- Staat
- FL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 07.11.2023
- Impfdatum
- 04.11.2021
- Beginn
- 28.10.2023
- Tage bis Beginn
- 723,0
- Dosis
- 2
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
COVID-19 pneumonia
Symptomtext
Hospitalization for acute hypoxemic respiratory failure with pneumonia secondary to COVID-19 on dates 10/28/2023- 11/3/2023. Treated with dexamethasone, Remdesivir, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 06.03.2023
- Impfdatum
- 12.02.2021
- Beginn
- 05.03.2023
- Tage bis Beginn
- 751,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Pt arrived to ER with shortness of breath. She has a PMH of CHF with diastolic dysfunction, obesity, and COPD. She was found to be COVID positive and was admitted with acute hypoxic respiratory failure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 29.11.2022
- Impfdatum
- 05.11.2021
- Beginn
- 25.11.2022
- Tage bis Beginn
- 385,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Pulmonary embolism
Symptomtext
Patient arrived to the local ER on 11-27-22 with complaints of SOB that started on 11-25-22. Patient was diagnosed with a Pulmonary Embolism and was admitted to the general ward on 11-28-22 for treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- Pancreatic Cancer and taking Chemo treatments
- Vorgeschichte
- HX GERD, HTN
- Andere Medikamente
- Aspirin 81 mg po daily atorvastatin po labetalol po Norco 7.5-325 mg po prn Valsartan/hctz po
- Allergien
- NKDA/ Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 31.10.2022
- Impfdatum
- 13.12.2021
- Beginn
- 25.10.2022
- Tage bis Beginn
- 316,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Acute respiratory failure
Asthenia
COVID-19
COVID-19 pneumonia
Computerised tomogram thorax abnormal
Cough
Dyspnoea
Fatigue
Hypoxia
Intensive care
Lung opacity
Malaise
Pneumonia
SARS-CoV-2 test positive
Symptomtext
COVID + 10/25/22 - Vaccination status - moderna x3 Discharge Summary HOSPITALIST Discharge Information: Discharge Provider: MD Primary Care Provider : Procedures to be scheduled by PCP: None Results/Procedures requiring PCP followup: None Admission Date: 10/25/2022 Discharge Date: 10/30/2022 Admitting Diagnoses: Acute hypoxemic respiratory failure due to COVID-19 Details of Hospital Stay PRESENTING PROBLEM: Acute hypoxemic respiratory failure due to COVID-19 [U07.1, J96.01] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: Patient is a 85 y.o. male who presents to hospital with shortness of breath. Patient attended a wedding 10 days ago where multiple people became sick, including his wife. He began to feel ill 3 days ago, with fatigue and cough. Symptoms gradually worsened and this morning he had a pulse ox of "50%" at home according to his wife. EMS was called and the patient brought to the ED. He required a NRB mask to maintain adequate sats in the ED. CT showed no signs of PE but bilateral ground glass and tree in bud opacities. COVID testing was positive. Because of his severe hypoxemia he was referred to the hospital and transferred to hospital for further evaluation and care. Patient was admitted to the critical care unit and treated with steroids remdesivir and empiric antibiotics to cover community-acquired pneumonia. He was managed with high-flow nasal cannula oxygen which was gradually weaned. He continued to have significant weakness hypoxia and shortness of breath. He underwent aggressive respiratory hygiene, physical occupational therapy. Gradually his symptoms did improve. He was weaned back down to his normal 2 L nasal cannula. He improved with physical therapy and was felt that he did not need subacute rehab. He completed a 5 day course of remdesivir and antibiotics. He is discharged in stable condition on dexamethasone for 3 more days. Home care will be arranged for him and he will follow up with primary care provider within the next week. He is instructed to continue to self isolate for 2 more days which will be 10 days from symptom onset.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertriglyceridemia Hypertension Lung cancer Type 2 diabetes mellitus Alzheimer's disease
- Andere Medikamente
- Ascorbic Acid (VITAMIN C PO) B Complex Vitamins (VITAMIN B COMPLEX) tablet Barberry-Oreg Grape-Goldenseal (BERBERINE COMPLEX PO) budesonide/formoterol (SYMBICORT) 160-4.5 MCG/ACT inhaler Cholecalciferol (D3 PO) Cyanocobalamin (B-12 PO) done
- Allergien
- penicillins
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 27.10.2022
- Impfdatum
- 26.10.2021
- Beginn
- 16.10.2022
- Tage bis Beginn
- 355,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acquired diaphragmatic eventration
Acute respiratory failure
Amyotrophic lateral sclerosis
Bronchial secretion retention
COVID-19
Computerised tomogram thorax abnormal
Condition aggravated
Dyspnoea
Hypoxia
Lung consolidation
Lung infiltration
Pleural effusion
Pneumonia
Polyuria
Positive airway pressure therapy
Pulmonary embolism
SARS-CoV-2 test positive
Sepsis
Symptomtext
Discharge Provider: DO Primary Care Provider: DO Admission Date: 10/16/2022 Discharge Date: Oct 27, 2022 PRESENTING PROBLEM: ALS (amyotrophic lateral sclerosis) (HCC) Pneumonia of both lower lobes due to infectious organism COVID-19 virus infection Sepsis (HCC) COVID-19 Acute respiratory failure with hypoxia (HCC) HOSPITAL COURSE: The patient is a 75-year-old male with a history of OSA on BiPAP, essential hypertension, prediabetes, who more recently was diagnosed with ALS in March of 2021. The patient did have dysphagia related to his ALS with placement of a PEG tube. In September of 2022 he was admitted to hospital with massive PE. The patient underwent thrombectomy, and was continued on anticoagulation, but had chronic respiratory failure requiring supplemental oxygen at 6 L/Min at discharge. Patient presented to Hospital on 10/16 with increasing shortness of breath and increasing O2 requirements. At the time of admission, CT scan of the chest showed no acute PE but did show consolidation of the left lower lobe as well as dense infiltrate in the right lower lobe and pleural effusion. Patient was also found to be positive for COVID. Patient was treated with broad-spectrum antibiotics, and started on dexamethasone and remdesivir. Pulmonary was consulted virtually. Patient was initially managed with high-flow nasal cannula and BiPAP at night. With cefepime and vancomycin. MRSA screen was negative and vancomycin was discontinued. Patient was switched from cefepime to Rocephin. Initially there was some discussion that the patient may require bronchoscopy, as there was significant mucus plugging seen on initial CT. Patient was noted to have advanced ALS, with dysphagia, being wheelchair-bound using Hoyer lift and slide board for transfers. Patient stated that he was adamant that he would not a tracheostomy, or chronic ventilator support. Given the patient's wishes it was felt there was no role for bronchoscopy, with pulmonary recommending continuing antibiotics, gentle diuresis and aggressive pulmonary toilet. Repeat CT chest was performed on 10/21 showing persistent consolidation in the left lower lobe, but clearing infiltrates in the right lower lobe. With treatment, the patient did have a slight improvement in his respiratory status, allowing a titration of his high-flow nasal cannula. Hospice was consulted for informational visit which occurred on 10/25/22. By morning of 10/10/2022 decision was made to the take patient home without hospice initiation and to continue restorative care. Long discussion had with patient, wife, his son who is a PA, about prognosis, treatment plan, supportive services that will be made available at this time. Patient has improved his O2 support needs down to 3 L at rest, and extra O2 support has been provided in case of increased needs during mobilization up to 12 L via nasal cannula. Repeat SLP evaluation determined that the patient is not swallowing Entocort in manner and is to be NPO except for pureed pleasure feeding infrequently. To continue PEG tube for feedings. Patient will have palliative Care, Home Health Care, respiratory services available at home and his daughter will also be available to provide some care support. Patient's prognosis is guarded at this time, but patient and wife are adamant about remaining DNI.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 11,0
- Labordaten
- -
- Aktuelle Erkrankungen
- Admission from 09/22/2022-9/30/2022 Hospital Discharge Provider: MD Primary Care Provider: DO Admission Date: 9/22/2022 Discharge Date: Sep 30, 2022 PRESENTING PROBLEM: Acute hypoxemic respiratory failure (HCC) Acute pulmonary embolism, unspecified pulmonary embolism type, unspecified whether acute cor pulmonale present (HCC) Acute respiratory failure with hypoxemia (HCC) HOSPITAL COURSE: 74-year-old male who presented to Hospital with acute shortness of breath and was found to have submassive bilateral pulmonary emboli with evidence of RV strain and transferred to hospital for further evaluation and treatment. Interventional Radiology evaluated the patient and felt he is an appropriate candidate for mechanical embolectomy which he underwent on 9/22. Post embolectomy he still required O2 6 l/min during day and BIPAP at night. Limited echo on 9/25 did not visualize RV, but showed intra-atrial shunt. He also had chronic elevation of the left hemidiaphragm, and probable some degree of respiratory muscle weakness due to ALS. Pulmonary has been consulted and recommended repeating CT PE study which was obtained. Repeat CT PE study showed improvement in overall clot burden and no new pathology. After re-evaluation, pulmonology did not believe that the patient required any sort of repeat thrombectomy and they believe that the patient's hypoxic respiratory failure was related to his underlying ALS and there was a component related to his interatrial shunt. It was suspected that he would simply need oxygen at discharge with continue use of incentive spirometer with hopes that he would be able to wean off of oxygen in the future. Patient was continued on supplemental oxygen and he was encouraged to use incentive spirometer. Eventually, he was thought to be an appropriate candidate for inpatient rehab and was transition to inpatient rehab on 09/30/2022 in stable condition.
- Vorgeschichte
- Mild intermittent asthma, uncomplicated Snoring Mild persistent asthma without complication Acute on chronic hypoxemic respiratory failure (HCC) Moderate persistent asthma without complication OSA (obstructive sleep apnea) Diaphragm, eventration HAP (hospital-acquired pneumonia) Essential hypertension, benign TIA (transient ischemic attack) Old myocardial infarction Atherosclerosis of aorta (HCC) Acute pulmonary embolism with acute cor pulmonale (HCC) Acute deep vein thrombosis (DVT) of femoral vein of left lower extremity (HCC) Dysphagia Diverticulosis of sigmoid colon Gastroesophageal reflux disease without esophagitis Slow transit constipation Moderate protein-calorie malnutrition (HCC) Unspecified inflammatory spondylopathy, lumbar region (HCC) Chronic pain of right knee Lumbar nerve root impingement ALS (amyotrophic lateral sclerosis) (HCC) Cervical myelopathy (HCC) Primary open-angle glaucoma, bilateral, mild stage Pure hypercholesterolemia Prediabetes Sepsis (HCC) Attention-deficit hyperactivity disorder, predominantly inattentive type Primary osteoarthritis of right knee Benign prostatic hyperplasia with urinary frequency Biceps muscle tear, left, subsequent encounter Degenerative disc disease, lumbar Major depressive disorder, recurrent, in partial remission (HCC) Adjustment disorder with mixed anxiety and depressed mood Abnormal gait Acquired hammer toe of right foot Weight loss Elevated troponin
- Andere Medikamente
- acetaminophen (TYLENOL) 32 MG/ML suspension albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization ALBUTEROL 108 (90 Base) MCG/ACT inhaler ALPRAZolam (XANAX) 0.25 MG tablet apixaban starter pack (ELIQUIS) 5 MG TBPK tablet atorvastatin (LIPI
- Allergien
- Environmental Amlodipine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 02.11.2021
- Beginn
- 03.04.2022
- Tage bis Beginn
- 152,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Cerebrovascular accident
Computerised tomogram
Fatigue
Magnetic resonance imaging
Muscular weakness
Symptomtext
My right arm started feeling weak. I was really tired, so I rested all day then I took my blood pressure and it 225/111. I went to ER & was told I had a stroke.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- CT Scan MRI Bloodwork
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Levothyroxine
- Allergien
- Penicillin Codeine Azithromycin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 10.04.2022
- Impfdatum
- 28.10.2021
- Beginn
- 01.04.2022
- Tage bis Beginn
- 155,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Cardiac disorder
Computerised tomogram thorax abnormal
Dyspnoea
Eructation
Fibrin D dimer increased
Musculoskeletal chest pain
Pain
Pulmonary embolism
Pulmonary infarction
Symptomtext
4/1/2022 thru 04/07/2022 and ongoing: Trouble beathing, severe pain in coastal ribs, excessive and painful belching/burping
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 2,0
- Labordaten
- 4/7/2022 - D-dimer lab results: Positive 4/7/2022 - CT Scan results: Bilateral Pulmonary Embolism with pulmonary infarcts and diastolic heart
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Thyroid
- Allergien
- Scallops, Seaweed, Zythromax, Aspirin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 21.11.2021
- Beginn
- 24.01.2022
- Tage bis Beginn
- 64,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Apraxia
Death
Haematemesis
Inappropriate schedule of product administration
Nausea
Pain in extremity
Symptomtext
1st dose on 11.21.2021 Moderna Lot 939904 - Soreness on arm. Taken Tylenol to resolve. No other issues on 11.21.2021. 2nd dose on 12.31.2021 Moderna Lot 041J21A - Soreness on arm. Taken Tylenol to resolve. No other issues on 12.31.2021. Vomiting blood, nausea and inability to open eyes on day 24 after 2nd Moderna Dose. Death at 11AM on 01.24.2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- severe vertigo
- Vorgeschichte
- severe vertigo diabetes high blood pressure
- Andere Medikamente
- allopurinol 100mg atenolol 50mg vitamin b plex celebrex 200 mg colace 100 mg ducolax 5 mg evista 60 mg loratadine 10 mg losartan 100 mg meclizine 25 mg metformin 500 mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 101,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 02.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Moderna Product on 12/31/2020, 01/28/2021, and 11/02/2021. It is not known if the individual had a specific symptom onset date. They tested positive for COVID-19 via antigen test on 11/09/2021 at the skilled nursing facility at which they were a resident. They were hospitalized 11/26/2021 until their death on 12/02/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 6,0
- Labordaten
- Positive COVID-19 antigen test on 11/09/2021 despite being vaccinated.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes Mellitus, Hypertension, Dementia, Anemia, Glaucoma, history of renal failure; Diastolic Heart Failure; the individual was a resident of a Skilled Long Term Care Facility at the time of the adverse event
- Andere Medikamente
- -
- Allergien
- Fentanyl; Tramadol; Household Dust
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 03.11.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 34,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram pulmonary abnormal
Anticoagulant therapy
Dyspnoea
Fibrin D dimer increased
Presyncope
Pulmonary embolism
Right ventricular dysfunction
Symptomtext
patient developed gradually progressive dyspnea. had a near syncopal event. found to have pulmonary embolism (moderate clot burden) with evidence of R heart strain and was hospitalized for monitoring. she is recovering and on anticoagulation. negative thrombotic risk panel.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 2,0
- Labordaten
- ddimer +. CTPA + for PE.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- migraine headaches
- Andere Medikamente
- vitamin D, omega 3, excedrin migraine, medical cannabis
- Allergien
- sulfanilamide
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 14.11.2021
- Impfdatum
- 22.10.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 21,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Anticoagulant therapy
Computerised tomogram thorax abnormal
Deep vein thrombosis
Pulmonary embolism
Thrombectomy
Symptomtext
Massive Pulmonary Embolism of the right lung, small PE in the Left lung, and DVT of the right femoral the week of November 8-12, being hospitalized on the 12th of November 2021. Resulting in Thrombolectomy and anticoagulated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 3,0
- Labordaten
- CT showed massive PE on the right side, smaller one on the left side November 12th, 2021 ER MD Interventional MD General/Primary Care
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- moderate HTN
- Andere Medikamente
- Lisinopril, Lipitor, Zyrtec , Prilosec, Tamsulosin ,
- Allergien
- ASA, Toradol
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
C-reactive protein
COVID-19
Cerebrovascular accident
Eye pain
Full blood count
Headache
Metabolic function test
Neoplasm
Ophthalmological examination
Red blood cell sedimentation rate normal
Symptomtext
Extreme headache began about 1 day after vaccine. Sharp pains in head and behind eye began about 4 days after vaccine and have continued now to 8-9 days after vaccine. Pain is extremely debilitating, was in bed for hours and sought medical care with concern for stroke or tumor. May need head MRI or CT yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- COVID test, vision screen, blood count, metabolic panel, ESR, CRP are all normal
- Aktuelle Erkrankungen
- Change in voice--breathy/raspy
- Vorgeschichte
- type 2 diabetes, high cholesterol, high blood pressure, urinary dysfunction
- Andere Medikamente
- Hydrochlorothiazide, pravastatin
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 01.12.2022
- Impfdatum
- 08.12.2021
- Beginn
- 03.06.2022
- Tage bis Beginn
- 177,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Superficial vein thrombosis
Ultrasound Doppler abnormal
Symptomtext
Superficial Thrombophlebitis: Complete thrombosis of all four superficial basilic veins.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Superficial vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Ultrasound
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- creatine monohydrate, whey protein.
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 33,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Syncope
Symptomtext
hospitalization with positive covid after syncopal episode
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- positive for sars covid 2 6/14/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 18.11.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 53,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Cardiac operation
Cardiomegaly
Chest X-ray abnormal
Cough
Dyspnoea
Echocardiogram abnormal
Headache
Intensive care
Laboratory test normal
Malaise
Nasopharyngitis
Pain
Pericardial drainage
Weight bearing difficulty
Symptomtext
The shot itself wasn't abnormal it was sore like normal. A month later I got a cold that lasted for a week then it cleared for two days. Then I started feeling sick cough, headache mainly the cough. Everyday it got worse harder to breath Jan 10 I lost the ability to bear weight. I took a few test they all came back negative. I went to my doctor, and she checked my lungs they were clear, and I went home. Jan 31 my dr. sent me for a chest x-ray and it showed I had a enlarged heart. I then went to a HCF they did a echocardiogram the assist kept making faces and told me I was very symptomatic. They did transfer me to the ER department. They gave me two IV and then send me by ambulance with lights to another facility where they did surgery inserted a needle pulling fluid off the heart. Then I was in cardiac ICU I was there until the 20th which is when I was discharged. Two weeks later I went to see the Cardiologist and he said everything was fine. The medication they put me on for my heart has created even more issues and now I have to see another dr. about that.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Osteoporosis
- Andere Medikamente
- Levothyroxine 25mcg; metoprolol 25mg; amlodipine besylate 5mg
- Allergien
- Penicillin; erythromycin; any sulfa drugs; calcium channel blockers; no corn starch or blue dye
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 09.04.2022
- Impfdatum
- 28.10.2021
- Beginn
- 06.04.2022
- Tage bis Beginn
- 160,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Activated partial thromboplastin time
Bell's palsy
Borrelia test negative
Differential white blood cell count normal
Electrocardiogram normal
Facial paralysis
Full blood count normal
International normalised ratio normal
Metabolic function test
Metabolic function test normal
Prothrombin time normal
Symptomtext
Bell?s Palsy: Left sided facial palsy discharged from ED 4/7/2022 on prednisone, valacyclovir, Systane complete eye drops & eye ointment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- 4/7 Lyme disease negative; CBC diff, APTT, PT-INR, CMP?..WNL; EKG normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism, osteoarthritis, BPH
- Andere Medikamente
- Synthroid, tamsulosin, ASA, Flonase, ibuprofen, medical marijuana
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 12.11.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 39,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
ADAMTS13 activity normal
Acute kidney injury
Antibody test negative
Anticoagulant therapy
Aspartate aminotransferase increased
Base excess
Bicytopenia
Biopsy skin abnormal
Blood alkaline phosphatase increased
Blood creatinine increased
Blood fibrinogen decreased
Blood folate normal
Blood gases
Blood lactate dehydrogenase increased
Blood pH increased
Blood smear test abnormal
Blood urine present
COVID-19
Symptomtext
hospital dc summary from 12/17/21 to dc on 4 Jan 2022: Anasarca, AKI on CKD III, Metabolic Alkalosis (likely due to diuresis). DDx: chronic cardio-renal injury vs TMA from gemcitabine (kidney function has been worsening progressively since the patient started it) vs interstitial nephritis from gemcitabine, Bactrim, or cephalosporins. Urine urate low, not consistent with TLS. Baseline creatinine 1.0-1.5. Creatinine on admit 2.93, today 2.45. Lasix, HCTZ, and lisinopril were held on admit. 12/17 Renal US with small bilateral kidneys, otherwise unremarkable. 12/4 Echo: EF 75%, hyperdynamic, otherwise unremarkable. 12/1 PET scan showed development of moderate sized bilateral pleural effusions, body wall edema, and lower extremity edema, compatible with volume overload. 12/17 UA with negative protein, +1 blood, +2 leukocytes, WBC 20-50, RBC 2/10, Protein/creatinine ratio 0.1. Started on a Bumex gtt at 2 mg/hr per renal, held 12/31. Received Chlorthiazide and Albumin 12/28 and 12/29. VBG (12/31) 7.46/43/44/29.7/6.2 BE/74.5 S/p IV Albumin 25g 25% x2 on 12/31 and 1/1. Nephrology consulted. S/p 1L 1/2NS @ 75 mL hr 1/4. Cr improved to 2.39 day of discharge. Continue to hold lasix, lisinopril, and HCTz at discharge. Hold bactrim ppx as well since Cr clearance <30. Follow up outpatient being arranged by nephrology. 2) Stasis dermatitis. Dermatology was consulted previously and skin biopsy was consistent with stasis dermatitis, so antibiotics were discontinued. 12/17 leg swab culture 12/17 w/ coag neg staph. Per findings are consistent with severe lower extremity edema rather than cellulitis. Would not recommend antibiotics, now signed off For stasis dermatitis, derm has recommended triamcinolone BID x2 weeks on and 2 weeks off, restarted 1/3. Continue tylenol, tramadol, gabapentin for pain. 3) Bilateral Lower Extremity Acute DVT, Hx of DVT/PE on lifelong anticoagulation, Factor V Leiden. US of all 4 extremities obtained 12/21, bilateral upper extrem neg for acute DVT. Acute occlusive thrombus of the distal right femoral vein extending into the popliteal veins, acute occlusive and nonocclusive thrombus at the left common femoral vein and acute thrombus in the upper deep femora, upper greater saphenous, femoral and popliteal veins. Her Apixaban was stopped 12/20 w/ worsening thrombocytopenia but she had otherwise been adherent to the medication regimen. S/p Heparin gtt 12/21-12/23. IR c/s for thrombolysis, pain has improved so will hold off for now. Continue Apixaban 5 mg BID resumed 12/23. Not considered an Apixaban failure as home dose was 2.5 mg daily. 4) Cutaneous T cell lymphoma. Diagnosed in September 2020. Follows with Hematology. Recently started cycle 4 of gemcitabine on 12/10, was scheduled to get dose 12/17. Hematology consulted, continue Allopurinol for TLS ppx ( decreased to 100 mg daily duet to renal function). Chemotherapy on hold. F/u outpatient arranged. 5) Bicytopenia. Likely related to recent chemotherapy. Worsening plt 12/20-- lowest was 37-- > now 128 (12/31). Folate, B12 nml, LDH mildly elevated 541-- >661, Haptoglobin <30. Peripheral smear w/o schistocytes, no evidence of TTP. Smear (12/27/21) with sezary cells, few schistocytes, ADAMTS13 normal. Fibrinogen 181. HIT Ab negative. Plt slowly improving. 6) Soft palate mass. ENT consulted, noted a maxillary tori that is likely chronic, no acute intervention 7) Chronic elevated AST and Alk phos. Stable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Acquired hypothyroidism Arthritis Breast cancer Cancer of skin Hypertension Vision decreased
- Vorgeschichte
- 1. COVID positive = 1/24/2022 2. Stage IVA CTCL with sezary syndrome with large cell transformation 3. Stasis dermatitis with large wounds on bilateral lower extremities 5. Daytime and nocturnal diaphoresis 6. Pulmonary edema and pleural effusions on CXR 7. Osteopenia 8. Hypertension 9. ECOG PS 2
- Andere Medikamente
- Current Outpatient Medications: ? acetaminophen (TYLENOL EXTRA STRENGTH) 500 mg tablet, Take one tablet by mouth every 4 hours as needed for Pain. Max of 4,000 mg of acetaminophen in 24 hours., Disp: 20 tablet, Rfl: 0 ? acyclovir (ZOVIRA
- Allergien
- pneumonia shot and Td shot
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 05.01.2021
- Beginn
- 02.02.2021
- Tage bis Beginn
- 28,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Catheterisation cardiac
Echocardiogram
Electrocardiogram
Myocarditis
X-ray
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 2,0
- Labordaten
- 12/13/2021 - EKG, Blood Test, echo cardiogram, cath lab, xray
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 26.12.2021
- Impfdatum
- 28.10.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 59,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Central venous catheterisation
Dyspnoea
Ejection fraction decreased
Endotracheal intubation
Hypotension
Ischaemic cardiomyopathy
Respiratory distress
Symptomtext
74-year-old presents from outside nursing home to this hospital's emergency room with shortness of breath and EMS transported the patient to hospital. He was in respiratory distress upon arrival. He was intubated by ER physician. Patient was hospitalized at Hospital and diagnosed with COVID-19 2 weeks ago. He also has ischemic cardiomyopathy with very low ejection fraction. He became hypotensive after intubation. Pt is now on IV pressors & has a central line in place.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory distress
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 24.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Disorientation
Dyspnoea
Hepatic enzyme abnormal
Hyperhidrosis
Impaired work ability
Nausea
Pericarditis
Syncope
Symptomtext
On 12/01/2021 I woke up with intense chest pain and short breath. I started sweating, felt nauseous, became disoriented and fainted. My partner called 911 and an ambulance took me to the ER. I saw a cardiologist on 12/10 & it was seen through ultrasound that I have pericarditis. I am currently at home taking medication as prescribed; I am unable to work or do much physical activity.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- Had high liver enzymes on 10/08 & 10/10
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 27.10.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac tamponade
Intensive care
Pericardial drainage
Pericardial effusion
Shoulder operation
Symptomtext
Pericardial effusion with some evidence of cardiac tamponade. Status post pericardiocentesis. Admitted to inpatient hospital unit with critical care and cardiology services.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- shoulder surgery in November
- Vorgeschichte
- -
- Andere Medikamente
- aspirin, atorvastatin, baclofen, calcium, D3, famotidine, gaba
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 07.12.2021
- Impfdatum
- 27.10.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 37,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Borrelia test
Scan
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- C-Scan and Lymes Test
- Aktuelle Erkrankungen
- CHF
- Vorgeschichte
- Obesity, diabetes, heart disease, chronic pain
- Andere Medikamente
- Gabapentin, metformin, metoprolol, losartan, rosuvastatin, Influenza Flu (seasonal) Fluzone Quadrivalent
- Allergien
- Penicillin, ace inhibitor,
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 27.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Eye contusion
Eye swelling
Head injury
Hyperhidrosis
Loss of consciousness
Nausea
Scratch
Skin laceration
Swelling
Symptomtext
11/13/2021 approximately 10:00 AM--symptoms wave 1: dizzy, light headed, weak, sweating and light nausea; approximately 10:30 AM wave 2 symptoms: blacked out (less than 10 minutes), hit on forehead (swelling, scratches and minor cuts on forehead and nose; glasses caused both areas around eyes to blacken and swell).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes, hypo thyroid, high blood pressure, high cholesterol, Adult Growth Hormone Syndrome
- Andere Medikamente
- Atorvastatin 80 mg?daily PM Buperprion 150mg?twice daily Diltiazem 24h ER(CD) 180 mg CP?once daily AM Escitalopram 5mg daily AM Levoxyl 125 mcg?daily AM Losartan Potassium 100mg?daily PM Meloxicam 7.5 mg?daily PM Nutropin?7mm daily & BD ste
- Allergien
- Penicillin Sulphur Tetracycline Humatrope Norditropin Voltaren/Diclofenac Sodium Topical Gel
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 06.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Deep vein thrombosis
Fibrin D dimer increased
Pain in extremity
Tenderness
Ultrasound scan
Symptomtext
11/10/21 Three days after the vaccination I noticed tenderness in back my rt knee. The tenderness increased over the next two days to an ache in my calf and thigh. Saturday Nov 13 I noted a fullness in the back of my rt knee, increased pain with walking and with flexion of my foot I took myself to the ER and testing revealed a blood clot DVT in rt popliteal vein. I have never had a blood clot or bleeding problem in my life. I stopped Estradiol immediately. I am now taking Eliquis blood thinner for 6 months
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- D-Dimer 4660 ultrasound rt legs revealed a DVT popliteal vein, right Complete blood count nl
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- mild asthma, HRT, depression, gerd,
- Andere Medikamente
- estradiol, loratadine, famotidine, citalopram, montelukast, symbicort, albuterol MDI
- Allergien
- vancomycin powder in incision
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 30.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac stress test
Chest X-ray
Chest pain
Computerised tomogram thorax
Echocardiogram
Electrocardiogram
Fibrin D dimer
Pericarditis
Ultrasound scan
Symptomtext
Patient presented 11/23/21, 1 month after booster shot, with chest pain, then again 11/29/21- found to be Pericarditis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- 2,0
- Labordaten
- 11/23/21- 11/24/21 CT chest, EKG, Chest Xray, NM stress test, 2D ECHO, DDimer 11/29/21-CT chest, EKG, Chest Xray Ultrasound, 2D ECHO
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Benign prostatic hyperplasia Frequent PVCs Kyphosis Nocturnal hypoxia Prediabetes
- Andere Medikamente
- flonase 1 spray Both nartes, daily prn, alfuzosin 10mg q 24, Multivitamin 1xdaily
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 19.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase normal
Albumin globulin ratio
Anion gap decreased
Anticoagulant therapy
Aspartate aminotransferase normal
Basophil count normal
Basophil percentage increased
Blood albumin decreased
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium decreased
Blood chloride increased
Blood creatinine increased
Blood glucose normal
Blood potassium normal
Blood sodium normal
Blood urea normal
Carbon dioxide decreased
Symptomtext
O VAS DUPLEX VENOUS LWR EXT RIGHT. Acute deep venous thrombosis right gastrocnemius and peroneal veins. Current treatment is Rivaroxaban 15 & 20 MG Tablet Therapy Pack.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Labs: O CBC WITH DIFF Collection Time: 11/16/21 3:20 PM Result Value Ref Range WBC 5.65 4.00 - 12.00 K/uL RBC 4.21 (L) 4.50 - 6.00 mil/uL Hgb 13.5 (L) 14.0 - 18.0 g/dL Hct 44.6 40 - 54 % MCV 105.9 (H) 80 - 98 fL MCH 32.1 27 - 33 pg MCHC 30.3 (L) 32 - 37 g/dL RDW 12.1 11.5 - 15.0 % Plt 163 150 - 450 K/uL Differential type Automated Abs neuts 3.40 1.80 - 7.80 K/uL Abs immature grans 0.01 0.00 - 0.07 K/uL Abs lymphs 1.51 0.80 - 3.30 K/uL Abs monos 0.51 0.10 - 1.00 K/uL Abs eos 0.15 0.00 - 0.40 K/uL Abs basos 0.07 0.00 - 0.20 K/uL Abs NRBCs 0.00 0.00 K/uL Neuts 60.2 % Immature grans 0.2 0.0 - 0.9 % Lymphs 26.7 % Monos 9.0 % Eos 2.7 % Basos 1.2 % NRBC 0.0 0.0 % Plt estimate Adequate RBC morphology Reviewed O COMPREHENSIVE METABOLIC PANEL Collection Time: 11/16/21 3:20 PM Result Value Ref Range Na 136 135 - 145 mmol/L K 4.7 3.6 - 5.3 mmol/L Cl 107 98 - 109 mmol/L CO2 22 21 - 32 mmol/L Anion gap w/o K 7 7 - 15 BUN 20 8 - 24 mg/dL Creatinine 1.57 (H) 0.7 - 1.5 mg/dL GFR non African Amer 44 (L) >59 mL/min GFR African American 53 (L) >59 mL/min Glucose 97 65 - 120 mg/dL SGOT/AST 26 5 - 40 IU/L Alk Phos 77 38 - 126 IU/L SGPT/ALT 31 6 - 60 IU/L Bilirubin total 0.3 0.2 - 1.4 mg/dL Protein 6.6 6.1 - 7.8 g/dL Albumin 3.2 3.2 - 5.0 g/dL Globulin (calc) 3.4 2.0 - 4.5 g/dL A:G Ratio 0.9 (L) >1.0 Calcium 8.7 8.5 - 10.5 mg/dL
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anemia
- Andere Medikamente
- oxybutynin 5 MG Tb24 Xylitol 550 MG Disk folic acid 1 MG Tab trazodone 150 MG Tabs citalopram 20 MG Tabs omeprazole 20 MG Cpdr Glucos-Chond-Hyal Ac-Ca Fructo (MOVE FREE JOINT HEALTH ADVANCE OR) Free Text Medication Entry (OTHER) vitamin d3
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Electric shock sensation
Feeling abnormal
Paraesthesia
Vaccination site erythema
Vaccination site reaction
Vaccination site swelling
Vaccination site warmth
Visual impairment
Symptomtext
Brain zaps like when you stop cold turkey or are weaning off SSRIs; Feels like you stuck your finger in a light socket; Like pins and needles when your arm falls asleep. This runs down and out of her arm.; Couldn't see when she would move her eyes; Raised, red area in the general area of the injection site; Raised area in the general area of the injection site; began as an area about the size of her palm, but it had grown after booster dose to the size of her palm plus up to the knuckle of her hand size; COVID arm (worse); Very warm to the touch, she can feel the heat through her clothing; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE REACTION (COVID arm (worse)), VACCINATION SITE WARMTH (Very warm to the touch, she can feel the heat through her clothing), ELECTRIC SHOCK SENSATION (Brain zaps like when you stop cold turkey or are weaning off SSRIs), FEELING ABNORMAL (Feels like you stuck your finger in a light socket) and PARAESTHESIA (Like pins and needles when your arm falls asleep. This runs down and out of her arm.) in a 41-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Hysterectomy. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced VACCINATION SITE REACTION (COVID arm (worse)), VACCINATION SITE WARMTH (Very warm to the touch, she can feel the heat through her clothing), VACCINATION SITE ERYTHEMA (Raised, red area in the general area of the injection site) and VACCINATION SITE SWELLING (Raised area in the general area of the injection site; began as an area about the size of her palm, but it had grown after booster dose to the size of her palm plus up to the knuckle of her hand size). On 07-Nov-2021, the patient experienced ELECTRIC SHOCK SENSATION (Brain zaps like when you stop cold turkey or are weaning off SSRIs), FEELING ABNORMAL (Feels like you stuck your finger in a light socket), PARAESTHESIA (Like pins and needles when your arm falls asleep. This runs down and out of her arm.) and VISUAL IMPAIRMENT (Couldn't see when she would move her eyes). On 07-Nov-2021, ELECTRIC SHOCK SENSATION (Brain zaps like when you stop cold turkey or are weaning off SSRIs), FEELING ABNORMAL (Feels like you stuck your finger in a light socket), PARAESTHESIA (Like pins and needles when your arm falls asleep. This runs down and out of her arm.) and VISUAL IMPAIRMENT (Couldn't see when she would move her eyes) had resolved. At the time of the report, VACCINATION SITE REACTION (COVID arm (worse)), VACCINATION SITE WARMTH (Very warm to the touch, she can feel the heat through her clothing), VACCINATION SITE ERYTHEMA (Raised, red area in the general area of the injection site) and VACCINATION SITE SWELLING (Raised area in the general area of the injection site; began as an area about the size of her palm, but it had grown after booster dose to the size of her palm plus up to the knuckle of her hand size) outcome was unknown. Concomitant medication of the patient was not reported. The patient received the booster dose into the muscle of her left, upper arm. The events visual disturbance, brain zaps, feeling abnormal and pins and needles lasted for about 2-3 hours. The only way she would find relief was to lay flat with her eyes closed. It had not happened since. Treatment information for rest of the events were not reported by the reporter. This case was linked to MOD-2021-072928, MOD-2021-072933 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hysterectomy.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 31.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 02.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test abnormal
Cardiac monitoring
Chest X-ray normal
Chest discomfort
Chest pain
Dyspnoea
Electrocardiogram
Hypopnoea
Monocyte count increased
Myocarditis
Neutrophil count increased
Painful respiration
Respiratory viral panel
Troponin increased
White blood cell count increased
Symptomtext
25 YR OLD MALE PRESENTS TO ED WITH CHEST PAIN, TIGHTNESS AND SHORTNESS OF BREATH SINCE HE RECIEVED SECOND COVID SHOT 2 DAYS AGO. PT NOTES HAS TO TAKE SHALLOW BREATHS DUE TO PAIN IN CHEST WHEN A NORMAL BREATH IS TAKEN. PT HAD BLOODWORK, RESPIRATORY PANEL, EKG, XRAY COMPLETED HERE IN THE ED. BLOODWORK RESULTS SHOWED AN ELEVATED TROPONIN AT 159(OVER 22 IS POSITIVE.) WITH A SECOND 2 HOUR TROPONIN ADDITIONALLY ELEVATED AT 176. IMPRESSION FROM XRAY SHOWS NORMAL CHEST XRAY BUT FINDINGS REPORTED IMAGE WAS OBSCURED BY OVERLYING WIRES FROM HEART MONITOR. WBC BLOODWORK SHOWED ELEVATED AT 16.1 (RANGE 1.1-6.1) MONOCYTES ELEVATED AT 2.6 (RANGE .2-1.0) IMMATURE NEUTROPHILS ELEVATED .06 (RANGE .00-.04) MD SUSPECTS MIOCARDITIS HEART ECHO SCHEDULED FOR TOMORROW. PT CURRENTLY ADMITTED WITH NO COMMUNICATED DISCHARGE DATE UNTIL ECHO RESULTS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 1,0
- Labordaten
- PT HAD BLOODWORK, RESPIRATORY PANEL, EKG, XRAY COMPLETED HERE IN THE ED. BLOODWORK RESULTS SHOWED AN ELEVATED TROPONIN AT 159(OVER 22 IS POSITIVE.) WITH A SECOND 2 HOUR TROPONIN ADDITIONALLY ELEVATED AT 176. IMPRESSION FROM XRAY SHOWS NORMAL CHEST XRAY BUT FINDINGS REPORTED IMAGE WAS OBSCURED BY OVERLYING WIRES FROM HEART MONITOR. WBC BLOODWORK SHOWED ELEVATED AT 16.1 (RANGE 1.1-6.1) MONOCYTES ELEVATED AT 2.6 (RANGE .2-1.0) IMMATURE NEUTROPHILS ELEVATED .06 (RANGE .00-.04) MD SUSPECTS MIOCARDITIS HEART ECHO SCHEDULED FOR TOMORROW
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 31.05.2023
- Impfdatum
- 10.11.2022
- Beginn
- 24.05.2023
- Tage bis Beginn
- 195,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram abnormal
COVID-19
Computerised tomogram abdomen abnormal
Computerised tomogram thorax abnormal
Dyspnoea
Peripheral artery occlusion
Pneumonia
SARS-CoV-2 test positive
Tachycardia
Symptomtext
Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: "Patient is a 91 YO year old female with past medical history of persistent atrial fibrillation, CAD, HTN, and subdural hematoma who presented with difficulty breathing and tachycardia. Patient was tested COVID positive. CT chest abdominal and pelvic show multifocal pneumonia. Given concern for bacterial pneumonia, patient was treated with Rocephin, and her breathing status has improved. Unfortunately, CT angiogram of the aorta and runoff shows complete occlusion of the left common femoral artery and Complete occlusion of the right profunda femoris . CTS surgical team was consulted, CTS recommends that patient may likely require left AKA and right BKA. Discussed and explained to her son, Son states he does not want any surgery for her. Son elected for hospice. He signed with hospice on 5/29."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 7,0
- Labordaten
- COVID-19 detected PCR on 5/24/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN (Chronic) Permanent atrial fibrillation (Chronic) Seborrheic keratosis Panic attack Hypothyroidism (Chronic Dyslipidemia (high LDL; low HDL) GERD Hiatal hernia History of ovarian cancer (Chronic) Heart palpitations Benign head tremor Vaginal atrophy Chronic low back pain Hammer toe of right foot Sciatica of right side Very large incisional hernia, without obstruction or gangrene (Chronic) Chronic pain of right knee (Chronic) Cervical radiculopathy History of right hip replacement (Chronic) Debility Anxiety and depression Low vitamin D level Osteopenia of both thighs Lichen sclerosus of vulva Atherosclerosis of aorta Chronic diastolic heart failure (Chronic) Diuretic-induced hypokalemia Venous insufficiency of both lower extremities CAD (coronary artery disease) (Chronic) History of traumatic subdural hematoma 10/2020 RLS (restless legs syndrome) Hematoma of left iliopsoas muscle Slow transit constipation Stage 3b chronic kidney disease Anemia GAD (generalized anxiety disorder) Intertrigo labialis Lactic acidosis Critical limb ischemia of both lower extremities Permanent atrial fibrillation with rapid ventricular response
- Andere Medikamente
- -
- Allergien
- Hydrochlorothiazide Ciprofloxacin Macrobid [nitrofurantoin Monohyd/m-cryst] Pcn [penicillins]
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 12.04.2023
- Impfdatum
- 03.11.2021
- Beginn
- 28.03.2023
- Tage bis Beginn
- 510,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Dyspnoea
Symptomtext
Presented to the ER with complaints of shortness of breath and chest pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Atrial fibrillation, Hypertension, Diabetes mellitus
- Andere Medikamente
- Glimepiride 4 mg po BID Gemfibozil 600 mg po BID Metoprolol Succinate ER 25 mg po daily Lisinopril-hydrochlorothiazide 20-12.5 mg po daily Metformin 500 mg po daily
- Allergien
- KNDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 02.03.2023
- Impfdatum
- 19.07.2022
- Beginn
- 17.02.2023
- Tage bis Beginn
- 213,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest tube insertion
Chest tube removal
Dyspnoea
Encephalopathy
Hypoxia
Leukocytosis
Respiratory disorder
SARS-CoV-2 test positive
Symptomtext
Discharge summary "Patient is a 89 YO male history of bronchiectasis, prior Pseudomonas empyema, Parkinson's disease presented with dyspnea. He was found severely hypoxic. Labs reveal COVID +. During his stay, he received 5 days of Remdesivir and steroids for COVID treatment. He was initially placed on Rocephin and Doxycycline. His hospitalization was complicated by worsening respiratory status with concern for rapidly progressive left sided loculated effusion with concern for empyema. Pulmonary and IR were consulted and patient underwent left sided chest tube placement. ID was consulted who transitioned patient to Cefepime and Flagyl for better anaerobic coverage. He received TPA/Dornase instillation as well. His hospitalization was further complicated by worsening encephalopathy and leukocytosis despite medical management. Goals of care discussion were done with assistance from Palliative and Hospice care team. Family (son and wife) has elected to transition patient to Comfort care with plans to discharge back to prior living arrangements with Hospice team. Chest tube removed morning of day of discharge as requested by family. "
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 12,0
- Labordaten
- COVID PCR positive test 2/17/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- * (Principal) Empyema lung Bronchiectasis (*) Paroxysmal atrial fibrillation (*) Essential hypertension Dyslipidemia (high LDL; low HDL) Parkinsons Coronary artery disease of native artery of native heart with stable angina pectoris Acute respiratory failure with hypoxia Pneumonia due to 2019 novel coronavirus Moderate protein-calorie malnutrition Emphysema of left lung Gram-negative pneumonia Acute renal failure (ARF)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 22.02.2023
- Impfdatum
- 05.03.2021
- Beginn
- 22.04.2022
- Tage bis Beginn
- 413,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
COVID-19 immunisation
Ear pain
Paraesthesia
SARS-CoV-2 test
Vaccination failure
Symptomtext
EAR PAIN; MUSCLE TINGLING; CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a 66 year old female. Initial information was processed along with additional information on 21-FEB-2023. The patient's height, and weight were not reported. The patient's past medical history included: ruptured spleen (ruptured spleen due to fall), fall, and splenectomy (total), and concurrent conditions included: drug allergy (Thimerosal reaction), and immunocompromised, and other pre-existing medical conditions included: The patient not had other conditions or medication. The patient was not pregnant at the time of vaccination. The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805025 expiry: UNKNOWN) dose was not reported, 1 total, administered at right arm on 05-MAR-2021 10:30 for covid-19 prophylaxis. Age at time of vaccination 64 years old. No concomitant medications were reported. The patient also received moderna covid-19 vaccine (elasomeran) (Dose number in series 2) (form of admin and route of admin was not reported, batch number: 939904, expiry: Unknown) dose was not reported, administered at right arm on 04-NOV-2021 for covid-19 prophylaxis. It was unknown whether the patient experienced any adverse events following vaccination with moderna covid-19 vaccine (elasomeran) (Dose number in series 2). The patient also received moderna covid-19 vaccine (elasomeran) (Dose number in series 3) (form of admin and route of admin was not reported, batch number: 001M21A, expiry: Unknown) dose was not reported, administered at right arm on 22-APR-2022 for covid-19 prophylaxis which was associated with revaccination with different covid-19 vaccine (Dose number in series 3). On 01-FEB-2023, Laboratory data included: COVID-19 virus test Positive (lateral flow test), the patient had covid-19 (confirmed covid-19 infection) (Dose number in series 3) and received non company suspect drug paxlovid (nirmatrelvir/ritonavir) (form of admin and route of admin was not reported, batch number: GF4083 expiry: Unknown) dose and frequency were not reported from 01-FEB-2023 to 05-FEB-2023 for covid-19 treatment. On an unspecified date, the patient had chills, sore throat, headache, runny nose, sneezing, watery eyes, diarrhea and poor appetite returned after feeling well for about 5 days (confirmed covid-19 infection) (Dose number in series 3). The patient also had muscle tingling and ear pain (Dose number in series 3). On 12-FEB-2023, Laboratory data included: COVID-19 virus test Positive (11 days after first positive lateral flow test) which leads to confirmed clinical vaccination failure (Dose number in series 1). The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, and elasomeran was not applicable; and action taken with nirmatrelvir/ritonavir was not reported. The outcome of the confirmed covid-19 infection, confirmed clinical vaccination failure, revaccination with different covid-19 vaccine, muscle tingling and ear pain was not reported. This report was serious (Other Medically Important Condition). This case was associated with a product quality complaint: 90000272070.; Sender's Comments: V0: 20230244175-confirmed clinical vaccination failure . The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event. Specifically: SPECIAL SITUATIONS. Therefore, this event is considered inconsistent with vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230201; Test Name: COVID-19 VIRUS TEST; Test Result: Positive ; Test Date: 20230212; Test Name: COVID-19 VIRUS TEST; Test Result: Positive
- Aktuelle Erkrankungen
- Drug allergy (Thimerosal reaction); Immunocompromised
- Vorgeschichte
- Medical History/Concurrent Conditions: Fall; Rupture of spleen (ruptured spleen due to fall); Splenectomy (total); Comments: The patient not had other conditions or medication. The patient was not pregnant at the time of vaccination.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 20.09.2022
- Impfdatum
- 27.10.2021
- Beginn
- 09.09.2022
- Tage bis Beginn
- 317,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Dyspnoea
Fatigue
Symptomtext
fatigue, SOB, light-headedness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 20.02.2021
- Beginn
- 18.08.2022
- Tage bis Beginn
- 544,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest pain
Gangrene
Limb injury
SARS-CoV-2 test positive
Symptomtext
89 year old female with history significant for CAD with stenting, HTN, PAD, DM type II, CKD stage III, HLD presents to the hospital with gangrenous left heel wound. RRT called overnight for complaints of chest pain, now resolved. Cardiology consulted for further evaluation. Patient seen and evaluated this afternoon. Had brief episode of CP early this morning though resolved on its own. No current CP at this time. No SOB, dizziness, palpitations, paresthesias. Safe to discharge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 19,0
- Labordaten
- 8/18 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 05.09.2022
- Impfdatum
- 25.02.2021
- Beginn
- 01.05.2021
- Tage bis Beginn
- 65,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Blood triglycerides
Diabetes mellitus
Glycosylated haemoglobin increased
Hypoaesthesia
Paraesthesia
Sciatica
Spinal X-ray
Symptomtext
i went to see a cardiologist about my symptoms of tingling and numbness in my legs, arms, and the right side of my face ion June 24, 2022. He took blood tests and x-rays of my back. My heart was normal, but he said my symptoms were due to sciatica. He also said my A1c was high and that I had diabetes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- x-rays of lower spine on June 24, 2022 A1c, Triglycerides on June 24, 2022
- Aktuelle Erkrankungen
- sciatica,
- Vorgeschichte
- thalassemia, cataract in right eye, sciatica
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 01.08.2022
- Impfdatum
- 06.05.2022
- Beginn
- 31.07.2022
- Tage bis Beginn
- 86,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Cough
Dyspnoea
Dyspnoea at rest
Mental status changes
Symptomtext
7-31-2022 patient presented to our ER with c/o SOB while resting. Pt was already aware that he had covid. Pt also c/o weakness, AMS and coughing. Pt was admitted for further evaluation and treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CVA, Diabetes, hyperlipidemia, hypertension, Heart disease with CABG
- Andere Medikamente
- Aspirin 81 mg po daily mirtazapine 15 mg po HS ramipril 10 mg po daily glipizide 5 mg po bid clopidogrel 75 mg po daily folic acid 1 mg po daily lexapro 5 mg po daily metoprolol succinate 50 mg po daily atorvastatin 40 mg po hs januvia 100
- Allergien
- penicillin sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 29.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Eczema
Scab
Urticaria
Symptomtext
Symptoms started within a couple of days of vaccine. I experienced what I thought was eczema related rash because my skin is sensitive and I thought I had used soap or a cleanser that was irritating my skin but it was behaving like hives. It was on my torso, legs, and it would shift around so it wasn't very consistent. At first it was on my torso, and then a few days later it was on my legs. A number of days later, I had it on the left side of my scalp and it presented more of shingles scabbing, and I've had shingles before in the past so I am familiar with it but I didn't have the pain aspect of it. It persisted for a number of weeks so I was a doctor and they thought it was an eczema reaction and they didn't tie it to the booster. Typically when I've had eczema reaction it appears in one place and antihistamines usually clears it up, but this time the antihistamine didn't help and it took 2 months to resolve. I've still been battling flare ups.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin B; vitamin D as I'm deficient in both
- Allergien
- Food allergies but nothing where I have an anaphylactic reaction coffee; almonds; watermelon; latex sensitivity; sodium lauryl sulfate
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 12.11.2021
- Beginn
- 14.01.2022
- Tage bis Beginn
- 63,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
Blood test
COVID-19
Cough
Dyspnoea
Exercise tolerance decreased
Laboratory test
Pain
Vaccine breakthrough infection
Wheezing
White blood cell count decreased
Symptomtext
2 months after vaccination, I started feeling body aches and loss of taste/smell. I started having a cough a week later. I began wheezing with any exertion and could not take a deep breath. I halted exercising to see if that would help. On March 1st, 2022, I went to the doctor and they prescribed Albuterol inhaler 2 puffs every 4 hours as needed. I then went back on 4-6-2022, and they prescribed an antibiotic (name unknown) and done lab work. I am still experiencing wheezing and shortness of breath at this time. I am still using the inhaler as well. I am reporting a case of breakthrough Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- I had heard on the news and radio that there was not enough Covid tests so if there were symptoms, to assume it was positive and to stay home to isolate. I had ordered home tests but they had not arrived by the time I started having symptoms so no Covid test was done. My doctor did obtain some bloodwork on 4-6-2022 that showed low white blood count but that was all. I have to follow up with the doctor this summer.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Vit D deficiency
- Andere Medikamente
- Vitamin D 3 125mcg/5000 IU daily
- Allergien
- BACTRIM
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 12.02.2021
- Beginn
- 20.03.2021
- Tage bis Beginn
- 36,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Heart rate increased
Sleep disorder
Tinnitus
Symptomtext
Rapid heart beat when going to sleep, and changes in my Tinnitus . After second Covid shot my heart rate would increase dramatically when trying to go to sleep. Too fast to even try to count for one second. Dr. ordered a heart monitor for three day recording period. Supposed to mark time on cell phone type unit. I worked as a Locomotive Engineer for twenty four years following a previous nine years as a Brakeman. My system is still attuned to going to a wide awake state anytime I'm awakened. In Lew of being, I included a note as to the times this rapid beat was happening. Their report was nonsense. I'm quite sure a rapid beat before a resting sleep rate would be quite noticeable. They did list one episode of 172 beats. Corporation $$$$$, too much of a hurry. I'm blind in my right eye and need glasses to operate their cell phone unit, plus I would have had to turn on brighter lights to see what I was doing. I also have trouble with my hands, arthritis from the years operating the locomotives. I also have to contend with the over five inches in height I've lost from railroading. I loath loss of sleep. I had a appointment Jan 6, 2022 CLINIC CARDIOLOGY. Dr. changed my prescription for METOPROLOL TARTRATE 25MG twice a day to METOPROLOL ER 50MG - 1 TAB AM and 1/2 TAB PM. The fast heart rate has slowed considerably, but the beat are really strong. The heart rate is still faster than it should be. I have had some nights without the fast heart rate, and nights with the slowed heart rate. A couple of nights of no fast heart rate to be awakened after falling asleep with faster than normal strong heart beat rate some of which really pulse. My dad, his brother and sister, and a cousin (dad's brother daughter) all died of cerebral aneurysms. Strong beats do concern me. Today up at 04:30am regular beat, 09am sleepy sitting in Morris Chair , 09:10am beat speeding up, 09:20am beat faster and stronger as close to sleep; 09:30am, more awake; 09:40am normal, up walking around. It's not unusual having this sleepy events happen in mornings and afternoons. I had kidney failure in the eighty's. I was sick and had multiple appointment with my general practitioner. He order a glucose test and the tech found blood cells in the urine. Sent for ivp x-rays. They were unable to see kidney, Ordered blood tests. Creatine was 15.3 and Bunn was 122. Dialysis Nurse told me "I've seen your blood work. You should be in bed puking, not up walking around". Nine dialysis treatments and they had my kidneys restarted, Had 70% then, last test in 2020 was 37%.. Failure was attributed to viral infection and Dyazide shut them down. I had a new physician after that. I do a lot reading on the net, but careful where. On computers if something goes in, something comes out! Never, never self help groups. Everything placed on the dinner table was homemade, vegatables were either fresh or frozen. That's why I felt that I wasn't in bed puking. Tinnitus - I've had Tinnitus for years. It's been a high pitched monotone. Quite loud at times. After the second Covid shot the monotone changed to a jet engine roar. After acouplke of months it would switch back and forth between the monotone and jet engine roar. After the fourth Covid shot, same as above but now I've had instances of what sounds like a radio talk show is on, except the talk is muffled and not understandable. Weird! I'd be amused if I could understand it. Today 05/15/22 tone is monotone again. 05/16/2022 up at 4:30am - monotone, 07am - jet sound; 08am - monotone. Personal history. Was married to my wife for fifty-five years. She expired in 2018 of stage four Parkinson's Disease. We have five children, three girls and two boys who have provided fourteen grand, great-grand children. My primary occupation was a Brakeman for nine years and then a Locomotive Engineer for twenty four years. My promotion exam to Locomotive Engineer was seven hours of verbal examination by the toughest examiner the company ever had. As a side note I never missed giving a complete correct answer. To keep my mind active on long road trips on the Company I would keep my station times in binary and, or hexadecimal form calculated enentirely in my mind. Raising five children meant I did a lot of side jobs including autobody work, engine work, all the building trades, welding landscaping, many others. Hobby's were Morris Style woodworking, stained glass, computers and gunsmithing. Even at eighty I make my own meals, wash my own clothes and drive a car (I avoid night time driving if possible). With this rapid heart beat I imagine a question would be - Why I have had the additional booster shots. My answer would be my current health status. On the railroad I was subjected to ultrafine silica sand dust from the locomotive wheel sanding. I have a mass in my lower left lung. It's in the lower left lung from all the hours leaning left to see towards the backward direction while switching cars. They want a ct scan but I have declined account I can no longer hold my arms over my head to preforn their scan. There is a design flaw with the diesel exhaut stacks and a attached spark arrester that forces the exhaust to enter the car body that then is then drawn into the cab by traction motor blowers located below the cab. Another design flaw with the train brake valve in most of their GP9's and GP&7's. When ever using the train brakes the train line air is exhausted directely into the cab of the locomotive. Trian line air is high pressure, 75-90 psi. The exhaust would be full of fine oil mist. My breathing is degrated from the above. I'm sixteen lustrums. I am diabetic. I have kidney disease. My BMI is high. (Loss of five inches doesn't help). One of the early studies of Covid deaths said a high percentage (70% ?) of those deaths of over 65 were of blood type A +. Wan'na guess my blood type. It's not just surving Covid, it's what your goning to have left. I started sheltering in 02 of 2020. I find it had the amount of people that believed the POTUS retoric he was putting out. I guess it reinforced what I've seen with people that are smart, or those especially proclaiming to be smart, that a good percentage are seriously short of common sense. I haven't had Covid. I'm alone 95% of the time, that doesn't bother me as on the RR I was alone a lot. I do miss the banter the wife and I had, though. One of the many favorite was when we were sitting under the eve of the garage. It was L shaped and offered protection from the cold Lake wind. This particular day was heavy overcast (fog) just above the tree tops. A group of geese from the rail yards, where a lot of grain was spilled from leaking grain cars, would fly to the Bay area. We could hear a group coming as they were honking excessively. They flew over us right at tree top level account of the heavy overcast. It was down right irratating all the noise. A few minutes later another group followed. This group was not honking and when they went overhead you could hear the wind flowing over their wing as they flapped, and the heavy breathing from keeping those heavy bodies in the air. After they passed my wife asked "Was that second group a different kind of goose?". I ansewered dryly "NO, Those were all Males". I instantely received a back hand slap on the shoulder. I miss those days. Ya, some of you are probably thinking right now, but in our house there wasn't any male or female jobs, and the worst thing any of those kids could say was "I don't know how". My energy was spent on the mechanical side of things, so if you would excuse my grammer and spelling I would appreciate it, and of the length of this, because standing is now limited, I sit a lot more for things like this. Even with hearing aids I have trouble with higher pitched voices (some females). As an Engineer I blew the whistle a lot. During the time I was a Brakeman a nineteen year old girl later subcumed follow a grade crossing collision. What was really chilling was, forty-five minutes after hitting the car, a baby started crying. The baby was up under the dashboard and the driver and passenger were not in a condition to tell us. As having been a Locomotive Engineer I'LL gladily admit to being whistle happy. I rarely talk about this part of my RR career.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Type 2 diabetes, Diabetic peripheral neuropathy, chronic renal
- Vorgeschichte
- Lumbosacral spondylosis without myelopathy with hx of right sided sciatica Lumbar post-laminectomy syndrom: History of bilateral knee arthroplasty both knees Mixed hyperlipidemia: Postate cance Essentialhypertension; Type 2 diabetes mellitus treated with insulin- hammertoes and peripheral neuropathy uses diabetic shoes; Diabetic peripheral neuropathy; Primary osteoarthritis of both knees; Non-proliferative diabetic retinopathy mild, without macular edema - right eye , mostly blind right eye. VitreoRetinal surgery - checks bs 4 x per; CRD (chronic renal disease), stage III stable, has seen nephrology
- Andere Medikamente
- METOPROLOL ER 50MG 1-AM, 1/2-PM; FAMOTIDINE TWICE DAILY; HYDROCODINE/ACETAM 7.5-325MG i use one in am, occasionally a second 2 or 3 times a month, prescribed every eight hours; PRAVASTATIN 80MG-BEDTIME; OTC- CETIIRIZINE HYDROCHLORIDE 10MG
- Allergien
- Milk Protein Extract, Metformin, Triamterene-Hctz, asprin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 04.03.2021
- Beginn
- 03.05.2022
- Tage bis Beginn
- 425,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Angiogram pulmonary abnormal
Arteriosclerosis coronary artery
Bronchiectasis
COVID-19
Cardiomegaly
Chest X-ray abnormal
Computerised tomogram abdomen
Computerised tomogram thorax abnormal
Condition aggravated
Cough
Dyspnoea
Interstitial lung disease
Lung opacity
Pneumonia
Pulmonary fibrosis
SARS-CoV-2 test positive
Symptomtext
Patient is 76-year-old female with chronic chronic interstitial lung disease, chronic hypoxic respiratory failure on 3 L nasal cannula at baseline who presents to the ER complaining of increased cough over the past 2 weeks a mostly nonproductive. History per limited records and patient's daughter who is present. Patient presents to the ER due to of cough is noted above for denies headache, currently short of breath, no chest pain, nausea vomiting diarrhea she has not been on recent antibiotics. She has had COVID vaccine series he has had 2 doses and unaware of any COVID positive contacts DISCHARGE: Patient is a pleasant 76 year old female with history of ILD on
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 96,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 11.11.2021
- Beginn
- 02.05.2022
- Tage bis Beginn
- 172,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Dyspnoea
Fatigue
Influenza A virus test
Influenza B virus test
Nausea
SARS-CoV-2 test
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID infection leading to hospitalization. Symptoms beginning 4/30/22 including: cough, SOB, fatigue, and nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- SARS-CoV-2 (COVID-19) and Influenza AB by Nucleic Acid Amplification
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Thyroid disease, hypertension, diabetes mellitus, coronary artery disease, chronic renal failure, end stage renal disease, hypercholesteremia, peripheral vascular disease
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 27.10.2021
- Beginn
- 09.04.2022
- Tage bis Beginn
- 164,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
Bronchospasm
COVID-19
Chest pain
Chills
Decreased appetite
Fatigue
Hyperhidrosis
Musculoskeletal chest pain
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I started getting symptoms of chills, sweats, body aches, and congestion. On the 4/10/2022 I had a fever with fatigue, no appetite, and loss of sense of smell. I got a negative COVID-19 test on 4/9/2022 then positive COVID-19 test on 4/10/2022. My symptoms lasted about 10 days but then after 14 days I still felt feverish and had fatigue. I tested negative on 4/26/2022 with a positive outcome. My husband is a physician and was prescribed medications. I still have congestion and bronchial spasm. I would have pains in my ribs and chest that would last for minutes and then it would go away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lupus; HTN
- Andere Medikamente
- Tylenol, Vitamin B12 twice a week
- Allergien
- Cymbalta, Monistat, Gluten Sensitivity, Latex
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 26.10.2021
- Beginn
- 21.03.2022
- Tage bis Beginn
- 146,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angina pectoris
COVID-19
Chest pain
Cough
Fatigue
Headache
Nasopharyngitis
Productive cough
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I woke up with sold symptoms on Monday. It was just a runny nose and headache. The next day I woke up with a bad cough, I was hacking and the cough was productive. I also had pain in my chest and my heart when I was coughing and it was making it hard to cough. I did a home test and was positive for COVID-19. I called my doctor and he got me on Paxlovid to treat me. I was able to recover but I was tired and had fatigue for a few weeks after recovering from COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Crohn's Disease
- Andere Medikamente
- Metoprolol Tartrate; Stelara
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 27.10.2021
- Beginn
- 22.04.2022
- Tage bis Beginn
- 177,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Blood creatinine increased
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Chronic kidney disease
Condition aggravated
Lung disorder
Oedema peripheral
SARS-CoV-2 test positive
Ultrasound Doppler normal
Symptomtext
Hospitalized 04/23/2022-04/26/2022; OCVID-19 positive 04/23/2022; fully vaccinated plus booster Discharge Provider: DO Primary Care Provider at Discharge: Admission Date: 4/23/2022 Discharge Date: 04/26/2022 Discharge disposition: Home Condition on discharge: Stable DETAILS OF HOSPITAL STAY: AKI (acute kidney injury) (HCC) [N17.9] Pneumonia due to COVID-19 virus [U07.1, J12.82] ADMISSION AND DISCHARGE DIAGNOSES: HOSPITAL COURSE: COVID-19 pneumonia CXR shows subtle patchy airspace disease at the lung bases laterally. This is nonspecific but is compatible with Covid 19 pneumonia. COVID-19 PCR was positive Cont. Decadron , Rx for 3 more days, pt did well and on room air quickly, do not feel need full course of Decadron considering onset of symptoms is less than 10 days ago Supportive care AKI on CKD stage 3. Resolved History of renal cancer status post left nephrectomy Creatinine is 2.33 on admit Creatinine was 1.74 on 10/20 Lab Results Component Value Date CREATININE 1.74 (H) 04/26/2022 CREATININE 1.64 (H) 11/01/2017 CREATININE 1.60 (H) 11/01/2017 Coronary artery disease Hyperlipidemia Will continue aspirin and statin Hypertension Cont. losartan and hydrochlorothiazide Will continue amlodipine Right lower extremity edema US negative for DVT USV Venous Lower Extremity Duplex Right Final Result There is no deep venous thrombosis in the visualized deep veins of the right lower extremity. * DR CHEST 2 VIEWS FRONTAL AND LATERAL Final Result There is subtle patchy airspace disease at the lung bases laterally. This is nonspecific but is compatible with Covid 19 pneumonia. The cardiac silhouette is within normal limits. No pneumothorax or significant pleural effusion. No other change. Physical exam on discharge: BP 152/74 | Pulse 50 | Temp 36.6 ?C (Oral) | Resp 16 | Ht 1.778 m | Wt 102.3 kg | SpO2 97% | BMI 32.36 kg/m? Physical Exam Alert No distress Non toxic appearing No scleral lesions Oral mucosa moist Neck supple RRR No respiratory distress. No wheezing Abdomen soft No lower extremity edema No gross neuro deficits appreciated Skin is warm, no diaphoresis Affect normal. Calm. No agitation I spent 35 minutes performing this hospital discharge. I have reviewed the instructions with the patient and/or surrogate decision maker, answering all questions to his satisfaction. Patient verbalized understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pneumonia due to COVID-19 virus Essential hypertension Coronary artery disease post PCI with stent Vitamin D deficiency Degenerative arthritis of right knee COVID Type 2 diabetes, uncontrolled, with neuropathy CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min Solitary right kidney Diabetic renal disease Renal osteodystrophy Dyslipidemia Hyperparathyroidism Major depressive disorder, recurrent episode, moderate Encounter for long-term (current) use of insulin History of left kidney cancer post nephrectomy Osteochondroma of right lower extremity Isolated proteinuria with other morphologic lesion ACE inhibitor-aggravated angioedema, initial encounter
- Andere Medikamente
- amLODIPine (NORVASC) 10 MG tablet aspirin 81 MG enteric coated tablet atorvastatin (LIPITOR) 80 MG tablet Blood Glucose Monitoring Suppl MISC busPIRone (BUSPAR) 10 MG tablet dexamethasone (DECADRON) 6 MG tablet donepezil (ARICEPT) 10 MG tab
- Allergien
- Ace Inhibitors Amaryl Humalog Tylenol
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 30.03.2022
- Impfdatum
- 05.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection
Mobility decreased
Pain
Symptomtext
severe pain and unable to use arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- 3 steriod shots given unsure of exact date
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- congestive heart failure
- Andere Medikamente
- furosemide, spironolactine, jantoven, levothyoxine, coreg, simvastatin, omeprazole, flunisolide, silenafil citrate, amiodarone, and finasteride,
- Allergien
- all ace inhibitors
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 22.03.2022
- Impfdatum
- 08.11.2021
- Beginn
- 03.02.2022
- Tage bis Beginn
- 87,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Dyspnoea
Heart rate decreased
Heart rate increased
Tinnitus
Symptomtext
After receiving dose #3, the booster shot I started to feel some things health-wise that I had not felt before. On or about the first week of February I started to feel dizzy on occasion. I noticed ringing in my ears and a feeling that my heart rate was low at times and high at other times. I started getting a little winded at times also. I had never had any kind of feeling like dizziness or a slow or rapid heart rate so I just figured that I was getting old. As time passed, I kept feeling this way and decided that maybe I should see a doctor so I made an appointment for March 24th at 11 am to see my personal physician.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- I have an appointment on 3-24-22 with my personal physician
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- I take 10mg Rosuvastatin each night to keep my cholesterol under control
- Andere Medikamente
- 10mg Rosuvastatin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 11.02.2021
- Beginn
- 23.02.2022
- Tage bis Beginn
- 377,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Hypoxia
Pneumonia
Symptomtext
Hospitalization for COVID19, pneumonia with hypoxemia 2/23/22-3/6/22. Treated with dexamethasone, baricitinib, Remdesivir, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily. Discharged to hospice 03/06/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- 12,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 02.03.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cough
Dyspnoea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 4,0
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 01.11.2021
- Beginn
- 17.02.2022
- Tage bis Beginn
- 108,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Alpha haemolytic streptococcal infection
Angiogram pulmonary normal
Arthralgia
Blood culture positive
Blood gases normal
Blood sodium decreased
COVID-19
Cellulitis
Chest X-ray normal
Computerised tomogram abnormal
Condition aggravated
Culture negative
Debridement
Depression
Dyspnoea
Enteral nutrition
Erythema
Eye excision
Symptomtext
Hospitalized; COVID-19 positive (2.17.22); fully vaccinated PLUS booster Discharge Provider: MD Primary Care Provider: MD Admission Date: 2/16/2022 Discharge Date: Feb 23, 2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Pneumonia [J18.9] HOSPITAL COURSE: Patient is a 68 y.o. female with a past medical history of CKD3, T2DM, hypothyroidism, asthma, bronchiectasis, HTN, NASH Cirrhosis, MVA in 2016 leading to multiple ortho surgeries and chronic osteomyelitis as well as subtotal colectomy and ileostomy, dysphagia requiring feeding tube, chronic pain, GERD, OSA on 2L nightly. Patient took a home COVID test a week prior to presentation due to symptoms of sore throat and congestion. She was noted to be positive. She presented to the ED on 2/17 with productive cough and shortness of breath. In the ED, patient was on 100% non-rebreather, although no desaturation documented. Labs were significant for elevated pro calcitonin of 0.72, VBG was unremarkable, mild hyponatremia of 132, normal WBC of 9.22. She was found to be COVID positive. CXR was unremarkable. Patient had mild swelling in her right lower extremity so US right lower extremity was obtained and was negative for DVT. CTA was obtained and showed mild left lower lobe pneumonia. Blood cultures were obtained. Patient was started on vancomycin and zosyn. She was admitted to medicine for further management. Patient was treated with zosyn for left lower lobe pneumonia given her history of pseudomonas. Dexamethasone was started for COVID. Remdesivir was not given as patient initially had symptoms a week prior and her renal function was borderline. Pulmonology was consulted and recommended treated COVID with 10 days of dexamethasone as well as continuing to cover for pseudomonas. Bronchopulmonary hygiene was encouraged with acapella and incentive spirometer. 1/2 blood cultures came back positive for gram positive cocci in pairs and chains which later speciated to micrococcus luteus and streptococcus salivarius/vestibularis. Patient was restarted on vancomycin when cultures came back positive prior to speciation. Repeat blood cultures were obtained and were negative. The positive culture was thought to be a contaminant. ID was consulted. Levofloxacin was added. Vancomycin and zosyn were discontinued. Patient had high ileostomy output and oral vancomycin was added per ID recs as patient had history of c diff infection. Patient's hospital stay was complicated by hyperglycemia due to steroid use. Was consulted and assisted with diabetes management. Patient continued to oxygenate well on room air during her admission. She was discharged home in stable condition with plans to complete 10 day course of dexamethasone, 10 day course of levofloxacin and oral vancomycin. CONSULTS / RECOMMENDATION: - Infectious disease was consulted and assisted with antibiotic management. - Pulmonary was consulted due to history of pseudomonas and recommended to cover for pseudomonas and continue with bronchopulmonary hygiene. - was consulted to assist with diabetes management, gave home insulin recommendations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- 1.19.22: Telemedicine appt - ID - Reason for follow-up: Right ankle infection, cellulitis Synopsis: Patient is a 68-year-old female with a history of CHF, liver cirrhosis, diabetes, CKD stage III, chronic right ankle osteomyelitis with hardware, status post hardware removal and antibiotic nail placement 5/13/2021. Intraoperative cultures were negative in May (though she had been on prolonged course of antibiotics prior to surgery) was positive for group B strep. She was last seen in ID clinic 6/23/2021 and at that time minocycline was decreased to once daily dosing for chronic suppression with plans to follow-up in 6 months. Old cultures from 2017 from the same area had grown enterococci, coagulase-negative staph and Peptostreptococcus. She now comes in with nausea vomiting chills since around 11/24. She was started on Keflex 500 mg twice daily for tenderness around the PEG tube and yellow drainage. Soon after that she noted increasing pain redness and swelling of the right ankle. Afebrile since admission and without leukocytosis. Empirically started on ceftriaxone and vancomycin with a transition to Unasyn after infectious disease saw the patient.. CT of the right lower extremity showed fluid collection surrounding the tibiotalar joint space with a fragmented appearance of the talus and irregular distal tibia. Status post I&D down to bone 12/2. Cultures were all negative from this procedure but histopathology showed focal acute osteomyelitis. She had another surgery on 12/8 where all the hardware was removed and she underwent significant debridement. Numerous cultures from that revealed no pathogens identified. Histopathology also did not show any acute infection at that time. While in the hospital she was on broad-spectrum antibiotics and she was ultimately discharged on ertapenem. Interval history: Since she was discharged in the hospital, we have not been able to see the patient. She had numerous acute issues including altered mental status/lethargy that was felt to be related to ertapenem. We made a change over to tigecycline but unfortunately for the past couple weeks she has had severe nausea that is ongoing and continuously progressive. She did discontinue the tigecycline on her own around 24 to 48 hours ago because of the vomiting. She had severe eye pain and underwent an enucleation procedure on 1/13/2022 at health Currently her ankle is actually looking pretty good. No drainage or pain. It cracks a fair amount when she pivots but in terms of her functionality she is about as good as she can get at this time. No fevers or altered mental status. I did discuss the case at length with orthopedic surgery as well as the patient/patient's husband. There is significant concern there is residual infection and we ultimately will not be able to get control of this without a more permanent solution 1.20.22 - possible UTI 2.3.22 - seen by palliative care team - intractable nausea / vomiting x3 weeks; diarrhea due to malabsorption (subtotal colectomy and end ileostomy in 2016); tube feedings at night; chronic pain syndrome; depression with anxiety 2.9.22 - Seen by cardiology for SVT 2.10.22 - seen by urology for kidney stones
- Vorgeschichte
- Retained orthopedic hardware Depression Anemia Bronchiectasis without complication (HCC) Pseudomonas aeruginosa colonization Eosinophilic syndrome Type 2 diabetes mellitus with stage 3b chronic kidney disease, with long-term current use of insulin (HCC) Regular astigmatism of both eyes Subclinical hypothyroidism S/P bariatric surgery Moderate persistent asthma Gastroesophageal reflux disease and esophageal dysmotility, with concern for recurrent aspiration Osteoporosis Cirrhosis of liver without ascites, unspecified hepatic cirrhosis type (HCC) Status post ileostomy (HCC) Depression with anxiety Benign essential hypertension Neuropathy of both feet Nephrolithiasis Chronic pain syndrome Lung nodules Bilateral carotid artery stenosis Hyperparathyroidism (HCC) Thrombocytopenia, unspecified (HCC) Chronic, continuous use of opioids Avascular necrosis of bone (HCC) Chronic osteomyelitis of right ankle (HCC) Stage 3b chronic kidney disease (HCC) NASH (nonalcoholic steatohepatitis) Sick sinus syndrome (HCC) Severe episode of recurrent major depressive disorder, without psychotic features (HCC) Intractable nausea and vomiting Steroid dependence (HCC) ACP (advance care planning) PSVT (paroxysmal supraventricular tachycardia) (HCC)
- Andere Medikamente
- albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler benzonatate (TESSALON) 200 MG capsule buPROPion (WELLBUTRIN XL) 150 MG 24 hr tablet Calcium Carbona
- Allergien
- CeftazidimeUnknown SpironolactoneOther Ertapenem Actonel [Risedronate]GI Upset DogsSneezing Fosamax [Alendronic Acid]GI Upset Horse-derived Products PremarinUnknown Trees / GrassSneezing
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 29.10.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 70,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
COVID-19
Chest X-ray
Chest discomfort
Chills
Cough
Dyspnoea
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Tested positive for Covid 01/07/2022. Onset of symptoms 01/08/2022. Fever >103 F for 4 days, persistent cough, chills, difficulty breathing. Went to ER and received IV steroids on 01/11/2022. Returned to the ER 01/17/2022 due to chest pressure and difficulty breathing. Was held at the hospital until 01/19/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- Chest X-ray 01/17/2022, Blood work 01/11/2022, 01/17/2022, 01/18/2022
- Aktuelle Erkrankungen
- Mast Cell Activation Syndrome, Asthma, Rheumatoid Arthritis
- Vorgeschichte
- Mast Cell Activation Syndrome, Asthma, Rheumatoid Arthritis
- Andere Medikamente
- Loratadine, famotadine, cromolyn, alvesco, methotrexate, nabumatone, folic acid
- Allergien
- crab, alcohol, apricots, doxycycline
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 27.10.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 64,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest pain
Dyspnoea
Neck pain
Pain
SARS-CoV-2 test positive
Symptomtext
12/30/21 @2130, patient experienced chest pain, centralized that radiated to the neck bilaterally, he then went to sleep. Had another episode with SOB and went to ER 12/31/21, Covid-19 positive incidentally- no s/s. Patient admitted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 23.10.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aphasia
Chills
Confusional state
Dyspnoea exertional
Feeling abnormal
Memory impairment
Nausea
Photophobia
Pyrexia
Tremor
Symptomtext
Body shakes, fever, cold chills, light sensitivity, nausea persisting for three days. Following the second dose, I became increasingly more forgetful and have developed a "brain fog" which makes it difficult to find the right words for sentences/am confused about trying to discern things from one another. I could have a thought and be trying to communicate something and the words would elude me. This has never happened to me prior to the COVID19 vaccine. I also began to experience a shortness of breath when trying to climb stairs or exert myself physically, which has also persisted since the second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 07.11.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 50,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Angiogram pulmonary
COVID-19
Chills
Cough
Decreased appetite
Dyspnoea
Emphysema
Fibrin D dimer
Headache
Interchange of vaccine products
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
From history and physical on 12/27/21: PT is a 70 y.o. female with HO AAA repair, HTN, HLP, COPD on 2 LPM oxygen chronically (also on azithromycin 3 times a week w/ her duo nebs) as well as prior breast cancer in 2016 (Stage IIIB (T4N1M0) ER positive, PR positive,. Completed 4 cycles of neoadjuvant chemotherapy with Taxotere Cytoxan and mastectomy, as well as adjuvant radiotherapy with Dr. who had headache 1 1/2 weeks ago and now has had cough and congestion since 12/20/2021 she describes fever, chills, shortness of breath and decreased appetite. She presented to the ED today with worsening shortness of breath, COVID positive, oxygen sats on presentation were 79%. Oxygen saturation 93-94% on 4 liters. ED w/u = COVID19 +; D dimer 2.12; CTa chest w/ pleural based density LUL (3x1cm) - malignancy vs radiation therapy change, consider PET if no radiation, no PE or focal infiltrated, mild emphysematous changes First dose vaccine = Janssen on 3/10/21 (Lot# 1805025), Moderna on 11/7/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 25.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Influenza
Nausea
Oropharyngeal pain
Post-acute COVID-19 syndrome
Pyrexia
Tinnitus
Symptomtext
She got her vaccine (booster), she felt like she was coming down with a mild case of the flu. She had long-haul symptoms from having COVID before. She felt feverish, mild sore throat, nausea. These symptoms lasted for about 2 days, and then it cleared and has been OK since other than the residual from having COVID. She had COVID in 2019 and has had residual symptoms from it. It was to the point that she could not walk and has had vertigo issues since then. She went to her PCP who told her that she did not have COVID. She then had to go to an ENT who told her that it was from long-term COVID. She did not have any problems with vertigo prior to having COVID. She just wants people to know if they get COVID virus and you can have extreme symptoms and that tinnitus has been severe and it has gradually gotten worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Tinnitus due to COVID virus.
- Vorgeschichte
- Asthma, tinnitus due to long haul COVID, vertigo due to long haul COVID.
- Andere Medikamente
- Meclizine.
- Allergien
- Penicillin, Sulfa, Mycin, cedar.
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 26.10.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Balance disorder
Cognitive disorder
Fall
Hallucination
Mobility decreased
Symptomtext
Had a fall the evening of 10/26/2021 after getting the vaccine. And then continued to show signs of progressing weakness, unsteadiness, impaired cognition for the next 7-10 days. Had several falls between 11/7 and 11/8/2021. Admitted to hospital on 11/8/2021. Unable to return to her prior living at our Assisted Living facility due to impaired cognition and mobility. Reported to have ongoing hallucinations and falls.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Hospitalization at Hospital
- Aktuelle Erkrankungen
- Diagnosed with Covid for the 2nd time on 09/10/2021. First episode of Covid was 11/11/2020.
- Vorgeschichte
- Osteoporosis; Atherosclerosis; CAD; CHF; CKD; HTN; GERD; Anxiety, Depression, Presence of pacemaker; Chronic Pain; Macular Degeneration; Hyperlipidemia; Type 2 Diabetes; Afib; Pulmonary hypertension; OSA; Polymyalgia rheumatica; Osteoarthritis; Hypothyroidism; IBS; Vit D deficiency; Non-Hodgkin lymphoma
- Andere Medikamente
- Acetaminophen; Amiodarone; Antacid; Bumetanide; Bupropion; Carvedilol; Eliquis; Fish Oil; Fluoxetine; Duoneb; Levothyroxine; Lorazepam; Guaifenesin; Nystatin Powder; Omeprazole; Oyster Shell Calcium w/ Vit D; Miralax; Tramadol; Vitamin D3
- Allergien
- Ezetimibe; Fenofibrate; Pitavastatin; Simvastatin; Sulfamethoxazole; Trimethoprim; Vytorin; Adhesive Tape; Alendronate; Tricor
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 25.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Dizziness
Kawasaki's disease
Pruritus
Rash
Rash erythematous
Rash papular
Urticaria
Symptomtext
A long term issue I have had from Kawasaki Disease is what I call a heart pinchy thing because it feels like my heart is being pinched. This would normally occur every couple of months and last for a few minutes. After I got the first shot, I have had the heart pinchy thing everyday. It's more of a dull ache in my heart instead of a sharp pain. I am also getting extremely dizzy when go from laying down to up. It's enough that I need to spend a minute or two regulating myself before I stand up fully. I received the second dose on November 23 (lot #065F21A) at a Clinic. The same day, I was getting itchy, and by that night I had a rash on my arms and abdomen. The next morning, I noticed hives all over my body with the majority of them looking like scratch marks. The hives were on my right leg, right arm, both hips, chest, back, and back of my neck. The rest of my skin that did not have scratch marks was covered with raised red bumps. I also had a large red spot on my left cheek. The hives started to fade on December 6, 2021. The heart pinchy thing and dizziness have not changed. I am able to provide pictures of the hives.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- I saw my primary care physician on December 8th, and she asked me to submit the report to VAERS. I am workin g on scheduling an appointment with my cardiologist in January 2022. One topic I would like to ask my cardiologist is if I contracted POTS as a result of having COVID in May 2021 and receiving the vaccine.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Diagnosed with Kawasaki Disease at age 5 (1984) Extremely sensitive to alcohol, medication, and anesthesia (I don't metabolize normally)
- Andere Medikamente
- Vitamin D supplement, women's multi-vitamin, essential oils as needed
- Allergien
- Codine, Zyrtec, sensitivity to steri strips
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Arthralgia
Blood test abnormal
Computerised tomogram abnormal
Dyspnoea
Headache
Hypoaesthesia
Impaired work ability
Inflammatory marker increased
Injection site pain
Intervertebral disc protrusion
Loss of bladder sensation
Myalgia
Sensory loss
Urinary incontinence
Urine analysis normal
Vaccination complication
Symptomtext
11/29/2021 Within 2 hours of receiving the shot - muscle aches, headache, joint pain, injection site sore, 11/30/2021 Headache, muscle aches, joint pain, injection site sore, shortness of breath, numbness of limbs and lower body 12/02/2021 Urinary incontinence, numbness from waist down, loss of feeling of need to urinate or have bowel movement, headache, muscle aches, joint pain, injection site sore, shortness of breath - went to Urgent Care to be seen. Due to numbness and urinary incontinence following the vaccine, this was seen as an adverse reaction to the Moderna vaccine and a referral to the ER was made immediately. She made arrangement to go to the ER for further review and testing. At ER, urine sample, blood work, CT scan. Bloodwork showed elevated inflammatory markers, blood work & urine show no infection, CT scan showed slipped disc in L4, L5, & S1(not related to vaccine reaction). Was referred to neurologist for further evaluation. 12/08/2021 Continued numbness from ribs down, urinary incontinence, numbness in limbs, headache. all adverse events have not cleared to date. cannot return to work at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 12/01/2021Blood work, urine sample, CT scan, neurology referral
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- sulfa
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Dizziness
Headache
Muscle spasms
Palpitations
Pyrexia
Vertigo
Symptomtext
Fever, Extreme dizziness, vertigo, loss of balance, headache, calf muscle cramping, racing heart, palpitations
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Lactose, Gluten, Sulfa
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest pain
Chills
Fatigue
Myalgia
Pyrexia
Symptomtext
Awoke from sleep with chest pain, rigors, fever 103F, muscle pain. These symptoms lasted 72 hours. Severe fatigue, muscle pain, and intermittent chest pain lasted 7 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 07.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Cough
Dyspnoea
Fatigue
Influenza virus test negative
Oxygen saturation decreased
Pain
SARS-CoV-2 test negative
Symptomtext
11-24-21 (next day) cough, chills, body aches; 11-25-21, Chills and cough; 11-26-21 felt a little better; 11-27-21, evening, significant decline in health, used rescue inhaler (seldom uses normally), O sats dropped to 84; 11-28-21, went to local Urgent Care and had negative flu/COVID, prescribed Zpak and prednisone and steroid shot, continued decline, went to a second Hospital at 11pm; 11-29-21 4:30am sent home from ER with AirDuo, returned to same hospital in the evening because he felt as though he was continuing to decline and did not get admitted but sent home. As of 12-7-21, resting heartrate varies between 100-120, still coughing, still shortness of breath, exhausted but slowly improving
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma, controlled
- Andere Medikamente
- adderall 30mg twice daily Singulair 10mg daily Multi-vitamin daily
- Allergien
- ceclor
- Vorherige Impfungen
- After previous 2 shot series of Pfizer, extremely tired for about 40 hours each
- Staat
- MN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 19,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Biopsy
Diarrhoea
Erythema
Hair disorder
Pain
Palpitations
Pustule
Swelling
Vomiting
Symptomtext
I had like a little infected hair on my leg, next to my chin below my knee. It was a little bump. The next day it had gotten bigger. The day after thanksgiving I had the ER doctor take a look at it. By Sunday night it was so huge and deep and it looked like it was dying. It had puss. I went to see the surgeon. They did a biopsy and it came back as possible vasculitis. I was supposed to have another biopsy today but I have been throwing up since 2 am, I also have diarrhea, and my body hurts. I do have a history of IGA deficiency, so my immune system is compromised. So they need to do another biopsy and send it to pathology. They might do that tomorrow if I am feeling better. All of those diagnosis that they list when I did the research on it actually says they present after having a new drug or medication in your system when you have a weaken immune system. I have been taking Keflex since it started getting really red and spreading and puss was coming out of it. Since I had the booster I have been having like palpitations and increased anxiety. On 10/25/2021 I tested positive for RSV. I also received the flu vaccine on the early part of October but I cannot remember the exact date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Biopsy- came back as possible vasculitis
- Aktuelle Erkrankungen
- On 10/25/2021 I tested positive for RSV
- Vorgeschichte
- Depression, Attention deficit disorder, PTSD, history of IGA deficiency, chronic pain in neck
- Andere Medikamente
- Cymbalta, Adderall, Xanax
- Allergien
- I cannot be given any Morphine
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 27.10.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Appendicitis
Arthralgia
Chest discomfort
Chest pain
Computerised tomogram
Computerised tomogram abdomen abnormal
Heart rate irregular
Palpitations
Symptomtext
Heart palpitations, irregular heartbeat, chest/shoulder tightness and pain, appendicitis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 1,0
- Labordaten
- CT Scan Heart 2021-11-22 CT Scan abdomen 2021-12-02
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, Hypothyroidism
- Andere Medikamente
- Armour Thyroid 120mg, Losartan Potassium 100mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
COVID-19
Dyspnoea
Exposure during pregnancy
Fatigue
Night sweats
Rash
Respiratory tract congestion
SARS-CoV-2 test positive
Tachycardia
Symptomtext
I received my first dose of Moderna 12/31/20 (registered nurse) and my second dose around 1/28/21. I received my Moderna booster on 11/1/21. On 11/10/21 I became symptomatic but thought it was due to pregnancy complications (severe shortness of breath and tachycardia with minimal exertion and night sweats without a fever). I?m currently 36wks pregnant (due 12/23/21). On 11/18/21 Myself, my husband, and my 2.5yr old tested positive via PCR for covid-19. My husband has received his Pfizer series and booster (10/4/21). Our contact and exposure risk is low. I have been out on medical leave due to a high risk pregnancy, my husband has been teleworking, and my daughter stays at home with with us. My husband stayed asymptomatic other than maybe fatigue. I developed severe congestion on the 19th that last 3 days straight. I have also had a covid rash on my left foot, shortness of breath, tachycardia, fatigue, and loss of taste and smell. It?s now nov 30 and I only have a rash and intermittent congestion left. We just had a high risk ultrasound yesterday 11/29 and baby appears fine at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 11/18/21 positive covid 19 PCR test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Inappropriate sinus tachycardia
- Andere Medikamente
- Prenatal vitamin qD
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Dizziness
Headache
Hyperhidrosis
Injection site pain
Injection site swelling
Lymph node pain
Lymphadenopathy
Migraine
Pyrexia
Symptomtext
This is my first booster (my second shot in the two dose shot gave me a reaction as well). I ran a high fever, above 100 degrees (I normally do not even have normal 98.6 temp), even though I did tylenol every 4 hours. My left arm at the injection site has been very tender since the shot, even 6 days later and was swollen at the injection site. My lymph nodes under my arm and up to my collarbone on my left side were also very painful and swollen. On Friday night, after hving run moderately high temp all day, I got very sweaty and plummeted in temperature down to 93.4. I have had an overall headache, different from my typical migraines, and have felt dizzy and off since getting the shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines, Fibromyalgia
- Andere Medikamente
- Estradiol, Propranolol, Ajovy, Cranberry, Elderberry, Goldenseal, B Supplement, Magnesium
- Allergien
- Advil, Ibuprofen, Aleve, Salmon
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 23.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anger
Dyspnoea
Pain in extremity
Symptomtext
This spontaneous case reported by a pharmacist, describes the occurrence of pain in extremity (sore arm after 3rd full dose), anger and dyspnea (shortness of breath after 3rd full dose) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 vaccine, batch/lot# 939904) for COVID-19 immunization. The patient's past medical history included cancer/chemotherapy/surgery (post cancer and chemotherapy, half her lungs removed due to cancer prior to vaccination). On Oct 27, 2021, patient received the third dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On Oct 27, 2021, patient experienced pain in extremity (sore arm after 3rd full dose) and dyspnea (shortness of breath after 3rd full dose). On Nov 15, 2021, patient experienced anger. At the time of the report, pain in extremity (sore arm after 3rd full dose): not resolved; anger and dyspnea (shortness of breath after 3rd full dose) outcome: unknown. The reporter did not provide any causality assessments, concomitant medication or treatment information. Patient visited the doctor and they are running tests.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Cancer/chemotherapy/surgery (post cancer and chemotherapy, half her lungs removed due to cancer prior to vaccination).
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 19.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Burning sensation
Chest X-ray normal
Electrocardiogram normal
Paraesthesia
Troponin normal
Symptomtext
Sharp heart stabbing pains were felt for 1 hour on Friday the 12th of November from 3-4PM PST. The pain lessened over the night but felt like burning/pins feeling every few minutes around the heart area. Saturday: Woke up fine but after 12:00PM, the pain came back and intensified where I couldn't handle it anymore so I went to an urgent clinic on Saturday the 13th. Ran EKG, Troponin test, and Chest X ray. EKG was fine, troponin was fine. Chest x ray was fine. I felt the pain every few minutes. Went to my primary doctor on Monday the 15th of November. After his examination, he recommended that I take Buspirone. I do take it and it has helped but I still feel the hear area pain a few times a day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- EKG, troponin level test, blood test and chest x ray.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Losartan
- Allergien
- acetaminophen
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Ophthalmic migraine
Ophthalmological examination
Photopsia
Visual impairment
Vitreous detachment
Vitreous floaters
Vitreous opacities
Symptomtext
Flashes in the corner of OS and floaters in OS for several days. Headache on 11/15/2021, 11/16/2021 and 11/17/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ophthalmic migraine
- Hospital-Tage
- -
- Labordaten
- Ophthalmology Impression/Plan: 1. Assessment: Other subjective visual disturbances. DFE done 11/16/2021 and 11/17/2021 and OCT normal findings. Normal floaters. No retinal detachment, holes or tears. HVF done 11/17/2021 normal findings. 2. Assessment: Other vitreous opacities. Vitreous detachment accounts for the patient's complaints. There is no evidence of retinal pathology. 3. Assessment: Ophthalmoplegic migraine, not intractable.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Spinal stenosis
- Andere Medikamente
- Calcium; Vitamin D; Magnesium; Zinc
- Allergien
- Tylenol 4
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Hypoaesthesia
Limb discomfort
Mobility decreased
Pain in extremity
Periarthritis
Rotator cuff syndrome
Shoulder injury related to vaccine administration
Symptomtext
SIRVA leading to frozen shoulder/rotator cuff injury
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Flushing
Interchange of vaccine products
Lip swelling
Paraesthesia oral
Symptomtext
Patient's first dose was the Janssen vaccine. This was her Moderna booster. She waited 20 minutes after vaccination at the pharmacy and was fine and left. She left and then shortly after started to experience lips swelling and tingling and facial flushing. She returned to pharmacy and was given 25mg of benadryl. Her facial flushing decreased. Lips still felt swollen but were no longer tingling. Lips did not appear swollen in appearance but felt that way to her. She remained at pharmacy for 30 minutes and after symptoms started to resolve, she left. She was given benadryl capsules to take at bedtime and was counseled to go to the ER if she experienced hives, shortness of breath or if she felt that throat was closing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Herpes zoster
Paraesthesia
Rash
Symptomtext
Shingles. First symptom appeared November 5, 2021 -- sensitive/tingly skin on right thigh. Saturday Nov 6 a rash appeared on right upper thigh, Sunday Nov 7 a second smaller rash appeared on right middle of thigh. Went to emergency room Wednesday Nov 10, diagnosed shingles, and treated with antiviral and lidocaine gel. No prior history of auto immune issues or other potential causes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Went to emergency room Wednesday Nov 10, diagnosed shingles (visual assessment by doctor, no additional testing), and treated with antiviral and lidocaine gel. No prior history of auto immune issues or other potential causes.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- nuvaring vitamin d omega 3 magnesium
- Allergien
- ceclor
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Axillary pain
Dyspnoea
Fatigue
Injection site pain
Injection site pruritus
Injection site rash
Muscular weakness
Neuralgia
Pain
Pain in extremity
Pyrexia
Tenderness
Symptomtext
LARGE RASH DIAMETER OF THE RASH WAS ABOUT THE SIZE OF AN ORANGE MAYBE SLIGHTLY BIGGER. JUST AROUND WHERE SHE RECEIVED THE SHOT, IT WAS PAINFUL, ITCHY. ARMPIT IS HURTING FOR 2 SOLID DAYS AND ITS PAINFUL TO TOUCH. FAIRLY NORMAL IMMUNE RESPONSE TO FIRST ONE. BOTH SHOTS SHE WAS EXHAUSTED FOR A WEEK, HAD SOME SOB. FIRST 24 HOURS SHE HAD RANDOM SHARP PAINS THAT RAN DOWN HER ARM, LEFT ARM. HER ARM WENT TO WEAK THAT SHE FELT LIKE SHE WAS GOING TO DROP HER PHONE. RESOLVED AFTER 24 HOURS. PAIN AREA WAS INSIDE OF THE LEFT ARM. BODY ACHES, FEVER, NEVER ABOVE 100.5. SHE STATES THAT HER SKIN HERS MORE OF NERVE PAIN. WENT AWAY WITHIN 24 HOURS. ALL OF HER JOINTS HURT. SHE STATES HER JOINT PAIN WAS COMPARABLE TO THE FLU BUT EXAGERATED. FIRST 24 HOURS WAS RANDOM NERVE PAIN THROUGHOUT ARMS. BODY HURTING REAL BAD HAPPENED SATURDAY MORNING. RUNNING LOW GRADE FEVER WAS RUN OFF AND ON THROUGHOUT SATURDAY NIGHT. AS OF TODAY IT IS JUST THE RASH THAT IS LEFT (11/15/2021). SHE IS RESTING AND STATES THAT SHE IS OKAY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HIGH BLOOD PRESSURE,
- Andere Medikamente
- IBUPROFEN X1. VITAMINS AND PROBIOTICS. ATENOLOL 25MG
- Allergien
- PENICILLIN, KEFLEX, GLUTEN
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Chills
Chromaturia
Condition aggravated
Headache
Injection site pain
Myalgia
Nausea
Pruritus
Rash
Retching
Symptomtext
Painful injection site Nausea some dry heaves Chills Headache Myalgia Arthralgia Weakness Body rash/itching Very dark urine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Hypothyroid
- Vorgeschichte
- Chronic pain High cholesterol
- Andere Medikamente
- Armour thyroid Hydrocodone Vivelle dot Lunesta
- Allergien
- Clindamycin
- Vorherige Impfungen
- Painful injection site Myalgia 74 7/21 2nd Moderna
- Staat
- SC
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Tremor
Symptomtext
Starting at 10pm I felt shaking, tremors; Headache is really bad, like a band was wrapped around my head; Chills/Starting at 10pm I felt shivering; Have fatigue; This spontaneous case was reported by a consumer and describes the occurrence of TREMOR (Starting at 10pm I felt shaking, tremors), HEADACHE (Headache is really bad, like a band was wrapped around my head), CHILLS (Chills/Starting at 10pm I felt shivering) and FATIGUE (Have fatigue) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. Previously administered products included for COVID-19 vaccination: Johnson and Johnson vaccine on 16-May-2021. Past adverse reactions to the above products included No adverse event with Johnson and Johnson vaccine. Concomitant products included GABAPENTIN, LEVOTHYROXINE SODIUM (SYNTHROID), PRAVASTATIN SODIUM (PRAVACHOL) and FAMOTIDINE for an unknown indication. On 06-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Nov-2021, the patient experienced TREMOR (Starting at 10pm I felt shaking, tremors), HEADACHE (Headache is really bad, like a band was wrapped around my head) and FATIGUE (Have fatigue). 06-Nov-2021, the patient experienced CHILLS (Chills/Starting at 10pm I felt shivering). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) for Adverse event, at an unspecified dose and frequency. At the time of the report, TREMOR (Starting at 10pm I felt shaking, tremors), CHILLS (Chills/Starting at 10pm I felt shivering) and FATIGUE (Have fatigue) outcome was unknown and HEADACHE (Headache is really bad, like a band was wrapped around my head) had not resolved. Treatment information was not provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- GABAPENTIN; SYNTHROID; PRAVACHOL; FAMOTIDINE.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Gait disturbance
Headache
Influenza like illness
Loss of personal independence in daily activities
Mobility decreased
Pain
Pain in extremity
Symptomtext
My left arm is still sore. And it went from my left arm to my whole body feeling sore and achy. The only way I know to describe how I felt was like if I had the flu. I had headaches and my body ached. And then I became so sore I could hardly move. And I'm still sore. It got to the point where my back was hurting so bad, I could hardly walk. If I laid down, I couldn't turn over on my own. That went on for about almost a week. The chiropractor has gotten me to where I can move with ease now. But my body is still sore. The first two shots I had no problems whatsoever. I can't say that it was the shot, but these symptoms were definitely not here before. Went to the ER but went home immediately as there was a lot of people at the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- N/A
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chest pain
Cough
Disorientation
Disturbance in attention
Dizziness
Dysarthria
Fatigue
Feeling abnormal
Hypoaesthesia
Hypoaesthesia oral
Impaired work ability
Tinnitus
Symptomtext
Started to feel dizzy with ringing in my ears and trouble focusing on work around 10am around 10:45 my face started to feel numb and I felt like I was going to pass out. Laid my head down for a bit and then called my PCP's office. While talking to the nurse, my speech was slurred and my tongue and the roof of my mouth started to feel numb. she advised me to take Benadryl and call 911. I took Benadryl called 911 they sent out EMS and they advised me that I was just injected with a live virus and this was the side effect of having COVID. That made no sense to me, she then instructed me to take DayQuil for the effects of having COVID. I told the EMT that I was not feeling like I had the flu I felt out of it and numb. She checked my vitals and lungs and said everything was good and that they could transport me to the Hospital ED but they were full and I would just be sitting there and it would be best to rest in my home. That if the Benadryl wore off or if things got worse, to go to urgent care. I slept and when I woke up the facial numbness was less and my tongue and mouth no longer felt numb. I was dizzy and my ears were still ringing and disoriented the entire day. The next day I was extremely tired and started to having coughing with chest pain when I would cough and by that evening I was having joint pain everywhere. Today I feel better, still have the coughing with chest pain. Following up with my PCP at 9:20am 11/04/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Season allergies, post nasal drip.
- Vorgeschichte
- None.
- Andere Medikamente
- Wellbutrin; Lexapro.
- Allergien
- Sulfa.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac flutter
Chest pain
Dizziness
Fatigue
Hypoaesthesia
Muscle spasms
Peripheral swelling
Swelling
Symptomtext
Chest pain, Dizziness, Fatigue, Heart fluttering, Muscle cramping, Numbness, Swelling from left side of neck, down arm and leg to left foot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Plantar Fasciitis
- Andere Medikamente
- Vitamin D
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 24.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Cardiac monitoring
Chest X-ray
Chest discomfort
Dyspnoea
Echocardiogram
Electrocardiogram
Exercise tolerance decreased
Gait disturbance
Heart rate increased
Symptomtext
Beginning on 10/25, my heart rate became high at rest. Normally it is around low 70s at rest, but it was over 100 from just sitting. On 10/26 I was unable to breathe in the morning, and went to the ER where they checked me for a heart attack. I did not have one, and they referred me to my cardiologist. Ever since then, I am unable to run as I normally do without my heart rate increasing for the rest of the day (I normally run at least ~30 miles per week with no issues as well as weight train). I am barely able to walk as much as I used to (I used to walk ~3 miles per day). I have shortness of breath and chest tightness even walking up and down my stairs. Nothing like this has ever happened to me before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- blood work, chest x ray, and EKG at ER on 10/26/21, EKG at cardiologist 10/28/21, heart monitor from cardiologist from 10/28 - 10/30/21, echocardiogram 11/1/21
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- high blood pressure (managed with medication, exercise, and diet), bipolar
- Andere Medikamente
- Loxapine 5 mg and 10mg, Lamictal 100mg, Lisinopril 30mg, Clonidine .2mg, magnesium 800mg
- Allergien
- Penicillin, percuset, doxyxycline
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Feeling hot
Flushing
Heart rate increased
Palpitations
Symptomtext
The next day after the vaccine around 2:30pm, I developed heart palpitation and my HR was at 90 beats a minute which continued to go up to about 115beats per minute which lasted for about 15minutes. I was warm and flush, so I reached out to the nurse line who advised to monitor and if it continued into the next day to call back. It remained high for a little while longer then began to lower on its own. Later that evening around 8pm it began to elevate again back to the 115 range but this time it calmed down a little quicker than before. The next day I was fine and no additional symptoms after that.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Metamucil
- Allergien
- Keflex Bacterium
- Vorherige Impfungen
- 2021-J&J -Rapid HR
- Staat
- WA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Arrhythmia
Atrial fibrillation
Blood test
Cardioversion
Discomfort
Dyspnoea
Echocardiogram
Fatigue
Feeling abnormal
Hypophagia
Lymph node pain
SARS-CoV-2 test negative
Somnolence
Vaccination complication
X-ray
Symptomtext
On Saturday I got real sore lymph nodes, fatigue, I slept, and I didn't eat or drink all day. I was miserable. On Sunday it was a little better, but I still had the same symptoms. On Monday I felt better that morning, but I had got an arrhythmia in my heart. I was in A-FIB. I monitored that throughout the day. I called the nurse hotline and took more of my metoprolol medication. The arrhythmia did not go away. The nurse told me to wait 24 hours. The next day I went to the ER at 2:00 this morning and they did a cardioversion. They converted me then I went home. The next day I woke up with a tight band around my thoracic area, but it wasn't from the cardioversion. I couldn't breathe and I am on medication for this. I am currently in hospital because I couldn't breathe good. It was very uncomfortable. They are keeping me here for one night so far. The doctors contributed my A-FIB from the COVID-19 shot because it triggered my condition. They prescribed prednisone 40mg 1xday. Since I have been taking that I'm breathing better now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- 1,0
- Labordaten
- Test were did on 10/28/2021 Cardioversion Echocardiogram X-ray Blood test IV COVID-19 test negative.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- COPD A-Fib
- Andere Medikamente
- Centrum Silver Vitamins Excedrin Vitamin D Magnesium Metropole Warfarin
- Allergien
- Sulfa Barbiturates Lasix Fluroxene Codeine
- Vorherige Impfungen
- COVID (2nd dose), mild aches and headaches (February 2021).
- Staat
- GA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 23.10.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Headache
Mobility decreased
Nausea
Pain in extremity
Peripheral swelling
Pruritus
Pyrexia
Tremor
Vaccine positive rechallenge
Symptomtext
Fever of 103 starting g at 4am the next day along with chills, shaking, headache, fatigue, nausea. Took motrin which helped bring fever down to 100-101 but fever returned all that day. The next morning (10/25), I had a fever of 101 with chills and headache. I stayed in bed those two days. By 10/26, I was better other than a sore and swollen arm. Arm is still slightly sore and itchy today 10/28
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UTI
- Vorgeschichte
- Anxiety/Depression
- Andere Medikamente
- Wellbutrin Lipitor Xanax
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- Vaccination was 2nd dose of Moderna on 2/13/21. Same adverse reactions as booster but not as severe as with booster. The booster
- Staat
- CO
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 24.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Condition aggravated
Coordination abnormal
Fall
Fatigue
Thirst
Symptomtext
Began with extreme chills, teeth chattering 0500 for 1 hour Accompanied by extreme thirst, 2 hours with drinking water Fatigue, slept until 1330 Walked into bathroom, lost coordination and muscle strength, fell onto floor No strength, laid on floor until 2230 Wife called 911, EMT's lifted to standing position, did assessment and left, stood and walked as normal Went to sleep, 9 hours, awoke with full function 0800
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Atrial fibrillation, asthma (mild)
- Vorgeschichte
- Psoriasis
- Andere Medikamente
- Xarelto, Flovent,
- Allergien
- None
- Vorherige Impfungen
- Extreme fatigue, slept ~36 hours
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dyspnoea
Fatigue
Myalgia
Nausea
Pruritus
Skin sensitisation
Symptomtext
I experienced itchiness, nausea, fatigue, muscle pain, skin sensitivity, shortness of breath and chest pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Yes
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Extra dose administered
Hot flush
Lip swelling
Paraesthesia oral
Symptomtext
Shortly after vaccine administration patient reported that her tongue felt tingly and that her face felt hot and flushed - upon examination her face was starting to look red, her pulse was steady at 77, and her tongue appeared normal (not engorged or swollen). She sat resting, after another 10 minutes her face had become more red and her lips started to redden, with minimal swelling. She reported no wheezing or chest tightness, besides some anxious breathing. She sat resting for approx 40 minutes total, and with time her baseline face color returned and she reported feeling a little better, though with still some tingling. She went home and took a benadryl. Upon followup today, she ended up calling her physician, who recommended benadryl until her symptoms cleared completely. She reported some tingling earlier today but by this evening was feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 26.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Immediate post-injection reaction
Migraine
Pain
Pain in extremity
Paraesthesia
Pyrexia
Symptomtext
Pain and tingling right after injection. Tingling from DVT could have been linked. Body aches, migraine, SOB starting at 3 am 3.26.2021, took advil at that time. 9am legs in excruciating pain sharp stabbing pains 9/10. 11 am 101.6 degrees 1:00 pm 102 fever. 2:00 feverish, pain 8/10. Biggest complaint now is fever, lower extremities, migraine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PTSD, anxiety and clinical depression, HTN
- Andere Medikamente
- Gabapentin 600 mg, Lexapro, Xanax 2 a week, medication for pulmonary embolism(2/16)asa, supplements, lisinopril Today he has taken zofran, and hydrocodone 7.5/500
- Allergien
- nkda, environmental
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 25.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Malaise
Pallor
Tremor
Symptomtext
PATIENT HAD AN APPOINTMENT FOR THE FIRST DOSE OF THE MODERNA VACCINE. THE VACCINE WAS ADMINISTERED INTO THE LEFT DELTOID, PATIENT WAS ADVISED TO SIT FOR 15 MINUTES TO MONITOR FOR ADVERSE EVENTS. PATIENT DID WAIT FOR A COUPLE OF MINUTES AND THEN LEFT THE PHARMACY. PATIENT RETURNED TO THE PHARMACY STATING THAT HE DID NOT FEEL GOOD. PATIENT WAS PALE AND SHAKING. PHARMACIST ASKED THE PATIENT IF HE HAD ANY DIFFICULTY BREATHING OR IF HE HAD ANY VISUAL DISTURBANCES, PATIENT SAID NO. PHARMACIST ALSO ASKED THE PATIENT IF HE HAD EATEN SINCE THE MORNING, PATIENT SAID NO. PHARMACIST QUICKLY GOT THE PATIENT A BOTTLE OF WATER AND A CHOCOLATE BAR. PATIENT DRANK THE WATER AND ATE THE CHOCOLATE. PHARMACIST STAYED WITH THE PATIENT TO MONITOR THE PATIENT, SOON THE PATIENT WAS NOT SO PALE ANYMORE. THE PHARMACIST AGAIN ASKED THE PATIENT IF HE WAS FEELING ANY BETTER, PATIENT SAID A LITTLE BIT. PHARMACIST CONTINUED TO MONITOR AND LET THE PATIENT KNOW IF HE FEELS DIZZY OR HAS ANY DIFFICULTY BREATHIING OR ANY VISUAL DISTURBANCES THE PHARMACIST WILL CALL AN AMBULANCE. THE PATIENT REQUESTED THE PHARMACIST CALL THE AMBULANCE. IMMEDIATELY THE PHARMACIST CALLED 911 AND ASKED FOR AN AMBULANCE. THE AMBULANCE ARRIVED AFTER A COUPLE OF MINUTES. THE EMT TOOK THE PATIENT WITH THEM, THE PATIENT WALKED OUT OF THE PHARMACY UNDER THE SUPERVISION OF THE EMT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 15.03.2023
- Impfdatum
- 17.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Feeling cold
Rash
Rash vesicular
Symptomtext
The night of the vaccine, I had the severe chills and unable to get warm. I was shivering everywhere. That passed ultimately and by the next day that was gone. In the next 2 days, the rash appeared. It was initially on my left forearm then got to my right forearm. It got worse over a few days and began to blister so I went to my doctor. He prescribed a course of tapering steroids. I was also given a topical cream, a lotion of sort that was also prescription. It may have been a steroid lotion. Those reduced the symptoms over a period of 4 to 5 days. The rash would come and go in small patches. Nothing severe compared to the initial rash, but that did last for some time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- PreserVision AREDS
- Allergien
- Cholera & Yellow Fever vaccine in late 1980s resulting in anaphylactic shock; Hay fever
- Vorherige Impfungen
- Cholera & Yellow Fever vaccine in late 1980s resulting in anaphylactic shock
- Staat
- KS
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 27.01.2023
- Impfdatum
- 20.01.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 27,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
Blood test
X-ray
Symptomtext
About four to six weeks after receiving the third dose (first booster) of Moderna, I started to experience unexplained joint pain. At first I thought I was just experiencing normal aches and pains, but they have continued throughout the past year. I am still seeing a rheumatologist because the pains are still unexplained. I have had multiple counts of blood work and X-Rays, but no one can seem to find the cause to the pains.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Blood work; X-rays
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type II Diabetes; High Blood Pressure (controlled)
- Andere Medikamente
- Lisinopril; ibuprofen; TYLENOL; tramadol; multivitamin
- Allergien
- BACTRIM
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 15.01.2023
- Impfdatum
- 27.06.2022
- Beginn
- 21.12.2022
- Tage bis Beginn
- 177,0
- Dosis
- 1
- Route/Site
- JET / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Pain in extremity
SARS-CoV-2 test
Symptomtext
Sore arm and tired for a day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid home test
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Synthroid, losartan, metoprolol, focus select eye
- Allergien
- codeine - itchy
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 14.12.2022
- Impfdatum
- 29.01.2021
- Beginn
- 01.11.2022
- Tage bis Beginn
- 641,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
Asthenia
Vomiting
Symptomtext
11/01/22 presents to ED for "abdominal pain, vomiting, weakness" PMHx of "HTN, dyslipidemia, hypothyroidism"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 29.10.2021
- Beginn
- 04.05.2022
- Tage bis Beginn
- 187,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aphonia
COVID-19
Cough
Fatigue
SARS-CoV-2 test positive
Throat clearing
Throat irritation
Symptomtext
I received a Moderna COVID-19 booster on 10/29/2021. On 5/4/2022, I noticed that I had a throat irritation and had to clear my throat repeatedly. Overnight, it developed into a loss of voice, and I was unable to speak on 5/5/2022. On 5/5/2022, I underwent both a rapid test and a PCR test at a clinic. Within an hour, I learned that I had a positive result. On 5/5/2022 and 5/6/2022, the symptoms worsened. My voice was back, but then I developed fatigue and a cough. The cough didn't finally go away until 5/20/2022. However, the fatigue lingered for about 2 weeks after that. I never had a fever, though.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 5/5/2022 clinical PCR test positive result; 5/5/2022 clinical antigen test positive result.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypertension; Pre-Diabetes; Hypothyroidism; Gastroesophageal Reflux Disease; Depression.
- Andere Medikamente
- Lisinopril; levothyroxine; PROTONIX; WELLBUTRIN XR; ZYRTEC; super B complex supplement; vitamin D; iron.
- Allergien
- Tree nuts; phenol.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 29.10.2021
- Beginn
- 02.11.2022
- Tage bis Beginn
- 369,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Cerebral atrophy
Chest X-ray normal
Computerised tomogram head abnormal
Cough
Electrocardiogram normal
Encephalopathy
Exposure to SARS-CoV-2
Face injury
Fall
Full blood count normal
Memory impairment
Metabolic function test normal
Pyrexia
SARS-CoV-2 test positive
Urine analysis normal
Symptomtext
Discharge Provider: MD Primary Care Provider : MD Admitting Service: Internal Medicine Service Admission Date: 11/2/2022 Discharge Date: 11/08/2022 PRESENTING PROBLEM: Acute encephalopathy HOSPITAL COURSE: Patient is an 82-year-old male with a past medical history significant for hypertension, PCA CVA, dementia, alcohol use disorder remotely who presented to the emergency department with a chief complaint of 2 falls in the 48 hours prior to admission. The patient tested positive for COVID-19 on 11/01/2022 with a home test. He had mild symptoms of fever and dry cough. His wife also was sick with COVID-19 and was unable to care for him due to generalized weakness and falls in the setting of dementia. His memory issues had worsened with his acute illness. He fell on the day prior to admission and hit his face per his wife's report. He was brought to the emergency department. In the emergency department, he was hemodynamically stable, not hypoxic and afebrile. Complete blood count and CMP were unremarkable. COVID-19 PCR was positive. Urinalysis was negative for infection. EKG showed normal sinus rhythm. Chest x-ray was unremarkable. CT head showed moderate volume loss and old right PCA CVA without acute process. He was given fluids and Tylenol. He was admitted to the hospitalist service for COVID-19 with fall and placement. PT/OT re-evaluated him on 11/07/2022. They recommended Home with home health, eventually discharged home in relatively stable condition on 11/08/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Oropharyngeal dysphagia Essential hypertension Mixed dementia (HCC) Ulcerative esophagitis Vitamin B 12 deficiency Macular degeneration Glaucoma Charcot-Marie-Tooth disease hyperlipidemia Moderate episode of recurrent major depressive disorder (HCC) Rhinophyma History of stroke History of alcoholism (HCC) Tubular adenoma Elevated bilirubin History of partial colectomy Advance care planning Weight gain Falls Generalized weakness
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet Ascorbic Acid (VITAMIN C GUMMIE PO) aspirin 81 MG enteric coated tablet Carboxymethylcellul-Glycerin (REFRESH OPTIVE) 0.5-0.9 % SOLN clopidogrel (PLAVIX) 75 MG tablet Cyanocobalamin (B-12 PO) escitalopr
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 06.11.2022
- Impfdatum
- 13.10.2022
- Beginn
- 13.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Headache
Injection site erythema
Injection site pain
Injection site swelling
Musculoskeletal pain
Nausea
Neck pain
Pain
Symptomtext
Pain at injection site, including redness and swelling. Pain in left shoulder, left side of neck and left shoulder blade down to but cheek. Headaches, nausea since receiving injection. Pain level has remained at 8 or higher.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Propranolol 10mg table, 1 table per day, PRN. (2) Gabapentin 600mg, take 1 tablet twice daily plus 2 at bedtime. (3) Valacyclovir 1mg tablet daily. (4) Diltiazem CD 240mg capsule. One capsule daily. (5) Hydrochloride Orothazide 12 mg table
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 05.11.2022
- Impfdatum
- 20.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Hot flush
Symptomtext
Severe hot flashes / chills off + on for about 4 wks. 2nd Booster; Just hot flashes had been reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Vit. D, calcium, Escitalopram 1/2 5 mg
- Allergien
- Benadryl, phenagren
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 01.11.2022
- Impfdatum
- 31.10.2021
- Beginn
- 28.06.2022
- Tage bis Beginn
- 240,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Ageusia
Anosmia
COVID-19
Cough
Fatigue
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
The symptoms lasted 2 weeks and were extreme congestion, a little sore throat, bad fatigue, cough, intermittent loss of taste and smell. A few days of low grade fever. After 3 days I went to the clinic and gave me PAXLOVID which I took the full course. I still have lingering sinus congestion and intermittently more fatigued than I normally would be.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High blood pressure; Prediabetes
- Andere Medikamente
- Amlodipine desolate; HCTZ; TRULICITY shot
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 31.10.2022
- Impfdatum
- 29.10.2021
- Beginn
- 03.08.2022
- Tage bis Beginn
- 278,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Diverticulitis
Dysphonia
Gastrointestinal pain
Myalgia
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I started getting muscle aches and the pain was not excruciating, but it felt like the flu. I almost lost my voice. I had a very sore throat. I did not lose my appetite. No fever. My blood pressure was normal. I was not bed ridden at all. On 8/3/2022, I took a COVID-19 home test and it was positive. On 8/3/2022, I was prescribed Paxlovid, which was worse than COVID-19. If I had to do it again, I would not go on the medication, Paxlovid. The COVID symptoms went away within a week. The Paxlovid symptom started when I began the medication. I have Diverticulitis only on my left side. When I started taking the Paxlovid the pain feeling was all the way all across my lower GI. When I completed the Paxlovid the pain in GI also resolved. I received the 4th Dose of Moderna 10/3/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gastrointestinal pain
- Hospital-Tage
- -
- Labordaten
- 8/3/2022- COVID-19 home test- positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- Atorvastatin; Losartan HCTZ; losartan; Tamsulosin; omeprazole; Carbidopa-levodopa; Vitamin D; Zinc; multivitamin; Low dose Aspirin; Antihistamine; Vitamin C
- Allergien
- hay fever
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 26.10.2021
- Beginn
- 19.05.2022
- Tage bis Beginn
- 205,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Malaise
Nausea
Pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I felt unwell Thursday night. The next morning felt worse and took a COVID-19 test and it was positive right away. I went to the COVID-19 clinic and was given PAXLOVID for the 5 days, it didn't make symptoms any worse or better. I had a severe headache at first achiness, runny nose, slight cough, nausea. I was extremely tired after the PAXLOVID for quite a while. Now I'm ok.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High blood pressure; High cholesterol
- Andere Medikamente
- Chlorhexidine; montelukast; simvastatin; potassium
- Allergien
- Doxycycline; amlodipine; latex; bee stings
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 27.10.2022
- Impfdatum
- 26.10.2021
- Beginn
- 13.09.2022
- Tage bis Beginn
- 322,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
My son let me know that he tested positive, and we all live in the same house. After a couple days, I started running a fever and tested positive for COVID-19 on 9/13/22. By the next morning I had a sore throat, and body aches. I called my doctor, and he told me about PAXLOVID, and I turned it down that day. I called back the next day and had them call it in. I started feeling better a couple days after taking it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 13SEP22 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Cholesterol
- Andere Medikamente
- LIPITOR; baby aspirin; vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 25.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
COVID-19
Headache
Pain in extremity
Pyrexia
SARS-CoV-2 test
Symptomtext
patient got COVID-19 during a week or so; pain in the arm; mild headache; low fever of 99 degree F; This spontaneous case was reported by a patient and describes the occurrence of PAIN IN EXTREMITY (pain in the arm), HEADACHE (mild headache), PYREXIA (low fever of 99 degree F) and COVID-19 (patient got COVID-19 during a week or so) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 prophylaxis. Concurrent medical conditions included Seasonal allergy (season allergies) and Glaucoma. Concomitant products included CALCIUM and PRAVASTATIN for an unknown indication. On 25-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Nov-2021, the patient experienced PAIN IN EXTREMITY (pain in the arm), HEADACHE (mild headache) and PYREXIA (low fever of 99 degree F). In August 2022, the patient experienced COVID-19 (patient got COVID-19 during a week or so). The patient was treated with IBUPROFEN for COVID-19, at an unspecified dose and frequency. On 27-Nov-2021, PAIN IN EXTREMITY (pain in the arm), HEADACHE (mild headache) and PYREXIA (low fever of 99 degree F) had resolved. In September 2022, COVID-19 (patient got COVID-19 during a week or so) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In November 2021, Body temperature: low fever of 99 degree F. In August 2022, SARS-CoV-2 test: (Positive) Positive. Patient did not have any medical history relating to mentioned AE and both Acute and had no chronic illnesses at the time of vaccination. Patient did not receive other vaccines within 1 month prior to Moderna COVID-19 vaccine. Concomitant medication included Medications for allergies, eye drops for glaucoma. Patient called doctor. Patient did not experienced a similar event in the past. This case was linked to MOD-2022-654642 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 202111; Test Name: fever of 99?F; Result Unstructured Data: low fever of 99 degree F; Test Date: 202208; Test Name: had COVID test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Glaucoma; Seasonal allergy (season allergies)
- Vorgeschichte
- -
- Andere Medikamente
- CALCIUM; PRAVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 27.10.2021
- Beginn
- 17.08.2022
- Tage bis Beginn
- 294,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Fatigue
Nausea
Symptomtext
Fatigue and nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 28.10.2021
- Beginn
- 28.07.2022
- Tage bis Beginn
- 273,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood pressure measurement
Feeling hot
Headache
Heart rate
Malaise
Nausea
Pain in extremity
Symptomtext
not feeling well after second Moderna booster; her body felt hot; felt a bit weak; a bit of nausea; sore arm; very bad headache; This spontaneous case was reported by a patient and describes the occurrence of MALAISE (not feeling well after second Moderna booster), FEELING HOT (her body felt hot), ASTHENIA (felt a bit weak), NAUSEA (a bit of nausea) and PAIN IN EXTREMITY (sore arm) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 052B22A and 939904) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. On 2Jun2022 patient tested positive to COVID-19, and 4 days later she tested negative. It was reported that no other vaccines were given within 1 month prior to Moderna COVID-19 vaccine. The patient's past medical history included Thyroidectomy (patient had no thyroid) on 09-Jan-2017. Previously administered products included for COVID-19 vaccination: Johnson & Johnson (Dose no : 1 Route of administration : Intramuscular Lot number : 1305029) on 22-Mar-2021. Past adverse reactions to the above products included No adverse event with Johnson & Johnson. Concurrent medical conditions included Drug allergy (Methylprednisolone) and Allergy to antibiotic (cephalosporins). Concomitant products included LEVOTHYROXINE SODIUM (SYNTHROID) for Thyroidectomy. On 28-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Jul-2022, received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 28-Jul-2022, the patient experienced FEELING HOT (her body felt hot), ASTHENIA (felt a bit weak), NAUSEA (a bit of nausea), PAIN IN EXTREMITY (sore arm) and HEADACHE (very bad headache). On 29-Jul-2022, the patient experienced MALAISE (not feeling well after second Moderna booster). On 28-Jul-2022, NAUSEA (a bit of nausea) and PAIN IN EXTREMITY (sore arm) had resolved. At the time of the report, MALAISE (not feeling well after second Moderna booster), FEELING HOT (her body felt hot) and HEADACHE (very bad headache) had not resolved and ASTHENIA (felt a bit weak) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 28-Jul-2022, Blood pressure measurement: 124/65. On 28-Jul-2022, Heart rate: 72 pulse was 72 bpm. The AE did not cause patient to seek medical care (office visit, Urgent care, ER, hospitalized). The patient did not experience a similar event in the past. After 2nd booster dose patient experienced a bit of nausea, and sore arm. She woke up at night and felt symptoms like having COVID-19. No treatment has been given for her symptoms. This case was linked to MOD-2021-368752 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 29-Jul-2022: Live Significant follow up received contains Reporter email id added, patient details, concomitant product updated, Event added, Case narrative updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220728; Test Name: Blood pressure; Result Unstructured Data: 124/65; Test Date: 20220728; Test Name: Pulse rate; Result Unstructured Data: pulse was 72 bpm
- Aktuelle Erkrankungen
- Allergy to antibiotic (cephalosporins); Drug allergy (Methylprednisolone)
- Vorgeschichte
- Medical History/Concurrent Conditions: Thyroidectomy (patient had no thyroid); Comments: On 2Jun2022 patient tested positive to COVID-19, and 4 days later she tested negative. It was reported that no other vaccines were given within 1 month prior to Moderna COVID-19 vaccine.
- Andere Medikamente
- SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 30.10.2021
- Beginn
- 24.07.2022
- Tage bis Beginn
- 267,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Influenza like illness
Malaise
Sepsis
Symptomtext
Admitted on 7-24-2022 for covid symptoms and sepsis. Patient stated that he had flu like symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes type II, Reflux, Sleep apnea, osteoarthritis, Hypertension, Enlarged prostate
- Andere Medikamente
- Losartan 25 mg po daily HCTZ 25 mg po daily Faixiga 10 mg po daily Nicotine patch 21 mg/ 24 hours Nicotine gum 2 mg prn
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 01.02.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 155,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
02/01/2022 Vaccination 07/06/2022 I started to experience cough, fatigue, sore throat, and sniffles. 07/07/2022 COVID-19 POSITIVE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Simvastatin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 78,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Nasopharyngitis
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Symptomtext
Contracted Covid. Felt like I had a very bad cold. Maybe a fever the first night, body aches, cough, sore throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 06/25/2022 - Went to local Pharmacy and tested positive and was given Paxlovid.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 28.10.2021
- Beginn
- 31.05.2022
- Tage bis Beginn
- 215,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthropathy
Asthenia
COVID-19
Fatigue
Feeling abnormal
Malaise
Muscle discomfort
Oropharyngeal pain
SARS-CoV-2 test positive
Varicella
Symptomtext
I became symptomatic on March 31. I had this overall yucky feeling. It was a feeling of overall malaise, fatigue and sore throat. I tested negative for 2 days prior to me testing positive on the 3rd day. I called my doctor to see if I could get antivirals but he was not helpful. I called all over to try to get a prescriptions for antivirals but was unsuccessful. I called my doctor back and got a telehealth appointment. The telehealth person prescribed the medication. I had developed a sore throat and I kept getting wreaker. I had some muscle and joint discomfort. I begin to take the antivirals that Tuesday. I stayed sick a lot longer than I think I would, had I gotten the antivirals sooner. I was prescribed PAXLOVID, taking 3 tablets twice a day for 5 days. It took me about a month to feel better. I contracted the chicken pox right as I was scheduled to get my fourth vaccine. My recovery was slow. I had to take 2 rounds of prednisone to get over the chicken pox. For 2 months afterwards, I was having health issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test-March 31st negative. COVID-19 home test-April 1st negative. COVID-19 home test-April 2nd positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Under Active Thyroid
- Andere Medikamente
- Vitamin D; levothyroxine
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 28.10.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vaccination site urticaria
Symptomtext
after first booster, developed a really big red welt at the site of the vaccination; This spontaneous case was reported by a patient and describes the occurrence of VACCINATION SITE URTICARIA (after first booster, developed a really big red welt at the site of the vaccination) in an 83-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 prophylaxis. Concurrent medical conditions included Gluten sensitivity (was not an allergy), Allergy to antibiotic (medication allergy to Cipro) and Drug allergy (medication allergy to Crestor). Concomitant products included VITAMINS NOS for an unknown indication. On 28-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VACCINATION SITE URTICARIA (after first booster, developed a really big red welt at the site of the vaccination). At the time of the report, VACCINATION SITE URTICARIA (after first booster, developed a really big red welt at the site of the vaccination) had resolved. Patient has not had a positive covid test. Concomitant products included Statin drug, Low dose beta blocker and Antibiotic. After first booster, patient developed a really big red welt at the site of the vaccination, lasted for 4 days before it subsided. No treatment was received and had no hcp notification. This case was linked to MOD-2022-587456, MOD-2022-587428, MOD-2022-587447 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to antibiotic (medication allergy to Cipro); Drug allergy (medication allergy to Crestor); Gluten sensitivity (was not an allergy)
- Vorgeschichte
- -
- Andere Medikamente
- VITAMINS NOS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 16.11.2021
- Beginn
- 25.04.2022
- Tage bis Beginn
- 160,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Tested positive for COVID starting on April 25, 2022 Initial symptoms of fever and headache; took Paxlovid from April 25, 2022 through April 30, 2022 tested negative on April 30, 2022 symptoms resumed on May 4, 2022 and tested positive again severe congestions through May 10th tested negative on May 15, 16, and 18th
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID tests: April 25th - positive April 30th - negative May 4th - positive May 11th - positive May 13th - positive May 15th - negative May 16th - negative May 18th - negative
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- IUD
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 06.11.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 29,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heavy menstrual bleeding
Malaise
Menstruation irregular
Von Willebrand's factor activity normal
Symptomtext
I previously experienced this adverse event after dose 2 in the series, but it went away after several months. Adverse event began again after having the Booster shot. Menorrhagia during period. Extremely heavy bleeding. Filling-up an ultra tampon and overnight pad every hour, for several days. In the past I would have heavy periods, but nothing like this and heavy days never lasted this long. Heavy days now last almost a week. Accompanied by passage of large clots - some as large as a golf ball. General feeling of unwell. Period timing also somewhat irregular now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Tested for a Von Willebrand bleeding disorder 2/16/2022 - came back negative. After 2nd shot of Moderna adverse reaction, I was tested via a vaginal ultrasound and transabdominal ultrasound to look for cause of heavy bleeding. 6/24/2021. That also came back normal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism with nodule
- Andere Medikamente
- Levothyroxine Zyrtec Iron Supplement
- Allergien
- None
- Vorherige Impfungen
- Same experience after Moderna 2nd shot 3/11/21
- Staat
- FL
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 29.10.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Chronic spontaneous urticaria
Mechanical urticaria
Mental disorder
Pruritus
Sleep disorder
Urticaria
Weight increased
Symptomtext
1. Hives, dermatographism, and pruritus severe enough that it interferes with sleep 2. Seen by Dr. and diagnosed with chronic spontaneous urticaria (12/21) 3. Have never had an history of urticaria, asthma, or allergies (aside from seasonal) 4. Was prescribed montelukast which did not improve symptoms 5. Seen by Dr. and prescribed regimen of Zytrec TID (2/22) 6. Have been on a regimen of Zyrtec TID since February, if not taking this regimen urticaria, dermatographia, and pruritus persists 7. Have experienced weight gain (114->121lbs) since starting this regimen and has impacted mental health; anxious about taking another dose of vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chronic spontaneous urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Previfem
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 05.11.2021
- Beginn
- 06.05.2022
- Tage bis Beginn
- 182,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Ear discomfort
Ear pain
Facial pain
Feeling abnormal
Headache
Malaise
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
COVID-19 symptoms started 05/06/22 and tested positive same day. Symptoms include sore throat, congestion, headache, fever, and that's mostly it. I had aches and chills with the fever but when the fever is gone, I don't have it. I have terrible congestion with ear clogging and a headache that has lasted longer than any migraine I've ever had. The fever is gone so I don't feel as bad. I still have a headache and I'm super congested, and my ears and face hurt. I have no cough and I'm not super fatigued. I did speak to a doctor just to see about protocol with medications and what was current. I am only taking Tylenol and cold medications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19-positive- 05/06/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines
- Andere Medikamente
- Pepcid Allegra
- Allergien
- Ibuprofen
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 02.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 28,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test
Burning sensation
Laboratory test normal
Pain
Pain in extremity
Peripheral swelling
Pruritus
Symptomtext
28 days after vaccine I was having coffee with a friend and felt a pinprick stinging sensation in my left hand in ring and middle fingers. Began having swelling, itchy, and burning in left hand. Went to dermatologist and he was baffled. Then went to the doctor and he tested me for arthritis, which was negative. He then recommended that I double my medication for my autoimmune disease and that cleared up the reaction after 12 weeks on increased dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Blood work
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Undifferentiated Connective tissue Syndrome Hashimoto's Raynaud's
- Andere Medikamente
- Hydroxychloroquine Prolia Armor Thyroid Estradiol Restasis eye Fluconazole Areds 2 Flax seed oil Turmeric Cumin
- Allergien
- Scallops
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 27.10.2021
- Beginn
- 12.04.2022
- Tage bis Beginn
- 167,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Nasal congestion
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID-19 Case: It was an intense sore throat and a cough. I had one day of a runny nose or nasal congestion. Cough I still have and fatigue. I was prescribed Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At Home COVID-19 - Negative but husband tested positive and I had the same symptoms he had so I know I had it.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- GERD, Urgency Incontinence, Arthritis
- Andere Medikamente
- Enalapril 10mg, Estradiol .5mg, Trospium 50mg, Trazadone 25mg, Calcium Citrate with Vitamin D 1000mg, Vitamin C 1000mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 27.10.2021
- Beginn
- 01.04.2022
- Tage bis Beginn
- 156,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye irritation
Fatigue
Periorbital inflammation
Throat irritation
Symptomtext
I had inflammation around my eyes. It felt like a slight eye irritation. I also had a slight throat irritation and some fatigue. Those symptoms lasted for about 2 days or less. I had a slight moment of feeling that again briefly but then the feeling didn't stick around. The symptoms showed up momentarily and they didn't stay. I am living with someone who is having symptoms of a sore throat and sinus issues so I could be either getting something from them or giving them something.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Sulfa drug; Erythromycin
- Vorherige Impfungen
- COVID-19 Vaccine 1st dose, the symptoms are what I reported through the V-Safe check in on my 1st dose. Unknown vaccine, I had f
- Staat
- AZ
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- Impfdatum
- 27.10.2021
- Beginn
- 10.03.2022
- Tage bis Beginn
- 134,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Diarrhoea
Fatigue
Myalgia
Pyrexia
SARS-CoV-2 test
Symptomtext
cough, fever, muscle aches, diarrhea, exhaustion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Covid tests,
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- COPD, Asthma, High Blood Pressure, Insulin Resistance
- Andere Medikamente
- Metformin 500, MG, Levothyroxine 100 MG, Trazodone 100 MG, Rosuvastatin 10 MG, Losartan 50MG, Mucinex OTC, CoQ10 supplement, Vitamin D3, Symbicort Inhaler 160/4.5 mcg
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 27.10.2021
- Beginn
- 04.02.2022
- Tage bis Beginn
- 100,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Cough
Feeling abnormal
Influenza like illness
Lethargy
Pyrexia
SARS-CoV-2 test positive
Sneezing
Symptomtext
I started getting symptoms of sneezing. That night I felt flu like symptoms with a low grade fever of 101.1. The next day for 2 days I was lethargic and some coughing. I was feeling some better by 2/7/2022 and got tested at a clinic. I did a rapid and PCR test and both were positive. I felt brain fog and loss of energy which lingered for months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19 test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High cholesterol, Hypothyroidism
- Andere Medikamente
- Amidine, Levothyroxine, Aspirin 81mg, Simvastatin
- Allergien
- Grape wine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Hypoaesthesia
Influenza like illness
Pain
Pyrexia
Symptomtext
After I got into my car in the parking lot, my arm started to feel numb. As I was driving home, the numbness spread to my neck and face. After 15 minutes the left side of my face was very numb, like when a person gets a shot at a dentist to numb the area before drilling. The numbness continued to spread to the rest of my face that evening. I also had side effects that were like I has the flu for three days, body aches, fever, chills, etc. The numbness has gone away in my arm and the right side of my face, but the left side of my face still feels numb many months later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi vitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 30.10.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Inflammation
Purpura
Rash
Symptomtext
I had an inflammatory response. I had a huge lump under arm pit; took a week to leave. I had a purplish rash all over- hands, feet and knees. Spoke with a dermatologist and prescribed a topical cream.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Metoprolol Metformin
- Allergien
- Topical lidocaine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Autoimmune disorder
Fear
Immunosuppressant drug therapy
Mechanical urticaria
Pain
Pruritus
Symptomtext
I have been diagnosed with a lifelong autoimmune disease/condition known as dermatographia urticaria which causes painful burning/itching flare ups on different parts of my body. Also anytime my system ha to work due to a real injury to the body ?a bee sting for example? the symptoms are exaggerated and frightening. The treatment is currently to take antihistamines as needed and as a immune suppression treatment and to always take them in the event I will need additional booster shots. There is apparently no cure and something I have to live with.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- This took a long time to diagnose, the Immunologist was funny able to shed some light on what has happening to me.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 20.04.2022
- Impfdatum
- 13.12.2021
- Beginn
- 11.04.2022
- Tage bis Beginn
- 119,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Eye pruritus
Nasal congestion
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I was coming home from out of state. I started to have a sore throat feeling and my eyes really started to itch. The next morning I woke and still had the sore throat, itchy eyes and congestion. I decided to do a rapid test and it came back positive. The same day I went to get a PCR test and the results came back the next day and they were positive. I'm down to a dry cough and congestion nose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- PCR 04/12/2022: Positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Eliquis 2.5mg twice daily
- Allergien
- Sulfa
- Vorherige Impfungen
- Dose 1 Moderna. 24 hour leg muscle fatigue.
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 24.10.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 68,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test
Blood test
Cardiac stress test
Swelling face
Urticaria
Symptomtext
I started getting some swelling in my lower jaw around the cheek area. It took a couple days to reduce. I called my doctor and was referred to allergist. After 5 days, I started getting hives. They comes around 11pm at night then they dissipate then they show back up in the morning an dissipate in the afternoon. I've tried taking antihistamine that doesn't work. Now I am getting the hives everyday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- Food allergy test; Blood test; Nuclear medicine stress test.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None; Arthritis
- Andere Medikamente
- Omeprazole Senior multivitamin Vitamin B6 Fish oil Probiotic Metamucil
- Allergien
- Penicillin; Premarin; Iodine; Definity, Sulfa; Nitrofurantoin; Ibuprofen; Doxycycline
- Vorherige Impfungen
- Shingles, 2010. 60 yrs old. I had frozen shoulder and then my lymph nodes swelled up and I had to have them surgically removed.
- Staat
- NY
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 08.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antinuclear antibody
Blood test
Full blood count
Histamine level
Mechanical urticaria
Thyroid function test
Symptomtext
Received Moderna booster on December 8. Developed dermatographic urticaria on December 23. Dermatographic urticaria has persisted since December 23 and is ongoing. Consulted with both a dermatologist and an allergist. Allergist advised that she had seen many patients with this reaction, specifically to the COVID-19 booster. Treatment plan is Zyrtec 10mg BID until hives resolve.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- Bloodwork, 2/3/22 CBC CMP Histamine Release Panel ANA Thyroid Function
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Celiac Disease.
- Andere Medikamente
- Birth Control Pill (Lo Loestrin Fe) Vitamin D, 2,000 UT
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hidradenitis
Lymphadenopathy
Rash
Rash erythematous
Symptomtext
Left Arm of vaccination, 24hours of vaccination lymph node inflamed under the Left arm with Dose 3. Contacted physician and they gave you directives of care and if it lasted greater than one month to come in. Then a month later went in for a visit since the issue was not resolved. Then 3-4 weeks after notice a rash and little balls or bumps under the skin like red bumps. Hidradenitis Suppurativa - clogging of the sweat gland ducts. Physician prescribed keflex antibiotics for 10 days and it lasted a week. Then she went back to the physician who then he extended for additional 7 days. No cure but treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Observation.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Vitamin D3 once every other week; Maxzide 25mg three times a week; Crestor 10mg once every evening; Milan once a day
- Allergien
- Aspirin and all NSAID
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 21.03.2022
- Impfdatum
- 09.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 20,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Abscess jaw
C-reactive protein abnormal
Pain
Swelling face
Symptomtext
Patient presented to the Emergency Room with progressive left facial swelling over 1 week - was found to have a mandibular abscess. He was admitted for intravenous antibiotic treatment. Patient did improve symptomatically with respect to swelling and pain. His CRP improved slightly. He was treated with intravenous Clindamycin throughout hospitalization and did discuss with oral surgeon on-call. Per oral surgery, the patient will be able to be discharged today and will have an appointment tomorrow in the oral surgery clinic for definitive treatment debridement of abscess and he will continue on his oral Clindamycin on discharge. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 19.03.2022
- Impfdatum
- 11.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Hives all over my body. They have gotten less intense over time but I am still experiencing them over 4 months later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Levothyroxin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 25.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
LEFT ARM IS STILL SORE!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure controlled w/medication, obesity
- Andere Medikamente
- Maxide, triamterene, losartan, vitamin D
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 18.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye pain
Herpes zoster
Pain
Rash
Symptomtext
Shingles (herpes zoster) on face. Pain beginning in eye on 11/20/21 and symptoms lasting ~3 weeks from onset. Symptoms including severe pain and rash. Diagnosed 11/27/21. Treated with valacylovir,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 27.10.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 56,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Fatigue
Headache
Rhinorrhoea
SARS-CoV-2 test
Sinusitis
Symptomtext
I had symptoms start on 12-22-2021 symptoms 5 days total. Headache, fatigue, 1 day little cough, 1 day runny nose. symptoms come and go. I then got a sinus infection one week after symptoms of Covid ended. Z-pack was prescribed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Rapid Test 12/24/2021 POS
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Neuropathy
- Andere Medikamente
- 1. Bupropion 150mg 2. Citalopram 40 MG 3. Horizant Gabapentin 600MG 4. Adreno Distress Guard 2 softgells in AM 5. Pro Omega 2000 6. Stool Softener Docusate sodium
- Allergien
- Shellfish Steven Johnsons/Antibiotic allergy to certain Antibiotics
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 05.10.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 97,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
Malaise
Nasopharyngitis
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
On 01/10/2022 was feeling unwell and call in urgent care and was tested 01/11/2022 positive COVID, 10 days later 01/22/2022 negative COVID. Experience with COVID mild case cold symptom and tested positive instance clinic and 10 days negative at rite aid drive through clinic. Entire family exposure to COVID and all vaccinated and boosted so did not have a serious issue with COVID case.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetes, Degenerative Disease, High Cholesterol, Bi- Polar, IBS C, Gerd
- Andere Medikamente
- Levothyroxine 75mcg once daily, Esomeprazole Magnesium 40mg once daily, Gabapentin 600mg twice daily, Atorvastatin 20mg once daily, Braylair 1.5 mg once daily, Miralax over the counter capful once daily in the morning, Metformin 500mg twice
- Allergien
- Depakote, Tegretol, Desipramine and Tylenol 3
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 27.10.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Abdominal pain
Autoimmune pancreatitis
Biliary obstruction
Biopsy pancreas abnormal
Blood bilirubin increased
Blood immunoglobulin G
Chromaturia
Computerised tomogram abdomen
Endoscopic retrograde cholangiopancreatography
Hepatic enzyme increased
Jaundice
Magnetic resonance imaging
Nausea
Pancreatitis
Stent placement
Ultrasound abdomen
White blood cell count increased
Symptomtext
Five Days later after Booster developed Jaundice abdominal pain nausea urine brown required to go to ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 5,0
- Labordaten
- Increase liver enzymes, increase bilirubin ,increase WBCC, CT scan abdominal US and MRI intrabiliary compatible with Pancreas inflammation and Biliary Obstruction resulting in emergency ERCP with Stent Insertion and biopsy of Pancreas showing Autoimmune Pancreatitis with IG G2 levels and require to be started in Prednisone for treatment.
- Aktuelle Erkrankungen
- Total Knee Replacement(September 20/2021
- Vorgeschichte
- Prostatic cancer stable 2012, Hyperlipidemia,osteoarthritis
- Andere Medikamente
- Lozartam, lipitor
- Allergien
- Iodine and Shrimp
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 29.10.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 62,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Cough
Headache
Myalgia
Nasal congestion
Pyrexia
SARS-CoV-2 test
Symptomtext
Congestion; Body ache; High feve /Body temperature 100 F; Cough; Headache; This spontaneous case was reported by a consumer and describes the occurrence of COUGH (Cough), NASAL CONGESTION (Congestion), MYALGIA (Body ache), HEADACHE (Headache) and PYREXIA (High feve /Body temperature 100 F) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for Prophylactic vaccination. Previously administered products included for Prophylactic vaccination: JANSSEN (Dose number in series 1, batch number: 1805031 and Route: right arm.) on 15-Mar-2021. Past adverse reactions to the above products included No adverse event with JANSSEN. On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Dec-2021, the patient experienced COUGH (Cough) and HEADACHE (Headache). On 31-Dec-2021, the patient experienced NASAL CONGESTION (Congestion) and MYALGIA (Body ache). 31-Dec-2021, the patient experienced PYREXIA (High feve /Body temperature 100 F). On 02-Jan-2022, MYALGIA (Body ache), HEADACHE (Headache) and PYREXIA (High feve /Body temperature 100 F) had resolved. At the time of the report, COUGH (Cough) and NASAL CONGESTION (Congestion) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 30-Dec-2021, SARS-CoV-2 test: negative (Negative) Negative. On 31-Dec-2021, Body temperature: 100 (High) 100 Fahrenheit. Lab test: COVID 19 polymerase chain reaction (PCR) test : Awaiting result. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211231; Test Name: Body temperature; Result Unstructured Data: 100 Fahrenheit; Test Date: 20211230; Test Name: COVID-19 test; Test Result: Negative ; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 25.10.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 64,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Headache
Muscular weakness
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Woke up 12/28/21 with a sore throat, headache, unproductive cough, and muscular weakness. Called Dr office and was advised to self-test for Covid and to take 600mg of Guafenesin 2x per day. Test was clearly positive. Started Tussin DM (Guafenesin plus dexbromethorphan), but switched to Mucinex (just guafenesin.) Treated headache with extra aspirin. Symptoms rmostly resolved after 2 days. Only some general fatigue remains after 1 month.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Flowflex COVID-19 Home Test - Definite Positive 12/28/2021
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypertension High Cholesterol Insulin dependent diabetes type 2 chronic allergies
- Andere Medikamente
- Aspirin low dose Metformin Insulin Simvastatin Valsartan +HCT Cinnamon Chromium Picolinate Zinc Magnesium Potassium Multi-vitamin for Sr Men Balanced B super complex Omega 3&5 fish oils Vit D3 Vit C Iron Fexofenadine
- Allergien
- Liraglutide and analogs
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 16.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
12 days after my 3rd dose of Moderna, I started to have hives that would appear and move all over my body. I went to Urgent care a few days later and the doctor attributed it to my booster shot. I saw my primary doctor two weeks later when the rash still hadn't gone away and was referred to an allergist who confirmed it was from my booster shot. I was told the hives should last 6-8 weeks before completely going away. It has been 3.5 weeks now and the hives are a lot less severe than they were. This could be because of a steroid pack I took last week or maybe they are just subsiding. If I take a antihistamine they don't bother me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- D3 1000 IU (25mcg) Prenatal multi+DHA (200mg)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 29.10.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 62,0
- Dosis
- 2
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Cough
Headache
Nasal congestion
Pain
Pyrexia
SARS-CoV-2 test
Symptomtext
BODY ACHES; CONGESTION; HIGH FEVER; HEADACHES; COUGH; This spontaneous report received from a patient concerned a female of unspecified age, race and ethnic origin. 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 not reported, batch number: 1805031, Expiry: unknown) dose was not reported, frequency one total administered at right arm on 15-MAR-2021 for prophylactic vaccination. It was unknown whether the patient had any adverse events following vaccination with covid-19 vaccine ad26.cov2.s (Dose number in series 1). The patient received a booster of non-company suspect vaccine included: mrna 1273 (form of admin and route of admin were not reported, batch number: 939904, expiry: unknown) dose was not reported, administered at right arm on 29-OCT-2021 for prophylactic vaccination (dose number in series 2). No concomitant medications were reported. On 30-DEC-2021, the patient experienced cough and headaches (Dose number in series 2). Laboratory data included: COVID-19 antigen test (NR: not provided) negative. On 31-DEC-2021, the patient experienced body aches, congestion, and high fever (Dose number in series 2). Laboratory data (dates unspecified) included: Body temperature (NR: not provided) 100 F. On 02-JAN-2022, Laboratory data included: COVID-19 polymerase chain reaction (PCR) test (NR: not provided) awaiting result. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The action taken with mrna 1273 was not applicable. The patient recovered from body aches, high fever and headaches on 02-JAN-2022 and had not recovered from cough and congestion. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211230; Test Name: COVID-19 antigen test; Result Unstructured Data: negative; Test Date: 20211231; Test Name: Body temperature; Result Unstructured Data: 100 F; Test Date: 20220102; Test Name: COVID-19 PCR test; Result Unstructured Data: awaiting result
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Pain in extremity
Symptomtext
Patient received a "booster dose" which was 0.25 ml instead of 0.5 ml intended for second dose. She only had a sore arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- 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: unbekannt
Erholt: nein
Chills
Headache
Injection site rash
Pain
Symptomtext
1st dose November 23, 2021 Dull, constant headache (occasionally intensifies) since receiving first dose that has yet to go away over 6 weeks later. 2nd dose December 21, 2021 Headache intensified significantly after dose for a few days (approximately 72 hours). It was more of an intense, throbbing headache. Would worsen upon bending down and the return back up. On December 22, 2021, also had bad body aches and chills (felt like I couldn?t get warm even inside with heat). Strange skin rash on the arm where vaccine was administered that lasted for a few days (approximately 72 hours) was noticed on December 23, 2021. As mentioned above, the dull, constant headache (occasionally intensifies) remains and has yet to go away over 6 weeks after the first administration. The headache is refractory to multiple interventions including ibuprofen, acetaminophen, eating, drinking water, massage, etc.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None yet as of time of VAERS submission. Contacting physician for office visit.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
patient has arm pain and pain running down the arm. patient also complains of forearm pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Headache
Injection site erythema
Injection site swelling
Myalgia
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Redness and swelling the next day at the injection site and got worse 3-4 and the swelling and redness was like the size of a baseball, body ache for a week. My husband tested positive on 4dec2021. I started with a runny nose, worst headache of my life and cant stare a screen only for 2 -3 mins and I have to stop. Muscle aches and I am so tired and dry cough and got a low fever that comes and goes as high as 100.6 which was yesterday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID - positive on 9dec2021
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Anemic chronic , Gastric Bypass Surgery
- Andere Medikamente
- Iron; Multivitamin and Ibuprofen
- Allergien
- No
- Vorherige Impfungen
- flu vaccines - flu like symptoms and fever happened only 2 or 3 times. I take it every year.
- Staat
- CO
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Feeling cold
Headache
Myalgia
Parosmia
Pyrexia
Symptomtext
fever 100- 102, shivering during night and couldn't get warm, very bad headache, very sore muscles throughout body, one hours episode of phantosmia (fourth one in three years) four hours after fever broke, 38 hours of reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Chronic lymphocytic leukemia, nonspecific interstitial pneumonitis, sleep apnea, irritable bowel syndrome, chronic constipation, esophageal reflux, hypogammaglobulinemia, arthritis, BPH (benign prostatic hyperplasia), degeneration of lumbar or lumbosacral intervertebral disc, allergic rhinitis
- Andere Medikamente
- bupropion, cetirizine, famotidine, finasteride, fish oil, fluticasone propionate, immune globulin, kristalose, linaclotide, multivitamins with minerals, pramipexole, tamulosiin, venlafaxine
- Allergien
- penicillin, cephalexin, Pepcid AC and other protein pump inhibitors pollen, animal dander,
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 22.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 9,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood immunoglobulin E
C-reactive protein
Full blood count
Mechanical urticaria
Red blood cell sedimentation rate
Urticaria
Symptomtext
entire body urticaria and dermatographia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- CBC, ESR, hsCRP, allergen igE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 30.10.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 24,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test negative
Arthralgia
Back pain
Blood test
Crying
Fatigue
Idiopathic urticaria
Myalgia
Urticaria
Symptomtext
The night of the vaccine, 10/30/2021, I had severe back pain up and down my spine, starting at 8:00 PM. That night also started fatigue muscle pain, joint pain that never stopped. The following week, I got a doctor's appointment. I went to the doctor crying about it because nothing was working. He prescribed Celebrex for the muscle pain. I only took one pill the day I got it and the next day and I did not take it after that. It did help with the joint pain. And tizanidine, I only took one night. The underlying fatigue, joint pain and muscle pain I just dealt with it until 11/23/2021 when the hives hit. I thought it was going to go away, full body hives. By Thursday night, I had a telehealth appointment. They prescribed prednisone, Zyrtec and on Friday. I had another telehealth appointment with my doctor. To continue the prednisone, continue the Zyrtec, and add Pepcid and get an allergy appointment. I had an allergy appointment on 12/06/2021. They told me to get off all the antihistamines prior to taking the allergy test. Now I am on Singulair, Allegra Zyrtec and Pepcid. When I don't have to take medication, then I will call that recovered from my adverse events. Diagnosis: Spontaneous idiopathic urticaria.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Skin allergy test for food, negative. Blood work done for today 12/07/2021
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Chronic fatigue syndrome in 2020 but they are just guessing
- Andere Medikamente
- Estradiol estrogen patch 1.0 ml Vitamin D-3 Omega-3
- Allergien
- Nickel
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Urticaria
Symptomtext
Urticaria 12 days following booster shot. Went to see an allergist today, possibly urticaria related to booster shot. Will start on prednisone and antihistamines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- PCOS
- Vorgeschichte
- None
- Andere Medikamente
- Metformin 1000mg twice a day Apri once a day Spinorolactone 50 mg once a day
- Allergien
- Dust
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 26.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Impaired work ability
Nausea
Parosmia
Taste disorder
Symptomtext
Sense of smell altered. Metallic/blood scent and/or rancid/rotten meat smell persists consistently. Altered perception of food flavoring resulting in consistent nausea. This issue with nausea results in loss of work/excessive sick days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- None yet - awaiting Dr. appointment.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hashimoto's disease, Hypogonadism, PTSD, Sleep apnea
- Andere Medikamente
- Synthroid; Solriamfetol; Wellbutren; Testosterone Inj.
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Purpura
Rash erythematous
Rash pruritic
Symptomtext
ITCHY RED RASH THAT BLEEDS EASILY ON DAILY BASIS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- COPD
- Andere Medikamente
- CYMBALTA, LASIX, SYNTHROID, PRAVASTATIN,ZETIA,VITAMIN B, IRON
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 07.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash erythematous
Urticaria
Symptomtext
One week and one day after moderna booster started getting hives. I have no known allergies. These hives have lessened in severity but I am going on two weeks of bright red welts on skin that will disappear only to reappear on another part of my body and can be several areas at a time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Gums were inflamed was on medrol pack starting on 10/14/2021
- Vorgeschichte
- Hypothyroid
- Andere Medikamente
- Synthroid Cytomel Progesterone N-acetyl cystine Low dose naltrexone Magnesium Prenatal vitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Symptomtext
My Sister, Brother, and I got moderna booster shots in left arm. Since shots have been having right shoulder pain in all of us
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 26.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Urticarial rash over the whole body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Bone spurs, left foot.
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec, Miralax, align probiotic
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Cough
Fatigue
SARS-CoV-2 test positive
Symptomtext
Patient received booster dose of Moderna 10/27/21 (unclear exactly when patient got 1st two doses due to not having information available). Patient became weak, tired, coughing and positive for COVID which led to admission 11/22/21. Patient is still admitted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- 3,0
- Labordaten
- + COVID 11/22/21
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 19.11.2021
- Impfdatum
- 13.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Peripheral swelling
Symptomtext
1 week after vaccination, pt experienced intense pain and swelling of the left thumb joint which lasted for awhile, and resolved by taking otc NSAID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DM2, HTN
- Andere Medikamente
- metformin, pantoprazole, atorvastatin, bystolic, vascepa, vitamin d 1000iu
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 19.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fall
Gait disturbance
Symptomtext
Dizziness, unstable gait, almost falling down, especially in the morning on awakening. Fully resolved by 11/06/21 before I could get into see a doctor
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none, pulse and BP were normal
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high cholesterol, arthritis, BPH
- Andere Medikamente
- lipitor testosterone
- Allergien
- doxycycline
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Neck pain
Pruritus
Symptomtext
On the second day of 3rd dose patient complains of pain in the neck. at the third day the patient state that she had pain in the area and itchy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- fibromyalgia, upper respiratory
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Discomfort
Pain
Pyrexia
Symptomtext
Body aches; Chills; Little fever; quite a bit discomfort; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (Body aches), DISCOMFORT (quite a bit discomfort), CHILLS (Chills) and PYREXIA (Little fever) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. Previously administered products included for COVID-19 vaccination: Pfizer vaccine (Patient the first dose of the Pfizer vaccine on 15Feb2021 Lot EL9266.) on 15-Feb-2021 and Pfizer vaccine (Patient the second dose of the Pfizer vaccine on 18Mar 2021 Lot EN6204) on 18-Mar-2021. Concurrent medical conditions included Cholesterol. On 09-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced DISCOMFORT (quite a bit discomfort). On 10-Nov-2021, the patient experienced PAIN (Body aches), CHILLS (Chills) and PYREXIA (Little fever). At the time of the report, PAIN (Body aches), DISCOMFORT (quite a bit discomfort), CHILLS (Chills) and PYREXIA (Little fever) outcome was unknown. No Concomitant medications were reported. No Treatment information was reported. This case was created for booster dose. Patient wanted to know if she could take any Aspirin product or Excedrin Most recent FOLLOW-UP information incorporated above includes: On 10-Nov-2021: Significant followup received on 10-NOV-2021 contains historical vaccine added, event coding updated. On 10-Nov-2021: Followup received on 10-NOV-2021 contains Non-Significant information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cholesterol.
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Nausea
Somnolence
Symptomtext
Chills, nausea, headache, sleepy Started 11:00 am Slept fine thru night and fine the next day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Nobe
- Andere Medikamente
- Levothyroxine Sodium 137 MC
- Allergien
- Betadine
- Vorherige Impfungen
- 2bd dose of modern a but only chills and tiredness lasting one afternoon after shot given
- Staat
- AR
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site induration
Injection site mass
Injection site reaction
Injection site warmth
Rash pruritic
Symptomtext
At injection site: red, itchy rash, hot skin, hard knot, about 3 inches in circumference
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- PCOS, prediabetes
- Andere Medikamente
- Multi-vitamin
- Allergien
- penicillin, wheat, milk
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 16.11.2021
- Impfdatum
- 24.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Pain in extremity
Sciatica
Symptomtext
Soreness in lower back and left leg (sciatica). Had pulled back prior to booster shot, but after booster conditions became dramatically worse (with pain extending down left leg).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Saw Orthopedic doctor on 11/1/2021. Started PT on 11/11/2021
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- BPH
- Andere Medikamente
- Rosuvastatin, Lovaza, multi-vitamin, COQ10, Vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Chills
Headache
Illness
Liver injury
Lymphocyte count
Lymphopenia
Nausea
Pyrexia
Vaccination complication
Symptomtext
She felt really sick; chills; fever; nausea; headache; laid me really flat; lymphopenia; liver damage; This spontaneous case was reported by a consumer and describes the occurrence of LIVER INJURY (liver damage) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In 2021, the patient experienced LIVER INJURY (liver damage) (seriousness criterion medically significant). 2021, the patient experienced LYMPHOPENIA (lymphopenia). On 30-Oct-2021, the patient experienced VACCINATION COMPLICATION (laid me really flat), ILLNESS (She felt really sick), PYREXIA (fever), NAUSEA (nausea) and HEADACHE (headache). 30-Oct-2021, the patient experienced CHILLS (chills). The patient was treated with NAPROXEN SODIUM (ALEVE) at a dose of 1 dosage form and DIPHENHYDRAMINE, PARACETAMOL (EXTRA STRENGTH TYLENOL PM) at a dose of 2 extra strength Tylenol. At the time of the report, LIVER INJURY (liver damage), VACCINATION COMPLICATION (laid me really flat), LYMPHOPENIA (lymphopenia), ILLNESS (She felt really sick), CHILLS (chills), PYREXIA (fever), NAUSEA (nausea) and HEADACHE (headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 01-Nov-2021, Blood test: elevated alt and ast which is indicative of liver (High) ALT increased she had blood work which showed an elevated ALT and AST which is indicative of liver damage.. On 01-Nov-2021, Lymphocyte count: low (Low) She also had some lymphopenia as her lymphocyte count was low.. On 04-Nov-2021, Blood test: counts were improving (normal) counts were improving. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient after receiving the booster dose it laid really flat. patient felt really sick with chills, fever, nausea, and headache and took 2 extra strength Tylenol, then took an additional 2 extra strength Tylenol 6 hours later. patient also took an Aleve the following morning.On Monday 1NOV2021 patient had blood work which showed an elevated ALT and AST which is indicative of liver damage. patient also had some lymphopenia as the lymphocyte count was low. The primary care doctor of patient advised her to stop taking her statins, NSAIDS, and Vitamins. patient had additional blood work on 4NOV2021 which showed these counts were improving Company's comment: This is a spontaneous case concerning a 66-year-old, female patient with no relevant medical history, who experienced the unexpected serious events of liver injury. The events occurred approximately 1 day after the third dose of using mRNA-1273 . The rechallenge was unknown since no information about the first dose was disclosed. The benefit-risk relationship of using mRNA-1273 is not affected by this report. This case was linked to MOD-2021-378182, MOD-2021-378200, MOD-2021-378201 (Patient Link).; Sender's Comments: This is a spontaneous case concerning a 66-year-old, female patient with no relevant medical history, who experienced the unexpected serious events of liver injury. The events occurred approximately 1 day after the third dose of using mRNA-1273 . The rechallenge was unknown since no information about the first dose was disclosed. The benefit-risk relationship of using mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211101; Test Name: blood work; Result Unstructured Data: ALT increased she had blood work which showed an elevated ALT and AST which is indicative of liver damage.; Test Date: 20211104; Test Name: blood work; Result Unstructured Data: counts were improving; Test Date: 20211101; Test Name: lymphocyte count; Result Unstructured Data: She also had some lymphopenia as her lymphocyte count was low.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Nausea
Pain in extremity
Pyrexia
Symptomtext
Fever, Nausea, Fatigue, Arm soreness Fever and nausea lasted one day. fatigue and arm soreness lasted 4 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- TYPE 2 DIABETES, ILLIOTIBIAL BAND SYNDROME
- Andere Medikamente
- METFORMIN, GLIMIPERIDE, FARXIGA, LOSARTIN, BABY ASPIRIN, CHLORTRIMETON, SIMVASTATIN
- Allergien
- STRAWBERRIES
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose
Blood glucose increased
Fatigue
Pain
Therapeutic response unexpected
Symptomtext
minor aches; sugar spike; minor tiredness; two days after the shot I was able to walk with ease; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (minor aches), BLOOD GLUCOSE INCREASED (sugar spike), FATIGUE (minor tiredness) and THERAPEUTIC RESPONSE UNEXPECTED (two days after the shot I was able to walk with ease) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. The patient's past medical history included Lyme disease in 2006. Concurrent medical conditions included Drug allergy (Metoprolol ER Succinate 100 mg), Drug allergy (Zyrtex), Drug allergy (Macrobid), Drug allergy (Nifedical XL), Drug allergy (Lisinopril), Lactose intolerance, Supraventricular tachycardia since 2006, AFib since 2006, Vertigo since 2006, Blood pressure, Cholesterol, Osteopenia since 2009, Pre-diabetic since 2009, Supraventricular tachycardia since 2006, Premature ventricular contractions since 2006 and Premature beat atrial since 2006. Concomitant products included LOSARTAN, DILTIAZEM, APIXABAN (ELIQUIS), ROSUVASTATIN, VITAMIN D [VITAMIN D NOS] and CORTISONE for an unknown indication. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Nov-2021, the patient experienced THERAPEUTIC RESPONSE UNEXPECTED (two days after the shot I was able to walk with ease). On an unknown date, the patient experienced PAIN (minor aches), BLOOD GLUCOSE INCREASED (sugar spike) and FATIGUE (minor tiredness). On 04-Nov-2021, THERAPEUTIC RESPONSE UNEXPECTED (two days after the shot I was able to walk with ease) had resolved. At the time of the report, PAIN (minor aches), BLOOD GLUCOSE INCREASED (sugar spike) and FATIGUE (minor tiredness) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood glucose: increased (High) increased. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment medications was not reported. Patient had experienced soreness , minor aches , minor tiredness and sugar spike on 24-NOV-2021. Patient was waiting to schedule two hip replacements when COVID gets under control. On 04-NOV-2021 patient was able to walk with ease at a good clip for a 1 1/2 walk. The cortisone shot had worn out by September 2021. After all 3 vaccines patient's sugar count spiked 15-30 points. Patient experienced soreness , swelling and slight tiredness in the past and described as other vaccines had soreness , swelling and slight tiredness. This case was linked to MOD-2021-029925, MOD-2021-380489 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 09-Nov-2021: Follow up received and events , event outcomes added
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood glucose; Result Unstructured Data: increased
- Aktuelle Erkrankungen
- AFib; Blood pressure; Cholesterol; Drug allergy (Zyrtex); Drug allergy (Nifedical XL); Drug allergy (Metoprolol ER Succinate 100 mg); Drug allergy (Macrobid); Drug allergy (Lisinopril); Lactose intolerance; Osteopenia; Pre-diabetic; Premature beat atrial; Premature ventricular contractions; Supraventricular tachycardia; Vertigo
- Vorgeschichte
- Medical History/Concurrent Conditions: Lyme disease
- Andere Medikamente
- LOSARTAN; DILTIAZEM; ELIQUIS; ROSUVASTATIN; VITAMIN D [VITAMIN D NOS]; CORTISONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- -
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Inappropriate schedule of product administration
Symptomtext
headache; inappropriate schedule of vaccine administered; This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (headache) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (inappropriate schedule of vaccine administered) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. No Medical History information was reported. On 30-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Oct-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (inappropriate schedule of vaccine administered). On 31-Oct-2021, the patient experienced HEADACHE (headache). On 30-Oct-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (inappropriate schedule of vaccine administered) had resolved. At the time of the report, HEADACHE (headache) outcome was unknown. Patient received Johnson & Johnson as her first dose. No concomitant medications was reported. no treatment was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Symptomtext
Rash on neck, arms, legs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Famotidine 20 mg, Vitamin D 25 mcg, Citracal+D, Centrum Adult
- Allergien
- Ibuprofen possibly, Pencillin
- Vorherige Impfungen
- Covid-19 Vaccine February 20 and March 13, 2021
- Staat
- MD
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 12.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Feeling abnormal
Influenza like illness
Myalgia
Symptomtext
not feeling up to par; with flu like symptoms that are not nearly as severe as after the 2nd shot; a little tired; feeling a little bit the the usual achy; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (not feeling up to par), INFLUENZA LIKE ILLNESS (with flu like symptoms that are not nearly as severe as after the 2nd shot), MYALGIA (feeling a little bit the the usual achy) and FATIGUE (a little tired) in a 70-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. No Medical History information was reported. On 04-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced MYALGIA (feeling a little bit the the usual achy). On an unknown date, the patient experienced FEELING ABNORMAL (not feeling up to par), INFLUENZA LIKE ILLNESS (with flu like symptoms that are not nearly as severe as after the 2nd shot) and FATIGUE (a little tired). At the time of the report, FEELING ABNORMAL (not feeling up to par), INFLUENZA LIKE ILLNESS (with flu like symptoms that are not nearly as severe as after the 2nd shot), MYALGIA (feeling a little bit the the usual achy) and FATIGUE (a little tired) outcome was unknown. Concomitant medication was not provided. Treatment information was not provided. This case was linked to MOD-2021-089432 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
PATIENT SAID RASH FROM FACE AND SPREAD TO ENTIRE BODY. RECOMMENDED TAKE BENADRYL AND IF NOT GET BETTER THEN GO TO ER OR SEE PRIMARY CARE DOCTOR.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- DON'T KNOW
- Vorgeschichte
- DON'T KNOW
- Andere Medikamente
- NOT AVAILABLE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- 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: nein
Fatigue
Headache
Insomnia
Product administered to patient of inappropriate age
Pyrexia
Symptomtext
PATIENT IS UNDER 18 YEARS OLD AND RECEIVED MODERNA INSTEAD OF PFIZER VACCINE. PATIENT REPORTED FEVER FOR 2 DAYS, TROUBLE SLEEPING, HEADACHES AND FATIGUE. PATIENT STATES SHE IS NOW ONLY HAVING TROUBLE SLEEPING SINCE HER VACCINATION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear pain
Fatigue
Injection site pain
Lymphadenopathy
Tinnitus
Symptomtext
Pain in right arm, swelling of lymph nodes under arm right ear and neck area. Right ear ringing and pain. extremely tired. This are the same issues I had previously after the 2nd dose of Moderna vaccine in 3/10/2021 (010m20a). My Lymph nodes on left side were swollen with same symptoms as above and continue to periodically swell on the left side only. Left arm has a hard lump still present at injection site. Went to urgent care and has prescribed antibiotics a few months ago. Appears that every time a get slight ill I have a lymph node flare up issue. Recent booster on 11/9/2021 appears to have cause this issue again but on the right side this time (same side as the injection)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Left eye swelling, redness and pain
- Vorgeschichte
- pituitary adenoma benign; arthritis
- Andere Medikamente
- Ritalin; Cabergoline (Dostinex); daily vitamin; turmeric supplement, ibuprofen Rx recent for eye Gentamicin Sulfate Ophthalmic Solution
- Allergien
- Walnuts and sulfur, lactose intolerance
- Vorherige Impfungen
- Probably as mention in previously. Delayed lymph flare up
- Staat
- NH
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 22.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Fatigue
Gait inability
Hyperhidrosis
Hypokinesia
Nausea
Rash
Rash erythematous
Rash pruritic
Tinnitus
Symptomtext
I could not stand/walk; Rash all over her chest, abdomen, back, arms (not at the injection site) and upper legs; Nausea; Had to lay down; Sweating without fever; Ringing in the ears; Extreme dizziness; rash developing on my abdomen and and chest that is red, raised and itchy; rash developing on my abdomen and and chest that is red, raised and itchy; I could not stand/walk; This spontaneous case was reported by a nurse and describes the occurrence of HYPERHIDROSIS (Sweating without fever), TINNITUS (Ringing in the ears), DIZZINESS (Extreme dizziness), RASH ERYTHEMATOUS (rash developing on my abdomen and and chest that is red, raised and itchy) and RASH PRURITIC (rash developing on my abdomen and and chest that is red, raised and itchy) in a 49-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Jaw disorder NOS (received Botox injections but have not since February 19th 2021). Concomitant products included FAMOTIDINE from 19-Mar-2021 to an unknown date for GERD, ACICLOVIR SODIUM (ACYCLOVIR ABBOTT VIAL) from 19-Jan-2010 to an unknown date for Herpes dermatitis, ROSUVASTATIN CALCIUM (CRESTOR) from 19-Jan-2014 to an unknown date for High cholesterol, TRETINOIN (RETIN A) from 19-Jan-2008 to an unknown date for Skin cancer, FISH OIL, ALLOPURINOL (ELAVIL [ALLOPURINOL]) from 19-Jan-2018 to an unknown date and ALOE VERA JUICE for an unknown indication. On 22-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Oct-2021, the patient experienced HYPERHIDROSIS (Sweating without fever), TINNITUS (Ringing in the ears), DIZZINESS (Extreme dizziness), RASH ERYTHEMATOUS (rash developing on my abdomen and and chest that is red, raised and itchy), RASH PRURITIC (rash developing on my abdomen and and chest that is red, raised and itchy), GAIT INABILITY (I could not stand/walk) and FATIGUE (Had to lay down). On 25-Oct-2021, the patient experienced RASH (Rash all over her chest, abdomen, back, arms (not at the injection site) and upper legs) and NAUSEA (Nausea). On an unknown date, the patient experienced HYPOKINESIA (I could not stand/walk). The patient was treated with CETIRIZINE HYDROCHLORIDE (ZYRTEC ALLERGY) (oral) on 26-Oct-2021 for Adverse event, at a dose of 10 milligram twice a day. On 24-Oct-2021, TINNITUS (Ringing in the ears), RASH ERYTHEMATOUS (rash developing on my abdomen and and chest that is red, raised and itchy) and RASH PRURITIC (rash developing on my abdomen and and chest that is red, raised and itchy) had not resolved, FATIGUE (Had to lay down) had resolved. On 25-Oct-2021, HYPERHIDROSIS (Sweating without fever), DIZZINESS (Extreme dizziness) and NAUSEA (Nausea) had resolved. At the time of the report, GAIT INABILITY (I could not stand/walk), HYPOKINESIA (I could not stand/walk) and RASH (Rash all over her chest, abdomen, back, arms (not at the injection site) and upper legs) was resolving. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Most recent FOLLOW-UP information incorporated above includes: On 02-Nov-2021: Significant Follow-up : new reporter added, height,weight, race, adverse events added conmeds events start and stop date added
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Jaw disorder NOS (received Botox injections but have not since February 19th 2021)
- Vorgeschichte
- -
- Andere Medikamente
- FISH OIL; ELAVIL [ALLOPURINOL]; FAMOTIDINE; ACYCLOVIR ABBOTT VIAL; ALOE VERA JUICE; CRESTOR; RETIN A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Erythema
Fatigue
Neck pain
Peripheral swelling
Skin warm
Symptomtext
My arm swelled to my elbow - red and hot. That lasted for 4 days. I had the chills for two days I was exhausted for two days. On the third day I had neck pain. No fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- High Blood Pressure and High Cholesterol
- Andere Medikamente
- Metoprolol ER Succinate 100mg, Rosuvastatin 40 mg, Losartan/HCTZ 50/12.5 mg. Lansoprazole 30 mg, Aspirin 81mg Multivitamin and vitamin d & C
- Allergien
- None
- Vorherige Impfungen
- The first two moderna covid shots but not as bad as the booster
- Staat
- FL
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Symptomtext
2 hours after the dose today she noticed a bruise at the injection site; This spontaneous case was reported by a consumer and describes the occurrence of INJECTION SITE BRUISING (2 hours after the dose today she noticed a bruise at the injection site) in an 81-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. Previously administered products included for an unreported indication: INFLUENZA VACCINE in October 2021. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Nov-2021, the patient experienced INJECTION SITE BRUISING (2 hours after the dose today she noticed a bruise at the injection site). At the time of the report, INJECTION SITE BRUISING (2 hours after the dose today she noticed a bruise at the injection site) outcome was unknown. Patient experienced Bruise with flu shot taken a couple of weeks ago and patient also stated she had not taken any treatments. No concomitant medications were reported. This case was linked to MOD-2021-372938 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Confusional state
Headache
Inappropriate schedule of product administration
Malaise
Nasopharyngitis
Pyrexia
Vaccination site pain
Symptomtext
woke up cold, very cold; not well; Inappropriate schedule of vaccine administered; confused in my head; arm is hurting/pain in arm; fever; headache; This spontaneous case was reported by a consumer and describes the occurrence of CONFUSIONAL STATE (confused in my head), NASOPHARYNGITIS (woke up cold, very cold), MALAISE (not well), VACCINATION SITE PAIN (arm is hurting/pain in arm) and PYREXIA (fever) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was provided by the reporter. Concomitant products included LEVOTHYROXINE SODIUM (SYNTHROID) for an unknown indication. On 28-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced CONFUSIONAL STATE (confused in my head), VACCINATION SITE PAIN (arm is hurting/pain in arm), PYREXIA (fever) and HEADACHE (headache). On 28-Oct-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). On 29-Oct-2021, the patient experienced NASOPHARYNGITIS (woke up cold, very cold) and MALAISE (not well). On 28-Oct-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. At the time of the report, CONFUSIONAL STATE (confused in my head), NASOPHARYNGITIS (woke up cold, very cold), MALAISE (not well), VACCINATION SITE PAIN (arm is hurting/pain in arm), PYREXIA (fever) and HEADACHE (headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In October 2021, Body temperature: 98.7 (High) 98.7. Patient reports her first dose was Johnson & Johnson (JNJ) - Lot # 1805029 done on 22March2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 202110; Test Name: Body temperature; Result Unstructured Data: 98.7
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 08.11.2021
- Impfdatum
- 31.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Feeling hot
Loss of personal independence in daily activities
Pain
Pain in extremity
Symptomtext
Patient sore for 4 days after receiving the Moderna vaccine on 10/31/2021. The pain came back on 11/08/2021. The new side effects included hot to the touch, pain radiating from shoulder to wrist of left arm and pain such that she cannot pick up her child.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blood test
Contusion
Headache
Insomnia
Laboratory test
Malaise
Pain
Pain in extremity
Pyrexia
Rash
Rash erythematous
Vascular access site bruising
Symptomtext
Very Sichwithin 12 hours. Body Aches, Fever of 101.3, inability to sleep Pain throughout body central located in left arm and in left side of body. 72 hours later, red rash of Left arm and bruising in both left and right arms that was not caused from any trauma. Also, SEVERE headaches that warranted a Dr. visit. Had blood drawn. Bruising now at blood draw site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Had lab work done, to include blood clotting risk. scheduled MRI for severe headaches.
- Aktuelle Erkrankungen
- COVID 22SEP21 to 1OCT21
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 08.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product preparation error
Vaccination site pain
Symptomtext
Her arm is sore; Shook it vigorously; This spontaneous case was reported by a nurse and describes the occurrence of VACCINATION SITE PAIN (Her arm is sore) and PRODUCT PREPARATION ERROR (Shook it vigorously) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Oct-2021, the patient experienced PRODUCT PREPARATION ERROR (Shook it vigorously). On an unknown date, the patient experienced VACCINATION SITE PAIN (Her arm is sore). On 27-Oct-2021, PRODUCT PREPARATION ERROR (Shook it vigorously) had resolved. At the time of the report, VACCINATION SITE PAIN (Her arm is sore) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medication was reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 08.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose
Body temperature
Diarrhoea
Heart rate
Pyrexia
Vomiting
Symptomtext
Diarrhea; fever of 101.1 deg F; Vomiting; This spontaneous case was reported by a consumer and describes the occurrence of DIARRHOEA (Diarrhea), PYREXIA (fever of 101.1 deg F) and VOMITING (Vomiting) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. Concurrent medical conditions included AFib and Type 2 diabetes mellitus. Concomitant products included INSULIN, LIRAGLUTIDE (VICTOZA) and METFORMIN for an unknown indication. On 30-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Oct-2021, the patient experienced DIARRHOEA (Diarrhea), PYREXIA (fever of 101.1 deg F) and VOMITING (Vomiting). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) for Fever, at an unspecified dose and frequency. At the time of the report, DIARRHOEA (Diarrhea) and VOMITING (Vomiting) had resolved and PYREXIA (fever of 101.1 deg F) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 30-Oct-2021, Blood glucose: 177 (High) blood sugar lever went up to 177 units from its usual 120 units.. On 30-Oct-2021, Body temperature: 101.1 (High) 101.1 degree F. On 30-Oct-2021, Heart rate: 101-103 breaths per minute (High) it only ranges from 70-90BPM prior to vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211030; Test Name: Blood sugar; Result Unstructured Data: blood sugar lever went up to 177 units from its usual 120 units.; Test Date: 20211030; Test Name: Body temperature; Result Unstructured Data: 101.1 degree F; Test Date: 20211030; Test Name: Heart rate; Result Unstructured Data: it only ranges from 70-90BPM prior to vaccination
- Aktuelle Erkrankungen
- AFib; Type 2 diabetes mellitus
- Vorgeschichte
- -
- Andere Medikamente
- INSULIN; VICTOZA; METFORMIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Symptomtext
Swelling; pain; redness itching at injection site. Red, itchy oval became 2" by 2 ?." Continued to itch after pain ceased. Still a little itchy 11/6/2021. Redness almost gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Renal insufficiency; depression
- Andere Medikamente
- Antidepressants; thyroid meds; sleeping aids
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Neuralgia
Symptomtext
Nerve pain about every 20 seconds in left ankle during the night when trying to sleep first and second nights after shots and continuing in morning after a second night
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- peripheral neuropathy
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 24.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Rash erythematous
Rash pruritic
Swelling
Symptomtext
Swollen, red, itchy spreading rash covered all right upper arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes, asthma, high blood pressure
- Andere Medikamente
- Glipizide, metformin, lisinopril, adderall, effexor, lamictal, vitamin d, vitamin b12, levothyroxine, ambien, zyrtec
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling hot
Rash erythematous
Rash pruritic
Symptomtext
Patient's right arm started feeling warm on Monday (11/1/2021) evening. By Tuesday morning she had also developed a red itchy rash.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- diabetes
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 22.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Hyperhidrosis
Nausea
Pruritus
Rash
Tinnitus
Symptomtext
dizziness, sweating without fever, nausea, ringing in ears and rash to chest, abdomen, upper legs within 24 hours from time of injection. Dizziness, sweating without fever, nausea subsided within 4 days of injection. Rash has worsened, ringing in the ears continues on occasion intermittently. Dr. visit on 10/26/2021 with prescription for Cetrizine 10MG BID ordered. No improvement of rash with antihistamine. Rash has spread more further down legs and now presenting on arms (not at injection site) going through cycles of flaring causing severe itching. I am 13 days out from injection and planning on going to urgent care for treatment of rash as antihistamine is not aiding in reducing rash.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- no medical tests completed
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Elavil, Fish oil, Aloe vera juice, crestor, acyclovioir, famotidine, multi-vitamin. retin-a
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site pain
Symptomtext
arm pain (injection site); This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (arm pain (injection site)) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. No Medical History information was reported. On 26-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 26-Oct-2021, the patient experienced VACCINATION SITE PAIN (arm pain (injection site)). At the time of the report, VACCINATION SITE PAIN (arm pain (injection site)) outcome was unknown. Concomitant medication information was not provided by the reporter. Treatment information was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Feeding disorder
Full blood count
Headache
Metabolic function test
Nausea
SARS-CoV-2 test
Vomiting
Symptomtext
Extreme nausea & headache, Unable to eat or drink without vomiting for two days, Given IV fluids (sodium chloride o.9% (2 bags), Ondansetron (Zofran) , Ketorolac (Toradol) on 10/29/2021 starting at 6:07 pm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Basic Metabolic Panel, CBC with Differential, Covid-19 NAAT
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- multi-vitamin po, calcuim1200 po
- Allergien
- Codeine Sulfate
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Injection site bruising
Injection site erythema
Injection site induration
Injection site pain
Injection site pruritus
Injection site rash
Injection site swelling
Symptomtext
Redness, soreness, hard swelling, rash (about 10 cm wide by 4 cm high) with intermittent itching. Applied cold pack (once only). All of the above began Day 1 following the injection; started to subside on Day 4, with only soreness and a yellow bruise at the injection site remaining on Day 5 following the injection (11/03/21).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Centrum Silver Women 55+ Cranberry concentrate, 50,000 mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
patient said she was feeling lightheaded and dizzy - I instructed her to remain seated and got a her a chilled bottle of water- she then remained seated and drank her water. I checked in on her every 5 minutes or so and after she drank her water she said she felt better and left
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none aware of
- Vorgeschichte
- anemia
- Andere Medikamente
- none aware of
- Allergien
- amoxicillin - rash - hasnt had since she was 4 years old
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
Chest discomfort
Cough
Fatigue
Injection site pain
Injection site swelling
Pyrexia
Rhinorrhoea
Symptomtext
Per Client, received second dose of Moderna COVID 19 vaccine in the left arm on 10/26/2021. Next day on 10/27/2021, left arm at site swollen and painful. Later in day on 10/27/2021, symptoms of fever, runny nose, slight loss of taste and smell, fatigue, intermittent cough and slight chest discomfort, for now over a week since vaccine on 10/26/2021. Client dose have underlying medical conditions and taking prescription medications. Client reported taking over the counter Tylenol for pain and fever. PHN provided COVID 19 vaccine education with Client. PHN recommend that Client follow up with PCP, go into Urgent Care, ER or call 911 for medical emergency. Per Client, will be follow up with PCP and COVID 19 test
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN
- Andere Medikamente
- Yes- Claritin
- Allergien
- Yes-Environmental
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 31.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Chills
Diarrhoea
Dysgeusia
Feeling abnormal
Headache
Nausea
Neck pain
Pain
Symptomtext
severe headache, nauseous, chills, metal taste in mouth, entire body aches and pains, diarrhea, sore neck and upper back, swimmy head
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- swimmy head, chills, fever, nausea, severe headache, diarrhea
- Staat
- WA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Extra dose administered
Malaise
Odynophagia
Oropharyngeal pain
Pain
Poor quality sleep
SARS-CoV-2 test negative
Tonsillar ulcer
Upper respiratory tract infection
Symptomtext
My booster was on Monday 10/25 and I felt great that day and Tuesday, but Wednesday night at 9-10PM, I realized had a really sore throat, but I went to bed and didn't sleep really well. I had aches and pains. When I got up, I took my temperature, and it was 100.00. I was achy, etc. My throat was really sore. I took a flashlight and looked at my throat. And I had 5-6 white spots or sores on my tonsils on the left side. It was very tender underneath my jaw. So I spent that day (Thursday) not feeling good. I took ibuprofen during the day and rested and drank fluids. I thought if I didn't feel good the next day, I would go see the doctor. I still felt crummy but I wasn't running a fever the next day but my throat still hurt. Hurt to talk and swallow. I went to see my doctor, he did a COVID-19 test which was negative, and he prescribed Dexamethasone and I was required to swish it around and swallow it and do that for 3-5 days. I've taken it for 3 days, and I didn't take any today. I do still feel raspy, and I still have the spots on my tonsil, but it isn't painful anymore. And my doctor put down on the diagnosis that it was an upper respiratory tract infection of unspecified type. Feeling back to normal now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test: Negative
- Aktuelle Erkrankungen
- Diarrhea
- Vorgeschichte
- Hypertension Osteoarthritis Anxiety Disorder
- Andere Medikamente
- Amlodipine 10mg once daily Metoprolol Succinate XL 25mg once daily Omeprazole 20mg once daily Sertraline 100mg once daily Hydrocodone 10mg once daily MS Contin 15mg once daily Vitamin D 1000IU once daily Probiotic Gummy Vitamins Gummy Calc
- Allergien
- Tetracycline Seasonal Allergies
- Vorherige Impfungen
- 2020 Flu Shot - had aches and pains, and fever, then I was fine after one day
- Staat
- CA
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Extra dose administered
Peripheral swelling
Pruritus
Fatigue
Induration
Symptomtext
Arm very swollen, red, hardness, very itchy especially at night. Kept ice compresses on at night. Took Tylenol one time at night. Feel fatigued from morning to night. Have never had a reaction to shot of any kind before ( including first two Maderna vaccinations prior to this last Maderna booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None yet.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Had Shingles in 2011 and still have pain. Have thyroid condition that is monitored every six months and do not take meds.
- Andere Medikamente
- None
- Allergien
- Ragweed, dust, milk, wool,
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Extra dose administered
Peripheral swelling
Pruritus
Fatigue
Induration
Symptomtext
Arm very swollen, red, hardness, very itchy especially at night. Kept ice compresses on at night. Took Tylenol one time at night. Feel fatigued from morning to night. Have never had a reaction to shot of any kind before ( including first two Maderna vaccinations prior to this last Maderna booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None yet.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Had Shingles in 2011 and still have pain. Have thyroid condition that is monitored every six months and do not take meds.
- Andere Medikamente
- None
- Allergien
- Ragweed, dust, milk, wool,
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 31.10.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Injection site pain
Lymphoedema
Pyrexia
Symptomtext
Right arm pain at injection site and headache started morning of 10/30/21. Fever and chills started night of 10/30/21. Lymphedema right axilla started night of 10/30/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- HTN.
- Andere Medikamente
- Lisinopril; Pantoprazole.
- Allergien
- Sulfa - Rash.
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 30.10.2021
- Impfdatum
- 28.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site induration
Injection site pruritus
Injection site warmth
Symptomtext
Left arm at the injection site has a large round red circle. It is red, firm to the touch, hot and a little itchy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 30.10.2021
- Impfdatum
- 30.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Symptomtext
Itchy sensation but no visible rash . 1 dose of oral benadryl 25mg given. Pt report improvement after 15 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 30.10.2021
- Impfdatum
- 26.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pruritus
Injection site warmth
Local reaction
Symptomtext
Localized reaction left upper arm 2-3" wide approx 5" long, erythematous, +pruritis, warmth.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Asthma, HTN, Depression/anxiety
- Andere Medikamente
- Magnesium, Calcium, aleve, acidophyllis Certirizine 10 mg; Advair 100/50; ecitalipram 20mg; Buproprion 300XL; HCTZ 25 mg, ; simvastatin 40mg; omeprozole 20mg
- Allergien
- opioids
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Feeling cold
Feeling hot
Injection site bruising
Insomnia
Malaise
Symptomtext
Patient reported not feeling well after receiving the vaccine for approximately five nights after vaccination patient reports feeling hot and cold waking her up at night, a bruise about the size of an orange at injection site, and loss of appetite.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- losartan, metoprolol clonazepam pantoprazole
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 28.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Headache
Myalgia
Nausea
Vomiting
Symptomtext
Severe Headache, nausea, vomiting, muscle aches, chills, red face,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Prolapse of mitral valve
- Andere Medikamente
- None
- Allergien
- Gluten
- Vorherige Impfungen
- Moderns 1st dose
- Staat
- WI
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dizziness
Symptomtext
THE PATIENT FELT FAINT ABOUT 5 MINUTES AFTER HIS VACCINATION WHILE WAITING FOR HIS WIFE TO GET VACCINATED. HE WAS ASKED TO SIT IN THE VACCINATION AREA CHAIR FOR OBSERVATION BY THE VACCINATING TECHNICIAN. AFTER ABOUT 10 MINUTES OF REST HE STILL FELT VERY WEAK AND WAS CLOSING HIS EYES AND SLIPPING OUT OF THE CHAIR. HE SAID HE COULD NOT FEEL HIS LEGS SO I (PHARMACIST ) ASKED HIM IF I COULD CALL EMERGENCY NUMBER. HE SAID YES. I CALLED THE EMERGENCY NUMBER FOR EMERGENCY ASSISTANCE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- NOT KNOWN
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE KNOWN
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 28.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Pain in extremity
Symptomtext
General fatigue and severe arm pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Cymbalta, Naltrexone, Truvada, Vitamin D
- Allergien
- Penicillin, Levofloxacin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Erythema
Peripheral swelling
Pyrexia
Staphylococcal infection
Symptomtext
Starting the day after immunization, patient had significant redness and swelling of his left upper arm that spread towards his elbow, accompanied by fever. Patient presented to his doctor 2 days later, for which his doctor sent him to the hospital emergency room for fear of blood clot. In Emergency Room it was determined patient had Staph infection, he was given IV antibiotics in the hospital and discharged with PO antibiotics. Patient was fully recovered within 2 days after starting antibiotics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Decreased appetite
Fatigue
Joint range of motion decreased
Nausea
Pain in extremity
Symptomtext
debilitating pain in arm, unable to raise arm the morning after the vaccine 10/26. Nausea and lack of appetite the second and third days 26th and 27th temperature between 100.4 and 101.9 for 2 days after vaccine 26th and 27th and fatigue. Still have some fatigue and soreness in the arm but no fever or nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- hay fever
- Vorgeschichte
- sicca, osteoarthritis
- Andere Medikamente
- Fluoxetine, nexium, tramadol, tylenol, methotrexate, prednisone, folic acid, b-complex, alpha lipoic acid, vit d, fish oil,
- Allergien
- almonds, sulfa drugs, cephalosporins, dilaudid
- Vorherige Impfungen
- Fever Moderna vaccine #2 03/10/2021
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Influenza like illness
Urticaria
Symptomtext
Within 2 hour, Severe upper body hives,urticaria, took bendryl 50 mg twice in next 24 hours. Day two, felt like I had the flu, temp of approx 100 degrees for about 8 hours. Short episode of diarrhea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hashimotas Obesity
- Andere Medikamente
- Advil,Tylenol,synthroid, levostatin,fosamax
- Allergien
- Nka
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
Patient recieved vaccine on Monday. Called pharmacy reporting that she had redness and swelling at immunization site that was growing in size. Pharmacist recommend patient go to urgent care to determine if injection site was infected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- -
- Andere Medikamente
- No record
- Allergien
- No known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Fatigue
Injection site erythema
Injection site pruritus
Injection site swelling
Pain
Pyrexia
Symptomtext
Low-grade fever, fatigue, general achiness, especially in leg/hips joints -- these symptoms started late morning the day after receiving the injection, and were gone the following day. Red swollen area below injection site, kind of itchy, but not really a rash -- this symptom started about the same time as the others, but is still there now (2 days after receiving injection).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None. I'm assuming the redness and swelling are not a big deal, unless it means the injection was given in the wrong spot on my arm, but how would I know that?
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Ulcerative colitis (asymptomatic), overweight, high cholesterol
- Andere Medikamente
- Mesalamine, rosuvastatin, premarin, mometasone, valacyclovir, Osteo-BiFlex, Vit C, multi-vitamin
- Allergien
- apples, nectarines, peaches, plums, cherries
- Vorherige Impfungen
- Felt the same achiness and general fatigue after my 2nd Moderna shot March 2021 (70 yrs old), also after the 2nd Shingrix shot M
- Staat
- WA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Diarrhoea
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Mild diabetes High cholesterol Thyroid High bp
- Andere Medikamente
- Met for in Levothyroxine Atorvastatin Lisinopril
- Allergien
- Cimetidine
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 24.10.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Headache
Pain in extremity
Vomiting
Symptomtext
vomiting for 8 hours, starting at 6 am on 10/27/21, headache, arm and shoulder pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure, high cholesterol
- Andere Medikamente
- benazepril 40mg, rosuvastatin 10mg
- Allergien
- adhesive, iodine
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Extra dose administered
Feeling abnormal
Swollen tongue
Symptomtext
Patient received 0.25ml dose of Moderna in left arm as a booster dose, boostrix in right arm at 1:00pm. Patient was told to remain in pharmacy for at least 15 minutes after dose and check in with us before leaving the store as per protocol. At approximately 1:15 patient reported that she felt "funny and kind of dizzy, and a little off". I asked patient is she was feeling any swelling of her face lips or tongue or any other way felt off, she reported that she did not. I got her a bottle of water and took her into the counseling room to observe, at which point she reported that she felt "like her tongue was swelling". She did not have any breathing or swallowing issues. We called 911 and I took her blood pressure which was 133/80 with a pulse of 70. I then contacted her doctor, and he immediately called me back on his personal cell phone. He asked if we had any solu-medrol, but we do not stock injectibles, and asked that we dispense 40mg of prednisone tablets to be given right away. At this point, the paramedics arrived and they were able to converse with the doctor over my cell phone. I did not dispense the prednisone as the paramedics had solu-medrol in their ambulance. Patient was transported to hospital for further evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 25.10.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Injection site erythema
Injection site induration
Tenderness
Symptomtext
Red and hard at the injection site, lump appeared under arm pit and became tender.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High cholesterol, osteoporosis.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 24.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bedridden
Chills
Headache
Symptomtext
Moderna Covid-19 Vaccine EAU I received my third shot of the Vaccine on Friday at about 4 PM. ( 10/22/2021). On Saturday morning about 9 AM I began to have chills, teeth chattering, and some head aches. At the time I was working in a boat yard and often on boats. I had a friend drive me home and I got home late morning. More headaches and continued chills and teeth chattering. I went to bed for the rest of the day and basically stayed in bed till this morning. I believe I am now OK but will take it easy today. The first two Moderna shots did not trouble me at all. This came as a surprise.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Quad BYPASS
- Andere Medikamente
- -
- Allergien
- Fentanyl
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 19.09.2023
- Impfdatum
- 19.11.2021
- Beginn
- 14.09.2023
- Tage bis Beginn
- 664,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 1 booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- positive covid pcr 9/14/23
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- CABG, Cardiac Stents, maze ablation of heart, Renal stent, Cholecystectomy, Hysterectomy, Partial, BSO
- Andere Medikamente
- unknown
- Allergien
- amoxicillin, penicillins
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 05.05.2023
- Impfdatum
- 30.10.2021
- Beginn
- 27.04.2023
- Tage bis Beginn
- 544,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 5/4/23
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Coronary Artery Disease, Diabetes, Hyperlipidemia, Hypertension, Renal Disease and Other (Afib)
- Andere Medikamente
- unknown
- Allergien
- iodinated contrast media
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 02.03.2023
- Impfdatum
- 29.10.2021
- Beginn
- 28.02.2023
- Tage bis Beginn
- 487,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 21.02.2023
- Impfdatum
- 29.10.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 33,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anti-cyclic citrullinated peptide antibody negative
Blood immunoglobulin A
Blood immunoglobulin G normal
C-reactive protein normal
COVID-19
Full blood count normal
Metabolic function test normal
Muscular weakness
Musculoskeletal stiffness
Rheumatoid factor negative
SARS-CoV-2 test positive
Shoulder operation
Vitamin B12 normal
Symptomtext
Approximately 12/01/2021, I began to notice intermittent stiffness and weakness in both hands upon waking. More recently, they symptom has been more consistent. I went to the doctor recently. I had surgery on September 22, 2022 on my shoulder and I also had COVID-19 right after that surgery, on October 5, 2022. I had an allergic reaction to medications during surgery, which lowered my immunity. I have an appointment with a neurologist in March.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anti-cyclic citrullinated peptide antibody negative
- Hospital-Tage
- -
- Labordaten
- 05OCT2022 COVID-19 test positive; 16JAN2023 CRP normal; 16JAN2023 vitamin B-12 normal; 16JAN2023 Rheumatoid Factor normal; 16JAN2023 Anti-CCP normal; 16JAN2023 AB,IGG and IGA normal; 16JAN2023 CBC normal; 16JAN2023 Metabolic Panel normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Calcium; vitamin D
- Allergien
- Penicillin; chlorhexidine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 20.02.2023
- Impfdatum
- 29.10.2021
- Beginn
- 16.02.2023
- Tage bis Beginn
- 475,0
- Dosis
- 3
- 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 3 vaccines Moderna 2/16/21 Lot# 031M201; Moderna 3/16/21 Lot# 040021A Moderna 1029/21 Lot# 939904
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 09.03.2021
- Beginn
- 10.09.2022
- Tage bis Beginn
- 550,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19 immunisation
Suspected COVID-19
Symptomtext
REVACCINATION WITH DIFFERENT COVID-19 VACCINE; SUSPECTED COVID-19; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned an adult female. The patient's height, and weight were not reported. The patient's concurrent conditions included: penicillin allergy, and other pre-existing medical conditions included: Patient was not pregnant at time of vaccination. The patient previously received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (first dose) (suspension for injection, route of admin not reported, batch number: 1805020 expiry: UNKNOWN) dose was not reported, 1 total administered on 09-MAR-2021, 17:00 at left arm for covid-19 prophylaxis. 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). It was unknown whether patient had any adverse events following vaccination with covid-19 vaccine ad26.cov2.s (Dose number in series 1). The patient additionally received non-company suspect vaccine included Spikevax (elasomeran) (Moderna)(Dose number in series 2) (second dose) (batch number: 939904 expiry: UNKNOWN, form of admin, route of admin, and were not reported) dose was not reported, administered on 24-OCT-2021 at left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with second dose of Spikevax (elasomeran) (Moderna) (Dose number in series 2). The patient additionally received non-company suspect vaccine included Spikevax (elasomeran) (Moderna)(Dose number in series 3) (third dose) (batch number: A57415B expiry: UNKNOWN, form of admin, route of admin, and were not reported) dose was not reported, administered on 10-JUN-2022 at left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with third dose of Spikevax (elasomeran) (Moderna) (Dose number in series 3). The patient additionally received non-company suspect vaccine included Spikevax (elasomeran) (Moderna)(Dose number in series 4) (fourth dose) (batch number: 1805020 expiry: UNKNOWN, form of admin, route of admin, and were not reported) dose was not reported, administered on 10-SEP-2022 at left arm for covid-19 prophylaxis which was revaccination with different COVID-19 vaccine (Dose number in series 4). Concomitant medications included bupropion, Unisom (diphenhydramine hydrochloride), estradiol, levothyroxine, losartan, and Valacyclovir (valaciclovir) for unspecified indication. On an unspecified date in 2022, the patient had COVID-19 for which patient had non-company suspect Paxlovid (form of admin, route of admin, and batch number were not reported, expiry: unknown) dose was not reported, administered from 28-NOV-2022 to 03-DEC-2022 for Covid-19 treatment. On 06-DEC-2022 at 18:00 (evening), the patient started experiencing rebound symptoms (suspected COVID-19 infection), required 2 more 5-day isolation periods (Dose number in series 4) and symptoms resolved on 23-DEC-2022 The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, elasomeran, elasomeran was not applicable and with paxlovid was drug withdrawn. The patient recovered from suspected covid-19 on 23-DEC-2022, and the outcome of revaccination with different covid-19 vaccine was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 immunisation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Penicillin allergy
- Vorgeschichte
- Comments: Patient was not pregnant at time of vaccination
- Andere Medikamente
- BUPROPION; VALACYCLOVIR [VALACICLOVIR]; LEVOTHYROXINE; LOSARTAN; ESTRADIOL; UNISOM [DIPHENHYDRAMINE HYDROCHLORIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 30.12.2022
- Impfdatum
- 12.03.2021
- Beginn
- 01.10.2022
- Tage bis Beginn
- 568,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
COVID-19 immunisation
SARS-CoV-2 test
Vaccination failure
Drug ineffective
Interchange of vaccine products
Symptomtext
REVACCINATION WITH DIFFERENT COVID-19 VACCINE; CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a 34 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: graves disease, and drug allergy (Vicodin, Doxycycline), and other pre-existing medical conditions included: Patient was not pregnant at the time of reporting. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805031, expiry: UNKNOWN) dose was not reported, 1 total administered on 12-MAR-2021 in left arm for covid-19 prophylaxis. Age at time of vaccination 32 years old. No concomitant medications were reported. The patient received non-company suspect vaccine Moderna covid-19 vaccine (elasomeran) (dose number in series 2) (form of admin, and route of admin were not reported, batch number: 939904, expiry: UNKNOWN) dose was not reported, administered on 31-OCT-2021 in left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse event following vaccination with Moderna covid-19 vaccine (elasomeran) (dose number in series 2). The patient additionally received non-company suspect vaccine Pfizer Biontech covid-19 vaccine (tozinameran) (dose number in series 3) (form of admin, and route of admin were not reported, batch number: 6H9703, expiry: UNKNOWN) dose was not reported, administered on 01-OCT-2022 in right arm for covid-19 prophylaxis which was revaccination with different covid-19 vaccine (dose number in series 3). On an unspecified date in 2022, the patient had COVID-19 infection (dose number in series 3) for which patient received non-company suspect Paxlovid (form of admin, route of admin, and batch number were not reported, expiry: unknown) dose was not reported, administered on 13-NOV-2022 for covid-19 treatment. Date of last dose of administration was 18-NOV-2022. On NOV-2022, Laboratory data included: COVID-19 virus test Negative. On 10-DEC-2022, the patient tested positive four weeks after testing negative following Paxlovid treatment (confirmed covid-19 infection) (dose number in series 3) which resulted to confirmed clinical vaccination failure (dose number in series 1). Laboratory data included: COVID-19 virus test Positive. The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, tozinameran was not applicable and with Paxlovid was drug discontinued. The patient had not recovered from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure and revaccination with different covid-19 vaccine was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint: 90000264857.; Sender's Comments: V0-20221258545-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
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202211; Test Name: COVID-19 VIRUS TEST; Test Result: Negative; Test Date: 20221210; Test Name: COVID-19 VIRUS TEST; Test Result: Positive
- Aktuelle Erkrankungen
- Drug allergy (Vicodin, Doxycycline); Graves' disease
- Vorgeschichte
- Comments: Patient was not pregnant at the time of reporting.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 10.11.2022
- Impfdatum
- 17.02.2021
- Beginn
- 12.09.2022
- Tage bis Beginn
- 572,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Aphasia
COVID-19
SARS-CoV-2 test positive
Symptomtext
09/12/22 admitted to inpatient rehabilitation unit for "aphasia" PMHx of "multiple medical problems including vasculopathy, prior CVA in 2013"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aphasia
- Hospital-Tage
- -
- Labordaten
- 09/16/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 07.11.2022
- Impfdatum
- 27.10.2021
- Beginn
- 03.11.2022
- Tage bis Beginn
- 372,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough case dose 1 Moderna 1/22/21 029L20A dose 2 Moderna 2/19/21 023M20A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ 11/3/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 01.10.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 61,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray
Computerised tomogram thorax abnormal
Cough
Mycobacterium avium complex infection
Neutrophil count increased
Respiratory tract congestion
White blood cell count increased
Symptomtext
Chronic Cough, MAI lung infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest X-ray
- Hospital-Tage
- -
- Labordaten
- Elevated WBC, elevated absolute neutrophils, chest xrays, CT chest
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic MAI lung infection diagnosis after months of coughing and congestion once CT was done on 9/29/2022
- Andere Medikamente
- Losardin, hydroclorizie, dexilant,synthroid, ambien,mobic,Tylenol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 21.10.2022
- Impfdatum
- 26.04.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 177,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 03.11.2021
- Beginn
- 20.09.2022
- Tage bis Beginn
- 321,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against, then tested positive for COVID-19. This resulted in ER visit and hospitalization.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 91,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 03.11.2021
- Beginn
- 21.09.2022
- Tage bis Beginn
- 322,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against, then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 20.09.2022
- Impfdatum
- 14.12.2021
- Beginn
- 19.09.2022
- Tage bis Beginn
- 279,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 9/20/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Asthma, Coronary Artery Disease, COPD, Hypertension, Reflux and Renal Disease
- Andere Medikamente
- unknown
- Allergien
- cephalexin monohydrate
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 28.10.2021
- Beginn
- 05.09.2022
- Tage bis Beginn
- 312,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after two vaccines Moderna 9/27/21 Lot# 040B21A; Moderna 10/28/21 Lot# 939904;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 30.08.2022
- Impfdatum
- 15.11.2021
- Beginn
- 27.08.2022
- Tage bis Beginn
- 285,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalization with covid; fully vaccinated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- positive covid pcr 8/27/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Asthma and Hypertension
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 11.08.2022
- Impfdatum
- 13.03.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19 immunisation
Interchange of vaccine products
No adverse event
Symptomtext
interchange of vaccine products; Revaccination with different covid-19 vaccine; No adverse event; This spontaneous case was reported by a patient and describes the occurrence of INTERCHANGE OF VACCINE PRODUCTS (interchange of vaccine products), COVID-19 IMMUNISATION (Revaccination with different covid-19 vaccine) and NO ADVERSE EVENT (No adverse event) in a 40-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for Prophylactic vaccination. Co-suspect product included non-company product COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) for Prophylactic vaccination. Concurrent medical conditions included Drug allergy. Concomitant products included LISDEXAMFETAMINE MESILATE (VYVANSE) from December 2017 to 12-Jun-2022, BUPROPION from December 2017 to 12-Jun-2022, TADALAFIL from October 2021 to 09-Jun-2022 and CETIRIZINE HYDROCHLORIDE (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) from December 2017 to 12-Jun-2022 for an unknown indication. On 13-Mar-2021, the patient received first dose of COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) (unknown route) 1 dosage form. On 23-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (interchange of vaccine products), COVID-19 IMMUNISATION (Revaccination with different covid-19 vaccine) and NO ADVERSE EVENT (No adverse event). At the time of the report, INTERCHANGE OF VACCINE PRODUCTS (interchange of vaccine products), COVID-19 IMMUNISATION (Revaccination with different covid-19 vaccine) and NO ADVERSE EVENT (No adverse event) outcome was unknown. No treatment medication were provided. This case was linked to MOD-2022-595341 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 immunisation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy
- Vorgeschichte
- -
- Andere Medikamente
- VYVANSE; BUPROPION; TADALAFIL; ZYRTEC [CETIRIZINE HYDROCHLORIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 28.07.2022
- Impfdatum
- 26.10.2021
- Beginn
- 21.07.2022
- Tage bis Beginn
- 268,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram
Metastasis
Neoplasm malignant
Tinnitus
Symptomtext
Tinnitus after each dose/even longer with booster/tinnitus got louder and worse with each dose/tinnitus in both ears/It was bad; diagnosed with cancer that has metastasized to other organs with unknown origination.; diagnosed with cancer that has metastasized to other organs with unknown origination.; This spontaneous case was reported by a patient and describes the occurrence of NEOPLASM MALIGNANT (diagnosed with cancer that has metastasized to other organs with unknown origination.) and METASTASIS (diagnosed with cancer that has metastasized to other organs with unknown origination.) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Penicillin allergy (breaks into a pink rash). Concomitant products included ACETYLSALICYLIC ACID (BABY ASPIRIN) for an unknown indication. On 26-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Jul-2022, the patient experienced NEOPLASM MALIGNANT (diagnosed with cancer that has metastasized to other organs with unknown origination.) (seriousness criterion medically significant) and METASTASIS (diagnosed with cancer that has metastasized to other organs with unknown origination.) (seriousness criterion medically significant). On an unknown date, the patient experienced TINNITUS (Tinnitus after each dose/even longer with booster/tinnitus got louder and worse with each dose/tinnitus in both ears/It was bad). At the time of the report, NEOPLASM MALIGNANT (diagnosed with cancer that has metastasized to other organs with unknown origination.), METASTASIS (diagnosed with cancer that has metastasized to other organs with unknown origination.) and TINNITUS (Tinnitus after each dose/even longer with booster/tinnitus got louder and worse with each dose/tinnitus in both ears/It was bad) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 13-Jul-2022, Computerised tomogram: hardening of organs. In medical history it was reported that patient was healthy until cancer. Patient had the following labs: CA 125, CEA Blood Level, and CA19-9. Patient was consulting Acupuncturist for tinnitus and Oncologist for cancer. No treatment medication was reported. Company Comment: This is a spontaneous case concerning a 79-year-old female patient with concomitant medication of Aspirin, who experienced the unexpected serious (medically significant) events of Neoplasm malignant with Metastasis, reported as cancer that has metastasized to other organs with unknown origin, which occurred approximately 8 months and 3 weeks after receiving a dose of mRNA-1273 as the third/booster dose of COVID-19 vaccine. Patient had received the first dose of mRNA-1273 vaccine and unspecified COVID-19 vaccine prior to booster dose of mRNA-1273 vaccine. It was reported that the patient also experienced loud tinnitus in both ears after each dose that persisted for 3 to 4 months, which became louder, worse, and longer in duration after each dose. Patient consulted an Acupuncturist for tinnitus and Oncologist for cancer. Patient had CA 125, CEA Blood Level, and CA19-9 tumor markers, however, no results were reported. Patient also underwent Computerised tomogram which showed "hardening of organs" and was scheduled for a biopsy. No further details about the treatments were provided. It was reported that patient still had residual effects of tinnitus and ongoing cancer. The concomitant intake of Aspirin remains as a confounder for the event Tinnitus. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to MOD-2022-613185 (Patient Link).; Sender's Comments: This is a spontaneous case concerning a 79-year-old female patient with concomitant medication of Aspirin, who experienced the unexpected serious (medically significant) events of Neoplasm malignant with Metastasis, reported as cancer that has metastasized to other organs with unknown origin, which occurred approximately 8 months and 3 weeks after receiving a dose of mRNA-1273 as the third/booster dose of COVID-19 vaccine. Patient had received the first dose of mRNA-1273 vaccine and unspecified COVID-19 vaccine prior to booster dose of mRNA-1273 vaccine. It was reported that the patient also experienced loud tinnitus in both ears after each dose that persisted for 3 to 4 months, which became louder, worse, and longer in duration after each dose. Patient consulted an Acupuncturist for tinnitus and Oncologist for cancer. Patient had CA 125, CEA Blood Level, and CA19-9 tumor markers, however, no results were reported. Patient also underwent Computerised tomogram which showed "hardening of organs" and was scheduled for a biopsy. No further details about the treatments were provided. It was reported that patient still had residual effects of tinnitus and ongoing cancer. The concomitant intake of Aspirin remains as a confounder for the event Tinnitus. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Computerised tomogram
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220713; Test Name: Cat Scan; Result Unstructured Data: hardening of organs
- Aktuelle Erkrankungen
- Penicillin allergy (breaks into a pink rash)
- Vorgeschichte
- -
- Andere Medikamente
- BABY ASPIRIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 27.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 106,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 101,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 27.10.2021
- Beginn
- 17.07.2022
- Tage bis Beginn
- 263,0
- 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 Moderan 9/29/21 Lot# 006cz1A; Moderna 10/27/21 Lot# 939904
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 04.11.2021
- Beginn
- 19.07.2022
- Tage bis Beginn
- 257,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 30.10.2021
- Beginn
- 14.07.2022
- Tage bis Beginn
- 257,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 1 booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 7/15/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Asthma, Coronary Artery Disease (RCA totalled, fills by collaterals), Congestive Heart Failure (HFpEF), COPD, CVA (residual right sided weakness ), Diabetes, Hyperlipidemia, Hypertension, Obstructive Sleep Apnea, Peripheral Vascular Dz (femoral PCI ), Reflux, Renal Disease (stage III), Thyroid (hypo ) and Other (afib; pulm HTN; neuropathy; RLS; MR; carotid artery stenosis )
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 14.04.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 90,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 03.11.2021
- Beginn
- 12.07.2022
- Tage bis Beginn
- 251,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 29.10.2021
- Beginn
- 11.07.2022
- Tage bis Beginn
- 255,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 13.03.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Suspected COVID-19
Vaccination failure
Symptomtext
SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient via other manufacture (pfizer) concerned a 41 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: drug allergy (not specified). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1802068 expiry: UNKNOWN) dose was not reported, 1 total administered at left arm on 13-MAR-2021 for prophylactic vaccination. Age at time of vaccination 40 years old. Concomitant medications included bupropion, cetirizine hydrochloride, lisdexamfetamine mesilate, and tadalafil. The patient additionally received non-company suspect Moderna (spikevax) vaccine (elasomeran) (dose number in series 2) (form of admin and route of admin were not reported, batch number: 939904 expiry: UNKNOWN) dose was not reported, 1 total administered at left arm on 23-OCT-2021 for prophylactic vaccination. Age at time of vaccination 40 years old. It was unknown whether patient had any adverse events following vaccination with first dose of non-company suspect Moderna (spikevax) vaccine (elasomeran) (dose number in series 2). The patient received second dose of non-company suspect Moderna (spikevax) vaccine (elasomeran) (dose number in series 3) (form of admin and route of admin were not reported, batch number: 026L21B expiry: UNKNOWN) dose was not reported, 1 total administered at left arm on 30-MAR-2022 for prophylactic vaccination. Age at time of vaccination 41 years old. On an unspecified date, the patient had Covid-19 symptoms (suspected covid-19 infection) (Dose number in series 3) which led to suspected clinical vaccination failure (Dose number in series 1). The patient additionally received non company drug Paxlovid (form of admin, route of admin and batch number were not reported and expiry: unknown) dose was not reported, administered on 14-JUN-2022 for covid-19 treatment. Patient received last dose of Paxlovid on 19-JUN-2022. On 22-JUN-2022, the patient experienced rebound covid infection three days after completion of paxlovid. The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, and elasomeran was not applicable. The patient had not recovered from suspected covid-19 infection, and the outcome of suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000239917.; Sender's Comments: V0: 20220657382-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
- Suspected COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy (not specified)
- Vorgeschichte
- -
- Andere Medikamente
- VYVANSE; BUPROPION; TADALAFIL; ZYRTEC [CETIRIZINE HYDROCHLORIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 28.06.2022
- Impfdatum
- 28.01.2021
- Beginn
- 20.06.2022
- Tage bis Beginn
- 508,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Hypertensive heart disease
SARS-CoV-2 test positive
Symptomtext
hospitalization. Positive for COVID 19 on admission for hypertensive heart disease
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- hypertensive heart disease end stage
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 03.11.2021
- Beginn
- 10.06.2022
- Tage bis Beginn
- 219,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 03.11.2021
- Beginn
- 15.06.2022
- Tage bis Beginn
- 224,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 02.11.2021
- Beginn
- 22.06.2022
- Tage bis Beginn
- 232,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 6/20/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Asthma, Migraines, Cervical and Lumbar Stenosis, Reflex Sympathetic Dystrophy Syndrome, Tobacco use
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 97,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 25.10.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Agitation
Aphasia
Confusional state
Disorientation
Memory impairment
Neuropsychiatric symptoms
Symptomtext
Pronounced and sudden increase in dementia symptoms -- memory difficulties, agitation, confusion, disorientation on waking, rocking, using incorrect words, not recognizing people
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Agitation
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CHF, kidney disease, obesity, high cholesterol, high blood pressure
- Andere Medikamente
- rosuvastatin, carvedilol, amlodipine, torsemide, levothyroxine
- Allergien
- scallops
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 24.10.2021
- Beginn
- 01.05.2022
- Tage bis Beginn
- 189,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
Initial COVID-19 infection prior to Paxlovid treatment; This spontaneous case was reported by an other health care professional and describes the occurrence of COVID-19 (Initial COVID-19 infection prior to Paxlovid treatment) in a 47-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. Concurrent medical conditions included Allergy. On 24-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In May 2022, the patient experienced COVID-19 (Initial COVID-19 infection prior to Paxlovid treatment). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 13-May-2022 to 18-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (Initial COVID-19 infection prior to Paxlovid treatment) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: positive (Positive) Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. patient was not other medications/products within 2 weeks of starting COVID-19 treatment. Patient had relapse of covid 5 days after finishing paxlovid. Became symptomatic again and tested positive again on antigen test on 22-May-2022. Treatment medication information was not provided. Company Comment: This is a spontaneous case concerning a 47-year-old female patient with no relevant medical history reported, who experienced the unexpected non-serious adverse event of special interest COVID-19, described as initial COVID-19 infection prior to Paxlovid treatment, which occurred approximately 7 months after receiving a dose of mRNA-1273 as the third dose of COVID-19 vaccine (no information disclosed on previous COVID-19 vaccinations). Patient was given a six-day-course of Paxlovid treatment for the initial COVID-19 infection. However, four days after the treatment with Paxlovid, patient became symptomatic again, then tested positive for COVID-19 antigen. Outcome of the event for the initial COVID-19 infection was unknown. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This is a spontaneous case concerning a 47-year-old female patient with no relevant medical history reported, who experienced the unexpected non-serious adverse event of special interest COVID-19, described as initial COVID-19 infection prior to Paxlovid treatment, which occurred approximately 7 months after receiving a dose of mRNA-1273 as the third dose of COVID-19 vaccine (no information disclosed on previous COVID-19 vaccinations). Patient was given a six-day-course of Paxlovid treatment for the initial COVID-19 infection. However, four days after the treatment with Paxlovid, patient became symptomatic again, then tested positive for COVID-19 antigen. Outcome of the event for the initial COVID-19 infection was unknown. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: antigen test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 04.02.2021
- Beginn
- 28.04.2022
- Tage bis Beginn
- 448,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
ADMITTED TO HOSPITAL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 01.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test abnormal
Cardiac monitoring abnormal
Cardiac stress test abnormal
Echocardiogram abnormal
Electrocardiogram abnormal
Fluid retention
Heart rate irregular
Ventricular extrasystoles
Symptomtext
A week after receiving the booster I went in for scheduled pre surgery testing. The testing showed irregular heart rate, irregular EKG, blood work was out of whack. My surgery was cancelled and I was scheduled to see a cardiologist. I wore a heart monitor for fourteen days, I went through a stress test and an echocardiogram. These test showed I have PVC's I fluid retention in my lower extremities. I am now on seven new medications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test abnormal
- Hospital-Tage
- -
- Labordaten
- Stress test, Echocardiogram.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Blood Pressure Medication Trazodone
- Allergien
- E.E.S Codeine
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 26.10.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Formication
Hypersensitivity
Magnetic resonance imaging
X-ray
Symptomtext
Within a month or so started to have hypersensitivity in both legs to vibrations wherever I am, the feeling of vibrations of items running being transferred up through my feet and legs. Shortly after that I started having spider crawling feelings in both legs, like my muscles in my legs are moving, this has continued up to this date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling abnormal
- Hospital-Tage
- -
- Labordaten
- X-ray, MRI.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Some arthritis , spinal chord but does not hinder movement. High blood pressure Atherosclerosis Thyroid - Hypo
- Andere Medikamente
- Rosuvastatin 10 MG Lisinopril 10 MG LevoTHYROxine 75 MCG, Aspirin 81 MG Coenzyme Q10 (Co Q10) 200 MG
- Allergien
- None known.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 25.10.2021
- Beginn
- 25.02.2022
- Tage bis Beginn
- 123,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Herpes zoster
Laboratory test
Symptomtext
So I ended up having Shingles in the back of my head four months (Feb. 24, 2022) after being vaccinated. It was on my left side of my face and shoulder.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- Swab the Shingles and cultures.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma
- Andere Medikamente
- Zyrtec 10mg, Omeprazole 20mg and Vyvanse 20mg.
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 26.10.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 61,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Feeling abnormal
SARS-CoV-2 test positive
Sternal injury
Symptomtext
On 12/26/21 I started with a dry cough. I do not think I ever had a fever, I just felt bad. ON 12/27/21 I got tested and on 12/29/21 I was informed that I tested positive for Covid 19. On 01/08/22 I took a Covid test and I was still positive. On 01/11/22 I went to doctor and was given medicine for my cough and was advised to keep taking Mucinex. On 01/13/22 from coughing so much I ended up damaging my sternum and had to go to the urgent care. Urgent care may have prescribed me steroids and antibiotics. Once I started taking the steroids and antibiotics, I noticed the next day I felt better. The cough continued to lingered for about another 2 weeks. I still have brain fog today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid test 12/27/21- Positive.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- Singulair; Celexa; Multivitamin; Hair skin & nails; Calcium; Glucosamine
- Allergien
- Codeine; Penicillin
- Vorherige Impfungen
- Moderna- 2nd dose
- Staat
- OH
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 15.04.2020
- Beginn
- 01.06.2020
- Tage bis Beginn
- 47,0
- Dosis
- 1
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tetanus. Ringing in my ears constantly
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 16.03.2021
- Beginn
- 21.03.2022
- Tage bis Beginn
- 370,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asymptomatic COVID-19
SARS-CoV-2 test positive
Symptomtext
He does have positive COVID test on 3/21 but is asymptomatic
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 30.11.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 24,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abortion spontaneous
Exposure during pregnancy
Foetal growth restriction
Inappropriate schedule of product administration
Symptomtext
Conception on 10/15/21 Miscarriage at 10 weeks pregnant Baby stop developing at 8 weeks - 12/10/21 2nd Covid vaccine administered on 11/30/21 Time from vaccination until development stop - 10 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abortion spontaneous
- Hospital-Tage
- -
- Labordaten
- Miscarriage/ death of my child
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 02.11.2021
- Beginn
- 16.01.2022
- Tage bis Beginn
- 75,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Symptomtext
I got the rash on my face that I got with the first two vaccines and then I got the Shingles 2 months after the Booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoporosis Hypothyroidism
- Andere Medikamente
- Synthroid 0.075, Calcium Multivitamin Omega # Vegetarian
- Allergien
- Penicillin Demerol Vancomycin Erythromycin Narcotic pain relievers, Latex, Shellfish
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 28.10.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 62,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anticoagulant therapy
Electrocardiogram abnormal
Heart disease congenital
Laboratory test
Magnetic resonance imaging
Transient ischaemic attack
Ultrasound scan
Symptomtext
I had a TIA/mini stroke on 12/29. I went to the ER that same day and received a bunch of tests. They determined there was no neurological damage or visible cause for the TIA. The only thing they found was a congenital heart defect. I was in the ER for 2 days and was discharged with a blood thinner. Soon after that I started taking a high cholesterol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anticoagulant therapy
- Hospital-Tage
- 2,0
- Labordaten
- Ultrasound, EKG, MRI
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Spironolactone, Oxcarbazepine, Estradiol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 27.10.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 66,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asymptomatic COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient presented to emergency department on 1/1/2022 following an intentional drug overdose. She was found to be COVID-19 positive during screening for admission. Patient was asymptomatic for COVID-19 during admission and required no treatment or supportive care for infection. Patient was discharged home on 1/8/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- 7,0
- Labordaten
- COVID-19 PCR test positive on 1/1/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Arthritis, depression, hypertension
- Andere Medikamente
- alendronate (FOSAMAX) 70 MG tablet aspirin (HALFPRIN) 81 MG tablet dorzolamide-timolol (COSOPT) 22.3-6.8 MG/ML ophthalmic solution latanoprost (XALATAN) 0.005 % ophthalmic solution mirtazapine (REMERON) 7.5 MG tablet naproxen (NAPROSYN) 500
- Allergien
- Azithromycin
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 30.12.2021
- Beginn
- 11.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested Positive for Covid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 28.10.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 50,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Confusional state
Hypoxia
SARS-CoV-2 test positive
Symptomtext
Case was vaccinated and boosted with Covid vaccine, then hospitalized for Covid 7 weeks after being boosted. Admitted 12/17/21 for confusion and weakness, found to be hypoxic and Covid positive. Required up to 4 litres of oxygen, and weaned back down to room air.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 13,0
- Labordaten
- Ordered Test: No Information Given Accession Number: Specimen Source: Nose (nasal passage) Specimen Site: Bilateral Nares Specimen Collection Date/Time: 12/17/2021 results:Resulted Test: SARS-CoV-2 (COVID19) RNA NAA+probe Ql (Resp) Coded Result: detected Numeric Result: Units: Text Result: Reference Range From: Reference Range To: Status: Final
- Aktuelle Erkrankungen
- A-fib HTN Prostate cancer Hypothyroidism
- Vorgeschichte
- A-fib HTN Prostate cancer Hypothyroidism History of Aortic valve replacement FOrmer smoker History of Covid infection in November 2020
- Andere Medikamente
- Atorvastaytin Cefdinir Chlorthalidone Ferrous gluconate Gabaentin Levothyroxine Losartan Metoprolol POotasium Chloride Warfarin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 29.10.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Coccydynia
Sitting disability
Symptomtext
Following the booster shot, I am experiencing now coccyx pain making it difficult to sit in addition to frozen shoulder pain that began after the 2nd vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Coccydynia
- Hospital-Tage
- -
- Labordaten
- The rheumatologist ruled out arthritis and other issues.
- Aktuelle Erkrankungen
- Only inflammation represented in both frozen shoulders which is ongoing - left is beginning to improve that became inflamed after the second vaccination on 2/21/21.
- Vorgeschichte
- Caused by vaccination - 2 frozen shoulders (left beginning to improve), Coccyx pain that began after the booster on 10/29/21, no other health conditions.
- Andere Medikamente
- Trazodone 200 mg, Estradiol 2 mg
- Allergien
- Penicillin, Gadolinium
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 12.11.2021
- Beginn
- 20.02.2022
- Tage bis Beginn
- 100,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalization; covid, fully vaccinated with booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 1,0
- Labordaten
- positive covid pcr 2/20/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Anemia, Chest Pain and Hypertension
- Andere Medikamente
- unknown
- Allergien
- Penicillin V, tramadol, aspirin, morphine, acetaminophen, hydrocodone, sertraline, sulfa
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 29.10.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 53,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Atrial fibrillation
Blood thyroid stimulating hormone normal
Electrocardiogram abnormal
Symptomtext
Episode of atrial fibrillation, first event on 12/20/21. Onset after lunch while on vacation. Seen in ER. treated with diltiazem and metoprolol with return to sinus rhythm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- 1,0
- Labordaten
- TSH was normal. ECG Atrial fibrillation at 150 bpm
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypothyroidism
- Andere Medikamente
- synthroid 75 mcg a day, alavert as needed, tylenol as needed, benadryl as needed
- Allergien
- sulfa
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 24.02.2021
- Beginn
- 01.02.2022
- Tage bis Beginn
- 342,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cough
Oxygen saturation decreased
Symptomtext
Low o2 saturations, DIB, cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Aortic insufficiency Atrial fibrillation CHF (congestive heart failure) DVT (deep venous thrombosis) (~03/2021) GERD (gastroesophageal reflux disease) Grade II diastolic dysfunction High cholesterol High risk medication use Hot flashes Hypothyroidism (~1980) Insomnia Interstitial pulmonary fibrosis Liver cancer (~1999) Mitral insufficiency Obesity (BMI 30-39.9) Primary osteoarthritis of right shoulder Pulmonary embolism (~03/2021) Rheumatoid arthritis Right hip pain Rotator cuff arthropathy of right shoulder Tricuspid insufficiency
- Andere Medikamente
- Omeprazole, Apixaban, Metoprolol
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 04.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 27,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abortion spontaneous
Exposure during pregnancy
Human chorionic gonadotropin
Pregnancy test positive
Symptomtext
Early Miscarriage at 5 weeks gestation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abortion spontaneous
- Hospital-Tage
- -
- Labordaten
- HGC 11/29/21 12 miu/ml HCG 12/01/21 3.7 miu/ml Positive at home pregnancy test 11/25/21
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hasimotos thyroid disease, high cholesterol and triglycerides, PCOS, anxiety/ depression
- Andere Medikamente
- levothyroxin 112 mcg, aspirin 81 mg, lexapro 10 mg, probiotic, prenatal vitamin daily
- Allergien
- sulfa
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 26.10.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bradycardia
Electrocardiogram ambulatory
Implantable cardiac monitor insertion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bradycardia
- Hospital-Tage
- -
- Labordaten
- Holter Monitor on 11/18/2021, Medtronix Linq implant on December 2021
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Losarton, thyroxin, fenobibtate
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 10.11.2021
- Beginn
- 06.02.2022
- Tage bis Beginn
- 88,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Asthenia
COVID-19
Symptomtext
Hospitalized with weakness found to have COVID 19 O2 sats were in the 80s and required oxygen. treated with dexamethasone
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 27.10.2021
- Beginn
- 05.02.2022
- Tage bis Beginn
- 101,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
fully vaccinated and boosted, COVID infection breakthrough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 27.02.2021
- Beginn
- 26.01.2022
- Tage bis Beginn
- 333,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Alanine aminotransferase increased
Anion gap
Aspartate aminotransferase increased
Blood bicarbonate decreased
Blood calcium increased
Blood chloride increased
Blood creatinine increased
Blood gases
Blood lactic acid
Blood magnesium increased
Blood potassium normal
Blood sodium increased
Blood urea increased
COVID-19
Cerebral atrophy
Chest X-ray abnormal
Computerised tomogram head abnormal
Confusional state
Symptomtext
77 year old man with PMH of dementia. He is acutely confused, history obtained from his wife who is a poor historian herself. Has had worsening confusion over the past week. Has had decreased PO intake for about 3 days. No fevers, chills. Has chronic sinus issues. Has a little bit of a cough. No CP. He has been constipated. No vomiting. He has been falling a lot lately. May have some coughing with eating. He has been vaccinated and boosted, moderna, booster on 12/10/21. On arrival to the ED, he had a T of 97.2, heart rate of 120, blood pressure 126/74. Labs show white count 15.9, hemoglobin 17, platelets 180. Chemistry with sodium 160, potassium 4.8, chloride 118, bicarb 17, anion gap 25, BUN 69, creatinine 3.4 (baseline 0.8 in 2020) calcium 11.4, magnesium 3.4, AST 107, ALT 45, lactate 6.5, procalcitonin 7.16, troponin 96. ABG on room air 7.47/27/68/95%. He is COVID positive. Chest x-ray with low lung volumes with possible left basilar infiltrate. CT head with severe cerebral atrophy with frontotemporal predominance in no acute intracranial process. PT IS INPATIENT AT THIS TIME.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alanine aminotransferase increased
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 797663
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 22.10.2021
- Beginn
- 16.01.2022
- Tage bis Beginn
- 86,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested positive for COVID-19 after being vaccinated with all three doses of the Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID test.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma
- Andere Medikamente
- Lorazepam 1/2mg, Atorvastatin 20mg, multivitamin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 03.11.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 54,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Parosmia
Symptomtext
Diesel exhaust smell present without source present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Parosmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- arthritis
- Andere Medikamente
- Cialis 5mg, lovastatin 20mg, vitamin C, D, fish oil, glucosamine chondroitin, multi vitamin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 03.11.2021
- Beginn
- 20.01.2022
- Tage bis Beginn
- 78,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 30.10.2021
- Beginn
- 19.01.2022
- Tage bis Beginn
- 81,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Hospitalized with covid after being fully vaccinated with a booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive covid PCR 1/19/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Coronary Artery Disease, COPD, Hyperlipidemia, Hypertension, Reflux, Thyroid and Other (migraine-Bipolar depression-Chronic respiratory failure with home oxygen-osteoporosis)
- Andere Medikamente
- unknown
- Allergien
- Amoxicillin, ampicillin, codeine, morphine, opana, penicillins, requip, sulfa, ultram, keflex, hydrocodone
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 27.10.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 64,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID BREAKTHROUGH CASE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID+ 12/30/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- dementia, hyperlipidemia, osteoarthritis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated the vaccines were still safe and effective but requested we make an official report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperature. A case opened with the vaccine manufacturer demonstrated the vaccines were still safe and effective but requested that we make an official report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 27.10.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 70,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine Breakthrough case. Boosted, Moderna 030A21A on 03/23/2021 and Moderna 004M20A on 02/15/2021. Booster Moderna 939904 on 10/27/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID test on 01/05/2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 02.01.2022
- Impfdatum
- 21.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
After my booster shot I got stereo tinnitus screaming in my head most of the day. However, there are a couple hours during the day that is is less noticeable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- Just had a doctor visit to discuss options December 27, 2021 but have not pursued treatment yet.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Accidental underdose
Inappropriate schedule of product administration
Symptomtext
First dose more than 35 days before second dose; first dose was 0.25 ml; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL UNDERDOSE (first dose was 0.25 ml) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (First dose more than 35 days before second dose) in a 46-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 939904 and 059H21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 27-Dec-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to .5 ml. On 02-Nov-2021, the patient experienced ACCIDENTAL UNDERDOSE (first dose was 0.25 ml). On 27-Dec-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (First dose more than 35 days before second dose). On 02-Nov-2021, ACCIDENTAL UNDERDOSE (first dose was 0.25 ml) had resolved. On 27-Dec-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (First dose more than 35 days before second dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was provided. No treatment medications was provided. Most recent FOLLOW-UP information incorporated above includes: On 28-Dec-2021: Non Significant follow up included reporter's email address.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 98,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered after stored greater than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated the vaccines were still safe and effective but requested that we report it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 30,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered was stored great than thirty days in refrigerated temperatures. A case opened with the vaccine manufacturer demonstrated that the vaccines were still safe and effective but requested that we report to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Heavy menstrual bleeding
Menstruation irregular
Symptomtext
Ten days after the third dose of the vaccine I got my period during that time, and it was very unusual. I passed large clots and it was very heavy. It started heavily immediately instead of slowly. It lasted about 4-5 days which was normal for me. I normally do not have large blood clots during that time. I also had some GI distress during that time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal discomfort
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- Lexapro; loratadine
- Allergien
- CT Contrast Dye; Red Dye Sensitivity; Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 28.12.2020
- Beginn
- 07.12.2021
- Tage bis Beginn
- 344,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nasopharyngitis
Respiratory tract congestion
Rhinorrhoea
Symptomtext
runny nose congestion, feels like a cold. starting 12/7/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nasopharyngitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Diabetes 2011, Hypertension, sleep apnea 1998. On CPAP, Obesity
- Andere Medikamente
- Taking Aspir-81 81 MG Tablet Delayed Release 1 tablet Orally Once a day, Taking Fish Oil 1000 MG Capsule 1 capsule Orally Once a day, Taking Lisinopril 40 MG Tablet 1 tablet Orally Once a day, Taking metFORMIN HCl 1000 MG Tablet 1 tablet Or
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 31,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Drug hypersensitivity
Symptomtext
On thurs. Nov. 25 I discovered a tick in my shoulder. The hotel where I was staying helped rmove it, and the ite was very red and irritated. I texted. Dr. andspoke with him on fri. Nov 26. He sent a prescription for 100 mg tabs of Doxycycline Hyclate which I began taking that day., to be taken 2x day on empty stomach. The medicine made me nauseous and caused vomiting. I kept trying to take it, but it kept making me sick. By Sunday eve. it caused vomiting again, and I called Dr. to prescribe a different antibiotic. I have never reacted to an antibiotic this way before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Drug hypersensitivity
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- obesity
- Andere Medikamente
- diovan/hct, synthroid, multivitamins, vit D coQ10, aspirin, zyrtec, pantaprazole, pepsid
- Allergien
- blue dyes, limonene, adhesive, fish, seafood, lactose
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Pt does not meet age requirements for Moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 17.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Pt does not meet age requirement for Moderna vaccine. She should have received the Adult Pfizer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 28.11.2021
- Impfdatum
- 23.10.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Patient has experienced tinnitus since the day following her vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- obesity, hypertension
- Andere Medikamente
- losartan
- Allergien
- latex, penicillin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 27.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
Mistakenly assumed patient was immunosuppressed because pt insisted doctor wanted her immunized immediately, after telling pt it was too early for routine booster shot. So patient got shot at less than 6 months and got full 0.5ml dose. The patient called our corporate office to complain of various side effects, unknown to me, and spoke to our Regional Pharmacy Leader.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- unkown
- Aktuelle Erkrankungen
- RHEUMATOID ARTHRITIS, SJOGRENS SYNDROME, OTHERS
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 26.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
12 year old received Moderna vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (12 year old received Moderna vaccine) in a 12-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. No Medical History information was reported. On 19-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Nov-2021, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (12 year old received Moderna vaccine). On 19-Nov-2021, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (12 year old received Moderna vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant and Treatment medication were reported. A 12-year-old patient received the first dose of Moderna COVID-19 vaccine on 19NOV2021 (Lot# 939904 & Exp. Date: 24MAR2022 ) instead of Pfizer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 21.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Symptomtext
patient had no reaction to the vaccine so thinks she got it subcutaneous
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- unknown
- Andere Medikamente
- n/a
- Allergien
- demerol, statins, niacin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 19.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
This is a vaccine administration error due to age.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
patient received a double dose of the booster; This spontaneous case was reported by a pharmacist and describes the occurrence of EXTRA DOSE ADMINISTERED (patient received a double dose of the booster) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. Concurrent medical conditions included Alzheimer's disease. On 09-Nov-2021, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 ml. On 09-Nov-2021, the patient experienced EXTRA DOSE ADMINISTERED (patient received a double dose of the booster). On 09-Nov-2021, EXTRA DOSE ADMINISTERED (patient received a double dose of the booster) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Alzheimer's disease
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Laboratory test
Platelet count
Postmenopausal haemorrhage
Symptomtext
Post menopausal bleeding
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Laboratory test
- Hospital-Tage
- -
- Labordaten
- Seeing doctor for tests and platelet count
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Omepersole Atorvastatin Glucosamine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cellulitis
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Levothyroxine 150mcg
- Allergien
- sulfa & penicillin
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vertigo
Symptomtext
Vertigo 3 days after vaccination. It is intermittent and still occurring 2 weeks after vaccination. I also got vertigo 3 days after my 2nd shot in February but was unsure if it was due to the vaccination. It last for a six weeks. It is intermittent and often depends on my position.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vertigo
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Synthroid, Lisinprol, HCZ
- Allergien
- None
- Vorherige Impfungen
- 2nd Covid age 50 February 2021
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Skin warm
Swelling
Symptomtext
2 1/2 inches in diameter swollen and red, hot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- no
- Andere Medikamente
- Cymbalta , zinc, vitamin c, d3
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Lymphadenopathy
Peripheral swelling
Symptomtext
Arm swollen and swollen lymph nodes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High blood and cholesterol Hypo thyroid
- Andere Medikamente
- Levothyroxine Losartan Vascepa Rosuvastatin Atenolol
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tinnitus in left ear. Started day after received booster dose of moderna vaccine. Tinnitus remains unchanged nearly two weeks later. Say my primary doctor today- physical exam normal. Received initial moderna covid vaccines 12/30/2020 and 1/25/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- Had physical exam with my primary doctor today, 11/10/21- normal.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- anxiety, depression, obesity, GERD
- Andere Medikamente
- blisovi, pantoprazole, multivitamin, vitamin d, lexapro, wellbutrin, loratadine, flonase
- Allergien
- NSAIDs
- Vorherige Impfungen
- Rash from second dose of moderna covid vaccine 1/25/2021
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient came to our pharmacy to get COVID booster vaccine ( moderna). We went through the questionnaires and found no problem so we gave the vaccine. Later, we were contacted by a family member. Daughter said she had gotten the booster 2 days ago and told us patient has memory problems. Patient received 2 doses of 0.25ml Moderna booster 2 days apart.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKWON
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 09.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental underdose
Symptomtext
a patient (1 patient) that is supposed to received his 1st dose of the Moderna covid19 vaccine but what they gave to the patient was a booster dose; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL UNDERDOSE (a patient (1 patient) that is supposed to received his 1st dose of the Moderna covid19 vaccine but what they gave to the patient was a booster dose) in a 41-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. No Medical History information was reported. On 25-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Oct-2021, the patient experienced ACCIDENTAL UNDERDOSE (a patient (1 patient) that is supposed to received his 1st dose of the Moderna covid19 vaccine but what they gave to the patient was a booster dose). At the time of the report, ACCIDENTAL UNDERDOSE (a patient (1 patient) that is supposed to received his 1st dose of the Moderna covid19 vaccine but what they gave to the patient was a booster dose) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was mentioned. No treatment medication was mentioned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inflammation
Symptomtext
Inflammation of the Face on the same side of injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inflammation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
There has not been a reported adverse event. A third dose (0.5 mL) was given instead of a booster dose (0.25 mL).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 04.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Swelling in lymph node of left armpit
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Glossopharyngeal neuralgia
- Andere Medikamente
- Gabapentin, Truvada, testosterone, multivitamin, omega3 tablets, glucosamine/chondroitin tablets
- Allergien
- None
- Vorherige Impfungen
- fever, aches, chills for one week following shingles vaccine
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Interchange of vaccine products
No adverse event
Symptomtext
Patient came in for a COVID-19 Booster. She received J& J as her first dose, and wanted the Moderna as her booster. Patient was administered 0.5ml dose instead of 0.25ml dose. Patient is immunocompromised with Lupus. No adverse reaction have been reported to us by the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Lupus
- Andere Medikamente
- Methotrexate
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
Patient was given a third Moderna dose of 0.5 mL when a third Moderna dose of 0.25 mL was indicated. This error was communicated to the patient. Patient denied experiencing side effects at time of injection and during the COVID-19 vaccine waiting period following administration of the vaccine. Paient was called by this individual on 11/03/2021 in the afternoon for a follow-up at which time he denied having negative signs/symptoms of receiving the 0.5 mL dose of Moderna. When asked how he was and had been feeling, he stated he felt "Wonderful!". No adverse effects were identified at the time of documentation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension and arthritis
- Andere Medikamente
- chlorthalidone for hypertension & celecoxib for arthritis
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- U
- Eingang
- 03.11.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Patient was administered a 3rd dose being a 0.5 mL Moderna dose on accident instead of the Pfizer booster; This spontaneous case was reported by a pharmacist and describes the occurrence of INTERCHANGE OF VACCINE PRODUCTS (Patient was administered a 3rd dose being a 0.5 mL Moderna dose on accident instead of the Pfizer booster) in an 80-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. No Medical History information was reported. On 23-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 23-Oct-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Patient was administered a 3rd dose being a 0.5 mL Moderna dose on accident instead of the Pfizer booster). On 23-Oct-2021, INTERCHANGE OF VACCINE PRODUCTS (Patient was administered a 3rd dose being a 0.5 mL Moderna dose on accident instead of the Pfizer booster) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Patient received first two doses of Pfizer vaccine. No side effects reported by pharmacist. First Pfizer dose on 30-Mar-2021 and second dose on 20-Apr-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Inflammation
Symptomtext
Inflammation of places where chronic shingles appeared.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Recurrent shingles.
- Vorgeschichte
- Chronic shingles.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 31.10.2021
- Impfdatum
- 28.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Lip swelling
Swelling face
Symptomtext
patient woke up following morning after vaccine with lips and face swelling. she went to urgent care and got Benadryl and Prednisone prescribed and felt relief after a few days. she is feeling ok now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.10.2021
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Received dose from vial punctured for more than 12 hours; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received dose from vial punctured for more than 12 hours) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939904) for COVID-19 vaccination. No Medical History information was reported. On 21-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received dose from vial punctured for more than 12 hours). On 21-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Received dose from vial punctured for more than 12 hours) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Total amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F)24 hours. It was at room temperature since the moment it was punctured and the vaccine was administered 24 hours after that. Concomitant medications was not provided by the reporter. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Incorrect dose administered
Interchange of vaccine products
Symptomtext
Gave 0.5 ml thinking that was correct dose for JJ booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes HTN , hypercholesterol
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 26.10.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient came 10/26/2021 to get her Moderna booster shot, second shot was given 05/12/2021, shot today was earlier than the recommended 6 month period
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 26.10.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Patient with cancer came for Moderna booster shot 10/26/2021. Patient was giving 0.25 ml of Moderna vaccine instead of 0.5 ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- cancer
- Vorgeschichte
- cancer
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
It had to be half (0.25ml) of the original dose for booster, but was given full dose (0.5ml) that are usually given to the immunocompromised patient. Followed up with the patient. No unusual ADR notified at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
It had to be half (0.25ml) of the original dose for booster, but was given full dose (0.5ml) that are usually given to the immunocompromised patient. Followed up with the patient. No unusual ADR notified at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 26.10.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- 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
Incorrect dose administered
No adverse event
Symptomtext
It had to be half (0.25ml) of the original dose for booster, but was given full dose (0.5ml) that are usually given to the immunocompromised patient. Followed up with the patient. No unusual ADR notified at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- 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
Incorrect dose administered
No adverse event
Symptomtext
It had to be half (0.25ml) of the original dose for booster, but was given full dose (0.5ml) that are usually given to the immunocompromised patient. Followed up with the patient. No unusual ADR notified at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 26.10.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
No unusual ADR notified at this time. It had to be half of the original dose for booster, but was given full dose that are usually given to the immunocompromised patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 26.10.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
No unusual ADR notified at this time. It had to be half (0.25ml) of the original dose for booster, but was given full dose (0.5ml) that are usually given to the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cardiac flutter
Heart rate increased
Symptomtext
Moderna COVID-19 Vaccine EUA Booster Dose. About 3 hours after the injection, started with heart flutter and rapid heart beat. Measured at home, then returned to pharmacy to check vitals with their equipment. Pharmacy is a hub for , with a doctor available by call. Spoke to pharmacist. Heart Rate went to 100, blood pressure went to 159/82. Episode lasted about three hours total, then subsided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac flutter
- Hospital-Tage
- -
- Labordaten
- None. At the three hour mark, vitals started to return to normal and were normal the following day.
- Aktuelle Erkrankungen
- Bacterial infection of the kidneys and intestine.
- Vorgeschichte
- Systemic Sclerosis, Lupus. Possible Hashimoto's Disease
- Andere Medikamente
- None. Finished doxycycline RX two weeks prior.
- Allergien
- Shellfish, fish, pork, Demerol, Paxil, erythromycin, codeine, Ambien, sulfa.
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 26.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Wrong product administered
Symptomtext
Patient had scheduled an appointment and filled out paperwork to receive flu shot. Was inadvertently given booster dose of Moderna COVID 19 vaccine. No adverse effects were reported, and patient was informed of error. Patient had completed doses 1 and 2 of Moderna vaccine 6 months prior, so timing was appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 22.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Gave 0.5ml for the 3rd dose instead of 0.25ml.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none.
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 22.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Gave 0.5ml dose instead of the 0.25ml dose for the 3rd dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- -
- Allergien
- none.
- Vorherige Impfungen
- -