VAERS Reports 1855194

VAERS 1562206

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 15.02.2023
Impfdatum: 22.11.2021
Beginn: 07.12.2022
Tage bis Beginn: 380,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Acute respiratory distress syndrome Acute respiratory failure Angiogram pulmonary Angiogram pulmonary normal Anticoagulant therapy Bacteraemia Blood culture Blood culture positive Blood gases Blood gases abnormal COVID-19 COVID-19 pneumonia Candida infection Central venous catheterisation Chest X-ray Chest X-ray abnormal Culture

Symptomtext

ACUTE KIDNEY INJURY; PULMONARY HYPERTENSION; SARS-COV-2 TEST POSITIVE; ACUTE RESPIRATORY DISTRESS SYNDROME; PULMONARY HYPERTENSION; SEPTIC SHOCK; GRAM STAIN POSITIVE; ACUTE RESPIRATORY FAILURE; ACUTE RESPIRATORY DISTRESS SYNDROME; HYPOKALAEMIA; LUNG OPACITY; BACTERAEMIA; HYPOKALAEMIA; COVID-19 PNEUMONIA; PULMONARY OEDEMA; LACTIC ACIDOSIS; RIGHT ATRIAL ENLARGEMENT; PULMONARY OEDEMA; BLOOD CULTURE POSITIVE; TOXIC ENCEPHALOPATHY; ANGIOGRAM PULMONARY NORMAL; VIRAL SEPSIS; PO2 DECREASED; COVID-19; LACTIC ACIDOSIS; CANDIDA INFECTION; TOXIC ENCEPHALOPATHY; HAEMATURIA; HYPERNATRAEMIA; HYPERGLYCAEMIA; LEUKOCYTOSIS; HYPERNATRAEMIA; LUNG INFILTRATION; LEUKOCYTOSIS; RIGHT VENTRICULAR ENLARGEMENT; LUNG INFILTRATION; ANTICOAGULANT THERAPY; LUNG OPACITY; CENTRAL VENOUS CATHETERISATION; MALNUTRITION; INTENSIVE CARE; RIGHT ATRIAL ENLARGEMENT; PROCALCITONIN; RIGHT VENTRICULAR ENLARGEMENT; CULTURE; ANTICOAGULANT THERAPY; ACUTE RESPIRATORY FAILURE; CENTRAL VENOUS CATHETERISATION; VIRAL SEPSIS; INTENSIVE CARE; MALNUTRITION; CHEST X-RAY ABNORMAL; COVID-19; ECHOCARDIOGRAM ABNORMAL; HAEMATURIA; SARS-COV-2 TEST POSITIVE; BLOOD GASES ABNORMAL; BLOOD CULTURE POSITIVE; BACTERAEMIA; PROCALCITONIN; ECHOCARDIOGRAM ABNORMAL; CULTURE; CANDIDA INFECTION; BLOOD GASES ABNORMAL; COVID-19 PNEUMONIA; GRAM STAIN POSITIVE; HYPERGLYCAEMIA; ANGIOGRAM PULMONARY NORMAL; SEPTIC SHOCK; PO2 DECREASED; CHEST X-RAY ABNORMAL; This spontaneous report received from a health care professional via Regulatory Authority Vaccine Adverse Event Reporting System (VAERS) (VAER reference number 2562206) on 27-JAN-2023 concerned an 85 year old male of an unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's concurrent conditions included: prostate cancer, and normocytic anemia. On an unspecified date, the patient previously received covid-19 vaccine ad26.cov2.s (Unspecified manufacturer) (Dose number in series 1) (suspension for injection,, route of admin, batch number not reported expiry: UNKNOWN) dose was not reported, 1 total administered for an unspecified indication. It was unknown whether patient had any adverse events following covid-19 vaccine ad26.cov2.s (Unspecified manufacturer) (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194 expiry: UNKNOWN) dose was not reported, 1 total administered on 22-NOV-2021 for an unspecified indication. Age at time of vaccination 85 years old. No concomitant medications were reported. On 07-DEC-2022, the patient experienced acute kidney injury, acute respiratory distress syndrome, acute /hypoxic respiratory failure. Initial O2 (Oxygen) saturation was around 70% on 5 L nasal cannula. He was placed on 15 L nonrebreather and O2 (Oxygen) saturation corrected to just above 90. The patient met signs and symptoms of septic shock with viral sepsis. The patient was started was on Levophed therapy and found to have a PO2 (Partial pressure of oxygen) of 38. Chest x-ray revealed abnormal multifocal opacities (Lung opacity) infiltrates (Lung infiltration). He was started on dexamethasone broad spectrum antibiotics and breathing treatments. Initial admission was to intensive care unit started on broad-spectrum antibiotics including vancomycin and cefepime. Cultures were obtained as well as procalcitonin and antibiotics were de-escalated Confirmed COVID-19 infection required aggressive steroid therapy. His acute renal failure on presentation was prohibitive of Remdesivir therapy. Echocardiogram was obtained with preserved ejection fraction (Abnormal). The patient was noted to have right ventricular enlargement and right atrial enlargement with moderate pulmonary hypertension. A CTA (Angiogram) was obtained and negative for pulmonary embolism. Initially the patient was treated with heparin infusion pending rule out of pulmonary embolism. A left femoral central venous line was removed (central venous catheterisation) following 3 of 4 blood cultures positive for gram stain positive cocci Vancomycin was continued throughout his inpatient stay based on this patient was adequately fluid resuscitated with improvement in his lactic acidosis and his AKI. Because of his leukocytosis and bacteremia he was not an appropriate candidate for baricitinib therapy. Ultimately patient had failed to respond to aggressive broad-spectrum antibiotics with O2 (Oxygen) support and Decadron therapy. Nebulizer therapies have been provided scheduled and as needed throughout his stay without significant improvement in his pulmonary function and was hospitalized for 11 days. The patient has been followed by pulmonary service Discharge diagnosis was Acute respiratory failure with hypoxia, Viral sepsis, Septic shock, ARDS, COVID-19 pneumonia, Possible superimposed bacterial pneumonia, Acute toxic metabolic encephalopathy due to sepsis and hypoxia. Pulmonary Edema on exam Blood culture contamination Pulmonary hypertension, Acute Hypernatremia, AKI, Lactic acidosis, Hypokalemia, Thrush Hematuria, Hyperglycemia Severe protein calorie (malnutrition) (Dose number in series 2). Laboratory data (dates unspecified) included: Oxygen saturation (NR: not provided) 70 %, and Oxygen saturation 90 (Dose number in series 2). Treatment medications (dates unspecified) included: vancomycin, cefepime, heparin, Levophed and dexamethasone. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the acute kidney injury, acute respiratory distress syndrome, acute respiratory failure, angiogram pulmonary normal, anticoagulant therapy, bacteraemia, blood culture positive, blood gases abnormal, covid-19, covid-19 pneumonia, candida infection, central venous catheterisation, chest x-ray abnormal, culture, echocardiogram abnormal, gram stain positive, haematuria, hyperglycaemia, hypernatraemia, hypokalaemia, intensive care, lactic acidosis, leukocytosis, lung infiltration, lung opacity, malnutrition, po2 decreased, procalcitonin, pulmonary hypertension, pulmonary oedema, right atrial enlargement, right ventricular enlargement, sars-cov-2 test positive, septic shock, toxic encephalopathy and viral sepsis was not reported. This report was serious (Hospitalization Caused / Prolonged). This report was associated with a product quality complaint: 90000269107. 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 received from department on 10-FEB-2023. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result.; Sender's Comments: V1: This follow up version updates- Product quality complaint investigation result. This updated information does not alter the causality of previously reported events. 20230161674- Acute kidney injury, pulmonary hypertension, septic shock, hypokalaemia, bacteraemia, lactic acidosis, pulmonary oedema, toxic encephalopathy, candida infection, haematuria, hyperglycaemia, hypernatraemia, leukocytosis, lung infiltration, lung opacity, malnutrition, right atrial enlargement, right ventricular enlargement, anticoagulant therapy, central venous catheterisation, intensive care, chest x-ray abnormal, echocardiogram abnormal, blood culture positive, procalcitonin, culture, blood gases abnormal, gram stain positive, angiogram pulmonary normal, po2 decreased. The event shows an incompatible temporal relationship. Therefore, this event is considered inconsistent with vaccine administration. V0: 20230161674- acute respiratory distress syndrome, acute respiratory failure, covid-19 pneumonia, viral sepsis, covid-19, sars-cov-2 test positive. The event is deemed to be scientifically implausible, i.e., there is scientific evidence against a drug/event relationship; AND there is no known class effect. Therefore, this event is considered inconsistent with vaccine administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: Test Date: 20221207; Test Name: ANGIOGRAM PULMONARY; Result Unstructured Data: negative for pulmonary embolism; Test Date: 20221207; Test Name: BLOOD CULTURE; Test Result: Positive ; Test Date: 20221207; Test Name: BLOOD GASES; Result Unstructured Data: Abnormal; Test Date: 20221207; Test Name: CHEST X-RAY; Result Unstructured Data: multifocal opacities infiltrates; Test Date: 20221207; Test Name: CULTURE; Result Unstructured Data: Not reported; Test Date: 20221207; Test Name: ECHOCARDIOGRAM; Result Unstructured Data: preserved ejection fraction; Test Date: 20221207; Test Name: SARS-COV-2 TEST; Test Result: Positive ; Test Date: 20221207; Test Name: GRAM STAIN; Result Unstructured Data: positive for cocci Vancomycin; Test Date: 20221207; Test Name: PO2; Result Unstructured Data: Decreased, 38; Test Date: 20221207; Test Name: PROCALCITONIN; Result Unstructured Data: Not reported; Test Name: OXYGEN SATURATION; Result Unstructured Data: 70 %; Test Name: OXYGEN SATURATION; Result Unstructured Data: 90
Aktuelle Erkrankungen: Normocytic anemia; Prostate cancer
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2577987

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: MI
Alter: 62,0
Geschlecht: F
Eingang: 08.02.2023
Impfdatum: 12.11.2022
Beginn: 20.12.2022
Tage bis Beginn: 38,0
Dosis: 2
Route/Site: - / -

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

Agitation Antiplatelet therapy Anxiety Blood creatinine increased Blood pressure systolic increased COVID-19 Cerebrovascular accident Computerised tomogram head abnormal Dysphagia Encephalopathy Full blood count abnormal Hypertension Hypokalaemia Intensive care Leukocytosis Magnetic resonance imaging abnormal Mental status changes Metabolic encephalopathy

Symptomtext

Provider d/c note: "63-year-old female past medical history of poorly controlled hypertension and medical noncompliance. She presented on 12/20 for chief complaint of altered mental status. On presentation patient was noted to be hypertensive systolics in the 240s creatinine 2.8 hypokalemic, complete blood count notable for leukocytosis. CT was performed showing nonspecific low attenuation in both cerebral hemispheres. Patient was admitted for workup of strokes and altered mental status. See initially admitted to the intensive care unit requiring IV blood pressure medications transferred to progressive care unit once titrated off of IV medications. Patient continued to be noncompliant with oral medications throughout her stay requiring IV supplementation to her blood pressure regimen. Patient was tested positive for COVID-19, family declined remdesivir and she was not requiring oxygen. Initial repeat CT was concerning for acute CVA right caudate head lacunar infarct, question microhemorrhage. Initial MRI was a poor study secondary to patient agitation. Repeat studies were obtained with IV medications for anxiety/sedation. MRI showed small attenuated acute infarcts right caudate nucleus right lateral ventricle, left temporal lobe. Patient was started on dual antiplatelets and seen by Neurology. MRI was obtained without large vessel occlusion or stenosis. Patient required prolonged stay secondary to encephalopathy edema secondary to new CVAs, COVID, metabolic encephalopathy. Renal function improved following IV fluids. Blood pressure regimen was titrated up former she no longer required IV medications. She was seen by PT and OT with recommendations for rehab. Family declined wanting to take patient home. Patient will be discharged on 21 day therapy dual antiplatelets followed by aspirin monotherapy. Discharge was delayed secondary to holiday difficulty with coordination of home care. Family choosing to pursue home care from primary outpatient. Patient had dysphagia which improved prior to discharge patient was able to eat normal diet."

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 13,0
Labordaten: Covid PCR dectected on 12/20/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular HTN, Benign* (401.1) Cerebrovascular accident (CVA) due to embolism of carotid artery (HCC) Integumentary Tinea capitis (110.0) Alopecia Other DISORDER, TOBACCO USE (305.1) Acute encephalopathy Hypertensive encephalopathy
Andere Medikamente: amLODIPine (NORVASC) 10 mg tablet Take 1 tablet by mouth daily. aspirin (LOW DOSE ASA) 81 mg chewable tablet Take 1 tablet by mouth daily. atorvastatin (LIPITOR) 40 mg tablet Take 1 tablet by mouth nightly. cloNIDine (CATAPRES-TTS-1) 0.
Allergien: No Know Allergies
Vorherige Impfungen: -

VAERS 2562206

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 18.01.2023
Impfdatum: 22.11.2021
Beginn: 07.12.2022
Tage bis Beginn: 380,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Acute respiratory distress syndrome Acute respiratory failure Angiogram pulmonary normal Anticoagulant therapy Bacteraemia Blood culture positive Blood gases abnormal COVID-19 COVID-19 pneumonia Candida infection Central venous catheterisation Chest X-ray abnormal Culture Echocardiogram abnormal Gram stain positive Haematuria Hyperglycaemia

Symptomtext

86-year-old male presented with hypoxic respiratory failure. Initial O2 saturation was around 70% on 5 L nasal cannula. He was placed on 15 L nonrebreather and O2 saturation corrected to just above 90. He met signs/symptoms of septic shock with viral sepsis. He was started on Levophed therapy and found to have a PO2 of 38 on arterial blood gas. Nasal swab was obtained and positive for COVID-19. Chest x-ray revealed multifocal opacities/infiltrates. He was started on dexamethasone, broad-spectrum antibiotics, and breathing treatments. Initial admission was to intensive care unit. Admitted started on broad-spectrum antibiotics including vancomycin and cefepime. Cultures were obtained as well as procalcitonin and antibiotics were de-escalated. Confirmed COVID-19 infection required aggressive steroid therapy. His acute renal failure on presentation was prohibitive of remdesivir therapy. Echocardiogram was obtained on 12 7 with preserved ejection fraction noted. He was noted to have right ventricular enlargement and right atrial enlargement with moderate pulmonary hypertension. A CTA was obtained and negative for pulmonary embolism. Initially he was treated with heparin infusion pending rule out of pulmonary embolism. A left femoral central venous line was removed following 3 of 4 blood cultures positive for gram-positive cocci. Vancomycin was continued throughout his inpatient stay based on this. He was adequately fluid resuscitated with improvement in his lactic acidosis and his AKI. Because of his leukocytosis and bacteremia he was not an appropriate candidate for baricitinib therapy. Ultimately he has failed to respond to aggressive broad-spectrum antibiotics with O2 support and Decadron therapy. Nebulizer therapies have been provided scheduled and as needed throughout his stay without significant provement in his pulmonary function. He has been followed by pulmonary service. Discharge diagnosis Acute respiratory failure with hypoxia Viral sepsis Septic shock ARDS COVID-19 pneumonia Possible superimposed bacterial pneumonia Acute toxic metabolic encephalopathy due to sepsis and hypoxia Pulmonary Edema on exam Blood culture contamination Pulmonary hypertension Acute Hypernatremia AKI Lactic acidosis Hypokalemia Thrush Hematuria Hyperglycemia Severe protein calorie malnutrition History of prostate cancer Normocytic anemia

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

VAERS 2504321

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 06.11.2021
Beginn: 21.10.2022
Tage bis Beginn: 349,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Bladder scan Blood creatinine increased Blood gases C-reactive protein increased COVID-19 Chest X-ray abnormal Dyspnoea Full blood count abnormal Haemoptysis Influenza virus test negative Leukocytosis Lung consolidation Malaise Pain Pneumonia bacterial Pneumonia viral

Symptomtext

Patient is a pleasant 66 y.o. male patient of DO with a PMHx of CAD s/p PCI in 2015, cAF on Eliquis presenting with hemoptysis, SOB. Acute hypoxic respiratory failure d/t, resolved Post-viral bacterial pneumonia +COVID-19 infection Hemoptysis 1 week of cough, malaise, body aches. Brief period of improvement before recurrence of worsening sxs. Cough now productive w small volume hemoptysis (streaked sputum) Afebrile, HR 75, BP 102/57, RR 27, satting 91% on 2L CBC w mild leukocytosis (WBC 12.6). Trop 7, ProBNP 1.2K. VBG 7.41/39.3. COVID+, influenza neg. Vaccinated x2, no boosters CXR (AP/LAT) with RML/RLL consolidation. No vascular congestion Currently on 2L supplemental O2, wean to goal SpO2 > 92% Abx coverage with Rocephin and Azithromycin, transition to Augmentin 10/22/22 Cont decadron but hold off on Remdesivir, course c/w post-viral PNA Strep pneu urine antigen + Procal 2.76, CRP 137, Scheduled Mucinex. Robitussin-DM, Tylenol, nebs PRN Vibratory PEP and IS ordered, encourage use Continue Augmentin and decadron for 10 days total Return precautions discussed Acute kidney injury, resolved Initial Cr 1.4 (baseline ~1.0) Likely prerenal from above in the setting of ACEi Gentle resuscitation with NS gtt @ 100cc/hr for 1L total Hold home Lisinopril Bladder scan w PVR if e/o urinary retention Avoid nephrotoxic agents, renally adjust meds Daily RFPs, strict I&Os, daily weights to monitor CAD s/p PCI in 2015 Chronic AF on Eliquis Continue home ASA, Lopressor, statin, Eliquis Discussed hold parameters for Lopressor and ACEi

Weitere VAERSDATA-Felder

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

VAERS 2427605

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 02.09.2022
Impfdatum: 16.12.2021
Beginn: 28.08.2022
Tage bis Beginn: 255,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Agitation Arrhythmia COVID-19 Cardiac failure congestive Chronic kidney disease Chronic obstructive pulmonary disease Condition aggravated Death Delirium General physical health deterioration Intensive care Positive airway pressure therapy Respiratory failure

Symptomtext

Discharge Provider: MD Primary Care Physician at Discharge: PA-C Admission Date: 8/28/2022 PRESENTING PROBLEM: Acute on chronic respiratory failure with hypercapnia (HCC) [J96.22] Acute on chronic respiratory failure with hypoxia and hypercapnia (HCC) [J96.21, J96.22] HOSPITAL COURSE: Patient is a 77-year-old male with a history of significant comorbid conditions including end-stage chronic obstructive pulmonary disease, systolic congestive heart failure, chronic kidney disease as well as chronic respiratory failure with hypoxia and hypercapnia. Patient was admitted to the hospital on August 28, 2022 for acute on chronic respiratory failure with hypoxia and hypercarbia in the setting of COVID-19 infection complicated by chronic obstructive pulmonary disease and congestive heart failure. Patient was also noted to have acute kidney injury superimposed on chronic kidney disease. The patient was admitted to the intensive care unit for treatment of respiratory failure with BiPAP. Patient's hospital course was complicated by agitation, delirium and cardiac arrhythmia. The patient struggled with the use of BiPAP which seemed to make him more agitated. With the patient's condition failed to improve, patient's family elected to transition patient into comfort and hospice care. This decision was made August 31, 2022. Patient was placed into comfort care order set with family at bedside. Patient expired peacefully today September 1, 2022 at 11:09 p.m.. Family was at bedside and present. Message sent primary care provider for notification.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: End stage COPD (HCC) Stage 3a chronic kidney disease (HCC) Penetrating ulcer of aorta (HCC) Acute on chronic systolic (congestive) heart failure (HCC) Acute on chronic respiratory failure with hypoxia and hypercapnia (HCC) Coronary artery disease AICD (automatic cardioverter/defibrillator) present Malignant neoplasm of posterior wall of urinary bladder (HCC) Abdominal aortic aneurysm (HCC) AKI (acute kidney injury) (HCC) Arrhythmia ATN (acute tubular necrosis) (HCC) Benign non-nodular prostatic hyperplasia without lower urinary tract symptoms Bilateral inguinal hernia without obstruction or gangrene, recurrence not specified Decreased cardiac ejection fraction Hypercholesteremia Left ventricular dysfunction Neuropathy S/P AAA repair Vitamin D deficiency Depression, recurrent (HCC) Elevated glucose Acute kidney injury superimposed on chronic kidney disease (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet acetaZOLAMIDE (DIAMOX) 250 MG tablet albuterol (PROVENTIL) 0.5% (5 mg/mL) nebulizer solution albuterol HFA (ALBUTEROL) 108 (90 Base) MCG/ACT inhaler aspirin 81 MG chewable tablet atorvastatin (LIPITOR)
Allergien: None
Vorherige Impfungen: -

VAERS 2394939

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: OH
Alter: 88,0
Geschlecht: M
Eingang: 28.07.2022
Impfdatum: 09.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Death Pyrexia Seizure

Symptomtext

Patient's daughter reported that her dad spiked a high fever the following day, which caused them to take him into the hospital. Once arriving at the hospital he developed seizures and eventually passed away. This was the limited information I was given.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ISOSORBIDE, CILOSTIZOL, NAPROXEN, CEPHALEXIN
Allergien: morphine
Vorherige Impfungen: -

VAERS 2364409

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: IL
Alter: 93,0
Geschlecht: M
Eingang: 11.07.2022
Impfdatum: 23.11.2021
Beginn: 15.02.2022
Tage bis Beginn: 84,0
Dosis: 1
Route/Site: IM / -

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

Acute respiratory failure Agitation Anticoagulant therapy Blood glucose increased Blood lactic acid normal COVID-19 Chest X-ray abnormal Computerised tomogram head normal Computerised tomogram thorax abnormal Confusional state Fall Heart rate increased International normalised ratio increased Lung consolidation Malaise Oxygen saturation decreased Pleural effusion Pneumonia

Symptomtext

J&J Dose 11/23/22 COVID Positive 2/20/22 2/20/22: The patient is a 92-year-old gentleman who has past medical history significant for vertebral fractures, diabetes, coronary disease, atrial fibrillation and recent COVID-19. It seems that he having problems at home and not doing well due to which he was admitted to a Medical Center. It seems he had a fall and possibly heart attack. It seems that he was at the Medical Center for 5 to 6 days and was sent to a nursing facility. He was admitted over that yesterday. Today morning it seems that he was confused and getting agitated. His pulse ox was also low at 89%. It seems that his lungs are crackly. He was subsequently sent to emergency room by ambulance for further evaluation. The patient is unable to give any history due to his current condition. He would wake up a little bit to verbal and pain stimuli but then go back to state of drowsiness. In the emergency room patient had chest x-ray that showed right-side effusion with bilateral areas of airspace disease. CT scan of the head showed no acute process. CT of the chest showed moderate to large side effusion with small left effusion with bibasilar consolidation. There is also left upper lobe airspace disease most likely consistent with pneumonia. His proBNP is elevated and his troponin at 10274 and 0.3 respectively. His INR is 1.3 and on Eliquis. His lactate was 2.1. His glucose was 213. His white count was 11.23. His heart rate was fast and have requested the ER to give some IV metoprolol. He also got Lasix 40 mg IV along with IV Levaquin. It seems that he was placed on BiPAP. Per the son he has lost some weight but he is not sure how much. 2/20/22: The patient was admitted with acute hypoxic respiratory failure, on BiPAP. Subsequently, weaned off the oxygen. The patient's family was in the process of transitioning him to Hospice as an outpatient. He was admitted, put on IV antibiotics and IV fluids for supportive treatment. Subsequently, the patient was accepted to Hospice, and he will be discharged over there today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: vertebral fractures diabetes CAD a fib recent COVID-19
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 2182593

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: NY
Alter: 47,0
Geschlecht: M
Eingang: 16.03.2022
Impfdatum: 06.11.2021
Beginn: 12.02.2022
Tage bis Beginn: 98,0
Dosis: 1
Route/Site: SYR / LA

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

Cerebrovascular accident Computerised tomogram Headache Magnetic resonance imaging Paraesthesia Vomiting

Symptomtext

Stroke- Vomiting, headache in back of head, tingling in arms and face after the second vomit. Vomited 3 times total. This started on 2/12 and I made it home and laid in bed thinking I had a stomach bug. Went to primary care doc on 2/15 and he said to go to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 7,0
Labordaten: CT Scans (2/15) MRI (2/17)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin C Zinc NAC Turmeric D3 Quercitin
Allergien: Teriyaki
Vorherige Impfungen: Flu vaccine/Date unknown

VAERS 2161971

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: CA
Alter: 68,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 19.11.2021
Beginn: 09.02.2022
Tage bis Beginn: 82,0
Dosis: 2
Route/Site: OT / -

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

Acute respiratory distress syndrome Blood pressure abnormal Deep vein thrombosis Dyspnoea Endotracheal intubation Oxygen saturation Pulmonary embolism Intensive care Mechanical ventilation Tracheostomy

Symptomtext

ACUTE RESPIRATORY DISTRESS SYNDROME; PULMONARY EMBOLISM; DEEP VEIN THROMBOSIS; This spontaneous report received from a health care professional concerned a 68 year old male. The patient's height, and weight were not reported. The patient was using a wheelchair due to mobility and pain issues. The patient's concurrent conditions included: chronic pain, and mobility issue. The patient had no known allergies to medications, food, or other products. Patient had no other illnesses at the time of vaccination and up to one month prior. The patient had no adverse event following any previous vaccine. The patient previously received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, intramuscular, batch number: 1808980, and expiry: UNKNOWN) dose was not reported, 1 total, administered on left arm on 10-JUL-2021 for prophylactic vaccination. No adverse events reported post primary vaccination (Dose number in series 1). The patient received booster dose of covid-19 vaccine ad26.cov2.s vaccine (Dose number in series 2) (suspension for injection, intramuscular, batch number: 1855194, and expiry: UNKNOWN) dose was not reported, 1 total, administered on left arm on 19-NOV-2021 at 12:00 for prophylactic vaccination. Concomitant medications included paracetamol for drug used for unknown indication. On 09-FEB-2022 at 17:00, after 2.5 months after booster dose, patient had been dyspneic for 36 hours. First responder noted oxygen saturation of 78 percent. Patient was transferred to the outside hospital emergency room for further treatment and care. Patient ended up being intubated, admitted to the ICU (Intensive Care Unit) and was diagnosed with pulmonary embolism and deep vein thrombosis. Patient had acute respiratory distress syndrome and was needing mechanical ventilation still for almost 3.5 weeks at the time of reporting, blood pressure support and tracheostomy (Dose number in series 2). On an unspecified date, the patient was hospitalized. Number of days of hospitalization was 24. No medical tests and laboratory results related to the adverse event(s) were performed before complaining of dyspnea (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the pulmonary embolism, deep vein thrombosis and acute respiratory distress syndrome was not reported. This report was serious (Hospitalization Caused / Prolonged, and Life Threatening).; Sender's Comments: V0: 20220316804-Covid-19 vaccine ad26.cov2.s- Acute respiratory distress syndrome, Pulmonary embolism, Deep vein thrombosis. 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 24,0
Labordaten: Test Date: 20220209; Test Name: Oxygen saturation; Result Unstructured Data: 78 %
Aktuelle Erkrankungen: Chronic pain; Mobility decreased
Vorgeschichte: Medical History/Concurrent Conditions: Wheelchair user; Comments: Patient had no known allergies to medications, food, or other products. Patient had no other illnesses at the time of vaccination and up to one month prior. The patient had no adverse event following any previous vaccine.
Andere Medikamente: ACETAMINOPHEN
Allergien: -
Vorherige Impfungen: -

VAERS 2161971

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: CA
Alter: 68,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 19.11.2021
Beginn: 09.02.2022
Tage bis Beginn: 82,0
Dosis: UNK
Route/Site: IM / LA

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

Acute respiratory distress syndrome Blood pressure abnormal Deep vein thrombosis Dyspnoea Endotracheal intubation Oxygen saturation Pulmonary embolism Intensive care Mechanical ventilation Tracheostomy

Symptomtext

ACUTE RESPIRATORY DISTRESS SYNDROME; PULMONARY EMBOLISM; DEEP VEIN THROMBOSIS; This spontaneous report received from a health care professional concerned a 68 year old male. The patient's height, and weight were not reported. The patient was using a wheelchair due to mobility and pain issues. The patient's concurrent conditions included: chronic pain, and mobility issue. The patient had no known allergies to medications, food, or other products. Patient had no other illnesses at the time of vaccination and up to one month prior. The patient had no adverse event following any previous vaccine. The patient previously received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, intramuscular, batch number: 1808980, and expiry: UNKNOWN) dose was not reported, 1 total, administered on left arm on 10-JUL-2021 for prophylactic vaccination. No adverse events reported post primary vaccination (Dose number in series 1). The patient received booster dose of covid-19 vaccine ad26.cov2.s vaccine (Dose number in series 2) (suspension for injection, intramuscular, batch number: 1855194, and expiry: UNKNOWN) dose was not reported, 1 total, administered on left arm on 19-NOV-2021 at 12:00 for prophylactic vaccination. Concomitant medications included paracetamol for drug used for unknown indication. On 09-FEB-2022 at 17:00, after 2.5 months after booster dose, patient had been dyspneic for 36 hours. First responder noted oxygen saturation of 78 percent. Patient was transferred to the outside hospital emergency room for further treatment and care. Patient ended up being intubated, admitted to the ICU (Intensive Care Unit) and was diagnosed with pulmonary embolism and deep vein thrombosis. Patient had acute respiratory distress syndrome and was needing mechanical ventilation still for almost 3.5 weeks at the time of reporting, blood pressure support and tracheostomy (Dose number in series 2). On an unspecified date, the patient was hospitalized. Number of days of hospitalization was 24. No medical tests and laboratory results related to the adverse event(s) were performed before complaining of dyspnea (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the pulmonary embolism, deep vein thrombosis and acute respiratory distress syndrome was not reported. This report was serious (Hospitalization Caused / Prolonged, and Life Threatening).; Sender's Comments: V0: 20220316804-Covid-19 vaccine ad26.cov2.s- Acute respiratory distress syndrome, Pulmonary embolism, Deep vein thrombosis. 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 24,0
Labordaten: Test Date: 20220209; Test Name: Oxygen saturation; Result Unstructured Data: 78 %
Aktuelle Erkrankungen: Chronic pain; Mobility decreased
Vorgeschichte: Medical History/Concurrent Conditions: Wheelchair user; Comments: Patient had no known allergies to medications, food, or other products. Patient had no other illnesses at the time of vaccination and up to one month prior. The patient had no adverse event following any previous vaccine.
Andere Medikamente: ACETAMINOPHEN
Allergien: -
Vorherige Impfungen: -

VAERS 2137097

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: WA
Alter: 61,0
Geschlecht: M
Eingang: 24.02.2022
Impfdatum: 22.12.2021
Beginn: 24.02.2022
Tage bis Beginn: 64,0
Dosis: 2
Route/Site: IM / LA

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

Angiogram cerebral normal Angiogram normal Cerebral haemorrhage Computerised tomogram head abnormal Electrocardiogram Hypoaesthesia Laboratory test Muscular weakness Thalamus haemorrhage

Symptomtext

Sudden onset of numbness to left face, left upper extremity, left lower extremity, with weakness in the left upper and left lower extremity. He presented to the emergency department and a code Nuro was initiated. I received a phone call from the radiologist stating that he has a significant 3.2 x 2.1 x 1.6cm brain hemorrhage on his non-contrast CT brain. A CT angiogram of his head and neck showed no evidence of aneurysm or other vascular lesion to account for the hemorrhage. It was a right thalamic hemorrhage. He was admitted to the hospital for further neurologic monitoring for expanding hemorrhage and to get follow up MRI exam. He will also likly need physical therapy/occupational therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: CT head, CT Angiogram head and neck, a plethera of lab tests and ECG all done on 2/24/22 in the ED, then admitted for further testing.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Baby aspirin
Allergien: None
Vorherige Impfungen: -

VAERS 1998675

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 22.11.2021
Beginn: 13.12.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: - / LA

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

Angiogram Angiogram cerebral Anticoagulant therapy Blindness Cerebrovascular accident Computerised tomogram head Magnetic resonance imaging head abnormal Neurological symptom

Symptomtext

CVA occipital lobe presenting with visual loss. She recovered fully . Symptoms occured suddenly 21 days post vaccination. Stroke confirmed on brain MRI. Treated with heparin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: 12/13/21 CT brain MRA brain 12/14/2021 12/13/21 CTA 12/13/21 MRI brain
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1888092

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: NY
Alter: 69,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 27.10.2021
Beginn: 15.11.2021
Tage bis Beginn: 19,0
Dosis: UNK
Route/Site: IM / -

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

Pulmonary embolism

Symptomtext

Pulmonary emboli. History of J & J on 3/31/2021 and on 10/27/2021 (booster).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: Thyroid nodules
Vorgeschichte: Diabetes, hyperlipidemia, HTN
Andere Medikamente: Lantus SQ, Losartan, Simvastatin
Allergien: -
Vorherige Impfungen: -

VAERS 1869512

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

kritisch

Staat: CA
Alter: 56,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 29.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy Cerebrovascular accident Dysarthria Echocardiogram Facial paralysis Muscular weakness Thrombectomy

Symptomtext

Patient received Janssen vaccine on 10/29/21. On 11/2/21 patient woke up at 4:00 am with left arm and right leg weakness, had slurred speech and face drop, transferred to ER, diagnosed with right MCA stroke, had thrombectomy diachged home on statins and Eliquis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: ECHO-Uknown; Patient admitted at local Hospital.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Nicoderm
Allergien: NKA
Vorherige Impfungen: -

VAERS 2685215

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: FL
Alter: 45,0
Geschlecht: F
Eingang: 22.09.2023
Impfdatum: 22.02.2022
Beginn: 23.08.2023
Tage bis Beginn: 547,0
Dosis: 1
Route/Site: IM / -

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

Abdominal pain upper Anticoagulant therapy COVID-19 Deep vein thrombosis Splenic infarction

Symptomtext

8/23/2023 - 8/30/2023 (7 days) Date of Admission: 8/23/2023 Discharge Date: 08/30/2023 Discharge Disposition: Home or Self Care past medical history of SLE, recent left lower extremity DVT with splenic infarct and discharged on 07/03/2023 on Eliquis, recent COVID-19 1 week prior to arrival, presented with worsening left upper quadrant pain over the past 1 week prior to arrival. Patient asymptomatic from this regard. No hypoxia or pneumonia noted. Continue supportive care. 2/22/2022 Janssen 1855194

Weitere VAERSDATA-Felder

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

VAERS 2430962

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 27.10.2021
Beginn: 25.08.2022
Tage bis Beginn: 302,0
Dosis: 2
Route/Site: - / -

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

Arterial catheterisation Asthenia Blood lactic acid increased Blood pressure decreased COVID-19 Chest X-ray abnormal Fall Hypotension Intensive care Lung infiltration Mobility decreased Physical deconditioning Pyrexia SARS-CoV-2 test positive Sepsis Sinus bradycardia White blood cell count decreased

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 8/25/2022 Discharge Date: 8/29/2022 PRESENTING PROBLEM: Severe sepsis [A41.9, R65.20] COVID [U07.1] Suspected COVID-19 virus infection [Z20.822] COVID-19 [U07.1] Sepsis [A41.9] HOSPITAL COURSE: Per ICU transfer summary: "Patient is a 73 year old with NIDDM, HTN, and GERD who presented to ED 8/25 with generalized weakness, fever and fall from standing. In ED, she was febrile to 39.1C with stable vitals. Labs were significant for LA 2.7, WBC 3800, and she was found to be COVID-19 positive. CXR was clear. She was given 4L NS and admitted for further care. After admission, her BP dropped and she was brought to ICU where arterial line was placed which showed adequate BP. She did not require vasopressors. She had episodes of sinus bradycardia (HR down into 30s, similar to a previous admission in 2019 for Influenza A) with some associated hypotension that improved with volume, overall improved over time. She continued to require only room air oxygen - CXRs did show some increased interstitial infiltrates 8/27 but improved by 8/28. No therapy for COVID was started. She has been very deconditioned - requiring assistance with mobility. PT/OT ordered." She was transferred to the Hospitalist service on 8/28/2022. She was evaluated by PT/OT who recommended home with assist as needed. Home valsartan-HCTZ was held on DC until she follow up with her PCP as an outpatient. She was discharged home in stable condition on 8/29/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: 10/6/2021-Thrush
Vorgeschichte: Hypertension associated with diabetes Hyperlipidemia associated with type 2 diabetes mellitus DM (diabetes mellitus) type II controlled, neurological manifestation Obesity (BMI 30-39.9) Cervical spine disease Posterior vitreous detachment of both eyes Posterior capsular opacification, obscuring vision, left Type 2 diabetes mellitus with both eyes affected by mild nonproliferative retinopathy without macular edema, without long-term current use of insulin Baastrup's syndrome Onychomycosis GERD (gastroesophageal reflux disease) Sinus bradycardia Dry eyes, bilateral COVID-19 Low blood pressure Severe sepsis Sepsis
Andere Medikamente: aspirin 81 MG tablet Cholecalciferol (VITAMIN D3) 2000 UNITS CAPS Omeprazole Magnesium (PRILOSEC OTC PO) tramadol-acetaminophen (ULTRACET) 37.5-325 MG per tablet
Allergien: Adhesive TapeRash NsaidsRash PenicillinsRash MetforminDiarrhea Zocor [Hmg-coa-r Inhibitors]Other
Vorherige Impfungen: -

VAERS 2404086

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: NJ
Alter: 33,0
Geschlecht: F
Eingang: 07.08.2022
Impfdatum: 19.01.2022
Beginn: 01.04.2022
Tage bis Beginn: 72,0
Dosis: 2
Route/Site: IM / LA

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

Thrombosis

Symptomtext

blood clot in leg 3 months after vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asplenia, hx of blood clots over past 4 years, malnourishment, iron deficiency, protein deficiency
Andere Medikamente: BUPRENORPHINE/NALOXONE 8MG/2MG TAB, CLONAZEPAM 1MG, MIRTAZEPINE 45MG
Allergien: -
Vorherige Impfungen: -

VAERS 2308530

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: AL
Alter: 18,0
Geschlecht: M
Eingang: 03.06.2022
Impfdatum: 01.06.2022
Beginn: 01.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Musculoskeletal disorder Syncope Unresponsive to stimuli

Symptomtext

REPORT OF 06/01/2022 18 year old male arrived at clinic with mother on 06/01/2022 to request Janssen Vaccine. Patient and mother provided with Janssen patient information packet to read and then allowed to ask questions. Both patient and mother stated they had reviewed the information and had no questions. Prior to receiving vaccine mother requested to see and inspect vaccine vial. Mother allowed to do so and was satisfied. At 1405 on 06/01/2022 RN gave vaccine Janssen Lot# 1855195 to left arm IM. At 1410 patient appeared to slump in a syncopal episode and did not respond to mother calling his name. RN called 911 to request assistance at this time with RN at patien

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2275249

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: OR
Alter: -
Geschlecht: M
Eingang: 13.05.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Biopsy bone marrow Epstein-Barr virus infection Guillain-Barre syndrome Haemorrhage subcutaneous Laboratory test

Symptomtext

MILD GUILLAIN-BARRE SYNDROME; BLEEDING UNDER THE SKIN; EPSTEIN-BARR VIRUS; This spontaneous report received from a patient concerned a 61 year old male of an unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's past medical history included: physical therapy, and acupuncture, and concurrent conditions included: shoulder rotator cuff injury. On an unspecified date, the patient previously received covid-19 vaccine ad26. cov2. s (dose number in series: 1) (suspension for injection, route of admin, and batch number were not reported, expiry: unknown) dose was not reported, 1 total administered on 01-MAY-2021 for prophylactic vaccination. On an unspecified date in 2021, post the vaccination, the patient experienced side effects and lingering pain was gone (dose number in series: 1). The outcome of side effects was not reported and lingering pain was gone was recovered. On 25-OCT-2021, the patient received covid-19 vaccine ad26.cov2.s (dose number in series: 2) (suspension for injection, route of admin not reported, batch number: 1855194, expiry: UNKNOWN) dose was not reported, 1 total administered for prophylactic vaccination. No concomitant medications were reported. On an unspecified date in 2021, the patient reported really, really sick, bleeding under the skin, mild Guillain-Barre Syndrome (GBS) and very serious Epstein-Barr Virus (EBV) (dose number in series 2). The patient stated to be in a good health. The patient's doctor had mentioned to him that bruising was normal when old and had discontinued some of patient's medications including ibuprofen. The patient had undergone numerous tests within a period of 3 months post vaccination. Laboratory data (dates unspecified) included: Bone marrow biopsy was negative for blood cancer, and unspecified tests indicated diagnosis of very serious Epstein-Barr Virus (EBV) and mild Guillain-Barre Syndrome (GBS) (dose number in series: 1). The patient's symptoms were pointing to blood cancer before the test results had arrived. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from bleeding under the skin, epstein-barr virus, and mild guillain-barre syndrome. This report was serious (Other Medically Important Condition). This case, involving the same patient is linked to 20220511951.; Sender's Comments: V0:20220513079-covid-19 vaccine ad26.cov2.s- Mild guillain-barre syndrome.. This event(s) is labeled per RSI and is therefore considered potentially related. 20220513079-covid-19 vaccine ad26.cov2.s-Bleeding under the skin. The event(s) has an unknown/unclear 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Laboratory test; Result Unstructured Data: Diagnosis of EBV and GBS; Test Date: 2021; Test Name: Bone marrow biopsy; Result Unstructured Data: negative for blood cancer
Aktuelle Erkrankungen: Rotator cuff injury
Vorgeschichte: Medical History/Concurrent Conditions: Acupuncture; Physical therapy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2147504

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: KY
Alter: 46,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 30.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Bell's palsy Blood immunoglobulin M Blood test abnormal Chills Cold-stimulus headache Computerised tomogram head Computerised tomogram neck Dizziness Electrocardiogram Electrophoresis protein Facial paralysis Guillain-Barre syndrome Headache Hemiparesis Immunology test Inflammation Magnetic resonance imaging Metabolic function test

Symptomtext

Initial reaction beginning day 1: fever of 103, most severe headache I've ever experienced, similar to a "brain freeze" when drinking something too cold, severe chills, body aches, dizziness, and blurry vision. Day 3: went to urgent care for right-sided weakness and my right foot had been asleep for 11 hours. Urgent care doctor suspected potential Guillain-Barre and it was strongly suggested to go to ER for neuro workup. The medical chart said "rare inflammatory immune response due to vaccine". I went home, hoping it would pass. Woke up on Day 5 with right-sided facial paralysis. Went to ER and had an MRI, CT of the head and neck to rule out stroke, EKG, and bloodwork. Suspected bells-palsy and loss of peripheral vision, medical chart included vaccine-related injury. Was referred to neurology, despite intense pressure to be admitted, we agreed that I would follow up with neuro. Appointment with neurologist and complete battery of tests resulted in a positive monoclonal IGM Lamda and positive for myasthenia gravis. Referred to Hematologist. Follow up bloodwork in January resulted in the monoclonal IGM Lamda had resolved itself and I was released from care of Hematologist. Follow up with neurologist, I have now been referred to have chest CT to rule out thymus gland issues. Still have ongoing symptoms of myasthenia gravis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: 11/3/21 Stroke CT & MRI, ECG, 11/11 protein electrophoresis, erythrocyte sedimentation rate, myasthenia gravis panel, immunology path order, CMP 1/20 Immunology path order
Aktuelle Erkrankungen: none. I was very healthy
Vorgeschichte: none
Andere Medikamente: multivitamin
Allergien: allergic to penicillin, ampicillin, and history of allergic reaction to a tdap vaccine.
Vorherige Impfungen: -

VAERS 2109302

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: FL
Alter: 43,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 03.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Computerised tomogram abnormal Pulmonary thrombosis Thrombosis

Symptomtext

blood clots in leg and lungs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 2,0
Labordaten: ct scan
Aktuelle Erkrankungen: check up with doctor which led to test for blood clots because i wanted to make sure there was not any clots prior to getting vaccine
Vorgeschichte: high blood pressure, type 2 diabetes
Andere Medikamente: bystolic 10 mg, vitamin D 3 500mg, asprin 81mg, irbesartan 300mg , mag oxide 400mg 3X daily, famotidine 40 mg, fish oil 1200 mg adderall 30 mg 3X daily, metformin er 500 mg 2X daily
Allergien: none
Vorherige Impfungen: -

VAERS 2101067

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: WA
Alter: -
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: -
Beginn: 03.02.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Anaphylactic reaction

Symptomtext

ANAPHYLAXIS/SHORTNESS OF BREATH/TIGHTNESS OF CHEST; This spontaneous report received from a patient concerned a 56 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: asthma since 11 years. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, expiry: 09-APR-2022) dose was not reported, 1 total administered on 01-FEB-2022 23:30 for prophylactic vaccination. Non-company suspect drugs included: prednisone ( form of admin, route of admin, and batch number were not reported) dose and frequency were not reported received on 01-FEB-2022 18:35, 20 mg and 03-FEB-2022 2.5mg for asthma. And patient reported she did not take Prednisone on 02-FEB-2022 really need to take every day for asthma, at least 5-10mg per day No concomitant medications were reported. On 01-FEB-2022, after receiving vaccine at 23:30 and prednisone at 18:35, the patient experienced anaphylaxis after 30 minutes and patient visited emergency care unit. On 03-FEB-2022, the patient experienced (Felt tightening in chest and shortness of breath) anaphylaxis, but not enough to use Epi-pen or go to urgent care. Treatment medications (dates unspecified) included: epinephrine for anaphylaxis. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of anaphylaxis/shortness of breath/tightness of chest was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0- 20220213102-Covid-19 vaccine ad26.CoV-2.s- Anaphylaxis/Shortness of breadth/tightness of chest. This event(s) is labeled per RSI and is therefore considered potentially related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma (Since age 11)
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2095982

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 23.11.2021
Beginn: 06.12.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Anticoagulant therapy COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chest pain Dyspnoea Fibrin D dimer increased Intensive care Lung opacity SARS-CoV-2 test positive Sepsis Treatment noncompliance

Symptomtext

12/6/2021 - presents to ED SOB/chest pain/severe dyspnea. Patient is on dialysis 3xs/wk but missed 1 day. Temp 98.6, HR 108, R 20, BP 215/122, SPO2 92%. D dimer 469. Sepsis/Covid pneumonia and need for urgent dialysis. Covid+ on admit. Patient dialyzed in ED. Following this, RA sat 99%, BP 212/112. Reglan, Tylenol, and Clonidine given - BP improved. Casirivimab/imdevimab given. CXR neg for PE.Prepared for discharge with Covid at home. 12/7- Subsequently presents chest pain/SOB to ED. T-101.5,R-22,HR-149, BP-188/126, O2 94% RA. Admit to ICU acute RF due to Covid. CXR shows groundglass bil pneumonia. Started ceftriaxone, azithromycin, heparin. Decadron continued. Not a candidate for Baricitinib/Remdesivir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: End stage Renal Disease on dialysis, Lupus, HTN. 12/9- Decadron d/c- Solu-medrol started. Baricitinib continued. Heparin IV to subcu. Dialysis continued. 12/10- O2 maintained on 2L. Clinically improved. 12/13 - Due for dialysis yesterday 12/12. Advised dialysis before discharge. Refused dialysis with a H/O non compliance. Left AMA.
Andere Medikamente: Bamlanivimab/etesevimab given. Tocilizumab not available. O2 to maintain sat above 90%. BP meds continued.
Allergien: Vancomycin
Vorherige Impfungen: -

VAERS 2088968

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: OR
Alter: 22,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 04.02.2022
Beginn: 04.02.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / AR

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

Dizziness Hyperacusis Nausea Skin discolouration Syncope Vomiting

Symptomtext

Patient initially experienced dizziness and remained seated. After approximately 5 minutes he fainted and remained sitting in chair, and did not hit body or head on floor. His companion and pharmacist made certain he sat back and did not faint again. He was able to converse and no signs of anaphylaxis. His skin color remained gray and ashy. He had some sips of water and stated he was nauseous. He vomited a few minutes later. He remained in the pharmacy area for 2.5 hours. During that time he was sensitive to noises, sometimes dizzy, and vomited a few more times. After about 2 hours he stated he could try some sips of Gatoraid and his color started returning. He was able to leave the pharmacy after 2.5 hours and arrived home safely. He stated he would also enter his data into V-Safe for tracking.

Weitere VAERSDATA-Felder

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

VAERS 2065831

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: MI
Alter: 50,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 13.12.2021
Beginn: 14.01.2022
Tage bis Beginn: 32,0
Dosis: 1
Route/Site: IM / RA

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

Bell's palsy Facial paresis

Symptomtext

4 weeks after, right facial weakness (Bell's palsy-7th cranial nerve right). steroid rx prednisone for one week. on 1-22-2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: no other acute illness
Vorgeschichte: hypertension, hyperlipidemia, GERD , hyperuricemia
Andere Medikamente: vitmain d 50,000iu per week amlodipine 5mg d, losartin 100mg one daily, allopurinol 100mg 2 daily , omeprazole 20mg d.
Allergien: none
Vorherige Impfungen: -

VAERS 2057569

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: NH
Alter: 47,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 22.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cold sweat Feeling cold Feeling hot Syncope Tremor

Symptomtext

Patient stated that he passed out, although I did not observe it. He stated he felt very warm, then very cold and broke out in a cold sweat. My technician said he was shaking at one point and thought it could have been a seizure. His wife was asked if she wanted an ambulance called and she said yes. He was sitting upright and responsive when paramedics arrived and all observed vitals were within normal limits. He declined to go to the hospital for further evaluation.

Weitere VAERSDATA-Felder

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

VAERS 2032107

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: PA
Alter: 29,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Fall Loss of consciousness

Symptomtext

AFTER INJECTION THE PATIENT GOT UP TO LOOK AT CARDS. WITHING 2 MINUTES HE PASSED OUT AND FELL TO THE FLOOR. 911 WAS CALLED AND THE PATIENT WAS TAKEN TO THE HOSPITAL

Weitere VAERSDATA-Felder

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

VAERS 2025727

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: ID
Alter: 39,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 30.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Facial paralysis Hypoaesthesia

Symptomtext

Patient began to experience numbness in hands, fingers and face, Facial numbness was worse on Left side. Patient then began to experience Left eye drooping. Left eye droop began to resolve on the morning of 12/4/2021. Patient was offered appointment with a provider and refused. She just wanted it reported to VAERS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lexapro
Allergien: None
Vorherige Impfungen: MMR vaccine when a child. Gets ill after flu vaccine refuses to have it.

VAERS 1995845

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: MA
Alter: 40,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 31.12.2021
Beginn: 31.12.2021
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

Patient has known syncopal history, but did not inform vaccinator. After vaccination, he had a near-syncopal event. Patient laid down with feet elevated. He received evaluation from EMS, but refused further treatment/transport.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: EMS evaluation.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKDA, NKA
Vorherige Impfungen: -

VAERS 1985757

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: CT
Alter: 26,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 14.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / LA

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

Abstains from alcohol Alanine aminotransferase normal Aspartate aminotransferase normal Blood creatine normal Blood glucose normal Blood potassium normal Blood sodium normal Blood thyroid stimulating hormone normal C-reactive protein decreased Chest X-ray Chest pain Dizziness Dyspepsia Dyspnoea Electrocardiogram abnormal Exercise tolerance decreased Fibrin D dimer decreased Glomerular filtration rate

Symptomtext

10 days following the first J&J vaccine, I experienced sudden onset chest pain and shortness of breath in addition to lightheadedness, faintness, and rapid heartbeat. The chest pain was relieved by aspirin 325 mg, however the pain would return once the aspirin wore off. I went to Hospital less than 48 hours later, where they performed a work up to rule out a pulmonary embolism. They ultimately sent me home with a broad diagnosis of heartburn and told me to follow up with my primary care provider "as needed." After reviewing the documentation in the Hospital notes, they failed to document that I had received the J&J vaccine 10 days prior to symptom onset and that my mother has a history of blood clots. Knowing that I did not have heartburn, I scheduled an appointment with a cardiologist who diagnosed me with pericarditis. I am currently being treated with high dose aspiring (325 mg TID) and colchicine 0.6 mg daily, no exercise/caffeine/alcohol for 1 month. Symptoms have started to improved after 1 week of treatment. Follow up with the cardiologist in another 3 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: 11/27/21: Hospital: EKG: Sinus rhythm with marked sinus arrhythmia. chest xray: FINDINGS:The lungs are clear. The cardiomediastinal silhouette is normal in size. There is no pleural effusion or pneumothorax. No acute osseous abnormality. Labs: PT 11.9, INR 1.0, glucose 95, Cr 0.9, GFR > 60, sodium 140, Potassium 4.0, AST 17, ALT 16, wbc 7.9, platelet count 217, hgb 13.9, hct 44.2%, troponin T < 6, D dimer < 150 12/17/21: Cardiologist: labs: TSH 2.16, troponin 7, CRP 0.4
Aktuelle Erkrankungen: none
Vorgeschichte: migraines
Andere Medikamente: vitamin D, oral contraceptive
Allergien: none
Vorherige Impfungen: -

VAERS 1971424

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: MI
Alter: 22,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
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 Nausea

Symptomtext

PATIENT'S MOTHER HAD CALLED AND ALERTED CLINIC THAT PATIENT HAS HISTORY OF SEIZURE ACTIVITY AFTER VACCINATIONS. PATIENT HAD LAYED DOWN ON THE FLOOR DURING OBSERVATION AND STATED HE WAS FEELING NAUSEATED. WAS VERBALLY RESPONDING APPROPRIATELY TO SIMPLE YES/NO QUESTIONS. NURSE ELEVATED FEET, PLACED ICE PACK BEHIND HEAD AND SECOND NURSE GOT PILLOW FOR HEAD. INITIAL BP 110/71 AT 1726. AT 1728, HE LOST CONSCIOUSNESS, NURSE DID STERNAL RUB & HE USED HIS HAND TO REMOVE NURSES HAND. BEGAN VERBALLY RESPONDING AGAIN TO SIMPLE YES/NO QUESTIONS WITHIN 2 MINUTES. WAS NOT ABLE TO OPEN EYES AT THE TIME. NOTED INVOLUNTARY MOVEMENT OF BOTH ARMS AND EYES WHILE STILL RESPONDING AT REDUCED LEVEL OF CONSCIOUSNESS. AT 1730, BP WAS 120/83. INVOLUNTARY MOVEMENTS REDUCING, AND CONTINUED TO IMPROVE UNTIL 1745 WHEN HE WAS ABLE TO OPEN HIS EYES, SIT UP, AND TAKE SIPS OF JUICE WITH BP 119/83. HAD STATED THIS IS TYPICAL RESPONSE PER HIS BASELINE REACTION TO VACCINES, HAS NOT REQUIRED EMERGENCY ASSISTANCE AND WAS A&O X3 AT TIME OF DEPARTURE WITH SISTER ACCOMPANYING AND DRIVING HIM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: HISTORY OF SEIZURE ACTIVITY AFTER VACCINATIONS
Andere Medikamente: UNKNOWN
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1967566

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: PA
Alter: 56,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 20.11.2021
Beginn: 17.12.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / -

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

Abdominal tenderness Alanine aminotransferase increased Anticoagulant therapy Aspartate aminotransferase increased Bilirubin conjugated increased Blood alkaline phosphatase increased Blood bilirubin normal Computerised tomogram abnormal Gastroenteritis Portal vein thrombosis Pyrexia Transaminases increased

Symptomtext

Presented to outside hospital ED with complaints of abdominal tenderness for about 9 days on 12/12. Was diagnosed with gastroenteritis and discharged home. Normal CT scan at that time. Presented again to the ED and was found to have fevers and transaminitis. CT scan showed left portal and right anterior portal vein thrombosis requiring admission and further workup. Patient was discharged on rivaroxaban for anticoagulation for at least 3 months and will have a follow up CT scan.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Portal vein thrombosis
Hospital-Tage: 3,0
Labordaten: CT scan as mentioned above 12/17 Direct Bili (12/17) = 2.0 Alk Phos (12/17) = 325 AST (12/17) = 52 ALT (12/17) = 79 Total Bili (12/17) = 3.0
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxine
Allergien: None
Vorherige Impfungen: -

VAERS 1958940

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: VA
Alter: 69,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 05.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: IM / LA

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

Hypoaesthesia Ischaemic stroke Magnetic resonance imaging head abnormal

Symptomtext

ACUTE STROKE DUE TO ISCHEMIA (HCC) NUMBNESS TO RIGHT SIDE OF FACE, CHEST, ARM, HAND, ABDOMEN, THIGH, LEG, FOOT, TOES

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 4,0
Labordaten: MRI 12/10/21 "PUNCTUATE FOCUS OF INFARC IN THE LEFT THAMAMUS"
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: CIPRO
Vorherige Impfungen: -

VAERS 1936339

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: TX
Alter: 65,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 29.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Bloody discharge Cough Eye irritation Eyelid margin crusting Lacrimation increased Lethargy Ocular hyperaemia Sinus congestion Thrombosis Vision blurred

Symptomtext

No health problems prior to vaccine: 1) now both eyes water constantly, are red and irritated, and are crusty when I wake up in the morning with cloudy vision. 2) Sinuses are constantly congested and discharge when I blow my nose is bloody and blood clots along with coughing. 3) Almost always lethargic during the day at work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Daily vitamins, EFA's, BCAA's
Allergien: NA
Vorherige Impfungen: -

VAERS 1929635

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: CA
Alter: 22,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Pallor Syncope

Symptomtext

syncope within 5 minutes of immunization. faint, white and sweating. had patient lie down, elevate legs and gave some water. He rested for 30 minutes and then was released.

Weitere VAERSDATA-Felder

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

VAERS 1928814

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: NC
Alter: 47,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Amnesia Confusional state Dizziness Echocardiogram Loss of consciousness Ultrasound scan

Symptomtext

Dizziness and passed out, became extremely confused and couldn't remember anything. Went to ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 1,0
Labordaten: yes, echocardiogram, sonogram of arteries
Aktuelle Erkrankungen: -
Vorgeschichte: autoimmune disorder
Andere Medikamente: cosentics
Allergien: -
Vorherige Impfungen: pt stated he has had reaction to the flu vaccine which landed him in the hospital

VAERS 1926054

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: CA
Alter: 85,0
Geschlecht: M
Eingang: 06.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Extra dose administered Syncope

Symptomtext

On 12/3/21 AT 12:20 pm patient presented to our pharmacy to get covid-19 booster vaccine for Janssen vaccine. after receiving the vaccine by nurse patient fainted. Ambulance was called for the patient and when they arrived patient started feeling better . Blood pressure reported by nurse was 119/56 mmHG. sitting. Patient denied need for hospitalization and was helped to go to his car after he started feeling better.

Weitere VAERSDATA-Felder

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

VAERS 1925045

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: SC
Alter: 40,0
Geschlecht: M
Eingang: 06.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Dizziness Fatigue Headache Hyperhidrosis Hypotension Loss of consciousness Pain in extremity Seizure Vomiting

Symptomtext

Immediately after (in the car in the parking lot) I began to sweat and get light headed. My wife who was in the car told me to pull over because she could see I didn?t look right. I pulled over, passed out and had a seizure. My wife called 911 and the paramedics came to check me out. BP was very low but everything else checked out ok. On the way home I threw up violently filling up the entire bag that the EMT had given me where my wife had to pull over and dump it out. I felt very weak, excruciating headache, and my head just didn?t feel right. Arm is very sore and still very fatigued with headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Paramedics checked vitals (BP, HR, BS)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamins: C, D, Zinc
Allergien: PCN
Vorherige Impfungen: -

VAERS 1922873

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: CA
Alter: -
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: -
Beginn: 21.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Blood pressure increased Blood pressure measurement Body temperature Breast pain Breast swelling Dizziness Headache Pain Pyrexia Syncope Vision blurred Visual field defect

Symptomtext

ELEVATED BLOOD PRESSURE; FAINTING; STINGING PAIN ALL OVER THE BODY/ BODY ACHES; BLURRY VISION IN LEFT EYE; PERIPHERAL VISION AFFECTED; HEADACHE; BREAST AREA SWOLLEN (LEFT ARM UNDERNEATH); BREAST PAIN (ON LEFT UNDER SIDE ARM BESIDE BREAST); DIZZINESS/ LIGHT HEADNESS; LOW GRADE FEVER; This spontaneous report received from a patient concerned a 43 year old female of unknown race and ethnicity. The patient's height, and weight were not reported. The patient's past medical history included: covid-19, and concurrent conditions included: asthma, and hypoglycemic. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194 and expiry: unknown) dose was not reported, 1 total, administered on left arm at 11-NOV-2021 for prophylactic vaccination (Dose number in series 1). No concomitant medications were reported. On 21-NOV-2021, the patient experienced low grade fever. On 23-NOV-2021, the patient experienced breast area swollen (left arm underneath), breast pain (on left under side arm beside breast) and dizziness/ light headness. On 24-NOV-2021, the patient experienced blurry vision in left eye, peripheral vision affected, headache. On 25-NOV-2021, the patient experienced stinging pain all over the body/ body aches (in front part of thigh/right leg, behind the knee on right knee, pains in stomach meeting chest area, chest pain and elbow and mid forearm, pain in mid-back on right side). On 27-NOV-2021, the patient experienced fainting, could not look down to see floor, paramedics called and offered ride to hospital which the patient declined. On an unspecified date, the patient experienced elevated blood pressure. Laboratory data (dates unspecified) included: Blood pressure (NR: not provided) 171/90 ELEVATED, and Body temperature (NR: not provided) 100.2 F. Treatment medications (dates unspecified) included: paracetamol, and ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from breast area swollen (left arm underneath), and breast pain (on left under side arm beside breast) on 25-NOV-2021, and low grade fever on 23-NOV-2021, was recovering from dizziness/ light headness, headache, stinging pain all over the body/ body aches, blurry vision in left eye, peripheral vision affected, and fainting, and the outcome of elevated blood pressure was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20211201944-Covid-19 vaccine ad26.cov2.s -Fainting. 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: Syncope
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: 171/90 ELEVATED; Test Name: Body temperature; Result Unstructured Data: 100.2 F, LOW GRADE FEVER
Aktuelle Erkrankungen: Asthma; Hypoglycemia
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1917729

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: FL
Alter: 27,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Loss of consciousness Pallor Syncope Tremor

Symptomtext

Patient fainted and fell over. Regained consciousness in ~30 seconds from falling. Emergency services was called, fire rescue happen to be shopping to arrived in about 5 minutes. When fire rescue was tending to the patient (maybe about 20 minutes after initial fall) the patient started to shake blacked out for a few seconds again. Patient was pale, but responsive. Fire rescue proceeded to take him away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No known illnesses
Vorgeschichte: No known chronic health conditions
Andere Medikamente: None known.
Allergien: No known drug allergies
Vorherige Impfungen: -

VAERS 1913454

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: AK
Alter: 52,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 02.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: IM / RA

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

Blood test Chest X-ray Chest pain Computerised tomogram Dyspnoea Pulmonary thrombosis Urine analysis Vaginal haemorrhage

Symptomtext

Was seen in the Emergency Department and they found a blood clot in one of my lungs. Was started on Xarelto starter pack and to follow up with PCP. 10 days after starting Xarelto I returned to the ER for chest pain and shortness of breath. Along with vaginal bleeding. followed up with PCP whom referred me to Gynacologist ASAP because I have been bleeding vaginally heavy and with clots since stating the Xarelto.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: -
Labordaten: Blood work, Chest xray, UA, CT,
Aktuelle Erkrankungen: -
Vorgeschichte: Rheumatoid Arthritis, Bipolar
Andere Medikamente: Lithium 300mg, Xeljans 11mg, multivitamin, Emberen,
Allergien: Lactose
Vorherige Impfungen: -

VAERS 1958417

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: NY
Alter: 37,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LL

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

Drug hypersensitivity Feeling hot Paraesthesia Syncope

Symptomtext

Patient fainted in waiting room after vaccination with no head injury. Patient remained in chair seated during incident. She became quickly responsive and drank water. She experienced warmth and tingling in hands that resolved by end of 30 minute , Observation window she denied paramedics being called

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No illness prior to vaccination
Vorgeschichte: sulfa and methylprednisolone allergy
Andere Medikamente: unknown
Allergien: -
Vorherige Impfungen: -

VAERS 1903962

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: MO
Alter: 32,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient received vaccination, and 7-10 min later she approached the counter and informed of being syncopetic, then she passed out to the floor. We immediately called 911 and performed an initial evaluation. She was conscious, and breathing almost immediately. We kept her on the floor on her back until EMS arrived. They evaluated her and she left the pharmacy on her own accord.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: There was a nurse in line to receive her vaccination and she checked her pulse.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1897311

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: VA
Alter: 44,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Disorientation Hyperhidrosis Loss of consciousness Pallor Syncope

Symptomtext

Patient fainted in the waiting room approximately 5 to 7 minutes after receiving Janssen COVID-19 vaccine. He was caught by his father and a bystander (preventing fall). Upon regaining consciousness, he began to experience loss of color, sweating and disorientation. I removed his hat and jacket and kept him upright with support to keep him from falling. He fainted/loss consciousness an additional 2 times (time between unknown). I was unable to get a BP reading on an automatic BP machine. I administered 0.3mg of epinephrine. Patient reported approximately 30-45 seconds later he was beginning to feel better. Diaphoresis improved and he began to regain color. EMTs arrived and took over care.

Weitere VAERSDATA-Felder

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

VAERS 1895074

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Feeling abnormal Malaise Presyncope

Symptomtext

Pt received Janssen Booster. Pt previously received Pfizer Covid Vaccine x1 and Janssen Covid Vaccine x1 30mins post vaccination pt was observed to be dizzy by observation RN. Pt had a near syncopal event. Pt escorted by w/c to triage area and assess by provider. Pt denies SOB, chest pain. Provider recommended to call 911 for further evaluation at the ER @11:30. Vitals: 160/101, 83, 18, 100% A&O x4, dizzy upon standing -- > 155/94, 83, 18. Pt d/c to ER via EMS w/ family member In ED: Pt reports that he noticed he was feeling "weird" and generally unwell Described as pre-syncope States similar s/s w/receipt of prev covid vax. However, endorses mild CP w/onset of s/s States s/s ongoing but gradually improving. NO further information available. Pt appears to have been discharged from ED without intervention.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: CAD s/p stent, COPD, HTN, OSA, HLD, GERD, Diverticulosis, Diverticulitis, anxiety, chronic CP
Andere Medikamente: Medications: albuterol sulfate (PROVENTIL HFA;VENTOLIN HFA) 90 mcg/actuation HFA inhaler Inhale 1 Inhalation by mouth every 6 (six) hours as needed for Wheezing or Shortness of Breath. aluminum-mag hydroxide-simethicone (MINTOX MAXIMUM STRE
Allergien: Allergies: Pfizer COVID Vaccine
Vorherige Impfungen: -

VAERS 1858477

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: CO
Alter: 39,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Anxiety Arthralgia Asthenia Blood fibrinogen Blood uric acid Bradypnoea Malaise Nausea Pallor Syncope C-reactive protein Cold sweat Fibrin D dimer Full blood count Hypoaesthesia Immediate post-injection reaction Laboratory test Loss of consciousness

Symptomtext

Immediate negative reaction. Feeling of imminent death. Nausea, cold sweat, numbness, tingling, pass out. Continuing joint / tendon pain, night sweats, weakness 2 weeks post vaccination. Pain inside of left leg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Diner Quan, PTT, Uris acid, fibrinogen, ptt, c reactive protein, chem 13, CBC 500
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No known
Vorherige Impfungen: -

VAERS 1858477

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: CO
Alter: 39,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Arthralgia Asthenia Blood fibrinogen Blood uric acid Bradypnoea Malaise Nausea Pallor Syncope C-reactive protein Cold sweat Fibrin D dimer Full blood count Hypoaesthesia Immediate post-injection reaction Laboratory test Loss of consciousness

Symptomtext

Immediate negative reaction. Feeling of imminent death. Nausea, cold sweat, numbness, tingling, pass out. Continuing joint / tendon pain, night sweats, weakness 2 weeks post vaccination. Pain inside of left leg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Diner Quan, PTT, Uris acid, fibrinogen, ptt, c reactive protein, chem 13, CBC 500
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No known
Vorherige Impfungen: -

VAERS 1891006

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Head injury Posture abnormal Skin laceration Syncope

Symptomtext

Patient received COVID booster shot and reported feeling light headed while sitting in observation about 5 minutes later. She fainted and fell backwards in the chair. She lost consciousness and hit her head on the pavement. She revived about 30 seconds later and had some confusion for about 1 minute, then was A &O x 3. Patient was assessed by staff and EMS was called and arrive 5 minutes later. She received a 3 inch diameter scrape on her forehead. Vital signs were within normal limits and stable. After consultation with EMS, patient was transported to hospital. After the incident, the patient reported that she has a history of syncope related to needles and vaccinations. This was not reported to staff prior to the vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: NKDA
Vorherige Impfungen: patient reported history of syncopal events following needles and vaccinations

VAERS 1888350

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: NC
Alter: 23,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

Patient passed-out after vaccinated.

Weitere VAERSDATA-Felder

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

VAERS 1885579

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 23.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 5,0
Dosis: UNK
Route/Site: - / -

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

Ischaemic stroke

Symptomtext

I63.9 - Ischemic stroke (CMS/HCC) I63.9 - Stroke determined by clinical assessment (CMS/HCC)

Weitere VAERSDATA-Felder

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

VAERS 1882689

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: HI
Alter: 23,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Loss of consciousness Syncope

Symptomtext

Patient was given first dose of Janssen Covid vaccine with no issues upon administration. He was sitting during observation period and fainted after about 10 minutes. I checked on him immediately and he was alert and responsive. EMS was called and they checked and cleared him.

Weitere VAERSDATA-Felder

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

VAERS 1877579

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: MA
Alter: 51,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 01.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / AR

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

Angiogram cerebral normal Aphasia Facial paralysis International normalised ratio increased Neurological examination normal Visual impairment

Symptomtext

within a few minutes after receiving vaccine he had a brief visual disturbance similar to the ones that preceded his stroke in 2010 by a few days. Then in the evening of November 4th after finishing supper he found himself unable to talk (expressive aphasia) even though he understood speech and knew what he wanted to say. Family noted a right facial droop. ambulance called and arrived within about 15 minutes. By the time the ambulance got him to General Hospital he had fully recovered. He had a negative CT angioram of the brain. It was compared to the 2010 CT angiogram. Neurologist in ER found him to have entirely normal neurological exam.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: He had a negative CT angiogram of the brain. It was compared to the 2010 CT angiogram inr 2.0 on 11/4 at hosptial inr 1.9 on 10/13
Aktuelle Erkrankungen: none
Vorgeschichte: paroxysmal atrial fibrillation implantable pacemaker history stroke 2010
Andere Medikamente: warfarin multivitamin vitamin D
Allergien: latex
Vorherige Impfungen: -

VAERS 1877463

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: MA
Alter: 41,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / RA

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

Cold sweat Dizziness Fatigue Loss of consciousness Paraesthesia Syncope Tunnel vision

Symptomtext

This was my booster (second) J&J vaccine. About five minutes after receiving the vaccine, while I was sitting for the waiting period, I fainted. It began with tunnel vision, cold sweat, and then I blacked out. My wife was with me at the time and was unable to revive me for about ten to fifteen seconds. The pharmacist who gave the injection was also present. After waking up, I was lightheaded and had tingling hands for another ten minutes. After about 20 minutes, I was ok to walk and felt only a little tired. I had this exact same reaction (fainting) when I got my first J&J vaccine in April 2021 (I filed a VAERS report at that time as well - Temporary VAERS E-Report No: 422631).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Daily over-the-counter multivitamin. No medications.
Allergien: Allergic to dairy and gluten.
Vorherige Impfungen: J&J Janssen covid vaccine, April 2021, age 41.

VAERS 1873777

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 1855194

schwer

Staat: OH
Alter: 32,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Joint injury Loss of consciousness Skin laceration

Symptomtext

THE PATIENT WAS GIVEN A SHOT OF THE J&J COVID VACCINE. AFTERWARDS HE WAS ADVISED TO SIT AND WAIT FOR ROUGHLY 15 MINUTES JUST TO MAKE SURE THAT HE DID NOT HAVE AN ALLERGIC REACTION TO THE VACCINATION. HE WENT OUT TO HIS VEHICLE AND GRABBED A BOTTLE OF WATER THEN CAME BACK INSIDE WHERE HE PASSED OUT BY THE GREETING CARD SECTION. THE FRONT END MANAGER GRABBED HIM A CHAIR, SAT HIM UP AND INFORMED ME ABOUT WHAT WAS GOING ON. WE OBSERVED HIM FOR SEVERAL MINUTES WHILE HE DRANK SOME WATER AND SAID THAT HE FELT BETTER. FRONT END MANAGER BEGUN ENTERING A REPORT. I INFORMED THE PATIENT TO SIT A LITTLE WHILE AND CONTINUE DRINKING WATER AND TO LET ME OR FRONT END MANAGER KNOW IMMEDIATELY IF HE STARTED FEELING WORSE AGAIN. HE SAT FOR A FEW MORE MINUTES UNTIL HE FELT BETTER AND THEN LEFT. THE PATIENT DID NOT HIT HIS HEAD BUT DID SUSTAIN SOME ABRASIONS TO THE LEFT LOWER ARM AND STRUCK HIS HIP WHEN HE FELL.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: NO KNOWN ILLNESSES
Vorgeschichte: NO KNOWN CONDITIONS
Andere Medikamente: NOT KNOWN
Allergien: NO KNOWN ALLERGIES
Vorherige Impfungen: -

VAERS 1867909

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Altered state of consciousness Hyperhidrosis Loss of consciousness Pulse abnormal

Symptomtext

Post 1st Janssen injection, became sweaty, semi conscious, thready pulse. Patient was sitting when he lost consciousness, did not fall to floor, remained in the chair when the medical staff attended to him. When he became conscious, he was provided water, which he drank, and he was transferred into a wheelchair and then moved unto the cot. While in the wheelchair he started to go in and out of consciousness again. Dr. tended to the patient, BP 110/60, weak pulse, EMS was called at 12:44. At 12:53 EMS arrived, patient was conscious and talking, BP 120. EMS asked the patient a series of questions, rechecked BP, and pulse - all within normal range. Patient was able to sit up and stand without feeling lightheaded and refused EMS transport. EMS left, the patients spouse left to move their vehicle closer to the mall entrance, patient was offered and accepted a granola bar, when his spouse arrived back at the clinic the patient was wheeled to the mall entrance door in the wheelchair, as recommended by EMS as precautionary, and then walked to his vehicle from the mall entrance door with his spouse. When patient left he was talking normally, responsive, and reported feeling well.

Weitere VAERSDATA-Felder

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

VAERS 1867627

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Abdominal pain upper Asthenia Contusion Cough Decreased appetite Diarrhoea Discomfort Dizziness Ear infection Eye pain Facial pain Fatigue Gait disturbance Head discomfort Headache Hyperhidrosis Hypersomnia Impaired driving ability

Symptomtext

Fifteen minutes after injection, I experienced tingling in my left arm from my elbow to my fingers and body aches within an our accompanied by a severe headache. In less than 15 hours, I had a temp of 99 (normal temp is 97) with continued headache, stomach cramps and diarrhea. Additional symptoms that followed beginning day 1 post vaccine (Oct 30, 2021) through today (Nov 13, 2021) included complete loss of appetite, skin sensitive to the touch that felt bruised, night sweats that left me completely drenched, extreme fatigue and weakness to the point I could barely function and missed 2.5 days of work, my face and eyes hurt to the touch when washing them in the shower, my headache became so unbearable I had to stay in bed, sore throat, ear infection, developed a cough, passed out in my kitchen, severe dizziness that made it hard for me to ambulate throughout my home, severe cramping in my legs, with extreme fatigue in my limbs to the point it was difficult to lift them, the back of my neck and shoulders were so heavy, I had a hard time holding up my head, couldn't drive for a week as my vision was blurry to the point of nausea and reading became almost impossible as the words blurred together and danced on the page. I had one day where I slept for 20 hours, with additional hours of sleep being between 12-15+ hours a night. I was unable to clean my house, do dishes, make my bed, do laundry, fix meals and on the days I did work, it was extremely difficult. Day ten (10) I developed a rash on my chest that migrated to areas on my back, torso, neck and from my groin on the inside of my legs to just below my knees; this rash is still active in some locations.

Weitere VAERSDATA-Felder

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

VAERS 1865941

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: NV
Alter: 31,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac assistance device user Eye movement disorder Fall Induration Pallor Seizure

Symptomtext

Other 11/12/2021 03:16 PM Communication: Pt was administered her first Janssen vaccine today by RN. After vaccine was administered, went to get her water while I sat with patient and informed her of Vsafe, Pt became very pale. I asked her if she wanted to lay down. She agreed. i went to look for an open room and as soon as I came back which was only a couple seconds later, I lifted patient up from the chair and pts eyes rolled back, she fell on me and started to convulse and her arms became hard. Then told me to put her on the floor. I yelled for help, the AED cart. I asked someone to call the paramedics and to bring over a Dr., came over to assist me with the AED cart. Dr then came over to access pt. Pt was recommended to go to ER but choose not to go. She did sign and AMA. I will send VAERS report online and Incident report will go in her chart. Waited with pt until her car ride came to pick her up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: ASTHMA, DEPRESSION
Vorgeschichte: -
Andere Medikamente: ZOLOFT, BIRTH CONTROL
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 1865224

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: -
Alter: 35,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

1min post vaccination, pt had a syncopal episode. Pt was noted to be pale. Vitals: @17:32 BP 108/80, HR 66, SpO2 98% -- > @17:55 110/80 Pt stable and released from the vaccination site. Janssen Booster after Moderna Primary Series

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH, Medications, Allergies unknown to this writer.
Andere Medikamente: PMH, Medications, Allergies unknown to this writer.
Allergien: PMH, Medications, Allergies unknown to this writer. Pt reported NKA
Vorherige Impfungen: -

VAERS 1857806

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: WA
Alter: 30,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 01.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Blepharospasm Eyelid function disorder Facial paralysis Vision blurred

Symptomtext

Right eye began twitching / clamping shut within 2 days time. AS of 11/10/21, eyelid appeared to droop; vision is blurred in right eye at times.Right side of face is asymetrical when compared to left. No other facial discrepancies; no other notable neurological symptoms noted by mother, who is LPN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: The only varaible is the 2nd / 'booster' dose of J&J liquid Patient is electing to monitor symptom at this time/ will notify PCP/clinic if condition does not spontaneously resolve.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: ASA 325mg for clotting prophylaxis
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 1243456

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: NC
Alter: 36,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abnormal dreams Depressed mood Hallucination Limb discomfort Movement disorder Arthralgia Dizziness Fatigue Immediate post-injection reaction Injected limb mobility decreased Injection site pain Mobility decreased Neck pain Pain Pain in extremity Paranoia Parosmia Sleep disorder

Symptomtext

Immediate pain in arm at the sight of the injection, feeling dizzy, faint, and fatigued. The day following the vaccine fever as high of 99.8, extreme fatigue, arm pain. Two days after vaccine arm pain got worse, radiating from mid-shoulder to lower shoulder, upper shoulder, across clavicle, and to neck. Five days after vaccine and pain is worse, limited mobility of arm, shoulder, and neck. Intense pain with attempts to move arm or neck.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Have reached out to doctor for testing and appointment, awaiting reply.
Aktuelle Erkrankungen: none
Vorgeschichte: polycystic kidney disease
Andere Medikamente: none
Allergien: food: garlic, lactose intolerant
Vorherige Impfungen: COVID Vaccine, Pfizer Lot#EW0150, age 35, 4/5/21, hallucinations, intrusive thoughts, paranoia, beginning at midnight after rece

VAERS 1855563

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: CO
Alter: 39,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Immediate post-injection reaction Syncope

Symptomtext

Syncopal episode started immediately after vaccination. Patient was laid down on the ground with feet elevated. He was given water and food. Patient did not hit his head. Patient made a full recovery after 15 minutes.

Weitere VAERSDATA-Felder

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

VAERS 1855071

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: CA
Alter: 30,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Angina pectoris Blood test Electrocardiogram abnormal Headache Hypoaesthesia Malaise Muscle contractions involuntary Nausea Pericarditis Pyrexia Syncope

Symptomtext

About 12 hours after vaccination, I fell very ill with headache, fever, and nausea. As time went on, my hands started to go numb along with my legs and face. My muscles began to seize violently and I collapsed to the ground. I was later revived by co-workers and EMS who came shortly after. Following this event, I started to experience pain in and around my heart the next morning. The next day, I went to urgent care where some tests were run and I was able to see a doctor. They sent me home saying 'all was normal'. However, the pain persisted and I made an appointment with the cardiologist. There, I explained my symptoms and the cardiologist looked at my EKG where they found something abnormal. It also became obvious that the urgent care had missed some things as well as not ordered/done all the necessary tests. I left the cardiologists with a diagnosis of Acute Pericarditis. I am currently receiving treatment for it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: At the urgent care, I was given an EKG as well as some bloodwork on 11/1/21. The cardiologist I met with on 11/9/21 noticed something on my EKG that the urgent care doctors missed as well as the fact that they had not done the proper blood work. As of today (11/9/21), I have given them more blood to be analyzed as well as scheduled an upcoming ultrasound of my heart. The EKG and the description of my symptoms are what the doctor diagnosed me with acute pericarditis with.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1853827

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: MA
Alter: 26,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Heart rate decreased Hypotension Loss of consciousness

Symptomtext

After patient received his J&J COVID shot he told my technician who administered the shot that he was feeling woozey and would like some water...just after asking for the water he passed out...my technician was able to wake him but he was unaware that he passed out...911 was called and he was assessed...his blood pressure was low at 106/70 and heart rate was extremely low at 50 bpm...the EMTs assessed him for several minutes before feeling that his heart rate and blood pressure had stabilized and he was ok to leave.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: see above
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: another vaccine which is unknown

VAERS 1850413

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: TN
Alter: 40,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Loss of consciousness Nausea Palpitations

Symptomtext

Heart racing, sweating, dizzy and nausea then I passed out around 11:53pm

Weitere VAERSDATA-Felder

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

VAERS 1847009

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: CT
Alter: 19,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Erythema Hyperhidrosis Loss of consciousness

Symptomtext

Patient was very nervous about getting the covid Janssen vaccine and worked himself into an anxious state prior to getting injected. Very soon after getting injected, possibly 5 minutes, he passed out while sitting upright in a chair in the pharmacy. He quickly, possibly 10 seconds, regained consciousness, at which point we called for EMS. He was given water, but soon after, possibly 5 minutes, he passed out again. This time I noticed he was very sweaty and red in the face. He regained consciousness easily as before, but I insisted he lay down on the floor this time. With the help of a couple other people, I lowered him gently to the floor, putting a sweatshirt under his head, and feet up on a chair, to raise above his heart. His color quickly returned to normal and he seemed very alert at this point. EMS arrived, they evaluated him, and determined he was fine. After about 15 minutes, he sat back into the chair, drank water, waited another 20 or so minutes, then chose to drive home. I requested he call when he got home, he did, without any further incident.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1834257

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: OH
Alter: 28,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cold sweat Head injury Skin warm Syncope

Symptomtext

patient was fine when walking out of vaccine room but walked half way down an isle and passed out. Patient stated he felt warm prior to passing out. He was warm and clammy. He hit his head but refused medical treatment. No blood. Advise him to monitor for concussion.

Weitere VAERSDATA-Felder

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

VAERS 1825841

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

schwer

Staat: AZ
Alter: 20,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Loss of consciousness Nausea

Symptomtext

PATIENT FAINTED ABOUT 5 MINUTES AFTER RECEIVING VACCINATION. PATIENT WAS SITTING ON A BENCH AFTER VACCINATION AND STATED SHE FELT LIKE SHE WAS GOING TO PASS OUT OR THROW UP. WE WERE ABLE TO CATCH HER BEFORE SHE FELL, LAID HER DOWN ON HER LEFT SIDE AND SHE WOKE BACK UP. AFTER WAKING UP SHE SAID SHE IS PRONE TO FAINTING AND WAS VERY NERVOUS TO GET THE VACCINATION. GOT THE PATIENT A BOTTLE OF WATER, SHE LAID ON THE BENCH AND DRANK THE WATER FOR ABOUT 20 MINUTES, SAT UP FOR A FEW MINUTES THEN LEFT THE STORE STATING SHE WAS FEELING FINE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NO DRUG ALLERGIES PER PATIENT
Vorherige Impfungen: -

VAERS 2702639

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: 54,0
Geschlecht: M
Eingang: 26.10.2023
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Amnesia Asthenia Balance disorder Blood test Brain fog Chest pain Insomnia Magnetic resonance imaging ear Magnetic resonance imaging head Magnetic resonance imaging heart Migraine Night sweats Tinnitus Visual impairment

Symptomtext

chest pain, night sweats, insomnia, brain fog, migraines, ringing ear, no energy, memory loss, balance problems, visual problems. etc.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: blood test, MRI, eye, ear, heart
Aktuelle Erkrankungen: 1st. Jessen and Jessen covid vaccine symptoms from first shot on 6/18/21, resulting in chest pain, brain fog, migraines, ringing ear, no energy, memory lose, etc.
Vorgeschichte: high blood pressure, heart problems
Andere Medikamente: carvedilol, lisinopril
Allergien: none
Vorherige Impfungen: -

VAERS 2659596

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

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: 1
Route/Site: IM / RA

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 2559481

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IN
Alter: 31,0
Geschlecht: M
Eingang: 13.01.2023
Impfdatum: 10.01.2022
Beginn: 08.01.2023
Tage bis Beginn: 363,0
Dosis: 1
Route/Site: IM / AR

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

Blood test normal Chest pain Electrocardiogram normal Heart rate increased Hypoaesthesia X-ray normal

Symptomtext

About one year after receiving the Johnson and Johnson vaccine, I experienced what I thought was a heart attack while at work. My chest was hurting, my pulse went up to 160 resting and my hands and feet went numb. My wife drove me to the ER and they ran multiple tests. I had blood work drawn, an EKG and an X-Ray. I was put on a saline drip while there, but that is it. The hospital was not able to locate anything that may have caused the complications I was experiencing. I went to see my PCP and she has set me up with a Cardiologist. I will not see them for another three weeks. I'm still experiencing a spike in my heartrate even while doing something as simple as going to another room. I have been put on restrictions from my PCP to try and rule out certain options as for what could be causing the spike in my heartrate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Blood work; EKG; X-Ray
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin; TYLENOL; ibuprofen; WELLBUTRIN XL
Allergien: Milk; STRATTERA
Vorherige Impfungen: -

VAERS 2554747

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 06.05.2021
Beginn: 21.11.2022
Tage bis Beginn: 564,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

11/21/22 presents to EC ED for "shortness of breath". PMHx of "factor V and CAD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/21/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2502004

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Dyspnoea Epistaxis Eye irritation Hypoaesthesia Hypoaesthesia oral Impaired work ability Injection site erythema Laboratory test abnormal Lacrimation increased Loss of personal independence in daily activities Muscle spasms Paraesthesia Tongue discomfort Tremor Vitreous detachment

Symptomtext

My arm became red at the site of the injection and my leg became very shaky and this lasted for the next three days like I had the flu. To this day of the report I have shortness of breath and numbness, tingling down my left arm and leg. My immune system seems to be compromised. I am having auto immune conditions now and my legs spasm and cramp. When I take my bike out to ride I have severe spasms in my chest and lack the ability to breath and pain like someone is sitting on my chest, to this day I cannot function in any capacity at all, I have had to take a leave of absence from my medical education and I am unable to work. In addition I have burning and numbness of my tongue and nose bleeds daily, my eyes are continually burning and watering of the eyes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Ophthalmologist ran several test and said I have posterior vitreous and detachment.
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure
Andere Medikamente: Lisinopril
Allergien: Latex
Vorherige Impfungen: -

VAERS 2467512

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IL
Alter: 24,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 24.01.2022
Beginn: 15.02.2022
Tage bis Beginn: 22,0
Dosis: 2
Route/Site: SYR / UN

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

COVID-19 Chest discomfort Chest pain Dizziness Dyspnoea Echocardiogram Ehlers-Danlos syndrome Electrocardiogram abnormal Fatigue Impaired work ability Joint dislocation Joint hyperextension Oxygen saturation decreased Poor peripheral circulation Post-traumatic neck syndrome Productive cough Tachycardia Total lung capacity

Symptomtext

Chronic, constant, non-relenting left chest pain. Chest tightness, constriction, and heaviness. Tachycardia. Extreme shortness of breath, where I can't function. Lightheadedness and Fatigue that make it difficult to work. I feel faint when I stand. Wheezing, chronic sputum following covid infection March 2020 has gotten worse. In the past 3 months, my oxygen has been dropping to as low as 88. I was a steady 99 before this booster, now I'm lucky if I get it up to 96. I can hardly carry a grocery bag without cutting off circulation in my fingers. I am not the same person I was before I took this vaccine. Covid damaged me, but I recovered. I have not recovered from this second booster, and the symtoms that emerged following vaccination. The reported date of adverse events is approximate. I was bedridden for the first 2 weeks following the booster, symptoms emerged during those first 2 weeks and never went away. Additionally, I seem to have developed Ehler's Danlos like-symptoms.2 instances of whiplash, confirmed by an ER visit from injuries obtained during looking in the mirror, and reinjuring when eating. Additionally, a hyperextended knee and dislocated rib. All within the last 6 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Abnormal EKG 09/22/2022 following several normal ones in past years. Waiting for results of Echocardiogram and Pulmonary Capacity tests. I have a prior echo to compare to as well from childhood.
Aktuelle Erkrankungen: Prior Diagnosis of mitral valve regurgitation prior to receiving booster, following 1 month post initial vaccination. Childhood asthma, never needed to use an inhaler, but following booster, I've needed to.
Vorgeschichte: HPB, Autoimmune disease of unknown specificity. Victim of Parkersburg DuPont Poisonings.
Andere Medikamente: Effexor, Lisinopril
Allergien: -
Vorherige Impfungen: Jansen Covid 19 primary vaccine

VAERS 2465340

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 30.09.2022
Impfdatum: 03.11.2021
Beginn: 26.09.2022
Tage bis Beginn: 327,0
Dosis: 2
Route/Site: - / -

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

Bronchial wall thickening COVID-19 COVID-19 pneumonia Cardiac failure acute Cardiac failure congestive Chest X-ray abnormal Chest pain Condition aggravated Cough Dyspnoea Echocardiogram abnormal Ejection fraction normal Left ventricular failure Leukocytosis Nasal congestion Pneumonia Pneumonitis Polyuria

Symptomtext

Admission Date: 9/26/2022 Discharge Date: 9/29/2022 ? Pneumonia due to COVID-19 virus HOSPITAL COURSE: Patient is a 69 y.o. male with past medical history significant for paroxysmal Afib on eliquis, CHF, PVD, T2DM, liver cirrhosis, Parkinson's disease who presented to the ED for concern of chest pain and shortness of breath. Associated cough, rhinorrhea, and nasal congestion. In the emergency department, vital signs were stable. Labs significant for WBC 15, Pro BNP 2600 (previous 2000), procal 0.04. COVID-19 PCR positive. CXR showed severe congestive changes and bronchial thickening concerning for CHF versus inflammatory infection process worse in the left lung than the right. He was started on azithromycin and Rocephin. He was admitted for further evaluation and management. With negative procal, antibiotics were discontinued. Decadron started for covid and possible CXR findings. He was continued on IV diuresis for acute on chronic diastolic heart failure. Repeat echo showed EF 57% (down from 67% previously) with findings consistent with RV pressure overload. He was transitioned back to home torsemide. Oxygen was weaned off. He was discharged home in stable condition with upcoming cardiology appointment scheduled. Of note, leukocytosis increasing, suspect steroid induced as infectious symptoms improving, no fever. Patient did not want to stay to be monitored further, return precautions given.

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Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Peripheral vascular disease (HCC) Low back pain Hyperlipidemia HTN (hypertension) DM (diabetes mellitus), type 2 (HCC) Persistent atrial fibrillation (HCC) Inguinal hernia Myalgia Depression Diverticulosis OSA (obstructive sleep apnea) Polycythemia vera/Myelodysplastic Syndrome (HCC) Anemia, iron deficiency Bilateral varicoceles CHF (congestive heart failure) (HCC) Hyperkalemia Type 2 diabetes mellitus with both eyes affected by moderate nonproliferative retinopathy without macular edema, with long-term current use of insulin (HCC) Bilateral leg edema Acute on chronic congestive heart failure, unspecified congestive heart failure type Chronic diastolic heart failure (HCC) PD (Parkinson's disease) (HCC) Hemifacial spasm Cholecystitis Acute on chronic combined systolic and diastolic CHF (congestive heart failure) (HCC) Primary pulmonary hypertension (HCC) Morbid (severe) obesity due to excess calories (HCC) Bilateral impacted cerumen Abrasion of left ear canal, initial encounter Atrial fibrillation, unspecified type (HCC) Chest pain Pneumonia due to COVID-19 virus Other cirrhosis of liver (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet acyclovir (ZOVIRAX) 200 MG capsule allopurinol (ZYLOPRIM) 300 MG tablet apixaban (ELIQUIS) 5 MG tablet carbidopa-levodopa (SINEMET) 25-100 MG per tablet empagliflozin (JARDIANCE) 25 MG tablet gabapentin
Allergien: None
Vorherige Impfungen: -

VAERS 2452981

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: -
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 26.08.2022
Beginn: 30.08.2022
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: - / -

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

Asthenia Cough Fatigue Hyperhidrosis Hypoaesthesia Paraesthesia Rhinorrhoea

Symptomtext

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: 1855194 expiry: UNKNOWN) dose was not reported, administered on 26-AUG-2022 for covid-19 prophylaxis. No concomitant medications were reported. On 2022, the patient experienced tingling of both arms from the elbow until the hands and in both legs from knees until the feet, and numbness of both arms from the elbow until the hands and in both legs from knees until the feet. On 30-AUG-2022, the patient experienced lot of runny nose, sweating, dry cough, weakness, and tiredness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from lot of runny nose, sweating, weakness, and tiredness on SEP-2022, and had not recovered from dry cough, tingling of both arms from the elbow until the hands and in both legs from knees until the feet, and numbness of both arms from the elbow until the hands and in both legs from knees until the feet. This report was non-serious.

Weitere VAERSDATA-Felder

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

VAERS 2446089

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 1855194

moderat

Staat: VA
Alter: 39,0
Geschlecht: M
Eingang: 15.09.2022
Impfdatum: 11.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Balance disorder Blood thyroid stimulating hormone increased Disturbance in attention Feeling abnormal Headache Impaired driving ability Migraine Pain in extremity Sleep disorder Tinnitus

Symptomtext

a. Starting 3-4 days after employer mandated Vaccine on 11NOV2021, began having the following symptoms: i. Day3, loss of balance, brain fog, pain in upper left thigh, migraines. ii. Day4, painful headaches, top of skull and temple/side of skull, ringing in ears increasing. 3. Patient reported on initial visit that he continued to have pain in thigh (inner and outer left thigh) near groin and down to femoral, and deep fascia. a. Pain would last approximately 1-5 minutes and would require patient to massage with great pressure (even stated that he was required to resort to striking his own leg with a closed fist on several occasions to alleviate the pain/pressure). 4. For the next 30+ days, Patient continued to experience pain in thighs and calves. a. Primarily pain was on left side, but also occurred on right side. b. This daily pain has lessened to approximately once a week 5. Ringing (tinnitus) in both ears was reported to have not subsided. a. Patient did not recall ever experiencing tinnitus prior to DEC 2021. This ringing has gradually gotten more disturbing 6. In first week of March 2022, the pain was so great in the thigh (while driving) that patient had to pull over on the side of the highway and walk it off. 7. Ringing has persisted since the last office visit (as of 18APR2022) and is impacting sleep and concentration. Ringing is noticeably louder and higher pitch. a. Patient has purchased a machine to sleep. Patient can not be in complete silence, and electricity signals from lights or electronic devices that emit buzz or whine are very disturbing to patient. 8. Upon initial visit: Patient notified physician ( Medical Associates) (ATN: Dr.) , physician stated that a follow up in a few months would be required. Subsequent follow up with missed due to work commitment. And patient made a new appointment (earliest possible to get in) with another physician slated for NOV2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Patient was unable to get into Primary Care provider until months after symptoms. Patient missed follow up appointment due to mandated work travel 3 months later. Patient had lab draw on 03JAN2022, showed elevated TSH. Patient has follow up with a new primary care physician scheduled for first week of NOV2022.
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Multi Vitamin
Allergien: UNK
Vorherige Impfungen: -

VAERS 2372157

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NJ
Alter: -
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain Acute kidney injury Amnesia Anaemia Arthralgia Asthenia Back pain Blood test abnormal Blood thyroid stimulating hormone Blood urea increased Cellulitis Cough Decreased appetite Dehydration Dyschromatopsia Ear discomfort Electrolyte imbalance Fall

Symptomtext

RECEIVED ONE DOSE J & J VACCINE ON NOV 1, 2021 MATTER OF 3-4 HOURS AFTER VACCINE DEVELOPED GENERALIZED JOINT PAIN - SO SEVERE NOTHING RELIEVED IT - NO MED, NO POSITION ETC. - SLIGHT NAUSEA SUBSIDED QUICKLY, GENERALIZED WEAKNESS, LETHARGY, UNSTEAD GAIT, LOSS OF APPETITE, SIGNIFICANT WT LOSS THIS LED TO 3-4 FALLS DURING THIS PERIOD OF 3 - 3 1/2 MONTHS IN WHICH I FURTHER DEVELOPED (L) SIDED ABDOMINAL PAIN WHICH PERSISTED ANTACIDS ETC NO EFFECT - NO CHANGE WITH ANTIBODIES ETC. - THIS CONTINUED SEVERAL DAYS BEFORE SUBSIDING AS TIME WENT ON - BILATERAL LOWER EXTREMITY MUSCLE CRAMPS (EVEN IN ANKLES) DEVELOPED PHLEBITIS/CELLULITIS IN ONE LOWER EXTREMITY WITH BILATERAL ANKLE EDEMA RX FOR KEFLEX PRESCRIBED BY MY PRIMAR MD VIA VERBAL CONTACT - UNABLE TO GO TO OFFICE IN MY CONDITION - THIS RESOLVED AFTER TREATMENT - STILL HAD "VEIN SORENESS" BOTH LOWER EXTREM JOINT / MUSCULAR PAIN SUBSIDED AFTER SEVERAL DAYS WITH EXCEPTION OF SCIATI (L) AND CERVICAL PAIN IN ADDITION (L) EAR / JAW AREA DISCOMFOR LASTED SEVERAL DAYS LATER IN THIS PERIOD DEVELOPED PELVIC PAIN - 72 YRS OLD SYMPTOMS REMINDED ME OF PRE-MENSTRUAL SYMPTOMS YEARS AGO HEADACHE, LOWER BACK PAIN SUBSIDED WITHIN A FEW DAYS HAD EPISODES OF AMNESIA (LOSS/MEMORY) COLOR VISION CHANGES - MULTIPLE DAYS OF NAPPING FREQUENTLY PLEASE NOTE NO FEVER, NO LOSS OF SMELL ETC. 11/29/21 TAKEN TO HOSPITAL - MD NEVER EXAMINED ME THIS WAS TOLD TO MEDICAL DIRECTOR OF ER - ORDERED BLOOD WORK ONLY NEVER EXPLAINED TO ME - AS A NURSE READ HOSPITAL PAPERS (DX AS ACUTE RENAL FAILURE, DEHYDRATION) ONLY TX GIVEN WAS 1 LITTER OF NORMAL SALINE AFTER HOURS OF WAITING FOR ATTENTION 21 DAYS AFTER VACCINE ADMINISTRATION ABLE TO SLEEP WITHOUT AWAKENING WITH EARLIER DESCRIBED JOINT/MUSCULAR PAIN 2 WKS AFTER VACCINE DEVELOPED SORENESS AT INJECTION SITE - NONE PREVIOUSLY SUBSIDED QUICKLY DEVELOPED BILATERAL HAND TREMORS NOT SURE OF DURATION OBTAINED MEDICAL RECORDS WHICH DIDN'T REVEAL TRUTH RE: MY LACK OF CARE RE: PHYSICAL EXA PLEASE NOTE SAME BLOOD TESTS WERE NORMAL (APROX) 1 MONTH PRIOR TO LABS DRAWN AT HOSPITAL HOSPITAL LABS INDICATED INCREASED LIVER ENZYMES LOW PLATELET COUNT, LOW PROTEIN, ELECTROLYTE IMBALANCE, LOW BLOOD COUNT (ANEMIA) INCREASED BUN / KIDNEY FUNCTION TESTS GROSSLY ABNORMAL FORGOT TO MENTION EPISODES OF COUGHING PERSIST PRODUCTIVE AND NON-PRODUCTIVE - NEEDED NEBULIZER TX INHALERS ETC. - COUGH LESSENED TIME BUT HAD FOR GOOD 3 MONTHS ALSO (L) THIGH PAIN NOTICED NO GROWTH OF HAIR SINCE ONSET OF THIS - VERIFIED BY BEAUTY INSTRURCTOR - NO GROWTH OF HAIR ON LOWER EXTREIMITES ALSO - SAID MY HAIR WASN'T AS FULL AS USUAL - THIS IS ONLY THING THAT HAS REMAINED 3 - 4 MONTHS AFTER INCIDENT ALL LABS BACK TO NORMAL PLEASE NOTE UNFORTUNATELY MD LISTED ON ER RECORD NEVER EXAMINED ME - JUST ORDERED LABS - TOO SICK TO VISIT MY PRIMARY PHYSICIAN SAW ME AFTER SYMPTOMS SUBSIDED

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Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: 11/29/21 CBC TSH METABOLIC PANEL
Aktuelle Erkrankungen: NONE
Vorgeschichte: HYPOTHYROIDISM, HTN, HIATAL HERNIA ASTHMA
Andere Medikamente: SYNTHROID, BENICAR, IBUPROFEN TAGAMET, VIT D
Allergien: NONE
Vorherige Impfungen: -

VAERS 2338818

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: VA
Alter: 30,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 29.10.2021
Beginn: 11.01.2022
Tage bis Beginn: 74,0
Dosis: 2
Route/Site: SYR / LA

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

Ageusia Arthralgia COVID-19 Cough Dysgeusia Dyspnoea Fatigue Feeling abnormal Headache Impaired work ability Malaise Oropharyngeal pain Pain Paraesthesia Peripheral coldness Pyrexia Rash Rhinorrhoea

Symptomtext

Starting 01/10/2022, I developed a rash across my chest and upper back, and a sore throat. On 01/11/2022, I went to work and I felt a little off but not enough to be off. I left in the middle of the day not feeling well. I had a fever spiking at around 102, a headache and body aches, joint pain and sore throat which worsened. The cough started either that night or the next day (01/12/2022). For about 3-4 days I would experience the same symptoms but nonstop. I tested positive on 01/12/2022. My temp started to subside around 01/15/2022 and it would remain at about 99F-100F for about a week. I still felt fatigued, body aches, cough, sore throat and runny nose until about 01/28 or 01/29. Then, I returned to work on 01/31/2022. It wasn't until then I noticed the "brain fog" which lasted for about a month. The last week of January my taste seemed to change and things started tasting funny/metallic. To this day, my taste has not returned and I have lost about 40 lbs due to being unable to tolerate most foods: dairy tastes sour/spolied, meat tastes rancid/bad, everything else has a chemical/dirt taste (breads and vegetables) and I am unable to tolerate sweets (make me nauseous). Also, around the 2nd week of being sick I developed extreme coldness in my hands and feet which would require extremely hot temperatures to rewarm them. To this day, I still get episodes of tingling coldness in my hands and feet but more intermittent (about 1x weekly now). During this episode, someone gave me a pulse ox to monitor my oxygen levels and the lowest they ever went were about 90% and, at that time, I was having shortness of breath and feeling very fatigued.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID PCR test (01/12/2022): Positive 2 at home tests COVD: Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Failing Gallbladder
Andere Medikamente: Nasonex, Trazadone PRN, Multivitamin, Vitamin D Gummy and Probiotic
Allergien: Penicillin and Amoxicillin, Sensitivity to Chlorhexidine
Vorherige Impfungen: -

VAERS 2323981

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: -
Alter: 21,0
Geschlecht: M
Eingang: 18.06.2022
Impfdatum: 19.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Echocardiogram abnormal Electrocardiogram normal Mitral valve prolapse

Symptomtext

pt started feeling chest pains apprx ~1 wk after vaccination, EKG normal, echo shows mitral valve prolapse

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Echocardiogram and EKG 4/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2298751

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NY
Alter: 54,0
Geschlecht: F
Eingang: 27.05.2022
Impfdatum: 24.11.2021
Beginn: 11.01.2022
Tage bis Beginn: 48,0
Dosis: 1
Route/Site: IM / LA

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

Cardiomegaly Dyspnoea Exercise tolerance decreased Fatigue Generalised oedema Heavy menstrual bleeding Hypertension Imaging procedure abnormal X-ray

Symptomtext

new onset HTN, generalized edema heavy menstrual cycle continued sob and fatigued, activity intolerance enlarged heart as shown on imaging studies completed on 2/21/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: twice daily blood pressure monitoring Xray
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Albuterol inhaler prn
Allergien: Penicillin and Sulfa drugs
Vorherige Impfungen: -

VAERS 2287184

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IL
Alter: 29,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 19.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Blood test abnormal Central nervous system function test normal Feeling of body temperature change Hypoaesthesia Immunisation reaction Laboratory test abnormal Neurological examination normal Pain Pain in extremity Paraesthesia Sensory disturbance Vitamin D decreased

Symptomtext

Beginning day after vaccine: constant numbness/tingling sensations and hot/cold sensations throughout legs from knee to feet, with intermingled pain; same sensations of pain and numbness throughout arms and torso but less constantly. These constant sensations lasted about 2 weeks (January 20-February 1, 2022). After that time the frequency of sensations slowly decreased but intensity of pain has increased. From February 1, 2022 to present: painful pinching sensations throughout body (on arms, legs, torso, feet, joints, head) which occur randomly and without warning; approximately 2-8 sensations/hour. Occasional numbness on various parts of body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Blood draw showed low Vitamin B & D. Neurology physical exam showed that nerve function appears normal. Neurologist stated that the sensations are an "over-active inflammatory response" to the vaccine and "should go away in a few months" (has not gone away yet). No treatment options given.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2287135

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IA
Alter: 58,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 02.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / -

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

Angiogram pulmonary abnormal Asthenia Blood sodium decreased COVID-19 Chest X-ray abnormal Cough Dyspnoea Fibrin D dimer Hilar lymphadenopathy Hyponatraemia Hypoxia Laboratory test abnormal Lung infiltration Myalgia Nausea Pneumonia Pneumonia viral Pyrexia

Symptomtext

COVID Vaccine Breakthrough Case J&J Dose 2/2/21 (1855194) COVID Positive 12/15/21 12/15/21: 58-year-old male with no past medical history except he has a chronic smoker. He presented to the emergency room this morning complaining of worsening SOB and associated cough of 5 days duration. He also complained of fever, nausea, occasional vomiting, generalized weakness and some myalgia. Patient received 1 dose of Johnson and Johnson COVID vaccine on 12/02/2021. At the emergency room he was quite febrile with a temperature of 104.2? F and hypoxic currently requiring 3-4 L of oxygen with O2 saturation of 100% but on room air saturation is 88%. Other vitals are normal. The laboratory test is significant for mild hyponatremia with Na 132 and D-dimer of 0.77. CT angiogram of the chest revealed no PE in the proximal vessels, mediastinal, bilateral hilar adenopathy and bilateral infiltrates right greater than left. 12/18/21: 58-year-old man who presented worsening shortness of breath, cough for 5 days duration. In the emergency department he was noted to be febrile and hypoxic on room air, COVID-19 rapid antigen and PCR was subsequently positive. Chest x-ray And CT pulmonary angiogram demonstrated bilateral viral pneumonitis and ruled out pulmonary embolism. was admitted to the hospitalist service where was started on anti-inflammatory agents, parenteral steroids and remdesivir with good effect. Clinical response was favorable with resolution of hypoxia, improvement in shortness of breath and cough. He has been successfully weaned to room air will be discharged today in stable medical condition to continue outpatient follow-up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: chronic smoker
Vorgeschichte: chronic smoker
Andere Medikamente: none
Allergien: NKA
Vorherige Impfungen: -

VAERS 2282902

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IA
Alter: 31,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chills Dyspnoea Pain Pyrexia

Symptomtext

I experienced shortness of breath, fever, body aches and chills.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypermobility Syndrome, Depression, Anxiety, ADHD
Andere Medikamente: Hydrocodone, Viibryd, Metformin
Allergien: Apples, Tape Adhesive, Steroids
Vorherige Impfungen: -

VAERS 2237303

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: OH
Alter: -
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: -
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

COVID-19 pneumonia Oxygen saturation decreased SARS-CoV-2 test Scan Vaccination failure

Symptomtext

This spontaneous report received from a patient concerned a 74 year old female of unknown race and ethnicity. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received Covid-19 vaccine ad26.cov2.s (unspecified manufacturer) (dose number in series 1) (suspension for injection, route of admin, batch number and expiry were not reported) dose, start therapy date were not reported, 1 total administered for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of Covid-19 vaccine ad26. cov2.s (dose number in series 1). The patient received Covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194, and expiry: UNKNOWN) dose was not reported, 1 total administered to right arm on 04-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 01-JAN-2022, the patient had a sore throat (dose number in series 2). On 03-JAN-2022, she went to the clinic and underwent polymerase chain reaction (PCR) Covid-19 test, the test came out positive (confirmed Covid-19 infection) which led to confirmed clinical vaccination failure (dose number in series 2). On JAN-2022, she started with a lot of coughing and decreased oxygen, laboratory data included: Oxygen saturation decreased (NR: not provided) decreased, so she returned to the clinic and they did a scan which was negative for clots, and positive for pneumonia (dose number in series 2). On 07-JAN-2022, the patient was administered with steroids and monoclonal antibody. The action taken with Covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from Covid-19 pneumonia, and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000225106. Sender's Comments: V0: 20220414785-COVID-19 VACCINE AD26.COV2.S-COVID-19 pneumonia. 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. 20220414785-COVID-19 VACCINE AD26.COV2.S- Confirmed clinical vaccination failure. 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: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: Test Date: 202201; Test Name: Scan; Result Unstructured Data: negative for clots; Comments: negative for clots; Test Date: 202201; Test Name: Oxygen saturation decreased; Result Unstructured Data: decreased; Test Date: 202201; Test Name: Scan; Result Unstructured Data: positive for pneumonia; Test Date: 20220103; Test Name: SARS-CoV-2 PCR test; Result Unstructured Data: Positive.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2218651

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / RA

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

Blood test Computerised tomogram Dyspnoea Fatigue Inflammation Laboratory test Magnetic resonance imaging Vocal cord disorder X-ray

Symptomtext

Breathing problems, shortness of breath, hospitalization. Fatigue, inflamation, damaged vocal chord

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 13,0
Labordaten: Cat scans, xrays, blood work,MRI, ent TESTING. HEART TESTING
Aktuelle Erkrankungen: back pain, asthma,
Vorgeschichte: hypertension, asthma
Andere Medikamente: amlodipine, baclifin, lisinopril, pantoprazole,
Allergien: codein
Vorherige Impfungen: polio 1961

VAERS 2201801

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IL
Alter: 50,0
Geschlecht: M
Eingang: 28.03.2022
Impfdatum: 23.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Diarrhoea Dyspnoea Influenza like illness Pyrexia

Symptomtext

Patient started having sever flu like type symptoms (fever, diarrhea), and experienced shortness of breath. resolved late 3-26-2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknon
Vorgeschichte: Afib per wife
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2189864

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: MI
Alter: 94,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 31.12.2021
Beginn: 18.03.2022
Tage bis Beginn: 77,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Chest X-ray abnormal Cough Dyspnoea Influenza virus test Pleural effusion Pulmonary congestion Respiratory syncytial virus test SARS-CoV-2 test positive

Symptomtext

cough and sob, tested positive on 3/18/22 for COVID

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Covid-19, Flu, RSV by NAA SARS CoV2 detected on 3/18/2022 CXR on 3/20/22: Low lung volumes with suggestion of pulmonary vascular congestion and small bilateral pleural effusions.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, obesity, AKI
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2179010

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Dizziness Investigation Tachycardia Vertigo White blood cell count

Symptomtext

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, gallbladder removal, and concurrent conditions included, irregular heart rhythm for years (reported as never waiver, never different), weak immunity, kidney problem, and sepsis, and other pre-existing medical conditions included patient was very sick from an unspecified date in JAN-2021 to on an unspecified date in APR-2021. Patient stated one day she even passed out and her heart stopped for a second. She was hospitalized and her white blood cell count was 22,000 (Unit not specified). She stated her heart rhythm still behaved the same way even after the sickness. Number of days hospitalized and discharge information was not reported. Patient looks younger than she was and she takes care of herself. She was very beautiful and slender. She is a very active person but since receiving the booster she was a very different person. The patient received Covid-19 vaccine ad26. cov2. s (suspension for injection, route of administration not reported, batch number: unknown, and expiry: unknown) dose was not reported, dose number in 01, 01 in total, administered on left arm on an unspecified date in JUL-2021 for prophylactic vaccination. On an unspecified date, following vaccination with Covid-19 vaccine ad26.cov2.s, it was unknown if patient had any side effects (dose number in series 01). The patient additionally received Covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration not reported, batch number: 1855194, and expiry: unknown) dose was not reported, dose number in series 02, 01 in total, administered on right arm on an unspecified date in NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, concern started since the rhythm was intermittent. Due to booster vaccine her heart beats faster than usual. According to patient rhythm mostly came from heart atrium but sometimes from ventricle. She had bad tachycardia, also had dizziness and vertigo (dose number in series was 02). Patient went to an electrophysiologist and got some tests done but she won't hear back. The action taken with Covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from bad tachycardia/heart beats faster than usual, and the outcome of dizziness and vertigo was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Test Name: Investigation; Result Unstructured Data: unknown; Test Name: WBC; Result Unstructured Data: 22000 (Unit not specified).
Aktuelle Erkrankungen: Cardiac arrhythmia; Immunodeficiency; Kidney disorder; Sepsis
Vorgeschichte: Medical History/Concurrent Conditions: Gallbladder removal; Comments: Patient was very sick from an unspecified date in JAN-2021 to on an unspecified date in APR-2021. Patient stated one day she even passed out and her heart stopped for a second. She was hospitalized and her white blood cell count was 22,000 (Unit not specified). She stated her heart rhythm still behaved the same way even after the sickness. Number of days hospitalized and discharge information was not reported. Patient looks younger than she was and she takes care of herself. She was very beautiful and slender. She is a very active person but since receiving the booster she was a very different person.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2166250

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: UT
Alter: 57,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 03.11.2021
Beginn: 20.01.2022
Tage bis Beginn: 78,0
Dosis: UNK
Route/Site: SYR / LA

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

Angiogram Arthralgia Chest X-ray abnormal Chest discomfort Chest pain Dyspnoea Fatigue Fibrin D dimer increased Pneumonitis Pulmonary mass

Symptomtext

Tightness in chest, pain across chest and shoulders, hard to get a deep breath, and fatigue. Because I have had two past blood clots I decided I should get checked and I had heard about the possibility of clots with that particular vaccine. Dr. determined because of my past history I needed a D-Dimmer if that was elevated I would need an x-ray and CTA. The result was elevated so I did the other test. CTA was clear, but the x-ray found a small nodule on left lung. I was told to start an aspirin regimen every day and take Ibprophen 4 times a day for a week to help inflammation in the lungs. After a week my breathing did improve. I still become winded at times. I was told to check on lung nodule again in 6 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: chest x-ray, D-dimmer blood test, CTA
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: armour thyroid, progesterone, DIM-Evail, sertraline
Allergien: none
Vorherige Impfungen: -

VAERS 2134380

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NJ
Alter: 60,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 10.02.2022
Beginn: 11.02.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Blood pressure increased Chills Crying Dyspnoea exertional Electrocardiogram Fatigue Headache Lymphadenopathy Rash Rash pruritic

Symptomtext

Patient stated that next morning 2/11 she woke up with fatigue, chills, swollen under Left arm (lymph node area on same side shot was given), also complained of headaches. chills went away on 2/13. On 2/14 felt weakness with SOB with walking. she saw Dr. on 2/12, her Blood pressure was elevated and they did EKG. she left crying office and went home. Dr. told her to fill out a Vaers form for the vaccine but she has no access to internet at home. So she came in to health department to report. She also developed a couple itchy bumps on bilateral ribs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: denied any. Did have covid-19 (12/22/21)
Vorgeschichte: -
Andere Medikamente: on blood pressure medicine since June 2021
Allergien: PCN
Vorherige Impfungen: -

VAERS 2112636

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NY
Alter: 46,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 10.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: JET / LA

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

Cough Dehydration Diarrhoea Dysphagia Myalgia Nasal congestion Nasal mucosal disorder

Symptomtext

Dehydration, Coughing, Stuffy nose, mucous, HARD TO SWALLOW, ACHING MUSCLES

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Yes. Supplements DIETARY
Allergien: No
Vorherige Impfungen: -

VAERS 1857462

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: -
Beginn: 01.08.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Asthenia Back pain Cyst Mass Pain B-cell lymphoma Biopsy Blood test Computerised tomogram abdomen Computerised tomogram thorax Injection site mass Injection site pain Mammogram Pain assessment Ultrasound scan Paraesthesia

Symptomtext

LUMP AT INJECTION SITE; LEFT SHOULDER PAIN AT INJECTION SITE; MARGINAL B CELL LYMPHOMA; This spontaneous report received from a patient concerned a 57 year old female 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 (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1855194, expiry: UNKNOWN) dose was not reported, 1 in total administered to left deltoid on 04-AUG-2021 for prophylactic vaccination. No concomitant medications were reported. Around early to mid August 2021, following vaccination with covid-19 vaccine ad26.cov2.s, the patient felt a pain in the right flank (towards the right hip). The patient visited a dermatologist around 10-Aug-2021 for the pain, who sent her for testing. On 19-Aug-2021, she received an ultrasound and showed 09 into 08 cm heterogenous mass just below the skin surface along the right flank. On 23-Sep-2021, Computed tomography (CT scan) of chest and abdomen was done for the initial complaint of the heterogenous mass on the right hip which had not shown that it was an unremarkable study. On 28-Sep-2021, patient also had a routine mammogram which came back fine. Around 15-Nov-2021, the patient also developed 2 masses on the right side flank (described as where a woman's bra strap would) and back side of the left shoulder. She described the masses as very dark in color, raised, and noticeable. The one the shoulder was smaller than a quarter and the 2 on the flank were larger than a quarter but felt bigger than it looked. Since the CT above was unremarkable, she made an appointment with her primary dermatologist to assess the right hip mass once more, but by this time she had developed the masses described above as being on the right flank and left shoulder so the dermatologist focused on those masses. She had a biopsy of the masses on the right flank and the left shoulder on 29-Nov-2021 by the primary dermatologist, which showed an atypical lymphoid infiltrate. The patient was diagnosed with marginal B-cell Lymphoma on 23-Dec-2021. On an unspecified date the patient had left shoulder pain at the injection site and a lump at the injection site that was still there, the pain was described as a 1/10 but noticeable (dose number in series 1). The patient also visited Cancer Centre on 18-JAN-2022 where she had another biopsy (of the right flank only) and blood work done. The biopsy results were pending, and the blood work came back normal with a couple of red flags. The action taken with covid-19 vaccine ad26.cov2.s was not reported. The patient had not recovered from marginal b cell lymphoma, left shoulder pain at injection site, and lump at injection site. This report was serious (Other Medically Important Condition). This case, involving the same patient is linked to 20220146890 (dose number in series 2).; Sender's Comments: V0: 20220145846- COVID-19 VACCINE AD26.COV2.S- MARGINAL B CELL LYMPHOMA. This event(s) is considered not related. The event(s) shows an incompatible temporal relationship.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20210819; Test Name: Diagnostic ultrasound; Result Unstructured Data: 09 X 08 cm heterogenous mass; Test Date: 20210923; Test Name: Abdomen CT; Result Unstructured Data: unremarkable; Test Date: 20210923; Test Name: Chest CT; Result Unstructured Data: unremarkable; Test Date: 20210928; Test Name: Mammogram; Result Unstructured Data: Fine; Test Date: 20211129; Test Name: Biopsy; Result Unstructured Data: atypical lymphoid infiltrate; Test Date: 20220118; Test Name: Blood test; Result Unstructured Data: Normal; Test Date: 20220118; Test Name: Biopsy; Result Unstructured Data: Not reported; Test Name: Pain scale; Result Unstructured Data: 1/10 but noticeable
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2082694

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IN
Alter: 56,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

COVID-19 pneumonia Chest X-ray Fatigue Hypoaesthesia Laboratory test Malaise Pain Pain in extremity Renal disorder Spinal X-ray Swelling Swelling face

Symptomtext

pt felt tired and unwell later in the day after receiving injection. body aches started the next day. she was hospitalized 11/21/21-11/29/21 at hospital for covid pneumonia. she was given remdesivir and dx'd with kidney damage and symptoms worsened with treatment. she was discharged and returned to same ER 12/14/21 for facial and neck swelling. went to ER 12/27/21 arm pain and numbness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 9,0
Labordaten: labs, chest xray, neck xray
Aktuelle Erkrankungen: n/a
Vorgeschichte: hypothyroidism
Andere Medikamente: synthroid
Allergien: codeine
Vorherige Impfungen: -

VAERS 2071980

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 20.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Electrocardiogram Headache Hypoaesthesia Paraesthesia

Symptomtext

The morning after I received the vaccine I started with a headache and numbness tingling in my fingertips/toes. the headaches continued mostly all the time for 3 weeks and then they started to diminish. I went to the ER per my Dr's request because of the headaches and chest pain, numbness and tingling . They did an EKG and told me to see headache specialist or my pcp about the HA. Date of ER visit 12/29/21. Still have nightly headaches which have improved but numbness/tingling in hands/feet continues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 12/29/21 EKG ER visit
Aktuelle Erkrankungen: NA
Vorgeschichte: occasional GERD-diet controlled, occasional constipation
Andere Medikamente: vitamin D, vitamin C
Allergien: NKA
Vorherige Impfungen: -

VAERS 2068547

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IN
Alter: 27,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / LA

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

Chills Decreased appetite Feeling abnormal Feeling cold Immediate post-injection reaction Injection site pain Insomnia Lymph node pain Migraine Mobility decreased Nausea Neck mass Rhinorrhoea Swelling

Symptomtext

Immediately after injection, there was pain in injection site and it became very sore. By 10PM the night of vaccination, I was shivering, freezing and couldn't sleep; kept waking up all night. Next morning (10/23) I was miserable: nauseous, I had a migraine/ headache and couldn't even get out of bed until after 11AM. I took Aleve since I had to get out of the house for my dog's vet appointment. I felt better after taking Aleve, but I had loss of appetite that day as well. On the evening of 10/24, I felt a lump in the left side of my neck, same side as injection site. It was swollen and sore lymph nodes that lasted a few days, along with sniffles. I spent more time sick post-vaccine than I did when I actually got Covid-19 in Feb 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Sprintec birth control, spironolactone for acne
Allergien: none
Vorherige Impfungen: -

VAERS 2065404

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: PA
Alter: 50,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 29.11.2021
Beginn: 15.12.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: SYR / RA

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

Hypoaesthesia Nerve conduction studies Paraesthesia

Symptomtext

Pins/needles in lower right arm. Numbness in right are. Occurred 3 times. The third time full feeling has not returned.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Nerve conduction test 1/19/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: High blood pressure
Andere Medikamente: Labetaol
Allergien: -
Vorherige Impfungen: -

VAERS 2051405

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: ID
Alter: 53,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 16.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: IM / RA

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

Condition aggravated Dyspepsia Gastritis Hypotension Inflammation Palpitations Prostatitis Tremor

Symptomtext

Around 2 weeks after injection I began having inflammation, first in my prostate, then throughout my abdomen and diaphragm area. I started to have heart palpitations, and episodes of low blood pressure. I also began having tremors and difficulty digesting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I visited a urologist on 1/13/2022. He diagnosed me with acute prostatitis, and prescribed 30 days of doxycycline 100mg 2X daily. This was my first visit to a medical doctor since 2014.
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypermobility; intermittent prostatitis.
Andere Medikamente: No prescriptions. Multivitamin/mineral; flaxseed oil. No herbal remedies.
Allergien: Sulfa drugs.
Vorherige Impfungen: -

VAERS 2047446

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: OR
Alter: 35,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dysphonia Paraesthesia oral Throat tightness

Symptomtext

Mouth started tingling, throat had feeling of tightness, voice changed. 50mg of liquid Benadryl, EpiPen. Observed in emergency department.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Ear infection
Vorgeschichte: Fibromyalgia, history of diabetes, seasonal allergies
Andere Medikamente: Cymbalta, low-dose naltrexone, Mastodon, Zyrtec
Allergien: Dairy, soy, lavender, potato, mold
Vorherige Impfungen: Pfizer Covid-19.

VAERS 2043350

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NY
Alter: 65,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 13.12.2021
Beginn: 16.01.2022
Tage bis Beginn: 34,0
Dosis: 2
Route/Site: UN / UN

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

Abdominal discomfort Abdominal pain Anxiety Blood glucose normal COVID-19 Chest pain Dyspnoea Foot operation Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

CHIEF COMPLAINT: pt states he tested positive for COVID 2 days ago. states he is "throwing up and everything". states he cant keep anything down. "i cant give it to my wife and stuff". also feels SOB and has 10/10 abd pain. HISTORY OF PRESENT ILLNESS: Patient is a 66-year-old male who presents to the emergency department with shortness of breath, chest pain, abdominal discomfort. Patient states that he had foot surgery about 2 weeks ago. He states that he had tested positive for COVID at that time. He states that he followed up few days ago and tested positive again for COVID. He states that he had been doing well until about 4 days ago when he started experiencing nausea, vomiting, shortness of breath. He states that he is feeling very anxious. Patient has a history of diabetes. He states that his blood sugar has been controlled in the 100s. He has not had any diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Asthma, chest pain, chronic ulcer of left foot, Cirrhosis, Diabetes mellitus, Hypertension, Stroke syndrome
Andere Medikamente: Unknown
Allergien: baclofen,
Vorherige Impfungen: -

VAERS 2034092

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: OH
Alter: 79,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 28.10.2021
Beginn: 16.12.2021
Tage bis Beginn: 49,0
Dosis: 2
Route/Site: OT / RA

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

Alopecia Injection site pain Mobility decreased Rash SARS-CoV-2 test Skin burning sensation

Symptomtext

COULDN'T LIFT/ MOVE HER RIGHT ARM; RASH TO HER CHEST, ARMS, LEGS; PAINFUL AT INJECTION SITE; HAIR STARTED FALLING OUT; SCALP IS SORE/BURNING; This spontaneous report received from a patient concerned a 79 year old female. The patient's weight was 145 pounds, and height was 62 inches. The patient's concurrent conditions included: sleep/anxiety, seasonal allergies, and environmental allergies, and other pre-existing medical conditions included: Patient was not pregnant at the time of report. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series: 1) (suspension for injection, route of admin not reported, batch number: 1802068 expiry: 23-AUG-2021) dose was not reported, 1 total, administered to right arm on 10-MAR-2021 for prophylactic vaccination. On an unspecified date, the patient was not feeling well following vaccination with covid-19 vaccine ad26.cov2.s and went to the Emergency Department and there had a positive COVID-19 PCR (polymerase chain reaction) test confirmation of COVID -19 infection. The patient was subsequently hospitalized for 3 days. On an unspecified date, the patient experienced confirmed clinical vaccination failure (dose number in series: 1). On 28-SEP-2021, Laboratory data included: COVID-19 PCR (polymerase chain reaction) test (NR: not provided) positive. The patient received covid-19 vaccine ad26.cov2.s (dose number in series: 2) (suspension for injection, route of admin not reported, batch number: 1855194 expiry: 09-APR-2022) dose was not reported, 1 total, administered to right arm on 28-OCT-2021 for prophylactic vaccination. Concomitant medications included alprazolam for sleep/anxiety. On an unspecified date, the patient experienced couldn't lift/ move her right arm, rash to her chest, arms, legs, and painful at injection site following vaccination with covid-19 vaccine ad26.cov2.s (dose number in series: 2). It was reported that the patient's hair/scalp felt strange ever since positive COVID diagnosis. The patient added that she was told by her HCP that if not for being vaccinated, she may have needed intubation. (dose number in series: 2) On 16-DEC-2021, the patient experienced hair started falling out, and scalp is sore/burning dose number in series: 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from rash to her chest, arms, legs, and painful at injection site, had not recovered from hair started falling out, and the outcome of couldn't lift/ move her right arm and scalp is sore/burning was not reported. This report was non-serious. This case, involving the same patient is linked to 20220104484. (dose number in series: 1)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Date: 20210928; Test Name: COVID-19 PCR test; Result Unstructured Data: positive
Aktuelle Erkrankungen: Anxiety (on Xanax for sleep/anxiety "for years", otherwise "very healthy"); Environmental allergy; Seasonal allergy.
Vorgeschichte: Comments: The patient was not pregnant at the time of vaccination.
Andere Medikamente: XANAX
Allergien: -
Vorherige Impfungen: -

VAERS 2032856

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IL
Alter: 62,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 12.11.2021
Beginn: 03.01.2022
Tage bis Beginn: 52,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram pulmonary abnormal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Diarrhoea Dyspnoea Lung consolidation Lung disorder Lung opacity Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

Vaccinated with J&J on 11/12/21. Presented to ER on 1/3/22. COVID positive on 12/29/21. who presented to ED with increasing work of breathing. Reports nausea with vomiting and diarrhea for several days. Patient denies fevers, chills, body aches, headaches, loss in sense of taste or smell. She had tested +ive for COVID 19 on December 29 stating symptom onset was three days prior to positive test. She received the Johnson and Johnson vaccine approx 4 months ago. CXR demonstrated bilateral pulmonary opacities. A CTA chest is ordered. Labs are all in process. She is to be admitted at this time for further management. Received ceftriaxone, azithromycin, dexamethasone, and remdesivir. Discharged on 1/12/22

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Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 9,0
Labordaten: 12/29/21 COVID19: positive 1/3/22 Chest xray: Bilateral pulmonary opacities likely representing COVID-19 pneumonia. 1/4/22 CTA chestL: Extensive bilateral airspace disease and ground-glass opacities most consistent with changes of COVID-19 pneumonia. Early changes of ARDS not excluded. More consolidative changes seen within the lower lobes which could also relate to COVID pneumonia but does raise the possibility of superimposed bacterial pneumonia.
Aktuelle Erkrankungen: -
Vorgeschichte: Diagnosis Date ? Acute seasonal allergic rhinitis due to pollen 6/23/2018 ? Allergic rhinitis ? Asthma ? Essential hypertension, benign ? Female stress incontinence 6/23/2018 ? GERD with esophagitis 6/23/2018 ? Hyperlipidemia ? Hyperlipidemia associated with type 2 diabetes mellitus 6/23/2018 ? Obesity ? Obesity (BMI 30-39.9) 6/23/2018 ? Type 2 diabetes mellitus ? Uncontrolled type 2 diabetes mellitus without complication, without long-term current use of insulin
Andere Medikamente: Aspirin, loratadine
Allergien: augmentin
Vorherige Impfungen: -

VAERS 2031550

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 06.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Full blood count Palpitations

Symptomtext

Palpitations that started 2 days after vaccine, occurring daily and lasted for 3 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Had CBC drawn on 12/23. Self monitored BP and heart rate. Notified doctor
Aktuelle Erkrankungen: cough
Vorgeschichte: none
Andere Medikamente: Vyvanse
Allergien: no
Vorherige Impfungen: -

VAERS 2024035

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: PA
Alter: 51,0
Geschlecht: U
Eingang: 11.01.2022
Impfdatum: -
Beginn: 08.01.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Chest pain Diarrhoea Fatigue Nasal congestion

Symptomtext

NOSE CLOGGED; CHEST PAIN (DULL) LIKE THE FEELING YOU GET AFTER YOU STUB YOUR TOE; DIARRHEA; FEELING VERY TIRED; This spontaneous report received from a patient concerned a 51 year old of unspecified sex. The patient's height, and weight were not reported. The patient's concurrent conditions included: abstains from alcohol, and smoker, and other pre-existing medical conditions included: Patient had no known allergies and 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: 1855194 expiry: UNKNOWN) dose was not reported, administered on 07-JAN-2022 for prophylactic vaccination. No concomitant medications were reported. On 08-JAN-2022, the patient experienced nose clogged. On 08-JAN-2022, the patient experienced chest pain (dull) like the feeling you get after you stub your toe. On 08-JAN-2022, the patient experienced diarrhea. On 08-JAN-2022, the patient experienced feeling very tired. Treatment medications included: chlorphenamine maleate/paracetamol/phenylephrine hydrochloride, and paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from diarrhea on 08-JAN-2022, and had not recovered from nose clogged, feeling very tired, and chest pain (dull) like the feeling you get after you stub your toe. This report was non-serious.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Abstains from alcohol; Smoker (About 5 cigarettes out of the 24 pack a day)
Vorgeschichte: Comments: Patient had no known allergies and no drug abuse or illicit drug usage.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2017531

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: WA
Alter: -
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: -
Beginn: 28.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Chest discomfort Chest pain Headache Myalgia Pain in extremity Paraesthesia Pruritus

Symptomtext

CHEST PAIN; ITCHY (FEELS NEED TO SCRATCH BODY); HEAVINESS IN THE CHEST; NUMBNESS AND TINGLING IN THE ARMS AND LEGS; SORE ARM; HEADACHE; MUSCLE ACHES; This spontaneous report received from a patient concerned a female of unspecified age. 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 admin not reported, batch number: 1855194, and expiry: UNKNOWN) dose was not reported, administered on 28-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 28-DEC-2021, the patient experienced sore arm, headache, and muscle aches. On 31-DEC-2021, the patient experienced chest pain, itchy (feels need to scratch body), heaviness in the chest, and numbness and tingling in the arms and legs. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sore arm, headache, and muscle aches, and had not recovered from numbness and tingling in the arms and legs, chest pain, itchy (feels need to scratch body), and heaviness in the chest. This report was non-serious. This report was associated with product complaint number.

Weitere VAERSDATA-Felder

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

VAERS 2010575

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NY
Alter: 56,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 28.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Impaired work ability Magnetic resonance imaging Mobility decreased Muscle spasms Pain Rash Spinal pain Swelling Vision blurred

Symptomtext

Spasms started Friday eve on October 30, 2021. First started with painful lines across from spine to each side. Then changed to bumps and advanced to large butterfly wing like raised sections from mid spine out. Pain is unbearable to which I have to sit down and not move. I am taking meds to stop spasms and pain. At one time when they first started pain was a 9 out of 10 being the worst my vision blurred. Over 2 months later I've been through MRI's, physical therapy, medications, target pain shots, and nerve block shots which have given me a quick temporary relief from spasms and pain. I am also out of work from and don't know when I'll be able to go back to work. My strength and mobility has been drastically limited. With simple walking and bending or lifting the spasms and pain come quickly, please help me.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: MRI's
Aktuelle Erkrankungen: Back injury at work
Vorgeschichte: None
Andere Medikamente: Naproxen 500 mg., Gabapentin 300 mg
Allergien: None
Vorherige Impfungen: -

VAERS 2007086

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: 30,0
Geschlecht: U
Eingang: 05.01.2022
Impfdatum: 07.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

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

Angina pectoris Chest pain Dyspnoea Fatigue Insomnia Pain

Symptomtext

1st night: Body Aches, Fatigue, Sleeplessness 2nd day: Body Aches, Fatigue, Sleeplessness, Shortness of breathe 3rd day: Fatigue, sharp pain in heart 4th day - 10th day: Fatigue, sharp pain in heart after jumping or any strenuous movements (immediate), Shortness of breathe Until now: shortness of breathe (unlike before, I become winded more quickly), heart is a little sensitive to physical activity, have not felt a sharp pain since the 4th - 10th day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2006043

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: FL
Alter: 43,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest discomfort Diarrhoea Discomfort Dizziness Ear discomfort Feeling cold Hypoaesthesia Injection site pain Nausea Paraesthesia Peripheral swelling Pyrexia Tinnitus Vision blurred

Symptomtext

-Pain in the injection site; nausea; low fever and diarrhea (started within 24 hours of injection) Resolved within a week; except diarrhea which still happening on an irregular basis. -Tingling sensation in my feet (started within 1st week after injection). Still happening on an irregular basis. -Decreased feeling in my thighs (outer area) (started within 1st week after injection). Still happening on an irregular basis. -Tingling and numbness in my hands (mostly fingers) (started within 1st week after injection). Still happening on an irregular basis. -Pressure in both ears and forehead (sometimes accompanied with ringing) (started within 24 hours of injection) Still happening on an irregular basis. -Fast Heartbeat (started within 5 minutes after injection) Still happening on an irregular basis. -Dizziness accompanied with a cold feeling rush thru my brain (started within 5 minutes after injection) Cold feeling rush thru my brain resolved within 4 weeks after injection. Dizziness still happening on an irregular basis. -Chest pressure (started within 24 hours of injection) Still happening on an irregular basis. -Leg Swelling (started within 1st week after injection). Still happening on an irregular basis. -Blurred Vision (started within 1st week after injection). Still happening on a regular basis.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None as of today (medical appointments will be scheduled in the upcoming days).
Aktuelle Erkrankungen: None
Vorgeschichte: Pre-Diabetic High Cholesterol
Andere Medikamente: Multivitamins
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2002718

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NY
Alter: 32,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose normal Dizziness Feeling abnormal Pallor Tremor Unresponsive to stimuli Vision blurred

Symptomtext

The patient stated that he felt dizzy after receiving the vaccine and did not feel good. Patient was pale but breathing normally but for less than 30 seconds the patient's eyes became unfocused and his body seemed to tremble and he was unresponsive to questions but never lost consciousness. After this, the patient recovered quickly. First responders evaluated the patient and the patient refused any medical treatment and stated that he felt better and left 30 mins after receiving the vaccination

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: EMTs took patient's blood glucose which was 74
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2000188

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IN
Alter: -
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 29.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Body temperature Dyspnoea Fatigue Feeling abnormal Nausea Pyrexia Vomiting

Symptomtext

SHORT OF BREATH ON ACTIVITY LIKE WALKING; FELT SO BAD, CHANGED SO QUICK; FEVER/LOW GRADE FEVER; TIREDNESS; NAUSEA; VOMITING; This spontaneous report received from a patient concerned a 45 year old female. The patient's height, and weight were not reported. The patient's past medical history included: covid-19, and intensive care unit (icu). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194 expiry: UNKNOWN) dose was not reported, administered on 29-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced short of breath on activity like walking, felt so bad, changed so quick, fever/low grade fever, tiredness, nausea, and vomiting. Laboratory data (dates unspecified) included: Body temperature (NR: not provided) 102.4 F. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from fever/low grade fever, and short of breath on activity like walking, and the outcome of felt so bad, changed so quick, tiredness, nausea and vomiting was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Result Unstructured Data: 102.4 F
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (In ICU for 5 days with COVID.); Intensive care (In ICU for 5 days with COVID.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1999845

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: WI
Alter: 41,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood creatinine Blood test Blood thyroid stimulating hormone Bradycardia C-reactive protein Chest X-ray normal Chest discomfort Chills Cold sweat Electrocardiogram ambulatory Electrocardiogram normal Fatigue Full blood count Heart rate increased Malaise Nausea Pain Pyrexia

Symptomtext

Initially after the shot I had the expected reactions (Fever to 102 degrees, body, aches, chill, nausea, fatigued) for about 2 days. The following weekend (November 13th) I was still very fatigued where slept up to 12 hours a night but all other symptoms had resided. On Sunday November 14th, as I was walking down the stairs I became out of breath (chest tightness) and my heart rate really fast (in the 140s per my smart watch). I sat down and became nauseous and clammy. I thought I was possibly dehydrated so I rested and drank more water. Throughout the next week these same symptoms continued to occur at random times with minimal exertion (even sitting at my desk working) about 4 more times. I stopped drinking coffee and any alcohol to see if it made an impact and I did not notice any difference. On Friday, November 19th I went in for my annual with my primary physician and I explained my symptoms along with the general fatigue and not feeling well. I took a chest xray (clear), blood test (all looked good) and and EKG. The EKG results came back with normal sinus rhythm but suggested left atrial enlargement. At that point, I was continuing to have these symptoms so a heart event monitor was ordered. I wore the monitor from November 23-December 2nd and continued to have symptoms during that time but they were becoming more infrequent. After the heart event monitor I began to start feeling better in general and began slowly exercising again moderately. I met with my physician on December 30th. The results of the test do show a normal sinus rhythm but there were some episodes of tachardia and brachardia along with my symptoms. The physician said there are other test that can be done to evaluate my symptoms but as I have not had any for a couple weeks now I will hold off on any further evaluations unless the symptoms occur again.

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Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: EKG, blood tests (CBC, THS, Erythrocyte Sed, Creatinine, Electrolytes, C-Reactive Protein) Chest x-ray: 11/19/21 COVID test: 11/19/21 negative Heart Event Monitor 11/23/21-12/2/21
Aktuelle Erkrankungen: None
Vorgeschichte: GERD, Depression/anxiety
Andere Medikamente: Citalopram 20 mg/Daily, B12 supplement daily, multivitamin daily, Mirena (in place)
Allergien: Amoxicillin, Nickle, steri-strips
Vorherige Impfungen: -

VAERS 1999810

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: SC
Alter: 45,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 09.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / LA

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

Condition aggravated Headache Hypertension Migraine Sciatica

Symptomtext

Sciatica (went to urgent care 2x for meds due to flare-up), high blood pressure (was under control with meds before the vaccine, then went up to 144/95, had to add another med to get it back under control), headache or migraine everyday since the vaccine.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Blood pressure: 11/19/21- 144/95 12/06/21- 145/95 12/08/21- 144/94
Aktuelle Erkrankungen: None
Vorgeschichte: Thyriod, high blood pressure, obese
Andere Medikamente: Amlodipine Besylate, Claritin, Levothyroxine
Allergien: Lisinopril, HCTZ, Sulfa
Vorherige Impfungen: -

VAERS 1988930

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: OR
Alter: 70,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Dyspnoea Interchange of vaccine products Skin warm

Symptomtext

Patient with history of multiple allergies and anaphylaxis. Previous anaphylaxis by report to first dose of Moderna vaccine, given initial dose of Janssen weeks later without reaction. Presented to mass vaccination site for booster dose of Janssen, administered in LD. Approximately 25 minutes post vaccination began feeling chest tightness, SOB, skin warming. 0.3 mg epinephrine administered per Epipen in R thigh and EMS called. Symptoms began to resolve immediately, patient reported feeling better with RR normalizing. BP upon discharge to EMS 152/82, P 86, RR 24. Patient initially declined transfer to ED, stated she wanted to go home. Educated patient on additional monitoring needed post epinephrine administration and potential return of symptoms, and she agreed. Patient transported to ED by EMS. Followed up with patient by phone on 12/29/2021, but no return call.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Multiple, unavailable at the time of report
Vorherige Impfungen: Anaphylaxis at 69, post Moderna COVID-19 vaccine. Unknown date, but approximately Feb-April 2020.

VAERS 1988195

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: SC
Alter: -
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: -
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Blood pressure measurement Cardiac stress test Chest pain Culture throat Echocardiogram Injection site pain Paraesthesia Sensory disturbance Vertigo

Symptomtext

PAIN IN CHEST/HEART AREA; TINGLING IN RIGHT AND LEFT HAND; TINY BIT SORE AT THE SITE; TINGLING IN NERVES; VERTIGO; SENSATION DOWN IN ARM AND HAND (BOTH SIDES); This spontaneous report received from a patient concerned a 70 year old male of unknown race and ethnic origin. The patient's height, and weight were not reported. The patient's past medical history included: Patient had a history of vertigo (rocks in ears) maybe 5 or 6 years ago, and stenosis back surgery with spinal stenosis surgery, had stents and concurrent conditions included: cardiac event (heart attack maybe). The patient had covid-19 vaccine ad26. cov2. s (suspension for injection, route of admin not reported, batch number: unknown, expiry: UNKNOWN, dose was not reported, 1 total administered on 22/Jun/2021 at right arm for prophylactic vaccination (dose number in series 1). The batch number was not reported and has been requested. On 22/JUN/2021, the patient experienced tingling sensation in right arm/hand which was decreasing. The tingling sensation was like when hand was going to sleep. Patient told a woman at work and she pushed on his back and he felt it in his hand. There was apparently a knot and the woman mashed on it and he could feel it in his hand. After that he came home and took 1/2 a naproxen and it was better. The tingling started in his arm and hand right side, then became mostly hands. In Jul/2021, patient experienced suspected clinical vaccination failure. He Had tingling sensation started around the same time as his vaccine likely after but he was not sure. On 25th/Oct/2021, Medicine doctor (MD) said it was carpel tunnel which was between his 2 vaccinations. Patient also noticed diminished energy very slight after the shot. He attributed it to his COVID-19 but he was not sure because he noticed it after his COVID-19. He had very poor sense of taste and smell. Patient had COVID-19 after his first dose of COVID shot, 3 weeks after. When he had COVID he lost his appetite. Lost weight 250 to 210lbs, due to decreased appetite. Patient noticed sore throat with mask use but noticed a sore throat with a different feel. Doctor diagnosed him with COVID-19 via a swab in the nose. 15 minutes later it came back positive (not sure the test he had). Events occurred on dose series 1. The patient received booster dose of covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, expiry: UNKNOWN) dose was not reported, 1 total, administered on 14/NOV/2021 at right arm for prophylactic vaccination (dose number in series 2). No concomitant medications were reported. On an unspecified date the patient experienced a tiny bit sore at the site of injection. It seem like that it responds to a half dose of naproxen sodium. Patient thought that it maybe the muscle in back was clamped down causing some tingling in his nerves. The patient experienced tingling in right and left hand. When he was up and moving none of the tingling bothers him. When his hands sit he can feel it. Nothing was going on with gut/bowel. On DEC/2021, the patient experienced vertigo (ongoing dizziness), sensation down in arm and hand (both sides) and started sense it in his left hand. On 17/DEC/2021, in morning the patient had sensation/pain which was not bad but does not normally get those, had it may be around 3 times. On an unspecified date, the patient experienced pain in chest/heart area. Events occurred on dose series 2. Laboratory data (dates unspecified) included: BP (NR: not provided) 117/91, Echocardiogram (NR: not provided) not reported, and Stress test (NR: not provided) not reported. Treatment medications (dates unspecified) included: naproxen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from vertigo, was recovering from tingling in right and left hand, and the outcome of tiny bit sore at the site, sensation down in arm and hand (both sides), tingling in nerves and pain in chest/heart area was not reported. This report was not serious. This case, involving the same patient is linked to 20211240502.; Sender's Comments: V0 Medical assessment comment not required as per standard operating procedure as the case assessed as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: BP; Result Unstructured Data: 117/91; Test Name: Nasopharyngeal swab; Result Unstructured Data: covid; Test Name: Stress test; Result Unstructured Data: not reported; Test Name: Echocardiogram; Result Unstructured Data: not reported
Aktuelle Erkrankungen: Cardiac disorder (When 51/52 had a cardiac event (heart attack maybe). Had stents put in. Has cardiac issues/chest area)
Vorgeschichte: Medical History/Concurrent Conditions: Back surgery; Stent placement; Vertigo (maybe 5-6 years ago)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1981161

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NY
Alter: 54,0
Geschlecht: F
Eingang: 26.12.2021
Impfdatum: 26.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest X-ray normal Chest discomfort Dyspnoea Fatigue Impaired work ability Loss of personal independence in daily activities Pain in extremity SARS-CoV-2 test negative

Symptomtext

11/28/2021: Hospital for SOB, prescribed Prednisone 20mg po twice daily x5days, Albuterol nebulizer and Albuterol inhalers 11/30/2021: Medical facility for continued SOB and leg pain-was told "my body is building antibodies and this is normal" 12/20/2021: ED for continued SOB, Xray completed, negative COVID test, given albuterol nebulizer x3, 12/24/2021: ED for SOB, given nebulizers x3, Prednisone 60mg po and continued steroid taper for SOB I have had continued shortness of breath with chest discomfort, fatigue and leg pain since taking the vaccine, which has resulted in missed time form work and at times an inability to complete normal daily task

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/20/2021: Chest Xray-negative 12/24/2021: repeat Chest Xray
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: none
Allergien: Penicillin Anaphylaxis Sulfa Drugs-Swellings
Vorherige Impfungen: -

VAERS 1976897

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: MA
Alter: 28,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 11.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Fibrin D dimer Hypersensitivity Immediate post-injection reaction Injection site pain Pain Pain in extremity Paraesthesia Pyrexia

Symptomtext

Arm immediately started hurting after injection ~11Am on a Saturday (knew that was normal), later that evening ~5:30PM after waking up from a nap, started to develop fever of 101 and severe pain in mostly arm, rest of body was aching (again, knew that was normal). Took following day to fully rest (Sunday). Starting Monday left leg started to have throbbing pain. Arm was still hurting. Throughout week, left leg and arm were hurting. A week later my leg ?throbbing? turned into a sharp pain. A week later I took myself to ER in concern I had a blood clot. Medical personnel took a blood sample for D Dimer test. My results came back within normal range. Later that evening after hospital visit, throbbing /sharp pain, turned into pins and needles sensation in both legs. Then it made its way throughout entire body. Pins and needles sensation in chest, legs, both arms, calfs. Took Asprin to sleep. Left arm continues to feel pins and needles sensation and like I have a flood pressure cuff around bicep. Called my primary care on Wed 12/22 and they had me come in for another blood test. I told her I had visited ER days prior in concerns pain in leg was blood clot (testing came back negative as mentioned above). Had my blood taken at a local healthcare facility around 1pm. Dr (NAME) said she was looking specifically liver and kidney functions. I was told everything looked great in terms of blood work. Dr suggested to me that I may have had an allergic reaction and recommended a combination of Claritin / Benadryl over the next several days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Local Hospital 12/19/2021-D dimer test Second health care facility 12/22 - full panel blood test I think
Aktuelle Erkrankungen: No
Vorgeschichte: Back problems (herniated disc in recovery >10years)
Andere Medikamente: Duloxetine (60mg), multivitamin
Allergien: Not that I?m aware of
Vorherige Impfungen: -

VAERS 1970366

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: FL
Alter: 47,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: -
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Balance disorder Blood pressure measurement Blood test Chest X-ray Chest pain Chills Computerised tomogram Dizziness Dyspnoea Electrocardiogram Feeling drunk Headache Heavy menstrual bleeding Hypertension Injection site pain Panic attack Polymenorrhoea

Symptomtext

HORRIBLE PAIN IN LEFT ARM AT INJECTION SITE; LOSING BALANCE; VERY HIGH BLOOD PRESSURE DUE TO PANIC ATTACKS; EARLY AND HEAVY PERIOD (ON DAY 20 OF MENSTRUAL CYCLE); EARLY PERIOD; CHEST PAIN THAT MOVED TO HER BACK; DIFFICULTY BREATHING; 2 HORRIBLE PANIC ATTACKS; DIZZINESS; FELT DRUNK; HEADACHE; SHIVERS; This spontaneous report received from a patient concerned a 47-year-old female. The patient's weight was 137 pounds, and height was 63 inches. The patient's past medical history was significant for chest pain after going on a trip. The patient's concurrent conditions included was drug allergy (Acetomycin (Penicillin) esomeprazole, oral steroids), stress, celiac disease, hormonal changes, perimenopause, nonsmoker, non-alcohol user, gluten intolerant, and exercising. Past products were benzylpenicillin, esomeprazole, and oral steroids for drug used for unknown indication. On 06-APR-2021, the patient received primary vaccination with covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of administration, batch number and expiry were not reported) dose was not reported, for prophylactic vaccination. No adverse events were reported following administration of covid-19 vaccine ad26.cov2.s. (Dose number in series 1). On 25-OCT-2021, the patient received a booster vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch/lot number: 1855194, and expiry: unknown) dose was not reported, 1 total, administered on right arm on for prophylactic vaccination. No concomitant medications were reported. On an unspecified date in OCT-2021, the patient experienced shivers. On 25-OCT-2021, the patient experienced dizziness (serious event) (dose number in series 2). On 25-OCT-2021, the patient experienced felt drunk, horrible pain in the left arm, headache (dose number in series 2). On 28-OCT-2021, the patient experienced chest pain that moved to her back, difficulty breathing and 2 horrible panic attacks (serious event) (dose number in series 2). On 29-OCT-2021, the patient could not go to work due to her symptoms. On 30-OCT-2021, the patient stated that she thought she was going to have a heart attack because of all the symptoms and visited urgent care. The patient stayed in urgent care for 3-4 hours. The following diagnostic and laboratory tests were performed while at the urgent care: test for blood clot was inconclusive, chest x-ray, electrocardiogram (EKG) every hour, and a bag of saline solution due to losing balance. A computerized tomography (CAT) scan was also performed to rule out pulmonary embolism. The result of all tests were reported by the patient to have come back as normal. At an unspecified time the patient was rushed to the Emergency Room (ER). On 31-OCT-2021, the patient experienced very high blood pressure due to panic attacks, early and heavy period (on day 20 of menstrual cycle), and losing balance. After returning from the hospital on 31-OCT-2021 she had early and heavy period (on day 20 of menstrual cycle), the patient was going through perimenopause but stated that her periods are normally late not early usually on day 25 or 26,28 or 30 (dose number in series 2). On 01-NOV-2021 the patient saw a cardiologist who saw her chart because her blood pressure was measured at the hospital and it was high 162/93 mmHg and told her that panic attacks can raise blood pressure. On an unspecified date, the patient also reported she experienced left arm hurting, the patient specified it as pain at the injection site for which she used ice and it resolved (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from chest pain that moved to her back, difficulty breathing, 2 horrible panic attacks, and dizziness on 01-NOV-2021, very high blood pressure due to panic attacks on 31-OCT-2021, felt drunk, and headache on 28-OCT-2021. The event of horrible pain in left arm at injection site resolved on an unspecified date. The outcome of shivers, early and heavy period (on day 20 of menstrual cycle), losing balance and early period was not reported. This report was serious (Other Medically Important Condition). This case, involving the same patient is linked to 20211223061.; Sender's Comments: V0: 20211219942-covid-19 vaccine ad26.cov2.s -chest pain that moved to her back, difficulty breathing, 2 horrible panic attacks, loosing balance, dizziness. 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: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20211031; Test Name: EKG; Result Unstructured Data: Not reported; Test Date: 20211031; Test Name: Chest X-ray; Result Unstructured Data: Not reported; Test Date: 20211031; Test Name: CAT scan; Result Unstructured Data: Normal; Test Date: 20211031; Test Name: Blood test; Result Unstructured Data: Inconclusive; Test Date: 20211101; Test Name: Blood pressure; Result Unstructured Data: 162/93 mmHg, high; Comments: elevate blood pressure
Aktuelle Erkrankungen: Abstains from alcohol; Celiac disease; Drug allergy (acetomycin (penicillin) esomeprazole oral steroids'); Exercise adequate; Gluten intolerance; Hormone level abnormal; Non-smoker; Perimenopause; Stress
Vorgeschichte: Medical History/Concurrent Conditions: Chest pain (Patient reported chest pain happened before when she came back from a trip but less severe.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1958979

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IN
Alter: 22,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Decreased appetite Immediate post-injection reaction Injection site discomfort Injection site pain Lymphadenitis Mobility decreased Somnolence

Symptomtext

Immediately following the injection, pain was experienced in the upper left arm where the vaccine was administered. The pain continued for 2-3 days and then subsided. On the drive home it felt like it was pulsing around the injection site some. The day after I began experiencing moderate drowsiness and limited appetite, so I laid on the couch and ate soup to try and recover. It eventually evolved in severe drowsiness three days following the vaccine and ultimately subsided 6 days following the injection. 2 days following the injection, the lymph nodes in the right side of my neck became inflamed, and it became very difficult to turn my head to the right. This continued until the sixth day post vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Food poisoning
Vorgeschichte: -
Andere Medikamente: Daily Multivitamin
Allergien: Penacyllin
Vorherige Impfungen: -

VAERS 1958846

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NM
Alter: 48,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 30.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Dyspnoea

Symptomtext

dyspnea which continues to increase

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: s/p Left Lower Lobectomy in July 2021
Andere Medikamente: Bupropion HCL 100mg daily Atorvastatin 20mg daily
Allergien: Codiene
Vorherige Impfungen: -

VAERS 1954100

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NJ
Alter: 59,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: -
Beginn: 29.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Asthenia Fatigue Feeling cold Headache Pain Paraesthesia

Symptomtext

WEAKNESS; THROBBING PAIN IN HANDS; FELT NEEDLES IN FINGER TIPS OF LEFT HAND; COLD BODY/FELT COLD ALL OVER BODY/HANDS BECAME VERY COLD AND WERE FREEZING; HEADACHE; FELT TIRED; This spontaneous report received from a patient concerned a 59 year old female of unspecified ethnicity. Initial information was processed along with the additional information received on 06-DEC-2021. The patient's height, and weight were not reported. The patient's past medical history included: cancer on unspecified date in 2014, she was also diagnosed with cancer in 2019, The patient was in remission from cancer. Chemotherapy has created peripheral nerve issues, but they had resolved. The patient was under the care of a neurologist and was normal. The patient previously received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 207A21A, expiry: UNKNOWN) dose was not reported, (dose number in series was 1), 1 total, administered on 12-APR-2021 to left arm for prophylactic vaccination. On an unspecified date, following vaccination with covid-19 vaccine ad26.cov2.s, the patient felt cold all over her body, had a headache and felt tired following vaccination (dose number in series was 1). The patient received booster dose of covid-19 vaccine ad26.cov2.s vaccine (suspension for injection, route of admin not reported, batch number: 1855194, expiry: UNKNOWN) dose was not reported, (dose number in series was 2), 1 total, administered on 29-NOV-2021 to left arm for prophylactic vaccination. No concomitant medications were reported. On 29-NOV-2021, the same night after vaccination with covid-19 vaccine ad26.cov2.s, the patient felt cold all over her body, had a headache and felt tired. Her hands and feet got colder and colder, the cold was extreme to the point of hurting. On 30-NOV-2021, later on morning while she was washing her hands in cool water, she felt needles in finger tips of her left hand and was resolved. 0n 03-DEC-2021, when she was washing her hands in cold water, her hands became very cold and were freezing. It took a long time over 15 minutes for them to warm up. This happened while she was at a grocery store. She tried to warm her hands by putting them in her pockets. When she got in her car, her hands started warming. She felt throbbing pain in hands as they were warming up. On an unspecified date, the patient also experienced weaknesses in certain areas that may have got triggered due to vaccination (dose number in series was 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from felt needles in finger tips of left hand, and the outcome of throbbing pain in hands, cold body/felt cold all over body/hands became very cold and were freezing, headache, felt tired and weakness was not reported. This report was non-serious. This report was associated with a product quality complaint (PQC): 90000205465. The suspected product quality complaint has been confirmed to be void (does not meet PQC criteria) based on the PQC evaluation/investigation performed. This case, involving the same patient is linked to 20211231019.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer (Remission from cancer); Cancer; Neuropathy peripheral (Chemo has created peripheral nerve issues, but they had resolved); Comments: The patient was under the care of a neurologist and was normal.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1950449

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: 27,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: -
Beginn: 28.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Aptyalism Asthenia Blood glucose Blood glucose increased Blood test Body temperature Chest pain Dizziness Dyspnoea Electrocardiogram Feeling abnormal Fibrin D dimer Haemoptysis Heart rate Heart rate increased Influenza like illness Lacrimation decreased Oxygen saturation normal

Symptomtext

SUSPECTED COVID-19; DISRUPTED SLEEP/DISTURBED SLEEP WOULD SLEEP FOR 4 HOURS THEN BE COMPLETELY WAKE; FELT SPACEY, BODY IS NOT TAKING NUTRIENT, ON THE VERGE OF DYING; DID NOT HAVE ALL MY THOUGHTS CONNECTED; ELEVATED HEART RATE 110-120 BEAT PER MINUTE; COUGHING BLOOD; DO NOT PRODUCE TEARS/ COULD NOT CRY; ELEVATED BLOOD GLUCOSE LEVELS 1.5 ABOVE REFERENCE RANGE; LEG TREMORS/UNCONTROLLABLE SHAKING OF LEGS; LOSS OF SALIVATION; INCREDIBLE CHEST PAIN/ DEEP ACHING ON THE SIDE OF CHEST; STRANGE BODY ODOUR METALLIC LIKE ONION; SHORTNESS OF BREATH/ DIFFICULTY BREATHING WITH NO MORE THAN 5 BREATHS PER MINUTE; LACK OF ENERGY; DIZZINESS; FLU LIKE SYMPTOMS, COUGHING MUCOUS, FATIGUE, FEVER, LOSS OF APPETITE, BODYACHE, HEADACHE; This spontaneous report received from a patient concerned a 27-year-old male of unspecified race and ethnicity. Initial information was processed along with the additional information received on 06-DEC-2021. The patient's weight was 177 pounds, and height was not reported. The patient's concurrent conditions included: panic attacks, and other pre-existing medical conditions included: The patient had no comorbidities. The patient had no medical conditions and concerns. The patient had no known allergies. The patient was an athlete run the ultramarathon 25,30,40 miles. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, and expiry: UNKNOWN) dose was not reported, 1 total administered on 28-OCT-2021 for prophylactic vaccination. (Dose number in series :1) No concomitant medications were reported. On 28-OCT-2021 the patient experienced reaction 8-10 hours after that never went away, the patient stated that he was basically on the verge of death, the patient reported that 8 hours after receiving the vaccine he started to feel severe body aches, headache, fever of 103 degree, loss of appetite, dizziness, muscle aches flu like symptoms, fatigue and exhaustion. On 29-OCT-2021, the patient after sleeping for 12 hours he stated "he felt short of breath, incredible chest pain, deep aching on the side of his chest, metallic taste and strange body odor, metallic like onion, this was a weekend, the patient had no appetite and no energy. On an unspecified date in NOV-2021, the patient experienced red spotting mostly in arms elbows very small some spots are larger than other, thick red elevated rash with epson salt/lavendar bath feels like pins and needles. On 01-NOV-2021, Laboratory data included: Brain scan NOS (NR: not provided) Not reported. On 03-NOV-2021, the patient experienced, the patient visited urgent care they did blood work and EKG with no remarkable findings. On 03-NOV-2021, the patient experienced loss of salivation. Laboratory data included: Blood test (NR: not provided) Normal, No remarkable findings, EKG (NR: not provided) No remarkable findings, and Fibrin D dimer (NR: not provided) Not elevated. The patient stated that he tried to resume life after that but felt so exhausted, he stated " forced myself to eat, tried on liquid diet orange juice, the patient drink's 2-3 gallons per day but was not salivating. On 03-NOV-2021, the patient visited emergency room. On 04-NOV-2021 the patient was treated for that by IV (intravenous) therapy of vitamin C 15mg but his body was not taking IV, he was told it was dripping so slowly (Patient did not provide any further details about where this IV treatment was initiated or the treating physician). On 05-NOV-2021, the patient visited emergency room, there was no remarkable finding and he was discharged, on the following day he started to feel uncontrollably shaking started in one leg. On 06-NOV-2021, the patient experienced leg tremors/uncontrollable shaking of legs. On 07-NOV-2021, the patient visited emergency room. On 07-NOV-2021, the patient experienced coughing mucous, coughing blood, do not produce tears/ could not cry, elevated blood glucose levels 1.5 above reference range. Laboratory data included: COVID-19 virus test negative (NR: not provided) negative. Laboratory data included: Blood glucose (NR: not provided) elevated, 1.5 above normal, Blood test (NR: not provided) No remarkable findings, and Respiratory rate (NR: not provided) 5 /min. On 08-NOV-2021, the patient experienced elevated heart rate 110-120 beat per minute. Laboratory data included: Heart rate (NR: not provided) elevated 110-120 beat per minute. It was reported that experienced elevated heart beat 110-120 beat per minute gone on for 2-3 weeks, patient stated what assisted in reducing his elevated heart beat Hydrocolon therapies, they flushed my colon twice which reduced his beat to 80 (so it is resolving), my heart rate was in the forties which is normal form. On 28-NOV-2021, Laboratory data included: Body temperature (NR: not provided) 103 F. On an unspecified date, the patient experienced disrupted sleep/disturbed sleep would sleep for 4 hours then be completely wake, felt spacey, body is not taking nutrients, on the verge of dying, also had disrupted sleep/would sleep for 4 hours then be completely wake, did not have all my thoughts connected and suspected covid, muscle ache, rash, metallic taste . Laboratory data (dates unspecified) included: Oxygen saturation normal (NR: not provided) normal. Treatment medications (dates unspecified) included: ascorbic acid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from elevated heart rate 110-120 beat per minute, was recovering from suspected covid-19, had not recovered from flu like symptoms, coughing mucous, fatigue, fever, loss of appetite, bodyache, headache, loss of salivation, and dizziness, and the outcome of incredible chest pain/ deep aching on the side of chest, shortness of breath/ difficulty breathing with no more than 5 breaths per minute, strange body odour metallic like onion, do not produce tears/ could not cry, lack of energy, elevated blood glucose levels 1.5 above reference range, leg tremors/uncontrollable shaking of legs, disrupted sleep/disturbed sleep would sleep for 4 hours then be completely wake, felt spacey, body is not taking nutrient, on the verge of dying, did not have all my thoughts connected and coughing blood was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000205463. The suspected product quality complaint has been confirmed to be voided (did not meet pqc criteria as this record describes adverse events and the reporter's concern that the lot number in vaccination card was causing more adverse events than any other lot numbers. this report does not allege a product quality complaint and does not meet the definition of a product quality complaint or explicitly allege a potency issue) based on the PQC evaluation/investigation performed.; Sender's Comments: V0: 20211210320-COVID-19 VACCINE AD26.COV2.S - Elevated heart rate 110-120 beat per minute, loss of salivation . 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: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20211101; Test Name: Brain scan NOS; Result Unstructured Data: Not reported; Test Date: 20211103; Test Name: EKG; Result Unstructured Data: No remarkable findings; Test Date: 20211103; Test Name: Blood test; Result Unstructured Data: No remarkable findings; Test Date: 20211103; Test Name: Fibrin D dimer; Result Unstructured Data: Not elevated; Test Date: 20211103; Test Name: Blood test; Result Unstructured Data: Normal; Test Date: 20211107; Test Name: COVID-19 virus test negative; Result Unstructured Data: negative; Test Date: 20211107; Test Name: Respiratory rate; Result Unstructured Data: 5 /min; Test Date: 20211107; Test Name: Blood test; Result Unstructured Data: No remarkable findings; Test Date: 20211107; Test Name: Blood glucose; Result Unstructured Data: elevated, 1.5 above normal; Test Date: 20211108; Test Name: Heart rate; Result Unstructured Data: elevated; Test Date: 20211128; Test Name: Body temperature; Result Unstructured Data: 103 F; Test Name: Oxygen saturation normal; Result Unstructured Data: normal
Aktuelle Erkrankungen: Panic attacks
Vorgeschichte: Comments: The patient had no comorbidities. The patient had no medical conditions and concerns. The patient had no known allergies. The patient was an athlete run the ultramarathon 25,30,40 miles.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938346

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: FL
Alter: -
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: -
Beginn: 16.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Chills Dysstasia Feeling cold Feeling hot Fibromyalgia Muscular weakness Pain Pain assessment Pain in extremity Pyrexia Toothache Tremor

Symptomtext

FIBROMYALGIA ATTACK; HANDS SHAKING; COULD NOT STAND; COLD FEELING; FINGERS HURT; BOTH LEGS VERY WEAK; CHILLS; FEVER FEELING; HOT FEELING; TOOTH ACHE; FELT A WAVE OF PAIN OVER THE ENTIRE BODY; This spontaneous report received from a patient concerned a 74-year-old white not Hispanic or Latino female. The patient's height, and weight were not reported. The patient's past medical history included: polymyalgia rheumatica, and concurrent conditions included: fibromyalgia The patient was previously treated with covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin, batch number: 204A21A expiry: 21-SEP-2021) dose was not reported, 1 total administered on 30-Apr-2021 for prophylactic vaccination (dose number series 1). On 17-May-2021 to 19-May-2021, the patient stated that she had a fibromyalgia attack but did not correlate this to the administration of the Janssen vaccine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194 expiry: 09-APR-2022) dose was not reported, 1 total, administered on left arm on 16-NOV-2021 at 13:30 for prophylactic vaccination (dose number series 2). No concomitant medications were reported. On 16-NOV-2021 at 23:00, the patient experienced hot, fever feeling which lasted about 15 minutes. She did not take her temperature. The patient then experienced a very cold feeling, hands shaking, and after 15 minutes it was resolved. Then the patient felt a wave of pain throughout her entire body that was very weird, unusual, not a muscle ache/pain. She tried to stand but both legs were very weak, and she could not stand. She then laid back down. The patient stated that the pain lasted 10 hours solid and would rate it as a 10 on the pain scale. She did not take any medications because she could not get up. Patient stated that every tooth in her mouth had a tooth ache, the fingertips hurt, and entire body hurt (dose series 2). After 10 hours it disappeared, and patient went into her normal attack of Fibromyalgia. For about 2-3 days she took it easy. Patient reported she was now experiencing her normal fibromyalgia pain and has not experienced anything else. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from hot feeling, hands shaking, cold feeling, chills, and fever feeling on 16-NOV-2021, and tooth ache, felt a wave of pain over the entire body, could not stand, fingers hurt, and both legs very weak on 17-NOV-2021, and the outcome of fibromyalgia attack was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20211116; Test Name: Pain scale; Result Unstructured Data: 10
Aktuelle Erkrankungen: Fibromyalgia
Vorgeschichte: Medical History/Concurrent Conditions: Polymyalgia rheumatica (Patient reported " went away 4 years after diagnosis")
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932472

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: MA
Alter: 43,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 24.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Cough Discomfort Dyspnoea Headache Hypoaesthesia Pain in extremity

Symptomtext

Alot of pressure headaches with numbness and heaviness on right side of face. Pain in legs, shortness of breath followed by sudden cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: N/A
Allergien: None
Vorherige Impfungen: -

VAERS 1929617

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cough Musculoskeletal chest pain Myalgia

Symptomtext

Chest muscle pain started at 6:15PM in bed while laying down. Deep cough no mucus with the chest wall pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: Bactrim, Levaquin
Vorherige Impfungen: Flu shot

VAERS 1923448

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: OR
Alter: 26,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest discomfort Chills Dyspnoea Feeling cold Heart rate increased Pain in extremity X-ray normal

Symptomtext

First night couldn?t breathe. Very tight chest. Extreme leg pain. Shivering. Couldn?t get warm. Fast heart beat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: X-ray way ok. But in progress of getting EKG and Blood test for myocarditis on December 6,2021
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Syeda
Allergien: None
Vorherige Impfungen: -

VAERS 1923231

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IA
Alter: 50,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chills Headache Myalgia Pyrexia Tremor

Symptomtext

Headache within 5 minutes - lasted 3 days Muscle aches about 6 hours after - lasted 2 days Fever and shaking chills about 10 hours after - lasted until next morning

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: hypothyroid, depression
Andere Medikamente: Levothyroxine, escitalopram, wellbutrin, omeprazole
Allergien: Latex
Vorherige Impfungen: -

VAERS 1921038

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: OH
Alter: 74,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Electrocardiogram Laboratory test Myalgia Vaccination site erythema Vaccination site swelling X-ray

Symptomtext

patient with severe myalgias in left arm and left leg lasting for several weeks following the vaccine. He also had significantly prolong redness and swelling at the vaccine site. He also developed dyspnea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: labs and xrays on 11/13, 11/22 and labs and EKG on 12/3
Aktuelle Erkrankungen: NONE
Vorgeschichte: DM, lumbar spondylosis, HTN, hyperlipidemia
Andere Medikamente: YES
Allergien: METFORMIN
Vorherige Impfungen: -

VAERS 1916585

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: PA
Alter: 65,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Mobility decreased Pain Pain in extremity

Symptomtext

Patient stated that after receiving the vaccine, he had regular arm pain. The arm pain then radiated to his shoulder and eventually down to his elbow in the coming days. He is still experiencing pain from his shoulder to elbow and cannot lift his arm past his shoulder without severe pain.

Weitere VAERSDATA-Felder

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

VAERS 1916048

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: -
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Balance disorder Body temperature Chest pain Cognitive disorder Dyspnoea Feeling abnormal Mental impairment Migraine Pain in extremity Paraesthesia Productive cough Pulmonary pain Pyrexia

Symptomtext

CHEST PAIN COMING AND GOING; CLOUDED THINKING; NUMBNESS AND STINGING IN LEFT, RIGHT ARM AND LEFT FINGERS; LOW GRADE FEVER; LUNGS HURT; ON AND OFF MIGRAINES; COUGHING A LOT CRUD / SPUTUM; CONSTANTLY GASPING FOR BREATH; COGNITIVE ABILITY OFF; EQUILIBRIUM OFF; FEELS LIKE RUNS INTO SHOULDER AND INTO DIAPHRAGM; DULL ACHE FROM RIGHT FOREARM TO ELBOW; This spontaneous report received from a patient concerned a 56 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: mental illness, chronic obstructive pulmonary disease, soap allergy, leukoplakia on voice box and larynx, degenerative disc disease, stenosis, spine and neck vertebra sciatica, pinched nerve, and asthma. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, expiry: Unknown) dose was not reported, 1 total, dose series of 1, administered on 19-NOV-2021 to left arm for prophylactic vaccination. No concomitant medications were reported. On 19-NOV-2021, patient experienced the continuous, severe headache and migraines on and off. Patient had 10-15 migraines since vaccination. Patient took no medicines for migraine in past. Patient reported that, migraine was debilitating and was not had light or noise when had migraine and was puts head in pillow. Patient took Imitrex for migraines. On 20-NOV-2021, the patient experienced lungs hurt. Patient experienced coughing up a lot of crud or sputum and constantly gasping for breath. Patient used the nebulizer and inhaler for chronic obstructive pulmonary disease (COPD) but did not helped. On 20-NOV-2021, the patient experienced blurred peripheral vision. Patient experienced the blurry vision and was able to saw only a dark shadows as equilibrium was off. Only time did not had this if looked straight out. On 20-NOV-2021, the patient experienced dizziness. Patient experienced dizziness when look down and stood up with feet spreads apart to prevent fall. On 20-NOV-2021, patient experienced the low grade fever which was lasted for 10-15 hours. Patient took 800 mg Ibuprofen 3 times and 81 mg aspirin. Patient body temperature was 104 F (fahrenheit). On 20-NOV-2021, patient experienced the vomiting. Vomiting was coming and going. Patient coughed as walking dog and was felt like acid reflux and stomach bile contents came up, felt like lump in throat and vomited a total of 3 times since first incident. On 22-NOV-2021, patient experienced numbness and stinging in left arm. The patient sit on hand and hands falls asleep, had three finger that was numb. Patient experienced the same sensation on right arm but a dull ache from forearm to elbow. On 23-NOV-2021, the patient experienced chest pains that was coming and going and felt like tightness in breast area and sternum. Patient taken Ibuprofen and then subsided in hour, felt like ran into shoulder and into diaphragm. On 23-NOV-2021, patient experienced the clouded thinking. Patient cognitive ability was off, mind was racing, felt cloudy and if thought of something sensation of mind was not grasping it. Patient tried to get medical exemption for not getting covid-19 vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from low grade fever on 21-NOV-2021, was recovering from on and off migraines, chest pain coming and going, lungs hurt, clouded thinking, numbness and stinging in left, right arm and left fingers and the outcome of coughing a lot crud / sputum, constantly gasping for breath, cognitive ability off, equilibrium off, dull ache from right forearm to elbow and feels like runs into shoulder and into diaphragm was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20211200601-covid-19 vaccine ad26.cov2.s-clouded thinking. 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: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20211120; Test Name: Body temperature; Result Unstructured Data: 104 F, Low grade fever
Aktuelle Erkrankungen: Asthma; Chronic obstructive pulmonary disease (Patient using nebulizer and inhaler.); Degenerative disc disease; Leukoplakia; Mental disorder; Pinched nerve; Sciatica; Soap allergy; Stenosis
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1914227

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NC
Alter: 51,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest discomfort Chills Fatigue Feeling abnormal Fibrin D dimer normal Insomnia Laboratory test Pain in extremity Paraesthesia Tremor

Symptomtext

I feel off, not myself. I had chest pressure/heaviness. Hands shaking, tremors at times, internal trembling. Cold chills. Arm soreness. Insomnia. Lower body tingling. Extremely fatigued. Some issues are better some still continue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Just lab work - D-dimer test (results came back normal)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1909370

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: MI
Alter: 46,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Anion gap Biopsy kidney abnormal Blood albumin decreased Blood calcium decreased Blood chloride increased Blood creatinine increased Blood glucose increased Blood potassium increased Blood sodium decreased Blood urea increased Carbon dioxide decreased Condition aggravated Glomerular filtration rate decreased Haematuria Kidney transplant rejection Transplant rejection

Symptomtext

Patient was admitted with acute renal failure, kidney biopsy showed Banff III TCMR in transplanted kidney. He is just over a year post kidney transplant. Patient got J&J 2nd vaccine on 16th and symptom of hematuria started on 11/17/21. Had received 1st dose in 3/2021 without any issues. Notably, one of his immunosuppression meds (cellcept) dose was reduced to 250mg BID recently for BKV viremia. There was no evidence of BKV in kidney biopsy. He had several triggers for rejection including CMV viremia few months back, BKV viremia, slightly decreased cellcept dose. But given temporal relation with vaccination with J&J, and the resultant severity of the rejection despite being on 2 other immunosuppression agents at good doses and no preceding DSA, raises the concern of if the vaccine had any role to play in triggering his immune system facilitating this degree of rejection. He is being treated for TCMR at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 7,0
Labordaten: Full kidney biopsy report and DSA are pending at this time. Results for patient 11/26/2021 08:34 Sodium: 135 (L) Potassium: 5.9 (H) Chloride: 107 CO2: 18 (L) Urea Nitrogen: 66 (H) Creatinine: 4.81 (H) Glucose: 126 (H) Calcium: 8.8 Albumin: 3.5 EGFR, Black: 16 (L) EGFR, Non-Black: 13 (L) Anion Gap: 10 11/27/2021 05:41 Sodium: 131 (L) Potassium: 5.6 (H) Chloride: 102 CO2: 16 (L) Urea Nitrogen: 80 (H) Creatinine: 4.72 (H) Glucose: 269 (H) Calcium: 8.7 Albumin: 3.4 (L) EGFR, Black: 16 (L) EGFR, Non-Black: 14 (L) Anion Gap: 13 (H) 11/28/2021 07:26 Sodium: 135 (L) Potassium: 5.4 (H) Chloride: 107 CO2: 19 (L) Urea Nitrogen: 84 (H) Creatinine: 4.39 (H) Glucose: 235 (H) Calcium: 9.1 Albumin: 3.5 EGFR, Black: 17 (L) EGFR, Non-Black: 15 (L) Anion Gap: 9 11/29/2021 07:10 Sodium: 137 Potassium: 5.6 (H) Chloride: 111 (H) CO2: 20 (L) Urea Nitrogen: 83 (H) Creatinine: 3.76 (H) Glucose: 191 (H) Calcium: 8.9 Albumin: 3.3 (L) EGFR, Black: 21 (L) EGFR, Non-Black: 18 (L) Anion Gap: 6 11/30/2021 07:27 Sodium: 137 Potassium: 4.9 Chloride: 110 (H) CO2: 20 (L) Urea Nitrogen: 81 (H) Creatinine: 3.22 (H) Glucose: 108 (H) Calcium: 8.8 Albumin: 3.2 (L) EGFR, Black: 25 (L) EGFR, Non-Black: 22 (L) Anion Gap: 8
Aktuelle Erkrankungen: - CMV viremia - BKV viremia
Vorgeschichte: Patient had end-stage kidney disease secondary to diabetic nephropathy, now status post a deceased unrelated donor kidney transplant on 10/31/2020. Diabetes mellitus (CMS/HCC) ? GERD (gastroesophageal reflux disease) ? Hyperlipidemia ? Hypertension ? Obesity ? Polycythemia ? Sleep apnea
Andere Medikamente: - aspirin (ECOTRIN LOW STRENGTH) 81 mg delayed release tablet Take 1 tablet (81 mg) by mouth once daily. 12/20/19 - atorvastatin (LIPITOR) 20 mg tablet Take 1 tablet (20 mg) by mouth at bedtime. 10/5/21 - cholecalciferol (VITAMIN D3
Allergien: - Simvastatin Not Specified Other (See Comments) - Sevelamer Carbonate Low GI Distress, Unknown
Vorherige Impfungen: -

VAERS 2571827

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: -
Alter: 43,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac flutter Chest discomfort Chest pain Dyspnoea Dyspnoea exertional Electrocardiogram normal Fatigue Headache Hypertension Hypoaesthesia Myalgia Neck pain Pain in extremity Palpitations Paraesthesia Pruritus Pyrexia Rash

Symptomtext

BlurredVision, Headache, Myalgia, Fever, SkinRash, Rash, UrticariaPruritus, Palpitations, HYPERtension Day 1 - Fever 103.6/bilateral neck pain; Day 2 - HA, R eye blurry/white lines, heart fluttering/chest tightness, R arm numb/tingly; Day 3 - chest pain/shortness of breath with exertion, palpitations; Day 4 - cont'd Narrative: Day 4 (cont'd) - "woke up with full rash and hives to neck back, itching, swelling of neck, increased SOB worse than day prior. Rash went up to face with swelling within hours and heart palpitations were worse, so went to urgent care at shopping center. BP 140/92 hr 123. Normal is 109/60 hr usually in 70. Explained adverse effects over days prior and that things have gotten way worse since. Dr. placed me on prednisone for swelling 20mg once a day to see if it would help with chest tightening and SOB. Day 5 - no change, followed orders Day 6 - rash persisted with itching, heart fluttering, SOB with deep breath, Rt arm still numb. Went to primary care and asked for EKG and chest x ray. I was only given the EKG which was normal sinus rhythm. Run down and so fatigued. Day 7 - headache with blurred vision in Rt eye getting worse. Pain in back of calf. Fatigued and feeling that head is about to explode. Will reach out to ophthalmology as recommended by occupational health."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: yes - "Flu shot really makes me sick"

VAERS 1901664

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: OR
Alter: 32,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: -
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Blood test Chills Dehydration Diarrhoea Dyspnoea exertional Food poisoning Gait inability Headache Hepatic enzyme Liver injury Migraine Muscle tightness Myalgia Pyrexia SARS-CoV-2 test Sluggishness Trismus Vision blurred

Symptomtext

MIGRAINES; COULD NOT WALK; JAW LOCKED OPEN; FOOD POISONING; LIVER DAMAGE; DEHYDRATED; HIPS AND KNEES STARTED LOCKING UP/ LOCKED UP MUSCLES; CHILLS; EXPLOSIVE DIARRHEA; FEVER; HEADACHE; SCIATIC/MUSCLE PAIN; BLURRED VISION LIKE LENS WITH RAIN DROPS ON IT/COULD NOT SEE; SLUGGISH/SLOW; OUT OF BREATH WHILE RUNNING/WORKING OUT; This spontaneous report received from a patient concerned a 32 year old female. The patient's weight was 127 pounds, and height was 70 inches. The patient's concurrent conditions included: latex skin sensitivity. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194 expiry: 09-APR-2022) dose was not reported, 1 total, administered on left deltoid on 03-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 03-NOV-2021, at evening the patient began to experience what she referred to as the regular side effects of fever, headache and chills, and then her hips and knees started locking-up by 7-9 pm, felt like sciatic/muscle pain, that cleared up. Patient went to urgent care to make sure all was ok. The patient experienced diarrhea the same evening on 03-Nov-2021 and it was bright yellow/explosive like food poisoning for 7 days, the patient felt miserable, dehydrated/urine dark. On 17-Nov-2021, two weeks after vaccination, the patient felt this was normal but had migraines with occasional diarrhea for 10 days after vaccination and reported that she could not walk until 1 pm the next day from those muscle cramps. The patient stated that jaw was feeling like it locked open as well. Patient added that, on an unspecified day in Nov-2021 she went back to urgent care because her vision was blurred like lens with rain drops on it, felt it was a temporary side effect and possibly just needed a smaller vaccine dose/dose adjustment. Patient had blood work on 17-Nov-2021 which showed liver damage and ALT/AST levels were high (elevated liver enzymes), where prior they were in normal range. HCP was able to palpate liver. Patient had bloodwork both in January and also 1 week prior to vaccination as she wanted to check prior to getting vaccinated if she was healthy and tested for covid-19 prior to vaccine. Patient stated that she had been to urgent care several times. On an unspecified date the patient experienced, blurred vision like lens with rain drops on it/could not see, sluggish/slow and could not walk and out of breath while running/working out. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from dehydrated, hips and knees started locking up/ locked up muscles, jaw locked open, chills, explosive diarrhea, fever, and sciatic/muscle pain, had not recovered from liver damage, migraines, and headache, and the outcome of blurred vision like lens with rain drops on it/could not see, sluggish/slow, food poisoning, could not walk and out of breath while running/working out was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20211154558-COVID-19 VACCINE AD26.COV2.S-Liver damage. 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: Dehydration
Hospital-Tage: -
Labordaten: Test Date: 202101; Test Name: Blood test; Result Unstructured Data: unknown; Test Date: 202110; Test Name: Blood test; Result Unstructured Data: unknown; Test Date: 20211117; Test Name: Hepatic enzyme; Result Unstructured Data: elevated; Test Date: 20211117; Test Name: Blood test; Result Unstructured Data: liver damage, high ALT/AST level; Test Name: SARS-CoV-2 test; Result Unstructured Data: unknown
Aktuelle Erkrankungen: Latex allergy
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1899698

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NJ
Alter: 55,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Chest pain Chills Cold sweat Feeling cold Grip strength decreased Headache Hypoaesthesia Immediate post-injection reaction Injection site pain Lethargy Pain Paraesthesia

Symptomtext

Immediate onset: Tingling and numbness in left arm down to 3 fingers on left hand with accompanying weakness of grip; sharp, deep pain at injection site. 4 hours after the injection: headache, chills, freezing cold, lethargy, cold sweats, throbbing and sharp shooting pains in left ankle. As of 11/24, chest pain on left side behind breast.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None yet
Aktuelle Erkrankungen: None
Vorgeschichte: RSD in left ankle post ankle fracture
Andere Medikamente: Women?s multi-vitamin
Allergien: Fluoroquinolones; penicillin
Vorherige Impfungen: -

VAERS 1897554

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: 30,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
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 Chest X-ray normal Chest pain Dizziness Electrocardiogram normal Hypoaesthesia Neck pain Tonsillar inflammation Urticaria

Symptomtext

Within the first 10 mins of the shot I had sharp chest pains, hives on my chest, face and neck, very sore neck (left side) from behind my ear to left clavicle and numbness on my jaw. I was instructed by my doctor to go to the nearest emergency. At the ER, I got light headed. 11/18 - had white spots on my tonsils and believed it was strep. Got swab and a culture test and it came back negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, chest scan and blood work came back negative. Before leaving the ER they gave me fluids and pain medicine via catheter in left arm.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Celexa 10MG
Allergien: None
Vorherige Impfungen: -

VAERS 1892702

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: -
Beginn: 19.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Bursitis Fatigue Feeling hot Paraesthesia Pruritus

Symptomtext

LEFT FOOT BECAME ITCHY; FLUID FILLED SPOT ON LEFT FOOT; LEFT FOOT BECAME WARM; LEFT FOOT TINGLY WHEN WALKS; FEELS LIKE DISSIPATING; This spontaneous report received from a patient concerned a 35 year old female. 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 admin not reported, batch number: 1855194, and expiry: 09-APR-2022) dose was not reported, administered on 17-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 19-NOV-2021, the patient experienced left foot became itchy. On 19-NOV-2021, the patient experienced fluid filled spot on left foot. On 19-NOV-2021, the patient experienced left foot became warm. On 19-NOV-2021, the patient experienced left foot tingly when walks. On 19-NOV-2021, the patient experienced feels like dissipating. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from left foot became itchy, fluid filled spot on left foot, left foot tingly when walks, left foot became warm, and feels like dissipating. This report was non-serious.

Weitere VAERSDATA-Felder

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

VAERS 1890216

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: ID
Alter: 57,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Expired product administered Paraesthesia oral Refusal of vaccination

Symptomtext

PT WAS ADMINISTERED A JANSSEN VACCINE OUTSIDE THE 6 HOUR WINDOW HELD AT 36-46 DEGREES FAHRENHEIT. THE 6 HOUR TIME FRAME WAS MISCALCULATED AND ADMINISTERED AT EXACTLY 7 HOURS. PT WAS MONITORED FOR 30 MINUTES AND PT NEVER EXHIBITED SYMPTOMS OF ANAPHYLAXIS OR DISTRESS. THE ERROR WAS CAUGHT BY MYSELF 30 MINUTES AFTER THE PT HAD LEFT. I CONTACTED JANSSEN AND THEY HAD NO GUIDANCE AND STATED TO MAKE MY BEST CLINICAL JUDGEMENT. THE CDC GUIDANCE ON COVID-19 VACCINE ADMIN ERRORS AND DEVIATIONS STATES THAT IF THE MANUFACTURER DOES NOT HAVE DATE TO SUPPORT THE STABILITY OF THE VACCINE TO REPEAT THE DOSE. I CONTACTED THE PT AND SHE STATED " I WILL NOT GET REVACCINATED, DUE TO ME ONLY GETTING IT BECAUSE MY WORK WANTS ME TO." THE PT THEN TOLD ME THAT SHE STARTED EXPERIENCING TINGLING OF THE TONGUE, LIPS, AND GUMS. PT DENIED SOB, DIFFICULTY BREATHING, AND SWELLING OF THE MOUTH/THROAT/FACE. ADVISED PT TO TAKE BENADRYL AND TO GO TO THE ER IMMEDIATELY BECAUSE IT SOUNDED LIKE SHE COULD POSSIBLY BE HAVING A REACTION. PT REFUSED. REEDUCATED THE IMPORTANCE OF GOING TO THE ER TO PT AND SHE REFUSED A SECOND TIME. PT STATES " MY DAUGHTER IS AND RN AND WILL MONITOR ME."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: NONE CONDUCTED.
Aktuelle Erkrankungen: PT STATED SHE HAD NO CURRENT ILLNESSES.
Vorgeschichte: PT STATED NO CHRONIC OR LONG-STANDING HEALTH CONDITION.
Andere Medikamente: UNKNOWN WHAT MEDICATIONS PT WAS TAKING.
Allergien: PT STATED AT THE TIME OF VISIT THAT SHE HAD ANAPHYLAXIS TO PENICILLIN, DOXYCYCLINE, ALEVE, GABAPENTIN, AND ERYTHROMYCIN.
Vorherige Impfungen: -

VAERS 1888084

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: GA
Alter: 66,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / -

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

Asthenia Confusional state Metabolic encephalopathy Mobility decreased Neurological examination normal Plasmapheresis Speech disorder

Symptomtext

After receiving vaccination, a day after patient became confused, unable to speak or move any of her extremities. On examination, patient was noted to have generalized weakness with power grade of 2/5 globally. A diagnosis of acute metabolic encephalopathy was made. Patient had extensive neurological work-up which was unremarkable. She received plasmapheresis for total of 5 sessions. Patient noted to have some mild improvement with treatment. IT was considered that patient had Covid-vaccine related reaction from covid vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 20,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, COPD, GERD, Type 2 diabetes mellitus, depression and anxiety
Andere Medikamente: Amlodipine, Nexium, Celebrex, Neurotin, Zanaflex, CBD oil , Zolpidem, Lisinopril
Allergien: Metformin, Sulfa containing medication, arformoterol
Vorherige Impfungen: -

VAERS 1870018

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: PA
Alter: 69,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Cough Dizziness Dyspnoea Fatigue Headache Heart rate increased Pyrexia Restlessness

Symptomtext

fatigue, fever ( around 99.5) , rapid heart beats, shortness of breath, almost fainting episodes, restlessness, headache, coughing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vitamins D, C, cardioloc 2.5 mg.
Allergien: allergy to penicillin
Vorherige Impfungen: -

VAERS 1868221

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: FL
Alter: 32,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Fatigue Headache Heart rate increased Pyrexia Tachycardia

Symptomtext

Tachycardia with resting heart rate around 120-128bpm. Heart rate would increase to around 150bpm with minimal exertion, such as walking 30? to the bathroom. Tachycardia continued until approximately 33hours post-vaccine. My resting heart rate is still higher than my normal by about 15bpm and continue to have elevated heart rate with minimal exertion (around 120bpm after walking 30? to bathroom). This is completely abnormal for me. A couple weeks ago I could walk 4 miles and my heart rate would never raise above 115bpm. Other typical symptoms: Fever for 36 hours Chills for 12 hours Fatigue for 36 hours Headache for 36 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma: well controlled
Andere Medikamente: None
Allergien: Azithromyacin : nausea and vomiting
Vorherige Impfungen: -

VAERS 1868025

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: 25,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Chills Computerised tomogram thorax normal Fatigue Heart rate increased Palpitations

Symptomtext

Typical symptoms presented as fatigue and chills. Then my heart started beating 120-165bpm sitting still and started palpitating 4-5 times per minute for 2 hours. Hospital gave me Ativan, beta blockers, minerals to get my heart to start beating properly again. I was in the hospital for about 8 hours, my heart eventually returned to normal. Normal CT scan for heart. Covid vaccine probably amped up an immune response and caused my heart rate to spike and not pump efficiently. Released from the hospital with fatigue but my heart is fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: IBS
Andere Medikamente: Allegra Antihistamine
Allergien: None
Vorherige Impfungen: -

VAERS 1865575

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Electrocardiogram Feeling abnormal Hypertension

Symptomtext

PT COMPLAINED OF MILD SOB AND FEELING WOBBLY. SHE WAS ADVICED IN THE PAST OF POTENTIAL REACTIONS TO VACCINE AND AGREED TO TAKE ONE TODAY. SHE WAS ON HER 28TH MINUTE OF OBSERVATION WHEN SHE HAD ONSET OF SYMPTOMS. NO TREATMENT WAS PERFORMED BUT VITALS WERE TAKEN ALL WITHIN NORMAL LIMITS, WITH EXCEPTION OF BP ON THE SECOND TIME TAKING IT, SHE WAS HYPERTENSIVE. PT WAS ASSESSED AND ADVISED TO SEEK MEDICAL ATTENTION AND GIVEN SYPTOMS TO BE CAUTIOUS OF.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: VITALS TAKEN, EKG, SPO2
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1865555

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: UT
Alter: 34,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Asthenia Chills Dysstasia Fall Feeling cold Hallucination Headache Myalgia Pyrexia Tremor

Symptomtext

Im very healthy, haven't been sick in 10+ years, workout, eat clean , have very good hygeine. 4 hours after injection I had shakes and shivers where I felt like I was freezing inside. 7 hours after the injection the shakes and shivers increasing got worse and with them came terrible muscle aches and following that a terrible headache started and with each hour proceeded to get worse to the point of being practically unbearable. 10 hours after a fever insued and I began hallucinating and could hardly stand up without falling over. 24 hours later the hallucinations and shaking stopped but the headache, muscle aches, and shivers persisted for 3 more days and I felt incredibly weak. A full week after the injection I feel fine and am back to normal and do not seem to have any lasting symptoms.

Weitere VAERSDATA-Felder

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

VAERS 1864835

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Computerised tomogram Condition aggravated Feeling hot Grip strength decreased Hypertension Hypoaesthesia Laboratory test Magnetic resonance imaging Muscular weakness Pain in extremity Paraesthesia Peripheral coldness Tachycardia X-ray

Symptomtext

Day 1 arm soreness and loss of ability to hold onto items of any weight such as a glass of water. Made serval messes 10/28/21 throughout the day requireing long periods of time to clean them up. I am LEFT HAND DOMINANT and was able to clean up the messes with the LEFT hand although the hand had lost approx 50% of control . Therefore the mess clean up took longer and was less than adequate, had to relcean several times and get assitance from others. The arm pain stopped after 2 days. The weakness also gradually made itself back to normal until 11/10/2021. At that time I woke up with a completely numb and tingling arm resembling storke as the arm was cold and unusable. I took a beta blocker Corgard as my heart was experiencing a tachy event along with high blood pressure event (HR 155 BP 184/100. Went to ER immediately. After approx 12 hours in the ER the arm began to stop tingling and had periods of extreme heat sensation as it was coming back to life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I had Cat Scan MRI xray Blood tests and complete stroke workup.
Aktuelle Erkrankungen: Tachycardia, Bradycardia, Heart Disease(Leaky Tricuspid valve and Mitral Moderate/Minimum), Lynch Syndrome Genetic Mutation,
Vorgeschichte: Tachycardia, Bradycardia, Heart Disease(Leaky Tricuspid valve and Mitral Moderate/Minimum), Lynch Syndrome Genetic Mutation,
Andere Medikamente: Corgard 81mg Aspirin Lorazapram Potassium and Magnesium Vitamin C
Allergien: None Known
Vorherige Impfungen: -

VAERS 1860874

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: FL
Alter: 38,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chapped lips Condition aggravated Extra dose administered Lip swelling Rash pruritic

Symptomtext

Booster for Janssen Lip swelling Itchy rash Chapped lips

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Venlafaxine ER 150 mg daily
Allergien: Cipro Sulfa
Vorherige Impfungen: 4/6/2021 Janssen 1 dose, lip swelling, hives

VAERS 1860672

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: MI
Alter: 43,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Chills Gait inability Headache Insomnia Pain Palpitations Tremor Vision blurred

Symptomtext

Headache, severe body aches, joint pain, chills, shaking to the point unable to walk, blurry vision, heart racing, insomnia,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Fibroids
Andere Medikamente: Zinc, vitamin b, probiotic, iron
Allergien: None
Vorherige Impfungen: -

VAERS 1858263

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Extra dose administered Hypoaesthesia

Symptomtext

44 year old female who states left arm numbness at the end of 15 min. observation period after receiving 2nd dose of Janssen (Johnson and Johnson), COVID-19 vaccine on 11/10/2021. States no reaction after 1st dose of COVID-19 vaccine in March of 2021, (Janssen, Johnson and Johnson). Vital signs at 1112 am are Blood pressure of 121/91, 99 percent 02 sat on room air, pulse of 81, breathing equal and unlabored. History of fibromyalgia. No known drug allergies. Currently on Lyrica. Denies any other medical history. States at 1118 am chest pressure at 2/10. Vital signs 126/80. O2 sat 99 percent on room air. Pulse of 80. EMS, (911), called for chest pain and left arm numbness. Four lead EKG completed at 1124. 02 at 2l via nasal cannula. Blood pressure 126/87, pulse of 76. At 1132 12 lead EKG completed, (no abnormalities noted) EMS arrived and report given by RN. Pt. evaluated by paramedics/EMD. 1135, pt. in ambulance bay for further evaluation. At 1147 pt. states chest pain and arm numbness subsided and evaluation completed by paramedics/EMS and left vaccine clinic to personal car under own accord in stable condition. Vital signs, Blood pressure, 128/75, O2 sat 100 percent on room air, pulse of 75. Report given to lead vaccine staff.

Weitere VAERSDATA-Felder

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

VAERS 1857369

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IL
Alter: 40,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Dyspnoea Headache Pyrexia

Symptomtext

Fever, headache and SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Advised to self quarantine
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Bupropion, Clonazepam, Vitamin D2
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1855313

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Chills Fatigue Insomnia Pain Pyrexia Tremor Vaccination complication

Symptomtext

Adverse reaction to J&J booster: Severe chills; shaking for 11 hours; no sleep; aches; fever; fatigue for 2 days. I had no reaction to the J&J vaccine, only reaction to booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None, Did not seek medical assistance. I do have an appointment scheduled with my NP Nov. 22, 2021.
Aktuelle Erkrankungen: No illness
Vorgeschichte: High blood pressure regulated by metoprolol
Andere Medikamente: Metoprolol tartrate
Allergien: Darvon, opioids
Vorherige Impfungen: -

VAERS 1851214

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: MA
Alter: 22,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Paraesthesia

Symptomtext

The patient presented to the Outpatient pharmacy requesting her first dose of the Janssen CV-19 vaccine (Lot# 1855194). After administration, patient was told to sit in the waiting area for observation for 15 minutes. After a few minutes, patient approached the pharmacist on duty and stated that she was experiencing tingling in her arm and neck. The pharmacist immediately informed the nurses in the clinic, who observed the patient. Nurses stated that there was no redness at the injection site, and that there was no discoloration in her arm. Patient stated to nurses upon observation that she was feeling better, and the nurses advised her to seek the ED if she experiences any other symptoms or issues later on. She verbalized understanding.

Weitere VAERSDATA-Felder

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

VAERS 1850945

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: GA
Alter: 48,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood creatine phosphokinase Chest X-ray Chest pain Dyspnoea Electrocardiogram Fibrin D dimer Full blood count Headache Injection site pain Lymphadenopathy Metabolic function test Pain Troponin I White blood cell count

Symptomtext

Chest pain 10 days. Left arm sharp pain which traveling from injection site to my heart area 5 days. Shortness on breath 10 days. Hurt to breath 7 days. Headache. Body ache 7 days. Left shoulder to the neck had sharp pain 5 days. Mid spinal cord had sharp pain intermittent 4 days. Neck glands swollen for 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 10/26/2021 D-Dimmer Troponin I EKG 12 or more leads w int & rpt Chest Xray EKG 12 or more leads w int & rpt CBC (Complete blood count) White blood cell differential Basic metabolic panel Creatine kinase Troponin I
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: No prescriptions. Vitamin B, C, E, Multi-vitamin.
Allergien: None I'm aware of.
Vorherige Impfungen: -

VAERS 1850732

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IN
Alter: 49,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Chills Headache Immediate post-injection reaction Pain Paraesthesia

Symptomtext

Immediately developed severe headache lasting 24hrs through night prevent sleep Developed significant body aches and some tingling in extremities x 24hrs Chills x24hrs

Weitere VAERSDATA-Felder

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

VAERS 1849333

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: 27,0
Geschlecht: M
Eingang: 07.11.2021
Impfdatum: 28.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / LA

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

Anxiety Aptyalism Blood test normal Chest pain Confusional state Decreased appetite Dyspnoea Fatigue Fibrin D dimer normal Headache Insomnia Myalgia Pyrexia Tremor

Symptomtext

Vaccinated 10/28 in the afternoon, fever, headaches, muscle aches, shortness of breath, and fatigue 10/29 evening; headache, loss of appetite, chest pain, fatigue 10/30; loss of appetite, fatigue, chest pain, shortness of breath, headaches, loss of salivation; 10/31 loss of appetite, chest pain, shortness of breath, headaches, loss of salivation, fatigue; 11/1 loss of appetite, chest pain, shortness of breath, headaches, loss of salivation, fatigue; 11/2 loss of appetite, chest pain, shortness of breath, headaches, loss of salivation, fatigue; 11/3 loss of appetite, chest pain, shortness of breath, headaches, loss of salivation, fatigue, difficulty sleeping ; 11/4 confusion, loss of appetite, chest pain, shortness of breath, headaches, loss of salivation, fatigue, shaking, difficulty sleeping; 11/5 loss of appetite, chest pain, shortness of breath, headaches, loss of salivation, fatigue, shaking, difficulty sleeping, anxiety, confusion, tremors; 11/6 loss of appetite, chest pain, shortness of breath, headaches, loss of salivation, fatigue, shaking, difficulty sleeping, anxiety, confusion, tremors; 11/7 loss of appetite, chest pain, shortness of breath, headaches, loss of salivation, fatigue, shaking, difficulty sleeping, anxiety, confusion, tremors

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Blood work on 11/3 came back normal, D Dimer was Normal; seeking more blood work soon.
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: N/a
Allergien: N/a
Vorherige Impfungen: -

VAERS 1849103

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: PA
Alter: 42,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Deafness Paraesthesia Somnolence Unresponsive to stimuli Vision blurred

Symptomtext

PATIENT GOT VERY SLEEPY, VISION BLURRED, FELT TINGLY, COULDN'T HEAR. 911 WAS CALLED AT THIS TIME. HE THEN BECOME UNRESPONSIVE . A STERNAL STIMULATION REVIVED HIM. WE KEPT HIM AWAKE, MONITORED HIS PULSE WHILE WE WAITED FOR EMS. PATIENT BECAME MORE ALERT AND COLOR RETURNED OVER NEXT FEW MINUTES. WHEN EMS ARRIVED HE WAS COHERENT AND TALKING. PARAMEDICS TOOK VITALS AND EXAMINED HIM. HE WAS RELEASED TO GO HOME NO HOSPITAL TRIP WAS NEEDED1

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NKA
Vorherige Impfungen: -

VAERS 1848711

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: VA
Alter: 59,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 01.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / -

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

Asthenia Chills Gastrooesophageal reflux disease Headache Hypotension Muscular weakness Musculoskeletal discomfort Pain

Symptomtext

Headache and severe weakness started around 5 pm. Difficult keeping head up. Blood pressure low. Reflux symptoms affecting heart. Discomfort lower right back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: BP. 100/60 Es tylenol for weakness and aches and pains and chills
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 DM , hayfever allergies. Mild asthma
Andere Medikamente: Trulicity, symbicort, COVID vitamins. Metformin
Allergien: Latex?
Vorherige Impfungen: -

VAERS 1846891

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: OH
Alter: 63,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Erythema Interchange of vaccine products Pruritus Urticaria

Symptomtext

Had allergic reaction to the Pfizer Covid vaccine on 3/10/2021 and advised by physician to get the JNJ vaccine as the second dose. 3:55 pm Following the JNJ vaccine she had itching and hives around the lt. nipple, itching and redness across the forehead, lt. arm, neck and waist. B/P 150/90, P. 93 O2 Sat 99%. Given Benadryl 50 mg po. 4:20 B/P 142/82, P. 82, O2 Sat 98%. Instructed to contact physician if she becomes worse or go to the emergency department. Told she may take another dose of Benadryl 50 mg later this evening as needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Allergic reaction with itching and hives.

VAERS 1846118

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: GA
Alter: 58,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Bradycardia Feeling hot Hyperhidrosis Hypotension Nasopharyngitis Peripheral coldness Speech disorder

Symptomtext

WITHIN FIVE MINUTES OF RECEIVING VACCINE, PATIENT APPROACHED COUNTER AND ASKED FOR A PLACE TO LIE DOWN. WE IMMEDIATELY SAT HIM IN A CHAIR WHILE PROCURING A COT. WE CHECKED BLOOD PRESSURE WITH AUTOMATIC BP MACHINE TWICE BUT PATIENT WAS TOO HYPOTENSIVE FOR MACHINE TO READ. PATIENT REPORTED THAT HE WAS VERY HOT. PATIENT WAS SWEATING PROFUSELY, HIS HANDS AND FOREHEAD FELT VERY COLD, HIS CHEST AND NECK FELT WARMER THAN USUAL. PATIENT WAS COHERENT, BUT SPEECH INDICATED SIGNS OF DISORIENTATION. WE PROVIDED WATER AND ICE PACKS. A VISITING PHYSICIAN JOINED THE EFFORTS AND CONFIRMED HE WAS HYPOTENSIVE AND BRADYCARDIC. WE PROVIDED 25MG OF ORAL LIQUID DIPHENHYDRAMINE TO PATIENT. EMS WAS ON SITE BY THIS TIME (PROBABLY FIFTEEN TO TWENTY MINUTES AFTER VACCINE ADMINISTRATION) AND EVALUATED PATIENT. PATIENT FELT BETTER AFTER ADMINISTRATION OF DIPHENHYDRAMINE. EMS STAYED WITH PATIENT UNTIL HE RETURNED TO NORMAL STATUS.

Weitere VAERSDATA-Felder

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

VAERS 1846111

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: WY
Alter: 61,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

Patient came into clinic to receive, J&J vaccine. No contraindication to getting the J&J vaccine. Vaccine was given to patient in Left Deltoid at 1121am on 11/04/2021. At approximately 1136am patient reports numbness and tingling in left hand. Vitals were taken at 1140am HR: 61, BP: 150/90, Oxygen: 90%, RR: 14. Patient reports known health history of hypertension, no respiratory distress, no difficulty breathing, no vision changes, no loss of consciousness. Had patient stay for observation, vitals were retaken at 1215pm, and were WNL. Patient reports tingling/numbness in hand is improving and referred to health care provider ASAP for further observations.

Weitere VAERSDATA-Felder

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

VAERS 1844296

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NC
Alter: 29,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Cough Dizziness Dyspnoea Fatigue Hypersensitivity Hypoaesthesia Irritability Memory impairment Nausea

Symptomtext

Lightheadedness, Extreme fatigue, Hypersensitivity to stimuli, Shortness of breath, Violent bouts of coughing, Nausea, Irritability, Numbness of extremities, Working memory interference

Weitere VAERSDATA-Felder

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

VAERS 1843467

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / AR

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

Anaemia Angiogram pulmonary abnormal Asymptomatic COVID-19 Blood sodium decreased Chronic obstructive pulmonary disease Condition aggravated Dyspnoea exertional Electrocardiogram abnormal Emphysema Fatigue Full blood count normal Haemoglobin decreased Hyponatraemia Hypoxia Metabolic function test abnormal Normocytic anaemia Oxygen saturation decreased Productive cough

Symptomtext

Hospitalized (10.29.21); COVID-19 positive (10.29.21); Fully vaccinated Discharge Provider: MD Primary Care Provider: MD (Inactive) Admission Date: 10/29/2021 Discharge Date: 10/30/21 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypoxia [R09.02] COPD exacerbation (HCC) [J44.1] Anemia, unspecified type [D64.9] COVID-19 virus detected [U07.1] COVID-19 virus infection [U07.1] HOSPITAL COURSE: Patient is a 82 y.o. male with a 31 pack year smoking history and COPD who presented to the ED with progressive exertional dyspnea for 1 month. Patient states he had productive cough with quarter sized pale green sputum on 10/1/21 and saw an urgent care provider who gave him a 5 day course of oral Azithromycin. He continued to have the cough and began developing SOB with exertion that was getting progressively worse. He got a CXR before seeing his pulmonologist on 10/13/21 which was negative for pneumonia, he was prescribed another 5 day course of Azithromycin with oral prednisone taper and nebulized albuterol for the diagnosis of Acute COPD exacerbation. His cough improved significantly, however his SOB with exertion persisted. 10/28/21 he states his exertional SOB was severe enough to warrant a hospital visit. Notes getting his Covid19 booster shot on 10/27/21. No other symptoms than SOB with exertion and fatigue. ED course: patient was afebrile with O2 sats in the 90's at rest, but desaturated to 89% when up and moving around. He tested positive for Covid19. Lungs clear bilaterally, no conversational dyspnea. CTA chest showed emphysematous changes with no evidence of infiltrates/pneumonia. ECG was NSR with PAC. His labs showed normocytic anemia with Hgb of 8.9. Troponins were normal. CMP showed hyponatremia with Na of 127. He was given solumedrol 125mg IV, and was admitted for Acute COPD exacerbation. Upon admission, patient remained afebrile with stable vitals within normal limits, and saturating in the upper 90's on room air. Hyponatremia improved with Na to 132, CBC stayed within normal limits, and patient was eating and drinking without difficulty. Patient remained asymptomatic with current Covid19 infection. Discussed need of pulmonary function testing to reassess COPD severity and likely home oxygen needs for exertion and potentially beneficial changes to his daily breathing treatments that are confirmed with repeated PFT's . Patient and wife preferred to rest at home with oral steroid taper and 2 days of oral antibiotics rather than remaining in hospital. Patient is medically and vitally stable for discharge home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: 10.1.21: Urgent Care visit - cough for 3 days, no other symptoms - dx: bronchitis 10.13.21: Pulmonary office visit - COPD exacerbation
Vorgeschichte: COPD with exacerbation (HCC) CAD (coronary artery disease) Carotid artery stenosis Chronic rhinitis HTN (hypertension) Supraventricular premature beats COPD with exacerbation (HCC)
Andere Medikamente: albuterol (PROAIR HFA) 108 (90 BASE) MCG/ACT inhaler albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization aspirin 81 MG tablet B Complex CAPS cetirizine (ZYRTEC) 10 MG tablet Cholecalciferol (VITAMIN D3) 400 UNITS CAPS finasteride (PROSCA
Allergien: Aggrenox [Aspirin-dipyridamole Er] Breo Ellipta [Fluticasone Furoate-vilanterol] DoxycyclineGI Upset Symbicort [Budesonide]
Vorherige Impfungen: -

VAERS 1842877

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NY
Alter: 50,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Burning sensation Chills Headache Hyperhidrosis Hypoaesthesia oral Injection site pain Pain Pain in extremity Paraesthesia oral Pyrexia

Symptomtext

Whole left arm(not just injection site)throbbing and burning for about 3 hours. Lips became numb and tingly and headache started around 11am . Chills, sweating and body aches started around 4pm. Fever began around 8pm and reached 102.8 degrees. 6am on 11/4 temperature dropped to 100.1. 10am on 11/4 temperature returned to normal level. Some weakness and body aches were still present at that time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: None- did not seek medical attention(my wide is a RN and took care of me.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1840364

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain Chest discomfort Chills Diarrhoea Pain Paraesthesia Pyrexia

Symptomtext

Tingleling in extremities, abdominal pain, fever, chills, body aches, chest pressure, diarrhea,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Multi-vitamin, vitamin d
Allergien: none
Vorherige Impfungen: -

VAERS 1839874

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: MD
Alter: 46,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 30.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Arthralgia Back pain Fatigue Injected limb mobility decreased Lymphadenopathy

Symptomtext

Severed joints pain, lower back pain, tiredness, swollen armpit lymph nodes, lacked of right arm movement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Seasonal allergy
Vorgeschichte: None active asthma, only triggers with dust, mites and pollen. Seasonal allergies
Andere Medikamente: Vitamins
Allergien: None
Vorherige Impfungen: -

VAERS 1835269

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: UT
Alter: 69,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: -
Beginn: 29.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Body temperature Fatigue Headache Medication error Pyrexia Tremor

Symptomtext

MUSCLE TREMORS; MEDICATION ERROR; HEADACHE; FEVER; FATIGUE; This spontaneous report received from a patient concerned a 69 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: alcoholic, and non smoker, and other pre-existing medical conditions included: The patient had no known allergies and did not have any 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: 1855194 expiry: UNKNOWN) dose was not reported, administered on 29-OCT-2021 for prophylactic vaccination. Concomitant medications included mrna 1273 for prophylactic vaccination. On 29-OCT-2021, the patient experienced muscle tremors. On 29-OCT-2021, the patient experienced medication error. On 29-OCT-2021, the patient experienced headache. On 29-OCT-2021, the patient experienced fever. On 29-OCT-2021, the patient experienced fatigue. Laboratory data included: Body temperature (NR: not provided) 100.6 F. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from fever, and fatigue, had not recovered from headache, and muscle tremors, and the outcome of medication error was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20211029; Test Name: Body temperature; Result Unstructured Data: 100.6 F
Aktuelle Erkrankungen: Alcoholic (less than 1/week (2-3 per month)); Non-smoker
Vorgeschichte: Comments: The patient had no known allergies and did not have any drug abuse or illicit drug use.
Andere Medikamente: MODERNA VACCINE
Allergien: -
Vorherige Impfungen: -

VAERS 1831940

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: CA
Alter: 36,0
Geschlecht: M
Eingang: 31.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Asthenia Chest discomfort Dizziness Dyspnoea Feeling abnormal Heart rate increased Hypoaesthesia Immediate post-injection reaction Injection site paraesthesia Paraesthesia Tinnitus Vision blurred

Symptomtext

Adverse Events: Within one minute of receiving the injection: -paresthesia occurred in right arm, and then across chest -accelerated heart rate Within 10 minutes of receiving injection: -Brain fog -Numbness in limbs -Tinnitus in left ear -Difficulty breathing -Dizziness and weakness -Vision blurred Treatment: Was immediately escorted to have Dr. and Nurses monitor myself for the next hour. Was checked for any signs of rashes - none were immediately seen Vitals were checked after 20 minutes of receiving injection: (Heart rate, temperature, blood O2 levels) - heart rate was slightly elevated; yet all appeared normal Additionally, I informed Medical staff that it appeared I might have also had a panic attack right after the injection; yet some of the adverse reactions were listed on the Jansen Vaccine information PDF, and are not associated with panic attacks. -Was given glucose to normalize blood sugar levels, and Maylox for GERD symptoms. -Condition began to improve; yet severe dizziness, numbness/tingling of limbs persisted for the next 48 hours, intermittently. -72 Hours after injection, felt tightness in chest, intermittently

Weitere VAERSDATA-Felder

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

VAERS 1831578

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: TX
Alter: 44,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Back pain Neck pain Paraesthesia

Symptomtext

Feet, legs are tingling with minor back and neck pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Non
Aktuelle Erkrankungen: Non
Vorgeschichte: Ulcerative colitis
Andere Medikamente: Mesalamine, Propecia, gummy multi- vitamins
Allergien: Non
Vorherige Impfungen: -

VAERS 1829676

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: NY
Alter: 33,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / LA

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

Burning sensation Dyspnoea Feeling hot Headache Hyperhidrosis Impaired work ability Mobility decreased Pain

Symptomtext

On 10/28/2021 at 1530 hrs I was forced to take the Covid shot or be fired from my place of work. With a 2 month baby at home I decided to get the shot to avoid work termination. Soon after the shot my left arm was burning and was very difficult to lift my arm. Keep in mind I already got Covid in March of 2020. The shot was by far worse than actually getting covid. That night I felt like I was on fire with hot sweats a really bad headache. In the morning I found it very difficult to breath out of my nose. Aches and pains all day and I had to call out of work. So far to say the least my out come was terrible and I cannot believe I was forced to take this shot. I am following up with my doctor once I can move around more to see if this shot had any other effects on my health. In the past with all the shots they gave me I never had a side effect like the Covid-19 vaccine Thanks again ...

Weitere VAERSDATA-Felder

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

VAERS 1829543

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: OR
Alter: 40,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Dyspnoea Flushing Heart rate increased Nausea Throat tightness Vomiting

Symptomtext

Shortness of Breath Chest Pain Throat Tightness/Closure Rapid Pulse Flushing Nausea/Vomiting Action taken: Antihistamine given., Epinephrine given., Physician contacted, and 911 called. Outcome: Patient transported to ED at 10:53 AM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: None
Vorgeschichte: Problem List 11 items DM 2 HTN (HYPERTENSION) DM 2 W HYPERGLYCEMIA CAD, PRESENCE OF STENT ADULT OBSTRUCTIVE SLEEP APNEA, SEVERE EPIGASTRIC ABDOMINAL PAIN FATTY LIVER ABNL URINARY ORGAN IMAGING THYROID DISORDER HX OF PANCREATITIS
Andere Medikamente: Outpatient Medications Hydrocortisone 2.5 % Top Lotn Apply to affected area(s) 2 times a day Aspirin (ECOTRIN LOW STRENGTH) 81 mg Oral TBEC DR Tab Take 1 tablet by mouth every morning for prevention metFORMIN (GLUCOPHAGE) 1,000 mg Or
Allergien: All tree nuts
Vorherige Impfungen: -

VAERS 1826076

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: -
Alter: 27,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / UN

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

Cough Diarrhoea Feeling cold Pain Paraesthesia

Symptomtext

At time of vaccine patient had tingly arm. Day after, patient could not get warm, had body aches, cough, diarrhea

Weitere VAERSDATA-Felder

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

VAERS 1825271

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: FL
Alter: 41,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Chills Condition aggravated Fatigue Flushing Headache Injection site pain Neck pain Pain

Symptomtext

injection site soreness chills body ache neck pain flushing headache weakness fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: vitamin D zinc
Allergien: pcn
Vorherige Impfungen: fatigue and weakness from seasonal flu shot

VAERS 1809004

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

moderat

Staat: IN
Alter: 21,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Dyspnoea Heart rate increased Paraesthesia oral Rash

Symptomtext

Super high heart rate, tingling lips, shortness of breath, rash. I went to the ER and got epinephrine

Weitere VAERSDATA-Felder

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

VAERS 2677636

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 29.08.2023
Impfdatum: 22.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 40,0
Dosis: 2
Route/Site: SYR / LA

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

Aphonia Endoscopy abnormal Inflammation Polymyalgia rheumatica

Symptomtext

I have developed PMR. Polymyalgia Rheumatica. It took me over a year to realize that was what was actually developing. It took a long time to come on full. I can't exercise and it caused inflammation throughout my body. I even was losing my voice because of it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Polymyalgia rheumatica
Hospital-Tage: -
Labordaten: I have my vocal cords checked, I also had an asthma test at the pulmonologist, I then had an endoscopy which the tissue samples showed the inflammation. Now I'm at a Rheumatologist and had bloodwork and everything else. The problem is that the cure for this is Prednisone. I'm allergic to that drug. Thank you for screwing with peoples health. I was a 100 percent very healthy adult.
Aktuelle Erkrankungen: None
Vorgeschichte: Now I have PMR which started the month after I received the 2nd J&J shot. I'm sick of this crap and the lying of the government and CDC. Pfizer Vaccine killer my father on 3/26/21 just a month after his 2nd pfizer shot.
Andere Medikamente: Nothing at time of vaccination
Allergien: I am allergic to Propylene Glycol, methyldibromo glutaronitrile, cobalt, corticosteroids Group A.
Vorherige Impfungen: -

VAERS 2597756

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: FL
Alter: 91,0
Geschlecht: F
Eingang: 16.03.2023
Impfdatum: 01.11.2021
Beginn: 22.02.2023
Tage bis Beginn: 478,0
Dosis: 2
Route/Site: IM / -

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

Asthenia COVID-19 Diarrhoea Nausea SARS-CoV-2 test positive

Symptomtext

Hospitalization: 2/22/2023 - 2/25/2023 (3 days); Presentation to the ED: nausea and diarrhea, generalized weakness COVID + date: 2/22/2023; Treatment: Remdesivir; Discharge to: HOME. 205A21A 4/11/2021; 1855194 11/1/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, DM2, CVD, peptic ulcer disease, HLD, hypertension, CKD 3
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2603186

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IN
Alter: 49,0
Geschlecht: F
Eingang: 15.03.2023
Impfdatum: 12.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / RA

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

Erythema Pain in extremity Phlebitis Thrombophlebitis

Symptomtext

covid booster given 11/12 then to ER 11/16 for right leg pain, redness and diagnosed with phelebitis and thrombophlebitis right lower extremity

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: neck, back pain, tinnitus
Vorgeschichte: GERD, back, neck pain
Andere Medikamente: Gabapentin, tylenol, ibuprofen, Norgestimate-Eth Estradiol
Allergien: shellfish, avelox, PCN, vancomycin
Vorherige Impfungen: -

VAERS 2577576

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: UT
Alter: 20,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 02.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Arthralgia Asthenia Blood test Depression Fatigue Hepatic enzyme increased Impaired work ability Joint range of motion decreased Magnetic resonance imaging Musculoskeletal stiffness Myalgia Nausea Neuralgia Scan Ultrasound scan X-ray

Symptomtext

About 2 weeks after injection I had joint pain, stiffness, weakness, physical fatigue, abdominal pain, depression, nausea, muscle and nerve pain, raised liver enzymes, limited range of motion in knees, elbows, fingers and wrists. I had to cut my work schedule down to cope. Treatment included medication: gabapentin, opiods, antidepressants, Nsaids, possibly infusion of benlysta, plaquenil. Lots of diagnostics testing that have taken time out of being able to work. No diagnoses have been formally made, but they speculate on PCOS as well as fibromyalgia, RA, lupus, Autoimmune hepatitis, myocitis/dermatomyosis, liver disease, etc.

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Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: Lots of diagnostics testing have been done, and the extensive list of results can be provided in a document upon request. I have done blood work, mris, xray, ultra sounds, fibroscans, and many doctors appointments.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diagnosis of JRA at age of 3, treated and in remission at age 11, no other issues until vaccine.
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2555797

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 07.04.2021
Beginn: 25.11.2022
Tage bis Beginn: 597,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Mental status changes Pyrexia SARS-CoV-2 test positive

Symptomtext

11/25/22 presents to ED for "altered mental status and fever". PMHx of "Alzheimer's dementia, kidney transplant on mycophenolate"

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Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 11/25/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2455989

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: FL
Alter: 99,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 15.11.2021
Beginn: 30.08.2022
Tage bis Beginn: 288,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Cough Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Hospitalization: 8/30/2022- ADMITTED, 9/6/2022- DISCHARGED. Presentation to the ED: congestion and a nonproductive cough and fever. She had a temperature of a 103? F on admission and was saturating at 93% on room air. COVID-19 + date: 8/30/22. Treatment: steroids, Remdesivir and increased O2 supply. Discharge to: SNF, (Skilled Nursing Facility).

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Praegender Schweregrund: Pyrexia
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, hyperlipidemia, hypothyroidism, osteoarthritis, osteoporosis, coronary artery disease.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2450712

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: PA
Alter: 40,0
Geschlecht: M
Eingang: 21.09.2022
Impfdatum: 11.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Arthralgia Foreign travel Gait disturbance General physical health deterioration Impaired work ability Joint swelling Laboratory test Polyarthritis

Symptomtext

PAIN IN RIGHT LEG JOINTS; This spontaneous report received from a consumer concerned a 40 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient was healthy and physically active individual with no notable medical history prior to receiving the vaccine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194 expiry: UNKNOWN) dose was not reported, administered on 11-NOV-2021 for covid-19 prophylaxis. Age at time of vaccination 40 years old. No concomitant medications were reported. On 2021, the patient experienced pain in right leg joints. Treatment medications (dates unspecified) included: naproxen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of pain in right leg joints was not reported. This report was non-serious. This case, involving the same patient is linked to 20220938918.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient was healthy and physically active individual with no notable medical history prior to receiving the vaccine.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2450712

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: PA
Alter: 40,0
Geschlecht: M
Eingang: 21.09.2022
Impfdatum: 11.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: SYR / AR

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

Arthralgia Foreign travel Gait disturbance General physical health deterioration Impaired work ability Joint swelling Laboratory test Polyarthritis

Symptomtext

PAIN IN RIGHT LEG JOINTS; This spontaneous report received from a consumer concerned a 40 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient was healthy and physically active individual with no notable medical history prior to receiving the vaccine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194 expiry: UNKNOWN) dose was not reported, administered on 11-NOV-2021 for covid-19 prophylaxis. Age at time of vaccination 40 years old. No concomitant medications were reported. On 2021, the patient experienced pain in right leg joints. Treatment medications (dates unspecified) included: naproxen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of pain in right leg joints was not reported. This report was non-serious. This case, involving the same patient is linked to 20220938918.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient was healthy and physically active individual with no notable medical history prior to receiving the vaccine.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2452079

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MI
Alter: 50,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 15.11.2021
Beginn: 08.09.2022
Tage bis Beginn: 297,0
Dosis: 2
Route/Site: - / -

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

Abdominal distension Abdominal pain Adult failure to thrive Alcohol rehabilitation Alcoholism Ammonia increased Anaemia Ascites Asthenia Blood thyroid stimulating hormone increased COVID-19 Chest X-ray normal Fall Haptoglobin decreased Hepatic cirrhosis Hepatic function abnormal International normalised ratio increased Nasal congestion

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 9/8/2022 Discharge Date: Sep 15, 2022 PRESENTING PROBLEM: Adult failure to thrive Failure to thrive in adult HOSPITAL COURSE: 51-year-old female with PMH significant for hereditary hemochromatosis/Dr. recurrent urinary tract infection/sepsis, seizures/status epilepticus/Keppra, alcohol abuse/quit 02/2022, cirrhosis/portal hypertension, chronic thrombocytopenia, chronic anemia, iron deficiency as well presents to ER 9/8 due to generalized weakness, abdominal pain multiple falls. Patient was at a alcohol rehab since July and was discharged from there on 09/08 and was asked to come directly to ER and she did. However when she got admitted there, she had to be transferred to acute hospital the second day due to sepsis related to urinary tract infection. She was there in the hospital for 1 month. After discharge back to alcohol rehab, she had to go to ER 2-3 times for swelling, abdominal swelling, paracentesis x2. She has been falling recently. Increased weakness and also has noted increased abdominal distension lower extremity edema. Presented with multiple falls and generalized weakness, likely related deconditioning. Even though family requested that patient be arranged with rehab, she did not qualify. Patient independently ambulating in the hallways. Patient with known cirrhosis, presented with decompensated cirrhosis (ascites, lower extremity edema, elevated ammonia and INR). Etiology is felt to be related to alcohol use, could be also from her history of hemachromatosis. She will need follow-up at GI office, office will arrange. She was noted to have ascites, empirically started on Rocephin for SBP prophylaxis but fluid studies were negative after paracentesis on 09/11. A 2.6 L. ultrasound was negative for thrombosis. Patient was started on Lasix/Aldactone and was instructed about 2 g salt restriction. He will need a screening EGD as outpatient. An EGD was scheduled for 9/12 however this was canceled after patient tested positive for COVID-19. Ammonia was 72 and was started on lactulose. Patient was noted to have fever along with nasal congestion sore throat, tested positive for COVID-19 but chest x-ray without infiltrates and patient is on room air. Patient received 3 days of remdesivir. TSH was noted to be 100 and free T4 low normal at 0.6. Home dosage to 175 mcg was increased to 200 mcg daily. Repeat free T4 ordered for 9/14 normal, as suggested by endocrinology. They recommend to continue current levothyroxine dose of 200 mcg daily and repeat TSH in 6 weeks. Patient's primary care can follow this. Patient noted to have anemia without any obvious bleeding. Occult blood however was positive and was 1 of the reasons why she was going to get EGD, this will have to be pursued as outpatient. No evidence of hemolysis. Haptoglobin was low but that is related to her liver dysfunction. Chronic alcoholism, recently discharged from alcohol rehab, reiterated about need for absolute alcohol cessation. Social work also evaluated patient. PTOT re-evaluation performed on 09/14 for patient's daughter continued to voice concerns of safety. Patient did well with this re-evaluation that they recommended no post hospital skilled care needs. With patient stable she was discharged home on 9/15/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: 11/1/2021- Surgical Procedure CONTROL BILATERAL EPISTAXIS
Vorgeschichte: Hemochromatosis Essential hypertension Acquired hypothyroidism Anxiety and depression Dense breast tissue on mammogram Thrombocytopenia Sleep disturbance Seizure Epilepsy, generalized tonic-clonic, intractable Sepsis Anemia due to other cause, not classified History of acute renal failure PTSD (post-traumatic stress disorder) Ascites due to alcoholic cirrhosis
Andere Medikamente: cyanocobalamin 100 MCG tablet ferrous gluconate (FERGON) 324 (38 Fe) MG tablet Folic Acid-Vit B6-Vit B12 2.5-25-1 MG TABS furosemide (LASIX) 20 MG tablet lactulose (CONSTULOSE) 10 GM/15ML solution levETIRAcetam (KEPPRA) 750 MG tablet levoth
Allergien: AtorvastatinHives EzetimibeHives Ace InhibitorsUnknown Lipitor [Atorvastatin Calcium]Cough Trazodone Vicodin [Hydrocodone-acetaminophen]Unknown Zetia [Ezetimibe]Cough
Vorherige Impfungen: -

VAERS 2429729

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 12.12.2021
Beginn: 31.08.2022
Tage bis Beginn: 262,0
Dosis: 1
Route/Site: UN / UN

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

Headache Visual impairment

Symptomtext

Visual disturbance, and headaches.

Weitere VAERSDATA-Felder

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

VAERS 1594325

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 61,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 19.11.2021
Beginn: 24.12.2021
Tage bis Beginn: 35,0
Dosis: 2
Route/Site: - / -

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

Blood test normal Foot operation Infusion site discolouration Infusion site infection Infusion site swelling Infusion site urticaria Nerve block Procedural vomiting Surgery Swollen tongue SARS-CoV-2 antibody test Therapy partial responder Weight decreased Tongue coated Vasodilatation

Symptomtext

NEUROMA; SWOLLEN TONGUE; WHITE TONGUE; IMMUNE SYSTEM DISORDER; LEFT FOOT LOOKED WHITE/LOSS OF PIGMENTATION; FELT HOT AND COLD; SKIN TINGLING/ LEFT FOOT FELT TINGLING; INFUSION SITE INFECTION; NAUSEA; VOMITING; This spontaneous report received from a patient concerned a 61 year old adult male. The patient's weight was 69.85 kilograms, and height was 72 inches. The patient's past medical history included: foot surgery (both feet), knee surgery, appendectomy, nausea, vomiting, impetigo (had in 3rd grade), rash on the face (the patient stated took a biopsy, it was a rash that felt like taking a piece of thread and dragging it across face. Red scaly, thought patient was having a severe reaction to Covid, the patient was on Triamcinolone, Mupirocin and Cephalexin a month or two before the 1st vaccine) and flu, and concurrent conditions included: heart valve defect, impetigo contagious, boils (impetigo, and boils both contagious and keeps on repeating), Morton neuroma (the patient stated it was inflammation of the main nerves on the pads of the foot, it was a result of the fat loss. The right foot was more prominent, and the patient had that procedure before), severe soy allergy, food allergy (green bean, bean sprouts, coffee gives nausea and vomiting), non-smoker, alcohol use (one drink per week) and immunocompromised, and other pre-existing medical conditions included: no adverse event after any previous vaccination, no vaccine and drug allergies. The patient had mild symptoms before 30 days prior to vaccination (booster dose). The family history included sister that had lupus, she had a kidney transplant, older brother had high blood pressure, the patient's mother had hives and did not had food allergies. The patient had no family history of allergy. The patient had no other suspected causes including co-administered vaccine(s)/risk factors. The patient had no substance abuse or use. The patient was working in banking. On an unspecified date before MAR-2020, the patient stated he saw cardiologist right before covid. The cardiologist saw a hiccup, that showed up in EKG (Electrocardiography). The patient had to wore heart monitor for 2 days. The echo (echocardiogram) showed cyst on the thyroid. The patient went to thyroid expert. The patient saw another cardiologist, had a stress test, nuclear test and sonogram, EKG, pressure of veins both arms and feet. Outcome of heart was 21 years younger than the chronological age. Patient had never tested positive for COVID. The patient had past history of similar event (patient had never taken the flu shot, when he did get the flu, he was under dressed, exposed). The patient had previously received ascorbic acid/ergocalciferol/folic acid/nicotinamide/panthenol/retinol/riboflavin/thiamine hydrochloride, zinc, and magnesium hydroxide. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin, and batch number: 1805022, expiry: unknown) dose was not reported, 1 total, administered at left deltoid on 08-MAR-2021 for covid-19 prophylaxis. Patient stated that he was calling due to the fact that he was sick previous to the vaccine but the vaccine seemed to help him get better. He stated that he tolerated the vaccine well and that since then he was about six months in. Patient stated that he was not recovering but rather his condition was worsening. He had seen 4 doctors recently and 3 whom he saw a year ago. He was terrific prior to the vaccine. The vaccine was great but then he was not so great and seem to be going back to the past where he was pre vaccination. He stated that his antibody level had never been above 28. The patient reported a low antibody level of 36-38 (consumer's partner had an antibody count of 140, and his friends had counted over 400), antibody test and result was 22 units unspecified. The patient was tested on 24-JUL-2021, received results on 07-AUG-2021. On 24-JUL-2021, the patient was tested with antibody test- IgG which showed low antibody level 36- 38 (partial responder to therapy). The patient also experienced weight loss from 165 lbs to 142 lbs (after receiving Janssen vaccine primary vaccination lost all his body fat, I lost 10 to 14 pounds, no body knew why). The patient stated that the vaccine increased his metabolism. Adipose filler (referring to injection procedure of fat) was added to both feet injectable for fat loss. Leneva that was for the feet somebody else's fat that was been sterilized and injected into patient. He ate ice-cream daily at bedtime for weight gain. On Aug-2021, the patient experienced right foot neuroma (his right food began hurting (date asked but unknown), he used to be a runner but with the pain in his right foot, it was painful to walk, they had to inject adipose filler to his right foot which felt great but 3 to 4 months later, all the fat dissolved, then they cut the bones shorter, cut the nerves and put in a screw to offset the pressure on the bones (dose number in series 1). The clinical diagnosis of the right foot condition was neuroma, the patient stated that condition of his right foot was improving however the screw does not allow toes to bend at one point but pain was lessened and still undergoing physiotherapy to reduce swelling when not walking). The patient had blood test on 27-AUG-2021 and the date on the report was 28-AUG-2021, with results ABS TD19 plus lymph (result 382 reference range: 12-645), ABS CD3 (result 1230 reference range 622-2402), ABS (absolute) CD4 plus helper (result 826 reference range 254-1519), percent CD19 plus lymphs (result 19.1 percent reference range 3.3 to 25.4 percent), percent CD3 plus lymphs (result 61.5 percent reference range 57.5 to 87.2 percent), percent CD4 plus lymphs (result 41.3 percent reference range 30.8 to 58.5 percent), CD4 / CD8 ratio (result 2.05 reference range 0.92 to 3.72), hemoglobulin (result 16.5 reference range 13.0 to 17.7), platelets (result 31 reference range 150 to 450)(dose number in series 1). Laboratory data (dates unspecified) included: SARS-CoV-2 test (NR: not provided) negative. The patient stated that skin became drier, putting on a lot of face cream. The patient stated that been to dermatologist as well. The dermatologist prescribed Triamcinolone Acetonide. The patient stated that he did not have to scratch. But felt his skin crawling and splotchy, it appears on knee, chest, front and back but never on the face, it was red and tingling. The patient stated that he would touch that and which would turn red. Last year after initial injection in AUG-2021, calluses was starting on the left foot (dose number in series 1). It was reported that the fat pad on patient feet was dissolved and got injections of adipose fat 1.5 vials. The patient went to many doctors, a cardiologist, cause they were looking for heart inflammation. The doctors told patient that everything was good, and no heart inflammation was found. The outcome of the increased metabolism, skin became drier, Skin tingling, low antibody count, calluses on left foot, low platelet counts, skin crawling and splotchy and weight loss was not reported and was recovering from neuroma. The patient received booster covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin, and batch number: 1855194, expiry: unknown) dose was not reported, 1 total, administered on 19-NOV-2021 for covid-19 prophylaxis. Concomitant medications included ascorbic acid/chondroitin sulfate/curcuma longa root/glucosamine sulfate/manganese gluconate, Vitamin supplements C, Zinc, Fe, D, B, E and fish oil, charcoal on occasion. On an unspecified date patient was confirmed with clinical condition called neuroma and on 24-DEC-2021 patient had surgery, vomiting afterwards and second foot surgery nerve block. As a result, patient's tongue was often swollen, and that turned white (dose number in series 2). The patient stated that he thought it was allergy. The patient's doctor thought it was allergic reaction to anesthesia. The patient stated IV (intra venous) in his left arm, 3 days later (27-DEC-2021), the patient stated where they connected the IV the marking was raised like a welt and the surgeon, anesthesiologist, his primary care provided thought it looked worse, like an infection (infusion site infection). The surgeon said looked like they had trouble finding the vein. It was raised and purple. The Primary care provider said infection, they recommended hydrocortisone. It was not itching, 10 days gone then, the vein looked like double in width it looks normal at the time of reporting, not black and blue. Antibiotic, Cephalexin was given to patient for surgery, doctor extended the prescription. Patient stated that after taking Duexis, pain pill, started throwing-up (after foot surgeries both times). On the week of 10-MAY-2022, patient Left foot felt tingling also felt hot and cold (dose number in series 2). On 19-MAY-2022, the left foot looked white so the patient thought it is something related to blood flow so on same day patient went to cardiologist who did blood pressure test on extremities and ankles, it was ok, the doctor thought it was food allergies. Patient told the doctor that he did not eat any new food that could trigger any allergies so the doctor ordered blood work and it came back normal, when asked about the date of blood work, patient answered last week. Patient exposed feet to the sun and it tanned but 2 days later the tan went away and the foot looked white again (dose number in series 2). The doctor ruled out vitiligo and diagnosed the condition as immune system related but the patient thinks that the immune system issue is related to receiving the Janssen COVID-19 vaccine that is his own perception but the doctor did not say it is related to receiving the Janssen COVID-19 vaccine. The loss of pigmentation started between the first and second left toes then to the dorsal side of the left big toes then spread to between toes 2,3 and 4 and now the top side of the left foot is turning white which the patient described as strange. The right foot is not affected by pigmentation issues but had an extensive surgery in AUG-2021, and it is undergoing physiotherapy (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from infusion site infection, and the outcome of surgery, swollen tongue, white tongue, skin tingling/ left foot felt tingling, nausea, vomiting, felt hot and cold, left foot looked white/loss of pigmentation and immune system disorder was not reported. This report was serious (Other Medically Important Condition). This case, involving the same patient is linked to 20210829077. This case, from the same reporter is linked to 20220137233, 20220136407 and 20220617665. Additional information was received from patient on 31-AUG-2022. The following information was updated and incorporated into the case narrative: patient concomitant condition (immunocompromised), past drugs (multivitamins, zinc, magnesium) added, patient weight updated from 71.66 to 69.85 kilograms. Upon review the following information was updated: vaccine indication updated to covid-19 prophylaxis, batch number statement removed.; Sender's Comments: V4- This version updates- patient concomitant condition (immunocompromised), past drugs (multivitamins, zinc, magnesium) added, patient weight updated from 71.66 to 69.85 kilograms. Upon review the following information was updated: vaccine indication updated to covid-19 prophylaxis, batch number statement removed. This follow up information received does not alter the assessment of prior company causality of previously reported events. 20220114730-COVID-19 VACCINE AD26.COV2.S-Neuroma Follow-up received regarding Clinical Details. The event(s) has an unknown/unclear 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.(Concurrent condition of neuroma)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Infusion site urticaria
Hospital-Tage: -
Labordaten: Test Date: 20210724; Test Name: SARS-COV-2 IGG ANTIBODY TEST; Result Unstructured Data: 36-38; Test Date: 20210827; Test Name: CD4/CD8 RATIO; Result Unstructured Data: 2.05; Test Date: 20210827; Test Name: PLATELET COUNT; Result Unstructured Data: 31; Test Date: 20210827; Test Name: HEMOGLOBIN; Result Unstructured Data: 16.5; Test Date: 20210827; Test Name: BLOOD TEST; Result Unstructured Data: Not reported; Test Date: 20220519; Test Name: BLOOD PRESSURE TEST; Result Unstructured Data: on extremities and ankles and it was ok.; Test Date: 202206; Test Name: BLOOD WORK; Result Unstructured Data: normal; Test Name: NUCLEAR TEST; Result Unstructured Data: Not reported; Test Name: SONOGRAM; Result Unstructured Data: Not reported; Test Name: STRESS TEST; Result Unstructured Data: Not reported; Test Name: ECHO; Result Unstructured Data: cyst on the thyroid; Test Name: EKG; Result Unstructured Data: Hiccup; Test Name: COVID-19 TEST; Result Unstructured Data: Negative; Test Name: ANTIBODY TEST; Result Unstructured Data: 22
Aktuelle Erkrankungen: Boil; Fat atrophy; Food allergy (green bean, bean sprouts, coffee makes nauseuos, and vomiting); Heart valve disorders; Immunocompromised; Impetigo contagious; Morton's neuroma; Non-smoker; Social alcohol drinker; Soy allergy
Vorgeschichte: Medical History/Concurrent Conditions: Appendectomy (In 1999); Flu; Foot surgery (2001 and 2007); Impetigo; Knee operation (Knee surgery in year 2001, and 2007, orthoscopic surgery as hit by car); Nausea; Rash on face (on Triamcinolone, Mupirocin and Cephalexin a month or two before the 1st vaccine); Vomiting; Comments: no adverse event after any previous vaccination, no vaccine and drug allergies. The patient had mild symptoms before 30 days prior to vaccination (booster dose). The family history included sister that had Lupus, she had a kidney transplant, Older brother had high blood pressure, the patient's mother had hives and did not had food allergies. The patient had no family history of allergy. The patient had no other Suspected causes including co-administered vaccine(s)/risk factors. Patient had never tested positive for COVID. The patient had no substance abuse or use. The patient had past history of similar event (patient had never taken the flu shot, when he did get the flu, he was under dressed, exposed).
Andere Medikamente: OSTEOFLEX [ASCORBIC ACID;CHONDROITIN SULFATE;CURCUMA LONGA ROOT;GLUCOSAMINE SULFATE;MANGANESE GLUCON
Allergien: -
Vorherige Impfungen: -

VAERS 2425241

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: -
Alter: 41,0
Geschlecht: M
Eingang: 31.08.2022
Impfdatum: 07.11.2021
Beginn: 23.08.2022
Tage bis Beginn: 289,0
Dosis: 1
Route/Site: UN / UN

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

Nausea Oropharyngeal pain Vomiting

Symptomtext

sore throat, nausea, vomiting

Weitere VAERSDATA-Felder

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

VAERS 2407463

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: VA
Alter: 32,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / AR

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

Chills Pain Pyrexia Vomiting

Symptomtext

104 fever, throwing up, body aches, chills

Weitere VAERSDATA-Felder

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

VAERS 2399973

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: AL
Alter: 65,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

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

Back pain Biopsy skin abnormal Erythema Induration Malignant melanoma Nerve injury Peripheral swelling Scar Skin cancer Surgery

Symptomtext

Hard bump the size of an eraser came up right below my right shoulder. Red spots were partly around the bump. Biopsy revealed melanoma and red spots were pre-melanoma. Since diagnosed, I have had three surgeries in the same spot. Oct 2021 1st surgery, received COVID booster in Nov. 2021, melanoma came back in March 2022. May 10 surgery. June 14 surgery margins clear. I am receiving Immunotherapy every 3 weeks for one yr. Prior to Oct. 2021, I have never had a melanoma. My dermatologist thought the spot was a bug bite but being cautious, she biopsied it. When the pathology report came back "melanoma", my dermatologist said in all her 50 years of practice, she has never seen a melanoma look like mine. Highly unusual. I was referred to a melanoma specialist/surgeon. According to my pathology report, Dr said my melanoma was very unusual an very aggressive! This cancer came up on my back only about 3-4 weeks after my first covid shot. I had surgery in Oct. 2021 and margins were clear. I had a covid booster shot in Nov. of 2021 and Dec. dermatologist check up was good. When I went back in March, 2022, for my 3 mo. check up, the cancer was back "in the scar" of where my surgery was on my back. My health was perfect before I took the covid vaccination. I will never take another one. I now suffer from back pain caused by nerve damage from my first surgery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Oct 2021 biopsy March 2022 biopsy
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lipitor - Alprazolam - calcium - B-12 (Estradiel - Noreth)
Allergien: Contrast dye
Vorherige Impfungen: Swine and flu shot given at same time. 2013? experienced anaphylaxis

VAERS 2396180

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MI
Alter: 36,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 05.11.2021
Beginn: 29.07.2022
Tage bis Beginn: 266,0
Dosis: 1
Route/Site: - / -

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

Oropharyngeal pain

Symptomtext

sore throat

Weitere VAERSDATA-Felder

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

VAERS 2393149

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 49,0
Geschlecht: M
Eingang: 27.07.2022
Impfdatum: 16.03.2022
Beginn: 18.03.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Angiogram Blood test Cardiac monitoring Cardiac stress test Computerised tomogram head Computerised tomogram neck Echocardiogram Electrocardiogram Headache Hyperacusis Laboratory test Magnetic resonance imaging Pain Tinnitus Ultrasound Doppler

Symptomtext

2 Days after vaccine administration, I developed severe tinnitus and ringing in bilateral ears, sound sensitivity and pain. I have suffered from severe headaches. Completed 2 courses of an oral steroids with no improvement.( 1 in April and 1 in June I have seen multiple ENTs, Neurologists, dentists, physical therapists and have had many diagnostic tests with no symptom improvement or other causative diagnosis. Symptoms persist with no change since onset on 3/18/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: I have had MRI's, MRA's, Cat scans of head and neck ,Carotid dopplers, stress tests, echocardiogram, EKG, Serum blood work and extended cardiac monitoring at home all in the month of May with repeated blood work in June
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2374887

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: OH
Alter: 61,0
Geschlecht: M
Eingang: 20.07.2022
Impfdatum: 22.03.2022
Beginn: 22.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypotonia Injection site pain Pain in extremity

Symptomtext

"My arm has hurt at the injection site since the minute they gave it to me and has never stopped hurting. I think they gave it to me in the tendon that goes into the muscle". "My left arm has pain and muscle loss". "The needle injection site hurts". "My whole left arm hurts from the injection site down".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: Patient states he went to clinic to his nurse practitioner who told him in patient's words "it stays in my body for 5 years". Patient denied provider doing any tests or follow-up.
Aktuelle Erkrankungen: Denied
Vorgeschichte: Denied
Andere Medikamente: Meloxicam
Allergien: No known allergies
Vorherige Impfungen: reports 15 years ago adverse event from tetanus shot (arm swelling and fever)

VAERS 2362790

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: AZ
Alter: 31,0
Geschlecht: F
Eingang: 08.07.2022
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain lower Abdominal pain upper Appendicectomy Appendicitis Chills Computerised tomogram abdomen abnormal Pain Ultrasound abdomen abnormal

Symptomtext

A few hours after receiving the vaccine, I experienced chills and body aches, and a stomach ache. The chills and body aches went away after taking ibuprofen. However, the stomach ache continued and gradually moved into the lower right quadrant. This pain was severe and continued the next day and night. The next morning I went to the emergency room and they diagnosed me with appendicitis and removed my appendix.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain lower
Hospital-Tage: 1,0
Labordaten: ultrasound and CT scan 11/12/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2319920

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: PA
Alter: -
Geschlecht: M
Eingang: 15.06.2022
Impfdatum: 16.04.2022
Beginn: 01.05.2022
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: - / -

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

Body temperature COVID-19 Cellulitis Injection site mass Injection site pain Lymph node pain Lymphadenopathy

Symptomtext

CELLULITIS; LUMP AT INJECTION SITE; BURNING HAS SPREAD TO LYMPH NODES; SWELLING TO LYMPH NODES; BURNING AT INJECTION SITE; COVID-19; This spontaneous report received from a patient concerned a male of an unspecified age, race and ethnicity. Initial information was processed along with additional information received on 06-JUN-2022. 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 admin not reported, batch number: 1855194 expiry: UNKNOWN) dose was not reported, 1 in total administered to the back of the left arm on 16-APR-2022 for prophylactic vaccination. No concomitant medications were reported. On MAY-2022, 3 weeks after vaccination the patient experienced covid-19 and had symptoms of fever of 102.4 F and headache. On 04-JUN-2022, the patient woke up with reaction to injection site. The patient experienced lump in injection site with burning, and the burning was spreading to lymph nodes under and there was swelling (swelling to lymph nodes). On an unspecified date, the patient went to urgent care and patient was diagnosed with cellulitis. Treatment medications (dates unspecified) included: cefalexin, 500 mg four times a day for 7 days. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from lump at injection site, burning at injection site, burning has spread to lymph nodes, and swelling to lymph nodes, and the outcome of covid-19 and cellulitis was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20220609638-COVID-19 VACCINE AD26.COV2.S-CELLULITIS. The event(s) has an unknown/unclear 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site mass
Hospital-Tage: -
Labordaten: Test Date: 202205; Test Name: BODY TEMPERATURE; Result Unstructured Data: 102.4 Fahrenheit
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2313012

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: OH
Alter: 85,0
Geschlecht: F
Eingang: 08.06.2022
Impfdatum: 21.12.2021
Beginn: 14.05.2022
Tage bis Beginn: 144,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Diarrhoea Headache Malaise Nausea Oropharyngeal pain SARS-CoV-2 test positive Viral sepsis Vomiting

Symptomtext

Patient presented with HA, malaise, N/V/D and tested positive for covid. She was dx with viral sepsis due to covid. The patient was given vanc/zosyn, decadron for sore throat, robutussin-DM, tylenol, zofran prn.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HLD, osteoporosis, HTN, CAD, CKD
Andere Medikamente: vitamin C, asa 81mg, lasix, lisinopril, lovastatin, multivit, vit d3,
Allergien: donepezil, levaquin, bactrim
Vorherige Impfungen: -

VAERS 2290488

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NH
Alter: 52,0
Geschlecht: M
Eingang: 23.05.2022
Impfdatum: 20.11.2021
Beginn: 19.05.2022
Tage bis Beginn: 180,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Chest X-ray Chills Cough Fatigue Headache Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I started getting symptoms of fever, chills, body aches, severe headache, and fatigue. I received a positive COVID-19 home test. Then I went and got a PCR test at a pharmacy which was positive as well. Then my symptoms progress to a cough. I went to the urgent care today to see if I had possible pneumonia. I had a chest x-ray done which has to be read by a radiologist. I did get some prescriptions for a cough suppressant and an inhaler. I still have a bad cough and congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 test positive. X-ray pending.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin
Allergien: NSAIDS
Vorherige Impfungen: -

VAERS 2267490

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NE
Alter: 69,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 04.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Arthritis Arthropathy Autoimmune disorder Blood test Fatigue Joint range of motion decreased Rash Skin haemorrhage Skin lesion Wound

Symptomtext

It started my Acute Arthritis skin legions open and bleeding. It is a on going symptoms and I have had this since the 1980's and the doctors have tried several different medications. The doctors said that they are running out of things to try. I have to have all of these bandages on my skin. It is very frustrating because I am having a lot of fatigue, joint discomfort, lost of range of motions, a lot of out breaks on my skin. This is autoimmune disorder of arthritis. Every since the second vaccine, I had notice that's when al of these symptoms have started all over again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Blood Panel Lab in December and March
Aktuelle Erkrankungen: No
Vorgeschichte: Arthritis and Heart Disease
Andere Medikamente: Atenolol 25mg Lisinopril 5mg Farxiag one tablet ADVAIR 250/50 Fluticasone Repatha 140mg every two weeks Aspirin 81mg Cranberry 900mg Vitamin 800UI Fish Oil 1200 Vitamin B 100mg Bio-Shield x2 Vitamin C 1000mg Stelara 45mg injection every two
Allergien: Penicillin Sulfate Fluoroquinolone Methotrexate Ixekizumab
Vorherige Impfungen: -

VAERS 2266507

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IL
Alter: 53,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 26.10.2021
Beginn: 01.02.2022
Tage bis Beginn: 98,0
Dosis: 2
Route/Site: IM / -

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

Blood creatine phosphokinase Blood thyroid stimulating hormone Epstein-Barr virus test Fatigue Full blood count General physical health deterioration Impaired work ability Laboratory test Metabolic function test Vitamin D

Symptomtext

My health has been steadily declining since I had the second vaccine. I am experiencing extreme fatigue and tiredness and am unable to do my daily work. I have been to my PCP, Oncologist, Endocrinologist and Allergist they cannot find a reason for why I am feeling this way. I am waiting to hear from my PCP for the referral for a Neurologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Epstein Barr panel all 3 test CPK Vitamin D levels Hormone level Complete Metabolic Panel CBC TSH
Aktuelle Erkrankungen: No
Vorgeschichte: Cancer Thyroid
Andere Medikamente: Tamoxifen Synthroid Gabapentin Spironolactone Calcium
Allergien: Seafood IV Contrast Media
Vorherige Impfungen: -

VAERS 2258345

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: FL
Alter: 45,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 27.10.2021
Beginn: 22.04.2022
Tage bis Beginn: 177,0
Dosis: 2
Route/Site: SYR / LA

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

Ageusia Anosmia COVID-19 Chills Constipation Diarrhoea Fatigue Gastrointestinal disorder Headache Hyperhidrosis Productive cough SARS-CoV-2 test positive Sinus congestion Sinus disorder Sputum discoloured Upper-airway cough syndrome Vomiting

Symptomtext

GI symptoms loss of taste and smell sinus congestion headache extreme fatigue post nasal drip leading to cough yellow and green flehm sinus chills and sweats diarrhea vomiting constipation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Covid 19 test-positive
Aktuelle Erkrankungen: No.
Vorgeschichte: No.
Andere Medikamente: No.
Allergien: No.
Vorherige Impfungen: -

VAERS 2251478

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: GA
Alter: -
Geschlecht: F
Eingang: 26.04.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Injection site pain

Symptomtext

SORE ARM, HURTING FOR A COUPLE OF DAYS AFTER RECEIVING INITIAL DOSE; This spontaneous report received from a patient concerned a female of unspecified age. 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 admin not reported, batch number: 1855194, and expiry: UNKNOWN) dose was not reported, administered on 07-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced sore arm, hurting for a couple of days after receiving initial dose. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sore arm, hurting for a couple of days after receiving initial dose. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2194313

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

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.

Weitere VAERSDATA-Felder

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 2174212

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MA
Alter: 41,0
Geschlecht: M
Eingang: 11.03.2022
Impfdatum: 21.01.2022
Beginn: 11.02.2022
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia

Symptomtext

Left hip pain consistent with arthritis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Gout, high blood pressure
Andere Medikamente: Allopurinol, ivermectin, multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2168300

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 29,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 17.02.2022
Beginn: 01.03.2022
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: IM / LA

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

Chills Hyperpyrexia Menstruation irregular Pain Stomatitis Vaginal haemorrhage Vulvovaginal mycotic infection

Symptomtext

High fever, chills, body aches x 72 hours. Treatment: Tylenol Vaginal yeast infection x 96 hours. Treatment: Fluconazole Mouth sores x 36 hours. Treatment: none Unusual vaginal bleeding, disruption to normal menstrual cycle x 14 days and counting. Treatment: none

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None.
Vorgeschichte: Endometriosis
Andere Medikamente: Vyvanse 50 mg Multi-vitamin Vitamin D 2000 IU
Allergien: Amoxicillin-rash Wasp sting-anaphylaxis
Vorherige Impfungen: -

VAERS 2155111

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Injection site pain

Symptomtext

Right arm has been painful and tender at the injection site ever since I got the shot on 12/2/21. I reported it to my doctor on 12/23/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Depression High cholesterol
Andere Medikamente: Effexor Atorvastatin
Allergien: NKA
Vorherige Impfungen: -

VAERS 2128321

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 19.02.2022
Impfdatum: 01.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Acquired immunodeficiency syndrome Chills HIV infection Hypoaesthesia Laboratory test Malaise Pyrexia Viral load White blood cell count decreased

Symptomtext

I became very sick. fever, chills, fingers numb, went to the ER and they told me I have HIV and am in the AIDS category. I am a heterosexual male, and have never done drugs or used a needle. I haven't had sex in 3 years and have only had sex with women. It makes no sense that I acquired HIV, I was fine until after I received the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: 14,0
Labordaten: CD4- 26, Viral load- 982,000, WBC-1.7
Aktuelle Erkrankungen: none
Vorgeschichte: Hypertension
Andere Medikamente: amlodipine 5mg
Allergien: amoxicillin, clyndamycin, lactose intolerant
Vorherige Impfungen: -

VAERS 2121096

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 19,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain upper Anxiety Constipation Dizziness Feeling cold Flatulence Headache Hyperhidrosis Nausea Nervousness Pallor Somnolence Tinnitus

Symptomtext

Client received her Janssen COVID booster vaccine (lot # 1855194, exp. 4.9.22) on 11.09.21 at 1645. At 1648, client reported that she was feeling dizzy, a little sleepy, had a ringing in the ear with her skin pale and diaphoretic, and was transferred to the anti-gravity chair in semi-fowler position at the vaccination room by vaccinator RN & PHN with A & O x 4. Second PHN came to assist with client. Client denied SOB or any signs and symptoms of anaphylaxis. Client told she didn?t eat since 0800 and had only a snack. At 1650, RN took client?s vitals: BP 86/56, P 50, O2 Sat. 99 %. At 1700, RN took client?s vitals: BP 105/69, P 87, O2 Sat. 99 %, R 15. Client denied any reactions to her first Janssen COVID dose except feeling a little sleepy with after received the vaccine. At 1700, she told she has headache, feeling a little sleepy, has no ringing in the ear, has no dizziness, has no SOB, has no redness, has no swelling on any parts of her body. Client drank water and juice provided without any issues. At 1705, client was transferred to a wheelchair to EMT station due to still feeling a little dizzy again. PHNs and RN continue to assist with client at the EMT station. At 1717, EMT took client?s vitals: BP 116/86, P 88, O2 Sat. 98 %. At 1717, client reported she has a lower stomach cramping with a pain level of a 7 due to client was not able to have a bowel movement. At 1720, client reported nauseous with A & O x 4 and that she has a history of constipation. At 1725, EMT took client?s vitals: BP 98/64, P 84, O2 Sat. 99 %, and client stated ?feeling nervous and anxious? with still having dizziness and lower stomach cramping and feeling cold. RN elevated her feet and client stated she had gas. At 1731, client reported all her symptoms are improving. At 1733, she sat up in the anti-gravity chair and EMT took her vitals: BP 98/76, P 83, O2 Sat. 99 %, T 97.4 F and denied any symptoms. PHN educated client on S/S of anaphylaxis and when to call EMS. Client verbalized understanding. At 1735, client got up from the anti-gravity chair unassisted and left the HCF vaccination site with her parents driving her home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115606

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: TN
Alter: 79,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: -
Beginn: 29.10.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Chills Headache

Symptomtext

CHILLS; LITTLE BIT OF HEADACHE; This spontaneous report received from a patient concerned a 79 year old female. The patient's height, and weight were not reported. The patient's past medical history included: explosive gallbladder, and atrial fibrillation. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number and expiry: unknown) dose was not reported, 1 total, administered on an unspecified date for prophylactic vaccination. On an unspecified date, following primary vaccination with covid-19 vaccine ad26.cov2.s, she experienced chills and a little bit of headache (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194, and expiry: unknown) dose was not reported, 1 total, administered on 29-OCT-2021 on right arm for prophylactic vaccination. No concomitant medications were reported. On 29-OCT-2021, after receiving the vaccine, the patient experienced chills, and little bit of headache. She put on a heating pad and went to bed and the next day she felt fine. She did not have any ache or soreness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from chills, and little bit of headache on 30-OCT-2021. This report was non-serious. This case, involving the same patient is linked to 20220217857 (dose number in series 1 case).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atrial fibrillation; Gallbladder perforation
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2084753

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: -
Beginn: 26.01.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Blood test Injection site swelling Lupus-like syndrome

Symptomtext

INJECTION SITE SWELLING; DRUG INDUCED LUPUS; This spontaneous report received from a patient concerned a 58 year old female The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported and batch number: Unknown and expiry: Unknown) dose was not reported, (dose number in series 1) 01 total, administered on 04-AUG-2021 for prophylactic vaccination. The patient developed lumps/tumors (diagnosed as marginal B-cell lymphoma) she had injection site pain which she was not sure whether due to the original or the booster and had injection site lump (dose number in series 1). The patient had not recovered from injection site pain, injection site lump and marginal B-cell lymphoma (dose number in series 1). The patient additionally received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194 and expiry: Unknown) dose was not reported, (dose number in series 2) 01 total administered in left deltoid on 19-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. The patient reported that she during that first dose that she received the booster and was not sure if it worsened her symptoms. On an unspecified date patient had injection site swelling which was rated as a 1/10 but it was noticeable and was still there. The patient did the blood work on 26-JAN-2022 with the diagnosis of drug induced lupus. She stated she spoke to health care professional (HCP) and she was stunned with the report, she stated she was going for additional testing in several days (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from injection site swelling, and the outcome of drug induced lupus was not reported (dose number in series 2). This report was serious (Other Medically Important Condition). This case, involving the same patient is linked to 20220145846.; Sender's Comments: 20220146890-COVID-19 VACCINE AD26.COV2.S-Drug induced lupus. 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: Injection site swelling
Hospital-Tage: -
Labordaten: Test Date: 20220126; Test Name: Blood test; Result Unstructured Data: drug induced lupus
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2079222

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain upper Adverse reaction Blood test Culture stool Diarrhoea Fatigue Nausea

Symptomtext

I Started Having Diarrhea Really Bad That Night And I Had Severe Stomach Pain & Nausea & So It Continued For About A Month & I Was Just Exhausted So My Husband Took Me To An Urgent Care & I Was Given Several Test & Diagnosed With Adverse Reaction To Vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: BLOODWORK, STOOL WORK.
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: Atorvastatin, Synthroid, Liothyronine, Calcitriol
Allergien: NONE
Vorherige Impfungen: -

VAERS 2074838

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NJ
Alter: 53,0
Geschlecht: F
Eingang: 30.01.2022
Impfdatum: 19.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: SYR / LA

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

Lymph node pain Lymphadenopathy Pain in extremity

Symptomtext

Pain in arm after injection up to 3 days. Enlarged left and right lymph nodes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Anemia
Andere Medikamente: None
Allergien: Rubber tires
Vorherige Impfungen: -

VAERS 2073112

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: ME
Alter: 22,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 17.11.2021
Beginn: 09.01.2022
Tage bis Beginn: 53,0
Dosis: UNK
Route/Site: SYR / LA

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

Contusion Injection site reaction Rash Rash vesicular

Symptomtext

Blister like rash starting at injection site and spreading down my arm. Rash has also started bruising.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: pseudotumor
Andere Medikamente: Zonegram (150mg), methylphenidate (54mg), sprintec (0.25mg), concerta (10mg)
Allergien: ibuprofen, grapes
Vorherige Impfungen: -

VAERS 2062716

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MI
Alter: 25,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 22.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Chest X-ray abnormal Cough Lung opacity Malaise Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

Patient is fully vaccinate. Presented to the ED with cough and sore throat. Patient is a 25-year-old female presenting here with covid symptoms. She started having them 6 days ago and did test positive for Covid. She's having body aches, chills, congestion, cough that is occasionally productive. BP 131/70 | Pulse 88 | Temp 98.6 ?F (37 ?C) (Oral) | Resp 20 | Ht 160 cm (5' 3") | Wt 79.4 kg (175 lb) | SpO2 98% | BMI 31.00 kg/m? CXR: Subtle bibasilar pulmonary opacities. These findings can be seen with atypical pneumonia such as Covid pneumonia. She has a history of asthma recommended a short course of steroids. Was given referral to Dr. for monoclonal antibody infusion. Discharged from ED. Proceed to the emergency department immediately with any new or worsening symptoms.

Weitere VAERSDATA-Felder

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

VAERS 2059524

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 60,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 06.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Fatigue

Symptomtext

This was the J&J booster. The first 24-30 hours post booster where just some fatigue, However my metatarsals, knees, hips, shoulders, hands to include the wrists and metacarpals and elbows and all muscle groups associated with these joints became very painful. I went to a local urgent care on 13Jan22, they said the symptoms I was experiencing would likely hang around 10-14 days. They had me d/c the ibprophen and use tylenol . I'm still having issues all day long. please advise!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: no labs
Aktuelle Erkrankungen: osteoarthritis
Vorgeschichte: osteoarthritis
Andere Medikamente: IBPROPHEN 800MG tid, cyclobenzophrine 10mg, x2 @ bedtime
Allergien: NKA
Vorherige Impfungen: -

VAERS 2059365

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: FL
Alter: 62,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 01.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Injection site pain

Symptomtext

long term weakness and pain at injection site ( tricep ) beginning week after shot and still present 80 days later

Weitere VAERSDATA-Felder

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

VAERS 2048789

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 26,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Feeling hot Visual impairment

Symptomtext

Patient, was given his first dose of the Janssen J&J vaccine my the staff pharmacist. He was then asked to wait for about 15 minutes just to make sure he was ok, and that he will be given his vaccine card. He then left the vaccine room and sat in the waiting area in front of the pharmacy. He then started to dose of on his chair, almost as if he was going to fall over. Pharmacist, then told me about it and I went out and spoke to patient. I held his shoulder and asked him if he was ok. He nodded, saying that he felt light headed. I then told Pharmacist to call 911. I kept talking to Patient, and asked him if he wanted some water - he said yes, I then gave him some water to drink. he darnk the water and said that he felt much better. The paramedics came, asked him if he wanted to go to the hospital, he refused their service saying that he was alright. I later gave him his vaccine and asked if he was feeling better and will be ok going home. He said he was feeling much better. I called Patient today (next day after the event) to check on him. He thanked me for the call and said that he was feeling much better. He explained to me that he had just felt hot right after receiving the vaccine, felt his vision narrowing and was light- headed. I told him that I was glad he was feeling much better and that I would report the incident to VAERS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None disclosed
Vorgeschichte: None Disclosed
Andere Medikamente: None disclosed
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2043239

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 19.03.2021
Beginn: 15.01.2022
Tage bis Beginn: 302,0
Dosis: 2
Route/Site: - / -

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

Asthenia COVID-19 Dizziness Fatigue SARS-CoV-2 test positive

Symptomtext

Found to be COVID positive on admission. Pt has a past medical history of ESRD and is on dialysis. He arrived to the ED with generalized weakness, dizziness, and increasing fatigue.

Weitere VAERSDATA-Felder

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

VAERS 2041975

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: AZ
Alter: -
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Burning sensation Cough Headache Muscle spasms Myalgia Pain Rhinorrhoea Skin laceration

Symptomtext

RUNNY NOSE; COUGH; CUTS ON NECK AND DIFFERENT PARTS OF THE BODY STARTED AFTER THE SHOT AND DID NOT GO AWAY; CUTS HAVE BURNING SENSATION; LITTLE SPASMS; CUTS HAVE PAIN; MUSCLE PAINS; HEADACHES; This spontaneous report received from a patient concerned a 64 year old male. 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 admin not reported, batch number: 1855194, expiry: UNKNOWN) dose was not reported, administered on 30-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced runny nose, cough, cuts on neck and different parts of the body started after the shot and did not go away, cuts have burning sensation, little spasms, cuts have pain, muscle pains, and headaches. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from cough, had not recovered from cuts on neck and different parts of the body started after the shot and did not go away, and the outcome of muscle pains, runny nose, headaches, cuts have burning sensation, little spasms and cuts have pain was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

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

VAERS 2040460

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: OR
Alter: 64,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Cough Interchange of vaccine products Pharyngeal swelling Pruritus Throat tightness Wheezing

Symptomtext

Patient received for her first 2 covid 19 vaccines the Pfizer vaccine. But she had systemic reactions to both of those doses. So an allergist recommended that she get the J&J vaccine for her booster dose. 5 minutes after recieving the dose she had generalized itching. PO Benadryl given; then about 10 minutes after that the symptoms worsened to wheezing, coughing, throat tightness and swelling. Epi IM given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Pfizer vaccine 3/30/21 and 4/20/21

VAERS 2030929

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 66,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

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

Product administration error Vaccination site pain

Symptomtext

This spontaneous report received from a patient concerned a 66 year old White not Hispanic or Latino female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient had no known drug allergy. The patient previously received with covid-19 vaccine ad26. cov2. s (Dose number in series 1, unspecified manufacturer) (suspension for injection, route of admin, and batch number were not reported) dose was not reported, 1 total administrated, therapy start date was not reported for prophylactic vaccination. No adverse events reported after covid-19 vaccine ad26. cov2. s. (Dose number in series 1) The patient received covid-19 vaccine ad26.cov2.s (Janssen, Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194, expiry: UNKNOWN) dose was not reported, 1 total, administered on 23-DEC-2021 in right arm for prophylactic vaccination. No concomitant medications were reported. On 23-DEC-2021, the patient took booster dose and thought it was improperly administered to her, that it was given on right arm but on the upper back part in the fatty area and not on the muscle (improper administration). The patient stated that she felt the needle seemed shorter and thicker than the first time she received it and that the syringe seemed bigger with more fluid. Patient felt that fatty part of her arm was sore after the injection but that it did go away in a few days. (Dose number in series 2) The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of soreness in fatty part of arm after the injection (also reported by patient that it went away in a few unspecified number of days) and received vaccine at upper right arm in fatty area and not on the muscle was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no known drug allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2029250

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 39,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 04.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Extra dose administered Injection site pain Myalgia Vomiting

Symptomtext

Immunocompromised (AIDS) patient received a dose of Moderna which is not currently authorized by written Agency/CDC guidelines as of 1/6/22. Janssen Dose #1 in April 2021. Janssen Dose #2 in November 2021. Received a full dose (0.5mL) of Moderna with Team on 01/04/2022. Current guideline for Janssen schedule is 1 dose only for Primary Schedule, no immunocompromised dose, and a booster dose 2 months from Primary Dose. Moderna Dose given by Team falls outside of this current guideline. I telephoned patient in the afternoon of 1/6/22, and he reported only moderate side effects. Soreness at injection site, myalgia, & vomiting. Did not have to visit PCP, UC, or ED. Otherwise felt decent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: AIDS
Vorgeschichte: AIDS
Andere Medikamente: HIV Anti-Virals
Allergien: None disclosed at time of assessment.
Vorherige Impfungen: -

VAERS 2024399

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 51,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 18.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Groin pain Neuralgia Pain Pain in extremity Sciatica Tenderness

Symptomtext

November 23?left hip sciatic pain mild to moderate. Took Tylenol and Advil throughout the day to relieve pain. November 24?continued left hip sciatica, spreading down the front left thigh and groin area. November 25?same and without Tylenol or Advil its aggravating. Still not a short acting pain but feels like a warning pain. December 1?pain is diminishing and can sleep through the night without adjusting to avoid pinching the nerve. Still a deep tinge in my left hip area and leg December 2?sciatic pain is likely and contained to the left side but there is now shingles like nerve pain but without a rash on both sides of my upper thighs. Hurts to touch and is a stinging-like pain. Pain relief from Advil lasted most of the day until bedtime. December 6?the flareup on the right side is gone for a few days but the sciatic nerve pain continues on the left side whenever a sleep, wake up, put on socks and pants on the left foot and leg, and sitting for extended periods over 15 minutes. December 8?same as last 2 days but with less intensity. Fully resolved by 12/15/2021

Weitere VAERSDATA-Felder

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

VAERS 2017448

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: AL
Alter: 63,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: -
Beginn: 02.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Arthralgia Body temperature Eye pain Herpes zoster

Symptomtext

PAIN IN THE RIGHT EYE SOCKET; JOINT PAIN; SHINGLES; This spontaneous report received from a patient concerned a 63 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient was previously treated with covid-19 vaccine ad26. cov2. s (suspension for injection, route of admin not reported, batch number: unknown, expiry: UNKNOWN) dose was not reported, 1 total administered on specified date in MAR-2021 for prophylactic vaccination (Dose series number 1). On MAR-2021, the patient experienced not much reaction (Dose series number 1). The outcome of not much reaction was not reported. The patient received booster of covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, expiry: unknown) dose was not reported, 1 total administered on 02-DEC-2021 at left arm for prophylactic vaccination ( Dose series number 2). No concomitant medications were reported. On 02-DEC-2021 (after 2 hours of vaccination), the patient had fever, chills and extreme fatigue with the booster shot which lasted for 3 days. On an unspecified day, the patient had fever of 101 and experienced body aches, big lumps on right side of head, itchy lumps, soreness, headache, pain in joints, sickness for 3 days and pain in the right eye socket. The patient went to physician and diagnosed with shingles (Dose series number 2). The physician prescribed an antiviral (valaciclovir) and she was taking Tylenol for the pain. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the shingles, pain in the right eye socket and joint pain was not reported. This report was non-serious. This case, involving the same patient is linked to 20211259385.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 20211202; Test Name: Body temperature; Result Unstructured Data: 101
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2001035

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IL
Alter: 42,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Headache

Symptomtext

Persistent whole head headache

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

VAERS 1999333

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Injection site pain

Symptomtext

Client reported her "arm in pain" around the injection site at 2:00PM. The client was provided a cool pack and placed it over the injection site. The client was alert and oriented to person, place, time, and situation. The client denied any other symptoms at that time. At 2:05PM the clients reported the pain was getting better. Around 2:10 PM the client reporting feeling light headed. Vitals obtained at 2:11PM were as follows: BP 121/89, HR 64, O2 98%. The client stated she last ate at noon. Reported clear vision. The client denied any current medications or known allergies. RN responded and provided education to the client regarding signs and symptoms of anaphylaxis and when to seek EMS. The client voiced understanding of this education. At 2:22PM the client declined repeat vitals and stated, "I feel fine." The client stated she was ready to leave the vaccination site. The client stood up, and denied felling light headed. The client left against medical advice at 2:22PM ambulating unassisted with a steady gait.

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

VAERS 1997705

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 60,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 30.10.2021
Beginn: 10.11.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: SYR / RA

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

Injection site pain Loss of personal independence in daily activities Pain

Symptomtext

Injection site upper arm constantly in pain , especially upon movement . Daily chores are difficult , exercise is difficult - dressing and lifting/carrying things is difficult and all of the above are painful . Scale of 1-10 , where 10 pain level is the worst , my daily pain is at a 7.

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Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Major depressive disorder , anxiety disorder, Lyme disease
Andere Medikamente: Alprazolam .5mg. As needed Paroxetine 20 mg. 1/2 tablet daily
Allergien: Shellfish, iodine, doxycycline, mold , some trees/grasses, gadolinium
Vorherige Impfungen: -

VAERS 1996745

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NJ
Alter: 30,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: -
Beginn: 27.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Antinuclear antibody positive Body temperature Chills Diarrhoea Headache Heart rate Heart rate increased Mental impairment Nausea Pain Photosensitivity reaction Pyrexia Skin burning sensation

Symptomtext

HARD TIME THINKING; BURNING IN THE ARM; FAST HEART RATE AROUND 120-130 BPM; SENSITIVITY TO LIGHT; BODY ACHES; CHILLS; DIARRHEA; HEADACHE (HEAD KILLING HER); FEVER OF 103F; NAUSEA; This spontaneous report received from a patient concerned a 30 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: non smoker, social drinker, penicillin allergy, iodine allergy, and drug allergy (Erythromycin Zoloft). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, expiry: 09-APR-2022) dose was not reported, 1 total, administered on 27-DEC-2021 at around 12:30 PM on left arm for prophylactic vaccination (Dose number in series 1). Concomitant medications included acetylsalicylic acid. On 27-DEC-2021, the patient experienced burning in the arm after the shot, patient took Benadryl because she was scared. Around at 19:00-20:00 patient started having symptoms of body aches, chills and fever 103 F (Fahrenheit), nausea, diarrhea, patient's watch recorded heart rate around 120-130 BPM (beats per minute) and her head was killing. The symptoms were getting worse until 02:30 or 03.00 in the morning. Her fever broke 100.9 F after she took Tylenol 500 mg (milligram). But at the time of reporting she was still experiencing headache (head killing her) and sensitivity to light. Tylenol was not helping her headache. Later at the time of reporting she reported that she had a hard time thinking. She called her doctor but haven't heard back from him. The patient had tested positive for ANA (Antinuclear antibodies) antibody. Treatment medications (dates unspecified) included: diphenhydramine hydrochloride, and paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from fever of 103f, had not recovered from headache (head killing her), sensitivity to light, and hard time thinking, and the outcome of burning in the arm, body aches, chills, diarrhea, fast heart rate around 120-130 bpm and nausea was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20211260926-covid-19 vaccine ad26.cov2.s -Hard time thinking. 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: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211227; Test Name: Body temperature; Result Unstructured Data: 103 F, fever; Test Date: 20211227; Test Name: Heart rate; Result Unstructured Data: around 120-130; Test Date: 20211228; Test Name: Body temperature; Result Unstructured Data: 100.9 F, fever; Test Name: Antinuclear antibodies present; Result Unstructured Data: POSITIVE
Aktuelle Erkrankungen: Drug allergy (Erythromycin and Zoloft); Iodine allergy; Non-smoker; Penicillin allergy; Social alcohol drinker
Vorgeschichte: Comments: Unknown
Andere Medikamente: ASPIRIN [ACETYLSALICYLIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 1996138

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 41,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 30.10.2021
Beginn: 16.12.2021
Tage bis Beginn: 47,0
Dosis: 1
Route/Site: IM / RA

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

Confusional state Dysarthria Dysphemia Fatigue Headache Irritability Speech disorder

Symptomtext

Difficulty Speaking, stuttering, slurring words, would automatically substitute words for other words I wanted to say, when trying to pronounce words, the wrong sounds would come out. B would become V sounds and vice verse, confusion, tired, headaches, and irritable for the last two weeks. I"m only finally starting to feel somewhat normal. though I'm not 100%.

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

VAERS 1991627

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: AZ
Alter: 66,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: -
Beginn: 29.10.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Fatigue Lethargy

Symptomtext

FATIGUE; NO ENERGY/LETHARGY; This spontaneous report received from a patient concerned a 66 year male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26.cov2.s (Janssen, dose number in series 1)(suspension for injection, route of admin not reported, batch number: 1805020, and expiry: UNKNOWN) dose was not reported, 1 total, administered on 17-MAR-2021 into left arm for prophylactic vaccination. On 18-MAR-2021, the patient had fatigue the next day for around 24 hours or less. The next day patient woke up fine (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (Janssen, Dose number in series 2)(suspension for injection, route of admin not reported, batch number: 1855194, expiry: UNKNOWN) dose was not reported, 1 total, administered on 29-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 29-OCT-2021, the patient experienced no energy/lethargy. On 30-OCT-2021, the patient experienced fatigue. (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from no energy/lethargy, and fatigue on 31-OCT-2021. This report was non-serious. This case, involving the same patient is linked to 20211247378 (Dose number in series 1 case).

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

VAERS 1987587

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 02.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Balance disorder Decreased appetite Disturbance in attention Fatigue Headache Nausea

Symptomtext

Headache, nausea, fatigue, difficulty with balance, difficulty with concentration, loss of appetite. Time - whole week.

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

VAERS 1985478

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: PA
Alter: 62,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 02.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Back pain Computerised tomogram Discomfort Hypoaesthesia Muscle spasms Pain Pain in extremity X-ray

Symptomtext

11/6 - left thigh becomes slightly numb - increases over next week 11/14 - 11/20 - lower back pain and cramping in left thigh - increasing discomfort through week 11/21 - pain in back escalates, along with severe cramps in left thigh 11/22 - Dr. - prescribed Naproxin and Methylprednisone 11/22 - 11/27 - pain continues 11/28 - pain increases 11/29 - Dr. refers me to Hospital. Admitted 9 pm. 12/2 - released from Hospital, prescribed oxycodone and prednizone, lidocane patches 12/3 - 12/28 pain and cramping continues, gradual attentuation of back pain, pain in thigh remains

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Praegender Schweregrund: Back pain
Hospital-Tage: 4,0
Labordaten: 11/29 - X-ray 12/01 - CAT Scan
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multi-vitamin, Omega 3
Allergien: None
Vorherige Impfungen: -

VAERS 1983831

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CT
Alter: 66,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: -
Beginn: 20.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Body temperature Pyrexia

Symptomtext

LOW GRADE FEVER; This spontaneous report received from a patient concerned a 66-year-old female of unknown race and ethnic origin. The patient's height and weight were not reported. The patient's concurrent conditions included: crawling sensation, drug allergy to latex, abstain alcohol, and nonsmoker. The patient previously received covid-19 vaccine ad26.cov2.S (suspension for injection, route of admin not reported, batch number: unknown, expiry: unknown ) dose was not reported, frequency one total administered on 10-APR-2021 for prophylactic vaccination (Dose number in series 1). It was unknown whether patient had any adverse event following vaccination with covid-19 vaccine ad26.cov2.s. (Dose number in series 1) The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194 expiry: 09-APR-2022) dose was not reported, frequency one total, vaccinated at left arm, administered on 19-DEC-2021 for prophylactic vaccination (Dose number in series 2). No concomitant medications were reported. On 20-DEC-2021, the patient experienced a low-grade fever. (Event occurred in Dose number in series 2). Laboratory data included: Body temperature (NR: not provided) 99 F. Treatment medications (dates unspecified) included: paracetamol (Tylenol) overnight for the fever. Patient reported that while reading through the paperwork that they gave her at the facility, then mentioned that She had a strange sensation in the back of her neck when she was sitting by her computer that goes away when she stands but did not know how to describe it to her doctor. When she read the paperwork, she saw the crawling sensation in the skin, so that reminded her of that feeling that she had had but did not know how to describe it. She stated that she wanted to clarify that she did not have this crawling sensation after the booster. She had this strange feeling (Crawling/tingling) for more than 2 years from the time of reporting. It comes and goes. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from low grade fever on 21-DEC-2021. This report was non-serious.

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Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Test Date: 20211220; Test Name: Body temperature; Result Unstructured Data: 99 F
Aktuelle Erkrankungen: Abstains from alcohol; Crawling sensation (for more than 2 years); Latex allergy; Non-smoker
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1983825

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: OH
Alter: -
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Arthralgia Pain in extremity

Symptomtext

PAIN IN BOTH KNEES; PAIN IN ARMS; This spontaneous report received from a consumer concerned a 78 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: Alzheimer's, non alcohol user, non smoker, and arthritis, and other pre-existing medical conditions included: The patient had no history of drug abuse or illicit drug usage. The patient had no known drug allergies. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number:1808980, and expiry: UNKNOWN) dose was not reported, 1 total, administered on 07-APR-2021 on right arm for prophylactic vaccination. No adverse events reported post primary vaccination (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number:1855194, and expiry: UNKNOWN) dose was not reported, 1 total, administered on 22-NOV-2021 on right arm for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the reporter noticed that her husband was in pain after receiving the booster dose with his expressions of ooos and ahhs. The patient was specifically experiencing pain in both his knees and arms (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the pain in both knees and pain in arms was not reported. This report was non-serious. This case, from the same reporter is linked to 20211240355, 20211240436, 20211240486 and 20211240211.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Abstains from alcohol; Alzheimer's disease; Arthritis; Non-smoker
Vorgeschichte: Comments: The patient had no history of drug abuse or illicit drug usage. The patient had no known drug allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1983821

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: OH
Alter: 68,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 22.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Arthralgia Insomnia Pain Pain in extremity

Symptomtext

PAIN HAS BEEN SO INTENSE; NOT GETTING ANY SLEEP; SHOULDERS WERE IN PAIN AGAIN; PAIN IS OCCURRING ALL THE WAY TO HER HAND/PAIN IN HAND IS NOT AS BAD AS SHOULDERS; This spontaneous report received from a patient concerned a 68 year female. The patient's height, and weight were not reported. The patient's concurrent conditions included: arthritis, breast cancer, diabetic, alcohol user, non smoker, and drug allergy to penicillin (anaphylaxis). The patient had no history drug abuse or illicit drug usage. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1808980 and expiry: 20-JUN-2021) dose was not reported,1 total, administered on 07-APR-2021 on left arm for prophylactic vaccination. On an unspecified date in APR-2021, the patient experienced pain in shoulders and worse (laid hand on top of shoulder and slide hand to deltoid area) and constant ache and soreness of muscles from both shoulders to both elbow (feels like been beat), pain in biceps (dose number in series 1). The patient was prescribed concomitant medications: diclofenac sodium arthritis pills and Advil for unknown indication. Nothing was helping the pain from massage and prescription medication. Primary care physician sent patient to see an orthopedic doctor in October. Orthopedic doctor injected both shoulders with concomitant medication prednisone for unknown indication. Within 3 days, left shoulder was better. She was pain free, until she received her next injection. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194, and expiry: UNKNOWN) dose was not reported,1 total, administered on 22-NOV-2021 on left arm for prophylactic vaccination. On an unspecified date in NOV-2021, within 48 hours after vaccination, the patient shoulders were in pain again, and pain was occurring all the way to her hand, pain in hand was not as bad as shoulders. Pain had been intense. She was not getting any sleep (dose number in series 2). She reached out to doctor for another prednisone shot. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the shoulders were in pain again, pain is occurring all the way to her hand/pain in hand is not as bad as shoulders, pain has been so intense and not getting any sleep were unknown. This report was non-serious. This case, involving the same patient is linked to 20211240436 (dose number in series 1). This case, from the same reporter is linked to 20211240355, 20211240211 and 20211241144.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Alcohol use (4-5 times per year); Arthritis; Breast cancer (in 30s); Diabetic; Non-smoker; Penicillin allergy
Vorgeschichte: Comments: The patient had no history of drug abuse or illicit drug usage.
Andere Medikamente: DICLOFENAC SODIUM; ADVIL [IBUPROFEN]; PREDNISONE
Allergien: -
Vorherige Impfungen: -

VAERS 1978905

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: OR
Alter: 43,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Chills Confusional state Dizziness Fatigue Feeling cold Headache Myalgia Nausea Pyrexia

Symptomtext

Confusion; I was freezing cold; Started to feel very fatigued; I was having chills; Light headed and dizzy/Mental fog; headache; Nauseous; Muscle aches; Felt the fever rising; This spontaneous case was retrieved on 18-Nov-2021 from Vaccine Adverse Event Reporting System (VAERS) (reference number: 1840394-1), reported by other non-healthcare professional (consumer) and concerned the 43-years old, female patient. The patient's relevant medical history was not reported. The patient's concomitant medications included Gabapentin for unreported indication. On 29-Sep-2021, the patient was vaccinated with Afluria Quadrivalent (influenza vaccine; dose: 'one' as reported, route of administration: intramuscular, anatomical location: right arm (RA), indication: not reported). The batch number was not reported. On the same day, patient was vaccinated with non-company co-suspect Janssen COVID-19 vaccine (covid-19 vaccine nrvv Ad26 (JNJ 78436735)dose: 'two' as reported, route of administration: intramuscular, anatomical location: left arm (LA), indication: not reported). The batch number was reported was 1855194. On 29-Sep-2021, about three hours after receiving Janssen Covid-19 vaccine and Afluria Quadrivalent vaccine, the patient started to feel very fatigued, headache, lightheaded, dizzy, and nauseous. The patient went to lay down and literally felt the fever rising in the body. The patient was freezing cold with muscle aches coming on and the headache getting more severe. The patient fell asleep and her husband woke her up in the night because she was having chills so bad that husband thought she was convulsing. The chills and fever went Thursday night into the next day, as reported. Most of the symptoms subsided by the next evening except for the headache, dizziness, confusion, and a mental fog, as reported. The patient stated that six days past the injection headache, dizziness, and mental fog did not go away. The patient was exhausted and could barely write the report. The patient had missed her work for the week because sick she was sick and stated that condition was awful. At the time of the initial reporting patient recovered from all events, except 'dizziness', 'headache' and ?feeling abnormal'. The reporter did not provide causality assessment. The case was assessed as non-serious. Company comment: A 43-years old, female patient was vaccinated with the suspect product Afluria Quadrivalent and non-company co-suspect Janssen COVID-19 vaccine. Within three hours after vaccination the patient developed dizziness, headache, fever, chills, fatigue, nausea, myalgia and was feeling cold. The patient additionally reported confusion. Causality is confounded by concurrent administration of co-suspect vaccine. Information regarding the underlying medical history has not been provided. Causality for confusional state is assessed as not related based on biological implausibility. Based on plausible time relationship causality for the remaining events is assessed as possibly related.; Sender's Comments: A 43-years old, female patient was vaccinated with the suspect product Afluria Quadrivalent and non-company co-suspect Janssen COVID-19 vaccine. Within three hours after vaccination the patient developed dizziness, headache, fever, chills, fatigue, nausea, myalgia and was feeling cold. The patient additionally reported confusion. Causality is confounded by concurrent administration of co-suspect vaccine. Information regarding the underlying medical history has not been provided. Causality for confusional state is assessed as not related based on biological implausibility. Based on plausible time relationship causality for the remaining events is assessed as possibly related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (Sulfa)
Vorgeschichte: -
Andere Medikamente: Gabapentin
Allergien: -
Vorherige Impfungen: -

VAERS 1975226

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: GA
Alter: 56,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain upper Oropharyngeal discomfort Pharyngeal swelling

Symptomtext

Stomach ache began in the morning after the vaccine. I awoke the following morning to my throat feeling different and had throat swelling after taking my morning medications, then used the first epinephrine shot (not an auto injector due to severe reaction to preservatives in auto injector). With each swallow of food or water during the day I experienced some throat swelling then used second epinephrine shot at 6:30pm after a meal. The process continued the filling day, Sunday, with two more epinephrine shots, one in the a.m and another in the p.m. After eating my nightly meal, there was no reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: I did not go to the ED/hospital due to my local one being unable to care for me. I did see my allergist.
Aktuelle Erkrankungen: None
Vorgeschichte: Anaphylaxis Food, environmental, chemical allergies
Andere Medikamente: Betapace, Singulair, Zyrtec, Claritin, Trazodone, Thyroid
Allergien: Tested allergic to many foods including peanuts, soy, fish, beef, beans, peas, gluten, preservatives, petroleum, chemicals
Vorherige Impfungen: -

VAERS 1974765

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: OH
Alter: 71,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 07.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: SYR / RA

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

Injection site pain

Symptomtext

Extreme soreness in right arm at injection site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Artorvastatin, Lisinopril
Allergien: none
Vorherige Impfungen: -

VAERS 1970456

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IN
Alter: -
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: -
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Asthenia Chills Fatigue Headache Pyrexia

Symptomtext

COLD CHILLS; FEVER; WEAK; HEADACHE; FEELING VERY TIRED; This spontaneous report received from a patient concerned a male of unspecified age. 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 admin not reported, batch number: 1855194, and expiry: UNKNOWN) dose was not reported, administered on 18-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On DEC-2021, the patient experienced cold chills, fever, weak, headache, and feeling very tired. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the fever, cold chills, weak, headache and feeling very tired was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

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

VAERS 2537356

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 10.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Diarrhoea Nasopharyngitis Pain

Symptomtext

Narrative: Patient received his 2nd dose of J&J on friday, called Monday reporting that since receiving the 2nd shot he had been having diarrhea, body aches, and head cold. Patient was advised to use OTC medications for relieve of symptoms and to seek more treatment at clinic if needed.

Weitere VAERSDATA-Felder

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

VAERS 1966636

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IL
Alter: 30,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 15.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Autoscopy Cough Euphoric mood Headache

Symptomtext

OUT OF BODY FEELING; FEELS HIGH LIKE FROM MARIJUANA; DRY COUGH; BRUTAL HEADACHE; This spontaneous report received from a patient concerned a 30 year old male. 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 admin not reported, batch number: 1855194 expiry: 09-APR-2022) dose was not reported, administered on 15-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On DEC-2021, the patient experienced dry cough, and brutal headache. On 15-DEC-2021, the patient experienced feels high like from marijuana. On 17-DEC-2021, the patient experienced out of body feeling. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the feels high like from marijuana, brutal headache, dry cough and out of body feeling was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

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

VAERS 1963648

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CO
Alter: 65,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 26.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / RA

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

Arthralgia Pain Pain in extremity Product administered at inappropriate site

Symptomtext

My arm was extremely sore after injection in the shoulder region, felt it was just a minor reaction and it would get better. But the soreness in my shoulder kept getting worse, with extreme pain, upon certain movements. I took ibuprofen for the pain, but it would just ease the symptoms and not take it away. After 3 weeks of pain I made an appointment with my physician, who felt it was due to injection being given in my rotor cuff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None so far.
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes, sinutitis,
Andere Medikamente: Metformin, Atorvastatin, Citalopram, Buspirone, 80mg aspirin
Allergien: No
Vorherige Impfungen: -

VAERS 2537463

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 19.12.2021
Impfdatum: 10.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Diarrhoea Nasopharyngitis Pain

Symptomtext

Narrative: Patient received his 2nd dose of j&J on friday, called Monday reporting that since receiving the 2nd shot he had been having diarrhea, bodyaches, and head cold. Patient was advised to use OTC medication for relieve of symptoms and to seek more treatment at facility if needed.

Weitere VAERSDATA-Felder

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

VAERS 1962476

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 07.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Headache Pain in extremity Thrombocytopenia Ultrasound Doppler

Symptomtext

thrombocytopenia, headache, pain in right leg

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 12/18/21 blood test 12/18/21 lower extremity venous doppler
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: multivitamins, probiotic, magnesium
Allergien: -
Vorherige Impfungen: -

VAERS 1961813

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 01.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Fatigue Feeling cold Feeling hot Headache Hyperhidrosis Musculoskeletal stiffness Oral herpes Pain Photophobia Pyrexia Sleep disorder Tension

Symptomtext

Upon receiving this vaccine, I had no immediate reactions. However, upon arriving home around 4:30pm, I realized that I had the cold chills. Around 6pm, I had a very intense headache. It was also at this time that I began to feel very tried and fatigue. By 10pm my entire body was tense, and hurting! Teeth were chattering because I was so cold and even the slightest LIGHT hurt my head. I woke up around 2am COVERED in sweat with a fever. Fever was 101.2 (my normal temp is 97.8). I had to change clothes TWICE due to soaking them through. I was not cold at this time. Just HOT. At 7:30am, I awoke with the same headache as the night before, accompanied by a fever blister. Chills started again around 11:30am. It is currently 12:56pm & I am suffering from the headache, chills & lots of stiffness throughout my back and neck still. I will continue to monitor my symptoms & report anything new.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Viral cold roughly 19 days ago.
Vorgeschichte: None
Andere Medikamente: Tylenol 500mg
Allergien: None
Vorherige Impfungen: -

VAERS 1956184

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: PA
Alter: 27,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 05.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain Arthralgia Fatigue Impaired work ability Nausea Pain

Symptomtext

Woke up 12/6 at 1am. Intense ABD pain. Got ready for work 5am. Intense body aches, ABD pain, nausea. Called off of work. Every day since 12/6, I have had extreme fatigue, body aches, and bilateral knee pain. I have NEVER had pain in my knees.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: I have not been seen by my pcp.
Aktuelle Erkrankungen: Endometriosis
Vorgeschichte: Endometriosis
Andere Medikamente: Calcium Ginkgo Bilbao Ginger root Omega 3 Vitamin c Super b complex Turkey tail Lions mane Zyrtec Qellbutrin Folate
Allergien: Sulfa Pcn Soy Apples Cherries
Vorherige Impfungen: -

VAERS 1951410

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: TX
Alter: 63,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 05.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Dermatitis contact Pain in extremity Pruritus Temperature intolerance

Symptomtext

First Adverse Symptom notice about a week after vaccination was that any drink that was hot (coffee, tea, hot chocolate) will produce a extremely itchy feeling of having a rash all over the body without showing visible signs. The solution had been stayed away from hot drinks and wait for ambient temperature-warm. Reaction is starting to go away after 5 weeks. Second Adverse symptom has been a sudden reaction to detergent (hard soap bar or liquid) but only to specific ones. Since not sure which one (s) wearing gloves had been the way of aggravating the skin break down and sensitive pain on both hands from the moment it did get started. It's healing in a very slow pace however I had to use gloves to keep the skin on the hands not dry since nothing else is working.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None done
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Benazepril, Simvastatin
Allergien: no
Vorherige Impfungen: -

VAERS 1944100

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: -
Alter: 20,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis

Symptomtext

4mins post vaccination pt reported dizziness flushing and sweating. Vitals: 9:50 104/62, 79, 17, 100% -- > 10:07 106/70, 83, 16, 100% Pt laid supine. Fluids provided. No further intervention needed. Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 1942603

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IN
Alter: 26,0
Geschlecht: M
Eingang: 12.12.2021
Impfdatum: 10.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia Chills Extra dose administered Feeling cold Headache Hyperhidrosis Injection site pain Injection site swelling Muscular weakness Nausea Pyrexia

Symptomtext

Booster shot 1:10 pm, middle of the night(am of 12/11/2021)-sweating, chills, weakness, feeling cold, muscle weakness, nausea, severe head ache, pain in left arm at injection site & swelling. Day of 12/11/2021- measured fever of 103, fever, sweating, chills, severe headache, nausea, weakness. 12/11 later that day(7 pm)took a Tylenol, fever started going down 102,100,99,98.6. side effects started going down. Left arm at injection spot still sore.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic on and off lower back pain on right side.
Andere Medikamente: Divalproex SOD DR 250 MG TAB- 2 by mouth every night. Cetirizine HCL 10 MG Tablet-1 everyday. SAMe 400 MG- 3 each night. Kroger Men?s Gummies mixed berry and strawberry Multivitamin- 2 a day.
Allergien: Allergy to: Soybeans
Vorherige Impfungen: -

VAERS 1941618

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 39,0
Geschlecht: M
Eingang: 11.12.2021
Impfdatum: 09.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Disorientation Headache Pyrexia

Symptomtext

head ache, slight fever, disorientation

Weitere VAERSDATA-Felder

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

VAERS 1934848

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MI
Alter: 62,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: -
Beginn: 22.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Apathy Fatigue Headache Hypersomnia Injection site pain Somnolence

Symptomtext

ON THE COACH TODAY THE ALL DAY; VERY TIRED AND EXHAUSTED; SLIGHT HEADACHE; THE INJECTION STING A LITTLE BIT; VERY DROWSY; SLEPT FOR 9.5 HOURS LAST NIGHT AND DID NOT WAKE UP TILL 9:30 MORNING; This spontaneous report received from a patient concerned a 62-year-old male of unspecified race and ethnic origin. The patient's weight was 200 pounds, and height was 69 inches. The patient's past medical history included: guillain-barre syndrome (GBS) (and cannot have the flu vaccine), and concurrent conditions included: diabetes (type II), alcohol use (3 beers per week), non-smoker, and blood pressure abnormal. The patient had no history of drug abuse or illicit drug use. The patient experienced diarrhea and throwing up when treated with potassium citrate, and sick and very nauseous when treated with cefalexin. The patient received vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of administration not reported, and batch number, expiry were not reported ) dose was not reported, 01 total, administered on 09-APR-2021 for prophylactic vaccination. No adverse evets reported. No adverse event reported following vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of administration not reported, batch number: 1855194, and expiry: 09-APR-2022) dose was not reported, 01 total administered on 22-NOV-2021 at 10:00 hours for prophylactic vaccination in right arm. No concomitant medications were reported. The patient was on blood pressure pill. On 22-NOV-2021, 3 hours following vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 2) the patient had slight headache, very tired, exhausted and was very drowsy. He slept for 9.5 hours last night (from the day of reporting) and did not wake up till 9:30 this (day of reporting) morning. He stated that, injection sting a little bit and the pharmacist told him that it was expected because it would go into the muscle. He was on the coach today the all day. The action taken with covid-19 vaccine ad26.cov2.s (dose number in series 2) was not applicable. The patient had not recovered from very tired and exhausted, slight headache, and on the coach today the all day, and the outcome of very drowsy, the injection sting a little bit and slept for 9.5 hours last night and did not wake up till 9:30 morning was not reported. This report was non-serious. This case, from the same reporter is linked to 20211154670.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Alcohol use (3 beer per week); Hypertension; Non-smoker; Type II diabetes mellitus
Vorgeschichte: Medical History/Concurrent Conditions: Guillain-Barre syndrome (that almost went on ventilator and was treated with plasmapheresis.); Comments: The patient had no history of drug abuse or illicit drug use. The patient was on blood pressure pill
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1933115

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: VA
Alter: 33,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Gait disturbance

Symptomtext

Went to bed and woke up after midnight with terrible joint pain. Shoulder joints hurt, knee joints hurt (I could barely walk), and the most serious issue was with my left wrist. I could barely move my fingers and when I was able to move my fingers, it felt like something in my wrist kept popping. I had to use my other hand to rotate my wrist around until it made a loud pop noise and then I was able to move my hand without it continuously popping and hurting. I went back to bed and woke up about 2 hours later with the same issue. The rest of my joints are better now, but I'm still having issues with my left wrist/hand. I can't always fully stretch my thumb, my wrist continues to pop randomly throughout the day and it's painful, sometimes my hand seizes up and I can't move it, and I have to wear a wrist brace during work because I work on a computer all day and it will randomly seize up without a brace on. I never had an issue with my wrist before until that night.

Weitere VAERSDATA-Felder

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

VAERS 1931264

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: -
Beginn: 11.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Pain in extremity

Symptomtext

ARM HURT TERRIBLE; This spontaneous report received from a patient concerned a 57 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient experienced terrible headache when treated with covid-19 vaccine ad26. cov2. s for prophylactic vaccination. (Dose number in series 1) The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, and batch number: 1855194 expiry: 09-APR-2022) dose was not reported, administered on 11-NOV-2021 for prophylactic vaccination.(Dose number in series 2) No concomitant medications were reported. On 11-NOV-2021, the patient experienced arm hurt terrible.(Dose number in series 2) The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of arm hurt terrible was not reported. This report was non-serious. This case, involving the same patient is linked to 20211145104 (Dose number in series 1). This case, from the same reporter is linked to 20211144980.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1927688

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: -
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Headache Urinary tract infection

Symptomtext

URINARY TRACT INFECTION; SLIGHT HEADACHE; This spontaneous report received from a patient concerned a 71 year old female. The patient's height, and weight were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, expiry: Unknown) dose was not reported, administered on MAR-2021 for prophylactic vaccination on left arm (dose number in series 1). No concomitant medications were reported. the patient did no have a sore arm. On MAR-2021, the patient experienced urinary tract infection and slight headache. (dose number in series 1) The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from slight headache, and the outcome of urinary tract infection was not reported. This report was non-serious. This case, involving the same patient is linked to 20211137873 (Dose number in series 2).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient did not have sore arm
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1927682

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: PA
Alter: -
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: -
Beginn: 09.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Headache Hyperhidrosis Nasal congestion Pyrexia

Symptomtext

STUFFY NOSE; STARTED TO SWEAT; FEVER; HEADACHE; This spontaneous report received from a patient concerned a 73 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, and batch number: 1808978) dose was not reported, administered on 29-MAR-2021 for prophylactic vaccination. On an unspecified date following vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 1), the patient experienced tired. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient received booster dose of covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194 expiry: UNKNOWN) dose was not reported, administered on 08-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 09-NOV-2021, the patient experienced stuffy nose, started to sweat, fever and headache.(dose number in series 2) Treatment medications (dates unspecified) included: chlorphenamine maleate/paracetamol/pseudoephedrine hydrochloride. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from fever, and headache, had not recovered from stuffy nose, and the outcome of started to sweat was not reported. This report was non-serious. This case, involving the same patient is linked to 20211127601 (Dose series in number 1).

Weitere VAERSDATA-Felder

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

VAERS 1926049

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MN
Alter: 53,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Injection site pain Neck pain Pain

Symptomtext

Patient stated she experienced pain at the site of the injection on her left arm. The pain is radiating to her neck (left-side). Patient stated she contacted her doctor via phone and her doctor thinks the pain could be related to the vaccine. Patient did not have an office visit scheduled with her doctor at the time of reporting this event to the pharmacy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Migraine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1924258

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: VT
Alter: 51,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 01.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chills Confusional state Dizziness Headache Injection site discolouration Insomnia Nausea

Symptomtext

Severe headache Insomnia Cold chills Black spot at injection site Confusion Difficult to think of words Thoughts jumbled Dizziness Nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety and mood
Andere Medikamente: Lamictal, diazepam,premarin
Allergien: -
Vorherige Impfungen: -

VAERS 1924146

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: -
Beginn: 10.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Headache Pyrexia Toothache

Symptomtext

HEADACHE; TOOTH PAIN/PIERCING PAIN; OVER NIGHT FEVER; This spontaneous report received from a patient concerned a 60 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: alcohol user, and non smoker, and other pre-existing medical conditions included: The patient had no known allergies, no history of drug abuse or illicit drug use. She was healthy. The patient received their initial vaccination (dose number in series 1) with covid-19 vaccine ad26. cov2.s (suspension for injection, route of admin, and batch number were not reported) dose was not reported, administered on 04-APR-2021 for prophylactic vaccination. No adverse event was reported after series one dose. The patient mentioned she did dental cleaning on 24-SEP-2021, where the hygienist was very hard on her. He triggered a broken tooth that she was waiting to fix the next year due to insurance coverage. That caused her severe pain. She suffered from that dental pain from 24-SEP-2021 to 24-OCT-2021, as constant pain like storm. The patient received booster dose (dose number series 2) covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration not reported, batch number: 1855194, expiry: unknown) dose was not reported, frequency time 1 total administered on 10-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 10-NOV-2021, the pharmacist injected the dose aggressively and the patient experienced over night fever which was not checked by thermometer. On 11-NOV-2021, the patient experienced headache, that went away same day at evening time. After booster dose, her tooth pain came back in the same area. That pain was still there till the day of report, it was piercing pain, from one tooth (lower jaw), toward the whole side of the mouth. At the same level of the initial pain patient told the dentist about the incident. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from over night fever, and headache on 11-NOV-2021, and had not recovered from tooth pain/piercing pain. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Alcohol use (occasional); Non-smoker
Vorgeschichte: Comments: The patient had no known allergies, no history of drug abuse or illicit drug use. She was healthy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1923858

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: PA
Alter: 46,0
Geschlecht: M
Eingang: 05.12.2021
Impfdatum: 01.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Acoustic stimulation tests Balance disorder Dizziness Ear discomfort Tinnitus Visual impairment

Symptomtext

Ringing and preasure in right ear increased. Mild ringing started in left ear. Dizziness Off-balance Vision changes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Hearing test and evaluation on 11/16/21. 2 week dose of Prednisone started on 11/16/21.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Meniere's disease
Andere Medikamente: Vitamin D; Calcium; BioFlex; Biotin; Vitamin B; Influenza Flu Vaccine
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1921161

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NH
Alter: 44,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dysgeusia Immediate post-injection reaction Injection site pain Nausea Tinnitus

Symptomtext

Tinnitus, nausea, muscle pain at injection site, metal taste in mouth, all occurring immediately and lasting at about 24 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1920225

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: PA
Alter: 20,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Immediate post-injection reaction Urticaria

Symptomtext

Patient presented with hives immediately after receipt of the vaccine. We gave her 50mg Benadryl by mouth. She was not in anaphylaxis so we sent her directly to follow up with her MD.

Weitere VAERSDATA-Felder

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

VAERS 1919233

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: AZ
Alter: 75,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / RA

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

Incorrect route of product administration Injection site pain

Symptomtext

INAPPROPRIATE ROUTE OF VACCINE ADMINISTRATION; BURNED/STUNG; This spontaneous report received from a patient concerned a 75 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient was previously treated with covid-19 vaccine (unspecified manufacturer) for prophylactic vaccination (dose number in series 1). No events reported. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, intravenous, batch number: 1855194 expiry: UNKNOWN) (unspecified manufacturer) dose was not reported, administered on 03-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 03-NOV-2021, following vaccination with covid-19 vaccine ad26.cov2.s booster dose the patient experienced inappropriate route of vaccine administration and burned/stung. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the inappropriate route of vaccine administration and burned/stung was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1912794

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IN
Alter: 47,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 29.11.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Axillary pain

Symptomtext

Severe soreness under left arm (armpit) I am just taking ibuprofen for pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, rheumatoid arthritis, high blood pressure , sleep apnea.
Andere Medikamente: Methotrexate , glipizide, metformin, leflunomide, clopidogrel, ezetimibe, hydroxychloroquin, folic acid, insulin, antioxidant vitamin.
Allergien: Mangos and the tetanus shot
Vorherige Impfungen: -

VAERS 1912196

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 12.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Headache Urinary tract infection

Symptomtext

URINARY TRACT INFECTION; SLIGHT HEADACHE; This spontaneous report received from a patient concerned a 72 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient experienced slight headache and urinary tract infection (both events dose number in series 1) when treated with covid-19 vaccine ad26. cov2.s for prophylactic vaccination on /MAR-2021 (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194 expiry: UNKNOWN) dose was not reported, 1 total, administered in left arm on 12-NOV-2021 (dose number in series 2) for prophylactic vaccination. No concomitant medications were reported. On an unspecified date in NOV-2021, the patient experienced urinary tract infection and slight headache from the booster dose ( both events dose number in series 2). The patient did not have sore arm, so she slept on it. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of urinary tract infection and slight headache was unknown. (also mentioned recovered from slight headache) This report was non-serious. This case, involving the same patient is linked to 20211137085.

Weitere VAERSDATA-Felder

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

VAERS 1912192

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: TX
Alter: 58,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: -
Beginn: 08.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Bedridden Body temperature Chills Hyperhidrosis Illness Insomnia Limb discomfort Lymph node pain Lymphadenopathy Pain Pyrexia

Symptomtext

WET AND SWEATY; COULD NOT GET OUT OF BED AND IT WAS A CHALLENGE TO GET OUT OF BED; SWOLLEN LYMPH NODE UNDER RIGHT ARM IN WHICH BOOSTER DOSE WAS RECEIVED ABOUT THE SIZE OF A BASEBALL; ACHY ALL OVER; SWOLLEN LYMPH NODE UNDER THE RIGHT ARM AND IT HURTS REALLY BAD; FEVER, FEVER OF 100 FAHRENHEIT; ARM HURT SO BAD, FROM SHOULDER TO FINGERS; REALLY SICK ABOUT 10 HOURS AFTER RECEIVING THE BOOSTER,AROUND 20:00; DID NOT SLEEP; COULD NOT PICK UP HER ARM, IT WAS LIKE A DEAD WEIGHT; CHILLS; This spontaneous report received from a patient concerned a 58 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. Patient received covid-19 vaccine ad26. cov2. s (suspension for injection, route of admin not reported, batch number and expiration date unknown ) dose was not reported, 1 total administered on 30-MAR-2021 on left arm for prophylactic vaccination (dose series 1). After receiving this shot patient experienced arm hurt a long time ( "for months") after the original shot in left arm, she could feel the needle sticking in her arm. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, and expiry: 09-APR-2022) dose was not reported, 1 total administered on 08-NOV-2021 on right arm at 10:00 for prophylactic vaccination (dose series 2). No concomitant medications were reported. Patient was really sick about 10 hours after receiving the booster, around 20:00. Patient's arm hurt so bad, from her shoulder to her fingers, she could not pick her arm up, it was like a dead weight. The pain got worse throughout the night, and she did not sleep. She had a fever and chills really bad that night. She did not take her temperature that night. On 09-NOV-2021 she could not get out of bed. She was achy all over. She also had a fever of 100F and chills. On same day patient took Aspirin, in the morning and afternoon. Patient had a swollen lymph node under the right arm, the arm she received the booster in, about the size of a baseball and it hurts really bad. The lymph node started swelling at night on 09-NOV-2021. At the time of reporting on 10-NOV-2021 patient had a fever around 100F and it was a challenge to get out of bed. Patient was wet and sweaty. Patient also took Aspirin coated 500mg, with food, 1 at a time, about 4 hours apart on 10-NOV-2021 in morning . The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from fever, fever of 100 Fahrenheit, swollen lymph node under right arm in which booster dose was received about the size of a baseball, and could not get out of bed and it was a challenge to get out of bed, and the outcome of really sick about 10 hours after receiving the booster, around 20:00, did not sleep, chills, achy all over, wet and sweaty, could not pick up her arm, it was like a dead weight, arm hurt so bad, from shoulder to fingers and swollen lymph node under the right arm and it hurts really bad was not reported. This report was non-serious. This case, involving the same patient is linked to 20211162567 (series 1).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211109; Test Name: Body temperature; Result Unstructured Data: 100 F
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1910054

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CO
Alter: 50,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 08.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 13,0
Dosis: UNK
Route/Site: SYR / RA

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

COVID-19 Chills Cough Nasal congestion Night sweats Pyrexia Rash SARS-CoV-2 test positive Upper-airway cough syndrome

Symptomtext

on 11/21/21 I had postnasal drip and a low cough. On 11/23/21 I had night sweats and the two symptom's became more prevalent. On 11/24//2021 I had a fever chills and tested positive for Covid-19. I had an extremely high fever for three days, cough, congestion and I developed a rash on my back. Stop prompting the vaccine if it doesn't work. I spent 10 days of my life isolated and sick due to an ineffective product.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Positive covid test on 11/24/21 after receiving my vaccine. Stop prompting the vaccine if it doesn't work. I spent 10 days of my life isolated and sick due to an ineffective product.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1908317

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MI
Alter: 34,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: -
Beginn: 11.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Abdominal pain upper Back pain Urinary retention

Symptomtext

UNABLE TO URINATE; LOWER BACK PAIN; STOMACH PAIN; This spontaneous report was received from a parent (mother) concerning her daughter, a 34 year old female. The patient's height, and weight were not reported. No past medical history and concurrent conditions were reported. On 08-APR-2021, the patient received initial Janssen COVID 19 vaccine shot for prophylactic vaccination (Janssen series 1). After initial shot, she had kidney problems started in MAY-2021. She felt really sick one day with headache, stomach ache, back ache, and throwing up. The patient went to the emergency room which revealed a 5 mm kidney stone that was taken out the next day. The patient had a headache for about a week after initial shot. The patient had not urinated on own after getting kidney stone out. In OCT-2021, she started urinating a little on her own. The patient received Covid-19 vaccine ad26.cov2.s (Janssen series 2 Booster dose) (suspension for injection, route of admin not reported, batch number: 1855194 and expiry: 09-APR-2022) dose was not reported, 1 total, administered on right arm on 11-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 11-NOV-2021, the patient had not urinated since receiving her booster vaccination (unable to urinate) and she sought advice from doctors but they found nothing wrong. The patient had also been experiencing lower back pain and stomach pain since 11-NOV-2021. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from unable to urinate, lower back pain, and stomach pain. This report was serious (Other Medically Important Condition). This case, involving the same patient is linked to 20211145488.; Sender's Comments: V0-20211144980-Covid-19 vaccine ad26.cov2.s- Unable to urinate. 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: Abdominal pain upper
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1906493

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 10.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: SYR / LA

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

Rash Swelling face Urticaria

Symptomtext

Swelling of face Bad shin hive-like rash on my face that has not gone away

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Thyroid
Andere Medikamente: One a Day Women's over 50+ Complete Multivitamins Leothyroxine 50 MCG 1 tablet daily Bupropin HCI XL 300 MG 1 tablet daily Trazadone 50 MG tablet daily
Allergien: bactrim
Vorherige Impfungen: -

VAERS 1904472

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: AK
Alter: 26,0
Geschlecht: F
Eingang: 28.11.2021
Impfdatum: 14.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Back pain Bladder pain Kidney infection Pyrexia Urinary tract infection Urine analysis

Symptomtext

Urinary tract infection. I woke up to extreme burning and pain around my bladder about a week after the booster. The pain did not go away like it usually does for UTIs, which I seem to be prone to. It continued for several days before I started feeling pain in my back and a slight fever. I went to the emergency room. They didn't think it had infected my kidneys yet and gave me antibiotics and antinausea medicine. However, I notice that drinking lots of water makes my back ache and a fever flare again. I am waiting to make sure to get through a few more days of antibiotics before returning to the hospital. There is no blood in my urine yet. I have beem drinking lots of water and cranberry juice, but still feel fairly miserable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Urine sample/processing at the hospital visit on 11.26.2021.
Aktuelle Erkrankungen: None
Vorgeschichte: Depression Anxiety Sensory Disorder Seasonal Allergies Asthma
Andere Medikamente: Trinessa Lo Vitamin D
Allergien: Penicillin Morphine
Vorherige Impfungen: Fever for 24 hours after the first Johnson/Johnson dose, but no UTI

VAERS 2571835

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: -
Alter: 44,0
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Dizziness Dysstasia Electrocardiogram Fatigue Laboratory test Muscular weakness

Symptomtext

Narrative: Pt received first dose of COVID vaccine (Janssen) at approx 1600. After approximately 15 minutes, pt reported feeling dizzy, lightheaded , and fatigued. Also reported BLE weakness. He attempted to stand and was unable to support himself. Pt provided with juice, VS monitored with BP 142/90, HR 92-99, SPO2 100^ on RA. He continued to feel week and dizzy. After another 15 minutes, pt was agreeable to be transferred to the ED for additional monitoring. In the ED, pt received IL NS. Labs and EKG were done. Full note from ED not available at time of this report. Pt discharged home in stable condition at 19:33

Weitere VAERSDATA-Felder

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

VAERS 1902017

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: 21.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / RA

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

Urticaria

Symptomtext

Per patient hives on chest, neck, shoulder, hand that started 5 days after vaccination

Weitere VAERSDATA-Felder

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

VAERS 1900026

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NC
Alter: 28,0
Geschlecht: M
Eingang: 25.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Pityriasis rosea Rash Urticaria

Symptomtext

After taking my Jansen booster shot, I developed rashes/ hives all over my body starting from my back and then slowly spreading to my chest, thighs, arms and legs (in that order) as days went by. The initial reaction was within 48 hours of my shot and it has been 9 days since the booster shot and the conditions dont seem to subside.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: It was diagnosed at pityriasis rosea by my doctor during the first visit and was prescribed antihistamines (Cetirizine, once a day). However, it continued to become worse and on my subsequent visit to urgent care, they gave me a shot of steroids and have prescribed me steroid tablets as well.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Vitamin B, D, K supplements.
Allergien: No allergies.
Vorherige Impfungen: -

VAERS 1897566

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MN
Alter: 49,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 05.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Rash

Symptomtext

rash all over body

Weitere VAERSDATA-Felder

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

VAERS 1896323

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IN
Alter: -
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: -
Beginn: 21.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Feeling of body temperature change Headache Malaise Pain in extremity SARS-CoV-2 test

Symptomtext

FEELS HOT/COLD; ARM SORENESS; NOT FEELING 100 PERCENT; HEADACHE; This spontaneous report received from a patient concerned a male of unspecified age. 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 admin not reported, batch number: 1855194 and expiry: UNKNOWN) dose was not reported, administered on 20-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 21-NOV-2021, the patient experienced feels hot/cold. On 21-NOV-2021, the patient experienced arm soreness. On 21-NOV-2021, the patient experienced not feeling 100 percent. On 21-NOV-2021, the patient experienced headache. Laboratory data included: COVID-19 virus test (NR: not provided) Negative. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from headache, feels hot/cold, and arm soreness, and the outcome of not feeling 100 percent was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 20211121; Test Name: COVID-19 virus test; Result Unstructured Data: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1894815

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: -
Alter: 39,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nausea

Symptomtext

8mins post vaccination pt reported nausea and dizziness. Vitals: 109/66, 53, 20 Pt stable and released from the vaccination site @15:10.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Allergies, Medications, and PMH unknown to this writer
Andere Medikamente: Allergies, Medications, and PMH unknown to this writer
Allergien: Allergies, Medications, and PMH unknown to this writer
Vorherige Impfungen: -

VAERS 1894512

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IN
Alter: 54,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Ear pain Head discomfort Headache Hypersomnia Musculoskeletal pain Pain Pain in extremity Pain in jaw

Symptomtext

6 days later, I've had a headache that feels like pressure all over my head, jaw, and ears. Also, I have 1 step from my back room to my kitchen that is usually easily maneuvered but my thighs hurt. My buttocks hurt. I feel achy and slept 11 hours 4 nights after my vaccine. I usually sleep 7.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: None. I'm debating calling my doctor tomorrow. I've been complaining and taking advil and tylenol for 6 days.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1890516

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NJ
Alter: 17,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Headache Product administered to patient of inappropriate age

Symptomtext

patient is age 17 , guardian reported client having a slight headache day after immunization which resolved itself, then no other side effects were encountered.

Weitere VAERSDATA-Felder

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

VAERS 1889866

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NC
Alter: 58,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / -

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

Dizziness Nausea

Symptomtext

Within 5-10 minutes I started feeling light-headed and slightly nauseous. I had taken an antihistamine 45 minutes before the injection due to a similar reaction after my first J&J vaccine. The symptoms worsened slightly so I took a second antihistamine about 45 minutes after the vaccine injection . This resolved the symptoms by about 1.5 hours after the vaccine injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Rheumatoid Arthritis, Celiac Disease, Hypothyroidism, Psoriasis
Andere Medikamente: Tirocint, Cytomel, Omega-3 Fish Oil, Calcium Citrate, Magnesium Citrate, Methyl B-12, CoQ10, Folate, Copper Glycinate, Iodine, Thorne Basic Nutrients, Carnityl, Phosphotidylserine, Alpha Lipoic Acid, Selenomethionine, Ferrasorb (iron), zinc
Allergien: Epinephrine (causes fainting), Polyethylene Glycol (causes long-lasting body rash)
Vorherige Impfungen: Throat tightening, nausea, light-headedness within 10 minutes following the first Janssen vaccine on 4/2/2021. I was 58 years ol

VAERS 1889440

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 29.10.2021
Beginn: 08.11.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: SYR / RA

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

Ageusia Anosmia Blood test normal COVID-19 Chills Fatigue Fibrin D dimer Hypersomnia Impaired healing Nasopharyngitis Pyrexia SARS-CoV-2 test positive Scratch Vomiting

Symptomtext

ER - 14Nov2021 - Leg - I had a scratch on my leg - the wound did not heal and went to ER because of this . There I got tested and also tested positive. 8-10 symptoms started. tested positive , fever, chills and threw up after 2-3 days I was over and had a simple head cold and fatique and slept on and off for a couple days . Still no taste and smell.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: 3,0
Labordaten: Covid - Positive D- dimer for embolism Bloodwork - normal
Aktuelle Erkrankungen: no
Vorgeschichte: heart patient and choric lupus and had hip replacement
Andere Medikamente: no
Allergien: Lactose intolerant , oxycodone
Vorherige Impfungen: -

VAERS 1885883

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: -
Alter: 29,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Malaise

Symptomtext

5mins post vacciantion, pt began to feel unwell. Vitals: 14:55 104/53, 79, 18, O2 Sat 100% -- > 15:00 109/59, 77, 18, 100%. Pt recovered quickly and was sitting upright. Pt stable and released from the vaccination site. Pt refused wheelchair transport to exit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Recent pregnancy and vaginal birth
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1880320

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IN
Alter: 48,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 20.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Headache

Symptomtext

Almost constant headaches since the vaccine. Primarily in the front part of my head, strongest in the front left. Very rare to ever have a headache in my entire life prior to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1877395

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: -
Alter: 21,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis

Symptomtext

10mins post vaccination pt c/o flushing/sweating and dizziness. Vitals 16:25 103/52, 70, 20, SpO2 100% -- > 16:35 109/55, 63, 20, 100% -- > 16:43 113/69, 55, 20, 100% Pt stable and released from vaccination site at 16:43. Pt refused wheelchair.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: PMH, Medications unknown to this writer
Vorgeschichte: PMH, Medications unknown to this writer
Andere Medikamente: PMH, Medications unknown to this writer
Allergien: NKA
Vorherige Impfungen: -

VAERS 1876459

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MD
Alter: 71,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Fatigue Headache

Symptomtext

Temp 99.5, dull headache, and feeling weak and tired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension Hypothyroid
Andere Medikamente: Levothyroxine 88 MCG daily----Calcium, Magnesium and Zinc daily Lisinopril HCTZ 10-12.5-mg daily Metoprolol succ ER 25mg daily Low dose Aspirin 81mg daily Vitamin D3 2000 IU daily
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1873976

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain upper Body temperature increased Dizziness Immediate post-injection reaction

Symptomtext

Patient complained about lightheaded sensation right after receiving the vaccination and her body temperature increased with some stomach pain. Watched the patient in increments of 5 minutes Treatment: Had her sit down in a dark room Gave her water

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1872818

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: FL
Alter: 51,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Arthralgia Chills Fatigue Feeling cold Feeling hot Muscle fatigue Myalgia Pyrexia

Symptomtext

Approximately nine hours after receiving the vaccine I began feeling fatigue in my muscles and joints. Within a half hour I start to feel cold and used a heating blanket to warm up. Despite being under a heating blanket, I began shivering and feeling pain and soreness in my muscles and joints. The shivering became severe and the pain increased. The shivering went on for about an hour and a half and finally started to subside. I was able to fall asleep, but woke up again about 30 minutes later and started to feel hot. I had a fever of 102.6, but felt like my insides were on fire. That went away approximately three hours later. I am still feeling a lot of fatigue, it my temperature seems to have leveled out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin and magnesium citrate
Allergien: None known
Vorherige Impfungen: Influenza symptoms from influenza shot approximately 2003, 2004

VAERS 1870131

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 26,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Headache Hot flush

Symptomtext

Hot flash , headache

Weitere VAERSDATA-Felder

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

VAERS 1869481

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: KS
Alter: 29,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Injection site erythema Injection site reaction Injection site swelling Injection site warmth Pain in extremity Urticaria

Symptomtext

arm is extremely sore- below injection site is very red, swollen, and hot to the touch. It looks like a giant welt, it has grown in size each day

Weitere VAERSDATA-Felder

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

VAERS 1868597

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IL
Alter: 49,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dry throat Dysphonia Urticaria

Symptomtext

Dry throat and later voice was scratchy and hoarse within 10 minutes of the vaccine Two hives two hours after the vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic idiopathic urticaria
Andere Medikamente: claritin 20 mg vit d3 4000IU
Allergien: shellfish nickel ?pfizer covid vaccine
Vorherige Impfungen: Covid 19 Pfizer #2 vaccine on 1/11/2021. dry throat and later scratchy voice and hoarse voice within 30 minutes of vaccines. One

VAERS 1866980

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NH
Alter: 25,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: -
Beginn: 10.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Body temperature Body temperature increased Pain

Symptomtext

SIGNIFICANTLY ELEVATED TEMPERATURE (NOT SURE WHAT THE TEMPERATURE WAS); PAIN IN THE ENTIRE BODY (TEETH HURTS, HAIR AND HEAD HURTS, LAYING ON THE PILLOW, CRYING DUE TO THE PAIN); This spontaneous report received from a parent concerned a 25 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: Hashimoto's thyroiditis. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1855194, expiry: UNKNOWN) dose was not reported, administered on 10-NOV-2021 16:00 for prophylactic vaccination. No concomitant medications were reported. On NOV-2021, treatment medications included: ibuprofen. On 10-NOV-2021, the patient experienced pain in the entire body (teeth hurts, hair and head hurts, laying on the pillow, crying due to the pain). On 11-NOV-2021, the patient experienced significantly elevated temperature (not sure what the temperature was). Laboratory data included: Body temperature (NR: not provided) Elevated. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from pain in the entire body (teeth hurts, hair and head hurts, laying on the pillow, crying due to the pain) on NOV-2021, and had not recovered from significantly elevated temperature (not sure what the temperature was). This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 20211111; Test Name: Body temperature; Result Unstructured Data: Elevated; Comments: Elevated
Aktuelle Erkrankungen: Hashimoto's thyroiditis
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1865925

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MI
Alter: 43,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Blood pressure increased Dizziness Throat irritation

Symptomtext

Patient received the vaccine at 5:35pm. Our intern, gave it to her and was in the consultation room for quite awhile (7-10 minutes) before she consulted me. said that the patient is sitting down in the room, but it having some throat itching. I then went into the room to help and talk with . I first asked her how she was feeling. She said "ok" but was having throat itching, but no other symptoms right now. I had the Epi-pen out and ready to administer if she were to have any other severe symptoms. We then talked extensively about her allergies and how she was very nervous to get the vaccine at all; she had put it off until the last minute and had done a lot of research with her doctor about which one to get so she could avoid 100% of her allergies. She saw that the J & J vaccine contained something of a yellow stain/dye, but upon further investigation, it was a plant derived oil and she was comfortable getting it. While we talked, I took her blood pressure and kept monitoring for any other symptoms (fainting, lip swelling, tongue swelling, etc.). She never experienced any other symptoms besides a little bit of lightheadedness that went away. Her blood pressure was elevated (170/110, 156/100) but was coming down each time. She stated that her blood pressure at home and in the office is usually 128/86 or around there. was very anxious at first, but calmed down immensely after sitting and talking with her for over an hour. We gave her water and she purchased a box of diphenhydramine 25mg and took two of them around 5:50pm. By 6:30pm she was much more calm and was comfortable leaving and meeting her husband who was right down the street. I told her to come back or call me if she needed anything else or had any other questions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown. Known past of anaphylaxis reaction to chlorhexidine and severe reactions to yellow dye.
Vorgeschichte: Severe allergies
Andere Medikamente: Unknown
Allergien: Prednisone, chlorhexidine, yellow dye
Vorherige Impfungen: -

VAERS 1865171

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IN
Alter: 41,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chills Feeling hot Hypoaesthesia Injection site pain Insomnia Pain Renal pain

Symptomtext

24 hours later: severe chills, aches, no fever. Severe pain throughout body but most severe in kidney area and at injection site. Numbness in left arm. After the chills went away after about 6 hrs., started burning up but again, no fever, still in pain. Insomnia. Treated with 2 Advil liquidgels and 1 benadryl.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Zero
Vorgeschichte: Hypertensive, asthma, obesity
Andere Medikamente: Metformin, metoprolo, hydrochlorothiazide.
Allergien: Demerol. Phenergen. Sulfa. Erithromycin. Peanuts.
Vorherige Impfungen: -

VAERS 1860669

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Cough Headache Injection site pain Oropharyngeal pain

Symptomtext

cough, sore throat, headaches, chest heaviness, still sore on vaccine site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: bronchitis, obesity
Andere Medikamente: Cepacol
Allergien: none
Vorherige Impfungen: Influenza Vaccine

VAERS 1860104

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IA
Alter: 72,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: -
Beginn: 03.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Dizziness Fatigue Hypersomnia

Symptomtext

FELT DIZZY; COULDN'T STAY AWAKE; FATIGUE; This spontaneous report received from a patient concerned a 72 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: allergies. The patient was previously treated with covid-19 vaccine ad26. cov2. s for prophylactic vaccination. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported and batch number: 1855194 expiry: 09-APR-2022) dose was not reported, administered on 03-NOV-2021 for prophylactic vaccination. Concomitant medications included dupilumab for allergies. On 03-NOV-2021, the patient experienced felt dizzy. On 03-NOV-2021, the patient experienced couldn't stay awake. On 03-NOV-2021, the patient experienced fatigue. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from felt dizzy, couldn't stay awake, and fatigue on 05-NOV-2021. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy multiple (patient had 30 different allergies).
Vorgeschichte: Comments: Unknown
Andere Medikamente: Dupixent
Allergien: -
Vorherige Impfungen: -

VAERS 1858816

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: SC
Alter: 36,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 07.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Dysuria Fatigue Headache Lethargy Myalgia

Symptomtext

Headache, chills, lethargy and exhaustion, muscle pain (back, arms, neck), and pain urinating -- originating around 3 AM which was 12 hours after vaccination, lasted until went to bed the day following vaccination around 8 PM. Symptoms much reduced the next morning (6 AM) and not detectable by the next day after.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: zinc, vitamin c
Allergien: -
Vorherige Impfungen: -

VAERS 1858426

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Dizziness

Symptomtext

Client received Booster dose of COVID vaccine Janssen (lot # 1855194, exp 04/09/2022) in left arm and Fluarix in right arm today at 9:05 am. At 9:10 client was sitting on park bend and stated she felt ?dizzy? to PHN. Client denied itchiness, denied nausea, skin was dry and appropriate to Ethnicity. Client stated she hasn?t eaten yet today, denies history of syncope with vaccines. Vitals taken at 9:20 am: BP 123/90, HR 87 bpm, SpO2 95%, RR 20. Client has no known allergies. Client reports history of chronic pain, Hypertension, Anxiety, and Depression. Client takes ibuprofen and antibiotics currently. Client reports primary PMD is doctor with facility. At 9:23 am PHN assisted client to lie down, and client ate some food. At 9:25 am client sat up, stated she ?felt better? and the dizziness was gone. Vitals taken at 9:30 am: 130/88, HR 86 bpm, SpO2 98%, RR 18. PHN educated client s/s of concern and when to call 9-1-1. Client stood up at 9:37 am and walked off with a steady gait.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: chronic pain, HTN, anxiety, depression
Andere Medikamente: ibuprofen and "anitbiotics"
Allergien: NKA
Vorherige Impfungen: -

VAERS 1856607

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MI
Alter: -
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: -
Beginn: 06.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Dizziness Faeces discoloured Malaise

Symptomtext

LIGHT HEADED; DARK BLACK COLOR STOOL; FELT LIKE SICK; This spontaneous report received from a patient concerned a 23 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no pain. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, and expiry: UNKNOWN) dose was not reported, administered on 05-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 06-NOV-2021, the patient experienced dark black color stool. On 06-NOV-2021, the patient experienced light headed. On 06-NOV-2021, the patient experienced felt like sick. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from light headed, and the outcome of dark black color stool and felt like sick was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

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

VAERS 1854066

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: NJ
Alter: 57,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Dizziness Hyperhidrosis Pain in extremity Pallor

Symptomtext

Patient reported he felt dizzy/lightheadedness few minutes after getting the covid-19 vaccine. He admits feelings of anxiousness in getting the vaccine, as he was scared to get the vaccine but he got the vaccine (Janssen) due to it being required for his job. His physical exam was normal except he was pale and diaphoretic. Blood pressure was 106/72 heart rate 62, oxygen saturation 99%.He was monitored for 35 minutes and reported feeling well. Blood pressure rose to 112/78. He left facility in stable condition with his wife. Charge nurse followed up with wife the next day 11/9 and patient was said to only be experiencing a sore arm. Stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension
Andere Medikamente: aspirin 25mg daily losartan 25mg daily
Allergien: -
Vorherige Impfungen: -

VAERS 1851229

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MN
Alter: 44,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Heart rate increased Hyperhidrosis Pyrexia

Symptomtext

Very high heart beat. Lasted about 4-6 hours. Fever - lasted appoximately 48 hours Constant sweating , still persisting over 80 hours after vaccine administration, yet no fever at this time.

Weitere VAERSDATA-Felder

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

VAERS 1850784

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: VT
Alter: 53,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 29.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Pruritus Urticaria

Symptomtext

HAVE BEEN EXPERIENCING ITCHY SPOTS ON LEFT ARM, LEFT HIP WITH HIVE LOOKING BUMPS FOR SEVERAL DAYS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: BUPROPION
Allergien: NONE
Vorherige Impfungen: -

VAERS 1849581

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chills Diarrhoea Fatigue Feeling cold

Symptomtext

Client reports receiving "Cansino" COVID-19 vaccine in April 2021. Client reports that one and a half days later, she experienced diarrhea, chills, felt cold and was fatigued for about 2 hours. Client reports that symptoms resolved after taking an Acetaminophen-like medication. Client reports drug allergies to "phedrines" medications. Elevated to Clinical Supervisor, who received approval from medical provider for client to receive Janssen COVID-19 vaccine, according to current Interim CDC Guidelines. Explained risks/benefits/emergency precautions to client who verbalizes understanding and provides this nurse with verbal consent to administer Janssen COVID-19 vaccine (Lot # 1855194). No adverse side effects noted or reported by client during 15 minute post-observation period. - , RN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: none reported by client
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1844536

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 02.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Pruritus

Symptomtext

Client reported itchiness to her left leg 6 hours after the Moderna shot. Two weeks later she reported general numbness and was treated by her MD with steroids. She currently experiences intermittent numbness when stressed out. MD approved her to get the Janssen and she received it on 11/3/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: cast material
Vorherige Impfungen: -

VAERS 1843180

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness

Symptomtext

After approximately 18 minutes, veteran endorsed feelings of lightheadedness/wooziness. S/s lasted for approximately 20 minutes; self resolved with veteran in reclined position, drank water. O2 sats stayed between 96-100% on RA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Lidocaine, nuts, sesame seeds, immunotherapy treatments
Vorherige Impfungen: -

VAERS 1842835

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: IN
Alter: 56,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Headache Myalgia Pyrexia

Symptomtext

Fever, full body muscle and joint pain, very bad headache. These all mostly cleared within 48 hours. Some muscle / joint pain still

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: head cold
Vorgeschichte: HBP, T2 diabetes
Andere Medikamente: Metformin, Tribenzor, Cialis
Allergien: none
Vorherige Impfungen: -

VAERS 1841219

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: FL
Alter: 40,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Decreased appetite Fatigue Headache Neck pain Pyrexia

Symptomtext

Headache, neck and joint pain, fatigue, mild fever ( <100), loss of appetite. Symptoms lasted for 24hrs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: None
Andere Medikamente: Vitamin C, Zinc, B12
Allergien: Dairy, Gluten, Eggs
Vorherige Impfungen: -

VAERS 1840630

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: AZ
Alter: 33,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fatigue Swelling Throat tightness

Symptomtext

Pt reported within 10 minutes of recieving vaccine that their throat felt a little tight and asked for some water. Asked patient to stay and gave them 50mg diphenydramine. Patient stayed and was observed for 40 more minutes and stated they weren't any worse or better but tired and wanted to go home. Called patient about 2 hours later and they stated they were okay but still a bit swollen. He put ice packs on for 20 minutes and it went down. Called patient 2 hours after that and they stated their symptoms completely resolved. He also stated that he works with various viruses at work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: OTC- Melatonin 3mg supplement
Allergien: Iodine and shellfish
Vorherige Impfungen: -

VAERS 1840394

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: OR
Alter: 43,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chills Confusional state Dizziness Fatigue Feeling abnormal Feeling cold Headache Impaired work ability Myalgia Nausea Pyrexia

Symptomtext

About 3 hours after the injection, i started to feel very fatigued, headache, light headed, dizzy, and nauseous. I went to lay down and I literally felt the fever rising in my body. I was freezing cold with muscle aches coming on and the headache getting more severe. I fell asleep and my husband woke me up in the night because I was having chills so bad that he thought I was convulsing. The chills and fever went thru the night into the next day. Most of the symptoms subsided by the next evening except for the headache, dizziness, confusion, and a mental fog. I am now 6 days past the injection and my headache, dizziness, and mental fog will not go away. I am exhausted and can barely write this. I am putting in sick days to miss work for the rest of the week. This is awful.

Weitere VAERSDATA-Felder

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

VAERS 1840085

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Chills Hyperhidrosis Injection site pain Myalgia Pyrexia

Symptomtext

Muscle aches and tendernes of the injection site all day chills from 5:45am-1:30pm fever of 99.8 to 103.7 from 7:26am-1:53pm heavy perspiration from 2:00pm-3:17pm (this all took place the day after the injection and only lasted that day.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, seasonal allergies
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1833408

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: OH
Alter: 47,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Arthralgia Dizziness Erythema Mouth swelling Nausea Swollen tongue Vision blurred

Symptomtext

swollen tongue and roof of mouth, face felt swollen (not sure it was it just felt like alot of pressure on the face) that lasted approx 4 hrs light headed, nauseated (lasted 24 hrs) and blurred vision that lasted 4 hrs. I had a 4in red line on my forearm/wrist with pain (not constant pain just every once in awhile i'd get a shooting pain in wrist ) that went away after approx 3 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: mens multivitamin (Code Age is the brand name)
Allergien: neosporan
Vorherige Impfungen: -

VAERS 1833404

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: TX
Alter: 31,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 01.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Chills Pain Pyrexia

Symptomtext

Persistent high fever (101.7-103.6 dF) lasting >24hrs and not responsive to Tylenol; chills; body aches; persistent abdominal pain after eating and drinking lasting one full week (through current and not resolved at time of report)

Weitere VAERSDATA-Felder

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

VAERS 1833105

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: FL
Alter: 36,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Headache Muscle tightness Pain in extremity

Symptomtext

Pain and tightness in my left leg Headache Sore arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Epilepsy
Andere Medikamente: Levetiracetam 500 mg
Allergien: -
Vorherige Impfungen: -

VAERS 1832374

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 31.10.2021
Impfdatum: 28.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Extra dose administered Hypoaesthesia Lymph node pain Lymphadenopathy Pain Pain in extremity

Symptomtext

Received booster vaccination on Thursday (10/28). Friday I felt achy but nothing that kept me down. On Sat. 10/30 I had at least a 4.5 x 3 inch lymphadenopathy under my left axilla. It was very prominent. I had no reaction with my first J&J shot. Today yet I still have soreness in my left arm. Nothing painful but I did not have that with my first shot. Today the lymphadenopathy is not as bad but still persists. The lymph node(s) are sore not painful. Yesterday I had some numbness in my distal hand but that seems to have resolved. I have never had any reactions to any type of vaccinations like this. Truly this type of reaction concerns me and makes me hesitant to ever get additional Covid vaccinations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Recent A. Flutter which is now in NSR
Andere Medikamente: Diltiazem Flecanide Apixaban
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1829646

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: SD
Alter: 74,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Injection site haemorrhage Product administered at inappropriate site

Symptomtext

The injection was suposed to go into deltoid muscle at my upper arm. They did not asperate but just gave me shot. when needle was removed their was blood on my arm so obviously a blood vessel was hit it was not given intermusclular. I have no side effects yet but there has been a lot of publicity about side effects caused by hitting a blood vessel by mistake. I wanted to report this now so If I develop cardiac or other new conditions you can relate these e vents together.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site haemorrhage
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no illnesses, long term conditions I have had 10 years or mor
Vorgeschichte: lots
Andere Medikamente: 21 orescriptions
Allergien: 15 to drugs plus insects,dust
Vorherige Impfungen: -

VAERS 1829507

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cough Interchange of vaccine products Nausea Pruritus Throat tightness Vomiting

Symptomtext

Pt had previous reaction to Moderna first dose on 7/8. Pt received Janssen dose to complete primary series. 40mins post vaccination, pt c/o Nausea, Vomiting, itching of the neck and arms, cough, throat tightness. Vitals:@18:30 BP 137/79, HR 68, RR 18 Pt had gradually worsening symptoms. no visible rash. Lungs CTAB, good air movement. @18:30 Pt was administered 25mg IM Benadryl to Right Deltoid Recommended pt go straight to urgent care for further observation as a precaution, accompanied by daughter. Recommended pt also f/u w/ PCP. It is unclear if the patient went to Urgent Care. Next visit known to this writer was 10/28 for dental concerns. No mention of continued symptoms at that visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Positive TB test, Depression, Abnormal Pap Smear in 2001, Severe Cervical Dysplasia 2003
Andere Medikamente: Unknown current medication list
Allergien: Allergies: Moderna Covid Vaccine
Vorherige Impfungen: -

VAERS 1827887

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: PA
Alter: 38,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Back pain Chills Cold sweat Headache Musculoskeletal discomfort Myalgia Neck pain Pain in jaw Pyrexia

Symptomtext

Fever of 100.00, muscle pain, head and neck pain, sore jaw, sore back, joint discomfort, chills, cold sweats.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Shellfish, but I was told by the vaccine administer that this was irrelevant as the vaccines do not cause allergic reactions.
Vorherige Impfungen: -

VAERS 1825626

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: TX
Alter: 39,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Fatigue Headache

Symptomtext

Morning of 10/26/2021, felt tired and with a headache (like a bad hangover). Rested during the day, plenty of fluids. Morning of 10/27/2021, mostly symptoms were gone. In the afternoon (around 5pm), headache came back. Took Tylenol and went to bed at some point Morning of 10/28/2021, no headache in bed, but about 30 minutes after getting out of bed, despite hydration, headache came back

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Zyrtec once a day
Allergien: Allergy to pollen - but pollen count is super low/non-existent this week, as per pollen reports Allergy to Aspirin, Levofloxacin
Vorherige Impfungen: Just sore arm after some vaccines, nothing too concerning

VAERS 1818732

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: CO
Alter: 55,0
Geschlecht: M
Eingang: 26.10.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Gastrointestinal disorder Heart rate increased Nausea Vomiting

Symptomtext

Patient's spouse contacted the pharmacy report husband was experiencing nausea. I discussed the prevalence of the GI side effects and mentioned the increased heart rate may be due the nausea and vomiting. I encouraged them to contact their provider.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Not on file
Allergien: No
Vorherige Impfungen: -

VAERS 1818418

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 01.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Cough Ear discomfort Eye inflammation Eye pain Headache Ocular hyperaemia Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test negative Swelling of eyelid Tinnitus

Symptomtext

On the night of the vaccine I started with fever, articulation pain (spine, knees, fingers), headache and loud ringing in left ear. This continued over the weekend (Saturday and Sunday). On Sunday night I developed pain in my right eye. On Monday morning, the right eyelid was swollen and my inside eye was a deep red color. It was oozing pus (at first I could not open my eyelid). On Tuesday morning, my left eye is also now swollen and red with pus. On Monday the fever and body aches have gone BUT I started with a very bad, continuous cough and sore throat that continues today (Tuesday). I am taking cough suppressant in order to sleep. Both eyes are inflamed, I believe due to the vaccine. My ears are sore (feeling of fullness and are ringing) I believe due to the vaccine. The vaccine made my previous mild cough much worse. On Tuesday I had a medical appointment with my health provider at health care, who advised me to report to this system.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Negative PCR test with MD. Taken on Tuesday, 19 October, negative result on Thursday 21st October.
Aktuelle Erkrankungen: one week prior: mild cold, cough (with NEGATIVE PCR TEST).
Vorgeschichte: ASTHMA IN PAST, OCCASIONAL OUTBREAKS OF ECZEMA DUE TO CHEMICALS/PERFUMES
Andere Medikamente: none
Allergien: Sensitivity to strong chemicals like cleaning products / perfumes (cause eczema) and some medicines cause asthma.
Vorherige Impfungen: -

VAERS 1815258

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: GA
Alter: 18,0
Geschlecht: M
Eingang: 25.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Fall

Symptomtext

Patient felt light headed and finally collapsed to the Ground.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Not known
Allergien: NKA
Vorherige Impfungen: -

VAERS 1807785

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

mild

Staat: MD
Alter: 31,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hyperhidrosis

Symptomtext

1 minute after administration of the vaccine the person became diaphoretic and complained of dizziness. His resp. rate was noted to be 22. BP checked @ 314p was 67/38, hr. 42. He was given water, then placed on the floor with his feet up. Spoke to my medical director Arsalan Sheikh who recommended calling 911. Informed pt. of same but he asked that they not be called. Called pts. wife and informed her of the situation. Rechecked BP @ 315, 70/39 hr. 42. After lying prone for 6 mins. he reported feeling much better BP 119/66 hr 52, oxygen sat. 95%. Please note the patient informed us upon entering for his shot that he didn't believe in it and was only getting it so that he could keep his job and appeared anxious.

Weitere VAERSDATA-Felder

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

VAERS 2702460

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MN
Alter: 36,0
Geschlecht: F
Eingang: 26.10.2023
Impfdatum: 30.11.2021
Beginn: 14.03.2022
Tage bis Beginn: 104,0
Dosis: 1
Route/Site: IM / UN

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

N-terminal prohormone brain natriuretic peptide increased

Symptomtext

03/03/2021 NT-PRO BNP Result 36 pg/ML 11/30/2021 COVID VACCINE 03/14/2022 NT-PRO BNP Result 80 pg/ML 10/09/2023 NT-PRO BNO Result 236 pg/ML

Weitere VAERSDATA-Felder

Praegender Schweregrund: N-terminal prohormone brain natriuretic peptide increased
Hospital-Tage: -
Labordaten: 03/03/2021 NT-PRO BNP Result 36 pg/ML 11/30/2021 COVID VACCINE 03/14/2022 NT-PRO BNP Result 80 pg/ML 10/09/2023 NT-PRO BNO Result 236 pg/ML
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Keflex
Vorherige Impfungen: -

VAERS 2701461

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: TN
Alter: 68,0
Geschlecht: F
Eingang: 25.10.2023
Impfdatum: 19.11.2021
Beginn: 29.09.2023
Tage bis Beginn: 679,0
Dosis: 2
Route/Site: - / -

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

Breakthrough COVID-19

Symptomtext

Covid-19 Breakthrough Infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breakthrough COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Chronic Anemia, CAD, Hypocalcemia, Hypochloremia, MI, PUD, CKD stage 3
Andere Medikamente: ASA, Hydrocodone-Acetaminophen, Levetiracetam, Metformin, Metoprolol, Omeprazole, Ondansetron, Pantoprazole, Prasugrel
Allergien: Ace Inhibitors, Cephalosporins, PCN, Tramadol
Vorherige Impfungen: -

VAERS 2678847

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 03.09.2023
Impfdatum: 04.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac discomfort Electrocardiogram normal Laboratory test normal

Symptomtext

Roughly one month after vaccine, started getting sharp rushes to heart at random points during the day (e.g., not during exercise or physical activity; even when sitting). Not painful, more like a dull pressure. But they are uncomfortable, and I never had them before the vaccine. These flashes last 1-2 seconds and then go away. Happen several times per day. They've continued to occur over the course of almost 2 years since I received the vaccine. The frequency of these flashes of dull pressure in my upper left chest / heart area have reduced significantly but they still happen from time to time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac discomfort
Hospital-Tage: -
Labordaten: Went to doctor. They did an ECG and other tests. Said they saw/found nothing wrong with my heart.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2672903

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 17.08.2023
Impfdatum: 30.10.2021
Beginn: 24.03.2023
Tage bis Beginn: 510,0
Dosis: 2
Route/Site: IM / LA

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

Atrial flutter Obstructive sleep apnoea syndrome

Symptomtext

ADULT OBSTRUCTIVE SLEEP APNEA, MILD 5/1/2023 ATRIAL FLUTTER, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2655687

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: GA
Alter: 38,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 14.03.2021
Beginn: 01.05.2023
Tage bis Beginn: 778,0
Dosis: UNK
Route/Site: - / LA

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

Cardiomyopathy Catheterisation cardiac abnormal Chronic left ventricular failure Ejection fraction decreased

Symptomtext

Left heart catheterization, non-ischemic cardiomyopathy, Ef estimated at 35% to 40% 5/01/2023 7:17 am Chronic systolic Heart failure

Weitere VAERSDATA-Felder

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

VAERS 2631780

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 12.05.2023
Impfdatum: 11.05.2022
Beginn: 22.06.2022
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: IM / LA

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

Atrial fibrillation Cardiac ablation

Symptomtext

Afib flare requiring cardiac ablation after booster covid vax.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atrial fibrillation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism, senile osteomalacia, mild intermittent asthma, Pure Hypercholesterolemia, nonrheumatic mitral
Andere Medikamente: See attach
Allergien: NKA
Vorherige Impfungen: -

VAERS 2603245

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IA
Alter: 24,0
Geschlecht: F
Eingang: 20.03.2023
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Interchange of vaccine products

Symptomtext

Patient came to clinic today to receive Janssen covid vaccine. This RN looked up patient is system and saw she had Pfizer dose on 08/27/2021. This RB educated and encouraged the completion of the Pfizer series. Patient reported she had a new employer that was recommending she now receive Janssen dose. This RN educated on the recommendations of boosters, and she would need a booster at 2 moths following the Janssen dose versus 6 months if she completed the Pfizer series. Patient declined the Pfizer dose and reported she only wanted Janssen. Patient educated about possible adverse effects and side effects. Patient verbalized understanding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Sulf
Vorherige Impfungen: -

VAERS 2581652

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 14.02.2023
Impfdatum: 02.12.2021
Beginn: 26.01.2023
Tage bis Beginn: 420,0
Dosis: 1
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after Janssen vaccine

Weitere VAERSDATA-Felder

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

VAERS 2574759

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MI
Alter: 54,0
Geschlecht: F
Eingang: 03.02.2023
Impfdatum: 02.11.2021
Beginn: 24.08.2022
Tage bis Beginn: 295,0
Dosis: 2
Route/Site: - / -

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

Body temperature COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient via a company representative concerned a 55 year old female. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1802072, expiry: unknown) dose was not reported, 1 total, administered on 11-MAR-2021 for covid-19 prophylaxis. It was unknown whether patient had any adverse event following vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient additionally received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194, expiry: unknown) dose was not reported, 1 total, administered on 02-NOV-2021 for covid-19 prophylaxis. Age at time of vaccination 54 years old. No concomitant medications were reported. On 24-AUG-2022, the patient got a fever out of nowhere of 104 (dose number in series 2). On 25-AUG-2022 and 26-AUG-2022, it was staying high could not break it. On 26-AUG-2022 (at night), the doctor called her husband and told him to have her get a PCR (polymerase chain reaction) even though none of the symptoms were there and all at home tests (covid-19 test) were negative. On 27-AUG-2022 (Saturday, in the morning), even the one she took (home test) was negative, the patient woke up and felt like a whole new person and nothing happened. Hence on same day, she went to the pharmacy (consumer value store) to get her PCR test. Patient further stated that, she went shopping (masked), went out to dinner, and felt fine, all was well. On 29-AUG-2022 (Monday), patient got up to go to work. Her husband asked her to take another test. She turned off her street and her husband called her and said it was positive which led to confirmed covid-19 infection and thus had confirmed clinical vaccination failure (dose number in series 2). Patient stated, she was shocked since she felt fine, no symptoms, no fever, nothing. She was absolutely fine. Her work said not to come in for 5 days. So she went back home and to her shock the pharmacy and department of health called within 10 minutes of each other that she had a positive PCR test. On 30-AUG-2022 (Tuesday), she lost some taste but she was fine, working out, working from home, not feeling ill at all (dose number in series 2). A friend told her to eat as much spicy food as she could handle, she did. On 31-AUG-2022 (Wednesday), she could taste everything again. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000269194.; Sender's Comments: V0: 20230163685- 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: Body temperature
Hospital-Tage: -
Labordaten: Test Date: 20220824; Test Name: BODY TEMPERATURE; Result Unstructured Data: 104; Test Date: 20220826; Test Name: COVID-19 VIRUS TEST (HOME TEST); Test Result: Negative ; Test Date: 20220827; Test Name: COVID-19 VIRUS TEST (HOME TEST); Test Result: Negative ; Test Date: 20220827; Test Name: SARS-COV-2 PCR TEST; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2521970

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: OH
Alter: 27,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 02.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: SYR / LA

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

Dysmenorrhoea Menstrual disorder

Symptomtext

Severe menstral cramping, changes in menstral cycle

Weitere VAERSDATA-Felder

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

VAERS 2468590

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: FL
Alter: 94,0
Geschlecht: F
Eingang: 04.10.2022
Impfdatum: 05.11.2021
Beginn: 01.10.2022
Tage bis Beginn: 330,0
Dosis: 2
Route/Site: IM / RA

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

Unevaluable event

Symptomtext

patient hospitalized

Weitere VAERSDATA-Felder

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

VAERS 2463260

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NJ
Alter: 56,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 10.12.2021
Beginn: 01.03.2022
Tage bis Beginn: 81,0
Dosis: 1
Route/Site: IM / UN

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

Tinnitus

Symptomtext

pt developed tinnitus (ringing in the ear) 3 months after receiving janseen covid19 vaccine

Weitere VAERSDATA-Felder

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

VAERS 2460619

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MI
Alter: 59,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 10.11.2021
Beginn: 20.09.2022
Tage bis Beginn: 314,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after two vaccines Janssen 3/14/21 Lot# 1805020; Janssen 11/10/21 Lot# 1855194

Weitere VAERSDATA-Felder

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

VAERS 2366564

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 08.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 23,0
Dosis: 1
Route/Site: - / RA

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

Neuropathy peripheral

Symptomtext

Peripheral neuropathy.

Weitere VAERSDATA-Felder

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

VAERS 2335701

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: SC
Alter: 59,0
Geschlecht: F
Eingang: 27.06.2022
Impfdatum: 28.10.2021
Beginn: 11.06.2022
Tage bis Beginn: 226,0
Dosis: 2
Route/Site: - / -

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

Blood pressure measurement Heart rate decreased Suspected COVID-19 Vaccination failure

Symptomtext

BEATS PER MINUTE HAD DROPPED BELOW 40; SUSPECTED COVID-19 INFECTION; SUSPECTED CLINICAL VACCINATION FAILURE; This spontaneous report received from a patient via other company (Pfizer) concerned a 60 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received with covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin was not reported, batch number: 1805022 and expiry: UNKNOWN) dose was not reported, 1 total administered on 16-MAR-2021 at 14:30 on right arm for prophylactic vaccination. Age at time of vaccination 59 years old. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194 and expiry: UNKNOWN) dose was not reported, 1 total administered on 28-OCT-2021 at 15:45 on right arm for prophylactic vaccination. No concomitant medications were reported. The patient received paxlovid (form of admin, route of admin not reported, batch number: GA8854 and expiry: unknown) dose was not reported, administered from 08-JUN-2022 to 12-JUN-2022 for treatment of COVID-19. On an unspecified date in 2022, the patient experienced suspected covid-19 infection which was suspected clinical vaccination failure (dose number in series 2). On 11-JUN-2022, the patient lwatch started giving her alerts in the middle of the night that her blood pressure per minute (blood pressure per minute) had dropped below 40 bpm (dose number in series 2). This happened while she was on the drug, Patient took all five days, when she stopped the drug it went away. Patient believe it only dropped her BPM about five points. Patient do not believe she was in any danger. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from beats per minute had dropped below 40 on 12-JUN-2022, and the outcome of suspected covid-19 infection and suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint, and reference number requested.; Sender's Comments: V0:20220647189-COVID-19 VACCINE AD26.COV2.S-Suspected clinical vaccination failure. 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. 20220647189-COVID-19 VACCINE AD26.COV2.S-Beats per minute had dropped below 40. 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: CONMEDS-OTHER SUSPECT DRUGS. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood pressure measurement
Hospital-Tage: -
Labordaten: Test Date: 20220611; Test Name: BLOOD PRESSURE; Result Unstructured Data: below 40 beats per minute
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2320457

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: ME
Alter: 73,0
Geschlecht: M
Eingang: 15.06.2022
Impfdatum: 07.06.2022
Beginn: 07.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Wrong product administered

Symptomtext

Patient came in for a Pfizer COVID Vaccine booster. Received Janssen by mistake.

Weitere VAERSDATA-Felder

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

VAERS 2277806

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IL
Alter: 28,0
Geschlecht: M
Eingang: 15.05.2022
Impfdatum: 10.05.2022
Beginn: 10.05.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Muscle twitching

Symptomtext

Immediately after receiving my booster shot for COVID-19, my calves started twitching. The twitching does not seem to be muscle related, but I could be wrong. It seems to be a nerve system reaction and it's been 5 continuous days of nonstop calf twitching. This is not normal and it is very concerning. I have a follow up appointment scheduled with my doctor to address this concern this coming week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Muscle twitching
Hospital-Tage: -
Labordaten: Not yet.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Finasteride for hair growth.
Allergien: None.
Vorherige Impfungen: -

VAERS 2273059

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MD
Alter: 37,0
Geschlecht: M
Eingang: 12.05.2022
Impfdatum: -
Beginn: 01.05.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Glycosylated haemoglobin Lip swelling Lip ulceration Oral herpes Suspected COVID-19 Vaccination failure

Symptomtext

SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID 19 INFECTION; COLD SORES; LIP SWELLING WITHOUT BREATHING INVOLVEMENT MORE PRONOUNCED ON THE BOTTOM LIP; LIP ULCER; This spontaneous report received from a pharmacist concerned a 37 year old male patient. Initial information was processed along with the additional information received on 10-MAY-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: type 2 DM (diabetes mellitus) without longterm use of insulin (The reporter stated controlled with A1c 6% on 16-FEB-2022, down from 8% on 21-DEC-2021), and autistic disorder of childhood onset, and other pre-existing medical conditions included: The reporter stated that patient had no known drug allergies. On 15-DEC-2021, the patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1855194, and expiry: UNKNOWN) dose was not reported, 01 total, administered to right arm for prophylactic vaccination. The patient age at time of vaccination was 37 years old. Concomitant medications included dextromethorphan hydrobromide/quinidine sulfate, famotidine, hyoscyamine, lorazepam, metformin, omeprazole, ondansetron, propranolol, and risperidone. On 21-DEC-2021, Laboratory data included: HbA1C (Haemoglobin A1C)(NR: not provided) 8 %. On 16-FEB-2022, Laboratory data included: HbA1C (Haemoglobin A1C) (NR: not provided) 6 %. On an unspecified date, the patient had suspected covid- 19 infection and suspected clinical vaccination failure. On 27-APR-2022, the patient was treated for covid-19 with non-company suspect drug Paxlovid (oral route of administration, batch number and expiry were not reported) dose and frequency were not reported. On 01-MAY-2022, on 3 day of medication the patient started lip swelling without breathing involvement, more pronounced on the bottom lip. 01-MAY-2022, the patient had lip ulcer. On an unspecified date, the patient experienced cold sores and improving by using Lysine and (LLT) Abreva on day 4 post non-company suspect drug (Paxlovid) . The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from lip swelling without breathing involvement more pronounced on the bottom lip, lip ulcer, and cold sores, and the outcome of suspected clinical vaccination failure and suspected covid 19 infection was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint: 90000230266.; Sender's Comments: V0-20220516356- Covid-19 vaccine ad26.cov2.s - Suspected clinical vaccination failure. 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: Glycosylated haemoglobin
Hospital-Tage: -
Labordaten: Test Date: 20211221; Test Name: HbA1C; Result Unstructured Data: 8 %; Test Date: 20220216; Test Name: HbA1C; Result Unstructured Data: 6 %
Aktuelle Erkrankungen: Autistic disorder; Type II diabetes mellitus (The reporter stated controlled with A1c 6% 2/16/22, down from 8% on 12/21/21.)
Vorgeschichte: Comments: The reporter stated that patient had no known drug allergies.
Andere Medikamente: NUEDEXTA [DEXTROMETHORPHAN HYDROBROMIDE;QUINIDINE SULFATE]; FAMOTIDINE; HYOSCYAMINE; LORAZEPAM; METFORMIN; OMEPRAZOLE; ONDANSETRON; PROPRANOLOL; RISPERIDONE
Allergien: -
Vorherige Impfungen: -

VAERS 2266522

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: GA
Alter: 46,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 23.12.2021
Beginn: 04.03.2022
Tage bis Beginn: 71,0
Dosis: 1
Route/Site: SYR / LA

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

Abortion spontaneous Chromosome analysis normal Gene mutation identification test Uterine dilation and curettage

Symptomtext

Unexplained miscarriage - no chromosome abnormalities

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abortion spontaneous
Hospital-Tage: -
Labordaten: D&C and genetic lab test 4/06/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Losartan. Synthroid
Allergien: -
Vorherige Impfungen: -

VAERS 2250118

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NC
Alter: 32,0
Geschlecht: F
Eingang: 25.04.2022
Impfdatum: 16.04.2022
Beginn: 16.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Interchange of vaccine products No adverse event

Symptomtext

No adverse event occurred. Recipient had received an initial series of Pfizer, a Moderna booster 12/10/21, and then a second booster of Janssen--which is not approved by the CDC. The individual was not eligible for a second booster and Janssen was incorrect.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2250082

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NC
Alter: 48,0
Geschlecht: F
Eingang: 25.04.2022
Impfdatum: 19.04.2022
Beginn: 19.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Extra dose administered No adverse event

Symptomtext

No adverse event occurred, however, this was an administration error. The recipient had received a dose of Janssen as an initial and booster, then received a second booster of Janssen--which is not approved yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2228383

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NJ
Alter: 39,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Heart rate increased Throat irritation

Symptomtext

Patient got Janssen vaccine after usual intake evaluation. She neglected to say she is allergic to citrate (one component of the vaccine) and realized it later while carefully reading the fact sheet while waiting 30 minutes. Nurse vaccinator monitored her carefully after she c/o a scratchy throat but was otherwise OK except an elevated pulse. Patient took two benedryls she had brought with her. She was anxious and still with scratchy throat, but no respiratory problems. She was encouraged to go to the ED but she did not want to go by EMS. Her husband was called and picked her up. I called at 4:30pm and she was doing well after a trip to the ED where she was given steroids. She was instructed to return to the ED if she had any CP, dizziness, SOB, or palpatations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anxiety
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: ASTHMA
Andere Medikamente: OMEPRAZOLE 40 MG ALBUTEROL HFA 90 MCG INHALOR FLONASE 50 MCG
Allergien: ASPIRIN, CITRATE, DYE, IBUPROFEN, MEPERIDINE AND PENICILLIN
Vorherige Impfungen: -

VAERS 2196501

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: -
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: 07.03.2022
Beginn: 08.03.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Burning sensation Chest discomfort Full blood count Glycosylated haemoglobin Haemoglobin Laboratory test Lipids Metabolic function test Platelet count

Symptomtext

Pt states recvd J & J vaccine 3/7/22 on left arm at Rite-Aid (Lot# 1855194). Pt reports "burning" chest discomfort the day after and regularly since 3/8/22. Pt is new with no prior cardiac disease. Pt denies SOB and left arm pain. Pt rates pain 4/10 and stable at that pain level.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Burning sensation
Hospital-Tage: -
Labordaten: 3/24/2022 LABS CBC (INCLUDES DIFF/PLT) COMPREHENSIVE METABOLIC PANEL HEMOGLOBIN A1C LIPID PANEL
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2190260

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: OH
Alter: 60,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 03.03.2022
Beginn: 14.03.2022
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: SYR / RA

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

Herpes zoster

Symptomtext

Severe case of Shingles approximately 2 weeks after receiving Johnson and Johnson Covid vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: Emergency room visit on 3/17/2022 at local Hospital
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine
Allergien: None
Vorherige Impfungen: -

VAERS 2208964

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NY
Alter: 13,0
Geschlecht: M
Eingang: 18.03.2022
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

GIVEN TO SOMEONE UNDER 18

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2208959

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NY
Alter: 16,0
Geschlecht: M
Eingang: 18.03.2022
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

j&J GIVEN TO SOMEONE UNDER 18

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2183544

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

COVID-19 TEST POSITIVE; This spontaneous report received from a consumer concerned a 48 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26. cov2. s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 206A21A, and expiry: 20-DEC-2021) dose was not reported, 1 total, administered at left arm on 08-APR-2021 for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26. cov2.s (dose number in series 1). The patient received booster covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194, and expiry: 08-JUL-2022) dose was not reported, 1 total, administered at left arm on 04-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient took Binax Now at home test laboratory data (dates unspecified) included: COVID-19 virus test (NR: not provided) and tested positive (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of covid-19 test positive was not reported. This report was non-serious. This case, from the same reporter is linked to 20220329517.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Name: COVID-19 virus test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2181401

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NJ
Alter: 49,0
Geschlecht: M
Eingang: 16.03.2022
Impfdatum: 03.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

COVID-19 TEST POSITIVE; This spontaneous report received from a patient concerned a 49 year old male of unspecified ethnicity. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26. cov2. s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 041A21A expiry: 18-DEC-2021) dose was not reported, 1 total, administered at left arm on 07-APR-2021 for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26. cov2.s. (dose number in series 1). The patient received booster dose of covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194 expiry: 08-JUL-2022) dose was not reported, 1 total, administered on 03-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient took Binax now at home test Laboratory data (dates unspecified) included: COVID-19 virus test (NR: not provided) and tested positive (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of covid-19 test positive was not reported. This report was non-serious. This case, from the same reporter is linked to 20220331195.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Name: COVID-19 virus test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2178551

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: WA
Alter: 17,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 11.02.2022
Beginn: 11.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient was vaccinated with the Janssen COVID-19 vaccine. He was not eligible to receive it as he is minor. Patient did not report having an adverse reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: No
Vorherige Impfungen: -

VAERS 2144849

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 22.11.2021
Beginn: 11.12.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: - / -

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

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

Symptomtext

Event occurred after Janssen vaccine; breakthrough case admission

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 12/11/2021 COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2134614

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 23.02.2022
Impfdatum: 17.11.2021
Beginn: 21.01.2022
Tage bis Beginn: 65,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19

Symptomtext

covid-19 illness

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 24,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2134600

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 27.03.2021
Beginn: 20.02.2022
Tage bis Beginn: 330,0
Dosis: 2
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Event occurred after full vaccination. Patient was diagnosed with Covid Tylenol Discharged Home

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 2,0
Labordaten: Covid test positive
Aktuelle Erkrankungen: -
Vorgeschichte: GERD, High BP, Obesity, Visual Impairment, IBS
Andere Medikamente: -
Allergien: cefoxitin, clindamycin, latex, tape
Vorherige Impfungen: -

VAERS 2125776

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: -
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: -
Beginn: 09.02.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Vaginal haemorrhage

Symptomtext

VAGINAL BLEEDING; This spontaneous report received from a health care professional (registered nurse) concerned a female of unspecified age, race and ethnicity. The patient's height, and weight were not reported. The patient's concurrent conditions included: post-menopause. The patient previously received covid-19 vaccine ad26. cov2. s (unspecified manufacturer) (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 171808 and expiry: unknown) dose was not reported, 1 total administered on unspecified date for prophylactic vaccination. The patient experienced side effects after her first shot (dose number in series 1). The patient received booster covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194, and expiry: unknown) dose was not reported, 1 total administered at left arm on 06-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 09-FEB-2022, the patient experienced vaginal bleeding (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of vaginal bleeding was not reported. This report was non-serious. This case, involving the same patient is linked to 20220242139.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaginal haemorrhage
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Postmenopause
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123737

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CO
Alter: 34,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

No adverse event Wrong product administered

Symptomtext

Patient came into the clinic for a Moderna booster (3rd shot). The actual vaccine given was 0.25 ml of Janssen. Patient was notified of the error on 2/17. Spoke with patient on 2/18 and he was not experiencing any adverse reactions.

Weitere VAERSDATA-Felder

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

VAERS 2123727

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CO
Alter: 30,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

No adverse event Wrong product administered

Symptomtext

Patient came into the clinic for a Moderna booster (3rd shot). The actual vaccine given was 0.25 ml of Janssen. Patient was notified of the error on 2/17. Spoke with patient on 2/18 and she was not experiencing any adverse reactions.

Weitere VAERSDATA-Felder

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

VAERS 2123563

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: WA
Alter: 17,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

Vaccine given to patient less than 18 years old. The vaccinator miscalculated the age of the patient when asked her birthdate. The patient was accompanied by parent. Both signed the pre-vaccination screening form, which stipulated the required age of 18 for the Janssen (Johnson & Johnson) vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None indicated on intake.
Vorgeschichte: None indicated on patient intake form.
Andere Medikamente: None indicated on patient intake form.
Allergien: None indicated on patient intake form.
Vorherige Impfungen: -

VAERS 2116328

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: OR
Alter: 27,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 02.12.2021
Beginn: 10.01.2022
Tage bis Beginn: 39,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

I started with a sore throat and fever of around 102 F. Managed that with Tylenol. I also had a lot of mucus and drainage. I got an at home test and it came out positive. Doctor said just stay home and treat the symptoms. I was out of work from 1/10-1/15 due to illness. I received Johnson & Johnson for my booster but had Moderna for my first 2 doses.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Prozac, Zyrtec
Allergien: Codeine, Seasonal
Vorherige Impfungen: I got the rabies series and I had the side effects that are common.

VAERS 2115615

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MD
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: -
Beginn: 07.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Off label use SARS-CoV-2 test Suspected COVID-19 Wrong technique in product usage process

Symptomtext

SUSPECTED COVID-19 INFECTION; OFF LABEL USE; WRONG TECHNIQUE IN DRUG USAGE PROCESS; 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: bronchitis, chronic sinus infection, and drug allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, and expiry: 09-APR-2022) dose was not reported, administered on 07-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 07-DEC-2021, the patient experienced off label use, and wrong technique in drug usage process. On 01-JAN-2022, the patient experienced suspected covid-19 infection. Laboratory data included: COVID-19 virus test (NR: not provided) Positive. Laboratory data (dates unspecified) included: COVID-19 virus test (NR: not provided) Negative, Negative. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from suspected covid-19 infection, and the outcome of off label use and wrong technique in drug usage process was not reported. This report was non-serious.; Sender's Comments: V0-Medical assessment comment not required as per standard procedure as the case was assessed as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: Test Date: 20220101; Test Name: COVID-19 virus test; Result Unstructured Data: Positive; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Test Name: COVID-19 virus test; Result Unstructured Data: Negative
Aktuelle Erkrankungen: Bronchitis; Chronic sinusitis; Drug allergy (singulair and doxycycline)
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2084812

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 01.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 24,0
Dosis: 2
Route/Site: OT / -

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

SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

TESTED POSITIVE FOR COVID; This spontaneous report received from a consumer concerned an 71 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1808978, expiry: 11-SEP-2021) dose was not reported, 1 total administered on 31-MAR-2021 to left arm for prophylactic vaccination. No adverse events were reported following administration of covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient additionally received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194, expiry: 09-APR-2022) dose was not reported, 1 total administered on 01-JAN-2022 to left arm for prophylactic vaccination. No concomitant medications were reported. On 25-JAN-2022, the patient tested positive for Covid with the Binax Now test when treated with covid-19 vaccine ad26.cov2.s (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of tested positive for Covid was not reported (dose number in series 2). This report was non-serious. This case was associated with a product quality complaint: 90000214055. 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.; Sender's Comments: V0 Medical assessment comment not required as per standard operating procedure as the case assessed as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20220125; Test Name: COVID-19 antigen test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2076076

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: FL
Alter: 60,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 12.11.2021
Beginn: 28.01.2022
Tage bis Beginn: 77,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19

Symptomtext

Vaccinated patient hospitalized with COVID-19.

Weitere VAERSDATA-Felder

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

VAERS 2075137

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: -
Beginn: 24.01.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Inappropriate schedule of product administration Off label use

Symptomtext

INAPPROPRIATE SCHEDULE OF VACCINE ADMINISTERED; OFF LABEL USE; This spontaneous report received from a patient concerned a 63 year old White, not Hispanic or Latino female. The patient's height, and weight were not reported. The patient's concurrent conditions included: non alcohol user, non smoker, tinnitus from medication she was on, neuropathies, neuralgias, flu (every year), immunocompromised, upper respiratory issues with infusions, sulfa drugs don't do well, multiple drug allergies/ allergic to lot of rheumatoid drugs, and autoimmune rheumatoid inflammatory disease due to vaccine for lyme disease. The patient had a past medical history of covid-19 on DEC-2020 and was hospitalized for 10 days.On 18-JUN-2021, the patient was previously treated with covid-19 vaccine ad26. cov2. s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1808982, expiry: unknown) dose was not reported, 1 total administered for prophylactic vaccination. The patient had no adverse events following vaccination with covid-19 vaccine ad26. cov2. s. (Dose number in series 1).On 02-NOV-2021, the patient was treated with covid-19 vaccine ad26. cov2. s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194, expiry: unknown) dose was not reported, 1 total administered for prophylactic vaccination. The patient received third dose of covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194, expiry: 09-APR-2022) dose was not reported, 1 total administered to left arm on 24-JAN-2022 for prophylactic vaccination which was an off label use, and inappropriate schedule of vaccine administered. (Dose number in series 2). Concomitant medications included abatacept (Orencia) 750 mg intravenous a month. The action taken with covid-19 vaccine ad26.cov2.s was not applicable.The outcome of the off label use and inappropriate schedule of vaccine administered was not reported.This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Abstains from alcohol; Drug allergy; Drug intolerance; Flu (Every year); Immunocompromised; Neuralgia; Neuropathy; Non-smoker; Rheumatoid arthritis; Tinnitus; Upper respiratory disorder.
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Comments: The patient had a history of covid-19 on DEC-2020 and was hospitalized for 10 days.
Andere Medikamente: ORENCIA.
Allergien: -
Vorherige Impfungen: -

VAERS 2068588

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 1855194

gering

Staat: KY
Alter: 50,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 16.11.2021
Beginn: 20.01.2022
Tage bis Beginn: 65,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Occupational exposure to SARS-CoV-2 SARS-CoV-2 test positive

Symptomtext

Covid positive through work contact. Not due for booster.

Weitere VAERSDATA-Felder

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

VAERS 2062905

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: KY
Alter: 27,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 12.11.2021
Beginn: 17.01.2022
Tage bis Beginn: 66,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Covid positive through work contact. Not due for booster

Weitere VAERSDATA-Felder

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

VAERS 2061259

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MD
Alter: 28,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 08.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 16,0
Dosis: UNK
Route/Site: SYR / LA

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

Menstruation delayed Pregnancy test negative

Symptomtext

Delayed periods since vaccination. Month of November period was two days late. Month of December was three days late. Month of January it is five days late and I have not had it yet. Three pregnancy tests have been negative the past three days. Have been trying to conceive since October but with the delayed periods and negative ovulations tests since November, It has not happened obviously.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Menstruation delayed
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: None
Allergien: No
Vorherige Impfungen: -

VAERS 2060276

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: OR
Alter: 61,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 08.11.2021
Beginn: 24.01.2022
Tage bis Beginn: 77,0
Dosis: 5
Route/Site: IM / LA

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

Extra dose administered Inappropriate schedule of product administration Interchange of vaccine products

Symptomtext

Pt had too many covid shots 12/19/2021pfizer, 1/8/2021 pfizer, 5/11/2021 janssen, 9/27/2021 pfizer, 1/24/2022 janssen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: na
Vorgeschichte: na
Andere Medikamente: na
Allergien: na
Vorherige Impfungen: -

VAERS 2057649

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: PA
Alter: 53,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dysphagia Head discomfort Hypoaesthesia Hypoaesthesia oral Magnetic resonance imaging Pharyngeal swelling Swollen tongue

Symptomtext

Numb lips, cheeks. Tongue, swollen throat Difficulty swallowing within 5min of shot, Took 4 benedryl withi. 10min and drank 8oz of water. Headed by car to hospital but symptoms were calming back down enroute. That night pressure built in head. Lasted about 30days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dysphagia
Hospital-Tage: -
Labordaten: Two doctor visits and MRI approx. 3 weeks after shots
Aktuelle Erkrankungen: -
Vorgeschichte: Mast cell disease, POTS
Andere Medikamente: Xolair, Allegra, zyrtec, celebrex, gabapentin, singular, ketotofin, naltrexone, Zantac, chromolyn, vitamins D, A, K, C, Bcomplex
Allergien: Phengren, penicillin, doxycyline, cephalosporkns, triptans, erythromycin, Reglan, keflex, spironolactone, clindomyocin, sulpha-drugs, avocado, latex, cinnamon, carrots, black pepper, red dye 40, MRI and CT contrast dyes
Vorherige Impfungen: -

VAERS 2039204

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IA
Alter: 44,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 08.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Tinnitus

Symptomtext

Tinnitus, loud ringing in my ears

Weitere VAERSDATA-Felder

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

VAERS 2038131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 1855194

gering

Staat: FL
Alter: 43,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 27.05.2021
Beginn: 10.01.2022
Tage bis Beginn: 228,0
Dosis: 2
Route/Site: IM / -

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

Unevaluable event

Symptomtext

patient hospitalized

Weitere VAERSDATA-Felder

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

VAERS 2037795

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 03.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 5,0
Dosis: UNK
Route/Site: - / -

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

Asthenia C-reactive protein COVID-19 Inflammatory marker test SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid breakthrough, first vaccine 3/30/21. Patient admitted 1/8/22 with worsening generalized weakness. Patient WC bound with history of DM, HTN, Obesity, Afib, GERD, PUD, OSA, arthritis and non healing left leg wound. Patient also came to hospital for possible rehab placement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: -
Labordaten: Covid 19 + on 1/8/22, CRP inflammatory H49.3A
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic LE weakness, WC bound, HTN, DM, Obese, Afib, GERD, OSA, PUD, non-healing left leg wound
Andere Medikamente: -
Allergien: Silvadene
Vorherige Impfungen: -

VAERS 2010732

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IA
Alter: 22,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Interchange of vaccine products

Symptomtext

Pt. falsified vaccine history and DOB stating he had never received a previous COVID vaccine. Due to incorrect DOB given, not able to find pt. in system. After dose given, attempted to enter pt. into system and discovered pt. under different DOB. Pt. had received first dose of Moderna vaccine on 1/5/22 at a different location. Staff called pt., who admitted he was untruthful so he could get the J&J vaccine today. Pt. states he has a job opportunity that requires him to be fully vaccinated, he was unaware when he received the Moderna yesterday that he had to wait 28 days to receive the second dose. Pt. stated he lied because he will lose the job if he waits that long. Nurse instructed pt. to contact PCP with any adverse reactions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: At time of vaccination, stated he had a runny nose that was baseline normal. After discovering pt. blatantly gave false information to obtain a dose of vaccine that should not have been received, pt. admitted he has been sick x 1 week.
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Denied every having a severe allergic reaction to anything during vaccine consent.
Vorherige Impfungen: -

VAERS 1996079

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: FL
Alter: 33,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 24.11.2021
Beginn: 29.12.2021
Tage bis Beginn: 35,0
Dosis: 1
Route/Site: SYR / LA

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

Abortion spontaneous

Symptomtext

Pregnancy Miscarriage on 12/29/21, symptoms occurred 5 weeks after Covid injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abortion spontaneous
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Vitamin d, prenatal vitamins
Allergien: -
Vorherige Impfungen: -

VAERS 2523940

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: -
Alter: 32,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1988202

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: -
Beginn: 19.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Activated partial thromboplastin time Blood test Dysgeusia Full blood count International normalised ratio Metabolic function test Prothrombin time

Symptomtext

This spontaneous report received from a patient concerned a 64 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: food allergy, pollen allergy, and sensitivity to medicines, and allergy to certain insects. The patient reported she had no drug allergies but she did not want the Moderna or Pfizer vaccine due to the PEG content. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 206A21A expiry: Unknown) dose was not reported, 01 total, administered on 30-JUL-2021 at left arm for prophylactic vaccination. On 30-JUL-2021, around midnight, the patient felt like her tongue tasted salty. On 31-JUL-2021, the patient experienced tiredness. On 14-AUG-2021, 2 weeks later, the patient was advised to go to ER (Emergency room) by someone from JNJ for a bruise on right arm even though injection was in left arm (dose number in series 1). At the hospital (ER) the patient had blood test and all was normal. Laboratory tests included APTT (NR: not provided) Not reported, Basic metabolic panel (NR: not provided) Not reported, Blood test (NR: not provided) Normal, CBC (NR: not provided) Not reported, INR (NR: not provided) Not reported, Prothrombin time (NR: not provided) Not reported. The patient recovered from tiredness on 31-JUL-2021, tongue tasted salty on 07-AUG-2021 and bruise in right arm on 18-AUG-2021 (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194, expiry: Unknown) dose was not reported, 01 total, administered on 10-DEC-2021 at left arm for prophylactic vaccination. No concomitant medications were reported. On 19-DEC-2021, in the morning, the patient experienced salty taste on tongue. On 20-Dec-2021, the patient experienced same sensation again (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from tongue tasted salty (dose number in series 2). This report was non-serious. This case, involving the same patient is linked to 20211245128.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Activated partial thromboplastin time
Hospital-Tage: -
Labordaten: Test Date: 20210814; Test Name: Basic metabolic panel; Result Unstructured Data: Not reported; Test Date: 20210814; Test Name: APTT; Result Unstructured Data: Not reported; Test Date: 20210814; Test Name: Blood test; Result Unstructured Data: Normal; Test Date: 20210814; Test Name: INR; Result Unstructured Data: Not reported; Test Date: 20210814; Test Name: CBC; Result Unstructured Data: Not reported; Test Date: 20210814; Test Name: Prothrombin time; Result Unstructured Data: Not reported
Aktuelle Erkrankungen: Drug hypersensitivity; Food allergy; Insect bite allergy; Pollen allergy
Vorgeschichte: Comments: The patient had no drug allergies but had sensitivity to medicines and allergies to certain insects.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1973975

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: OH
Alter: -
Geschlecht: U
Eingang: 23.12.2021
Impfdatum: -
Beginn: 16.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Poor quality product administered

Symptomtext

ADMINISTRATION OF VACCINE STORED OUTSIDE RECOMMENDED CONDITIONS (FOR 5 HOURS AT ROOM TEMPERATURE); This spontaneous report received from a pharmacist concerned a patient of unspecified age and sex. 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 admin not reported, batch number: 1855194, and expiry: 09-APR-2022) dose was not reported, administered on 16-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 16-DEC-2021, the patient experienced administration of vaccine stored outside recommended conditions (for 5 hours at room temperature). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of administration of vaccine stored outside recommended conditions (for 5 hours at room temperature) was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1971313

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 08.11.2021
Beginn: 17.12.2021
Tage bis Beginn: 39,0
Dosis: 1
Route/Site: SYR / RA

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

Amenorrhoea Blood test

Symptomtext

No period (menstruation) cycle after vaccination. In 25 years the patient has never missed or been late (not even a day) on a menstruation cycle and it has completely stopped. Full blood work was completed and there were no other conditions found, nor is patient in peri menopause.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Amenorrhoea
Hospital-Tage: -
Labordaten: Full blood panel completed 11/24/2021
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1967784

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: GA
Alter: 58,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 29.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Tinnitus

Symptomtext

Chronic tinnitus starting 11/3/2021 through 12/21/2021

Weitere VAERSDATA-Felder

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

VAERS 1966598

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MI
Alter: 47,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 17.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: OT / -

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

CONFIRMED CLINICAL VACCINATION FAILURE; POSITIVE PCR CONFIRMED COVID-19 VACCINE AFTER BOOSTER DOSE OF JANSSEN COVID-19 VACCINE; This spontaneous report received from a patient concerned a 47 year old male. The patient's height and weight were not reported. The patient had no significant medical history. The patient was previously vaccinated with covid-19 vaccine ad26. cov2.s (suspension for injection, route of admin not reported, batch number: 1802068, expiry: 23-AUG-2021) dose was not reported, 01 total was administered on 23-MAR-2021 on left arm for prophylactic vaccination (dose number in series 1). The reporter had not reported any adverse events following vaccination (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194 expiry: 09-APR-2022) dose was not reported, 01 total was administered on 17-NOV-2021 on left arm for prophylactic vaccination (dose number in series 2). No concomitant medications were reported. On 29-NOV-2021 or 30 NOV-2021 (exact date not mentioned) the patient tested self (rapid test) found negative as his wife started to show symptoms to Covid. On 02-DEC-2021, following vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 2), the patient had cold like symptoms, little/light cough, feeling cold. On the same day, the patient reported a positive coronavirus disease (COVID)-19 test for himself on self (rapid) test when he retested after he began experiencing loss of smell. On 04-DEC-2021, laboratory test was performed and he had positive polymerase chain reaction (PCR) confirmed covid-19 vaccine after booster dose of Janssen covid-19 vaccine (confirmed clinical vaccination failure). He reported that, the lab result for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was detected abnormal (Ab). He was treated with zinc, vitamin C, multivitamin and reported that he always wore a mask, prior to and after vaccination whenever leaving the house. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from positive PCR confirmed covid-19 vaccine after booster dose of Janssen covid-19 vaccine and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). The case was associated with product quality complaint (PQC): 90000205848. This case, involving the same patient is linked to 20211220582 and 20211217118, 20211217766 (wife's case).; Sender's Comments: V0:20211217227-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

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202111; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Test Date: 20211202; Test Name: COVID-19 virus test; Result Unstructured Data: negative; Test Date: 20211204; Test Name: COVID-19 PCR test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no significant medical history
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1959702

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: OH
Alter: 21,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine was administered to patient 5 hours after after vial was punctured and left at room temperature. (exceeding 2 hours room-temp limit)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1948238

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: VA
Alter: 64,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 17.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Hypoacusis Tinnitus

Symptomtext

Blocked/Muffled Hearing in Right Ear. Increasingly-Constant Ringing in Ear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypoacusis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Mild Asthma
Andere Medikamente: Vitamin's C, B-complex, E. Nugenix.
Allergien: Tylox
Vorherige Impfungen: -

VAERS 1947727

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MN
Alter: 42,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 13.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Incorrect route of product administration Shoulder injury related to vaccine administration

Symptomtext

Per email from Customer Care, patient stated - ?I received my COVID booster shot at the Pharmacy on Sat, Nov 13. I've just returned from the doctor and have been told that I have SIRVA (Shoulder Injury Related to Vaccine Administration) due to the vaccine being given improperly. I don't know the full extent of the damage yet but will be seeing an orthopedist for a prognosis and course of treatment. Some action needs to be taken with the Pharmacist at the this Cub. At the very least, she needs to be retrained on how to properly give a vaccine shot in the arm. Mine was given too far up on the shoulder. I'm sure I can't be the only one who received the shot incorrectly.?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect route of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1946759

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: -
Geschlecht: U
Eingang: 14.12.2021
Impfdatum: -
Beginn: 12.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Off label use Wrong device used

Symptomtext

SUBCUTANEOUS NEEDLE WAS USED TO ADMINISTER INTRAMUSCULAR VACCINE; OFF LABEL USE; This spontaneous report received from a pharmacist concerned a patient of unspecified age and sex. 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 admin not reported, batch number: 1855194, and expiry: UNKNOWN) dose was not reported, administered on 12-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 12-DEC-2021, the patient experienced subcutaneous needle was used to administer intramuscular vaccine. On 12-DEC-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the subcutaneous needle was used to administer intramuscular vaccine and off label use was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938334

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: OH
Alter: -
Geschlecht: U
Eingang: 10.12.2021
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

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

Incorrect dose administered Syringe issue

Symptomtext

INJECT LIQUID, IT LEAKED OUT; INCOMPLETE DOSE ADMINISTERED; This spontaneous report received from a patient concerned a patient of unspecified age, sex, 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 (dose number series 1) for prophylactic vaccination of unspecified manufacturer. No adverse event was reported after receiving dose series 1. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194, expiry: unknown) dose, 01 total was administered on 24-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 24-NOV-2021 at 12:10 PM, the booster shot the patient received had a potentially defective syringe (batch number: 1054572) (B-D Integra Syringe 3ml 25gx1 REF 305270). Further it was reported that, the joint between the needle and the cylinder was loosen, and when the health care professional (HCP) pushed the piston to inject liquid, it leaked out from that joint which might have resulted in incomplete dose administration (both events dose number in series 2). The HCP found another shot and it worked. The suspected defective product was discarded. The action taken with covid-19 vaccine ad26.cov2.s (dose number in series 2) was not applicable. The outcome of inject liquid, it leaked out and incomplete dose administered was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1935247

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: AK
Alter: 43,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Deafness bilateral Tinnitus

Symptomtext

Tinnitus/Hearing loss in both ears but it more prevalent in my left ear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deafness bilateral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 1934840

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: -
Beginn: 18.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Therapeutic response unexpected

Symptomtext

UNEXPECTED BENEFIT; This spontaneous report received from a patient concerned a 72 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patients received their initial vaccination with covid-19 vaccine ad26.cov2.s (manufacturer not specified) (dose series 1) (suspension for injection, route of admin, batch number, and expiry date were not reported) dose, start therapy date were not reported, administered for prophylactic vaccination. No adverse events were reported (dose series 1). The patient received booster dose of covid-19 vaccine ad26.cov2.s (dose series 2) (suspension for injection, route of admin not reported, batch number: 1855194 expiry: 09-APR-2022) dose was not reported, administered on 18-NOV-2021 on left arm at 11:30 am for prophylactic vaccination. No concomitant medications were reported. On 18-NOV-2021, the patient experienced unexpected benefit (dose series 2). He reported that his peripheral neuropathy went away, there was no tingling, sharp pains out of no where, no numbness or cramping in feet. His feet felt great and were still feeling great at the time of reporting. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of unexpected benefit was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Therapeutic response unexpected
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929183

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NY
Alter: 17,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 05.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Gave Janssen covid vaccine instead of Pfizer Covid vaccine by mistake.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid 19
Vorgeschichte: none
Andere Medikamente: None
Allergien: none
Vorherige Impfungen: -

VAERS 1928381

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MA
Alter: 57,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 04.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Hyperhidrosis Pallor

Symptomtext

Patient received second dose of J&J Vaccine on 12/4/2021. Approximately 14 minutes after vaccination the patient reported feeling diaphoretic and exhibited pale skin. Patient denied chest discomfort or SOB. Vitals were stable. Cold compress was applied, apple juice was given. The patient was monitored an additional 15 minutes without incident. Patient left the clinic stable and reported feeling well. Patient was notified to notify PCP of incident.

Weitere VAERSDATA-Felder

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

VAERS 1925413

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: PA
Alter: 61,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 02.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: IM / RA

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

Herpes zoster

Symptomtext

Small patch of shingles on side of middle phalanx of right ring finger.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin C; Vitamin B-complex
Allergien: Keflex
Vorherige Impfungen: -

VAERS 1925026

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: WI
Alter: 62,0
Geschlecht: M
Eingang: 06.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Syringe issue Underdose

Symptomtext

SYRINGE MALFUNCTIONED, WHEN INJECTING THE DOSE OF VACCINE MOST OF IT LEAKED OUT ONTO PATIENTS ARM

Weitere VAERSDATA-Felder

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

VAERS 1915830

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Interchange of vaccine products Wrong product administered

Symptomtext

The patient incorrectly received the Janssen vaccine instead of her second dose of Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1913865

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: AL
Alter: 17,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

No adverse event Product administered to patient of inappropriate age

Symptomtext

17 YEAR OLD INADVERTENTLY GIVEN JANSSEN VACCINE NO ADVERSE EFFECTS REPORTED

Weitere VAERSDATA-Felder

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

VAERS 1913776

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 18,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 21.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Interchange of vaccine products Wrong product administered

Symptomtext

client signed up for Pfizer vaccine. At Vaccine station she was asked if she was getting Janssen, She said yes. Janssen administered. When vaccinator looked at label says she received Pfizer. At this instance she was asked again what dose she was looking for and she say Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1913464

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: TX
Alter: 49,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Erythema Flushing Hot flush

Symptomtext

face flushing, redness of the neck , hot flashes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Nkda
Allergien: NKDA
Vorherige Impfungen: she used to get rash, used antihistamine OTC

VAERS 1913366

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IN
Alter: 54,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Wrong product administered

Symptomtext

Wrong vaccine given. Pt came in wanting Pfizer but instead was given J&J. Pt was checking in at the window and a card stating Pfizer was placed on the table for another nurse to take and administer vaccine. Nurse brought pt back into vaccine room to administer vaccine. Nurse asked pt if he had any allergies which he stated tomatoes and stated he did not have trouble breathing. Nurse then stated you are getting your first J&J vaccine. Pt stated nothing.). J&J vaccine was administered into Rt delt. Nurse then gave pt his vaccine card and information sheet on the vaccine. Pt asked what he needed to do if he wasn't in the area on 12/27/21 and nurse stated I gave you) the J&J vaccine. Pt replied by stating that he wanted the Pfizer vaccine and that he would have a reaction to this vaccine. Nurse stated that she told him what he was getting prior to giving it and pt said nothing. Nurse then asked if) he wanted to speak with someone and he stated he did. Nurse stepped out of the room and notified CMA and Nursing Administrator, RN of what had occurred. They went into the room and spoke with Administrator, RN and Health Officer, notified of the incident.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1905453

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 04.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

COVID vaccine breakthrough case

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID positive 11/27/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1902058

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: PA
Alter: 76,0
Geschlecht: M
Eingang: 26.11.2021
Impfdatum: 30.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / UN

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

Angiogram Atrial fibrillation COVID-19 Chest X-ray Electrocardiogram Fibrin D dimer Full blood count Laboratory test Troponin

Symptomtext

Became ill with COVID 7 days later, then developed a-fi b 8 days later

Weitere VAERSDATA-Felder

Praegender Schweregrund: Angiogram
Hospital-Tage: -
Labordaten: CBC, CHEM 7 d-dimer, troponin CHEst xray EKG cta of chest
Aktuelle Erkrankungen: none
Vorgeschichte: NIDDM, HTN, Thrombocytopenia
Andere Medikamente: Metoprolol, Aspirin Metformin
Allergien: NKA
Vorherige Impfungen: -

VAERS 1897042

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: KY
Alter: 53,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

CLIENT STATED HE HAD NOT RECEIVED A COVID VACCINE & REQUESTED JANSSEN TODAY. AFTER ADMINISTERING VACCINE, WHEN ENTERING VACCINE DOSE GIVEN INTO database IT WAS FOUND THAT CLIENT HAD RECEIVED A MODERNA VACCINE AT ANOTHER FACILITY ON 6/16/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 1893417

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: ID
Alter: -
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: -
Beginn: 19.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Off label use Poor quality product administered

Symptomtext

This spontaneous report received from a physician concerned an adult female.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 admin not reported, batch number: 1855194, expiry: 09-APR-2022) dose was not reported, administered on 19-NOV-2021 for prophylactic vaccination. No concomitant medications were reported.On 19-NOV-2021, the patient experienced janssen covid 19 vaccine administered after 1 hour past 6 hours expiration, and off label use.The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the janssen covid 19 vaccine administered after 1 hour past 6 hours expiration and off label use was not reported.This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1893198

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: -
Geschlecht: U
Eingang: 23.11.2021
Impfdatum: -
Beginn: 18.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Poor quality product administered Product storage error

Symptomtext

THE REFRIGERATOR WAS LEFT OPEN AND UNOPENED VIAL STORED FOR 15 MINUTES WHICH HAD A TEMPERATURE EXCURSION OF 47.44 DEGREES F; ADMINISTRATION OF VACCINE THAT WAS STORED OUTSIDE OF THE RECOMMENDED STORAGE CONDITIONS; This spontaneous report received from a health care professional concerned a patient of unspecified age and sex. 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 admin not reported, batch number: 1855194, expiry: 09-APR-2022) dose was not reported, administered on 18-NOV-2021 15:20 for prophylactic vaccination. No concomitant medications were reported. On 18-NOV-2021, the patient experienced administration of vaccine that was stored outside of the recommended storage conditions. On an unspecified date, the patient experienced the refrigerator was left open and unopened vial stored for 15 minutes which had a temperature excursion of 47.44 degrees f.The action taken with covid-19 vaccine ad26.cov2.s was not applicable.The outcome of the administration of vaccine that was stored outside of the recommended storage conditions and the refrigerator was left open and unopened vial stored for 15 minutes which had a temperature excursion of 47.44 degrees f was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1889909

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: OH
Alter: 27,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Interchange of vaccine products

Symptomtext

Patient had appointment for Janssen vaccine. He presented with passport and no Data was found. When checking out patient, I reviewed that this was the first COVID vaccine the patient has had. He stated he had not gotten a vaccine for COVID before. After vaccination, the patient was asking about Janssen after having had the vaccine series. The patient then made us aware that he received this vaccine with last dosing sometime in September 2021. He had no documentation to show this. I suggested he report all of his vaccines to the agency program and contact his provider with any other concerns.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1889012

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: PA
Alter: 66,0
Geschlecht: M
Eingang: 21.11.2021
Impfdatum: 15.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Blood urine present

Symptomtext

Dark colored / blood? in urine about 24 hours after injection. Resolved by later in the same day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood urine present
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Allopurinol 300 mg, Omega 3, Red Yeast Rice
Allergien: None
Vorherige Impfungen: -

VAERS 1887658

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: UT
Alter: -
Geschlecht: U
Eingang: 20.11.2021
Impfdatum: -
Beginn: 16.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Poor quality product administered Product temperature excursion issue

Symptomtext

45 TOTAL VIALS INVOLVED IN TEMPERATURE EXCURSION; ADMINISTRATION OF EXPIRED VACCINE; This spontaneous report received from a health care professional concerned a patient of unspecified age and sex. 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 admin not reported, batch number: 1855194 expiry: 09-APR-2021) dose was not reported, administered on 16-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 16-NOV-2021, the patient experienced administration of expired vaccine. On an unspecified date, the patient experienced 45 total vials involved in temperature excursion. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administration of expired vaccine and 45 total vials involved in temperature excursion was not reported. This report was non-serious. This case, from the same reporter is linked to 20211143086 and 20211139494.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1883995

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: FL
Alter: 83,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: -
Beginn: 28.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Poor quality product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED (PUNCTURED VIAL OF VACCINE WAS EXPIRED FOR 6 HOURS PRIOR TO BEING ADMINISTERED); This spontaneous report received from a consumer concerned an 83 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no medical history. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, and expiry: 28-OCT-2021) dose was not reported, administered on 28-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 28-OCT-2021, the patient experienced expired vaccine administered (punctured vial of vaccine was expired for 6 hours prior to being administered). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered (punctured vial of vaccine was expired for 6 hours prior to being administered) was not reported. This report was non-serious. This case, from the same reporter is linked to 20211139224.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no medical history.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1883982

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: FL
Alter: 39,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: -
Beginn: 28.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Expired product administered

Symptomtext

ADMINISTERED EXPIRED VACCINE; This spontaneous report received from a health care professional concerned a 39 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient had no medical history. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, and expiry: 28-OCT-2021) dose was not reported, administered on 28-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 28-OCT-2021, the patient experienced administered expired vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of administered expired vaccine was not reported. This report was non-serious. This case, from the same reporter is linked to 20211139710.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no medical history.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1880974

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 38,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 01.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Tinnitus

Symptomtext

Loud ringing in ears started 48 hours after shot. Has continued several weeks later.

Weitere VAERSDATA-Felder

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

VAERS 1877046

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MI
Alter: 19,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Immunisation Syringe issue Underdose

Symptomtext

on 11/5/21 I went to push in the plunger to administer the vaccine, the vaccine gushed out of the syringe instead of going into the patient. I wasn't sure what to do at the time, so I let the patient go so I could contact my clinical pharmacist specialist and also call Janssen. They advised me to administer the vaccine again, but the patient had already left. I called him to come back, and he was not able to come back that day. So I reached out again to Janssen and our clinical specialist to see if I should just administer it as soon as possible. Janssen could not give me that information, but my clinical specialist advised that if an unknown amount was administered, it should be repeated. I called the patient on 11/10/21 to come back in, and he finally came back on 11/16/21 for his repeat dose.

Weitere VAERSDATA-Felder

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

VAERS 1873884

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: -
Alter: 17,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

Pt received the J&J vaccine at age 17 instead of the approved 18 years old.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1873774

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NH
Alter: 36,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 15.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Hypoaesthesia

Symptomtext

numbness on the left side of her face without paralysis of the face

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypoaesthesia
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: immune thrombocytopenia
Vorgeschichte: immune thrombocytopenia
Andere Medikamente: none
Allergien: doxycycline, sulfonamides, amoxicillin
Vorherige Impfungen: -

VAERS 1873318

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 04.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / LA

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

Acoustic stimulation tests Tinnitus

Symptomtext

Ringing in ear. Worse at night, sleeping, but constant. Also happened after first dose in March 2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic stimulation tests
Hospital-Tage: -
Labordaten: ear test Summer, 2021
Aktuelle Erkrankungen: Rheumatoid arthritis high Blood pressure regulated -normal with meds
Vorgeschichte: rheumatoid arthritis, thryroid nodules
Andere Medikamente: Methotrexate Losartin
Allergien: misc foods, dust
Vorherige Impfungen: same for covid first shot in March, 2021

VAERS 1873251

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IA
Alter: 17,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

one dose of Janssen COVID-19 vaccine (.5mL) was given to a patient under age 18

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1873223

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IA
Alter: 13,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

one dose of Janssen COVID-19 vaccination was given to an individual under the age of 18.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1872906

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: VA
Alter: 73,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 30.10.2021
Beginn: 11.11.2021
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: IM / LA

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

Hypoaesthesia

Symptomtext

11/11/2021- Left side of my face is numb. 11/12/2021- Went to the doctor and informed to give it more time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypoaesthesia
Hospital-Tage: -
Labordaten: No medical test done
Aktuelle Erkrankungen: No other illnesses at the time
Vorgeschichte: High Blood Pressure
Andere Medikamente: Amlodipine Losartan Atorvastatin Hydrochlorothiazide Low Dose Aspirin
Allergien: I have no allergies
Vorherige Impfungen: -

VAERS 1872012

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 16.11.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Poor quality product administered

Symptomtext

OUTSIDE OF REFRIGERATED TEMPERATURE 6 HOURS; This spontaneous report received from a pharmacist concerned multiple patients. 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 admin not reported, batch number: 1855194, expiry: UNKNOWN) dose, start therapy date were not reported for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced outside of refrigerated temperature 6 hours. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of outside of refrigerated temperature 6 hours was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1868037

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Pharyngeal hypoaesthesia Pharyngeal swelling Throat irritation

Symptomtext

About an hour after the vaccines, felt a tickle in my throat and slight swelling on left side of throat. Took a couple benadryl, but swelling continued to worsen and spread to about 3/4 across my throat at 1.5 hours. Throat felt like it was touching as if I was swallowing food or drink, even when I wasn't eating/drinking. Sucked on ice chips to sooth and slow swelling. Also started to get numb on the left side of lips and face (like after a local at the dentist for fillings/crowns) at 1.75 hours. No issues with breathing occurred, so went into urgent care (arrived at 2 hour mark). Urgent care decided it was an acute reaction, not severe and gave me a steroid injection, at 2.5 hour mark, and said to continue Benadryl at home. Head to the ER if symptoms worsen or any trouble breathing. Item 21 unavailable to completely report at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal hypoaesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Tachycardia, Stenosis, Migraines, Allergies, Osteoarthritis
Andere Medikamente: None
Allergien: Tetracycline, Imitrex, Immunology shots, Tomatillos, Mango
Vorherige Impfungen: -

VAERS 1867894

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: -
Alter: 50,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Interchange of vaccine products

Symptomtext

Client presented to the vaccination site on 11/13/2021. The client notified PHN that he received a both doses of the Novavax COVID vaccine during a clinical trial on 4/29/2021 and 5/25/2021. PHN submitted a medical consult via text message to Vaccine Operations Leads, requesting to proceed with the COVID vaccine Janssen. Patient reported no medical conditions and takes vascepa, atorvastatin, and multivitamin. Approval to proceed with COVID vaccine Janssen was obtained from medical consult team via text message from Vaccine Operations Lead per Dr. Client received COVID vaccine Janssen Lot#1855194 on 11/13/2021. The client did not report any symptoms during the 15 minute observation period. Vaccinator Pharmacist educated client on possible adverse reactions and when to seek medical care. The client left the vaccination site at 1300 walking with steady gait.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: vascepa, atorvastatin
Allergien: -
Vorherige Impfungen: -

VAERS 1867798

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dysphagia Pharyngeal swelling Supine position Vision blurred

Symptomtext

Patient received the booster dose of the Janssen COVID vaccine (lot 1855194) and the Fluarix influenza vaccine (lot 7557A) at approximately 1625. At 1655, patient reported to Paramedic and PHN feeling like her throat was swelling and dysphagia. PHN noted patient no use of accessory muscles or difficulty speaking. Vital signs: blood pressure 142/86, O2 99%, pulse 86, respirations 16. Patient reported allergy to PEG causing hives and throat tightness for which she takes oral Benadryl with good effect. Medical condition includes arthritis. Patient takes Truvy weight loss supplement. PHN offered Benadryl IM, patient consented. PHN administered Benadryl 50mg IM at 1656. PHN educated on remaining for 30min monitoring from time of medication administration, to follow up with provider, and ER precautions. Patient called sister to arrange for transportation. At 1700, patient reported improved dysphagia and able to drink water provided by site with no difficulty. At 1703, vital signs: blood pressure 136/72, O2 99%, pulse 84, respirations 14. At 1708, vital signs: blood pressure 136/78, respirations 16, O2 99%, pulse 82. Patient reported blurry lights. Patient moved unassisted to zero-gravity chair with no difficulty and placed supine closely monitored by PHN. At 1720, vital signs: blood pressure 128/84, respirations 14, O2 99%, pulse 76. Patient reported all symptoms had resolved and starting to feel drowsy due to Benadryl. Patient's sister arrived at site. Patient left walking with steady gait at 1746 accompanied by sister to drive her home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dysphagia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: arthritis
Andere Medikamente: Truvy weight loss supplement
Allergien: PEG
Vorherige Impfungen: -

VAERS 1865517

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Interchange of vaccine products No adverse event

Symptomtext

Client presented to the vaccination site on 11/04/21. The client notified RN that she received a single dose of CanSino COVID vaccine on 4/30/21. RN submitted a medical consult via text message to Vaccine Operations Leads, requesting to proceed with the COVID vaccine Janssen. Per CDC guidance, approval to proceed with COVID vaccine Janssen was obtained from medical consult team via text message from Vaccine Operations Lead . Client received COVID vaccine Janssen 11/04/21 Lot# 1855194. The client did not report any symptoms during the 15 minute observation period. RN educated client on possible adverse reactions and when to seek medical care

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: NKA
Vorherige Impfungen: -

VAERS 1865456

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 40,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Interchange of vaccine products

Symptomtext

Client presented to the vaccination site on 11/04/2021. The client notified RN that he received a single dose of COVID-19 vaccine in another country on 4/21/2021. RN submitted a medical consult via text message to vaccine operations leads, requesting to proceed with the COVID-19 vaccine Janssen. Per CDC guidance, approval to proceed with COVID-19 vaccine Janssen was obtained from medical consult team via text message from lead vaccine operations. Client received COVID-19 vaccine Janssen Lot#1855194 on 11/04/2021. The client did not report any symptoms during the 15-minute observation period. RN educated client on possible adverse reactions and when to seek medical care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: None reported
Allergien: Aspirin/Silica
Vorherige Impfungen: -

VAERS 1865253

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

Client presented to the vaccination site on 11/04/2021. The client notified nurse that she received a single dose of CanSino, COVID vaccine in country on 04/20/21. A medical consult via text message to Vaccine Operations Leads, requesting to proceed with the COVID vaccine Janssen. Per CDC guidance, approval to proceed with COVID vaccine Janssen was obtained from medical consult team via text message from Vaccine Operations Lead. Client received COVID vaccine Janssen on 11/04/2021. The client did not report any symptoms during the 15-minute observation period. Nurse educated client on possible adverse reactions and when to seek medical care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none reported
Vorgeschichte: none reported
Andere Medikamente: none reported
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1858103

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NY
Alter: 39,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 06.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / RA

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

Tinnitus

Symptomtext

intense ringing in ears. everyone sounds like robots with echos.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: mitrial valve prolapse, mild asthma
Andere Medikamente: entresto 24/26 mg tablets
Allergien: wheat allergy
Vorherige Impfungen: -

VAERS 1855555

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MO
Alter: 50,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Cough Feeling hot Hypersensitivity Wheezing

Symptomtext

Within approximately 10 minutes post injection , patient was seated and waiting for 30 minutes when she started a deep cough and wheezing. Offered her water - which she accepted. She stated her chest felt tight and she felt hot. She said this is how she went into an allergic reaction. EpiPen was readied for use. Asked if she used any rescue inhalers to treat these reactions. she said she had in the past. She was given an albuterol inhaler, which she said she had used before. She took one inhalation. She refused an EpiPen stating she did not need it yet. She also refused oral OTC benadryl. Her wheezing started declining i n about 15 minutes. Coughing gradually reduced in intensity. Patient sat for another hour as we kept checking on her about every 5 minutes. She was very calm and stated that she was okay. We released her about 1 & 1/2 hours post vaccination. She stated she was okay to go. Advised her to immediately call 911 if she had any further symptoms thru the night. She stated that she was returning home and not going to work or any other activity. Reaction would be described as similar to an acute asthma attack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest discomfort
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: none known
Vorgeschichte: Allergic reactions
Andere Medikamente: unknown
Allergien: Penicillin - anaphylactic Environmental- anaphylactic
Vorherige Impfungen: -

VAERS 1855343

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

No adverse event

Symptomtext

patient had vaccine 6 mo ago- no reactions at this time with Janssen vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1852046

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 07.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

No adverse event

Symptomtext

Patient presented to the vaccination site on 11/07/21. The client notified RN that she received the complete series of Janssen COVID vaccine. First dose was given on 4/04/21 and second dose was given on 4/27/21. RN submitted a medical consult via text message to Vaccine Operations Leads, requesting to proceed with the COVID vaccine Janssen. Per CDC guidance, Dr approved to proceed with COVID vaccine Janssen was obtained from medical consult team via text message from, RN, Vaccine Operations Lead. Client received COVID vaccine Janssen Lot# 1855194 on 11/07/21. The client did not report any symptoms during the 15 minute observation period. RN educated client on possible adverse reactions and when to seek medical care. The client left the vaccination site at 1501 unassisted and with a steady gait.

Weitere VAERSDATA-Felder

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

VAERS 1851410

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 42,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

Client presented to the vaccination site on 11/04/2021. The client notified RN that he received COVID vaccine on 02/2021 in. RN submitted a medical consult via text message to Vaccine Operations Leads, requesting to proceed with the Janssen COVID vaccine. Per CDC guidance, approval to proceed with COVID vaccine Janssen was obtained from medical consult team. Client received COVID vaccine (Janssen, Lot# 1855194) on 11/04/2021 at 11:37 am. The client did not report any symptoms during the 30 minute observation period. RN educated client on possible adverse reactions and when to seek medical care. The client left the vaccination site at 12:10 pm, walking with steady gait.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1851390

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 46,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

Client presented to the vaccination site on 11/04/2021. The client notified RN that he received COVID vaccine on 04/29/2021. RN submitted a medical consult via text message to Vaccine Operations Leads, requesting to proceed with the Janssen COVID vaccine. Per CDC guidance, approval to proceed with COVID vaccine Janssen was obtained from medical consult team. Client received COVID vaccine (Janssen, Lot# 1855194) on 11/04/2021 at 12:04 pm. The client did not report any symptoms during the 30 minute observation period. RN educated client on possible adverse reactions and when to seek medical care. The client left the vaccination site at 12:40 pm, walking with steady gait.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1851362

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

Client presented to the vaccination site on 11/04/2021. The client notified Marisela RN that she received COVID vaccine on 04/29/2021 in another country. RN submitted a medical consult via text message to Vaccine Operations Leads, requesting to proceed with the Janssen COVID vaccine. Per CDC guidance, approval to proceed with COVID vaccine Janssen was obtained from medical consult team. Client received COVID vaccine (Janssen, Lot# 1855194) on 11/04/2021 at 11:59 am. The client did not report any symptoms during the 30 minute observation period. RN educated client on possible adverse reactions and when to seek medical care. The client left the vaccination site at 12:30 pm, walking with steady gait.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1851332

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 37,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

Client presented to the vaccination site on 11/04/2021. The client notified RN that he received 1st Sputnik COVID vaccine(Lot # I-980521) on 07/27/2021, and 2nd Sputnik dose(Lot # II-37-0721) on 09/15/2021. RN submitted a medical consult via text message to Vaccine Operations Leads, requesting to proceed with the Janssen COVID vaccine. Per CDC guidance, approval to proceed with COVID vaccine Janssen was obtained from medical consult team via text message from (Privacy) RN, Vaccine Operations Lead . Client received COVID vaccine (Janssen, Lot# 1855194) on 11/04/2021. The client did not report any symptoms during the 30 minute observation period. RN educated client on possible adverse reactions and when to seek medical care. The client left the vaccination site at 12:55pm, walking with steady gait.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1851302

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Interchange of vaccine products No adverse event

Symptomtext

Patient presented to the vaccination site on 11/04/2021. The client reports that she received a single dose of CanSino COVID vaccine on 05/01/2021. RN submitted a medical consult via text message to Vaccine Operations, requesting to proceed with the Janssen COVID vaccine. Per CDC guidance, approval to proceed with COVID vaccine Janssen was obtained from medical consult team from Vaccine Operations Lead. Client received COVID vaccine (Janssen, Lot# 1855194) on 11/04/2021. The client did not report any symptoms during the 30 minute observation period. RN educated client on possible adverse reactions and when to seek medical care. The client left the vaccination site at 12:15pm, walking with steady gait.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1851167

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

Client presented to the vaccination site on 11/04/2021. The client notified RN that she received a single dose of COVID vaccine on 04/30/2021. RN submitted a medical consult via text message to Vaccine Operations Leads, requesting to proceed with the Janssen COVID vaccine. Per CDC guidance, approval to proceed with Janssen COVID vaccine was obtained from medical consult team via text message from RN, Vaccine Operations Lead . Client received COVID vaccine Janssen at 11:35 am. The client did not report any symptoms during the 30 minute observation period. RN educated client on possible adverse reactions and when to seek medical care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1849612

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 38,0
Geschlecht: M
Eingang: 07.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Inappropriate schedule of product administration Interchange of vaccine products No adverse event

Symptomtext

On 11/5/21 at approximately 11:16 AM, 38 year old, male client ( DOB 07/12/1983) arrived to County operated vaccine site and requests to receive Janssen COVID-19 vaccine. Client reports receiving one dose of Moderna vaccine at 11:00 AM on 2/11/21. Client reports that at 1:00 AM on 2/11/21, and for 3 days thereafter, he began to experience swelling of lips, hives, and denies experiencing SOB. Client reports HR of 145 while experiencing these symptoms. He reports going to Urgent Care at 9:00 am on 2/11/21, which informed client to hydrate. Client denies receiving treatment or any medications from Urgent Care, and denies taking Benadryl or any medications for these symptoms. Client reports following up with PCP who recommended that client receive a non-mRNA COVID-19 vaccine in the future. Elevated concern to Clinical Supervisor, who completed medical consult, with approval by Doctor to administer Janssen COVID-19 vaccine to client at this time, and Doctor recommends observation time of 30 minutes. Janssen (Lot# 1855194) administered to client by this nurse at 11:16 AM on 11/5/21. No adverse reactions of side effects reported by client or noted by EMT during post-observation period. Explained risks, benefits, and emergency precautions to client who verbalized understanding. - RN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Client denies
Vorgeschichte: Client denies
Andere Medikamente: Client denies
Allergien: Client denies
Vorherige Impfungen: -

VAERS 1849553

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 54,0
Geschlecht: M
Eingang: 07.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Extra dose administered Interchange of vaccine products No adverse event

Symptomtext

On 11/5/21, 54 year old male client (patient) arrived to vaccination site and asked to receive Janssen Booster COVID-19 dose. He reports and shows documentation of completing 2-dose series of Pfizer COVID-19 vaccines in February/March 2021. Client reports history of pericarditis "years ago", and reports experiencing symptoms of pericarditis which included inflammation and swelling, especially after receiving 2nd dose of Pfizer. Client reports consulting with his cardiologist in the past for pericarditis symptoms, and reports that his cardiologist recommended that client take "Naproxen" when these symptoms arise (client reports symptoms last occurring "years ago". Client reports taking Naproxen (BID) for a few days, and reports that swelling/inflammation subsided. Client requests to receive Janssen booster, instead of Pfizer booster dose at this time. Elevated inquiry to Clinical Supervisor, who receives approval from Medical Provider Dr. to administer Janssen booster dose to client at this time. This nurse explained to client risks/benefits/emergency precautions post-observation. Client verbalizes understanding and provides consent to receive Janssen booster (Lot #1855194), which was administered by this nurse at 1:16 PM on 11/5/21. - RN. No Adverse reactions noted during 15-minute post-observation period. Explained potential risks and side effects to client, explained emergency protocol to client. Client verbalized understanding. - RN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: Client reports history of pericarditis "years ago". Client reports speaking with cardiologist regarding this condition.
Andere Medikamente: Hx of OTC Naproxen; client denies taking medications at this time.
Allergien: none reported
Vorherige Impfungen: -

VAERS 1848951

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IL
Alter: 19,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

This vaccine was stored at room temperature outside of 2 hours. The vial was opened around 3PM and the vaccine was administered around 530PM. I did not realize this was incorrect until 11/5/21. I have contacted my managers and the manufacturer who did not have stability data past 2 hours and advised to use clinical judgement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1848946

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IL
Alter: 70,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 30.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / RA

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

Product storage error

Symptomtext

This vaccine was stored at room temperature outside of 2 hours. The vial was opened around 1115AM and the vaccine was administered around 245PM. I did not realize this was incorrect until 11/5/21. I have contacted my managers and the manufacturer who did not have stability data past 2 hours and advised to use clinical judgement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1848941

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IL
Alter: -
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 16.08.1957
Beginn: 05.11.2021
Tage bis Beginn: 23.457,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered Product storage error

Symptomtext

This vaccine was stored at room temperature outside of 2 hours. The vial was opened around 11AM and the vaccine was administered around 2PM. I did not realize this was incorrect until 11/5/21. I have contacted my managers and the manufacturer who did not have stability data past 2 hours and advised to use clinical judgement. The patient's first 2 doses were Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1848928

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IL
Alter: 34,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 28.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

This vaccine was stored at room temperature outside of 2 hours. The vial was opened around 1235AM and the vaccine was administered around 3PM. I did not realize this was incorrect until 11/5/21. I have contacted my managers and the manufacturer who did not have stability data past 2 hours and advised to use clinical judgement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1848920

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IL
Alter: 24,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 26.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: - / LA

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

Expired product administered Product storage error

Symptomtext

This vaccine was stored at room temperature outside of 2 hours. The vial was opened around 11AM and the vaccine was administered around 246PM. I did not realize this was incorrect until 11/5/21. I have contacted my managers and the manufacturer who did not have stability data past 2 hours and advised to use clinical judgement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1848915

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IL
Alter: 47,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 26.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered Product storage error

Symptomtext

This vaccine was stored at room temperature outside of 2 hours. The vial was opened around 11AM and the vaccine was administered around 207PM. I did not realize this was incorrect until 11/5/21. I have contacted my managers and the manufacturer who did not have stability data past 2 hours and advised to use clinical judgement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1848902

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: IL
Alter: 52,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 26.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: IM / RA

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

Expired product administered Product storage error

Symptomtext

This vial was kept at room temperature for more than 2 hours. At the time, I did not realize this vial is only good for 2 hours at room temperature. I contacted the manufacturer and they did not have any stability data for me and said to use clinical discretion. The vial was opened around 11AM and the patient was vaccinated around 330PM. The patient was not contacted yet and I am awaiting further instruction on this as per a conversation with my immunization specialist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1848154

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: WA
Alter: -
Geschlecht: U
Eingang: 06.11.2021
Impfdatum: -
Beginn: 03.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Poor quality product administered

Symptomtext

ADMINISTRATION OF THE JANSSEN COVID-19 VACCINE AFTER IT HAD BEEN PUNCTURED AND LEFT AT ROOM TEMPERATURE FOR 4 HOURS; This spontaneous report received from a pharmacist concerned a patient of unspecified age and sex. 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 admin not reported, batch number: 1855194, and expiry: 09-APR-2022) dose was not reported, administered on 03-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 03-NOV-2021, the patient experienced administration of the janssen covid-19 vaccine after it had been punctured and left at room temperature for 4 hours. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of administration of the janssen covid-19 vaccine after it had been punctured and left at room temperature for 4 hours was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1848140

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: MA
Alter: -
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: -
Beginn: 02.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Eye swelling Mass Ocular hyperaemia Periorbital swelling

Symptomtext

LEFT EYE SWOLLEN; PUFFINESS IN LEFT EYE; RIGHT EYE WAS REDDIDSH BUT NOT SWOLLEN/REDNESSS IN LEFT EYE; BAGGY LUMP IN LEFT EYE; This spontaneous report received from a patient concerned a 50 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Generally healthy, saw physician for checkup in 2020 routine. Patient had no drug or non-drug allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1855194, expiry: UNKNOWN) dose was not reported, administered on 01-NOV-2021 07:20 for prophylactic vaccination. No concomitant medications were reported. On 02-NOV-2021, the patient experienced left eye swollen. On 02-NOV-2021, the patient experienced puffiness in left eye. On 02-NOV-2021, the patient experienced right eye was reddidsh but not swollen/rednesss in left eye. On 02-NOV-2021, the patient experienced baggy lump in left eye. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from left eye swollen, puffiness in left eye, and right eye was reddidsh but not swollen/rednesss in left eye, and the outcome of baggy lump in left eye was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye swelling
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Generally healthy, saw physician for checkup in 2020 routine. Patient had no drug or non-drug allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1846489

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 19,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Interchange of vaccine products No adverse event

Symptomtext

Patient presented to the vaccination site on 11/02/21. The client notified RN that he received a complete series of Sputnik first dose was given on 6/18/21 and second dose was given on 7/17/21 COVID vaccine. RN submitted a medical consult via text message to Leads, requesting to proceed with the COVID vaccine (Janssen). Per CDC guidance, approval to proceed with COVID vaccine (Janssen) was obtained from medical consult team via text message from (RN), Lead . Client received COVID vaccine (Janssen) Lot#1855194 on 11/02/21. The client did not report any symptoms during the 30 minute observation period. RN educated client on possible adverse reactions and when to seek medical care. The client left the vaccination site unassisted and with a steady gait at 1220.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1838740

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NE
Alter: -
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: -
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Poor quality product administered Product storage error

Symptomtext

INCORRECT PRODUCT STORAGE; THE VACCINE WAS KEPT IN THE FREEZER WHEN RECEIVED (THE POSSIBILITY OF BEING FROZEN TWICE) AND LATER INJECTED; This spontaneous report received from a health care professional concerned a male of unspecified age. 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 admin not reported, batch number: 1855194, expiry: 09-APR-2022) dose was not reported, administered on OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On OCT-2021, the patient experienced the vaccine was kept in the freezer when received (the possibility of being frozen twice) and later injected. On 26-OCT-2021, the patient experienced incorrect product storage. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the the vaccine was kept in the freezer when received (the possibility of being frozen twice) and later injected and incorrect product storage was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1831837

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: NM
Alter: 42,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chest discomfort Feeling hot Hypoaesthesia Tinnitus

Symptomtext

Patient complained of numbness in right hand and arm about 20 minutes after dose was given. Shortly after she began complaining of tightness in the chest and ringing in the ears. She was given benadryl and monitored. She complained of being hot and was given an ice pack. She stayed for 1 hour and 30 minutes under supervision. When she left she was not symptomatic and was accompanied by her spouse.

Weitere VAERSDATA-Felder

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

VAERS 1829641

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Interchange of vaccine products No adverse event

Symptomtext

Client received the 1st COVID vaccine (unknown lot and expiration) on 04/22/2020 and is requesting to receive 1st dose of Janssen. EMT took vitals (blood pressure: 150/82, heart rate: 66, respirations: 16, and oxygen saturation 97%) for baseline information and a possible medical consult. Per patient underlying conditions are hypertension and diabetes, allergic to penicillin and currently taking losartan and metformin. Per patient no adverse reactions noted after vaccine administration. Per CDC Guidance, patient is approved to receive primary dose of Janssen. Patient received and completed 15 minutes of observation, no adverse reactions noted. PHN provided education regarding ER precautions, follow up with MD, and educated on the use of V-Safe. VAERS completed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: DM and hypertension
Andere Medikamente: metformin and losartan
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1829456

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

No adverse event

Symptomtext

Client received the 1st dose Sinovac vaccine on 07/27/2021 and 2nd dose Sinovac vaccine on 08/25/2021. Client reported to Lead RN that she would like to receive the Janssen Booster. Client reported no adverse reaction to the Sinovac vaccine series. Lead RN provided medical consult to RN Supervisor. RN Supervisor received approval for the Janssen vaccine booster dose from County. Client received the Janssen Booster (lot#1855194) at 1025 in the L deltoid. No adverse reaction was observed during clients observation period of 15 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1829420

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Extra dose administered Interchange of vaccine products No adverse event

Symptomtext

Client received the 1st dose Sinovac vaccine on 07/30/2021 and 2nd dose Sinovac vaccine on 08/25/2021. Client reported to Lead RN that he would like to receive the Janssen Booster. Client reported no adverse reaction to the Sinovac vaccine series. Lead RN provided medical consult to RN Supervisor. RN Supervisor received approval for the Janssen vaccine booster dose from County MD. Client received the Janssen Booster (lot#1855194) at 1020 in the L deltoid. No adverse reaction was observed during clients observation period of 15 minutes.

Weitere VAERSDATA-Felder

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

VAERS 1821809

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: WY
Alter: 27,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Tinnitus

Symptomtext

At 12:44pm patient complained of Tinnitus, patient vitals were taken, BP: 120/90, HR: 86, RR: 14, Pulse: 68, O2: 93%. Patient denied s/s of hearing loss, dizziness, vision changes, difficulty breathing, and said he felt fine other than the ringing in his ears. Waited 15 minutes and Patient reported no improvement with Tinnitus. Rechecked vitals at 01:10pm BP: 120/90, HR: 89, RR: 12, O2: 93%, Patient still denies any s/s of hearing loss, dizziness, vision changes, difficulty breathing. Patient was alert and oriented no signs of confusion, skin looked normal no pallor or sweat visible. Patient education on Tinnitus and encouraged to see Primary Provider ASAP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONe
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1813487

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: SC
Alter: 77,0
Geschlecht: M
Eingang: 23.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Extra dose administered Product storage error

Symptomtext

Patient was administered a booster dose that may have been administered outside of the room temperature window. Janssen is good for 2 hours at room temperature. Vial was out of the refrigerator for longer than 2 hours time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Ace Inhibitors, ARBs, Metoclopramide, Meperidine, Proton Pump inhibitors- per patient Rx profile, however, not verified
Vorherige Impfungen: -

VAERS 1813475

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 1855194

gering

Staat: SC
Alter: 51,0
Geschlecht: M
Eingang: 23.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine may have been administered outside of the room temperature window. Janssen is good for 2 hours at room temperature. Vial was out of the refrigerator for longer than 2 hours time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No record of prior illnesses
Vorgeschichte: No record of long standing illnesses
Andere Medikamente: Do not have a record of Medications patient is currently or previously taking.
Allergien: No record of known allergies
Vorherige Impfungen: -