- Staat
- TN
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 10.08.2023
- Impfdatum
- 29.06.2022
- Beginn
- 08.12.2022
- Tage bis Beginn
- 162,0
- Dosis
- 4
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Breakthrough COVID-19
Death
Symptomtext
Breakthrough Covid Death
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- HTN, DM type II, Hypothyroidism, Lewy body Demetia,
- Andere Medikamente
- Propranolol, Lisinopril, ASA, Benzonatate, Famotidine, Metformin, Levothyroxine, Insulin, Melatonin, Rivastigmine.
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 26.07.2023
- Impfdatum
- 19.01.2021
- Beginn
- 07.02.2023
- Tage bis Beginn
- 749,0
- Dosis
- 4
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Patient deceased
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- CVA, Anemia, Anxiety, BPH, Bursitis, DM type II, PVD, Seizure disorder,
- Andere Medikamente
- Jardiance, Lotrisone, Narcan, Trazodone, Allopurinol, Celexa, Plavix, Flomax, Vit D3, Calcitriol, Pepcid, Coreg, Gabapentin, Bumex, Torsemide, Percocet, Omeprazole, Nitroglycerin.
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 24.05.2023
- Impfdatum
- 15.07.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 165,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deep vein thrombosis
Hypertension
Hypotension
Pulmonary embolism
Symptomtext
I26.99 ACUTE PULMONARY EMBOLISM 12/27/2022 HTN (HYPERTENSION) I82.403 ACUTE DVT OF BILAT LEGS, UNSPECIFIED VEINS 12/27/2022 HTN (HYPERTENSION) I95.9 HYPOTENSION 12/27/2022 HTN (HYPERTENSION)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 23.05.2023
- Impfdatum
- 15.07.2022
- Beginn
- 19.05.2023
- Tage bis Beginn
- 308,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
SARS-CoV-2 test positive
Symptomtext
Hospitalized with covid; fully vaccinated with 2 boosters. Pt. expired.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 2,0
- Labordaten
- Positive covid pcr 5/18/23
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Hypertension, Obstructive Sleep Apnea, Thyroid and Other (allergic rhinitis, BPH, colon polyps, HTN, Lymphoma of skin, OSA on CPAP, Osteoarthritis, history of kidney stones, hypothyroidism, glaucoma.)
- Andere Medikamente
- unknown
- Allergien
- ciprofloxacin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 14.04.2023
- Impfdatum
- 02.08.2022
- Beginn
- 27.03.2023
- Tage bis Beginn
- 237,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Angiogram pulmonary abnormal
Anticoagulant therapy
Antiphospholipid antibodies negative
Antithrombin III abnormal
Beta-2 glycoprotein antibody negative
Blood alkaline phosphatase increased
Blood bicarbonate normal
Blood creatinine normal
Blood culture negative
Blood gases abnormal
Blood pH increased
Blood sodium decreased
Blood urea normal
C-reactive protein increased
COVID-19
Calcium ionised
Cardiolipin antibody negative
Symptomtext
Patient is a 77 y.o. female patient, DO with history of cataract, HTN who presents as transfer from alternate ED for SOB 2/2 recent COVID 19 infection as direct admit to our facility. COVID-19 Infection Acute respiratory failure with hypoxia Superimposed bacterial pneumonia Presumed COPD, not in acute exacerbation AF, WBC 20-- >11.4, PCT 2.66, CRP 346.7; needed 3 L NC but now on RA 3/17: Positive COVID test, completed OP course of paxlovid 5 days VBG at Hospital: ph 7.45, pCO2 36.7, pO2 27, hCO3 25.7 CTPA at ER: No evidence of central PE. Moderate centrilobular emphysema Blood cultures 3/27 NGTD ID following; started decadron, rocephin, azithromycin 3/27 On 2L NC this AM. Home O2 eval prior to discharge Recommend OP PFT and OSA eval Home with albuterol inhaler Continue steroids for total 10d course. Will transition to PO abx Liver lesion Branched portal vein thrombosis Found incidentally on imaging. No abdominal complaints or hx of liver disease. LFTs normal. GGT 49. ALP 80. iCa 4.0 CTAP 3/27: Abnormal, subtle 2 cm area of decreased attenuation within the dome of the liver concerning for hepatic tumor AFP, hepatitis negative MRI liver: branch portal vein thrombosis w/ mild associated inflammation. Few small rounded foci of nonenhancement contiguous with the thrombosed veins in the peripheral liver dome which would make tiny developing abscesses difficult to exclude. No drainable abscess. Small hemangioma in anterior right hepatic lobe Hypercoagulable panel ordered. Thrombosis likely 2/2 COVID, but cannot exclude underlying disorder. No hx of blood clots, prolonged bleeding, or fmhx. GI and hematology following, recommend initiating anticoagulation, heme consult, repeat MR towards the end of the week Heme consulted, JAK2, BCR-ABL, lupus anticoag, cardiolipin ab, beta-2 glycoperotein ab ordered. Initiated heparin gtt 3/28. Will hold on transition to DOAC pending imaging results Hypercoag work up negative so far except Factor VIII of 285, antithrombin III of 81 MR liver 3/30: Re-demonstration of thrombosis of RPV branches. Areas of hypoenhancement are less conspicuous and are inconsistent with abscesses. May represent areas of improving periportal inflammation. Will transition to DOAC 6 months. Close f/u with GI and PCP Pulmonary nodule History of tobacco use Incidently found on imaging. Hx of distant tobacco use. On RA at home CTPA: Small 4 mm left upper lobe pulmonary nodule Recommend interval f/u CT in 12 months Bilateral renal cysts Incidently found on imaging. No hx of renal dx or symptoms Cr 0.69 on admission. BUN 12 CT: simple 2 cm left renal cyst MR: left renal cyst 2.5 cm without evidence of internal enhancement and there are multiple small bilateral renal cysts which are too small to characterize but not overtly suspicious No interventions indicated Continue to monitor kidney function Pancreatic cystic lesions Incidentally found on imaging. No hx of pancreatitis, jaundice, weight loss, anemia, or abdominal complaints. Abd S, NT, ND, w/ no palpable mass MR: Sub-centimeter cystic lesions in the pancreas may represent dilated ductal side branches or side branch IPMNs. No main ductal dilatation Recommend MRI/MRCP 2 years Hyponatremia Na 122 on arrival now 136; continue to hold HCTZ Essential Hypertension Controlled; continued home clonidine but hold HCTZ
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 17.03.2023
- Impfdatum
- 21.01.2021
- Beginn
- 15.03.2023
- Tage bis Beginn
- 783,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
Dyspnoea
Exposure to SARS-CoV-2
SARS-CoV-2 test positive
Symptomtext
Pt presents with shortness of breath. There have been a few cases of COVID at the center. She has a PMH of COPD and CHF. She tested positive for COVID and was admitted for acute hypoxic respiratory failure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 23.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Cardiac pacemaker insertion
Influenza like illness
Myocardial infarction
Chest pain
Chills
Fatigue
Headache
Pyrexia
Symptomtext
flu like symptoms, heart attack; stent placed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- lisinopril
- Allergien
- aspirin, sulfa
- Vorherige Impfungen
- Moderna 3/22/2021, 4/19/2021, 11/29/2021
- Staat
- MN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 30.12.2022
- Impfdatum
- 08.06.2022
- Beginn
- 30.10.2022
- Tage bis Beginn
- 144,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
Cough
Dyspnoea
Fatigue
Oropharyngeal pain
Pneumonia
SARS-CoV-2 test positive
Symptomtext
Patient with history of lung cancer in remission. She was seen in the ED on 10/30 with cough, shortness of breath, fatigue, and sore throat. She was tested for COVID in the ED by PCR and was positive. Patient was admitted from 10/30 - 11/1 with RLL pneumonia, COVID-19, and acute hypoxic respiratory failure. She was initially on 3L O2 but was able to be weaned down to room air. She was discharged home. Patient has received the primary COVID vaccine series and two boosters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 13.12.2022
- Impfdatum
- 14.06.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 141,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute respiratory failure
Asthenia
COVID-19
COVID-19 pneumonia
Chest X-ray normal
Confusional state
Death
Electrocardiogram normal
Hallucination
Hypokalaemia
Hyponatraemia
Hypoxia
Laboratory test abnormal
Malaise
Mental status changes
Nasal congestion
Pyrexia
Rhinorrhoea
Symptomtext
Adverse event information provided in this submission, is per a report received by the Public Health Department from a submitting facility. Covid-19 vaccination information is from Immunization Registry. Moderna 1/26/2021 Lot # 043L20A Moderna 2/22/2021 Lot # 011M20A Moderna 12/15/2021 Lot # 045J21A Moderna 6/14/2022 Lot # 059A22A Patient presented to the Hospital 11/2/2022 accompanied by family. Patient is positive for COVID-19 and started on antivirals 11/1/2022. He presented to ER with altered mental status, generalized weakness and hypoxia. Symptoms and fever started 11/1/2022. Family stated patient was more confused. He was seen in urgent care 11/1/2022. He was set up on home health monitoring. The home health care technician who came over to set up home health monitoring checked patient?s pulse ox and it was found to be in the 80s. The patient was directed to the ER for evaluation. Normal EKG. Elevated Troponin to 500. He became increasingly unwell in the past 24 to 48 hours with fever, increasing confusion, increasing weakness, nasal congestion, rhinorrhea. He was also said to be hallucinating. He tested positive for COVID-19 on 11/1/2022. He was taken to urgent care and was started on Paxlovid. He was brought to the ER because of increasing weakness and hypoxia. In the ER, he was placed on oxygen. Routine labs showed hyponatremia and hypokalemia, he received a bolus of normal saline and potassium supplement. He was febrile with a temperature 102 ?F. Chest x-ray was unremarkable. No leukocytosis, kidney and liver function unremarkable. Patient?s daughter was at bedside as patient is not a good historian. He denied headache, dizziness, chest pain, dyspnea, abdominal pain, nausea, vomiting, joint aches etc. Patient developed Acute hypoxic resp failure; found to be hypoxic 83% on 3L oxy mask overnight. Needed 1 5 L NRB mask to keep 02 sat > 90 %. It got worse in the and patient required up to 25 Liters. POA directed no further treatment. Given his advanced dementia and worsening resp failure from covid 19 pneumonia. Patient was placed on hospice care. Family agreed for that. ----- Patient expired 11/9/22 @ 2015
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 7,0
- Labordaten
- EKG Chest X-Ray lab work
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Essential hypertension, coronary artery disease, GERD, dyslipidemia and dementia
- Andere Medikamente
- unknown
- Allergien
- unknown if patient had any allergies
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 02.12.2022
- Impfdatum
- 14.07.2022
- Beginn
- 26.11.2022
- Tage bis Beginn
- 135,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
Inguinal hernia
Inguinal hernia repair
SARS-CoV-2 test positive
Symptomtext
Death on 11/26/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Positive Covid test on 10/29/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Complications of small bowel obstruction; OSC: bilateral inguinal hernia repair 10/24/2022; COVID-19; atrial fibrillat
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 22.08.2022
- Impfdatum
- 09.04.2021
- Beginn
- 20.08.2022
- Tage bis Beginn
- 498,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
COVID-19
Dyspnoea
Osteomyelitis
Positive airway pressure therapy
SARS-CoV-2 test positive
Tachypnoea
Toe amputation
Symptomtext
Pt arrived with increased shortness of breath and acute hypoxic respiratory failure. He was recently hospitalized and discharged on 7/26 for osteomyelitis status post bilateral toe amputation, and his hospital course was complicated by AKI. Pt was found to be tachypneic and required BIPAP and was COVID positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 25.07.2022
- Beginn
- 08.08.2022
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Bundle branch block left
Cardiac arrest
Coma
Computerised tomogram head normal
Echocardiogram
Ejection fraction normal
Electrocardiogram abnormal
Electroencephalogram
Hypokinesia
Hypoxic-ischaemic encephalopathy
Resuscitation
Shock
Troponin
Symptomtext
Patient presented with out of hospital cardiac arrest 8/8/22. She suffered VT arrest with shock x2 then asystole then ROSC. She suffered hypoxic ischemic encephalopathy. She underwent targeted temperature management to 33C and was rewarmed. Cardiology was consulted. She was started on heparin for ACS protocol. She remains comatose with prognosis still pending.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- CT brain 8/9 negative for acute pathology troponin 8/9-10: 0.32--0.33--0.34--0.29 EKG 8/9 with chronic left bundle branch block, no new ST elevations TTE 8/9 with EF 45-50% and mid inferolateral and lateral hypokinesis; worsened from prior 7/2022 with EF 55-60 and no wall motion abnormalities EEG 8/9-10 with burst suppression pattern while off sedation
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- ESRD on PD prior PCI on aspirin and goal directed management
- Andere Medikamente
- amlodipine bumetanide doxazosin losartan carvedilol ezetimibe furosemide atorvastatin insulin aspirin 81mg sucroferric oxyhydroxide caliltriol fluoxetine
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 18.06.2022
- Impfdatum
- 04.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Angiogram pulmonary
Blood test abnormal
Chest X-ray
Computerised tomogram thorax abnormal
Deep vein thrombosis
Dizziness
Dyspnoea
Echocardiogram abnormal
Ejection fraction
Electrocardiogram
Pulmonary embolism
Scan with contrast
Tricuspid valve incompetence
Ultrasound Doppler abnormal
Symptomtext
Ten days after receiving my second booster, as recommended by the CDC and doctors, I became very light headed and out of breath, needing to sit or lie down. Then throughout the morning, I was short of breath and light headed. I went to my doctor's office, who recommended I go to the Emergency Department of our local hospital. After CT imaging and bloodwork, it was determined I had a large Pulmonary embolism in my right lung and a smaller one in my left lung. After imaging of my legs, DVTs were also discovered there. Exactly 10 days after my 3rd dose (first booster) I also was diagnosed with a DVT (blood clot). I had never had a blood clot prior. Both of these occurances happened exactly 10 days after each vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 1,0
- Labordaten
- 12-LEAD ECG 12-LEAD ECG CT ANGIO CHEST WITH AND WITHOUT CONTRAST X-RAY PORTABLE CHEST SINGLE FRONTAL VIEW VASCULAR ULT VENOUS DUPLEX LOWER EXTREMITY COMPLETE BILATERAL VASCULAR ULT VENOUS DUPLEX UPPER EXTREMITY LIMITED LEFT ECHOCARDIOGRAM 2D WITH IMAGE ENHANCEMENT AGENT AS NEEDED All performed on 6/14/2022 Imaging: CT of the chest reviewed, and standing demonstrates bilateral PE, the largest clot burden is in the right pulmonary artery. Patient does not have a saddle pulmonary embolus. Dopplers: New superficial venous thrombosis at the left cephalic vein near the antecubital fossa. Persistent deep venous thrombosis at the left internal jugular vein/subclavian vein junction. Deep venous thrombus identified the distal femoral vein and popliteal vein extending to the distal segments of the deep calf veins Echocardiogram: 1. Normal left ventricular systolic function. The left ventricular ejection fraction is 50-55% by visual estimation 2. Normal right ventricular systolic function. No evidence of right ventricular strain. 3. There is moderate tricuspid regurgitation 4. The estimated right ventricular systolic pressure is 35.5 mmHg.
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- Metastatic Breast Cancer
- Andere Medikamente
- Dexamethsone, Linzess, synthroid, b vitamins, fish oil supplement, calcium, Vitamin D
- Allergien
- Versed, Sancuso, caphlexin
- Vorherige Impfungen
- Ten days after first booster for Covid, I was diagnosed with a DVT.
- Staat
- PA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 09.06.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 92,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram head
Echocardiogram
Electroencephalogram
Magnetic resonance imaging
Magnetic resonance imaging head
Partial seizures
Symptomtext
Sudden onset partial simple focal seizures Treated with Keppra
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Partial seizures
- Hospital-Tage
- 4,0
- Labordaten
- Cat Scan on Brain, MRI on brain and carotids, echocardiogram and EEG during stay in Hospital from September 13-16
- Aktuelle Erkrankungen
- Second Covid infection from May 14 to May 23rd prior to third booster on June 9, 2022
- Vorgeschichte
- None
- Andere Medikamente
- Levothyroxin
- Allergien
- contrast dyes and opioids
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 16.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Eyelid disorder
Headache
Sensory disturbance
Symptomtext
On 6/4/22 I started having a headache and it continued the next day and on 6/6/22 I woke up and noticed my face felt weird and I couldn't close my left eyelid and I thought I slept wrong on my left side and after 15 minutes it did not go away so I went to an urgent care clinic to rule out stroke. They examined me and they could tell it was Bell's Palsy and gave me a prescription for some medication for it and that was prednisone and antiviral. I still have the Bell's Palsy as of today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Feeling abnormal
Malaise
Syncope
Symptomtext
PER PATIENT GOT THE VACCINE ON 06/03/22 AT 09:31 AM, PATIENT LEFT FOR CITY THE NEXT DAY. ON 06/10/22 PATIENT FAINTED IN KITCHEN. PATIENT ALSO STATED HE WAS FEELING NOT GOOD AFTER VACCINE ('' UNEASY FEELING, TIRED ''). PATIENT WAS DISCHARED ON 06/12/22 FROM HOSPITAL. PER PATIENT HOSPITALIST TOLD HIM NEXT TIME FOR VACCINE HE WILL HAVE TO GO TO DOCTOR SO YHE CAN BE OBSERVED AFTER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 3,0
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 09.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Headache
Limb mass
Loss of consciousness
Myalgia
Pain in extremity
Taste disorder
Symptomtext
symptoms knocked her out, symptoms knocked her on her butt; bad taste; hard knot in arm; arm is hurting, arm is sore; muscles and joints are achy; headache; muscles and joints are achy; This spontaneous case was reported by a patient and describes the occurrence of LOSS OF CONSCIOUSNESS (symptoms knocked her out, symptoms knocked her on her butt) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 09-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced LOSS OF CONSCIOUSNESS (symptoms knocked her out, symptoms knocked her on her butt) (seriousness criterion medically significant), TASTE DISORDER (bad taste), LIMB MASS (hard knot in arm), PAIN IN EXTREMITY (arm is hurting, arm is sore), ARTHRALGIA (muscles and joints are achy), HEADACHE (headache) and MYALGIA (muscles and joints are achy). At the time of the report, LOSS OF CONSCIOUSNESS (symptoms knocked her out, symptoms knocked her on her butt), TASTE DISORDER (bad taste), LIMB MASS (hard knot in arm), PAIN IN EXTREMITY (arm is hurting, arm is sore), ARTHRALGIA (muscles and joints are achy), HEADACHE (headache) and MYALGIA (muscles and joints are achy) outcome was unknown. No concomitant drug was reported. It was reported that patient did not experience side effects from the other doses. It was reported that patient experienced side effects from the 2nd booster dose of the Moderna COVID-19 vaccine on 09Jun2022. Patient talked to several people who some reported side effects and some did not. No Treatment medications were reported. Company comment This spontaneous case reported by a patient concerns a 70-year-old female patient with no medical history reported, who experienced the unexpected serious event of loss of consciousness and other non-serious events, which occurred on an unknown date after receiving the fourth dose of mRNA-1273, thus latency between vaccination and the event cannot be assessed. The patient reports that after the 2nd booster dose, the symptoms knocked her out. She reports her arm was sore, hard knot, when she tried to move her arm the muscles and joints were achy. She also had headache and bad taste. She did not experience side effects from the other doses. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.; Sender's Comments: This spontaneous case reported by a patient concerns a 70-year-old female patient with no medical history reported, who experienced the unexpected serious event of loss of consciousness and other non-serious events, which occurred on an unknown date after receiving the fourth dose of mRNA-1273, thus latency between vaccination and the event cannot be assessed. The patient reports that after the 2nd booster dose, the symptoms knocked her out. She reports her arm was sore, hard knot, when she tried to move her arm the muscles and joints were achy. She also had headache and bad taste. She did not experience side effects from the other doses. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 12.06.2022
- Impfdatum
- 11.06.2022
- Beginn
- 12.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chills
Fall
Feeling abnormal
Feeling cold
Gait disturbance
Heart rate increased
Hypoaesthesia
Inappropriate schedule of product administration
Loss of consciousness
Pharyngeal swelling
Speech disorder
Tremor
Symptomtext
Early in the morning Hours, I stopped playing Video games due to annoyance and an Elevated Heart Rate. Started to watch TV, 3-4 mins into a show I started Shivering and Shaking uncontrolably for over an Hour. When I first started shaking i figured i was just cold but my throat started to swell up and my chest felt like it was being squeezed, i was having a very hard time just walking or talking for that matter. when i was laying down with my girlfriend toying to get warm, my hand feel went numb on and off for a while. i did eventually fall asleep. when i woke up to use the bathroom, on my way back peeing, i blacked out in the hallway to my bedroom and fell. i woke up feeling better but i do not feel great.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- I haven't seen a medical specialist yet.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- Bees/wasp
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 11.06.2022
- Impfdatum
- 11.06.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Hyperhidrosis
Lethargy
Syncope
Symptomtext
Patient initially recevied Janssen covid vaccine on 3/22/21 and came in today to get booster dose of Moderna. She has a history of feinting after vaccinations. After the injection patient felt lightheaded and about a minute later she said she was going to feint and she did. Paramedics were called at this point. Patient was out for about 10 seconds and never stopped breathing. She came too and broke out into a sweat. She continued to be lethargic (almost like she wanted to sleep). Whenever I called her name she would open her eyes and when asked if she could hear me she would respond "yes". Paramedics came and transported her to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- anxiety depression
- Andere Medikamente
- wellbutrin, alprazolam
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AS
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 14.12.2023
- Impfdatum
- 06.06.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 15,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Butterfly rash
Condition aggravated
Dysgeusia
Granulomatous rosacea
Rash
Rash erythematous
Rash papular
Skin exfoliation
Skin texture abnormal
Symptomtext
Metallic taste after 6/6/22 Moderna, 8/1/22 Moderna & 12/27/22 Mod. Bivalent Facial rash that never fades and became progessively worse after each covid vax Pinkish butterfly facial rash 2-weeks after 1st dose Bright red, swollen facial rash forehead, nose, checks, chin within 1-2 weeks of 2nd dose Deep purple / red facial rash, scaly, swollen, and tough texture to skin in affected area Knobby painful nuckles on fingers 2-3 months after Moderna bivalent. Speaking with DERM, they believe this is Granulomatus Rosacea Before, after, & current photos if needed. Prior to covid-19 vaccination, I have never experienced any rash or skin issues on my face. My first cousin had the same after 2 pfizer. 1 yr. to resolve.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hashimotos, MRI neg extreme elev. cortisol, un-dx connective tissue disorder, hypertension
- Andere Medikamente
- BP and Thyroid
- Allergien
- thimerosal
- Vorherige Impfungen
- Rash after flu shots. Elevated BP and acute kidney failure 4-days after 2020 flu shot
- Staat
- MN
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 24.07.2023
- Impfdatum
- 28.06.2022
- Beginn
- 10.05.2023
- Tage bis Beginn
- 316,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cardiac failure
Cardiac failure acute
Cardiac failure congestive
Condition aggravated
Dyspnoea
Left ventricular failure
Oedema peripheral
SARS-CoV-2 test false positive
SARS-CoV-2 test negative
Symptomtext
The patient has a history of COPD, pulmonary embolism, and stroke. She was seen in the ED on 5/10/23 for worsening difficulty breathing and bilateral lower extremity edema over the past three days. A COVID PCR test done in the ED resulted positive. Ultimately, she was admitted 5/10/23 - 5/14/23. During admission, she was placed on ceftriaxone and azithromycin. Discharge diagnoses include shortness of breath, bilateral lower extremity edema, acute on chronic diastolic CHF, and mild to moderate HFpEF exacerbation, among other diagnoses. Of note, the provider felt the COVID-19 result was a false positive, as a repeat COVID-19 test did result negative. Of note, the patient has recieved the primary COVID vaccine series and two boosters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 26.06.2023
- Impfdatum
- 15.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 12,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Acoustic stimulation tests
COVID-19
Condition aggravated
Respiratory tract congestion
SARS-CoV-2 test positive
Throat irritation
Tinnitus
Symptomtext
On about 6/27/2022 or 6/28/2022, I experienced head congestion and a scratchy throat. I took a home antigen test and got a positive result on 6/30/2022. On 7/1/2022, I went to an urgent care clinic to be retested for confirmation, and I tested positive on the PCR test they gave me. I was visiting a relative at this point, and I self-isolated from the rest of my family until I tested negative on 7/5/2022. On the flight back home afterwards, I made it a point to mask; I had also worn a mask during the flight to my relative's home city. In October 2022, I began experiencing a buzzing noise in both ears. I didn't really pay attention until November 2022, though. I went to my PCP, who suggested that I undergo a hearing test and see a specialist. On 12/16/2022, I saw an otolaryngologist, who administered a hearing test. I had previously undergone a hearing test in September 2019, and it was then found that I had had some hearing loss. After the 12/16/2022 hearing test, the otolaryngologist concluded that my hearing had not deteriorated considerably since September 2019. The doctor confirmed that I had tinnitus. He couldn't offer a cure or a treatment, but he did tell me that another patient of his had tried taking lipo-flavonoid, and they had had decreased buzzing in the ears. I took lipo-flavonoid for three months, and there was no change. I've recently begun undergoing acupuncture therapy, because I have heard that it can sometimes help. However, in the six weeks I have received the treatments, I have noticed no change.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 30JUN2022 home antigen test, positive result; 01JUL2022 PCR test, positive result; 05JUL2022 home antigen test, negative result; SEPT2019 Hearing test, hearing loss detected in both ears; 16DEC2022 Hearing test, no deterioration in hearing detected
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Psoriatic Arthritis; Tinnitus; Sleep Apnea
- Andere Medikamente
- Amlodipine besylate; clopidogrel bisulfate; ramipril; rosuvastatin calcium; ezetimibe; HUMIRA injections; triamcinolone acetonide topical cream; vitamin C; glucosamine chondroitin; turmeric
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 21.06.2023
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Dyspnoea
Feeling abnormal
Wheezing
Symptomtext
6/16/2022 About eight hours after my vaccination, I started having a cough and wheezing. It felt like I was closing up and was having trouble breathing, like an asthma attack. I thought maybe it was allergies. The not being able to breathe became worse and I had to use my inhaler a lot. My doctor prescribed Prednisone and a medication for the cough. This lasted about a week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Venous Insufficiency; Hypertension; Obesity; Osteo Arthritis
- Andere Medikamente
- Levothyroxine, Spironolactone HCTZ, Multi Vitamin, Vitamin D, Calcium, Melatonin, CBD Tincture with THC, Apple Cider Vinegar, Tums , Probiotic
- Allergien
- Percodan, Compazine Suppository
- Vorherige Impfungen
- Flu Vaccine, 10/31/20, I had the most pain in my arm, shoulder and it lasted 9 days.
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 10.03.2023
- Impfdatum
- 18.07.2022
- Beginn
- 01.03.2023
- Tage bis Beginn
- 226,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anticoagulant therapy
Blood lactic acid normal
Blood potassium decreased
COVID-19
Chronic obstructive pulmonary disease
Condition aggravated
Cough
Electrolyte substitution therapy
International normalised ratio increased
Leukocytosis
Procalcitonin normal
Symptomtext
Discharge Provider: MD Primary Care Provider: MD Admission Date: 3/1/2023 Discharge Date: 3/5/2023 Clinical Narrative: Patient was admitted for acute chronic obstructive pulmonary disease exacerbation and COVID-19, however his cough has much improved, he has remained on room since the day after he was admitted and saturating in the mid 90s, he denies any chest pain. He was started on IV remdesivir on admission and has completed 4 days. He remains afebrile with no shortness of breath no chest pain. Leukocytosis today is felt to be reactive from steroids would repeated procalcitonin lactic acid today which but normal. Physician at the extended care facility to repeat complete blood count within 1 week. Examination reveals no wheeze, since he is on room air with no shortness of breath we may discontinue steroids today on discharge since he has had a total of 4 days Decadron He was evaluated by General surgery during this admission to assist with these bilateral Unna boot He was evaluated by PT/OT for history of falls and will be transferred to extended care facility for rehabilitation Patient is on Coumadin for anticoagulation and he was subtherapeutic on admission, with subsequently bridged with Lovenox, his INR however today is 2.7 so we will discontinue Lovenox bridge. Potassium was 3.2 this morning and he received a total of 40 mEq of potassium replacement Please see the following problem-list oriented Hospital Course below: No new Assessment & Plan notes have been filed under this hospital service since the last note was generated. Service: Hospitalist
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- History of prostate cancer History of kidney stones Esophagitis Sleep apnea, unspecified COPD with acute exacerbation Essential hypertension OSA (obstructive sleep apnea) Coronary artery disease involving native coronary artery of native heart without angina pectoris Type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin Protein S deficiency Arthritis Current use of anticoagulant therapy Balance disorder Chronic gout History of DVT (deep vein thrombosis) History of pulmonary embolism Zenker's diverticulum Dysphagia, unspecified type Cellulitis of both lower extremities Cellulitis Chronic obstructive pulmonary disease Zenker's diverticulum Protein S deficiency Type 2 diabetes mellitus without complications Non-pressure chronic ulcer of left lower leg, with fat layer exposed Non-pressure chronic ulcer of calf, right, with fat layer exposed PAD (peripheral artery disease) Pre-ulcerative corn or callous Venous ulcer of ankle, right Pressure injury of deep tissue of left calf COVID-19 virus infection Acute viral tracheitis Recurrent falls Venous stasis ulcers of both lower extremities
- Andere Medikamente
- acetaminophen (TYLENOL 8 HOUR) 650 MG extended release tablet allopurinol (ZYLOPRIM) 100 MG tablet atorvastatin (LIPITOR) 40 MG tablet blood glucose test strips Elastic Bandages & Supports (MEDICAL COMPRESSION STOCKINGS) MISC furosemide (L
- Allergien
- Avelox [Moxifloxacin]Hives, Shortness of Breath Pain MedicationsNausea Only
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 02.07.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 177,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
12/26/22 presents to ED for "breathing problem". PMHx of "adenocardinoma of colon, DMT2 and HTN"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 12/26/22 SARS-CoV-2 (COVID-19) detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 16.01.2023
- Impfdatum
- 15.07.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 48,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood urine present
Chest pain
Haematuria
Scan myocardial perfusion
Ultrasound pelvis abnormal
Uterine mass
Symptomtext
I was experiencing some chest pains. I went to see my doctor, who ordered test, I have had a series of stress test that involved radiation while going through the test. I am awaiting the results of the stress test. I had a pelvic ultrasound that showed a mass on my uterus. I have an MRI schedule, January 23, to determine if it is just a fibroid. I have an appointment for an endoscopy of my bladder to determine where the blood (hematuria) in my urine is coming from.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Ultrasound,
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Skin Lupus; Knee Arthritis
- Andere Medikamente
- Amlodipine; Losartan; Multivitamin; Trazadone; Vitamin B-12; Thiamine
- Allergien
- Lisinopril; Iron;
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 13.06.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 196,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 12/26/2022 - 1/9/2023 (14 days) Presentation to the ED: shortness of breath. COVID + date: 12/26/22 Treatment: remdesivir. Discharge to: Hospice/Home. 013M20A 3/3/2021 046A21A 3/31/2021 026D21A 10/22/2021 059A22A 6/13/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension, hyperlipidemia, hypothyroidism, and asthma/COPD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 12.01.2023
- Impfdatum
- 13.07.2022
- Beginn
- 26.08.2022
- Tage bis Beginn
- 44,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthritis
COVID-19
Musculoskeletal stiffness
Paranasal sinus discomfort
Pneumonia
Pyrexia
SARS-CoV-2 test positive
Sinus headache
Throat irritation
Symptomtext
It started with a slight tickle in the back of my throat then I started getting a sinus pressure headache. I thought it was sinuses related, then I had a slight fever that was barely above 100. I started taking medications for that and just felt like I had a sinus infection. It wouldn't go away so I started talking ADVIL, MUCINEX and other sinus medication. It never moved from my head into my chest or anything. I went to my doctor and I asked for medication for my sinuses. They did a COVID-19 test and I actually came back positive. I can't remember if they gave me medication, but I went home and stayed in bed and kept testing until I was negative. The headache eventually went away and I wasn't super tired. I just kept testing positive until it finally stopped. That was pretty much it with the COVID-19 infection. It was pretty mild. Right after Christmas, I came down with pneumonia and it's still in my chest a little bit. I tested myself again to see if it was COVID-19 but it was negative. With my hands, nobody in my family has this type of problem. I had gotten surgery for my knuckle in 2021 before receiving the third dose of the COVID-19 vaccine. I had a blister on my knuckle and it had caused pressure on my nail, so I had to get surgery for that. It's happening on the other hand, but currently not impacting the nail bed. My fingers are stiffer than they used to be and I've been diagnosed with arthritis. Recovered from COVID-19 infection, still lingering symptoms from Pneumonia, not recovered from the hands.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- 31AUG2022 COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- CENTRUM SILVER women's 50+ multivitamin; NATURE'S MADE vitamin B complex; OCUVITE; vitamin C
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 17.10.2022
- Beginn
- 18.12.2022
- Tage bis Beginn
- 62,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Blood test normal
Dysgeusia
Echocardiogram normal
Nasopharyngitis
Paraesthesia
SARS-CoV-2 test negative
Taste disorder
Symptomtext
My booster was 10/17/2022. By 12/18/2022, I lost my sense of taste. I feel like I always have a metal taste in my mouth. I can taste salty better than sweet, but normal things that should taste good do not. I've never had this issue before. Between the time of getting my booster and having this symptom, I did have cold, but it was not COVID-19. I tested myself for COVID-19 and I took a second COVID-19 test as well and both were negative. It was around 12/10/2022, that I developed my cold and then it was around 6 or 7 days later when I developed this taste issue. I was also at this time, experiencing a little tingling in my right and a bit in my left. I went to the doctor, and they had no explanation for it. They did a blood test, and everything was normal. I have looked up loss of taste and cannot find anything that makes sense that could be causing this. I have no idea if this is related to the booster. I had COVID-19 in May of 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- 12DEC2022 - At Home COVID-19 Test - Negative; 21DEC2022 - At Home COVID-19 Test - Negative; 23DEC2022 - Blood Test - Nothing Abnormal Found; 23DEC2022 - Echocardiogram - Nothing Abnormal Found
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoarthritis
- Andere Medikamente
- Sertraline
- Allergien
- Gluten Sensitivity
- Vorherige Impfungen
- 12/01/2021- Age: 59 First Moderna COVID-19 booster - Extended fatigue and flu like symptoms.
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 30.12.2022
- Impfdatum
- 29.12.2021
- Beginn
- 20.12.2022
- Tage bis Beginn
- 356,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Dyspnoea
Symptomtext
Hospital Course and Significant Findings: 81 yo M with history of DM2, chronic anemia, HLD, prior colon cancer, COPD, ESRD on HD, tobacco user who presented with progressive shortness of breath x1 week found to have COVID-19. I kept the patient for 48 hours to ensure that she was stable from a respiratory standpoint. She did not require more than 2 L supplemental oxygen, and she was discharged on 1 L. Also, she had hemodialysis on 12/20 and 12/22. She was officially discharged on 12/21, but we were unable to secure hemodialysis chair for 12/22 so she stayed overnight for hemodialysis before transferring to Facility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 07.06.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 149,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Decreased appetite
Exercise tolerance decreased
Fatigue
Loss of personal independence in daily activities
Mobility decreased
Nasal congestion
Paranasal sinus hypersecretion
SARS-CoV-2 test positive
Symptomtext
Starting 11/03/2022, I felt like I was getting the flu and I had a strange cough. I was tired but didn't have a fever. I stayed in bed for 48 hours and when I got up I did not have an appetite. I tested negative with a COVID-19 at home test on 11/05/2022 and I waited 48 hours before I tested myself again. On 11/07/2022, I tested myself again and was positive. I started coughing pretty severely but never at any point did I develop a fever. I would eventually test negative on 11/12/2022 with an at home COVID-19 test and ended up leaving the house on 11/14/2022 after testing negative again. I did call my doctor on 11/15/2022 to get some relief from the severe cough and was prescribed some cough medicine. I stayed in bed on 11/16/2022 and 11/17/2022 and I had a telehealth visit on 11/18/2022 for a follow up. At that time, I still had the nasal congestion, sinus drainage, severe fatigue and a cough. The symptoms slowly started to get better and by 11/24/2022 I felt well enough to have people over for the holiday but my cough was still quite persistent. It has slowly been improving since then and I have started back with some regular exercise at this point, and resumed more of my normal daily activities.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- At-home COVID-19 test (11/05/2022): negative; at-home COVID-19 test (11/07/2022): positive; at-home COVID-19 test (11/12/2022): negative; at-home COVID-19 test (11/14/2022): negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure; Hypothyroidism
- Andere Medikamente
- Levothyroxine; HCTZ; vitamin D3; vitamin B12
- Allergien
- None
- Vorherige Impfungen
- To each COVID-19 vaccine, I had a 36 hour reaction consisting of fatigue and body aches
- Staat
- AZ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Hypoaesthesia
Malaise
Tremor
Symptomtext
Headache chills fingers went numb up to knuckles shaking uncontrollably sick for three days, will never get vaccinated again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Propranolol; multivitamin; vitamin B; vitamin D; omega 3
- Allergien
- Penicillin
- Vorherige Impfungen
- 2nd dose Moderna and 1st
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 04.12.2022
- Impfdatum
- 06.06.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 38,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Mechanical urticaria
Pruritus
Symptomtext
Dermographism relapse. I was diagnosed with dermographism and general skin itchyness in 2007. I took Loratadine (Claritin) for it, but gradually stopped taking Claritin every day with no issues. After my 2nd booster, the dermographism symptoms returned. I talked to my doctor about it during a physical on 7/21/2022 and he prescribed Cetirizine (Zyrtec). I put 2 and 2 together after reading this site which is not scientific, but made me think there could be a link: website
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Prior Covid vaccinations: Moderna 020B21A on 28 Mar 2021, Moderna 008C21A on 25 April 2021, Pfizer FH8927 (unclear writing) on 1 Dec 2021.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.12.2022
- Impfdatum
- 30.06.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
C-reactive protein increased
Fatigue
Gait disturbance
Hypoaesthesia
Laboratory test
Loss of personal independence in daily activities
Mobility decreased
Pain
Pain in extremity
Paraesthesia
Red blood cell sedimentation rate increased
Screaming
Sleep disorder
Symptomtext
I had body aches, numbness and tingling and radiating pain to bilateral feet, lower extremities, hands and arms. Pain radiates from feet to hips and hands to arms and shoulder areas. The pain was so bad I could not walk. Fatigue set in but could not sleep due to pain. If I fell asleep, I would wake up yelling in pain. Basically, I could not really function and spent most of my time in bed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Many labs were completed. CRP was 28.3 and sed rate of 30. Tests were done 10/20/2022
- Aktuelle Erkrankungen
- Diabetes and Covid -19 June 1st, 2022.
- Vorgeschichte
- Diabetes
- Andere Medikamente
- cetirizine, citalopram, Nexium, humalog insulin, Levemir insulin, zofran prn, triamterene-hydrochlorothiazide,
- Allergien
- Elmiron
- Vorherige Impfungen
- Information is in Vaers. Aching, elevated temps.
- Staat
- WI
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 10.11.2022
- Impfdatum
- 05.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Diuretic therapy
Dyspnoea
Hypervolaemia
Oxygen saturation decreased
Renal impairment
SARS-CoV-2 test positive
Symptomtext
94 y.o. female with history of CAD, HTN, HLD, HFpEF, a fib on Eliquis, AS s/p TAVR, and OSA who presents with shortness of breath and signs of volume overload. Also tests positive for COVID-19. Did get diuresed with improvement of symptoms. Intermittently desaturating, started on steroids. Does not qualify for Remdesivir due to renal function.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 23.09.2022
- Impfdatum
- 28.07.2022
- Beginn
- 28.08.2022
- Tage bis Beginn
- 31,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anaemia
Angiogram pulmonary abnormal
Anticoagulant therapy
Aspartate aminotransferase increased
Atrial fibrillation
Blood alkaline phosphatase increased
Blood magnesium normal
Body temperature increased
Brain natriuretic peptide increased
C-reactive protein increased
Cough
Dyspnoea
Echocardiogram
Electrocardiogram QRS complex prolonged
Electrocardiogram abnormal
COVID-19
COVID-19 pneumonia
Cardiac telemetry
Symptomtext
Patient was vaccinated and receive Pfizer: 2/24/2021 EN6200, Pfizer: 3/17/2021 ER2613 Moderna: 12/1/2021 045J21A Moderna: 7/3/2022 059A22A This patient presented to the Emergency Department via EMS with a complaint of cough and tachycardia, COVID-positive. The patient's husband was currently admitted to the hospital with COVID. She took a home COVID test which was positive. Her son called EMS because she appeared to be having worsening dyspnea and cough. The patient stated that she felt generally fatigued but did not feel short of breath per se. She denied chest pain, abdominal pain, vomiting, and diarrhea. Noted to have slight swelling of bilateral lower extremities on review of systems. EMS reported a temp of 102 on their arrival. EMS also found the patient to be tachycardic with atrial fibrillation and she was given diltiazem 10 mg in route. The patient stated she had no history of atrial fibrillation. No previous EKGs available to evaluate. Echocardiogram from 2016 states the patient was in sinus rhythm. Patient admitted 8/28/22. This patient presented to ER with cough, dyspnea, and tachycardia. The patient was febrile at 99.4 with heart rate of 130, blood pressure of 121/56, respirate of 18, pulse ox 93% on room air. The patient did not appear to have significant increased work of breathing or tachypnea but was audibly rhonchorous. Lungs were rhonchorous bilaterally. Heart rate was irregular and tachycardic. No significant edema of the lower extremities on my exam. Stat EKG showed atrial fibrillation 120 bpm with a wide-complex QRS, poor R wave progression, no previous EKG available for comparison. The patient CBC showed normal white blood cell count, anemia with a hemoglobin of 8.9, slightly down from 9.3 earlier this month, magnesium was slightly low 1.5 and this was repleted with IV magnesium. Troponin was elevated at 70. BNP was elevated at 2700. CMP showed mild hypokalemia and elevations of alkaline phosphatase at 1700 and AST of 45, consistent with the patient's previous results on August 5, but otherwise normal liver function tests. The patient's D-dimer was elevated at 1410. A CT angiogram was obtained which was negative for pulmonary thromboembolic disease. Patchy bibasilar infiltrates; left worse than right likely pneumonia associated tiny bilateral pleural effusions were seen. It was determined she warranted IV antibiotics which were empirically initiated. Patient was admitted to hospital for further work-up and management. The patient's heart rate improved on the diltiazem drip and she was transferred to the stepdown bed in stable condition. Unknown when patient was discharged from 8/28/22 admission. Readmitted on 9/4/22 from nursing home (UNKNOWN NAME OF NURSING HOME) with worsening shortness of breath and hypoxia. Patient was on oral antibiotics at the nursing home. In ER, needed oxygen 3L per nasal cannula. Per notes, on exam the patient had rales throughout the lungs without JVD or peripheral edema. Chest x -ray shows worsening right middle lobe infiltrate. Cefepime for IV antibiotics was given for worsening pneumonia and recent hospitalization. States that her shortness of breath is continued to increase despite treatment at the nursing home. Labs done today showed elevated white blood cell count, BNP, and D-dimer. Of note the patient had a elevated D-dimer while in the hospital and had a CT scan at that time which showed no evidence of PE. Patient completed a course of dexamethasone. She was also started on Coumadin for anticoagulation while in the hospital. She denied vomiting or abdominal pain. She denied any diarrhea. Patient started on Zosyn and doxycycline. Continue both antibiotics while awaiting sputum culture. Problem list per hospital note of Probable superimposed bacterial pneumonia -Recently completed 5-day course of ceftriaxone and azithromycin -Presented back with worsening respiratory symptoms and chest image findings COVID-19 pneumonia with hypoxia -Symptom onset date on 8/23/2022 -Received COVID-19 vaccines and boosted last with Moderna on 7/3/2022. -Dexamethasone was started on 8/28 -Currently on 2 L of supplemental oxygen. -High CRP at 31, BNP of 3,360 Leukocytosis -WBC elevated at 31 -Most likely related to above. Health department has no further information on this patient?s hospitalization or outcome or current condition. Please contact Hospital for further information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- -
- Labordaten
- Lab work including D-dimer and troponin CT-angiogram chest x-ray Echo cardiogram Telemetry
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- ? Arthritis ? Brain bleed (* ) slip fall in basement fell hitting back of head ? Colon polyp ? Diarrhea ? Diverticulitis ? Diverticulosis ? Enlargement of lymph nodes ? GERD (gastroesophageal reflux disease) (* ) ? Hip prosthesis implantation- left ? Hypertension ? Irritable bowel syndrome (IBS ) ? Mild intermittent asthma ? Osteopenia
- Andere Medikamente
- UNKNOWN
- Allergien
- doxycycline eggs Lisinopril
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 24.02.2021
- Beginn
- 15.08.2022
- Tage bis Beginn
- 537,0
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest discomfort
Dyspnoea
Inflammatory marker test
Malaise
Pain
Palpitations
Productive cough
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
58y.o. female developed symptoms 3 days prior to presentation, felt unwell, developed chest pressure, fever, congestion, runny nose, body aches, productive cough, shortness of breath, mild palpitations. Initial home covid test was negative. Then repeated 2 days later, showed positive. Vaccinated and boosted. Last in July 2022. Covid 19. Patient was at high risk due to immunosuppressants post renal transplant and diabetes. She was stable, no hypoxia. Inflammatory markers were monitored. She was started Remdesivir for 3 days. All other medical issues were managed as prior to hospital stay.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 1,0
- Labordaten
- 8/15 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 30.08.2022
- Impfdatum
- 27.05.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 70,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chiropractic
Cough
Dizziness
Dyspnoea
Dyspnoea exertional
Ear congestion
Ear discomfort
Ear pain
Eye pain
Fatigue
Feeling abnormal
Headache
Malaise
Nasal discomfort
Pain
Paranasal sinus hypersecretion
Paranasal sinus inflammation
Symptomtext
I received my second Moderna booster for COVID-19 on 5/27/2022. On around 8/5/2022, I started to feel a little run down and mentally foggy. I then began to have a runny nose, sinus drainage in the throat, and ear pressure. I thought that maybe these symptoms were caused by the barometric pressure, so I didn't give them much thought. I then developed a headache around 8/12/2022. It was an unusual headache, as it affected an area that usually isn't affected whenever I have headaches. I thought that maybe I had dislocated a vertebra in my neck, so I saw my chiropractor on 8/18/2022. He adjusted my neck, but it brought no relief for my headache, my inner ear congestion, or my sinus drainage. On 8/19/2022, I woke up feeling fine, though I still had a headache and inner ear congestion; however, I wasn't as fatigued as I was previously. Around noon that day, I felt a burning sensation in my nose and the sensation of liquid moving in my ears. A short time later, I sneezed three times, and I thought that I had a sinus infection. After the sneezing, I then developed sinus inflammation, coughing, and eye pain. I began to feel unwell, because I also felt a little dizzy and my headache worsened. Shortly thereafter, I developed a fever of 99.9 and extreme body aches and earaches. At this point, I still thought that my symptoms were caused by a sinus infection and ear infection and that the body aches were the result of the fever. I also had an aching sensation in my eyes, and I couldn't keep them open on account of the pain. The body aches were among the worst things I've ever experienced in my life. When my partner came home, he told me that I needed to take a home COVID-19 test, so I did and the result was positive. The aforementioned symptoms gradually worsened. At about 6 PM on 8/19/2022, I called my doctor's office, and she told me to take OTC MUCINEX and TYLENOL. She also told me to drink copious amounts of water and to keep an eye on my oxygen levels. She told me that I was to immediately go to the ER if my oxygen levels dropped below 90 or if I felt worse in any way. We discussed the possibility of taking an antiviral, but she was hesitant to prescribe an antiviral on account of my pre-existing health issues and the possible side effects of the medication. She told me that if I felt worse or didn't feel any better by 8/22/2022, she and the other doctors on her team would discuss the possibility of prescribing me an antiviral. As it turns out, though, by the time 8/22/2022 rolled around, I felt somewhat better. I still had a cough and congestion, but the headache, fever, and body aches were gone. I think that TYLENOL really helped. The MUCINEX has also reduced the cough somewhat and seems to have gotten rid of the earache. I took a home COVID-19 test on 8/29/2022, and the result was negative. I then took another on 8/30/2022 and got another negative result. At the time of this writing, the body aches, fever, and headache are gone, but I still feel extremely fatigued and have brain fog. The nasal sinus on the right side and both of my ears still have a feeling of pressure, though it's not painful. My oxygen levels never dropped below 90, but I have still experienced shortness of breath. If I exert myself in any way, I easily develop shortness of breath and have to periodically stop to rest and catch my breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 8/19/2022 home COVID-19 positive result; 8/29/2022 home COVID-19 test negative result; 8/30/2022 home COVID-19 test negative result.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Graves Disease; Post-Ablative Hypothyroidism; Hyponatremia; vitamin D Deficiency; Heart Disease; Hypertension; Tremors from Graves Disease Nerve Damage; Bipolar Disorder; Post-Traumatic Stress Disorder; Hypercholesterolemia; Meniere's Disease; Eye Irritation and Pressure from Graves Disease.
- Andere Medikamente
- Baby aspirin; losartan potassium; metoprolol tartrate; SYNTHROID; oxcarbazepine; trazodone; venlafaxine; prazosin; PRALUENT; centrum silver multivitamin; magnesium bisglycinate; probiotic complex; super B complex; vitamin D3; coQ10; krill o
- Allergien
- Doxycycline; penicillin; ciprofloxacin; sulfa drugs; XANAX; ace inhibitors; adhesive tape with silicone; alprazolam; atorvastatin; rosuvastatin; simvastatin; baclofen; bupropion; clindamycin; iron; latex; naratriptan; rescinnamine; sulfamethoxazole-trimethoprim; sulfasalazine; morphine; tramadol; hydrocodone acetaminophen; tramadol; acetaminophen.
- Vorherige Impfungen
- After I got my first Moderna booster, I experienced extreme chills and extreme fatigue. They only lasted overnight, and I felt f
- Staat
- MO
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 09.08.2022
- Impfdatum
- 09.08.2022
- Beginn
- 09.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Fall
Feeling hot
Malaise
Pain in extremity
Symptomtext
Patient stated his arm was already sore and that he didn't feel very well. He stated he was short of breath and feeling hot. He tried to stand up and fell to the ground. He did not lose consciousness and was immediately given a dose of PO diphenhydramine liq 50 mg. He was taken to the ER for further observation. The ER doctor states that his diagnosis is a non-anaphylactic allergic reaction to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none noted
- Vorgeschichte
- none noted
- Andere Medikamente
- unknown
- Allergien
- Patient marked no severe allergic reactions, but did verbally tell me he had a history of anaphylactic reaction at hospital but he wasn't sure what he was allergic to.
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 20.06.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 37,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest pain
Fatigue
Headache
Malaise
Nasopharyngitis
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I woke up in the morning and felt like I was coming down with a mild cold. I had a slight headache, scratchy throat, achy chest, fatigue, congestion, and body ache. I took TYLENOL, and ADVIL to help relive those symptoms. I took an at home COVID-19 test that came back negative. I continued to have mild symptoms and re took a COVID-19 test on 7/30/2022 that came back positive. I went to an urgent care that same day and they prescribed me PAXLOVID. I am still experiencing the same symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 test- positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes Type 2
- Andere Medikamente
- Metformin; RYBELSUS
- Allergien
- Thiomersal
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 30.07.2022
- Impfdatum
- 18.07.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anxiety
Blood thyroid stimulating hormone normal
Chills
Dizziness
Fatigue
Full blood count normal
Impaired work ability
Lymphadenopathy
Metabolic function test normal
Nausea
Pain in extremity
Paraesthesia
Pregnancy test negative
SARS-CoV-2 test negative
Tremor
Vertigo
Symptomtext
Day 1-4 significant lymph node swelling (arm pit), significant arm pain and fatigue followed by day 5-9 of dizzyness/vertigo, extreme fatigue, nausea, arm/leg tingling , intermittent shaking/chills but not fever, significant anxiety. Went to urgent care on day 5 7/22 and received 1 L NS fluid bolus, CBC/BMP labs checked, pregnancy test . All labs WBL, pregnancy test normal. Dizzy/vertigo and fatigue continued thru next 6 days and symptoms began to resolve day 9. Seen by PCP on 7/26 for physical exam, tested for COVID and lab work done (TSH) to rule out thyroid disorder. TSH normal and negative for COVID. Unable to work for 1 week due to debilitating symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- CBC, BMP (7/22) TSH (7/28) and COVID lab work done (7/26), Results all negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma -currently well controlled on current medication regime
- Andere Medikamente
- Mirtazapine, Wixela inhalor, Allegra, Montekulast, pre-natal multivitamin, Vit D with calcium, Elderberry supplement
- Allergien
- Lactase /dairy
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 28.07.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Pain in extremity
Symptomtext
Arm soreness, unable to lift arm. Started few hours after administration on 7/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 27.07.2022
- Impfdatum
- 28.06.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 23,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest discomfort
Condition aggravated
Cough
Discomfort
Electrocardiogram abnormal
Headache
Malaise
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Sneezing
Tachycardia
Ventricular extrasystoles
Symptomtext
I received my second Moderna booster for COVID-19 on 6/28/2022. On the night of 7/21/2022, I had an onset of sneezing, sore throat, and headache. On 7/22/2022, I then developed a fever, headaches, general malaise, and discomfort. Those symptoms remained until 7/23/2022, when I developed a cough. On 7/22/2022, I took a home test for COVID-19, and the result was positive. On 7/24/2022, I developed chest tightness. On 7/25/2022, I arranged to receive Bebtelovimab monoclonal antibodies. On the night of 7/26/2022, I experienced periods of wide complex rhythm, which were noted on Kardia. I had them at least 2 or 3 times,; the longest lasted for 10 seconds, and another lasted for about 8 seconds. After these resolved, I resumed a normal sinus rhythm with occasional premature ventricular contractions. I have had premature ventricular contractions for several years now, so this was not unusual. However, the wide complex rhythm was atypical for me, and I wonder if it could have been precipitated by the monoclonal antibodies I received. At the time of this writing, I am still not fully recovered from COVID-19, though I am making steady progress.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 7/22/2022--home COVID-19 test--positive result
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypertension; Paroxysmal Atrial Fibrillation.
- Andere Medikamente
- Ramipril; Flecainide; Hygroton; Amlodipine; Eliquis; Rosuvastatin; CoQ10; Magnesium.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Headache
Hypoaesthesia
Paraesthesia
Pyrexia
Sleep disorder
Tremor
Symptomtext
Mom of patient called the pharmacy on 7/20 to report that at 4am that morning, patient woke up with 100.9 degree Fahrenheit fever and large movement shaking that was uncontrollable. She also started having a feeling of numbness in her face as well as tingling in her hands and feet. Several hours later she had headache and upset stomach only.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 17.06.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Cardiac monitoring
Chills
Electrocardiogram
Extrasystoles
Headache
Pain
Palpitations
Pyrexia
Symptomtext
I received my 2nd booster shot on 06/17/2022 and my adverse event started on 06/18/2022 at around 05:00PM. I had fever 101.05; chills; slight headache; body aches lasted for 4 days. On 06/22/2022 no fever I started heat palpation with skipping beats. I went to the clinic the same day just to check if this was normal. On 06/29/2022 I went to the clinic back because my heart palpation was still there. They did EKG. 07/06/2022 I went to a cardiologist she did blood test; EKG; and heart monitor. My heart palpation is going away naturally. Am still recovering as of now 07/11/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- EKG; blood work; heart monitor.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure; Asthma; Pulmonary hypertension; Cholesterol
- Andere Medikamente
- BENICAR; spironolactone; cranberry capsules; BREO ELLIPTA
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 02.07.2022
- Impfdatum
- 30.06.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Feeling hot
Gait disturbance
Pain
Pyrexia
Tremor
Symptomtext
Started getting a few mild aches about 11:00pm. To bed @ midnight. Woke up suddenly with chills,severe aches,body hot. Teeth chattering so hard I had to clamp them tight and body shaking so hard and uncontrollably. I could barely walk to the bathroom I was shaking so hard. Lasted at least an hour maybe more before starting so subside. Had a 100 degree fever all day. Still had bad aches all day gradually subsiding by about 5:00pm. Not sure I'll get another vaccine!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Levothyroxin,meloxicam,pramipexole,alendronate,metronidazole,triamcinolone,fosamax.Womens multi vit,calcium,k-2,fish oil, gaviscon,glucosamin/chondrointin/msm,d-3,b-12,iron,vit-c,imodium,omeprazole,aspirin,advil,voltaren,hydrocortisone
- Allergien
- no
- Vorherige Impfungen
- 71 yr/ Pfizer,covid 3-2-21/Pfizer,covid 3-23-21/Pfizer,covid12-30-21,similar reaction but not the shaking/teeth chattering
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 28.06.2022
- Impfdatum
- 28.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenopia
Dyspnoea
Hyperhidrosis
Tremor
Vertigo
Symptomtext
56-year-old female 15 minutes post vaccine (Post Moderna booster vaccine) at 9:30 am client complained of "head spinning", Client stated no history of past vaccine reactions and no history of anxiety. Client states she has eaten this morning. Son used as interpreter. Nurse assisted in assessment of symptoms with blood pressure as first reading, 9:34 am BP: 62/42 RR: 48 HR: 52. Nurse and son assist client to anti-gravity chair for further assessment and observation. Client became diaphoretic and shaking. Instructed to deep breathe. Son gave client (mom) sips of water per her request. 9:39 am, BP: 113/69 HR: 68. Nurses continued to observe client for additional complications. Client continues to tremble. Next set of vital signs during observation: 9:43 am BP: 124/76 HR: 83. Client was given juice, breathing improved and less diaphoretic. Client continues to stay oriented x 4. Vital signs at 9:48 BP: 123/84 HR: 81 RR: 30. Client verbalizes that she is "feeling better" and eyes feel heavy. Client states she would like to go home. Last set of vitals before client is sent home: 9:53 am BP: 129/92 HR: 75 RR: 17. Client left observation area on own steady gait. Reviewed patient education with son instructing to call emergency services if symptoms return or worsen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 10.06.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Chest X-ray normal
Chest discomfort
Chest pain
Electrocardiogram normal
Hypoaesthesia
Symptomtext
Patient experienced chest pain and tightness approximately 15 mins after administration of a Moderna booster dose. Patient experienced numbness down through his hands and still feels the same way nearly 2 weeks later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Patient went to the Emergency department where they did an EKG, chest X-Ray and blood work, but found nothing abnormal.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 09.06.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Fall
Hypotension
Labile blood pressure
Symptomtext
About 18 hrs after the injection trying to get out of the chair she fell . She felt weak all over. Paramedics arrived and put her on the bed . It took several hrs to regain strength so that she could get up. Was not taken to ED to no specific treatment other then resting. Visit to physician to discuss further was not until 6/17/22. Of note she has labile BP and sometimes very low with weakness but low BP was not reported as part of this event. Reports also feeling generally weak the day after her second Moderna vaccine also with a fall but this was a more significant event. Was okay after the 1st and 3rd vaccinations. All were Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- CKD, GERD, HTN, Hx breast CA, Hx TIA, osteoarthritis
- Andere Medikamente
- ASA, atenolol, famotidine, lisinopril, atorvastatin
- Allergien
- triamcinolone
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 10.06.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Hypertension
Malaise
Palpitations
Symptomtext
Pt had High Blood Pressure, palpitation, and felt sick after moderna shot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pt mentioned that she takes medicine for tremors. She had to take it after the moderna shot because she got tremors from getting it.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Moderna - from the 3rd shot from Pharmacy.
- Staat
- NC
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 22.06.2023
- Impfdatum
- 21.06.2022
- Beginn
- 01.03.2023
- Tage bis Beginn
- 253,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint stiffness
Joint swelling
No adverse event
Pain in extremity
Symptomtext
I did not have an adverse reaction to the vaccine. In 03/2023, I woke up unable to close my hands. I have swollen joints and pain in both hands. I have seen my doctor and I have referred to a specialist. I take two Advil each night before going to bed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 19.05.2023
- Impfdatum
- 16.06.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 46,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Facial pain
Magnetic resonance imaging head normal
Trigeminal neuralgia
Symptomtext
Began experiencing sharp, sporadic, excruciating pain on L side of face, in 08/2022. Saw dentist on 09/09/2022, who ruled out TMJ. Appointment with PCP, at the time, the MD on 09/22/2022. Dr. diagnosed condition as Trigeminal Neuralgia, she prescribed Carbamazepine 200 mg 3 x a day. Referred me to a Dr. Neurologist, appt on 10/03/2022, he concurred with diagnosis and the prescribed medication, he scheduled MRI for 10/17/2022. I experienced an allergic reaction to Cabamazepine, visited Urgent Care on 10/07/2022, for shot and medication, stopped Cabamazepine. Started taking Advil and Extra Strength Tylenol 3 times a day, and mouth guard at night. I saw Dr. on 11/23/2022 for MRI results. No abnormalities on MRI.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial pain
- Hospital-Tage
- -
- Labordaten
- MRI on 10/17/2022 of brain, no abnormalities found.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraine Headache Herpes
- Andere Medikamente
- ;Hydrochlorothiazide 25mg 1 day; Multi Vitamin
- Allergien
- Motrin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 20.03.2023
- Impfdatum
- 23.06.2022
- Beginn
- 13.03.2023
- Tage bis Beginn
- 263,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Laboratory test
Malaise
Symptomtext
Symptom onset 3/13/23. Treatment includes admission with therapy, labs, and assessment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes, HTN
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 03.02.2023
- Impfdatum
- 08.06.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Chills
Feeling abnormal
Pain
SARS-CoV-2 test negative
Symptomtext
I received my 4th dose of Moderna on 06/08/2022. I didn't feel any reaction till the 3rd day. I was surprised. I had body aches, upset stomach, and chills, I felt vey miserable. I went to my doctors office after few day. My doctor told me that it was very common after receiving vaccines. She probably prescribed me TYLENOL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 03FEB2023 COVID-19 test negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Omeprazole
- Allergien
- Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 20.01.2023
- Impfdatum
- 21.07.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 110,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Nasal congestion
Oropharyngeal pain
Productive cough
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Throat irritation
Symptomtext
I thought I was just getting a cold. It started as a scratchy throat that developed into a sore throat. Then I started getting a runny and stuffy nose. I was sneezing for a while and it developed into coughing where I would spit up phlegm. I had a slight headache but no fever. I tested for COVID-19 on November 08, 2022 and it was positive. I called my doctors office the next day and spoke with the nurse who gave me instructions over the phone. I went to the doctor at the end of November to see if I was all clear and they said that I seemed to have recovered. I was not prescribed any medications, I just took over the counter Mucinex.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Test-November 08, 2022-Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Arthritis; Sciatica; Foot Drop; Acid Reflux; High Blood Pressure
- Andere Medikamente
- Gabapentin; Pantoprazole; Hydrochlorothiazide; Amlodipine; Methimazole; One a Day Women's; Cod Liver Oil Tablets; Goalie Apple Cider Vinegar Gummies; Vitamin D3
- Allergien
- Tomato's; Strawberries
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 11.07.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 169,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Fatigue
Feeling abnormal
Malaise
Respiratory tract congestion
SARS-CoV-2 test positive
Sinus headache
Throat irritation
Symptomtext
I received my 4th dose on 07/11/2022 at 01:00PM. My COVID-19 infection symptoms started on 12/27/2022 at 08:00PM. I had a lot of congestions, scratchy throat, and sinus headache. I thought it was my sinus that was bothering me so I did a telehealth with a doctor who prescribed me with Z-PAK for 5 days. With the symptoms I had I was feeling bad so I took the COVID-19 home test on 12/30/2022 which turned out to be positive. On 12/31/2022 I went to the urgent care after testing positive they didn't prescribe me with any medication but they advised me to take BOIRON OSCILLOCOCCINUM for 3 days. As of today 01/11/2023 I still have little fatigue and congestions but rest of the other symptoms resolved. I am recovering as of now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 30DEC2022 COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Kidney Tendinitis; Reflux Disease
- Andere Medikamente
- PEPCID; PROZAC; WELLBUTRIN; vitamin D
- Allergien
- Sulfa
- Vorherige Impfungen
- COVID-19 vaccines 2nd and 4th dose, fever, chills, and nausea for 1 day and half.
- Staat
- MN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 07.06.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 146,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Diarrhoea
Heart rate irregular
SARS-CoV-2 test positive
Sepsis
Symptomtext
Patient brought to the ED on 10/31 with generalized weakness that started the same morning. He lives at an assisted living facility, and the nurse checked his vitals and found that this heart was irregular so advised he come to the ED. Additionally the patient reported about 2 episodes of diarrhea per day for the past two weeks. In the ED, he was found to have a fever of 100.3 F and oxygen saturations at 88-90% on room air. He tested positive for COVID-19 by PCR. He was admitted to the hospital 10/31 - 11/3 for sepsis with COVID-19 infection resulting in acute diarrhea. Patient has received the primary vaccine series and two boosters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 13.06.2022
- Beginn
- 02.10.2022
- Tage bis Beginn
- 111,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I had my vaccination on 06/13/2022. I started to experience fever achiness cough on 10/02/2022. I tested COVID-19 positive on 10/03/2022. I was prescribed PAXLOVID and I currently feel fine on 01/09/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 10/03/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Losartan; amlodipine; multivitamins
- Allergien
- N/A
- Vorherige Impfungen
- COVID-19 achy and nausea
- Staat
- PA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 01.06.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 171,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Nasal congestion
Pyrexia
SARS-CoV-2 test positive
Symptomtext
In November of 2022 I began to have fever in the middle of the night. The following night I had a fever again and a stuffy nose. I was unable to reach my doctor until the next Monday but I tested positive for COVID-19 on a home test.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19, positive, 11/19/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; Hypothyroidism
- Andere Medikamente
- Hydrochlorothiazide; levothyroxine; calcium; ginseng; vitamin C; vitamin D; vitamin K; multivitamin; elderberry; sea moss; probiotics
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 27.06.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 148,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest discomfort
Headache
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID-19 on 11/22/2022. I had a headache, fever, sore throat, chest discomfort, and body aches. The headache was the worst symptom. I contacted my doctor and was prescribed 5 days' worth of PAXLOVID. I started feeling better after taking PAXLOVID, but that only lasted for 2 days and then I started feeling worse than I did originally. I am feeling better now, but still have quite a bit of fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 22NOV2022 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Heart Disease
- Andere Medikamente
- Aspirin; rosuvastatin; tadalafil
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 23.12.2022
- Impfdatum
- 22.06.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 82,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
In September 2022 my breakthrough COVID-19 infection started with sore throat then a cough that was painful. I had a fever for about 48 hours that remained low-grade as well as chest congestion. At Urgent Care I was prescribed Paxlovid and took that for 5 days. The cough remained for two weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Home COVID-19, negative, 092022; Home COVID-19, positive, 092022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Parkinsons; Enlarged Prostate
- Andere Medikamente
- Sinemet; Flomax; Vitamin C; Occuvite; Iron; Azilect
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 18.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arthritis
Blood test
Bursitis
Electromyogram
Exercise tolerance decreased
Nodal osteoarthritis
Oral pain
Pain in extremity
Pain of skin
Skin discomfort
Tenderness
Symptomtext
Prior to my first injection, I did not suffer with arthritis. Within a month, I was unable to do yoga exercises as easily as I had prior to my first injection., After my second, it got worse and I had to go to an osteopath and starting getting cortisone injections in my hips due to arthritis and bursitis. Thinking it was only old age, I continued with my Moderna injections. My distal joints on my right hand were struck with arthritis for which I will need surgery and the final booster brought on Heberden Nodes in my distal joints. I now suffer with excruciating pain in my hands, scalp and mouth that when touched, feel like my skin has been peeled off and vinegar poured on it. I have a neurologist appointment in February to diagnose this issue. No more boosters for me!!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oral pain
- Hospital-Tage
- -
- Labordaten
- Bloodwork EMG (nerve conduction test)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PBC
- Andere Medikamente
- OLMESARTAN URSODIOL PANTOPRAZOLE GABAPENTEN MILK THISTLE EXTRACT PROBIOTIC CITRACAL PLUS MAGNESIUM POTASSIUM VITAMIN C
- Allergien
- SOFT SHELL FISH
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 20.12.2022
- Impfdatum
- 20.06.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 135,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Influenza A virus test negative
Influenza virus test negative
Oropharyngeal pain
Pain
Pyrexia
Respiratory syncytial virus test negative
SARS-CoV-2 test negative
Streptococcus test negative
Symptomtext
I had a fever of 101F, chills, body aches, extreme sore throat. I went to the doctor they tested me for COVID-19, strep, influenza, RSV. All tests came back negative, I was advised to go home get plenty of rest, drink fluids and it should clear itself up. In a couple of days I was feeling much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- RSV; Influenza A & B; Strep; COVID-19; all came back negative.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Omeprazole; iron; vitamin B-12
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 14.12.2022
- Impfdatum
- 30.07.2022
- Beginn
- 02.10.2022
- Tage bis Beginn
- 64,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Ear infection
Fatigue
Influenza virus test negative
Laboratory test normal
Oropharyngeal pain
SARS-CoV-2 test negative
Sinusitis
Symptomtext
I have a sore throat, cough, and fatigue. I have developed a sinus infection and a double ear infection This has lasted for about two and a half months so far. I was prescribed doxycycline and ZITHROMAX. I am feeling better, but I still have a cough that won't go away. I tested negative for COVID-19, flu, and Pneumonia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 24OCT2022 COVID-19 test negative; 24OCT2022 flu test negative; 24OCT2022 Pneumonia test negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Penicillin; sulfa
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 27.07.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Myalgia
Symptomtext
About a week after I developed sore muscles and joints which is worst in my shoulders.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Atorvastatin and Metoprolol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 06.12.2022
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Formication
Hypoaesthesia
Pruritus
Rash
Rash erythematous
Spider vein
Symptomtext
I was not observed after the shot. About 7 minutes later I got a sudden and severe itch on my left lower jaw with a bright red rash, my left nostril felt like ants crawling over it, the rash then spread a lighter red up my cheeks, over my chin, and to the right side of my face. Once it spread the itch went away, the itch lasted about 7 minutes. The rash then turned brighter and no longer spread, the brightest spots were along my jawline and followed a line to the other side of my jaw and was very dense (it looked like a severe sunburn) the rash on my cheeks and chin were not as bright (it looked like I got slapped repeatedly on both cheeks) it also showed what appeared to be spider veins on my cheeks that were bright red. We were stuck in traffic and couldn?t get to ER the rash lasted an hour and complete disappeared, it left a numb internal feeling on my right cheek, I took a Benadryl and this feeling went away in 5 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Stuck in traffic
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- CRPS/RSD and Dystonia in left hand which affects left arm for 11 years. Diagnosed with MS 11 years ago, then told a year later that the brain lesions didn?t change and I don?t have MS, doctors attribute my neurological issues of Dystonia with the radiation injury to my hand which affects my walking at sporadic times.
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 13.09.2022
- Beginn
- 13.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Erythema
Pain in extremity
Swelling
Symptomtext
Pt received a COVID Vaccine at the Health Dept on 09/13/2022 then came to our facility to see a provider on 11/15/2022 for arm and shoulder pain. Pt requested that we report the incident due to she continues to have Pain in that arm and shoulder. She stated that the swelling and redness are gone but she believed that is the cause of her shoulder pain. Provider is treating pt for shoulder pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Naproxen
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 22.11.2022
- Impfdatum
- 28.07.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 41,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
I began symptoms on 09/07/2022 with a sore throat. I contacted my healthcare provider over their messaging system. Later that day, I did a home test and tested positive. My doctor returned my phone call the next morning 09/08/2022 and they told me that I did not necessarily qualify for any medication because I didn't have any long standing health conditions, but because of my age, they prescribed PAXLOVID. I picked up the prescription on 09/08/2022 and began taking the dosage for 5 days. On 09/09, I had a runny nose. 09/10 and 09/11 I had a dry cough. On 09/12, I felt great with no symptoms at all. I took my last dose of PAXLOVID on 09/13 in the morning. 09/18, I developed symptoms again such as sneezing, coughing and a sore throat. I tested positive again. I took over the counter medication on 09/18 and 09/19. On the 19th, I started to feel somewhat better. On 09/25/2022, I did another home test and tested negative. I had a dry cough for another 10 days after that.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 09/07/2022 at home COVID-19 test positive; 09/18/2022 at home COVID-19 test positive; 09/25/2022 at home COVID-19 test negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 11.10.2022
- Impfdatum
- 13.06.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Acupuncture
Arthralgia
Asthenia
Chiropractic
Exercise tolerance decreased
Fatigue
Grip strength decreased
Hypoaesthesia
Influenza like illness
Injection site pain
Massage
Pain
Pain in extremity
Symptomtext
Covid19 Adverse side effects after receiving 3rd booster shot: I am a 64 year old male. I am reporting a serious adverse side effect after receiving a third booster shot. I previously had made an earlier attempt to file this complaint but my online form was stopped and rejected after 20 minutes. I find this a bad policy by the CDC and it should be corrected. Detail of incident: My first Covid vaccine was 4/26/21 with the J&J (Lot #1808980) I experienced no adverse side effects. My second shot (booster) was 10/27/21 with the Moderna (Lot#023F21A or 032F21A) I experienced mild (fatigue, flu like symptoms) for about 36 hours after injection. Then nothing further. My third booster was 6/13/22 with Moderna (Lot#059A22A) I experienced injection site soreness later the same day and the following day only because the shot was administered closer to the interior of my left upper shoulder, and higher up on my brachii biceps. The soreness dissipated within 2-3 days. However, about 5 days since receiving that booster shot I started having pain in my left wrist, palm, and fingers. (pain, numbness and loss of grip strength) I regularly bicycle for exercise and good health and had not experienced any pain or diminished grip strength ever prior to this date. I decided to monitor the pain and continue daily rides. After several more days the symptoms only got worse and bicycling seems to aggravate the pain, numbness and lack of strength. I tried a number of OTC topical pain relief products, but none were of any effect to reduce the pain. Further the wrist/hand was much more painful in the morning after sleeping. Additionally, there developed a correlation of soreness/numbness at my elbow area and the interior shoulder area where the nerves pass through. I thought that the lost of grip strength and the pain when using the left hand warranted a visit to the doctor. Unfortunately, its almost impossible to see a doctor immediately and I had to wait about 2 weeks before getting seen. In the interim I continued to try topical pain relief, with no further effect, physical massage, chiropractic, and acupuncture to see if this would relieve or resolve the wrist/hand pain and weakness. None were successful other than temporally/nominal reduction in pain. I spoke to all of these health care workers that the pain in the left wrist/hand developed within days of receiving the Covid19 booster shot. I was hoping that they knew of any connection between the shot and the problem. None had any information to offer or an explanation as to how the problem may have developed, nor a cause for recovery. The CDC public website list ?known adverse side effects?, and one that is listed is Guillain-Barr? Syndrome (GBS). It specifically notes ?men over 50? and ?having received the J&J?. Which in my case I am over 50 and received the J&J. I have not suffered any injury to my left arm/hand. The only recent cause and effect was getting the booster and then shortly there after developing hand/wrist pains, which according to the Doctor after being examined; were caused by nerves, not muscle or bone damage. The medical facility (a very large hospital) doctor knew little about Covid19 side effects and dismissed my concerns and offered no follow up. Which is why I am filing this complaint approximately 4 months after the last shot. The physical problem has not cleared up on its own and has gotten to the point where I can not grasp and close my left hand and fingers. This is very troubling to someone who uses their hands as an artist. I request a response to my filing this complaint and sincerely hope that there is a medical remedy available. I can be reached at any of the following contact points. I could use any and all help that you can offer. Thank you.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none currently, doctor's notes available as needed
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- None: other than underactive thyroid syndrome
- Andere Medikamente
- Levothyroxine, Acyclovir, Asprin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 10.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 18,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Cough
Exposure to SARS-CoV-2
Headache
Loss of personal independence in daily activities
Malaise
Night sweats
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I do not know where I was exposed to COVID-19 but I was at an outdoor event and in contact with a lot of people, but I have no idea where I got it. I first had a runny nose and cough. I could tell that I was more sick than just a regular cold. The symptoms were not very bad but enough that I could tell that this was different. I was supposed to fly internationally 5 days later but I rescheduled that flight before I even got test results. I took multiple home tests that were negative. I took a PCR test at a local pharmacy on 06/30/2022. I received positive results a few days later. I experienced a severe lack of energy. I had one day of a really bad headache. I did not have any fever but did have sore throat, some coughing, and night sweats. I was very relieved that it did not move into my lungs due to my existing asthma. I had a telehealth visit and was prescribed Paxlovid and began taking it on 07/02/2022. I took my last dose on the morning of 07/06/2022. After beginning the medication, cough, sore throat, and runny nose only lasted 1-3 days. My headache had already improved before beginning the Paxlovid. The lack of energy lasted for around 2 weeks after the onset of my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 06/30/2022 PCR COVID-19 test-positive; At home COVID-19 test- negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Migraines
- Andere Medikamente
- Zyrtec; Albuterol Inhaler as needed; Sumatriptan as needed; Calcium Magnesium Zinc
- Allergien
- Penicillin; Sulfa based antibiotics
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 09.09.2022
- Impfdatum
- 09.06.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 49,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse reaction to the vaccine. I tested positive for COVID-19 via home test on 07/28/2022. We had traveled out-of-state for a family gathering and got sick from that trip. I wasn't running a temperature but I just didn't feel good. I contacted my doctor and was prescribed Paxlovid. My symptoms was not bad so I'm not sure that it really helped me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Home test for COVID-19 was positive on 07/28/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Allergies and pre-diabetic
- Andere Medikamente
- None
- Allergien
- Latex; codeine; sulfa; tetracycline
- Vorherige Impfungen
- 2nd Shingles vaccine I had bad aches and flu like systems.
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 25.08.2022
- Impfdatum
- 13.07.2022
- Beginn
- 15.08.2022
- Tage bis Beginn
- 33,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Cough
Decreased appetite
Discomfort
Exercise tolerance decreased
Exposure to SARS-CoV-2
Extra dose administered
Fatigue
Head discomfort
Impaired work ability
Nasopharyngitis
Oropharyngeal pain
Photophobia
Rhinorrhoea
SARS-CoV-2 test positive
Sinus congestion
Sinus headache
Symptomtext
I received my second Moderna booster for COVID-19 on 7/13/2022. On the morning of 8/15/2022, I felt like I had a really bad head cold. I didn't think much of it, because there was a head cold that was being spread around at my workplace. I had a sinus headache, sinus congestion, fatigue, and an itchy throat. I felt the same way on 8/16/2022. On 8/17/2022, the symptoms were worse. I began to have a runny nose and a bit of a cough. I was also even more fatigued. I didn't feel like working, but I had to go to work, because we were short-staffed. I just took some ADVIL sinus and went to work. I went to work and felt a little bit better. At around 10 AM, though, I got a text from my sister, whom I had recently visited. In the text, she informed me that she had tested positive for COVID-19. I immediately put on a mask and informed my manager that I needed to go home. I went home and took a COVID-19 test, which yielded a positive result. I stayed home afterwards. I called and emailed my doctor to inform her of my test results and to ask for suggestions. Because I had had asthma when I was a child, the doctor prescribed me an albuterol inhaler, which I didn't need. She also prescribed me benzonatate. She recommended that I also buy some OTC medicines like MUCINEX and AFRIN nasal spray, plus a NETI POT. I obtained all of these by the end of the day. I stayed at home and followed the doctor's orders. On 8/18/2022, I felt even worse than before. My fatigue, cough, and head congestion were more intense. I had a sensitivity to light. My nose was running constantly. My sore throat also hurt worse than before. I used the NETI POT and took the medicine, which helped some, but not much. Of all the medicines, the benzonatate helped the most, because it got rid of the cough. I wasn't sleeping well during this period; I would wake up multiple times at night. This was largely due to generalized discomfort. The worst day was probably 8/19/2022. I had zero energy and had to make an effort to get up and eat and drink water. I still had a severe cough and a severe sinus headache. I still had a runny nose. On 8/20/2022, I started to feel a little better. The headache was less severe. The fatigue was also less severe. On 8/21/2022, I felt fine enough to go for a walk, though I still had a cough and fatigue. I still had a headache, though it was manageable. When I was walking, I had to pause every 15 minutes or so to rest and catch my breath. On 8/22/2022, I felt significantly better. I felt less fatigued. I wasn't coughing as much. The headache was now more of a feeling of pressure rather than pain. The sore, scratchy throat was also gone. On 8/23/2022, I felt much better and took another home COVID-19 test. The result was positive, though the line was very faint. I also went for a walk that day. Unlike the previous walk, though, I never had to pause to rest. On 8/24/2022, I felt pretty much felt back to normal. I took another home test, and I finally got a negative result. On that day, I actually went for a run. The run was slower than my usual speed, and I had to slow down and walk at one point. However, I did feel well enough to help a friend move. At the time of this writing, I still pretty much feel normal. I'm usually a very active person. I am gradually resuming my previous activity levels, though it will take some time to rebuild my stamina. Throughout my illness, I drank copious amounts of water. I also consumed protein shakes, because I didn't feel much like eating, but I knew I had to ensure I still received nutrients.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 8/17/2022 home COVID-19 test positive result; 8/23/2022 home COVID-19 test positive result; 8/24/2022 home COVID-19 test negative result.
- Aktuelle Erkrankungen
- Common Cold.
- Vorgeschichte
- Attention Deficit Hyperactivity Disorder; Depression; Anxiety.
- Andere Medikamente
- CONCERTA; cetirizine hydrochloride.
- Allergien
- Gluten; dairy.
- Vorherige Impfungen
- When I got my first Moderna booster in for COVID-19, I started getting periods twice a month. I have a Nexplanon implant, and pr
- Staat
- IL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 18.08.2022
- Impfdatum
- 23.07.2022
- Beginn
- 06.08.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash papular
Rash pruritic
Urticaria
Symptomtext
Patient reported approximately 3 to 4 weeks after first booster, a rash appeared like bug bites affecting hands, feet, legs and trunk for about 2 months. She did not relate this to the first booster. Patient reported approximately two weeks after second booster, a rash/hives of increased severity appeared in varying areas of trunk and arms for a few hours. They were red and raised after possibly itching, then disappeared and reappeared in different places.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- ASA, Ibuprofen, Penicillin, Pseudoephedrine
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 17.08.2022
- Impfdatum
- 29.06.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Dizziness
Fatigue
Feeling abnormal
Symptomtext
fatigue, lightheaded, generalized weakness, brain fog
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 15.08.2022
- Impfdatum
- 18.06.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 25,0
- Dosis
- 5
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dysphagia
Extra dose administered
Eye pruritus
Hypersensitivity
Malaise
Oropharyngeal pain
SARS-CoV-2 test positive
Upper respiratory tract congestion
Symptomtext
Extreme sore throat to the point where I could barely swallow. It started out with allergy symptoms, dry cough and a little bit of itchy eyes and stuffy head on the 13th. On the 15th I tested positive and my throat was so sore I could barely swallow. Within 20 hours I got Paxlovid and by the 17th the severity of the soreness started decreasing. I positive for 22 days. Seven days after Paxlovid I tested negative. Two days after I tested positive with increased symptoms. I was prescribed Acyclovir and a round of antibiotics. I started a second round of Paxlovid on the Aug 2 nd, and tested negative on Aug 6th.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- COVID-19 antigen positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- I don't have a spleen; Hypoactive thyroid; Ulcerative Colitis; Low testosterone
- Andere Medikamente
- I do not disclose
- Allergien
- No
- Vorherige Impfungen
- 2nd and 3rd shots of Moderna I had mild COVID symptoms - fever and aches.
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 06.07.2022
- Beginn
- 31.07.2022
- Tage bis Beginn
- 25,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Headache
SARS-CoV-2 test
Secretion discharge
Sneezing
Symptomtext
coughing, sneezing, headache, mucus. took Paxlovid, lasted around 5 days. Still a little coughing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- n/a, self tested
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure and cholesterol
- Andere Medikamente
- Benazepril-HCTZ 20-12.5, amLODIPine BESYLATE 5mg, simvastattin 20mg., 81 mg aspirin, cetirizine hydrochloride
- Allergien
- diavan
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 08.08.2022
- Impfdatum
- 15.07.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 20,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Fatigue
Headache
Laboratory test abnormal
Nasal congestion
Pain
Symptomtext
It started with two days of an intense headache which didn't go away with medication. On the third day I had the headache. nasal congestion and fatigue. I then tested positive on the third day of the symptoms. The symptoms have just been a few days of nasal congestion and on day 4 the headache went away. Today is day 5 and I just have a slight cough and nasal congestion. I have also had body aches the whole time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Osteoarthritis, Hypertension.
- Andere Medikamente
- Diclofenac Sodium, Triamterene Hydrochlorothiazide, Lexapro, Allegra.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 03.08.2022
- Impfdatum
- 28.07.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Poor quality product administered
Product colour issue
Symptomtext
Her arm is killing her; The vaccine that she received looked orange brown in the syringe; The vaccine that she received looked orange brown in the syringe/ saw vial which had pink cap and said 12 years and up; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Her arm is killing her), POOR QUALITY PRODUCT ADMINISTERED (The vaccine that she received looked orange brown in the syringe) and PRODUCT COLOUR ISSUE (The vaccine that she received looked orange brown in the syringe/ saw vial which had pink cap and said 12 years and up) in a 37-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059A22A) for COVID-19 vaccination. Patient had no allergies. The patient's past medical history included COVID-19 (Yes, tested positive for COVID-19) in January 2022. On 28-Jul-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 28-Jul-2022, the patient experienced PAIN IN EXTREMITY (Her arm is killing her), POOR QUALITY PRODUCT ADMINISTERED (The vaccine that she received looked orange brown in the syringe) and PRODUCT COLOUR ISSUE (The vaccine that she received looked orange brown in the syringe/ saw vial which had pink cap and said 12 years and up). At the time of the report, PAIN IN EXTREMITY (Her arm is killing her), POOR QUALITY PRODUCT ADMINISTERED (The vaccine that she received looked orange brown in the syringe) and PRODUCT COLOUR ISSUE (The vaccine that she received looked orange brown in the syringe/ saw vial which had pink cap and said 12 years and up) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. No concomitant medications were reported. Patient stated that before vaccination she saw the vial which had a pink cap and said 12 years and up. The Pharmacist filled up the syringe and kept pushing back the syringe. Then pharmacist administrated the vaccine. Patient started getting suspicious because her arm was killing her. The caller explained that she wanted to know what was injected to her, but did not want to start a commotion. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 29-Jul-2022: Follow up received contains QE number updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (Yes, tested positive for COVID-19); Comments: Patient had no allergies.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 23.07.2022
- Beginn
- 23.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Product administered at inappropriate site
Symptomtext
Shot allegedly given to high on arm,. Patient currently has had pain since shot for 5 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 03.06.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Patient reported a rash developed on entire body 2 days after receiving her second booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Sertraline, bupropion, Vraylar, doxepin
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 29.07.2022
- Impfdatum
- 25.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Fatigue
Muscle rigidity
Symptomtext
After I went to bed on the 25th of July, two hours later I woke up with a cough, and my body went regid! It lasted about 10 seconds. Then two hours later the same thing! This happened 5 or 6 times in the night, and lasting 10 seconds. The next day I was exhausted all day and slept most of the day. It took two days to get over this I have always had some unpleasant reactions to the Covid 19 shots and vaccines. This was by far the worst.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Chronic Sinus Polyps
- Andere Medikamente
- simvastatin Citirizine Nucala Levoxthyroxine Vit D3 Citalopram Potassium Omeprazole Magnesium Miralax Biotin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 27.07.2022
- Impfdatum
- 25.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
Pt reports showering Tuesday night and when she came out of the shower she noticed hives on her face. She then stated she wasn't sure if it was hives, but she had red bumps that formed all over her face. She didn't take anything to treat it, it went away on its own the same day. Patient was counseled to keep an eye on it and to report if any other symptoms occur.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- n/a
- Andere Medikamente
- N/A
- Allergien
- Penicillins and sulfa antibiotics
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 21.07.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site discolouration
Injection site mass
Injection site pain
Symptomtext
FORMED A SMALL BUMP AFTER VACCINATION, THE NEXT DAY IT BECAME LITTLE DARK AND PT COMPLAINED ABOUT PAIN. GAVE AN ICE PACK TO APPLY RIGHT AFTER VACCINATION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discolouration
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 20.06.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of personal independence in daily activities
Pain
Sleep disorder
Substance use
Symptomtext
The night of the vaccine, I noticed that I was achy. I woke up the next day in pain at 5AM. I was in extreme pain. I had aches and pain all throughout my whole body that was severe. It affected my normal activities. I tried marijuana to help with the pain. The pain did go away. I went to bed but then by noon, about 24 hours later I was achy again but not as severe. I tried marijuana again and the second dose of that of that helped and the pain went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Peptic Ulcer
- Andere Medikamente
- N/A
- Allergien
- Aloe; Onions; Sulfa; Neomycin
- Vorherige Impfungen
- DTap- arm swollen and hot at site in 1973
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 14.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Dysgeusia
Immunisation reaction
Swollen tongue
Symptomtext
had a little bit of a reaction to it; had a weird metal taste in her mouth which the metal taste continued for 2 weeks; some mild, minimal swelling under the tongue; dizziness; This spontaneous case was reported by a patient and describes the occurrence of IMMUNISATION REACTION (had a little bit of a reaction to it), DYSGEUSIA (had a weird metal taste in her mouth which the metal taste continued for 2 weeks), SWOLLEN TONGUE (some mild, minimal swelling under the tongue) and DIZZINESS (dizziness) in a 30-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 14-Jun-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 14-Jun-2022, the patient experienced IMMUNISATION REACTION (had a little bit of a reaction to it), DYSGEUSIA (had a weird metal taste in her mouth which the metal taste continued for 2 weeks), SWOLLEN TONGUE (some mild, minimal swelling under the tongue) and DIZZINESS (dizziness). At the time of the report, IMMUNISATION REACTION (had a little bit of a reaction to it), SWOLLEN TONGUE (some mild, minimal swelling under the tongue) and DIZZINESS (dizziness) outcome was unknown and DYSGEUSIA (had a weird metal taste in her mouth which the metal taste continued for 2 weeks) had resolved. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. No concomitant medication reported. Patient reported that she was told to wait around longer at the vaccination facility for monitoring purpose and later gave her an antihistamine & something for dizziness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 21.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Insomnia
Nerve compression
Pain
Pain in extremity
Symptomtext
couldn't sleep; patient was told maybe had a pinched nerve and that maybe came from neck; get unbelievably pain in his arm, crying howbad the pain was on his arm; severe pain; This spontaneous case was reported by a patient family member or friend and describes the occurrence of PAIN (severe pain), INSOMNIA (couldn't sleep), NERVE COMPRESSION (patient was told maybe had a pinched nerve and that maybe came from neck) and PAIN IN EXTREMITY (get unbelievably pain in his arm, crying howbad the pain was on his arm) in a 31-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059a22a) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer (Dose-1) on 05-Apr-2021, Pfizer (Dose-2) on 26-Apr-2021 and Pfizer (1st Booster dose) on 06-Aug-2021. Past adverse reactions to the above products included No adverse event with Pfizer, Pfizer and Pfizer. On 21-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In June 2022, the patient experienced PAIN (severe pain). On 05-Jul-2022, the patient experienced INSOMNIA (couldn't sleep), NERVE COMPRESSION (patient was told maybe had a pinched nerve and that maybe came from neck) and PAIN IN EXTREMITY (get unbelievably pain in his arm, crying howbad the pain was on his arm). The patient was treated with IBUPROFEN (MOTRIN [IBUPROFEN]) at an unspecified dose and frequency; PARACETAMOL (TYLENOL) at an unspecified dose and frequency; CORTISONE at a dose of cortisone in his neck; PREDNISONE at a dose of prednisone shot pack and GABAPENTIN at an unspecified dose and frequency. At the time of the report, PAIN (severe pain), INSOMNIA (couldn't sleep), NERVE COMPRESSION (patient was told maybe had a pinched nerve and that maybe came from neck) and PAIN IN EXTREMITY (get unbelievably pain in his arm, crying howbad the pain was on his arm) had not resolved. No concomitant medication information provided. Patient did not have any allergies. It was reported that the patient was very healthy. It was reported that, following vaccination with the second booster the patient had severe pain on the 27 or 28-Jun-2022, on 05-Jul-2022 went to the emergency room, patient was told that maybe he had a pinched nerve in the emergency room, and that maybe came from his neck in a orthopedic walking clinic. The patient was given "all kind of medicines". Patient took steroid shot and 2 more shots as treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 01.06.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Myalgia
Nasal congestion
Oropharyngeal pain
Pain
Paranasal sinus discomfort
SARS-CoV-2 test positive
Symptomtext
My wife and kids had it before I did. Starting 07/05/2022, I developed fatigue, sore throat, muscle aches and body soreness. By saturday, 07/09/2022, I decided to take an At-Home COVID-19 test which came back positive. Then, the symptoms have been consistent, except I have developed nasal congestion and sinus pressure. By saturday I was feeling a little better but still present. I tested myself earlier today (07/14/2022) and was still positive. I am feeling mostly better but I still am having fatigue and nasal congestion. I was able to speak to my PCP on 07/13/2022 and they recommended Paxlovid. However, since I was already starting to feel better I declined it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At-home COVID-19 test (07/09/2022): Positive; At-home COVID-19 test (07/14/2022): Positive; PCR test (07/14/2022): awaiting results
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure; Obesity; Depression; Anxiety
- Andere Medikamente
- Fluvoxamine; Clonazepam; Metoprolol; Vitamin D; Men's Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 07.06.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Decreased appetite
Fatigue
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Vaccine breakthrough infection
Symptomtext
On 7-11-2022, I started having a temp of 98.8, chills, fatigue, loss of appetite, runny nose and a scratchy throat. Later that morning, I took a home Covid19 test with positive results. I called the doctors office later that afternoon and left a message with their tele service. The next morning on 7-12, they doctors office called me back and prescribed Paxlovid. I started taking the Paxlovid on 7-12 and have had 2 doses of it. I am not taking anything over the counter for symptoms. I am reporting my breakthru case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 7-11-2022 home Covid19 test with positive results
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, Hypertension, Atrial Fibrillation, High Cholesterol
- Andere Medikamente
- Metoprolol, Triamterene/HCTZ, Xarelto, Simvastatin, Zolpidem, Asmanex inhaler, Ventolin inhaler, Potassium Chloride, Multivitamin, Calcium with Vitamin D, Claritin, Vit D3, Tylenol ES as needed
- Allergien
- Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 07.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Injection site erythema
Injection site pain
Symptomtext
redness on resident's chest, observed some redness on resident's upper chest, resident denies itchiness. Resident had received Moderna booster shot on 7/7/22 and also noted redness on injection site, Rt deltoid and tender to touch. CRNP gave order for Loratidine 10 mg daily for 3 days. CRNP will be here to assess resident tomorrow. Message left to resident's daughter to call bac
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Resident had PNA on 6/14/2022 and was treated
- Vorgeschichte
- SICK SINUS SYNDROME SPONDYLOSIS WITHOUT MYELOPATHY OR RADICULOPATHY, LUMBAR REGION TREMOR, UNSPECIFIED UNILATERAL INGUINAL HERNIA, WITHOUT OBSTRUCTION OR GANGRENE, RECURRENT UNSPECIFIED ABNORMALITIES OF GAIT AND MOBILITY UNSPECIFIED ATRIAL FIBRILLATION UNSPECIFIED FALL, SEQUELA VENTRICULAR PREMATURE DEPOLARIZATION VITAMIN D DEFICIENCY, UNSPECIFIED WEAKNESS
- Andere Medikamente
- Loratadine Tablet 10 MG Metoprolol Succinate ER Tablet Extended Release 24 Hour 25 MG Atorvastatin Calcium Tablet 40 MG Biotin Tablet 5000 MCG Ergocalciferol Capsule 1.25 MG (50000 UT) Amiodarone HCl Tablet 200 MG Midodrine HCl Tablet 10 MG
- Allergien
- : traMADol, Penicillins, Sulfa Antibiotics
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 27.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site discolouration
Injection site erythema
Injection site reaction
Injection site swelling
Rash pruritic
Symptomtext
Pt reported increase swelling, erythema and pruritic rash at site of Moderna injection (Booster #2). Reports same type of reaction following Moderna injection (Booster #1). On most recent virtual visit, pt noted to have 6cm X 5 cm brownish hyperpigmented well circumscribed area around injection site. Pt reports similar reaction with first booster and resolved with time on its own.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discolouration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- GAD
- Andere Medikamente
- OTC Tumeric and Vit D3 supplements
- Allergien
- NKDA
- Vorherige Impfungen
- similar reaction noted with Moderna booster #1 (had no reaction with PFR primary series)
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 10.07.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Incorrect dose administered
Pain
Pyrexia
Swelling
Symptomtext
Patient came in to receive 2nd booster. had received 3 doses of Pfizer. Pharmacist on duty recommended Moderna. Pharmacist administered 0.5ml dose instead of the recommended 0.25ml dose. Patient later complained of high fever >101, body aches fatigue and swelling in the armpit of the injection site arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 05.07.2022
- Impfdatum
- 17.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 11,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Insomnia
Myalgia
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Tested positive for COVID 12 days after second booster, on 6/29/2022, though symptoms began one day prior. Do not know if infection related to vaccine or not. Symptoms were body aches, chills, heavy congestion, and sleeplessness for about 3 days. Sore muscles have persisted through now, 7/5/2022 (although hard to tell whether soreness simply due to being isolated and sedentary for extended period).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Positive at-home antigen tests on 6/29, 7/3, and 7/5.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Corneal erosion, macular pucker
- Andere Medikamente
- Daily multi-vitamin (iron free), Lotemax eye drops (T/Th/Su)
- Allergien
- Amoxycillin (rash)
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 02.07.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Nodule
Pain in extremity
Pruritus
Symptomtext
A large knot formed in my arm and it was very red and sore with severe itching. It is still sore with a medium knot in my arm and very itchy as of 7/2/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- I haven't gone to the doctor yet, I will go back to the clinic today since the knot is still there and it itches so bad. 07/2/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- no medications taken at the time or within a week
- Allergien
- Latex, Hydromorphone
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 27.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Symptomtext
I got a rash the day after my second booster. It was about 3 inches long and 2 inches wide. This did not happen with the first 3 and all were Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension well controlled
- Andere Medikamente
- Losartan 100mg QD, Famotidine 20mg daily as needed, Ibuprofen 600mg qd as needed
- Allergien
- milk
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 20,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Feeling abnormal
Infection
Nasopharyngitis
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Sinus operation
Sinus pain
Symptomtext
I had congestion like a head cold, sinus drainage, and a sore throat but up in the sinus cavity. I also had soreness. I didn?t have any fever and just a little bit of a cough. That started on the 20th of June. My infection kept hanging on and I tested on the 22nd and came back positive. Two days later on the 24th, I wasn?t feeling any better. I called the health department, and I had a previous episode several years ago of a pertussis cough. I was worried about this moving into my lungs, so I was prescribed Paxlovid and I started that the night of the 24th which I finished yesterday morning. Unfortunately, I am still congested and it?s hanging on and doesn?t want to go away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test - Positive on 06/22/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D; Fish Oil; Lipitor
- Allergien
- Macadamia nuts
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Headache
Myalgia
Nasal congestion
SARS-CoV-2 test positive
Symptomtext
Tested positive for COVID-19 on 6/18/2022 using an at-home antigen test. Symptoms: headache, nasal congestion, muscle pain, fatigue Spoke to PCP on 6/19/2022 over the phone; he called in a prescription for Paxlovid Took Paxlovid orally from 6/19/2022 to 6/24/2022 along with Tylenol and Ibuprofen All symptoms except fatigue have subsided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Escitalopram (20mg daily), Vitamin D (4,000 IU daily)
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 08.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 8,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Headache
Infection
Polymerase chain reaction
Pyrexia
Respiratory tract congestion
Symptomtext
Breakthrough infection began with mild cough led by fever, chills, headache and congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- PCR, nasal swab - swab.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Thyroid
- Andere Medikamente
- SYNTHROID; vit D; vit C
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- -
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 10.06.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Facial pain
Inflammation
Injection site inflammation
Injection site pain
Oral pain
Somnolence
Pain in jaw
Toothache
Symptomtext
Right side of her mouth was severely hurting; Shortly after that she became very sleepy; This spontaneous case was reported by a patient and describes the occurrence of SOMNOLENCE (Shortly after that she became very sleepy) and ORAL PAIN (Right side of her mouth was severely hurting) in a female patient of an unknown age who received mRNA-1273 (Spikevax) for COVID-19 prophylaxis. No Medical History information was reported. On 10-Jun-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 10-Jun-2022, the patient experienced SOMNOLENCE (Shortly after that she became very sleepy). On 11-Jun-2022, the patient experienced ORAL PAIN (Right side of her mouth was severely hurting). The patient was treated with PARACETAMOL (TYLENOL) in June 2022 for Mouth pain, at an unspecified dose and frequency. At the time of the report, SOMNOLENCE (Shortly after that she became very sleepy) and ORAL PAIN (Right side of her mouth was severely hurting) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. No concomitant medication information was provided. Patient received her first dose of Moderna vaccine and shortly after that she became very sleepy, so Patient went to sleep and woke up the next day and the right side of her mouth was severely hurting. Patient stated that she can now only eat soft foods. Patient reached out to the pharmacy and they told her that there was nothing that they could give her to reject the vaccine and told her to take Tylenol for her pain. Patient went to her primary care physician on the day of the appointment to discuss the risks of getting the vaccine. Patient was concerned that this would affect her daily life especially since she considered herself to be healthy prior to receiving the vaccine. Patient consulted with a lawyer and wanted to know what needs to be done to correct the situation before she takes the next steps.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 17.06.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Feeling cold
Lymphadenopathy
Nausea
Vomiting
Symptomtext
severe joint pain, chills, nausea, vomiting, swollen lymph nodes above clavicle
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- highly controlled asthma (no attacks in 10+ years)
- Andere Medikamente
- Alvesco
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 06.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Pruritus
Symptomtext
Swollen right axillary lymph node. Pruritus of the abdomen and thorax as well as both arms. No difficulties with breathing nor visibile rash are present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 20.06.2022
- Impfdatum
- 14.06.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Headache
Injection site erythema
Injection site induration
Injection site mass
Injection site warmth
Photophobia
Symptomtext
SEVERE HEADACHE, LIGHT SENSITIVITY, HARD LUMP AT INJECTION SITE, RED SKIN REACTION, FELT HOT AROUND INJECTION SITE. ONSET WAS WITHIN 12 HOURS OF SHOT AND TOOK 5 PLUS DAYS TO RESOLVE. PATIENT DID NOT SEEK MEDICAL ATTENTION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- SURGERY
- Vorgeschichte
- HIGH BLOOD PRESSURE, CHRONIC PAIN, HYPOTHYROIDISM,
- Andere Medikamente
- MAG OXIDE, ELIQUIS, OXYCODONE, METOPROLOL, LEVOTHYROXINE, LISINOPRIL, ARANSP, CETIRIZINE, SODIUM BICARBONATE, ALLOPURINOL, METHANAMINE HIPP, CALCITRIOL, PHENAZOPYRIDINE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 18.06.2022
- Impfdatum
- 09.06.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Gait disturbance
Vertigo
Symptomtext
It's worst when I'm lying down/The room is spinning when lying down.; difficulty walking/walking into walls/I was walking sideways; dizziness; This spontaneous case was reported by a patient and describes the occurrence of VERTIGO (It's worst when I'm lying down/The room is spinning when lying down.), GAIT DISTURBANCE (difficulty walking/walking into walls/I was walking sideways) and DIZZINESS (dizziness) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. It was unknown that patient ever had COVID + test or diagnosis. Previously administered products included for Product used for unknown indication: Pfizer (Dose Number: 1st dose Lot number: EW0161 Dose: full dose) on 17-Apr-2021, Pfizer (Dose Number: 2nd dose Lot number: ER8736 Dose: full dose) on 08-May-2021 and Pfizer (Dose Number: 1st booster Lot number: FJ1611 Dose: booster dose) on 08-Nov-2021. Past adverse reactions to the above products included No adverse event with Pfizer, Pfizer and Pfizer. Concurrent medical conditions included Hypertension and Diabetes. On 09-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Jun-2022, the patient experienced GAIT DISTURBANCE (difficulty walking/walking into walls/I was walking sideways) and DIZZINESS (dizziness). On 14-Jun-2022, the patient experienced VERTIGO (It's worst when I'm lying down/The room is spinning when lying down.). At the time of the report, VERTIGO (It's worst when I'm lying down/The room is spinning when lying down.) and DIZZINESS (dizziness) had not resolved and GAIT DISTURBANCE (difficulty walking/walking into walls/I was walking sideways) was resolving. Concomitant medications was not provided by the reporter. It was unknown that recent change in status such as improvement or worsening. Adverse event did not cause patient to seek medical care (office visit, Urgent care, ER, hospitalized). Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Diabetes; Hypertension
- Vorgeschichte
- Comments: It was unknown that patient ever had COVID + test or diagnosis.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Heart rate increased
Injection site erythema
Injection site swelling
Injection site warmth
Pain in extremity
Pyrexia
Symptomtext
After the first 12 hours I experienced for about 12 hours the typical side effects of elevated heartrate, fever and chills. This was very unpleasant. I also experienced a sore arm. A few days later, I noticed where the injection site that my arm was very red and swollen and warm to the touch. This is about 3 inches in diameter and is still there, although starting to subside. My arms is still a little swollen. This is the first time this has happened with all of the Moderna vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Anxiety
- Andere Medikamente
- Paxil
- Allergien
- N/A
- Vorherige Impfungen
- Multiple vaccinations for possible exposure to sewage exposure. Gamma Globulin and Typhoid. I was about 23 years old.
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 16.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Injection site rash
Pain in extremity
Symptomtext
Patient husband reported patient (wife) experiencing rash at injection site and lower leg pain. Advised to alternate tylenol/motrin for pain management and to see PCP for further evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 08.06.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Pain in extremity
Swelling
Symptomtext
Patient came to the store because she received the Moderna vaccine 5 days earlier and has had pain and swelling in her arm. However the swelling is in the armpit, not at the injection site. We directed the patient to a free county clinic since she has no primary Dr and no insurance coverage.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 09.06.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspepsia
Headache
Heart rate increased
Injection site pain
Pyrexia
Symptomtext
Fever, headache, rapid heart rate, lower leg cramps, Acid indigestion, very dry mouth These adverse events started around midnight (which was around 12 hours after the injection) and continued for at least 4+ hours during the night. The fever and headache was intense. I took 2 ibuprofen in the morning . Also the site of the injection was extremely painful. I also had similar events that lasted much longer after my 1st Moderna injection on 1/29/2021 and they also started about 12 hours after the injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- One A Day Women?s 50+ multivitamin Phillips Colon Health Daily Probiotic Aspirin 81 mg Stool Softener
- Allergien
- None
- Vorherige Impfungen
- Fever, headache, sore joints, felt like the flu 74 years old 01/29/2021 Covid 19 vaccine Moderna #1 injection
- Staat
- CO
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Injection site urticaria
Symptomtext
Pain at injection site, redness and swelling at injection site, hives, itchiness on left bicep. Treatment: drink water, take Claritin Allergy 24-hour, take Ibuprofen, rest
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Breast cancer survivor
- Andere Medikamente
- Trazadone, Bupropion XL, Tamoxifen Citrate, D3, Atorvastatin, Levothyroxine, Iron, Hydrochlorothiazide
- Allergien
- Bactrim, Morphine, Penicillin, Keflex, Fluorouracil
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 07.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
patient reports recurrent rash on face in the ensuing 4 days after vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Urticaria
Symptomtext
Patient developed hives 5 days after receiving vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 21.12.2023
- Impfdatum
- 29.07.2022
- Beginn
- 20.12.2023
- Tage bis Beginn
- 509,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test
Symptomtext
hospitalized with covid; fully vaccinated with 1 booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 1,0
- Labordaten
- positive covid pcr 12/18/20
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- HTN, HLD, Dementia, CAD
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 08.11.2023
- Impfdatum
- 16.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 01.09.2023
- Impfdatum
- 09.08.2022
- Beginn
- 09.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 01.09.2023
- Impfdatum
- 26.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 01.09.2023
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.09.2023
- Impfdatum
- 26.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 01.09.2023
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 01.09.2023
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 01.09.2023
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 01.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 01.09.2023
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 01.09.2023
- Impfdatum
- 26.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 01.09.2023
- Impfdatum
- 18.07.2022
- Beginn
- 18.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 01.09.2023
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.09.2023
- Impfdatum
- 06.07.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 01.09.2023
- Impfdatum
- 14.07.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Patient received vaccine after BUD
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 01.09.2023
- Impfdatum
- 08.07.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 01.09.2023
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 01.09.2023
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 01.09.2023
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received a vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 01.09.2023
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 31.08.2023
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 11.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 31.08.2023
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 26.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 31.08.2023
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 31.08.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 08.07.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 31.08.2023
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 31.08.2023
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccinr after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 08.07.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 08.07.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 31.08.2023
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 25.07.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 31.08.2023
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 18.08.2023
- Impfdatum
- 20.10.2022
- Beginn
- 12.08.2023
- Tage bis Beginn
- 296,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthma
Wheezing
Symptomtext
Patient without oxygen requirement at present. No indications for COVID-19 specific therapy. Saturating well on room air with SpO2 greater than 94%. Treated with Decadron 6 mg daily for mild wheezing/asthma, currently resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthma
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension, hyperlipidemia, non-insulin dependent type 2 diabetes mellitus, chronic kidney disease stage 2, restless
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 13.07.2023
- Impfdatum
- 25.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Anosmia
Magnetic resonance imaging head normal
Symptomtext
Anosmia - Lost sense of smell within days of booster shot. Not sure of exact date but, I have no recollection of smelling anything in the month of September so, I lost my sense of smell within days of the 08/25/22 injection date. I had not head trauma, injuries, or infections at the time of the injection or thereafter to account for the loss of smell that followed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anosmia
- Hospital-Tage
- -
- Labordaten
- Examined by Ear Nose & Throat Surgeon on 03/24/2022 - No abnormal findings MRI of the Brain and Brain Stem on 05/16/2023 - No abnormal findings
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- I had long-term heart burn post Covid contracted in Dec 2021 which the Omniprazole cured.
- Andere Medikamente
- Omniprazole
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 06.06.2023
- Impfdatum
- 05.06.2022
- Beginn
- 05.04.2023
- Tage bis Beginn
- 304,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
SARS-CoV-2 test positive
Symptomtext
I had no symptoms but it took a week before the test was negative. I had absolutely nothing I tested for COVID-19 due to my wife's positive test.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test-Positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Coronary artery disease
- Andere Medikamente
- Atorvastatin; Clopidogrel; Metoprolol; Isobirol Mononitrate; Ranolazine; Lisinopril; Alpurinol; Amlodopine; Budesonide; Nitroglycerin PRN
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 91,0
- Geschlecht
- M
- Eingang
- 02.06.2023
- Impfdatum
- 16.06.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 186,0
- Dosis
- 4
- 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 4 vaccines Moderna 2/14/21 lot# 038K20A; Moderna 3/14/21 lot# 044A21A; Moderna 10/27/21 lot#939904 ; Moderna 6/16/22 lot# 059A22A;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 08.03.2023
- Impfdatum
- 08.06.2022
- Beginn
- 03.03.2023
- Tage bis Beginn
- 268,0
- Dosis
- 5
- 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 5 vaccines Moderna 1/14/21 Lot# 025J20A and 011L20A, Moderna 2/11/21 Lot# 025J20A; Moderna 11/20/21 Lot# 013F21A; Moderna 6/8/22 Lot# 059A22A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 26.06.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 39,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Inappropriate schedule of product administration
No adverse event
Symptomtext
No adverse event; Inadvertently administered 51 doses of the monovalent vaccines/ expiration date 13Jul2022 and Date of administration of vaccine was 26Jul2022; 1st dose on 27-Jun-2022 and 2nd dose on 04-Aug-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Inadvertently administered 51 doses of the monovalent vaccines/ expiration date 13Jul2022 and Date of administration of vaccine was 26Jul2022), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st dose on 27-Jun-2022 and 2nd dose on 04-Aug-2022) and NO ADVERSE EVENT (No adverse event) in an 86-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 004M21A and 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 26-Jun-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 04-Aug-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 04-Aug-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Inadvertently administered 51 doses of the monovalent vaccines/ expiration date 13Jul2022 and Date of administration of vaccine was 26Jul2022) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st dose on 27-Jun-2022 and 2nd dose on 04-Aug-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Inadvertently administered 51 doses of the monovalent vaccines/ expiration date 13Jul2022 and Date of administration of vaccine was 26Jul2022), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st dose on 27-Jun-2022 and 2nd dose on 04-Aug-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Inadvertently administered 51 doses of the monovalent vaccines/ expiration date 13Jul2022 and Date of administration of vaccine was 26Jul2022) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st dose on 27-Jun-2022 and 2nd dose on 04-Aug-2022). No concomitant product was reported. It was reported by a pharmacy staff that 51 doses were inadvertently administered of the monovalent vaccines with lot number 004M21A, expiration date 13-Jul-2022. No treatment information was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704260 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704260:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 27.01.2023
- Impfdatum
- 22.06.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure fluctuation
Symptomtext
Long-term blood pressure variation (swings). I monitor my blood pressure regularly because of adverse reactions to several drugs, including oral birth control pills and medications to control depression. After receiving my fourth COVID vaccine, which I was told was the Moderna bivalent but which was apparently not available then, I began having large swings in blood pressure after years of stability at 120/70 (except for medication-induced elevation). For the most part the BP was elevated, anywhere from 140s/80s to 160s/90s, but it would also dip low. In the fall (~Oct, 2022 I began reducing my nortriptylene and eventually got off it entirely, with no reduction in blood pressure swings. I began lisinopril (5 mg/day, now increased to 7.5 mg/day, taken at bedtime) which was previous successful in reducing SSRI-induced elevated BP, and this has reduced BP to, in general, 130s/80s, but I still experience wide swings, mostly elevations, especially towards the end of the day as the lisinopril wears off.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure fluctuation
- Hospital-Tage
- -
- Labordaten
- Monitoring of blood pressure at home: daily Documentation of high blood pressure at primary care provider's office: 11/22/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Major depressive disorder
- Andere Medikamente
- nortriptylene (5 mg/day), duloxetine (20 mg/day), aspirin (81 mg/day), Vit D (2000/day)
- Allergien
- sulfa antibiotics
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 20.01.2023
- Impfdatum
- 17.01.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
monovalent Moderna Covid 19 bivalent vaccine booster dose instead of a bivalent booster dose on 1/17/2023; No adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of WRONG PRODUCT ADMINISTERED (monovalent Moderna Covid 19 bivalent vaccine booster dose instead of a bivalent booster dose on 1/17/2023) and NO ADVERSE EVENT (No adverse event) in a 60-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. Previously administered products included for COVID-19 prophylaxis: Moderna COVID-19 Vaccine (Lot number 037K20A, expiration date was 22-Jun-2021, route of administration: Right Arm ) on 29-Dec-2020, Moderna COVID-19 Vaccine (Lot number 043L20A, expiration date was 07-Jul-2021, route of administration: Right Arm ) on 26-Jan-2021, Moderna COVID-19 Vaccine (Booster dose, Lot number 047C21A, expiration date 7-Nov-2021, route of administration: Left Arm ) on 26-Oct-2021, Moderna COVID-19 Vaccine (2nd Booster dose, Lot number 066K21A, expiration date 7-Jul-2022 and route of administration: Left Arm ) on 25-Apr-2022. Past adverse reactions to the above products included No adverse event with Moderna COVID-19 Vaccine, Moderna COVID-19 Vaccine, Moderna COVID-19 Vaccine and Moderna COVID-19 Vaccine. On 17-Jan-2023, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced WRONG PRODUCT ADMINISTERED (monovalent Moderna Covid 19 bivalent vaccine booster dose instead of a bivalent booster dose on 1/17/2023) and NO ADVERSE EVENT (No adverse event). At the time of the report, WRONG PRODUCT ADMINISTERED (monovalent Moderna Covid 19 bivalent vaccine booster dose instead of a bivalent booster dose on 1/17/2023) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for WRONG PRODUCT ADMINISTERED (monovalent Moderna Covid 19 bivalent vaccine booster dose instead of a bivalent booster dose on 1/17/2023). No concomitant medicine were reported. It was reported that the patient received a 0.25ml Pediatric Dose instead of a 0.5ml Adult dose. No treatment medicine were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 16.01.2023
- Impfdatum
- 13.10.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 62,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bronchitis
Ear infection
Influenza virus test negative
Respiratory tract congestion
SARS-CoV-2 test negative
Sinusitis
Symptomtext
I had congestion that led to a sinus and ear and progressed to bronchitis. I was tested for COVID-19, influenza both came back negative. I was given antibiotic medication to help get rid of the sinus and ear infection. I am still battling the bronchitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bronchitis
- Hospital-Tage
- -
- Labordaten
- 3 PCR COVID-19 test negative, influenza - negative
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 14.01.2023
- Impfdatum
- 26.05.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 8,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthritis
Blood test
Inflammatory marker test
Polyarthritis
X-ray limb
Symptomtext
Since receiving the vaccine, I have had multiple site of arthritis inflammation, including both knees and my right foot. I have never had any issues with arthritis prior. The symptoms have gotten increasingly worse as well since receiving the bivalvent Moderna booster on 9/9/2022. Lot # AS714SB. I have needed cortisone shot treatments and have my third visit to orthopedics Monday, 1/16,2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthritis
- Hospital-Tage
- -
- Labordaten
- X-rays of left knee and right foot.,anticipate x-rays of my right knee at above listed visit. Blood work for inflammatory markers.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension History of thyroidectomy
- Andere Medikamente
- Losartan 50mg daily Levothyroxine 88 mcg daily Estradiol patch two times weekly
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 09.01.2023
- Impfdatum
- 06.10.2022
- Beginn
- 07.01.2023
- Tage bis Beginn
- 93,0
- Dosis
- 4
- 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 in the ER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 02.01.2023
- Impfdatum
- 29.06.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Herpes ophthalmic
Symptomtext
Ocular shingles
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes ophthalmic
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Slight hypertension
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 22.11.2022
- Impfdatum
- 02.11.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Symptomtext
Given Moderna Bivalent Booster on 11/2/2022 before Primary Series was complete. No adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- Administered Moderna Primary Series dose on 11/8/2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 05.09.2022
- Beginn
- 05.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
No adverse event; possible administration of Moderna monovalent booster instead of bivalent booster; This spontaneous case was reported by a nurse and describes the occurrence of WRONG PRODUCT ADMINISTERED (possible administration of Moderna monovalent booster instead of bivalent booster) and NO ADVERSE EVENT (No adverse event) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 05-Sep-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Sep-2022, the patient experienced WRONG PRODUCT ADMINISTERED (possible administration of Moderna monovalent booster instead of bivalent booster). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, WRONG PRODUCT ADMINISTERED (possible administration of Moderna monovalent booster instead of bivalent booster) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for WRONG PRODUCT ADMINISTERED (possible administration of Moderna monovalent booster instead of bivalent booster). No concomitant medication was provided. It was reported that patient had received a Moderna COVID-19 booster on 5 Sep 2022. However, it was incorrectly recorded as a Pfizer booster on her vaccination card by the provider. Treatment medication was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 08.07.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 55,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Impaired driving ability
Vertigo
Symptomtext
I developed severe vertigo on September 14, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Impaired driving ability
- Hospital-Tage
- -
- Labordaten
- I went to urgent care on Sept.28, 2022 and had neurological tests done and was referred to a head neck surgeon. I had the head neck surgeon appointment on Oct.4, 2022 and was prescribed Sudafed and anti nausea medication. On Oct.12, 2022 I was prescribed Prednisone to help with vertigo symptoms and was referred to a neurologist whom I will see on Dec. 28, 2022. I am still suffering from vertigo and can't drive.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Migraine
- Andere Medikamente
- none
- Allergien
- Latex, Erythromicin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Symptomtext
Monovalent Covid-19 (Pfizer and Moderna) boosters were administered to 24 patients after FDA removed their authorization; these errors occured from 9/1/22 to 9/7/2022. No more monovalent booster vaccines administeredafter we received the Bivalent Boosters on 9/8/2022. No adverse event noted. RN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 01.11.2022
- Impfdatum
- 15.06.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 76,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Computerised tomogram
Diplopia
Heart valve incompetence
Magnetic resonance imaging head
Rectal haemorrhage
Symptomtext
Double Vision, Went to ER for a possible TIA. ER wanted to do an Echo Cardiogram, but I had that done the next week. Cat scan and MRI of the head were performed. Blood tests were run. Overnight in the hospital where they put me on a Statin and advised to use a low dose aspirin. Saw my doctor 9/3/22, who ordered an Echo Cardiogram for 9/22. This revealed a leaky left valve. Stain and aspirin exacerbated unrelated rectal bleeding, leading to blood loss and a hematologist consult.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- 2,0
- Labordaten
- I didn't see the test results.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Gp Gastro Puresis; Fibromyalgia; Osteo Arthritis; Stroke
- Andere Medikamente
- Omeprazole; Vitamin D3, Multivitamin; Presvision; Vitamin B; Tums
- Allergien
- Dust
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 27.10.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Symptomtext
Monovalent Covid-19 (Pfizer and Moderna) boosters were administered to 24 patients after FDA removed their authorization; these errors occured from 9/1/22 to 9/7/2022. No more monovalent booster vaccines administeredafter we received the Bivalent Boosters on 9/8/2022. No adverse event noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Hypothyroidism; Anemia; High Cholesterol; Hiatal Hernia; Gastritis; Vitamin D deficiency.
- Andere Medikamente
- Tylenol
- Allergien
- N.K.A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 27.10.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Symptomtext
Monovalent Covid-19 (Pfizer and Moderna) boosters were administered to 24 patients after FDA removed their authorization; these errors occured from 9/1/22 to 9/7/2022. No more monovalent booster vaccines administeredafter we received the Bivalent Boosters on 9/8/2022. No adverse event noted. RM,RN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- Mixed Hyperlipidemia; Obesity; Hypertension; Chronic Kidney Disease Stage 3; HYPERBETALIPOPROTEINEMIA; Vit D deficien
- Andere Medikamente
- unknown
- Allergien
- N.K.D.A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 27.10.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Symptomtext
Monovalent Covid-19 (Pfizer and Moderna) boosters were administered to 24 patients after FDA removed their authorization; these errors occured from 9/1/22 to 9/7/2022. No more monovalent booster vaccines administeredafter we received the Bivalent Boosters on 9/8/2022. No adverse event noted. RN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 19.10.2022
- Impfdatum
- 01.06.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 44,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Irritable bowel syndrome
Symptomtext
Developed IBS and continue to have trouble. Went to primary care doctor and gastroentorolgist. They said wait and see if gets better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Irritable bowel syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 22.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient received 0.5mL of moderna (original monovalent) vaccine, instead of bivalent moderna dose. Patient has been informed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 22.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Patient received 0.5mL of moderna (original monovalent) vaccine, instead of bivalent moderna dose. Patient has been informed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient received 0.5mL of moderna (original monovalent) vaccine, instead of bivalent moderna dose. Patient has been informed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Propoxyphene, phenobarbitol
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 22.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient received 0.5mL of the original moderna vaccination, instead of the bivalent booster. Patient was informed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 22.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient received 0.5mL of the original moderna vaccination, instead of the bivalent booster. Patient was informed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 22.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient was incorrectly given the monovalent moderna vaccine, instead of the bivalent moderna vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Administered Moderna Monovalent .25ml as booster dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Victoza
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Moderna Monovalent .25 ml given as booster dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Keflex- Rash
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
Administered .25 ml of Moderna monovalent as booster. No adverse effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
Administered 0.25 Moderna Monovalent as booster dose. No adverse reaction noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- Paxil- Rash
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 10.08.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
vaccine was given after the 30 day beyond use date; No adverse event; vaccine was given after the 30 day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine was given after the 30 day beyond use date), PRODUCT STORAGE ERROR (vaccine was given after the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) in a 33-year-old male patient who received mRNA-1273 (Spikevax) (batch nos. 052B22A and 059A22A) for COVID-19 vaccination. No Medical History information was reported. On 10-Aug-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 07-Sep-2022, received second dose of mRNA-1273 (Spikevax) (Intramuscular) dosage was changed to 1 dosage form. On 07-Sep-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine was given after the 30 day beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vaccine was given after the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine was given after the 30 day beyond use date), PRODUCT STORAGE ERROR (vaccine was given after the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (vaccine was given after the 30 day beyond use date) and PRODUCT STORAGE ERROR (vaccine was given after the 30 day beyond use date). No Concomitant medications were provided. It was reported that the second dose of the vaccine was given after the 30 day beyond use date. That patient had not reported any symptoms. No additional doses were administered in response at that time. Patient received Monovalent product from Individual vial with vial size of 5.5 mL. Vial was initially stored in the refrigerator on 6 Aug 2022 and did not undergo temperature excursions. No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 11.06.2022
- Beginn
- 06.09.2022
- Tage bis Beginn
- 87,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Insomnia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I received my second Moderna booster for COVID-19 on 6/11/2022. On the evening of 9/6/2022, I developed a persistent cough. I thought it was caused by allergies, and I had trouble sleeping that night. (As a matter of fact, I have had trouble sleeping ever since.). On 9/7/2022, I called my PCP's office to try to book an appointment, but they were booked up. They offered to do a telehealth visit, but I declined, as I have a number of allergies anyway. Through the following days, my cough became more persistent, and I developed a runny nose. On the night of 9/9/2022, I took a home COVID-19 test and got a positive result. On 9/10/2022, I went to an urgent care, and they gave me a number to call to inquire about getting medication. I called the number, and I was prescribed PAXLOVID, which I started taking that night. While I was at the urgent care, I also underwent a rapid test for COVID-19 and got another positive result. Since I've begun taking the PAXLOVID, the symptoms have begun diminishing. It got rid of the runny nose, though I still have a cough. I'm taking OTC EQUATE cold and flu medicine and ADVIL, and they are helping ease the cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test 9/9/2022 positive result; 9/10/2022 rapid test for COVID-19 at urgent care clinic positive result.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypercholesterolemia.
- Andere Medikamente
- Atorvastatin; men's multivitamin; fish oil; vitamin D; vitamin C.
- Allergien
- None.
- Vorherige Impfungen
- With the first 2 Moderna vaccines and the second Moderna booster for COVID-19, I had chills, lethargy, and muscle aches for abou
- Staat
- GA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 09.09.2022
- Impfdatum
- 09.06.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 85,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Paranasal sinus hypersecretion
Respiratory tract congestion
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
So on Friday 9/2/22 I just had a little bit of drainage but I get that with my sinuses and drank an Emergence and on Sunday I was lying down and when I got up I felt like my sinuses were full. On Monday I was feeling congested and I took a home COVID-19 test and it was positive and I went to the urgent care and took a PCR COVID -19 test and it was positive and they prescribed me a Anti-viral Molunpiravir and a nose spray. I am totally better an walked 2.5 miles this morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test Home Positive 9/5/22 COVID -19 PCR test Positive 9/5/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin; Caltrate;
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 22.08.2022
- Beginn
- 15.08.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Demyelinating polyneuropathy
Inflammation
Symptomtext
patient was admitted on 8-15-22 with weakness which was found to be acute inflammatory demyelinating polyneuropathy. The patient was then transferred to the Inpatient rehab unit on 8-30-22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 06.09.2022
- Impfdatum
- 25.07.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Atrial fibrillation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anticoagulant therapy
- Hospital-Tage
- -
- Labordaten
- 2 visits to the Emergency Room. Eliquis 5mg started along with Multaq 400mg. Multaq stopped 7/4/2022 and Amiodorone 400mg started. As of today 9/6/2022 still in afib. Appt on Thu 9/8/2022 with my Cardiologist.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN
- Andere Medikamente
- Lobatelol, Nefedepine, Losartan, Pravastatin, HCTZ, 40meq K
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 29.08.2022
- Impfdatum
- 24.06.2022
- Beginn
- 30.07.2022
- Tage bis Beginn
- 36,0
- Dosis
- 4
- 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 4 vaccines Moderna 2/20/21 Lot# 031L20A; Moderna 3/20/21 Lot# 030A21A; Moderna 12/1/21 Lot# 013F21A; Moderna 6/24/22 Lot# 059A22A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 23.08.2022
- Impfdatum
- 04.06.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Administration Error: Patient is received, which comes to administer his 2nd dose of Moderna, which must have received 0.5ml, however the nurse administered 0.25ml as if it were a booster dose. The patient is notified that he must be inoculated again with 0.25ml to complete the dose that the patient was supposed to receive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 18.08.2022
- Impfdatum
- 23.06.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 50,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asymptomatic COVID-19
SARS-CoV-2 test positive
Symptomtext
Pt w/out s/s associated with Covid. Pt in hospital w/other concerns. Pt +Covid PCR while in hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 13.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint injury
Laboratory test
Symptomtext
Felt like "rubber band snapped" at her ankle. Being evaluated for tendonitis or rupture
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Joint injury
- Hospital-Tage
- -
- Labordaten
- pending
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Lipitor 20, Cozaar 50, Norvasc 5, Glipizide ER 5, Januvia 50
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 06.08.2022
- Impfdatum
- 30.06.2022
- Beginn
- 30.07.2022
- Tage bis Beginn
- 30,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
Tested positive for Covid after her 1st dose; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (Tested positive for Covid after her 1st dose) in a 26-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059A22A) for COVID-19 vaccination. No Medical History information was reported. On 30-Jun-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 30-Jul-2022, after starting mRNA-1273 (Spikevax), the patient experienced COVID-19 (Tested positive for Covid after her 1st dose). At the time of the report, COVID-19 (Tested positive for Covid after her 1st dose) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 30-Jul-2022, SARS-CoV-2 test: (Positive) Positive. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. No concomitant medications were reported. It was reported that patient has not gotten her 2nd dose. Patient wanted to know how long after testing negative could she get her 2nd dose. No treatment medications were reported. Company Comment: This spontaneous case concerns a 26 year old female patient with no medical history reported , who experienced non-serious , unexpected , AESI of Covid 19 which occurred one month post vaccination with the dose 1 of mRNA-1273 vaccine. This patient test positive for SARS-COV 2 test last July 30, 2022. Treatment information , results of other laboratories/diagnostic procedures were not reported and there was no report if any medical consult was done. Outcome of the event is unknown. The benefit -risk relationship of mRNA -1273 ( Moderna Covid 19 Vaccine) is not affected by this report.; Sender's Comments: This spontaneous case concerns a 26 year old female patient with no medical history reported , who experienced non-serious , unexpected , AESI of Covid 19 which occurred one month post vaccination with the dose 1 of mRNA-1273 vaccine. This patient test positive for SARS-COV 2 test last July 30, 2022. Treatment information , results of other laboratories/diagnostic procedures were not reported and there was no report if any medical consult was done. Outcome of the event is unknown. The benefit -risk relationship of mRNA -1273 ( Moderna Covid 19 Vaccine) is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220730; Test Name: COVID-19 virus test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 05.08.2022
- Impfdatum
- 24.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; The vaccine was given 1 day past beyond use date of 23-Jun-2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vaccine was given 1 day past beyond use date of 23-Jun-2022) and NO ADVERSE EVENT (No adverse event) in a 56-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 24-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vaccine was given 1 day past beyond use date of 23-Jun-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vaccine was given 1 day past beyond use date of 23-Jun-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (The vaccine was given 1 day past beyond use date of 23-Jun-2022). No concomitant medications were reported. It was reported that vaccine was given 1 day past beyond use date of 23-Jun-2022. The moderna was contacted and the lot was analyzed. It was stated that as per moderna this lot was still active and patient was not needed to be revaccinated. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 04.08.2022
- Impfdatum
- 03.08.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
wrong dose given
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
- 03.08.2022
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 01-Jul-2022 past the BUD date 23-Jun-2022/ administration error) and NO ADVERSE EVENT (No adverse event) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 vaccination. It was unknown if the patient was ever diagnosed with or tested COVID-19 positive. It was also unknown if there was any acute illness at the time of vaccination or any chronic or long-standing health conditions of the patient. On 01-Jul-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 01-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 01-Jul-2022 past the BUD date 23-Jun-2022/ administration error). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 01-Jul-2022 past the BUD date 23-Jun-2022/ administration error) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 01-Jul-2022 past the BUD date 23-Jun-2022/ administration error). Concomitant medications details were not reported. It was reported vaccine was administered 8 day past the BUD of 23 Jun 2022. Reporter further reported that as per Moderna, the product was still active and patient need not to be re-vaccinated. The event did not cause patient to seek the medical care. There was no other potential caused. It was unknown if patient same event in past. The treatment details were not reported. This case was linked to US-MODERNATX, INC.-MOD-2022-599989 (E2B Linked Report). Sender's Comments: US-MODERNATX, INC.-MOD-2022-599989: Master case.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if the patient was ever diagnosed with or tested COVID-19 positive. It was also unknown if there was any acute illness at the time of vaccination or any chronic or long-standing health conditions of the patient.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 24.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vaccine was given one day past BUD) and NO ADVERSE EVENT (No adverse event) in a 75-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 24-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vaccine was given one day past BUD). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vaccine was given one day past BUD) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (The vaccine was given one day past BUD). No concomitant medication was reported. It was unknown that the patient ever got COVID-19. BUD date was given as 23-Jun-22. No treatment information were provided. This case was linked to MODERNATX, INC.-MOD-2022-599989 (E2B Linked Report). Sender's Comments: MODERNATX, INC.-MOD-2022-599989:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Product administration error
Symptomtext
No adverse event; The vaccine was given BUD; Administration error; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vaccine was given BUD), PRODUCT ADMINISTRATION ERROR (Administration error) and NO ADVERSE EVENT (No adverse event) in an 88-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. It was also unknown if there was any acute illness at the time of vaccination or any chronic or long standing health conditions of the patient. On 27-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 27-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vaccine was given BUD) and PRODUCT ADMINISTRATION ERROR (Administration error). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vaccine was given BUD) and NO ADVERSE EVENT (No adverse event) outcome was unknown and PRODUCT ADMINISTRATION ERROR (Administration error) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (The vaccine was given BUD) and PRODUCT ADMINISTRATION ERROR (Administration error). No concomitant medication was reported. It was unknown if the patient was ever diagnosed with or tested COVID-19 positive. BUD date was given as 23-Jun-22. Reporter further reported that as per Moderna, the lot was still active and patient need not to be re-vaccinated. No treatment medication was reported. This case was linked to US-MODERNATX, INC.-MOD-2022-599989 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-599989:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was also unknown if there was any acute illness at the time of vaccination or any chronic or long standing health conditions of the patient.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 26.06.2022
- Beginn
- 26.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
No adverse event; The vaccine was given 2 days past BUD; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vaccine was given 2 days past BUD) and NO ADVERSE EVENT (No adverse event) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 26-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 26-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vaccine was given 2 days past BUD). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vaccine was given 2 days past BUD) had resolved and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (The vaccine was given 2 days past BUD). No concomitant medication were provided No treatment details were provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (This vaccine was given 4 days past the beyond use date of 23-Jun-22) and NO ADVERSE EVENT (No adverse event) in an 86-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 27-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 27-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (This vaccine was given 4 days past the beyond use date of 23-Jun-22). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (This vaccine was given 4 days past the beyond use date of 23-Jun-22) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (This vaccine was given 4 days past the beyond use date of 23-Jun-22). No concomitant drug information was provided. Beyond use date of the product was reported as 23-Jun-2022. It was unknown if the patient was ever diagnosed with or tested COVID-19 positive. It was also unknown if there was any acute illness at the time of vaccination or nay chronic or long standing health conditions of the patient. Reporter further reported that as per Moderna, the product was still active and patient need not to be re-vaccinated. No treatment drug information was provided. This case was linked to MOD-2022-599989 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 02.07.2022
- Beginn
- 02.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Product administration error
Symptomtext
No adverse event; administration error; The vaccine was given 9 days past BUD; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT ADMINISTRATION ERROR (administration error), EXPIRED PRODUCT ADMINISTERED (The vaccine was given 9 days past BUD) and NO ADVERSE EVENT (No adverse event) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 vaccination. No Medical History information was reported. On 02-Jul-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 02-Jul-2022, the patient experienced PRODUCT ADMINISTRATION ERROR (administration error) and EXPIRED PRODUCT ADMINISTERED (The vaccine was given 9 days past BUD). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, PRODUCT ADMINISTRATION ERROR (administration error) had resolved and EXPIRED PRODUCT ADMINISTERED (The vaccine was given 9 days past BUD) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for PRODUCT ADMINISTRATION ERROR (administration error) and EXPIRED PRODUCT ADMINISTERED (The vaccine was given 9 days past BUD). No concomitant drug information was provided. Beyond use date of the product was reported as 23-Jun-2022. It was unknown if the patient was ever diagnosed with or tested COVID-19 positive. It was also unknown if there was any acute illness at the time of vaccination or any chronic or long standing health conditions of the patient. Reporter further reported that as per Moderna, the product was still active and patient need not to be re-vaccinated. No treatment drug information was provided. This case was linked to MOD-2022-599989 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vaccine was given 7 days past beyond use date of 23-Jun-2022) and NO ADVERSE EVENT (No adverse event) in a 52-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 30-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 30-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vaccine was given 7 days past beyond use date of 23-Jun-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vaccine was given 7 days past beyond use date of 23-Jun-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (The vaccine was given 7 days past beyond use date of 23-Jun-2022). No concomitant medications were reported. It was reported that vaccine was given 7 days past beyond use date of 23-Jun-2022. The moderna was contacted and the lot was analyzed. It was stated that as per moderna this lot was still active and patient was not needed to be revaccinated. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 24.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 24-Jun-2022 past the BUD date 23-Jun-2021.) and NO ADVERSE EVENT (No adverse event) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 vaccination. No Medical History information was reported. On 24-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 24-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 24-Jun-2022 past the BUD date 23-Jun-2021.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 24-Jun-2022 past the BUD date 23-Jun-2021.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 24-Jun-2022 past the BUD date 23-Jun-2021.). Concomitant medications details were not reported by the reporter. It was reported vaccine was administered 1 day past the BUD. The event did not cause patient to seek medical care. Treatment details were not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 50,0
- Geschlecht
- U
- Eingang
- 29.07.2022
- Impfdatum
- 20.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vaccine was put in the refrigerator on 15-Jun-2022 for more than 30 days and administered on 20-Jul-2022; administered with the vaccine that has been stored in the refrigerator for more than 30 days; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with the vaccine that has been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (The vaccine was put in the refrigerator on 15-Jun-2022 for more than 30 days and administered on 20-Jul-2022) in a 50-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 20-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with the vaccine that has been stored in the refrigerator for more than 30 days). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vaccine was put in the refrigerator on 15-Jun-2022 for more than 30 days and administered on 20-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered with the vaccine that has been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (The vaccine was put in the refrigerator on 15-Jun-2022 for more than 30 days and administered on 20-Jul-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications details were not reported by the reporter. Patient had received first booster. Pharmacist reported that they administered 7 doses of the COVID-19 vaccine that had been stored in the refrigerator for more than 30 days. The vaccine was initially stored in the refrigerator on 15-Jun-2022 and administered on two dates 3 doses on 19-Jul-2022 and 4 doses on 20-Jul-2022. Treatment details were not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 84,0
- Geschlecht
- U
- Eingang
- 29.07.2022
- Impfdatum
- 20.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was put in the refrigerator on 15-Jun-2022 and administered on 20-Jul-2022; Administered with the vaccine that has been stored in the refrigerator for more than 30 days; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that has been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (Vaccine was put in the refrigerator on 15-Jun-2022 and administered on 20-Jul-2022) in an 84-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 20-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that has been stored in the refrigerator for more than 30 days). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was put in the refrigerator on 15-Jun-2022 and administered on 20-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that has been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (Vaccine was put in the refrigerator on 15-Jun-2022 and administered on 20-Jul-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication list was not provided. The patient received second booster on 20 Jul 2022. The vaccine was put in the refrigerator on 15 Jun 2022. 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
- WV
- Alter
- 65,0
- Geschlecht
- U
- Eingang
- 29.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was put in the refrigerator on 15-Jun-2022 and administered on 19-Jul-2022; Administered with the vaccine that has been stored in the refrigerator for more than 30 days; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that has been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (Vaccine was put in the refrigerator on 15-Jun-2022 and administered on 19-Jul-2022) in a 65-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 19-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that has been stored in the refrigerator for more than 30 days). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was put in the refrigerator on 15-Jun-2022 and administered on 19-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that has been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (Vaccine was put in the refrigerator on 15-Jun-2022 and administered on 19-Jul-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient was administered second booster on 19-Jul-2022. Concomitant medication list was not provided. Vaccine was put in the refrigerator on 15-Jun-2022. 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
- VA
- Alter
- 45,0
- Geschlecht
- U
- Eingang
- 28.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that has been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (Vaccine was put in the refrigerator on 15-Jun-2022, patient administered Moderna vaccine on 19-Jul-2022) in a 45-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 19-Jul-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 19-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that has been stored in the refrigerator for more than 30 days). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was put in the refrigerator on 15-Jun-2022, patient administered Moderna vaccine on 19-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that has been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (Vaccine was put in the refrigerator on 15-Jun-2022, patient administered Moderna vaccine on 19-Jul-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 52,0
- Geschlecht
- U
- Eingang
- 28.07.2022
- Impfdatum
- 20.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vaccine was put in the refrigerator on 15-Jun-2022 for more than 30 days and administered on 20-Jul-2022; Administered with the vaccine that had been stored in the refrigerator for more than 30 days; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that had been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (The vaccine was put in the refrigerator on 15-Jun-2022 for more than 30 days and administered on 20-Jul-2022) in a 52-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 20-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that had been stored in the refrigerator for more than 30 days). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vaccine was put in the refrigerator on 15-Jun-2022 for more than 30 days and administered on 20-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that had been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (The vaccine was put in the refrigerator on 15-Jun-2022 for more than 30 days and administered on 20-Jul-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided by the reporter. The patient received second booster. 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
- WV
- Alter
- 75,0
- Geschlecht
- U
- Eingang
- 28.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was put in the refrigerator on 15-Jun-2022, patient administerd Moderna vaccine on 19-Jul-2022; administered with the vaccine that has been stored in the refrigerator for more than 30 days; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with the vaccine that has been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (Vaccine was put in the refrigerator on 15-Jun-2022, patient administerd Moderna vaccine on 19-Jul-2022) in a 75-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 19-Jul-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with the vaccine that has been stored in the refrigerator for more than 30 days). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was put in the refrigerator on 15-Jun-2022, patient administerd Moderna vaccine on 19-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered with the vaccine that has been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (Vaccine was put in the refrigerator on 15-Jun-2022, patient administerd Moderna vaccine on 19-Jul-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication details were not reported by the reporter. Treatment details was not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 66,0
- Geschlecht
- U
- Eingang
- 28.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Administered with the vaccine that has been stored in the refrigerator for more than 30 days; Administered with the vaccine that has been stored in the refrigerator for more than 30 days; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that has been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (Administered with the vaccine that has been stored in the refrigerator for more than 30 days) in a 66-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 19-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that has been stored in the refrigerator for more than 30 days). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Administered with the vaccine that has been stored in the refrigerator for more than 30 days). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine that has been stored in the refrigerator for more than 30 days) and PRODUCT STORAGE ERROR (Administered with the vaccine that has been stored in the refrigerator for more than 30 days) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications details were not reported by the reporter. Patient had received second booster. Pharmacist reported that they administered 7 doses of the COVID-19 vaccine that had been stored in the refrigerator for more than 30 days. The vaccine was initially stored in the refrigerator on 15-Jun-2022 and administered on two dates 19-Jul-2022 (3 doses on 11:11AM, 11:15AM, 02:27PM), 20-Jul-2022 (4 doses on 09:43AM, 01:31PM, 03:05 PM, 06:18 PM). Treatment details were not reported by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 25-Jul-2022: Follow-up received as patient details and product information was updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 06.07.2022
- Beginn
- 24.07.2022
- Tage bis Beginn
- 18,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated and fully boosted. COVID breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 26.07.2022
- Impfdatum
- 25.07.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
PATIENT WAS GIVEN 0.25 ML OF MODERNA (ADULT) VACCINE. NURSING STAFF SPOKE WITH THE PATIENT'S MOTHER TO INFORM HER OF THE ERROR. PATIENT'S MOTHER STATED THAT THE PATIENT IS DOING FINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Patient was given 0.25 mL IM of the right thigh (Moderna Adult - Lot #059A22A)
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial was stored in refrigerator on 26-May-2022 and administered on 27-Jun-2022; Vaccine administered 1 days after beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered 1 days after beyond use date) and PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 26-May-2022 and administered on 27-Jun-2022) in a 62-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 vaccination. Patient had never been diagnosed with/ tested positive for COVID-19. Patient did not have acute illnesses at the time of vaccination and up to one month before vaccine. Concurrent medical conditions included Blood pressure, Cholesterol and Coagulation disorder. Concomitant products included METOPROLOL for Blood pressure, ATORVASTATIN for Cholesterol, CLOPIDOGREL BISULFATE (PLAVIX) for Coagulation disorder. On 27-Jun-2022 at 10:00 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 27-Jun-2022 at 10:00 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered 1 days after beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 26-May-2022 and administered on 27-Jun-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered 1 days after beyond use date) and PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 26-May-2022 and administered on 27-Jun-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Number of doses or vails were reported as 7. The patient had reported no side effects. The vial did not undergo any temperature excursion. No treatment details were provided. This case was linked to MODERNATX, INC.-MOD-2022-601207 (E2B Linked Report).; Sender's Comments: MODERNATX, INC.-MOD-2022-601207:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood pressure; Cholesterol; Coagulation disorder
- Vorgeschichte
- Comments: Patient had never been diagnosed with/ tested positive for COVID-19. Patient did not have acute illnesses at the time of vaccination and up to one month before vaccine.
- Andere Medikamente
- METOPROLOL; ATORVASTATIN; PLAVIX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 28.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered 2 days beyond use date) and PRODUCT STORAGE ERROR (Vaccine administered 2 days after beyond use date) in a 55-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. Concurrent medical conditions included Diabetes. Concomitant products included METFORMIN for an unknown indication. On 28-Jun-2022 at 8:00 PM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 28-Jun-2022 at 8:00 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered 2 days beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine administered 2 days after beyond use date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered 2 days beyond use date) and PRODUCT STORAGE ERROR (Vaccine administered 2 days after beyond use date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient born with twins. Number of doses/vials was reported as 7. On 26-May-2022, the vial was initially stored in the refrigerator. Vaccine was administered from 26-Jun-2022 to 4-Jul-2022. Vial did not undergo any temperature excursions. No treatment drug were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Diabetes
- Vorgeschichte
- -
- Andere Medikamente
- METFORMIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 23.07.2022
- Impfdatum
- 29.06.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial was stored in refrigerator on 26-May-2022 and administered on 29-Jun-2022; Vaccine administered 3 days after beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered 3 days after beyond use date) and PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 26-May-2022 and administered on 29-Jun-2022) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 29-Jun-2022 at 10:30 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 29-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered 3 days after beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 26-May-2022 and administered on 29-Jun-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered 3 days after beyond use date) and PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 26-May-2022 and administered on 29-Jun-2022) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. The patient had never been diagnosed with or tested positive for COVID 19. Acute illness at the time of vaccination and up to one month before was reported as none. No concomitant medications were reported. The number of doses or vails were reported as 7. The vial was initially stored in the refrigerator on 26-May-2022. The vial had not undergone any temperature excursion. The patient had reported no side effects. Treatment details were not reported by the reporter. This case was linked to MOD-2022-601207 (E2B Linked Report).; Sender's Comments: MOD-2022-601207:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 23.07.2022
- Impfdatum
- 29.06.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
the vial was initially stored in the refrigerator 26May2022; Vaccine administered 3 days after beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered 3 days after beyond use date) and PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator 26May2022) in a 21-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 vaccination. The patient had never diagnosed or tested positive for COVID-19. It was reported that patient had no acute illness at the time of vaccination and up to one month before. No chronic or long standing health conditions were reported. On 29-Jun-2022 at 11:00 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 29-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered 3 days after beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator 26May2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered 3 days after beyond use date) and PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator 26May2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication information provided. No other vaccines were given to patient when Moderna vaccine was administered. No other vaccines were received within one month prior to any dose of Moderna Covid-19 vaccine. On 26-May-2022 vial was initially moved to refrigerator. The vial did not undergone any temperature excursion. No treatment medication information provided. This case was linked to US-MODERNATX, INC.-MOD-2022-601207 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-601207:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had never diagnosed or tested positive for COVID-19. It was reported that patient had no acute illness at the time of vaccination and up to one month before. No chronic or long standing health conditions were reported.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 28.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine administered 2 days after beyond use date; Vaccine administered 2 days after beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered 2 days after beyond use date) and PRODUCT STORAGE ERROR (Vaccine administered 2 days after beyond use date) in a 55-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 vaccination. Patient had been never diagnosed or tested positive for Covid-19. Non acute illness at the time of vaccination and upto one month before. No other vaccines given on the same day as moderna covid-19 vaccine. No other vaccines received within one month prior to any dose of moderna covid-19 vaccine. Concurrent medical conditions included Asthma. Concomitant products included MONTELUKAST SODIUM (SINGULAIR) and AZELASTINE for Asthma. On 28-Jun-2022 at 8:00 PM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 28-Jun-2022 at 8:00 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered 2 days after beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine administered 2 days after beyond use date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered 2 days after beyond use date) and PRODUCT STORAGE ERROR (Vaccine administered 2 days after beyond use date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. The patients had reported no side effects. Number of doses or vails were reported as 7. The vial was initially stored in the refrigerator on 26-May-2022. The vial did not undergo any temperature excursion. Treatment details were not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma
- Vorgeschichte
- Comments: Patient had been never diagnosed or tested positive for Covid-19. Non acute illness at the time of vaccination and upto one month before. No other vaccines given on the same day as moderna covid-19 vaccine. No other vaccines received within one month prior to any dose of moderna covid-19 vaccine.
- Andere Medikamente
- SINGULAIR; AZELASTINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial was initially stored in the refrigerator on 14Jun2022 and dose administered on 15-Jul-2022; Administered a Moderna Covid-19 vaccine two days after 30 day expiration; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered a Moderna Covid-19 vaccine two days after 30 day expiration) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 14Jun2022 and dose administered on 15-Jul-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Jul-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 15-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered a Moderna Covid-19 vaccine two days after 30 day expiration). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 14Jun2022 and dose administered on 15-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered a Moderna Covid-19 vaccine two days after 30 day expiration) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 14Jun2022 and dose administered on 15-Jul-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Vial was initially stored in the refrigerator on 14-Jun-2022. Vial did not undergo any temperature excursions. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient received 0.25mL Moderna COVID-19 vaccine (red cap) booster dose on 07/22/2022. His primary vaccination was Pfizer-BioNTech COVID-19 vaccine on 11/04/2021 and 12/10/2021. CDC recommends children ages 5-17 who received Pfizer-BioNTech primary series get Pfizer-BioNTech for a booster dose. In this case, Moderna is not indicated as a booster dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 18.07.2022
- Beginn
- 18.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
The quality related event is a dose administration error. Review of the patient history reveals the person received four covid-19 vaccine doses previously on 03/04/21; 04/01/21; 11/19/21; and 06/09/2022. The new booster dose today on 7/18/22 is dose number 5 which is an error. The recipient reports no adverse response to the dose number 5.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
This vaccine was given 7 dayS past the BUD (6/23/22). Moderna was contacted and the lot was analyzed. Per Moderna this lot was still active and the patient did not need to be revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 26.06.2022
- Beginn
- 26.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
This vaccine was given 3 dayS past the BUD (6/23/22). Moderna was contacted and the lot was analyzed. Per Moderna this lot was still active and the patient did not need to be revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 24.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
This vaccine was given 1 day past the BUD (6/23/22). Moderna was contacted and the lot was analyzed. Per Moderna this lot was still active and the patient did not need to be revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 24.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
This vaccine was given 1 day past the BUD (6/23/22). Moderna was contacted and the lot was analyzed. Per Moderna this lot was still active and the patient did not need to be revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 02.07.2022
- Beginn
- 02.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
This vaccine was given 9 days past the BUD (6/23/2022). Moderna was contacted and the lot was analyzed. Per Moderna this lot was still active and the patient did not need to be revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine given 8 days past the BUD (6/23/2022). Moderna contacted and lot analyzed. Per Moderna, this lot was still active. The patient did not need to be revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product use issue
Symptomtext
This vaccine was given 4 days past the BUD (6/23/22). Moderna was contacted and the lot was analyzed. Per Moderna this lot was still active and patient did not need to be revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product use issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
This vaccine was given 4 days past the BUD (6/23/22). Moderna was contacted and the lot was analyzed. Per Moderna this lot was still active and patient did not need to be revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- 07.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Gait disturbance
Hypotonia
Loss of proprioception
Muscular weakness
Symptomtext
bilateral lower leg weakness/floppiness/poor proprioception in ?stocking? distribution, from knees down. symmetrical. needed to lift knees high, for feet to clear the floor, as i walked to sit down. duration: 3 to 5 minutes. sudden onset; complete resolution of symptoms within 5 minutes. no other associated symptoms. no recurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gait disturbance
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- polymyalgia rheumatica
- Vorgeschichte
- hypercholesterolemia polymyalgia rheumatica
- Andere Medikamente
- zoloft 25mg a day atorvastatin 20mg a day
- Allergien
- sulfa allergy
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 23.06.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Test positive for Covid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Self test kit provided
- Aktuelle Erkrankungen
- Diabetic type 2 Thyroid replacement Injury from car t- boning my car ...still in PT.
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Ozempic, Metformin, Synthroid Vitamin C, D3 , CoQ 10 , zinc, biotin
- Allergien
- Mango Penicillin Propofol
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 14.07.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient signed up for a Shingrix Vaccine, and the vaccine given was a 4th Booster Shot, indicated for persons >50 yrs old. Patientsa last 'Booster' was provided 1/2022. Greater than 5 months prior, so on time for COVID series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown, none listed
- Vorgeschichte
- Unknown, none listed
- Andere Medikamente
- None
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 08.06.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 33,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
SARS-CoV-2 test
Symptomtext
patient received a Moderna vaccine that was open since the 8Jul2022; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received a Moderna vaccine that was open since the 8Jul2022) in a 45-year-old male patient who received mRNA-1273 (Spikevax) (batch nos. 059A22A and 059A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Jun-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 11-Jul-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 11-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received a Moderna vaccine that was open since the 8Jul2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received a Moderna vaccine that was open since the 8Jul2022) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 15-May-2022, SARS-CoV-2 test: Positive. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications was not provided by the reporter. The patient received a Moderna vaccine that was open since 08-Jul-2022, on the 11-Jul-2022. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220515; Test Name: COVID + test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 14.07.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Patient's mom insisted on getting Moderna booster instead of Pfizer booster for her 12 years old kid. The intern gave the patient 0.25ml of Moderna vaccine but upon re-checking administration guideline, that has not been approved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- no need. spoke with mother, patient has no side effects.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 08.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Full blood count abnormal
Platelet count decreased
Symptomtext
Lowered platelet count, will wait and watch with frequent CBCs to monitor
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Full blood count abnormal
- Hospital-Tage
- -
- Labordaten
- CBC; platelet count at 20,000; 7/12/22
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- ITP; SLE
- Andere Medikamente
- Azelastine 0.1%; hydroxychloroquine 200mg; mycophenolic 360mg x 2 daily; D3; calcium; multivitamin; probiotic; allerclear
- Allergien
- Shellfish/plankton
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 12.07.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Dose administered after 30-day Use By Date; the vial was initially stored in the refrigerator 26May2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date) and PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator 26May2022) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date) and PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator 26May2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date) and PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator 26May2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication reported. No treatment medication reported. On 26 May 2022, the vial was initially stored in the refrigerator. Between 26 Jun 2022 to 04 Jul 2022 vaccines were administered. to 7 patients.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 21.06.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
Patient hospitalized with COVID while vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 21.06.2022
- Beginn
- 03.07.2022
- Tage bis Beginn
- 12,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
Patient hospitalized with COVID while vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 01.07.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Contusion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Contusion
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Diabetes, hypertension, degenerative joint disease, gastric polyps, bilateral sciatica
- Andere Medikamente
- Lyrica, Flonase, Pravachol, metoprolol tartrate, estradiol, pioglitazone, cholecalciferol, docasahexaenoic acid-epa, empagliflozin, pepcid, linagliptin, lisinopril, metformin,
- Allergien
- Gabapentin, Ibuprofen, latex
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 04.07.2022
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
No adverse events were reported. The patient received a 2nd booster despite not being eligible. She is under the age of 50 and reports she is not immunocompromised.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 28.06.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Parosmia
Symptomtext
Patient had the 4th dose of Moderna on 6/28/22 and then Patient started experiencing parosmia (unusal / strange smell) the day after on 6/29/22. He states that he could smell other things normally, but there would be a strong chemical like smell lingering and it wouldnt go away. Only until about 7/2/22 that strong chemical smell started fading away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Parosmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
The patient received a 2nd booster 4th immunization for Covid 19 vaccine. Moderna Lot# 059A22A exp 6/30/22 . They were not elgible . They were 42 years old
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Diabetic
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 22.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Depressed level of consciousness
Eyelid function disorder
Hyporesponsive to stimuli
Symptomtext
Patient's wife states that the patient was not alert, could not open eyes, and would only answer the simplest of questions for 3 days after 2nd booster dose of Moderna vaccine. The patient had 4 total doses of Moderna and only had this reaction on the last dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Depressed level of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Unknown
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 29.06.2022
- Impfdatum
- 27.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bacterial test negative
Blood urine present
Burning sensation
Genitourinary symptom
Micturition urgency
Muscle spasms
Pollakiuria
Urinary tract infection
Urine analysis
Symptomtext
Urinary symptoms of spasm. Burning. Frequency. Urgency starting around 4:00 pm day of vaccine. Continued through night. Went to ER on 6/28 with worsening of symptoms. Was given Pyridium 200mg 3x?s a day for 2 days. Lower UTI was diagnosed. Still having symptoms but not quite as bad today (6/29).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bacterial test negative
- Hospital-Tage
- -
- Labordaten
- Urinalysis showing 1+ blood. No bacteria.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes. Asthma. Hypertension. Hyperlipidemia. OSA.
- Andere Medikamente
- Hyzaar, Metformin, Levothyroxine, Atenolol, Lipitor, Protonix, Potassium, Multivitamin, Baby Aspirin, Trulicity
- Allergien
- Penicillin, Ultram, Codeine, Erythromycin, Betadine, Duragesic, Scallops
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- 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
Symptomtext
Patient came into vaccine clinic looking for covid vaccine to complete series after receiving first Janssen vaccine on 3/11/2021. Nurse administered moderna dose of 0.5mL to patient?s right deltoid at 10:23am. Nurse told patient a 10-15-minute waiting period after the covid vaccine as per CDC guidelines and patient agreed. After 10-15 minutes patient advised nurse of no ill-being and walked away with no visible signs and symptoms of distress. When reviewing paperwork data entry clerk noticed that instead of a booster dose of 0.25 mL, a full dose of 0.5 mL was administered. Nurse was not able to advise patient of dosage error due to patient leaving. When returned to the office, primary nurse notified and supervisor notified of found error. Protocol orders include notifying patient of error, filling an incident report, and completing a VAERS report. Nurse called Patient at 2:20pm at employment number provided of dosage error, possible adverse reactions, and emergency needs if applicable. Patient given opportunity to ask questions, patient acknowledged and no further questions asked. Nurse gave patient office phone number to contact nurse of any further questions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Dx of Bell's Palsy
- Vorgeschichte
- None.
- Andere Medikamente
- At this moment, patient was taking a medication for Bell's Palsy but did not recall the medication.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 09.06.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Administration error: A 37-year-old female patient with a dose of Janssen and a booster of Moderna receives a second booster of the Moderna vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- No chronic conditions
- Andere Medikamente
- No medications at the time of vaccination
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Incorrect timing of administration: Pt was given dose 2 moderna 0.5ml at day 21 instead of day 28.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetic
- Andere Medikamente
- glimepiride, methocarbamol, meloxicam, neurontin, metformin, amitriptyline
- Allergien
- none
- Vorherige Impfungen
- fainted at dose 1 moderna 5/23/22
- Staat
- UT
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 21.06.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
patient received a dose of moderna, was suppose to get 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
- UT
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 21.06.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
patient received moderna dose. was suppose to get 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
- -
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 19.06.2022
- Impfdatum
- 18.06.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
pt was given 2nd booster at age 49 instead of 50. she did not meet booster requirements (immunocompromised) but dr had told her to get booster. rph did not catch age discrepency until after boost was given 0.25ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 18.06.2022
- Impfdatum
- 14.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental overdose
Inappropriate schedule of product administration
Symptomtext
Gave 0.5 mL instead of 0.25 mL/ This was the patient's 3rd dose; Inappropriate schedule of vaccine administered; This spontaneous case was reported by an other health care professional and describes the occurrence of ACCIDENTAL OVERDOSE (Gave 0.5 mL instead of 0.25 mL/ This was the patient's 3rd dose) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059A22A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Johnson & Johnson vaccine (1st Dose: Johnson & Johnson) on 19-Mar-2021 and Pfizer (2nd Dose: Pfizer) on 27-Dec-2021. Past adverse reactions to the above products included No adverse event with Johnson & Johnson vaccine and Pfizer. On 14-Jun-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 14-Jun-2022, the patient experienced ACCIDENTAL OVERDOSE (Gave 0.5 mL instead of 0.25 mL/ This was the patient's 3rd dose) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). At the time of the report, ACCIDENTAL OVERDOSE (Gave 0.5 mL instead of 0.25 mL/ This was the patient's 3rd dose) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product was provided by the reporter. Patient has not reported any adverse reactions to the dose. No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental overdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 17.06.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Administration error: Patient receives 0.25ml dose of the Moderna vaccine, instead of receiving 0.5ml according to the guidelines established by the regulatory authority, due to the conditions and medications that he presents at vaccination day. The dose is completed with an additional 0.25 ml minutes after the administration error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- Rheumatoid Arthritis
- Andere Medikamente
- Enbrel
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 16.06.2022
- Impfdatum
- 10.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye irritation
Hypersensitivity
Insomnia
Swelling
Uveitis
Symptomtext
I woke up Tuesday with eye feeling very irritated. By night time it was so bad I couldn't sleep. I went to the eye doctor and she told me I could have internal uveitis and a severe allergic reaction gave me something she prescribed a steroid and then it got better and the swollen is gone and the irritation is almost gone. I went back to the doctors today to get rechecked and she said it confirmed that it got way better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye irritation
- Hospital-Tage
- -
- Labordaten
- Eye exam, Tonality exam
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Environmental allergies
- Andere Medikamente
- Azelastine; CHA nasal solution
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Was only 17 years and 9 months of age at the time vaccine was given. No known adverse reaction at time of administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
There actually were no adverse event or reactions. I am filling out this form b/c I realized that this pt was under 50 years old and not immunocompromised. The 2nd booster was given, but technically he didn't qualify to receive the 2nd booster. I alerted his staff. He is in a group home
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 93,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 07.06.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient received 4th booster dose on 4//15/22 but presented to vaccine clinic requesting a booster. Agency and vaccine card had conflicting information due to some providers not reporting doses. Administered another booster on 6/7/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.06.2022
- Impfdatum
- 09.06.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
the vial stored post puncture in fridge; Expired Vaccine Administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Vaccine Administered) and PRODUCT STORAGE ERROR (the vial stored post puncture in fridge) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 059A22A) for COVID-19 vaccination. No Medical History information was reported. On 09-Jun-2022 at 1:20 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 09-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Vaccine Administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (the vial stored post puncture in fridge). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Vaccine Administered) and PRODUCT STORAGE ERROR (the vial stored post puncture in fridge) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. One dose was administered. The vial was initially stored in the refrigerator on 31-May-2022. The vial was first punctured on 08-Jun-2022 at 2:48 PM. The vial did not undergo any temperature excursions. The vial was exposed to room temperature range (8 degree Celsius to 25 degree Celsius = 46 degree Celsius to 77 degree Fahrenheit) for 15 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 11.06.2022
- Impfdatum
- 09.06.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Moderna Covid vaccine was wrongly given to person under 18 years old (patient was 17 years old at the time)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 08.06.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
Symptomtext
16 yo patient received Moderna instead of Pfizer for first dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 06.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Patient signed up to receive Pfizer COVID vaccine and was given Moderna 0.25ml booster vaccine instead
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -