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1230008

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: AL
Alter: 73,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 11.03.2021
Beginn: 16.04.2021
Tage bis Beginn: 36,0
Dosis: 1
Route/Site: IM / RA

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

Angiogram pulmonary normal Cardio-respiratory arrest Chest pain Death Fibrin D dimer increased Resuscitation

Symptomtext

PATIENT DIED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism
Andere Medikamente: Hydrochlorothiazide 12.5mg, Levothyroxine 125mcg, Losartan 100mg
Allergien: None listed at pharmacy
Vorherige Impfungen: -

VAERS 1230008

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: AL
Alter: 73,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 11.03.2021
Beginn: 16.04.2021
Tage bis Beginn: 36,0
Dosis: UNK
Route/Site: IM / RA

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

Angiogram pulmonary normal Cardio-respiratory arrest Chest pain Death Fibrin D dimer increased Resuscitation

Symptomtext

PATIENT DIED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism
Andere Medikamente: Hydrochlorothiazide 12.5mg, Levothyroxine 125mcg, Losartan 100mg
Allergien: None listed at pharmacy
Vorherige Impfungen: -

VAERS 1251202

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: AL
Alter: 48,0
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: 19.03.2021
Beginn: 27.03.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / RA

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

Computerised tomogram thorax abnormal Deep vein thrombosis Erythema Hysterectomy Pain in extremity Peripheral swelling Pulmonary embolism Thrombosis Ultrasound scan abnormal

Symptomtext

Events: Vaccine was given on 3/19/21; Hysterectomy on 3/25/21; blood clots diagnosed on 3/30/21 Left forearm was swollen, with a light reddish tint to it, and tender. After getting an ultra sound on my forearm a DVT was found and I was sent to the emergency room. I then had a CT scan done of my chest and it was discovered I had several pulmonary emboli. I was admitted to the hospital and put on a heparin drip. I am currently taking Eliquis and will be following up with a pulmonologist and a hematologist in a week or two.

Weitere VAERSDATA-Felder

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

VAERS 1201178

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: -
Alter: -
Geschlecht: U
Eingang: 23.04.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / AR

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

Angiogram Computerised tomogram Dyspnoea Fibrin D dimer Pain in extremity Pulmonary embolism Ultrasound scan X-ray Thrombosis

Symptomtext

BLOOD CLOTS; This spontaneous report received from a company representative via social media post and concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose, start therapy date were not reported, one total dose is administered for prophylactic vaccination. The batch number was not reported. Per procedure, no follow up will be requested. No concomitant medications were reported. On an unspecified date, the subject experienced blood clots. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of blood clots was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: This patient reported via social media to have blood clots and to have received the COVID-19 vaccine ad26.cov2.s. No other information provided. There is insufficient information to make a meaningful assessment. Additional information will be requested.

Weitere VAERSDATA-Felder

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

VAERS 1238463

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MN
Alter: 58,0
Geschlecht: M
Eingang: 21.04.2021
Impfdatum: 12.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy Chest pain Computerised tomogram thorax abnormal Dizziness Dyspnoea Fatigue Laboratory test Pulmonary embolism

Symptomtext

3/26 office appointment: New onset right and left sided chest pain with associated shortness of breath, fatigue and intermittent lightheadedness. Labs drawn. CT scan showed Scattered small occlusive and nonocclusive emboli within small distal pulmonary artery branches bilaterally. Started on apixaban. Has appointment with Hematology on 4/29

Weitere VAERSDATA-Felder

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

VAERS 1233202

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 54,0
Geschlecht: F
Eingang: 20.04.2021
Impfdatum: 10.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: IM / LA

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

Cerebrovascular accident Computerised tomogram Fall Hypoaesthesia Magnetic resonance imaging Thrombosis Ultrasound Doppler Ultrasound scan

Symptomtext

Patient states that while vacationing, 3 weeks and 1 day after receiving her Janssen vaccine, she woke up at 8:30am with numbness in her left foot. When attempting to stand she fell to floor. After checking her blood pressure and blood sugar she took 2 tylenol and sat down to rest. Around 10:30am she began to have numbness in her left hand and on the left side of her face. She was taken by ambulance at that time to Hospital. While there they ran a number of tests and scans diagnosing her with have a stroke caused by a small blood clot in right side of her brain. She was admitted to the hospital and was not discharged until 4/3/2021. Upon returning home, she has been seeing her PCP, APRN and a neurologist. She has since been released on 4/19/2021 to go back to work and has no residual side effects from stroke. She states she is now on blood pressure and cholesterol medication and is taking a daily baby Aspirin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: Patient states that Hospital performed 2 CT scans, MRI, Echo, and Carotid doppler. She states "they saw a small blood clot on the right side of my brain."
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1233011

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: IL
Alter: 79,0
Geschlecht: M
Eingang: 20.04.2021
Impfdatum: 06.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / -

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

Asthenia Cardiac arrest Fall Hip fracture Open reduction of fracture

Symptomtext

Janssen vaccine received 3/6/2021. Had a fall from sudden onset weakness 3/9/21 broke hip then ORIF and cardiac arrest. Now at skilled nursing facility

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 10,0
Labordaten: many
Aktuelle Erkrankungen: Parkinsons, Amyloidosis, Atrial Fibrillation
Vorgeschichte: see above
Andere Medikamente: Coumadin
Allergien: Penicillin, Sulfa, Myecitin's
Vorherige Impfungen: -

VAERS 1225587

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: MA
Alter: 40,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 19.03.2021
Beginn: 17.04.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: IM / -

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

Activated partial thromboplastin time Brain natriuretic peptide Chest X-ray Computerised tomogram abdomen Computerised tomogram thorax Angiogram pulmonary abnormal Back pain Computerised tomogram thorax abnormal Dyspnoea Infarction Electrocardiogram Full blood count International normalised ratio Metabolic function test Prothrombin time Infection Lung consolidation Platelet count normal

Symptomtext

Patient presented to the ED on 4/18/2021 with one day of shortness of breath and mid-thoracic, pleuritic back pain, found to have bilateral pulmonary emboli. He was started on apixaban 10mg BID for this at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: CT pulmonary angiogram 4/18/2021 " 1. Pulmonary emboli within segmental branches of the right lower and left lower lobes. 2. Consolidation within the right lung base distal to the embolus, which represent infarct versus infection. 3. No acute abnormality within the abdomen or pelvis. " Platelet count 230 on 4/18/2021 Workup related to this event is ongoing.
Aktuelle Erkrankungen: Presentation to the ED on 3/29/2021 for right knee pain
Vorgeschichte: None per report
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1216452

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 10.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: SYR / LA

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

Pulmonary embolism Respiration abnormal Ventilation/perfusion scan

Symptomtext

within 10 days I had severe breathing problems that lasted about 4 days, had test that revealed blood clots in my lungs about a week after

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: VQ scan that revealed several blood clots in my lungs on 3/24/2021
Aktuelle Erkrankungen: -
Vorgeschichte: afib
Andere Medikamente: albutarol amLODIPine atorvaSTATIN'BUMETAMIDE vit d dorzolamide iron levothyroxine metoprolol omeprazole potassium metamucil warfrin
Allergien: mprphone loratab
Vorherige Impfungen: -

VAERS 1215369

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 56,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 15.03.2021
Beginn: 07.04.2021
Tage bis Beginn: 23,0
Dosis: UNK
Route/Site: IM / RA

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

Activated partial thromboplastin time Angiogram Brain natriuretic peptide Deep vein thrombosis Full blood count International normalised ratio Metabolic function test Prothrombin time Pulmonary embolism Ultrasound Doppler

Symptomtext

DVT right lower extremity and pulmonary embolism: was hospitalized for 2days with a Heparin Drip and discharged home with Eliquis 10mg twice a day. Home meds discontinued: all BP meds, Ibuprofen, Tylenol, and Torodol. Follow up appointments with Dr. oncologist. Also had to cancel upcoming ventral hernia repair after having to wait 3 years due to complications with bowel obstructions and had to lose weight before surgery due to high risk. Now will have to wait longer until cleared medically, primary physician instructed me that it would be 6months or more before being cleared.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: CT angio, Lower extremity doppler, ultrasound, PTT, PT/INR, CBC, BMP, BNP
Aktuelle Erkrankungen: Polycythemia vera, bladder cancer, hypertension, GERD
Vorgeschichte: Polycythemia vera, bladder cancer, hypertension, GERD
Andere Medikamente: Losartan/HCTZ, Norvasc, Metoprolol, Magnesium, Vitamin D, Vitamin B12, Potassium, Protonix, Carafate, Macrobid, Zofran, aspirin, zyrtec
Allergien: Levaquin, Lisinopril, Sulfa, Lortab, Loracet
Vorherige Impfungen: -

VAERS 1208968

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: KY
Alter: 61,0
Geschlecht: F
Eingang: 14.04.2021
Impfdatum: 19.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / LA

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

Cerebrovascular accident Confusional state Dementia Disorientation Electrolyte imbalance Neurological symptom Urinary tract infection

Symptomtext

Traveled and reported to family that she was disoriented and having some confusion. Was evaluated at ED, had some electrolyte imbalance and UTI. Once resolved, she continued to have neurological symptoms and was diagnosed with a stroke, including early onset dementia per telephone interview with daughter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 6,0
Labordaten: See #18
Aktuelle Erkrankungen: None
Vorgeschichte: COPD
Andere Medikamente: Daily meds - Venlafaxine 150 mg, Oxybutynin 5 mg, Ropinirole, Valsartan/HZT 325/10
Allergien: NKA, NKDA
Vorherige Impfungen: -

VAERS 1208502

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: FL
Alter: 63,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 22.03.2021
Beginn: 05.04.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Patient deceased 04/06/2021. Reported by family member.

Weitere VAERSDATA-Felder

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

VAERS 1202622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 1805025

kritisch

Staat: CO
Alter: 62,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 05.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: SYR / LA

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

Blister Blood test Computerised tomogram Pain Pain in extremity Pulmonary embolism Rash X-ray

Symptomtext

Severe pain in right side radiating up to shoulder. Diagnosed as a Pulmonary Embolism. On April 7, 10 days after second Pfizer Covid vaccination shot, (administered on March 26), patient developed severe pain in her left leg. Numerous tests for blood clots proved negative and on April 10 she developed a rash and blisters which is believed to be Shingles.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Blood work, Cat scan, X-Ray
Aktuelle Erkrankungen: -
Vorgeschichte: Multiple Myeloma
Andere Medikamente: Revlimid, Trintellix, Simvastatin, CoQ10, Vitamin D, MultiVitamin, Biotin
Allergien: -
Vorherige Impfungen: -

VAERS 1202570

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: TX
Alter: 60,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 04.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

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

Cerebrovascular accident Condition aggravated Platelet count decreased Transfusion

Symptomtext

Good morning, I have the patient in the hospital. We have had to give her 2 transfusion in the last 2 weeks and 2 days. The patient also had a more pronounced stroke system. We read today that people with the systems of low platelets and stoke system need to report. I have called everyone and have had no help. I believe it has to be the health department.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: stroke
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1202401

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: CO
Alter: 49,0
Geschlecht: M
Eingang: 13.04.2021
Impfdatum: 12.03.2021
Beginn: 08.04.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: - / -

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

Alanine aminotransferase increased Angiogram cerebral abnormal Arteriogram carotid abnormal Aspartate aminotransferase increased Blood albumin decreased Blood alkaline phosphatase increased Blood bilirubin normal Blood glucose normal Blood urea increased COVID-19 pneumonia Cardiac ventricular thrombosis Catheterisation cardiac abnormal Cerebral infarction Cerebrovascular accident Chest X-ray abnormal Confusional state Coronary artery disease Coronary artery occlusion

Symptomtext

Janssen COVID-19 Vaccine EUA: patient presents to emergency department with altered mental status and confusion three days after being discharged from a different hospital for COVID-19 infection. In emergency department diagnosed with stroke, left ventricular thrombus, subacute anterior myocardial inferction with totally occluded mid LAD, and COVID-19 infection. Underwent cardiac catheterization and transferred to current facility for higher level of care and testing- currently remains hospitalized on anticoagulation and oxygen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 6,0
Labordaten: In emergency department: Cardiac catheterization: complete occlusion of mid lAD with faint collaterals, subacute versus chronic; mild coronary artery disease Brain MRI: patchy acute infarcts in bilateral anterior ciculation suspicious for embolic infarcts over six horus in age; MS plaques similar to previous exams; no intracranial mass or lesion TTE: left ventricular thrombus Head/neck CTA: multiple small infarcts of both cerebral hemispheres, continued maturation of multifocal infarction predominanatly involving the left frontal operculum Chest x-ray: COVID-19 pneumonia Cardiac MRI: acute myocardial infarction, left ventricle mild dilation, biventricular thrombi Extremity ultrasound (when admitted): no evidence of DVT bilaterally Electrolytes: glucose 109 mg/dL, BUN 22 mg/dL, rest within normal limits CBC: WBC 12.5 19*9/L, rest within normal limits Troponin: 6.80 ng/mL Alkaline phosphatase: 146 U/L, AST 80 U/L, ALT 147 U/L, direct bili 0.3 mg/dL, albumin 2.8 g/dL, total protein 5.5 g/dL EKG sinus rhythm, left anterior fasicular block, probable recent anteroseptal infarct
Aktuelle Erkrankungen: none reported
Vorgeschichte: multiple sclerosis, neurogenic bladder, chronic fatigue
Andere Medikamente: amlodipine, dextroamphetamine-amphetamine, ocrelizumab, valacyclovir
Allergien: none reported
Vorherige Impfungen: -

VAERS 1201229

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 1805025

kritisch

Staat: AL
Alter: 71,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 12.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / UN

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

Computerised tomogram thorax Dyspnoea Dyspnoea exertional Pleuritic pain Pulmonary embolism Thrombectomy

Symptomtext

SOB, DOE, pleuritic chest pain x2 weeks progressively worsened, the patient presented to hopsital and was later transferred to secondary hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: CTA chest revealed saddle pulmonary embolus, IR was consulted and pulmonary thrombectomy was performed (starting Pa pressures 66/27 with ending Pa pressures 45/20)
Aktuelle Erkrankungen: Hypercholesterolemia Vertigo
Vorgeschichte: -
Andere Medikamente: Meclizine
Allergien: PCN, Codeine, shellfish, sulfa drugs
Vorherige Impfungen: -

VAERS 1168291

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: IL
Alter: 71,0
Geschlecht: M
Eingang: 05.04.2021
Impfdatum: 30.03.2021
Beginn: 05.04.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: - / -

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

Agonal rhythm Blood glucose normal Breath sounds abnormal Cardiac arrest Chest pain Chronic obstructive pulmonary disease Condition aggravated Death Dyspnoea Endotracheal intubation Mobility decreased Oxygen saturation decreased Physical deconditioning Pulse absent Pupil fixed Resuscitation

Symptomtext

3/22/21 Admission HPI: 71 y.o. male with a history of poorly controlled diabetes mellitus and COPD. He presented to my office today acutely with a several day history of increasing shortness of breath. He has increased his prednisone at home recently and been increasing the frequency of his DuoNebs. Despite this, he states that his oxygen saturations have been staying in the low 80s. He has a hard time walking due to the shortness of breath. He states previous to about a week ago he was doing very well. He denies any fever. He denies any known exposure to coronavirus (COVID-19). In the office today his oxygen saturations were 88% on 4 L. Because of his failure of outpatient therapy, he will be admitted to the hospital for further evaluation and treatment. This patient has a history of severe respiratory decompensation that happens very quickly. Therefore, it is medically urgent we get him into the hospital. 3/25/21 Admission HPI71 y.o. male with a known history of severe COPD and type 2 diabetes mellitus. He came to my office with a several day history of increasing shortness of breath. He had increased his oral steroids and breathing treatments at home and despite this was still having oxygen saturations in the low to mid 80s on 2-4 L of supplemental oxygen. In my office he was extremely diminished and had basically failed outpatient therapy. Therefore he was admitted to inpatient status for acute treatment of a severe COPD exacerbation requiring IV antibiotics and IV steroids. He was admitted and treated with IV treatments. He did recover nicely. However, he was found to be extremely physically deconditioned. Because of this he was thought to be an excellent candidate for swing bed and is being transitioned to swing bed. 4/5/21 ER Practitioner Note: Upon arrival to ED trauma room I found patient to be in cardiac arrest, CPR in progress. History is that EMS was called to the scene for a patient with chest pain. Shortly after arrival at his home patient developed a cardiac arrest. They followed standard ACLS protocol and the patient was intubated. Blood sugar normal. As CPR was given, medications were administered consisting of epinephrine and 1 mg in 2 different doses along with 1 amp of bicarb. IV access via an IO. Patient was then transported to the emergency department. Upon arrival, CPR was continued and oxygen supplied via endotracheal tube with good tube placement verified by auscultation and good sat readings. Monitor was placed and patient demonstrated initially a sinus rhythm but there was no pulse. Therefore, diagnosis was PEA and no reversible causes were identified. ACLS protocol was followed with epinephrine 1 mg IV every 5 min. He received a total that including EMS, 5 mg of epinephrine and 1 amp of bicarb. Monitor at this point revealed the rhythm changed to an agonal rhythm. When CPR was given, there was good results from the CPR. However, CPR discontinued and there is no pulse and patient had an agonal rhythm for several minutes, pupils were fixed but not dilated year. Lungs demonstrating clear bilateral breath sounds when he was bagged via the endotracheal tube. No external signs of any trauma noted. The patient's sister is here and she is a registered nurse. We had discussed management at this point with her and all were in agreement that the code be terminated. At 1015, patient was pronounced deceased.. ACLS protocol was followed. See nursing record for medication and vital sign details. Code outcome: Deceased CC time 20 minutes.

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Medications Prior to Admission Medication Sig Dispense Refill Last Dose ? allopurinol (ZYLOPRIM) 300 MG tablet 2 times daily Unknown at Unknown time ? amLODIPine (NORVASC) 10 MG tablet Take 1 tablet by mouth once daily 30 tablet 0 Unk
Allergien: Allergies Allergen Reactions ? Codeine ? Hydrochlorothiazide ? Maxzide [Hydrochlorothiazide W/Triamterene] Renal failure ? Nitroglycerin Blood pressure drops
Vorherige Impfungen: -

VAERS 1168142

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: IL
Alter: 72,0
Geschlecht: F
Eingang: 05.04.2021
Impfdatum: 08.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: - / -

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

Asthenia Death Dyspnoea Haemoptysis Malaise Nausea Vomiting Weight decreased

Symptomtext

ER 3/17 HPI: 72 y.o. female who presents with generalized weakness and not feeling well. Patient states that she had her 1st dose of COVID-19 vaccine about a week ago and since then has not felt well. She denies fever or chills, she denies any arthralgias or myalgias, she has had some nausea and vomiting but none in the last couple of days. There has been no diarrhea. There have been no urinary symptoms. 3/22/21 Inpt Admission hpi 72 y.o. female who presents with shortness of breath and hemoptysis. Patient has known history of COPD and also has a history of squamous cell carcinoma of the lung that is in remission. Patient reports she has noticed increasing shortness of breath for the past several weeks. She states the got worse around the noon time today. Patient reports she began having some hemoptysis today. Patient denies any chest pain or palpitations. Patient denies any fevers or chills. Patient denies any sinus congestion or nasal drainage. Patient denies any headaches, myalgias, or loss of sense of taste and smell. Patient does report a 4 day history of intermittent diarrhea. She denies any nausea or vomiting. Patient has had COVID-19 vaccination. Of note, patient's family reports she has lost 10 lb in the past 30 days. 3/30/21 Deceased

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Current Outpatient Medications: ? albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulizer solution, Take 1 vial (2.5 mg) by nebulization every 4 hours as needed for Wheezing, Disp: 360 mL, Rfl: 11 ? aspirin 325 MG tablet, Take 325 mg by mout
Allergien: sulfa abx
Vorherige Impfungen: -

VAERS 1112120

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

kritisch

Staat: IL
Alter: 76,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 09.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / -

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

Alanine aminotransferase increased Albumin globulin ratio Aspartate aminotransferase increased Asthenia Blood albumin decreased Blood alkaline phosphatase Blood bilirubin increased Blood calcium decreased Blood chloride decreased Blood creatine phosphokinase increased Blood creatinine increased Blood lactic acid Blood potassium decreased Blood sodium Blood urea increased Computerised tomogram thorax abnormal Cough Dizziness

Symptomtext

3/18/21 ER Triage Nurse Note: "To er via EMS for eval of weakness and dizziness. States he started with sore throat and head congestion last week. Seen PCP Monday 03-15-21. Started amoxil. Took it for 2 days and became dizzy so he quit taking it. Dizziness got worse and came to ER." 3/18/21 ER HPI: 76 y.o. male who presents with c/o weakness cough and fever for the past seven days. Pt report sx are mod better with rest and worse with movement. Transferred to Hospital, dx: pneumonia dt covid-19 virus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: Final Result EXAMINATION: CTA of the chest CLINICAL HISTORY: 76 years Male,elevated ddimer COMPARISON: There is no prior similar study available for correlation. TECHNIQUE: Axial imaging along with 2-D and 3-D postprocessing performed from the level of the thoracic inlet to the kidneys following the administration of IV contrast and utilizing CTA protocol. This exam was performed according to our departmental dose-optimization program, which includes automated exposure control, adjustment of the mA and/or kV according to patient size and/or use of iterative reconstruction technique. IV CONTRAST: 100 mL TOTAL DLP: 953 mGy-cm FINDINGS: There are filling defects in the bilateral segmental and subsegmental pulmonary arteries. There is a small right pleural effusion. The heart is enlarged. There is no pericardial effusion. The thoracic aorta is within normal limits. Severe peripheral groundglass opacities identified predominantly in the lower lungs. There are several small stones in the gallbladder. Multiple cysts identified in the visualized right kidney. IMPRESSION: Multiple bilateral segmental and subsegmental PE Large bilateral groundglass opacities worrisome for severe Covid pneumonia. Correlate with clinical findings. Multiple small gallstones. Multiple right renal cysts EKG nsr no acute changes no st changes normal axis CBC W AUTO DIFF Collection Time: 03/18/21 9:57 AM Result Value Ref Range White Blood Cell Count 5.4 4.8 - 9.6 THOUS/uL Red Blood Cell Count 4.86 4.33 - 5.59 MIL/uL Hemoglobin 12.6 (L) 13.1 - 16.8 GM/DL Hematocrit 36.9 (L) 38.8 - 49.0 % Mean Corpuscular Volume 75.9 (L) 82.7 - 94.4 FL Mean Corpuscular Hemoglobin 25.9 (L) 27.7 - 32.6 PG Mean Corpuscular Hemoglobin Conc 34.1 32.4 - 35.7 G/DL Rdwcv 15.9 (H) 11.6 - 13.9 % Rdwsd 43.6 36.0 - 46.1 FL Platelet Count 157 154 - 364 THOUS/uL Mean Platelet Volume 9.8 8.7 - 11.7 FL Nucleated Red Blood Cells 0.0 0.0 /100 WBC'S Abs NRBC 0.0 0.0 THOUS/uL Seg 86.0 (H) 46.9 - 70.0 % Lymphs 9.0 (L) 19.1 - 41.2 % Monocytes 5.0 (L) 6.1 - 12.3 % Neutrophils Absolute Count 4.6 1.7 - 8.7 THOUS/uL Lymphocytes Absolute Count 0.5 (L) 0.8 - 5.6 THOUS/uL Monocytes Absolute Count 0.3 0.1 - 1.0 THOUS/uL RBC Morphology NORMAL NORMAL Differential Type AUTO Platelet Estimate ADEQUATE ADEQUATE COMPREHENSIVE METABOLIC PANEL Collection Time: 03/18/21 9:57 AM Result Value Ref Range Glucose 102 (H) 65 - 100 MG/DL Blood Urea Nitrogen 27 (H) 7 - 18 MG/DL Creatinine 1.4 (H) 0.7 - 1.3 MG/DL Sodium 128 (L) 136 - 145 MMOL/L Potassium 3.0 (L) 3.5 - 5.1 MMOL/L Chloride 90 (L) 98 - 107 MMOL/L Co2 25 21 - 32 MMOL/L Calcium 8.6 8.5 - 10.1 MG/DL Protein Total 7.2 6.4 - 8.2 G/DL Albumin 3.2 (L) 3.4 - 5.0 G/DL A/G Ratio 0.8 0.8 - 2.0 Alkaline Phosphatase 86 46 - 116 U/L Alt (SGPT) 50 16 - 63 U/L AST(SGOT) 79 (H) 15 - 37 U/L Bilirubin, Total 1.1 (H) 0.2 - 1.0 MG/DL GFR Comment IF PATIENT IS AFRICAN AMERICAN, MULTIPLY RESULT BY 1.16 Est GFR 48 (L) >90 ML/MIN/1.73sq.m LACTIC ACID, SERUM Collection Time: 03/18/21 9:57 AM Result Value Ref Range Lactate 1.5 0.4 - 2.0 MMOL/L TROPONIN Collection Time: 03/18/21 9:57 AM Result Value Ref Range Troponin I 0.11 (H) 0.00 - 0.06 ng/mL D-DIMER,QUANTITATIVE Collection Time: 03/18/21 9:57 AM Result Value Ref Range D-Dimer 1,550 (HH) 0 - 400 NG/ML FEU CK (CPK) CREATINE PHOSPHOKINASE Collection Time: 03/18/21 9:57 AM Result Value Ref Range Creatine Kinase Total 694 (HH) 39 - 308 U/L SEDIMENTATION RATE (SED RATE) Collection Time: 03/18/21 9:57 AM Result Value Ref Range Sedimentation Rate, Erythrocyte 31 (H) 0 - 15 MM/HR INFLUENZA A AND B ANTIGEN Collection Time: 03/18/21 9:58 AM Specimen: NARES Result Value Ref Range Influenza A NEGATIVE NEGATIVE Influenza B NEGATIVE NEGATIVE FHC COVID ANTIGEN Collection Time: 03/18/21 9:59 AM Result Value Ref Range FHC COV AG PRESUMPTIVE POSITIVE REPORTED TO URINALYSIS WITH REFLEX TO CULTURE, IF INDICATED Collection Time: 03/18/21 11:08 AM Specimen: URINE,CLEAN CATCH (CCMS) Result Value Ref Range Glucose UA NEGATIVE NEGATIVE MG/DL Protein UA 2+ (A) NEGATIVE MG/DL Bilirubin UA NEGATIVE NEGATIVE Urobilinogen UA 0.2 0.2 - 1.0 MG/DL pH UA 5.5 5.0 - 8.0 Blood UA 2+ (A) NEGATIVE Ketones UA 2+ (A) NEGATIVE MG/DL Nitrite UA NEGATIVE NEGATIVE Leukocyte Esterase UA NEGATIVE NEGATIVE UR Appearance CLEAR CLEAR Specific Gravity UA 1.025 1.000 - 1.030 Color YELLOW YELLOW Site CCMS Comment, Urine Culture NOT INDICATED RBC Urine 0 to 5 <3 /HPF WBC Urine 0 to 5 <5 /HPF Bacteria RARE (A) NONE /HPF Mucus RARE /LPF
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Current Outpatient Medications: ? amoxicillin (AMOXIL) 875 MG tablet, Take 1 tablet (875 mg) by mouth 2 times daily for 7 days, Disp: 14 tablet, Rfl: 0 ? atenolol (TENORMIN) 25 MG tablet, Take 1 tablet (25 mg) by mouth daily, Disp: 30 ta
Allergien: Allergen Reactions ? Darvocet-N 100 [Kdc:Acetaminophen+Sorbitan+Propoxyphene
Vorherige Impfungen: -

VAERS 2686130

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: OH
Alter: 79,0
Geschlecht: M
Eingang: 26.09.2023
Impfdatum: 11.03.1921
Beginn: 09.05.2021
Tage bis Beginn: 36.584,0
Dosis: 1
Route/Site: - / -

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

Asthenia Disability Gait inability Pain Peripheral swelling Gait disturbance Muscular weakness Pain in extremity Walking aid user Syncope

Symptomtext

2 MONTHS AFTER THE INJECTION STARTED TO HAVE PAIN AND WEAKNESS TO MY RIGHT LEG. SINCE THEN I HAVE HAD A LOT OF PAIN IN THE RIGHT LEG AND CANNOT WALK. HAVE TO USE A WALKER ALL THE TIME TO GET AROUND - SOMETIMES A CANE TOO

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: BUSPIRONE, LISINOPRIL JANUVIA, ASPIRIN STOOL SOFTNER
Allergien: METFORMIN - HIVES/SKIN RASH PENICILLIN - CAUSES DEATH
Vorherige Impfungen: -

VAERS 2686130

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: OH
Alter: 79,0
Geschlecht: M
Eingang: 26.09.2023
Impfdatum: 11.03.1921
Beginn: 09.05.2021
Tage bis Beginn: 36.584,0
Dosis: UNK
Route/Site: - / -

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

Asthenia Disability Gait inability Pain Peripheral swelling Gait disturbance Muscular weakness Pain in extremity Walking aid user Syncope

Symptomtext

2 MONTHS AFTER THE INJECTION STARTED TO HAVE PAIN AND WEAKNESS TO MY RIGHT LEG. SINCE THEN I HAVE HAD A LOT OF PAIN IN THE RIGHT LEG AND CANNOT WALK. HAVE TO USE A WALKER ALL THE TIME TO GET AROUND - SOMETIMES A CANE TOO

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: BUSPIRONE, LISINOPRIL JANUVIA, ASPIRIN STOOL SOFTNER
Allergien: METFORMIN - HIVES/SKIN RASH PENICILLIN - CAUSES DEATH
Vorherige Impfungen: -

VAERS 2583979

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: WI
Alter: 54,0
Geschlecht: F
Eingang: 18.02.2023
Impfdatum: 11.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain upper Asthenia Autoimmune disorder Chest X-ray Chest discomfort Computerised tomogram Contusion Dyspnoea Feeling abnormal Gait disturbance Gastrointestinal pain Headache Hypertensive crisis Laboratory test Loss of consciousness Magnetic resonance imaging Musculoskeletal chest pain Myalgia

Symptomtext

Muscle pain, weakness, tinnitus, headache, BP 200 range hypertension crisis, difficulty breathing, chest tightness, couldn?t walk, loss of bladder control, GI and upper right side pain, autoimmune phenomenon, vasculitis, chest wall muscle pain, neuropathy hands and feet, snow vision, brain fog, lost consciousness 1x and woke to husband clearing vomit from my mouth to start CPR, bruising of unknown origin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: MRI, CT, chest X-ray, lots of labs. Autoimmune attack on liver and thyroid.
Aktuelle Erkrankungen: None
Vorgeschichte: None before vaccinated
Andere Medikamente: Vit D
Allergien: None before vaccinated
Vorherige Impfungen: -

VAERS 2522328

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 33,0
Geschlecht: F
Eingang: 03.12.2022
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Abdominal distension Abdominal pain Airway secretion clearance therapy Allergy to vaccine Anisocoria Blindness Blood pressure measurement Bradycardia Bronchoalveolar lavage Bronchoscopy Corneal scar Device occlusion Dry eye Dyspnoea Endotracheal intubation COVID-19 Colostomy Condition aggravated

Symptomtext

INTENSIVE CARE; DYSPNOEA; HYPOTENSION; CORNEAL SCAR; IIIRD NERVE DISORDER; DEVICE OCCLUSION; INCREASED BRONCHIAL SECRETION; DRY EYE; LAGOPHTHALMOS; ENDOTRACHEAL INTUBATION; MENTAL STATUS CHANGES; EXPOSURE KERATITIS; NEUROTROPHIC KERATOPATHY; HYPOTENSION; NYSTAGMUS; IIIRD NERVE DISORDER; OXYGEN SATURATION DECREASED; INCREASED BRONCHIAL SECRETION; SACCADIC EYE MOVEMENT; OXYGEN SATURATION DECREASED; STRABISMUS; VISUAL FIELD DEFECT; PYREXIA; LAGOPHTHALMOS; BLINDNESS; SACCADIC EYE MOVEMENT; BRADYCARDIA; PYREXIA; CORNEAL NEOVASCULARISATION; ABDOMINAL DISTENSION; CORNEAL OPACITY; ABDOMINAL PAIN; PARALYSIS; INTENSIVE CARE; SEIZURE; SARS-COV-2 TEST POSITIVE; VOLVULUS; NYSTAGMUS; ABDOMINAL DISTENSION; SEIZURE; ABDOMINAL PAIN; VOLVULUS; AIRWAY SECRETION CLEARANCE THERAPY; BRONCHOALVEOLAR LAVAGE; ALLERGY TO VACCINE; BRONCHOSCOPY; ANISOCORIA; NEUROTROPHIC KERATOPATHY; BRONCHOALVEOLAR LAVAGE; BLINDNESS; BRONCHOSCOPY; BRADYCARDIA; COLOSTOMY; CORNEAL OPACITY; CONDITION AGGRAVATED; PARALYSIS; CORNEAL SCAR; AIRWAY SECRETION CLEARANCE THERAPY; DEVICE OCCLUSION; ALLERGY TO VACCINE; DRY EYE; ANISOCORIA; DYSPNOEA; COVID-19; ENDOTRACHEAL INTUBATION; COLOSTOMY; EXPOSURE KERATITIS; CONDITION AGGRAVATED; COVID-19; CORNEAL NEOVASCULARISATION; SARS-COV-2 TEST POSITIVE; MENTAL STATUS CHANGES; This spontaneous report received from a parent by a Regulatory Authority, Vaccine Adverse Event Reporting System (VAERS) concerned a 34 year old female of an unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's past medical history included: brain damage, cervical spine fracture, colostomy, colostomy (Good stool output overall Stoma viable some retraction), hemolacria, blood clots, intracranial hemorrhage, motor vehicle accident, ocular nystagmus, headache, sigmoid volvulus subdural hematoma, seizures and paralysis (lasting 80) and concurrent conditions included: anal fistula, anisocoria, bilateral profound visual loss, sigmoid volvulus (s p end), corneal pannus of both eyes, corneal scar, opacity, depression, dry eyes bilateral, exotropia of both eyes, exposure keratopathy, gastroesophageal reflux disease, pressure ulcer, hypertropia of right eye, lagophthalmos of eyelids of both eyes, neurotrophic keratoconjunctivitis of right eye, localized visual field defect (bilateral), paralytic strabismus (associated with right partial oculomotor nerve palsy), tremor, seizure, saccadic eye movement deficiency, drug allergy (amoxicillin, ampicillin) and covid-19 ad26 vaccine allergy. The personal history of other diseases of the nervous system and sense organs. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025, expiry: UNKNOWN) dose was not reported, 1 total administered to the right arm on 10-MAR-2021 for an unspecified indication. Age at time of vaccination 33 years old. Concomitant medications included adderall (amfetamine aspartate/amfetamine sulfate/dexamfetamine saccharate/dexamfetamine sulfate), baclofen, cetirizine, senna-docusate (docusate sodium/sennoside a and b), escitalopram, guaifenesin, duo-neb (ipratropium bromide/salbutamol sulfate), lacosamide, lactulose, levetiracetam, melatonin, memantine, montelukast, oxybutynin, hypotears (retinol palmitate), eye solution, soothe eye solution, salbutamol and valproic acid. It was reported that on 10-MAR-2021, the patient had COVID-19 PCR test (sars-cov-2 test positive) which confirmed positive result (covid-19). On 23-AUG-2022, the patient experienced blindness, corneal neovascularization, corneal opacity, paralysis, seizure, volvulus, abdominal distension, abdominal pain, allergy to vaccine, anisocoria, bronchoalveolar lavage, colostomy, condition aggravated, corneal scar, device occlusion, dry eye, endotracheal intubation, exposure keratitis, iiird nerve disorder, increased bronchial secretion, lagophthalmos, neurotrophic keratopathy, nystagmus, saccadic eye movement, strabismus and visual field defect. On 23-AUG-2022, Laboratory data included: Airway secretion clearance therapy not reported, Bronchoalveolar lavage not reported, Bronchoscopy not reported, Colostomy not reported, Intubation Not reported, and Oxygen saturation (NR: not provided) 85%. It was reported that on 23-AUG-2022, the patient was presented to hospital due to worsening shortness of air (dyspnoea) and as per the patient's mother the patient became febrile (pyrexia) in the morning of admission (on 28-AUG-2022) and upon checking her oxygen saturation, it was noted to be 85% (oxygen saturation decreased). The patient was placed on 5 L home oxygen and brought to the hospital. The patient was found to have covid. She was initially admitted to the hospital medicine service, however it was noted to have decreased mentation (mental status changes) which required emergent intubation (endotracheal intubation). Post intubation the patient had a bronchoscopy with BAL performed. On 24-AUG-2022 into 25-AUG-2022, the patient became hypotensive and was given 1 liter IVF (Intravenous fluid) but remained hypotensive and was started on norepinephrine. Shortly after initiation of norepinephrine, the patient became bradycardic and therefore the patient was transitioned to epinephrine and BP and heart rate improved. The patient's mother mentioned the patient had similar issues two times prior while on norepinephrine. On 25-AUG-2022, early morning the patient was weaned off of epinephrine and extubated (device occlusion) to HFNC (High flow nasal cannula) (airway secretion clearance therapy). On 26-AUG-2022 the patient was transitioned from HFNC to 5L NC and broad spectrum abx were stopped. On 29-AUG-2022, the patient was upgraded to ICU (intensive care) status for closer monitoring. On 30-AUG-2022, the patient was hypotensive with SBP in the 70s was given 1 liter IVF (Intravenous fluid) transitioned back to HFNC (High flow nasal cannula) and repeat infectious workup was obtained. On 31-AUG-2022, the patient was transitioned back to regular NC and downgraded back to progressive care on 01-SEP-2022. On 04-SEP-2022, the patient was dropped her SpO2 (oxygen saturation) to 75%, on 4L NC NT suction was performed but catheter clogged due to secretions. The patient was placed on a NRB and SpO2 (oxygen saturation) improved to 96% and transitioned to 80% and 40L HFNC and initiated on mucomyst nebs. The patient stayed in the ICU and her oxygen was weaned down to 2L NC PRN over the past few days. The patient was continued getting mucomyst nebs, albuterol nebs, hypertonic saline nebs, chest PT (Chest physical therapy) and cough assist. These interventions due help with her secretions. It was reported that the patient's mother had all these modalities for airway clearance (airway secretion clearance therapy) at home and the patient had remained hemodynamically stable on midodrine and has tolerated RA mostly during the day with 2L PRN at night. It was reported that the patient will be discharged home with current neb treatments as well as oxygen to use PRN, home health services will resume and the team has reviewed the care plan new medications with her mother. On 04-SEP-2022, Laboratory data included: Oxygen saturation (NR: not provided) 75 %. Laboratory data (dates unspecified) included: Blood pressure improved, Heart rate improved, Oxygen saturation (NR: not provided) 80 %, 96 %, and Oxygen saturation down to 2L. The patient was hospitalized on 23-AUG-2022 for 19 days. Treatment medications (dates unspecified) included: norepinephrine, and epinephrine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from blindness, bradycardia, corneal neovascularisation, corneal opacity, paralysis, seizure, volvulus, abdominal distension, abdominal pain, airway secretion clearance therapy, allergy to vaccine, anisocoria, bronchoalveolar lavage, bronchoscopy, covid-19, colostomy, condition aggravated, corneal scar, device occlusion, dry eye, dyspnoea, endotracheal intubation, exposure keratitis, iiird nerve disorder, increased bronchial secretion, intensive care, lagophthalmos, mental status changes, neurotrophic keratopathy, nystagmus, oxygen saturation decreased, sars-cov-2 test positive, saccadic eye movement, strabismus, visual field defect, and pyrexia, and had not recovered from hypotension. This report was serious (Hospitalization Caused / Prolonged). This report was associated with a product quality complaint: 90000253946. The suspected product quality complaint has been confirmed to be the reported allegation was not confirmed and the root cause was determined to be not manufacturing related. Batch and lot tested and found within specifications based on the PQC evaluation/investigation performed. Additional information received from Complaint department on 30-NOV-2022. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result.; Sender's Comments: V2:Follow up information in this version updates, product quality complaint investigation result added.. This updated information does not change the causality of the previously reported events. 20220951222 -Covid-19 vaccine ad26.cov2.s- Blindness ,Anisocoria ,Volvulus ,Abdominal distension, Abdominal pain, Colostomy ,Corneal scar, Corneal neovascularisation ,Corneal opacity ,Dry eye ,Exposure keratitis ,IIIrd nerve disorder ,Lagophthalmos, Neurotrophic keratopathy ,Nystagmus ,Saccadic eye movement ,Strabismus ,Visual field defect , Bradycardia, Airway secretion clearance therapy ,Bronchoalveolar lavage., Bronchoscopy ,COVID-19,Condition aggravated ,Device occlusion, Dyspnoea, Endotracheal intubation, Hypotension, Increased bronchial secretion ,Intensive care, Mental status changes ,Oxygen saturation decreased ,SARS-CoV-2 test positive ,Pyrexia ,Allergy to vaccine . The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). Therefore, this event(s) is considered unassessable. 20220951222-covid-19 vaccine ad26.cov2.s- Paralysis ,Seizure . The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: MEDICAL HISTORY. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 19,0
Labordaten: Test Date: 20210310; Test Name: SARS-COV-2 TEST; Test Result: Positive ; Test Date: 20220823; Test Name: BRONCHOALVEOLAR LAVAGE; Result Unstructured Data: not reported; Test Date: 20220823; Test Name: BRONCHOSCOPY; Result Unstructured Data: not reported; Test Date: 20220823; Test Name: COLOSTOMY; Result Unstructured Data: not reported; Test Date: 20220823; Test Name: ENDOTRACHEAL INTUBATION; Result Unstructured Data: Not reported; Test Date: 20220823; Test Name: AIRWAY SECRETION CLEARANCE THERAPY; Result Unstructured Data: not reported; Test Date: 20220823; Test Name: OXYGEN SATURATION; Result Unstructured Data: 85 %; Comments: decreased; Test Date: 20220829; Test Name: INTENSIVE CARE; Result Unstructured Data: for closer monitoring; Test Date: 20220904; Test Name: OXYGEN SATURATION; Result Unstructured Data: 75 %; Test Name: OXYGEN SATURATION; Result Unstructured Data: 80 %; Test Name: BLOOD PRESSURE; Result Unstructured Data: improved; Test Name: HEART RATE; Result Unstructured Data: improved; Test Name: OXYGEN SATURATION; Result Unstructured Data: down to 2L; Test Name: OXYGEN SATURATION; Result Unstructured Data: 96 %
Aktuelle Erkrankungen: Allergy to vaccine; Anal fistula; Anisocoria; Corneal opacity; Corneal scar; Depression; Drug allergy (amoxicillin, ampicillin); Dry eyes; Exotropia; Exposure keratopathy; Gastrooesophageal reflux disease; Hypertropia; Lagophthalmos; Neurotrophic keratoconjunctivitis; Pannus (corneal); Paralytic strabismus (associated with right partial oculomotor nerve palsy); Pressure ulcer; Saccadic eye movement; Seizure; Sigmoid volvulus (s p end); Tremor; Vision loss; Visual field defect (bilateral)
Vorgeschichte: Medical History/Concurrent Conditions: Brain damage; Cervical vertebral fracture; Clot blood; Colostomy (Good stool output overall Stoma viable some retraction.); Colostomy; Headache; Hemolacria; Intracranial hemorrhage; Motor vehicle accident; Nystagmus; Paralysis (lasting 80); Seizures; Sigmoid volvulus; Subdural hematoma; Comments: The personal history of other diseases of the nervous system and sense organs.
Andere Medikamente: ALBUTEROL [SALBUTAMOL]; ADDERALL; BACLOFEN; CETIRIZINE; ESCITALOPRAM; GUAIFENESIN; LACOSAMIDE; LACTULOSE; LEVETIRACETAM; MELATONIN; MEMANTINE; MONTELUKAST; OXYBUTYNIN; HYPOTEARS [RETINOL PALMITATE]; SENNA AND DOCUSATE SODIUM; VALPROIC ACID;
Allergien: -
Vorherige Impfungen: -

VAERS 2440771

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 33,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 10.03.2021
Beginn: 23.08.2022
Tage bis Beginn: 531,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal distension Abdominal pain Airway secretion clearance therapy Allergy to vaccine Anisocoria Blindness Bradycardia Bronchoalveolar lavage Bronchoscopy COVID-19 Colostomy Condition aggravated Corneal neovascularisation Corneal opacity Corneal scar Device occlusion Dry eye Dyspnoea

Symptomtext

Hospital course: Patient is a 34 y.o. female with a PMH significant for TBI 2/2 MVC in 2018, spastic quadriparesis, and seizures who presented to the hospital on 8/23 due to worsening shortness of air. Per the patient's mother, the patient became febrile the morning of admission and upon checking her O2 sat, it was noted to be 85%. She was placed on 5L home O2 and brought to the hospital. The patient was found to have COVID. She was initially admitted to the hospital medicine service, however was noted to have decreased mentation requiring emergent intubation. Post intubation the patient had a bronchoscopy with BAL performed. On the night of 8/24 into 8/25, the patient became hypotensive, was given 1L IVF, but remained hypotensive and was started on norepinephrine. Shortly after initiation of norepinephrine, the patient became bradycardic therefore the patient was transitioned to epinephrine and BP and heart rate improved. Per the patient's mother, the patient has had similar issues two time prior while on norepinephrine. On the early morning of 8/25, the patient was weaned off of epinephrine and extubated to HFNC. On 8/26, the patient was transitioned from HFNC to 5L NC and broad spectrum abx were stopped. On 8/29, the patient was upgraded to ICU status for closer monitoring. On 8/30, the patient was hypotensive wit SBP in the 70s, was given 1L IVF, transitioned back to HFNC, and repeat infectious workup was obtained. On 8/31, the patient was transitioned back to regular NC and downgraded back to progressive care on 9/1. On 9/4, the patient dropped her SpO2 to 75% on 4L NC. NT suction was performed, but catheter clogged due to secretions. The patient was placed on a NRB and SpO2 improved to 96%. The patient was then transitioned to 80% and 40L HFNC and initiated on mucomyst nebs. The patient stayed in the MICU and her oxygen was weaned down to 2L NC PRN over the past few days. She has continued getting mucomyst nebs, albuterol nebs, hypertonic saline nebs, chest PT, and cough assist. These interventions due help with her secretions. The patient's mother does have all these modalities for airway clearance at home and they are wanted to take the patient home. She has remained hemodynamically stable on midodrine and has tolerated RA mostly during the day with 2L PRN at night. The patient will be discharged home with current neb treatments as well as oxygen to use PRN. Home health services will resume and the team has reviewed the care plan/new medications with her mother. She states that she feels like the patient's care can be managed by them at home. She will follow up with her PCP in 1-2 weeks for further management. Discharge Disposition/Condition Disposition: Home with Home Health Condition: Stable (s/sx potential problems absent or manageable)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 19,0
Labordaten: COVID-19 PCR confirmed positive on 03/10/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: ? Anal fistula ? Anisocoria 03/02/2022 ? Bilateral profound visual loss 03/02/2022 ? Brain damage ? Cervical spine fracture 03/04/2019 ? Colostomy in place 10/21/2021 Sigmoid volvulus (s/p end colostomy 10/17) Good stool output overall Stoma viable, some retraction ? Corneal pannus of both eyes 03/02/2022 ? Corneal scar and opacity 05/05/2022 ? Depression ? Dry eyes, bilateral 03/02/2022 ? Exotropia of both eyes 03/02/2022 ? Exposure keratopathy 05/05/2022 ? GERD (gastroesophageal reflux disease) ? Hemolacria 08/27/2020 ? History of blood clots 06/12/2019 ? History of pressure ulcer ? Hypertropia of right eye 03/02/2022 ? Intracranial hemorrhage 03/05/2019 ? Lagophthalmos of eyelids of both eyes 05/05/2022 ? MVA (motor vehicle accident) ? Neurotrophic keratoconjunctivitis of right eye 05/05/2022 ? Ocular nystagmus 03/23/2021 ? Other localized visual field defect, bilateral 03/02/2022 ? Paralytic strabismus associated with right partial oculomotor nerve palsy 03/02/2022 ? Personal history of other diseases of the nervous system and sense organs History of tremor ? Personal history of other specified conditions History of headache ? Personal history of other specified conditions History of seizure ? Saccadic eye movement deficiency 03/02/2022 ? Seizures ? Sigmoid volvulus 10/15/2021 Presented 10/14 with abdominal distension, pain, found to have a sigmoid volvulus. Underwent sigmoid end colostomy 10/17. ? Subdural hematoma 03/11/2019
Andere Medikamente: albutoerol adderall baclofen cetirizine escitalopram guaifenesin duo-neb lacosamide lactulose levetiracetam melatonin memantine montelukast oxybutynin hypotears eye solution soothe eye solution senna-docusate valproic acid
Allergien: COVID-10 AD26 vaccine (Janssen) amoxicillin ampicillin
Vorherige Impfungen: Covid-19 Ad26 Vaccine(janssen), adverse event was: Per patient family, patient had a reaction of seizures, paralysis (lasting 80

VAERS 2398044

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 56,0
Geschlecht: F
Eingang: 01.08.2022
Impfdatum: 24.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 38,0
Dosis: 1
Route/Site: IM / LA

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

Anaemia Anti-thyroid antibody increased Blood creatinine decreased Blood culture negative Blood thyroid stimulating hormone decreased Chest X-ray Computerised tomogram Computerised tomogram thorax Diarrhoea Fibrin D dimer Hepatic enzyme increased Illness Intensive care International normalised ratio increased Lymphadenopathy Monocyte count increased Neutrophil count increased Night sweats

Symptomtext

High Fevers (5 illness events leading Up to Hospitalization Starting in 5/2021 Hospitalization 4/8/2022 8 days Cardiac ICU Severely Swollen Glands Night Sweats Diarrhea Weight Loss Thyroiditis Severe Pericarditis (Requiring operative pericardial window) local Medical Center Pneumonia (Requiring Operative Thoracotomy) Left Lung local Medical Center Anemia High Platelets High Monocytes High Neutrophils Negative Blood Culture x 2 Low Creatinine Multiple Cat Scans Chest and Lungs with Contrast and without Multiple Chest X-rays

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Praegender Schweregrund: Intensive care
Hospital-Tage: 8,0
Labordaten: High WBC 17-28 High Liver Enzymes High TSH .0005 Low ESR 53 High SARS CoV-2 Covid 19 Not Detected INR 1.2 Anti Thyroid Peroxidase 172 High D Dimer 5.19 High Cat scans x-rays
Aktuelle Erkrankungen: Hashimotos' Thyroiditis Controlled
Vorgeschichte: None
Andere Medikamente: NP Thyroid 180 mg , Vivelle Patch, progesterone 100mg nightly
Allergien: None
Vorherige Impfungen: -

VAERS 2214042

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 72,0
Geschlecht: M
Eingang: 04.04.2022
Impfdatum: 05.03.2021
Beginn: 20.02.2022
Tage bis Beginn: 352,0
Dosis: UNK
Route/Site: IM / LA

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

Acute sinusitis Angiogram cerebral abnormal Apnoeic attack Arteriogram carotid abnormal Blood culture negative Blood thyroid stimulating hormone increased COVID-19 Carotid artery stenosis Chest X-ray normal Chronic sinusitis Computerised tomogram head abnormal Cortisol normal Electroencephalogram normal Encephalopathy Endotracheal intubation Extubation Haemoglobin decreased Hypotension

Symptomtext

Patient presents with acute encephalopathy. Patient was hypothermic, hypotensive with SBP 79, and encephalopathic. Patient had apneic episodes and was subsequently intubated for airway protection in setting of encephalopathy. Lab work notable for hemoglobin 6.6, TSH of 15, and initial troponin of 164. Patient had CXR without focal consolidation, repeat CXR showing ETT in appropriate position. Patient had CTH and CTA H/N with 50% stenosis of right proximal ICA at bifurcation and chronic versus acute sinusitis. ER consulted Neurology for evaluation of encephalopathy. In ER patient received acyclovir, vancomycin, ceftriaxone, and ampicillin as well as 2L IVFs. MICU was consulted given respiratory failure 2/2 encephalopathy for admission. For his altered mental status workup infectious workup which was negative including peritoneal fluid with a total cell count 5 stain without organisms, blood cultures were negative, UA did not suggest UTI, and negative chest x-ray. CT head did show acute sinusitis for which she received a course of Rocephin. Eeg not show seizure, TSH 15 but normal T4, normal cortisol. Patient did develop shock and required pressors but this was suspected to be sedation related. Patient was extubated on February 26th to eventually room air. Discharge Disposition/Condition Disposition: Home Condition: Stable (s/sx potential problems absent or manageable)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Shock
Hospital-Tage: 12,0
Labordaten: COVID PCR confirmed positive on 2/20/22
Aktuelle Erkrankungen: N/A
Vorgeschichte: Past Medical History He has no past medical history on file. Per review of prior records seen on care everywhere patient has a history of CAD s/p CABG in 2000 and 2008, T2DM on insulin, and anemia of chronic disease.
Andere Medikamente: apixaban aspirin atorvastatin bumetinide clopidogrel dorzolamide-timolol ergocalciferol ferrous sulfate multiviatmine gabepntin gentamicin cream levothyroxine metoprolol succinate tamsulosin amlodipine docusate hydralazine insulin 70-3
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2173289

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 59,0
Geschlecht: M
Eingang: 11.03.2022
Impfdatum: 31.03.2021
Beginn: 19.01.2022
Tage bis Beginn: 294,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia COVID-19 Chest discomfort Cough Fall Fatigue Nausea Presyncope Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient presented to ED after a fall from his couch. He states he was feeling weaker than usual, he rolled off the couch while trying to get up and fell on the floor. Denies any dizziness, HA or loss of consciousness. Constitutional: Positive for fatigue and fever. Negative for appetite change, chills, diaphoresis and unexpected weight change. HENT: Negative for congestion. Respiratory: Positive for cough and chest tightness. Negative for shortness of breath and wheezing. Cardiovascular: Negative for chest pain, palpitations and leg swelling. Gastrointestinal: Positive for nausea. Negative for abdominal pain, blood in stool, constipation, diarrhea and vomiting. He did not require treatment for COVID19 infection. Falls were thought to be due to presyncope with possible BPPV. Originally had acute rehab recs, but he improved clinically while inpatient and will discharge home with his wife and son who understand his isolation precautions. Discharge Disposition/Condition Disposition: Home Condition: Stable (s/sx potential problems absent or manageable)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 6,0
Labordaten: COVID PCR confirmed positive ono 1/19
Aktuelle Erkrankungen: N/A
Vorgeschichte: Past Medical History: Diagnosis Date ? Personal history of other diseases of the nervous system and sense organs History of cataract ? Personal history of other diseases of the nervous system and sense organs History of neuropathy ? Personal history of other endocrine, nutritional and metabolic disease History of diabetes mellitus
Andere Medikamente: aspirin atorvastatin clopidogrel lisinopril pantoprazole carvedilol
Allergien: penicillin metformin dapagliflozin
Vorherige Impfungen: -

VAERS 2098546

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 09.02.2022
Impfdatum: 09.03.2021
Beginn: 04.02.2022
Tage bis Beginn: 332,0
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy Atrial fibrillation Blindness Cerebellar stroke Chronic obstructive pulmonary disease Dyskinesia Electroencephalogram normal Endotracheal intubation Lethargy Nystagmus Positive airway pressure therapy Respiratory acidosis Seizure like phenomena

Symptomtext

Patient is a 78 yo M with hx paroxysmal atrial fibrillation, dilated cardiomyopathy with systolic and diastolic CHF, arthrosclerotic heart disease, mixed hyperlipidemia, moderately differentiated invasive ductal carcinoma of the left breast in a male s/p bilateral mastectomy, history of alcoholism and peptic ulcer who presented with lethargy and seizure like activity. No reported focal neurological deficits. Patient did have some visual loss that was improving early in hospitalization. Patient found to have bilateral occipital lobe and right cerebellar stroke. Patient started on ASA, continued eliquis, lipitor. Patient with worsening lethargy and respiratory acidosis in PM on 2/6. Suspect multifactorial in setting of ativan from CIWA protocol, COPD. Patient intubated on 2/6 after patient did not improve with BiPAP. Patient started on steroids. Patient has been on precedex and fentanyl for sedation. After intubation patient was noted to have seizure like activity with vertical nystagmus and jerking of extremities. Patient loaded on keppra and started on 500 mg BID for maintenance. STAT EEG and did not show epileptic activity on 2/7 or 2/8 but patient having intermittent seizure like activity. Keppra increased to 1000 mg BID. Routine exam may have not captured event. We cannot do continuous EEG monitoring at or facility. No recurrent episodes since increasing keppra. Hospitalization also complicated by Afib w/ RVR. Tikosyn discontinued due to QTC prolongation and diltiazem gtt started 2/7. Pt transferred for higher level of care to hospital on 2/8.

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

VAERS 2074158

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 70,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 12.03.2021
Beginn: 01.06.2021
Tage bis Beginn: 81,0
Dosis: 1
Route/Site: OT / -

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

Brain oedema Dementia Alzheimer's type Fall Gait inability Head injury Inadequate diet Pneumonia Thrombosis Ultrasound scan Weight decreased

Symptomtext

VACCINE SPEEDED UP ALZHEIMERS; NOT EATING WELL; LOOSING WEIGHT (WENT DOWN TO 66 LBS); PNEUMONIA; COULD NOT WALK; DIAGNOSED WITH WATER IN BRAIN; CUTS IN HEAD/CUT IN FOREHEAD; MULTIPLE FALLS/FELL 5 TIMES/FELL IN THE NURSING HOME; BLOOD CLOTS FROM KNEE DOWN/BLOOD CLOT IN LEG (PROBABLY RIGHT LEG); This spontaneous report received from a consumer concerned a 77 year old female. The patient's weight was 76 pounds, and height was not reported. The patient's past medical history included: stroke, and thyroid, and concurrent conditions included: alzheimer's dementia, advance rheumatoid arthritis, memory loss, cigarette smoker, no alcohol use, and sulfa allergy, and other pre-existing medical conditions included: The patient had no drug abuse or illicit drug usage. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025 and expiry: 25-MAY-2021) dose was not reported, 1 total administered on 12-MAR-2021 for prophylactic vaccination. Concomitant medications included Levothyroxine for thyroid disorder. On JUN-2021 (3 months after receiving the vaccine), the patient experienced multiple falls and could not walk, patient would take little tiny steps then falls. The patient was misdiagnosed with thyroid problems for 2 weeks then admitted to hospital on 13-JUN-2021 and stayed for 2 days, then spent two and half weeks in for walking but was still falling and reported rehab was unsuccessful. The patient had direct nursing care because she was not making any progress, the patient then had home therapy which showed significant progress. The patient was not eating well when she was at the hospital in JUN-2021 and was loosing weight (went down to 66 pounds) and experienced stomach shrunk, the patient was on a chopped up diet and was prescribed a pill to increase her apatite but they could not afford it, then when patient went to home (date unspecified), started eating better, smaller more frequent meals and did not need to have a feeding tube and gained back 10lbs. The patient also experienced slurred speech (date unspecified) and had speech therapy with home therapy. On 04-JUL-2021, the patient fell 5 times and had cuts in head. On 05-JUL-2021, the patient went to the emergency room and admitted and stayed in the hospital for 11 days. During the admission on 08-JUL-2021, the patient was diagnosed with water in brain by neurologist. The patient also fell in the nursing home on 16-JUL-2021 and on 31-JUL-2021. On 11-AUG-2021, the neurologist wrote a letter to patient stating that patient can no longer make health or financial decisions or drive, and was also prescribed Donepezil and another memory medication for the signs of memory problems. The patient was performed with lumbar puncture to drain water from brain by surgeon (date unspecified) but it was reported that, water keeps coming back, the reporter was told a shunt is required to prevent water from coming, back but a specialist advised against the procedure and did not recommend the shunt as that water acts like a cushion for the brain inside the skull and the shunt would cause blood clots especially with vaccine, with complications the brain would bleed, and could lead to death. The reporter reported that (date unspecified) , the patient has to wear diapers for urination secondary to Alzheimer's and reported vaccine speeded up the process of aging/vaccine speeded up Alzheimer's. On 01-NOV-2021, the patient admitted to hospital with a diagnosis of pneumonia and was discharged on 06-NOV-2021 with Mucinex (guaifenesin) and recovered around 13-NOV-2021. On 13-NOV-2021, the patient noticed that the right leg was swollen and patient taken to the emergency room and was performed with an ultrasound and diagnosed with blood clots from knee down. The patient was not admitted but discharged with 30 days supply of Eliquis (apixaban) and a prescription of Eliquis was 10 mg one in the morning and one in the evening for 6 month. Laboratory data included: Diagnostic ultrasound (NR: not provided) Not reported. The reporter also reported that (date unspecified), the patient memory is coming back about 90%, eats better, still leans backsword so can fall anytime, and speech still slurred. On an unspecified date, the patient experienced confusion. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from pneumonia on 13-NOV-2021, was recovering from multiple falls/fell 5 times/fell in the nursing home, could not walk, not eating well, and loosing weight (went down to 66 lbs), had not recovered from diagnosed with water in brain, and blood clots from knee down/blood clot in leg (probably right leg), and the outcome of vaccine speeded up alzheimer's and cuts in head/cut in forehead was not reported. This report was serious (Hospitalization Caused / Prolonged, and Other Medically Important Condition).; Sender's Comments: V0: 20220154205-COVID-19 VACCINE AD26.COV2.S- Pneumonia, diagnosed with water in brain, blood clots from knee down/blood clot in leg (probably right leg), multiple falls/fell 5 times/fell in the nursing home, cuts in head/cut in forehead, could not walk, not eating well, loosing weight (went down to 66 lbs), stomach shrunk. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). 20220154205-COVID-19 VACCINE AD26.COV2.S-vaccine speeded up Alzheimer's. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: MEDICAL HISTORY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20211113; Test Name: Diagnostic ultrasound; Result Unstructured Data: Not reported
Aktuelle Erkrankungen: Abstains from alcohol; Cigarette smoker; Dementia Alzheimer's type; Memory loss; Rheumatoid arthritis; Sulfonamide allergy
Vorgeschichte: Medical History/Concurrent Conditions: Stroke; Thyroid disorder; Comments: The patient had no drug abuse or illicit drug usage
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 1236955

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: -
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Aphasia Blood test Computerised tomogram Eyelid function disorder Facial paralysis Computerised tomogram head normal Condition aggravated Dysphonia Facial paresis Headache Guillain-Barre syndrome Human herpesvirus 6 infection Immunoglobulin therapy Lumbar puncture abnormal Magnetic resonance imaging Lumbar puncture normal Magnetic resonance imaging normal Neck pain

Symptomtext

MILLER-FISHER SYNDROME; This spontaneous report was received from literature. This report concerned a 32 year old male of unknown race and ethnicity. The objective of the study was to describe the relationship between Covid 19 vaccination and Miller Fisher Syndrome. Miller-Fisher syndrome (MFS) is a rare variant, estimated to affect 1 to 2 in 1,000,000 cases of GBS (Guillain Barre Syndrome). The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: No significant medical history presented with progressive facial motor and sensory dysfunction. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number was not reported) 1 total, dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On an unspecified date, the patient experienced miller-fisher syndrome and presented with progressive facial motor and sensory dysfunction. He received the Johnson & Johnson COVID-19 vaccination 18 days prior. For three days, he had blurry vision, eye pain, and dysarthria. Then, over 24 hours, he became unable to smile and drink/eat due to facial weakness. In the Emergency Department, the patient was afebrile and hemodynamically stable. Lab work was unremarkable. Physical exam demonstrated significant facial diplegia including inability to fully close the eyes, raise the eyebrows, and smile. Magnetic Resonance Imaging and Magnetic Resonance Angiogram head and neck did not reveal any abnormalities. The patient underwent lumbar puncture which revealed an albumino cytologic dissociation with negative cultures and antibodies against GQ1B. The patient was monitored in the ICU (intensive care unit) and improved with IVIg (Intravenous immune globulin). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovered from miller-fisher syndrome. The authors emphasized that at this time, The link between COVID-19 and GBS remains uncertain and clinicians should avoid drawing associations between both, but should remain vigilant in their practice, especially in recently immunized patients. The benefits of vaccination continue to far outweigh the small risk of GBS.(Guillain Barre Syndrome). This report was serious (Hospitalization Caused / Prolonged, and Life Threatening).; Sender's Comments: V0 20220117568-COVID-19 VACCINE AD26.COV2.S-myocarditis. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Test Name: Lumbar puncture; Result Unstructured Data: albuminocytologic dissociation; Comments: albuminocytologic dissociation with negative cultures andantibodies against GQ1B; Test Name: Magnetic resonance imaging head; Result Unstructured Data: no abnormalities; Test Name: Magnetic resonance imaging neck; Result Unstructured Data: no abnormalities; Test Name: Physical examination; Result Unstructured Data: significant facial diplegia; Test Name: Lab test; Result Unstructured Data: unremarkable
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No significant medical history presented with progressive facial motor and sensory dysfunction.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1236955

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: -
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

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

Aphasia Blood test Computerised tomogram Eyelid function disorder Facial paralysis Computerised tomogram head normal Condition aggravated Dysphonia Facial paresis Headache Guillain-Barre syndrome Human herpesvirus 6 infection Immunoglobulin therapy Lumbar puncture abnormal Magnetic resonance imaging Lumbar puncture normal Magnetic resonance imaging normal Neck pain

Symptomtext

MILLER-FISHER SYNDROME; This spontaneous report was received from literature. This report concerned a 32 year old male of unknown race and ethnicity. The objective of the study was to describe the relationship between Covid 19 vaccination and Miller Fisher Syndrome. Miller-Fisher syndrome (MFS) is a rare variant, estimated to affect 1 to 2 in 1,000,000 cases of GBS (Guillain Barre Syndrome). The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: No significant medical history presented with progressive facial motor and sensory dysfunction. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number was not reported) 1 total, dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On an unspecified date, the patient experienced miller-fisher syndrome and presented with progressive facial motor and sensory dysfunction. He received the Johnson & Johnson COVID-19 vaccination 18 days prior. For three days, he had blurry vision, eye pain, and dysarthria. Then, over 24 hours, he became unable to smile and drink/eat due to facial weakness. In the Emergency Department, the patient was afebrile and hemodynamically stable. Lab work was unremarkable. Physical exam demonstrated significant facial diplegia including inability to fully close the eyes, raise the eyebrows, and smile. Magnetic Resonance Imaging and Magnetic Resonance Angiogram head and neck did not reveal any abnormalities. The patient underwent lumbar puncture which revealed an albumino cytologic dissociation with negative cultures and antibodies against GQ1B. The patient was monitored in the ICU (intensive care unit) and improved with IVIg (Intravenous immune globulin). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovered from miller-fisher syndrome. The authors emphasized that at this time, The link between COVID-19 and GBS remains uncertain and clinicians should avoid drawing associations between both, but should remain vigilant in their practice, especially in recently immunized patients. The benefits of vaccination continue to far outweigh the small risk of GBS.(Guillain Barre Syndrome). This report was serious (Hospitalization Caused / Prolonged, and Life Threatening).; Sender's Comments: V0 20220117568-COVID-19 VACCINE AD26.COV2.S-myocarditis. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Test Name: Lumbar puncture; Result Unstructured Data: albuminocytologic dissociation; Comments: albuminocytologic dissociation with negative cultures andantibodies against GQ1B; Test Name: Magnetic resonance imaging head; Result Unstructured Data: no abnormalities; Test Name: Magnetic resonance imaging neck; Result Unstructured Data: no abnormalities; Test Name: Physical examination; Result Unstructured Data: significant facial diplegia; Test Name: Lab test; Result Unstructured Data: unremarkable
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No significant medical history presented with progressive facial motor and sensory dysfunction.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1981643

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: MA
Alter: 75,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 29.03.2021
Beginn: 08.12.2021
Tage bis Beginn: 254,0
Dosis: 1
Route/Site: IM / LA

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

Ageusia COVID-19 Chest X-ray abnormal Dyspnoea Lung opacity Pulmonary oedema SARS-CoV-2 test positive

Symptomtext

patient presented to HCF ED on 12/8/21 with SOB and loss of taste, found to be covid positive. Patient is fully vaccinated and also received a booster. Admission CXR was significant for diffuse interstitial- like opacities likely representing edema. Patient was appropriately treated for covid and responsed well. Patient was discharged home on 12/15/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: 7,0
Labordaten: covid positive on 12/13/21 chest x ray impression on 12/8/21- diffuse interstitial-like opacities likely representing edema
Aktuelle Erkrankungen: N/A
Vorgeschichte: DVT, HFpEF, CKD, asthma, obesity
Andere Medikamente: acetaminophen, atorvastatin, calcium-vitamin d3, cetirizine, citalopram, diclofenac gel, furosemide, guifenesin, hydroxyzine, levothyrixine, losartan, multivitamin, olanzapine, pantoprazole, proair, senna, simethicone, spironolactone, symbi
Allergien: lisinopril
Vorherige Impfungen: -

VAERS 1963492

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 63,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 16.03.2021
Beginn: 17.10.2021
Tage bis Beginn: 215,0
Dosis: 1
Route/Site: IM / LA

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

Computerised tomogram head Ophthalmological examination abnormal Retinal vascular thrombosis Sudden visual loss

Symptomtext

Sudden loss of vision 10/17/21. Went to ER. Had CT scan of brain to rule out stroke. Was seen by ophthalmologist same day. Diagnosed with blood clot of optic nerve left eye.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Retinal vascular thrombosis
Hospital-Tage: -
Labordaten: Eye Exam. CT scan of brain
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, high cholesterol
Andere Medikamente: Metformin, Atorvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 1908316

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: -
Alter: -
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 23.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Acoustic stimulation tests Cardiac function test Congenital hydrocephalus Foetal exposure during pregnancy Foetal heart rate decreased Neonatal seizure SARS-CoV-2 test Spina bifida Urinary tract infection neonatal Vesicoureteric reflux

Symptomtext

URINARY TRACT INFECTION; FOETAL EXPOSURE DURING PREGNANCY; KIDNEY REFLUX; SPINA BIFIDA; HYDROCEPHALUS; SEIZURE; LOW FETAL HEART RATE; This solicited pregnancy report received from a consumer concerned a female of unspecified age, race and ethnicity. The patient was enrolled in a non-company sponsored study Registry number: C05587). The patient's weight was 2.95 kilograms, and height was not reported. No past medical history or concurrent conditions were reported. The patient initiated treatment with covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025 expiry: UNKNOWN) dose was not reported, 1 total, administered on 23-MAR-2021 for covid-19 immunisation. Concomitant medications included amitriptyline hydrochloride, atorvastatin calcium, and sertraline hydrochloride. The baby route of administration was transplacental. On 07-JUN-2021, the mother had prenatal ultrasound which showed open neural tube defect. On 24-AUG-2021, at gestational age 38 weeks and three days, the mother delivered a live, full-term, female neonate by caesarean method of delivery (C-section). Primary reason for the C-section was low fetal heart rate. Mother spent two days in the hospital for the delivery. The neonate spent more than 10 days in the Neonatal Intensive Care Unit (NICU) after delivery due to birth defects. Neonate was born with spina bifida (myelomeningocele) and hydrocephalus. She was treated with endoscopic third ventriculostomy with choroid plexus cauterization (ETV/CPC), which failed. On 15-SEP-2021, the neonate developed a urinary tract infection (UTI), treated with amoxicillin. On 29-OCT-2021, the baby had shunt placement procedure for treatment of hydrocephalus. Shunt placement had a long recovery. The baby experienced seizures post-surgery, treated with Keppra (levetiracetam) and Vimpat (lacosamide). On 14-NOV-2021, the baby was hospitalized for UTI. Treatment required catheter and amoxicillin, administered every 4 hours as kidney infection prophylaxis because of kidney reflux. On the same day, the baby was tested for SARS-CoV-2 virus. Result was negative. On unspecified date patient was hospitalized for unspecified number of days. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the low fetal heart rate, hydrocephalus, spina bifida, urinary tract infection, seizure, kidney reflux and foetal exposure during pregnancy was not reported. The reporter considered the causality between covid-19 vaccine ad26.cov2.s, and low fetal heart rate, hydrocephalus, spina bifida, seizure, urinary tract infection, and kidney reflux as not related. The reporter did not provide a causality assessment between covid-19 vaccine ad26.cov2.s, and foetal exposure during pregnancy. Company causality between covid-19 vaccine ad26.cov2.s, and spina bifida, hydrocephalus, seizure, low fetal heart rate, urinary tract infection, kidney reflux, and foetal exposure during pregnancy was not related. This report was serious (Hospitalization Caused / Prolonged, and Congenital Anomaly/Birth Defect). This parent/child case is linked to 20210800843.; Sender's Comments: V0: 20211157053-covid-19 vaccine ad26.cov2.s -Spina bifida. This event(s) is considered not related. The event(s) shows an incompatible temporal relationship. 20211157053-covid-19 vaccine ad26.cov2.s -Hydrocephalus, Seizure, Low fetal heart rate, Urinary tract infection, Kidney reflux. . This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: UNDERLYING DISEASE-Spina bifida. 20211157053-covid-19 vaccine ad26.cov2.s -Foetal exposure during pregnancy. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neonatal seizure
Hospital-Tage: -
Labordaten: Test Date: 202108; Test Name: Hearing test; Result Unstructured Data: unknown; Test Date: 202108; Test Name: Cardiac function test; Result Unstructured Data: unknown; Test Date: 20211114; Test Name: SARS-CoV-2 test; Result Unstructured Data: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: ATORVASTATIN CALCIUM; AMITRIPTYLINE HYDROCHLORIDE; ZOLOFT
Allergien: -
Vorherige Impfungen: -

VAERS 1861119

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 11.03.2021
Beginn: 09.11.2021
Tage bis Beginn: 243,0
Dosis: 1
Route/Site: - / -

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

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

Symptomtext

The patient had a syncope episode on 11/9/21 and fell. She was brought to the hospital and tested positive for COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: COVID+ by PCR on 11/9/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1785241

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 22.03.2021
Beginn: 22.04.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: IM / UN

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

COVID-19 Intensive care

Symptomtext

Admission to critical care hospital with COVID-19 diagnosis on admission

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Morbid obesity, Anxiety, Hyperlipidemia, Hypertension
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1765239

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 14.03.2021
Beginn: 30.09.2021
Tage bis Beginn: 200,0
Dosis: 1
Route/Site: IM / -

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

Endotracheal intubation Hypotension Leukocytosis Mental status changes Pneumonia Respiratory distress Respiratory failure Urine output decreased

Symptomtext

9/30/21: ED for AMS and hypoxic respiratory failure. Hx limited and mainly obtained from EMR review and ED physician. Pt was emergently intubated on arrival to the ED d/t saturating in the 60s. In the ED pt was found to have leukocytosis w/ PNA and was tx w/ Vanc and Cef. Patient has developed sustained hypotension at the time when she was in respiratory distress and getting intubated. Currently patient is on norepinephrine. Her urine output has been declining. Please note: Patient received J&J vaccine on 3/14/2021 Lot # 1805025

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN
Andere Medikamente: -
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 1744516

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 69,0
Geschlecht: F
Eingang: 29.09.2021
Impfdatum: 03.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Back pain Blindness Dizziness Dyspnoea Fatigue Headache Muscle spasms Nausea Palpitations Seizure

Symptomtext

Severe vision loss in both eyes (over 50% in left eye about 50% in right eye), severe headaches, dizziness, nausea, heart palpatations, extremely fatigue, shortness of breathe, back aches, muscles cramps, seizures

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: various medical test performed
Aktuelle Erkrankungen: None
Vorgeschichte: Heart failure, COPD, blood clots
Andere Medikamente: Blood thinners
Allergien: Ragweed, Sulfa drugs, codine
Vorherige Impfungen: -

VAERS 1708425

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 17.09.2021
Impfdatum: 20.03.2021
Beginn: 16.09.2021
Tage bis Beginn: 180,0
Dosis: 1
Route/Site: - / -

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

Deep vein thrombosis Peripheral swelling Ultrasound scan

Symptomtext

Patient reported to the ER on 09/16/2021 with left leg swelling. Diagnosed with an acute DVT of the left leg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Venous US done in the ER, on 09/16/2021.
Aktuelle Erkrankungen: HTN, Hyperlipidemia, chronic epixtasis
Vorgeschichte: HTN, Hyperlipidemia, chronic epixtasis
Andere Medikamente: Losartan/HCTZ 50/12.5 mg daily; Omega 3-6-9; Amlodipine 10 mg daily
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1947386

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: AZ
Alter: 58,0
Geschlecht: M
Eingang: 07.09.2021
Impfdatum: 05.04.2021
Beginn: 23.08.2021
Tage bis Beginn: 140,0
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy Bradykinesia Cardiac disorder Cold sweat Coronary arterial stent insertion Flushing Gait disturbance Intensive care Intracardiac thrombus Laboratory test

Symptomtext

On 8-23-2021 at 115AM while at work is when the first symptom happened. I felt flushed and had cold sweats, body went into slow motion. Like when I walked it felt like I was wading through mud. Called security, they called 911. Transported by EMT's to emergency surgery to implant stent into LAD region of heart. I spent 1 day in ICU, move to room day 2, go released on 3rd day. Now I have a damaged heart with a stent. I'll need to take blood thinners for life due to a blood clot going to my heart. This event, is the one and only symptom that I had. This is 138 days from vaccine to this event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 3,0
Labordaten: Testing is ongoing. Can supply any and all information up to date. When I know where to send it to? Thank you
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1641207

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 55,0
Geschlecht: F
Eingang: 27.08.2021
Impfdatum: 21.03.2021
Beginn: 18.07.2021
Tage bis Beginn: 119,0
Dosis: 1
Route/Site: - / -

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

Asthenia Bilevel positive airway pressure COVID-19 Condition aggravated Cough Dyspnoea Endotracheal intubation Fatigue Intensive care Myasthenia gravis Palpitations Pyrexia SARS-CoV-2 test positive

Symptomtext

55 years old female, seen and examined on July 19, 2021 1:00 a.m., with history of asthma, CAD, hyperlipidemia, hypertension, myasthenia gravis. Here for evaluation of progressive short of breath, dry cough, generalized weakness for which she believes might having a MG flare up, started about 5 days ago, per patient she received Johnson & Johnson vaccine back in March. She also developed subjective fever, palpitations. 7/23/21: intubated due to increased fatigue while on BiPAP 7/30/21: transferred to Hospital ICU 8/15/21: remains intubated, not tolerating weaning of sedation, afebrile 8/22/21: awaiting Trach/PEG

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: SARS COV2 PCR positive 7/18/2021
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, CAD, hyperlipidemia, hypertension, myasthenia gravis, former smoker
Andere Medikamente: albuterol, cetirizine, ferrous sulfate, Flonase, CellCept...
Allergien: NKA
Vorherige Impfungen: -

VAERS 1554431

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 33,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 24.03.2021
Beginn: 09.04.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: SYR / RA

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

Heavy menstrual bleeding Thrombosis

Symptomtext

Extremely heavy periods since the vaccine. Often with huge golf ball size blood chunks. I?ve had PCOS under control and this is not my normal to bleed as much and as often as I have been since the vaccine. I will have 3-4 extremely heavy days, soaking through pads, heavy to change menstrual cup once an hour with it filled each time (previously was having to only change 2-3 times a day).

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Crohns Disease, PCOS
Andere Medikamente: None
Allergien: None, gluten sensitivity
Vorherige Impfungen: -

VAERS 1497157

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TX
Alter: -
Geschlecht: F
Eingang: 23.07.2021
Impfdatum: -
Beginn: 23.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

COVID-19 Cough Diarrhoea Fatigue Guillain-Barre syndrome Headache Myalgia Nausea Urinary tract infection Vomiting

Symptomtext

UTI; GUILLAIN BARRE SYNDROME; COUGH; MUSCLE PAIN; VOMITING; DIARRHEA; TIREDNESS; NAUSEA; HEADACHE; This spontaneous report received from a consumer concerned herself a 40 year old female. Initial information was processed with additional information received on 21-JUL-2021 via a telephone outreach with the patient. The patient's height, and weight were not reported. The patient's concurrent conditions included asthma, diabetes (Type II), pollen allergy, tobacco use (3-4 cigarettes daily and vaping), no drug abuse or illicit drug use, no alcohol use. She reports a semi-active lifestyle; with no recent infectious illnesses or traveling. The patient was not recently vaccinated or hospitalized 6 weeks prior to onset of the event. She also did not have any of the following prior the the events: common cold, flu, or infection with Epstein-Barr, Herpes simplex, Herpes Zoster, adenovirus infection, cytomegalovirus, respiratory syncytial virus infection, coxsackievirus, diarrhea or bloody diarrhea, Lyme disease. Her HIV status was negative. The patient's family history included maternal grandmother with ovarian and breast cancer; no known neurological or autoimmune family history. The patient's last menstruation was 03-JUN-2021; and did not have her period last month. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025) dose was not reported, administered on 22-MAR-2021 in her right arm for prophylactic vaccination. No concomitant medications were reported. On 23-MAR-2021, 1 day after receiving the vaccine, the patient experienced diarrhea, tiredness, nausea, vomiting and headache (also reported as a week after the vaccination). She stated all symptoms worsened at night more than during the day. On 29-MAR-2021, the patient experienced cough and muscle pain. She stated muscle pain relief with a muscle relaxant. On 13-JUL-2021, the patient reported being diagnosed with Guillain-Barre Syndrome, and was not hospitalized. Both her arms and legs had pain, weakness bilateral; she was falling and dropping things from her hands due to the weakness. She reported the symptoms as starting gradually, spreading and becoming worse. The patient also had problems with her left eye blurry, shortness of breath, left jaw weak when chewing, trouble swallowing both liquids and solids. On an unspecified date, the patient also experienced urinary tract infection (UTI) and frequent urination. Laboratory data (dates unspecified) included: COVID-19 as negative. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from Guillain-Barre Syndrome, cough, diarrhea, tiredness, nausea, headache, muscle pain and vomiting. The outcome of UTI was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: This spontaneous report received from a consumer concerned herself, a 40-year-old female, who experienced Guillain Barre syndrome (GBS), with symptoms starting approximately 3 days after vaccine. Concurrent conditions included asthma, diabetes, tobacco use. She reports no recent infections or travel. The patient was not recently vaccinated with other products. She also did not have any of the following prior the events: common cold, flu, or infection with Epstein-Barr, Herpes simplex, Herpes Zoster, adenovirus infection, cytomegalovirus, respiratory syncytial virus infection, coxsackievirus, diarrhea or bloody diarrhea, Lyme disease. Her HIV status was negative. There was no known neurological or autoimmune family history. No concomitant medications were reported. On day 1, the patient experienced diarrhea, tiredness, nausea, vomiting and headache (also reported as a week after the vaccination). She stated all symptoms worsened at night more than during the day. On day 7, the patient experienced cough and muscle pain. On day 113, the patient reported being diagnosed with Guillain-Barre Syndrome (date of diagnosis not specified) and was not hospitalized. Both her arms and legs had pain, weakness bilateral; she was falling and dropping things from her hands due to the weakness. She reported the symptoms as starting gradually, spreading and becoming worse. The patient also had problems with her left eye blurry, shortness of breath, left jaw weakness when chewing, trouble swallowing both liquids and solids. On an unspecified date, the patient also experienced urinary tract infection (UTI) and frequent urination. COVID-19 testing was negative (date unknown). The occurrence of GBS could represent background incidence of such events in the general population. Considering the temporal relationship, the event is assessed to have an indeterminate relationship with vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: Test Name: COVID-19; Result Unstructured Data: Negative
Aktuelle Erkrankungen: Asthma; Pollen allergy; Tobacco user (3-4 cigarettes per day and vaping); Type II diabetes mellitus
Vorgeschichte: Comments: Does the patient have any allergies? :: Yes Provide details of the allergies :: pollen allergy. Was there drug abuse or illicit drug usage? :: No Does the patient consume alcohol? :: No Does the patient smoke? :: Yes Provide details of cigarettes(indicate consumption per day, week, month) :: 3-4 cigarettes per day.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1490879

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: IL
Alter: 41,0
Geschlecht: F
Eingang: 21.07.2021
Impfdatum: 06.03.2021
Beginn: 28.03.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: SYR / RA

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

Asthenia Dysmenorrhoea Menstruation irregular Oligomenorrhoea Thrombosis

Symptomtext

Since the vaccination, my menstrual cycles are not the same. They last way longer and I pass very large blood clots that are not normal for me, to the point that I feel very weak. They have been like this every month since, the pain it?s excruciating at times and I?m not someone that complains, but this doesn?t feel normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1341442

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: UT
Alter: 55,0
Geschlecht: M
Eingang: 17.07.2021
Impfdatum: -
Beginn: 18.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Bell's palsy Blood test Chills Guillain-Barre syndrome Headache Myalgia Tremor Laboratory test Magnetic resonance imaging Nerve conduction studies Pyrexia

Symptomtext

GUILLEN BARRE SYNDROME; BELLS PALSY/FACE DROOPING; CHILLS; HEADACHES/EXCRUCIATING HEADACHES; FEVER; This spontaneous report was received from a consumer and concerned a 55 year old male. The patient's height and weight were not reported. The patient's concurrent conditions included drug allergy. Other relevant history included general good health and a marathon runner. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025, expiry: 09-JUL-2021) dose was not reported, administered on 17-MAR-2021 to left arm for prophylactic vaccination. No concomitant medications were reported. On 18-MAR-2021, the patient experienced fever, chills and headaches. On 14-APR-2021, patient thought he had eaten something that had burned his lip. On 18-APR-2021, the patient experienced bells palsy/face drooping. His "lip going numb" then "face started drooping". He went to the emergency room. The doctors proceeded with an MRI and "all sorts of bloodwork." Patient also had "leg started to have twitching" and then started to have excruciating headaches ", "back started hurting on around the 22nd or 23rd of April" and "his legs and feet were numb" and "just couldn't get his utensils", "body weakness and headaches." He went to a neurologist and had a nerve conducting study and "it looked like it was GBS and chronic inflammatory." On 27-MAY-2021, Guillen Barre syndrome was diagnosed. Treatment medications included: ibuprofen, gabapentin, sodium chloride, paracetamol, naproxen, and plasma infusions to help with GBS. At the neurologist, the patient had 5 treatments of plasma. He was having reactions with the infusion including "light headedness or headaches." He was given saline and the doctors told him to "stay hydrated and also was suggested acetaminophen and ibuprofen." He was also having "extreme weakness" with the plasma therapy. The neurologist was looking into the diagnosis and determined as it "is a reaction to the vaccine". The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of Guillen Barre syndrome was not reported. The patient recovered from Bells Palsy/face drooping on 23-APR-2021, and fever and chills on an unspecified date, and had not recovered from headaches/excruciating headaches. This report was serious (Other Medically Important Condition). This case, from the same reporter is linked to 20210726629.; Sender's Comments: V0: This spontaneous report received from a consumer concerns a 55 year old male, who was noted to have bell's palsy and diagnosed with Guillain-Barre syndrome (GBS) 32 and 71 days, respectively, after receiving the Janssen Covid-19 vaccine. Patient's height and weight were not reported. The patient's past medical/surgical history, concurrent conditions and concomitant medications were not reported. Information on smoking history, illicit drug use and alcohol abuse were not provided. Patient has drug allergy, unspecified. Patient had fever, chills and headache one day after receiving the vaccine. Thirty-two (32) days post vaccine, the patient's face started to droop and was noted to have bells palsy. He sought consult at the emergency room and was worked up on. No results provided. Patient started experiencing twitching of his legs, excruciating headaches and back pains. Later, his legs and feet started to get numb, described as not being able to get his utensils. His body started to get weak and he still was experiencing headaches. He went to a neurologist and had a nerve conducting study. Seventy-one (71) days after receiving the vaccine, patient was diagnosed with Guillain-Barre Syndrome (GBS). Treatment medications included: ibuprofen, gabapentin, sodium chloride, paracetamol, naproxen, and plasma infusions. Information regarding other potential etiologies was insufficient, and the occurrence of Bells Palsy and GBS could represent background incidence of such events in the general population. Considering the temporal relationship, the event is assessed to have an indeterminate relationship with vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Date: 20210527; Test Name: Laboratory test; Result Unstructured Data: Guillen Barre Syndrome; Test Name: Blood test; Result Unstructured Data: not reported; Test Name: Nerve conduction studies; Result Unstructured Data: GBS and chronic inflammatory; Test Name: MRI; Result Unstructured Data: not reported
Aktuelle Erkrankungen: Drug allergy (Erythromycin, sulfa)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1341442

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: UT
Alter: 55,0
Geschlecht: M
Eingang: 17.07.2021
Impfdatum: -
Beginn: 18.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Bell's palsy Blood test Chills Guillain-Barre syndrome Headache Myalgia Tremor Laboratory test Magnetic resonance imaging Nerve conduction studies Pyrexia

Symptomtext

GUILLEN BARRE SYNDROME; BELLS PALSY/FACE DROOPING; CHILLS; HEADACHES/EXCRUCIATING HEADACHES; FEVER; This spontaneous report was received from a consumer and concerned a 55 year old male. The patient's height and weight were not reported. The patient's concurrent conditions included drug allergy. Other relevant history included general good health and a marathon runner. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025, expiry: 09-JUL-2021) dose was not reported, administered on 17-MAR-2021 to left arm for prophylactic vaccination. No concomitant medications were reported. On 18-MAR-2021, the patient experienced fever, chills and headaches. On 14-APR-2021, patient thought he had eaten something that had burned his lip. On 18-APR-2021, the patient experienced bells palsy/face drooping. His "lip going numb" then "face started drooping". He went to the emergency room. The doctors proceeded with an MRI and "all sorts of bloodwork." Patient also had "leg started to have twitching" and then started to have excruciating headaches ", "back started hurting on around the 22nd or 23rd of April" and "his legs and feet were numb" and "just couldn't get his utensils", "body weakness and headaches." He went to a neurologist and had a nerve conducting study and "it looked like it was GBS and chronic inflammatory." On 27-MAY-2021, Guillen Barre syndrome was diagnosed. Treatment medications included: ibuprofen, gabapentin, sodium chloride, paracetamol, naproxen, and plasma infusions to help with GBS. At the neurologist, the patient had 5 treatments of plasma. He was having reactions with the infusion including "light headedness or headaches." He was given saline and the doctors told him to "stay hydrated and also was suggested acetaminophen and ibuprofen." He was also having "extreme weakness" with the plasma therapy. The neurologist was looking into the diagnosis and determined as it "is a reaction to the vaccine". The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of Guillen Barre syndrome was not reported. The patient recovered from Bells Palsy/face drooping on 23-APR-2021, and fever and chills on an unspecified date, and had not recovered from headaches/excruciating headaches. This report was serious (Other Medically Important Condition). This case, from the same reporter is linked to 20210726629.; Sender's Comments: V0: This spontaneous report received from a consumer concerns a 55 year old male, who was noted to have bell's palsy and diagnosed with Guillain-Barre syndrome (GBS) 32 and 71 days, respectively, after receiving the Janssen Covid-19 vaccine. Patient's height and weight were not reported. The patient's past medical/surgical history, concurrent conditions and concomitant medications were not reported. Information on smoking history, illicit drug use and alcohol abuse were not provided. Patient has drug allergy, unspecified. Patient had fever, chills and headache one day after receiving the vaccine. Thirty-two (32) days post vaccine, the patient's face started to droop and was noted to have bells palsy. He sought consult at the emergency room and was worked up on. No results provided. Patient started experiencing twitching of his legs, excruciating headaches and back pains. Later, his legs and feet started to get numb, described as not being able to get his utensils. His body started to get weak and he still was experiencing headaches. He went to a neurologist and had a nerve conducting study. Seventy-one (71) days after receiving the vaccine, patient was diagnosed with Guillain-Barre Syndrome (GBS). Treatment medications included: ibuprofen, gabapentin, sodium chloride, paracetamol, naproxen, and plasma infusions. Information regarding other potential etiologies was insufficient, and the occurrence of Bells Palsy and GBS could represent background incidence of such events in the general population. Considering the temporal relationship, the event is assessed to have an indeterminate relationship with vaccination.

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Date: 20210527; Test Name: Laboratory test; Result Unstructured Data: Guillen Barre Syndrome; Test Name: Blood test; Result Unstructured Data: not reported; Test Name: Nerve conduction studies; Result Unstructured Data: GBS and chronic inflammatory; Test Name: MRI; Result Unstructured Data: not reported
Aktuelle Erkrankungen: Drug allergy (Erythromycin, sulfa)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1415523

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: IN
Alter: 22,0
Geschlecht: F
Eingang: 21.06.2021
Impfdatum: 18.03.2021
Beginn: 18.03.2021
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 approximately 5 minutes after administration.

Weitere VAERSDATA-Felder

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

VAERS 1390015

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: CO
Alter: 34,0
Geschlecht: F
Eingang: 10.06.2021
Impfdatum: 10.06.2021
Beginn: 10.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hot flush Nausea Syncope

Symptomtext

Approx 5 min after administration of vaccine, patient was sitting in post vaccine waiting area when she fainted. Customers near the waiting area assisted her while alerting the pharmacist. She was regaining consciousness as I got to her side. Assisted her to chair, gave Gatorade and candy then later cold bottle of water. Patient stated she was having waves of "hot flashes and nausea" which remained constant over the next 30-45 minutes. She called her husband to drive her home. She left with him at approx. 7:15 pm.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none at this time, recommended seeking care if symptoms worsen
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: pt stated she had rash after mmr several years ago, did not indicate this on consent form.

VAERS 1377760

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: AL
Alter: 61,0
Geschlecht: F
Eingang: 07.06.2021
Impfdatum: 30.03.2021
Beginn: 18.05.2021
Tage bis Beginn: 49,0
Dosis: 1
Route/Site: IM / UN

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

Asthenia COVID-19 Chest X-ray abnormal Condition aggravated Cough Exposure to SARS-CoV-2 Lethargy Pneumonia Pyrexia Rhinorrhoea SARS-CoV-2 test positive Seizure Tremor Wheezing

Symptomtext

Patient presented to PCP on 05/18/2021 office from group home with C/O cough, runny nose, lethargic, fever, lungs rattling, uncontrollable shaking. Patient had a seizure the night before and had been having weak spells and coughing and fever since that time. Patient admitted to hospital on 05/18/2021 and chest Xray showed pneumonia. Patient tested for COVID-19 on 05/21/2021 after learning of potential exposure at group home and result was positive.

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Praegender Schweregrund: Seizure
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: Seizure disorder, Autism, T2DM, OA, chronic allergic rhinitis, peripheral neuropathy, GERD, urinary incontinence
Andere Medikamente: Aspirin, Tegretol XR, Colace, Estrace, Amaryl, Mobic, Glucophage, Mylicon, Prilosec, Dilantin, Lyrica, Topamax, Desyrel, Zyrtec, Breztri inhaler, Ayr nasal spray
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 1376504

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: ND
Alter: 69,0
Geschlecht: F
Eingang: 06.06.2021
Impfdatum: 10.03.2021
Beginn: 09.04.2021
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: UN / UN

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

Intensive care

Symptomtext

Case was hospitalized and admitted to the ICU

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Praegender Schweregrund: Intensive care
Hospital-Tage: 5,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: syncope, cardiovascular disease, Diabetes
Andere Medikamente: unknown
Allergien: Bee stings, tomatos
Vorherige Impfungen: -

VAERS 1369563

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: KY
Alter: 77,0
Geschlecht: M
Eingang: 02.06.2021
Impfdatum: 31.03.2021
Beginn: 25.05.2021
Tage bis Beginn: 55,0
Dosis: 1
Route/Site: SYR / UN

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

Deep vein thrombosis Peripheral swelling Ultrasound scan abnormal

Symptomtext

Swelling of left leg. Ultrasound left lower extremity (06/01/2021) showed extensive occlusive DVT. Started Xarelto on 06/01/2021. 15mg twice daily for 21 days. Appointment to see vascular surgeon on 06/04/2021.

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound left lower extremity (06/01/2021) showed extensive occlusive DVT. Started Xarelto on 06/01/2021. 15mg twice daily for 21 days. Appointment to see vascular surgeon on 06/04/2021.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Amlodipene
Allergien: None
Vorherige Impfungen: -

VAERS 1366787

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: AZ
Alter: -
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: -
Beginn: 21.05.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Abdominal pain Gastric disorder Pain in extremity Thrombosis

Symptomtext

BLOOD CLOT; BELLY BUTTON PAIN; LOWER LEG PAIN; STOMACH PROBLEMS; This spontaneous report received from a patient concerned a 57 year old white(Not Hispanic or Latino) female. The patient's height, and weight were not reported. No past medical history was reported. The patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025,expiry: UNKNOWN) dose was not reported, administered on 09-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 21-MAY-2021, the patient experienced stomach problems(pain, cramping, bloating). On an unspecified date, the patient experienced blood clot, belly button pain, and lower leg pain. The patient did not made any changes to diet and no new medications took since getting the vaccine. The patient had tried yogurt and probiotic. Treatment medications (dates unspecified) included: bismuth subsalicylate for unknown indication. On 28-May-2021, she started taking turmeric, but so far nothing had resolved the issues. The patient had a tele visit with family doctor of medicine and would go next week wednesday. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from blood clot, and lower leg pain, and had not recovered from stomach problems, and belly button pain. This report was serious (Other Medically Important Condition). This case, from the same reporter is linked to 20210556734.; Sender's Comments: V0 20210556510- COVID-19 VACCINE AD26.COV2.S- blood clot. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no known allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1261176

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: TN
Alter: 51,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 16.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: SYR / RA

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

Arterial thrombosis Fatigue Hypoaesthesia Lymphadenopathy Pain in extremity Cardiopulmonary exercise test Catheterisation cardiac Computerised tomogram Coronary artery disease Echocardiogram Electrocardiogram Microvascular coronary artery disease Swelling Thrombosis Ultrasound scan

Symptomtext

Both sides of my neck were very swollen. There was extreme pain on my right arm. The pain was severe and numbness in my finger. I went to the ER and they said I have radial thrombus, a clot in the radial artery. Before the shot, my heart was checked multiple times and I was fine. After the shot, my coronary arteries are now very small. There are now luminal changes inside my coronary arteries which are still now very small. I now have been diagnosed with CAD. I had a heart cath on March 29. My arm is still in a lot of pain. My neck is still swollen.

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Praegender Schweregrund: Arterial thrombosis
Hospital-Tage: -
Labordaten: CT Cardiopulmonary test Multiple EKG Ultrasound Transthoracic Echo cardiogram
Aktuelle Erkrankungen: -
Vorgeschichte: Autoimmune disease Asthma
Andere Medikamente: Prednisone
Allergien: Compazine Pork, citrus fruit, walnuts, melons, hazelnuts, and oranges
Vorherige Impfungen: -

VAERS 1261176

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: TN
Alter: 51,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 16.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 14,0
Dosis: UNK
Route/Site: - / -

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

Arterial thrombosis Fatigue Hypoaesthesia Lymphadenopathy Pain in extremity Cardiopulmonary exercise test Catheterisation cardiac Computerised tomogram Coronary artery disease Echocardiogram Electrocardiogram Microvascular coronary artery disease Swelling Thrombosis Ultrasound scan

Symptomtext

Both sides of my neck were very swollen. There was extreme pain on my right arm. The pain was severe and numbness in my finger. I went to the ER and they said I have radial thrombus, a clot in the radial artery. Before the shot, my heart was checked multiple times and I was fine. After the shot, my coronary arteries are now very small. There are now luminal changes inside my coronary arteries which are still now very small. I now have been diagnosed with CAD. I had a heart cath on March 29. My arm is still in a lot of pain. My neck is still swollen.

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Praegender Schweregrund: Arterial thrombosis
Hospital-Tage: -
Labordaten: CT Cardiopulmonary test Multiple EKG Ultrasound Transthoracic Echo cardiogram
Aktuelle Erkrankungen: -
Vorgeschichte: Autoimmune disease Asthma
Andere Medikamente: Prednisone
Allergien: Compazine Pork, citrus fruit, walnuts, melons, hazelnuts, and oranges
Vorherige Impfungen: -

VAERS 1337783

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: WI
Alter: 23,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 16.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chills Pain Syncope

Symptomtext

I woke up around 12:30 in the morning and felt achy. I fainted twice after getting out of bed. I experienced severe aches and body chills. I felt fine the day after better.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: I did not have any medical tests completed.
Aktuelle Erkrankungen: I did not have any other illnesses.
Vorgeschichte: I have anxiety and mild IBS.
Andere Medikamente: I was taking Zoloft and a norethindrone .35 mg.
Allergien: I am allergic to Penicillin.
Vorherige Impfungen: I experience being light headed after receiving the meningitis vaccine when I was 18 in 2015.

VAERS 1337051

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: TX
Alter: 51,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 19.03.2021
Beginn: 13.04.2021
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: IM / RA

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

Deep vein thrombosis Fibrin D dimer normal Full blood count normal Pain in extremity Ultrasound Doppler Ultrasound Doppler abnormal

Symptomtext

Patient has had chronic intermittent pain on her left lower leg for the past 5 years. However, she has noticed more pain on the left lower leg since having the COVID-19 Janssen vaccine on 3/19/2021. She is a chronic smoker. Thus, a left lower extremity arterial doppler was done on 5/20/2021 which incidentally revealed a DVT in the gastronemius vein of the left lower extremity. A subsequent bilateral US venous doppler of both lower extremities was done which revealed no DVT. Therefore, a repeat venous doppler of the left lower extremity was ordered for today, 5/21/2021, and remains pending at this time. Of note, patient was started on eliquis on 5/20/2021 (10 mg BID for the first 7 days with subsequent decrease to 5 mg BID thereafter). She will be referred to a hematologist for continued management.

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: CBC on 4/13/2021 revealed normal values for hemoglobin, hematocrit, white blood cells, and platelets. D-dimer on 4/13/2021 was noted to be 0.36 mcg/ml which is in the normal range. Left lower extremity arterial doppler done on 5/20/2021 revealed a DVT in the gastronemius vein. Bilateral lower extremity venous doppler done on 5/20/2021 revealed no evidence of DVT's bilaterally. A repeat venous doppler of the left lower extremity is ordered for 5/21/2021. Results are pending at this time.
Aktuelle Erkrankungen: none
Vorgeschichte: Hyperlipidemia Asthma: as a child, but not maintained on any medications as an adult; Gastroesophageal Reflux Disease: maintained on zantac prn; Type 2 Diabetes: dx'd in 2006; initially gestational DM. presently not on any medications. diet controlled at this time.; Allergies: allergy testing was done 2004; received immunotherapy in the past; stopped after less than a month secondary to anaphylaxis; Depression diagnosed in her 20's. now in full remission and maintained on lexapro daily
Andere Medikamente: Zantac 150 mg oral tablet [1 tab PO BID prn for GERD] Lexapro 20 mg oral tablet [Take 1 tablet(s) by mouth daily] Pravastatin 40 mg oral tablet [Take 1 tablet(s) by mouth at bedtime] traZODone 50 mg oral tablet [TAKE 1 TABLET BY MOUTH AT BE
Allergien: Penicillins: anaphylaxis Influenza Vaccine, Recombinant: anaphylaxis Lipitor: Myalgias (Adverse Reaction)
Vorherige Impfungen: A past influenza vaccine resulted in anaphylaxis. Age of patient at the time of the adverse event is unknown.

VAERS 1312664

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: IL
Alter: 59,0
Geschlecht: F
Eingang: 13.05.2021
Impfdatum: 14.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Asthenia Feeling hot Hyperhidrosis Hypersomnia Loss of consciousness

Symptomtext

10 minutes after receiving injection felt body heating up like blood was boiling, sweating eventually passed out. 8 weeks later still low energy levels and llengthy sleeping times

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Recently contacted physician for new patient appointment
Aktuelle Erkrankungen: Hashimotos. Elevated cholesterol
Vorgeschichte: Hashimotos. Elevated cholesterol
Andere Medikamente: Adderall 10 mg
Allergien: Pennecillin
Vorherige Impfungen: -

VAERS 1311195

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: FL
Alter: 18,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 12.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Loss of consciousness

Symptomtext

Pt received vaccine and sat down in observation and passed out after 3 mins in observation. Pt monitored for an additional 30 minutes then cleared by medical professional to go home with parent.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No PMHx
Vorgeschichte: None
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1309969

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

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Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 12.05.2021
Impfdatum: 13.03.2021
Beginn: 09.04.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / RA

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

Back pain Computerised tomogram head Guillain-Barre syndrome Immunoglobulin therapy Lumbar puncture abnormal Magnetic resonance imaging spinal abnormal Magnetic resonance imaging thoracic Muscular weakness Subacute inflammatory demyelinating polyneuropathy

Symptomtext

Acute Inflammatory Demyelinating Polyneuropathy/Guillain-Barre Syndrome, 6-day in-patient hospital admission, IVIG for 5 days, outcome undetermined as yet. Initial symptoms include severe low back pain for a week followed by bilateral leg weakness and ascending paralysis.

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Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 6,0
Labordaten: Spinal tap, lumbar MRI, Thoracic MRI, Brain CT Scan, numerous neurological clinical exams, other?
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin daily
Allergien: None
Vorherige Impfungen: -

VAERS 1229878

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: WA
Alter: 58,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: -
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / RA

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

Carotid artery dissection Carotid artery occlusion Cerebral artery occlusion Embolic stroke Physical examination Syncope Thrombosis

Symptomtext

BLOOD CLOT; COLLAPSED; This spontaneous report received from a consumer concerned a 58 year old white and Not Hispanic or Latino male. The patient's height, and weight were not reported. The patient's had perfect health in NOV-2020 or DEC-2020. The patient was a teenage runner in terms of heart condition. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, expiry: UNKNOWN) dose was not reported, 1 total, administered on 19-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 01-APR-2021, the patient was hundred percent fine but then he collapsed and was taken to the hospital. He was diagnosed with a blood clot and immediately surgery was attempted to break the clot. But, the patient died subsequently. The cause of death was blood clot. It was unknown if autopsy was performed. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the collapsed was not reported. This report was serious (Death, and Other Medically Important Condition).; Sender's Comments: V0: 20210506470-JANSSEN COVID-19 VACCINE Ad26.COV2.S- Blood clot, Collapsed. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).; Reported Cause(s) of Death: BLOOD CLOT

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Praegender Schweregrund: Embolic stroke
Hospital-Tage: -
Labordaten: Test Date: 2020; Test Name: Physical examination; Result Unstructured Data: In perfect health as Heart of a teenage runner
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1229878

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: WA
Alter: 58,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: -
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / -

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

Carotid artery dissection Carotid artery occlusion Cerebral artery occlusion Embolic stroke Physical examination Syncope Thrombosis

Symptomtext

BLOOD CLOT; COLLAPSED; This spontaneous report received from a consumer concerned a 58 year old white and Not Hispanic or Latino male. The patient's height, and weight were not reported. The patient's had perfect health in NOV-2020 or DEC-2020. The patient was a teenage runner in terms of heart condition. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, expiry: UNKNOWN) dose was not reported, 1 total, administered on 19-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 01-APR-2021, the patient was hundred percent fine but then he collapsed and was taken to the hospital. He was diagnosed with a blood clot and immediately surgery was attempted to break the clot. But, the patient died subsequently. The cause of death was blood clot. It was unknown if autopsy was performed. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the collapsed was not reported. This report was serious (Death, and Other Medically Important Condition).; Sender's Comments: V0: 20210506470-JANSSEN COVID-19 VACCINE Ad26.COV2.S- Blood clot, Collapsed. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).; Reported Cause(s) of Death: BLOOD CLOT

Weitere VAERSDATA-Felder

Praegender Schweregrund: Embolic stroke
Hospital-Tage: -
Labordaten: Test Date: 2020; Test Name: Physical examination; Result Unstructured Data: In perfect health as Heart of a teenage runner
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1229878

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: WA
Alter: 58,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: -
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Carotid artery dissection Carotid artery occlusion Cerebral artery occlusion Embolic stroke Physical examination Syncope Thrombosis

Symptomtext

BLOOD CLOT; COLLAPSED; This spontaneous report received from a consumer concerned a 58 year old white and Not Hispanic or Latino male. The patient's height, and weight were not reported. The patient's had perfect health in NOV-2020 or DEC-2020. The patient was a teenage runner in terms of heart condition. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, expiry: UNKNOWN) dose was not reported, 1 total, administered on 19-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 01-APR-2021, the patient was hundred percent fine but then he collapsed and was taken to the hospital. He was diagnosed with a blood clot and immediately surgery was attempted to break the clot. But, the patient died subsequently. The cause of death was blood clot. It was unknown if autopsy was performed. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the collapsed was not reported. This report was serious (Death, and Other Medically Important Condition).; Sender's Comments: V0: 20210506470-JANSSEN COVID-19 VACCINE Ad26.COV2.S- Blood clot, Collapsed. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).; Reported Cause(s) of Death: BLOOD CLOT

Weitere VAERSDATA-Felder

Praegender Schweregrund: Embolic stroke
Hospital-Tage: -
Labordaten: Test Date: 2020; Test Name: Physical examination; Result Unstructured Data: In perfect health as Heart of a teenage runner
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1309770

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: AL
Alter: -
Geschlecht: M
Eingang: 11.05.2021
Impfdatum: 18.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / LA

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

Oedema peripheral Pain in extremity Thrombosis Ultrasound Doppler abnormal

Symptomtext

On 4/15/21 came into office with bilateral edema in both lower legs as well as pain x 2 weeks. sent for doppler- Diagnosed with occlusive thrombus in R lower leg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Venous doppler on 4/15/21 showing occlusive thrombus R lower leg
Aktuelle Erkrankungen: none
Vorgeschichte: Hyperlipidemia, hypertension, sleep apnea, Hypogonadism
Andere Medikamente: Dyazide 37.5 mg-25 mg capsule; lisinopril 20 mg-hydrochlorothiazide 12.5 mg tablet; metformin 500 mg tablet; pseudoephedrine-guaifenesin ER 60 mg-600 mg tablet, extend release 12hr; sertraline 100 mg tablet; Tamsulosin 0.4 mg capsule; testo
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1275502

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: PA
Alter: 28,0
Geschlecht: F
Eingang: 30.04.2021
Impfdatum: 07.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Dizziness No adverse event Syncope

Symptomtext

Hours after receiving the vaccine, I became dizzy, and nearly fainted several times. This was resolved once j was able to lay down and elevated my legs. I had no adverse effects in the first 15 minutes after the vaccine, the fainting spells were several hours after I was vaccinated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tylenol, 500mg
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1240651

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TN
Alter: 62,0
Geschlecht: M
Eingang: 28.04.2021
Impfdatum: 12.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: SYR / RA

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

Arthralgia Back pain Catheterisation cardiac abnormal Computerised tomogram Coronary arterial stent insertion Delirium Guillain-Barre syndrome Hallucination Impaired self-care Magnetic resonance imaging Lumbar puncture Pain in extremity Paralysis

Symptomtext

Guillain Barre Syndrome final diagnosis. 4 weeks in hospital first week after vaccine severe pain in legs, back and shoulders. Took 7 days to diagnose. During that time he was waiting diagnosis he had several MRI?s Ct scans etc. Heart cath requiring a stint. Delirium and Hallucinations . Now he is totally dependent on everyone to take care of him. Paralyzed from neck down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 40,0
Labordaten: Everyday starting from 3/21/2021
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 diabetes
Andere Medikamente: Insulin for type 2 diabetes.
Allergien: None known
Vorherige Impfungen: -

VAERS 1240651

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TN
Alter: 62,0
Geschlecht: M
Eingang: 28.04.2021
Impfdatum: 12.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 7,0
Dosis: UNK
Route/Site: - / -

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

Arthralgia Back pain Catheterisation cardiac abnormal Computerised tomogram Coronary arterial stent insertion Delirium Guillain-Barre syndrome Hallucination Impaired self-care Magnetic resonance imaging Lumbar puncture Pain in extremity Paralysis

Symptomtext

Guillain Barre Syndrome final diagnosis. 4 weeks in hospital first week after vaccine severe pain in legs, back and shoulders. Took 7 days to diagnose. During that time he was waiting diagnosis he had several MRI?s Ct scans etc. Heart cath requiring a stint. Delirium and Hallucinations . Now he is totally dependent on everyone to take care of him. Paralyzed from neck down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 40,0
Labordaten: Everyday starting from 3/21/2021
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 diabetes
Andere Medikamente: Insulin for type 2 diabetes.
Allergien: None known
Vorherige Impfungen: -

VAERS 1263525

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 62,0
Geschlecht: M
Eingang: 27.04.2021
Impfdatum: 30.03.2021
Beginn: 16.04.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / RA

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

Blood test Pain in extremity Platelet count Thrombosis Ultrasound scan

Symptomtext

Left leg pain started about 4/16/21. Reports evaluated by nurse practitioner at the medical office of primary care provider on 4/23/21. Ultrasound ordered a hospital and diagnosed with a blood clot in the left leg on 4/23/2021. Placed on a "blood thinner" to take orally BID for one month then once daily for undetermined duration. States MD is not considering the vaccination as the reason for the blood clot because of the duration of time between when the vaccine was given and the onset of the blood clot. When asked, pt reports a platelet count was done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultrasound and blood test.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1262540

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: VA
Alter: 55,0
Geschlecht: F
Eingang: 27.04.2021
Impfdatum: 07.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Eye swelling Gait disturbance Headache Ocular discomfort Thrombosis

Symptomtext

blood clot in my left eye, swelling of the eye and under the eye. headaches at the base of my skull so bad nothing helped. Joint pain so bad I couldn't walk for 2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Psoriasis
Andere Medikamente: Zoloft, Otezla, allergy pill, ginko biloba; Cholest-off; Vit D
Allergien: Sulfur drugs, azo standard, bee stings, honey
Vorherige Impfungen: -

VAERS 1262422

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TX
Alter: 94,0
Geschlecht: F
Eingang: 27.04.2021
Impfdatum: 16.03.2021
Beginn: 26.04.2021
Tage bis Beginn: 41,0
Dosis: UNK
Route/Site: IM / RA

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

Back pain Pain in extremity Thrombosis

Symptomtext

RESIDENT COMPAINED OF PAIN TO BILATERAL THIGHS AND LOWER BACK SENT TO ER. NOTIFIED BY ER, PATIENT HAS BLOOD CLOTS IN ABDOMIN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 1,0
Labordaten: UNKNOWN
Aktuelle Erkrankungen: NONE
Vorgeschichte: E03.9 HYPOTHYROIDISM, UNSPECIFIED 3/25/2019 Present on Move-in 9/12/2019 update F03.90 UNSPECIFIED DEMENTIA WITHOUT BEHAVIORAL DISTURBANCE 3/25/2019 Present on Move-in 9/12/2019 update Z91.81 HISTORY OF FALLING 3/25/2019 9/12/2019 update M62.81 MUSCLE WEAKNESS (GENERALIZED) 3/25/2019 Present on Move-in 9/12/2019 update H54.0 BLINDNESS, BOTH EYES 3/25/2019 5/15/2020 update M84.459A PATHOLOGICAL FRACTURE, HIP, UNSPECIFIED, INITIAL ENCOUNTER FOR FRACTURE 3/25/2019 5/21/2020 update F05 DELIRIUM DUE TO KNOWN PHYSIOLOGICAL CONDITION 3/25/2019 5/21/2020 update M19.90 UNSPECIFIED OSTEOARTHRITIS, UNSPECIFIED SITE 3/25/2019 5/21/2020 update S72.352D DISPLACED COMMINUTED FRACTURE OF SHAFT OF LEFT FEMUR, SUBSEQUENT ENCOUNTER FOR CLOSED FRACTURE WITH ROUTINE HEALING
Andere Medikamente: ASPIRIN 81MG TAB CHEW TAB CHEW 1 TABLET(S) EVERY DAY BY ORAL ROUTE(Indications for Use: heart health) Pharmacy Active 12/18/2020 09:00 3/27/2021 There is a black box warning associated with this order. Please click to view details. FUROS
Allergien: nka
Vorherige Impfungen: -

VAERS 1261180

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 32,0
Geschlecht: F
Eingang: 27.04.2021
Impfdatum: -
Beginn: 12.04.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Chills Decreased appetite Dizziness Headache Nausea Neck pain Pain Syncope Vomiting

Symptomtext

SYNCOPE EPISODE; NECK PAIN; LOSS OF APPETITE; BODY ACHE; DIZZINESS; VOMITING; CHILLS; HEADACHE; NAUSEA; This spontaneous report received from a health care professional concerned a 32 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included penicillin allergy, hepatitis C, HIV, opioid dependence, polysubstance abuse, and depression. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025, and expiry: UNKNOWN) dose was not reported, administered on 12-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 12-APR-2021 about one hour after the vaccination, the patient experienced neck pain, loss of appetite, body ache, dizziness, vomiting, chills, headache, and nausea. On 13-APR-2021, the patient experienced syncope episode and other symptoms got worsened. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from syncope episode, chills, neck pain, loss of appetite, headache, nausea, vomiting, body ache, and dizziness. This report was serious (Other Medically Important Condition). This case, from the same reporter is linked.; Sender's Comments: V0- covid-19 vaccine ad26.cov2.s-syncope. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: MEDICAL HISTORY, UNDERLYING DISEASE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Dependence on opiates; Depression; Hepatitis C; HIV infection; Penicillin allergy; Polysubstance abuse
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1256511

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: WI
Alter: 57,0
Geschlecht: F
Eingang: 25.04.2021
Impfdatum: 19.03.2021
Beginn: 02.04.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Peripheral swelling Skin warm Thrombosis Ultrasound scan

Symptomtext

Left lower medial aspect swelling , warmth and thrombosis noted. Placed on Naproxen 500mg BID Compression stockings Heat and Cold compresses

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultrasound done on 4/6/21 negative for DVT Scheduled to get more testing on 5/5/21 and see vascular surgeon
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: omeprazole, zinc, vit d
Allergien: -
Vorherige Impfungen: -

VAERS 1252210

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TX
Alter: -
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: -
Beginn: 10.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Fatigue Myalgia Nausea Presyncope Vertigo

Symptomtext

VERTIGO BUT NOT DIZZINESS; WHEN LEANS OVER ALMOST FAINT; INCREASED JOINT MUSCLE PAIN (HAS ARTHRITIS); TIREDNESS; SLIGHT NAUSEA; This spontaneous report received from a patient concerned a female of unspecified age. The patient's height, and weight were not reported. The patient's concurrent conditions included arthritis, and other pre-existing medical conditions included the patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 09-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 10-MAR-2021, the subject experienced vertigo but not dizziness. On 10-MAR-2021, the subject experienced when leans over almost faint. On 10-MAR-2021, the subject experienced increased joint muscle pain (has arthritis). On 10-MAR-2021, the subject experienced tiredness. On 10-MAR-2021, the subject experienced slight nausea. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from vertigo but not dizziness, when leans over almost faint, tiredness, slight nausea, and increased joint muscle pain (has arthritis). This report was non-serious.; Sender's Comments: MAC not required per standard procedure as the case assessed as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Arthritis
Vorgeschichte: Comments: The patient had no known allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1246863

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: IL
Alter: 62,0
Geschlecht: F
Eingang: 23.04.2021
Impfdatum: 24.03.2021
Beginn: 02.04.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: SYR / UN

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

Dyspnoea Pulmonary thrombosis

Symptomtext

Shortness of breath, blood clot in lungs

Weitere VAERSDATA-Felder

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

VAERS 1242694

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 51,0
Geschlecht: F
Eingang: 22.04.2021
Impfdatum: 08.03.2021
Beginn: 19.04.2021
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest X-ray Computerised tomogram Gait disturbance Hypoaesthesia Impaired driving ability Lacunar infarction Magnetic resonance imaging head abnormal Scan with contrast Thrombosis Ultrasound scan

Symptomtext

03/19/21 woke up with numbness on whole right side of body (head to toe). Referred to ER by Family Physician on 03/20/21. admitted to hospital for testing. MRI confirmed a blood clot caused a Lacuna Infarcts Event (type of mini stroke) The patient continues to have numbness and difficulty walking, driving and has affected her normal daily activities. The patient will be required to start Plavix and baby aspirin. Waiting for requirement for Prolong numbness which affects her daily activity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 2,0
Labordaten: Chest Xray 03/20/21 CT scan with and without contrast 03/20/21 MRI with and without contrast 03/20/21 Echo with and without Bubble test 03/21/21 Cholesterol panel 03/21/21 Misc Blood work-specific test unknown
Aktuelle Erkrankungen: UVitis - Retasert Implant Colon Rectal Cancer - Surgically removed no treatment or prescription required
Vorgeschichte: Hypertension - no issues with daily Medication
Andere Medikamente: Lisinapril 10mg daily Montelukast 10mg daily Timolol Maleate 1 drop both eyes 2 times per day Venlafaxine 75mg daily Vitamin D3 25mcg daily Biotin 10,000mcg
Allergien: MRI dye
Vorherige Impfungen: -

VAERS 1239782

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: IL
Alter: 60,0
Geschlecht: M
Eingang: 21.04.2021
Impfdatum: 10.03.2021
Beginn: 13.04.2021
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Cardiac ventricular thrombosis Catheter directed thrombolysis Chest pain Dizziness Dyspnoea Headache Impaired work ability Intensive care Middle ear effusion SARS-CoV-2 test negative Sinusitis

Symptomtext

Tues 4/13/21- Headache and dizziness started about 4p. Wed 4/14/21- Could not go to work because of headache and dizziness. Made appt for 4/15 at 6:45a with Dr Thur 4.15/21- Awoke with intense headache and dizziness. Ready to go to appt but emergency room called at 6:37 to switch to a Virtual appt. I never received a call so I walked to the office. They told me they would not see me as I had Covid 19 symptoms. Went to airport and received a Negative Covid test. Went o Clinic and was diagnosed with fluid in the ears and a sinus infection. Went to work and only stayed 2 hours. Drove myself to the emergency room with weakness, shortness of breath and intense pain under the sternum. Diagnosed with a blood clot in the right ventricle. The cardiac cath lab removed it. Was in intensive care Thur-Sat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac ventricular thrombosis
Hospital-Tage: 3,0
Labordaten: 4/15/21 to 4/17/21 - see Hospital records.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Atorvastatin, levothyroxine, meloxicam; Vitamins A, B, C, D & E. Fish Oil, CoQ10, Turmaric, Osteo Bi-Flex
Allergien: none
Vorherige Impfungen: -

VAERS 1233450

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: MS
Alter: 50,0
Geschlecht: M
Eingang: 20.04.2021
Impfdatum: 19.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: SYR / LA

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

Back pain Pain in extremity Peripheral swelling Thrombosis

Symptomtext

A week and a half after taking the Janssen COVID shot I had a knot and pain come up in my lower back. After going to the chiropractor two times the knot and pain ended up in my right leg. I then went to Urgent Care where they diagnosed me with a large blood clot. They sent me to imaging and after scanning the area confirmed that there was a blood clot in my right leg. Urgent Care then set me up with a specialist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Imaging Thursday April 15, 2021, Urgent Care Thursday April 15, 2021.
Aktuelle Erkrankungen: none
Vorgeschichte: Pre-diabetic
Andere Medikamente: Flomax, Metformin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1233121

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: MN
Alter: 58,0
Geschlecht: M
Eingang: 20.04.2021
Impfdatum: 12.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain Computerised tomogram abnormal Laboratory test Thrombosis

Symptomtext

Received shot on 3/12. Starting having pain in chest on 3/22. Was diagnosed with blood clots in the lungs on 3/26 via blood test and CT scan.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Multiple blood test and CT scan ran on 3/26 identified blood clots in my lungs
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1231210

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: IN
Alter: 57,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 12.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Electrocardiogram Pain in extremity Palpitations Thrombosis Ultrasound scan

Symptomtext

I received the vaccine on 3-12-21 and woke up 3-15-21 with pain in the bottom of my left foot. I scheduled an apt with my PCP on 3-16-21. My PCP scheduled an ultrasound on 3-24-21 where the nurse discovered blood clots in my lower left leg. I started taking Eloquis later that afternoon. I then had an apt with a blood dr. on 4-9-21 where she drew blood for tests. I was experiencing my heart racing and she scheduled me an apt with a cardiologist on 4-13-21 where the cardiologist suspected that the clots had moved into my lungs. The cardiologist did an EKG on the same day. I have a heart echo scheduled for 5-7-21. I am experiencing side effects from Eloquis so 4-19-21 I switched to Xeralto.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultrasound 3-24-21; Blood Draw 4-9-21 ; EKG 4-13-21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1230134

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: DC
Alter: 44,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 28.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / -

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

Chest X-ray abnormal Chest pain Computerised tomogram thorax abnormal Dyspnoea Echocardiogram Thrombosis

Symptomtext

Started to feel chest pain and shortness of breath 3 days after the vaccine. Ended up in the hospital 5 days after the vaccine and diagnosed with blot clots in the lungs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 1,0
Labordaten: xray ct scan ekg ultra sound of heart
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Reclipsen birth control and symbicort
Allergien: -
Vorherige Impfungen: -

VAERS 1228668

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 17.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test abnormal Embolic stroke Headache Scan brain Thrombosis Urinary incontinence Vomiting

Symptomtext

My symptoms i had sever headache! Once April 1st Hit! Thats Was the day I Had a Heart stroke at store, i don?t remember anything and once i woke up i was at the hospital, and they told me that i had a heart stroke because i had lots of blood clots in my body. And they told me i vomit and peed myself durong the whole situation i went in store

Weitere VAERSDATA-Felder

Praegender Schweregrund: Embolic stroke
Hospital-Tage: 3,0
Labordaten: Hospital did everything even scans of my head and nothing. The only thing they told me was blood clots and also loww Blood count. !! Never ever in my life had that!
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Yodo
Vorherige Impfungen: Janssen

VAERS 1225799

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 53,0
Geschlecht: F
Eingang: 18.04.2021
Impfdatum: 03.04.2021
Beginn: 11.04.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / RA

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

Computerised tomogram Thrombosis Ultrasound scan vagina Urine analysis Vaginal haemorrhage

Symptomtext

4/11/2021 830PM I NOTICED MOISTURE IN MY UNDERWEAR. WENT INTO BATHROOM , PANTIES BLOODIED, BRIGHT RED AND A QUARTER SIZED CLOT WAS INTHE TOILET. I SUFFERED NO PAIN. HOWEVER I HAD A TOTAL HYSTERECTOMY IN 1997, AND SHOULD NOT HAVE ANY BLEEDING WHATSO EVER. TOOK A SHOWER, ADVISED MY HUSBAND OF THE INCIDENT. WENT TO BED , 230AM 4/12/2021 SAME THING HAPPENS, ONLY NOW I AM WIPING BRIGHT RED BLOOD AND I FELT A LARGER SIZED CLOT LEAVE MY BODY. I WENT TO THE ER IMMEDIATELY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: 4/12/2021 3A PRESENTED TO ER DEPT...VAGINAL EXAM CONFIRMS BLEEDING BUT COULD NOT DETERMINE IT'S SOURCE. ALSO UNDERWENT VAGINAL ULTRASOUND AND PELVIC CT SCAN W/ CONTRAST. NEITHER EXAM COULD GIVE REASON FOR THE BLEEDING. LABS WERE ALSO TAKEN, BUT UNDISCOVERABLE. I WAS LATER RELEASED AND ASK TO FOLLOW UP WITH PRIMARY CARE / GYN. 4/16/2021 SAW MY PRIMARY. SHE DID URINALYSIS AND RECTAL EXAM , BOTH NORMAL. NO EVIDENCE OF BLADDER OR RECTAL BLEED. I ADVISED PCP OF THE RECENT DATA OF THE J &J VACCINATION...WHICH WAS DISCOVERED AFTER MY ER VISIT.
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: TYLENOL IBUPROFEN
Allergien: NONE
Vorherige Impfungen: -

VAERS 1222534

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 61,0
Geschlecht: F
Eingang: 17.04.2021
Impfdatum: 10.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: - / RA

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

Anxiety Aphasia Brain scan normal Echocardiogram normal Fatigue Feeling abnormal Gait inability Laboratory test normal Loss of consciousness Memory impairment Speech disorder Tinnitus Transient ischaemic attack Ulcer Vertigo Visual impairment

Symptomtext

Presented as a TIA (mini stroke) Had vision issues, difficulty speaking, vertigo, could not walk, passed out and taken to hospital by ambulance . Began at around 10am. Felt like I was dying. Placed on Stroke Unit. Scans and tests all negative for stroke and Drs. thought could be panic attack or TIA. Since then my lingering effects point to TIA, Seemed to clear up around 2pm with gradual improvement through the day. Still experiencing some side effects including tinnitus, memory and word retrieval issues, fatigue, anxiety. DO NOT HAVE PANIC ATTACKS. The only time I have had a panic attack was at 26 after the death of my mother.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 1,0
Labordaten: Brain scan, heart echo, loads of labs, all day of event. I am basically recovered...yet performing at about 75% of normal activity. Struggling with multi tasking, memory, etc.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Basic daily vitamins including vitamin C, D, Zinc and Host Defense Stamets 7
Allergien: Sulpha Drugs
Vorherige Impfungen: NO...but I have a son who had a severe reaction to an MMR that was reported in the late 90s. Just thought that was worth mention

VAERS 1219538

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TN
Alter: 56,0
Geschlecht: F
Eingang: 16.04.2021
Impfdatum: 20.03.2021
Beginn: 10.04.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / UN

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

Bell's palsy Computerised tomogram Magnetic resonance imaging

Symptomtext

Bells palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: 2,0
Labordaten: MRI, CT scan
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1216273

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 180 50 25

schwer

Staat: TX
Alter: 42,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 06.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Feeling cold Migraine Muscle spasms Pruritus Rash Seizure Tremor

Symptomtext

Muscle Seizures 5-6 hours post vaccine. Full body muscle spasms/seizures that lasted 5-6 hours. Ice cold extremities. Violent shakes. Migraines over the course of the following 4 days and a itchy rash over my face, neck and torso that lasted a full 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Spherocytosis
Andere Medikamente: Probiotic, folate, vitamin d, NAC, Beta TCP
Allergien: Iodine
Vorherige Impfungen: -

VAERS 1216189

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: CA
Alter: 78,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 01.04.2021
Beginn: 02.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Back pain Brain natriuretic peptide increased Echocardiogram abnormal Emphysema Gait inability Haemoglobin decreased Heart rate increased Hypoxia Intracardiac thrombus Leukocytosis Lumbar vertebral fracture Peripheral artery thrombosis Platelet count decreased Procalcitonin normal Pulmonary hypertension Thrombosis prophylaxis Tricuspid valve incompetence Troponin increased

Symptomtext

78 year old woman admitted with severe back pain, inability to ambulate and leukocytosis on 3/31/21. History of hypertension, CHF, obesity, chronic kidney disease, and back pain. Work up included multiple consults. The patient was placed on SQ heparin for VTE prophylaxis. Acute L5 fracture was found along with emphysematous changes. Neurosurgical evaluation- no surgery was necessary. During the first 24 hours (before receiving the vaccine), the patient's Hg dropped 9.3 to 6.8 and platelets dropped 130K to 61 K with no apparent bleeding source. PRBC transfusion was given. GI consult was obtained the patient was scheduled to have EGD the following morning (day 3). Cardiology was obtained for elevated troponin and hypoxia. An echo obtained on day 2 showed moderate elevated pulmonary artery pressure, mild to moderate tricuspid regurgitation, and normal sized right atrium and ventricle. The patient received the Janssen vaccine upon request the morning of hospital day 2 (4.1.21 at 11:02). At 11:37PM on 4/1/21 the patient received 5mg IV metoprolol for elevated HR of 132 (BP 129/67). At 0128 on 4/2/21 the patient's heart rate dropped into the 60's and then declined further requiring cardiac resuscitation. The attempt was unsuccessful and the patient expired at 01:43 on 4/2/21. An autopsy was conducted (results available on 4/13/21) showed a 4 cm clot in the patient's right atrium and a mural thrombus in her femoral artery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Peripheral artery thrombosis
Hospital-Tage: 3,0
Labordaten: Hg dropped from 9.3 on admission to 6.8 and subsequently 6.4 with no apparent bleeding source. Platelets dropped from 130K to 61K to 59K. WBC on admission was 22.9; troponin rose on day 2 from 0.067 to 0.174. Procalcitonin 0.95 on admission increased to 1.40 on day 2. BNP on day 2 was 157.
Aktuelle Erkrankungen: To ED with acute back pain, constipation, recent root canal, had received tramadol and Medrol dosepak at Urgent Care
Vorgeschichte: Hypertension, congestive heart failure, obesity, back pain, chronic kidney disease not requiring dialysis
Andere Medikamente: Prednisone, Metoprolol, amlodipine, furosemide
Allergien: Penicillin, Sulfa
Vorherige Impfungen: -

VAERS 1214440

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 16.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: SYR / LA

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

Disorientation Dizziness Facial spasm Headache Loss of consciousness Muscle twitching Nausea Pain Vomiting projectile

Symptomtext

experienced a sudden pain to the forehead. Pain increased from 0-100 very rapidly, I became very nauseated to the point of having projectile vomit. Experienced blackout segments. Took 1 dose of 100mg Sumatriptan at about 930pm and tried to sleep w/the immense pain. Took 2nd dose at about 12am. Pain did not dissipate but fell asleep. When i woke up pain was gone but felt very sore, dizzy and disoriented. Fast forward to April 9th while laughing uncontrollably the right side of my face spasmed/cramped closing my right eye and contracting my right cheek as if having Bell's Palsy. I have never experienced this before. Face did not continue to droop but has left a tick/twitch sensation under my right eye.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: NONE. I have an MRI scheduled for 04212021
Aktuelle Erkrankungen: week before had been to the DR with pain and was prescribed prednisone
Vorgeschichte: migraines
Andere Medikamente: Aimovig (monthly), Amitiptyline, Sumatriptan
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1213007

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 69,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 28.03.2021
Beginn: 12.04.2021
Tage bis Beginn: 15,0
Dosis: UNK
Route/Site: - / -

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

Deep vein thrombosis Ultrasound Doppler abnormal

Symptomtext

DVT of left popliteal vein per Venous US 4/14/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Venous Ultrasound 4/14/21
Aktuelle Erkrankungen: COPD s/p Covid Hypertension CKD
Vorgeschichte: COPD s/p Covid Hypertension CKD
Andere Medikamente: Nifedipine ER 30 Trelegy Montelukast Albuterol HFA Albuterol via neb
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1209678

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: NJ
Alter: 29,0
Geschlecht: F
Eingang: 14.04.2021
Impfdatum: 10.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Gaze palsy Nausea Pain Pyrexia Syncope Vomiting

Symptomtext

Nausea, vomiting, fever, dizziness, headache, body ache, fainting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: -
Allergien: Amoxicillin, penicillin, tetracycline, eurethamiacin, Mango, papaya, kiwi, apples
Vorherige Impfungen: -

VAERS 1209248

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: OH
Alter: 41,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 06.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Electrocardiogram Fatigue Hypersomnia Road traffic accident Syncope

Symptomtext

I received the dose at 5:35am on 3/6/21 went home slept most of the day woke up and felt tired, 8:00pm on 3/6/21 I left for work drove a few miles up the road and fainted and crashed my vehicle.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Ekg and blood work completed
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes
Andere Medikamente: Humalog/ synjardy/ fluxtine
Allergien: None
Vorherige Impfungen: -

VAERS 1208372

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: CO
Alter: 41,0
Geschlecht: F
Eingang: 14.04.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Syncope

Symptomtext

Approximately 5 minutes after receiving the shot, got light headed and fainted

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: seasonal allergies
Vorgeschichte: none
Andere Medikamente: allergy medicine
Allergien: seasonal allergies
Vorherige Impfungen: -

VAERS 1208222

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 22.03.2021
Beginn: 12.04.2021
Tage bis Beginn: 21,0
Dosis: UNK
Route/Site: IM / LA

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

Diverticular perforation Intensive care Mechanical ventilation Surgery Unresponsive to stimuli

Symptomtext

Per res. being taken to surgery for a perforated diverticulum. ICU, resident had made it through surgery, resident is off the vent, not really responsive at this time and will be keeping a close eye on him.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: BENIGN NEOPLASM OF COLON, ACUTE CYSTITIS WITHOUT HEMATURIA, UNSPECIFIED DEMENTIA WITHOUT BEHAVIORAL DISTURBANCE, PERSONAL HISTORY OF TRAUMATIC BRAIN INJURY, IDIOPATHIC ASEPTIC NECROSIS OF RIGHT FEMUR, CHRONIC OBSTRUCTIVE PULMONARY DISEASE, ATHEROSCLEROTIC HEART DISEASE OF NATIVE CORONARY ARTERY WITHOUT ANGINA PECTORIS, BENIGN PROSTATIC HYPERPLASIA WITH LOWER URINARY TRACT SYMPTOMS, PERIPHERAL VASCULAR DISEASE, RETENTION OF URINE, ALCOHOL DEPENDENCE, PRESENCE OF UROGENITAL IMPLANTS, ALLERGIC RHINITIS, UNSPECIFIED, OBESITY, ACUTE PYELONEPHRITIS, ALCOHOLIC POLYNEUROPATHY, SPONDYLOSIS WITHOUT MYELOPATHY OR RADICULOPATHY, CERVICAL REGION, INSOMNIA, MIXED HYPERLIPIDEMIA, DISORDER OF ARTERIES AND ARTERIOLES, ALCOHOLIC HEPATITIS WITHOUT ASCITES, IDIOPATHIC ASEPTIC NECROSIS OF LEFT FEMUR, PREDIABETES, ELEVATED PROSTATE SPECIFIC ANTIGEN [PSA]
Andere Medikamente: Aspirin, B complex, Donepezil, escltalopram, Fish oil, Flonsae, duoneb, maalox, melatonin, metoprolol, plavix, resveratrol, rosuvastatin, multivit w/ minerals, flowmax, tylenol.
Allergien: Simvastatin, Penicillins
Vorherige Impfungen: -

VAERS 1203985

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 24.03.2021
Beginn: 03.04.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: SYR / LA

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

Erythema Pain in extremity Peripheral swelling Phlebitis Thrombosis Ultrasound scan abnormal

Symptomtext

Pain, reddness, swelling in right leg, below the knee, when I got up in the morning. Symptoms continued over the weekend. Called Dr. on Monday, April 5, 2021 and got an appointment for the following day. Dr. diagnosed it as phlibitis and sent me for an ultr sound. Prescribed Xarelto 15 mg twice a day for 21 days, then decrease to 20 mg daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultra sound confirmed blood clots
Aktuelle Erkrankungen: None
Vorgeschichte: pollen allergies causes nasal drip and slight asthma
Andere Medikamente: Rosuvastatin 10 mg every other day, D3 2000IU daily, Calcium 750 mg daily
Allergien: Tetenus
Vorherige Impfungen: Tetenus at age 10 caused anaphyllaxis // Shringrex 8-1-2018 high fever, dizzy, heart palpitations

VAERS 1202017

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: AL
Alter: 57,0
Geschlecht: M
Eingang: 13.04.2021
Impfdatum: 09.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / RA

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

Blood test Computerised tomogram head normal Dysphagia Echocardiogram normal Facial paralysis Hypoaesthesia Magnetic resonance imaging head normal Scan with contrast normal Speech disorder Transient ischaemic attack

Symptomtext

Received vaccine on 3/9/21. Started experiencing facial numbness , difficulty with speech and swallowing on 3/16/21 around 11pm. Had facial drooping of the mouth and eye on my left side of face. Went to Hospital ER around 5:30 am on 3/17/21 as symptoms did not subside. I was later placed in stroke observation unit. I had 2 MRI's, CT scan and Echo tests ran. i was diagnosed with TIA. All test were negative for a cause. I sent a total of about 26 hours hospitalized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 2,0
Labordaten: 2 MRI's with and w/o contrast. Ct scan with contrast and Echo scan with bubble test...as well as complete blood workup.. All test performed on 3/17/21.
Aktuelle Erkrankungen: POSSIBLE PROSTATITIS
Vorgeschichte: CONTROLLED HYPERTENSION
Andere Medikamente: LISINOPRIL/HCTZ 20/12.5MG, FAMOTIDINE 40MG
Allergien: NO KNOWN DRUG ALLEGERIES
Vorherige Impfungen: -

VAERS 1201645

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: AR
Alter: 69,0
Geschlecht: M
Eingang: 13.04.2021
Impfdatum: 09.03.2021
Beginn: 02.04.2021
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: IM / RA

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

Blindness unilateral Computerised tomogram Ischaemic stroke Musculoskeletal disorder

Symptomtext

PATIENT SUFFERED AN ISCHEMIC OCCIPITAL LOBE STROKE, CONFIRMED BY CT SCAN, ON 4/2/2021. PATIENT WAS TRANSFERRED TO AND ADDMITTED TO HOSPITAL. PATIENT WAS NOT ADMITTED TO THE ICU PER HIS WIFE. PATIENT WAS RECENTLY TRANSFERED TO REHAB WHERE IS HE IS CURRENTLY AS OF 4/13/2021. PATIENT LOST VISION IN LEFT EYE AS WELL AS FUNCTION IN HIS LEFT ARM PER THE PATIENTS WIFE. PATIENT IS REGAINING SIGHT AND STRENGTH IN BOTH HIS LEFT EYE AND ARM BUT PROGRESS IS SLOW, PER HIS WIFE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 11,0
Labordaten: CT SCAN ON 4/2/2021
Aktuelle Erkrankungen: NONE
Vorgeschichte: HYPERTENSION, INSULIN DEPENDENT TYPE 2 DIABETES, HYPERLIPIDEMIA, HISTORY OF MULTIPLE STROKES
Andere Medikamente: NONE AT THE TIME OF VACCINATION
Allergien: IODINE, SHELLFISH
Vorherige Impfungen: -

VAERS 1201482

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 52,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 05.03.2021
Beginn: 04.04.2021
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal wall operation Hernia repair Skin operation Thrombosis

Symptomtext

Patient had the vaccine on 3/5/21. She then had major abdominal surgery which included abdominal reconstruction, hernia repair and excess skin removal on 3/19/21. She was released from the hospital on 3/22/21. She was readmitted on 4/4/21 for blood clots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: On 3/19/2021 she had surgery for abdominal reconstruction, hernia repair and excess skin.
Vorgeschichte: She was diagnosed with covid-19 on 6/24/2020
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1086197

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TX
Alter: 23,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 08.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood pressure decreased Chills Hypoaesthesia Syncope Vision blurred Vomiting

Symptomtext

syncope

Weitere VAERSDATA-Felder

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

VAERS 1198478

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: IL
Alter: 34,0
Geschlecht: M
Eingang: 12.04.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Headache Muscle spasms Muscle twitching Seizure Tremor

Symptomtext

Began with cramping/convulsing of my left thigh, then my right and within a split second all the muscles in my body were convulsing for about 3-5 minutes. I had a headache and small tremors following that episode. Tylenol helped but side effects did not dissipate until the following morning 3/11 at 10AM. Fresh air helped also.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fluoxetene Albuterol Trazadone
Allergien: sulfa, amoxicillin and celcor
Vorherige Impfungen: -

VAERS 1186918

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: WI
Alter: 26,0
Geschlecht: M
Eingang: 09.04.2021
Impfdatum: 26.03.2021
Beginn: 27.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Alcohol test Amnesia Analgesic drug level Bacterial test Blood culture Blood magnesium CSF cell count CSF glucose CSF lactate CSF protein Chest X-ray Chills Clostridium test Computerised tomogram Computerised tomogram head Concussion Differential white blood cell count Drug screen

Symptomtext

Only minor chills before bed, 11pm. Muscle aches, felt as tightness in IT bands, made remaining asleep difficult. Got up to use the bathroom around 5am. Upon finishing peeing while standing, I lost consciousness, falling. As a result of the fall, I fractured my cheek bone, cut open my ear, later requiring three stitches, and was concussed, resulting in a loss of memory. I was nonresponsive when my fiance found me immediately following the crash, and was rushed to the hospital via ambulance. Upon arrival to the hospital, my fever was found to be 102 F. As a result of the fall, I have a cheek bone fracture, three stiches in my ear, and a concussion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: That morning of 03/27, in order to evaluate the extent of the injuries and rule out contributing factors, I received the following lab tests: - Acetaminophen level - Alcohol - CBC with differential - Cell count, CSF (performed 2 times) - Comprehensive metabolic panel - Covid-19 PCR - Culture, CDF with gram stain - Glucose, CSF - Lactate - Magnesium - Protein, CSF - Prothrombin Time/INR - Salicylate - Troponin - Urinalysis with Microscopy - Culture, blood, bacteria and yest (performed 2 times) - Drug screen, urine - CT cervical spine W/O IV contrast -CT Head W/O IV contrast - ECG - 12 Lead - X-ray chest single view - Lumbar Puncture
Aktuelle Erkrankungen: None
Vorgeschichte: alopecia universalis
Andere Medikamente: Zyrtec
Allergien: None
Vorherige Impfungen: -

VAERS 1186733

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 25,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / UN

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

Dizziness Fall Head injury Loss of consciousness Skin laceration

Symptomtext

Received a call from Lead RN, patient received J & J vaccine @ 1555, patient walked over to the observation area and sat down. At 1600 patient told her wife she was feeling light headed, patient slumped over in chair and fell off the chair hitting the gravel pavement. Per RN patient lost consciousness for a few seconds, small laceration noted to the side of her head. EMS called at 1602, arrived at 1610, evaluated by EMS, per patient she does not want to be transported to the hospital. Patient left site with wife at her side, in stable condition.

Weitere VAERSDATA-Felder

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

VAERS 1186151

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: IL
Alter: 64,0
Geschlecht: M
Eingang: 09.04.2021
Impfdatum: 15.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / -

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

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

Symptomtext

Severe COVID-19 infection with ARDS. Requiring mechanical ventilation, paralysis and flolan nebulization.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory distress syndrome
Hospital-Tage: 4,0
Labordaten: SARS-CoV-2 Rapid positive on 4/5/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1177331

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TN
Alter: 24,0
Geschlecht: M
Eingang: 07.04.2021
Impfdatum: 05.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Headache Pain Syncope

Symptomtext

Headache, body aches, chills starting about 12 hours after injection and lasting until about 48 hours later; fainted in the bathroom about 20 hours after the injection

Weitere VAERSDATA-Felder

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

VAERS 1170469

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 34,0
Geschlecht: M
Eingang: 05.04.2021
Impfdatum: 02.04.2021
Beginn: 02.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Head injury Hyperhidrosis Loss of consciousness Nausea Visual impairment

Symptomtext

Patient received vaccine and five minutes after injection he began to see dots, slowly progressed to the floor and passed out. Patient reports hitting his head. After recovering patient states he woke up with healthcare personnel making sure he was ok. He describes his experience as taking deep breaths, he felt chills, sweats and nausated. He refused further treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: IBS, Syncope
Andere Medikamente: Bentyl
Allergien: Sulfa, Aspirin
Vorherige Impfungen: -

VAERS 1170172

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 25,0
Geschlecht: M
Eingang: 05.04.2021
Impfdatum: 05.04.2021
Beginn: 05.04.2021
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

About 5 minutes after administering Jassesn COVID 19 vaccine the patient began to lose consciousness and rested his head on the table. The patient was then assisted down to the floor. Within 2 minutes the patient was alert and oriented, 911 was activated. PT reported dizziness. Patient asked about medical history which entail WPW, and no medications. EMS assessed and took vital signs. PT refused to go to the hospital. Patient monitored for an additional 30 minutes, and escorted downstairs.

Weitere VAERSDATA-Felder

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

VAERS 1169761

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TX
Alter: 34,0
Geschlecht: F
Eingang: 05.04.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cold sweat Hyperhidrosis Loss of consciousness Pallor

Symptomtext

Date: 3/22/2021 Problem: Notes: Time: 12:40P Upon arrival to nurses station. Patient noted pale, clammy & sweaty. BP 60/33 HR 48, RR18. Call placed to EMS Patient awake, alert &oriented x 3. Vaccinator stated that patient loss consciousness approx. 1-2 minutes after receiving vaccine. Patient states that she had a granola/ breakfast bar for breakfast & had not eaten lunch. Patient feet elevated to elevate patient BP. EMS Arrival pending. Will continue to monitor. Time: 12:50p EMS Arrived. Patient assessed by HFD. Patient declined to go to hospital. Snacks & water provided to patient. Patient rested an additional 15 minutes. Will continue to monitor. Time: 1320 Patient went home with fianc? in stable condition.

Weitere VAERSDATA-Felder

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

VAERS 1160975

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TX
Alter: 26,0
Geschlecht: M
Eingang: 02.04.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Syncope

Symptomtext

Date: 3/23/2021 Problem: Syncope Notes: Client requested a bottle of water upon returning with the water client noted to fall out of his chair. Staff was able to reach him before he hit the ground, guiding his head downward off setting some of the impact from the fall. Client states he does not remember the fall. He also states he has a history of fainting when he gives blood. AAOx3 T 97.4 P68 R18 BP 124/72 O2 97% RA Client monitored for an additional 30 minutes. States he feels fine after 30 mins. T98.0 P72 R20 BP 126/70 O2 98% RA. Client left facility AAOx3 via personal vehicle.

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: -

VAERS 1160706

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: MO
Alter: 21,0
Geschlecht: M
Eingang: 02.04.2021
Impfdatum: 01.04.2021
Beginn: 01.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Dizziness Loss of consciousness Vital signs measurement

Symptomtext

Patient received vaccine and immediately felt dizzy and almost lost consciousness. He was brought in a wheelchair and vital signs taken. Patient refused transport to hospital. Advised to call 911 if any issues persist. Patient left to go home.

Weitere VAERSDATA-Felder

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

VAERS 1124795

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: GA
Alter: 18,0
Geschlecht: M
Eingang: 01.04.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Bradyphrenia Computerised tomogram Electrocardiogram Electroencephalogram Eye contusion Fall Headache Magnetic resonance imaging Seizure Unevaluable event

Symptomtext

PATIENT WANTED MODERNA BUT RECEIVED JANSSEN

Weitere VAERSDATA-Felder

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

VAERS 1147830

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 1805025

schwer

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 30.03.2021
Impfdatum: 30.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Condition aggravated Fall Loss of consciousness Seizure

Symptomtext

At approximately 1238 patient was noted to be on floor, experienced fall from chair. 911 called. came to patient. Pt placed in recumbent position. noted to be having seizure regained consciousness. Airway not obstructed no s/s if respiratory destress noted. Regain consciousness after 2 seconds. Vs bp130/82, O298% on RA, HR 72, RR 28. Denies pain or discomfort. Pt alert and oriented able to state his name date location. Mae x34 l neurologically intact. did not give Epi . No s/s of anaphylaxis noted. please patient and become a position. Ambulance and fire department on site at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hx of. Seizure
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1145737

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: -
Geschlecht: F
Eingang: 30.03.2021
Impfdatum: 11.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: UN / -

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

Chills Cough Headache Loss of consciousness Nausea Pain Pyrexia

Symptomtext

PASSED OUT ONCE (Passed out, Loss of consciousness) COUGHING OUT (Coughing, Cough) CHILLS (Chills, Chills) NAUSEA (Nausea, Nausea) FEVER (Fever, Pyrexia) HEADACHE (Headache, Headache) This spontaneous report received from a patient concerned a female of unspecified age. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, expiry: UNKNOWN) dose was not reported, administered on 11-MAR-2021 14:00 for prophylactic vaccination. No concomitant medications were reported. On 11-MAR-2021, after getting the vaccine, the patient experienced achiness throughout the body, coughing out, chills, fever, headache and nausea. On 12-MAR-2021, the patient also passed out once. The action taken with covid-19 vaccine ad.26.cov2.s was not applicable. The patient recovered from passed out once, and fever on 12-MAR-2021, and chills on MAR-2011, had not recovered from headache, and achiness throughout the body, and the outcome of nausea and coughing out was not reported. The reporter causality between covid-19 vaccine ad26.cov.2.s and passed out once, coughing out, achiness throughout the body, chills, nausea, fever, headache was possible. The company causality between covid-19 vaccine ad26.cov2.s and passed out once, coughing out, achiness throughout the body, chills, nausea, fever, headache was possible. This report was serious (Other Medically Important Condition).

Weitere VAERSDATA-Felder

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

VAERS 1144623

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 18,0
Geschlecht: F
Eingang: 29.03.2021
Impfdatum: 29.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Incontinence Pallor Seizure

Symptomtext

At 1428, patient mother alerted medical staff, stating her daughter had a seizure. Upon arrival, daughter was sitting upright in passenger seat, mother holding her, eyes open, appearing pale. No convulsions , incontinence, or other seizure activity noted. EMS notified and arrived within a minute and evaluated patient. No medications or additional treatment given. Patient ambulated to EMS stretcher with one person assistance. Awake and talking. Patient transported via ambulance at 1437.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Wisdom tooth extraction
Vorgeschichte: none
Andere Medikamente: Ibuprofen, tylenol
Allergien: nka
Vorherige Impfungen: -

VAERS 1139892

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: NY
Alter: 29,0
Geschlecht: M
Eingang: 27.03.2021
Impfdatum: 23.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

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

Dizziness Dysstasia Fall Loss of consciousness

Symptomtext

Severe dizziness, unable to stand for almost 4 hours. Ended up collapsing due to dizziness and momentary loss of consciousness due to fall and dizziness

Weitere VAERSDATA-Felder

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

VAERS 1137019

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: NY
Alter: 22,0
Geschlecht: M
Eingang: 26.03.2021
Impfdatum: 26.03.2021
Beginn: 26.03.2021
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 Tonic clonic movements

Symptomtext

Patient passed out and began seizing within 5 minutes of vaccine administration sitting down on chair. Tonic, clonic motions for 5 seconds. No foaming at the mouth. Patient was taken off chair, held on the ground until seizure ended. Patient gained consciousness after a minute. Given water, snacks, air and EMS was called. EMS assessed situation, and allowed patient's girlfriend to pick him up from site and drive back home.

Weitere VAERSDATA-Felder

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

VAERS 1134642

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: CA
Alter: 24,0
Geschlecht: M
Eingang: 25.03.2021
Impfdatum: 25.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Dry skin Head injury Loss of consciousness Musculoskeletal stiffness Pallor Skin warm Vital signs measurement

Symptomtext

Patient received Janssen COVID-19 vaccine at 123pm on 3/25/2021. Patient directed to observation area and fell backwards out of chair at 127pm on 3/25/2021. After falling backwards out of chair patient had a full body stiffening episode and was noted to be bleeding from his head. Bleeding controlled with gauze held by an RN. Patient initially GCS 13 and unable to answer questions appropriately, manual blood pressure 118/60 HR 50 SpO2 89% on room air, patient pale and dry. Patients legs raised by RN and pressure to laceration on top of forehead continued to be held by RN. After 5-7 minutes patient GCS increased to 15 and he was alert and oriented x 4, manual blood pressure 114/60 HR 62 SpO2 97% on room air, patient pink warm and dry. Fire arrived on scene at 147pm and Ambulance shortly after. Fire and Ambulance given report by RN on site while other RN on site continued holding pressure to laceration on forehead with gauze.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Unknown. Patient transported by EMS to hospital.
Aktuelle Erkrankungen: None per patient
Vorgeschichte: None per patient
Andere Medikamente: None per patient
Allergien: None per patient
Vorherige Impfungen: -

VAERS 1120196

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: MA
Alter: 27,0
Geschlecht: F
Eingang: 21.03.2021
Impfdatum: 20.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Pallor Presyncope Tinnitus Tremor

Symptomtext

Pt had a near syncopal episode after injection. Ringing in ears, pale, shaky, light headed. We lied pt down, BP was 90/60 then increased to 110/70 with rest and a snack.

Weitere VAERSDATA-Felder

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

VAERS 1120141

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: MA
Alter: 30,0
Geschlecht: F
Eingang: 21.03.2021
Impfdatum: 20.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Pallor Presyncope

Symptomtext

Pt had a near syncopal event after the injection. She became pale, light headed BP 102/60. She lied down for 20 min and improved

Weitere VAERSDATA-Felder

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

VAERS 1118280

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: GA
Alter: 44,0
Geschlecht: M
Eingang: 20.03.2021
Impfdatum: 20.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Eye movement disorder Feeling abnormal Hyperhidrosis Lethargy Loss of consciousness Syncope

Symptomtext

Patient was given shot and asked to wait in pharmacy area at least 15 minutes. Within about 5-10 minutes his girlfriend comes to the pharmacy window and tells me he's feeling bad. By the time I get to his chair he is very lethargic and slumped over. I sit him up in the chair and his head rolls back and his eyes have rolled back in his head. I place him on the floor and instructed my staff to call 911. The patient presented with sweats and was unresponsive for about 10-20 seconds. When he came to he asked how he got on the floor. The patient never had any trouble breathing heart rate was steady the entire time. When EMS arrived they checked him out and was fine. He refused transport to the hospital. He walked out of the store after about 30 minutes from the point of his passing out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: unknown
Allergien: nka
Vorherige Impfungen: -

VAERS 1116829

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: IL
Alter: 42,0
Geschlecht: M
Eingang: 19.03.2021
Impfdatum: 19.03.2021
Beginn: 19.03.2021
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

Pt had a syncopal episode following covid-19 vaccine. Pt states he has had similar episodes following needle injections. Pt was closely monitored for 30 min following syncopal event. Pt stated that he felt much better and was discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Covid 19 J&J Vaccine
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1115946

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 89,0
Geschlecht: M
Eingang: 19.03.2021
Impfdatum: 18.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Blood glucose Blood test Chest X-ray Computerised tomogram head Dysarthria Facial paralysis Full blood count Hypotonia Urine analysis

Symptomtext

resident began to experience stroke like symptoms at approximately 0300, resident noted with slurred speech, left arm and leg flacid, facial drooping to left side of face. B/P 193/116. transferred to ER for evaluation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: CBC WBC-6.8, HGB-12.3,HCT-36.4. Sodium-138, Potassium-3.8,BUN-24, Creatnine-1.4, glucose-89. Lipids-Chol-172, HGBA1C-89, TSH-1.01. Chest Xray- negative, CT of head- old right occipital infarct. Lactic acid- 1.1. Urinalysis- trace blood,nitrites negative, rare bacteria
Aktuelle Erkrankungen: Atrial Fibrillation, Chronic Kidney Disease, Hypertension, Rheumatoid Arthritis, ASHD, Alzheimer's
Vorgeschichte: Atrial Fib
Andere Medikamente: Aricept 10mg at bedtime, ASA 81 mg daily, Centrum Silver daily, Cyclobenzaprine 10mg at bedtime, Mirtatazapine 15mg at bedtime, Memantine 10mg twice daily, Naproxen 500mg twice daily, Saline Nasal spray twice daily, Norco 5-325mg every 6
Allergien: Hydromorphone, Oxymorphone, Norvasc, Percogesic
Vorherige Impfungen: -

VAERS 1115660

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: UT
Alter: 57,0
Geschlecht: F
Eingang: 19.03.2021
Impfdatum: 18.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Fall Seizure Syncope

Symptomtext

DURING THE 15 MINUTE OBSERVATION PERIOD, ABOUT 5 TO 10 MINUTES POST VACCINE THE PT FAINTED WHILE SITTING IN HER CHAIR AND FELL OUT OF THE CHAIR. I INSTRUCTED A TECH TO 911 WHILE RAN TO THE PT. AS I TOUCHED HER TO FEEL FOR A PULSE SHE REGAINED CONSCIOUSNESS. I EXPLAINED WHAT HAPPENED AND ASKED HER TO STAY WHERE SHE WAS AT UNTIL PARAMEDICS CAME. SHE WAS ALERT AND ABLE TO ANSWER QUESTIONS. THE PARAMEDICS ARRIVED ABOUT 5 MINUTES LATER. THEY GOT HER UP AND SHE HAD A SEIZURE. THE TOOK HER TO AND UNKNOW HOSPITAL

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: -
Vorgeschichte: BP
Andere Medikamente: SOMETHING FOR BP, KNOWN DRUG
Allergien: NO KNOWN DRUG ALLERGIES
Vorherige Impfungen: -

VAERS 1109342

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TX
Alter: 34,0
Geschlecht: M
Eingang: 17.03.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
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

Reports dizziness, fainted for few minutes. history of same symptom with venipuncture. BP: 71/42; Repeat: 110/69 HR: 57 Sp02: 97% Refused to be transported to ER, refusal form signed. Seen and cleared by EMS

Weitere VAERSDATA-Felder

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

VAERS 1109072

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TX
Alter: 39,0
Geschlecht: M
Eingang: 17.03.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
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

Reports he fainted for few minutes. History of similar symptom with venipuncture. BP: 134/94 and 150/103 ( repeat) Fingerstick: 121 HR: 60 Sp02: 99% RA Refused to be transported by EMS to ER. Refusal form signed by patient Seen and cleared by EMS,

Weitere VAERSDATA-Felder

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

VAERS 1108784

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: AZ
Alter: 63,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
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

PATIENT FAINTED AND WAS UNCONSCIOUS FOR A FEW SECONDS ONLY. SHE GAIND CONSCIIOUSNESS VERY QUICKLY. 911 WAS CALLED

Weitere VAERSDATA-Felder

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

VAERS 1108163

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: FL
Alter: 32,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 14.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Blood glucose decreased Diarrhoea Dizziness Loss of consciousness Nausea Pyrexia

Symptomtext

On the night of Monday 15, I started to have a fever over 102.2 degrees. Took Ibuprofen for the fever. At 3:00 AM of the same day started to feel weak. On that moment I lost consciousness and passed out. In my opinion, I experimented a down on sugar, which had never happened before. My husband was able to catch me and sat me on the floor. A minute after I recovered and my husband gave me fruit (Melon) to raise my blood sugar. On that moment I had lots of nauseas and diarrhea. I was feeling weak and dizzy all night and the next day. Today Wednesday March the 17 I have been feeling much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Haven't realized any test yet.
Aktuelle Erkrankungen: -
Vorgeschichte: Allergies and Asthma
Andere Medikamente: Cetirizine
Allergien: Sulfa, Seafood, shrimp, Dust, Grass, Pets, and certain trees.
Vorherige Impfungen: -

VAERS 1106671

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TN
Alter: 42,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Loss of consciousness Pallor

Symptomtext

Notified by pharmacy technician that patient had 'passed out' in parking lot. Patient found lying on the ground, pale but awake. Patient had been instructed to wait in the store for 15 minutes after vaccination in case of any adverse reaction but, per police, decided to wait in the car instead. He then began to feel lightheaded and decided to come back into the clinic. He passed out on his way. Civilian notified policeman that patient was passed out and EMS was called. EMS arrived shortly after I went out to parking lot to check on the patient. Patient was alert and oriented for EMS, reported history of HTN. He continued to c/o feeling lightheaded and BP per EMS was 77/48mmHg. Patient taken by ambulance for further evaluation and treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None listed
Vorgeschichte: HTN
Andere Medikamente: (unknown)
Allergien: None
Vorherige Impfungen: -

VAERS 1099323

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TN
Alter: 39,0
Geschlecht: M
Eingang: 14.03.2021
Impfdatum: 14.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Condition aggravated Hyperhidrosis Loss of consciousness Skin discolouration

Symptomtext

BEFORE GIVING THE JANSSEN COVID VACCINE (LOT # 1805025 EXP 5/25/21), THE PATIENT HAD STATED THAT THE LAST FEW TIMES HE GOT A SHOT OR HAD A BLOOD DRAW HE GOT REALLY SICK AND EVEN PASSED OUT. THE VACCINE WAS GIVEN WITHOUT INCIDENT AND PATIENT SAID HE FELT OK. HE TRADED PLACES WITH HIS GIRLFRIEND AND SAT IN A CHAIR IN THE EXAM ROOM. IT WAS NOT UNTIL AFTER I HAD ALREADY GIVEN HIS GIRLFRIEND HER VACCINE THAT HE SAID THAT HE WAS FEELING FUNNY. HIS COLORING CHANGED AND HE WAS DIAPHORETIC. I GOT A PAPERTOWEL WITH COOL WATER ON IT AND PLACED ON HIS NECK AND ANOTHER ONE FOR HIS FOREHEAD. AFTER A MINUTE OR SO, HE DID PASS OUT WHILE IN THE CHAIR. HE WAS OUT FOR ABOUT 30 SECONDS AND THEN CAME BACK TO AND WAS ALERT AND ORIENTED X 4 BUT STILL FELT VERY WEAK. I GAVE HIM A WATER TO SIP ON. HIS GIRLFRIEND STAYED AT HIS SIDE THE WHOLE TIME. HIS O2 WAS 100% AND HIS PULSE 53. HE SAID THAT HE HAD EATEN SHORTLY BEFORE COMING TO GET HIS VACCINE BUT THEN LATER ASKED FOR AN APPLE BECAUSE HE WAS ON A CLEANSE DIET AND REALLY HAD NOT EATTEN MUCH. THE PCT WENT TO GET HIM AN APPLE. AFTER EATING THE APPLE AND SITTING FOR AN ADDITIONAL 20 MIN HE FELT WELL ENOUGH TO LEAVE. STILL WITH HIS GIRLFRIEND AND HIS GIRLFRIEND COMMITTED TO DRIVING HIM SO HE DID NOT HAVE TO. HE LEFT WITH NO ASSISTANCE.

Weitere VAERSDATA-Felder

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

VAERS 1097740

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: AK
Alter: 33,0
Geschlecht: M
Eingang: 13.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Presyncope

Symptomtext

Patient went into a vasovagal response with sweating about 8 minutes after the shot. patient came back to consciousness after 7 seconds after pharmacist checked pulse made sure the patient was upright and used applied tension technique. Patient was then given fluids and lime soda that helped the patient come back to total consciousness. We continued to monitor patient for an extra 30 minutes and called family to pick him to ensure that he does not drive. Moreover, I recommended that the patient does not go snowboarding as he was thinking of heading to the mountains today.

Weitere VAERSDATA-Felder

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

VAERS 1096316

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: CA
Alter: 43,0
Geschlecht: M
Eingang: 13.03.2021
Impfdatum: 08.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fear Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Additional Details: Patient did experience fainting with Janssen, though important to note that patient said he has fainted before in past with vaccinations. He said he is fearful of them and it is more \"mental\"" and does not attribute it to the vaccine itself."

Weitere VAERSDATA-Felder

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

VAERS 1096310

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: CA
Alter: 20,0
Geschlecht: F
Eingang: 13.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
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-Mild, Systemic: Fainting / Unresponsive-Mild

Weitere VAERSDATA-Felder

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

VAERS 1095334

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 12.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Seizure

Symptomtext

She has history of seizures and was given the vaccine and then had a seizure. She was transferred to local ER for further evaluation. She was given Ativan and has been discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: TYPE 2DM, ANXIETY,STROKE,RA,SEIZURES
Vorgeschichte: TYPE 2DM, RA, SEIZURES,STROKE, ANXIETY
Andere Medikamente: CLONAZEPAM, HYDROCHLOROTHIAZIDE,LAMICATL,AMBIEN,TRAMADOL,ESTRADIOL,METFORMIN,GABAPENTIN,VENLAFAXINE,TOPIRAMATE,AGGRENOX
Allergien: SULFA,NSAIDS
Vorherige Impfungen: -

VAERS 1095066

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: IL
Alter: 84,0
Geschlecht: F
Eingang: 12.03.2021
Impfdatum: 09.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / -

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

Alanine aminotransferase normal Albumin globulin ratio Amnesia Arteriogram carotid abnormal Aspartate aminotransferase normal Basophil percentage decreased Bilirubin urine Blood albumin decreased Blood alkaline phosphatase normal Blood calcium decreased Blood chloride normal Blood creatine phosphokinase normal Blood creatinine normal Blood culture negative Blood glucose normal Blood lactic acid Blood magnesium normal Blood potassium normal

Symptomtext

On the morning of admission, patient had another episode. She was sitting at the kitchen table and then slumped forward unconscious. She has no memory of the episode. Daughter is unsure how long she was unconscious for. She was taken to the ER via ambulance. Head CT in the ER showed only age-related changes. Chest x-ray showed an increase in infiltrate. Influenza test negative. Rapid COVID-19 test negative. Urinalysis only had 2+ leukocyte esterase. White count of 3.3. Cardiac enzymes negative. BNP normal. remains hospitalized at Hospital - inpatient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 3,0
Labordaten: US Carotid Duplex Doppler Collected: 03/12/21 0934 Order Status: Completed Updated: 03/12/21 1452 Narrative: PROCEDURE: CAROTID DOPPLER ULTRASOUND CLINICAL INDICATION: Syncope. COMPARISON: None. TECHNIQUE: This examination was performed using a duplex scanner combining Doppler and real-time. Multiple Doppler samples were obtained at different points along the carotid arteries in the neck. Special attention was paid to the proximal portions of both internal carotid arteries. The Doppler samples were analyzed using a spectral analyzer. FINDINGS: There is no evidence of hemodynamically significant stenosis was within the common carotid arteries. There is mild calcification of the bilateral common carotid arteries and carotid bulbs. Peak systolic velocities within the proximal, mid and distal right ICA are 56 cm/s, 86 cm/s and 103 cm/sec, respectively. Peak systolic velocities within the proximal, mid and distal left ICA are 87 cm/s, 82 cm/s and 85 cm/sec, respectively. The ICA to CCA ratio on the right is 1.9. The ICA to CCA ratio on the left is 1.3. Anterograde flow is demonstrated in both vertebral arteries. IMPRESSION: No sonographic evidence of hemodynamically significant stenosis in the internal carotid arteries in the neck. Mild calcification of the bilateral distal common carotid arteries and carotid bulbs. Blood culture Collected: 03/10/21 1629 Order Status: Completed Specimen: BLOOD, VENOUS Updated: 03/12/21 1028 Specimen Type BLOOD, VENOUS Special Handling NONE Culture Result NO GROWTH 2 DAYS Specimen Status Report PENDING Blood culture Collected: 03/10/21 1629 Order Status: Completed Specimen: BLOOD, VENOUS Updated: 03/12/21 1028 Specimen Type BLOOD, VENOUS Special Handling NONE Culture Result NO GROWTH 2 DAYS Specimen Status Report PENDING Urine culture Collected: 03/10/21 1046 Order Status: Completed Specimen: URINE, VOIDED Updated: 03/12/21 0908 Specimen Type VOIDED Special Handling NONE Reflexed from W12781 Culture Result MIXED FLORA, SUGGESTIVE OF CONTAMINATION Specimen Status Report 03/12/2021 FINAL Basic metabolic panel (Abnormal) Collected: 03/12/21 0508 Order Status: Completed Specimen: Blood Updated: 03/12/21 0536 Glucose 93 65 - 100 MG/DL Blood Urea Nitrogen 11 7 - 18 MG/DL Creatinine 0.8 0.5 - 1.0 MG/DL Sodium 139 136 - 145 MMOL/L Potassium 3.8 3.5 - 5.1 MMOL/L Chloride 106 98 - 107 MMOL/L Co2 22 21 - 32 MMOL/L Calcium 8.4Low 8.5 - 10.1 MG/DL GFR Comment IF PATIENT IS AFRICAN AMERICAN, MULTIPLY RESULT BY 1.16 Est GFR 68Low >90 ML/MIN/1.73sq.m CBC w Auto Diff (Abnormal) Collected: 03/12/21 0508 Order Status: Completed Specimen: Blood Updated: 03/12/21 0520 White Blood Cell Count 3.6Low 4.3 - 10.5 THOUS/uL Red Blood Cell Count 4.24 3.93 - 5.07 MIL/uL Hemoglobin 12.4 11.8 - 14.8 GM/DL Hematocrit 37.6 35.6 - 45.0 % Mean Corpuscular Volume 88.7 83.5 - 95.9 FL Mean Corpuscular Hemoglobin 29.2 27.4 - 32.0 PG Mean Corpuscular Hemoglobin Conc 33.0 31.5 - 34.7 G/DL Rdwcv 13.2 11.8 - 14.2 % Rdwsd 42.7 37.2 - 47.8 FL Platelet Count 237 167 - 402 THOUS/uL Mean Platelet Volume 9.7 8.8 - 12.0 FL Nucleated Red Blood Cells 0.0 0.0 /100 WBC'S Abs NRBC 0.0 0.0 THOUS/uL Differential Type AUTO Neutrophils 49.5 34.0 - 67.9 % Lymphs 33.0 20.4 - 48.6 % Monocytes 13.9High 5.0 - 11.5 % Eos 2.5 1.0 - 5.4 % Basos 0.3 0.2 - 1.3 % Neutrophils Absolute Count 1.8Low 2.1 - 6.6 THOUS/uL Lymphocytes Absolute Count 1.2 1.2 - 3.9 THOUS/uL Monocytes Absolute Count 0.5 0.3 - 0.8 THOUS/uL Eosinophils Absolute Count 0.1 0.1 - 0.4 THOUS/uL Basophils Absolute Count 0.0 0.0 - 0.1 THOUS/uL Imm Gran 0.8High 0.1 - 0.7 % Abs Imm Gran 0.03 0.0 - 0.1 THOUS/uL Basic metabolic panel (Abnormal) Collected: 03/11/21 0510 Order Status: Completed Specimen: Blood Updated: 03/11/21 0623 Glucose 100 65 - 100 MG/DL Blood Urea Nitrogen 13 7 - 18 MG/DL Creatinine 0.8 0.5 - 1.0 MG/DL Sodium 138 136 - 145 MMOL/L Potassium 3.4Low 3.5 - 5.1 MMOL/L Chloride 106 98 - 107 MMOL/L Co2 22 21 - 32 MMOL/L Calcium 8.1Low 8.5 - 10.1 MG/DL GFR Comment IF PATIENT IS AFRICAN AMERICAN, MULTIPLY RESULT BY 1.16 Est GFR 68Low >90 ML/MIN/1.73sq.m CBC with Auto Diff (Abnormal) Collected: 03/11/21 0510 Order Status: Completed Specimen: Blood Updated: 03/11/21 0601 White Blood Cell Count 4.1Low 4.3 - 10.5 THOUS/uL Red Blood Cell Count 3.91Low 3.93 - 5.07 MIL/uL Hemoglobin 11.6Low 11.8 - 14.8 GM/DL Hematocrit 34.7Low 35.6 - 45.0 % Mean Corpuscular Volume 88.7 83.5 - 95.9 FL Mean Corpuscular Hemoglobin 29.7 27.4 - 32.0 PG Mean Corpuscular Hemoglobin Conc 33.4 31.5 - 34.7 G/DL Rdwcv 13.2 11.8 - 14.2 % Rdwsd 42.9 37.2 - 47.8 FL Platelet Count 211 167 - 402 THOUS/uL Mean Platelet Volume 9.7 8.8 - 12.0 FL Nucleated Red Blood Cells 0.0 0.0 /100 WBC'S Abs NRBC 0.0 0.0 THOUS/uL Differential Type AUTO Neutrophils 63.4 34.0 - 67.9 % Lymphs 20.4 20.4 - 48.6 % Monocytes 13.8High 5.0 - 11.5 % Eos 1.2 1.0 - 5.4 % Basos 0.5 0.2 - 1.3 % Neutrophils Absolute Count 2.6 2.1 - 6.6 THOUS/uL Lymphocytes Absolute Count 0.8Low 1.2 - 3.9 THOUS/uL Monocytes Absolute Count 0.6 0.3 - 0.8 THOUS/uL Eosinophils Absolute Count 0.1 0.1 - 0.4 THOUS/uL Basophils Absolute Count 0.0 0.0 - 0.1 THOUS/uL Imm Gran 0.7 0.1 - 0.7 % Abs Imm Gran 0.03 0.0 - 0.1 THOUS/uL EKG Resulted: 03/11/21 Order Status: Completed Updated: 03/11/21 0551 Urinalysis with reflex to culture, if indicated (Abnormal) Collected: 03/10/21 2039 Order Status: Completed Specimen: URINE,CATH INDWELLING Updated: 03/10/21 2136 Glucose UA NEGATIVE NEGATIVE MG/DL Protein UA NEGATIVE NEGATIVE MG/DL Bilirubin UA NEGATIVE NEGATIVE Urobilinogen UA 0.2 0.2 - 1.0 MG/DL pH UA 7.0 5.0 - 8.0 Blood UA TRACEAbnormal NEGATIVE Ketones UA NEGATIVE NEGATIVE MG/DL Nitrite UA NEGATIVE NEGATIVE Leukocyte Esterase UA NEGATIVE NEGATIVE UR Appearance CLEAR CLEAR Specific Gravity UA 1.015 1.000 - 1.030 Color YELLOW YELLOW Site CATH INDWELLING Comment, Urine Culture NOT INDICATED WBC Urine 0 to 5 <5 /HPF Squamous Epithelial RARE <5 /HPF PROTIME (PROTHROMBIN TIME) Collected: 03/10/21 1600 Order Status: Completed Specimen: Blood Updated: 03/10/21 1529 PROTIME 12.3 10.3 - 12.6 SEC INR 1.0 0.9 - 1.1 Comment: Recommended therapeutic ranges or oral anticoagulant is and INR of 2.0 to 3.0. An INR of 2.5 to 3.5 is recommended to prevent recurrent MI. Lactic Acid, Serum Collected: 03/10/21 1109 Order Status: Completed Specimen: Blood Updated: 03/10/21 1157 Lactate 1.2 0.4 - 2.0 MMOL/L Magnesium Collected: 03/10/21 1105 Order Status: Completed Specimen: Blood Updated: 03/10/21 1150 Magnesium 2.1 1.8 - 2.4 MG/DL CK (CPK) Creatine Phosphokinase Collected: 03/10/21 1105 Order Status: Completed Specimen: Blood Updated: 03/10/21 1150 Creatine Kinase Total 34 26 - 192 U/L CKMB [244331649] Collected: 03/10/21 1105 Order Status: Completed Specimen: Blood Updated: 03/10/21 1150 Creatine Kinase-MB 0.3 0.0 - 3.6 NG/ML Troponin Series Collected: 03/10/21 1105 Order Status: Completed Specimen: Blood Updated: 03/10/21 1150 Troponin I 0.00 0.00 - 0.06 ng/mL Comment: 0.1 to 0.5 ng/mL shows an increased risk of AMI. 0.6 to 1.5 or greater is suggestive of AMI. Comprehensive metabolic panel (Abnormal) Collected: 03/10/21 1105 Order Status: Completed Specimen: Blood Updated: 03/10/21 1150 Glucose 104High 65 - 100 MG/DL Blood Urea Nitrogen 21High 7 - 18 MG/DL Creatinine 0.9 0.5 - 1.0 MG/DL Sodium 138 136 - 145 MMOL/L Potassium 4.1 3.5 - 5.1 MMOL/L Chloride 105 98 - 107 MMOL/L Co2 27 21 - 32 MMOL/L Calcium 8.7 8.5 - 10.1 MG/DL Protein Total 6.4 6.4 - 8.2 G/DL Albumin 2.7Low 3.4 - 5.0 G/DL A/G Ratio 0.7Low 0.8 - 2.0 Alkaline Phosphatase 63 46 - 116 U/L Alt (SGPT) 21 14 - 59 U/L AST(SGOT) 18 15 - 37 U/L Bilirubin, Total 0.7 0.2 - 1.0 MG/DL GFR Comment IF PATIENT IS AFRICAN AMERICAN, MULTIPLY RESULT BY 1.16 Est GFR 59Low >90 ML/MIN/1.73sq.m FHC COVID Antigen Collected: 03/10/21 1041 Order Status: Completed Updated: 03/10/21 1149 FHC COV AG PRESUMPTIVE NEGATIVE PRESUMPTIVE NEGATIVE XR Chest Portable Collected: 03/10/21 1115 Order Status: Completed Updated: 03/10/21 1133 Narrative: EXAMINATION: Frontal view of the chest CLINICAL HISTORY: 84 years Female,syncope COMPARISON: 3/8/2021 FINDINGS: The cardiomediastinal size and contour are normal. The lungs are hyperinflated with a flattened diaphragm. Slight increase in right basal infiltrate. There is a small right pleural effusion. IMPRESSION: Slight increase in right basal infiltrate. Small right effusion. Brain Natriuretic Peptide (BNP) Collected: 03/10/21 1109 Order Status: Completed Specimen: Blood Updated: 03/10/21 1132 B-Type Natriuretic Peptide 94 0 - 100 PG/ML EXAMINATION: UNENHANCED CT OF THE HEAD CLINICAL HISTORY: 84 years Female,Syncope COMPARISON: There is no prior similar study available for correlation. TECHNIQUE: Axial imaging and 2-D reformatting performed without IV contrast. This exam was performed according to our departmental dose-optimization program, which includes automated exposure control, adjustment of the mA and/or kV according to patient size and/or use of iterative reconstruction technique. TOTAL DLP: 1085 mGy-cm FINDINGS: The mastoid air cells, middle ears and visualized paranasal sinuses are clear. There is no mass effect, midline shift, intracranial hemorrhage, hydrocephalus or acute blurring of the gray-white interface. There are mild bilateral symmetric periventricular hypodensities. There is mild cerebral atrophy.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Current Outpatient Medications on File Prior to Encounter Medication Sig Dispense Refill ? amoxicillin-clavulanate (AUGMENTIN) 875-125 MG per tablet Take 1 tablet by mouth 2 times daily for 7 days 14 tablet 0 ? azithromycin (ZITHROMAX) 250
Allergien: nka
Vorherige Impfungen: -

VAERS 1094532

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 41,0
Geschlecht: M
Eingang: 12.03.2021
Impfdatum: 11.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Feeling hot Hyperhidrosis Hypoaesthesia Hypotonia Loss of consciousness Paraesthesia Syncope Urinary incontinence

Symptomtext

Upon wakening this morning pt reports L arm numbness, tingling and flaccidity. pt walked to kitchen and he began feeling sweaty and hot, the next thing he awoke laying in the floor after passing out . Pt was incontinent of urine during event. He now reports some mild shortness of breath but no acute distress or known injuries from syncope episode. pt advised to go to the ER. Pt's states his wife is on her way home and will drive him to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: going to ER today 3-12-21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: unknown
Allergien: None
Vorherige Impfungen: -

VAERS 1094025

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: WI
Alter: 34,0
Geschlecht: F
Eingang: 12.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Immediate post-injection reaction Loss of consciousness Mental status changes Vision blurred

Symptomtext

Client got very quiet and lost eye focus immediately after vaccination. She reported feeling dizzy around 2 minutes after vaccination. After reclining client, they lost consciousness about 9 minutes after vaccination for 3 minutes. EMS was activated, upon regaining consciousness, clients mental status was still altered per staff report. Client was then transported via EMS to local ER.

Weitere VAERSDATA-Felder

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

VAERS 1093366

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nausea Presyncope

Symptomtext

Patient had a vasovagal response shortly after vaccination, while in the observation area. Reported dizziness and nausea. Patient was given water and asked to lay in supine position in exam room. After 20 minutes, patient felt better and was able to leave the clinic.

Weitere VAERSDATA-Felder

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

VAERS 1092968

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: CO
Alter: 37,0
Geschlecht: M
Eingang: 11.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Presyncope

Symptomtext

Vagal reaction. Fully recovered after laying flat and drinking water. Monitored for 30 minutes after reaction

Weitere VAERSDATA-Felder

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

VAERS 1092339

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Dizziness Loss of consciousness Nausea Nervousness Pallor Syncope

Symptomtext

After getting vaccinated and escorted to waiting area patient fainted out of chair and hit head on floor. She was briefly unconscious and pale for a few minutes after coming back to consciousness. She remained on the floor feeling dizzy, shaky, and nauseous until she was taken to the hospital by paramedics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Patient had not eaten all day due to travel.
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1089709

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: AZ
Alter: 64,0
Geschlecht: M
Eingang: 10.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Contusion Dyspnoea Eye movement disorder Pallor Peripheral swelling Syncope

Symptomtext

After receiving the vaccine with in minutes the patients left arm began to swell and bruise. He began to become pale and his eyes rolled back into his head and passed out. He woke up a min later and had SOB. Very pale and almost threw up. Paramedics and Firefighters were called. The eveulated the patients and gave him a liter of sodium choride. His Heart Rate was in the 30's. After several min and a liter of fluid, patient was alert. Once stable he was transported to Hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Nothing
Vorgeschichte: High Blood Pressure
Andere Medikamente: Lisinopril
Allergien: None
Vorherige Impfungen: -

VAERS 1087595

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: VA
Alter: 60,0
Geschlecht: F
Eingang: 10.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Seizure

Symptomtext

Patient experienced a seizure lasting 2-3 minutes approximately 1-2 minutes after receiving the vaccine. patient has a history of seizures/epilepsy.

Weitere VAERSDATA-Felder

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

VAERS 1081625

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: MN
Alter: 64,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 08.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyskinesia Fear of injection Loss of consciousness Staring Unresponsive to stimuli

Symptomtext

Patient seemed to pass out. Reported fear of needles. Happened about 13 minutes after vaccine was administered. She wasn't responsive to voice for short time period with a blank stare. Once she snapped out of it, she jerked and then we tried to make her more comfortable. EMS was contacted to verify patient was okay. Patient did not want to go to hospital or ER.

Weitere VAERSDATA-Felder

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

VAERS 1079181

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: IL
Alter: 38,0
Geschlecht: M
Eingang: 07.03.2021
Impfdatum: 05.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Flushing Hypoacusis Syncope Vision blurred

Symptomtext

I fainted the following evening after my vaccination. I felt fine all day and after dinner started to feel flush, vision became blurry and had trouble hearing. Within 3 minutes I fainted. Felt fine after coming to, and have felt fine so far the next day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Omeprazole Finestride Vitamin D3 Men's Multi-Purpose Vitamin
Allergien: -
Vorherige Impfungen: -

VAERS 1078592

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: IL
Alter: 25,0
Geschlecht: F
Eingang: 06.03.2021
Impfdatum: 05.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Fatigue Loss of consciousness Myalgia Pyrexia

Symptomtext

Violent muscle aches that were not settled by medication, far beyond normal muscle aches from illness. Began exactly 6 hours following vaccine and continued for approximately 12 hours. Fever for 24 hours. Fatigue, black outs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lamictal Ortho Tri Cyclen Lo
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1075378

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

schwer

Staat: KY
Alter: 35,0
Geschlecht: M
Eingang: 05.03.2021
Impfdatum: 05.03.2021
Beginn: 05.03.2021
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 increased Cold sweat Fall Head injury Hyperhidrosis Lip injury Loss of consciousness Pallor

Symptomtext

PATIENT RECEIVED VACCINATION AND WAS THEN ASKED TO SIT IN LOBBY. AFTER BEING SEATED PATIENT PASSED OUT AND FELL OUT OF CHAIR, HITTING HIS HEAD AND BITING HIS LIP IN THE PROCESS. 911 WAS CALLED AND EPI PEN WAS RETRIEVED. PATIENT CAME TO AND WAS PALE, SWEATY, AND HAD CLAMMY HANDS. PATIENT REPORTED NO DIFFICULTY IN BREATHING OR FEELING OF THROAT SWELLING SO EPI PEN WAS NOT ADMINISTERED. BP WAS CHECK AND WAS EXTREMELY ELEVATED. AMBULANCE ARRIVED A FEW MOMENTS LATER AND EMTS ASSESSED PATIENT. PATIENTS BP HAD RETURNED TO NORMAL RANGE, COLOR WAS IMPROVED AND HE WAS NO LONGER SWEATING. EMTS ASKED PATIENT IF HE WANTED TO BE TAKEN TO THE ER FOR FURTHER EVALUATION AND PATIENT REFUSED. PATIENT SAT IN THE PHARMACY FOR A FEW MORE MINUTES AND WAS THEN DRIVEN BACK TO WORK.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BLOOD PRESSURE, HEART RATE, EYE EXAM
Aktuelle Erkrankungen: SINUS INFECTION
Vorgeschichte: HIGH BLOOD PRESSURE
Andere Medikamente: AMOXICILLIN, NORVASC, XYZOL
Allergien: CECLOR
Vorherige Impfungen: -

VAERS 2716108

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 23,0
Geschlecht: F
Eingang: 21.11.2023
Impfdatum: 08.03.2021
Beginn: 28.01.2022
Tage bis Beginn: 326,0
Dosis: 1
Route/Site: IM / UN

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

Chills Cough Headache Pyrexia Tachycardia

Symptomtext

Patient was admitted for COVID related symptoms including fever, chills, cough, headache. She had maternal and fetal tachycardia and maternal fever on admission. She underwent the sepsis protocol. All her symptoms resolved and she was afebrile >24 hours. She was stable prior to discharge.

Weitere VAERSDATA-Felder

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

VAERS 2679304

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 53,0
Geschlecht: F
Eingang: 05.09.2023
Impfdatum: 10.03.2021
Beginn: 20.01.2022
Tage bis Beginn: 316,0
Dosis: 1
Route/Site: IM / RA

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

Anticoagulant therapy C-reactive protein increased COVID-19 pneumonia Chest X-ray abnormal Dyspnoea Fibrin D dimer Lung infiltration Positive airway pressure therapy Pyrexia Serum ferritin increased

Symptomtext

Presented with SOB/fever; DX: Covid PNA Labs: D-Dimer: 0.62; CRP: 11.6; Ferritin: 368 CXR: bil infiltrates TX: Steroids, remdesivir, lovenox, zinc, singulair; Initially on 5 LPM NC; went up to Bipap and High Flow O2 (60/80); back down to 3 LPM NC at d/c; cont O2 @ home

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2672950

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 56,0
Geschlecht: M
Eingang: 17.08.2023
Impfdatum: 08.03.2021
Beginn: 12.01.2022
Tage bis Beginn: 310,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Coronavirus pneumonia Hypoxia

Symptomtext

Chief Complaint: Hypoxia. Diagnosed with COVID on 1/6. Coronavirus pneumonia. We will start him on moderate dose of steroid as he is requiring 4 L so far. Increase the dose of steroid accordingly. He is not a candidate for Remdesivir

Weitere VAERSDATA-Felder

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

VAERS 2659596

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 45,0
Geschlecht: M
Eingang: 21.07.2023
Impfdatum: 29.10.2021
Beginn: 08.01.2023
Tage bis Beginn: 436,0
Dosis: 2
Route/Site: IM / LA

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

Back pain Blindness Chest pain Headache Muscular weakness Vein disorder

Symptomtext

Vein bulging initially with leg weakness. Then in 2023 after having COVID, severe headaches and loss of vision, chest pain and back pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 5/15/2023
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: testosterone
Allergien: NSAID, Penicillin
Vorherige Impfungen: -

VAERS 2618358

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 68,0
Geschlecht: M
Eingang: 20.04.2023
Impfdatum: 07.05.2021
Beginn: 28.02.2023
Tage bis Beginn: 662,0
Dosis: UNK
Route/Site: IM / LA

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

Blood sodium increased COVID-19 Chest pain Dehydration Escherichia urinary tract infection Renal disorder SARS-CoV-2 test positive

Symptomtext

He had two vaccines that I am aware of: J and J at Health dept 5-7-21 and Pfizer on 11-26-21 at this locatioin pharmacy Nursing Home resident sent to ER 2-2-2023 with what they thought was chest pain (he is unable to give history) , did not have MI, had dehydration, covid and renal issues and found to have E coli UTI and was rehydrated. Also had high sodium. On 2-7-23 he tested + for covid and had to be kept for five days and then ended up being transferred to med center to consider Peg tube. His course was complicated and he was sent to hospice for further care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HYPERTENSION, SCHIZOPHRENIA, SPEECH IMPEDIMENT, GERD, CHRONIC CONSTIPATION, LEFT SIDED WEAKNESS
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2585380

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 64,0
Geschlecht: F
Eingang: 22.02.2023
Impfdatum: 05.03.2021
Beginn: 22.04.2022
Tage bis Beginn: 413,0
Dosis: 1
Route/Site: - / -

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

COVID-19 COVID-19 immunisation Ear pain Paraesthesia SARS-CoV-2 test Vaccination failure

Symptomtext

EAR PAIN; MUSCLE TINGLING; CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a 66 year old female. Initial information was processed along with additional information on 21-FEB-2023. The patient's height, and weight were not reported. The patient's past medical history included: ruptured spleen (ruptured spleen due to fall), fall, and splenectomy (total), and concurrent conditions included: drug allergy (Thimerosal reaction), and immunocompromised, and other pre-existing medical conditions included: The patient not had other conditions or medication. The patient was not pregnant at the time of vaccination. The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805025 expiry: UNKNOWN) dose was not reported, 1 total, administered at right arm on 05-MAR-2021 10:30 for covid-19 prophylaxis. Age at time of vaccination 64 years old. No concomitant medications were reported. The patient also received moderna covid-19 vaccine (elasomeran) (Dose number in series 2) (form of admin and route of admin was not reported, batch number: 939904, expiry: Unknown) dose was not reported, administered at right arm on 04-NOV-2021 for covid-19 prophylaxis. It was unknown whether the patient experienced any adverse events following vaccination with moderna covid-19 vaccine (elasomeran) (Dose number in series 2). The patient also received moderna covid-19 vaccine (elasomeran) (Dose number in series 3) (form of admin and route of admin was not reported, batch number: 001M21A, expiry: Unknown) dose was not reported, administered at right arm on 22-APR-2022 for covid-19 prophylaxis which was associated with revaccination with different covid-19 vaccine (Dose number in series 3). On 01-FEB-2023, Laboratory data included: COVID-19 virus test Positive (lateral flow test), the patient had covid-19 (confirmed covid-19 infection) (Dose number in series 3) and received non company suspect drug paxlovid (nirmatrelvir/ritonavir) (form of admin and route of admin was not reported, batch number: GF4083 expiry: Unknown) dose and frequency were not reported from 01-FEB-2023 to 05-FEB-2023 for covid-19 treatment. On an unspecified date, the patient had chills, sore throat, headache, runny nose, sneezing, watery eyes, diarrhea and poor appetite returned after feeling well for about 5 days (confirmed covid-19 infection) (Dose number in series 3). The patient also had muscle tingling and ear pain (Dose number in series 3). On 12-FEB-2023, Laboratory data included: COVID-19 virus test Positive (11 days after first positive lateral flow test) which leads to confirmed clinical vaccination failure (Dose number in series 1). The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, and elasomeran was not applicable; and action taken with nirmatrelvir/ritonavir was not reported. The outcome of the confirmed covid-19 infection, confirmed clinical vaccination failure, revaccination with different covid-19 vaccine, muscle tingling and ear pain was not reported. This report was serious (Other Medically Important Condition). This case was associated with a product quality complaint: 90000272070.; Sender's Comments: V0: 20230244175-confirmed clinical vaccination failure . The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event. Specifically: SPECIAL SITUATIONS. Therefore, this event is considered inconsistent with vaccine administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20230201; Test Name: COVID-19 VIRUS TEST; Test Result: Positive ; Test Date: 20230212; Test Name: COVID-19 VIRUS TEST; Test Result: Positive
Aktuelle Erkrankungen: Drug allergy (Thimerosal reaction); Immunocompromised
Vorgeschichte: Medical History/Concurrent Conditions: Fall; Rupture of spleen (ruptured spleen due to fall); Splenectomy (total); Comments: The patient not had other conditions or medication. The patient was not pregnant at the time of vaccination.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2577393

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: ND
Alter: 60,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 10.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / UN

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

Arthralgia C-reactive protein Disability Full blood count Malaise Metabolic function test Mobility decreased Red blood cell sedimentation rate Swelling

Symptomtext

severe joint pain, swelling, disabling symptoms with generalized malaise (mostly wrists and hands). Most severe malaise for 7-10 days, not able to get out of bed, but joints symptoms not resolving for more than 6 months.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: cbc, cmp, esr, crp.
Aktuelle Erkrankungen: Polymyalgia rheumatica
Vorgeschichte: polymyalgia rheumatica, hyperlipidemia
Andere Medikamente: prednisone 5-8 mg, vitamin D
Allergien: Latex, ped dander.
Vorherige Impfungen: -

VAERS 2570041

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 51,0
Geschlecht: F
Eingang: 29.01.2023
Impfdatum: 12.03.2021
Beginn: 01.06.2021
Tage bis Beginn: 81,0
Dosis: 1
Route/Site: IM / RA

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

Acoustic stimulation tests Condition aggravated Meniere's disease Tinnitus Vertigo

Symptomtext

Approximately 3 months after vaccine, I developed an echo in my left ear resulting in a significant decrease in speech discernment. I also experienced an increase in meneire?s vertigo attacks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Hearing test
Aktuelle Erkrankungen: -
Vorgeschichte: Meneires disease
Andere Medikamente: Yes
Allergien: Sulpha drugs, Augmentum
Vorherige Impfungen: -

VAERS 2536731

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: DC
Alter: 50,0
Geschlecht: M
Eingang: 19.12.2022
Impfdatum: 21.03.2021
Beginn: 14.04.2021
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Tongue haematoma

Symptomtext

Hematomas on my tongue. I first started getting oral hematomas in 2003 subsequent to several vaccination and medical errors; for example, there were dosage errors in the Anthrax and Pneumovax vaccine administered to me. Also in 2003, I was given the wrong dosage for the malaria medication Lariam (once daily instead of once weekly). I also have photographs I took of my hematomas after the J& J vaccine. Also, I had no outbreak of hematomas between 2016 and and my J&J vaccine in 2021 after I started supplementing with vitamin D3/K2. However, these hematomas came back after receiving the J&J vaccine, and also after getting the Moderna jab in December 2021. Consequently, I have not had a COVID vaccine since December 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Idiopathic hypersomnia.
Vorgeschichte: Chronic Fatigue Syndrome, PTSD.
Andere Medikamente: Acetyl Carnitine, Alpha Lipoic Acid, Gamma Linolenic Acid, N-Acetyl Cysteine, Magnesium, Zinc, Kelp / Bladderwrack, Liposomal vitamin C, Vitamin D3/K2.
Allergien: Adverse reaction (severe hives lasting a week) to Anthrax vaccine while administered in 2003 and Wellbutrin in 2014. Also, allergic rhinitis diagnosed in 2001.
Vorherige Impfungen: Anthrax vaccine (hives) / Pneumovax

VAERS 2449597

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 06.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Acoustic stimulation tests COVID-19 Cardiac function test Foetal exposure during pregnancy Pneumonia respiratory syncytial viral Premature baby SARS-CoV-2 test

Symptomtext

PNEUMONIA DUE TO RSV; PREMATURE BIRTH; FOETAL EXPOSURE DURING PREGNANCY; COVID-19; This solicited pregnancy report received from a consumer concerned a female neonate of an unspecified race and ethnicity. The patient was enrolled in a non-company sponsored study C-VIPER: COVID 19 Vaccines Pregnancy Exposure Registry. The patient's weight was 3.51 kilograms (7 pounds and 12 ounces) and height was not reported. No concurrent conditions were reported. The maternal medical history of the patient's mother (44 years old) included anxiety, low blood pressure. The maternal obstetrical history of the patient's mother included five previous pregnancies of which four resulted in live newborn. The body mass index (BMI) for the patient's mother was 19.68. The mother had no history of tobacco use, however reported history of alcohol and recreational drug use. Maternal first day of the last menstrual period (LMP) for the patient's mother was calculated to be 10-AUG-2020, the estimated delivery date (EDD) was reported to be 17-MAY-2021. The mother had singleton pregnancy and on 10-MAY-2021 at gestational age of 39 weeks, the mother delivered vaginally live, pre-term female neonate and the mother spent two days in the hospital for the delivery. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, transplacental, batch number: 1805025 and expiry: UNKNOWN) dose was not reported, 1 total administered on 06-MAR-2021 for covid-19 immunisation. Concomitant medications included zyrtec (cetirizine hydrochloride) (drug started on 10-AUG-2020), pepcid AC (famotidine) (drug started on 15-NOV-2020) and minerals nos/vitamins nos. On 06-MAR-2021, the patient had foetal exposure during pregnancy. Duration of the event, foetal exposure during pregnancy was reported as 66 days. On 10-MAY-2021, the patient had premature birth. On MAY-2021, cardiac function test and hearing test were performed and results were unknown (not reported). On 16-OCT-2021, the patient experienced pneumonia due to RSV (Respiratory syncytial virus). On 16-OCT-2021, the patient was hospitalized. The number of days of hospitalization was not reported. It was unknown if the patient was discharged. On 06-FEB-2022, the patient was diagnosed with covid-19 and on the same day laboratory data included: SARS-CoV-2 test and result was not reported. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from foetal exposure during pregnancy on 10-MAY-2021, and the outcome of pneumonia due to RSV, premature birth and covid-19 was not reported. The reporter considered the causality between covid-19 vaccine ad26.cov2.s, and pneumonia due to RSV, premature birth, foetal exposure during pregnancy, and covid-19 as not related. This report was serious (Hospitalization Caused / Prolonged, and Other Medically Important Condition). This parent/child case is linked to 20210726619.; Sender's Comments: V0: 20220918409-covid-19 vaccine ad26.cov2.s-Pneumonia due to RSV. The event(s) shows an incompatible temporal relationship. Therefore, this event(s) is considered not related. 20220918409-covid-19 vaccine ad26.cov2.s-Premature birth. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: MEDICAL HISTORY(Advanced maternal age and high parity). Therefore, this event(s) is considered not related. 20220918409-covid-19 vaccine ad26.cov2.s-Foetal exposure during pregnancy. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia respiratory syncytial viral
Hospital-Tage: -
Labordaten: Test Date: 202105; Test Name: HEARING TEST; Result Unstructured Data: not reported; Test Date: 202105; Test Name: CARDIAC FUNCTION TEST; Result Unstructured Data: not reported; Test Date: 20220206; Test Name: SARS-COV-2 TEST; Result Unstructured Data: not reported
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; PEPCID AC
Allergien: -
Vorherige Impfungen: -

VAERS 2426566

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 77,0
Geschlecht: F
Eingang: 01.09.2022
Impfdatum: 13.03.2021
Beginn: 21.07.2022
Tage bis Beginn: 495,0
Dosis: 1
Route/Site: - / -

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

Blood creatinine increased COVID-19 Cough Decreased appetite Dyspnoea Feeling abnormal Fluid intake reduced Haemoglobin decreased Haemophilus test positive Lung infiltration Pneumonia Pneumonia bacterial Pyrexia SARS-CoV-2 test positive Sputum culture positive Sputum discoloured Staphylococcus test positive Transfusion

Symptomtext

79 y.o. Admit Date: 7/21/2022 Discharge Date: 7/28/2022 Principal Dx/ Final Dx: Pneumonia of left lower lobe due to infectious organism Relevant Inpt Dx: Principal Problem: Pneumonia of left lower lobe due to infectious organism Active Problems: Hypothyroidism COVID-19 Acute renal failure superimposed on stage 3 chronic kidney disease Coag negative Staphylococcus bacteremia T2DM (type 2 diabetes mellitus) Benign essential HTN Follow-up Recommendations: #1 please take medication as prescribed #2 please keep follow-up appointments HPI: As per Dr Note: "Patient is a 79 y.o. female who presents to ED with c/o cough, fever and shortness of breath for 4-5 days. Was seen on 7/18 and COVID + (had 1 dose J&J). Had blood cx then with 2/4 bottles coag neg staph, was called back to ED. States she has been feeling worse, now having thick yellow sputum production. Not eating/drinking well. Does have h/o CKD, her Cr is above baseline, also has LLL infiltrate. ED workup more c/w bacterial pneumonia but also has COVID, will admit. Family at bedside and assists w/history." Hospital Course: Patient presented with cough and shortness breath. She was found to have left lower lobe pneumonia related to Covid 19 infection. She was also found to have Haemophilus influenza in her sputum cultures. MRSA screen was positive. She was started on empiric antibiotics which were gradually weaned to Omnicef and doxycycline based on culture and sensitivity data. She completed the course of ampicillin and Decadron. Gradually her symptoms improved and was considered suitable for discharge home. Rehabilitation/nursing home placement was offered but family preferred to take him home with home health services. During her hospital stay her hemoglobin dropped to 6.6 requiring one unit of blood transfusion. She was evaluated by gastroenterology and no EGD was recommended at this time. Her hemoglobin remained stable after initial blood transfusion. She was started on Protonix. Potassium and magnesium were appropriately replaced while inpatient. Unresolved issues requiring follow up (w/ labs or studies): Follow-up BMP next week for potassium levels Consults: CONSULT TO SOCIAL WORK CONSULT TO GASTROENTEROLOGY CONSULT TO SOCIAL WORK CONSULT LUNG HEALTH ADVISOR Significant Diagnostic Studies: Chest x-ray with the left lower lobe pneumonia Covid 19 positive Hypokalemia Hypomagnesemia Operations: None Wound care recs: None Disposition: Home with home health Discharge Condition: good Discharge Medications: Current Discharge Medication List START taking these medications Details cefdinir (OMNICEF) 300 mg capsule Take 1 Capsule by mouth Twice a day for 3 days. Qty: 6 Capsule, Refills: 0 Associated Diagnoses: Pneumonia of left lower lobe due to infectious organism doxycycline monohydrate (MONODOX) 100 mg capsule Take 1 Capsule by mouth Twice a day for 3 days. Indications: pneumonia Qty: 6 Capsule, Refills: 0 Associated Diagnoses: Pneumonia of left lower lobe due to infectious organism potassium chloride SA (KLOR-CON) 20 mEq tablet Take 1 Tablet by mouth Once Daily for 3 days. Qty: 3 Tablet, Refills: 0 Associated Diagnoses: Hypokalemia pantoprazole (PROTONIX) 40 mg DR tablet Take 1 Tablet by mouth Once Daily for 30 days. Qty: 30 Tablet, Refills: 0 Associated Diagnoses: Gastroesophageal reflux disease with esophagitis, unspecified whether hemorrhage CONTINUE these medications which have CHANGED Details magnesium chloride (SLOW-MAG) 71.5 mg DR tablet Take 2 Tabs by mouth Twice a day for 30 days. Qty: 120 Tablet, Refills: 0 Associated Diagnoses: Hypomagnesemia CONTINUE these medications which have NOT CHANGED Details cyanocobalamin-salcaprozat sod 1,000 mcg Tab Take by mouth. levocetirizine (XYZAL) 5 mg tablet Take 5 mg by mouth Once Daily. ergocalciferol (VITAMIN D2) 50,000 unit CAPSULE Take 1 Capsule by mouth Every week. Qty: 12 Capsule, Refills: 3 Associated Diagnoses: Vitamin D deficiency levothyroxine (SYNTHROID) 50 mcg tablet Take 1 Tablet by mouth Once Daily. Qty: 90 Tablet, Refills: 3 Associated Diagnoses: Nontoxic diffuse goiter rosuvastatin (CRESTOR) 40 mg tablet Take 1 Tablet by mouth Once Daily. Qty: 90 Tablet, Refills: 3 Associated Diagnoses: Mixed hyperlipidemia clopidogreL (PLAVIX) 75 mg tablet Take 1 Tablet by mouth Daily. Qty: 90 Tablet, Refills: 3 Associated Diagnoses: Coronary artery disease involving native coronary artery of native heart without angina pectoris metoprolol (LOPRESSOR) 25 mg tablet Take 75 mg by mouth Twice a day. amitriptyline (ELAVIL) 50 mg tablet Take 1 Tab by mouth Daily.

Weitere VAERSDATA-Felder

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

VAERS 2213685

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 23.04.2022
Impfdatum: -
Beginn: 17.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Asthenia Blood pressure measurement Body mass index Body surface area Body temperature Condition aggravated Injection site pain Muscular weakness Initial insomnia Mammogram Middle insomnia Mobility decreased Muscle spasms Pain Pain in extremity Swelling

Symptomtext

DECREASED MOBILITY; DIFFICULTY INITIATING SLEEP; NOCTURNAL AWAKENING; NOCTURNAL PAIN; SPASMS; SWELLING; RIGHT ARM SEVERE PAIN; PAIN AT THE INJECTION SITE; WEAKNESS; This spontaneous report received from a patient via health care professional via a Regulatory Authority VAERS (Vaccine Adverse Event Reporting System) (VAERS ID 1856008) concerned a 54 year old female of an unspecified ethnicity. The patient's weight was 65.31 kilograms, and height was 162 centimeters. The patient's past medical history included: broken bone, joint injury, low back pain, back surgery, hernia repair, and cesarean section, and concurrent conditions included: arthritis, asthma, depression, insomnia, migraine, thyroid disease, non-smoker (no passive smoke exposure), postmenopausal, alcohol user (occasionally), caffeine user, latex allergy, and sulfa (sulfonamide antibiotics) allergy, and other pre-existing medical conditions included: The patient was not allergic to egg, neomycin and gelatin. The patient's family history includes father had cancer (unspecified) and diabetes mellitus, and mother and sister had cancer(unspecified). The patient was not pregnant at the time of vaccination. The patient was married and does not needed interpreter. The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 1), (suspension for injection, intramuscular, batch number: 1805025, expiry: UNKNOWN) dose was not reported, 1 total administered on 17-MAR-2021 to right deltoid for an unspecified indication. Age at time of vaccination 54 years old. No concomitant medications were reported. On 17-MAR-2021, the patient experienced decreased mobility, difficulty initiating sleep, nocturnal awakening, nocturnal pain, spasms, swelling, right arm severe pain, pain at the injection site, and weakness (Dose number in series 1). it was reported that right arm pain occurs constantly and was stable. The pain was aching, sharp and piercing. The pain was aggravated by bending, lifting and movement. There was no reliving factors as per reported. On 25-MAY-2021, Laboratory data included: Mammogram (NR: not provided) not reported. On 15-DEC-2021, the patient received additional Pfizer Covid-19 vaccine (dose number in series 2), (form of admin, route of admin, and batch number were not reported), dose was not reported, administered for an unspecified indication. It was unknown whether patient had any adverse events following vaccination (dose number in series 2). On 25-MAR-2022 at 15:30, the patient visited the physician office. On 25-MAR-2022, Laboratory data included: Blood pressure (NR: not provided) 96/60 mmHg, Body mass index (NR: not provided) 24.72 kg/m2, Body surface area (NR: not provided) 1.72 m2, and Body temperature (NR: not provided) 98 F. Treatment medications included: levosalbutamol hydrochloride (inhale 3 millimliter by nebulization route every 8 hours for cough and shortness of breath, as needed). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from pain at the injection site, weakness, right arm severe pain, decreased mobility, difficulty initiating sleep, nocturnal awakening, nocturnal pain, spasms, and swelling. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20210525; Test Name: Mammogram; Result Unstructured Data: not reported; Test Date: 20220325; Test Name: Body surface area; Result Unstructured Data: 1.72 m2; Test Date: 20220325; Test Name: Body mass index; Result Unstructured Data: 24.72 kg/m2; Test Date: 20220325; Test Name: Body temperature; Result Unstructured Data: 98 F; Test Date: 20220325; Test Name: Blood pressure; Result Unstructured Data: 96/60 mmHg
Aktuelle Erkrankungen: Alcohol use (occasionally); Arthritis; Asthma; Caffeine consumption; Depression; Insomnia; Latex allergy; Migraine; Non-smoker (no passive smoke exposure); Postmenopause; Sulfonamide allergy; Thyroid disorder
Vorgeschichte: Medical History/Concurrent Conditions: Back surgery; Cesarean section; Fracture bone; Hernia repair; Joint injury; Low back pain; Comments: The patient was not allergic to egg, neomycin and gelatin. The patient's family history includes father had cancer (unspecified) and diabetes mellitus, and mother and sister had cancer(unspecified). The patient was not pregnant at the time of vaccination. The patient was married and does not needed interpreter.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2243207

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: -
Alter: 60,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 01.04.2021
Beginn: 27.07.2021
Tage bis Beginn: 117,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Cough Dyspnoea Exposure to SARS-CoV-2 SARS-CoV-2 test positive

Symptomtext

8/3/21 PMH of diabetes mellitus, type II; presents for cough and SOB after exposure and positive covid test at urgent care

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 7/27/21 SARS-CoV-2 (COVID-19) by PCR Detected by Labs
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2218082

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: OH
Alter: 71,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 09.03.2021
Beginn: 23.07.2021
Tage bis Beginn: 136,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Chemotherapy Dyspnoea Pleural effusion SARS-CoV-2 test positive

Symptomtext

Janssen COVID vaccine received on 3/9/2021 She was at hospital for chemo treatment on 7/19/2021 and tested positive for COVID-19 tested due to shortness of breath Hospitalized on 7/26/2021 with trace of left pleural effusion

Weitere VAERSDATA-Felder

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

VAERS 2216023

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 57,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 02.02.2022
Beginn: 06.02.2022
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Mobility decreased Muscular weakness

Symptomtext

PATIENT STATES SHE HAD LOST USE OF BOTH LEGS FOR APPROXIMATELY 2-4 WEEKS AFTER RECEIVING VACCINE. STATES THAT SHE STILL HAS LASTING EFFECTS OF WEAKNESS IN BOTH LEGS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: NOT AT THIS TIME
Aktuelle Erkrankungen: NO
Vorgeschichte: HYPOTHYROIDISM; HYPERLIPIDEMIA; DIABETES TYPE II; DEPRESSION; HYPERTENSION
Andere Medikamente: PRAVASTATIN; VITAMIN D; METFORMIN; NORAVASC; EFFEXOR; METOPROLOL; LEVOTHYROXIN
Allergien: NKA
Vorherige Impfungen: -

VAERS 2196938

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: -
Alter: 58,0
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: 19.03.2021
Beginn: 10.01.2022
Tage bis Beginn: 297,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

01/10/22 presents to ED for "cough shortness of breath". PMHx of " type 2 diabetes, renal transplant, hypertension, peripheral vascular disease status post right BKA"

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 2192141

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CO
Alter: 56,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 18.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test normal Burning sensation Chest X-ray normal Chills Dyspnoea Fatigue Insomnia Muscle spasms Myalgia Pain Pyrexia

Symptomtext

I had extreme pain all over my body. I was in agonizing pain for a week and for 2 weeks before it was reduced. I had fever and chills. I had intense burning pain all over. It felt like my body was on fire. I was on Percocet for 2 weeks straight. I have severe fatigue, fever, aches, and short of breath. My muscles burn and cramp up. I get tired so easily and can hardly sleep. I have tried potassium, calcium, and ibuprofen but nothing has helped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Bloodwork- normal; Chest x-rays- normal.
Aktuelle Erkrankungen: None
Vorgeschichte: Sarcoidosis; Eosinophilic Syndrome; Mild Asthma
Andere Medikamente: Singulair 10mg; Amitriptyline 5mg; Albuterol Inhaler, as needed; Hydroxyzine 25mg
Allergien: Xolair; Hay Fever
Vorherige Impfungen: -

VAERS 2189047

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 81,0
Geschlecht: M
Eingang: 19.03.2022
Impfdatum: 29.10.2021
Beginn: 16.03.2022
Tage bis Beginn: 138,0
Dosis: UNK
Route/Site: - / -

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

Asthenia COVID-19 Gait inability Hypotension Leukocytosis SARS-CoV-2 test positive Urinary tract infection Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 03/21/2021. 82 y/o with PMHX of CAD/CABG, DM, HTN, HLD, Metastatic prostate cancer, chemotherapy, Left nephrostomy tube presents to ED via EMS on 3/7/2022. Pt was receiving home PT and after assessed by the therapist, pt was found to have generalized weakness, inability to walk and hypotension so EMS called. In ED, Pt hypotensive, with Leukocytosis/UTI, possible sepsis, ARF. Room air sat 95%, afebrile. Covid test not done on admission. However, pre-procedure Covid test performed on 03/16/2022 -positive. Repeat test on 3/18/2022 also positive. Pt on IV ABX and IVF's.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19- Detected on 03/16/2022 and 03/18/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: CAD/CABG, DM, HLD, HTN, Metastatic prostate cancer, chemotherapy, Left nephrostomy tube
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2152568

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 54,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 02.04.2021
Beginn: 04.01.2022
Tage bis Beginn: 277,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain Atrial fibrillation COVID-19 Chest X-ray abnormal Dyspnoea Endotracheal intubation Intestinal perforation Lung opacity Mechanical ventilation Peritonitis Pleural effusion Pneumonia aspiration Positive airway pressure therapy SARS-CoV-2 test positive Vomiting

Symptomtext

Patient received J&J vaccine on 4/2/21. COVID positive on 1/4/22 and presented to ER on 1/14/22. Presented to outside hospital for abdominal pain and shortness of breath found to have perforated bowel, b/l pleural effusions, and afib RVR.Then transferred to a HCF. Admitted for peritonitis. Incidentally covid positive. Patient had episode of emesis while on ventilator 1/18. Patient extubated to Optiflow and required re-intubation likely secondary to aspiration pneumonia from emesis. Extubated to optiflow 1/25. Placed back on BiPAP 1/30. Stable thereafter. Discharged on 2/18/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 35,0
Labordaten: 1/4/22 COVID19: positive 1/15/22 chest xray: Moderate size right pleural effusion with support devices as described above 2/8/22 chest xray: Continued bibasilar opacification, right greater than left.
Aktuelle Erkrankungen: -
Vorgeschichte: Tobacco abuse GERD
Andere Medikamente: none
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 2110769

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 52,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 01.04.2021
Beginn: 04.04.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / -

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

Arthralgia Condition aggravated Flatulence Gastrointestinal disorder

Symptomtext

I had suffered from mild joint pain, and also had occasional stomach issues, especially gas. The severity of these issues went up considerably since the vaccine, and seemed to be made even worse after the booster that I received on 11-22-21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I've gone to my GP as well as physical therapist for these issues.
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2095786

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 61,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 09.03.2021
Beginn: 01.02.2022
Tage bis Beginn: 329,0
Dosis: 1
Route/Site: IM / RA

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

Acute kidney injury Blood creatinine increased Blood urea increased Chest X-ray abnormal Cough Dyspnoea Pleural effusion

Symptomtext

Acute Renal failure, Creatinine 4.3, BUN 33, hemo dialysis x3 weekly. Pt has been unable to find transportation to dialysis over the last several days. Pt complaints of SOB x3 days with cough. O2 saturation 99-100% on RA, Chest Xrays showing bilateral layering pleural effusions with no significant acute interstitial airspace disease.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, CAD, Type II DM, COPD, ESRD on dialysis
Andere Medikamente: -
Allergien: Darvocet
Vorherige Impfungen: -

VAERS 2088280

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MS
Alter: 64,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 30.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Condition aggravated Injection site swelling Neuropathy peripheral Rash Rash pruritic

Symptomtext

Itchy rash appeared on neck, swelling at injection site and worsened neuropathy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure; asthma; chemo (04/2019)
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2082491

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CO
Alter: 61,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 13.05.2021
Beginn: 21.06.2021
Tage bis Beginn: 39,0
Dosis: 1
Route/Site: SYR / AR

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

Bundle branch block left Cardiac monitoring Cardiac stress test Chest X-ray Echocardiogram Electrocardiogram Feeling abnormal Heart rate increased Nasopharyngitis Palpitations SARS-CoV-2 antibody test positive SARS-CoV-2 test negative

Symptomtext

I felt poorly in mid-June 2021 about 5 or 6 weeks after the vaccination, I remember feeling chest palpitations and racing pulse and cold-like symptoms and went to a local clinic to be tested for COVID19. I tested negative for having COVID 19 but had the long term antibodies for it. I late November 2021, I was having racing pulse (around 1600) several times throughout the evenings and night and the triage nurse for my PCP wanted me to go to the ER. I went to a local Hospital (approximately 12-05-2021) and was diagnosed with a Left Bundle Branch Block. I have never had a Left Bundle Branch Block before and have been told that this may have occurred as a result of taking the J & J vaccination. I have since seen a private cardiologist at a local office and did a 30 day heart monitor to check for issues such as A-Fib from mid- December 2021 into January 2022. I do not yet have results. My appointment with the cardiologist is scheduled for February 11, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 2,0
Labordaten: The local Hospital ran tests such as EKG, Echocardiogram, NM heart stress test, chest x-ray, etc. and said that I now have a Left Bundle Branch Block. I did a 30 day heart monitor to check for issues such as A-Fib from mid- December 2021 into January 2022 through HCF. I do not yet have results. My appointment with the cardiologist is scheduled for February 11, 2022.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma and Allergies (weak respiratory system)
Andere Medikamente: Vitamin D, 50,000 IU, once weekly; Zetia, 10 mg., 1x daily; Famotidine, 40 mg., 1x daily; Levothyroxine, 150 mcg., 1x daily; Singular, 10 mg, 1x daily; Pantoprazole, 40 mg, 1x daily; multivitamin 1x daily; Ancestral Supplements Grassfed
Allergien: -
Vorherige Impfungen: -

VAERS 2079090

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 23.03.2021
Beginn: 03.01.2022
Tage bis Beginn: 286,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Chest X-ray Chest pain Fatigue Nausea Pain Pyrexia

Symptomtext

Patient is fully vaccinated. Boosted on 12/22/2021. COVID + at ED visit on 1/3/2022. 53-year-old female with a history of liver transplant. Patient presents to the emergency department with concern of covid infection. Patient states that her symptoms started 2 days ago. She is having body aches, fatigue, feeling feverish, nausea. She is on chronic immunosuppressants for her transplant. She does have bilateral chest pain worse with deep inhalation and cough. Denies any shortness of breath, hemoptysis, lower extremity swelling, history of PE or DVT. CXR: Chest appears as stated without evidence of a suspicious pleural or parenchymal abnormality. Normal EKG. Discharged home stable

Weitere VAERSDATA-Felder

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

VAERS 2047824

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MN
Alter: 71,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 17.01.2021
Beginn: 17.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest discomfort Chest pain Dyspnoea Headache Nausea Peripheral coldness

Symptomtext

I LEFT THE VACCINE FACILITY AND I ONLY GOT ABOUT A MILE AWAY & I STARTED FEELING THIS BURNING & TIGHTNESS IN MY CHEST WHEN I WOULD BREATHE SO I FOUND A PLACE TO SIT DOWN AND I HAD SHORTNESS OF BREATH SO I CONTINUED WALKING THEN WHEN I GOT HOME I WOKE UP IN THE MIDDLE OF THE NIGHT & BOTH OF MY LEGS FELT LIKE THEY WERE FREEZING COLD SO I TURNED ON MY ELECTRIC BLANKET & IT TOOK ABOUT 2 HRS BEFORE THEY FELT WARM I WAS LAID UP IN BED FOR THE NEXT 36 HRS & I JUST RESTED & SLEPT I HAD A HEADACHE FOR MOST OF THE TIME & WAS VERY NAUSEOUS.I CALLED MY DR THE NEXT DAY & WAS TOLD TO MAKE APPT & HE REFERRED ME TO AN ALLERGIST.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: GERD CH0LESTEROL SQUAMOUS CELL CARCINOMA BLOOD CLOTS/LUNGS
Andere Medikamente: ATORVASTATIN PANTOPRAZOLE ASPIRIN ALPHA INTERFERON 2B
Allergien: SULFA DRUGS CATS
Vorherige Impfungen: -

VAERS 2027886

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 53,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 11.03.2021
Beginn: 18.11.2021
Tage bis Beginn: 252,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Chest X-ray normal Chest pain Cough Fatigue Laboratory test normal SARS-CoV-2 test positive

Symptomtext

Patient tested positive for COVID on 11/17/2021. Fully vaccinated and also vaccinated with a booster. 52-year-old female presents complaining of cough and fatigue.Admits to some chest aching but denies any chest pain with exertion. Denies any leg pain, leg swelling, shortness of breath.She was given IVF, Toradol, Tylenol, and Decadron. CXR negative for acute process. Labs reviewed, no significant abnormalities. Pt agreed to giving Dr. clinic her information for monoclonal antibody infusion.Told to return to ED for any new, worsening, changing or persistent symptoms.

Weitere VAERSDATA-Felder

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

VAERS 2020901

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 55,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 10.03.2021
Beginn: 11.11.2021
Tage bis Beginn: 246,0
Dosis: 1
Route/Site: - / -

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

Back pain COVID-19 Chest pain Cough Dyspnoea Electrocardiogram normal Nasal congestion Nausea Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Troponin normal

Symptomtext

Pt tested positve for COVID on 11/11/2021.Chief complaint, cough, nasal congestion. 56y.o. male presenting to the emergency department for chest pain. Patient also admits to shortness of breath. Patient admits to congestion and rhinorrhea for 1 week. Positive for back pain and nausea. Troponin normal, EKG normal sinus rhythm, no signs of ischemia, no arrhythmia and non-specific ST-T changes. Treatment: Decadron and Toradol. Stable for discharged. Discharged to home.

Weitere VAERSDATA-Felder

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

VAERS 1966622

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 60,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 21.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / -

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

Hypoaesthesia Muscle spasms Pain in extremity Paraesthesia Neurological examination Plantar fasciitis Ultrasound scan

Symptomtext

Sharp and excruciatingly pain on lower right and left leg, both right and left leg/foot have continuous numbness and tingling sensation since receiving the vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Visited ER on 3/22/2021 and was informed it was a muscle spasm. They checked for blood clot but none was detected. Pending appointment to see a neurologist.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetic type 2
Andere Medikamente: Metformin
Allergien: None
Vorherige Impfungen: -

VAERS 1966622

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 60,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 21.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / -

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

Hypoaesthesia Muscle spasms Pain in extremity Paraesthesia Neurological examination Plantar fasciitis Ultrasound scan

Symptomtext

Sharp and excruciatingly pain on lower right and left leg, both right and left leg/foot have continuous numbness and tingling sensation since receiving the vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Visited ER on 3/22/2021 and was informed it was a muscle spasm. They checked for blood clot but none was detected. Pending appointment to see a neurologist.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetic type 2
Andere Medikamente: Metformin
Allergien: None
Vorherige Impfungen: -

VAERS 1988650

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: -
Alter: 56,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 10.03.2021
Beginn: 13.10.2021
Tage bis Beginn: 217,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Cardiac failure congestive Dyspnoea exertional Left ventricular failure SARS-CoV-2 test positive

Symptomtext

This patient was admitted to the emergency room, was COVID-19 positive even though the patient was immunized. The patient was saturating in the mid 90s on room air. Dyspnea on exertion. Congestive heart failure, systolic with exacerbation. Consultation was made for Pulmonary and Cardiology. His medications were adjusted. Discharged to home.

Weitere VAERSDATA-Felder

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

VAERS 1968095

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 91,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 22.03.2021
Beginn: 07.12.2021
Tage bis Beginn: 260,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Chills Cough Dyspnoea Headache Myalgia Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

BREAKTHROUGH COVID-19 VACCINE HOSPITALIZATION She was vaccinated with Janssen vaccine in March 2021. Rapid testing for covid-19 was positive on 12/7/21 after having symptoms of fever, chills, muscle aches, headache, cough and shortness of breath. She was then hospitalized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS-COV2 RAPID ASSAY=POSITIVE
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: HYPERTENSION
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 1939452

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 44,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 11.03.2021
Beginn: 05.12.2021
Tage bis Beginn: 269,0
Dosis: 1
Route/Site: IM / LA

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

Ageusia Anosmia Asthenia COVID-19 COVID-19 pneumonia Hypophagia Hypoxia SARS-CoV-2 test positive

Symptomtext

Symptoms started 11/27, states she had holiday facilities with her family the few days prior.She lost her sense of taste and smell. She has been feeling weak and not able to take in much p.o. intake. COVID-19 (+) on 12/5 with pneumonia. Hypoxia/78% on RA on admission.

Weitere VAERSDATA-Felder

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

VAERS 1939350

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 44,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 03.05.2021
Beginn: 03.12.2021
Tage bis Beginn: 214,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Chills Decreased appetite Dyspnoea Nausea Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

Patient presented to emergency department on 12/3/2021 after getting positive COVID-19 test result earlier that day. He was shortness of breath, fevers, chills, nausea/vomiting, and loss of appetite. He was admitted for further management. He was treated with supplemental oxygen and dexamethasone. He was discharged home on 12/5/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: Patient reported COVID-19 test positive on 12/3/2021.
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, morbid obesity, GERD
Andere Medikamente: albuterol (PROAIR HFA) 108 (90 BASE) MCG/ACT HFA inhaler budesonide-formoterol (SYMBICORT) 80-4.5 MCG/ACT inhaler hydrochlorothiazide (HYDRODIURIL) 25 MG tablet lisinopril (PRINIVIL) 10 MG tablet montelukast (SINGULAIR) 10 MG tablet
Allergien: None known
Vorherige Impfungen: -

VAERS 1927675

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Acoustic stimulation tests Foetal exposure during pregnancy Neonatal dyspnoea Premature baby

Symptomtext

Birth at gestational age 36 weeks; Problems with breathing; Foetal exposure during pregnancy; This solicited pregnancy report received from a consumer concerned a female Neonate of unspecified age. The patient's mother was enrolled in a non-company sponsored study, with unknown race and ethnicity. The patient's weight was 2.38 kilograms, and height was 48 centimeters. No past medical history or concurrent conditions were reported. The maternal (mother age was 32 Years old) medical history included anxiety, asthma, depression, polycystic ovary syndrome. The mother had body mass index (BMI) of 35.422. The mother had no relevant obstetrical history and no history of tobacco, alcohol or recreational drug use. The patient's mother initiated treatment with covid-19 vaccine ad26.cov2.s (suspension for injection, route not provided, batch number: 1805025, expiry: Unknown) dose was not reported, administered on 22-MAR-2021 for covid-19 immunisation (Dose number in series 1). neonate route of administration was transplacental. Concomitant medications included amoxicillin/clavulanic acid, salbutamol sulfate, sertraline hydrochloride and prenatal multivitamins. On 22-MAR-2021, the patient experienced foetal exposure during pregnancy. On unspecified date in OCT-2021, the patient experienced problems with breathing. Laboratory data included: Hearing test (NR: not provided) Unknown. At gestational age 36 weeks and two days, the mother delivered a live, premature, female neonate via caesarean method of delivery (C-section). Primary reason for C-section was reported as labor not progressing. Labor was induced due to pre-eclampsia. The mother spent five days in the hospital for the delivery. The neonate was admitted in the Neonatal Intensive Care Unit (NICU) due to problems with breathing. No birth defects, genetic or inherited disorders have been diagnosed since birth. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from foetal exposure during pregnancy on 12-OCT-2021, and the outcome of problems with breathing and birth at gestational age 36 weeks were not reported. The reporter considered the causality between covid-19 vaccine ad26.cov2.s, and birth at gestational age 36 weeks, and problems with breathing as not related. The reporter did not provide a causality assessment between covid-19 vaccine ad26.cov2.s, and foetal exposure during pregnancy. Company causality between covid-19 vaccine ad26.cov2.s, and foetal exposure during pregnancy, birth at gestational age 36 weeks, and problems with breathing was not related. This report was serious (Other Medically Important Condition). This parent/child case is linked to 20210727879.; Sender's Comments: V0: 20211205280- JANSSEN COVID-19 VACCINE Ad26.COV2.S- Birth at gestational age 36 weeks. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: MEDICAL HISTORY OF MOTHER (Pre-Eclampsia). 20211205280- JANSSEN COVID-19 VACCINE Ad26.COV2.S- Problems with breathing. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: MEDICAL HISTORY (Premature birth). 20211205280-JANSSEN COVID-19 VACCINE Ad26.COV2.S- Foetal exposure during pregnancy. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neonatal dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 202110; Test Name: Hearing test; Result Unstructured Data: Unknown
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ALBUTEROL [SALBUTAMOL SULFATE]; AUGMENTINE [AMOXICILLIN;CLAVULANIC ACID]; ZOLOFT
Allergien: -
Vorherige Impfungen: -

VAERS 1921692

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 43,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 18.03.2021
Beginn: 26.11.2021
Tage bis Beginn: 253,0
Dosis: 1
Route/Site: IM / UN

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

Ageusia Anosmia COVID-19 Cough Hypotension Hypoxia Lung infiltration Procalcitonin normal Pulmonary imaging procedure abnormal SARS-CoV-2 test positive

Symptomtext

She was diagnosed with COVID on November 22nd, she has symptoms on November 21st which included cough and loss of taste and smell. Patient was doing relatively well after the 22nd and was scheduled for a monoclonal antibodies morning. When she arrived to the facility they noted she was hypotensive on a wrist cuff blood pressure monitor to the center down to the ER. Her blood pressure was stable in the ER however they found her to be hypoxic with a saturation in the 70s. Placed on 2 L of oxygen with the a good response in her saturations. Workup over there was negative for pneumonia however imaging revealed bilateral patchy infiltrates. Procal was negative. Patient was transferred here for further management on 11/26/21 as their hospital did not have any bed availability. Patient denies any chest pain lightheadedness fevers or chills. She denies any dyspnea either. When she arrived to our facility her saturation was 84% on room air so she was placed back on 2 L of oxygen.Treated with dexamethasone, remdesevir, oxygen support. Gradually started to feel well. Weaned off oxygen prior to discharge. Discharged on 11/29/21

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Praegender Schweregrund: Hypotension
Hospital-Tage: 3,0
Labordaten: 11/22/21 COVID19: positive
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety, Breast cancer (HCC) (2014), Diabetes mellitus (HCC), Hypertension, and Obesity. Hx of DVT and PE
Andere Medikamente: Bupropion, buspirone, levothyroxine, lorazepam, losartan, metoprolol tartrate, trazodone, venlafaxine, vitamin D3, warfarin
Allergien: Lactose
Vorherige Impfungen: -

VAERS 1894310

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 18.03.2021
Beginn: 18.11.2021
Tage bis Beginn: 245,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Chest X-ray abnormal Cough Dyspnoea Pulmonary congestion SARS-CoV-2 test positive

Symptomtext

short of breath, cough beginning around 11/18/21, then presented to ER and tested positive for covid

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS-CoV-2 (COVID-19) by NAA, Micro detected 11/22/21 Chest xray 11/22: IMPRESSION: Question possibility of a right lower lobe infiltrate and mild congestion. Follow-up recommended
Aktuelle Erkrankungen: -
Vorgeschichte: s/p hip replacement
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1889441

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 49,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 10.03.2021
Beginn: 15.11.2021
Tage bis Beginn: 250,0
Dosis: UNK
Route/Site: IM / LA

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

COVID-19 Dyspnoea Fatigue Haemoptysis Headache Myalgia Productive cough Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient is a 50 y.o. male with PMH of pneumoconiosis, RA chronically on steroids who presented to the hospital for worsening shortness of breath, fever, and was recently tested positive for covid-19 Constitutional: Positive for fatigue and fever. Negative for chills. HENT: Negative for congestion. Eyes: Negative for visual disturbance. Respiratory: Positive for cough (Productive) and shortness of breath. Typically wears oxygen only as needed at night though prior to admission requiring 2-3L constantly. Also prior to admission had been started on dexamethasone as outpatient on 11/9 without improvement. Treated with remdesivir x5d and continued on dexamethasone 6mg daily. Noted to have fevers this admission with significant cough productive of sputum with streaks of blood, severe myalgias, and headaches. Managed symptomatically with anti-tussives, NSAIDs, scheduled acetaminophen and oxycodone (at home takes Norco PRN). Discharge Disposition/Condition Disposition: Home Condition: Stable (s/sx potential problems absent or manageable)

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: COVID PCR positive on 11/15/21
Aktuelle Erkrankungen: N/A
Vorgeschichte: He has a past medical history of Hypoglycemia, unspecified, Other nonspecific abnormal finding of lung field, Personal history of other specified conditions, Rheumatoid arthritis, unspecified, and Unspecified disorder of nose and nasal sinuses.
Andere Medikamente: albuterol neb albuterol inhaler ascorbic acid tablet budesonide-formoterol cholecalciferol escitaolopram famotidine gabapentin hydorxyzine pamoate ibuprofen pantoprazole sucralfate thiamine tiotropium inhaler zinc sulfate dexamethasone hy
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1885942

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 18.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Cardiac stress test Chest pain Dyspnoea Headache Influenza like illness Pain Pyrexia Vomiting

Symptomtext

Fever, headache, body aches, vomit, weakness. Severe flu like symptoms for 36 hours after the shot. Incident of Shortness of breath and chest pain 6 months after. Followed up with my doctor.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Sept 2021 heart stress test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multi vitamin/ calcium/C/D
Allergien: None
Vorherige Impfungen: -

VAERS 1858118

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 1805025

moderat

Staat: TX
Alter: 69,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 22.03.2021
Beginn: 10.10.2021
Tage bis Beginn: 202,0
Dosis: UNK
Route/Site: IM / UN

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

COVID-19 Pneumonia Respiratory failure SARS-CoV-2 test positive

Symptomtext

pneumonia, resp. failure, COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN
Andere Medikamente: unknown
Allergien: Ace inhibitors; hydrocodone
Vorherige Impfungen: -

VAERS 1846857

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 51,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 12.03.2021
Beginn: 30.10.2021
Tage bis Beginn: 232,0
Dosis: 1
Route/Site: IM / UN

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

COVID-19 Chills Cough Dysphonia Dyspnoea Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Patient tested positive for COVID 19 on 10/30/2021 symptoms reported: Fever 102.5, chills, sore throat, congestion, hoarseness, shortness of breath, cough

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID 19 rapid antigen testing positive on 10/30/2021
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1840044

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 18.03.2021
Beginn: 29.10.2021
Tage bis Beginn: 225,0
Dosis: 1
Route/Site: IM / -

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

Atypical pneumonia COVID-19 Chest X-ray abnormal Chest discomfort Dyspnoea Fatigue Lung opacity Myalgia Pneumonia viral SARS-CoV-2 test positive

Symptomtext

10/29 tested positive at dr office for covid, symptoms have included worsening shortness of breath, fatigue, myalgias, and chest tightness. pt presented to EC with worsening SOB

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Praegender Schweregrund: Atypical pneumonia
Hospital-Tage: -
Labordaten: Results CORONAVIRUS (COVID-19) ? OFFICE Status: Final result Next appt: 12/13/2021 at 04:15 PM in Internal Medicine Ref Range & Units 5 d ago SARS-CoV-2, NAA Negative Positive Abnormal Comment: Positive: SARS-CoV-2 detected Testing identified the presence of SARS-CoV-2 (the virus that causes COVID-19) in the patient's sample. chest x ray: FINDINGS: There are bilateral patchy airspace opacities worst at the lung bases. No pneumothorax or effusion. IMPRESSION: 11/2/21 Patchy bilateral airspace opacities suspicious for atypical/viral pneumonia. Correlate for Covid 19.
Aktuelle Erkrankungen: -
Vorgeschichte: morbid obesity, hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1828702

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 16.03.2021
Beginn: 27.10.2021
Tage bis Beginn: 225,0
Dosis: 1
Route/Site: - / -

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

Cough Dyspnoea Respiratory disorder

Symptomtext

Pt. came in with difficulty breathing, cough, and respiratory issues; Pt. is on Zinc Sulfate, Pantoprazole; Lovenox; Vitamin C; Inpatient

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

VAERS 1825334

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 96,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 11.03.2021
Beginn: 27.10.2021
Tage bis Beginn: 230,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia COVID-19 Cough Hypersomnia Hypertension Hypotension Hypoxia Mobility decreased Oxygen saturation decreased Pyrexia Respiratory symptom SARS-CoV-2 test positive Sneezing Somnolence

Symptomtext

To ED with weakness and low blood pressure. She notes that she has been experiencing upper respiratory symptoms including cough, sneezing, and fever that started yesterday. She reports that her temperature 10/26 was 102. Originally presented to Hospital today for evaluation. Upon arrival she was noted to be hypertensive and ultimately was given 0.2 mg of clonidine and discharged home with pending COVID-19 test. Reportedly, she had normal oxygen saturations at that evaluation. Since evaluation, the daughter reports continued/progressive somnolence to the point they had difficulty getting her from the vehicle back into her house. Given continued somnolence, she brings her mother to ED for further evaluation. Upon arrival to the ED, she is noted to be hypotensive with SBP of 80. She has responded well to IVF bolus. The patient is able to awaken and talk but quickly falls back asleep. She is found to be COVID-19 positive as well as hypoxic with oxygen saturations in the low 90s.

Weitere VAERSDATA-Felder

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

VAERS 1800226

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 61,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: -
Beginn: 28.04.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Anxiety Asthenia Fatigue Feeling abnormal Insomnia Nausea Palpitations Tinnitus Vertigo

Symptomtext

VERTIGO; RACING HEART; ANXIETY; NOT FEELING QUITE LIKE SELF; TROUBLE SLEEPING AT NIGHT; NAUSEA; FELT TIRED; TINNITUS; NO ENERGY; This spontaneous report received from a patient concerned a 61 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: glaucoma, and other pre-existing medical conditions included: Patient had no pertinent medical history. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025 expiry: 23-AUG-2021) dose was not reported, administered on 24-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 28-APR-2021, the patient experienced vertigo. On 28-APR-2021, the patient experienced racing heart. On 28-APR-2021, the patient experienced anxiety. On 28-APR-2021, the patient experienced not feeling quite like self. On 28-APR-2021, the patient experienced trouble sleeping at night. On 28-APR-2021, the patient experienced nausea. On 28-APR-2021, the patient experienced felt tired. On 28-APR-2021, the patient experienced tinnitus. On 28-APR-2021, the patient experienced no energy. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from vertigo, racing heart, anxiety, not feeling quite like self, nausea, felt tired, and no energy on 23-JUN-2021, and trouble sleeping at night on 11-OCT-2021, and had not recovered from tinnitus. This report was non-serious.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Glaucoma (Glaucoma drops in eyes every day.)
Vorgeschichte: Comments: Patient had no pertinent medical history.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1788097

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WI
Alter: 64,0
Geschlecht: M
Eingang: 15.10.2021
Impfdatum: 12.03.2021
Beginn: 11.10.2021
Tage bis Beginn: 213,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Chest X-ray abnormal Confusional state Diarrhoea Dyspnoea Lung infiltration Lung opacity SARS-CoV-2 test positive

Symptomtext

Patient originally diagnosed with COVID on 10/4/21. Patient presented to ER on 10/7, 10/9 and was admitted 10/11/21 for progressively worsening symptoms. Patient has symptoms of confusion, shortness of breath, diarrhea, and patchy infiltrates on left lung. Patient was admitted overnight for observation and supportive therapy and discharged the next day. Patient was treated with Dexamethasone.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: COVID NP Swab positive 10/1/2021 10/9/21 Chest Xray Interval progression of patchy opacities in the lower lobes concerning for worsening pneumonia.
Aktuelle Erkrankungen: COPD
Vorgeschichte: COPD
Andere Medikamente: aspirin low dose 81mg, lipitor 80mg, clonazepam 1 mg, propranolol 10mg, umeclidinium-vilanterol 62.5-25mcg, albuterol
Allergien: Urethane
Vorherige Impfungen: -

VAERS 1784844

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 81,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 12.03.2021
Beginn: 27.08.2021
Tage bis Beginn: 168,0
Dosis: 1
Route/Site: IM / UN

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

COVID-19 COVID-19 pneumonia Cancer in remission Chest X-ray abnormal Cough Decreased appetite Dyspnoea Fatigue Lung infiltration SARS-CoV-2 test positive

Symptomtext

Chief Complaint: SOB, Cough, Fatigue, No Appetite, COVID+ Patient tested positive for COVID-19 on 08/13/21 and had Regeneron infusion on 08/19/21. Patient had recent chest XR indicating left lower lobe infiltrate and was sent by MD for COVID pneumonia. In remission for prostate cancer.

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

VAERS 1783128

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 42,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 05.04.2021
Beginn: 11.05.2021
Tage bis Beginn: 36,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Insomnia Limb discomfort Pain Paraesthesia Sensory disturbance

Symptomtext

felt the medicine immediately travel into the area of my armpit. Soreness for 3 days. Insomnia for 2 days. 6 weeks post injection my left arm (shoulder) started going numb and tingling. Feeling of "dead arm" and heavy arm. Pain that lasted approx 4 -5 days. Took iron and magnesium supplements which helped. The same numbness and tingling returned again about 5-6 weeks later. The supplements didn't help as much the 2nd time. Symptoms returned again, but I can't remember how far apart the third time, they weren't as strong, and dissipated faster. I did call my Dr after the 2nd time and she recommended an U/S but my insurance isn't good, and it was too far away and too expensive.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: chronic idiopathic urticaria hashimotos
Andere Medikamente: Adderall 30 mg XR
Allergien: sunflower (plant) seeds, oil
Vorherige Impfungen: -

VAERS 1773400

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 69,0
Geschlecht: F
Eingang: 09.10.2021
Impfdatum: -
Beginn: 13.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Blood pressure measurement Echocardiogram Hypertension Insomnia Pruritus Rash

Symptomtext

HIGH BLOOD PRESSURE; COULD NOT SLEEP AT NIGHT; RASH; ITCHINESS ON ONE SPOT AROUND THE HEART; This spontaneous report received from a patient concerned a 69 year old female The patient's height, and weight were not reported. The patient's concurrent conditions included: high blood pressure, diabetes, no alcohol use, and non-smoker, and patient had no known allergies. Patient had no drug abuse or illicit drug use. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and expiry: 23-AUG-2021) dose was not reported, 1 total, administered on 11-MAR-2021 for prophylactic vaccination on left arm. No concomitant medications were reported. On 13-MAR-2021, the patient experienced rash and itchiness on one spot around the heart which resolved in 3 weeks. Three to four weeks after vaccination on 01-APR-2021, the patient experienced high blood pressure and could not sleep at night. Patient's daughter who was a nurse took her to the hospital. They tested her for brain bleed and stroke all negative. Patient also underwent Laboratory data included: Blood pressure (NR: not provided) high (250/150), Echocardiogram of the heart (NR: not provided) negative, and Eosinophils (NR: not provided) really elevated. They said that was because of the vaccine. They raised the dose of her blood pressure medication and added a second one and it took 2 weeks before her blood pressure came back to her normal. They released her the same day and sent her to a cardiologist which mentioned the same thing that it was because of the vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from high blood pressure on 15-APR-2021, itchiness in one spot around the heart, and rash on 01-APR-2021, and could not sleep at night. This report was serious (Other Medically Important Condition). This case, from the same reporter is linked to 20211011824.; Sender's Comments: V0 20211012327-COVID-19 VACCINE AD26.COV2.S-high blood pressure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: MEDICAL HISTORY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20210401; Test Name: Blood pressure; Result Unstructured Data: high (250/150); Test Date: 20210401; Test Name: Eosinophils; Result Unstructured Data: really elevated; Test Date: 20210401; Test Name: Echocardiogram; Result Unstructured Data: negative
Aktuelle Erkrankungen: Abstains from alcohol; Blood pressure high; Diabetes; Non-smoker
Vorgeschichte: Comments: Patient had no known allergies. Patient had no drug abuse or illicit drug use.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1744420

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 29.09.2021
Impfdatum: 10.03.2021
Beginn: 28.09.2021
Tage bis Beginn: 202,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Chest X-ray abnormal Cough Dyspnoea Dyspnoea exertional Interstitial lung disease SARS-CoV-2 test positive Sputum purulent

Symptomtext

hospitalized 9/28/21 with shortness of air, SARS-CoV-2 positive 9/28/21. Multiple high risk comorbidities for severe COVID-19 disease including type 2 diabetes mellitus, chronic obstructive pulmonary disease, obstructive sleep apnea on nocturnal CPAP, and atherosclerotic coronary vascular disease with previous coronary artery bypass grafting. Brought to ER after calling paramedics with increasing shortness of breath. O2 saturation on room air in the emergency department 84%. Symptomatic over the last 8 days with increasing cough and exertional dyspnea. Patient reports green purulent sputum production. Unaware of hemoptysis. Failed on pulmonary appointment with Dr. The patient's wife died of acute respiratory failure 1 week ago. It is uncertain as to whether or not this was Covid related. Chest x-ray in the emergency department with interstitial infiltrates predominant late in a lower lobe distribution consistent with COVID-19

Weitere VAERSDATA-Felder

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

VAERS 1719152

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AZ
Alter: 68,0
Geschlecht: F
Eingang: 21.09.2021
Impfdatum: 16.03.2021
Beginn: 27.04.2021
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: SYR / LA

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

Amnesia Head discomfort Paraesthesia

Symptomtext

Memory lost, pressure and tingling on right side of head.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vitamins
Allergien: Garlic; Morphine; and Oxycodine
Vorherige Impfungen: -

VAERS 1715343

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 83,0
Geschlecht: F
Eingang: 20.09.2021
Impfdatum: 05.04.2021
Beginn: 17.09.2021
Tage bis Beginn: 165,0
Dosis: 1
Route/Site: IM / -

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

Asthenia Cough Hypotension Nasal congestion Nausea Nervousness Pulmonary congestion Respiratory symptom SARS-CoV-2 test negative Vomiting

Symptomtext

9/17/21: Patient arrived at the ER due to the last couple days she has had persistent nausea with multiple episodes of nonbloody, nonbilious vomit as well as generalized weakness and reports feeling more shaky than usual. She states she spoke with her nephrologist in regards to her symptoms who referred her to the ED for further management. She reports over the last week she has had upper respiratory symptoms of a cough, nasal congestion, chest congestion and states she saw her PCP who prescribed her antibiotics, a Medrol Dosepak and albuterol inhaler and reports her symptoms have actually improved. She states during the visit with her PCP she tested negative for COVID at that time. Please note: Patient received J&J vaccine on 4/05/2021 Lot # 1805025 Blood pressure with borderline hypotension, and O2 saturations ranging between 92 and 94% on room air. At this time will admit patient under inpatient status for continued monitoring and treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, CKD, CAD/CABG, pacemaker, hyperlipidemia, thoracic abdominal aortic aneurysm and CVA
Andere Medikamente: -
Allergien: Aspirin, contrast dye, heparin
Vorherige Impfungen: -

VAERS 1708579

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: UT
Alter: 64,0
Geschlecht: F
Eingang: 17.09.2021
Impfdatum: 18.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: SYR / RA

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

Adverse reaction Asthma Computerised tomogram normal Computerised tomogram thorax Condition aggravated Inhalation therapy Loss of personal independence in daily activities

Symptomtext

24 hours after the vaccination - I started having severe asthma attacks and it continues. Some days are better than other days. I went through a period were it did not bother me. But here we are today and it's horrific. It has definitely limited my ability to function in a normal way. I have seen several doctors and have gotten different medications and have not gotten anywhere with them: Azelastine- nasal spray, Fluticasone- inhaler, Flovent-inhaler, Symbicort-inhaler. All of these have been non-effective or I have had an adverse event to them. ENT, DR, he ordered a sinus CT- no abnormalities. Dr, an allergy/asthma specialist, I started allergy session last October before I got COVID -19 and before the vaccine. Our belief was the allergy shot would help me with the asthma, but so far it has not . When my PCP was not available I also saw PA, she gave me a breathing treatment. I have been referred by Dr. to see Dr, a pulmonary specialist who specializes on Long-Haul COVID, and I have an appointment on 09/28/2021. I had COVID-19 December 2020 I had a pretty good case of it and then I got the shot in March. I asked Dr, but he said to ask the long-haul pulmonary specialist the question: They talked a lot about people getting booster shots , I am very concerned about getting the booster because of the AE reaction I had from the original vaccine which may do more of the same to me. I am al worried about getting COVID again because I am in such a bad situation with my asthma, that I may not be able to fight it again if I got the actual disease.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Sinus CT-no abnormalities ; Chest CT- no abnormalities.
Aktuelle Erkrankungen: No
Vorgeschichte: Breast cancer 12 years ago not a current situation; diagnosed with asthma, like 10 years ago. I was given Singulair and I have not had any asthma attacks after taking the Singulair.
Andere Medikamente: Omeprazole; Effexor; Amoxicillin; Pepcid; Singulair; Trazodone; Baby Aspirin; Zyrtec; One a day Vitamins Womens; Citracal; Vitamin D-3; Fish Oil Pearls; Magtech Magnesium
Allergien: Extensive pollen allergy; Rocephin injectable antibiotic
Vorherige Impfungen: -

VAERS 1704777

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 63,0
Geschlecht: M
Eingang: 16.09.2021
Impfdatum: 19.03.2021
Beginn: 12.08.2021
Tage bis Beginn: 146,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 pneumonia Cardiomegaly Chest X-ray abnormal Chills Cough Dyspnoea Hypoxia Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Presented to ED with fever, chills, bodyaches and shortness of breath on 8/16/21. Onset was 8/12/2021. Did receive the J&J vaccine. Was placed on 4L and given tylenol, dexamethasone, morphine and zofran. Diagnosed with COVID-19 pneumonia with hypoxia and admitted. Ceftriaxone, doxycycline, dexamethasone, Lovenox,and remdesivir started. Repeat/follow-up chest x-ray obtained on 08/19/2021 did not show any worsening pathology. PRN tessalon perles was given for distressing cough. He continued to maintain adequate respiratory saturations on ambient air without need for supplemental oxygen therapy throughout his hospital stay. The patient was ultimately discharged home in stable, improved condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 4,0
Labordaten: 8/16/21 chest xray: cardiomegaly 8/19/21 chest xray: similar to 8/16/21 8/16/21 COVID19: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis, Cardiomegaly, Coronary atherosclerosis of unspecified type of vessel, native or graft, Diabetes mellitus, Former smoker, Hematuria, Hypercortisolism, Hypertension, Insomnia, MI (myocardial infarction), Obesity, Class II, BMI 35-39.9, Osteoarthritis, Pain in limb, Pure hypercholesterolemia, Stones, urinary tract, and Stroke.
Andere Medikamente: Norco, multiple vitamin, fish oil, quetiapine, allourinol, amlodipine, benazepril, clopidogrel, glipizide, hydrochlorothiazide, metformin, mifepristone, potassium chloride, rosuvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 1700159

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 35,0
Geschlecht: M
Eingang: 15.09.2021
Impfdatum: 25.03.2021
Beginn: 06.09.2021
Tage bis Beginn: 165,0
Dosis: 1
Route/Site: IM / AR

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

Anxiety COVID-19 Condition aggravated Cough Depression Diarrhoea Drug screen Electrocardiogram Headache Nausea SARS-CoV-2 test positive Self-injurious ideation Suicidal ideation Vomiting

Symptomtext

Hospitalized 9.14.21 ; COVID-19 positive 9.6.21; fully vaccinated HISTORY OF PRESENT ILLNESS: HPI and hx obtained from patient and chart review. Patient is a 35 y.o. male with pmhx of depression and anxiety who presented with a chief complaint of suicidal ideation. Patient reports worsening symptoms of depression and feeling hopeless facility thoughts of harming himself for the past week. He reports that the past a year he has had multiple stressors in his life. Stressors include being in jail the common going to rehab not being able to see his children, and the death of his brother 2 years ago due to suicide. His depression symptoms include not being able to stay asleep poor appetite, feeling down depressed and hopeless. He has taken multiple medications in the past for his depression he does not remember which ones he has tried. He reports that last week after he was tested positive for COVID-19 his depression symptoms got worse. Yesterday he took a half a tablet of Suboxone because he was anxious, after he took it he to the rest of the bottle out. He reports being on Suboxone in the past but has not taken it in a year. He reports a history of alcohol use and heroin use but has not consumed in 4 years. Today he had thoughts of harming himself, but did not have a plan. He wants help for his depression. In regards to his COVID symptoms he reports having a headache, nausea, cough, diarrhea that started on 09/05. He went to the emergency department and that is where he tested positive for COVID on 09/07. He now denies any fevers, chills, difficulty breathing. He reports having some mild nausea. Brief ED course: Vitals were stable on arrival to the emergency department. Spoke with social Work . General medicine will admit patient for further evaluation and workup. CHIEF COMPLAINT: Suicidal ideation ASSESSMENT/PLAN: Patient is a 35 y.o. male with PMH of depression/anxiety . He presented to the emergency department due to suicidal ideation. # Suicidal ideation Patient reports that the last year has been hard for him. He has multiple stressors including being in jail, being in rehab, not being able to be there for his children, as well recent death his brother 2 years ago due to suicide. He reports that this week his depression has gotten significantly he thinks due to recent diagnosis COVID. He reports today that she have follow-up ending his life, but did not have a specific plan. He reports not wanting to take any medications. Plan: - video monitoring - social work consult- Plan for him to touch base with network, patient agreeable to inpatient psych treatment but no facility open for covid patients. - urine drug screen - EKG given his recent Suboxone use # COVID-19 positive Patient tested positive for SARS-CoV-2 on 9/6/2021. He reports some nausea, mild cough, and headache but no other symptoms. Symptoms started on 9/5. He does not qualify for remdesivir or steroids. - Continue to monitor

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: ED 9.6.21 and 9.13.21 Headache, vomiting COVID-19 positive 9.6.21
Vorgeschichte: Hospital Suicidal ideation Non-Hospital Chronic low back pain Back pain Chronic pain Overuse syndrome Elbow pain, right Headache Gastritis Fracture of wrist Migraine headache Contusion Pain at surgical incision Pain due to any device, implant or graft Dermatitis Wrist pain, right Wrist swelling Opioid use disorder, severe, on maintenance therapy (HCC) Bipolar II disorder (HCC)
Andere Medikamente: Hospital Medications acetaminophen (TYLENOL) tablet 1,000 mg acetaminophen (TYLENOL) tablet 1,000 mg acetaminophen (TYLENOL) tablet 500 mg acetaminophen (TYLENOL) tablet 500 mg bisacodyl (DULCOLAX) suppository 10 mg magnesium hydroxide (MIL
Allergien: Benadryl Crea Penicillins Propoxyphene GI Upset Tramadol GI Upset Ketorolac Tromethamine Nausea Only
Vorherige Impfungen: -

VAERS 1694569

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: OH
Alter: 62,0
Geschlecht: F
Eingang: 13.09.2021
Impfdatum: 11.03.2021
Beginn: 01.08.2021
Tage bis Beginn: 143,0
Dosis: UNK
Route/Site: IM / LA

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

Blood test COVID-19 Computerised tomogram thorax Cough Dyspnoea Headache Human rhinovirus test positive Muscle spasms Pneumonia Rhinovirus infection SARS-CoV-2 test positive X-ray

Symptomtext

Coughing, headache, severe leg cramps, trouble breathing. Double pneumonia, Covid 19, & Rhino virus. X-rays, lung CT scan, blood tests, 3 different antibotics, breathing treatments, cough & cold meds.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: August 4, xray August 4, blood tests September 1, lung CT September 3, blood tests, xrays September 21-another lung CT scan scheduled
Aktuelle Erkrankungen: N/A
Vorgeschichte: Since Covid positive, battling double pneumonia
Andere Medikamente: Sentraline 50 mg
Allergien: Nuts
Vorherige Impfungen: -

VAERS 1666764

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: GA
Alter: 55,0
Geschlecht: M
Eingang: 02.09.2021
Impfdatum: 12.03.2021
Beginn: 10.08.2021
Tage bis Beginn: 151,0
Dosis: 1
Route/Site: SYR / UN

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

COVID-19 pneumonia

Symptomtext

Patient was hospitalized for over a week with COVID Pneumonia. Patient doesn't know how he was exposed but doctor said he was lucky to be living. Patient has COPD, Congestive heart failure and a host of other pre-existing conditions

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Patient was hospitalized for over a week with COVID Pneumonia.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1666035

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 71,0
Geschlecht: F
Eingang: 02.09.2021
Impfdatum: 05.03.2021
Beginn: 06.08.2021
Tage bis Beginn: 154,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain lower COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Colectomy Colon neoplasm Colostomy Computerised tomogram abnormal Condition aggravated Fine motor skill dysfunction Hiatus hernia Intestinal perforation Large intestine perforation Ostomy bag placement Ovarian cancer Ovarian clear cell carcinoma Pathology test Pelvic abscess

Symptomtext

Received COVID vaccine on 3/5/21, tested positive for COVID on 8/7/21 8/6/21:Patient is a 72 y.o. female with a history of HTN, COPD, HLD who presents to the Emergency Department for evaluation of bowel perforation. Patient reports she started having lower abdominal pain approx 1 week ago. States her pain went away after a few days. 2 days ago her pain returned, and has progressively worsened. Seen at the hospital today, had CT scan that showed findings concerning for bowel perforation with stool contamination, abscess, and possible malignancy. Patient denies hx of previous abdominal surgeries. States her pain is tolerable as long as she remains still. Denies fever, chills, body aches, chest pain, palpitations, shortness of breath, wheezing, dizziness, lightheaded, syncope, dysuria. 72y female with COPD and no known history of cancer who presents with abdominal pain and CT findings consistent with feculent perforation of the sigmoid colon, sigmoid mass with concern for metastasis, and 2 large pelvic abscesses. Patient is hemodynamically stable, but given that pain is consistent with peritonitis and with the findings of free air within her hiatal hernia, will plan to take patient to OR emergently for lap sigmoid ectomy with end colostomy. Risks, benefits, and alternatives of the procedure were discussed with the patient. Patient elected to proceed to the OR. Code status discussed and patient is full code. Patient will be posted as an A and will be admitted to colorectal surgery following the procedure. #Perforated sigmoid mass #Intra-pelvic feculent abscesses - To OR as A for laparoscopic sigmoidectomy, end colostomy, and all other indicated - NPO - IVF @ 100 - zosyn 3.375 IV - Dilaudid for pain control - Admit to colorectal surgery following procedure - Consent signed and in chart 8/17/21 Discharge Summary: Hospitalization Admit Date/Time: 8/6/2021 5:05 PM Discharge Date: 08/17/21 No address on file Chief Concern, Brief History of Present Illness, and Hospital Course Patient is a 72 y.o. female with COPD who presented to ED with abdominal pain, evidence of bowel perforation. They were evaluated and found to have perforated sigmoid mass and intra-pelvic feculant abscess. They were taken to the operating room on 8/6 for emergent laparoscopic sigmoidectomy and end colostomy. Patient found to have involvement of left ovary and tube as well as small bowel; therefore, left SPO and SBR performed as well. The patient tolerated the procedure well and was subsequently extubated and transferred to the PACU for recovery. After recovery, the patient was transferred to the floor. Patient's COVID test was positive, so she was transferred to COVID unit. She received aggressive respiratory therapy. With her COPD, she was high risk for severe infection; however, her respiratory status has slowly improved. She is now on 1L O2 nc. Of note, she was vaccinated. The patient's hospital course was otherwise uncomplicated and it was felt that the patient had reached maximal benefit from hospitalization. They were deemed appropriate for discharge to acute rehab. On the day of discharge the patient's pain was controlled on oral medications, they were ambulating, voiding appropriately, passing flatus and stool in ostomy bag, and tolerating oral intake. Patient becoming more comfortable with changing ostomy bag herself, but struggles with dexterity. Has some deconditioning. Of note, her pathology returned as likely ovarian cancer. She will follow up outpatient with Dr. The patient was discharged on 08/12/21 to rehab and will return to clinic in 1 month with Dr. Discharge Diagnosis Medical Problems Active and Resolved Hospital Problems Hospital Aspiration pneumonitis (CMS/HCC) Overview Addendum 8/16/2021 7:55 AM by MD -confirmed by CXR -speech consulted- no dysphagia, okay for regular diet and thin liquids -monitor for signs of pneumonia -no concern for pneumonia COPD (chronic obstructive pulmonary disease) (CMS/HCC) Overview Signed 8/14/2021 11:54 AM by MD Complicates all aspects of care Increases risk for severe COVID infection Clear cell carcinoma (CMS/HCC) Overview Signed 8/14/2021 11:55 AM by MD -thought to be gyn primary * (Principal) Bowel perforation (CMS/HCC) Overview Addendum 8/16/2021 7:56 AM by MD -s/p lap colectomy, end colostomy, SBR, and left salpingo-oophorectomy (8/7) -Path: HIGH-GRADE CARCINOMA WITH CLEAR CELL AND SARCOMATOID DIFFERENTIATION, INVOLVING FALLOPIAN TUBE, OVARY, COLON MUSCLE WALL AND MESENTERY. ONE LYMPH NODE NEGATIVE FOR METASTASIS (0/1). Dr. discussed with Dr., will see outpatient. -IS/OOB, Flutter Valve for IS -Regular diet, HLIV -PT/OT: acute recs, appreciate visits - Pending insurance approval to ARF, medically stable for discharge - SW states she will require transportation to rehab facility due to Covid (+) COVID-19 Overview Addendum 8/14/2021 11:53 AM by MD -On 3L O2 at home in past, now on 1L nasal cannula -Duo-nebs PRN for wheezing -formal consult to RT -chest physiotherapy and airway clearance

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, COPD, HLD, GERD
Andere Medikamente: alendronate, aspirin effervescent, ergocalciferol, ferrous sulfate, pantoprazole, pravastatin, polyethylene glycol
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1481338

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CA
Alter: 63,0
Geschlecht: M
Eingang: 31.08.2021
Impfdatum: 27.03.2021
Beginn: 16.04.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Hypoaesthesia Paraesthesia Peripheral swelling Pruritus

Symptomtext

At the time the shot was administered, no side effects. But shortly, about a month afterward, symptoms started to surface. The first symptom I encountered was severe itching around the right nipple. It was all the time, especially after I would shower. The next one showed up in my right arm, numbness, and tingling, from my shoulder down to my fingers. So I had the iching and numbness and tingling, going on at the same time. Both of these issues lasted from April until June/July. I went to the pharmacist and then to my doctor. The numbness and itching dissipated around the last of July, but now the issue I am currently experiencing is joint pain in my right knuckles. Everything has returned to normal, with the exception of the pain in my right knuckles. My index finger has swelling across the top of the joint.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: High Blood Pressure and Diabetes Medications
Allergien: None.
Vorherige Impfungen: -

VAERS 1655781

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 57,0
Geschlecht: M
Eingang: 30.08.2021
Impfdatum: 17.03.2021
Beginn: 09.08.2021
Tage bis Beginn: 145,0
Dosis: 1
Route/Site: IM / LA

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

Abnormal behaviour Acute kidney injury Aggression Blood beta-D-glucan increased Blood creatinine normal Blood potassium normal Blood sodium decreased Blood urea normal COVID-19 Chest X-ray abnormal Chest pain Costochondritis Cough Dyspnoea Haemoglobin decreased Haemophilus test positive Immunosuppression Ischaemia

Symptomtext

Patient vaccinated 3/17/2021, admitted 8/9, tested positive for Covid 8/9 left AMA 8/16/2021 History Of Present Illness A 57 y.o. homeless male, smoker, with a PMH of AIDS (CD4 102 on 7/31), CAD s/p CABG and PCI, HTN, polysubstance abuse who presents with a chief complaint of dyspnea and chest pain. Of note, he presented for similar concerns yesterday and left AMA and was also previously admitted from 7/31 - 8/1 for chest pain, fentanyl overdose and an AKI. He was evaluated by cardiology during this time who felt his elevated troponin was due to global ischemia from polysubstance abuse. His chest pain was reproducible and felt to be secondary to costochondritis and chronic cough possibly from undiagnosed COPD. His CXR did show interstitial infiltrates that had been present since February 2020 so PJP, beta glucan and sputum cultures were obtained. Beta glucan was elevated and sputum cultures eventually grew H. Influenzae but PCP testing was negative. He was discharged in stable condition. Further history unable to be obtained from patient as he is sleeping and rouses to provide one word responses but refuses to wake up and participate further. He does endorse coming in for "his breathing" and also for his chest. According to ED provider note, the patient reported "intermittent chest pain and a cough productive of white/yellow sputum" since last discharge. Also reported noncompliance with anti-retrovirals and bactrim prophylaxis. Denied fever, palpitations, lightheadedness, N/V or diarrhea or any other symptoms. LEFT AGAINST MEDICAL ADVICE Hospitalization Admit Date/Time: 8/9/2021 5:00 AM Discharge Date: 08/16/21 Chief Concern, Brief History of Present Illness, and Hospital Course 57-year-old gentleman with past medical history of HIV, coronary artery disease SP CABG, hypertension polysubstance abuse presented with complaint of having chest pain and dyspnea. Upon arrival, Pt was hemodynamically stable with BP 130/90, RR 21, HR 90 and Temp 36.8. Labs were remarkable for Hb 11.5, WC 3.16, Plts 117, Na 133, K 4.2, BUN 18, Cr 1.04. Patient was incidentally found to be COVID positive and was admitted for it. For COVID-19 in setting of Johnson & Johnson vaccination, Patient did not require any oxygen and was not started on dexamethasone and remdesivir. Patient was given regeneron on 8/13 as per ID reccs. Patient has COVID-19 infection in setting of immunosuppression and will require quarantine for 20 days Patient has history of bipolar schizophrenia and is impolite staff. Psychiatry was consulted and patient has been uncooperative with them. Patient is complaining of having persistent neck pain and was started on Neurontin along with Tylenol, ibuprofen and baclofen. Neurology was consulted who recommended MRI with further evaluation as O/P as no acute finding present. Infectious disease was consulted and patient was started on Geneovya, Bactrim and valacyclovir. During entire hospital stay, pt had extensive behavioral issues. He was impolite towards hospital staff, was swearing and cursing at nurses, had threatening attitude, had frequent outbursts of profanity. He was repeatedly counseled to have nice attitude and behavior towards staff. He was counseled at least three times not to leave against medical advise. Tried to find a place where patient can quarantine safely and not be a risk to heath of others, called mayors office, local charities and multiple other places but were unsuccessful. Pt was not happy with care he was getting and was unhappy about the fact that hospital cannot arrange place for him. Pt was extensively counseled to complete his quarantine in hospital but was was unwilling and wanted to leave. He was provided with clothes, list of his appointments and medication. He was unwilling to sign AMA papers and left against medical advice.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: 7/29 seen in ED, suspected admit due to overdose of fentanyl 7/30 seen in ED, left AMA discharged 8/1 for 3 month hx of chest pain, brough to ED by policy after found walking on highway, requested discharge 8/5 admit for penumonia, left AMA, other hospital 8/8 admit to ED for chest pain, left AMA
Vorgeschichte: HIV, polysubstance abuse, HTN, CAD
Andere Medikamente: albuterol, amlodipine, ammonium lactate, aspirin, capsacicin-menthol, multivitamin, rosucastatin, bactrim DS, terazosin, Spiriva, amitriptyline, certirizine, darunavir, Genvoya, hydroxyzine, valacyclovir, ibuprofen
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1636466

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 46,0
Geschlecht: M
Eingang: 26.08.2021
Impfdatum: 13.03.2021
Beginn: 24.08.2021
Tage bis Beginn: 164,0
Dosis: 1
Route/Site: IM / UN

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

Chest pain Pain in extremity Polymerase chain reaction positive

Symptomtext

Patient presented to facility with chest pain radiating to left arm. Patient ruled out non-infectious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: PCR test came back positive on 8/24/21.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1628556

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 52,0
Geschlecht: F
Eingang: 24.08.2021
Impfdatum: 08.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / LA

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

Chest X-ray normal Cough Dyspnoea Fatigue Headache Influenza virus test negative Malaise Respiratory tract congestion SARS-CoV-2 test negative Wheezing

Symptomtext

After vaccine, that night felt very tired, next day had a bad headache from noon to 7 p.m. On 3/14/21, developed a cough and severe congestion with wheezing in lungs. Went to urgent care facility. Was tested for COVID-19 and flu. Both tests were negative. Given a steroid shot and antibiotics. Followed up with primary care giver, on March 23, 2021, because I wasn't feeling any better and still had a cough and a lot of congestion, was given Mucinex. Returned to primary care giver, on 4/6/21 because I still wasn't feeling well and had a cough with wheezing and congestion, and was prescribed amoxicillin 875-potassiumclavulanate 1.25 mg, and more mucinex. - 4/14/21, I went back to my primary care giver at Family Medicine, due to congestion and coughing and not feeling well, and was prescribed albuterol sulfate for my nebulizer and a chest x-ray was done at the clinic and results showed no pneumonia. - On Saturday, 4/17/21, I awoke with severe congestion, coughing, trouble breathing, and wheezing, so I went to Urgent Care. Urgent Care did a covid test and a flu test with a negative result for both. Urgent Care also did a chest x-ray and saw shadows that they thought were pneumonia, so they gave me a steroid shot and Levaquin antibiotics. - On May 4, 2021, I went back to my primary care giver at Family Medicine, due to severe coughing and wheezing again?. and I was prescribed pseudoephedrine and they referred me to an allergist. -I saw the allergist, Doctor L. on May 14, 2021, and I underwent allergy testing that resulted in the need for two allergy shots weekly beginning June 4, 2021. I have the allergy shots every Friday now. -On July 28, 2021, I developed a dry cough. -On July 29, 2021, by mid-day, I was coughing a lot and had a lot of congestion. -I again saw my primary care giver at Regional Medicine on July 30, 2021, and was prescribed Mucinex and a z-pack antibiotics and sent to Family Clinic for a covid test which resulted in a negative result. -On August 3, 2021, there were no improvements, I actually felt worse, so I went back to my primary care giver and a chest x-ray was administered with a negative result for pneumonia, was prescribed Augmentin antibiotics and steroids for what they thought could be a sinus infection that was causing drainage that caused coughing and congestion. -On August 5, 2021, I still did not feel any better, so I was seen at my primary care giver, Family Medicine and they sent me to Family Clinic, for a covid test which resulted with a negative result, so I was prescribed Levaquin antibiotics and another steroid. -On August 11, 2021, I was still sick with extreme coughing and congestion, so I underwent another covid test at Family Clinic, with a negative result and the care giver at the testing center at Family Clinic listened to my lungs and said they sounded really bad and she prescribed a stronger steroid and sent me to the Hospital for a chest x-ray because she thought it was a false covid test or pneumonia. The chest x-ray came back clear with no pneumonia -August 18, 2021, I followed up with my primary care giver at Family Medicine, and I was told my lungs still sounded bad and they didn't know why, therefore, they are referring me to a pulmonary specialist and I have an appointment there on 10/12/21. I still continue to cough and have congestion. I continue to use my nebulizer 2-3 times daily per doctor's orders.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Covid tests: 3/14/21, 4/17/21, 7/30/21, 8/5/21, 8/11/21 -had both rapid and send off tests with negative results for all. Chest x-rays -4/14/21, 4/17/21, 8/3/21, 8/11/21-clear resul
Aktuelle Erkrankungen: None
Vorgeschichte: chronic bronchitis, mild COPD
Andere Medikamente: albuterol inhaler, albuterol nebulizer solution, symbicort, diclofenac, Flonase, furosemide Lasix, Tylenol, garlic supplement, Mucinex, hydroxyzine HCI, levocetirizine (xyzal), montelukast (singular), omeprazole, triamcinolone acetonide cre
Allergien: flexril, shrimp, egg plant, pollen, mold, grass, pet dander cats, dogs, feathers, Phoma, Stemphylium, Ash, Birch, Elm, Hickory, Maple, Histamine, Dust Mite DF, Dust Mite DP, Mold Mix, Grass Mix, Ragweed, Tree Mix, Weed Mix, Oak Mix, Walnut, Cocklebur, Pig Weed, Plantain, Mosquito, Aspergillus, Botrytis, June/KY Blue grass, Orchard grass, Red Top grass, Timothy grass.
Vorherige Impfungen: Flu shot - made me very sick, developed flu symptoms.

VAERS 1583135

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: OK
Alter: 41,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 15.03.2021
Beginn: 12.04.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: SYR / LA

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

Pain Paraesthesia

Symptomtext

I started feeling a tingling/shooting pain going from my elbow up to my shoulder/underarm and down to my hand. I've never felt this before. It is still happening. It happens several times a day. The only time I haven't noticed it happen is when I'm lying in bed.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothroidism Hashimoto's
Andere Medikamente: Synthroid Adderall Multi-vitamin
Allergien: Pertussis vaccine
Vorherige Impfungen: Swollen leg at first Pertussis vaccine when a baby.

VAERS 1582978

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 73,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 09.03.2021
Beginn: 01.08.2021
Tage bis Beginn: 145,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain COVID-19 Chills Diarrhoea Dyspnoea Fatigue Nausea Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

VACCINATED WITH JANSSEN VACCINE IN MARCH OF THIS YEAR. WENT TO HOSPITAL ER ON 8/15/21 WITH A 2 WEEK HISTORY OF SYMPTOMS WHICH INCLUDED: CHILLS, RUNNY NOSE, FATIGUE, SHORTNESS OF BREATH, NAUSEA, ABDOMINAL PAIN AND DIARRHEA. RECEIVED MONOCLONAL ANTIBODY TREATMENT WHILE IN ER AND WAS ADMITTED THE SAME DAY. SHE IS NOT IN ICU OR ON THE VENTILATOR. HER HUSBAND TESTED POSITIVE ON 8/6/21 AND HE WAS HOSPITALIZED ON 8/14/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: MOLECULAR AMPLIFICATION TEST RT PCR POSITIVE FOR SARS-COV-2
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: HYPERTENSION, CHRONIC LUNG DISEASE (COPD), ASTHMA AND FORMER SMOKER
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 1489525

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 66,0
Geschlecht: M
Eingang: 21.07.2021
Impfdatum: -
Beginn: 05.05.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Chills Decreased appetite Mobility decreased

Symptomtext

COULD NOT MOVE LEGS, ARMS AND UPPER BODY; LOSS OF APPETITE; CHILLS; This spontaneous report received from a consumer concerned a 66 year old male. The patient's height, and weight were not reported. The patient's past medical history included aneurysm in 2012 (rupture killed the nerve with one leg), the aneurysm changed the way he was walking and problems walking and concurrent conditions included ex-alcohol user (Stopped drinking 2 years ago), non-smoker, rheumatoid arthritis, and blood thinner. The patient had no known allergies. The patient had no history of drug abuse or illicit drug use. The patient was previously treated with prednisone. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, expiry: UNKNOWN) dose was not reported, 1 total, administered on 03-MAR-2021 in left deltoid for prophylactic vaccination. Concomitant medications included infliximab for rheumatoid arthritis. The last dose of infliximab was in FEB-2021. The patient did not discuss getting the vaccine with rheumatoid arthritis doctor. On 05-MAY-2021, the patient had more limited movement until could not move legs and was not walking good. It went up from legs to arms, upper body (coded as could not move legs, arms and upper body). The patient went to emergency room at hospital and stayed in hospital for 1 week. The patient went to rehabilitation one week after for physical therapy. The patient was about ninety percentage back to where he was before the vaccine. The patient also experienced chills and loss of appetite. The symptoms lasted 3 weeks and went away. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from loss of appetite, and chills, and was recovering from could not move legs, arms and upper body. This report was serious (Hospitalization Caused / Prolonged).; Sender's Comments: V0: 20210730947-JANSSEN COVID-19 VACCINE Ad26.COV2.S- Could not move legs, arms and upper body. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: MEDICAL HISTORY, UNDERLYING DISEASE.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: Anticoagulant therapy; Ex-alcohol user (did not use any more. Stopped drinking 2 years ago.); Non-smoker; Rheumatoid arthritis
Vorgeschichte: Medical History/Concurrent Conditions: Aneurysm (rupture killed the nerve with one leg. It changed the way he was walking); Difficulty in walking; Comments: The patient had no known allergies. The patient had no history of drug abuse or illicit drug use.
Andere Medikamente: REMICADE
Allergien: -
Vorherige Impfungen: -

VAERS 1478583

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 55,0
Geschlecht: F
Eingang: 16.07.2021
Impfdatum: 05.03.2021
Beginn: 27.03.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: IM / LA

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

Blood cholesterol normal Chest discomfort Dizziness Dyspnoea Electrocardiogram Exercise tolerance decreased Fatigue Feeling hot Full blood count normal Hyperhidrosis Injected limb mobility decreased Injection site pain Injection site swelling Laboratory test normal Paraesthesia Rectal haemorrhage Temperature regulation disorder Thyroid function test normal

Symptomtext

Initial side effect was swelling and pain at injection site 18 days after vaccination, could not raise arm, tingling sensation to the finger tips. Following this, I was having tightness of the chest, shortness of breath, dizziness, and unable to exercise. This lasted about 45 days. My blood pressure which is normally 105/70 went to 155/105 for a few days. I have since had an ECG done and waiting on further work up. Around 30 days, I had profuse blood coming from my rectum for 36 hours. My temperature regulation is still not back to normal. I get extremely hot, especially at night ever since the vaccination and I am still heat intolerant, sweating profusely and get overheated easily to the point of feeling like I will pass out. Just the past couple of weeks I can actually jog a little bit but still tire very easily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: I recently had a full work up at my GP, Chem, CBC, UA, Chol Panel and Thyroid. Everything now appears pretty much my normal from previous years. ECG, normal on initial reading, waiting on the final from the cardiologist.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin C, Mulltivitamin, Aspirin 81 mg, Calcium, Vit D3, CoQ10
Allergien: Penicillin Wasp stings
Vorherige Impfungen: -

VAERS 1474782

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 57,0
Geschlecht: M
Eingang: 15.07.2021
Impfdatum: 23.03.2021
Beginn: 23.04.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: SYR / LA

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

Hypoaesthesia Muscular weakness Paraesthesia

Symptomtext

About 1 month after receiving the J&J Covid vaccine patient noticed numbness/tingling in the smaller 3 fingers of his right hand. Around the same time, he noticed weakness in his right hand also. He received his vaccine in his left deltoid.

Weitere VAERSDATA-Felder

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

VAERS 1470819

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 28,0
Geschlecht: F
Eingang: 14.07.2021
Impfdatum: 29.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Condition aggravated Eczema Eczema eyelids Erythema Pain Sleep disorder

Symptomtext

I?ve always had eczema, but after the vaccine it became MUCH MUCH worse. It?s so bad. Both of my eyes look like someone punched them. My neck and chin are red as well and some on my arms. It?s so painful, it keeps me awake at night. It?s the worst it?s ever been in my life.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I?m doing patch testing next month August 9th, 11th and 13th. I?m now using topical steroids multiple times per week. I constantly have to take Benadryl and Zyrtec. I can?t drink alcohol or smoke marijuana or it gets much worse.
Aktuelle Erkrankungen: I?ve always had eczema
Vorgeschichte: Eczema
Andere Medikamente: Klonopin .5 mg as needed, Benadryl and Zyrtec as needed
Allergien: NSAIDS, Tylenol, Aspirin, Montelukast
Vorherige Impfungen: -

VAERS 1470655

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 65,0
Geschlecht: M
Eingang: 14.07.2021
Impfdatum: 13.03.2021
Beginn: 23.06.2021
Tage bis Beginn: 102,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

Tingling feeling in hands and feet that started 3 months after vaccine was administered. Tingling has subsided in feet after 2nd week. I now only have slight numbness in both my thumbs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1455095

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 07.07.2021
Impfdatum: 03.04.2021
Beginn: 03.04.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / LA

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

Chills Dyspnoea Electrocardiogram Fatigue Lymphadenopathy Palpitations Peripheral swelling

Symptomtext

11:30PM - Chills late that night and up for an hour for them - went to go to bed with a lot of clothes and lots of blankets but I fell asleep. Morning they were gone. Slightly after that, I had some fatigue but nothing major. I was pretty normal. Then I noticed a few weeks later some swelling under my arms - lymph nodes swollen. I was very aware that they were touching. That seemed to last for a couple of months. I have just become aware the last few weeks that those symptoms with the swollen lymph nodes are gone. About 6 weeks to two months ago - I have been getting pounding heart and a bit of difficulty breathing. May be related stress. It comes and goes and then about a month ago I started a stress reduction supplement protocol and started doing meditation but they were still there and so I went to the doctor. She did an EKG and general physical and she didn't find anything that showed up abnormal with heart. The heart pounding and the breathing issues I'm still noticing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG - doctor's office - Tuesday 22nd of June
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Supplements - didn't take any that morning of vaccine. Around that time - Zinc/ Vit D/ Vit C - immune boosting; CBD stuff- sometimes; Sometimes I take digestive enzymes
Allergien: reaction to Penicillin about 20 years ago - rash
Vorherige Impfungen: -

VAERS 1438000

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 30.06.2021
Impfdatum: 08.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Arthralgia Headache Mobility decreased Musculoskeletal stiffness Nausea Pain Palpitations Pyrexia

Symptomtext

14 hours after injection I had normal reactions of headache, nauseous, fever, body ache, but I also had every joint hurt even my knuckles I couldn't bend my fingers neck was stiff I couldn't turn my head and I had the heart palpitations like a racing heart.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: I did not go to dr
Aktuelle Erkrankungen: none
Vorgeschichte: anxiety/depression
Andere Medikamente: lexapro
Allergien: none
Vorherige Impfungen: -

VAERS 1430521

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 28.06.2021
Impfdatum: 31.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Dizziness Myalgia Pain in extremity Palpitations Paraesthesia Pyrexia

Symptomtext

First 5 days-fever, pain joints muscles lightheaded Since to date- racing heart and pulse. Severe dizzy spells. Intense pain and tingling I n legs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure. Type 2 diabetes
Andere Medikamente: Losartin and Januvia
Allergien: Sulfide
Vorherige Impfungen: -

VAERS 1424381

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 32,0
Geschlecht: F
Eingang: 24.06.2021
Impfdatum: 20.03.2021
Beginn: 21.05.2021
Tage bis Beginn: 62,0
Dosis: 1
Route/Site: IM / LA

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

Heart rate increased Injection site pain Supraventricular tachycardia

Symptomtext

I experienced two months after my J&J vaccine- soreness to my left arm with pain that lasted two weeks. I also experienced SVT, supraventricular tachycardia, my heart rate went up to 103 bpm and my heart rate could not go down. I went to ER where they helped my heart rate go down and I am still being monitored for SVT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Supraventricular tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Rheumatoid arthritis, Hypermobile EDS
Andere Medikamente: Nortriptyline 150mg, Neurontin 2700mg, Hydrocodone 30mg, OTC Tylenol
Allergien: -
Vorherige Impfungen: Tetanus vaccine- experience a fever of 102F when I received this vaccine.

VAERS 1399908

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CO
Alter: 49,0
Geschlecht: M
Eingang: 15.06.2021
Impfdatum: 10.03.2021
Beginn: 20.04.2021
Tage bis Beginn: 41,0
Dosis: N/A
Route/Site: IM / LA

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

Computerised tomogram Headache Hypoaesthesia Magnetic resonance imaging abnormal Paraesthesia Vision blurred

Symptomtext

Six weeks after the vaccine I started to get headaches. It is a dull headaches at the back of my head where my neck connect. I have not been able to find any medication that helps. I have the headache all day every day. Occasionally my eyes get blurry and I get some numbness and pins and needles on the right side of my face. I have been experiencing these headaches for ten weeks to date. I have seen a Neurologist and other specialists.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: CT Scans MRI
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Disc Disease
Andere Medikamente: Atorvastatin Clopidogrel Sertraline Omeprazole Flonase Allergy
Allergien: -
Vorherige Impfungen: -

VAERS 1388561

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AZ
Alter: 71,0
Geschlecht: F
Eingang: 10.06.2021
Impfdatum: 25.03.2021
Beginn: 10.04.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / LA

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

Arrhythmia Heart rate increased Hypertension Oxygen saturation decreased X-ray

Symptomtext

Extremely high blood pressure and high heart rate and low oxygen levels. Incidents have happened 4-10-21, 4-28-21, 5-22-21 & 6-1-2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: On 5-22-21 went to Urgent Care, they took X-ray and the Dr. said since it was going to be 2 hours he was going to call what was wrong as pneumonia. I was not getting any better so I did a tele visit with Dr. and he saw the X-ray report I downloaded and he said I did not have pneumonia and he wanted to see me on 5-31-21 so I schedule it for 6-1-21. That morning I woke up to extremely high blood pressure and high heart rate and was still that way when I went in to his office. I was in cardiac arrhythmia, so I ordered a prescription of Pacerone to control my heart rate, which I found out my Drug insurance would not cover the cost and it would be $906.00 because they don't carry the generic. The pharmacy was able to run it through Goodrx and it tool the price down to $42.75. My MD referred me to a cardiologist which I was suppose to see today but his office called and cancelled my appointment until next Thursday. Now I have a call into my Dr. because my blood pressure is pretty good, but my heart rate is in the low 40's and when I just walk around my oxygen goes down close to 80 .
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, COPD, Diabetic, Hemochromatosis & Restless Leg Syndrone
Andere Medikamente: Atenolol, Lisinopril, Omperzole, Methocaramol, Ropinrole, Celecolix, Solifenacin, Metformin,Rosuvastin, Venalaxine, Mutli-Vitamin, Glucosamine, Chrondrotin & MSN, Calcium, Fiber, Omega 3 Salmon oil, Cinnamon,& Baby Asprin
Allergien: Evista, Niacin, and Spriva
Vorherige Impfungen: -

VAERS 1377813

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 74,0
Geschlecht: M
Eingang: 07.06.2021
Impfdatum: 16.03.2021
Beginn: 21.05.2021
Tage bis Beginn: 66,0
Dosis: 1
Route/Site: IM / AR

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

COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chills Cough Dyspnoea Exposure to SARS-CoV-2 Lung opacity Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient presented to PCP on 05/21/21 from group home with C/O cough, dyspnea, fever, and chills with known exposure to COVID-19. Rapid test in office was positive for COVID-19. Chest Xray showed ground-glass opacities consistent with COVID pneumonia. Patient admitted to the hospital on 05/21/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: COPD, HTN, Hypothyroidism, OA, dementia, anxiety, depression, Schizoaffective disorder, H/O pulmonary embolism, chronic constipation, neurogenic bladder, diverticulosis of colon
Andere Medikamente: Duoneb neb, Albuterol neb, Ayr nasal spray, Risperdal, Klonopin, Neurontin, Ferrous sulfate, Lopressor, Ultram, MVI, Imdur, Synthroid, Anoro Ellipta inhaler, Remeron, Aricept, Fibercon, Xarelto, Protonix, Dilantin, Miralax, Flonase nasal sp
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1377792

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 50,0
Geschlecht: F
Eingang: 07.06.2021
Impfdatum: 24.03.2021
Beginn: 20.05.2021
Tage bis Beginn: 57,0
Dosis: 1
Route/Site: IM / AR

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

COVID-19 COVID-19 pneumonia Chest X-ray abnormal Exposure to SARS-CoV-2 Oropharyngeal pain Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Patient presented to PCP from group home residency on 05/20/2021 complaining of fever up to 100.9, body aches, sore throat, runny nose with known exposure to COVID-19. Rapid test in office was positive for COVID-19. Chest Xray findings consistent with COVID pneumonia. Patient admitted to hospital on 05/20/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: COPD, T2DM, HTN, Cerebral palsy
Andere Medikamente: Mobic, Singulair, Synthroid, Prinivil, Advair, Flonase, Albuterol neb, Seroquel, Zoloft, Glucophage, Zyrtec
Allergien: Penicillin, Aspirin
Vorherige Impfungen: -

VAERS 1377779

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 47,0
Geschlecht: M
Eingang: 07.06.2021
Impfdatum: 26.03.2021
Beginn: 20.05.2021
Tage bis Beginn: 55,0
Dosis: 1
Route/Site: IM / AR

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

COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Exposure to SARS-CoV-2 Lung opacity Oropharyngeal pain Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Wheezing

Symptomtext

Patient presented to PCP office on 5/20/21 from residence at group home with C/O body aches, fever up to 100.2, runny nose, sore throat, wheezing, and coughing. Known exposure to COVID-19 at group home. Rapid test done in office positive for COVID-19. Patient admitted to hospital on 05/20/21 and chest Xray positive for ground-glass opacities consistent with COVID pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: COPD, GERD, Spina bifida, HTN, hypothyroidism
Andere Medikamente: Claritin, Protonix, Colace, Ferrous sulfate, MVI, Symbicort, Zovirax, Flonase nasal spray
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1368615

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MO
Alter: 60,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 15.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: - / -

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

Angiogram pulmonary abnormal Anti-cyclic citrullinated peptide antibody negative Antineutrophil cytoplasmic antibody negative Antinuclear antibody Antinuclear antibody negative Aspergillus test negative Blood creatinine decreased Brain natriuretic peptide normal Bronchoscopy normal C-reactive protein Chest pain Computerised tomogram thorax abnormal Culture negative Cytology normal Dyspnoea Fungal test negative Haemoptysis Laboratory test normal

Symptomtext

Patient developed hemoptysis, chest pain, and shortness of breath and was admitted to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: CT angiogram of the chest on 3/19/2021: "ground glass opacities throughout the right lung that may represent alveolar hemorrhage" Strep pneumoniae Ag: negative Legionella Ag: negative COVID pcr nasal: negative respiratory viral panel: negative ANA, quantiferon gold, ANCA: negative Jo-A antibody: negative SCL-70 ab: negative Anti-CCP; negative Histoplasma Ag; negative Aspergillus Ag: negative Fungitell: negative Blastomyces Ab: negative Anti-Ro and La ab: negative WBC: 11.9 Cr: 0.4 U/a: normal, no blood CRP <5.0 ESR: 4 BNP: 72 Bronchoscopy: negative respiratory culture, pneumonia PCR panel, AFb and fungus; cytology negative; 28WBC in cell count
Aktuelle Erkrankungen: none
Vorgeschichte: HLD, HTN
Andere Medikamente: zocor, aldcactone
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1358316

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CO
Alter: 38,0
Geschlecht: F
Eingang: 28.05.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Atrial fibrillation Blood cholesterol increased Condition aggravated Headache Hypoaesthesia Pyrexia Renal failure Renal function test abnormal Thyroid disorder Thyroid hormones increased

Symptomtext

On 03/10/2021 bad headache, fever, leg arm went numb . Headache lasted for three days, other symptoms went away after 24 hours. I had several A-VIB events in the 24 hours, and went into kidney failure, and was hospital for three days. The Thyroid, Cholesterol and kidney failure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: The test ran were blood labs-levels of thyroid, cholesterol and kidneys were high, and put in hospital for three days. Kidney Fuction has never went back to normal.
Aktuelle Erkrankungen: At the time I was diagnosed with A-Vib
Vorgeschichte: Just the A-Vib
Andere Medikamente: I was taking a daily aspirin 325mg, Flukicide as needed(not taken on the day) Diltizam for a-vib two diff ones, did not take either the day of the vaccination.
Allergien: I am allergic to grapefruit, codeine, and mold.
Vorherige Impfungen: -

VAERS 1350442

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 08.04.2021
Beginn: 17.05.2021
Tage bis Beginn: 39,0
Dosis: N/A
Route/Site: IM / -

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

Blood albumin decreased Blood calcium increased Blood chloride decreased Blood sodium decreased Blood urea increased C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram thorax Fibrin D dimer increased Full blood count abnormal Haematocrit decreased Haemoglobin increased Hilar lymphadenopathy Immature granulocyte count Lung infiltration Lung opacity

Symptomtext

Pt received vaccine on 4/8/2021. Pt was diagnosed with COVID-19 on 5/17/2021. Pt was admitted to the hospital on 5/21/2021 for pneumonia secondary to COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: 5/21 chest x-ray positive for bilateral diffuse infiltrates consistent with COVID pneumonia, CMP significant for sodium 128, chloride 95, BUN 22, calcium 8.0, albumin 2.9, and total protein 5.7. CBC significant for hemoglobin 11.7, hematocrit 34.5, MCV 78.9, MCH 26.8, immature granulocytes 0.8, lymphocytes 59.9. 5/22 CT angio thorax significant for bilateral multifocal groundglass opacities and reactive hilar lymphadenopathy, CMP sodium 131, chloride 96, BUN 26, Calcium 8.5. 5/23 CMP significant sodium 132, chloride 96, BUN 26, calcium 8.0. 5/24 CMP significant sodium 128, chloride 94, BUN 22, calcium 8.0; d-dimer 470. 5/25 CMP significant chloride 95; CRP 26.2; CBC significant WBC 29.38, MCH 26.6
Aktuelle Erkrankungen: -
Vorgeschichte: History of chronic lymphocytic leukemia, age-related osteoporosis, history of breast cancer
Andere Medikamente: vitamin D, vitamin B12
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 1347303

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 60,0
Geschlecht: F
Eingang: 25.05.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Dyspnoea Pain in extremity Ultrasound Doppler

Symptomtext

I had trouble breathing for two days and had a sore arm within 5 minutes of having the injection. And pain in my left leg is still ongoing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Doppler Ultrasound done on my leg
Aktuelle Erkrankungen: -
Vorgeschichte: Neurogastrointestinal disease Enteric nerve disease Asthma
Andere Medikamente: Multivitamins Magnesium Vitamin D3 Iron Omega 3 Claritin Xanax Qvar inhaler Nasonex
Allergien: Insulin sensitivity
Vorherige Impfungen: I have difficult breathing for 24 hours from flu vaccines

VAERS 1346600

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: GA
Alter: 31,0
Geschlecht: F
Eingang: 25.05.2021
Impfdatum: 03.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Burning sensation Discomfort Dysmenorrhoea Headache Mucosal dryness Musculoskeletal stiffness Myalgia Pain in extremity Paraesthesia Pelvic pain Sensitive skin Skin burning sensation Swelling Urinary straining

Symptomtext

The Tuesday after vaccination, I had physical discomfort and pain inside like period cramps. It felt like there was a tampon inserted weirdly, I tried a yeast infection solution with yogurt on a tampon. Later that week I had pelvic bone pain like I had strained to hard using the bathroom. Friday I got a hyper sensitive spot on upper right thigh, diagnosed as paresthesia, the swelling and discomfort around pelvis was still there. Saturday the swelling and discomfort on the insides started going down, both legs experienced pain, It felt as If I had done a workout and pulled my muscle. I typically have a high threshold for pain, No change on Sunday. Monday the back of right knee stated aching, sensitivity in left thigh. Both muscles on outside of legs felt like I had done a workout and needed stretched, On the 13th the aching traveled from the back of knees to calves I went to the Hospital. Myalgia and paresthesia and acute vaginitis. Shot of Toradol in left arm, which did nothing. Did ultrasound with normal results, no blood clots. The 14th my legs were comfortable as long as I was moving, started having a sharp stinging in left calf. The soles of my felt felt blistered but no visible blisters. Significant headache. I wore compression socks. I got a weird Charlie horse in left foot toes, top of right foot got really sensitive also. Volotoral is a topical pain cream that I had I used it on specific areas, of pain. Thursday the 15th the left outside of my foot was still sore, my calves had gotten better, the outside of the calf still had hypersensitivity. The muscles on the back of my knee's and calves were still sore. While driving my Hip and thighs for aching. Ankles are popping a lot. Fri-Sun following I had leg stiffening and muscle soreness mainly in the left side, went for a walk that weekend and while walking they felt ok, until I stopped walking. Mon-tue after I had a headache that felt like my brain was burning near the left temple area.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: None, occasional allergy pill
Allergien: shellfish, ceclor
Vorherige Impfungen: -

VAERS 1337611

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WA
Alter: 46,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 21.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Chills Condition aggravated Depression Feeling abnormal Headache Hot flush Nausea Pain Pain in extremity Pyrexia Vaccination complication Vomiting

Symptomtext

The main adverse event, depressive episode, lasting 8 weeks post vaccination. The other side effects I had: chills (lasted 3 days), hot flashes (lasted 2-3 days), fever (lasted 3 days), nausea (lasted for 5 days), vomiting, brain fog (lasted 3 weeks), body aches (lasted for 5 days), headaches (lasted 5 days), left sore arm (lasted 3 days). I consulted with my psychiatrist about my symptoms. As of today I am still recovering from the depressive episodes. .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic migraines, treated for depression/anxiety, hypothyroidism
Andere Medikamente: Topomax, Trintellix, Levothyroxine
Allergien: High dose of NSAID, dialudid, penicillin, peaches, hay fever, rag weed
Vorherige Impfungen: -

VAERS 1337191

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 51,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 16.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Differential white blood cell count Full blood count Headache Hypoaesthesia Laboratory test abnormal Metabolic function test Migraine Paraesthesia Parosmia SARS-CoV-2 test negative Taste disorder Urine analysis Vision blurred Visual impairment Vomiting

Symptomtext

On the 17th I suffered a severe migraine at 2:00 AM went down the hallway and threw up most of the day. My vision was off and it felt like the top of my head was about to explode. I went to the Walk-in clinic to get treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: 1,0
Labordaten: I a COVID-19 test and it came back negative along with a CDC with a differential/Metabolic panel and a POCT performed urine dipstick. Some of the tests came back abnormal and I do have the results as well. I still have numbness and tingling in the right arm, blurred vision in my right eye, sense of smell/taste is not the same and am still having issues.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: I take a anti-depressant at night around 9pm.
Allergien: No
Vorherige Impfungen: -

VAERS 1337017

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 42,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 12.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: SYR / LA

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

Chills Depressed mood Diarrhoea Feeling hot Impaired work ability Influenza like illness Malaise Mobility decreased Nausea Pain SARS-CoV-2 test negative Tremor

Symptomtext

Started that day chills and three four hours hot and shaky. I could not work a couple days feeling like very very sick, nauseous. three or four days and went away slow. Missed work last week, diarrhea, getting sick off and on since the covid shot feeling like the flu. But tests negative. Sometimes I am perfectly fine, sometimes very sick and very down. Happens randomly. Could not even get up from the bed. Still taking nausea pills and pills for pain, body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: COVID test every time feeling unwell - but all have been negative.
Aktuelle Erkrankungen: none
Vorgeschichte: migraine
Andere Medikamente: none
Allergien: naratriptan
Vorherige Impfungen: Tetnus, two years ago

VAERS 1336832

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WI
Alter: 26,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 13.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Asthma Blood culture negative Chest X-ray normal Chest pain Chills Computerised tomogram normal Culture urine negative Differential white blood cell count abnormal Dyspnoea Electrocardiogram normal Fatigue Heart rate increased Malaise Myalgia Pyrexia SARS-CoV-2 test negative Systemic inflammatory response syndrome White blood cell count increased

Symptomtext

Experienced 2 days of worsening fever, chills, myalgias, mild chest pain, fatigue and malaise. Went to the ER after having a low grade fever, chills, shortness of breath, mild chest pain, and an elevated resting heart rate. Was diagnosed with SIRS as a response to the covid vaccine and hospitalized for observation. Was discharged the next day. Diagnosed with SIRS, possibly due to the COVID vaccine with a secondary diagnosis of asthma.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: EKG, Blood cultures, urine culture, Covid 19 test, CT scan, chest x-ray. Everything came back normal, except for an elevated WBC of 21.39. Manual differential found bands at 13%
Aktuelle Erkrankungen: Occasional allergies.
Vorgeschichte: Anxiety and potentially allergy induced asthma (in the process of being confirmed by a medical professional)
Andere Medikamente: Zyrtec for allergies (as needed), tylenol and aleve for fever and chills (as needed).
Allergien: Hazelnut
Vorherige Impfungen: -

VAERS 1336546

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 02.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Mobility decreased Pain Pain in extremity Periarthritis Swelling X-ray

Symptomtext

Pain in left upper arm about 10 days after injection, shooting down arm to hand, reduced mobility of the arm, didn't improve for 3 weeks thus saw my own doctor. She referred to orthopaedic doctor. Saw him on 5/12/2021, he diagnosed adhesive capsulitis in left shoulder possibly caused or exacerbated by the swelling due to the vaccination in that same area. Revisit in 3 weeks after dr. visit. Taking ibuprofen to reduce inflammation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: X-rays of shoulder 5/12/2021 - showed no degenerative joint disease.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1334372

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 61,0
Geschlecht: M
Eingang: 20.05.2021
Impfdatum: 08.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: SYR / RA

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

Blood test normal Chest X-ray normal Dyspnoea

Symptomtext

About 10 days after the shot I could not breath. It came on over the course of a few hours to the point that my doctor told me to go to the ER. There they administered a nebulizer and a prescription for prednisone for 4 days which helped. 24 hours after the prednisone prescription was complete, the breathing difficulty resurfaced and I was back in the ER again. This time they gave me a longer course of prednisone (10 days) that reduced over that time. Once that course was complete the breathing difficulty started again, but not to the point of an ER visit. My GP then prescribed a smaller dose of Prednisone over 6 days combined with an inhaler. That has helped. I don't really know if this is related to the vaccine. My suspicion is that the vaccine may have revved up my immune system and because of my autoimmune disease it attached my airway. But that is just a guess.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: The ER performed chest x-rays and a full compliment of blood tests and all were normal.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism Stage 3 Kidney disease Undefined autoimmune disease (speckled positive blood test result) Pre-hypertensive
Andere Medikamente: Levothyroxine, Atorvastatin, Hydrochlorothiazide, Lisinopril, Vitamin D3, Probiotic
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 1333992

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 20.03.2021
Beginn: 16.05.2021
Tage bis Beginn: 57,0
Dosis: 1
Route/Site: - / -

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

Arthralgia Bacterial test positive COVID-19 Confusional state Cough Depression Essential hypertension Fall Joint dislocation Joint dislocation reduction Nitrite urine present SARS-CoV-2 test positive

Symptomtext

Paraphrase from provider discharge to swing bed note: 83 y/o female brought to ED for fall and left shoulder pain. Baseline dementia, poor historian, early onset Parkinson's Disease. Fully vaccinated for COVID-19, showing no obvious symptoms of COVID. Cough, no dyspnea per review of systems. Problem list includes: Anterior shoulder dislocation, reduction. COVID-19. Essential Hypertension, Acute confusion, baseline dementia, urine + for nitrite and bacteria, started on macrobid. Depression. Unable to enter required fields for Q.#21, Hospitalization. Currently Hospitalized

Weitere VAERSDATA-Felder

Praegender Schweregrund: Essential hypertension
Hospital-Tage: -
Labordaten: COVID-19 PCR test 5/16/2021
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Parkinson's Disease, Hypertension, dementia
Andere Medikamente: Unknown
Allergien: Vicodin, Suprax, Cedax, Benadryl, PCN, quinine, VIoxx, Bextra
Vorherige Impfungen: -

VAERS 1331135

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 38,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: 05.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / LA

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

Amnesia Arthralgia Blood creatine phosphokinase increased Blood test Chest X-ray Chest pain Chills Head discomfort Pain Pyrexia

Symptomtext

Ever since the shot, that night - severe chills, fever. A week later, I went to ER - I was still having short term memory loss, chest pain and body aches and joint pains I have been scheduled for a Rheumatologist; Neurologist. I'm still taking prednisone until I can get to the Rheumatologist. As long as I'm on the prednisone, I'm all right but as soon as I come off it I get symptoms back of pressure in my head, all my joints start hurting and have short term memory loss.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: ER - - Chest x-rays, bloodwork - CPK levels were elevated after the vaccine
Aktuelle Erkrankungen: no
Vorgeschichte: type 2 diabetes
Andere Medikamente: Trulicity - for type 2 diabetes
Allergien: no
Vorherige Impfungen: -

VAERS 1330867

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 55,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 10.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: IM / RA

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

Anxiety Blood test normal Computerised tomogram normal Eating disorder Electrocardiogram normal Headache Inflammation Muscle disorder Muscular weakness Neuralgia Sleep disorder Tremor

Symptomtext

I developed severe headaches which turned into a lot of inflammation. There was nerve pain throughout my body. I wasn't able to sleep or eat for almost 7 days. I was experiencing nerve pain and tremors. They weren't continuous, but they would come and go. Inside I felt like there were quivering muscle sensations and weakness. The pain that was associated with the nerve pain would not go away. I have started to experience severe anxiety. I feel like I'm experiencing PTSD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: I had CT scans and different bloodwork. There were EKG's performed, but all results have come back normal. I was given an antibiotic for a possible UTI. I was also given a series of steroids that really helped with the pain.
Aktuelle Erkrankungen: I did not have any other illnesses.
Vorgeschichte: I do not have any chronic or long standing health conditions.
Andere Medikamente: I take Levothyroxine (125 mg, half a dose every other day), Valtrex 500mg per day, Bupropion (generic Wellbutrin) 150mg once per day and Pantoprazole 40mg daily.
Allergien: I have an allergy to iodine.
Vorherige Impfungen: -

VAERS 1329144

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 65,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: -
Beginn: 14.05.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Dyspnoea

Symptomtext

INCREASED SHORTNESS OF BREATH; This spontaneous report received from a patient concerned a 65 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included chronic obstructive pulmonary disorder, occasional social alcohol user, smoker, and shortness of breath, and other pre-existing medical conditions included the patient had no known allergies and no known drug abuse or illicit drug usage. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 13-MAY-2021 for prophylactic vaccination. Concomitant medications included acetylsalicylic acid, atorvastatin, budesonide/formoterol fumarate/glycopyrronium bromide, and hydrochlorothiazide/losartan potassium. On 14-MAY-2021, the subject experienced increased shortness of breath. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from increased shortness of breath. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Chronic obstructive pulmonary disease; Shortness of breath; Smoker (No more than 1/2 pack/day; hasn't had a cigarette in two days.); Social alcohol drinker (Maybe twice a month- will split a beer)
Vorgeschichte: Comments: the patient had no known allergies and no known drug abuse or illicit drug usage
Andere Medikamente: ASPIRIN [ACETYLSALICYLIC ACID]; ATORVASTATIN; LOSARTAN/HYDROCHLOROTHIAZIDE; BREZTRI AEROSPHERE
Allergien: -
Vorherige Impfungen: -

VAERS 1328007

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MA
Alter: 26,0
Geschlecht: F
Eingang: 18.05.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Dizziness Dyspnoea Headache Impaired driving ability Mobility decreased Pyrexia Sleep disorder

Symptomtext

103 fever,, dizziness, weakness, unable to walk or lift arms, shortness of breathe , severe headache Stayed at doctors office for 1.5 hours, took ibuprofen to lower temp and had to have my husband leave work to come and get me as I was unable to drive. Woke up in the middle of the night with same symptoms and had to take more ibuprofen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lithium, buspirone
Allergien: Geodan
Vorherige Impfungen: -

VAERS 1314974

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: UT
Alter: 32,0
Geschlecht: F
Eingang: 13.05.2021
Impfdatum: 19.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Dyspnoea Feeling hot Heart rate increased Heart sounds abnormal Oropharyngeal discomfort

Symptomtext

About 2 minutes after receiving the vaccine, while parked, I started getting very light headed, felt dizzy, and my heart starting beating extremely fast, and then slowed down and started beating very very hard, and felt like it was going to pound out of my chest. I then had a warm sensation in my throat and started feeling like it was getting harder to breathe. I rolled down my Window, and looked for someone to wave over for assistance, but there were cars in the way, so I closed my eyes and focused on breathing deep and slowly to see if that would make it any better. After about 5 minutes my heart rate went back to normal, I felt I could breathe normally, and wasn't so light headed anymore. I should have reported this to someone when they told me I could leave, but I wasn't sure if it was an actual allergic reaction. Or if it was just a stress reaction. I felt like I should at least report it here, because I was completely fine before the injection, during the injection, and right after, until about 2 minutes after being parked.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Daily multivitamin
Allergien: Benedryl
Vorherige Impfungen: -

VAERS 1311217

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 57,0
Geschlecht: F
Eingang: 12.05.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Arthritis Burning sensation Chest pain Dizziness Flushing Headache Hypoaesthesia Injury Insomnia Joint range of motion decreased Joint space narrowing Loss of personal independence in daily activities Magnetic resonance imaging Musculoskeletal discomfort Myalgia Nausea Neck pain

Symptomtext

Vaccine high up in left shoulder joint area & sideways towards body. Immediate severe burning pain, flushing, dizziness, faintness, chest pain, BP 180/115. Incident report was filed by nurses. Paramedics onsite attended patient; documentation was signed by patient. Felt like arm ripped off and put back on. Severe pain left shoulder to elbow, neck, scapula: continunous for 6 weeks, no sleep. Moderate pain at 8 weeks. Pins & needles top-trunk 4wks. 2 weeks out: lump on top of L shoulder for 1 week. 2.5 weeks out: burning rash in armpit for 1 week. 8+ wks of numb/tingling in L hand pinky & ring fingers, limited range of motion w/popping, crunching in shoulder when move left arm. Headache, nausea, muscle aches for 5 days post vaccine. On 3/29/21, 3/30/21, 4/16, 4/19, 4/30/21 sought medical attention @ internal med. doctor & orthopedic doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 4/27/21 MRI: see more p. 2 4/27/21 MRI - report showed 5x5 tear (interstitial) supraspinatus fibers @ junction middle & anterior 1/3 aspect, suprasinous/infraspinatus tendinosis; narrowing of achromialhumeral space w/subacromial subdeltoid bursa inflammation; basically damage to rotator cuff, impingement/frozen shoulder. Constant pain which worsens with use of arm. Cannot put weight on it, cannot lift with it, limited range of motion, hard to wash hair, difficult to use keyboard w/left hand for work, cannot resume normal health/fitness activities or play piano or violin as of 5/12/21 w/o pain.
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure, mild asthma
Andere Medikamente: lisinopril, estradiol
Allergien: PEG (Biaxin, Clarithromycin-antibiotics)
Vorherige Impfungen: -

VAERS 1289204

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 05.05.2021
Impfdatum: 03.04.2021
Beginn: 02.05.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Cardiac failure congestive Condition aggravated Pneumonia SARS-CoV-2 test positive

Symptomtext

COVID+ Pneumonia and CHF exacerbation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1285785

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 55,0
Geschlecht: M
Eingang: 04.05.2021
Impfdatum: 31.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Back pain Hypoaesthesia Hypoaesthesia oral Neck pain Pain in extremity Paraesthesia Peripheral swelling

Symptomtext

Numbness in nose and upper lip shortly after receiving shot. Both arms pain and numbness and tingling. Back and neck pain. Arm swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Neck and back injury from car accident.
Andere Medikamente: Celecoxib. Gabapentin. Baclofen. Cyclobenzaprine. Hydro app 10-325
Allergien: None
Vorherige Impfungen: -

VAERS 1284922

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MN
Alter: 58,0
Geschlecht: F
Eingang: 04.05.2021
Impfdatum: -
Beginn: 11.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Chills Dehydration Headache Nausea Pain assessment Positron emission tomogram

Symptomtext

DEHYDRATION; SEVERE HEADACHE; NAUSEA; MASSIVE CHILLS; This spontaneous report received from a patient concerned a 58 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included migraines. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and expiry: 25-MAY-2021) dose was not reported, 1 total administered on 10-MAR-2021 at left arm for prophylactic vaccination. No concomitant medications were reported. Right after Vaccine administration no side effects but the patient spent the next day at Emergency Room. On 11-MAR-2021, the patient was sicker than dog and had experienced dehydration, massive chills, severe headache, and nausea. On the same day PET scan was performed for headache and pain was 10/10. Patient was given cold medicine and 2 unspecified intravenous medication. After that patient was well enough to go home. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from dehydration, massive chills, severe headache, and nausea on 11-MAR-2021. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20210458937-COVID-19 VACCINE AD26.COV2.S-DEHYDRATION. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). 20210458937-COVID-19 VACCINE AD26.COV2.S-20210458937-COVID-19 VACCINE AD26.COV2.S-SEVERE HEADACHE, NAUSEA, MASSIVE CHILLS. This event(s) is labeled per RSI and is therefore considered potentially related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: Test Date: 20210311; Test Name: PET scan; Result Unstructured Data: unknown; Test Date: 20210411; Test Name: Pain scale; Result Unstructured Data: 10/10
Aktuelle Erkrankungen: Migraine
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1283075

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: NV
Alter: 35,0
Geschlecht: F
Eingang: 03.05.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Body temperature increased Dizziness Fatigue Feeling cold Headache Nausea Pain Tremor

Symptomtext

30 Minutes later had slight headache, around a hour later head ache got worse and little light headed. starting at approximately 9pm I started to feel very light headed, head ache, nauseaus around 11 started shaking un controllably and really cold and fever. was shaking and freezing all night highest fever was 104.4 checked around 6am. because couldn't find my temporal thermometer. Called and reported the problems. Talked to my doctor and told me to monitor and if doesn't get better to go to ER. around 10am I felt a little better and temp stayed around 101. by the next evening tempurature was around 98 degrees and only had muscle aches, fatigue and head ache. Felt alot better around Sunday afternoon.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Only spoke with doctor on the phone and then follow conversation Monday.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Only allergy I know of is red cedar, bee stings, and rodent urine.
Vorherige Impfungen: I will sometimes get flu like symptoms from flu shot

VAERS 1271011

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 26.03.2021
Beginn: 27.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Cardiac stress test normal Chest X-ray normal Chills Echocardiogram normal Electrocardiogram normal Fatigue Gastrointestinal disorder Hypertension Lethargy Pyrexia Rash erythematous Rash pruritic SARS-CoV-2 test negative Skin discolouration Troponin increased Ultrasound abdomen

Symptomtext

Very high fever for 3 weeks; Shivers; Extreme fatigue; Lethargy; GI problems; Increased level of traponin; Very dark and itchy red rash; Very high blood pressure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: 3,0
Labordaten: In hospital 3/31/21-4/02/21 covid test - negative Lung Xray - normal Blood work - elevated traponin Stress test - normal ECG - normal Echocardiogram - normal Abdominal ultrasound - 04/27 21 no results yet
Aktuelle Erkrankungen: none
Vorgeschichte: osteoporosis
Andere Medikamente: Fluoxetine 20mg; irbesartan HCTZ 300/12.5; clopidogrel 75 mg; atorvastin 40mg; Vitamin D3; probiotics
Allergien: Amoxicillin & zithromax (orally, stomach upset)
Vorherige Impfungen: -

VAERS 1264886

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 27.04.2021
Impfdatum: 01.04.2021
Beginn: 01.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Ageusia Angiogram Anosmia Chest X-ray Chest pain Coagulation test abnormal Dizziness Dysgeusia Dyspnoea Electrocardiogram Erythema Fatigue Full blood count Hypoaesthesia oral Nausea Pallor Pruritus

Symptomtext

04/01/2021 - Vaccinated at 3:00 pm . Waited 15 mins and then returned home. Around 3:30 pm I developed a metallic taste in my mouth. Around 3:35 pm I became very itchy with no rash or hives. Itching feeling felt like it was below the skin. Approx 3:45 pm I called called Primary Care Physician and let them know what going on. Around 4:05 pm my lips, tongue and mouth felt numb ( Novocaine like ) Around 4:15 pm My Dr's office called me back and after describing my symptoms they told me to go to to the ER. Immediately Went to Emergency Department. Was seen by doctor and others. Skin had now began going back and forth from pale to red. Itching had increased . Skin color began changing going from bright red to pale white and then back and forth. I was also now very light headed and very nauseous along with. I still had the metal taste in my mouth, was extremely itchy, and my lips and tongue were still numb. Around 5:14 pm they gave me Pepsid, Vistaril, Deltasone. We stayed there about another hours and I was released. Was give a script for Deltasone that I had filled that night. I went home and went to bed. 04/02 - Woke up and had lost all sense of taste and smell. I was still itchy, tired, nauseous, lips and tongue we still numb. I called my Dr and they said they would see me on Monday 04/05. The symptoms continued all weekend and on Sunday 04/04 i developed a burning feeling in my lungs. Monday 04/05 I went to see the Dr . The Dr prescribed hydrOXYzine . I did not do well on so it was changed to Zytec. Rested and tried to take it easy. Feeling in the lips and tongue came back. No longer nauseous . I was still light headed from time to time. My lungs were still bunring and I was very short of breath. On 04/23 went to the doctor because I still am not better. My lungs were still burning, I was tired all of the time, I and I was still light headed from time to time. They did blood work, EKG and a chest X ray. On 04/24 I had a CTA because ( abnormal coagulation profile shortness of breath. I was prescribed Albuterol in hopes it will be better. I have a follow up on 05/10 unless things get worse. 04/27 This are not worse, but they are not really improved. I am still tired all of the time. I still have shortness of breath, my lungs are still burning, and I still get light headed from time to time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 04/22 - complete blood work and chest x-ray 04/23 - CPT 71275 because of R791 Abnormal coagulation profile from 04/22 test results
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Vitamin D3 - 25mcg (1000 Ut) Capsules , Multivitamin, Vitamin C - 500mg Chewtabs, Zinc - 50mg Tablets , Black Elderberry(Berry-Flower) - 575mg Capsules
Allergien: Amoxicillin, Benadryl, MSG,Nutrasweet ,Sulfa Drugs, Latex Sensitivity
Vorherige Impfungen: Tdap 10/2019 - fu like symptoms for over a week ( tired, headache) . Injection site pain and swelling. 2017 & 2018 Flu Vaccine.

VAERS 1264595

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CO
Alter: 35,0
Geschlecht: F
Eingang: 27.04.2021
Impfdatum: 18.03.2021
Beginn: 05.04.2021
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Hypoaesthesia Incontinence Magnetic resonance imaging Nausea Platelet count decreased Red blood cell count decreased Somnolence Speech disorder Tremor Vomiting

Symptomtext

sleepy, not operable, incontinent, nausea, vomiting, tremors in hands, numbness in legs, speech issues

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: low plateleyt and red blood cell count, mri
Aktuelle Erkrankungen: -
Vorgeschichte: hypothyroidism
Andere Medikamente: levothyroxine, Adderall,
Allergien: penicillin, shellfish, bees
Vorherige Impfungen: -

VAERS 1256728

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 64,0
Geschlecht: M
Eingang: 25.04.2021
Impfdatum: 26.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / RA

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

Arrhythmia Blood test Cardiac assistance device user Cardioversion Echocardiogram Electrocardiogram abnormal Ventricular tachycardia

Symptomtext

6 days after receiving the Covid19 J&J vaccine I had sustained arrhythmia of 142bpm for 2 hours & received emergency intervention at the Hospital and 1 night observation. They were able to cardiovert me with abimondiron drip. 17 days later my heart started racing again & I received 2 consecutive shocks from my internal defibrillator and was transported to the hospital and stayed 1 night for observation. 22 days after receiving the above vaccine, I again developed a ventricular tachycardia rhythm & received 2 consecutive shocks and was transported to the hospital and stayed 2 nights. I do have a history of v-tach but prior to being vaccinated it had been two years without any incident of VTach or therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: 4,0
Labordaten: Defibrillator download; Echocardiagram, EKG, multiple blood work for levels 4-1-21; 4-12-21; & 4-17-21
Aktuelle Erkrankungen: none
Vorgeschichte: Congestive heart failure; Type II Diabetes; one kidney (former cancer)
Andere Medikamente: Aldactone 25 mg 1x daily; Amaryl 4 mg 1x day; Coreg 25 mg 2x day; Eiquis 5 mg. 2xday; Entresto 97/103 2xday; Lanoxin 0.125 1xday; Lasix 20 mg as needed; Levemir 30-40 units as needed; Betapace 120 mg 1x day; Januvia 100 mg 1x day; Viagra 10
Allergien: none
Vorherige Impfungen: -

VAERS 1253721

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AZ
Alter: -
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: -
Beginn: 24.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Dizziness Dyspnoea

Symptomtext

TROUBLE BREATHING; DIZZINESS; This spontaneous report received from a patient concerned a female of unspecified age. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and expiry: UNKNOWN) dose was not reported, administered on 24-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 24-MAR-2021, the subject experienced trouble breathing. On 24-MAR-2021, the subject experienced dizziness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from trouble breathing, and dizziness. This report was non-serious.

Weitere VAERSDATA-Felder

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

VAERS 1253247

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: -
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Arthralgia Chest pain Myalgia

Symptomtext

CHEST PAIN; HIPS AND SHOULDERS HURTS; MUSCLE ACHES; This spontaneous report received from a patient concerned a 43 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included the patient had no known drug allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025, expiry: UNKNOWN) dose was not reported, administered on 17-MAR-2021 09:30 a.m. vaccinated at right deltoid for prophylactic vaccination. No concomitant medications were reported. On 17-MAR-2021 21:30 p.m., the subject experienced chest pain. On 17-MAR-2021 21:30 p.m., the subject experienced hips and shoulders hurts. On 17-MAR-2021 21:30 p.m., the subject experienced muscle aches. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from muscle aches, chest pain, and hips and shoulders hurts. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no known drug allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1253121

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: UT
Alter: -
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: -
Beginn: 15.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Chest pain Heart rate increased Pyrexia

Symptomtext

FEVER; INCREASED HEART RATE; CHEST PRESSURE AND CHEST PAIN; This spontaneous report received from a patient concerned a 34 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included latex allergy, and inflammation of the sternum.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025, expiry: UNKNOWN) dose was not reported, administered on 15-MAR-2021 for prophylactic vaccination. Concomitant medications included ibuprofen for inflammation of the sternum, and propranolol for inflammation of the sternum. On 15-MAR-2021, the subject experienced increased heart rate. On 15-MAR-2021, the subject experienced chest pressure and chest pain. On 16-MAR-2021, the subject experienced fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from increased heart rate, and fever on 16-MAR-2021, and had not recovered from chest pressure and chest pain. This report was non-serious.; Sender's Comments: V0: Medical Assessment comment not required as per standard procedure as the case assessed as non-serious

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Costochondritis; Latex allergy
Vorgeschichte: Comments: Unknown
Andere Medikamente: IBUPROFEN; PROPRANOLOL
Allergien: -
Vorherige Impfungen: -

VAERS 1252845

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: -
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: -
Beginn: 12.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Fatigue Injection site pain Mobility decreased Nausea Pain Pyrexia

Symptomtext

CAN HARDLY MOVE; COMPLETE BODY ACHE; ARM HURT VERY BAD; FATIGUE; NAUSEA; FEVER; This spontaneous report received from a patient concerned a female of unspecified age. The patient's height, and weight were not reported. The patient's concurrent conditions included pancreatic cancer, sulfa allergy, penicillin allergy, narcotic allergy, codeine allergy, and macrobids allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and expiry: UNKNOWN) dose was not reported, administered on 12-MAR-2021 for prophylactic vaccination on left arm. No concomitant medications were reported. On 12-MAR-2021, the subject experienced can hardly move. On 12-MAR-2021, the subject experienced complete body ache. On 12-MAR-2021, the subject experienced arm hurt very bad. On 12-MAR-2021, the subject experienced fatigue. On 12-MAR-2021, the subject experienced nausea. On 12-MAR-2021, the subject experienced fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from fever on 14-MAR-2021, was recovering from can hardly move, and had not recovered from fatigue, complete body ache, nausea, and arm hurt very bad. This report was non-serious.; Sender's Comments: V0: Medical assessment comment not required as per standard procedure since case was assessed as non serious.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergic reaction to antibiotics; Drug allergy; Pancreatic cancer (Pancreatic Cancer (received chemo. last Wednesday)); Penicillin allergy
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1252222

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TN
Alter: -
Geschlecht: U
Eingang: 24.04.2021
Impfdatum: -
Beginn: 13.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Injected limb mobility decreased Injection site hypoaesthesia

Symptomtext

RIGHT ARM COULD NOT LIFT-UP; NUMB ON THE RIGHT ARM WHERE THE VACCINE WAS GIVEN; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, once toatal administered on 08-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-MAR-2021, the subject experienced right arm could not lift-up. On 13-MAR-2021, the subject experienced numb on the right arm where the vaccine was given. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the numb on the right arm where the vaccine was given and right arm could not lift-up was not reported. This report was non-serious.; Sender's Comments: V0: Medical assessment comment not required as per standard procedure since case was assessed as non serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1250768

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: -
Geschlecht: M
Eingang: 24.04.2021
Impfdatum: -
Beginn: 10.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Body temperature Chest pain Chills Flushing Headache Heart rate increased Nausea Pyrexia

Symptomtext

FAST HEART BEAT; FEVER; NAUSEA; CHILLS; HEADACHE; RIGHT SIDED CHEST PAIN; FLUSHED FACE; This spontaneous report received from a patient concerned a male. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 10-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 10-MAR-2021, the subject experienced flushed face. On 11-MAR-2021, Laboratory data included: Body temperature (NR: not provided) 99 deg, and Heart rate increased (NR: not provided) 100 bpm. On 11-MAR-2021 01:30:00, the subject experienced right sided chest pain. On 11-MAR-2021 01:30:00, the subject experienced chills. On 11-MAR-2021 01:30:00, the subject experienced headache. On 11-MAR-2021 02:00:00, the subject experienced nausea. On 11-MAR-2021 05:00:00, the subject experienced fever. On 11-MAR-2021 05:30:00, the subject experienced fast heart beat. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from flushed face on 10-MAR-2021, chills on 11-MAR-2021 02:00:00, nausea on 11-MAR-2021, and fever on 11-MAR-2021 05:30:00, had not recovered from headache, and the outcome of right sided chest pain and fast heart beat was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20210311; Test Name: Heart rate increased; Result Unstructured Data: 100 bpm; Test Date: 20210311; Test Name: Body temperature; Result Unstructured Data: 99 deg
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1109397

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MN
Alter: 65,0
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: -
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Cough Dyspnoea Muscle tightness Musculoskeletal chest pain Pain Painful respiration Vomiting

Symptomtext

LEFT RIB CAGE PAIN; MUSCLE TIGHTNESS; DIFFICULTY BREATHING; COUGH; This spontaneous report received from a patient concerned a 65 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included autoimmune hepatitis. The patient experienced drug allergy when treated with erythromycin, and morphine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 11-MAR-2021 13:50 on left arm for prophylactic vaccination. No concomitant medications were reported. On MAR-2021, the subject experienced cough. On MAR-2021, the subject experienced difficulty breathing. On 14-MAR-2021, the subject experienced left rib cage pain. On 14-MAR-2021, the subject experienced muscle tightness. Treatment medications (dates unspecified) included: ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from left rib cage pain, and difficulty breathing, and the outcome of cough and muscle tightness was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Autoimmune hepatitis (Patient was on dietary supplement for 15 days.Body reacted weird to it so stopped and Six months later was nauseated. Pt was on liver transplant list for several months.)
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1109397

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MN
Alter: 65,0
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: -
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Cough Dyspnoea Muscle tightness Musculoskeletal chest pain Pain Painful respiration Vomiting

Symptomtext

LEFT RIB CAGE PAIN; MUSCLE TIGHTNESS; DIFFICULTY BREATHING; COUGH; This spontaneous report received from a patient concerned a 65 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included autoimmune hepatitis. The patient experienced drug allergy when treated with erythromycin, and morphine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 11-MAR-2021 13:50 on left arm for prophylactic vaccination. No concomitant medications were reported. On MAR-2021, the subject experienced cough. On MAR-2021, the subject experienced difficulty breathing. On 14-MAR-2021, the subject experienced left rib cage pain. On 14-MAR-2021, the subject experienced muscle tightness. Treatment medications (dates unspecified) included: ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from left rib cage pain, and difficulty breathing, and the outcome of cough and muscle tightness was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Autoimmune hepatitis (Patient was on dietary supplement for 15 days.Body reacted weird to it so stopped and Six months later was nauseated. Pt was on liver transplant list for several months.)
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1249167

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 23.04.2021
Impfdatum: -
Beginn: 11.04.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Dyspnoea Oxygen saturation Rash Solar lentigo

Symptomtext

SHORTNESS OF BREATH; LIVER SPOTS; RASH LEFT THIGH; This spontaneous report received from a patient concerned a 62 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included copd. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 09-APR-2021 for prophylactic vaccination. Concomitant medications included oxygen for copd. On 11-APR-2021, the subject experienced shortness of breath. On 11-APR-2021, the subject experienced liver spots. On 11-APR-2021, the subject experienced rash left thigh. Laboratory data included: O2 saturation (NR: not provided) 97 %. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from shortness of breath, had not recovered from rash left thigh, and the outcome of liver spots was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210411; Test Name: O2 saturation; Result Unstructured Data: 97 %
Aktuelle Erkrankungen: COPD (uses 2.5l of oxygen via nasal canula)
Vorgeschichte: Comments: Unknown
Andere Medikamente: OXYGEN
Allergien: -
Vorherige Impfungen: -

VAERS 1247659

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 22,0
Geschlecht: F
Eingang: 23.04.2021
Impfdatum: 08.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

AST to platelet ratio index increased Alanine aminotransferase increased Chills Condition aggravated Contusion Dizziness Fatigue Headache Laboratory test Nausea Petechiae Platelet count decreased Platelet morphology Vision blurred Vomiting

Symptomtext

Janssen COVID-19 Vaccine EUA 8pm 3/8/21: Nausea, vomiting, chills began; slept for 10+ hours 8 am 3/9/21: Fatigue, nausea, headache; noticed petechiae on arms and abnormal bruising on legs 8 am 3/10/21: Blurry vision, headache (unlike usual throbbing headaches, consistent pain on top of head), lightheaded/dizzy 10 am 3/10/21: Asked friend to drive me to ED at Hospital; Labs were drawn showing platelet count of 42K and I was released from ED and told to follow up with Hematologist

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Labs at Hospital: Platelet count was 42K (When healthy, my usual platelet count is over 150K) Follow-up labs on 3/11/21 with Doctor: Platelet count 38K, Platelet morphology: Few large; Elevated AST and ALT liver enzymes: AST= 125, ALT= 148
Aktuelle Erkrankungen: N/A
Vorgeschichte: Immune Thrombocytopenia Purpura (ITP): Low platelets (Diagnosed at age 3)
Andere Medikamente: Wellbutrin 150 mg, Pristiq 100 mg, Vyvanse 20 mg
Allergien: N/A
Vorherige Impfungen: Varicella 11/03/1999; Diagnosed with ITP within 1 month of receiving vaccine

VAERS 1247589

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 47,0
Geschlecht: F
Eingang: 23.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test normal Chills Decreased appetite Electrocardiogram normal Fatigue Pain Palpitations

Symptomtext

On April 8, 2021, around 7pm I began to experience body aches, fatigue, and loss of appetite. By 8pm I began to experience chills along with continue body aches, fatigue, and loss of appetite. At 11pm that night, I was awaken as my heart was pounding very hard. I was still experiencing the body aches, fatigue, chills, and loss of appetite. This continued all through the night into the next day. April 9, 2021. On April 10, 2021, the body aches and chills subsided however I continued to feel fatigue, loss of appetite and I could still feel my heart beating hard. These symptoms continued through Tuesday April April 14, 2021 when I went to see the doctor. I started to get my appetite back later that week after my doctor appointment however I continue to feel heart palpitations and fatigue. I went for a follow up doctor appointment on April 21, 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: April 14, 2021 -BP reading 142/90; EKG - normal; and Blood work all came back normal April 21, 2021 - BP reading 122/86 My doctor has scheduled me to see a cardiologist and to have an ultra sound of my heart which is scheduled for Monday, May 3, 2021.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: No
Allergien: Vicadin Ambien
Vorherige Impfungen: -

VAERS 1242719

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IN
Alter: 45,0
Geschlecht: F
Eingang: 22.04.2021
Impfdatum: 25.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain upper Dyspnoea Headache Oedema peripheral

Symptomtext

headache, bilateral lower extremity edema, stomach pain, shortness of breath

Weitere VAERSDATA-Felder

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

VAERS 1242450

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 67,0
Geschlecht: F
Eingang: 22.04.2021
Impfdatum: 15.03.2021
Beginn: 20.04.2021
Tage bis Beginn: 36,0
Dosis: 1
Route/Site: - / -

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

Alanine aminotransferase normal Albumin globulin ratio normal Aspartate aminotransferase decreased Basophil count normal Blood albumin normal Blood alkaline phosphatase increased Blood bilirubin normal Blood calcium normal Blood chloride increased Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium normal Blood urea normal Carbon dioxide normal Chest X-ray abnormal Chest discomfort Chest pain

Symptomtext

4/20/21 ER HPI: 67 y.o. female who presents with complaint of shortness of breath since yesterday night when she went to bed and describes it as heaviness associated with lower chest pain both back and front. Patient says shortness of breath is worse with lying down and with activity. Patient also complained of cough that is nonproductive. No fever or chills, no nausea vomiting and no abdominal pain. Patient has been off her Coumadin is since for 04/09/2021 for back injection for back pain. Patient said the the shortness of breath is similar to the last time she had blood clot.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CTA Chest For Pulmonary Embolism w Contrast [245811813] Collected: 04/20/21 1327 Order Status: Completed Updated: 04/20/21 1348 Narrative: EXAMINATION: CTA Chest with Intravenous Contrast, Axial Imaging with Coronal and Sagittal 2-D imaging as well as 3-D MIP reconstructions. 80 mL Omnipaque 300 was administered intravenously. was administered intravenously for the post-contrast images. INDICATION: Elevated d-dimer 1330. History of pulmonary emboli. COMPARISON: PA and lateral chest x-ray 4/20/2021 and CT chest, abdomen and pelvis without contrast 7/6/2017. CTA CHEST FINDINGS: There is submaximal contrast opacification of the pulmonary arteries related to timing of imaging with regards to the phase of contrast, which may lower the sensitivity and specificity in evaluation of pulmonary emboli, especially in the distal subsegmental branches. Allowing for the limitations, no gross evidence of pulmonary emboli in the adequately opacified pulmonary arteries. Main pulmonary artery measures 3.2 cm in diameter. Aorta is age-appropriate without aneurysm. Direct origin of the left vertebral artery from the aortic arch proximal to the origin of the left subclavian artery, a normal variant. Mild atherosclerotic calcifications in the aortic arch and in the proximal left anterior descending coronary artery. Heart size is normal with no pericardial effusion. No pathologic adenopathy is seen in the chest. Nonspecific hypodense lesions in the included lower left lobe of thyroid measuring up to 1 cm, with the thyroid incompletely included on this exam. Minimal scarring in the lung apices. Minimal atelectasis or scarring in the anterior lingula or possibly artifact due to volume averaging with pericardial fat pad. No acute infiltrate, consolidation, pleural effusion or pneumothorax. No suspicious pulmonary nodule is visualized. Partially included upper abdominal organs are unremarkable. Stable chronic compression deformity approximately T5 and T8 vertebral bodies since chest x-ray of 9/30/2019, with suspected slight progression of compression fracture of T5 vertebral body since chest x-ray of 9/12/2018, with the compression deformity of T5 vertebral body new since CT chest exam of 7/6/2017. No acute osseous abnormality. IMPRESSION: 1. Limited evaluation for pulmonary emboli due to submaximal contrast opacification of the pulmonary arteries. Allowing for the limitations, no pulmonary emboli in the relatively adequately opacified central pulmonary arteries with limited evaluation of the distal subsegmental branches. 2. Nonspecific hypodense lesions in the partially included inferior left lobe of thyroid measuring up to 1 cm, which appear new since 2017. Suggest thyroid ultrasound exam for further evaluation. 3. Chronic compression deformities of T5 and T8 vertebral bodies, stable since at least 9/30/2019, with T5 compression fracture new since 7/6/2017. 4. Incidental direct origin of the left vertebral artery from the aortic arch, a developmental variant. Coronary artery calcifications. This CT exam was performed using one or more of the following dose reduction techniques: automated exposure control, adjustment of the mA and/or kV according to patient size, and/or use of iterative reconstruction technique. Radiation Dose: 607.8 mGy*cm total DLP Electronically signed by: Doctor 4/20/2021 1:47 PM CDT Workstation: 109-01249NK APTT [245811811] Collected: 04/20/21 1231 Order Status: Completed Specimen: Blood Updated: 04/20/21 1312 APTT 27.5 25.4 - 38.4 SEC Protime (Prothrombin Time) [245811810] Collected: 04/20/21 1231 Order Status: Completed Specimen: Blood Updated: 04/20/21 1312 PROTIME 11.3 10.3 - 12.6 SEC INR 0.9 0.9 - 1.1 Comment: Recommended therapeutic ranges or oral anticoagulant is and INR of 2.0 to 3.0. An INR of 2.5 to 3.5 is recommended to prevent recurrent MI. Protime (Prothrombin Time) [245811798] Collected: 04/20/21 1218 Order Status: Completed Specimen: Blood Updated: 04/20/21 1312 PROTIME 11.2 10.3 - 12.6 SEC INR 0.9 0.9 - 1.1 Comment: Recommended therapeutic ranges or oral anticoagulant is and INR of 2.0 to 3.0. An INR of 2.5 to 3.5 is recommended to prevent recurrent MI. Brain Natriuretic Peptide (BNP) [245811799] Collected: 04/20/21 1218 Order Status: Completed Specimen: Blood Updated: 04/20/21 1301 B-Type Natriuretic Peptide 22 0 - 100 PG/ML D-dimer, quantitative [245811805] (Abnormal) Collected: 04/20/21 1218 Order Status: Completed Specimen: Blood Updated: 04/20/21 1259 D-Dimer 1,330High Panic 0 - 400 NG/ML FEU Comprehensive metabolic panel [245811797] (Abnormal) Collected: 04/20/21 1218 Order Status: Completed Specimen: Blood Updated: 04/20/21 1246 Glucose 108High 65 - 100 MG/DL Blood Urea Nitrogen 16 7 - 18 MG/DL Creatinine 0.9 0.5 - 1.0 MG/DL Sodium 141 136 - 145 MMOL/L Potassium 4.0 3.5 - 5.1 MMOL/L Chloride 107 98 - 107 MMOL/L Co2 25 21 - 32 MMOL/L Calcium 8.9 8.5 - 10.1 MG/DL Protein Total 7.4 6.4 - 8.2 G/DL Albumin 3.5 3.4 - 5.0 G/DL A/G Ratio 0.9 0.8 - 2.0 Alkaline Phosphatase 131High 46 - 116 U/L Alt (SGPT) 24 14 - 59 U/L AST(SGOT) 14Low 15 - 37 U/L Bilirubin, Total 0.3 0.2 - 1.0 MG/DL GFR Comment IF PATIENT IS AFRICAN AMERICAN, MULTIPLY RESULT BY 1.16 Est GFR 66Low >90 ML/MIN/1.73sq.m Troponin Series [245811800] Collected: 04/20/21 1218 Order Status: Completed Specimen: Blood Updated: 04/20/21 1246 Troponin I 0.00 0.00 - 0.06 ng/mL Comment: 0.1 to 0.5 ng/mL shows an increased risk of AMI. 0.6 to 1.5 or greater is suggestive of AMI. XR Chest 2 View [245811802] Collected: 04/20/21 1229 Order Status: Completed Updated: 04/20/21 1246 Narrative: EXAMINATION: AP and lateral radiograph(s) of the chest CLINICAL HISTORY: 67 years Female,Shortness of breath COMPARISON: There is no prior similar study available for correlation. FINDINGS: The cardiomediastinal size and contour are normal. There is mild to moderate atherosclerotic disease The lungs are clear with no pneumothorax, pleural effusion or focal airspace consolidation. There is 20% compression deformity of a single mid thoracic vertebral body of uncertain age. IMPRESSION: No acute cardiopulmonary process Mild to moderate atherosclerotic disease 20% compression deformity of a single mid thoracic vertebral body of uncertain age Electronically signed by: Doctor 4/20/2021 12:45 PM CDT Workstation: 109-0082SB8 CBC w Auto Diff [245811796] (Abnormal) Collected: 04/20/21 1218 Order Status: Completed Specimen: Blood Updated: 04/20/21 1228 White Blood Cell Count 9.3 4.3 - 10.5 THOUS/uL Red Blood Cell Count 4.27 3.93 - 5.07 MIL/uL Hemoglobin 11.9 11.8 - 14.8 GM/DL Hematocrit 38.2 35.6 - 45.0 % Mean Corpuscular Volume 89.5 83.5 - 95.9 FL Mean Corpuscular Hemoglobin 27.9 27.4 - 32.0 PG Mean Corpuscular Hemoglobin Conc 31.2Low 31.5 - 34.7 G/DL Rdwcv 17.0High 11.8 - 14.2 % Rdwsd 55.8High 37.2 - 47.8 FL Platelet Count 213 167 - 402 THOUS/uL Mean Platelet Volume 9.2 8.8 - 12.0 FL Nucleated Red Blood Cells 0.0 0.0 /100 WBC'S Abs NRBC 0.0 0.0 THOUS/uL Differential Type AUTO Neutrophils 71.0High 34.0 - 67.9 % Lymphs 18.4Low 20.4 - 48.6 % Monocytes 7.2 5.0 - 11.5 % Eos 1.8 1.0 - 5.4 % Basos 0.5 0.2 - 1.3 % Neutrophils Absolute Count 6.6 2.1 - 6.6 THOUS/uL Lymphocytes Absolute Count 1.7 1.2 - 3.9 THOUS/uL Monocytes Absolute Count 0.7 0.3 - 0.8 THOUS/uL Eosinophils Absolute Count 0.2 0.1 - 0.4 THOUS/uL Basophils Absolute Count 0.1 0.0 - 0.1 THOUS/uL Imm Gran 1.1High 0.1 - 0.7 % Abs Imm Gran 0.10 0.0 - 0.1 THOUS/uL
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Current Outpatient Medications: ? albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulizer solution, Take 2.5 mg by nebulization 4 times daily., Disp: , Rfl: ? albuterol (PROVENTIL, VENTOLIN) 90 MCG/ACT inhaler, Inhale 1 Puff by mouth every
Allergien: Allergen Reactions ? Morphine Hallucinations and Headache ? Codeine Rash ? Lovenox Other/Unknown (See Comments) Abdominal wall hematoma
Vorherige Impfungen: -

VAERS 1241804

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 51,0
Geschlecht: F
Eingang: 22.04.2021
Impfdatum: 12.04.2021
Beginn: 19.04.2021
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 Burning sensation Chills Hypersensitivity Immediate post-injection reaction Miliaria Muscular weakness Paraesthesia Peripheral swelling Pruritus Pyrexia Rash macular Skin warm

Symptomtext

Immediately felt weakness in arm/hand of injection with tingling in hand. Minutes later tingling in left foot. Tingling continues to occur but less frequently. Early morning the next day (4/13) had chills and fever. Fever continued through early afternoon. On 4/19 both feet felt like they were on fire and the soles itched like crazy. Went away after an hour. Around 5:30 am red spots appeared on the bottoms of feet which were very warm. This went away. Throughout the day I had red spots on my feet and legs that would be red, warm, and some itchy that would come and go. My thighs had spots that appeared to be heat rash. At 7:30 pm areas on feet were bright red, warm and slightly swollen.Diagnosed with allergic

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Blood work.
Aktuelle Erkrankungen: sinus congestion 3 weeks prior, fully recovered at the time of
Vorgeschichte: none
Andere Medikamente: biotin
Allergien: none
Vorherige Impfungen: -

VAERS 1240522

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: GA
Alter: -
Geschlecht: F
Eingang: 22.04.2021
Impfdatum: -
Beginn: 15.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Breast pain Chest pain Mammogram Pain in extremity Ultrasound scan

Symptomtext

PAIN ON LEFT BREAST; PAIN IN LEFT SIDE OF CHEST ON SIDE OF INJECTION; PAIN UNDER LEFT ARM; This spontaneous report received from a patient concerned a female of unspecified age. The patient's weight, height, and medical history were not reported.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and expiry: UNKNOWN) dose was not reported, administered on 13-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 15-MAR-2021, the subject experienced pain on left breast. On 15-MAR-2021, the subject experienced pain in left side of chest on side of injection. On 15-MAR-2021, the subject experienced pain under left arm. Laboratory data (dates unspecified) included: Diagnostic ultrasound (NR: not provided) awaiting result, and Mammogram (NR: not provided) awaiting result. Treatment medications (dates unspecified) included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from pain on left breast, pain in left side of chest on side of injection, and pain under left arm. This report was non-serious.; Sender's Comments: V0: Medical assessment comments not required as per standard procedure as the case is assessed as non serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: Diagnostic ultrasound; Result Unstructured Data: awaiting result; Test Name: Mammogram; Result Unstructured Data: awaiting result
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1240517

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CO
Alter: -
Geschlecht: M
Eingang: 22.04.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Arthralgia Fatigue Headache Nausea Palpitations Pruritus

Symptomtext

PALPITATIONS; ITCH; JOINT ACHE; TIRED; HEADACHE; NAUSEA; This spontaneous report received from a patient concerned a 57 year old male. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025,expiry: UNKNOWN) dose was not reported, administered on 21-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the subject experienced palpitations, itch, joint ache, tired, headache, and nausea. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the palpitations, tired, headache, itch, joint ache and nausea was not reported. This report was non-serious.; Sender's Comments: V0: Medical Assessment comment was not required as per standard procedure as the case assessed as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1238854

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: ND
Alter: 51,0
Geschlecht: F
Eingang: 21.04.2021
Impfdatum: 10.03.2021
Beginn: 03.04.2021
Tage bis Beginn: 24,0
Dosis: N/A
Route/Site: - / LA

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

Back pain Blood test normal Chest X-ray normal Electrocardiogram normal Heart rate increased Hypertension Malaise Palpitations

Symptomtext

Saturday, April 3, my heart rate went up and I didn't feel well. My blood pressure was a little high. I did not go into the doctor at that time. My heartrate went basically normal that night. But it was doing things like that for a few days off and on after that. Two weeks ago this Thursday, (8th) I did go to ER - my back was starting to hurt and my blood pressure was high. I was prescribed a medication for heart palpitations - Propranolol. I've taken it a couple of weeks. The heart palpitations have not gone away. I'm having them quite a bit. I have to hit the button on the Zio Patch every time I have symptoms and I've had quite a few. Note: Shingrix vaccine on April 11th, injection on my left arm; and that was dose 1 or 2 - Lot # 444M2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: EKG - lots of bloodwork and a chest x-ray - - April 8th - tests came back normal that I wasn't having a heart attack. I have a 2 week heart monitor I'm on - Zio Patch
Aktuelle Erkrankungen: no
Vorgeschichte: history of cancer - breast cancer - I've gone through treatments
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 1236031

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 68,0
Geschlecht: F
Eingang: 21.04.2021
Impfdatum: -
Beginn: 09.04.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Blood pressure measurement Hypertension Influenza like illness

Symptomtext

BLOOD PRESSURE KEEPS GOING UP; FLU LIKE SYMPTOMS/CHILLS/HEADACHE; This spontaneous report received from a patient concerned a 68 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included hypertension, hypokalemia, anxiety, depression, penicillin allergy, non alcoholic, and non-smoker, and other pre-existing medical conditions included the patient was not pregnant at the time of reporting. the patient had no history of drug abuse or illicit drug usage. The patient experienced drug allergy when treated with lisinopril, and ibuprofen for drug used for unknown indication. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, expiry: UNKNOWN) dose was not reported, administered on 09-APR-2021 for prophylactic vaccination. Concomitant medications included paracetamol for prevention. On APR-2021, Laboratory data included: Blood pressure (NR: not provided) 140s (unit not specified). On 09-APR-2021, the subject experienced blood pressure keeps going up. On 09-APR-2021, the subject experienced flu like symptoms/chills/headache. Laboratory data included: Blood pressure (NR: not provided) 156/78 mmHg. Laboratory data (dates unspecified) included: Blood pressure (NR: not provided) 120s (unit not specified). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from flu like symptoms/chills/headache, and had not recovered from blood pressure keeps going up. This report was non-serious.; Sender's Comments: V0: Medical Assessment comment was not required as per standard procedure as the case assessed as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 202104; Test Name: Blood pressure; Result Unstructured Data: 140s (unit not specified); Test Date: 20210409; Test Name: Blood pressure; Result Unstructured Data: 156/78 mmHg; Test Name: Blood pressure; Result Unstructured Data: 120s (unit not specified)
Aktuelle Erkrankungen: Abstains from alcohol; Anxiety; Depression; Hypertension; Hypokalemia; Non-smoker; Penicillin allergy
Vorgeschichte: Comments: The patient was not pregnant at the time of reporting. The patient had no history of drug abuse or illicit drug usage.
Andere Medikamente: TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 1232311

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 51,0
Geschlecht: F
Eingang: 20.04.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Alopecia Chest discomfort Dyspepsia Feeling hot Gastrointestinal disorder Gastrooesophageal reflux disease Immediate post-injection reaction Palpitations Paraesthesia

Symptomtext

Immediately after injection. I felt a heat go from my head to toes and down my arms into my hands. My lower legs, feet, hands, left arm and chest begin to tingle. After sitting a few minutes it did not get worse. The tingling is not constant now, but I am still having it. Seems like I have it in the left arm more often than anywhere else. Within 20 minutes of the shot I began having gastrointestinal issues., that progressed. It built into strong chest pressure, acid reflux and indigestion. I got into the Dr on March 25. He prescribed Nexium. I am now having significant hair loss and have started having heart palpitations. I am waiting on his response as to what tests are needed to proceed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Possible Penicillin Allergy
Vorherige Impfungen: -

VAERS 1231770

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 32,0
Geschlecht: F
Eingang: 20.04.2021
Impfdatum: -
Beginn: 12.04.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Chest discomfort Chills Decreased appetite Dyspepsia Nausea Oropharyngeal pain Pain Tremor

Symptomtext

BODY ACHES; LOSS OF APPETITE; DYSPEPSIA; UPPER CHEST DISCOMFORT; SORE THROAT; CHILLS; NAUSEA; SHAKING; This spontaneous report received from a health care professional concerned a 32 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included iodine allergy, personality disorder, alcohol dependence, opioid dependence, seizure, and adjustment disorder.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 12-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 12-APR-2021, the subject experienced shaking. On 12-APR-2021, the subject experienced chills. On 12-APR-2021, the subject experienced nausea. On 13-APR-2021, the subject experienced body aches. On 13-APR-2021, the subject experienced loss of appetite. On 13-APR-2021, the subject experienced dyspepsia. On 13-APR-2021, the subject experienced upper chest discomfort. On 13-APR-2021, the subject experienced sore throat. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from body aches, loss of appetite, dyspepsia, nausea, chills, shaking, upper chest discomfort, and sore throat. This report was non-serious. This case, from the same reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Adjustment disorder; Alcohol dependence syndrome; Dependence on opiates; Iodine allergy; Personality disorder; Seizure
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1231329

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MN
Alter: 67,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 05.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Sleep disorder Tremor

Symptomtext

I began having chills and shakiness at about 7 PM. I could not warm up. Took a hot bath still could not get warm. Turned up my electric blank in bed and still could not warm up. Finally about 1 Am I got up and took an oral dose of Thera Warming Flu. It knocked out the chills immediately and I was finally able to sleep. I had no arm pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Estradiol. multi vitamin, Caltrate, Vitamin B and Magnesium
Allergien: House Dust, Grain Dust, Paper molds Perfumes
Vorherige Impfungen: -

VAERS 1230683

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 41,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: -
Beginn: 25.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Arthralgia Fatigue Feeling abnormal Hypoaesthesia Migraine Nausea Pain in extremity Paraesthesia Pyrexia

Symptomtext

BRAIN FOG; MIGRAINE; TIRED; NAUSEA; TINGLING IN HANDS; NUMBNESS IN HANDS; ARM HURT; VERY SHARP STABBING PAIN IN RIGHT SHOULDER; FEVER >103; This spontaneous report received from a patient concerned a 41 year old female. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and expiry: UNKNOWN) dose was not reported, administered on 25-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 25-MAR-2021, the subject experienced tingling in hands. On 25-MAR-2021, the subject experienced numbness in hands. On 25-MAR-2021, the subject experienced arm hurt. On 25-MAR-2021, the subject experienced very sharp stabbing pain in right shoulder. On 25-MAR-2021, the subject experienced fever >103. On 25-MAR-2021, the subject experienced nausea. On 26-MAR-2021, the subject experienced migraine. On 26-MAR-2021, the subject experienced brain fog. On 26-MAR-2021, the subject experienced tired. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from arm hurt, and nausea on 25-MAR-2021, and fever >103 on 28-MAR-2021, and was recovering from numbness in hands, migraine, brain fog, tired, very sharp stabbing pain in right shoulder, and tingling in hands. This report was non-serious. This case is associated with PQC number: 90000175693.; Sender's Comments: V0: Medical assessment comment not required as per standard procedure as the case assessed as non-serious

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1230278

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 67,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 10.03.2021
Beginn: 14.04.2021
Tage bis Beginn: 35,0
Dosis: 1
Route/Site: IM / RA

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

Dyspnoea Fibrin D dimer increased

Symptomtext

ELEVATED D-DIMER, SOB

Weitere VAERSDATA-Felder

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

VAERS 1229312

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 56,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 08.03.2021
Beginn: 17.04.2021
Tage bis Beginn: 40,0
Dosis: 1
Route/Site: - / -

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

Alanine aminotransferase normal Albumin globulin ratio normal Aspartate aminotransferase normal Basophil count decreased Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium normal Blood chloride normal Blood creatine phosphokinase MB normal Blood creatinine normal Blood glucose increased Blood magnesium normal Blood potassium normal Blood sodium normal Blood thyroid stimulating hormone normal Blood urea normal Carbon dioxide normal

Symptomtext

4/17/21 ER HPI: 56 y.o. male who presents with asymptomatic tachycardia. The patient purchased a home blood pressure monitoring device approximately 2 weeks ago and at that time he noted that the machine recorded his pulse at 150-160 beats per minute. The patient has repeatedly taking his blood pressure at home with this device and every time and has recorded his pulse in the same range. He denies fevers chills chest pain palpitations syncope lightheadedness peripheral edema or dyspnea. He presents today for evaluation of this as the machine again indicated that his pulse was 100 50-160 beats per minute

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: CKMB [247900288] Collected: 04/17/21 0923 Order Status: Completed Specimen: Blood Updated: 04/17/21 1003 Creatine Kinase-MB 0.8 0.0 - 3.6 NG/ML Troponin Series [247900289] Collected: 04/17/21 0923 Order Status: Completed Specimen: Blood Updated: 04/17/21 1003 Troponin I 0.00 0.00 - 0.06 ng/mL Comment: 0.1 to 0.5 ng/mL shows an increased risk of AMI. 0.6 to 1.5 or greater is suggestive of AMI. Comprehensive metabolic panel [247900293] (Abnormal) Collected: 04/17/21 0923 Order Status: Completed Specimen: Blood Updated: 04/17/21 1003 Glucose 147High 65 - 100 MG/DL Blood Urea Nitrogen 18 7 - 18 MG/DL Creatinine 1.2 0.7 - 1.3 MG/DL Sodium 139 136 - 145 MMOL/L Potassium 4.7 3.5 - 5.1 MMOL/L Chloride 104 98 - 107 MMOL/L Co2 28 21 - 32 MMOL/L Calcium 9.2 8.5 - 10.1 MG/DL Protein Total 7.5 6.4 - 8.2 G/DL Albumin 4.0 3.4 - 5.0 G/DL A/G Ratio 1.1 0.8 - 2.0 Alkaline Phosphatase 96 46 - 116 U/L Alt (SGPT) 50 16 - 63 U/L AST(SGOT) 25 15 - 37 U/L Bilirubin, Total 0.7 0.2 - 1.0 MG/DL GFR Comment IF PATIENT IS AFRICAN AMERICAN, MULTIPLY RESULT BY 1.16 Est GFR 67Low >90 ML/MIN/1.73sq.m Magnesium [247900294] Collected: 04/17/21 0923 Order Status: Completed Specimen: Blood Updated: 04/17/21 1003 Magnesium 2.2 1.8 - 2.4 MG/DL TSH Third Generation [247900299] Collected: 04/17/21 1000 Order Status: Completed Specimen: Blood Updated: 04/17/21 1003 TSH 2.57 0.30 - 3.04 uIU/mL D-dimer, quantitative [247900291] Collected: 04/17/21 0923 Order Status: Completed Specimen: Blood Updated: 04/17/21 1001 D-Dimer <100 0 - 400 NG/ML FEU XR Chest Portable [247900296] Collected: 04/17/21 0935 Order Status: Completed Updated: 04/17/21 1000 Narrative: EXAMINATION: PORTABLE CHEST SINGLE VIEW, 4/17/2021 at 0926 hours CLINICAL INFORMATION: Tachycardia COMPARISON: None FINDINGS: The cardiomediastinal silhouette is upper limits of normal in size. There is no significant consolidation or effusion. Osseous structures are without acute abnormality. IMPRESSION: Negative. CBC w Auto Diff [247900292] Collected: 04/17/21 0923 Order Status: Completed Specimen: Blood Updated: 04/17/21 0938 White Blood Cell Count 7.7 4.8 - 9.6 THOUS/uL Red Blood Cell Count 4.98 4.33 - 5.59 MIL/uL Hemoglobin 15.8 13.1 - 16.8 GM/DL Hematocrit 46.0 38.8 - 49.0 % Mean Corpuscular Volume 92.4 82.7 - 94.4 FL Mean Corpuscular Hemoglobin 31.7 27.7 - 32.6 PG Mean Corpuscular Hemoglobin Conc 34.3 32.4 - 35.7 G/DL Rdwcv 12.7 11.6 - 13.9 % Rdwsd 42.7 36.0 - 46.1 FL Platelet Count 202 154 - 364 THOUS/uL Mean Platelet Volume 9.1 8.7 - 11.7 FL Nucleated Red Blood Cells 0.0 0.0 /100 WBC'S Abs NRBC 0.0 0.0 THOUS/uL Differential Type AUTO Neutrophils 60.7 34.0 - 67.9 % Lymphs 27.6 19.1 - 41.2 % Monocytes 9.6 6.1 - 12.3 % Eos 1.3 0.9 - 7.6 % Basos 0.5 0.2 - 1.5 % Neutrophils Absolute Count 4.7 2.7 - 5.8 THOUS/uL Lymphocytes Absolute Count 2.1 1.1 - 3.3 THOUS/uL Monocytes Absolute Count 0.7 0.4 - 0.9 THOUS/uL Eosinophils Absolute Count 0.1 0.1 - 0.6 THOUS/uL Basophils Absolute Count 0.0 0.0 - 0.1 THOUS/uL Imm Gran 0.3 0.2 - 0.9 % Abs Imm Gran 0.02 0.0 - 0.1 THOUS/uL
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Current Outpatient Medications: ? atorvaSTATin (LIPITOR) 10 MG tablet, Take 10 mg by mouth daily, Disp: , Rfl: ? cholecalciferol (VITAMIN D) 25 MCG (1000 UT) tablet, Take 1,000 Units by mouth daily, Disp: , Rfl: ? metFORMIN (GLUCOPHAG
Allergien: nka
Vorherige Impfungen: -

VAERS 1228142

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: -
Geschlecht: U
Eingang: 19.04.2021
Impfdatum: -
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Chills Fatigue Headache Pain Paraesthesia

Symptomtext

CHILLS; BODY ACHES; HEADACHE; Fatigue; TINGLING IN BOTH HANDS; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, expiry: UNKNOWN) dose was not reported, administered on 08-MAR-2021 to right deltoid for prophylactic vaccination. No concomitant medications were reported. On MAR-2021, the subject experienced tingling in both hands. On MAR-2021, the subject experienced fatigue. Treatment medications included: ibuprofen. On 08-MAR-2021, the subject experienced chills. On 08-MAR-2021, the subject experienced body aches. On 08-MAR-2021, the subject experienced headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from tingling in both hands, and fatigue on MAR-2021, and chills, body aches, and headache on 08-MAR-2021. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1227105

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: NV
Alter: -
Geschlecht: F
Eingang: 18.04.2021
Impfdatum: 09.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Feeling abnormal Feeling jittery Hypoaesthesia Paraesthesia

Symptomtext

HANDS NUMBNESS ESPECIALLY FINGERS TIPS; FEELING OFF; BODY TINGLING; JITTERY; This spontaneous report received from a patient concerned a female of unspecified age. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025, and batch number: 1805025 expiry: UNKNOWN) .5 ml, administered on 09-MAR-2021 11:00 to Left Arm for prophylactic vaccination. No concomitant medications were reported. On 09-MAR-2021, the subject experienced body tingling. On 09-MAR-2021, the subject experienced jittery. On 09-MAR-2021 17:30, the subject experienced feeling off. On 09-MAR-2021 18:00, the subject experienced hands numbness especially fingers tips. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from hands numbness especially fingers tips, and jittery, and had not recovered from feeling off, and body tingling. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1225558

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TN
Alter: 40,0
Geschlecht: M
Eingang: 18.04.2021
Impfdatum: 15.03.2021
Beginn: 06.04.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: - / RA

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

Arthralgia Back pain Dyspnoea Erythema Mobility decreased Pain in extremity

Symptomtext

Starting from 04/07/21, Sudden waist and back pain, cannot straighten up the body. When straighten up the body feels breathing difficulties . After 3-4 days there?s a continuous pain in both thigh and the calf, and red marks are spawning on the legs.

Weitere VAERSDATA-Felder

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

VAERS 1224199

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 18.04.2021
Impfdatum: 03.04.2021
Beginn: 03.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain Amnesia Asthenia Back pain Burning sensation Chills Disturbance in attention Fatigue Feeling abnormal Headache Hyperhidrosis Loss of personal independence in daily activities Mobility decreased Nausea Pain Pyrexia

Symptomtext

8 hours severe symptoms started: over 100 fever, nausea, every muscle, organ, ligament and fiber in body felt on fire and with severe pain, so bad I could barely move. Chills and sweats. Heart rate for all night over 100. Had profound weakness. It was so bad I could not go from laying to sitting up without someone pulling me up to sitting. I was so weak I could not life the water glass and could not twist open orange juice container. Extremely fatigued and in pain with nausea and weakness the next few days. Long hauler symptoms came back and Day 2 had a severe headache & abdominal pain started, abdominal and back pain most days and can be significant. Day 6 Mack truck fatigue and cycling of fatigue symptoms since immunization. Day 7 severe headache. Neuro symptoms returned with memory loss, brain fog, in ability to concentrate and inability to finish tasks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: platelet test abnormal elevated on 4/13 426
Aktuelle Erkrankungen: Long Covid - diagnoses: Clinical Covid, leukoencephalopathy, hallucinosis, Charles Bonnet
Vorgeschichte: Long Covid - Diagnoses: Clinical Covid, leukoencephalopathy, hallucinosis, Charle Bonnet possible mitochondrial dysfunction and prior 1999 interstitial lung disease
Andere Medikamente: Amantadine Atorvstatin Ubiquinol Vitamin C
Allergien: -
Vorherige Impfungen: can have swelling, redness and malaise from immunizations

VAERS 1223993

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 51,0
Geschlecht: F
Eingang: 17.04.2021
Impfdatum: 06.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / LA

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

Paraesthesia

Symptomtext

Entire left arm has a tingling/ buzzing sensation. It comes and goes about 3 times a day. There is no regular pattern. It lasts a few seconds but strong enough for me to feel it going from top of the arm to the wrist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Hypothyroidism: taking levothyroxine .025 mg at the time of vaccination.
Vorgeschichte: Moderately high blood pressure
Andere Medikamente: Losartan 50 mg Zyrtec 10 mg Vitamin D 5000 iu
Allergien: Sulfa Yam
Vorherige Impfungen: -

VAERS 1220448

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 16.04.2021
Impfdatum: 24.03.2021
Beginn: 16.04.2021
Tage bis Beginn: 23,0
Dosis: 1
Route/Site: IM / RA

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

Dyspnoea Heavy menstrual bleeding Migraine Swelling

Symptomtext

1) EXTENDED MENSTRUATION 2) MIGRAINES 3) SWELLING OF EXTREMITIES 4) DIFFICULTY BREATHING

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1220198

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 16.04.2021
Impfdatum: 03.04.2021
Beginn: 04.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Discomfort Dyspnoea Headache Injection site pain Myalgia Peripheral swelling

Symptomtext

"Janssen COVID-19 Vaccine EUA" Night of April 4th, severe headache began at 9pm. Took an Aleve, but it did not help. Went to bed to sleep it off. Woke up and the headache was gone the next morning. Have not had any more headaches. Experienced muscle soreness in arm of injection and at the injection spot. Then whole body muscle soreness/heaviness began on April 5th for 3 days. I had swelling in both legs for only one day, on April 12th. First day I noticed I was experiencing shortness of breath was April 6th. Became out of breath walking a small incline. Shortness of breath continues to current, April 16th, perhaps a bit worse, where I seem that a natural breath requires a bit of work. So far, I have no

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none done to date
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure, Glaucoma, Chronic Low Back Pain, Seasonal Allergies
Andere Medikamente: Diovan HCT 160/12.5, Latanoprost, Symbicort 160/4.5, Ecotrin 81mg, Folic Acid 400mg, Vitamin D3 2000 UI, Black Cohosh, Claritin 10mg
Allergien: Sucrose intolerance, Lactose intolerance
Vorherige Impfungen: -

VAERS 1217997

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 37,0
Geschlecht: M
Eingang: 16.04.2021
Impfdatum: -
Beginn: 23.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Asthenia Dizziness Dyspnoea Fatigue Headache Malaise SARS-CoV-2 test

Symptomtext

SHORT OF BREATH; DIZZY; FEELING EXTREMELY SICK; FATIGUED; A HEADACHE; FEELING WEAK RIGHT AFTER VACCINATION; This spontaneous report received from a patient concerned a 37 year old male. The patient's height, and weight were not reported. The patient's past medical history included covid, and concurrent conditions included non alcoholic, and non smoker, and other pre-existing medical conditions included the patient had no known allergies, no drug abuse or illicit drug usage. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, expiry: UNKNOWN) dose was not reported, administered on 23-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 22-MAR-2021, Laboratory data included: COVID-19 virus test (NR: not provided) Negative. On 23-MAR-2021, the subject experienced feeling weak right after vaccination. On 25-MAR-2021, the subject experienced short of breath. On 25-MAR-2021, the subject experienced dizzy. On 25-MAR-2021, the subject experienced feeling extremely sick. On 25-MAR-2021, the subject experienced fatigued. On 25-MAR-2021, the subject experienced a headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from feeling weak right after vaccination, feeling extremely sick, fatigued, dizzy, a headache, and short of breath. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210322; Test Name: COVID-19 virus test; Result Unstructured Data: Negative
Aktuelle Erkrankungen: Abstains from alcohol; Non-smoker
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (In APR 2020); Comments: The patient had no known allergies, no drug abuse or illicit drug usage.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1207304

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: ND
Alter: -
Geschlecht: U
Eingang: 16.04.2021
Impfdatum: -
Beginn: 10.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Hypoaesthesia Musculoskeletal stiffness Paraesthesia

Symptomtext

NUMBNESS IN ARM, FINGERS AND LEG; This spontaneous report received from a pharmacist concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 10-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 10-MAR-2021, the subject experienced numbness in arm, fingers and leg. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from numbness in arm, fingers and leg. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1188195

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: -
Alter: -
Geschlecht: U
Eingang: 16.04.2021
Impfdatum: -
Beginn: 12.03.2021
Tage bis Beginn: -
Dosis: N/A
Route/Site: IM / LA

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

Body temperature Feeling jittery Headache Influenza like illness Migraine Condition aggravated Nausea Restlessness Panic attack Pyrexia

Symptomtext

PANIC ATTACK; ALARMING UPTICK IN MIGRAINE ACTIVITY; LESS SEVERE HEADACHE; NAUSEA; TEMPERATURE ELEVATION; RESTLESSNESS; JITTERINESS; FLU LIKE SYMPTOMS; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's height, and weight were not reported. The patient's concurrent conditions included migraine.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, 1 total, administered on 12-MAR-2021 14:30 for prophylactic vaccination. Concomitant medications included sumatriptan for migraine. On 12-MAR-2021, the subject experienced restlessness. On 12-MAR-2021, the subject experienced jitteriness. On 12-MAR-2021, the subject experienced flu like symptoms. On 12-MAR-2021, the subject experienced alarming uptick in migraine activity. On 12-MAR-2021, the subject experienced less severe headache. On 12-MAR-2021, the subject experienced nausea. On 12-MAR-2021, the subject experienced temperature elevation. Laboratory data included: Body temperature (NR: not provided) 99.7 degree. On 13-MAR-2021, the subject experienced panic attack. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from temperature elevation on 2021, and the outcome of restlessness, nausea, jitteriness, flu like symptoms, less severe headache, panic attack and alarming uptick in migraine activity was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20210312; Test Name: Body temperature; Result Unstructured Data: 99.7 degree
Aktuelle Erkrankungen: Migraine (That was the first of 4 major migraines since receiving the vaccine. The patient experienced last migraine was on Sunday.)
Vorgeschichte: Comments: Unknown
Andere Medikamente: IMITREX [SUMATRIPTAN]
Allergien: -
Vorherige Impfungen: -

VAERS 1188195

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: -
Alter: -
Geschlecht: U
Eingang: 16.04.2021
Impfdatum: -
Beginn: 12.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Body temperature Feeling jittery Headache Influenza like illness Migraine Condition aggravated Nausea Restlessness Panic attack Pyrexia

Symptomtext

PANIC ATTACK; ALARMING UPTICK IN MIGRAINE ACTIVITY; LESS SEVERE HEADACHE; NAUSEA; TEMPERATURE ELEVATION; RESTLESSNESS; JITTERINESS; FLU LIKE SYMPTOMS; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's height, and weight were not reported. The patient's concurrent conditions included migraine.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, 1 total, administered on 12-MAR-2021 14:30 for prophylactic vaccination. Concomitant medications included sumatriptan for migraine. On 12-MAR-2021, the subject experienced restlessness. On 12-MAR-2021, the subject experienced jitteriness. On 12-MAR-2021, the subject experienced flu like symptoms. On 12-MAR-2021, the subject experienced alarming uptick in migraine activity. On 12-MAR-2021, the subject experienced less severe headache. On 12-MAR-2021, the subject experienced nausea. On 12-MAR-2021, the subject experienced temperature elevation. Laboratory data included: Body temperature (NR: not provided) 99.7 degree. On 13-MAR-2021, the subject experienced panic attack. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from temperature elevation on 2021, and the outcome of restlessness, nausea, jitteriness, flu like symptoms, less severe headache, panic attack and alarming uptick in migraine activity was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20210312; Test Name: Body temperature; Result Unstructured Data: 99.7 degree
Aktuelle Erkrankungen: Migraine (That was the first of 4 major migraines since receiving the vaccine. The patient experienced last migraine was on Sunday.)
Vorgeschichte: Comments: Unknown
Andere Medikamente: IMITREX [SUMATRIPTAN]
Allergien: -
Vorherige Impfungen: -

VAERS 1171064

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 47,0
Geschlecht: F
Eingang: 16.04.2021
Impfdatum: -
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

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

Chest discomfort Chest pain Fatigue Hyperhidrosis Migraine Dizziness Headache Injection site bruising Myalgia Pain Palpitations Tachycardia Nausea Neck pain Tinnitus

Symptomtext

BODY ACHES; TINNIUTS; HEART RACING; TACHYCARDIA; DIZZINESS; SWEATING; CHEST TIGHTNESS/CHEST PRESSURE; BRUISING AT INJECTION SITE; HEADACHE; MYALGIA; FATIGUE; This spontaneous report received from a patient concerned a 47 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included allergic to bees.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unk) dose was not reported, administered on 01-APR-2021 11:00 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 01-APR-2021, the subject experienced tachycardia. On 01-APR-2021, the subject experienced dizziness. On 01-APR-2021, the subject experienced sweating. On 01-APR-2021, the subject experienced chest tightness/chest pressure. On 01-APR-2021, the subject experienced bruising at injection site. On 01-APR-2021, the subject experienced headache. On 01-APR-2021, the subject experienced myalgia. On 01-APR-2021, the subject experienced fatigue. On 01-APR-2021 14:00, the subject experienced tinniuts. On 01-APR-2021 14:00, the subject experienced heart racing. On an unspecified date, the subject experienced body aches. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from tachycardia, sweating, chest tightness/chest pressure, bruising at injection site, myalgia, and fatigue on 04-APR-2021, dizziness on 01-APR-2021, and headache on 03-APR-2021, was recovering from heart racing, had not recovered from tinniuts, and the outcome of body aches was not reported. This report was non-serious.; Sender's Comments: V0: Medical Assessment comment was not required as per standard procedure as the case assessed as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Insect bite allergy (high risk allergic to bees)
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1216526

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CA
Alter: 20,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 01.04.2021
Beginn: 01.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Body temperature increased Chills Fatigue Headache Migraine Nausea Vomiting

Symptomtext

Developed dull headache within 2 hours of vaccine with fatigue. By 6-7 hours later, her headache escalated to a severe migraine and she had chills, nausea, vomiting and a temp of 101. Severe symptoms lasted for 24 hours and she didn't feel better until 4 days later. By 5th day felt fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: History of migrain headaches
Vorgeschichte: Migraine headaches
Andere Medikamente: Unisom prn Excedrin Migraine prn
Allergien: None
Vorherige Impfungen: -

VAERS 1212919

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: GA
Alter: 41,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 22.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Full blood count normal Hypoaesthesia Injection site hypoaesthesia Pain in extremity Paraesthesia

Symptomtext

Numbness starting from the injection site (upper left arm) and surrounding area, noticed about a week after the shot. Then numbness continued progressing down my upper arm, and into the front of my lower arm. This is accompanied by pins and needles kind of tingling and an intermittent heavy aching feeling along my entire left arm (picture the feeling of dental numbing wearing off). On 4/14/2021, I noticed the numbness is now also in my left thumb. Arm appears to function normally at this time, but worried about the increasing loss of sensation. Went to doctor who performed a complete blood count and recommended monitoring as she felt nothing could be immediately done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Complete blood count 04/14/2021 - normal
Aktuelle Erkrankungen: vaginal yeast infection
Vorgeschichte: none known
Andere Medikamente: women's multivitamin
Allergien: bee venom, povidone
Vorherige Impfungen: -

VAERS 1212280

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TN
Alter: 69,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 20.03.2021
Beginn: 09.04.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain

Symptomtext

Complaints of chest pain. She went to ER. She was sent home and said no heart attack. She then had another episode of chest pain on 04/11/21 and went to ER and was sent home and told to see cardiologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: History of heart disease with a heart attack in 2014 with stent She has had 5 other stents since then. Last being on 12/01/2020. History of 3 back surgeries.
Andere Medikamente: Routine daily meds- Aspirin, Avastatin, Nitro patch, Naproxin, "pain killers"-unsure name
Allergien: Oxycodone
Vorherige Impfungen: -

VAERS 1212243

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 34,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 17.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Headache Migraine On and off phenomenon

Symptomtext

Severe migraine 2 weeks after vaccine, and then on and off headaches or migraines that last 24-48 hours and do not respond to Tylenol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Met with PCP 4/14/2021 who mentioned it?s unlikely the migraines are linked to the Janssen vaccine and prescribed migraine medications.
Aktuelle Erkrankungen: No illnesses
Vorgeschichte: TMJ and neck muscle pain - over 10 years of pain on and off.
Andere Medikamente: Birth control pill, pre-natal, CoQ10, magnesium supplements
Allergien: None that I?m aware of
Vorherige Impfungen: -

VAERS 1211179

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CO
Alter: 50,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 10.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: SYR / LA

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

Dyspnoea Platelet count increased

Symptomtext

Shortness of breath, difficulty breathing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: High platelet count at 462,000
Aktuelle Erkrankungen: None
Vorgeschichte: Heart attack on Oct 3, 2020.
Andere Medikamente: Prasugrel, Metoprolol Tartrate, Atorvastatin, Vitamin D, Baby Asprin, one a day Vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1207003

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: NJ
Alter: 46,0
Geschlecht: F
Eingang: 14.04.2021
Impfdatum: 18.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Back pain Hypoaesthesia Magnetic resonance imaging head normal Magnetic resonance imaging normal Multiple sclerosis Multiple sclerosis relapse Muscular weakness Neuralgia Pain in extremity Paraesthesia Sensory loss

Symptomtext

Arm pain, shoulder pain, numbness, tingling, nerve pain, arm weakness, armpit pain, loss of feeling in fingers, back pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: MRI - brain, neck, spine to see if pain if related to a MS flair ups - negative 4/8/2021
Aktuelle Erkrankungen: -
Vorgeschichte: multiple sclerosis
Andere Medikamente: gilenya, cymbalta, meloxicam, vitaman b-12, vitamin d, baby aspirin,
Allergien: cipro
Vorherige Impfungen: -

VAERS 1206011

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 46,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 29.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Injected limb mobility decreased Pain Pain in extremity

Symptomtext

Soreness in left arm persists after two weeks and is worse when arm is raised laterally.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1205446

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WA
Alter: 76,0
Geschlecht: M
Eingang: 13.04.2021
Impfdatum: 15.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 17,0
Dosis: UNK
Route/Site: IM / LA

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

Mobility decreased Pain in extremity X-ray normal

Symptomtext

Pt states that about 3 weeks after the vaccine, pt experienced pain in his right calf where he did not feel like he can put any weight on it. Pt states going to the doctor to check on the leg, ran tests, and also did an xray. Pt states the Dr did not find a clot and mentioned that perhaps it was a sprain/strain. The pt did not agree that it was a sprain and wanted the pharmacy to report this adverse event. No other side effects were reported. Recommended that pt goes back to doctor to get leg checked out some more.

Weitere VAERSDATA-Felder

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

VAERS 1204170

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CA
Alter: 39,0
Geschlecht: M
Eingang: 13.04.2021
Impfdatum: 03.04.2021
Beginn: 03.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test normal Chills Computerised tomogram normal Hypoaesthesia Paraesthesia Pyrexia Sleep disorder

Symptomtext

Later on that evening around 10:30pm I started having chills. Around 1am I woke up with high fever of 103 my body was very hot. By 5am the fever broke I was at normal temperature I felt better and was able to sleep. On 04/8/2021 around 6pm I went to reach out for something & I couldn't feel my arm my legs then I felt that my face was numb as well It was only left side. I felt tingling . It lasted for like 4 or 5 seconds. I went to the ER they did some lab work & a CT scan and everything came back normal. I will be scheduling an MRI as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: CT scan- normal blood work- normal
Aktuelle Erkrankungen: -
Vorgeschichte: asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1201152

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CO
Alter: 38,0
Geschlecht: M
Eingang: 13.04.2021
Impfdatum: 20.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: SYR / LA

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

Dehydration Headache Sleep disorder

Symptomtext

I have woken up in the middle of the night three times with a terrible headache. I attributed it to possible dehydration even though I was hydrated. The issue occurred sporadically over three weeks after the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: I have not sought medical attention as I do not have a medical provider.
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Finasteride
Allergien: NA
Vorherige Impfungen: -

VAERS 1200792

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: DC
Alter: 25,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 28.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chills Dehydration Headache Nausea Pain Pyrexia Vomiting

Symptomtext

Severe chills occurred approximately 6 hours after receiving vaccine. High fever (101) also occurred within the same timeframe. Approximately 8 hours after receiving the shot, severe and sudden nausea occurred, causing the patient to violently vomit in the middle of the night. Patient awoke the next morning, about 15 hours after receiving the shot, with body aches, chills, minor low grade fever, headache, and dehydration. After 24 hours, the patient felt fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Spironolactone
Allergien: None
Vorherige Impfungen: -

VAERS 1198861

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: VA
Alter: 65,0
Geschlecht: F
Eingang: 12.04.2021
Impfdatum: 18.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Asthenia Chills Condition aggravated Dizziness Dysstasia Erythema Headache Hyperhidrosis Malaise Nausea

Symptomtext

3/18 vaccination 3/19 4am woke up I felt sick I had a HA, Nauseas, dizzy, hard to stand, hard to keep eyes open to even go to the bathroom. I tried to go back to sleep. When I woke up, I took it easy. I did get the chills and sweats thru the day; skin turns really red (MCAS). That symptoms still comes and goes. The chills, regulating body temperature, has flared back up after being dormant for years. 3/30 I saw MD. She wanted to defer for 4-6 weeks after vaccination to see if symptoms were still persisting or leveling out. I have since canceled every sort of appt since then as I don't have the energy. *I am on the very tail end of an opioid withdrawal; tramadol. I have taken for 6 years, 400 mg weened down to 100 mg this last year, down to 12.5.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: MD deferred for 4-6 weeks post vaccination.
Aktuelle Erkrankungen: -
Vorgeschichte: hypothyroidism, diabetes II, depression, PTSD, mass cell activation syndrome (MCAS), ADD
Andere Medikamente: Synthroid, liophyronine; ozempic, pristiq, lithium, prazosin, hydroxyzine, clonidine, omeprazole, cimetidine, loprazolam, Vyvanse,
Allergien: sephalosporonine (anaphylaxis reaction)
Vorherige Impfungen: every previous vaccine; flu 2009, 2013, 2018 (hospitalized; fluids)

VAERS 1197532

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 12.04.2021
Impfdatum: -
Beginn: 28.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Adverse event Fatigue Pain Palpitations

Symptomtext

FATIGUE; BODY ACHES; HEART PALPITATIONS; LOW GRADE; This spontaneous report received from a patient concerned a 63 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included g6pd deficiency.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and expiry: UNKNOWN) dose was not reported, administered on 27-MAR-2021 to left arm for prophylactic vaccination. No concomitant medications were reported. On 28-MAR-2021, the subject experienced body aches. On 28-MAR-2021, the subject experienced heart palpitations. On 28-MAR-2021, the subject experienced low grade. On 29-MAR-2021, the subject experienced fatigue. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body aches, heart palpitations, low grade, and fatigue on 2021. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: G6PD deficiency (The lowest levels of 0.3.)
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1171198

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: -
Geschlecht: M
Eingang: 12.04.2021
Impfdatum: -
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Arthralgia Chest pain Fatigue Hyperhidrosis Injection site pain Diarrhoea Headache Myalgia Migraine Pain Tremor Vomiting Nausea Pain in extremity Pyrexia Respiratory rate increased Sensory disturbance

Symptomtext

CHEST/SHOULDER TIGHTNESS; DIARRHEA; VOMITING; ARM SORENESS; EXTREME FATIGUE; LOW GRADE FEVER; HEADACHE; MYALGIA; NAUSEA; SWEATING; BREATHING RATE INCREASED; This spontaneous report received from a consumer concerned a 48 year old male. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 01-APR-2021 on right arm for prophylactic vaccination. No concomitant medications were reported. On 01-APR-2021, the subject experienced sweating. On 01-APR-2021, the subject experienced breathing rate increased. On 01-APR-2021, the subject experienced diarrhea. On 01-APR-2021, the subject experienced vomiting. On 01-APR-2021, the subject experienced arm soreness. On 01-APR-2021, the subject experienced extreme fatigue. On 01-APR-2021, the subject experienced low grade fever. On 01-APR-2021, the subject experienced headache. On 01-APR-2021, the subject experienced myalgia. On 01-APR-2021, the subject experienced nausea. On 03-APR-2021, the subject experienced chest/shoulder tightness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sweating, and breathing rate increased, chest/shoulder tightness, diarrhea, vomiting, arm soreness, low grade fever, headache, myalgia, and nausea on 03-APR-2021, and was recovering from extreme fatigue. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1194993

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WA
Alter: 57,0
Geschlecht: F
Eingang: 11.04.2021
Impfdatum: 09.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / UN

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

Dizziness Groin pain Myalgia Pain in extremity Paraesthesia

Symptomtext

she felt dizzy 10 minutes post vaccine after standing up...this subsided minutes later. (note: patient used to give herself injections , so not fearful of injection) , now patient has severe muscle pain from groin, down legs and into feet with tingling, bilateral. far more intense than she's ever experienced. feels 'foggy', not like herself, having a harder time concentrating, and very tired all the time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none. she did mention her issues at a routine office appt, but he didn't seem responsive I encouraged her to make an appointment specifically for her leg and foot pain and tingling.
Aktuelle Erkrankungen: none
Vorgeschichte: migraine gastroparesis
Andere Medikamente: apap 500mg tabs
Allergien: heparin, norpine,benztropine,cumarin,diazepam, diphenhydramine, erythromycin,hydromorphone, ursodiol, lamotrigine, neuromuscular blocking agents, prednisone, prochlorperazine, sertraline, trimethobenzamide, carbamazepine, dexamethasone, dicyclomine, domperidone, pregabalin, fentanyl, hydroxyzine, nortriptyline, olanzapine, oxycodone, sulfa antibiiotics, tegaserod, trazodone,nefazodone, warfarin, metoclopramide, buspirone, amoxicillin, clonazepam, diazepam, ibuprofen
Vorherige Impfungen: -

VAERS 1192939

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 11.04.2021
Impfdatum: 13.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / LA

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

Body temperature increased Cyclic vomiting syndrome Headache Malaise Mobility decreased Pain in extremity Pyrexia

Symptomtext

At 4 AM the following day I woke up with a severe headache and fever. I attempted to take 2 extra strength Tylenol which seemed to trigger cyclic vomiting every 15-20 minutes for approximately 4 hours. After this, I vomited once an hour for another 4 hours. I was finally able to sip water and sleep after this. I also took my first temperature once feeling better and it was 99.9F. My normal temp is in the 97s and I?m sure it was much higher during the vomiting. My fever broke approximately 12 hours after the first symptoms. Headache lasted approximately 36 hours and resolved the next day, although a milder one did come back off and on for a couple more days. I did not have much pain in the arm I received the injection in.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: NA. I thought I should go to urgent care but I was too sick to get out of bed and hopes the symptoms would resolve and they did.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, hypertension, disability due to failed ankle fusion with chronic back/leg pain.
Andere Medikamente: Levothyroxine, liothyronine, venlafaxine, Orphenadrine, losartan, vit C, vit B complex, calcium, fish oil
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1190405

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 10.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain upper Asthenia Body temperature increased Chills Fatigue Feeling hot Immediate post-injection reaction Nausea Pain in extremity Pyrexia Tremor

Symptomtext

felt fine except for immediate arm pain. Within a few hours (by 6 pm) started having uncontrollable shaking and chills and was freezing. I was extremely tired. so went to bed at 9 but was feeling quite nauseas as though I had food poisonings and freezing. Wore 3 fleece jackets and two pairs of paint 2 pairs of socks. . At 11 pm woke up feeling extremely hot and my temperature was 104.5. I called my local physician and my physician. I tried getting the fever down with ice packs and cold drinks and no luck. The local doctor got back to me right away and said take 2 tylenol. At midnight it was still 104.3. By 1 am it went down to 103. By 2 am down to 102. Next day was weak and exhausted and still had a 102 fever. Took tylenol twice during day due to feeling like I had the flu. Exhausted went to bed at 9 pm and slept for 12 hours. Woke up today exhausted low grade fever, still have mild stomach ache and nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: vitamin c, zinc, vitamin D
Allergien: peanuts, emycin, sulfur
Vorherige Impfungen: -

VAERS 1189889

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 39,0
Geschlecht: F
Eingang: 10.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Feeling cold Immediate post-injection reaction Migraine Pain Pain in extremity Vaccination site pain Vision blurred Vomiting

Symptomtext

Very bad chills, puking, nausea, migraine, body aches, very sore left arm. At time of injection of vaccine it hurt and my arm started hurting. About 20 mins after vaccine I was slightly dizzy and vision a little blurry. I sat down a few more minutes. About 3 hours later that even is when the chills, body aches, migraine started. All thru that night I was in pain. Next day still felt like my head was in a vice with a migraine. The chills had gone away. still had body aches just not as severe. Day 3 after vaccine. SLight headache (nothing like the vice headache) , arm is still very sore. body aches have subsided considerably. I treated with taking Tylenol and using a heating pad on my arm and back to help with body aches and pain,.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: I did not go the ER or see treatment.
Aktuelle Erkrankungen: None
Vorgeschichte: Bi cuspid arortic valve Heart murmur
Andere Medikamente: Birth Control
Allergien: Lactose intolerant No allergies to medications
Vorherige Impfungen: -

VAERS 1189578

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 59,0
Geschlecht: F
Eingang: 10.04.2021
Impfdatum: 02.04.2021
Beginn: 03.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Feeling abnormal Feeling cold Headache Influenza like illness Loss of personal independence in daily activities Movement disorder Pain Pyrexia Thirst Tremor

Symptomtext

FYI, Approx. 1:00 AM woke up with high fever and could hardly move. Whole body hurt very bad. Shaking from chills . Bad headache. Very thirsty. Definitely flu like symptoms, but worse. Turned electric blanket on, very cold, and just tried to sleep. Only getting out of bed to use restroom and more water. Straight back to bed. I did not vomit, nor did I have diarrhea. Could not stand it any longer Saturday PM approx. 10:00 took two Advil. Woke up Sunday 8:00 AM felt much better. Still had slight symptoms, but I could do chores. My brother kept checking on me. Came to let my dog out. My brother wanted me to call 911 but I can not afford that. It was holiday weekend, I wanted to die, didn?t care. I get the flu shot every year. I have a high pain tolerance, very rare for me to be sick. If I needed a second dose. I would NOT get it. If I would have known it was that bad, I would not have signed up to get it. Thank you.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: None
Vorgeschichte: No
Andere Medikamente: Synthesis 100 MCG daily Lovastatin 40 MG daily
Allergien: NO
Vorherige Impfungen: -

VAERS 1183741

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: -
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: -
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Chills Dyspnoea

Symptomtext

DIFFICULTY BREATHING/SHORTNESS OF BREATH; CHILLS; This spontaneous report received from a patient concerned a female of unspecified age. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and expiry: 01-APR-2021) dose, start therapy date were not reported for prophylactic vaccination. No concomitant medications were reported. On APR-2021, the subject experienced chills. On 01-APR-2021, the subject experienced difficulty breathing/shortness of breath. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the chills and difficulty breathing/shortness of breath was not reported. This report was non-serious.; Sender's Comments: V0: Medical assessment comment is not required as per standard procedure as case assessed as non-serious.

Weitere VAERSDATA-Felder

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

VAERS 1183597

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 11.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 9,0
Dosis: N/A
Route/Site: SYR / LA

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

Chest discomfort Depressed mood Dyspnoea Oropharyngeal pain Pyrexia SARS-CoV-2 test negative Streptococcus test negative

Symptomtext

Continued fever, heaviness in my chest, breathlessness, sore throat, feeling really down

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: General vitals, covid test, strep test. Vitals looked good except for low grade fever, covd and strep test came negative
Aktuelle Erkrankungen: None
Vorgeschichte: Sarcoidosis
Andere Medikamente: Thyroid supplement, multivitamins, Vit D3
Allergien: Allergic to Propylene Glycol, Sulpha drugs, Erythromycin
Vorherige Impfungen: -

VAERS 1180066

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 74,0
Geschlecht: M
Eingang: 08.04.2021
Impfdatum: 08.03.2021
Beginn: 06.04.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: - / -

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

Alanine aminotransferase increased Albumin globulin ratio Aspartate aminotransferase increased Basophil count decreased Basophil percentage Blood albumin decreased Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium decreased Blood chloride decreased Blood creatinine increased Blood glucose normal Blood potassium normal Blood sodium decreased Blood urea normal Brain natriuretic peptide normal Chest X-ray normal Dyspnoea

Symptomtext

4/6/12 ER HPI: 74 y.o. male who presents with complaint of shortness of breath that is worse after eating for 3 weeks. Patient said he had received a his copied vaccine 3 weeks ago. No cough, no chest pain, no abdominal pain nausea vomiting, no palpitations and no fever or chills Shortness of Breath: Started 3 weeks ago and getting worse. Received covid vaccine 3 weeks ago and started then. No cough. Dyspnea on exertion. No fever. Early am he has had runny noses. No inhalers or nebs. Not smoker

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Comprehensive metabolic panel [200568102] (Abnormal) Collected: 04/06/21 2105 Order Status: Completed Specimen: Blood Updated: 04/06/21 2214 Glucose 128High 65 - 100 MG/DL Blood Urea Nitrogen 17 7 - 18 MG/DL Creatinine 1.6High 0.7 - 1.3 MG/DL Sodium 132Low 136 - 145 MMOL/L Potassium 3.5 3.5 - 5.1 MMOL/L Chloride 95Low 98 - 107 MMOL/L Co2 26 21 - 32 MMOL/L Calcium 8.4Low 8.5 - 10.1 MG/DL Protein Total 7.1 6.4 - 8.2 G/DL Albumin 3.4 3.4 - 5.0 G/DL A/G Ratio 0.9 0.8 - 2.0 Alkaline Phosphatase 49 46 - 116 U/L Alt (SGPT) 50 16 - 63 U/L AST(SGOT) 46High 15 - 37 U/L Bilirubin, Total 0.4 0.2 - 1.0 MG/DL GFR Comment IF PATIENT IS AFRICAN AMERICAN, MULTIPLY RESULT BY 1.16 Est GFR 42Low >90 ML/MIN/1.73sq.m NOVEL CORONAVIRUS SARS-COV-2 BY PCR [200568111] Collected: 04/06/21 2116 Order Status: Completed Updated: 04/06/21 2205 SARS-COV-2 Source NASOPHARYNGEAL SARS-COV-2 By PCR Not Detected Not Detected Comment: THIS TEST HAS BEEN VALIDATED BUT FDA'S INDEPENDENT REVIEW OF THE VALIDATION IS PENDING. THIS TEST IS PERFORMED AS A LABORATORY DEVELOPED TEST, INDEPENDENT REVIEW OF THE VALIDATION UNDER THE FDA'S EMERGENCY USE AUTHORIZATION (EUA) AUTHORITY WILL BE PERFORMED ACCORDING TO CURRENT GUIDANCE REQUIREMENTS. ********** WE WILL CONTINUE TO FOLLOW FEDERAL AND STATE REQUIREMENTS FOR BOTH NOTIFICATION OF RESULTS AND ANY CONFIRMATORY TESTING D-dimer, quantitative [200568107] (Abnormal) Collected: 04/06/21 2105 Order Status: Completed Specimen: Blood Updated: 04/06/21 2148 D-Dimer 402High 0 - 400 NG/ML FEU EKG [200568103] Resulted: 04/06/21 Order Status: Completed Updated: 04/06/21 2142 XR Chest 2 View [200568105] Collected: 04/06/21 2107 Order Status: Completed Updated: 04/06/21 2139 Narrative: XR CHEST 2 VIEWS CLINICAL INFORMATION: Shortness of breath TECHNIQUE: PA and lateral views. 2 images. COMPARISON: Chest radiograph October 27, 2014 FINDINGS: Lungs and pleura: Normal lung inflation. No focal consolidation, pleural effusion or pneumothorax Heart and mediastinum: Cardiomediastinal silhouette is normal size. Normal pulmonary vasculature Bones and chest wall: No suspicious osseous abnormalities Lines and tubes: None. IMPRESSION: No acute cardiopulmonary disease. Electronically signed by: MD 4/6/2021 9:38 PM : 109-1082 Brain Natriuretic Peptide (BNP) [200568104] Collected: 04/06/21 2105 Order Status: Completed Specimen: Blood Updated: 04/06/21 2137 B-Type Natriuretic Peptide 13 0 - 100 PG/ML CBC w Auto Diff [200568101] (Abnormal) Collected: 04/06/21 2105 Order Status: Completed Specimen: Blood Updated: 04/06/21 2113 White Blood Cell Count 3.9Low 4.8 - 9.6 THOUS/uL Red Blood Cell Count 4.09Low 4.33 - 5.59 MIL/uL Hemoglobin 13.5 13.1 - 16.8 GM/DL Hematocrit 37.3Low 38.8 - 49.0 % Mean Corpuscular Volume 91.2 82.7 - 94.4 FL Mean Corpuscular Hemoglobin 33.0High 27.7 - 32.6 PG Mean Corpuscular Hemoglobin Conc 36.2High 32.4 - 35.7 G/DL Rdwcv 12.2 11.6 - 13.9 % Rdwsd 40.6 36.0 - 46.1 FL Platelet Count 165 154 - 364 THOUS/uL Mean Platelet Volume 9.9 8.7 - 11.7 FL Nucleated Red Blood Cells 0.0 0.0 /100 WBC'S Abs NRBC 0.0 0.0 THOUS/uL Differential Type AUTO Neutrophils 47.2 34.0 - 67.9 % Lymphs 35.2 19.1 - 41.2 % Monocytes 15.5High 6.1 - 12.3 % Eos 0.8Low 0.9 - 7.6 % Basos 1.0 0.2 - 1.5 % Neutrophils Absolute Count 1.8Low 2.7 - 5.8 THOUS/uL Lymphocytes Absolute Count 1.4 1.1 - 3.3 THOUS/uL Monocytes Absolute Count 0.6 0.4 - 0.9 THOUS/uL Eosinophils Absolute Count 0.0Low 0.1 - 0.6 THOUS/uL Basophils Absolute Count 0.0 0.0 - 0.1 THOUS/uL Imm Gran 0.3 0.2 - 0.9 % Abs Imm Gran 0.01 0.0 - 0.1 THOUS/uL
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Current Outpatient Medications: ? aspirin 325 MG tablet, Take 325 mg by mouth daily Takes 1/2 tablet, Disp: , Rfl: ? Cholecalciferol (VITAMIN D) 1000 UNITS CAPS, Take 5,000 Units by mouth daily, Disp: , Rfl: ? lisinopril-hydrochloroth
Allergien: Allergen Reactions ? Novocain
Vorherige Impfungen: -

VAERS 1179764

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 31,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Blood pressure increased Dizziness Fatigue Palpitations

Symptomtext

Patient states feeling light headed. BP taken at 11:57 am 139/100 given bottle of water monitored. 12:02 136/103, 12:12 am BP 140/104 advised patient relax and stop talking on the phone. 12:18 pm 136/103 am given bottle of Gatorade: stated slight dizziness, 12:28 pm BP 135/96, HR 72, 12:40 pm 130/99, HR 72, 12:54 pm 118/95, 1:30 pm BP 126/97. Patient states feeling a little tired dizziness has lessened. No other symptoms voiced or noted. Color is good. Patient ambulated to car with out any S/S of distress. Advised to call 911 if SOB, light headed, dizziness, chest palpitations or BP goes exceeds 100 diastolic., RN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1161172

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CO
Alter: 54,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: -
Beginn: 24.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Back pain Hypoaesthesia Injection site pain Neck pain Pain in extremity Paraesthesia

Symptomtext

NECK PAIN; TINGLING IN LEFT FOREARM AND HAND; NUMBNESS IN LEFT FOREARM AND HAND; FOREARM PAIN; PINCH AT LEFT ELBOW; PINCH AT INJECTION SITE; This spontaneous report received from a consumer concerned a 54 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included the patient had no known drug allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 24-MAR-2021 at left arm for prophylactic vaccination. No concomitant medications were reported. On 24-MAR-2021, the subject experienced neck pain. On 24-MAR-2021, the subject experienced tingling in left forearm and hand. On 24-MAR-2021, the subject experienced numbness in left forearm and hand. On 24-MAR-2021, the subject experienced forearm pain. On 24-MAR-2021, the subject experienced pinch at left elbow. On 24-MAR-2021, the subject experienced pinch at injection site. On 30-MAR-2021, treatment medications included: diclofenac. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from forearm pain, pinch at injection site, tingling in left forearm and hand, numbness in left forearm and hand, neck pain, and pinch at left elbow. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no known drug allergies
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1161172

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CO
Alter: 54,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: -
Beginn: 24.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Arthralgia Back pain Hypoaesthesia Injection site pain Neck pain Pain in extremity Paraesthesia

Symptomtext

NECK PAIN; TINGLING IN LEFT FOREARM AND HAND; NUMBNESS IN LEFT FOREARM AND HAND; FOREARM PAIN; PINCH AT LEFT ELBOW; PINCH AT INJECTION SITE; This spontaneous report received from a consumer concerned a 54 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included the patient had no known drug allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 24-MAR-2021 at left arm for prophylactic vaccination. No concomitant medications were reported. On 24-MAR-2021, the subject experienced neck pain. On 24-MAR-2021, the subject experienced tingling in left forearm and hand. On 24-MAR-2021, the subject experienced numbness in left forearm and hand. On 24-MAR-2021, the subject experienced forearm pain. On 24-MAR-2021, the subject experienced pinch at left elbow. On 24-MAR-2021, the subject experienced pinch at injection site. On 30-MAR-2021, treatment medications included: diclofenac. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from forearm pain, pinch at injection site, tingling in left forearm and hand, numbness in left forearm and hand, neck pain, and pinch at left elbow. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no known drug allergies
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1177935

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 54,0
Geschlecht: M
Eingang: 07.04.2021
Impfdatum: -
Beginn: 29.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Body temperature Dehydration Dizziness Dyspnoea Pain in extremity Pyrexia Sluggishness

Symptomtext

FEEL SLUGGISH; BREATHING KIND OF HEAVY, OUT OF BREATH A LITTLE BIT; DEHYDRATED; TEMPERATURE 98.8; ARM SORENESS; LIGHTHEADED, DIZZINESS; This spontaneous report received from a patient concerned a 54 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included moderate asthma, penicillin allergy, and egg and chicken allergy, and other pre-existing medical conditions included that patient got flu shot in 2011 and had fever afterwards, but usually never gets fevers. patient had allergies (took shots as kid) and stated some complaints "could be pollen". The patient received covid-19 vaccine (suspension for injection, route of admin not reported, batch number: 1805025, expiry: UNKNOWN) dose was not reported, administered on 29-MAR-2021 at10:15 in right arm for prophylactic vaccination. Concomitant medications included loratadine. On 29-MAR-2021, the subject experienced lightheaded, dizziness. On 29-MAR-2021, the subject experienced arm soreness. On 30-MAR-2021, Laboratory data included: Body temperature (NR: not provided) 98.8 F, 97.1 F. Treatment medications included: paracetamol. On 30-MAR-2021 20:00, the subject experienced temperature 98.8. On an unspecified date, the subject felt sluggish and experienced breathing kind of heavy, out of breath a little bit, and dehydrated. The action taken with covid-19 vaccine was not applicable. The patient recovered from temperature 98.8 on 31-MAR-2021, had not recovered from arm soreness, and the outcome of feel sluggish, lightheaded, dizziness, breathing kind of heavy, out of breath a little bit and dehydrated was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: Test Date: 20210330; Test Name: Body temperature; Result Unstructured Data: 97.1 F; Test Date: 20210330; Test Name: Body temperature; Result Unstructured Data: 98.8 F
Aktuelle Erkrankungen: Allergic asthma; Food allergy; Penicillin allergy
Vorgeschichte: Comments: It was reported that patient got flu shot in 2011 and had fever afterwards, but usually never gets fevers. Patient has allergies (took shots as kid) and stated some complaints "could be pollen".
Andere Medikamente: CLARITIN [LORATADINE]
Allergien: -
Vorherige Impfungen: -

VAERS 1177835

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: -
Geschlecht: F
Eingang: 07.04.2021
Impfdatum: -
Beginn: 24.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Chills Injection site pain Paraesthesia Pyrexia

Symptomtext

TINGLING IN LEFT AND RIGHT ARMS AND FINGERS; FEVER; PAIN AT INJECTION SITE; CHILLS; This spontaneous report received from a patient concerned a female of unspecified age. The patient's height, and weight were not reported. The patient's past medical history included surgery in left arm. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered to left arm on 24-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 24-MAR-2021, the subject experienced fever. On 24-MAR-2021, the subject experienced chills. On 24-MAR-2021, the subject experienced pain at injection site. On 27-MAR-2021, the subject experienced tingling in arms and fingers. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from fever, chills, and pain at injection site on 26-MAR-2021, and had not recovered from tingling in arms and fingers. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arm operation
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1176638

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: -
Geschlecht: F
Eingang: 07.04.2021
Impfdatum: -
Beginn: 24.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Dizziness Nausea Tremor

Symptomtext

WOBBLY/SHAKY LEGS; DIZZINESS; NAUSEA; This spontaneous report received from a patient concerned an 82 year old female. The patient's height, and weight were not reported. The patient's past medical history included knee replacement, hip replacement, dizziness and concurrent conditions included arthritis, heart problem, broken leg, allergic to vancomycine, allergic to penicillin, and allergic to sulfas. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, expiry: 25-MAY-2021) dose was not reported, administered on 23-MAR-2021 at right arm for prophylactic vaccination. Concomitant medications included vitamins nos for drug used for unknown indication and atenolol for heart problems. On 24-MAR-2021, the subject experienced nausea. On 28-MAR-2021, the subject experienced wobbly/shaky legs. On 28-MAR-2021, the subject experienced dizziness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from nausea on 24-MAR-2021, and had not recovered from wobbly/shaky legs, and dizziness. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergic reaction to antibiotics (dizziness from the left ear following allergic reaction to vancomycine.); Allergic reaction to antibiotics; Arthritis; Broken leg; Heart disorder; Penicillin allergy
Vorgeschichte: Medical History/Concurrent Conditions: Dizziness (dizziness from the left ear following allergic reaction to vancomycine.); Hip replacement (Had 1 hip replacement.); Knee replacement (Had 4 knee replacements.)
Andere Medikamente: ATENOLOL; VITAMINS
Allergien: -
Vorherige Impfungen: -

VAERS 1172924

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TN
Alter: 36,0
Geschlecht: F
Eingang: 06.04.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Dyspnoea Oropharyngeal pain Pharyngeal swelling

Symptomtext

Patient called the office to mention an adverse event. She states about a minute after receiving the shot, she noticed that her throat became sore and her chest began to hurt. She did not mention anything to the provider and waited the 20 minute waiting period. As she was driving home, she began to develop some shortness of breath and she felt that her throat was started to swell a little. When she got home, she took 1 dose of OTC Claritin and within in hour, she was feeling much better. She did not have to take any other medications and has not had any reactions since the vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1169676

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 68,0
Geschlecht: F
Eingang: 05.04.2021
Impfdatum: 08.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: - / -

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

Back pain Chest pain Condition aggravated Fibrin D dimer increased Pain

Symptomtext

3/29/21 ER HPI: 68 y.o. female who presents with 3 day history of left anterior chest pain. The pain radiates into her back. Pain has been constant and severe at times. It has no relieving or exacerbating factors. Patient denies fever chills cough dyspnea diaphoresis nausea or vomiting. She denies prior similar history. Patient has taken nothing for the pain 4/2/21 ER presentation - flexed to clinic 4/2/21 Clinic HPI: 68 y.o. female who presents today for suspected shingles vs laceration that is infection on her L posterior back. She was seen in the ER for anterior chest wall pain on 03/29 which had started 3 days prior and then saw Dr. again yesterday for follow-up. He gave her a steroid shot and treated her with oral prednisone. In the ER, patient had elevated D-dimer but this was thought to be from her renal insufficiency. She had no other symptoms that suggested pulmonary embolism. No CT angiography of chest was done due to renal insufficiency.The rest of her workup was negative. Rash broke out the day she saw Dr. but didn't mention it to him at that visit. There was no rash on her anterior chest wall where she was hurting at the time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Lungs are clear of active infiltrate. The cardiac silhouette is within normal limits. Pulmonary vessels are within normal limits. No pleural fluid. No pneumothorax. Multiple metallic shrapnel fragments again demonstrated within the soft tissues of the left upper quadrant abdomen and visualized left arm with prior open reduction and internal fixation of left humerus. IMPRESSION: No active cardiopulmonary disease or significant interval change from 10/22/2019 . Electronically signed by: MD 3/29/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Current Outpatient Medications: ? aspirin 81 MG chewable tablet, Take 81 mg by mouth daily, Disp: , Rfl: ? Calcium Carbonate-Vitamin D3 (CALCIUM 600/VITAMIN D) 600-400 MG-UNIT TABS, Take, Disp: , Rfl: ? furosemide (LASIX) 20 MG tablet
Allergien: Allergen Reactions ? Arthrotec [Diclofenac-Misoprostol] Hives ? Gabapentin Other/Unknown (See Comments) and Depression States "made me crazy" ? Ibuprofen Rash
Vorherige Impfungen: -

VAERS 1168900

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 35,0
Geschlecht: F
Eingang: 05.04.2021
Impfdatum: -
Beginn: 15.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Chills Dizziness Migraine Nausea Pain Pyrexia

Symptomtext

BODY ACHES; DIZZY; MIGRAINE; CHILLS; NAUSEA; FEVER; This spontaneous report received from a patient concerned a 35 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included unknown. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and expiry: UNKNOWN) dose was not reported, administered on 15-MAR-2021 12:30 to left deltoid for prophylactic vaccination. No concomitant medications were reported. On 15-MAR-2021 20:00, the subject experienced body aches. On 15-MAR-2021 20:00, the subject experienced dizzy. On 15-MAR-2021 20:00, the subject experienced migraine. On 15-MAR-2021 20:00, the subject experienced chills. On 15-MAR-2021 20:00, the subject experienced nausea. On 15-MAR-2021 20:00, the subject experienced fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from nausea on 16-MAR-2021, and had not recovered from chills, body aches, migraine, fever, and dizzy. This report was non-serious. This parent/child case is linked to 20210336338.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1168158

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 37,0
Geschlecht: F
Eingang: 05.04.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Paraesthesia oral Swollen tongue Vital signs measurement

Symptomtext

Date: 3/22/2021 Problem: Tongue Feeling Funny Notes: Client States it feels like her tongue is swelling. Upon assessment. Client oxygen level is 98% RA. No swelling noted to clients face, neck, or tongue. T 98.9 P 86 R 18 BP 140/88. Client monitored for 30 mins. No longer c/o tongue swelling. Client states she feels fine. No swelling to face/ neck/tongue noted. T 98.4 BP 140/82 R18 P 70 O2 98% RA. AAOx3 Client left facility via Personal vehicle.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1167205

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 52,0
Geschlecht: M
Eingang: 04.04.2021
Impfdatum: 03.04.2021
Beginn: 04.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Feeling cold Tremor

Symptomtext

Uncontrollable shaking/chills and slight breathing difficulty at the same time. I couldn't hold a full glass of water without having the water shake out of the glass. I am in good health, was fully hydrated and exercise on a regular basis. This symptom is not listed on the published symptom list and I had no idea this could possibly be the outcome of the vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1161021

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WA
Alter: 44,0
Geschlecht: F
Eingang: 02.04.2021
Impfdatum: 09.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Asthenia Axillary pain Chills Cold sweat Headache Hypoaesthesia Influenza like illness Mobility decreased Muscular weakness Myalgia Pain Pain in extremity Paraesthesia Skin burning sensation Tremor

Symptomtext

As soon as the shot was administered in the deltoid muscle within 3 seconds my axillary node was on fire and I couldn't put my arm at rest. Extremely painful in my armpit. The injection nurse said that is not normal and gave me a sheet to report to the CDC scan code. My entire left arm was on fire within a minute. She had me sit for 30 minutes. I had no other reaction. My arm was subsiding a little bit to toleration. I went home and rested, drank a ton of water. I went to bed and woke up at 2 am in a cold sweat, I felt like I was freezing and could not stop shaking. My teeth chattered. My husband put on many blankets and helped me get warm. He said I was burning up. My muscles were so weak and painful, joints hurt and extreme head ache. I took some Advil and he warmed me up. My left arm was numb up my left side of my neck and my left cheek. I took the day off work. In addition, in the morning I felt like my left leg and foot had minor numbness and prickles. I could walk but it was colder and prickled on the foot each step. The next day I was 50% better and made it to work barely. It took me 3 days to recover from the flu like symptoms. My left arm continued to feel numb and had bouts of prickles and tingling. The muscles were hard to use in my left arm and I really didn't use it at all. Over the course of 2 weeks things have improved. I still have not recovered feeling in my left pinky and ring finger. They are weaker still today. Every morning my left arm is numb for a little while (I don't sleep on my left side) but recovers to about 75% except my pinky and ring finger. My left neck and cheek have a warming prickle feeling every morning for about a half hour. They mostly wake up to entirety. My L foot at the bottom has period/episodic prickles. Daily my left arm is colder and is weaker than before. I am a high school teacher so I don't have to use my left arm very much but it is causing pain and negative sensations and is reducing the amount of use of my left arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None. The regulatory authority said I need to report this to the CDC and the Health Department. The health dept sent me here.
Aktuelle Erkrankungen: none
Vorgeschichte: Right Sided Aortic Arch
Andere Medikamente: Estrogen patch. .025 Vit D Fish Oil multi-vitamin magnesium Co-Q10
Allergien: none
Vorherige Impfungen: -

VAERS 1158948

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 02.04.2021
Impfdatum: 01.04.2021
Beginn: 01.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Dyspnoea Pain Pyrexia

Symptomtext

Extreme body aches, high fever, uncontrollable chills, shortness of breath

Weitere VAERSDATA-Felder

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

VAERS 1158071

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TN
Alter: 29,0
Geschlecht: M
Eingang: 01.04.2021
Impfdatum: 31.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Nausea Pyrexia Tremor

Symptomtext

12 hours later I began to suffer from shaking, fever, chills, nausea. This continued off and on for about 14 hours. I used Advil around 10am and it broke my fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multi-Vitamin
Allergien: Penicillin allergy.
Vorherige Impfungen: -

VAERS 1157004

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WI
Alter: 46,0
Geschlecht: F
Eingang: 01.04.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood lactic acid normal COVID-19 Chest X-ray Chills Dyspnoea Electrocardiogram normal Fatigue Full blood count normal Headache Heart rate increased Laboratory test normal Metabolic function test normal Pain Palpitations Pyrexia Urine analysis

Symptomtext

I experienced chills, fever, headache, body aches, feeling very tired, racing heartbeat, and difficulty breathing. I called the on-call nurse line and was advised to go to the emergency room due to my fast heartbeat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: In the ER, they did an EKG, chest x-ray, COVID-19 test, urinalysis, CBC W auto differential, comprehensive metabolic panel, blood cultures, and lactic acid blood reflex. All tests came back normal/negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Mild allergy to amoxicillin
Vorherige Impfungen: -

VAERS 1156768

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 30,0
Geschlecht: F
Eingang: 01.04.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / LA

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

Back pain Body temperature increased Decreased appetite Dysstasia Hyperhidrosis Nausea Pain Pain in extremity Spinal pain Tremor Vomiting

Symptomtext

soreness in arm, 8 hours after the injection I had a temperature of 100.4, body soreness especially in back and spine, experienced shakes followed by sweating, loss of appetite/nausea, difficulty standing/moving. I used ice packs down spine to ease soreness, took a melatonin around 10pm, woke up at midnight and vomited, took 500 mg of Tylenol (symptoms lessened after Tylenol), continued to take Tylenol every 4-5 hours until symptoms were gone, approximately 24 hours after injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Lo-loestrin, valacyclovir 500 mg tablet
Allergien: no
Vorherige Impfungen: -

VAERS 1156012

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 50,0
Geschlecht: F
Eingang: 01.04.2021
Impfdatum: 15.03.2021
Beginn: 28.03.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / RA

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

Electrocardiogram Headache Hot flush Palpitations

Symptomtext

Racing heart rate, hot flashes, head ache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG 4/1-no changes
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines, allergies
Andere Medikamente: Synthroid, noritryptolyne, ajovy, Flonase, melatonin, vitamin B2, vitamin C
Allergien: None
Vorherige Impfungen: -

VAERS 1153086

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 29,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: -
Beginn: 10.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Chills Dehydration Dizziness Feeding disorder Fluid intake reduced Hyperhidrosis Myalgia Nausea Noninfective gingivitis Oral mucosal blistering Pharyngitis Pharyngitis streptococcal Pyrexia

Symptomtext

DEHYDRATION; CANNOT EAT DUE TO BLISTERS AND INFLAMED GUMS; CANNOT DRINK DUE TO BLISTERS AND INFLAMED GUMS; DIZZY/LIGHTHEADED; INFLAMED GUMS; MOUTH BLISTERS; INFLAMED, SWOLLEN AND SORE THROAT; SWEATS; CHILLS; FEVER; MUSCLE ACHES; NAUSEA; This spontaneous report received from a patient concerned a 29 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included alcohol user (Social once in a month), and non smoker, and other pre-existing medical conditions included patient had no known drug allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025, and expiry: UNKNOWN) dose was not reported, administered on 10-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 10-MAR-2021, the patient experienced sweats, chills, fever, muscle aches, nausea. On 12-MAR-2021, the patient experienced mouth blisters, inflamed, swollen and sore throat and the patient was given steroid shot. On 13-MAR-2021, the patient experienced dizzy/lightheaded, inflamed gums. On an unspecified date, the patient experienced dehydration, cannot eat due to blisters and inflamed gums, and cannot drink due to blisters and inflamed gums. The patient was given IV for dehydration. Laboratory data (dates unspecified) included: Streptococcal sore throat (NR: not provided) Negetive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from inflamed, swollen and sore throat on 13-MAR-2021, and sweats, chills, fever, muscle aches, and nausea on 12-MAR-2021, had not recovered from mouth blisters, dizzy/lightheaded, and inflamed gums, and the outcome of dehydration, cannot eat due to blisters and inflamed gums and cannot drink due to blisters and inflamed gums was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20210329079-covid-19 vaccine ad26.cov2.s -Mouth blisters, Inflamed Swollen and sore throat, Cannot eat due to blister, Cannot drink due to blisters, Dizziness, Dehydration, Inflamed gums, Sweats, Chills. These events are considered unassessable. The events have a compatible/suggestive temporal relationship, are unlabeled, and have unknown scientific plausibility. There is no information on any other factors potentially associated with the events. 20210329079-covid-19 vaccine ad26.cov2.s -Fever, Muscle aches, Nausea. These events are labeled and are therefore considered potentially related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: Test Name: Streptococcal sore throat; Result Unstructured Data: Negetive
Aktuelle Erkrankungen: Alcohol use (social(once a month)); Non-smoker
Vorgeschichte: Comments: patient had no known drug allergies
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1152804

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 59,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 30.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Body temperature decreased Chest X-ray Diarrhoea Dizziness Dry mouth Electrocardiogram Full blood count Hypoaesthesia Hypotension Metabolic function test Oxygen saturation Paraesthesia Tachycardia

Symptomtext

25 minutes post injection hypotension, tachycardia (116), lowered body temp.(96.8), dizziness, dry mouth, numbness and tingling in hands. Arrived at Hospital ER 2 hours post injection. Symptoms subsided about 2.5 hours post injection. Similar but milder symptoms on the morning of 03/31 with diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: EKG, chest x-ray, complete blood count (CBC), basic and comprehensive metabolic profile, cardiac enzymes, pulse oximeter, heart monitor. All results returned normal
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: vitamin D, Viviscal vitamin supplement
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1152074

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 91,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 15.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 9,0
Dosis: UNK
Route/Site: - / -

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

Chest pain Dyspnoea

Symptomtext

91 y.o. female who presents with difficulty breathing onset 1 week ago. States symptoms have worsened the last couple of days and has developed intermittent chest pain, at times on the right lower chest and today on the left upper chest. Patient does have a history of stage III kidney disease, hypertension and was told many years ago that she had congestive heart failure. 3/31/21 admitted observation dx chest pain , sob

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Current Outpatient Medications: ? amLODIPine (NORVASC) 5 MG tablet, Take 1 tablet (5 mg) by mouth daily, Disp: 90 tablet, Rfl: 3 ? aspirin 81 MG tablet, Take 81 mg by mouth daily, Disp: , Rfl: ? Blood Glucose Monitoring Suppl (EASY TOU
Allergien: pcn
Vorherige Impfungen: -

VAERS 1150757

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 1805025

moderat

Staat: MS
Alter: 73,0
Geschlecht: U
Eingang: 31.03.2021
Impfdatum: 26.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Cancer surgery Diabetes mellitus Hypertension

Symptomtext

None stated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, high blood pressure, cancer surgery
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1148528

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: UT
Alter: 60,0
Geschlecht: F
Eingang: 30.03.2021
Impfdatum: 19.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Affect lability Asthenia Cough Dry mouth Dyspnoea Feeling abnormal Hypersensitivity Hypervigilance Hypokinesia Illiteracy Increased viscosity of upper respiratory secretion Loss of proprioception Pain Somnolence Thirst

Symptomtext

Sensitivity started within four hours of dose. Autistic sensitivities to maximum. Scrambling of all senses including proprioception to the point of not being able to move from standing or sitting. By hour seven, all sensory inputs were too overwhelming to do anything but shut down and sleep. 911 was not an option because they don't let you sleep, and ERs are overwhelming already, before maximizing all inputs. 7.5 mg hydrocodone for overwhelming pain and sensitivity, allowed sleep. On waking, sensitivity was lessened, but the pain started, 18 hours after the vaccination. Emotional lability for three days. Average aching of arm and injection site were not above expected levels. "Brain fog" and lack of ability to articulate (another autism symptom) started within that first seven hours, and diminished over next ten days. Not yet gone as of today Dry mouth; overproduction of thick 'chunky' mucus that wouldn't cough out, treated with guaifenesin, lasted three days. Shortness of breath and cough associated with that mucus also diminished after three days. Not completely gone ten days later. Excessive thirst, onset two hours after vaccine, lasted two days. Hyperalert (can't sleep without drugs), hyperactive despite weakness, and hypervigilant (extreme startle reflexes) lasted three days as well. Sleep was achieved with hydrocodone and THC. All over body pain, feelings of immune mobilization (coming down with) for two days were not above expected levels. No fainting or other collapse at time of injection, or later. Knowing that severe over-stimulation is exacerbated in a medical setting, it was decided not to seek medical support for three days of systemic symptoms that would have easily merited hospitalization.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: EDS; Autism
Andere Medikamente: Potassium Cl 20 mEq/day; THC 3.25 mg/day; Magnesium Cl 1800 mg/day; multi vitamin; garlic extract; turmeric curcumin; flax oil.
Allergien: No allergies proper. Extreme sensitivities
Vorherige Impfungen: Shingrix 2018, similar neurological overwhelm, but nowhere near as much. Sought medical support, which made all of the symptoms

VAERS 1148453

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 43,0
Geschlecht: M
Eingang: 30.03.2021
Impfdatum: 08.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / -

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

Condition aggravated Hypertension

Symptomtext

On March 15 my blood pressure spiked even taking my medication. My BP was out of control even with medication. I contacted my Dr. asked me to double my high blood pressure medication and has worked since. I do have a follow up appointment with her. Prior to the vaccine I was taking one BP pill with no issues for 8 years.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: High Blood pressure Bells Palsy
Andere Medikamente: Lisinopril- 10mg Hydrochlorothiazide- 12.5mg
Allergien: -
Vorherige Impfungen: -

VAERS 1148427

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AR
Alter: 24,0
Geschlecht: F
Eingang: 30.03.2021
Impfdatum: 30.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Anxiety Blood pressure increased Headache Nausea Tachycardia

Symptomtext

Patient began having anxiety, nausea, headache, tachycardia, elevated BP. Patient was walked to nursing staff for further observation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: morphine, mango
Vorherige Impfungen: -

VAERS 1145475

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: -
Geschlecht: F
Eingang: 29.03.2021
Impfdatum: 29.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Electrocardiogram Flushing Nausea Palpitations Vital signs measurement

Symptomtext

Patient c/o palpitations, flushing, heart-racing and butterflies in her stomach. Fire-Rescue performed vitals: BP-134/73 P:87 sitting and BP: 154/70 P-87 standing. EKG presents a normal sinus rhythm. The patient signed a refusal for transport with the Fire-Rescue crew and drove away shortly after.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: NONE
Vorgeschichte: None
Andere Medikamente: Hormone Replacement medications for Menopause. Testosterone-Creme, Citalopram 10mg
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1141702

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TN
Alter: 57,0
Geschlecht: F
Eingang: 28.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain Arthralgia Condition aggravated Diarrhoea Dizziness Fibromyalgia Headache Migraine Myalgia Nausea Pain Pyrexia

Symptomtext

Beginning around 5 hours following the vaccine, I had the worst flareup of my fibromyalgia symptoms I have had in 7 years. Crushing pain all over body, joints and muscles. Stabbing headache similar to a migraine. Dizziness. Diarrhea for 1 day; abdominal pain for nearly two weeks. Intermittent nausea for nearly two weeks. Felt like I had a fever, although the thermometer said 99.7. The feverish feeling lasted for 3 days. The crushing pain lasted for nearly two weeks. The dizziness was intermittent for two weeks. Got a full-blown migraine headache 4 days after vaccine. Please note: I did NOT take my nightly aspirin dose for 2 days prior to vaccine so as to not affect the immune response. I restarted my nightly dose at 11 PM, 6 hours following the vaccine. Still had all the above-mentioned symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Fibromyalgia Hypothyroidism Hashimoto's thyroiditis Vestibular migraine Arthritis
Andere Medikamente: Armour thyroid
Allergien: Sulfa, nortryptilline, elavil, Monosodium glutamate
Vorherige Impfungen: -

VAERS 1141551

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MD
Alter: 24,0
Geschlecht: F
Eingang: 28.03.2021
Impfdatum: 28.03.2021
Beginn: 28.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Neuralgia Paraesthesia Vision blurred

Symptomtext

Blurred vision, list of vision, intense shivering and tingling. Peripheral neuropathic tingling in feet and fingers. Patient reported similar incidents when younger.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: BP 116/81 HR 82
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1139598

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 40,0
Geschlecht: F
Eingang: 27.03.2021
Impfdatum: 21.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Fatigue Mobility decreased Pain Pyrexia Vaccination site inflammation

Symptomtext

Fever, body aches, inflammation of vaccine site limiting arm mobility, tiredness

Weitere VAERSDATA-Felder

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

VAERS 1138429

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 29,0
Geschlecht: F
Eingang: 26.03.2021
Impfdatum: 22.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / LA

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

Adverse reaction Blood creatine phosphokinase decreased Dizziness Eosinophil percentage decreased Fatigue Full blood count normal Hypoaesthesia Impaired work ability Joint contracture Loss of personal independence in daily activities Lymphocyte count decreased Lymphocyte percentage decreased Malaise Mean cell haemoglobin concentration normal Monocyte percentage increased Muscular weakness Nausea Pain

Symptomtext

I received the vaccine at 1:30 pm in the afternoon on 3/22/21 and immediately afterwards I felt fine. I waited my 15 minutes and had no signs of a reaction and was free to go. Later in the afternoon, around 3:15 pm, I began to feel a little fatigued and my arm was sore. Around 6:00 pm that same night, I developed a low grade temp of 99.8, I was very fatigued, had achiness all over, as well as my arm was very warm and tender. I was unable to sleep through the night of 3/22/21 into 3/23/21 and got out of bed around 4: 30 am on 3/23/21 and had to call into work due to the pain. The pain was not an achiness but sharp throughout my whole body. Around 9:00 am, I took a pain reliever and was able to sleep for a few hours. Upon waking up around 1:30-2:00 pm, I was still hurting and was then nauseated as well. I tried to drink water and ate a few crackers to settle my stomach with no relief. At 5:15 pm on 3/23/21, I went to the bathroom and got in the shower to try to help with the pain. After a few minutes in the shower, I became extremely lightheaded and felt like I was going to be sick. I sat down in the bathtub and hollered for my mother to come help me because at this point, I felt like I needed to go to the hospital. Upon sitting down in the bathtub, I began to profusely vomit and started to lose feeling in my legs. My mother entered the bathroom and I explained what was happening and soon after my hands contracted and were stuck in an abnormal position. The pain was unbearable and I was unable to move them from that position. I was unable to get myself out of the bathtub so my mom then called for an ambulance. These symptoms occurred somewhere around 5:20-5:21 pm and EMS was called at 5:22 pm. After a few minutes, I was able to regain movement of my legs but my hands and fingers were still contracted and unmovable. I was able to help my mother enough to put my clothes on and to make my way outside to the front porch to get fresh air. After getting outside, I was accompanied by my mother and my neighbor whom is a nurse. My neighbor looked at my hands and noticed they were discolored and she attempted to straighten out my fingers to no avail. The pain in my fingers was sharp and excruciating but there was also a pins and needle type pain as well. I remained outside until EMS arrived. I was then transported to Hospital where I was seen in the ER for this. Upon arrival to the ER, the physician ordered labs and fluids and stated that apparently he had seen at least 2 other cases that day with a similar reaction to the vaccine. He explained that I was having an adverse reaction to the vaccine and that my hands should return to normal within 24-48 hours. I was then discharged home. As of 3/24/21, I was able to straighten my left hand out and my right hand, my fingers would straighten out, but they would return to a curled resting position. As of 3/25/21, I returned to work and I have some weakness in both hands with a slight discoloration of each hand as well. I am a nurse and work in an office and the physicians in my office commented on the color of skin upon seeing them. I was still very achy and fatigued. My arm was still sore and tender as well. As of today, 3/26/21, I am still achy as well as tired. My right hand has improved some but still returns to a curled resting position. The color of my hands has improved as well. I am a nurse and have seen many things throughout my career. This experience has been absolutely terrifying and I still have no answers as to why this happened to my body. I did my part by being vaccinated and was terrified that I was going to lose my life to it. I pray this does not happen to anyone else.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: All tests/labs were completed on 3/23/21: CBC W Auto Diff Lab- Results normal except for the following: White Blood Cell Count: 3.7 THOUS/uL (Low) Mean Corpuscular Hemoglobin Concentration: 32.9 G/DL (low) Lymphs: 16.8% (Low) Monocytes: 12% (High) Eos: 0.0% (Low) Lymphocytes Absolute Count: 0.6 THOUS/uL (Low) Comprehensive Metabolic Panel-Normal Creatine Kinase Total-Normal (44 U/L)
Aktuelle Erkrankungen: N/A
Vorgeschichte: Postural Orthostatic Tachycardia Syndrome (POTS syndrome) Cervical Dystonia Interstitial Cystitis Rheumatoid Arthritis
Andere Medikamente: Propanolol Celexa Synthroid Flexeril Sulfasalazine Vitamin D
Allergien: Ciprofloxacin Penicillin Codeine Cardizem
Vorherige Impfungen: -

VAERS 1137460

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 1805025

moderat

Staat: IN
Alter: 31,0
Geschlecht: F
Eingang: 26.03.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Erythema Eye pain Migraine Pain in extremity Pyrexia

Symptomtext

Extreme migraine, extreme eye pain, both arms in pain, full body turned blood red, extremely high fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Morphine and latex
Vorherige Impfungen: -

VAERS 1137432

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 82,0
Geschlecht: F
Eingang: 26.03.2021
Impfdatum: 15.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthritis Condition aggravated Gait inability Pain Walking aid user X-ray abnormal

Symptomtext

She received the vaccine, no problems initially, no real arm soreness. The next morning when she woke up she could not walk, had to hold onto something to walk, and has a lot of pain, and has not improved even with taking pain medications. There has been no improvement from the pain. There are times that she feels just a little better, but then returns back to where it was. She went to the ER on 3/17/21, they said that she had arthritis which she had but she has not had this type of pain until the vaccination. They gave her some pain medicine which did not help at all. She again is taking some pain medication now but the pain is still there. She can stand on her leg and it doesn't hurt, but when she moves her leg is when it hurts. She is now using a walker which she did not have to use before the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: X-ray that showed arthritis.
Aktuelle Erkrankungen: None.
Vorgeschichte: Osteoarthritis, high blood pressure, osteoporosis.
Andere Medikamente: Oxybutynin, Gabapentin, Carvedilol, probiotic, magnesium, apple cider vinegar, biotin, red yeast rice, vitamin E, cranberry, multi-gummies, calcium.
Allergien: Morphine.
Vorherige Impfungen: -

VAERS 1137306

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 26.03.2021
Impfdatum: 01.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 13,0
Dosis: N/A
Route/Site: IM / LA

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

Injected limb mobility decreased Pain

Symptomtext

Limited range of motion in left arm. Extreme pain with some movements. Started physical therapy 3/25/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Centrum Silver Multivitamin
Allergien: None known
Vorherige Impfungen: -

VAERS 1137051

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 47,0
Geschlecht: M
Eingang: 26.03.2021
Impfdatum: 26.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Blood glucose Bradycardia Dizziness Hypotension

Symptomtext

Patient felt lightheadedness and dizziness about 10 minutes after receiving COVID 19 vaccine. Patient bradycardic and hypotensive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Blood glucose, VS
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: NA
Allergien: None
Vorherige Impfungen: -

VAERS 1133711

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AZ
Alter: 58,0
Geschlecht: F
Eingang: 25.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Body temperature increased Dizziness Headache Nasopharyngitis Nausea Palpitations Tremor

Symptomtext

Experienced immediate body shakes from cold (severe) and unable to stop physically shaking until a heated blanket was used on the highest setting for about an hour; temperature 101.8; nausea; headache; dizziness; weakness; heart pounding. Felt weak and shaky for three days after fever broke. Fever broke two and a half days after vaccine administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No illnesses prior.
Vorgeschichte: Lupus; HBP; hypothyroidism; anxiety
Andere Medikamente: Lisinopril, Paroxetine, Levothyroxine, Amlodepine, general vitamin and zinc supplement
Allergien: Compazine - anaphylactic response - throat/tongue swelling
Vorherige Impfungen: -

VAERS 1132411

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 74,0
Geschlecht: M
Eingang: 25.03.2021
Impfdatum: 09.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / -

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

Chills Cough Dyspnoea Eating disorder

Symptomtext

3/25/21 To er for eval of cough, chills, shortness of breath x 2 days. States he had Covid January 2020 that left his lungs in " bad condition". Had his Johnson and Johnson Covid vaccine 2 weeks ago. Has not been drinking or eating much in the last 2 days

Weitere VAERSDATA-Felder

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

VAERS 1131865

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: HI
Alter: 25,0
Geschlecht: M
Eingang: 25.03.2021
Impfdatum: 23.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Body temperature increased Dizziness Dyspnoea Injection site pain Paraesthesia

Symptomtext

Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: Pt presented with a temperature of 99.1F after running from another pharmacy to our pharmacy. Shot was given at 1:10PM and within 5 minutes after pt's arrival time. Pt reported light headed, hard breathing and tingling in hands after 5 minutes of shot. Offered Epipen but pt refused. Continued to monitor pt, All adverse reactions were gone after 15 minutes. Pt was contacted after 24 hours and have no chief complaints except soreness at injection site.

Weitere VAERSDATA-Felder

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

VAERS 1131298

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CO
Alter: 50,0
Geschlecht: F
Eingang: 24.03.2021
Impfdatum: 23.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Chills Ear pain Feeling cold Headache Pain Paraesthesia Pyrexia

Symptomtext

tingling down arm up neck (left side) pain in left ear then moving accross forehead into head pain extreme headache chills, fever shot up to 102 hands and face freezing for hours while high temp. Up all night in extreme pain and with fever weakness body aches internal pain, migraine. took some oxy and ibuprofen in the early evening when pain got too bad to bear around I think 7pm. That helped, fever went down to 99, then the meds wore off chills and pain returned. Started taking oxy and ibuprofen every hour on the hour from 2am until 2pm following day when I was then able to sort of sleep for 2 hours. Stopped taking meds. Took NAC to protect against all that ibuprofen. Took warm bath with bathsalts. Still feel sick but head pain and muscle aches have receeded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: sub clinical hashimotos, no spleen, migraine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1130449

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 58,0
Geschlecht: M
Eingang: 24.03.2021
Impfdatum: 09.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: IM / -

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

Alanine aminotransferase increased Amylase decreased Aspartate aminotransferase normal Basophil count decreased Basophil percentage Bilirubin urine Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium decreased Blood chloride normal Blood creatine phosphokinase MB normal Blood creatine phosphokinase normal Blood creatinine normal Blood glucose normal Blood magnesium normal Blood potassium normal Blood sodium normal

Symptomtext

3/24/21 ER HPI: 58 y.o. male who presents with shortness of breath, palpitations, chest pressure, and hemoptysis. Patient has known history of atrial fibrillation and coronary artery disease. Patient reports he was out in his yard approximately 1 hour ago this evening picking up some items when he bent over and started feeling palpitations. Patient states the palpitations caused a pressure in the center of his chest. He then became short of breath. He then states he got into a coughing fit and coughed up some blood. Patient states he knew something was not right so he told his wife to bring him to the ER. Currently here in ER patient continues to complain of palpitations and trash pressure. Patient currently gives his pain as 6/10. It is nonradiating. Patient reports shortness of breath but denies any lightheadedness, dizziness, nausea, vomiting, or diaphoresis. Of note, patient reports he has been having acid reflux and belching tonight. He states his wife had given him two Pepcid earlier.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: CTA Chest For Pulmonary Embolism w Contrast [245598176] Collected: 03/23/21 0139 Order Status: Completed Updated: 03/23/21 0215 Narrative: EXAM DESCRIPTION: CT CHEST ANGIOGRAPHY WITH IV CONTRAST CLINICAL INFORMATION: Age: 58 years Gender: Male Indication: Shortness of breath Additional history: Hemoptysis COMPARISON: None. TECHNIQUE: Procedure: CT Angiography of the Chest Protocol: Pulmonary embolus Reformats: Coronal and sagittal Intravenous Contrast: 80 mL Omnipaque 300 without documented adverse reaction Image Quality: Adequate Multiple coronal computer generated 3D reconstructions (MIPS) of the pulmonary arteries were included. This exam was performed according to our departmental dose optimization program, which includes automated exposure control, adjustment of the mA and/or kV according to patient size and/or use of iterative reconstruction technique. Dose Range: Up-to-date CT equipment and radiation dose reduction techniques were employed. FINDINGS: Pulmonary arteries: No pulmonary embolus Lungs and pleura: Mild right basilar groundglass airspace opacities and mild bronchiectasis is seen.. Heart: Normal heart size. No pericardial effusion . Aorta: Normal Mediastinum and hila: Normal Chest wall: Normal Lower neck: Normal IMPRESSION: Negative for pulmonary embolus. Mild right basilar bronchiectasis and mild groundglass airspace opacities which may represent atypical infection versus pulmonary contusion in the setting of trauma. Electronically signed by: MD 3/23/2021 2:13 AM CDT Influenza antigen [245598168] Collected: 03/23/21 0149 Order Status: Completed Specimen: Nasopharyngeal Updated: 03/23/21 0214 Influenza A NEGATIVE NEGATIVE Influenza B NEGATIVE NEGATIVE NOVEL CORONAVIRUS SARS-COV-2 BY PCR [245598178] Collected: 03/23/21 0150 Order Status: Sent Specimen: Nasopharyngeal Updated: 03/23/21 0200 Urine Drug Screen Medical - 10 Panel [245598187] Collected: 03/23/21 0118 Order Status: Completed Specimen: Urine Updated: 03/23/21 0143 Amphetamines Screen, Urine NEGATIVE NEGATIVE Barbiturate Screen, Urine NEGATIVE NEGATIVE Benzodiazepine Screen, Urine NEGATIVE NEGATIVE Cocaine Metabolites Urine NEGATIVE NEGATIVE Methamphetamine, UR NEGATIVE NEGATIVE Methadone Screen, Urine NEGATIVE NEGATIVE Opiate Screen, Urine NEGATIVE NEGATIVE Oxycodone Scr Qual,UR NEGATIVE NEGATIVE Phencyclidine Screen Urine NEGATIVE NEGATIVE Propoxyphene NEGATIVE NEGATIVE THC NEGATIVE NEGATIVE TCA - Tricyclic Antidepressants Urine, Qualitative NEGATIVE NEGATIVE Urinalysis with reflex to culture, if indicated [245598186] (Abnormal) Collected: 03/23/21 0119 Order Status: Completed Specimen: URINE,CLEAN CATCH (CCMS) Updated: 03/23/21 0139 Glucose UA NEGATIVE NEGATIVE MG/DL Protein UA NEGATIVE NEGATIVE MG/DL Bilirubin UA NEGATIVE NEGATIVE Urobilinogen UA 0.2 0.2 - 1.0 MG/DL pH UA 5.0 5.0 - 8.0 Blood UA TRACEAbnormal NEGATIVE Ketones UA NEGATIVE NEGATIVE MG/DL Nitrite UA NEGATIVE NEGATIVE Leukocyte Esterase UA NEGATIVE NEGATIVE UR Appearance CLEAR CLEAR Specific Gravity UA <1.006 1.000 - 1.030 Color YELLOW YELLOW Site CCMS Comment, Urine Culture NOT INDICATED RBC Urine 0 to 5 <3 /HPF WBC Urine 0 to 5 <5 /HPF Squamous Epithelial RARE <5 /HPF D-dimer, quantitative [245598173] Collected: 03/23/21 0101 Order Status: Completed Specimen: Blood Updated: 03/23/21 0137 D-Dimer 244 0 - 400 NG/ML FEU Brain Natriuretic Peptide (BNP) [245598172] (Abnormal) Collected: 03/23/21 0101 Order Status: Completed Specimen: Blood Updated: 03/23/21 0137 B-Type Natriuretic Peptide 110High 0 - 100 PG/ML Magnesium [245598167] (Abnormal) Collected: 03/23/21 0101 Order Status: Completed Specimen: Blood Updated: 03/23/21 0136 Magnesium 1.7Low 1.8 - 2.4 MG/DL CKMB [245598170] Collected: 03/23/21 0101 Order Status: Completed Specimen: Blood Updated: 03/23/21 0136 Creatine Kinase-MB 1.7 0.0 - 3.6 NG/ML Troponin Series [245598171] Collected: 03/23/21 0101 Order Status: Completed Specimen: Blood Updated: 03/23/21 0136 Troponin I 0.03 0.00 - 0.06 ng/mL Comment: 0.1 to 0.5 ng/mL shows an increased risk of AMI. 0.6 to 1.5 or greater is suggestive of AMI. Comprehensive metabolic panel [245598164] (Abnormal) Collected: 03/23/21 0101 Order Status: Completed Specimen: Blood Updated: 03/23/21 0136 Glucose 136High 65 - 100 MG/DL Blood Urea Nitrogen 13 7 - 18 MG/DL Creatinine 0.9 0.7 - 1.3 MG/DL Sodium 138 136 - 145 MMOL/L Potassium 3.9 3.5 - 5.1 MMOL/L Chloride 100 98 - 107 MMOL/L Co2 21 21 - 32 MMOL/L Calcium 8.5 8.5 - 10.1 MG/DL Protein Total 7.6 6.4 - 8.2 G/DL Albumin 4.0 3.4 - 5.0 G/DL A/G Ratio 1.1 0.8 - 2.0 Alkaline Phosphatase 64 46 - 116 U/L Alt (SGPT) 43 16 - 63 U/L AST(SGOT) 21 15 - 37 U/L Bilirubin, Total 0.5 0.2 - 1.0 MG/DL GFR Comment IF PATIENT IS AFRICAN AMERICAN, MULTIPLY RESULT BY 1.16 Est GFR >90 >90 ML/MIN/1.73sq.m Amylase [245598165] Collected: 03/23/21 0101 Order Status: Completed Specimen: Blood Updated: 03/23/21 0136 Amylase 40 25 - 115 U/L Lipase [245598166] Collected: 03/23/21 0101 Order Status: Completed Specimen: Blood Updated: 03/23/21 0136 Lipase 92 73 - 393 U/L CK (CPK) Creatine Phosphokinase [245598169] Collected: 03/23/21 0101 Order Status: Completed Specimen: Blood Updated: 03/23/21 0136 Creatine Kinase Total 124 39 - 308 U/L CBC w Auto Diff [245598163] (Abnormal) Collected: 03/23/21 0101 Order Status: Completed Specimen: Blood Updated: 03/23/21 0117 White Blood Cell Count 11.7High 4.8 - 9.6 THOUS/uL Red Blood Cell Count 5.18 4.33 - 5.59 MIL/uL Hemoglobin 15.6 13.1 - 16.8 GM/DL Hematocrit 46.0 38.8 - 49.0 % Mean Corpuscular Volume 88.8 82.7 - 94.4 FL Mean Corpuscular Hemoglobin 30.1 27.7 - 32.6 PG Mean Corpuscular Hemoglobin Conc 33.9 32.4 - 35.7 G/DL Rdwcv 12.9 11.6 - 13.9 % Rdwsd 42.5 36.0 - 46.1 FL Platelet Count 198 154 - 364 THOUS/uL Mean Platelet Volume 11.4 8.7 - 11.7 FL Nucleated Red Blood Cells 0.0 0.0 /100 WBC'S Abs NRBC 0.0 0.0 THOUS/uL Differential Type AUTO Neutrophils 68.8High 34.0 - 67.9 % Lymphs 18.0Low 19.1 - 41.2 % Monocytes 10.0 6.1 - 12.3 % Eos 1.7 0.9 - 7.6 % Basos 0.9 0.2 - 1.5 % Neutrophils Absolute Count 8.1High 2.7 - 5.8 THOUS/uL Lymphocytes Absolute Count 2.1 1.1 - 3.3 THOUS/uL Monocytes Absolute Count 1.2High 0.4 - 0.9 THOUS/uL Eosinophils Absolute Count 0.2 0.1 - 0.6 THOUS/uL Basophils Absolute Count 0.1 0.0 - 0.1 THOUS/uL Imm Gran 0.6 0.2 - 0.9 % Abs Imm Gran 0.07 0.0 - 0.1 THOUS/uL
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Current Outpatient Medications: ? aspirin 81 MG EC tablet, Take 81 mg by mouth Nightly, Disp: , Rfl: ? atorvaSTATin (LIPITOR) 20 MG tablet, Take 20 mg by mouth Nightly, Disp: , Rfl: ? gabapentin (NEURONTIN) 300 MG capsule, Take 1,200 mg by
Allergien: nka
Vorherige Impfungen: -

VAERS 1130201

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 61,0
Geschlecht: F
Eingang: 24.03.2021
Impfdatum: 14.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Arthralgia Blood pressure increased Chills Condition aggravated Decreased appetite Dry mouth Full blood count normal Headache Insomnia

Symptomtext

Elevated blood pressure 230/170 for over 24 hours. Dry mouth, Feeling of unease. Chilled, Insomnia. Loss of appetite. Joint pain, Headache for 6 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: CBC normal
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis, Allergies, Hypertension
Andere Medikamente: Trelegy, Hydrochlorothiazide, Zyrtec, Xiidra, Dorzolomide Hydrochloride-Timolol, Advil, Passion flower, Garlic, Biotin, Cal Mag Zinc, B12, D3, Allergy shot immunotherapy
Allergien: Shellfish, Aspirin, Dogs, Cats, Tres, Grasses, Mold
Vorherige Impfungen: -

VAERS 1129090

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: -
Alter: 64,0
Geschlecht: F
Eingang: 24.03.2021
Impfdatum: 20.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Chills Fatigue Headache Myalgia Pyrexia Tremor

Symptomtext

Extreme fatigue and muscle ache throughout body, fever, chills and shaking, intense headache. Vaccine was administered at 9:30 am. Symptoms began around 3:30 pm and lasted until approximately 5:00 am the next day.

Weitere VAERSDATA-Felder

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

VAERS 1127701

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 35,0
Geschlecht: M
Eingang: 23.03.2021
Impfdatum: 18.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / -

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

Chills Decreased appetite Impaired work ability Pain Tremor Vomiting

Symptomtext

recieved jansen covid 19 shot on 3-18-21 11:56 am and felt fine the rest of the day then woke up that night around 1:30am throwing up alot,after about 20 mins in bathroom tried to lay back down and was shaking cause i had the chills after about 30 mins i had to throw up again laid back down with the chills fell back asleep. woke up friday morning to try to get ready for work i tried to eat a couple pieces toast and threw it back up and body aches and chills and throwing up i called into work and laid back down . i woke up at noon with body aches but as the day progressed i started to feel better went to bed . i woke up sat feeling good and continue to feel fine lasted total about 24 hrs.

Weitere VAERSDATA-Felder

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

VAERS 1125430

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 19,0
Geschlecht: F
Eingang: 23.03.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dysphonia Paraesthesia oral Pharyngeal paraesthesia Pruritus Vital signs measurement

Symptomtext

5:40pm - vaccine given 5:50pm - patients arm and legs begin itching, slight tingling of the tongue 6:00pm - Diphenhydramine injection given IM/RA 50mg/mL. BP 135/95, O2 Sat 96-97%. Dr was contacted via telephone (and continued on the phone until patient left the facility.) 6:25pm - Patient states that itching of extremities seems to be getting a little better, but tingling of tongue seems to be getting worse and now throat is tingling, voice sounds "raspy". Epinephrine 0.3mg was administered via EpiPen to the left thigh, at the direction of Dr. 6:40pm - Patient was transferred via ambulance to ER for observation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Patient had a past anaphylactic reaction to a DEPO injection
Vorherige Impfungen: -

VAERS 1123283

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 1805025

moderat

Staat: VA
Alter: 55,0
Geschlecht: F
Eingang: 22.03.2021
Impfdatum: 19.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Erythema Throat tightness

Symptomtext

Patient received Janssen covid-19 vaccine on 03/19/21 at 0800 pm. She was fine and about 5 minutes later, she complained she feels like her throat was closing. She also mentioned it hurts to breathe, her neck turned red in color and her heart rate was140s. I injected patient with the Epi pen in her left thigh. Patient responded to the Epi, her heart rate was came down to low 100s after a few minutes and deep breathing. 911 was activated, EMT came and transported patient to another Emergency Room.

Weitere VAERSDATA-Felder

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

VAERS 1122554

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WI
Alter: 33,0
Geschlecht: F
Eingang: 22.03.2021
Impfdatum: 19.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Chills Dizziness Fatigue Feeling abnormal Feeling cold Hyperhidrosis Injection site bruising Injection site pain Nausea Paraesthesia Pyrexia Vomiting

Symptomtext

Vaccinated at 12:00 19Mar2021. Sore arm started a couple hours afterward and is still present. Started experiencing fogginess and feeling cold at 1:00 am 20Mar2021. Went to bed at 1:00 and dreamed of being sick until waking up at 8:30 am 20Mar2021. Woke up and was very weak (could not push toothpaste through toothpaste tube), almost passed out in trying, so I sat on the floor. Tried getting back to bed and was extremely nauseous and started vomiting. After that, I had the sweats/fever/chills for a couple hours (until ~11:00am), and was fatigued until 4:00 pm. Spent most of the day sleeping, unable to do anything. Today, 22Mar2021, feel slight tingling on palm of left hand and fingers. Injection site is still sore and bruised

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: no
Vorgeschichte: Asthma, cold hives
Andere Medikamente: Vitamin D supplements
Allergien: no
Vorherige Impfungen: -

VAERS 1122073

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 54,0
Geschlecht: F
Eingang: 22.03.2021
Impfdatum: 21.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Chills Fatigue Headache Pyrexia Tremor

Symptomtext

Violent chills began just after midnight on 3/22 (my whole body was shaking and teeth were chattering uncontrollably). Noted fever of 101.5 at 1:30 am with extreme fatigue/weakness, headache. As of 8:30 am, still had fever, 101.7. I took Tylenol at 8:30 am and as of 9:27 am, my temperature is 100.7

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Medications: penicillin and amoxicillin Food: bivalval shellfish (mussels, clams, oysters, squid and octopi)
Vorherige Impfungen: -

VAERS 1120717

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: NJ
Alter: 31,0
Geschlecht: F
Eingang: 21.03.2021
Impfdatum: 13.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: SYR / LA

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

Hypoaesthesia oral Injection site erythema Injection site pruritus Paraesthesia oral Pruritus Rash

Symptomtext

Started at 2:00pm with itching and redness on left arm at the injection site. By 6:30pm rash/hives spread to legs, arms, feet, stomach and back. Severe itching. Took 25mg of Benadryl at 6:30pm. Rash appeared to subside. By 10:30pm rash and severe itching returned on legs, feet, back, stomach and arm. Felt tingling and numbness in tongue. Took additional 25mg of benadryl and called 911. Paramedics arrived and assessed vitals. Rash began to subside. Sunday 3/21 had residual internal itching all over body.

Weitere VAERSDATA-Felder

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

VAERS 1117191

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AR
Alter: 70,0
Geschlecht: F
Eingang: 19.03.2021
Impfdatum: 19.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Palpitations

Symptomtext

Took Benadryl 50mg prophylactically prior to vaccine. 5 min after shot experienced heart racing, mild air hunger and SOB. 15 min after symptoms started to subside. At 30-36 min later felt normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, Hypothyroid, Asthma
Andere Medikamente: Levothyroxin .25mg Metoprolol XL 25mg Vitamins C,D, B12, Methylfolate
Allergien: Fish/Seafood, NSAID'S, Sulfa, Quinolones, Valtrex, Z-pak, Mantoux skin test, Hepatitis B vaccine, Sulfites, Aspertame, Tartrazine
Vorherige Impfungen: Mantoux and Hepatitis B

VAERS 1116887

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AZ
Alter: 57,0
Geschlecht: F
Eingang: 19.03.2021
Impfdatum: 19.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Hypoaesthesia Muscle tightness Neuralgia Paraesthesia Pharyngeal hypoaesthesia Pharyngeal paraesthesia

Symptomtext

Tingling, slight numbness in left arm, hand and face, quite vague, less noticeable in throat muscles. Symptoms remind me of shingles-caused neuralgia which I sometimes experience on left side. Facial tingling, feeling of tightness in muscles, including inner ear are less familiar to me. Symptoms appear to change in degree--slight to more noticeable--as this first day wears on. (Now nearly five hours since vaccine.) I have gone about day as normal, eating and exercising, drinking plenty of water.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Thyroiditis, gluten intolerance
Andere Medikamente: None
Allergien: Gluten, slight reaction to raw peanuts
Vorherige Impfungen: -

VAERS 1116672

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TN
Alter: 67,0
Geschlecht: F
Eingang: 19.03.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / LA

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

Arthralgia Cold sweat Dizziness Hypotension Injection site erythema Injection site pain Malaise Myalgia Pain in extremity Pallor Throat tightness Vision blurred

Symptomtext

15-20 minutes after the injection, I started feeling a tightness in back of my throat; I broke out in cold sweat. I started getting dizzy and very whoozy. I felt my vision starting to close in. I thought I was going to pass out. I got the attention of the person across me to get an attendant and they brought me a chair with wheels. Two people got me up (and I'm not a big person) - they were worried I was going down and I was taken to exam room. They said I was white as a sheet. She checked my eyes and throat a few times and checked my blood pressure. It was lower than normal but she didn't seem really concerned about it - 104 over 60 something which is low for me. She gave me water to sip. She gave me very cold compresses to put on my forehead. They watched me pretty good. She had the epi-pen ready. She watched me and I sat in there and nurse came in a quite a few times to check me for about an hour. About an hour later the tightness went away and I started feeling myself again. We went home. I went to sleep. I woke up at night to go to bathroom and I was still a little woozy but I didn't fall. Next day, I just didn't feel well. My left arm was starting to hurt - was no swelling; it was a little red at injection site. It hurt just a little. I was woozy. My eyes couldn't focus as well. I felt out of it. I drank a lot of water and took a nap. Yesterday, I felt pretty decent but still woozy somewhat. I tried to run errands with my husband - just wasn't quite right. Today, much better but I'm not quite myself yet. Just a little wooziness - weird feeling. Yesterday, I did feel a soreness in the back of my right calf muscle. It wasn't warm to the touch or swollen. I don't have it anymore, it went away. It could have been a muscle thing from the first day of the vaccine when I got home and I got up and almost fell down. I do still have some achiness in joints. Especially in my knees - which isn't normal because they are replaced.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: Ulcerative Colitis; Meniere's disease; Allergies -seasonal; dust; mold; cats; arthritis: Macular Degeneration; Osteopenia I took a lot of Prednisone when I was young but they think that they had an affect on me on my joints.
Andere Medikamente: Lomotil (I'm taking the generic) - it slows down my digestive process; Hydrochlorothiazide - for Meniere's disease - helps to alleviate my ear that feels plugged up and helps with tinnitus; As needed: Azelastine HCI - for allergies; Albut
Allergien: Supha; Rocephin; Aspirin - high doses - can have an adverse reaction to that (when I got my second knee replaced) that's when I got tinnitus. I avoid Ibuprofen by mouth. Flu Vaccine - always have a reaction to flu vaccine every year - that were normal reactions - but a few years ago I got it and that is when I had an ear problem that took me through needing getting steroid shots etc. Allergies - seasonal; dust; mold; cats
Vorherige Impfungen: flu vaccine - symptoms that happened a week later - that happened with my ear. Several years ago.

VAERS 1116589

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 41,0
Geschlecht: F
Eingang: 19.03.2021
Impfdatum: 11.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain Dizziness Fatigue

Symptomtext

Started on day 5. Began day feeling extreme fatigue, dizziness, chest pain. Went to emergency room for chest pain. No indication of heart attack per ER. Extreme fatigue lasted for 3 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Emergency room visit on 2/16/21
Aktuelle Erkrankungen: -
Vorgeschichte: Type 1 Diabetic Rheumatoid Arthritis
Andere Medikamente: Insulin dependent type 1 diabetic Novalog-Insulin Pump Ozempic
Allergien: Sulpha drugs
Vorherige Impfungen: -

VAERS 1115793

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 32,0
Geschlecht: F
Eingang: 19.03.2021
Impfdatum: 14.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Cough Fatigue Headache Nausea Oropharyngeal pain Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test negative Streptococcus test negative Tremor

Symptomtext

Within 7 hours I was violently shaking with chills. I was shaking so bad my body was in pain. This lasted about 6 hours. The highest fever I ever recorded was 100.6 but it felt much higher. I had nausea, body aches, headache, and exhaustion for a full 24 hours. Within 48 hours, my chills and aches were mostly gone, but a sore throat, cough, and congestion developed. As of this morning, Friday 19 March, I?m still exhausted, but all other symptoms have finally resided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: I did get a Covid (rapid and PCR) and strep test done on Thursday the 19th. Both came back negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Anthrax, mid 20s, unable to move arm that was for approx 36 hours and tingling in fingers

VAERS 1114740

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 57,0
Geschlecht: M
Eingang: 19.03.2021
Impfdatum: 10.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Chest pain

Symptomtext

SUDDEN ONSET CHEST PAIN PT WAS TRANSFERRED FROM LOCAL ED TO ANOTHER FACILITY WITH AN ICU BED AVAILABLE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: D. DIMER 1.16MG/L
Aktuelle Erkrankungen: NONE
Vorgeschichte: TIA,OSTEOARTHRITIS
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1112586

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 39,0
Geschlecht: F
Eingang: 18.03.2021
Impfdatum: 18.03.2021
Beginn: 18.03.2021
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 Discomfort Paraesthesia Road traffic accident Vital signs measurement

Symptomtext

Complaint of left sided deficit( numbness and tingling on cheek, forearm and leg, left side feels heavier than right side.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Assess by EMS and NP: Required further evaluation. Called 911 to transfer patient to ED, VSS; B/P 142/96; HR 105, 100 02 sat room air. Blood sugar 128. Repeat B/P 125/68 HR 101
Aktuelle Erkrankungen: None
Vorgeschichte: Motor vehicle accident 2 and half years ago
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1112288

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 45,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 18.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Tremor

Symptomtext

Lightheaded, shaky; B/P-135/78, P- 78, pulse ox- 95%; cleared by onsite nursing supervisor Client reports past history of fainting with blood draws

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension
Andere Medikamente: Losartan 50mg daily
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1109385

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WI
Alter: 40,0
Geschlecht: M
Eingang: 17.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Abdominal discomfort Abdominal pain Appendicectomy Appendicitis Computerised tomogram abnormal Delirium Dizziness Eructation Headache Infection Lethargy Pain Pyrexia Tremor Vomiting White blood cell count abnormal

Symptomtext

On March 11th at around 10pm I experienced severe shaking, fever, headache and delirium. The next day I improved but had a fever on and off of 99.1. I felt like I was stable, but felt dizziness increasing, and was lethargic through the weekend. Then on Monday the 15th, I had a noticeable cramp in my right abdomen. At around 8pm CST I began feeling like I needed to burp and that I had GI problems. The problems increased that night at around 10pm I had pain where the cramp started. Two hours later I started throwing up because of the pain and feeling of too much air inside of me. I could not stop vomiting after 2 hours so went to the Hospital ED at around 2:30 AM Tuesday the 16th. I was admitted after a CT scan showed and white cell counts confirmed and infection and drastically enlarged appendix. I was diagnosed with an appendicitis and they immediately scheduled me for surgery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: 1,0
Labordaten: CT scan on the 16th. Appendectomy on the 16th. Released back home on the same day.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lexapro and Allegra
Allergien: None
Vorherige Impfungen: -

VAERS 1109361

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 36,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Pharyngeal paraesthesia Tremor

Symptomtext

hand tremors tingling in the throat Denies SOB, chest pain BP: 146/108 HR 70 Sp02: 97% Refused hospital transport, signed refusal form, seen and cleared by EMS

Weitere VAERSDATA-Felder

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

VAERS 1108345

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 28,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Fall Head injury Headache Hyperhidrosis Immediate post-injection reaction Nausea Panic attack Skin mass Vomiting

Symptomtext

Immediately after vaccination, pt was sitting in chair in clinic lobby, she states she felt like she was having a panic attack and that is the last thing she remembers. She fell out of chair and hit her head on the clinic floor. Staff responded to pt lying in the lobby floor with a quarter sized red knot on left side of forehead. Pt complained of a headache, was found to be diaphoretic and had nausea and small amount of emesis but had moderate nausea for 30 minutes after event. Vitals were obtained and WNL. EMS was called and pt agreed to be transported to ER for evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: transported to ER via EMS
Aktuelle Erkrankungen: hx of panic attack
Vorgeschichte: Diabetes, hx of panic attacks
Andere Medikamente: unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1106758

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 53,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal discomfort Abdominal pain upper Back pain Chills Dysarthria Fatigue Gastritis Headache Pain Paraesthesia oral Tremor

Symptomtext

At 7:00pm started to feel fatigued and back was sore, slight headache. 7:50pm started shivering uncontrollably and chattering teeth very hard (painful )temp was normal. Unable to talk clearly. Could not stop shaking. Drove to ER, but episode stopped once we arrived. Decided to go home. 10:32pm spiked 102.1 fever, bad ache and body aches. Took tylenol. 12:30am 102.9 fever. Took tylenol again 3ish fever at 101.9 Fever broke next day around 8:30pm. Gastriris attack next day. Stomach very upset and painful. Lip felt tingly and jaw felt like is was quivering, but no visible movement. Still experiencing phantom trembling feeling in lips, jaw and face to dat. Stomach pain resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia, Undifferentiated Connective Tissue Disease and IBS
Andere Medikamente: Amitriptyline 25mg, LDN (Naltrexone) 4.5mgs, Omeprazole 40 mg,Turmeric 600 mg, Methyl Folate 680 mcg, Methyl B12 100mcg, Magnesium 140 mg Calcium 238mg, D3 125mcg, p-5-p (B6) 1.5 mg. Red Clover 400mg, MACA 1900mg, Acetyl L-Carnitne HCL 400m
Allergien: Sulpha drugs - Hives, Latex - rash, Egg - rash, Gluten- runny nose
Vorherige Impfungen: -

VAERS 1106665

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: OH
Alter: 62,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 09.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Influenza Malaise Mobility decreased Pyrexia Vomiting

Symptomtext

3p received infection. 8:15 severe chills, vomiting until 2am. From 2am through the next day fever ( 100c) with it breaking through the night. Mild flu the next day with general Malaise. The chills were so intense that I was constricted for much of the time with little relieve. I would call them violent chills with a tetany kind of full body involvement. Never have I experienced chills like I have described. I?ve never had a reaction to vaccines and tend have a high tolerance. I did not contact my physician but spoke to colleagues who suggested report the experience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Vitamin D Roloxifene 60 mg Atorvastatin 20mg Whole food multi vitamin
Allergien: NKA
Vorherige Impfungen: -

VAERS 1105117

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 13.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / UN

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

Atelectasis Chest X-ray abnormal Cough Fatigue Haemoglobin normal Haemoptysis Lung opacity Myalgia Pneumonia White blood cell count increased

Symptomtext

Patient received vaccine on 3/13, initially had fatigue and myalgia the day after, which resolved, but also on 3/14 began having mild intermittent coughing, nonproductive, occurring every two hours or less. Patient began having some blood in his sputum since this morning at 4AM, and that occurred twice more with intervals of a few hours, both continuously improving and less blood. No other symptoms. No history of TB, no exposure to sick contacts, no recent travel. Unlikely a pulmonary embolus given normal vital signs and no risk factors. Patient was doing outdoor work in his yard for the past few days before the symptom onset and was working on mulch and compost. Although unlikely to have fungal infection currently, may be bacterial pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: Labs within normal limits, including normal hemoglobin. Patient has mild elevation of WBC 11, which is consistent with his previous labs. Chest x-ray shows a retrocardiac opacity which may represent atelectasis vs pneumonia. Given patient's symptoms, will treat for community acquired pneumonia with amoxicillin
Aktuelle Erkrankungen: none
Vorgeschichte: hyperlipidemia
Andere Medikamente: atorvastatin 10 mg daily
Allergien: none
Vorherige Impfungen: -

VAERS 1105071

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 14.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Feeling cold Headache Pyrexia Tremor Vomiting

Symptomtext

Extreme cold. Body shakes, low grade temp, headache and vomiting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Calcium w/Vitamin D Protonix Crestor Benadryl
Allergien: pcn
Vorherige Impfungen: -

VAERS 1102819

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: FL
Alter: 54,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
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 Dyspnoea Hypertension Hypoxia Nausea Tachycardia Vital signs measurement

Symptomtext

After client was vaccinated, she reported weakness, dizziness, SOB and nausea. ALS crew onsite took vitals - patient was initially tachycardic, hypoxic to 75% O2 sats with SOB, and hypertensive. Medics placed client on 10L of O2 via nonrebreather. 10:45 VS 161/117 100% 102 HR, 10:54 VS 157/88 96% on O2, 70 HR, 11:00 VS 145/72, 96% on RA, 63 HR. Patient refused for ALS crew to take her to the ER. Pt was alert and oriented x 3. Husband and sister at patient's side. Pt left with sister and refused afain to go with the crew.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: lupus, seizures
Andere Medikamente: Plaquenil, Keppra, Duloxetine, Topamax, Synthroid, Htz
Allergien: tylenol, motrin, pepto bismol
Vorherige Impfungen: -

VAERS 1102498

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 68,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 15.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Tachycardia Vital signs measurement

Symptomtext

Lightheadedness and tachycardia noted 20 minutes after administration of Covid Vaccine. Emergency drugs available. Airway assessment done, vital signs obtained, cold, damp cloth placed on patient's head and neck. Husband requested EMS to transport patient to ER for further evaluation. Patient stable when EMS arrived.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Transported to ER for further evaluation
Aktuelle Erkrankungen: Did not mention
Vorgeschichte: Did not have due to mass vaccination site.
Andere Medikamente: Did not mention
Allergien: answered no to the questionaire
Vorherige Impfungen: -

VAERS 1101785

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 60,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 08.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Facial discomfort Fatigue Feeling hot Limb discomfort Pain Paraesthesia

Symptomtext

About 5pm after I began feeling achy and fatigued. The next day after I developed the tingly, pins and needles sensation that came and went in both legs, my face, arms and both hand area which I am still experiening today but not as frequent as it was when it began. When it happens its not always in the same spots and doesnt occurs at the same times its as if it alternates and now I also get a hot sensation at the top of my ears periodically which doesnt last very long but it does occur

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: Hypertension, PSVT, High Cholesterol, Acid Reflux
Andere Medikamente: Metoprolol 25mg, Nexium 40mg, Vit D, Crestor 5mg, Flomag, Multivitamin Vit. C
Allergien: cinnamon, parmasean, ZTac, Erythromiocin, Aspirin, Doxycycline
Vorherige Impfungen: -

VAERS 1101480

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 43,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Headache Hypoaesthesia Injection site discomfort Injection site erythema Injection site hypoaesthesia Injection site joint pain Injection site pain Injection site paraesthesia Injection site pruritus Musculoskeletal stiffness Myalgia Neck pain Pain in extremity

Symptomtext

On-going pain, redness, itching and burning sensation at the injection site as well as stiffness, discomfort, tingling, mild numbness and joint pain, and headache from the day of injection, at the time of writing this report including the days in between injection and reporting. Initial swelling an hour after injection on 3/11/21 was the diameter of a quarter; swelling as of 3/15/21 is approximately 4.5 inches in diameter. The surface temperature of the injection site remains approximately 98.1 degrees. In addition, I am experiencing noticeable numbness and tingling on the left side of my body including facial muscles surround eye, mid face, left hand radiating out to all 4 fingers, left thigh, and left calf. I am experiencing joint and muscle pain on the left side of my neck, left shoulder, left upper arm, left elbow, left hip, knee and ankle.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Metoprolol Succinate, Lisinopril, Amlodipine besylate
Allergien: The only known allergies are lactose and Demerol.
Vorherige Impfungen: -

VAERS 1101315

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WI
Alter: 36,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 11.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Asthenia Chills Head discomfort Injection site pain Injection site swelling Pain Tension Tremor

Symptomtext

Approximately 7.5 hours after the vaccine I woke up with severe/violent chills/shakes. Fever unknown. I sat in a hot bath for about an hour and they stopped. When I got out I took ibprophen and went back to bed. Soon they started again and I piled on a weighted blanket to get them to calm down and eventually fell asleep. I also had a lot of head heaviness and pressure during this time. The next morning I woke up with body aches from all the tensing up and felt week and still had head pressure. By midday I was back to normal. Still some injection site soreness and swelling her today, Monday 3/15.

Weitere VAERSDATA-Felder

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

VAERS 1100959

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 36,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Paraesthesia Rash Urticaria

Symptomtext

Patient presented to nurse at vaccination clinic with rash on abdomen, rash with hives on both arms, neck and face. Patient complained of tingling in her arms and hands. No complaints of respiratory distress or symptoms. Epinephrine and Benadryl given IM. EMS transported to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No current illnesses.
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1098637

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 44,0
Geschlecht: M
Eingang: 14.03.2021
Impfdatum: 13.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Electrocardiogram Hypertension Injection site pain Pain in extremity

Symptomtext

pt has h/o htn and take 4 different meds. he has taken all of his meds today . pt received his covid vaccine on 03/13/2021 in the left shoulder and he woke up this morning with pain in the left shoulder radiating down his arm and it originates at the site of the vaccine. pt denies substernal chest pain , dyspnea , doe. he has h/o elevated blood pressures at the level seen today (180/100) when he has poor sleep and he had poor sleep last night due to pain at injection site. no CAD hx. pain is not changed with walking but will be worsened by moving his left arm. PE: a+ox3, in moderate pain left arm: injection site clean and intact. left arm is neurovascularly intact. no bony deformity of the shoulder lung: normal respiratory status, cv rrr no mgr Signed on 3/14/2021 at 11:54am

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Performed EKG and started IV with Normal saline infusing.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN
Andere Medikamente: amlodipine, hydrochlorothiazide,
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1098424

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: GA
Alter: 62,0
Geschlecht: M
Eingang: 14.03.2021
Impfdatum: 08.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Disturbance in attention Dizziness Fatigue Feeling abnormal Gait disturbance Hypoaesthesia Limb discomfort Motor dysfunction Muscular weakness Paraesthesia

Symptomtext

Day 1: 11 hours after injection - severe fatigue, dizziness, diminished ability to mentally focus, severe weakness in legs and diminished ability to control legs. Legs intermittently felt numb and at time with "pins and needles" tingling. Knee joints felt as if in danger of flexing backwards. Arms were similarly affected but not as drastically as legs. Arms had better function and control than legs but with marked weakness. Day 2: Some improvement. Able to go to work but still have fatigue and leg weakness persist. It takes additional mental and physical effort to walk. Walking does not feel automatic or safe like it was before. Still have high level of fatigue. Symptoms improve some later in the afternoon. Days 3

Weitere VAERSDATA-Felder

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

VAERS 1097533

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MO
Alter: 37,0
Geschlecht: F
Eingang: 13.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased Dizziness Eye movement disorder Hypotension Mydriasis Respiration abnormal

Symptomtext

Patient reported feeling dizzy. She asked for some water, which was provided. Went to check on patient a minute later and her eyes were fluttering and her breathing altered. She did not respond to me. Her pupils dilated dramatically and she slumped over. I called for a nurse and we lowered her to the floor together. Blood pressure was low (around 100/60) Her pupils started to return to normal and she was able to converse with us. Blood pressure increased slightly but was erratic. Emergency service responders made call to take to hospital because blood pressure would not stabilize

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1097486

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 45,0
Geschlecht: F
Eingang: 13.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Dyspnoea Headache Hyperhidrosis Skin burning sensation Thirst

Symptomtext

10 hrs afterwards I had the worst chills I have ever had for 2 hrs then my body was on fire for 2 hrs. I was drenched in sweat had to change my clothes twice and a severe headache. I felt some mild discomfort in my breathing and I was extremely thirsty. All of this lasted about 5 hrs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma and allergies
Vorgeschichte: None
Andere Medikamente: Vit C and Multi Vit and Elderberry
Allergien: None
Vorherige Impfungen: -

VAERS 1097223

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AL
Alter: 60,0
Geschlecht: M
Eingang: 13.03.2021
Impfdatum: 11.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Palpitations

Symptomtext

PATIENT WAS CALLED BY OUR PHARMACY TO CHECK IF PATIENT WAS OK AFTER ADMINSTERING THE VACCINE. PATIENT REPORTED HE WENT TO THE EMERGENCY ROOM THE EVENING AFTER HE GOT THE SHOT. HE REPORTED A HEART RATE OF OVER 120. HE STATED THAT HE FELT HIS HEART RACING AND DECIDED TO GO TO THE EMERGENCYROOM AND WAS OK AFTER THAT. THE PATIENT DID NOT TELL HIM WHAT HE WAS TREATED WITH.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: NONE
Vorherige Impfungen: -

VAERS 1096998

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WI
Alter: 48,0
Geschlecht: M
Eingang: 13.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea

Symptomtext

Client reported shortness of breath with gradual onset within 30 minutes of vaccination. Monitored by paramedics and symptoms resolved without treatment.

Weitere VAERSDATA-Felder

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

VAERS 1096922

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AZ
Alter: 61,0
Geschlecht: F
Eingang: 13.03.2021
Impfdatum: 12.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / RA

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

Chills Cold sweat Dizziness Nausea Pyrexia Tremor Vomiting

Symptomtext

3/13/21 03:00 am, chills, shakes 3/13/21 04:00 am, fever 102, threw up 3/13/21 07:00 am, dizziness, cold sweats, nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure, high cholesterol
Andere Medikamente: Valsartan-HCTZ 80-12.5 mg 1/2 every day Rosuvastatin Calcium 5 mg 1/day Bayer low dose aspirin 81 mg 1day Vitamin C 500 mg chewable 1/day One A Day Womens 50+ vitamin 1/day
Allergien: none
Vorherige Impfungen: -

VAERS 1096828

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 55,0
Geschlecht: M
Eingang: 13.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Discomfort Dizziness Fatigue Headache Injection site pain Lip pruritus Myalgia Pain of skin Paraesthesia Paraesthesia oral Pruritus Pyrexia Restlessness

Symptomtext

Around 7:00 P.M. on March 12, 2021 approximately 9 hours after receiving the Jansen COVD-19 vaccine in my left arm. I developed extreme fatigue, muscle aches, skin hurt to the touch of anything including clothing, headache, and fever 101.5. I had to go to bed and was very weak. I took ibuprofen and Tylenol for the discomfort. I slept 14 hours and was able to get up at 11:00 A.M. on March 13, 2021. The soreness at the site of the injection is not problematic. There were other odd symptoms overnight I would awake with strange nerve like sensations tingling and itching that occurred on the bottom of the left foot, upper lip, and neck. I also had several episodes of restlessness that was so bad that I had to stand for a few minutes before being able to lay down again. The worst is the skin hurting and headache. I have also had a few dizzy episodes since getting out of bed this morning. It passes if I sit down or hold onto something. None of these symptoms are normal for me and I cannot remember having a reaction to any vaccinations that I have received in the past. I hope this helps with your study.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: PVCs that are controlled with Atenolol.
Andere Medikamente: Atenolol 25 mg daily, Clarain-D 12 hour daily, Excedrin, Tylenol and Ibuprofen
Allergien: None
Vorherige Impfungen: -

VAERS 1096753

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WI
Alter: 29,0
Geschlecht: F
Eingang: 13.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Headache Hypoaesthesia Nail discolouration Paraesthesia Peripheral coldness Pyrexia Vomiting

Symptomtext

5:50pm to around 8:30pm constant shivering no matter how many layers to heat up body. Fingers and toes tingling and numb from cold. (It was 70 degrees in the house). Fingers under nails discolored bluish. 8:30pm shivering stopped, started getting a fever and headache, vomiting around 9:30pm. Vomiting started and stopped within an hour. 9:30pm to 4:20am (this morning) fever, severe headache. 4:20am to 10:30am severe headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None. Stayed home.
Aktuelle Erkrankungen: None.
Vorgeschichte: Childhood asthma (somewhat as an adult). Amxiety being diagnosed currently.
Andere Medikamente: None.
Allergien: Claritin (allergy medicinee) - gives a rash.
Vorherige Impfungen: -

VAERS 1096548

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 29,0
Geschlecht: M
Eingang: 13.03.2021
Impfdatum: 05.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Disorientation Dysstasia Gait inability Hypoaesthesia Hypoaesthesia oral Muscular weakness Pain in extremity Paraesthesia Paraesthesia oral Pyrexia Sensory disturbance Sleep disorder

Symptomtext

First three days 102 fever, legs were in so much pain I could not walk or get up. The fourth and fifth day my lips and face would become tingly/numb and my left arm would get weak and I would feel a little disoriented, my sleep has been pretty disturbed. It felt like I was having a stroke. I did not have a stroke, I continue to occasionally feel the above symptoms, a little less potent than they were, they might be going away, I can't tell. I will be calling my doctor if it continues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Nothing yet since I haven't felt in an emergency situation yet. just need rest and I usually feel better . If it continues into next week, I'm calling my doctor.
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: Omeprazole 40mg, daily multivitamin
Allergien: Penicillin, latex, sulfates
Vorherige Impfungen: -

VAERS 1095302

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 63,0
Geschlecht: M
Eingang: 12.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Blood glucose normal Tremor

Symptomtext

I started feeling mildly shaky sometime between 10:16 PM and 10:32 PM. I am a diabetic, so I took a blood glucose reading to determine if my blood glucose levels were low (which can cause mild shakiness). They were not (reading was 172 mg/dL), but by the time I took that reading at 10:32 my shakiness had increased from onset, and I was so shaky at 10:35 PM that I was not sure if I could take my bedtime injection of Levemir safely. I was only able to do so by injecting myself and then letting the insulin rest on the palm of my hand (rather than hold it firmly as I usually do). Although the shakiness began to subside several minutes later, I was unable to fully control my toothbrush in my mouth when brushing my teeth. I then got in bed, and the shakiness was gone by around 11:00 PM (I didn't record the exact time).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes Hypothyroidism
Andere Medikamente: Levothyroxine Sodium Novolog Levemir Atorvastatin Calcium 81mg asipirin Vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 1094930

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 25,0
Geschlecht: M
Eingang: 12.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Condition aggravated Dizziness Fear of injection Feeling hot

Symptomtext

Patient began feeling dizzy and hot about 10 minutes after receiving vaccination. Notified staff, Dr assisted patient to floor with his feet elevated. VS done, juice and crackers given, Patient stated, "This happens all the time. I have anxiety about needles." Left clinic in no distress, no dizziness.

Weitere VAERSDATA-Felder

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

VAERS 1092648

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IN
Alter: 36,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 08.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chills Fatigue Feeling cold Feeling hot Muscle spasms Pain Pyrexia Tremor

Symptomtext

At 2:50 am on 3/9/21 (about 7.5 hours after receiving the vaccine), I awoke to my body shaking intensely. It felt like a muscle spasm or like electricity was being pulsed through my body. First it would happen in one leg, and then the leg would curl up under my body. Then it would spasm in my chest and my arms would be drawn inward. Then the other leg, or sometime multiple locations at once. I didn't feel cold at the time. This lasted for 40 minutes total. I took 1000 mg Acetaminophen at 3:00 am. Then, as the shaking lessened, I became very cold. I put on lots of clothes and laid on a heating pad under my comforter. Sometime later, I became very hot. Throughout the night into the morning, I felt feverish and chilled back and forth. At 6:00 am I took 200 mg Ibuprofen. I then spent the rest of the day with fever, chills, and body aches. Everything was achy and I was very tired. I slept well that night. The next day I was fatigued.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Acidophilus, Bifidus, Vitamin D3, Vitamin B-6, Zinc, Magnesium, AlliBiotic CF
Allergien: None
Vorherige Impfungen: -

VAERS 1092128

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: MD
Alter: 26,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 06.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Balance disorder Chills Feeling hot Influenza Initial insomnia Pain Paraesthesia Pyrexia Tremor

Symptomtext

Around 8 pm (about 6 hours after receiving the vaccine) I started to feel typical flu symptoms such as chills and aches, and I had some body shaking as well. I was in bed that night and the symptoms kept getting stronger, and around 11 pm I started to feel tingling throughout my body, mostly in my hands and feet. It was very uncomfortable to lay still and I felt I'd never be able to fall asleep if I couldn't lay still. I took 10mg of Z-Quil around 11:30 pm. My body and skin was also starting to get very hot, I never took my body temperature but I probably had a fever. I put a cold compress on my forehead. I also took 1000 mg acetaminophen and 400 mg Advil. I got up to use the bathroom and I could walk but my balance was off and I felt tingling up my legs. I laid back in bed with the cold compress again and the tingling in my hands and feet increased. I tried walking around again and again felt tingling up my legs. I sat on the edge of my bed moving my feet around which helped the tingling, but when I laid down again the tingling kept coming back. I took another 10mg of Z-Quil and 0.25mg xanax (prescription for anxiety). I finally decided to move to a chair with lots of pillows so I could sit upright since that helped reduce the tingling. I finally fell asleep sometime after 12:30 am. I woke up in the chair around 2 am and was feeling better - no tingling, no body shaking, chills and aches were reduced and body temperature didn't feel as high. I was then able to sleep in bed for the rest of the night. The next day I still had aches and chills and a fever but it was manageable with Advil or acetaminophen, and by Monday (March 8) I was able to go to work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety, OCD
Andere Medikamente: 300 mg sertraline, birth control pill, daily multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1092095

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: AZ
Alter: 80,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dyspnoea Hypoaesthesia

Symptomtext

Vaccine given at 545 PM, pt left the clinic and came back at 623 with complaints of shortness of breath and facial numbness. Vitals were 150/80 97% on RA HR 80 and RR 18. At 630 PM vitals were 115/65 HR 92 100% on RA and RR 18. Pt reported all symptoms had resolved by that time and left the clinic.

Weitere VAERSDATA-Felder

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

VAERS 1091600

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Dysgeusia Paraesthesia oral Tongue discomfort Tongue pruritus

Symptomtext

My tongue started feeling itchy, I have a metal taste in my mouth. It has been this way since about an hour after I got the shot. Itchy has turned into like a tingling but also the feeling it you "burn" your tongue. It is not uncomfortable but a symptom that was not listed on the affects

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Penicillin, Strawberries, Avocados, Jalapenos, Lavender, Cedar, Grass, Eucalyptus, adhesives
Vorherige Impfungen: -

VAERS 1091445

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WI
Alter: 31,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal discomfort Chills Dizziness Injection site pain Migraine Pain Sleep disorder Tremor

Symptomtext

From 6pm-5am I experienced a terrible migraine, horrible body aches (every joint and muscle was throbbing), upset stomach, uncontrollable shaking/chills, and light headedness. Could only sleep short spurts after taking 400 mg of Ibuprofen. 24 hours after the vaccination, my body is still achey, sore at injection site, and uneasy stomach.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fish oil, potassium, magnesium, iron, multi vitamin, Claritin
Allergien: None
Vorherige Impfungen: Flu shot- age ~23, unsure of date and brand: vomiting, chills

VAERS 1090569

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: KY
Alter: 45,0
Geschlecht: M
Eingang: 11.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Feeling hot Nasopharyngitis Palpitations Sleep disorder Tremor

Symptomtext

Nine hours after receiving vaccine I started "trembling, shaking." Not convulsing, more like really cold. My temperature read 97.2 degrees. My normal temperature is 98.6 degrees. Shaking stopped around 11:30 p.m. I woke up at 3:15 a.m. very hot with my heartbeat racing. I did not measure heartbeat rate. I woke up this morning at 5:30 a.m. with no side effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Nexium Potassium 99 mg Mens One A Day Multi-Vitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1089229

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: TX
Alter: 32,0
Geschlecht: M
Eingang: 10.03.2021
Impfdatum: 08.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chest X-ray Dyspnoea Electrocardiogram Fatigue Laboratory test Respiratory rate decreased

Symptomtext

tiredness, breathing heavy, low raspatory rate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: ekg, chest xray, lab panel
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, sleep apnea, chronic gastroparesis,
Andere Medikamente: omeprazole 20mg, lisinopril 20mg, atorvastatin 20mg, singulair 10mg, albuterol 90mcg, vitamin d2 1250 mcg,
Allergien: -
Vorherige Impfungen: -

VAERS 1088910

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IN
Alter: 29,0
Geschlecht: F
Eingang: 10.03.2021
Impfdatum: 09.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Erythema Fatigue Gait disturbance Impaired work ability Malaise Migraine Myalgia Pain Pyrexia Thirst

Symptomtext

Around 3:15 in the afternoon, I began experiencing severe aches and muscle pains, combined with a growing migraine. Not realizing what it may be related to, I took two ibuprofen and I've acetaminophen. By the time I around home around 6:30, I could barely hold myself up. I ate dinner, which only helped minimally, and by 8 pm felt like death. My husband notice I looked red and felt my forehead, immediately going for the thermometer. I had a fever of 100.5. We eventually got me into bed after downing a lot of water, but the pain would not ease up. The pain was too excruciating. At 10:30 my husband came to bed and we took my temp again which was 101.6. To help me sleep I took another Tylenol. At 5:45 my work alarm went off and I checked my temp again; still 101.6. I got a cold pack for my migraine and went back to sleep. Slowly throughout the day my fever dwindled, until it finally broke in the early afternoon. By 4:15, as I am writing this, all that's left is done tiredness, thirst, and a small bit of achiness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Mental illness and disabilities
Vorgeschichte: Knee and ankle joint problems ADHD Low blood pressure
Andere Medikamente: Straterra 100 mg Lexapro 20 mg Lyrica 75 mg x2/ day Vitamin D3 25 mcg (1000 IU) Iron 65 mg Allegra 180 mg Omega-3 540 mg Seroquel 25 mg Melatonin 10 mg Ibuprofen as needed Acetaminophen as needed Flonase as needed
Allergien: Prozac (potential anaphylaxis) Adderall (hives) Amoxicillin (nausea, fever, vomiting) Nickle Corn Pollen (may contribute to mild corn allergy, still being tested) Significant seasonal allergies
Vorherige Impfungen: -

VAERS 1088851

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 10.03.2021
Impfdatum: 08.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Herpes zoster Pain

Symptomtext

Patient complained of a shingles flare the day after receiving vaccine and also described intensification of chronic pain, above and beyond normal, for the two days since her vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1087261

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: WI
Alter: 34,0
Geschlecht: F
Eingang: 10.03.2021
Impfdatum: 09.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Headache Injection site pain Pain Palpitations Pyrexia

Symptomtext

Fever of 102, chills, aches, minor heart racing, injection site pain, headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Central post stroke pain syndrome, anxiety
Andere Medikamente: Lorazepam prn, ERIN birth control
Allergien: None
Vorherige Impfungen: -

VAERS 1084612

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: OH
Alter: 65,0
Geschlecht: F
Eingang: 09.03.2021
Impfdatum: 08.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hypotension Injection site pain Pain in extremity

Symptomtext

Patient received Janseen COVID vaccine. The first 1/2 of the vaccine was given easily IM to the left deltoid and then the patient complained of severe arm pain, tensed her muscles, and the last 0.25ml was difficult to inject. Then the patient became hypotensive 90/45, dizzy, and felt like she was going to pass out. She was laid in the supine position, given a cool cloth for her forehead and monitored for approx. 45 minutes. Her blood pressure remained 90/60, 96/56 at discharge. Her heart rate ranged from 55-65, regular. Her son came to take her home as we did not feel comfortable with the patient driving. The patient was continuously monitored by the NPs and APCT. She ambulated without difficulty and was discharged home. She was given information for V-safe to report her reaction and advised to follow up in the ER for any SOB, difficulty breathing, difficulty swallowing, syncope, CP, etc.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: HTN, anxiety
Andere Medikamente: citalopram, blood pressure medication (patient does not remember name)
Allergien: NKA
Vorherige Impfungen: -

VAERS 1080993

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: VA
Alter: 55,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 07.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Pyrexia Tremor

Symptomtext

Severe shaking started at 11 PM and continued for over an hour. Including teeth shattering. Had a low grade fever also.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Omeprazole Vitamin D Atenolol Statin Multi Vitamin
Allergien: none
Vorherige Impfungen: -

VAERS 1080464

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: SD
Alter: 58,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 07.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Chills Headache Pain Paraesthesia Pyrexia

Symptomtext

Tingling started at fingertips felt it go thru my whole body to my toes. Severe headache, fever, chills, body/joint aches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Will notify my family doctor when clinic opens
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Blood pressure med & high cholesterol med
Allergien: Penicillin, oxycodone
Vorherige Impfungen: -

VAERS 1077371

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

moderat

Staat: IL
Alter: 38,0
Geschlecht: F
Eingang: 06.03.2021
Impfdatum: 05.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Blood pressure increased Dizziness Palpitations

Symptomtext

Patient had sudden onset of sensation of palpations and light headedness "lasting one second" in middle of night on the day after receipt of COVID-19 vaccine. Felt urgent need for medical treatment & came to our ER. Has had similar episodes previously that have been partly diagnosed as anxiety though without light-headedness. Vitals in ER HR 141, BP 147/101. Believed to be sinus tachycardia. Has been prescribed venlafaxine, lorazepam, and metoprolol previously for this. Has seen cardiologist but per patient no specific diagnosis. As yet, patient has received a fluid bolus in ER.

Weitere VAERSDATA-Felder

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

VAERS 2620380

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: IL
Alter: 47,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 06.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 56,0
Dosis: 1
Route/Site: SYR / LA

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

Acoustic stimulation tests Headache Pain in jaw Tinnitus Toothache

Symptomtext

Tinnitus - 24/7 since onset, sound of varying degrees of volume Symptoms also include pain in teeth and jaw, headaches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: ENT Appt - Hearing Test - 07/21/2021 ENT Appt - Hearing Test - 08/16/2021
Aktuelle Erkrankungen: n/a
Vorgeschichte: Sensitive GI with upset stomach
Andere Medikamente: Bupropion, naltrexone (combination helps constant upset stomach), D3
Allergien: Dairy, Tert-butylhydroquinone (tBHQ)
Vorherige Impfungen: -

VAERS 2593111

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 08.03.2023
Impfdatum: 19.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Injection site pain Pain

Symptomtext

She recalls that when she had the injection, it "was very painful going in" and pain increased in severity over time, after a few weeks "the pain morphed" from injection site pain to more profuse anterior shoulder and arm pain, pointing from the R AC joint down biceps region. She states "pain is 24/7" and "it does not go away", though it does improve at rest. She describes a constant, dull ache, with worst when lying down in supine with the arm unsupported at her side

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2526867

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 08.12.2022
Impfdatum: 06.04.2021
Beginn: 30.11.2022
Tage bis Beginn: 603,0
Dosis: 1
Route/Site: - / -

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

Anticoagulant therapy Arthralgia Asthenia COVID-19 Chest X-ray normal Cough Device breakage Fall Femur fracture Gait disturbance Joint injury Limb injury Pain in extremity Plantar fasciitis Productive cough SARS-CoV-2 test positive Walking aid user X-ray abnormal

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 11/30/2022 Discharge Date: 12/4/2022 COVID positive date: 11/30/2022 PRESENTING PROBLEM: Weakness [R53.1] Generalized weakness [R53.1] COVID [U07.1] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 77 y.o. male with prior medical history of hypertension, ischemic cardiomyopathy, type 2 diabetes, hyperlipidemia, atrial fibrillation (on Eliquis), arthritis and iron deficiency anemia. He presented to the hospital on 11/20/2022 for evaluation of weakness. The patient fell /at home on 11/26/2022. He was evaluated in the emergency department at that time and found to have a right femur fraction that was deemed inoperable. The patient was instructed to weight bear as tolerated and follow up outpatient with Orthopedics. The patient noted that he had more difficulty ambulating at home which got progressively worse over the past few days thus he proceeded to present back for evaluation on 11/30. Endorses a cough and sputum production but notes that this has been ongoing for 3 weeks and not much different from his baseline. Denies any known exposures to COVID-19 however did test COVID 19 positive in the emergency department. Physical therapy and occupational therapy consult were completed and recommended SAR.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: Emergency visit 11/26/2022 notes: Patient is a 77-year-old male that presents after a trip and fall. He notes he was at church and was pushing a trash can up ramp when he accidentally tripped and fell and landed on some chairs. He landed on his right hip and had pain. He was able to get up, ambulate and actually drive himself home but had worsening pain and comes in for reevaluation. He has very mild injury to his right shoulder but denies any pain elsewhere. He is anticoagulated on Eliquis but notes his fall was minor and had no injury to his head or neck. Has had no confusion or nausea or vomiting. He otherwise denies any other pain in his chest, ribs, back, or other extremities. An x-ray of his hip and femur was performed that does show concern for a some trochanteric proximal femur fracture that is periprosthetic. Chest x-ray was performed as well and is unremarkable. His concern for proximal femur fracture around the prosthesis was discussed with Dr. orthopedic surgery. We discussed that this is nonoperative at this time point with outpatient follow-up. He is able to ambulate with us and with a walker which he uses at baseline. He will be given pain control believe he can follow-up with orthopedic surgery on an outpatient basis after discussion with orthopedic surgery. He was discharged home in stable condition. Emergency 11/28/2022 HISTORY OF PRESENT ILLNESS: Patient presents to the ER by ambulance complaining of some right shoulder pain left heel pain. He was involved in a fall last Saturday at church and was seen another facility. They did find that he had an acute non operative proximal femur fracture on the right that did go into his prosthesis. He is evaluated by the Orthopedic Service and again they thought it was a non op and he can use his walker at home. He has been doing this. He said he did tell about his shoulder pain but nobody x-rayed it. He has also been complaining at 2 days of left heel pain as well. He has not had any new falls he says. Denies any new numbness or tingling. He does not know if he actually injured the shoulder with the fall but the next day it was hurting him. MEDICAL DECISION MAKING: Supervising Physician: DO Right shoulder film did not show any acute fracture dislocation. We did place a lidocaine patch. Patient will take Tylenol for pain use cool or warm compresses. Left heel x-ray did show he did have a spur. There is no other acute findings. I did discuss possibility of gel heel cups. He will follow up as needed. He is comfortable the plan. Questions were addressed and answered to his satisfaction. He will continue to use his walker at home and follow-up with Orthopedic Service as already been discussed on his previous visit to the outlying facility.
Vorgeschichte: Sinusitis Hypertension Atrial fibrillation, persistent Ischemic cardiomyopathy PVC (premature ventricular contraction) Class 2 obesity in adult Arthritis Anemia Iron deficiency anemia Gross hematuria Type 2 diabetes mellitus Hyperlipidemia Hematuria At risk for falls Generalized weakness with fall Femur fracture, right
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet apixaban (ELIQUIS) 5 MG tablet aspirin 81 MG enteric coated tablet Blood Glucose Monitoring Suppl MISC carvedilol (COREG) 25 MG tablet Contour Next Test Strips ENTRESTO 24-26 MG TABS ferrous sulfate 325
Allergien: Metformin Sulfa Drugs Lovenox [Lmw Heparin
Vorherige Impfungen: -

VAERS 2270953

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 11.03.2021
Beginn: 11.02.2022
Tage bis Beginn: 337,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

02/12/22 presents to ED for "nausea with vomiting". PMHx of " HTN, HLD, hypothyroidism"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: 02/15/22 SARS-CoV-2 (COVID-19) by NAA detected 02/12/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2243482

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 20.04.2022
Impfdatum: 08.03.2021
Beginn: 25.08.2021
Tage bis Beginn: 170,0
Dosis: UNK
Route/Site: - / -

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

Bile output decreased COVID-19 Nausea SARS-CoV-2 test positive

Symptomtext

8/25/21 PMH of afib, HTN, AAA repair, pancreatitis, and acute cholangitis. General surgery being consulted for decreased output from his biliary drain and nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: 8/25/21 SARS-CoV-2 (COVID-19) by NAA, Micro Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2214240

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 18.03.2021
Beginn: 19.01.2022
Tage bis Beginn: 307,0
Dosis: UNK
Route/Site: - / -

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

Abdominal pain Back pain COVID-19 SARS-CoV-2 test positive

Symptomtext

01/19/22 presents to ED for "abdominal pain and back pain". PMHx of "PSC cirrhosis"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: 01/19/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2211746

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: MI
Alter: 58,0
Geschlecht: M
Eingang: 01.04.2022
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia

Symptomtext

patient had shoulder pain on vaccinated arm for a couple months. also had with the moderna vaccine (as a booster) on 11/1/21

Weitere VAERSDATA-Felder

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

VAERS 2209241

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: TX
Alter: 61,0
Geschlecht: M
Eingang: 31.03.2022
Impfdatum: 25.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Fatigue Headache Pain in extremity Pyrexia

Symptomtext

Headache, fever, sore arm, tired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: mild cholesterol
Andere Medikamente: 10 mg Atorvastatin 81 mg aspirin multivitamin 500 mg Vitamin C
Allergien: None
Vorherige Impfungen: -

VAERS 2194313

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: IN
Alter: 48,0
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 19.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / LA

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

Arthritis Injection Limb discomfort Musculoskeletal discomfort Pain X-ray abnormal

Symptomtext

Discomfort started a few weeks after first vaccine in my right big toe. Felt as if needed to "pop" but never could. Saw my family physician, thinking it might be gout, however after exam he diagnosed arthritis and prescribed a topical cream. I received the booster on 10/26/21 of the J&J. Within 4 days of receiving the booster I began a more severe discomfort in my right ankle- almost as if I had rolled/sprained my ankle. I tried home remedies- wrapping, ice, elevation, ibuprofen but there was no relief and shooting pain when going down steps. This time I went to an orthopedic specialist- who confirmed the original diagnosis and added the arthritis diagnosis for the ankle as well. I received two cortisone shots one in the joint of my big toe and another in the ankle. This relieved the pain from the arthritis. The doctor said I could get these shots every three months.... It is currently the end of March and the pain is starting to resurface now that the cortisone shot is coming to a conclusion. Because there is no other place to list it- I received the booster at on 10/26/2021 at 10:00am lot number is above.

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Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: X-ray to determine arthritis
Aktuelle Erkrankungen: NA
Vorgeschichte: High Cholesterol
Andere Medikamente: Vitamin D3 1000mg; Vitamin C 1000mg; Rosuvastatin 10mg
Allergien: Bee stings
Vorherige Impfungen: -

VAERS 1180602

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: KY
Alter: 48,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 07.04.2021
Beginn: 22.01.2022
Tage bis Beginn: 290,0
Dosis: 1
Route/Site: IM / RA

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

Chills Dizziness Headache Pain COVID-19 SARS-CoV-2 test positive

Symptomtext

Tested Positive for Covid

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

VAERS 2141986

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: MI
Alter: 58,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 18.03.2021
Beginn: 08.12.2021
Tage bis Beginn: 265,0
Dosis: 1
Route/Site: OT / -

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

COVID-19 Malaise SARS-CoV-2 test SARS-CoV-2 test positive Transient ischaemic attack Vaccination failure

Symptomtext

TRANSIENT ISCHAEMIC ATTACK; CONFIRMED CLINICAL VACCINATION FAILURE; COVID-19; SARS-COV-2 TEST POSITIVE; MALAISE; This spontaneous report received from a health care professional by a Regulatory Authority (VAERS FDA, US-VAERS-1944320-OGNM-20211224160546) on 24-DEC-2021 and concerned a 58 year old male of unknown race and ethnic origin. The patient's height, and weight were not reported. The patient's concurrent conditions included: type 2 diabetes, obesity, and nephrolithiasis. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025 expiry: UNKNOWN) dose was not reported, 1 total administered on 18-MAR-2021 for an unspecified indication (Dose number in series 1). Drug start period was 265 days. No concomitant medications were reported. On 08-DEC-2021, the patient experienced symptoms of transient ischaemic attack, confirmed clinical vaccination failure, covid-19 , sars-cov-2 (Severe acute respiratory syndrome coronavirus 2)test positive, malaise, and was hospitalized (date unspecified). Laboratory data included: SARS-CoV-2 test (NR: not provided) positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the malaise, sars-cov-2 test positive, transient ischaemic attack, covid-19 and confirmed clinical vaccination failure was not reported. This report was serious (Hospitalization Caused / Prolonged). This report was associated with a product quality complaint: 90000208902. The suspected product quality complaint has been confirmed to be the reported allegation was not confirmed and the root cause was determined to be not manufacturing related based on the PQC evaluation/investigation performed. Additional information was received from Central Complaint Vigilance on 22-FEB-2022. The following information was updated and incorporated into the case narrative: product quality complaint investigation result was added.; Sender's Comments: V1:This version is created to update the information regarding Product quality complaint investigation result was added, This updated information does not change the causality of the previously reported events. 20211255599-covid-19 vaccine ad26.cov2.s- transient ischaemic attack, covid-19, sars-cov-2 test positive, malaise. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). 20211255599-covid-19 vaccine ad26.cov2.s- confirmed clinical vaccination failure . This event is considered not related. The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event than the drug. Specifically: SPECIAL SITUATIONS

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Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Test Date: 20211208; Test Name: SARS-CoV-2 test; Result Unstructured Data: positive
Aktuelle Erkrankungen: Nephrolithiasis; Obesity; Type II diabetes mellitus
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2057481

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: FL
Alter: 60,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 14.03.2021
Beginn: 19.01.2022
Tage bis Beginn: 311,0
Dosis: UNK
Route/Site: - / -

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

Asthenia Atelectasis Back pain COVID-19 Chest X-ray abnormal Nausea Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. Vaccinated on 03/14/2021. 60 y/o PMH chronic Pancreatitis and biliary obstruction with stent, HTN, Chronic pain opiod dependent, anxiety , CKD stage 4 and recently diagnosed with breast malignancy presents to ED with c/o fever, back pain, weakness and nausea worsening past 3 days. t-103, O2 2L NC, CXR-subsegmental atelectasis lower lobes. Treated with steroids and abx.

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Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19 -Detected 01/19/2022
Aktuelle Erkrankungen: -
Vorgeschichte: CKD stage 4, HTN, Hypothyroid, Pancreatitis, Breast BX positive for malignancy
Andere Medikamente: -
Allergien: ASA, Cipro, contrast dye, codeine, darvocet, Fentanyl, Iodine, Morphine, NSAIDS, Percocet, Vicodin
Vorherige Impfungen: -

VAERS 2027685

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: MI
Alter: 57,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 17.03.2021
Beginn: 17.11.2021
Tage bis Beginn: 245,0
Dosis: 1
Route/Site: - / -

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

Abnormal behaviour COVID-19 Dizziness Leukocytosis SARS-CoV-2 test positive

Symptomtext

Patient is COVID positive 11/17/2021. Fully vaccinated. Presented to the ED for dizziness and "not acting himself" + for leukocytosis. Decision to discharge patient. Patient told to return to ED for any worsening symptoms.

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

VAERS 2014468

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: -
Alter: 30,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 13.03.2021
Beginn: 07.01.2022
Tage bis Beginn: 300,0
Dosis: UNK
Route/Site: SYR / RA

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

Discomfort Disorientation Fatigue Headache Illness Lethargy Loss of personal independence in daily activities Nausea Pain Pyrexia

Symptomtext

At approximately 18:00 I phoned my father to pick me up as I was unable to care for my son per my symptoms of intense headache, lethargy, nausea, full-body aches, fever, and disorientation. I instructed him to take me to the hospital if I should become non-responsive. He caretook for me (ice pack, etc.) and supervised me for the next 72 hours where I was completely stricken to bed. Most of this Friday evening and Saturday I was agonizing in pain and discomfort. I believe the fever held for Friday and the majority of Saturday where it dropped to a low-grade fever. By Sunday, symptoms had begun to subside but did not cease. I had to call out of work on Monday. By Monday evening I had mostly returned to normal save for exhaustion from the experience. There were 3 witnesses to this event and it was the most severely I have been ill in my life that I can remember. I was too disoriented that weekend to navigate reporting system (I did start) but feel it is my responsibility to do so. Though not formally indicated below, I did fear for my life and safety and informally consulted with a physician following the event.

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

VAERS 2010694

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: NY
Alter: 67,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 09.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Alopecia Arthralgia Asthenia Blood test abnormal Fatigue Headache Inflammatory marker increased Magnetic resonance imaging head Magnetic resonance imaging normal Myalgia Pain in extremity Pyrexia Red blood cell sedimentation rate increased Renal impairment Stress Swelling face Vision blurred

Symptomtext

Starting that evening of the vaccine, I had a mild fever. Then, I developed a headache, severe joint pain and muscle pain that night. I waited 2 weeks to see if it would go away on its own. It did not, so I called the doctor and they did blood work. It showed elevated sed rate/inflammatory markers and was put on steroids off and on for at least 3 months. I ended up seeing a vascular surgeon to check on my leg to make sure the pain was not coming from poor circulation. Told to wear compression socks. I was sent to see a urologist due to decreased kidney function. Increasing fluids helped my kidney function to come back normal. Also, I developed blurry vision and swelling around the eyes, so I saw an ophthalmologist to rule out any issues. I was given steroid eye drops and I used them for a bit of time off and on as well. Also, I felt weak/tired during this event. I was sent to see a neurologist and get an MRI of the head to ensure I did not have a blood clot for the severe headaches. My hair started falling out around the same time, and was seen by a dermatologist who said it was likely due to severe medical stress. I had to use rogaine to help the hair grow back. My SED rate has not gone back to normal, hence why I was told to get a different booster shot.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: MRI of head: came back normal; Lots of blood work: Showing elevated inflammatory markers and decreased kidney function. SED rate is still coming back abnormal.
Aktuelle Erkrankungen: None
Vorgeschichte: Polymyalgia rheumatica; Asthma and seasonal allergies
Andere Medikamente: Emergen-C with Zinc and B vitamins; Vitamin D; Magnesium; Mushroom Caps
Allergien: Penicillin; Erythromycin; and Brimonidine
Vorherige Impfungen: 40 years ago thyroiditis due to small pox vaccine and autoimmune issues since then

VAERS 1992523

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: -
Alter: 56,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 16.03.2021
Beginn: 26.12.2021
Tage bis Beginn: 285,0
Dosis: 1
Route/Site: - / -

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

Abdominal discomfort Abdominal pain Asthenia COVID-19 Cough Dry skin Fatigue Feeding disorder Hyperglycaemia Illness Laboratory test abnormal Nausea Pyrexia SARS-CoV-2 test positive Upper respiratory tract infection Vomiting

Symptomtext

ADMISSION: 12262021: co illness x 1.5 weeks. sts "it feels like when I had DKA", abd pain n/v, unable to eat since Thursday, this is 3rd MD visit since illness onset, on Mon began abx for shortness of breath, cough, BA, chills, fatigue, & fever. Denies increased urine output. Presents to the emergency department today for nausea, vomiting, fever, and generalized abdominal discomfort. Patient is a type 2 diabetic controlled on multiple medications, initially metformin for years, then oral and eventually added insulin a year or two ago. He states a week and a half ago he had URI symptoms and tested COVID negative, got a Zpak from his PCP last Monday. Cough has persisted and fatigue. Felt weak today and felt "like when I had DKA before" and came back to the ED. On room air, COVID swab positive, lab not c/w DKA but dry and hyperglycemic. States had Johnson and Johnson vaccine last March and has not gotten booster because "I'm sick every time I think about making an appointment to get it". DISCHARGE: 12272021: no discharge instructions posted at this time.

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

VAERS 1978460

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: HI
Alter: 73,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 26.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Limb discomfort Malaise

Symptomtext

DISCOMFORT IN ARM; NOT FEELING WELL; This spontaneous report received from a patient concerned a 73 year old male. The patient's height, and weight were not reported. The patient's past medical history included: myocarditis and pericarditis in 1970. The patient was previously treated with covid-19 vaccine ad26. cov2. s(suspension for injection, route of admin not reported, batch number: 1805025 expiry: UNKNOWN) dose was not reported,1 total administered on 26-MAR-2021 to right arm for prophylactic vaccination.(Dose number in series 1). On 26-MAR-2021, the patient had discomfort in arm, and was not feeling well which lasted a few days (events occurred on dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A expiry: UNKNOWN) dose was not reported,1 total administered on 12-NOV-2021 for prophylactic vaccination (Dose number in series 2). No adverse events reported with booster dose. No concomitant medications were reported. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from discomfort in arm, and not feeling well. This report was non-serious.

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Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Myocarditis; Pericarditis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1944320

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: MI
Alter: 58,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 18.03.2021
Beginn: 08.12.2021
Tage bis Beginn: 265,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Malaise SARS-CoV-2 test positive Transient ischaemic attack

Symptomtext

symptoms of TIA and covid 19, 12/8/21

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Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: SARS-CoV-2 (COVID-19) by NAA, Micro detected 12//21
Aktuelle Erkrankungen: -
Vorgeschichte: type 2 diabetes, obesity, nephrolithiasis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1880612

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: TX
Alter: 63,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 08.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Feeling abnormal Pain Pyrexia

Symptomtext

From post vaccine 7 hours through 48 hours, I had aches, chills, low grade fever (below 101) and felt bad. This resolved eventually. I took Tylenol to help.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension Low Thyroid
Andere Medikamente: Lisinopril HCTZ 10mg 12.5mg Estradiol Levothyroxine 50mcg Desvenlafaxine ER 100mg Atenolol 50mg Montelukast 10mg Fish Oil Red yeast rice Melatonin
Allergien: Lodine
Vorherige Impfungen: -

VAERS 1862349

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: IL
Alter: 52,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 06.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 23,0
Dosis: 1
Route/Site: SYR / LA

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

Blood fibrinogen increased C-reactive protein increased Carbon dioxide normal Dry skin Fatigue High density lipoprotein increased Inflammation Low density lipoprotein decreased Mean cell haemoglobin concentration decreased Nodule

Symptomtext

Extreme and Prolonged Exhaustion with Inflammation throughout body. Inflammation mostly in right and left legs, knee and ankle area. nodules on top of both knees and right forearm. Dry skin spots on legs.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: May 3, 2021 Blood Testing: full CBC, Chem and Lipid Panel with out of range results of MCHC=31.8, LDL=135, HDL=3.1, CO2=30 9-22-2021 Blood Testing C REative Protein high 9.2 10-14-2021 Fibrinogen high 616.40
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Adderall 15 mg, Vitamin D, Vitamin B
Allergien: None
Vorherige Impfungen: -

VAERS 1814869

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: AL
Alter: 39,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 18.03.2021
Beginn: 28.03.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Antinuclear antibody increased Balance test Blood test normal Dizziness Feeling abnormal Magnetic resonance imaging normal Meniere's disease Vertigo Vestibular disorder

Symptomtext

Vaccine received on 3/18/2021 Brain fog and dizziness started on 3/28/2021 Progressively worsened until first intense vertigo episode on 5/3/2021. After this date, dizziness is constant. (1st) ENT prescribed meclizine, it did not help. Also prescribed prednisone, 21 days of strong dosage followed by 10 days tapering off. It helped a little, but did not fix anything. Episodes seemed to be worse around menstrual cycle, lasting days. Audiologist did balance test on Aug 19, 2021 and found uncompensated vestibular dysfunction and CNS involvement. Referred to PT for Vestibular Rehab (did 4 weeks), it didn?t help. Referred to neurologist; he was useless. Currently waiting to see 2nd neurologist. Ever since the balance test on Aug 19, I have had 3-5 intense vertigo and inner ear episodes every single week. Every. Single. Week.

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: May 12, 2021-ENT Dr. prescribed prednisone for a month (21 days followed by 10 days tapering off) May 18, 2021- MRI; came back clear June 2, 2021- Dr diagnoses me with Menieres Disease. I have another inner ear fullness and popping/vertigo episode and he prescribed me 10 days of steroids; it didn?t fix anything. August 19, 2021- Balance test; found uncompensated vestibular dysfunction and CNS involvement. August 27, 2021- bloodwork from general practitioner; came back clear August 21, 2021- received acupuncture; did not help September 1, 2021- started vestibular physical therapy; 4 concurrent weeks with no change September 8, 2021- started new ENT; does NOT think I have Menieres Disease. October 7, 2021- started me on triamterene (diuretic) with low sodium diet; blood work. Has helped just a little bit but not much. October 14, 2021- Dr. says bloodwork came back with high ANA levels. Awaiting what we?re going to do next.
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: Multivitamin Chlorophyll Turmeric Super Lysine Sacc B probiotic
Allergien: NONE
Vorherige Impfungen: -

VAERS 1804482

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: AL
Alter: 57,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Headache Musculoskeletal stiffness Ocular discomfort

Symptomtext

Headaches and stiff neck for 2 weeks and blocked oil glands in right eye.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes Epilepsy
Andere Medikamente: Tegretol Victoza Atenolol Estradiol
Allergien: N/A
Vorherige Impfungen: -

VAERS 1785590

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: KY
Alter: 57,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 09.03.2021
Beginn: 01.10.2021
Tage bis Beginn: 206,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Pain in extremity Peripheral swelling

Symptomtext

Pain in knees. some swelling, and pain in lower legs. States MD ruled out blood clots

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: chf, IBS, high blood pressure, anemic, hypothyroid, digenerative disc disease,
Andere Medikamente: actos, glimepiride, gardience, libteroxin, omperazole, aspirin, losartan, amipine, potassium, metropzole, carbamazeime, ducalax, simtcione, loperamide, fiber, imodium
Allergien: Fish iodine
Vorherige Impfungen: -

VAERS 1776829

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1805025

mild

Staat: -
Alter: 48,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 24.03.2021
Beginn: 01.10.2021
Tage bis Beginn: 191,0
Dosis: UNK
Route/Site: - / -

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

Ageusia Anosmia Cough Fatigue Nasal congestion Pyrexia

Symptomtext

fever, loss of taste and smell; fatigue, cough and nasal congestion

Weitere VAERSDATA-Felder

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