- Staat
- -
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 11.08.2023
- Impfdatum
- 28.12.2021
- Beginn
- 06.02.2023
- Tage bis Beginn
- 405,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Symptomtext
ACUTE ST ELEVATION MI, UNSPECIFIED ACUTE NON ST ELEVATION MI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 14.02.2023
- Impfdatum
- 27.12.2021
- Beginn
- 14.02.2023
- Tage bis Beginn
- 414,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
SARS-CoV-2 test positive
Symptomtext
admitted to Medical Center on 2.2.2023 expired 2.14.2023 covid-19 positive 1.20.2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 07.11.2022
- Impfdatum
- 07.10.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 28,0
- Dosis
- 2
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute respiratory failure
Anticoagulant therapy
Asthenia
Blood creatinine
Blood urea
Brain natriuretic peptide
COVID-19
Chills
Computerised tomogram thorax abnormal
Condition aggravated
Cough
Dehydration
Depression
Dyspnoea
Dyspnoea exertional
Fatigue
Fibrin D dimer increased
Hypophagia
Symptomtext
Chief Complaint: Cough and shortness of breath Additional Medical History: Patient is a 78-year-old male with a history of coronary artery disease, asthma, COPD, arthritis and depression. He presented to the emergency room by EMS complaining of worsening cough and shortness of breath over the last 3 days. Patient states 3 days ago he developed a cough which has progressively become worse. He states the cough is productive at times of yellowish colored sputum. He feels short of breath especially with seen when he is coughing or moving around. He denies fever or chills or sick contacts with similar symptoms. The shortness of breath became significant just prior to arrival at which point he called EMS. EMS arrived on the scene to find the patient hypoxic at 85% on room air. He was transported to the hospital. On 2 L nasal cannula he is oxygenating at 93 to 95%. He is otherwise alert and appropriate. He is in mild distress on presentation. He denies any chest discomfort or swelling of his lower extremities. He quit smoking 25 years ago. Associated Symptoms: cough, depression, fatigue, palpitations, shortness of breath, sputum, weakness, wheezing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- 2:40 PM patient did respond nicely to oxygen through the nasal cannula at 2 L/min. He will have a full work-up for pneumonia including cardiac enzymes, BNP and D-dimer. He will have blood cultures, lactic acid and COVID testing. Patient will have a nebulizer treatment and steroid given here in the emergency room while we await further testing. 3:11 PM patient is positive for COVID. He also has an elevated D-dimer over 900. Patient will have routine CTA of the chest for further evaluation to rule out a pulmonary embolism. He will require admission for further care and treatment. He continues to rest comfortably at this time and oxygenating well on nasal cannula. 4:59 PM CT of the chest shows multifocal pneumonia with a right lower lobe consolidation. No evidence of pulmonary embolism. The case was discussed with Dr. who accepted the admission for further care and treatment. Problem 1: Acute respiratory failure due to COVID-19 Plan 1: The patient presented with a 3-4 days history of upper respiratory symptoms including productive cough shortness of breath shaking chills. Patient was found to have COVID 19. The patient is vaccinated and booster which make his risk of deterioration less severe. He responded nicely to oxygen continue with the steroids oxygen breathing treatment. Problem 2: Bilateral pneumonia Plan 2: Superimposed on COVID-19. The CT scan clearly showed bilateral scattered focal consolidation consistent with bacterial pneumonia. Patient does have leukocytosis and tachycardia consistent with sepsis. The patient received the fluids antibiotics steroids awaiting culture and sensitivity to adjust oral antibiotics. Problem 3: Dehydration, moderate Plan 3: Patient had decreased p.o. intake and he has a bump in his BUN and creatinine. He received bolus in the emergency room I will continue with the fluid resuscitation. His tachycardia already improved. Problem 4: DVT prophylaxis
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- CAD Asthma arthritis COPD arrhythmia
- Andere Medikamente
- Not Currently Taking Home Medications.
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 22.10.2022
- Impfdatum
- 23.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase increased
Aspartate aminotransferase increased
Asthenia
Blood glucose normal
Blood potassium decreased
Cardiac arrest
Death
Diaphragmatic disorder
Differential white blood cell count
Dyspnoea
Fibrin D dimer
Full blood count
Gait inability
Haemoglobin increased
Intensive care
International normalised ratio normal
Mean platelet volume increased
Muscle spasms
Symptomtext
Couldn't walk for first 2 days after whole body felt like Charley horses, weak and short of breath . Stayed short of breath and weak until 1/11/2022. This day he went into cardiac arrest and died.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- CBC with different, high hemoglobin, high mpv, low RDW,low potassium,high glucose 154,high AST,high ALT, d dimer. 28, INR .97,Troponin I HS 6.2, mild asymmetric elevation of the right hemidiaphragm, ventricular tachycardia, critical care for 60 mins
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypothyroidism, high bp, diabetes, copd
- Andere Medikamente
- Lisinopril, lovastatin ,metformin,metoprolol, omeprazol,vibryd,vit d3, vit b12
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 07.08.2022
- Impfdatum
- 19.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram
Anticoagulant therapy
Atrial fibrillation
Cardiac ablation
Cardiac failure congestive
Cardioversion
Cough
Deep vein thrombosis
Dyspnoea
Electrocardiogram
Exercise tolerance decreased
Fluid retention
Magnetic resonance imaging
Nausea
Pain in extremity
Palpitations
Peripheral swelling
Polyuria
Symptomtext
Shortness of breath, heart palpitations, cough, exercise intolerance, some nausea/vomiting, pain in left lower leg, fluid retention, swelling in feet. Symptoms progressed in severity. Admitted to hospital week of Feb 6 for five days. Diagnosed with deep vein thrombosis is left leg. Pulmonary embolisms. Congestive heart failure. Tachycardia. Atrial fibrillation. Treated with blood thinner, diuretics, beta blockers. Cardioversion. Catheter radiofrequency atrial ablation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 5,0
- Labordaten
- EKG, Electro-cardiogram, ultrasound, MRI, angiogram - week of Feb 6, 2022.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- Moderna Covid-19, May 3, 2021, age 53, shortness of breath, heart palpitations, exercise intolerance, swelling in feet.
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 17.01.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 169,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asymptomatic COVID-19
Cerebrovascular accident
Hypertensive encephalopathy
Mental status changes
SARS-CoV-2 test positive
Symptomtext
Pt presented to hospital with altered mental status with acute cva, and hypertensive encepalopathy. Related to lack of gaudianship and placement pt has an extended hopital stay and tested positive for covid asymptomatic, Pt was able to be discharged to a residential facility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 163,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- schizophrenia, afib, cva, htn , hld, hypothyroidism
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 04.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 27,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19 pneumonia
Death
Symptomtext
Death secondary to COVID-19 pneumonia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- BRAIN TUMOR, NOT BIOPSIED; ACUTE METABOLIC ENCEPHALOPATHY10; COVID-19 PNEUMONIA
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 22.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram
Angiogram pulmonary abnormal
Anticoagulant therapy
Deep vein thrombosis
Pain in extremity
Peripheral swelling
Pulmonary embolism
Subclavian vein thrombosis
Ultrasound Doppler abnormal
Symptomtext
Developed swelling and pain in left arm shortly after vaccine. DVT US 1 month later revealed DVT of subclavian vein and CT PE showed pulmonary embolism. Treated with Eliquis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- Ultrasound vascular upper extremity venous 2/8/22 CT angiogram upper extremity left 2/13/22 CT angiogram chest 2/10/22
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Question of celiac disease, dilated aortic root, mitral valve prolapse, vitamin D deficiency
- Andere Medikamente
- vitamin D supplement 1000 IU
- Allergien
- gluten sensitive, sulfa antibiotics
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 53,0
- Geschlecht
- U
- Eingang
- 22.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cerebrovascular accident
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anxiety
COVID-19
Chest pain
Death of relative
Depressed mood
Dizziness
SARS-CoV-2 test positive
Symptomtext
He came to the hospital with a chief complaint of left-sided chest pain. Patient also reported some dizziness associated with that. Pain is less in the left lateral chest wall. Patient reports that recently his wife passed away so he is feeling very down and anxious. He reports that his chest pain may have something to do with that. He denies any fevers, chills, cough, shortness of breath, palpitations, abdominal pain, nausea, vomiting, burning or painful urination, diarrhea. Patient however denies any severe depressive symptoms or suicidal ideations. Tested positive on 01/16/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death of relative
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension, hyperlipidemia, history of DVT and PE currently not on anticoagulation due to high risk for bleeding, BPH, depression, chronic GERD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Cerebrovascular accident
Feeding tube user
Symptomtext
patient received booster shot on 12/22/21. then had a stroke on 1/1/22. he is still hospitalized and now on a feeding tube
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- DIABETES CARDIAC DISORDER
- Vorgeschichte
- -
- Andere Medikamente
- TERAZOSIN 5MG FINASTERIDE 5 TRULICITY 4.5MG/0.5ML METOPROLOL TART 50MG FENOFIBRATE 145MG ELIQUIS 5MG LEVEMIR GLIMEPERIDE 2MG
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 16.08.2023
- Impfdatum
- 14.12.2021
- Beginn
- 08.02.2023
- Tage bis Beginn
- 421,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Facial paresis
Ischaemic stroke
Symptomtext
ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY LEFT FACIAL MUSCLE WEAKNESS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 22.06.2023
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
Blood test
Chest X-ray
Echocardiogram
Electrocardiogram
Loss of consciousness
Malaise
Myalgia
Pain
Pain in extremity
Pain in jaw
Tinnitus
Unresponsive to stimuli
Urine analysis
Vomiting
Symptomtext
Boby aches, muscle aches, over all not feeling well, then started having ringing in my ears get louder and louder. I went to the ER about a week ago 6/10/23 over my heart, I blacked out, was unresponsive and shocking on my own vomit. ER diagnosis was I was in AFIB, my jaws and arm was killing me. I was treated with aspirin and various medication then able to go home with medication. I the new cardiologist/APN on 6/12/23
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- EKG, echo, blood work, UA, chest xray
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- osteoporosis
- Andere Medikamente
- magnesium, Citrucel/d3
- Allergien
- ranitidine, probiotics
- Vorherige Impfungen
- to other COVID vaccines , same symptoms stated
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 22.12.2022
- Impfdatum
- 10.01.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 108,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Gait disturbance
Implantable cardiac monitor insertion
Joint injury
Palpitations
Sciatica
Syncope
Ventricular extrasystoles
Walking aid user
Symptomtext
Syncope on 4/28/22. Injured L knee. Treatment consisted of ice, elevation and compression at home. Recovered over the next 12 weeks. Lingering intermittent sciatica, occasionally severe and disabling. Walking with cane occasionally required until 11/15/2022. In late May, early June patient experienced heart palpitations, premature ventricular contractions. Urgent Care arranged transport to ED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Cardiac workup at local Medical Center on 6/3/2022. Loop recorder implanted. Cardiac followup ongoing as of 12/22/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, hypercholesterolemia, hypothyroid, gout
- Andere Medikamente
- Allopurinol, hyzaar, flomax, synthroid, claritin, atorvastatin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 18.09.2022
- Impfdatum
- 08.07.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 64,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Body temperature increased
Communication disorder
Computerised tomogram head abnormal
Electroencephalogram normal
Endotracheal intubation
Fall
Intensive care
Loss of consciousness
Movement disorder
Subarachnoid haemorrhage
Ultrasound Doppler normal
Unresponsive to stimuli
Symptomtext
Patient had a fall with Loss of Consciousness. Head CT showed bilateral subarrachnoid hemorrhage. Transferred to neuro critical care. Repeat stability head scans showed worsening bleed. Patient intubated on day 2 for airway protection. EEG negative for seizures. Elevated temps with no known source of infection yet. Duplex upper and lower extremities (negative). Patient unable to communicate, follow commands or move upper extremities or lower extremities purposefully.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- A-fib (on coumadin), CAD, CHF, DM2, HTN, Parkinson's and neuropathy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Amiodarone and Spironalactone
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arrhythmia
Cardiac monitoring abnormal
Dry eye
Myocarditis
Palpitations
Periorbital oedema
Schirmer's test abnormal
Ventricular tachycardia
Symptomtext
myocarditis, palpitations, arrhythmia, ventricular tachycardia, periorbital edema, keratoconjunctivitis sicca
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Schirmer's test confirmed dry eye. Zio patch confirmed ventricular tachycardia.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 04.03.2022
- Beginn
- 26.03.2022
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Blood test normal
Deep vein thrombosis
Erythema
Induration
Oedema
Peripheral swelling
Superficial vein thrombosis
Tenderness
Ultrasound Doppler abnormal
Symptomtext
I developed swelling (pitting edema) and pain in my left lower extremity, as well as tenderness, redness, and induration along the course of my greater saphenous vein. This occurred three weeks after my Moderna booster. I was seen three days later in the emergency department and was diagnosed with both superficial thrombophlebitis of my greater saphenous vein and a deep venous thrombosis (DVT) of my left common femoral vein. I was started on Xarelto that day. One month later, my symptoms persist, although they are slightly improved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Doppler ultrasound of left lower extremity confirming DVT of left common femoral vein and superficial thrombophlebitis of left greater saphenous vein, 3-29-22. Bloodwork was unremarkable (although d-dimer was not performed).
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Multiple sclerosis (very mild, not limiting me in any way)
- Andere Medikamente
- Vitamin D, vitamin B12, omega-3, turmeric, multivitamin
- Allergien
- Dilantin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
C-reactive protein increased
Chest discomfort
Echocardiogram normal
Electrocardiogram normal
Pericarditis
Symptomtext
Several hours after receiving the Moderna booster (02/25/2022), patient developed acute chest discomfort. She didn't know what to do, therefore waited and then sought treatment 03/01/2022 with PCP. Echocardiogram, CRP and EKG obtained. Trialed off Wellbutrin to see if this was the cause without improvement. Since seeking medical evaluation and treatment she has not had significant alleviation of her symptoms. Seen by cardiology 04/21/2022 with continued chest discomfort that has not significantly alleviated since it started. Diagnosed with Acute pericarditis and currently undergoing treatment with ibuprofen and colchicine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- Echocardiogram - no acute abnormal findings (03/01/2022) EKG - no acute or abnormal findings (03/01/2022) CRP - elevated (03/01/2022) Repeat CRP - normalized (03/18/2022) Repeat EKG - no acute or abnormal findings (04/21/2022)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- thyroid cancer (currently in the process of treatment), depression with anxiety, obesity
- Andere Medikamente
- Wellbutrin, levothyroxine, magnesium oxide, calcitriol, Wegovy (weight loss med)
- Allergien
- Yeast
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 10.03.2021
- Beginn
- 10.03.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Dizziness
Electric shock sensation
Electromyogram
Erythema
Gait inability
Headache
Laboratory test
Lethargy
Lymphadenopathy
Magnetic resonance imaging
Neurological examination
Pain in extremity
Surgery
Symptomtext
3/10/2021 first dose moderna 15 minutes post vaccine onset of headache, lightheadedness, euphoric. 1 week later back pain with increasing pain from back down to lower left extremities pain 10+/10 and felt like "electricity" in body leading to pt being unable to ambulate. by lymph node surgery date on 3/25/21 patient was able to ambulate again. Second Moderna dose on 04/ 10/21 pt continued to experience lethargy and mobility issues. Neurologist consult 06/2021 work up done. Booster dose 12/27, during dose administration pt felt as if a "nerve was hit". Reported redness and swollen lymph odes on left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- EMG 07/12/2021 MRIx2 7/12/2021 12/14/2021 PCP lab work
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Post traumatic osteochondritis dissecans Arthritis Fibromyalgia glaucoma Plantar fasciitis caporal tunnel ACDF Anterolisthesis and retro spondylothesis spinal stenosis behcet Syndrome
- Andere Medikamente
- Lisinopril 20mg daily bystolic 10mg Gabapentin 300mg 3x a day Flexarul 10mg PRN Vit D 5000 U daily B complex Hair nails skin nature's bounty Centrum silver meloxican eye drops latanoprost 0.0005 nightly
- Allergien
- prednisone, mood changes
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Chest discomfort
Dyspnoea
Echocardiogram
Myocarditis
Symptomtext
Shortness of breath, chest pressure. I have Myocarditis due to vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 2,0
- Labordaten
- Echocardiogram 1-24 and another one 3-1-22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- History of Stroke in 12-2020
- Andere Medikamente
- ASA 81 mg
- Allergien
- Cipro, Bactrim, Sulfa
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Cardiac function test normal
Epistaxis
Injection site rash
Injection site swelling
Lip swelling
Product administered to patient of inappropriate age
Syncope
Urine analysis normal
Symptomtext
Pt arrived at school vaccination clinic for second primary vaccination and requested Moderna. I corrected pt stating she was ineligible to receive Moderna due to her age. Her mother stated she received Moderna for her first vaccine, produced a vaccine card confirming, and her record also confirmed. I confirmed with DOH that the next steps were to administer the age-appropriate second vaccine to the patient (Pfizer 12+) and assure her pediatrician is made aware of the situation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 10.02.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
C-reactive protein
Chest pain
Differential white blood cell count
Echocardiogram
Electrocardiogram abnormal
Full blood count
Metabolic function test
Myocarditis
Electrocardiogram
Fatigue
N-terminal prohormone brain natriuretic peptide
Red blood cell sedimentation rate
Respiratory viral panel
Troponin T
Troponin
Symptomtext
myocarditis; This spontaneous case was reported by a consumer and describes the occurrence of MYOCARDITIS (myocarditis) in a 24-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced MYOCARDITIS (myocarditis) (seriousness criteria hospitalization and medically significant). At the time of the report, MYOCARDITIS (myocarditis) was resolving. Not Provided DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, C-reactive protein: results not reported result not reported. On an unknown date, Electrocardiogram abnormal: abnormal (abnormal) Abnormal (ECG) and (EKG).. On an unknown date, Full blood count: results not reported results not reported. On an unknown date, Metabolic function test: results not reported results not reported. On an unknown date, N-terminal prohormone brain natriuretic peptide: results not reported results not reported. On an unknown date, Red blood cell sedimentation rate: results not reported results not reported. On an unknown date, Respiratory viral panel: results not reported results not reported. On an unknown date, Troponin T: results not reported performed 2 times. results not reported.. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment medications was provided by the reporter. Patient was admitted to the emergency room last night with chest pain. According to him it was determined that he had developed myocarditis due to the covid booster vaccine he received. He was released today and was at home recovering. On an unknown date, patient had hospital visit and got the doctor's note indicating the cause of his condition. Company Comment: This is a spontaneous case concerning a 24-year-old, male patient with no medical history reported, who experienced the expected serious AESI Myocarditis which occurred on an unknown date after the third dose of mRNA-1273 vaccine. Patient was admitted to the emergency room with chest pain. According to him it was determined that he had developed myocarditis due to the covid booster vaccine he received. Investigations like C-reactive protein, Electrocardiogram abnormal, Full blood count, Metabolic function test, N-terminal prohormone brain natriuretic peptide, Red blood cell sedimentation rate, Respiratory viral panel and Troponin T results were not reported. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.. Most recent FOLLOW-UP information incorporated above includes: On 02-Feb-2022: Patient DOB, lab data and events added.; Sender's Comments: This is a spontaneous case concerning a 24-year-old, male patient with no medical history reported, who experienced the expected serious AESI Myocarditis which occurred on an unknown date after the third dose of mRNA-1273 vaccine. Patient was admitted to the emergency room with chest pain. According to him it was determined that he had developed myocarditis due to the covid booster vaccine he received. Investigations like C-reactive protein, Electrocardiogram abnormal, Full blood count, Metabolic function test, N-terminal prohormone brain natriuretic peptide, Red blood cell sedimentation rate, Respiratory viral panel and Troponin T results were not reported. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Test Name: C-reactive protein; Result Unstructured Data: result not reported; Test Name: Abnormal electrocardiogram; Result Unstructured Data: Abnormal (ECG) and (EKG).; Test Name: CBC and differential; Result Unstructured Data: results not reported; Test Name: basic metabolic panel; Result Unstructured Data: results not reported; Test Name: nt-probnp test; Result Unstructured Data: results not reported; Test Name: sedimentation rate (ESR); Result Unstructured Data: results not reported; Test Name: COVID PANDEMIC respiratory viral order; Result Unstructured Data: results not reported; Test Name: troponin T; Result Unstructured Data: performed 2 times. results not reported.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 23.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Arteriogram coronary normal
Catheterisation cardiac normal
Chest pain
Myocarditis
Symptomtext
Substernal chest pain approx three days after booster shot. Admitted to a local Medical Center for Myocarditis. Spent 3 days in hospital then released under Dr care. Still undergoing follow-ups with additional perscriptions
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 3,0
- Labordaten
- 1/11/22- In hospital Angio Cath with all vessels clear. Placed on anti-inflammatories.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, High Cholesterol
- Andere Medikamente
- Simvastatin, Olmasartin HCTZ
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient fainted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- checked patient blood pressure per automatic monitor - initial reading 80/50 and gradually increased back to normal
- Aktuelle Erkrankungen
- None Reported
- Vorgeschichte
- None Reported
- Andere Medikamente
- None
- Allergien
- No known allergies
- Vorherige Impfungen
- Pt described similar reaction to previous immunization at age 14 - does not remember vaccine involved
- Staat
- AR
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Seizure
Symptomtext
Seizure reported by wife
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Seizure
Symptomtext
I had 3 seizures after the vaccine within 6 hours of the booster shot; Interchange of vaccine products; This spontaneous case was reported by a patient and describes the occurrence of SEIZURE (I had 3 seizures after the vaccine within 6 hours of the booster shot) in a 54-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Epilepsy and Lupus syndrome. Previously administered products included for Product used for unknown indication: janssen on 21-Apr-2021. Past adverse reactions to the above products included No adverse event with janssen. Concomitant products included PREDNISOLONE, LEVOTHYROXINE SODIUM (SYNTHROID), CLOPIDOGREL BISULFATE (PLAVIX), VERAPAMIL and IBUPROFEN for an unknown indication. On 27-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Dec-2021, the patient experienced SEIZURE (I had 3 seizures after the vaccine within 6 hours of the booster shot) (seriousness criterion medically significant). 27-Dec-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). The patient was treated with LORAZEPAM in December 2021 for Seizure, at an unspecified dose and frequency. On 27-Dec-2021, INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) had resolved. At the time of the report, SEIZURE (I had 3 seizures after the vaccine within 6 hours of the booster shot) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Company comment: This spontaneous case concerns a 54-year-old female patient with a relevant medical history of Epilepsy and Systemic lupus erythematosus, who experienced the unexpected serious (medically significant) event of Seizure after mRNA- 1273 vaccine, booster dose of the vaccination schedule. Interchange of vaccines products occurred since the patient had received initial schedule of vaccination with Janssen COVID-19 Vaccine. The events occurred on the day after the booster dose of mRNA- 1273 vaccine. The patient experienced 3 seizures after the vaccine within 6 hours of the booster shot. Very limited information is available regarding baseline health condition before vaccination, diagnostic work-up and other potential precipitating factors. Previous history of Epilepsy and Systemic lupus erythematous remain as confounder. The benefit-risk relationship of mRNA- 1273 vaccine is not affected by this report.; Sender's Comments: This spontaneous case concerns a 54-year-old female patient with a relevant medical history of Epilepsy and Systemic lupus erythematosus, who experienced the unexpected serious (medically significant) event of Seizure after mRNA- 1273 vaccine, booster dose of the vaccination schedule. Interchange of vaccines products occurred since the patient had received initial schedule of vaccination with Janssen COVID-19 Vaccine. The events occurred on the day after the booster dose of mRNA- 1273 vaccine. The patient experienced 3 seizures after the vaccine within 6 hours of the booster shot. Very limited information is available regarding baseline health condition before vaccination, diagnostic work-up and other potential precipitating factors. Previous history of Epilepsy and Systemic lupus erythematous remain as confounder. The benefit-risk relationship of mRNA- 1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Epilepsy; Lupus syndrome
- Andere Medikamente
- PREDNISOLONE; SYNTHROID; PLAVIX; VERAPAMIL; IBUPROFEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Seizure
Symptomtext
Pt reported to have 2 small seizures at approximately 6:20 P.M. Pt reported to be recovered per conversation 12/28/2021 at 4:30 p.m.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seizure disorder
- Andere Medikamente
- Tomiramate, Pirmella 1/35
- Allergien
- None listed
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Disorientation
Dizziness
Hyperhidrosis
Nausea
Pallor
Syncope
Symptomtext
After patient recieved booster dose of Moderna, patient complained of dizziness and then fainted. Patient regained consciousness after a few moments, but was disoriented, pale, sweating, and nausated. Stayed & monitored patient until all symptoms resolved and patient was able to leave on his own accord. Patient did not require any additional medical assistance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 24.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Lip swelling
Malaise
Pallor
Syncope
Symptomtext
Patient received first dose of the moderna covid vaccine. He was fine receiving the vaccine but about 5 minutes later did not feel well and fainted. By the time I got out there he had come to but was pale, clammy and had swollen lower lip. After about 5 minutes and a bottle of water he regained his color and felt ok enough to leave on his own. Paramedics arrived but did not treat patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 18.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adverse event
Confusional state
Flushing
Hyperhidrosis
Loss of consciousness
Syncope
Symptomtext
Systemic: Confusion-Severe, Systemic: Lost awareness and consciousness-Medium, Systemic: Flushed / Sweating-Medium, Additional Details: Patient receives COVIDSHIELD on September 7th in (Privacy) . This was not accurately relayed to pharmacy technician who administered a full dose of Moderna(0.5)ml to patient. Patient apparently passed out in his chair until technician realized he was sweating. He was given water to drink and was okay after 30 minutes. We called the CDC and was advised it was an adverse event and not administration error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 17.04.2023
- Beginn
- 18.04.2023
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Dizziness
Headache
Loss of personal independence in daily activities
Mobility decreased
Nausea
Symptomtext
splitting headache, nausea, dizziness, & extreme weakness all day on the 18th. I had to get help from my husband to get down the stairs. I was unable to participate in anything on the 18th.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lamictal 250 mg po once daily Trazodone 150 mg po hs prn insomnia
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 16.01.2023
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Disorientation
Dizziness
Immediate post-injection reaction
Lethargy
Mobility decreased
Oedema peripheral
Pain
Peripheral swelling
Pyrexia
Symptomtext
Immediately my left arm swelled even around and under my arm pit. Became dizzy and disoriented feverish and aching terribly all over ,it was the booster shot. In bed for about 2 weeks lethargic and aching. Went to my doctor
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Osteoporosis, asthma, asthma ptsd
- Vorgeschichte
- Asthma osteoporosis and PTSD
- Andere Medikamente
- Cymbalta ,vit d , Ambien, Clonazepam, nasonex, tylenol
- Allergien
- Fish Trifexor Fabric bandaids
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 10.02.2021
- Beginn
- 27.11.2022
- Tage bis Beginn
- 655,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
11/27/22 presents to ED for "shortness of breath". PMHx of "asthma, hypertension, left bundle branch block, cardiomyopathy, and gout"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 11/29/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 03.03.2021
- Beginn
- 15.08.2022
- Tage bis Beginn
- 530,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dizziness
Feeling of despair
Gait disturbance
Hypotension
SARS-CoV-2 test positive
Unresponsive to stimuli
Walking aid user
Symptomtext
75y.o. female who presents to hospital 8/15 presents with a c/o of dizziness. Pt states she was standing at the kitchen sink and suddenly got dizzy. Then she went to go sit on the toilet and still felt dizzy and then went to lay down using her walker and could "barely make it." Pt lives with her daughter. Pt's daughter states she felt like her mother was despondent - however she could answer the questions she was asking her. The daughter called EMS and pt was found to be hypotensive 79/37, given IVF bolus. During EMS ride, daughter states the pt had an unresponsive episode. Has hx of vertigo, although this episode felt different. Pt states her symptoms lasted about 1 hour. Pt states she was covid+ 2 weeks ago and her PCP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- 3,0
- Labordaten
- 8/15 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 22.08.2022
- Impfdatum
- 09.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Arrhythmia
Asthenia
Asthma
Blood folate
Cough
Dehydroepiandrosterone test
Fatigue
Feeling abnormal
Lip swelling
Lymphadenopathy
Oropharyngeal pain
Palpitations
Vitamin B12 decreased
Vitamin B12 deficiency
Symptomtext
Heart palpitations at rest. Stabbing heart pain, arrhythmia and aching heart pain. Vitamin B12 deficient and B12. Chronic Fatigue. Head fog and loss of energy with recurrent sore throat, cough, swollen lip glands and viral induced asthma.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- B12, Folic acid and DHEA.
- Aktuelle Erkrankungen
- Patient was showing signs of long Covid after becoming ill in November of 2021. Patient was complaining of "tightness" in chest probable cause viral induced asthma.
- Vorgeschichte
- Hiatal hernia, History of San Joaquin Valley fever, Oral herpes.
- Andere Medikamente
- Acyclovir - 400MG twice daily Supplements: Vitamins - A, B Complex, C, D and E Minerals: Copper, Magnesium, Selenium, and Zinc Vitamins and Minerals taken once every other day to avoid getting too much.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 21.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anti-muscle specific kinase antibody negative
Antiacetylcholine receptor antibody
Aphasia
Asthenia
Ataxia
Blood creatine phosphokinase decreased
Blood creatinine normal
Blood glucose increased
Blood lactate dehydrogenase normal
Computerised tomogram abdomen abnormal
Condition aggravated
Coordination abnormal
Diverticulitis
Dizziness
Electromyogram
Electrophoresis protein normal
Fine motor skill dysfunction
Glomerular filtration rate decreased
Symptomtext
I feel that thought this all started after the first dose. I felt a loss of stamina and strength. The 3rd dose, I noticed all the symptoms I had got worse more quickly. The progression of symptoms seemed to escalate and increase in severity over time. They symptoms that I'm talking about are losing words, generalized pain which includes aching and sharp shooting pain in the limbs, weakness, incoordination, mild ataxia, wooziness bordering on vertigo, headaches, decrease fine motor skills of my hands, forgetfulness. This prompted me to get thoroughly evaluated. I've been seen multiple times by my primary, neurology, and a spine specialist. I've had all kinds of lab work and imaging studies. The labs have been normal. I had a MRI of my brain and MRI of my neck and lower back. There were changes in the neck and lower back that would account for some of my symptoms, but not all of them. I had steroid injections in neck to see if it would help. All I can say is that I feel as though since I received the vaccine, things have precipitously gotten worse. The tinnitus got really bad. too.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 02/11/2022 Brain MRI - Normal; 03/20/2022 Cervical Spine MRI - C6 and C7 and C5 and C6 Severe Bilateral Foramina; 03/21/2022 Blood Chemistry - High Blood Sugar and Low EGFR; 03/21/2022 Vitamin D - Insufficient; 03/21/2022 A1C -High; 03/21/2022 Lipid Profile - Normal; 03/29/2022 COVID-19 PCR - Negative; 04/12/2022 Protein Electrophoresis - Normal; 04/12/2022 Creatine Kinase - Low; 04/12/2022 LDH - Normal; 06/03/2022 Muscle Specific Kinase Antibodies by RIA - Normal; 06/03/2022 Acetyl Choline Receptor Modulating Antibodies - Normal; 06/03/2022 A1C- High, 06/16/2022 Vitamin B6 - Normal; 06/16/2022 Vitamin B1 - Normal; 06/20/2022 Creatinine with Reflex EFGR - Normal; 06/21/2022 CT Scan of Abdomen and Pelvis - Showed Diverticulitis; 07/06/2022 EMG - No results yet
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Fibromyalgia; Mild Obesity; Lichen Planopilaris; Anxiety; Arthritis of Neck and Back; Hypersensitivity to Sound; Hypersensitivity to Smells; Tinnitus
- Andere Medikamente
- Ativan; Gabapentin; Sertraline
- Allergien
- Wellbutrin; Kiwi
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arthralgia
Discomfort
Hypoaesthesia
Injected limb mobility decreased
Injection site pain
Loss of personal independence in daily activities
Neck pain
Pain
Sleep disorder
Symptomtext
After IM (COVID -19) injection to Left arm experienced severe deltoid area pain as if bone was "fragmented" within days pain radiated to upper arm / shoulder and eventually neck area (left sided). Pain continued and I started to have limited mobility of arm. Difficult to move arm backwards (limited) Unable to fasten bra for my left arm currently is unable to extend backwards Limited with range of motion Still experience discomfort and on occasion arm goes numb. Unable to sleep on my left side due to excruciating pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- Seen by my Primary Doctor
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Overall good health
- Andere Medikamente
- Daily vitamins Vitamin D Zinc Calcium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 26.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Dyspnoea exertional
Feeling abnormal
Pain in extremity
Symptomtext
I received my 3rd dose of Moderna as was required by my employer. I began experiencing labored breathing after a run the day after new years. I mention this because I had a pretty laid back holiday with my boyfriend and his children. I began expereiencing pains in my left arm maybe a month later. The shoulder began to hurt, and then when that stopped the elbow joint began to ache, and then my pinky knuckle began ache as well. I had not changed anything in my normal routine, except maybe to slow down considering I was feeling a bit slow. I chocked it up to age and getting older, but will be getting check ed out for arthristis or some other condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamins, acidophilus, d3, alpha brain from onnit
- Allergien
- N/A
- Vorherige Impfungen
- I felt sluggish after the 2nd dose. Not as prominent.
- Staat
- NC
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Condition aggravated
Glycosylated haemoglobin increased
Lymphadenopathy
Pain
Pain in extremity
Peripheral swelling
Stress
Symptomtext
First Vaccine in April 2021 and May 2021: Swelling occurred in lymph nodes and in September the swelling became even worse, and the intensity of pain also increased, as well as pain in my chest, prompting me to seek out medical care. The increase in swelling and symptoms lead to more surgeon meetings, Medical Center surgeon and Healthcare, and in November they were going to remove the lymph node, however the size of the lymph node began to reduce, and the surgery was cancelled. I still do have the swelling however the symptoms are no longer consistent however they do come back with stimulation if I do any physical work and lifting heavy objects causes great pain including any stress that comes on will trigger symptoms worsening. Swelling increases as well if physical exertion is done and lymph node swelling has stayed baselined since October in regard to size. I did have a mammogram September 2021, done and they ruled out breast tumors and it showed that lymph nodes were the main culprit. I also had a biopsy done with the lymph node as well. For about a year I have had cloudy urine. I have now developed swelling in my feet and it gets to a point where it is extremely painful, and I did have to reach out to urgent care due to the pain February 2022. I have been given Lasix as a prescription and try to limit the use. I have had an increase in my A1C as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Mammogram: Showing no tumor Biopsy of Lymph node was performed.
- Aktuelle Erkrankungen
- Continued swelling from first COVID-19 vaccines in lymph nodes.
- Vorgeschichte
- Asthma Hypersomnia Seasonal Allergy Continued swelling from first COVID-19 vaccines in lymph nodes.
- Andere Medikamente
- Advair Inhaler Claritin Flonase PRN Adderall Generic for Hyposomnia Vitamin D 50,000iu once a week
- Allergien
- Seasonal Allergy
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 22.03.2022
- Beginn
- 26.03.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
Chest discomfort
Chest pain
Dyspnoea
Feeling abnormal
Gait disturbance
Nerve injury
Pain in extremity
Thinking abnormal
Symptomtext
I experienced pain and nerve damage in my left leg from thigh up which made it difficult to walk, shortness of breathe, chest pain/tightness, foggy brain at random including losing my train of though i.e. where I am or what I'm doing, loss of smell which is still muted as of now. I am still experiencing shortness of breath and loss of smell, with the brain fog last occurring 2 months ago. I was prescribed an alvesco mcg inhaler for the shortness of breathe and told to smell items i.e. flowers 5 times daily to help regain my sense of smell.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Womens Multivitamin
- Allergien
- Unknown chili spice
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 30.04.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphasia
Blood test
Dysstasia
Fatigue
Feeling abnormal
Gait disturbance
Headache
Memory impairment
Mobility decreased
Palpitations
Urinary tract infection
Vertigo
Symptomtext
30 minutes after I woke up on 1/13/2022, the day after the vaccination, I started experiencing severe vertigo. I could not stand or walk by myself. I could I sit upright. These symptoms lasted for 24 hours. I woke up on 1/14/2022 and the vertigo was gone. For the first couple of days after this incident I was exhausted and feeling very out of it. I thought this would pass given what just happened. Feb I went to the Dr. because my heart was racing and I felt off. I also developed my first UTI. I am still experiencing several of the symptoms described above 4 months later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Blood work conducted in March
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Fatigue, brain fog / memory issues, developed UTI, headache, achy, cannot always find the right words when speaking
- Andere Medikamente
- PremPro, Metoprolol ER Succinate
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Affective disorder
Arthralgia
Condition aggravated
Laboratory test normal
Pain
Pain in extremity
Symptomtext
Pt has been suffering with anosmia, mood disorder and rheumatologic sequala of long-covid since 12/2020. Pt had significant worsening of pain and mood disorders following covid booster as listed above. Pt has had worsening of pain in hand and shoulder joints following injection, requiring additional SSRI and anti-inflammatory medications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- none since booster. Prior (9/21) rheumatologic w/u neg
- Aktuelle Erkrankungen
- Long covid
- Vorgeschichte
- Long covid starting 12/7/2020, asthma, hypothyoidism, obesity.
- Andere Medikamente
- levothyroxine, proAir, singulair, metformin, naproxen, flonase, vit B6 and B12, celexa
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 30.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Condition aggravated
Eczema
Lymphadenopathy
Symptomtext
I experienced flares at the site of eczema (neck, cheeks, fold of arms, armpits) following the booster shot, as I had following my second vaccine. Similarly to my first two doses of the vaccine, I am currently experiencing persistent swelling in my lower abdominal area, independent of my menstrual cycle. While the eczema reaction and lymph swelling in my left armpit has subsided, my lower abdomen remains swollen/protruding. While there has not been pain resulting in hospitalization, it is troubling to have my stomach distended in this manner for such a protracted period of time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Eczema
- Vorgeschichte
- Eczema (Atopic dermatitis)
- Andere Medikamente
- Moducare (plant sterols), for eczema
- Allergien
- Meat allergy, latex, neosporin
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 13.04.2022
- Impfdatum
- 07.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Chest X-ray
Dizziness
Dyspnoea
Electrocardiogram
SARS-CoV-2 test
Sleep disorder
Urine analysis
Symptomtext
Both instances I woke up n the middle of the night with difficulty breathing. Both instances I felt light headed. Went to ER both times. They didn't figure out the issues. My PCP thought it could be allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- EKG; Chest x-ray; Blood work; Urine test; COVID test; Breathing treatment
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Allergies
- Andere Medikamente
- Montalucus Claritin
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 03.04.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Hypoaesthesia
Paraesthesia
Pruritus
Swelling face
Urticaria
Symptomtext
After my second dose of the Moderna vaccine, I experienced extreme facial swelling the following morning (03/31/21). The next day, I experienced numbness and tingling in my right leg that lasted 10+ hours. I received my booster shot (03/10/22) and starting that night and every single day since receiving it, I have broken out in large patches of extremely itchy hives on my neck, chest, stomach, groin, backs of my knees, back, shoulders, and my hands and feet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- After my strange reactions to my second dose, I contacted my PCP and had blood work done to check for an allergic reaction (4/2/21) but at that point it came back normal. Currently, I have been in communication with my PCP?s nurse through app, and am waiting to hear back from an allergy specialist.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Bactrim
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Condition aggravated
Fatigue
Interchange of vaccine products
Phlebitis
Tinnitus
Symptomtext
On Monday, March 21, 2022, I got the Moderna booster at 2:00 PM. Tinnitus started up again within an hour. * I was very tired that evening but otherwise fine. Tuesday night, March 22, at 9:00 PM, when I went to wash my face, I noticed a bulging vein going down the middle of my forehead toward my nose, about 2+ inches long! Prior, I have never seen even the slightest trace of a vein in that area. By 10:30 PM, it was reduced by half in length. There was no pain but the presence of it was worrisome. Wednesday evening, March 22, it was 2+ inches long again and worrisome. As of March 23, it had remained like that and I had a video appt. with my doctor's office at 4:30 PM. The doctors were not worried about vein. By Friday, March 25, it was completely gone, so no doubt a side effect of the booster. In addition to this, I also had a recurrence of tinnitus about an hour after the booster. * Tinnitus had developed three months after the second Pfizer vaccine that I had on 3/16/2021. By January, 2022, it was tapering off, and by mid February, was intermittent and infrequent. I no longer had it until getting the Moderna booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Audiology test in early 2022.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- MAI, GERD
- Andere Medikamente
- Sertraline 100 mg.; levothyroxine, 50 mcg; famotidine 40 mg; biotin 12,000 mcg. These are each taken at different times in the day, but none were at the same time of the Moderna booster.
- Allergien
- hard shellfish, such as clams and oysters
- Vorherige Impfungen
- Pfizer vaccine on 2/23/21 and 3/16/21. Tinnitus developed three months after second vaccine. Age 73,
- Staat
- AZ
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 26.01.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 62,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Malaise
Mobility decreased
Symptomtext
Upon completing audits for my facility, I realized patient had been given booster shot two months too soon by a MA. No adverse effects have been voluntarily reported to clinic by patient to the best of my knowledge. Personally spoke to patient and informed her of the administration error. She stated she has been feeling fine but she did mention she felt extremely sick post vaccine administration and was unable to get out of bed for two days. Patient stated all post side effects have since subsided and she is feeling fine. I recommended she be seen by her PCP and explain the situation so that she can be appropriately examined.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None to my knowledge
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 27.03.2022
- Impfdatum
- 19.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Tinnitus
Symptomtext
This was full dose booster per dr recommendation and prescription due to being immunocompromised. Increased tinnitus to preexisting tinnitus. Previous vaccinations for Covid have also elicited tinnitus which did lessen. This is worst tinnitus I?ve experienced and does not currently appear to be lessening
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None at present m. Intend to get hearing test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ESRD received kidney transplant, obstructive sleep apnea, anxiety and depression
- Andere Medikamente
- mycophenolic acid, prednisone, Envarsus XR, vitamind D3, folic acid, vitaminB12, biotin, escitalopram, Zolpidem,
- Allergien
- Vancomycin, chloraprep skin prep, Lamictal, ancef, levoquin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Fatigue
Induration
Injection site nodule
Injection site pain
Insomnia
Laboratory test
Nodule
Pain
Pruritus
Skin warm
Symptomtext
The day of the vaccination I had a knot that came up at injection site and wrapped around to my underarm. It was hard, hot, burning and itchy all the time. I took ibuprofen for the pain and ice pack. I had it for a week and it is still a little tender at injection site. I'm also very tired. I have had several tests and nothing is wrong but I am extremely tired all the time and having difficulty sleeping.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- I saw my primary care physician for the difficulty in breathing. He added Nebulizer.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, PTSD
- Andere Medikamente
- Cymbalta, Clonazepam, Asthma
- Allergien
- Tribenzor
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 22.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Heart rate increased
Palpitations
Symptomtext
After getting vaccine I felt pressure and palpitations- it was uncomfortable and I felt it for 1.5-2 weeks. I checked my blood pressure it was ok but my heart rate was in the high 90's-100's which was different.; with the second vaccine I felt like I had the flu for 24hrs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN, Hyperlipidemia, high Cholesterol, Cardiac Arrhythmia (PVC's), Migraines
- Andere Medikamente
- Metoprolol, Losartan, ASA, Vit C, Zinc, B-12, Turmeric, Probiotic & Prebiotic
- Allergien
- Lisinopril
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 12.03.2022
- Impfdatum
- 13.01.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 34,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Cough
Diarrhoea
Dry mouth
Dysphonia
Fatigue
Headache
Hyperhidrosis
Illness
Loss of personal independence in daily activities
Mobility decreased
Musculoskeletal chest pain
Myalgia
Nasal discomfort
Nausea
Pyrexia
Rhinorrhoea
SARS-CoV-2 test
Symptomtext
voice has been in and out lately; The drainage is almost 24/7; She has to keep her mouth open a lot because it's too dry, even if she drinks gallons of water.; so sick; sweats all over my legs for hours; back was hurting; can't even get out of bed/couldn't lay on my side or my back/hardly go to her fridge or bathroom; coughing every night 11 PM to 3 AM/dry hacking cough; fever/highest was 100; hurting so bad in my costal muscles near my ribs/ ribs were so sore; hurting so bad in muscles near ribs; sinus/sinus part wasn't bad for a brief moment [when vomiting]/sinus came back the next day; diarrhea [constantly]; vomiting [constantly]; tired/Fatigue; nausea; headache; it felt like a train hit my nose; come home from work / couldn't work the whole day; sniffles that day [after second dose]; This spontaneous case was reported by a consumer and describes the occurrence of DYSPHONIA (voice has been in and out lately), RHINORRHOEA (sniffles that day [after second dose]), NASAL DISCOMFORT (it felt like a train hit my nose), SINUS DISORDER (sinus/sinus part wasn't bad for a brief moment [when vomiting]/sinus came back the next day) and COUGH (coughing every night 11 PM to 3 AM/dry hacking cough) in a 34-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 045L21A and 066H21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 13-Jan-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 16-Feb-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 16-Feb-2022, the patient experienced RHINORRHOEA (sniffles that day [after second dose]). On 17-Feb-2022, the patient experienced NASAL DISCOMFORT (it felt like a train hit my nose), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (come home from work / couldn't work the whole day), FATIGUE (tired/Fatigue), NAUSEA (nausea) and HEADACHE (headache). On 22-Feb-2022, the patient experienced DIARRHOEA (diarrhea [constantly]) and VOMITING (vomiting [constantly]). On 23-Feb-2022, the patient experienced SINUS DISORDER (sinus/sinus part wasn't bad for a brief moment [when vomiting]/sinus came back the next day). On 05-Mar-2022, the patient experienced MUSCULOSKELETAL CHEST PAIN (hurting so bad in my costal muscles near my ribs/ ribs were so sore) and MYALGIA (hurting so bad in muscles near ribs). On an unknown date, the patient experienced DYSPHONIA (voice has been in and out lately), COUGH (coughing every night 11 PM to 3 AM/dry hacking cough), SECRETION DISCHARGE (The drainage is almost 24/7), DRY MOUTH (She has to keep her mouth open a lot because it's too dry, even if she drinks gallons of water.), ILLNESS (so sick), HYPERHIDROSIS (sweats all over my legs for hours), BACK PAIN (back was hurting), MOBILITY DECREASED (can't even get out of bed/couldn't lay on my side or my back/hardly go to her fridge or bathroom) and PYREXIA (fever/highest was 100). The patient was treated with EUCALYPTUS GLOBULUS OIL, MENTHOL (ROBITUSSIN COUGH DROPS) for Thrush, at an unspecified dose and frequency. At the time of the report, DYSPHONIA (voice has been in and out lately), RHINORRHOEA (sniffles that day [after second dose]), NASAL DISCOMFORT (it felt like a train hit my nose), SINUS DISORDER (sinus/sinus part wasn't bad for a brief moment [when vomiting]/sinus came back the next day), MUSCULOSKELETAL CHEST PAIN (hurting so bad in my costal muscles near my ribs/ ribs were so sore), SECRETION DISCHARGE (The drainage is almost 24/7), DRY MOUTH (She has to keep her mouth open a lot because it's too dry, even if she drinks gallons of water.), ILLNESS (so sick), HYPERHIDROSIS (sweats all over my legs for hours), BACK PAIN (back was hurting), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (come home from work / couldn't work the whole day), DIARRHOEA (diarrhea [constantly]), MYALGIA (hurting so bad in muscles near ribs), PYREXIA (fever/highest was 100), VOMITING (vomiting [constantly]), FATIGUE (tired/Fatigue), NAUSEA (nausea) and HEADACHE (headache) outcome was unknown and COUGH (coughing every night 11 PM to 3 AM/dry hacking cough) and MOBILITY DECREASED (can't even get out of bed/couldn't lay on my side or my back/hardly go to her fridge or bathroom) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: negative (Negative) negative. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided by the reporter. This case was linked to MOD-2022-506685 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Negative ; Result Unstructured Data: negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 29.12.2020
- Beginn
- 02.03.2022
- Tage bis Beginn
- 428,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
Abdominal pain lower
Anaemia
Appendicectomy
Appendicitis
Appendicitis perforated
Atelectasis
Body temperature increased
COVID-19
Chronic kidney disease
Computerised tomogram abnormal
Diarrhoea
Endotracheal intubation
Extra dose administered
Flatulence
Goitre
Hyperglycaemia
Hyponatraemia
Symptomtext
A 63-year-old female, resident of facility, gets her healthcare through the Health System. She is a kidney transplant patient and sees a nephrologist in city, who follows that. She went to the Clinic on Friday, February 25th, complaining of vaginal itching. She was given a topical cream and an antibiotic for UTI. She went back home and later that same day began having significant abdominal pain. So, she returned to the clinic and for unclear reasons, they tested her for COVID and found her to be COVID positive. She says she has had 4 vaccinations for COVID, has had no respiratory symptoms. She said they really did not address her abdominal pain that night. They had arranged for her to come back today to the clinic to receive sotrovimab because of her COVID positive test. However, she told them about her ongoing abdominal pain, which has been fairly constant since last Friday, and they directed her to the emergency room instead. There, her COVID test was negative and she underwent a CT scan indicating appendicitis. Therefore, she was sent here, apparently not having General Surgery anywhere closer. At the time of her transfer, it was relayed that she also had pneumonia, pyelonephritis, and it was initially suggested they may try Medical Center in city because of her kidney transplant status. They apparently contacted the Medical Center, but they could find no record of her having a transplant there, and declined the transfer. So, she was eventually accepted here. She says that her vaginal itching has cleared up, but she continues to have significant right lower quadrant abdominal pain. She had some nausea, vomiting, and diarrhea when it first started but this has since stopped. She was noted to have temp of 102 at the outside facility. DISCHARGE: 3/6/2022 Transferred from hospital for surgery 1. Acute appendicitis with microperforation. continued meropenem which was started at the outside hospital, until appendix removed, General Surgery consultation appreciated, Doctor took to OR 3/3; can now stop abx 2. Stage 4 chronic kidney disease with renal transplant status. Will continue her cyclosporine and mycophenolate. Do not know her baseline renal function, but certainly she is in the stage IV CKD range right now. She was on 3 days perioperative hydrocortisone in replace of prednisone Back to oral prednisone 3/6 am 3. Chronic anemia, stable 4. Mild hyponatremia, resolved 5. Type 2 diabetes mellitus with hyperglycemia. Hold glipizide. Sliding scale insulin. Stopped DKA protocol, chronic metabolic acidosis due to CKDz 6. Obesity with obstructive sleep apnea. Continue home CPAP if we can find her settings and/or machine for when extubated *** this is likely reason for reintubation post-op 7. Recurrent urinary tract infection. The air seen in the transplanted kidney on CT clinically does not appear to be consistent with emphysematous pyelonephritis. She has been on broad-spectrum antimicrobials anyway in the form of meropenem. 8. Atelectasis. She is not hypoxemic, no evidence of bacterial pneumonia. Again, as above, she will be on fairly broad antibiotic coverage. 9. Rheumatoid arthritis with Sjogren syndrome. She is immunosuppressed. She has chronic changes, but nothing that looks like acute synovitis. 10.Multinodular goiter seen on imaging, chronic and she says they are just following this for now and has an endocrinologist she sees 11.History of Clostridium difficile colitis. Monitored with her being on broad antibiotic therapy, never had diarrhea here. 12.Hypertension. She is normotensive currently
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 02.03.2022
- Impfdatum
- 02.03.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pharyngeal paraesthesia
Pharyngeal swelling
Symptomtext
Patient arrived for Moderna Booster at 1530. Reports hx of "mild throat swelling" after first shot that resolved with liquid Tylenol. Received second dose without complication. Cleared by HCP to receive booster. At 1544, pt complained of slight throat tingling and requested Benadryl. Provided 50mg Benadryl. Counseled to avoid driving, operating heavy machinery, or anything requiring concentration due to sedating effects. Monitored closely for additional 25 minutes with complete resolution of symptoms. Pt left accompanied by partner and was instructed to seek emergency services if his symptoms recur.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pharyngeal paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Bee stings, latex
- Vorherige Impfungen
- Moderna 1st dose on 3/5/21, stated his throat had "mild swelling," but resolved with "liquid Tylenol"
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 27.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Dyspnoea
Rash
Rash erythematous
Symptomtext
I started getting little rashes on 02/12/2022 then it started getting worse like bigger red rashes then a few days later my breathing started becoming off, like at night time when I lay down I can?t breath well (feels like my asthmas coming back) now it?s when I?m walking places I start not being able to breath well. I?ve been taking Benadryl daily since it started.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- I tested positive for covid on 02/03/2022 but was unaware of having it until my job told me on 2/10/2022 that I tested positive on 02/03/2022
- Vorgeschichte
- My asthma seems to be coming back
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 23.12.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Burning sensation
Chest X-ray normal
Erythema
Mechanical urticaria
Pain
Paraesthesia
Pruritus
Symptomtext
Extreme itching, burning under skin, pins-and-needles, tingling. Painful. Extreme redness when itched or scratched. Diagnosed by allergist/immunologist with dermatographia. Treatment: prescribed Claritin (double dose) Outcomes: Condition still ongoing 7 weeks after shot. Claritin alleviates some itching, but not the burning or pins-and-needles sensation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Routine bloodwork conducted to eliminate other conditions (1/10). Bloodwork normal. Chest X-ray clear. (1/12) Palpation of neck/throat showed no concerns.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Magnesium, Vitamin D, CBD oil
- Allergien
- None known.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Cough
Dizziness
Dyspnoea
Impaired work ability
Tremor
Symptomtext
Shortness of breath, cough, chest tightness, dizziness, weakness, shaky, took Benadryl and had took took take time off of work. The symptoms lasted for two weeks before relief began.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Migraines and hypertension
- Andere Medikamente
- Verapamil, metoprolol, Pepcid, topamax, K10 extended release, multi vitamin
- Allergien
- Eggs, shellfish
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Crying
Dizziness
Fatigue
Nausea
Palpitations
Pharyngeal swelling
Swollen tongue
Tremor
Symptomtext
10 mins slight chest pains, went to walk it off after 15 mins. Around 40 mins after while driving was dizzy, fatigue and nausea, around 47 mins after while driving throat closing and back of tongue swelling which turned into crying and uncontrollably shaking and heart racing at around 60-65 mins only had chest pain again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, psoriasis, psoriatic arthritis
- Andere Medikamente
- Naproxen, cyclobenzaprine, xeljanz, magnesium, b6, multivitamin, fenugreek , birth control
- Allergien
- Humira, latex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Dysphagia
Dyspnoea
Hypoaesthesia
Hypoaesthesia oral
Oropharyngeal discomfort
Symptomtext
Patient had chest tightness and grabbing her chest , states her throat feel funny, hard to swallow. Oxygen 99% on room air. 15 min later, her tongue states is numb and chest tightness is worse. Patient grabbing on her neck. Blood pressure was 177/92. Heart rate was 98. Respirations was 18. EpiPen administered and 911 called. Patient placed on 2L nasal cannula. Patient states shortness of breath, but oxygen at 99% , still states hard time swallowing , and grabbing on her chest. Switched to nonrebreather mask at 5L. Blood pressure was 160/91. Heart rate was 88. Oxygen saturation was 100%. Respiration was 18. Patient left via ambulance, paramedics were present, patient continued to have chest tightness and numbness in extremities and shortness of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HTN (HYPERTENSION) DM 2 BILAT TMJ DISORDER IRRITABLE BOWEL SYNDROME CKD STAGE 1 GERD (GASTROESOPHAGEAL REFLUX DISEASE)
- Andere Medikamente
- Rosuvastatin (CRESTOR) 20 mg Oral Tab Linagliptin (TRADJENTA) 5 mg Oral Tab metFORMIN (GLUCOPHAGE) 1,000 mg Oral Tab glipiZIDE (GLUCOTROL) 10 mg Oral Tab amLODIPine (NORVASC) 5 mg Oral Tab Metoprolol Tartrate (LOPRESSOR) 50 mg Oral Tab Levo
- Allergien
- Ace Inhibitors [Angiotensin-converting Enzyme Inhibitors] Hctz [Hydrochlorothiazide] Hydrocodone-acetaminophen
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site mass
Injection site pain
Muscular weakness
Paraesthesia
Symptomtext
The patient complained of a lump at the injection site, pain, muscle weakness and tingling down her left arm the morning after her vaccine. She treated it with ice and heat. Her symptom persisted and on day 4 she was seen by employee health and referred to a physician for evaluation and treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Celica Disease
- Andere Medikamente
- Paxil 20 mg oral, Protonix 20 mg oral
- Allergien
- Diazepam, Gluten, Hydrocodone, Morphine Sulfate, Penicillins Class
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 29.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Condition aggravated
Eye pain
Headache
Herpes zoster
Inflammation
Myalgia
Pain
Rash
Rash pruritic
Rash vesicular
Swelling of eyelid
Symptomtext
The day after I received the booster, I was in bed with joint pain and muscle aches all day. I expected this, as this happed with my first two shots. What I did not expect is that within the next week, I got an ear-splitting headache only on my right side - right above my ear. I could feel that something was inflamed. I took Excedrin to dull the pain. The headache, however has NOT gone away and now I broken out in a shingles type rash on my head, but ONLY the RIGHT side of my head. It's itchy, painful, blistering and now into it's second week, is finally showing signs of starting to go away. I have been treating the "shingles" with Melaleuca oil and have been taking an Oregano supplement as a natural antibiotic. Those, combined with over the counter aspirin are keeping the edge off the pain, but this is getting old. This morning (1/29), my right eye was almost swollen shut, after taking one Excedrin and going outside into cool weather, my right eye has been getting better, but it's still fairly swollen. There is a pulsing pain behind my right eye, so I know the inflammation hasn't totally gone away yet. Happy to talk with someone to answer questions - but the end result is, I want this cleared up asap.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Have not had any tests, as my insurance is major medical only and these tests may have run into the thousands, which I cannot afford.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Adverse reaction
Pharyngeal paraesthesia
Swollen tongue
Symptomtext
Covid-19 vaccine administered and patient experienced an adverse reaction: EPINEPHrine (Epipen) administered and 911 called and Ambulance transport Patient came into clinic stating she has some tingling after first Moderna Vaccine, did not escalate. Second Moderna vaccine patient stated they had anaphylaxis 35 mins after getting the vaccine as seen in note from ED on 4/27/2021. Today, patient got the 3rd dose of the Moderna vaccine at 10:05am, patient started to feel tingling in her throat and tongue swelling about 10 mins after vaccine administration. I observed patients mouth and was not able to see throat and tongue was swollen. Patient denied difficultly breathing and swallowing, chest pain, dizziness. EPI pen was given in her left anterior lateral thigh @10:17am. Patient was monitored closely and 911 was called. After 5 mins patient stated that the swelling was persistent and slightly worsening. Tongue did appear slightly more swollen; however, EMS had arrived to transport patient to hospital. Patient stable throughout encounter. Care was transferred to EMS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pharyngeal paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Multiple sclerosis Anxiety state Paresthesias Local infection of wound Atypical squamous cells of undetermined significance (ASC-US) on cervical Pap smear Nausea Pain in female pelvis Cyst of left ovary Right inguinal hernia Immunoglobulin G subclass deficiency CVID (common variable immunodeficiency) Recurrent sinusitis SLE (systemic lupus erythematosus) Right hip pain Fibroadenoma Breast mass, right
- Andere Medikamente
- acyclovir (ZOVIRAX) 400 mg tablet albuterol 5 mg/mL nebulizer solution albuterol 90 mcg/actuation HFA inhaler ALPRAZolam (XANAX) 0.25 mg tablet amLODIPine (NORVASC) 5 mg tablet azelastine (ASTELIN) 137 mcg nasal spray belimumab (Benlysta) 2
- Allergien
- Hydrocodone-acetaminophen- Hives, rash, itching, pruritic, headache Cephalexin- Red Man Syndrome Codeine- Itching, pruritis Doxycycline- Hives/urticaria, Other (Specify with Comments) Immune Globulin (Human) (Igg)- Hives/urticaria Vancomycin- Rash, Red Man Syndrome Adhesive- Rash Cephalosporins- Hives/urticaria, Rash, Swelling, Other (Specify with Comments) Fluticasone Propion-salmeterol- Palpitations, Other (Specify with Comments) Sulfamethoxazole-trimethoprim- Rash, Red Man Syndrome, Other (Specify with Comments) Vancomycin Analogues Other (Specify with Comments), Rash
- Vorherige Impfungen
- 4/27/21- Anaphylaxis
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Pruritus
Urticaria
Symptomtext
Patient c/o of hives/itchiness and mild sob the night after vaccination at 9 pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Chronic Asthma
- Andere Medikamente
- n/a
- Allergien
- codeine
- Vorherige Impfungen
- -
- Staat
- AS
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Dyspnoea
Feeling cold
Hyperventilation
Stomatitis
Symptomtext
0953 - pt returned to room stating that she felt cold, dizzy, SOB (felt like she just exercised), weird feeling in mouth, light headed. VS 192/116, 97.5, 38, 98, 99% RA 0955 - called Rapid Response to come 0957 - VS 184/110, 83, 36 same symptoms, breathing feels like sh over-exerted exercising, feeling a little better, still has weird feeling in mouth 1000 - rapid response arrived. VS done BP still elevated, RN decided to take her to ER. Left @ 1003
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Tdap - red streaking immediately, passed out
- Staat
- -
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Joint lock
Loss of personal independence in daily activities
Mobility decreased
Symptomtext
Left Shoulder locking up and inability to bend elbow or put his coat on after the injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysarthria
Dyskinesia
Eye movement disorder
Fatigue
Feeling abnormal
Headache
SARS-CoV-2 test negative
Tremor
Symptomtext
pt said he felt bad, gave him water, he started weaving in the chair, then he was slurring his words, he said he was tired, eyes rolled up a few times, we kept him talking. He was shaking and having tardine dyskinesia like movements. He then said his head hurt. Stated not diabetic, has had seizures previously, and a family member tested postivie earlier in the day but he is negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- prior seizures but not with vaccine, traumatic head injury and broken neck
- Andere Medikamente
- baclofen was all he told us
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Cardiac murmur
Dyspnoea
Electrocardiogram abnormal
Symptomtext
On or about 12/29/2021 I began to have severe shortness of breath. I scheduled an appointment with my internist on 1/6/2022 who scheduled me for an EKG on 1/7 after hearing a murmur during my visit. The EKG confirmed the atrial fibrillation and I was referred to cardiologist Dr. who confirmed the diagnosis and began treatment with Eliquis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Please see above.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension and obesity
- Andere Medikamente
- Perindopril - 4mg; Prevastatin - 20mg; Amlodipine Besaylate - 10mg; Levothroxine - 25 mcg; Hydrochlorothizide - 12.5 mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Dyspnoea
Pain
Pain in extremity
Symptomtext
chest pain with radiation into arms bilaterally, shortness of breath, intermittent chest discomfort 2x days prior to hospitalization.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- hypertension, psoriatic arthritis, palpitations
- Vorgeschichte
- hypertension, psoriatic arthritis, palpitations
- Andere Medikamente
- betamethason lotion, folic acid, gabapentin, lxekizumab (last dose 12/16/2021), losartan, methotrexate (on hold 14d post COVID vaccine on 1/8/2022), sildenafil
- Allergien
- lisinopril
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 16.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood glucose increased
Blood magnesium normal
Burning sensation
Butterfly rash
Chest pain
Condition aggravated
Differential white blood cell count
Dyspnoea
Electrocardiogram P wave
Electrocardiogram PR interval
Electrocardiogram QRS complex
Electrocardiogram QT interval
Electrocardiogram T wave abnormal
Fatigue
Feeling hot
Fibrin D dimer normal
Full blood count
Injection site pain
Symptomtext
Around 45 minutes to an hour after my vaccine my lupus malar rash appeared on my face, bright red and burning hot, then spreading to my cheeks, chin, nose and forehead. A couple hours later a chain of events started. The back of my head and neck felt like they were covered in hot, prickly heat. There was no redness or rash at site. My arm that received the shot hurt from my neck down to my fingers. I then started to get heart palpitations almost constantly. I was extremely tired so I layed down. The entire left side of my body hurt including my leg. I got tmj pain in my right jaw and lost feeling in my right hand. I took my temperature and it was only 99.5 F. I slept for hours. Woke up with no heart palpitations but everything else stayed the same. The next morning my heart palpitations came back. I still had loss of feeling in right hand and extreme fatigue, face redness and pain down my left side. Everything else had dissipated. I called my doctors office and spoke to a nurse in triage who recommended I go the the ER. At this time I had started to have shortness of breathe and cramping in the center of my chest. I went to hospital where they took my blood and did and ECG. I was then sent home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Tests performed on 01/15/2022 at Hospital. My ECG said as follows: Rate-68, Pr-163, Qrsd-91, qt-388, etc-414, p-14, qrs-11, t-42, Sinus rythym non specific t wave abnormality. D dimer normal, tronopin quant normal, thyroid normal, magnesium normal, basic metabolic, high glucose, cbc with diff, low mch, low mchc.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Fibromyalgia, lupus, interstitial cystitis, irritable bowel syndrome
- Andere Medikamente
- Nexium, spironolactone, tizanidine, hydroxychloroquine, hydrocodone, probiotic
- Allergien
- Sulfa, steroids, toradol
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Herpes zoster
Pain
Rash
SARS-CoV-2 test
Symptomtext
Rash underneath the breast and I didn't think much of it. I was helping my sister-in-law move and I talked to my mom, and she said that that has happened to her before. As you get older you get hotter underneath there. My grandmother also has gotten them there and she suggested creams. But it progressively got worse. It was on Monday that I woke up, I noticed that it was not getting any better and it had spread. I sent a photo to my gynecologist, and she said that it was Shingles. I went to visit her, and she confirmed it was Shingles and prescribed medication for 10 days. I had a hard time with the booster because I also had a problem with the first vaccine as well. I also had aches and pains with that first vaccine as well as this booster. I can't say that I got this from the booster, but I can't rule it out as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- COVID test 2 days ago - waiting for lab results
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 Diabetes, Kidney Disease (controlled, went back to normal range), Seizures (controlled with medication)
- Andere Medikamente
- Metformin, Atorvastatin, Tegretol, Gabapentin, Citalopram, Folic Acid , Nexium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anxiety
Asthenia
Condition aggravated
Heart rate increased
Hypertension
Symptomtext
I felt weak and anxious, pulse was high. Home blood pressure monitor showed high blood pressure and pulse of 98. I called for an ambulance. EMT person measured blood pressure to be Systolic-195 Diastolic-95. EMT person advised me that the hospital is filled and I will wait there many hours to be examined by an MD. I decided to stay home and take an extra Amlodipine tablet, and sleep aid pill "Relaxium". EMT stayed and observed me while my blood pressure decreased to a safe level. EMT advised me to buy a new blood pressure device for accuracy. MD advised me to not take many BP readings one after another and to relax, and increased my Amlodipine daily dosage.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 01/08/2022 Blood Pressure 195/95 mm[Hg] measured by EMT. 01/11/2022 Blood Pressure 150/78 mm[Hg] measured by MD.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure, high cholesterol
- Andere Medikamente
- Amlodipine, Vitamin A,B6,B12,C,D3,K2, Folate, Fish oil, Nattokinase, Quercetin, Zinc, Magnesium, Niacin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase increased
Albumin globulin ratio
Anion gap
Aspartate aminotransferase
Basophil count decreased
Bilirubin conjugated
Blood albumin increased
Blood alkaline phosphatase
Blood calcium normal
Blood chloride normal
Blood creatinine normal
Blood glucose normal
Blood potassium normal
Blood sodium normal
Blood urea nitrogen/creatinine ratio
Brain natriuretic peptide increased
COVID-19
Carbon dioxide normal
Symptomtext
Beginning on/around 12/26/2021: - Chest pain - Shortness of breath - Feelings of having a fast-beating, fluttering, or pounding heart
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 5,0
- Labordaten
- 12/30 - Chest X-Ray 12/31 - D?DIMER,QUANTITATIVE ?D?DIMER? 12/31 - Echocardiogram Narrative Value Ref Range % Performed At DEPARTMENT OF CARDIOLOGY Pathologist Signature DEPARTMENT OF CARDIOLOGY - 12/31/2021 2:03 PM Transthoracic Echocardiographic Report Gender: M Study Date: 12/31/2021 12:15:06 PM Ht(Cm): 185 Wt(Kg): 325.7 BSA: 4.09 Location: Heart Rate: 100 BMI: 95.16 Procedures: Echocardiographic Report: 93306 - Echocardiography, transthoracic, real-time with image documentation (2D), includes M-mode recording; when performed, complete, with spectral Doppler echocardiography, and with color flow Doppler echocardiography. Indications: A-Fib/Flutter, and Technically difficult study due to limited acoustic windows. Findings: Left Ventricle: Mildly dilated left ventricle. Moderately depressed left ventricular systolic function. LV Ejection Fraction is visually estimated 30-35 %. Right Ventricle: Mildly dilated right ventricle. Mildly depressed right ventricular systolic function. Left Atrium: Mildly dilated left atrium. Right Atrium: The right atrium is normal in size. Mitral Valve: The mitral valve demonstrates normal leaflet morphology. There is moderate mitral valve regurgitation. Aortic Valve: Normal appearance and function of the aortic valve. Tricuspid Valve: Tricuspid valve not well visualized. Pulmonic Valve: Pulmonic valve not well Pericardium: Normal pericardium with Aorta: Not well visualized. IVC: Not well visualized. Measurements: 2D/M Mode Measurement LVIDd 2D LVIDs 2D IVSd 2D LVPWd 2D Value 6.5 5.7 1.00 1.00 Normal Range [4.2-5.9]cm [2.3-3.9]cm [0.60-1.00]cm [0.60-1.00]cm Doppler Measurement Value AV Peak Vel 140.0 AV Mean Vel 99.2 AV Peak PG 6.0 AV Mean PG 5.0 Normal Range [ 100.0 - 170.0 ] cm/sec [ 70.0 - 90.0 ] cm/sec [2.0-9.0]mmHg [2.0-4.0]mmHg Conclusions: visualized. no pericardial effusion. AVA Vmax AVA VTI 3.6 [ 2.0 - 4.0 ] cm2 3.3 [ 2.0 - 4.0 ] cm2 1. Technically difficult study due to limited acoustic windows. 2. Mildly dilated left ventricle. Moderately depressed left ventricular systolic function. LV Ejection Fraction is visually estimated 30-35 %. 3. Mildly dilated right ventricle. Mildly depressed right ventricular systolic function. 4. The mitral valve demonstrates normal leaflet morphology. There is moderate mitral valve regurgitation. Electronically Signed By: 2021-12-31 14:02:59 Procedure Note ? 12/31/2021 Formatting of this note might be different from the original. Transthoracic Echocardiographic Report Patient Name: Gender: MStudy Date: 12/31/2021 12:15:06 PM Ht?Cm?: 185 Wt?Kg?: 325.7 BSA: 4.09 Heart Rate: 100 BMI: 95.16 Procedures: Echocardiographic Report: 93306 ? Echocardiography, transthoracic, real?time with image documentation ?2D?, includes M?mode recording; when performed, complete, with spectral Doppler echocardiography, and with color flow Doppler echocardiography. Indications: A?Fib/Flutter, and Technically difficult study due to limited acoustic windows. Findings: Left Ventricle: Mildly dilated left ventricle. Moderately depressed left ventricular systolic function. LV Ejection Fraction is visually estimated 30?35 %. Right Ventricle: Mildly dilated right ventricle. Mildly depressed right ventricular systolic function. Left Atrium: Mildly dilated left atrium. Right Atrium: The right atrium is normal in size. Mitral Valve: The mitral valve demonstrates normal leaflet morphology. There is moderate mitral valve regurgitation. Aortic Valve: Normal appearance and function of the aortic valve. Tricuspid Valve: Tricuspid valve not well visualized. Pulmonic Valve: Pulmonic valve not well visualized. Pericardium: Normal pericardium with no pericardial effusion. Aorta: Not well visualized. IVC: Not well visualized. Measurements: 2D/M Mode Doppler Measurement Value Normal Range Measurement Value Normal Range LVIDd 2D 6.5 [ 4.2 ? 5.9 ] cm AV Peak Vel 140.0 [ 100.0 ? 170.0 ] cm/sec LVIDs 2D 5.7 [ 2.3 ? 3.9 ] cm AV Mean Vel 99.2 [ 70.0 ? 90.0 ] cm/sec IVSd 2D 1.00 [ 0.60 ? 1.00 ] cm AV Peak PG 6.0 [ 2.0 ? 9.0 ] mmHg LVPWd 2D 1.00 [ 0.60 ? 1.00 ] cm AV Mean PG 5.0 [ 2.0 ? 4.0 ] mmHg AVA Vmax 3.6 [ 2.0 ? 4.0 ] cm2 AVA VTI 3.3 [ 2.0 ? 4.0 ] cm2 Conclusions: 1. Technically difficult study due to limited acoustic windows. 2. Mildly dilated left ventricle. Moderately depressed left ventricular systolic function. LV Ejection Fraction is visually estimated 30?35 %. 3. Mildly dilated right ventricle. Mildly depressed right ventricular systolic function. 4. The mitral valve demonstrates normal leaflet morphology. There is moderate mitral valve regurgitation. Electronically Signed By: 2021?12?31 14:02:59 Performing Organization Address CARDIOLOGY Lab Results (12/31): D?DIMER, QUANTITATIVE ?D?DIMER? ? Final result ?12/31/2021 12:03 PM? Component D?Dimer Value 0.59 ?H? Comment: Reference Range Comment: . <0.50 Negative . 0.50 - 2.00 Possible Thrombotic Event . >2.00 Suggestive of DIC Increases in D-Dimer concentration observed with thromboembolic events can be variable due to localization, extension and age of thrombus. Therefore, a thromboembolic event cannot be excluded with certainty solely on the basis of a D-Dimer concentration being within the reference range of ostensibly healthy persons. Results of this test should always be interpreted in conjunction with the patient's medical history, clinical presentation and other findings. Ref Range <0.50 ug/mLFEU Performed At Pathologist Signature Specimen Blood ? BLOOD Performing Organization Address Phone Number CORONAVIRUS ?COVID?19?, PCR, RAPID ?CORONAVIRUS ?COVID?19?, NAA, RAPID? ? Final result ?12/31/2021 12:50 AM? Component Value Ref Range Performed At Pathologist Signature Patient No Symptomatic Specimen Nasopharyngeal ? NASOPHARYNGEAL Performing Organization Address SARS?CoV?2,RNA, Negative Negative Rapid Comment: A positive result for COVID-19 indicates that RNA from SARS-CoV-2 was detected and the patient is infected with virus and presume to be contagious. Laboratory result should always be considered in the context of clinical observations and epidemiological data in making a final diagnosis and patient management decisions. A negative test result for this test means SARS-CoV-2RNA was not present in the specimen above the limit of detection, However, a negative result does not rule out COVID-19 and should not be used as the sole basis for treatment or patient management decisions. A negative result does not exclude the possibility of COVID-19. When diagnostic testing is negative, the possibility of a false negative should be considered if the context of a patient's recent exposures and the presence of clinical signs and symptoms consistent with COVID-19. If COVID-19 is still suspected based on exposure history together with other clinical findings , re- testing should be considered. This laboratory is certified under the Clinical Laboratory Improvement as qualified to perform moderate to high complexity clinical laboratory testing. This assay is for in vitro diagnostic use under the FDA Emergency Use Authorization and should be used for clinical purposes. SCANNED RESULT: GENERAL NON?INTERFACED LAB ?GENERAL NON INTERFACED LAB? ? Final result ?12/31/2021 12:00 AM? Narrative This result has an attachment that is not available. XRAY CHEST 1 VIEW FRONTAL PORTABLE ? Final result ?12/30/2021 11:57 PM? Anatomical Region Laterality Modality Chest, Body N/A Computed Radiography Specimen Impressions IMAGING CENTER AND DEPARTMENT - 12/31/2021 6:08 AM Cardiomegaly with findings suggesting pulmonary edema. Reviewed and Interpreted 12/31/2021 6:08 AM Narrative IMAGING CENTER AND DEPARTMENT AT - 12/31/2021 6:08 AM EXAM: XRAY CHEST 1 VIEW FRONTAL PORTABLE DATE: 12/30/2021 11:57 PM HISTORY: Chest Tightness. TECHNIQUE: Single frontal view of the chest was obtained. COMPARISON: None FINDINGS: The lung volumes are low. There is pulmonary vascular congestion and mild bilateral interstitial opacities with pulmonary cephalization. No large pleural effusion or pneumothorax. The heart size is enlarged. The bones are intact. Procedure Note 12/31/2021 Formatting of this note might be different from the original. EXAM: XRAY CHEST 1 VIEW FRONTAL PORTABLE DATE: 12/30/2021 11:57 PM HISTORY: Chest Tightness. TECHNIQUE: Single frontal view of the chest was obtained. COMPARISON: None FINDINGS: The lung volumes are low. There is pulmonary vascular congestion and mild bilateral interstitial opacities with pulmonary cephalization. No large pleural effusion or pneumothorax. The heart size is enlarged. The bones are intact. IMPRESSION: Cardiomegaly with findings suggesting pulmonary edema. Reviewed and Interpreted 12/31/2021 6:08 AM Performing Organization IMAGING CENTER AND DEPARTMENT MEDICAL CENTER Phone Number TROPONIN I ? Final result ?12/30/2021 11:30 PM ? Component Troponin I Value 0.02 Comment: <=0.04 ng/mL: NEGATIVE - repeat testing in four to six hours if clinically indicated. 0.041-0.39 ng/mL: Suspicious for myocardial injury. Serial measurement may be necessary to confirm or exclude the diagnosis of acute coronary syndrome. Repeat testing in four to six hours if indicated. 0.40 ng/mL or greater: Consistent with myocardial injury. Clinical and laboratory correlation recommended. Ref Range 0.00 ? 0.04 ng/mL Performed At Pathologist Signature Specimen Performing Organization Address Phone Number PROTIME?INR ?PROTHROMBIN TIME? ? Final result ?12/30/2021 11:30 PM? Component Value Ref Range Performed At Pathologist Signature Prothrombin Time 14.0 11.3 ? 15.4 sec. INR 1.1 <1.3 Comment: The new Thromboplastin Reagent for PT testing and Coumadin monitoring has an International Sensitivity Index (ISI) of 1.27. Specimen Blood ? BLOOD Performing Organization The International Normalized Ratio (INR) will continue to be reported for each PT. The change in the PT seconds does not affect the INR or the recommendations for oral anticoagulant therapy. Recommendations as outlined by the College of Chest Physicians: New Populations INR Value PT VALUE (sec) Low-intensity OAC therapy 1.5-2.0 18.1-22.7 Moderate-intensity OAC therapy 2.0-3.0 22.7-31.2 High-intensity OAC therapy 2.5-3.5 or 27.0-35.2 3.0-4.0 31.2-39.1 BRAIN NATRIURETIC PEPTIDE ?B?TYPE NATRIURETIC PEPTIDE ?BNP?? ? Final result ?12/30/2021 11:30 PM? Component B?Type Natriuretic Peptide Specimen Blood ? BLOOD Value 543 ?H? Ref Range 0 ? 100 pg/mL Performed At Pathologist Signature Phone Number Performing Organization Address COMPREHENSIVE METABOLIC PANEL ?METABOLIC PANEL, COMPREHENSIVE ?CMP?? ? Final result ?12/30/2021 11:30 PM? Component Value Sodium 141 Chloride 105 Anion Gap 16.0 Ref Range 136 ? 145 mEq/L 94 ? 108 mEq/L Performed At Pathologist Signature Glucose Random 107 65 ? 110 mg/dL Potassium 4.0 3.5 ? 5.1 mEq/L Total Co2 24 22 ? 30 mEq/L Calcium 9.0 8.8 ? 10.5 mg/dL Calculated 300 278 ? 305 mOsm/kg Osmolality LAB Bun 18 LAB 8 ? 26 mg/dL 6.4 ? 8.5 G/dL 2.4 ? 3.5 G/dL 0.0 ? 0.3 mg/dL 38 ? 126 IU/L 15 ? 37 U/L Creatinine 1.1 0.7 ? 1.2 mg/dL Bun/Creatinine Ratio Total Protein Globulin Direct Bilirubin Alkaline Phosphatase Aspartate Aminotransferase Specimen Blood ? BLOOD 16 8.0 4.3 ?H? 0.2 44 44 ?H? Estimated GFR > 60 >60 Albumin 3.7 3.5 ? 5.0 g/dL A/G Ratio 0.9 ?L? 1.0 ? 2.0 Total Bilirubin 1.0 0.4 ? 2.0 mg/dL Alanine 112 ?H? 17 ? 63 IU/L Aminotransferase LAB Performing Organization Phone Number CBC WITH DIFFERENTIAL ? Final result ?12/30/2021 11:30 PM? Component Value WhiteBloodCount 9.4 Ref Range 4.5 ? 11.0 x1000 14 ? 18 G/dL 78 ? 97 fl 33 ? 37 % 150 ? 500 x1000/uL Performed At Pathologist Signature Red Blood Count 4.76 4.4 ? 6.0 Mill/uL Hemoglobin Mean Corpuscular Volume Mean Corpuscular Hgb Conc Platelet Count 13.1 ?L? 85.8 32.1 ?L? 200 Hematocrit 40.9 ?L? 45 ? 52 % Mean Corpuscular 27.6 ?L? 28 ? 32 pg Hemoglobin RBC Distribution 15.7 ?H? 11.6 ? 14.6 % Width Mean Platelet 8.0 7.4 ? 10.4 fl Volume Type Of Differential Lymphocyte Eosinophil Neutrophil Monocyte Basophil Specimen Blood ? BLOOD AUTO 3.1 0.1 58.4 7.5 0.3 Seg Neutrophil 5.5 1.8 ? 8.4 x10*3/uL 0.9 ? 5.5 x10*3/uL 0.0 ? 0.6 x10*3/uL Monocyte 0.7 0.1 ? 0.9 x10*3/uL Basophil 0.0 0.0 ? 0.2 x10*3/uL 40 ? 76 % 2.0 ? 8.0 % 0.0 ? 2.0 % Lymphocyte 32.7 20 ? 50 % Eosinophil 1.1 0.0 ? 5.0 % Performing Organization Address Phone Number
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Morbid obesity, depression, binge-eating disorder
- Andere Medikamente
- Prescriptions: Metformin (500 mg), Atorvastatin (40mg), Valcyclovir (500mg) Supplements: Vitamin C, Vitamin D, Vitamin B12, Calcium/Magnesium, Chromium, Iron, Co-Q10, Omega3, Probiotic, Centrum Multivitamin for Men, Green Coffee Bean Extrac
- Allergien
- Codeine, Dairy Milk (liquid only)
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Full blood count normal
Gait disturbance
Head discomfort
Headache
Hemiparesis
Hypoaesthesia
Mobility decreased
Paraesthesia
Visual impairment
Vitreous floaters
Symptomtext
Pressure at the back of head. I felt numbness in left side of my face. Weakness on my left side. It was hard to lift up my left arm or even walk. I had a headache. I saw seeing floaters (black out) in my left eye. Occasional tingling in my face.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- blood test - normal, complete blood count
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- none
- Allergien
- amniotomy, Cipro, flagyl, Latex, Ambien
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Blood test normal
Chest pain
Chills
Electrocardiogram normal
Myalgia
Pain
Pyrexia
Tachypnoea
X-ray normal
Symptomtext
Myalgia, Fever, Tachypnea & Angina Narrative: In addition to fever/chills/body aches, after my booster I also had chest pain and shortness of breath. Employee received booster on 12/14. The other symptoms were gone by 12/16 but the chest pain remained. Employee went to the ED on the mainland 12/22 and EKG, XRAY, and bloodwork was normal. Chest pain has improved 12/22 but not back to normal yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Injection site hypoaesthesia
Injection site paraesthesia
Injection site warmth
Pyrexia
Symptomtext
redness in arm vaccine was received in, that progressed to under the arm and onto the back. Site has heat, tingling and numbness in area. Patient has ran low grade fever post vaccination (100.2). Patient contacted physician and received cephalexin for possible cellulitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- leukemia
- Vorgeschichte
- leukemia
- Andere Medikamente
- no
- Allergien
- penicillin allergy
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 07.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site erythema
Injection site paraesthesia
Symptomtext
redness and tingling in injection site arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Nausea
Tremor
Symptomtext
Patient reported feeling nausea, weakness, and shaking after receiving Moderna booster. Patient was then placed in reclined position, offered water, and monitored for 30 minutes. After monitor, patient reported feeling better, nausea, shaking, and weakness was much improved and felt normal. Patient was able to walk independently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- hypertension
- Vorgeschichte
- hypertension
- Andere Medikamente
- blood pressure medicine
- Allergien
- none
- Vorherige Impfungen
- Pfizer vaccine, 2/4/2021
- Staat
- MA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Injection site warmth
Oropharyngeal pain
Pharyngeal paraesthesia
Symptomtext
At approx 10-13 min throat pain/tingling. Given zyryec. Resolved around an hour. Day 2 left arm localized at site approx 5-6cm redness/raised/warm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pharyngeal paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Upper respiratory infection
- Vorgeschichte
- HTN, hyperlipdemia
- Andere Medikamente
- At approx 10-12 minutes had throat pain/tingling. 2nd day approx 5cm raised, red warm at site.
- Allergien
- Latex, contact derm
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Burning sensation
Hypertension
Malaise
Panic attack
Symptomtext
Patient came to pharmacy to get Moderna booster. After her shot she told the certified immunizing technician that she didn't feel good. The patient told me she thought she was having a panic attack. Her neck and forehead were burning up. She thought her blood pressure went up. I gave her 2 cold packs to put on her neck and forehead. I gave her a bottled water and took her blood pressure. Her blood pressure was a little high, but she started to feel better after 10-15 minutes. She said she had a much worse reaction to the 2nd dose of Moderna but she didn't indicate anything on her patient form.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Moderna 2nd dose over 6 months ago.
- Staat
- NJ
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 16.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 16,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Brain natriuretic peptide increased
C-reactive protein increased
COVID-19
Chest X-ray abnormal
Cough
Decreased appetite
Dyspnoea
Leukopenia
Pleural effusion
SARS-CoV-2 test positive
Thrombocytopenia
Symptomtext
92-year-old female with a PMH significant for CAD s/p CABG 2v/PIC, CM (EF 45-50%-10/2021), PAF, systolic/diastolic CHF, HTN, HLD, lymphoma, vaccinated Moderna x2 who presented to the ER for complaints of weakness, dry cough, SOB and decreased appetite for about 2 days reason for which she presented to the ER for further evaluation. In the ER, laboratory data revealing BNP 1026, leukopenia, thrombocytopenia and elevated CRP. CXR read as increased interstitial markings with central pulmonary vascular prominence and small bilateral pleural effusions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 3,0
- Labordaten
- 01/01/02022 - SARS-CoV-2 Antigen (++)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CAD s/p CABG 2v/PIC, CM (EF 45-50%-10/2021), PAF, systolic/diastolic CHF. HTN HLD, lymphoma CABG, , LHC s/p PCI to the RCA, Bone marrow biopsy, cholecystectomy, Upper endoscopy and colonoscopy. Smoking Status Never Smoker.
- Andere Medikamente
- amiodarone (Pacerone) 200 mg Tablet Directions: 1 tablet oral daily (Active) apixaban 2.5 mg Tablet Directions: 1 tablet oral every twelve hours (Active) atorvastatin (Lipitor) 40 mg Tablet Directions: 1 tablet oral daily at bedtime
- Allergien
- ezetimibe
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood electrolytes normal
Blood test normal
Dehydration
Dizziness
Fatigue
Hypoaesthesia
Hypovolaemia
Laboratory test normal
Nausea
Orthostatic hypotension
Pain in extremity
Peripheral coldness
Symptomtext
Woke up with extreme dizzyness, nausea and cold/numb hands. After consulting with a doctor over the phone, was advised to go to the ER to check vitals and be examined. Blood pressure dropped when I stood up, after being screened for heart and stroke (negative), blood tests for anemia and electrolytes (negative), was given IV fluids. Determined that I had "vascular depletion" / dehydration (likely from antibody reaction / drawing on vascular system). Additional symptoms included fatigue and sore arm).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- Medical tests available (blood test for anemia and electrolytes).
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- Sulfa and codeine
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 02.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
C-reactive protein increased
Chest pain
Dizziness
Dyspnoea
Dyspnoea exertional
Feeling abnormal
Headache
Malaise
Troponin
Symptomtext
He has not been feeling well since. Last night developed chest pain and shortness of breath. Waves of pain to the top of his head described as "zappy." Causes him to feel like his thinking is foggy as well. Has been feeling dizzy off and on. Walking to Er brought on pain the chest and dyspnea. All symptoms seem to come in waves.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Trop 0.06 CRP 5.6
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Feeling abnormal
Migraine
Myalgia
Nausea
Pyrexia
SARS-CoV-2 test
Vaccination complication
Vaccination site erythema
Vaccination site induration
Vaccination site pain
Vaccination site warmth
Symptomtext
still sore; fever; nausea; achy all over; joint pain; Really bad reaction; felt horrible/She felt bad; Migraine 10/10; hot/still warm; hard/ It was initially hard as a rock; Her arm became red/ It is still red/still has a 4x5 inch mark; This spontaneous case was reported by a nurse and describes the occurrence of VACCINATION COMPLICATION (Really bad reaction), FEELING ABNORMAL (felt horrible/She felt bad), MIGRAINE (Migraine 10/10), VACCINATION SITE WARMTH (hot/still warm) and VACCINATION SITE INDURATION (hard/ It was initially hard as a rock) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for Product used for unknown indication: Pfizer Vaccine (First shot, LOT- Ej1685, Intramuscular.) on 21-Dec-2020, Pfizer Vaccine (Second shot and LOT- EL1283) on 07-Jan-2021. Past adverse reactions to the above products included No adverse event with Pfizer Vaccine and Pfizer Vaccine. On 26-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 27-Dec-2021, the patient experienced VACCINATION COMPLICATION (Really bad reaction), FEELING ABNORMAL (felt horrible/She felt bad), MIGRAINE (Migraine 10/10), VACCINATION SITE WARMTH (hot/still warm), VACCINATION SITE INDURATION (hard/ It was initially hard as a rock), VACCINATION SITE ERYTHEMA (Her arm became red/ It is still red/still has a 4x5 inch mark), PYREXIA (fever), NAUSEA (nausea), MYALGIA (achy all over) and ARTHRALGIA (joint pain). On 30-Dec-2021, the patient experienced VACCINATION SITE PAIN (still sore). On 29-Dec-2021, VACCINATION COMPLICATION (Really bad reaction), FEELING ABNORMAL (felt horrible/She felt bad), MIGRAINE (Migraine 10/10), VACCINATION SITE INDURATION (hard/ It was initially hard as a rock), PYREXIA (fever), NAUSEA (nausea), MYALGIA (achy all over) and ARTHRALGIA (joint pain) had resolved. At the time of the report, VACCINATION SITE WARMTH (hot/still warm), VACCINATION SITE ERYTHEMA (Her arm became red/ It is still red/still has a 4x5 inch mark) and VACCINATION SITE PAIN (still sore) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In December 2021, SARS-CoV-2 test: negative (Negative) She got a COVID test and it was negative. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient's weight was reported as 175 and units were not reported. No concomitant information was reported. Patient Tried to put heat and lots of steroid cream for events. Patient had stated that she still has a 4x5 inch mark in the left deltoid and initially it was hard as rock.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Test Date: 202112; Test Name: COVID-19 Test; Test Result: Negative ; Result Unstructured Data: She got a COVID test and it was negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Blood test
Burning sensation
Condition aggravated
Myalgia
Pain
Pain in extremity
Peripheral swelling
Symptomtext
Muscle and joint pains, swelling below the fingers, burning and aching from the fingers to the shoulders. It may her Chronic Pain Syndrome worse and she believes it is full blown in her left hand and arm. Went to the ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- yes blood work
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic Regional Pain Syndrome
- Andere Medikamente
- trazodone 50mg, lyrica 50mg, tizanidine 2mg, metoprolol 25mg, np thyroid 30mg, vit b12 2500mg, clonidine 0.1mg, peroxitan 10mg, venlafaxine 150mg,
- Allergien
- latex, nicen, regular thyroid meds
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 27.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Hypotension
Symptomtext
Patient felt dizzy and started to sweat. I advise patient to lay down and give him cold compress. I check his blood pressure and it was low . i observe him and call 911. After while he was feeling good and EMS checked and he was doing fine. He left after 45 minutes and he was feeling fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- First moderna vaccine
- Staat
- IN
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 06.12.2023
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Patient stated her arm hurt the day the shot was given. She stated it was the covid Moderna vaccine that has caused her problems. She has had arm pain ever since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 13.04.2023
- Impfdatum
- 30.03.2022
- Beginn
- 23.02.2023
- Tage bis Beginn
- 330,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Impaired work ability
Loss of personal independence in daily activities
Malaise
SARS-CoV-2 test positive
Symptomtext
My adverse began 23FEB2023 I started to feel a little sick at work but not bad enough to go home at 6pm I went home and continued to be sick on Friday I did not go to work, Nyquil was very hopeful I started to feel much better. I took a home COVID-19 test which was positive and missed church a play and work. I was back to work by Tuesday. For the next four or five weeks I had a cough and it is now resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- 25FEB2023 COVID-19 Test-Positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 06.02.2023
- Impfdatum
- 26.01.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 248,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain of skin
Pruritus
Skin atrophy
Symptomtext
PT STATED SKIN TISSUE ATROPHY OF THE LEFT ARM WAS FIRST NOTICED BY HER BOYFRIEND IN OCTOBER. SINCE THEN IS BEEN ACHY AND ITCHY AND PROGRESSLY GOTTEN WORSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain of skin
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 18.01.2023
- Impfdatum
- 05.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 27,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exposure during pregnancy
Injection site pain
Pain in extremity
Swelling
X-ray
Symptomtext
Severe constanst pain in right arm that extends from upper shoulders to fingers. Some swelling 11 weeks pregnant at time of vaccine given Treatment of pain with lidocaine patches in addition to the tylenol. Patient also was referred to physical therapy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Patient was sent for x-ray
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Ibuprofen and Tylenol
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 09.01.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 357,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Allodynia
Anosmia
Bedridden
COVID-19
Chills
Malaise
Nausea
Pain
Productive cough
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
The following morning after receiving the vaccine I was bed ridden, terrible allodynia, nausea, chills and body aches. These symptoms lasted for ten days. The allodynia was the most horrific symptom. I had these same symptoms for the first dose. I started not feeling well on 01/01/2023 with a slight cough and progressed from there. I tested for COVID-19 on 01/02/2023 and 01/03/2023 with two different manufacturers and they were negative. On 01/04/2023 I tested positive for COVID-19 with a home test. I tested again on 01/05/2023 with another manufacturer home test and it was positive. I had stuffy head; a wet cough and I lost my sense of taste and smell. I was not eligible for the prescription for PAXLOVID since I was outside the window. As of today, I have improved but I still having symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 04JAN2023 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Famotidine; NATURES natural sleep aid; multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 20.12.2022
- Impfdatum
- 21.12.2021
- Beginn
- 06.09.2022
- Tage bis Beginn
- 259,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Headache
Lethargy
Night sweats
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
On Monday after a camping trip, I was feeling lethargic. I took some ibuprofen because I was also very sore. I took a nap in the middle of the day. I spoke with my doctor on Wednesday. Tuesday, September 6, 2022, I felt better but developed a sore throat and a bit of a cough. My headache and body aches went away. Tuesday night I tested positive for COVID-19. I was prescribed Paxlovid. I did not test negative for about 2 weeks. Thursday night I had a mild sore throat and felt like I had a night fever/night sweat. My sore throat diminished over time as well as my headache. I never felt out of breath or lethargic around the house.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Home COVID-19, positive, 09062022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 08.12.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Myalgia
Symptomtext
Muscular pain, worsen by time, almost a year and I feel worst every day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Muscular pain, headache, dizziness
- Vorgeschichte
- Thyroid Gastrointestinal
- Andere Medikamente
- None
- Allergien
- Penicillin Sulfa
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 21.11.2022
- Impfdatum
- 04.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram normal
Eye pain
Headache
Magnetic resonance imaging normal
Pain in extremity
Symptomtext
I've had headaches around my upper right temple and eye since the 3rd dose. I didn't get any treatment until after the most recent 5th vaccine. They gave me antibiotics and thought that maybe I had a sinus infection. They did a CT scan and MRI and they didn't find anything. After the 5th dose, they sent me to an ear nose and throat specialist, and he gave me allergy medication. That didn't help either. My arm has also been really painful and sore along with the headaches since that 5th shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- CT scan normal results; MRI scan normal results
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- TYLENOL; CENTRUM multivitamin; simvastatin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 22.01.2021
- Beginn
- 07.08.2022
- Tage bis Beginn
- 562,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Agitation
Arthralgia
Asymptomatic COVID-19
Bone deformity
Fibula fracture
Homicidal ideation
Joint injury
Rhabdomyolysis
SARS-CoV-2 test positive
Soft tissue swelling
Suicidal ideation
X-ray limb abnormal
Symptomtext
Patient is a 81-year-old male was admitted with complaints of ankle pain. Patient was attempting to move from 1 chair to the other he hit his ankle he did not lose consciousness. Because of the pain he brought to the ER when he came to the ER patient vitals have been stable. Trauma work-up done including left foot x-ray no acute process. Right foot x-ray diffuse soft tissue edema chronic deformity of mid right fibula compatible with healed fracture left ankle x-ray diffuse soft tissue edema. He was found to have AKI, rhabdo. Asymptomatic Covid 19 on routine screening for discharge at the request for SAR. He was kept on Ativan, Haldol and Thorazine for agitation. He was certified by the psychiatrist. Currently awaiting placement. Incidentally, patient was noted to have swabbed positive for COVID-19. He is currently admitted as psych facility will not take him till he is off COVID precautions. He does not have any upper respiratory symptoms at this time. No fevers or chills. No chest pain or shortness of breath. He mentions to have received 2 doses of the vaccine in 2021. When I examined the patient, he did not want to go into details of why he was having homicidal and suicidal ideations. Pt medically cleared for discharged via EMS transportation. DCP coordinated and arranged by psych. No other needs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- 22,0
- Labordaten
- 8/26 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 05.09.2022
- Impfdatum
- 12.02.2022
- Beginn
- 23.08.2022
- Tage bis Beginn
- 192,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pruritus
Rash
SARS-CoV-2 test
Vaccination site pain
Symptomtext
rashes, rashes got bad, new rashes on the forehead ,face and wrist; muscle soreness on the injection site; she still has the itchiness; This spontaneous case was reported by a patient and describes the occurrence of PRURITUS (she still has the itchiness), RASH (rashes, rashes got bad, new rashes on the forehead ,face and wrist) and VACCINATION SITE PAIN (muscle soreness on the injection site) in a 39-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 052B22A, 068H21A and 066H21A) for COVID-19 vaccination. The patient's past medical history included COVID-19 (She had the worst symptoms for 2 weeks and symptoms lingered for about 2 months) on 31-Dec-2021. On 12-Feb-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Mar-2022, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 23-Aug-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to .25 milliliter. In 2022, the patient experienced PRURITUS (she still has the itchiness). On 23-Aug-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced VACCINATION SITE PAIN (muscle soreness on the injection site). On 30-Aug-2022, the patient experienced RASH (rashes, rashes got bad, new rashes on the forehead ,face and wrist). The patient was treated with PREDNISONE for Allergic reaction, at a dose of 20 milligram once a day and IBUPROFEN for Allergic reaction, at a dose of 1-2 pills. On 26-Aug-2022, VACCINATION SITE PAIN (muscle soreness on the injection site) had resolved. At the time of the report, PRURITUS (she still has the itchiness) and RASH (rashes, rashes got bad, new rashes on the forehead ,face and wrist) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 31-Dec-2021, SARS-CoV-2 test: (Positive) Positive. Patient height reported as 5. No other vaccines was given within 1 month prior to Moderna COVID-19 vaccine. No concomitant medications was reported. Patient did not experienced a similar event in the past. Patient had new rashes appeared on her forehead, face and wrist on 1-Sep-2022. It was reported that patient will see a specialist for the rashes. Patient had gone to emergency room on 31-Aug-2022. Patient was given steroid for her allergic reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211231; Test Name: COVID-19; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (She had the worst symptoms for 2 weeks and symptoms lingered for about 2 months)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 29.08.2022
- Impfdatum
- 29.12.2021
- Beginn
- 22.08.2022
- Tage bis Beginn
- 236,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 11.01.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 146,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
COVID-19
Cough
Decreased appetite
Ear swelling
Fatigue
Insomnia
Malaise
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
I had a fever, head congestion, swelling in my ears, chest congestion and coughing. I took an at-home COVID-19 test on 06/06/2022 that came back positive. I called my doctor and informed her and she prescribed me Prednisone and Bactrim. And still to this day, I have a cough and extreme fatigue that I can't get rid of since I contracted COVID-19. I can't sleep, I've lost my appetite, my joints are hurting daily, I just can't seem to get back to full 100% wellness since then.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test: 06/06/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Arthritis
- Andere Medikamente
- Estradiol; Singulair; Flonase; Cetirizine; Advair; Albuterol; Wellbutrin; Buspar; Trazadone
- Allergien
- Penicillin; Erythromycin; Fish
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 21.12.2021
- Beginn
- 15.01.2022
- Tage bis Beginn
- 25,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Alopecia
Biopsy skin abnormal
Exfoliative rash
Pain of skin
Pruritus
Psoriasis
Rash erythematous
Rash pruritic
Skin disorder
Skin exfoliation
Symptomtext
Received booster COVID Moderna shot on 12/21/2021 and in January 2022 I started having scalp issues. Itchy, flaky, some pain. Went to Derm in January 2022 and they said could be dermatitis. Scalp did not heal and also started to get red itchy, flaky, scaly spots on my body. Went back to derm in March for a biopsy- Psoriasis. Have never had it. Noone in my family has it. I have done nothing at all that would affect my immune system except for the COVID vaccine. I am full of psoriasis and have lost half my hair.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exfoliative rash
- Hospital-Tage
- -
- Labordaten
- 3/14/2022 Biopsy by shave method. Result- Psoriasis
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Pre Diabetic
- Andere Medikamente
- Sertraline, Losartan, Folic Acid, Vit D, Metformin.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 02.12.2021
- Beginn
- 28.03.2022
- Tage bis Beginn
- 116,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Discomfort
Feeling hot
Muscle spasms
Peripheral swelling
Pruritus
Swelling
Swollen tongue
Urticaria
Vomiting
Symptomtext
3/28 - swollen tongue, diarrhea, itchy 4/7 - vomit, diarrhea, hives 4/22 - diarrhea, itchy, uncomfortable 4/26 - diarrhea, vomit, hives 4/30 - diarrhea, hives, swollen feet 5/4 - hives 5/10 - diarrhea, vomit, cramps, hot 5/13 - swollen, hives 5/21 - diarrhea, swollen tongue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Zoloft
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 21.12.2021
- Beginn
- 22.04.2022
- Tage bis Beginn
- 122,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chills
Cough
Myalgia
Pyrexia
Symptomtext
chills, fever, cough, myalgias
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 13.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
having persistent rashes on his chest; This spontaneous case was reported by a pharmacist and describes the occurrence of RASH (having persistent rashes on his chest) in a 69-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 31-Mar-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced RASH (having persistent rashes on his chest). At the time of the report, RASH (having persistent rashes on his chest) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. The patient has received his second booster dose of the Moderna Covid-19 vaccine. No concomitant medication was reported. Treatment information include patient talked to his HCP who recommended allergy medications and topical steroids and topical creams which have provided temporary relief.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 01.05.2022
- Impfdatum
- 12.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Asthenia
Fatigue
Myalgia
Symptomtext
Extreme Fatigue Weakness Muscle Aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypothyroid Psoriatic Arthritis
- Andere Medikamente
- Levothyroxine Enbrel
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Computerised tomogram normal
Feeling abnormal
Head discomfort
Pyrexia
Sinoscopy
Symptomtext
The Moderna dose #3 was given late afternoon, by 10:00 pm I began to have chills, fever and felt like I had been run over by a truck. It drug on until the end of March -the fever subsided but my joints were sore and I had congestion in my head. I took 3 rounds of antibiotics, two steroid rounds.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- They scoped my sinuses and did a CT scan of my sinuses. All showed infections but no blockages or polyps. I went to PT for my joints. I didn't go to the doctor until the 3rd week on January 2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- GIRD; Osteoarthritis
- Andere Medikamente
- Ibuprofen Mucinex Pantoprazole
- Allergien
- Sulfa
- Vorherige Impfungen
- Fever and chills for 8 hours from Moderna doses 1 and 2.
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 17.04.2022
- Impfdatum
- 31.01.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Arthralgia
Cognitive disorder
Disturbance in attention
Exercise tolerance decreased
Fatigue
Feeling abnormal
Pain in extremity
Symptomtext
No reaction immediately following vaccine other than sore arm. Approximately a week later: Joint pain, and pretty bad brain fog. Joint pain subsided after 3 weeks. Brain fog still present, worse when attempting to workout. I'll workout and a few hours later I'm hit with a big wave of brain fog, difficulty concentrating, diminished cognitive ability and fatigue. I've also notice coffee no longer provides me with clarity (doesn't wake me up as it used to). Anxiety has definitely increased.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- IBS/GERD following 2nd dose (6/04/2021)
- Andere Medikamente
- Vitamin D, Fish oil
- Allergien
- None
- Vorherige Impfungen
- Pfizer 2nd dose, 06/04/2021; symptoms began approximately 2 weeks after: GI issues, joint pain, fatigue, itchiness, brain fog an
- Staat
- NJ
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 17.02.2022
- Beginn
- 27.02.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Urticaria
Symptomtext
She got her vaccine she had no reaction that day. Her hives started 10 days after the booster vaccine, it was pretty much all over her body. It was on her upper arms, the side of her stomach, her stomach, her butt side, her hips, thighs and also intense itching on her feet and palms. It started off as hives/bumps, then over about 2 weeks it wasn't seen at wheels or hives, but persistent itching, and the same amount of itching on her upper forearms, back, hips, palms and feet. Hives and urticaria which lasted all of March until today. She spoke to a dermatologist who told them what was happening. Her hives did mildly calm down midway through March and they told her to take daily histamines and prescribed a low dose cream to apply (Triamcinolone). This cream did not help her whole situation, but did relieve her itching some, but the itching was in various locations and would be moving. She has not seen the dermatologist herself, and has just been following their instructions to take a daily antihistamines and to wait it out. The antihistamines relieve her itching when she's taking something like Zyrtec, and some don't work as well as others such as Allegra. She is taking Zyrtec which works better for her. She is worried that these medications are not solving this problem, and is worried that it is an internal problem from the booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.01.2022
- Tage bis Beginn
- 32,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Ageusia
Arthralgia
Chest discomfort
Chills
Cough
Diverticulitis
Ear discomfort
Ear pain
Fatigue
Headache
Oropharyngeal pain
Otorrhoea
Respiratory tract congestion
Symptomtext
I developed symptoms of COVID 19 on 12/30/21 with chills, cough, congestion, sore throat, ear ache, loss taste, chest tightness, headaches, joint pain, abdominal pain, fatigue, which lasted 7 to 10 days. I still have a lingering cough and ear ache/clogged/drainage. It has exacerbated diverticulitis attacks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; COPD; hypothyroidism, half of thyroid, two parathyroid removed
- Andere Medikamente
- Levothyroxine, Levastatin, Women's daily vitamin, started taking zinc and vitamin d at symptom onset.
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 21.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test negative
Urticaria
Symptomtext
Have had hives spontaneously (different places on body at random times) since 10 days after dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- Food allergy test is 1/18/22. No food allergies found
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Tinnitus
Symptomtext
Pt reported dizziness, hearing ringing and feeling anxious prior to vaccine admin. Admin in private cot area. NO LOC. Pt stated she was not driving home. Pt refused vital signs. Observed 30min w/ no additional adverse effects. Pt stable and released from the vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: HTN, DM, GERD, Fatty liver, Obesity, Adjust disorder w/ mixed Anxiety and Depression, IDA, Positive PPD
- Andere Medikamente
- Medications: Medication Sig ? acetaminophen (TYLENOL) 500 MG tablet Take 2 tablets by mouth every 6 (six) hours as needed (Mild pain (1 - 3/10) or Temp equals or greater than 100.4 F or 38 C.). ? aluminum-mag hydroxide-simethicone (MAALOX
- Allergien
- Allergies: NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Pruritus
Rash
Symptomtext
Pt reported itching and slight rash. NO SOB, no Swelling. Pt was given 25mg PO Benadryl @14:00. Pt was advised to take 2nd 25mg dose at home if itchiness continues and see medical attention if condition worsens or develop SOB. Pt stable and released from the vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Gallstones s/p cholecystectomy
- Andere Medikamente
- N/A
- Allergien
- Allergies: Influenza Vaccine, Shrimp
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 15.03.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burn oral cavity
Oral discomfort
Pain
Peripheral swelling
Rash
Swelling face
Symptomtext
On 01/15/2022, patient presents for swelling of face, rash/ burning sensation on tongue/ mouth. Patient states swelling on face started on 01/12/2022. It's resolving now per patient. Swelling on BLE has also resolved per patient. He is here to get something for burning sensation in his mouth when he eats. Patient denies N/V, CP, SOB, or difficulty breathing. Patient to start VISCOUS LIDOCAINE, avoid acidic, spicy, hot foods for oral lesion. Patient to discontinue BP meds and go to ER for evaluation. Patient started on LIDOCAINE VISCOUS HCl SOLUTION, 2% 15ML as needed for pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- N.K.D.A.
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 11.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood bicarbonate
Immunisation reaction
Pruritus
Urticaria
Symptomtext
Symptoms began with itching sensation in the scalp and neck, exploded into full body hives (urticaria) forming blisters. Treatment on February 24 included injection of epinephrine and oral antihistamines and steroids. The cycle of Prednisone, Famotidine, and cetirizine has conclude (lasted a total of 14 days), but hives have not completely subsided and still persist, appearing on the arms, lower abdomen, between legs and glutes, and scalp. Topical treatment with hydrocortisone cream helps with the itching sensation and will cause the location to revert to normal over a few hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- No medical or lab tests performed. Diagnosed with urticaria on February 24 by Dr. at the Hospital ER. Follow-up session with allergist Dr. has linked the urticaria to the vaccine booster.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyperuricemia; Acute viral bronchitis
- Andere Medikamente
- None
- Allergien
- Contact allergy to mercury
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 03.03.2022
- Impfdatum
- 09.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Laboratory test normal
Pruritus
Urticaria
Symptomtext
Hives all over my body . Given IV steroids and IV Benadryl. Itchiness went away given oral steroids for 5days 60mg. On Benadryl every 6hrs and Pepcid 25mg BID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Autoimmune ruled out - results negative. No allergies to medications and food allergies
- Aktuelle Erkrankungen
- Asthma
- Vorgeschichte
- -
- Andere Medikamente
- Birth control, multivitamins
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 20.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Symptomtext
Painful and extremely swollen lymph nodes in neck by left collar bone and in left armpit. Larger than a quarter since 02/23/2022. Still large and painful on 02/28/2022 (today).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- N/A. If pain persists in the next few days I'll be back at the doctors office.
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- Fibromyalgia, depression, anxiety, ADHD, endometriosis, history of HPV and precancerous cells in cervix.
- Andere Medikamente
- Pregabalin, Methylphenidate
- Allergien
- phenergan, latex, surgical glue, bandaid glue, possibly bleach or hydrogen peroxide.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 22.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dermatologic examination
Erythema
Pruritus
Swelling
Symptomtext
-Itchy red, raised spots on trunk, then arms, move around to different areas - Lasts 1 hour - Tends to happen mostly in the evenings, around 5pm - Current tx: cetirizine 10 mg once daily
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Urgent care visit-jan 11th Dermatology appt- feb 7th Allergy appt- march 4th 2022 (upcoming).
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Influenza like illness
Injection site induration
Injection site pruritus
Laboratory test
Malaise
Neck pain
Pain
Skin reaction
Symptomtext
Mostly the local skin reaction: harden at injection site, 4 inches in diameter. By third day it was gone, some itching, flu like systems, hurt all over. I felt like I was fighting something half. Headache and neck pain. I may have taken ibuprofen when my neck hurt.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Lab work 01/12/2022, additional labs on 01/13/2022.
- Aktuelle Erkrankungen
- Being evaluated for heart disease and vitamin D
- Vorgeschichte
- Normal range with medication: depression, GERD, low thyroid, high cholesterol,
- Andere Medikamente
- Protonics, Lipitor, Levoxyl, Toprol, Prozac, Baby Aspirin- two a day
- Allergien
- Codeine, latex, IV tape, sulfur
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Pruritus
Urticaria
Symptomtext
Hives, itching, and burning that occurs everyday all throughout the day since 2/7/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- There are not any other illnesses.
- Vorgeschichte
- There are not any chronic or long-standing health conditions.
- Andere Medikamente
- -
- Allergien
- There are not any known drug allergies
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 22.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Lymph node pain
Lymphadenitis
Pain in extremity
Symptomtext
Patient stated that about one week after her first dose of Moderna, she experienced a sore arm and pain in the lymph nodes under her arm pit and near her clavicle. She said they were inflamed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 27.12.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Symptomtext
1 week after vaccine; patient complains of constant pain in deltoid muscle. no loss of range of motion detected. pain flares when muscle is used.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Pain
Sleep disorder
Symptomtext
In the middle of the night woke up with body aches. Pain in my knees which I never had for 1 week ago. Saw Dr. 01/19/2022 prescribed Naproxen which was taken for two weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Biaxin and Ibuprofen
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 21.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 11,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Fatigue
Pollakiuria
Weight decreased
Symptomtext
Pt reported to pharmacy about 8 weeks after receiving Moderna booster dose at our pharmacy. He reported for the last 6 weeks he had fatigue, extensive weight loss, lack of appetite, frequent urination. Pt stated vaccination was only change to regular lifestyle. I recommended immediate follow up at nearby urgent care clinic, but patient seemed hesitant to go.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- unknown
- Andere Medikamente
- Pt stated he did not take any medications
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 05.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inflammation
Mechanical urticaria
Pain
Pruritus
Urticaria
Symptomtext
10 days after my Moderna booster my body began to itch throughout the day and by 6pm I started to break out in hives along my right side under my armpit and down along my rib cage. This continued for six days along with serious body pains from inflammation, I am currently on day 33 and still super itching and hives at night time but dermatographia throughout the day. I?ve been treating with Zyrtec and Benadryl as recommended from a doctor on a call where he confirmed the hives but did not want to refer me to an allergist unless I began to go into anaphylaxis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin C 500mg and 500mg MSM daily
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Feeling cold
Influenza like illness
Urticaria
Symptomtext
Patient reports that she noticed hives starting in the evening of 1/28/22. She states that the hives were localized to her upper body only, mainly on her torso, back, and neck. She reports fatigue and general cold and flu like symptoms Friday and Saturday after vaccination. Patient took benadryl for rash, states that it began to fade on Sunday 1/30/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest discomfort
Pain
Rash erythematous
Rash pruritic
SARS-CoV-2 test positive
Symptomtext
1/9 It started with upper arm and shin rash that was red, raised, and itchy. At that point called my PCP and was advised over the phone to wait it out. Advised to keep hydrated and started using hydrocortisone cream. Opted to get a CoVid test because of the rash, chest congestion, and body ache. Rash lasted for 5-6 days and has not returned. The other symptoms subsided as well. No additional issues and I am fully recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- 1/12 Received a CoVid PCR test(positive)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- PCOS
- Andere Medikamente
- Kirkland Signature Multi Vitamin, Zyrtec, Pepcid ac, Metformin
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Heavy menstrual bleeding
Pyrexia
Symptomtext
Chills headache low grade fever. Menstrual period has increased from 5 days too 9 days with heavy bleeding. Fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Sinusitis from allergies, IBS
- Andere Medikamente
- Duloxatine, singular, Allegra, daily vitamins, probiotics, Prilosec
- Allergien
- Tetracycline, latex sensitivity, nickel and metal allergies, preservative allergies
- Vorherige Impfungen
- Menstrual changes
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 26.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Diarrhoea
Headache
Musculoskeletal discomfort
Oral discomfort
Tenderness
Vaccination site inflammation
Vaccination site irritation
Vaccination site pruritus
Vaccination site swelling
Vomiting
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of ORAL DISCOMFORT (Left side of mouth, jaw, neck, and left shoulder felt weird), MUSCULOSKELETAL DISCOMFORT (Left side of mouth, jaw, neck, and left shoulder felt weird), TENDERNESS (Arm tender shot sight became itchy, inflamed, and irritated), VACCINATION SITE IRRITATION (Arm tender shot sight became itchy, inflamed, and irritated.\) and DIARRHOEA (Severe vomiting and diarrhea) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 26-Dec-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 31-Dec-2021, the patient experienced DIARRHOEA (Severe vomiting and diarrhea) and VOMITING (Severe vomiting and diarrhea). On 03-Jan-2022, the patient experienced ORAL DISCOMFORT (Left side of mouth, jaw, neck, and left shoulder felt weird), MUSCULOSKELETAL DISCOMFORT (Left side of mouth, jaw, neck, and left shoulder felt weird), ARTHRALGIA (Left side of mouth, jaw, neck, and left shoulder felt weird) and HEADACHE (Headaches). On 07-Jan-2022, the patient experienced TENDERNESS (Arm tender shot sight became itchy, inflamed, and irritated), VACCINATION SITE IRRITATION (Arm tender shot sight became itchy, inflamed, and irritated), VACCINATION SITE INFLAMMATION (Arm tender shot sight became itchy, inflamed, and irritated), VACCINATION SITE PRURITUS (Arm tender shot sight became itchy, inflamed, and irritated) and VACCINATION SITE SWELLING (Shot site was raised and the size of a half dollar). On 05-Jan-2022, DIARRHOEA (Severe vomiting and diarrhea) and VOMITING (Severe vomiting and diarrhea) had resolved. At the time of the report, ORAL DISCOMFORT (Left side of mouth, jaw, neck, and left shoulder felt weird), MUSCULOSKELETAL DISCOMFORT (Left side of mouth, jaw, neck, and left shoulder felt weird), TENDERNESS (Arm tender shot sight became itchy, inflamed, and irritated), VACCINATION SITE IRRITATION (Arm tender shot sight became itchy, inflamed, and irritated), VACCINATION SITE INFLAMMATION (Arm tender shot sight became itchy, inflamed, and irritated), ARTHRALGIA (Left side of mouth, jaw, neck, and left shoulder felt weird), VACCINATION SITE PRURITUS (Arm tender shot sight became itchy, inflamed, and irritated), VACCINATION SITE SWELLING (Shot site was raised and the size of a half dollar) and HEADACHE (Headaches) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered DIARRHOEA (Severe vomiting and diarrhea) and VOMITING (Severe vomiting and diarrhea) to be related. No further causality assessments were provided for ORAL DISCOMFORT (Left side of mouth, jaw, neck, and left shoulder felt weird), MUSCULOSKELETAL DISCOMFORT (Left side of mouth, jaw, neck, and left shoulder felt weird), TENDERNESS (Arm tender shot sight became itchy, inflamed, and irritated), VACCINATION SITE IRRITATION (Arm tender shot sight became itchy, inflamed, and irritated), VACCINATION SITE INFLAMMATION (Arm tender shot sight became itchy, inflamed, and irritated), ARTHRALGIA (Left side of mouth, jaw, neck, and left shoulder felt weird), VACCINATION SITE PRURITUS (Arm tender shot sight became itchy, inflamed, and irritated), VACCINATION SITE SWELLING (Shot site was raised and the size of a half dollar) and HEADACHE (Headaches). No concomitant medications were provided by the reporter. No treatment medications were provided by the reporter. This case was linked to MOD-2022-467332 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 21.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Disturbance in attention
Fatigue
Feeling abnormal
Headache
Symptomtext
I had COVID-19 within a month before being vaccinated. I had a very mild case and did not believe I was sick until I tested positive. I felt fine after COVID-19 and returned to work. The vaccine was mandated and I did not want to loose my job so I took the 1st vaccine. Now, I am exhausted all the time, it's hard for me to concentrate, I have headaches every day and my left arm feels weird. I believe all this is from the vaccine because I was fine even after having COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- COVID-19 - I had super mild symptoms to the point that I did not think I was sick. The week after my isolation I felt fine too. It was not until I got vaccinated that I started to not feel good.
- Vorgeschichte
- HTN
- Andere Medikamente
- amlodipine 10mg, black cohosh, hyaluronic acid
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 21.01.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Mechanical urticaria
Pruritus
Skin swelling
Symptomtext
Dermatographic urticaria. Random outbursts of itchy red lines/patches all over body. Skin easily swelling up with any scratching. Zyrtec was taken to treat itchiness and swelling of the skin but only relieves the symptoms for about 12hrs even though medication is for 24hrs. A Zyrtec has to be taken daily in order to reduce itchiness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- COVID-19
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Feeling abnormal
Headache
Oral herpes
Pain in extremity
Rash macular
Urticaria
Symptomtext
I got the shot and then I went to work that night at 6:30 PM and I was kind of fine up until morning time when I had a sore arm. I know it was sore by time I left work which was around 7 AM. Then I had achy joints and a little headache and just a kind of blah feeling. I guess it started around 3 or 4 AM so it was 12-13 hours after shot and that day around 24 hours after shot in the afternoon I went to take a shower and noticed I had a huge hive on my left forearm. I started checking the rest of my body and it was also across upper back and I had big splotches on lower back that started off as red dots everywhere. It was also under my breast and on my chest and then I took my shower and later on throughout the day they got bigger and smoothed out. I developed a cold sore by Saturday (2 days after) and my body was going nuts. I still have a faint hive on forearm and all other symptoms resolved within a day except the cold sore and the hives and those took a little longer to resolve. I took Benadryl for multiple days and reported symptoms to my Doctor via email. When I reported to my Doctor it was just an FYI for my chart just incase I couldn't get any more vaccines and I wanted to make sure it was documented.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Rheumatoid Arthritis, fibromyalgia, primary biliary cholangitis (autoimmune liver disease).
- Andere Medikamente
- Ursodiol, Baclofen, omeprazole, Vitamin D, Possibly a Percocet or tramadol, Tylenol
- Allergien
- Sulfa, Prednisone, Hydroxychloroquine, Wellbutrin, Penicillin, possibly an allergy to wheat but not sure if it's wheat or gluten.
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Immediate post-injection reaction
Laboratory test
Menstruation irregular
Pruritus
Throat irritation
Vertigo
Vertigo positional
Symptomtext
Immediately after injection, I had an allergic reaction itchiness in my throat and lymph nodes. The vaccine triggered my period the same day which was weird because my menstrual cycle just ended a week prior. I thought it was just spotting, but when I got home, I had a regular flow like a monthly period. The nurse practitioner there told me to take Benadryl. My roommate got me Benadryl and went to get food and went home. I woke up with intense vertigo for the next couple of days. The room was spinning around me; all the way to Sunday, I had severe vertigo and couldn't go to school all the way until 01/31/2022. I went to class on 02/01/2022. I went to class fine on 02/02/2022, but had a sharp headache after dinner that evening. The vertigo returned the following Thursday, 02/03/2022 and I couldn't go to class that Thursday until this Monday, 02/07/2022. I called my doctor who told the nurse practitioner to do a check-up as they diagnosed me with BPPV (benign paroxysmal positional vertigo). No medication would aid proper treatment to aid my recovery; I was given worksheets to exercise my brain for when experiencing vertigo episodes. I was also suggested to see an acupuncturist to help with treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Cranial pressure brain exam: 02/07/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Benadryl, Tylenol
- Allergien
- shrimp, lobster, jackfruit
- Vorherige Impfungen
- 04/10/2021, Janssen, COVID-19, allergic reaction & hives & throat swelling & back pain & fever, age 24.
- Staat
- NJ
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Rash
Rash erythematous
Rash papular
Rash pruritic
Urticaria
Symptomtext
Skin Rashes or hives developed on arm first and then all over body. Rashes appear in groups as large red swollen patches on skin and then disappear after a few hours. Rashes are itchy and create a burning sensation. Health care provider prescribed Benadryl and Prednisone 20mg. Rashes still persist on 3rd day after appearing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 03.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pain in extremity
Symptomtext
Patient said that she had regular pain and soreness for a day or two after vaccination, that went away after a few days. About a week after, she said she started to experience a pain and soreness radiating down her arm that intensified when she raises her arm. This was reported via the phone. She says there does not have any visual redness or irritation. Will follow up with her doctor if it does not improve
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Mechanical urticaria
Pain
Rash
Rash papular
Rash pruritic
Skin warm
Symptomtext
Approximately 2 weeks after my Moderna Covid-19 booster shot, I woke with rashes all over my body that were warm to the touch and incredibly itchy. Upon scratching to soothe the itchiness, I developed raised marks that became hot to the touch and would sting/ itch more than before. I believe the correct term for this is Dermatographia. As of 2/7/2022 it has not gone away and after doing research, this is something that has happened to others as well after the moderna booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Nickel, fabric softener, very strong scents
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 17.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Disturbance in attention
Headache
Lethargy
Pain
Raynaud's phenomenon
Taste disorder
Symptomtext
04/11/2020 - Had COVID-19. Ran fever for 5 weeks, lost taste and smell, body aches and pains, confusion, lethargy, headache, GI symptoms, sinus symptoms, respiratory symptoms, etc. I slowly began to get some taste and some smell back. I still do not have full sense of smell and taste back. Certain things I cannot smell. I also have problems with concentration. I have had extreme difficulty with mental focus and clarity, an attention deficit. 11/17/2021 - Received first vaccine of Moderna. 20 minutes after receiving the shot, I began to have a headache and lips tingled and went numb. 11/18 - Headache, sinus problems, fever, aches and pains, lethargy all set in and by that evening I went to bed and was unable to get out of bed until 11/21. This was intense and very much felt like when I was sick with COVID the year before. Sore achy arm, body aches and headaches lasted over a week. 12/17/2021 - Received second vaccine of Moderna. 3 AM of 12/18 the intolerable headache set in. Body aches, pains, headache, lethargy lasted until 12/20. The symptoms hit quicker, but also left quicker. Today, I continue to not taste and smell everything, aka I no longer smell poop (It smells like iron or pennys), I have extreme difficulty concentrating - definitely have an attention deficit, and now have experience Raynaud's Phenomenon. Raynaud's first occurred 1/11/22 to some of my toes. This has now happened a total of 3 times to my toes and one time to a finger. I have no history of Raynaud's and have no family history of Raynaud's. This has me concerned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN
- Andere Medikamente
- None
- Allergien
- PCN, Morphine, Sulfa eye drops, some band-aids/tape
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 20.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Gastrooesophageal reflux disease
Pruritus
Urticaria
Full blood count normal
Hot flush
Hyperhidrosis
Mechanical urticaria
Metabolic function test
Symptomtext
An itchy scalp/Itchiness on back; She has clusters of hives everywhere; Acid reflux; Anywhere she scratched on her body it turned red; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (An itchy scalp/Itchiness on back), URTICARIA (She has clusters of hives everywhere), GASTROOESOPHAGEAL REFLUX DISEASE (Acid reflux) and ERYTHEMA (Anywhere she scratched on her body it turned red) in a 47-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Jan-2022, the patient experienced PRURITUS (An itchy scalp/Itchiness on back), URTICARIA (She has clusters of hives everywhere), GASTROOESOPHAGEAL REFLUX DISEASE (Acid reflux) and ERYTHEMA (Anywhere she scratched on her body it turned red). The patient was treated with CETIRIZINE HYDROCHLORIDE (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) at an unspecified dose and frequency and FAMOTIDINE (PEPCID [FAMOTIDINE]) at an unspecified dose and frequency. At the time of the report, PRURITUS (An itchy scalp/Itchiness on back), URTICARIA (She has clusters of hives everywhere), GASTROOESOPHAGEAL REFLUX DISEASE (Acid reflux) and ERYTHEMA (Anywhere she scratched on her body it turned red) outcome was unknown. Concomitant product use was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 20.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Gastrooesophageal reflux disease
Pruritus
Urticaria
Full blood count normal
Hot flush
Hyperhidrosis
Mechanical urticaria
Metabolic function test
Symptomtext
An itchy scalp/Itchiness on back; She has clusters of hives everywhere; Acid reflux; Anywhere she scratched on her body it turned red; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (An itchy scalp/Itchiness on back), URTICARIA (She has clusters of hives everywhere), GASTROOESOPHAGEAL REFLUX DISEASE (Acid reflux) and ERYTHEMA (Anywhere she scratched on her body it turned red) in a 47-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Jan-2022, the patient experienced PRURITUS (An itchy scalp/Itchiness on back), URTICARIA (She has clusters of hives everywhere), GASTROOESOPHAGEAL REFLUX DISEASE (Acid reflux) and ERYTHEMA (Anywhere she scratched on her body it turned red). The patient was treated with CETIRIZINE HYDROCHLORIDE (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) at an unspecified dose and frequency and FAMOTIDINE (PEPCID [FAMOTIDINE]) at an unspecified dose and frequency. At the time of the report, PRURITUS (An itchy scalp/Itchiness on back), URTICARIA (She has clusters of hives everywhere), GASTROOESOPHAGEAL REFLUX DISEASE (Acid reflux) and ERYTHEMA (Anywhere she scratched on her body it turned red) outcome was unknown. Concomitant product use was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Fatigue
Impaired work ability
Insomnia
Rash
Rash erythematous
Rash pruritic
Urticaria
Symptomtext
8 days post vaccine, 01/07/2022, it started all over again, exactly like the 2nd dose of the Moderna ( VAERS reported summited),the hives/rash were in my ears, groin, everywhere, worse than the 2nd dose. It was itchy red, burning. I It was horrible. 01/08/2021, I called my doctor, she immediately prescribed prednisone on that day, I started with Prednisone 60 mg, drop down and tapered down to 0 mg and I still have the rash till this day, 01/31/2022. I still have the hives. I am completely exhausted. I cannot sleep. I am up scratching, it 's horrible. I have missed work.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Not yet with this one.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Lexapro 5 mg od Flonase 50 mcg nasal spray od Levocetirizine 5 mg od
- Allergien
- sulfa antibiotics latex
- Vorherige Impfungen
- Flu vaccine, Fall 2018, mild rash, only on my face and chest. Moderna dose 2, 05/07/2021, rash all over, cleared up on 06/25/202
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Rash
Rash maculo-papular
Symptomtext
Patient received Pfizer for their initial series in January 2021. Patient recently received a Moderna booster. Patient subsequently developed a maculopapular rash on neck ~ 24 hours after receiving Moderna. Symptoms resolved over several days with no intervention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Lacrimation increased
Oropharyngeal pain
Throat irritation
Symptomtext
Throat pain, itchy throat, watery eyes, redness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- No known illness
- Vorgeschichte
- alopecia
- Andere Medikamente
- acyclovir vacyclovir
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Lymph node pain
Lymphadenopathy
Pain in extremity
Pyrexia
Symptomtext
Patient is complaining about severely swollen and painful lymph nodes in the axilla in the arm that the vaccine was given. She also complained of fever that lasted about 24 hours, slight bruise at the injection sight and that her arm really hurts. She is taking acetaminophen and has iced the axilla. I suggested she take ibuprofen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Birth Control Pills
- Allergien
- none
- Vorherige Impfungen
- almost fainted after 1st dose of Moderna and vomitted after second dose
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Eye pruritus
Ocular hyperaemia
Symptomtext
Pt administered Pfizer 3 dose primary series and Moderna Booster. Pt developed itching and redness in the eyes. Pt carries her own benadryl and Epi. Pt took benadryl 25mg PO @10:04 Vitals: 148/69, 70, 20, 100% @10:22 pt is feeling much better w/ ice packs applied to eye area. @10:30 pt contacted husband to meet her at observation area prior to release from vaccination site @10:35 Pt stable and released from the vaccination site accompanied by husband.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Chronic migraine without aura, intractable, without status migrainosus Coarctation of aorta Hypertensive disorder Generalized abdominal pain, N/V Ovarian torsion Proctitis Endometriosis Idiopathic mast cell activation syndrome H/O sinusitis Hymenoptera allergy H/O migraine Common variable immunodeficiency Chronic ethmoidal sinusitis Asthma Samter's triad GERD (gastroesophageal reflux disease)
- Andere Medikamente
- Medications: calcium carbonate-vitamin D3 600 mg(1,500mg) -500 unit Cap Take by mouth. calcium polycarbophil 500 mg Chew Take by mouth. estradiol (ESTRACE) 1 MG tablet TAKE 1 TAB (1 MG TOTAL) BY MOUTH 2 TIMES A DAY loratadine (CLARITI
- Allergien
- Allergies: Adhesive Tape-Silicones Itching Albuterol Itching (eyes) Aspirin Other (See Comments) Aspirin Dl-Lysine Other (See Comments) Chocolate Flavor Unable to obtain Cromolyn Difficulty breathing Ibuprofen Rash Immune Globulin,Gamma (Igg) Human Vomiting, diarrhea, numb hands, soreness around kidney, dizzy Latex Itching Levofloxacin Swelling and difficulty breathing Rash. Metoclopramide Hcl Altered mental status or confusion Morphine Stop breathing Omalizumab Chest tightness, conjunctivitis Zileuton
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site rash
Symptomtext
Patient developed mild rash around injection site. No other signs or symptoms of anaphylaxis. Treated with 50mg PO diphenhydramine in clinic and given PO diphenhydramine and hydrocortisone cream for home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysstasia
Fatigue
Gait disturbance
Headache
Nausea
Pain
Sleep disorder
Vomiting
Symptomtext
On January 22 at approximately 2:00am I woke up with severe body aches and nausea where I vomited at that point. As the morning progresses my body aches got much worse in addition to having a severe headache. I continued to vomit through out the day and was barely able to stand or walk, along with being very fatigued. These symptoms continued through out the entire day and did not subside until late the next morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- Upper Respiratory Infection 3 weeks prior
- Vorgeschichte
- No
- Andere Medikamente
- Yes, multi-vitamin (Ritual)
- Allergien
- Seasonal and topical allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypersensitivity
Pain
Peripheral swelling
Pruritus
Skin hyperpigmentation
Skin lesion
Skin warm
Urticaria
Symptomtext
Had delayed hypersensitivity reaction which was pretty severe. Started with typical soreness then developed small wheal on day 2 (about 2cm diameter). Rapidly progressed by that night to almost entirety of upper deltoid. At it?s maximal spread was probably 13 cm across. Main symptom was severe pruritis and and fairly hot and swollen. Now have hyperpigmentation in the area where lesion was which I assume is post inflammatory
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Adhd Mild sleep apnea BMI 35 Anxiety Intermittent HTN
- Andere Medikamente
- Concerta
- Allergien
- Nickel, some medical adhesives, mosquitos, dust mites
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Peripheral swelling
Pruritus
Swollen tongue
Symptomtext
PT EXPERIENCED SWALLOWEN FEET AND TONGUE THE NEXT MORNING. UNCONTROLLABLE ITCHING ALL OVER THE BODY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pruritus
Urticaria
Symptomtext
Patient called back 45 minutes after getting their second Moderna Booster shot reporting itchy welts on their legs. Patient then reported that they had a similar reaction to the first shot, but did not report it on the informed consent form when they filled it out because they did not attribute it to the shot. It took about 2 weeks for it to go away the first time. I told patient to take Benadryl right now and then every 6 hours. I also told patient to monitor the hives, if it spreads to the face, to seek emergency care. Since there is a possibility, that it can obstruct breathing. The patient reported no breathing problems at this time and did not have any problems after getting shot during the 15 min wait period. The patient will report their reactions to V-safe from the handouts given during the immunization.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Pruritus
Pyrexia
Urticaria
Vomiting
Symptomtext
I got my moderna booster on January 7th. I had high fever muscle aches and vomiting next 2 days. But I knew already as I had same side effects on 2nd dose. But, after 1 weeks, I woke up in morning, I had very bad itching. After talking with doctor, it was diagnosed as hives. As I am not allergic to anything, and I didn't took anything new in that week. I suspect it is because of vaccination. Now I have hives since last 4 days, and it is all over my body. Face, eye, arms legs, hand palms and feet, everywhere. I am taking antihistamines Cetirizine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High cholesterol LDL
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Muscle spasms
Pyrexia
Symptomtext
CHILLS AND FEVER, FATIGUE, AND SEIZURE-LIKE CRAMPING THAT LASTED 2-3 MINUTES. CRAMPING RESOLVED AFTER DRINKING WARM WATER. SIDE EFFECTS EXPERIENCED 1/19/2022 AT AROUND 6:40AM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Peripheral swelling
Pruritus
Symptomtext
8 days after shot left arm swollen dark red over 8 inches in diameter and itching severely.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Stomach issues
- Andere Medikamente
- None
- Allergien
- Green peppers, oranges, silk tape
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Inappropriate schedule of product administration
Myalgia
Symptomtext
Booster was given approximately a month early. Patient experience known side effects of the vaccine like fatigue and muscle aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None to this writer's knowledge
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Heart rate increased
Injection site erythema
Injection site swelling
Pain
Pruritus
Urticaria
Symptomtext
swelling,redness at injection site, pain,hives,headache,itching,increased heart rate
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- corneal transplant rejection, transplant induced glaucoma
- Vorgeschichte
- keratoconus,hypothyroidism,ptsd,pcos
- Andere Medikamente
- predisone,sertraline,spironolactone,singulair,combigan,rocklatan,dorzolanide,levothyroxine
- Allergien
- penicillin,amoxicillin,Keflex,
- Vorherige Impfungen
- covid-19 moderna first dose & second dose 01/07/2021,02/04/2021 same reaction as described.
- Staat
- NC
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Injection site swelling
Pyrexia
Symptomtext
Pt. states that after receiving the 2nd dose of Moderna 01/14/2022, started experiencing symptoms 1 hr later of fever, chills, headaches, and Left arm swellings at the injection site. No noted Primary visit/communications. Pt. still experiencing symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Psoriasis
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eczema
Pruritus
Rash
Rash pustular
Symptomtext
rash small bumps on legs and arms. itchy. pus filled when scratched. took benadryl. dry patches from rash still present. eczema like.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- tylenol and benadryl
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Urticaria
Symptomtext
hives/rash 8x 10 inch area right buttock without accompanying pruritis, some hives left buttock and bilaterally inner thighs benadryl 50mg PO hydrocortisone cream 1% applied topically resolving at time of this report
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- chronic psoriasis flare suprapubic area 3cmx5cm cold sore to mouth x1
- Vorgeschichte
- back pain anemia psoriasis HSV-1
- Andere Medikamente
- phentermine 1 tab PO daily for weight loss fluoxetine 1 tab PO daily for depression acetaminophen 1000mg PO prn back pain iron 65mg 1 tab PO daily for anemia omeprazole 1 tab daily for heartburn acyclovir 400mg 3 tabs PO daily prn coldsore
- Allergien
- Clearasil brand acne OTC topical- angioedema eyes Stridex brand acne OTC topical- angioedema eyes Abalone- severe nausea/vomiting
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 21.04.2021
- Beginn
- 01.05.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Heavy menstrual bleeding
Nausea
Polymenorrhoea
Symptomtext
Increased frequency of menstrual cycle and bleeding heavier after completing second dose. Also experiencing headaches and nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Gait disturbance
Muscular weakness
Pain
Pain in extremity
Symptomtext
pt reported feeling extremely tired and achy, especially her legs (feeling weak/could barely walk) at work later that night after receiving the vaccine. reports going home and sleeping over the next day and says she feels a lot better today, although her arm is sore. pt did not seek medical attention for her reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- covid-19 infection
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Pain in extremity
Peripheral swelling
Symptomtext
having headache, chills, arm soreness and swelling 5 days later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- s/p TURP on 11/4/21
- Vorgeschichte
- HTN, Hyperlipemia, Prediabetes, Sever obesity, Palpitations, Dysphagia, Urinary retention,
- Andere Medikamente
- Zocor, Prinzide, multi vitamin, melatonin
- Allergien
- KNDA, KNFA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Erythema
Pruritus
Urticaria
Symptomtext
Patient reported mild redness and itching to both inner aspect of both arms. Hives. No SOB, A&Ox3 Vitals: 16:05 140/75, 76, 18; O2Sat 100%. Patient given Benadryl 25mg PO @16:10. No progression of hives or development of other unusual symptoms. At 16:17 stable; thereby released from the vaccination site accompanied by husband and daughter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hysterectomy, GERD
- Andere Medikamente
- Black cohosh 80mg PO daily
- Allergien
- Seafood, chicken, hibiscus, shrimp, chlorhexidine
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Nausea
Swelling face
Symptomtext
Patient received 3rd dose of Moderna vaccine. When the patient arrived in the observation staging area, the patient complained of dizziness and ?light headed?, and felt like vomiting. Patient was assessed. Vitals were Heart rate-75, Respirations-14, SpO2-93% on room air. BP-120/60. Patient then stated that she had a reaction with the two previous does, and it required transport by ambulance to the hospital. Patient appeared to have facial swelling. Patient denied difficulty breathing and hives. Patient has a history of Neuropathy. Patient stated that she did not want an ambulance called, nor want further treatment by us and left the premises by vehicle.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Neuropathy
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- Moderna, 1st and 2nd dose
- Staat
- RI
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 07.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Nausea
Pyrexia
Respiratory tract congestion
Symptomtext
RN reported that she suddenly feared she may have given 1mL instead of 0.5mL after the shot.RN is not sure why she suddenly felt that way except for a sudden doubt that came to her mind. It is quite likely that patient did just receive the correct 0.5mL dose and that the RN's worry was unfounded.Patient was called the following morning to check in on his symptoms if any by RN.Patient noted to have a fever,congestion and nauseau during the night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site rash
Injection site swelling
Symptomtext
Right arm swelling at injection site, redness/rash at injection site. Localized to right arm injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
Decreased appetite
Eczema
Fatigue
Headache
Lymphadenopathy
Nausea
Neck pain
Ovulation disorder
Pain in extremity
Symptomtext
Headache: onset 8 hours after booster dose, lasted for 72 hours, moderate in severity. Left adnexal lymphadenopathy : vaccine given in L deltoid, onset within 8 hours after booster dose, lasted for 5-7 days, moderate to severe swelling, looked like a chicken egg protruding from armpit. Fatigue: onset 8-12 hours after booster dose, lasted 3-4 days, moderate-to-severe. Full body arthralgia: onset 8-12 hours after booster dose, severe, lasted for 4-5 days, pain felt in back, hips, legs, neck, hands, nearly every joint. Nausea and loss of appetite: onset 24 hours post booster, lasted for 2-3 days, moderate severity. Eczema on webbing between fingers bilaterally: onset 1 week after booster dose, lasted 2 weeks, moderate severity. Delayed LH surge: onset 19 days after booster, cycle day 1 on 12/18/2021, typically have LH surge on day 14-15 of menstrual cycle, LH surge delayed to cycle day 17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Moderna vaccine, 2nd dose of primary series, given 2/13/2021
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Rash
Urticaria
Symptomtext
Covid Arm. Large 3x3cm rash on bicept area, Smaller 2x2 cm rash lateral arm, Welt at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Zyrtec
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Malaise
Nausea
Rash
Symptomtext
Patient reported to IMMZ department on 1/3/22 at around 9am regarding concern for reaction to 2nd dose of Moderna vaccine received 12/30/21. Patient states they did not feel s/s 15 mins after administration and went home fine. Sometime after, patient stated she started feeling "sick" and "nauseous", "something is not right", which prompted her to present to the hospital 1/1/22. Upon her presentation today, patient noted to have a localized swelling and redness noted on L arm (6x8cm), noted to be below the usual site for injection on the medial part of deltoid. Patient c/o mild nausea, denies CP, SOB, or any other acute s/s. Patient was then seen by the doctor as a walk in, with a differential diagnosis of local reaction vs early cellulitis. Per MD, patient was prescribed a diclofenac gel to use along with the advice to use ice packs and tylenol to manage pain and swelling on L arm injection site. ER precautions given by provider if symptoms acutely worsen. If rash persists, patient to return to clinic to reassess need for abx. Patient verbalized understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Presented to hospital 1/1/22 due to concern for allergic reaction to 2nd dose of Moderna vaccine received on 12/30/21. Otherwise, no acute illnesses nor hospitalizations up to one month prior.
- Vorgeschichte
- DM type 2, mixed hyperlipidemia, COPD mixed type, gastritis and duodenitis, low back pain, seasonal allergies/rhinorrhea, Hepatitis C without hepatic coma, breast malignant neoplasm, asthma, beta thalassemia trait
- Andere Medikamente
- Acetaminophen 500mg PRN, aspirin 81mg qd, atorvastatin 10mg, dulera 200mcg-5mcg aerosol inhaler 2 puffs BID, fluticasone propionate 50mcg nasal spray suspension, metformin 1000mg qd, mirtazapine 15mg, omepreazole 40mg qd, ProAir HFA 90mcg a
- Allergien
- Ibuprofen - rash
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Eating disorder
Feeling cold
Hyperhidrosis
Mouth ulceration
Pyrexia
Symptomtext
12/27/2021 @ 10:30 vaccination. 08:00PM I started to overall low grade fever, chills, sweats, I couldn't get warm enough. 12/28/2021 102 temperature. I stayed home. 12/30/2021 Mouth ulcerations started to appear. I woke up and they were all over my mouth. 1/1/2022 ER, Dr. stated it was due to the booster vaccination and that they would go away on their own. Visual observations. Prescribed numbing medication. I never took as pharmacy was closed due to the holiday. I used orgel and mouthwash. Presently, 1/4/2022, significantly better. Still on roof of mouth. I was able to eat some solid food starting yesterday. 12/23/2021 - shot of steroids for the ongoing cough from 11/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- 11/23/2021 COVID, neg; dry cough, congestion, low grade fever 11/30/2021 Dr. prescribed a cough medicine (presently still have lingering cough)
- Vorgeschichte
- Asthma; GERD
- Andere Medikamente
- -
- Allergien
- Biaxin; Bees
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Pain
Symptomtext
woke up with chills, body aches, no fever. Lasted until the early afternoon
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Received the flu shot at the same time as the Moderna booster on a weekly course of flucanazole
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Flushing
Nausea
Symptomtext
Primary series: Pfizer Vaccinated: 11:25AM Reaction: 11:30AM Patient complained of flushed/dizziness, felt slightly nauseous 5 minutes after vaccination Vitals: @11:27: 85/66, 52, 12 -> @11:32: 89/48, 71, 12 -> @11:40: 94/53, 71 HR -> @11:45: 87/48 -> @11:47: 95/53, HR 71 -> @11:50: 103/58 Patient reported feeling much better and released from vaccination site at 11:50AM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No Known PMH
- Vorgeschichte
- No Known PMH
- Andere Medikamente
- No Known Medications
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site pruritus
Injection site rash
Injection site warmth
Symptomtext
Pink rash an inch below injection site on left arm the size of a dollar coin. Warm to the touch, slight pain, a little itchiness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Fever, chills, nausea, sore injection arm
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Injection site warmth
Symptomtext
Customer came in with red area on arm where vaccine had been given. She said it was swollen and was warm to the touch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Symptomtext
Itching and hives down both arms and back
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Loss of personal independence in daily activities
Musculoskeletal pain
Pain
Pain in extremity
Sleep disorder
Symptomtext
Patient says very sore arm woke her from sleep 12 hours after her vaccine dose. Pt says, 10 days after vaccine, she is still having significant arm pain from shoulder blade down. She says arm has dull pain if she doesn't move it, but has severe "spear-like" pain if she moves the arm. She says it has affected her daily function.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- ear infection, upper respiratory infection, finished antibiotic about one week prior to vaccine dose
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- prednisone (swelling, etc)
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dermatitis contact
Pruritus
Symptomtext
Pt has Latex allergy, and was given the Moderna Booster. She had a reaction to the band aid used, which was latex free. Pt still has some itching 3 days later, nothing has been applied to the allergy site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Immediate post-injection reaction
Symptomtext
Immediately post vaccination pt reported feeling dizzy. Pt reports she has a hx of this issue w/ injections. Pt reports taking Klonopin before vaccination @11:45 Vitals: 106/73, 72, 20, 100% Pt stable and released from the vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: B12 deficiency Bipolar disorder, current episode mixed, mild Acquired hypothyroidism Acute recurrent maxillary sinusitis Allergic rhinitis Anxiety Family history of diabetes mellitus Menorrhagia with regular cycle Severe episode of recurrent major depressive disorder, without psychotic features Fainting w/ injections
- Andere Medikamente
- Medications: clonazePAM 1 mg tablet take by mouth doxycycline hyclate (Vibramycin) 100 mg capsule TAKE 1 CAPSULE BY MOUTH TWICE DAILY WITH FOOD fluticasone propionate (Flonase) 50 mcg/actuation SpSn spray 1 Spray by Nasal route 2 time
- Allergien
- Allergies: Amoxicillin (burning eyes), Animal Dander, Mite Extract, Mold, Propranolol (photosensitivity), venlafaxine (hives)
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Pruritus
Somnolence
Urticaria
Symptomtext
Moderna COVID-19 Vaccine EUA: I developed itchy hives only on my neck (front). Waking up the next day hives were still visible but no longer itching. Next morning experienced marked drowsiness and muscle aches. Tylenol helped.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Iodine dye
- Vorherige Impfungen
- Pfizer 2nd dose on May 6th. Exhaustion, muscle aches and headaches.
- Staat
- -
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Symptomtext
Pfizer Primary; Moderna Booster 10mins post vaccination pt reported dizziness. Vitals: 16:53 124/76, 66, 17, 100%, 98.0F -- > 17:00 133/78, 60, 18, 100%, 98.2 Pt stable and released from the vaccination site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Pyrexia
Symptomtext
The potential AE is a fever of 101.2 degrees Fahrenheit.; This spontaneous case was reported by a consumer and describes the occurrence of PYREXIA (The potential AE is a fever of 101.2 degrees Fahrenheit.) in a 22-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PYREXIA (The potential AE is a fever of 101.2 degrees Fahrenheit.). At the time of the report, PYREXIA (The potential AE is a fever of 101.2 degrees Fahrenheit.) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: 101.2 (High) 101.2 degrees fahrenheit. No concomitant medication was reported. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: 101.2 degrees fahrenheit
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site pain
Symptomtext
soreness on his arm; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (soreness on his arm) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066h21a) for COVID-19 vaccination. No Medical History information was reported. On 22-Dec-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Dec-2021, the patient experienced VACCINATION SITE PAIN (soreness on his arm). At the time of the report, VACCINATION SITE PAIN (soreness on his arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medications include Heart and diabetic medications. No Treatment medications were provided. Most recent FOLLOW-UP information incorporated above includes: On 23-Dec-2021: Non-Significant Follow Up
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Diarrhoea
Dysphagia
Oropharyngeal pain
Vaccination site pain
Symptomtext
sore throat on right side; hard to swallow; diarrhea; soreness in my injection arm; real bad chills; This spontaneous case was reported by a consumer and describes the occurrence of OROPHARYNGEAL PAIN (sore throat on right side), DYSPHAGIA (hard to swallow), DIARRHOEA (diarrhea), VACCINATION SITE PAIN (soreness in my injection arm) and CHILLS (real bad chills) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. The patient's past medical history included COVID-19 on 26-Nov-2020. Previously administered products included for COVID-19 vaccination: Pfizer COVID-19 vaccine in February 2021 and Pfizer COVID-19 vaccine in March 2021. Past adverse reactions to the above products included No adverse event with Pfizer COVID-19 vaccine and Pfizer COVID-19 vaccine. On 20-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Dec-2021, the patient experienced OROPHARYNGEAL PAIN (sore throat on right side), DYSPHAGIA (hard to swallow), DIARRHOEA (diarrhea), VACCINATION SITE PAIN (soreness in my injection arm) and CHILLS (real bad chills). The patient was treated with EUCALYPTUS GLOBULUS OIL, MENTHOL (HALLS) for Adverse event, at an unspecified dose and frequency. At the time of the report, OROPHARYNGEAL PAIN (sore throat on right side), DYSPHAGIA (hard to swallow), DIARRHOEA (diarrhea), VACCINATION SITE PAIN (soreness in my injection arm) and CHILLS (real bad chills) outcome was unknown. Concomitant medication of the patient was not reported. Due to the real bad chills, the patient had to put on a jacket, socks and gloves along with 5 blankets on her. The patient took Halls cough drop, which helped some.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Injection site pain
Lymphadenopathy
Pain in extremity
Symptomtext
Pt. states that after receiving the 3rd dose of Moderna 12/22/2021, started experiencing symptoms 12/23/2021 of fatigue, soreness of the injection arm, and Left under arm area swollen (Lymphnoid). 12/25/2021 Left arm pain throughout, self-treating with Tylenol. No noted Primary visit/communications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HBP
- Andere Medikamente
- Synthroid, Lasinapril, Vitamin D3
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 24.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site mass
Symptomtext
ERYTHERMA/REDISH AND LUMPY FEEL ON THE LEFT ARM AROUND THE INJECTION SIDE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Full blood count
Laboratory test normal
Metabolic function test
Urticaria
Symptomtext
8 days after receiving my first COVID booster, I developed severe systemic urticaria. Mildly responsive to Benadryl. Currently ongoing for 60 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- Basic metabolic profile and CBC labs all normal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anxiety, depression
- Andere Medikamente
- Sertraline 50mg Vitamin D 2000 IU
- Allergien
- None known.
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Vaccination complication
Symptomtext
Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Additional Details: COVID ARM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
3 days after the vaccine the patient called the pharmacy to report minor swelling and red patches on her arm around the injection site. She is going to monitor her arm for worsening conditions and call her doctor if it does not improve.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- ARTHRITIS, HYPOTHROIDISM, ANGINA PECTORIS, HYPERTENSION, HYPERLIPIDEMIA,
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pyrexia
Unresponsive to stimuli
Symptomtext
High Fever day after vaccination and pt was transported to Hospital VIA ambulance. He was not respndeing to wife trying to wake him up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Influenza like illness
Muscular weakness
Pain
Pain in extremity
Symptomtext
Lightning shooting pain through injected arm. Flu like symptoms for approximately 12 hours. Severe arm weakness, that resolved after about 18 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Burning sensation
Chills
Dizziness
Musculoskeletal discomfort
Nausea
Neck mass
Peripheral swelling
Pyrexia
Rash
Rash pruritic
Swelling
Throat irritation
Urticaria
Vaccination complication
Vomiting
Symptomtext
9hrs post vaccination pt presented to the ED w/ shakiness, sob, pruritic rash to chest and arms, nausea. Pt had Moderna Booster dose @ 11:45 , an hour after pt started to have a Fever, then chills and now broke out with diffused rash, also having Nausea. Pt said 1st dose no problem , 2nd dose had all the above symptoms except hives. 12hrs post vaccination Pt then with itchy rash to neck/chest/extremities. No tongue/lip swelling, no sob or wheezing No chest pain or palpitations + nausea, + vomiting, no diarrhea Pt given dexamethason 10mg IM x1, Diphenhydramine 25mg PO x2, Zofran 4mg ODT x1 and discharged home. 12/18 Pt re-presents to ED now w/ hives extending all over body. Reports itchy throat but denies fever, SOB, troubles swallowing. Also notes that she feels like there is a lump developing on the right side of her neck and that the rash is much worse over her neck. She denies any lip/face/tongue swelling, wheezing, shortness of breath, nausea, vomiting, diarrhea. Pt was given methylprednisolone 125mg IV x1, Epi 0.3mg IM x1, famotidine 20mg PO x1 Prednisone 40mg POx1, Cetirizine 10mgx1, calamine lotion and triamcinolone 0.1% ointment. Pt was admitted for observation. 12/19 Pt developed dizziness and fever to 38.3C She calls a rash as hives but never had wheels. Rash was always a lacy pattern with extreme itching and burning sensation. Initially noted it on her arms and spread all over her body now involving her groin, hands and feet on the palmar/plantar aspects. Her last temperature was 100 ?F at home last night. Had vomiting on 1217 but none since. Having right-sided neck swelling that is causing some discomfort from outside but denies any shortness of breath or hoarseness of voice or sore throat. She feels like her fingers and toes are also swollen. Did not notice any rash or burning sensation in her mouth. Currently not having any urinary symptoms of burning micturition, frequency. Patient had already noted much improvement in her rash after she got the cocktail in ED. Likely reactive rash to Moderna booster vaccination. Unlikely DRESS to Bactrim as no indication for such on laboratory evaluation and also timing correlates more with the booster vaccine. Patient with significant improvement after she received Cetrizine, Pepcid, prednisone and epinephrine in ED. No concern for mucosal involvement. Patient had already noted much improvement in her rash after she got the cocktail in ED as mentioned below. Pt discharged w/ the following: calamine-zinc oxide 8-8 % topical susp Apply to affected areas as needed for Other (itching). cetirizine 10 MG tablet Take 1 tablet by mouth daily. famotidine 40 MG tablet Take 1 tablet by mouth daily for 10 days. hydrOXYzine HCL 25 MG tablet Take 1 tablet by mouth every 6 (six) hours as needed for Itching. predniSONE 20 MG tablet Take 2 tablets by mouth daily for 4 days. triamcinolone 0.1 % ointment Apply to affected areas 2 (two) times daily as needed for Other (itching).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- Recent hx: UTI on Septra DS 1 tab BID 12/10-12/19
- Vorgeschichte
- PMH: Thrombocytopenia, presumed amoxicillin induced.
- Andere Medikamente
- Medications: Septra DS 1 tab BID 12/10-12/19
- Allergien
- Allergies: Amoxicillin (hives)
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Dizziness
Fatigue
Insomnia
Nausea
Pain
Symptomtext
Dizziness, imbalance, nausea (without vomiting), body aches, sleeplessness, extreme fatigue. lasted almost 24 hours. Not getting any more of these vaccines if I am going to react like this, I do not want any more of this being put in my body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Parathesis (feet), intermittent post concussion syndrome, fecal incontinence due to nerve damage from bladder removal
- Andere Medikamente
- Advil, Vitamin C, zinc sulfate, multivitamin, melatonin
- Allergien
- none
- Vorherige Impfungen
- Moderna Vaccine. age 61. Vaccine date 5-26-21. Body aches, fatigue
- Staat
- FL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Lymphadenopathy
Symptomtext
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Lymph Node Swelling-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Symptomtext
Lightheadedness. Patient is to report to MD and pharmacy should any further symptoms present themselves.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None documented.
- Vorgeschichte
- None documented.
- Andere Medikamente
- None documented.
- Allergien
- None documented.
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Ear pain
Pain
Vomiting
Symptomtext
Patient reports waking up at 4am morning after receiving the vaccine with body aches, vomiting, diarrhea, and ear pain. Utilizing acetaminophen and hydration with water to ease symptoms. Still experiencing symptoms. She is currently awaiting call back from oncologist to rule out other causes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Anemia per patient.
- Vorgeschichte
- Anemia per patient.
- Andere Medikamente
- Unknown.
- Allergien
- Sulfa antibiotics: hives. Amoxicillin: hives.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site rash
Symptomtext
Arm soreness, itchy red and like a small rash at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Prazosin, rexulti, vitamin d, cetirizine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Nausea
Vomiting
Symptomtext
Systemic: Nausea-Severe, Systemic: Vomiting-Severe, Systemic: Weakness-Medium, Additional Details: pt got flu and moderna booster. felt nausiated and vomited. sat down to be monitored for 30 mins and condition would not go away. emergency services called. pt vomited again when ems arrived and was taken to the hospital. on later check in pt was still in hospital, doing well bit still vomiting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- U
- Eingang
- 30.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Myalgia
Vaccination site lymphadenopathy
Vaccination site pain
Symptomtext
body aches; sore arm at injecti on site; swollen lymph nodes under arms on the side booster was received (left ); tender lymph nodes under arms on the side booster was received (left ); This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (body aches), VACCINATION SITE PAIN (sore arm at injection site), VACCINATION SITE LYMPHADENOPATHY (swollen lymph nodes under arms on the side booster was received (left )) and LYMPH NODE PAIN (tender lymph nodes under arms on the side booster was received (left )) in a 29-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In November 2021, the patient experienced MYALGIA (body aches), VACCINATION SITE PAIN (sore arm at injection site), VACCINATION SITE LYMPHADENOPATHY (swollen lymph nodes under arms on the side booster was received (left )) and LYMPH NODE PAIN (tender lymph nodes under arms on the side booster was received (left )). In November 2021, MYALGIA (body aches) had resolved. At the time of the report, VACCINATION SITE PAIN (sore arm at injecti on site) had not resolved and VACCINATION SITE LYMPHADENOPATHY (swollen lymph nodes under arms on the side booster was received (left )) and LYMPH NODE PAIN (tender lymph nodes under arms on the side booster was received (left )) was resolving. Concomitant medication of the patient was not reported. No treatment information was provided by the reporter. Symptoms started about 4-6 hours after receiving of booster. Body aches lasted about 48 hours; lymph nodes still swollen and tender, started to decrease and arm still slightly sore.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 20.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Chills
Cold sweat
Headache
Myalgia
Pyrexia
Symptomtext
Low-grade fever/ (98.8); Body aches; Headache; Chills; Cold sweats; This spontaneous case was reported by an other health care professional and describes the occurrence of COLD SWEAT (Cold sweats), PYREXIA (Low-grade fever/ (98.8)), CHILLS (Chills), MYALGIA (Body aches) and HEADACHE (Headache) in a 31-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Flu shot (Left arm) on 02-Nov-2021, Pfizer (Dose 2) and Pfizer (Dose 2). Past adverse reactions to the above products included Headache with Pfizer; Low grade fever with Pfizer; and No adverse reaction with Flu shot. Concurrent medical conditions included Anxiety and Acne. Concomitant products included SPIRONOLACTONE from 15-Oct-2020 to an unknown date for Acne, ESCITALOPRAM OXALATE (LEXAPRO) from 15-Oct-2020 to an unknown date for Anxiety, LEVONORGESTREL (MIRENA) from 23-Nov-2018 to an unknown date for an unknown indication. On 20-Nov-2021 at 10:00 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 50 microgram. On 20-Nov-2021 at 5:00 PM, the patient experienced COLD SWEAT (Cold sweats), CHILLS (Chills) and HEADACHE (Headache). On 20-Nov-2021 at 7:00 PM, the patient experienced PYREXIA (Low-grade fever/ (98.8)) and MYALGIA (Body aches). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) from 20-Nov-2021 to 21-Nov-2021 for Adverse event, at an unspecified dose and frequency. On 21-Nov-2021 at 11:00 AM, COLD SWEAT (Cold sweats), PYREXIA (Low-grade fever/ (98.8)), CHILLS (Chills), MYALGIA (Body aches) and HEADACHE (Headache) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 20-Nov-2021, Body temperature: 98.8 (High) Low grade fever. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered PYREXIA (Low-grade fever/ (98.8)), MYALGIA (Body aches) and HEADACHE (Headache) to be probably related. No further causality assessments were provided for COLD SWEAT (Cold sweats) and CHILLS (Chills). Reporter stated that her race was also Most recent FOLLOW-UP information incorporated above includes: On 24-Nov-2021: Patient's demographics, Historical vaccines, Patient's medical history, Concomitant and Treatment medications, Vaccine start date, Time and Batch number, Reporter's causality were updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211120; Test Name: Body temperature; Result Unstructured Data: Low grade fever
- Aktuelle Erkrankungen
- Acne; Anxiety
- Vorgeschichte
- -
- Andere Medikamente
- LEXAPRO; MIRENA; SPIRONOLACTONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Injection site erythema
Injection site pain
Injection site swelling
Pain
Symptomtext
headache, body ache (primarily back) - started ~ 10 hours after injection; almost fully resolved by day 2 after injection sore injection site, swollen injection site, red injection site - slight improvement 2 days after injection site but not resolved yet
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- swollen lymphnode in underarm after flu shot this year on same side as shot
- Staat
- -
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 19.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Myalgia
Vaccination site pain
Symptomtext
Muscle aches; Fatigue; General pain at the site of injection; This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (Muscle aches), FATIGUE (Fatigue) and VACCINATION SITE PAIN (General pain at the site of injection) in a 27-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) 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 MYALGIA (Muscle aches), FATIGUE (Fatigue) and VACCINATION SITE PAIN (General pain at the site of injection). At the time of the report, MYALGIA (Muscle aches), FATIGUE (Fatigue) and VACCINATION SITE PAIN (General pain at the site of injection) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant product use was provided by the reporter. No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Fatigue
Lymphadenopathy
Symptomtext
Booster dose of .5cc Patient c/o Exhaustion also pain and swelling in armpit-lymph nodes only on injection side
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- 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
- 57,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- 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
- 26,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- 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
- 51,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- 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
- 29,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- 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
- 47,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 19.02.2022
- Beginn
- 19.02.2022
- 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
- 23,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- M
- Eingang
- 02.11.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- M
- Eingang
- 02.11.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- 02.11.2023
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- 02.11.2023
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- M
- Eingang
- 02.11.2023
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- M
- Eingang
- 02.11.2023
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- 02.11.2023
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- M
- Eingang
- 02.11.2023
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- M
- Eingang
- 02.11.2023
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- 02.11.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- 02.11.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- M
- Eingang
- 02.11.2023
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- 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
- 48,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- 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
- 63,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- 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
- 63,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- 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
- 23,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- 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
- 23,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- 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
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
- 20,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- 20,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- 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
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
- 31,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- 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
- 31,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- 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
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
- 57,0
- Geschlecht
- U
- Eingang
- 02.11.2023
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- 57,0
- Geschlecht
- U
- Eingang
- 02.11.2023
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- 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
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
- 31,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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
- 31,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
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
- 73,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- 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
- 73,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- 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
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
- 75,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- 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
- 75,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- 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
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
- 22,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- 22,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
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
- 35,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- 02.11.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
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
- 02.11.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 24.08.2023
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- 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
- 51,0
- Geschlecht
- M
- Eingang
- 24.08.2023
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- 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
- 29,0
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- 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
- 47,0
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- 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
- -
- Geschlecht
- U
- Eingang
- 08.08.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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
No adverse event
Symptomtext
No Adverse Event; Vaccine was administered to 8 patients after 1 day of expiry; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry) and NO ADVERSE EVENT (No Adverse Event) in an adult patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 prophylaxis. Medical History or Condition were not reported. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 05-Apr-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry) 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 EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry). Reported patients were both male and female, none of the patients reported being pregnant or breastfeeding. Concomitant product use was not provided by the reporter. Expiry date of the vaccine was 04-Apr-2022. All of the vaccine administered were boosters. Suspect vaccine dosage text was reported as unknown. Treatment information was not provided. This case contains information about patient 1st out of 8 adult patients. This case was linked to US-MODERNATX, INC.-MOD-2023-735647, US-MODERNATX, INC.-MOD-2023-735653, US-MODERNATX, INC.-MOD-2023-735657, US-MODERNATX, INC.-MOD-2023-735666, US-MODERNATX, INC.-MOD-2023-735674, US-MODERNATX, INC.-MOD-2023-735682, US-MODERNATX, INC.-MOD-2023-735693 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-735666:5 out of 8 patients US-MODERNATX, INC.-MOD-2023-735657:4 out of 8 patients US-MODERNATX, INC.-MOD-2023-735647:2 out of 8 patients US-MODERNATX, INC.-MOD-2023-735653:3 out of 8 patients US-MODERNATX, INC.-MOD-2023-735674:6 out of 8 patients US-MODERNATX, INC.-MOD-2023-735682:7 out of 8 patients US-MODERNATX, INC.-MOD-2023-735693:8 out of 8 patients
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Medical History or Condition were not reported.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.08.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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
No adverse event
Symptomtext
No adverse event; Vaccine was administered to 8 patients after 1 day of expiry; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 prophylaxis. Medical History or Condition was not reported. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry) and NO ADVERSE EVENT (No adverse event) outcome was unknown. Not Provided 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 EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry). Reported patients were both male and female, none of the patients reported being pregnant or breastfeeding. Concomitant product use was not provided by the reporter. Expiry date of the vaccine was 04-Apr-2022. All of the vaccine administered were boosters. Suspect vaccine dosage text was reported as unknown. Treatment information was not provided. This case contains information about patient 8th out of 8 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-735621 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-735621:Master case, Patient 8 out of 8
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Medical History or Condition was not reported.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.08.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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
No adverse event
Symptomtext
no adverse event; Vaccine was administered to 8 patients after 1 day of expiry; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry) and NO ADVERSE EVENT (no adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 prophylaxis. Medical History or Condition were not reported. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry) and NO ADVERSE EVENT (no adverse event) outcome was unknown. Not Provided 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 EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry). Reported patients were both male and female, none of the patients reported being pregnant or breastfeeding. Concomitant product use was not provided by the reporter. Expiry date of the vaccine was 04-Apr-2022. All of the vaccine administered were boosters. Suspect vaccine dosage text was reported as unknown. Treatment information was not provided. This case contains information about patient 7th out of 8 adult patients. This case was linked to US-MODERNATX, INC.-MOD-2023-735621 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-735621:Master case, Patient 1
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Medical History or Condition were not reported.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.08.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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
No adverse event
Symptomtext
No adverse event; Vaccine was administered to patient after 1 day of expiry; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to patient after 1 day of expiry) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 prophylaxis. It was reported that HCP did not describe medical history or condition. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to patient after 1 day of expiry). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to patient after 1 day of expiry) and NO ADVERSE EVENT (No adverse event) outcome was unknown. Not Provided 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 EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to patient after 1 day of expiry). Reported patients were both male and female, none of the patients reported being pregnant or breastfeeding. Concomitant product use was not provided by the reporter. Expiry date of the vaccine was 04-Apr-2022. All of the vaccine administered were boosters. Suspect vaccine dosage text was reported as unknown. Treatment information was not provided. This case contains information about patient 6th out of 8 adult patients. This case was linked to US-MODERNATX, INC.-MOD-2023-735621 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-735621:Master case, patient 6 out of 8
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was reported that HCP did not describe medical history or condition.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.08.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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
No adverse event
Symptomtext
no adverse event; Vaccine was administered to 8 patients after 1 day of expiry; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry) and NO ADVERSE EVENT (no adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 prophylaxis. HCP did not describe Medical History or condition. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry) and NO ADVERSE EVENT (no adverse event) outcome was unknown. Not Provided 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 EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry). Reported patients were both male and female, none of the patients reported being pregnant or breastfeeding. Concomitant product use was not provided by the reporter. Expiry date of the vaccine was 04-Apr-2022. All of the vaccine administered were boosters. Suspect vaccine dosage text was reported as unknown. Treatment information was not provided. This case contains information about patient 5th out of 8 adult patients. This case was linked to US-MODERNATX, INC.-MOD-2023-735621 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-735621:Master case, 5 out of 8 patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: HCP did not describe Medical History or condition.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.08.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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
No adverse event
Symptomtext
no adverse event; Vaccine was administered to patient after 1 day of expiry; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to patient after 1 day of expiry) and NO ADVERSE EVENT (no adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to patient after 1 day of expiry). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to patient after 1 day of expiry) and NO ADVERSE EVENT (no adverse event) outcome was unknown. Not Provided 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 EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to patient after 1 day of expiry). No concomitant medication was reported. Patients were both male and female, none of the patients reported being pregnant or breastfeeding. No treatment information was reported. This case contains information for patient 4 out of 8. This case was linked to US-MODERNATX, INC.-MOD-2023-735621 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-735621:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.08.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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
No adverse event
Symptomtext
no adverse event; Vaccine was administered to 8 patients after 1 day of expiry; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry) and NO ADVERSE EVENT (no adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 prophylaxis. HCP did not describe Medical History or Condition. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry) and NO ADVERSE EVENT (no adverse event) outcome was unknown. Not Provided 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 EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry). Reported patients were both male and female, none of the patients reported being pregnant or breastfeeding. Concomitant product use was not provided by the reporter. Expiry date of the vaccine was 04-Apr-2022. All the vaccine administered were boosters. Suspect vaccine dosage text was reported as unknown. Treatment information was not provided. This case contains information about patient 3rd out of 8 adult patients. This case was linked to US-MODERNATX, INC.-MOD-2023-735621 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-735621:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: HCP did not describe Medical History or Condition.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.08.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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
No adverse event
Symptomtext
no adverse event; Vaccine was administered to 8 patients after 1 day of expiry; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry) and NO ADVERSE EVENT (no adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 prophylaxis. Medical History or Condition was not reported. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry) and NO ADVERSE EVENT (no adverse event) outcome was unknown. Not Provided 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 EXPIRED PRODUCT ADMINISTERED (Vaccine was administered to 8 patients after 1 day of expiry). Reported patients were both male and female, none of the patients reported being pregnant or breastfeeding. Concomitant product use was not provided by the reporter. Expiry date of the vaccine was 04-Apr-2022. All of the vaccine administered were boosters. Suspect vaccine dosage text was reported as unknown. Treatment information was not provided. This case contains information about patient 2nd out of 8 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-735621 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-735621:Master case, 2 out of 8 patients
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Medical History or Condition was not reported.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 07.08.2023
- Impfdatum
- 19.01.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 320,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Breakthrough COVID-19
SARS-CoV-2 test positive
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 3/24/21 lot# 038A21A; Moderna 4/21/21 lot# 040B21A; Moderna 1/19/22 lot# 066H21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 01.08.2023
- Impfdatum
- 03.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 1/14/21 lot# 01J20A; Moderna 2/1/21 lot# 013M20A; Moderna 12/3/21 lot# 066H21A;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 05.07.2023
- Impfdatum
- 04.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 2/10/21 lot# 01520A; Modern 3/10/21 lot# 030A21A; Moderna 1/4/22 lot# 066H21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 05.07.2023
- Impfdatum
- 20.12.2021
- Beginn
- 09.08.2022
- Tage bis Beginn
- 232,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 3/1/21 lot# 010A21A; Moderna 4/2/21 lot# 018B21A; Moderna 12/20/21 lot# 066H21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 02.06.2023
- Impfdatum
- 14.01.2022
- Beginn
- 23.08.2022
- Tage bis Beginn
- 221,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 2/24/21 lotA3 010A21a; MOderna 3/24/21 lot# 047A21a; Moderna 1/14/22 lot# 066h21a
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- -
- Geschlecht
- U
- Eingang
- 31.05.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Product temperature excursion issue
Symptomtext
HCP stated patience received a vaccine after a temperature excursion; The maximum temperature reached is 22.1 F. The minimum temperature reach was unknown; No adverse event; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (HCP stated patience received a vaccine after a temperature excursion), PRODUCT STORAGE ERROR (The maximum temperature reached is 22.1 F. The minimum temperature reach was unknown) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (HCP stated patience received a vaccine after a temperature excursion), PRODUCT STORAGE ERROR (The maximum temperature reached is 22.1 F. The minimum temperature reach was unknown) and NO ADVERSE EVENT (No adverse event). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (HCP stated patience received a vaccine after a temperature excursion), PRODUCT STORAGE ERROR (The maximum temperature reached is 22.1 F. The minimum temperature reach was unknown) 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 PRODUCT TEMPERATURE EXCURSION ISSUE (HCP stated patience received a vaccine after a temperature excursion) and PRODUCT STORAGE ERROR (The maximum temperature reached is 22.1 F. The minimum temperature reach was unknown). No concomitant medication was reported. It was unknown patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. 1st lot number 066H21A. The excursion in the freezer was between the beginning of January to November 2022 for a total of 123 hour 10 minutes not in a row. Something was wrong with the freezer and the temperature kept changing. 2nd lot number 002M21A. The expiration date was 11-Sep-2022. The excursion in the freezer was between the beginning of January to November 2022 in 15 minutes increments in a course of a few hours. 3rd lot number 215K22A and the expiration date is 19-Aug-2023. The excursion in the freezer was between 10March2023 to 01May2023. No treatment information was reported. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 15.05.2023
- Impfdatum
- 28.12.2021
- Beginn
- 14.05.2023
- Tage bis Beginn
- 502,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 1 booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 5/14/23
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Atrial Fibrillation HFpEF CAD DM2 HTN HLD CKD3
- Andere Medikamente
- unknown
- Allergien
- morphine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 05.04.2023
- Impfdatum
- 19.01.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 300,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case after 2 vaccines Janssen 4/5/21 Lot# 043A21A; Moderna 1/19/22 Lot# 066H21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 07.03.2023
- Impfdatum
- 30.12.2021
- Beginn
- 01.03.2023
- Tage bis Beginn
- 426,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- positive covid pcr 2/27/23
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- COPD, Kidney Disease, Peripheral Neuropathy
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 13.02.2023
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 09.02.2023
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 08.02.2023
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse Event, Vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 08.02.2023
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 06.02.2023
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 13.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19 immunisation
Interchange of vaccine products
No adverse event
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of INTERCHANGE OF VACCINE PRODUCTS (as a patient received 1 dose of the Pfizer COVID19 vaccine and a second dose of the Moderna COVID19 vaccine), COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) and NO ADVERSE EVENT (No adverse event) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066h21a) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: PFIZER BIONTECH COVID-19 VACCINE (Dose 1) on 06-Aug-2021. Past adverse reactions to the above products included No adverse event with PFIZER BIONTECH COVID-19 VACCINE. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for INTERCHANGE OF VACCINE PRODUCTS (as a patient received 1 dose of the Pfizer COVID19 vaccine and a second dose of the Moderna COVID19 vaccine) and COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine). No concomitant medication information was provided. No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 immunisation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Patient received Pfizer dose (dose #1) from pharmacy on 8/6/2021 and received Moderna (dose #2) from different pharmacy on 12/30/2021 when it should have been a second dose of Pfizer, not Moderna for the primary series. Patient did not have any ill effects, symptoms, or side effects. Patient came in on 1/23/2023 to get Moderna Bivalent Booster dose, and that is when the error with the primary series was identified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- None needed
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- unknown
- Andere Medikamente
- Unknown
- Allergien
- Contrast dye, latex bandaids
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Symptomtext
This spontaneous case was reported by another health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No Adverse Event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). This case contains information for the 13 out of 13 elderly patients described by the reporter. Concomitant Medication use information was not provided by reporter. The age group of the patients were mostly over 65. It was unknown that if patient receive any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was reported that the 13 patients received an expired Moderna vaccine. The dose administered after manufacturer date of expiry. The dates of administration of vaccine were reported as 14 April 2022, 21 April 2022, and 28 April 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Symptomtext
This spontaneous case was reported by another health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. In April 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In April 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) outcome was unknown. Not Provided This case is for 12th patient from 13 patient's case. Concomitant product use was not provided by the reporter. It was unknown if patient receive any other vaccines in the 4 weeks prior to COVID-19 vaccine. Vials went from freezer to room temperature on days of administration. Dates of administration of vaccine were 14-Apr-2022, 21-Apr-2022, and 28-Apr-2022. Vial did not undergo any temperature excursions. 13 doses total given from 3 vials. Multi dose vial size was 5.5mL. Age group of patients were mostly over 65 and they did report all of them in the website. 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
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. In April 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In April 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) outcome was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. In April 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In April 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) outcome was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Symptomtext
No Adverse Event; They have given patient an expired Moderna vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have given patient an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. In April 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In April 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have given patient an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have given patient an expired Moderna vaccine) 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 assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have given patient an expired Moderna vaccine). This case is for 7th patient from 13 patient's case. Concomitant product use was not provided by the reporter. It was unknown if patient receive any other vaccines in the 4 weeks prior to COVID-19 vaccine. Vials went from freezer to room temperature on days of administration. Dates of administration of vaccine were 14-Apr-2022, 21-Apr-2022, and 28-Apr-2022. Vial did not undergo any temperature excursions. 13 doses total given from 3 vials. Multi dose vial size was 5.5mL. Age group of patients were mostly over 65 and they did report all of them in the VAERS website. Treatment information was not provided. This case was linked to US-MODERNATX, INC.-MOD-2023-696547 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-696547:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have given patient an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. In April 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In April 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have given patient an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have given patient an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) outcome was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Symptomtext
; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) ( No Medical History information was reported. In April 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In April 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) outcome was unknown. Not Provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Symptomtext
No Adverse Event; They have given 13 patients an expired Moderna vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. In April 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In April 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No Adverse Event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). This case contains information for the 8 out of 13 Elderly patients described by the reporter. No concomitant information was reported. Vail never put in the fridge. Vials went from freezer to room temperature on days of administration. Dates of administration of vaccine were 14Apr2022, 21Apr2022, and 28Apr2022. Vial did not undergo any temperature excursions. 13 doses total given from 3 vials. Multi dose vials of 5.5mL. Age group of patients were mostly over 65 and they did report all of them in the VAERS website. No treatment information was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-696547 (E2B Linked Report). Reporter did not allow further contact; Sender's Comments: US-MODERNATX, INC.-MOD-2023-696547:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Symptomtext
No Adverse Event; They have given 13 patients an expired Moderna vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. In April 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In April 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No Adverse Event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). This case was considered as 5th patient out 13 patients. It was reported that age group of patients were mostly over 65. No concomitant medication information provided. It was unknown if patient had received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was reported that 13 doses total given from 3 vials. Vial size was multidose vials 5.5mL. It was reported that vial was never put in the fridge. Vials went from freezer to room temperature on days of administration. Dates vaccine was administered were reported as 14-Apr-2022, 21-Apr-2022 and 28-Apr-2022. The vials did not undergo any temperature excursions. No treatment information provided. This case was linked to US-MODERNATX, INC.-MOD-2023-696547 (E2B Linked Report). Reporter did not allow further contact; Sender's Comments: US-MODERNATX, INC.-MOD-2023-696547:master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Symptomtext
No Adverse Event; They have given 13 patients an expired Moderna vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. In April 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In April 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No Adverse Event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). This case was considered as 4th patient out 13 patients. It was reported that age group of patients were mostly over 65. No concomitant medication information provided. It was unknown if patient had received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was reported that 13 doses total given from 3 vials. Vial size was multidose vials 5.5mL. It was reported that vial was never put in the fridge. Vials went from freezer to room temperature on days of administration. Dates vaccine was administered were reported as 14-Apr-2022, 21-Apr-2022 and 28-Apr-2022. The vials did not undergo any temperature excursions. No treatment information provided. This case was linked to US-MODERNATX, INC.-MOD-2023-696547 (E2B Linked Report). Reporter did not allow further contact; Sender's Comments: US-MODERNATX, INC.-MOD-2023-696547:master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. In April 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In April 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) outcome was unknown. Not Provided Dates vaccine was administered were reported as 14-Apr-2022, 21-Apr-2022 and 28-Apr-2022. The vials did not undergo any temperature excursions. No treatment information provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Symptomtext
No Adverse Event; They have given 13 patients an expired Moderna vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. In April 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In April 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine) and NO ADVERSE EVENT (No Adverse Event) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No Adverse Event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have given 13 patients an expired Moderna vaccine). This case was considered as 2nd patient out of 13 patients. It was reported that age group of patients were mostly over 65. No concomitant medication information provided. It was unknown if patient had received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was reported that 13 doses total given from 3 vials. Vial size was multidose vials 5.5mL. It was reported that vial was never put in the fridge. Vials went from freezer to room temperature on days of administration. Dates vaccine was administered were reported as 14-Apr-2022, 21-Apr-2022 and 28-Apr-2022. The vials did not undergo any temperature excursions. No treatment information provided. This case was linked to US-MODERNATX, INC.-MOD-2023-696547 (E2B Linked Report). Reporter did not allow further contact; Sender's Comments: US-MODERNATX, INC.-MOD-2023-696547:master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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
No adverse event
Product storage error
Symptomtext
Product storage error; No Adverse Event; 13 patients administered an expired Moderna vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (13 patients administered an expired Moderna vaccine), PRODUCT STORAGE ERROR (Product storage error) and NO ADVERSE EVENT (No Adverse Event) in an elderly patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 prophylaxis. No Medical History information was reported. In April 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In April 2022, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (13 patients administered an expired Moderna vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Product storage error) and NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (13 patients administered an expired Moderna vaccine), PRODUCT STORAGE ERROR (Product storage error) 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 (13 patients administered an expired Moderna vaccine) and PRODUCT STORAGE ERROR (Product storage error). Concomitant medication was not reported. It was unknown if patient receive any other vaccines in the 4 weeks prior to COVID-19 vaccine. Vials went from freezer to room temperature on days of administration. Dates of administration of vaccine were 14Apr2022, 21Apr2022, and 28Apr2022. Vial did not undergo any temperature excursions. 13 doses total given from 3 vials. Multi dose vials of 5.5mL. Age group of patients were mostly over 65 and they did report all of them in the VAERS website. This case was related to patient number 1 out of 13patients. Treatment drug was not reported. This case was linked to US-MODERNATX, INC.-MOD-2023-697081, US-MODERNATX, INC.-MOD-2023-697097, US-MODERNATX, INC.-MOD-2023-697115, US-MODERNATX, INC.-MOD-2023-697138, US-MODERNATX, INC.-MOD-2023-697140, US-MODERNATX, INC.-MOD-2023-697170, US-MODERNATX, INC.-MOD-2023-697183, US-MODERNATX, INC.-MOD-2023-697200, US-MODERNATX, INC.-MOD-2023-697201 (E2B Linked Report). Reporter did not allow further contact; Sender's Comments: US-MODERNATX, INC.-MOD-2023-697097: US-MODERNATX, INC.-MOD-2023-697081: US-MODERNATX, INC.-MOD-2023-697138: US-MODERNATX, INC.-MOD-2023-697140: US-MODERNATX, INC.-MOD-2023-697115: US-MODERNATX, INC.-MOD-2023-697201: US-MODERNATX, INC.-MOD-2023-697183: US-MODERNATX, INC.-MOD-2023-697170: US-MODERNATX, INC.-MOD-2023-697200: US-MODERNATX, INC.-MOD-2023-697213:Master case US-MODERNATX, INC.-MOD-2023-697333:Master case US-MODERNATX, INC.-MOD-2023-697284:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
pt was given an expired vaccine due to local vaccine recording having incorrect manufactures expiration date listed on site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
pt was given an expired vaccine due to having incorrect manufactures expiration date listed on site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- 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
pt was given an expired vaccine due to local vaccine recording having incorrect manufactures expiration date listed on site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- 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
pt was given an expired vaccine due to local lot corordinator having incorrect manufactures expiration date listed on site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- 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
pt was given an expired vaccine due to data having incorrect manufactures expiration date listed on site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- 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
pt was given an expired vaccine due to immunization system having incorrect manufactures expiration date listed on site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
pt was given an expired vaccine due to local vaccine coordinator having incorrect manufactures expiration date listed on site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- 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
pt was given an expired vaccine due tolocal vaccine coordinator having incorrect manufactures expiration date listed on site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- 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
pt was given an expired vaccine due to data having incorrect manufactures expiration date listed on site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- 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
pt was given an expired vaccine due to having incorrect manufactures expiration date listed on site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- 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
pt was given an expired vaccine due to having incorrect manufactures expiration date listed on website
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- 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
pt was given an expired vaccine due to website having incorrect manufactures expiration date listed on site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- 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
patient given an expired vaccine. had incorrect manufactures expiration date in the system
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 07.01.2023
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Vaccine stored longer than recommended time post puncture (up to 28 days)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 21.11.2022
- Impfdatum
- 03.01.2021
- Beginn
- 03.01.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient received vaccine dose at 16 years of age
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 14.11.2022
- Impfdatum
- 10.03.2021
- Beginn
- 24.10.2022
- Tage bis Beginn
- 593,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
SARS-CoV-2 test positive
Symptomtext
Pt to ED 10/24 for possible syncope. Pt COVID+ 10/24, to start remdesivir for 5 days, denies shortness of breath. 10/26 pts oxygen sat, 78% on 5LNC. 10/17 Pt SpO2 was mid 80s while pt was laying flat in bed on left side. 10/28 pt with occasional non-prod cough. Pt discharged 10/31.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 8,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 diabetes mellitus with hypoglycemia ...
- Andere Medikamente
- amLODIPine (NORVASC) 10 MG PO ...
- Allergien
- Hydrocodone
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 02.11.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine vial store for longer than recommended post puncture of vial (potentially up to 28 days) no adverse reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Latex, amoxacillin, Lisinopril, PCN
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 24.10.2022
- Impfdatum
- 27.01.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 263,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case after three vaccinations Moderna 4/9/21 Lot# 025B21A; Moderna 5/7/21 Lot# 043B21A; Moderna 1/27/22 Lot# 066H21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 27.09.2022
- Impfdatum
- 26.01.2022
- Beginn
- 25.09.2022
- Tage bis Beginn
- 242,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ test on 9/26/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 26.09.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.09.2022
- Tage bis Beginn
- 243,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 9/23/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 07.09.2022
- Impfdatum
- 07.02.2022
- Beginn
- 06.09.2022
- Tage bis Beginn
- 211,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough case dose 1 3/26/21 Moderna 030A21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ on 9/6/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 03.08.2022
- Impfdatum
- 23.12.2021
- Beginn
- 02.08.2022
- Tage bis Beginn
- 222,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Fully vaccinated patient tested positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 03.08.2022
- Impfdatum
- 23.12.2021
- Beginn
- 02.08.2022
- Tage bis Beginn
- 222,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 23.12.2021
- Beginn
- 24.07.2022
- Tage bis Beginn
- 213,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVOID vaccine breakthrough case. Moderna 3/12/21 044A21A, 4/9/21 018B21A, and boosted on 12/23/2021 066H21A.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID test on 7/24/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 21.07.2022
- Impfdatum
- 10.06.2021
- Beginn
- 21.07.2022
- Tage bis Beginn
- 406,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
hospitalization
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 24.01.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 174,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case. Moderna 1/23/21 012L20A, 2/20/21 004M20A and bossted on 1/24/22 066H21A.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID test on 7/17/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 13.01.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 174,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Inappropriate schedule of product administration
Product storage error
Symptomtext
Vial was stored in refrigerator on 02-Jun-2022 and administered on 06-Jul-2022; Moderna COVID vaccine from a vial that had exceeded its 30 day working expiration.; Second dose 10-Feb-2022 and booster dose 06-Jul-2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna COVID vaccine from a vial that had exceeded its 30 day working expiration.), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Second dose 10-Feb-2022 and booster dose 06-Jul-2022) and PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 02-Jun-2022 and administered on 06-Jul-2022) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 059M21A, 068H21A and 066H21A) for COVID-19 prophylaxis. Concurrent medical conditions included Drug allergy (Methadone), Chronic pain since 13-Nov-2017, Hyperlipidemia since 05-Oct-2020, Hypertension since 17-Jan-2017, Anxiety disorder since 18-Oct-2021, Goiter since 21-Dec-2018 and Erectile dysfunction. Concomitant products included HYDROCODONE from 03-Mar-2022 to an unknown date and SULINDAC from 21-Sep-2020 to an unknown date for Chronic pain, SILDENAFIL from 19-Apr-2022 to an unknown date for Erectile dysfunction, PROPRANOLOL HYDROCHLORIDE (PROPRANOLOL SANDOZ) from 02-Jul-2018 to an unknown date for Hypertension, VITAMINS NOS (MULTIVITAMINUM) from 18-Nov-2005 to an unknown date for Supplementation therapy. On 13-Jan-2022 at 8:16 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 10-Feb-2022 at 9:19 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to .5 milliliter. On 06-Jul-2022 at 8:01 AM, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to .25 milliliter. On 06-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna COVID vaccine from a vial that had exceeded its 30 day working expiration.) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Second dose 10-Feb-2022 and booster dose 06-Jul-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 02-Jun-2022 and administered on 06-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna COVID vaccine from a vial that had exceeded its 30 day working expiration.), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Second dose 10-Feb-2022 and booster dose 06-Jul-2022) and PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 02-Jun-2022 and administered on 06-Jul-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient had never been diagnosed with/ tested positive for COVID 19. Acute illness at the time of vaccination and up to one month before was reported as none. Patient received a booster dose of vaccine from a vial that had exceeded its 30 day working expiration. No adverse events noted at the time of reporting. Number of doses and vials were reported as 15 doses and 3 red cap vials. Vial was initially stored in the refrigerator on 02-JUN-2022 The vial did not undergo any temperature excursions. Treatment details were not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Anxiety disorder; Chronic pain; Drug allergy (Methadone); Erectile dysfunction; Goiter; Hyperlipidemia; Hypertension
- Vorgeschichte
- -
- Andere Medikamente
- PROPRANOLOL SANDOZ; HYDROCODONE; SULINDAC; SILDENAFIL; MULTIVITAMINUM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 13.01.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 174,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Inappropriate schedule of product administration
Product storage error
Symptomtext
Vaccine was stored on 2Jun2022 and administered on 6Jul2022; Moderna COVID vaccine from a vial that had exceeded its 30 day working expiration.; second dose 10-Feb-22 and booster dose 6-Jul-22; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna COVID vaccine from a vial that had exceeded its 30 day working expiration.), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (second dose 10-Feb-22 and booster dose 6-Jul-22) and PRODUCT STORAGE ERROR (Vaccine was stored on 2Jun2022 and administered on 6Jul2022) in a 49-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 059M21A, 068H21A and 066H21A) for COVID-19 prophylaxis. Patient had no known allergies. On 13-Jan-2022 at 8:34 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 10-Feb-2022 at 8:37 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to .5 milliliter. On 06-Jul-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to .25 milliliter. On 06-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna COVID vaccine from a vial that had exceeded its 30 day working expiration.) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (second dose 10-Feb-22 and booster dose 6-Jul-22). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was stored on 2Jun2022 and administered on 6Jul2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna COVID vaccine from a vial that had exceeded its 30 day working expiration.), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (second dose 10-Feb-22 and booster dose 6-Jul-22) and PRODUCT STORAGE ERROR (Vaccine was stored on 2Jun2022 and administered on 6Jul2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant drug information was provided. The patient had never been diagnosed with/ tested positive for COVID 19. Acute illness at the time of vaccination and up to one month before was reported as none. Patient received a booster dose of vaccine from a vial that had exceeded its 30 day working expiration. No adverse events noted at the time of reporting. Number of doses and vials were reported as 15 doses and 3 red cap vials. Vial was initially stored in the refrigerator on 02-JUN-2022 The vial did not undergo any temperature excursions. Treatment details were not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient had no known allergies.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- 21.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
got COVID; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (got COVID) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066h21a) for COVID-19 vaccination. Concurrent medical conditions included Blood pressure and Anxiety. On 21-Dec-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In December 2021, the patient experienced COVID-19 (got COVID) (seriousness criterion hospitalization). The patient was hospitalized from sometime in December 2021 to 06-Jan-2022 due to COVID-19. The patient was treated with VITAMIN D NOS at an unspecified dose and frequency and OXYGEN at an unspecified dose and frequency. At the time of the report, COVID-19 (got COVID) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient was not known of any allergies. No other vaccines given within 1 month prior to Moderna COVID-19 vaccine. Patient was not on any concomitant regular or prescribed medication and reported no medication at all. Patient did not experience a similar event in the past. It was reported that the symptoms were improved. It was also reported that patient had to be on oxygen 24 hours, received all kinds of medication, went to a lung doctor and few doctors more and also reported that right now had 3 different inhalers, Oxygen when needed, CPAP machine which patient had problems to get adjusted with, blood pressure medication, sleep medication, anxiety medication, nasal spray, took cold medication. The patient was hard to stop coughing and had problems with yellow mucus and congestion. Company Comment: This spontaneous case concerns a 57-year-old female patient with no reported medical history, who experienced the unexpected, serious adverse event of special interest COVID-19 on an unknown date after receiving the first dose of mRNA-1273 vaccine that led to hospitalization. Latency between vaccine and event cannot be established. Patient experienced COVID-19 on the same month of vaccination. Patient presented with cough, yellow mucus, and congestion. She was treated with Vitamin D, nasal spray, inhalers, and unspecified medications for blood pressure, sleep, and anxiety. Management also included oxygen support and continuous positive airway pressure CPAP. SARS-CoV-2 test was not reported. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This spontaneous case concerns a 57-year-old female patient with no reported medical history, who experienced the unexpected, serious adverse event of special interest COVID-19 on an unknown date after receiving the first dose of mRNA-1273 vaccine that led to hospitalization. Latency between vaccine and event cannot be established. Patient experienced COVID-19 on the same month of vaccination. Patient presented with cough, yellow mucus, and congestion. She was treated with Vitamin D, nasal spray, inhalers, and unspecified medications for blood pressure, sleep, and anxiety. Management also included oxygen support and continuous positive airway pressure CPAP. SARS-CoV-2 test was not reported. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anxiety; Blood pressure
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
vaccine was administered to the patient at 1 month short of 18 yrs with parental consent. No post vaccine reaction .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- Irregular menses Anxiety Depressed
- Vorgeschichte
- Anxiety
- Andere Medikamente
- Zoloft 25 mg tablet SIG: take 1 tablet (25 mg) by oral route once daily for 30 days DISP: (30) Tablet with 0 refills Prescribed on 03/08/2022 Tri-Lo-Sprintec oral tablet 0.18/0.215/0.25 mg-25 mcg SIG: take 1 tablet by oral route once
- Allergien
- No Known Drug Allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 17.06.2022
- Impfdatum
- 14.01.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 154,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated with one booster. COVID breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
vials were stored in the refrigerator and thawed on same day of administration; Vial was expired on 04-APR-2022 and administered on 13-MAY-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vial was expired on 04-APR-2022 and administered on 13-MAY-2022) and PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vial was expired on 04-APR-2022 and administered on 13-MAY-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vial was expired on 04-APR-2022 and administered on 13-MAY-2022) and PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported No treatment medications were reported HCP stated that there was no information about side effects after administration of expired dose. The vial did not undergone any temperature excursion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 04-Apr-2022 and administered on 25-May-2022.; doses were administered after the expiration date/Administered after 30-day use by date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (doses were administered after the expiration date/Administered after 30-day use by date) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and administered on 25-May-2022.) in a 38-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 25-May-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 25-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (doses were administered after the expiration date/Administered after 30-day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and administered on 25-May-2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (doses were administered after the expiration date/Administered after 30-day use by date) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and administered on 25-May-2022.) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. The reporter stated that vaccine their office administered were expired at the time of administration. The vials were thawed on same day of administration and the vial did not undergo any temperature excursions. The patient had no known reactions at office. The patient's weight was reported as 230 with unknown units. 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
- FL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.06.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
vials were stored in the refrigerator and thawed on same day of administration; Vacccine was expired on 04-Apr-2022 and was administered on 20-May-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) and EXPIRED PRODUCT ADMINISTERED (Vacccine was expired on 04-Apr-2022 and was administered on 20-May-2022) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 20-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vacccine was expired on 04-Apr-2022 and was administered on 20-May-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration). At the time of the report, PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) and EXPIRED PRODUCT ADMINISTERED (Vacccine was expired on 04-Apr-2022 and was administered on 20-May-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient weight was reported as 180. Patient received Booster 2. No concomitant medications were reported. It was reported that the Vials was thawed on the same day of vaccine administration date. Vials did not undergo any temperature excursions. No treatment information were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 07.06.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was expired on 04-Apr-2022 and administered on 22-APR-2022; Vaccine was expired on 04-Apr-2022 and administered on 22-APR-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 22-APR-2022) and PRODUCT STORAGE ERROR (Vaccine was expired on 04-Apr-2022 and administered on 22-APR-2022) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 22-APR-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was expired on 04-Apr-2022 and administered on 22-APR-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 22-APR-2022) and PRODUCT STORAGE ERROR (Vaccine was expired on 04-Apr-2022 and administered on 22-APR-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient's weight was reported as 120 with unknown units. No concomitant medications were reported by the reporter. It was reported that patient was administered with booster 1 dose. It was reported that they were unsure if doses were administered after the expiration date. Number of doses/vials were 27 doses. Vials thawed on the same day of administration. Date(s) of administration of vaccine was since 06-Apr-2022 until 25-May-2022 Vial did not undergo any temperature excursions. No known reactions were reported in office. No treatment medications were reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 07.06.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 04-Apr-2022 and stored in the refrigerator on same day of administration; Vaccine was expired on 04-Apr-2022 and administered on 13-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and stored in the refrigerator on same day of administration) and EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 13-Apr-2022) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 13-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and stored in the refrigerator on same day of administration). At the time of the report, PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and stored in the refrigerator on same day of administration) and EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 13-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient's weight was reported as 136. No concomitant medication information was provided. HCP stated they administered expired doses of the Moderna COVID-19 Vaccine to 27 patients. It was reported that the vials were thawed on the same day of administration. The vails had not undergone ay temperature excursion. It was also reported that patient had no known reactions in office. No treatment medication information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
vials were stored in the refrigerator and thawed on same day of administration; Doses were administered after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) and EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date) in a 60-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration). At the time of the report, PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) and EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient's weight was reported as 200. Concomitant medications were not reported. The patient had received booster 1. The patient had no known reactions. The vials were thawed on same day of administration. The vials did not undergo any temperature excursions. Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration; The vial was expired on 04-Apr-2022 and administered on 25-Apr-2022 and 25-May-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vial was expired on 04-Apr-2022 and administered on 25-Apr-2022 and 25-May-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration) in a 78-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vial was expired on 04-Apr-2022 and administered on 25-Apr-2022 and 25-May-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vial was expired on 04-Apr-2022 and administered on 25-Apr-2022 and 25-May-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. Patient had no known reactions at office. The vial was thawed same day of administration. The vials did not undergo any temperature excursions. No adverse events were reported. 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
- FL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
vials were stored in the refrigerator and thawed on same day of administration; Vaccine was administered after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after the expiration date) and PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) in a 66-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after the expiration date) and PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient weight was reported as 169. Concomitant medications were not reported. The patient had received booster 1. The patient had no known reactions. The vials were thawed on same day of administration. The vials did not undergo any temperature excursions. Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
vial first expired then stored in refrigerator on same date of administration; doses were administered after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (doses were administered after the expiration date) and PRODUCT STORAGE ERROR (vial first expired then stored in refrigerator on same date of administration) in an 80-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (doses were administered after the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vial first expired then stored in refrigerator on same date of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (doses were administered after the expiration date) and PRODUCT STORAGE ERROR (vial first expired then stored in refrigerator on same date of administration) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. The patient had received booster 1. The patient had no known reactions. The vial did not undergo any temperature excursions. It was stated that the vial was thawed on the same day of administration. Treatment medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial expired on 04-Apr-2022, vial thawed on 26-Apr-2022 and administered on 26-Apr-2022; Doses were administered after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date) and PRODUCT STORAGE ERROR (Vial expired on 04-Apr-2022, vial thawed on 26-Apr-2022 and administered on 26-Apr-2022) in a 66-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 26-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial expired on 04-Apr-2022, vial thawed on 26-Apr-2022 and administered on 26-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date) and PRODUCT STORAGE ERROR (Vial expired on 04-Apr-2022, vial thawed on 26-Apr-2022 and administered on 26-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient's weight was reported as 233. The patient received booster 1 on 26-Apr-2022. Concomitant medication list was not provided. The vial was initially stored in the refrigerator: vials thawed on the same day of administration, 26-Apr-2022. Number of doses/vials- 27 doses.The vial did not undergo any temperature excursions. No known adverse reactions in office. Treatment information was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
vials were stored in the refrigerator and thawed on same day of administration; Doses were administered after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date) and PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) in a 75-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 07-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date) and PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient's weight was reported as 254. The patient had received booster one dose. No concomitant medications were reported. It was reported that the Vials was thawed on the same day of vaccine administration date. It was reported that vial did not undergo any temperature excursion. It was reported that patient had no known reaction in the office after receiving the dose. 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
- 74,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration; The vial was expired on 04-Apr-2022 and administered on 07-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vial was expired on 04-Apr-2022 and administered on 07-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vial was expired on 04-Apr-2022 and administered on 07-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vial was expired on 04-Apr-2022 and administered on 07-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. The weight of patient was reported as 192. Patient received second booster. Date the vial was initially stored in the refrigerator, was the same day vials were thawed. The vial did not undergo any temperature excursions. It was reported that patient did not experienced any known reactions. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Dose was administered beyonf 30 days of use; Doses were administered after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date) and PRODUCT STORAGE ERROR (Dose was administered beyonf 30 days of use) in a 61-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Dose was administered beyonf 30 days of use). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date) and PRODUCT STORAGE ERROR (Dose was administered beyonf 30 days of use) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient was administered with booster 2. No concomitant medications information was reported. HCP stated they administered expired doses of the Moderna COVID-19 Vaccine to 27 patients. Number of doses/vials: 27 doses Vials were thawed on the same day of administration Date(s) of administration of vaccine- since 06-Apr-2022 until 25-May-2022 The vial did not undergo any temperature excursions. There were no known reactions in office. 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
- FL
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 07.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
vials were stored in the refrigerator and thawed on same day of administration; Vaccine was expired on 04-Apr-2022 and was administered on 06-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) and EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and was administered on 06-Apr-2022) in an 87-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and was administered on 06-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration). At the time of the report, PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) and EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and was administered on 06-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient's weight was reported as 109. Concomitant medications were not reported. The patient had received booster 1. The patient had no known reactions. The vials were thawed on same day of administration. The vials did not undergo any temperature excursions. Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 06.06.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Moderna booster was accidentally administered too soon, 2 months after 2nd Moderna dose instead of 5 months after 2nd dose. We had initially believed we were administering a 2nd Moderna dose and not a booster, but found out this week that the same client's first dose was under a separate profile in system.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 16.04.2022
- Beginn
- 16.04.2022
- 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 was expired on 04-Apr-2022 then stored in refrigerator on same date of administration; Vaccine was expired on 04-Apr-2022 and administered on 16-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 16-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine was expired on 04-Apr-2022 then stored in refrigerator on same date of administration) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 16-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was expired on 04-Apr-2022 then stored in refrigerator on same date of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 16-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine was expired on 04-Apr-2022 then stored in refrigerator on same date of administration) outcome was unknown. Not provided. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient weight had been reported as 232. No concomitant medications were reported. The HCP (health care professional) stated that they had administered an expired doses of the Moderna COVID-19 Vaccine to 27 patients. The date of the vial that was initially stored in the refrigerator was the same day when the vials were thawed. The vial had not undergone any temperature excursions. The patient had no known reactions at office. 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
- FL
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 04.06.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
doses were administered after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (doses were administered after the expiration date) in a 47-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (doses were administered after the expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (doses were administered after the expiration date) outcome was unknown. Not provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient weight was reported as 160. No concomitant medications were reported. Total number doses were 27 , vial was initially stored in the refrigerator and thawed same day of administration. Vial did not undergo any temperature excursions. 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
- 47,0
- Geschlecht
- M
- Eingang
- 04.06.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration; Doses were administered after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration) in a 47-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigrator on same day of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigrator on same day of administration) outcome was unknown. Not provided. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. Patient weight has been reported as 185. HCP stated they administered expired doses of the Moderna COVID-19 Vaccine to 27 patients. Dose administered after 30-day Use By Date or after manufacturer date of expiry. Date the vial was initially stored in the refrigerator, was the same day vials were thawed. The vial didn't undergo any temperature excursions No treatment information were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 04.06.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
vials were stored in the refrigerator and thawed on same day of administration; Vaccine was expired on 04-Apr-2022 and administered on 26-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 26-Apr-2022) and PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 26-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 26-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 26-Apr-2022) and PRODUCT STORAGE ERROR (vials were stored in the refrigerator and thawed on same day of administration) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient weight was reported as 240. Concomitant medications were not reported. On 26-Apr-2022, the patient received a first booster dose (Lot: 066H21A) of Moderna vaccine. Reported that doses were administered after the expiration date/Administered after 30-day use by date. It was reported that patient didn't experienced any known reactions. The vials were thawed the same day of administration. The vials did not undergo any temperature excursions. Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 04.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was expired on 04-Apr-2022 and administered on 17-May-2022; Vaccine was expired on 04-Apr-2022 and administered on 17-May-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 17-May-2022) and PRODUCT STORAGE ERROR (Vaccine was expired on 04-Apr-2022 and administered on 17-May-2022) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 17-May-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was expired on 04-Apr-2022 and administered on 17-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 17-May-2022) and PRODUCT STORAGE ERROR (Vaccine was expired on 04-Apr-2022 and administered on 17-May-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. The reporter stated that vaccine their Office administered were expired at the time of administration. The vials were thawed on same day of administration and the vial didn't undergo any temperature excursions. On 17-May-2022, the patient received first booster dose of expired vaccine. The patient had no known reactions at office. 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
- FL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 04.06.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vials were stored in refrigerator even after expiration date/vials were stored in the refrigerator and thawed on same day of administration; Vaccine was administered on 13 Apr 2022 and expired on 04 Apr 2022.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered on 13 Apr 2022 and expired on 04 Apr 2022.) and PRODUCT STORAGE ERROR (Vials were stored in refrigerator even after expiration date/vials were stored in the refrigerator and thawed on same day of administration) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered on 13 Apr 2022 and expired on 04 Apr 2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vials were stored in refrigerator even after expiration date/vials were stored in the refrigerator and thawed on same day of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered on 13 Apr 2022 and expired on 04 Apr 2022.) and PRODUCT STORAGE ERROR (Vials were stored in refrigerator even after expiration date/vials were stored in the refrigerator and thawed on same day of administration) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. The weight of patient was reported as 180. Patient received second booster. Date the vial was initially stored in the refrigerator, was the same day vials were thawed. The vial did not undergo any temperature excursions. It was reported that patient did not experienced any known reactions. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 04.06.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 04-Apr-2022 and kept in the refrigrator on same day of administration; Doses were administered after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigrator on same day of administration) in a 76-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigrator on same day of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses were administered after the expiration date) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigrator on same day of administration) outcome was unknown. Not provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient weight was reported as 175. No concomitant medications were reported. Total number doses were 27, vial was initially stored in the refrigerator and thawed same day of administration. vial did not undergo any temperature excursions. It was reported that there were no known reactions. 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
- 73,0
- Geschlecht
- F
- Eingang
- 04.06.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- 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 expired on 04-Apr-2022 and kept in the refrigrator on same day of administration; Vaccine was expired on 04-Apr-2022 and administered on 13-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 13-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigrator on same day of administration) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 13-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigrator on same day of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 13-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigrator on same day of administration) outcome was unknown. Not provided. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient weight was reported as 180 Concomitant medications were not reported. Patient had received 2nd booster dose. Patient had reported no adverse events.28 patients may have received the expired Moderna COVID-19 vaccine The vials were thawed the same day of administration. The vials did not undergo any temperature excursions Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 04.06.2022
- Impfdatum
- 16.04.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
vial first expired then stored in refrigerator on same date of administration; Vaccine was expired on 04-Apr-2022 and administered on 16-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 16-Apr-2022) and PRODUCT STORAGE ERROR (vial first expired then stored in refrigerator on same date of administration) in a 63-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 16-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vial first expired then stored in refrigerator on same date of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 04-Apr-2022 and administered on 16-Apr-2022) and PRODUCT STORAGE ERROR (vial first expired then stored in refrigerator on same date of administration) outcome was unknown. Not provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient weight was reported as 240. Concomitant medications were not reported. The patient had received 2nd booster dose. Patient had reported no adverse events. 28 patients might had received the expired Moderna COVID-19 vaccine. The vials were thawed the same day of administration. The vials did not undergo any temperature excursions. Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 04.06.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration; The vial was expired on 04-Apr-2022 and administered on 25-Apr-2022 and 25-May-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vial was expired on 04-Apr-2022 and administered on 25-Apr-2022 and 25-May-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration) in a 43-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 066H21A and 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Apr-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 25-May-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 25-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vial was expired on 04-Apr-2022 and administered on 25-Apr-2022 and 25-May-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vial was expired on 04-Apr-2022 and administered on 25-Apr-2022 and 25-May-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and kept in the refrigerator on same day of administration) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Patient weight was reported as 265. No concomitant medications were provided. The patient received 1st and 2nd dose. HCP stated they administered expired doses of the Moderna COVID-19 Vaccine to 27 patients. Dose administered after 30-day Use By Date or after manufacturer date of expiry. The vial was initially stored in the refrigerator and was thawed same day of administration. The vials did not undergo any temperature excursions. No adverse events were reported. 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
- FL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 04.06.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 04-Apr-2022 and administered on 22-Apr-2022, doses were administered after the expiration date/Administered after 30-day use by date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (doses were administered after the expiration date/Administered after 30-day use by date) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and administered on 22-Apr-2022.) in a 71-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (doses were administered after the expiration date/Administered after 30-day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and administered on 22-Apr-2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (doses were administered after the expiration date/Administered after 30-day use by date) and PRODUCT STORAGE ERROR (Vaccine expired on 04-Apr-2022 and administered on 22-Apr-2022.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. The reporter stated that vaccine their office administered were expired at the time of administration. The vials were thawed on same day of administration and the vial didn't undergo any temperature excursions. On 22-Apr-2022, the patient received first booster dose of expired Moderna vaccine. The patient had no known reactions at office. The patient's weight was reported as 99 with unknown units. 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
- NJ
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 03.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
pt received an exp dose of moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
pt received an exp dose of moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 03.06.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
pt received an exp dose of modera vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
pt received an exp dose of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
pt was given an exp vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
pt was given exp covid vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 17.12.2021
- Beginn
- 14.05.2022
- Tage bis Beginn
- 148,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 28.05.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
Freezer temperature never reached an acceptable range and was always warm by at least 2 degree C; Possible administration of invalid dose to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Freezer temperature never reached an acceptable range and was always warm by at least 2 degree C) and POOR QUALITY PRODUCT ADMINISTERED (Possible administration of invalid dose to patients) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Freezer temperature never reached an acceptable range and was always warm by at least 2 degree C) and POOR QUALITY PRODUCT ADMINISTERED (Possible administration of invalid dose to patients). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Freezer temperature never reached an acceptable range and was always warm by at least 2 degree C) and POOR QUALITY PRODUCT ADMINISTERED (Possible administration of invalid dose to patients) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not provided. It was reported that there are 4 days temperature data (between 4/1/2022 and 4/4/2022) for the freezer storage unit, however it never reached an acceptable range and was always warm by at least 2 degree C. Between 2/22/21 to 4/26/22 there is no other temperature data available. Total 6640 doses of COVID-19 Moderna Vaccine were received by this facility during this time period and LOT numbers were provided (057M21A, 025L21B, 066H21A, 069H21A, 027H21B, 032F21A, 011F21A, 004F21A, 025C21A, 017C21A, 002C21A, 042B21A, 031B21A, 027B21A, 026B21A, 016B21A, 008B21A, 045A21A, 001B21A, 029A21A, 025A21A, 001A21A). Some vials may have been moved to a refrigerator at some point. There is no temperature data for that storage unit. Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 27.05.2022
- Impfdatum
- 18.11.2021
- Beginn
- 22.05.2022
- Tage bis Beginn
- 185,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
COVID 19; On 22-May-2022 symptoms returned, runny nose, sore throat headache, without fever and patient tested positive for SARS-Cov-2 again; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (On 22-May-2022 symptoms returned, runny nose, sore throat headache, without fever and patient tested positive for SARS-Cov-2 again) and COVID-19 (COVID 19) in a 45-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. Previously administered products included for Drug use for unknown indication: PENICILLIN NOS. Past adverse reactions to the above products included Allergy with PENICILLIN NOS. Concurrent medical conditions included Bicuspid aortic valve. Concomitant products included LISDEXAMFETAMINE MESILATE (VYVANSE) from 01-May-2022 to 11-May-2022, CELECOXIB (CELEXA [CELECOXIB]) from 01-May-2022 to 22-May-2022 and AMFETAMINE ASPARTATE, AMFETAMINE SULFATE, DEXAMFETAMINE SACCHARATE, DEXAMFETAMINE SULFATE (ADDERALL) from 01-May-2022 to 10-May-2022 for an unknown indication. On 18-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-May-2022, the patient experienced COVID-19 (On 22-May-2022 symptoms returned, runny nose, sore throat headache, without fever and patient tested positive for SARS-Cov-2 again). On an unknown date, the patient experienced COVID-19 (COVID 19). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 12-May-2022 to 16-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (On 22-May-2022 symptoms returned, runny nose, sore throat headache, without fever and patient tested positive for SARS-Cov-2 again) had not resolved and COVID-19 (COVID 19) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 19-May-2022, SARS-CoV-2 test: negative (Negative) Negative. On 22-May-2022, SARS-CoV-2 test: positive (Positive) Positive. The patient was taking other medications/products within 2 weeks of starting COVID-19 treatment. Patient was tested negative for SARS-Cov-2 on 19 May 2022. On 22 May 2022 the symptoms returned which included runny nose, sore throat headache, without fever and tested positive for SARS-Cov-2 again. Company comment: This spontaneous case concerns a 45-year-old male patient with no relevant medical history who experienced the unexpected non serious AESI of COVID 19 which occurred unknown days after the administration of third dose of mRNA-1273 vaccine in COVID 19 vaccination series. Patient received NIRMATRELVIR, RITONAVIR (Paxlovid) for 5 days as treatment for COVID 19 from 12-May to 16-May. Patient tested negative for COVID 19 on 19-May. 3 days later the symptoms returned, runny nose, sore throat headache, without fever, and patient again tested positive for COVID 19 on 22-May. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 45-year-old male patient with no relevant medical history who experienced the unexpected non serious AESI of COVID 19 which occurred unknown days after the administration of third dose of mRNA-1273 vaccine in COVID 19 vaccination series. Patient received NIRMATRELVIR, RITONAVIR (Paxlovid) for 5 days as treatment for COVID 19 from 12-May to 16-May. Patient tested negative for COVID 19 on 19-May. 3 days later the symptoms returned, runny nose, sore throat headache, without fever, and patient again tested positive for COVID 19 on 22-May. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220519; Test Name: Covid test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220522; Test Name: Covid test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Bicuspid aortic valve
- Vorgeschichte
- -
- Andere Medikamente
- VYVANSE; CELEXA [CELECOXIB]; ADDERALL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- 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
Pt given full dose moderna (0.5ml) supposed to be given half dose (0.25ml)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- 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
Symptomtext
administered with expired vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vials were not stored in the refrigerator and directly thawed them from the freezer before administration. The vial did not undergo any temperature excursions. 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
- NJ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- 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
Symptomtext
administered with expired vaccine; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. The vial did not undergo any temperature excursions. The vial was initially not stored in the refrigerator they directly thaw them from the freezer before administration. No treatment medication were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- 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
Symptomtext
Administered with expired vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered with expired vaccine) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered with expired vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered with expired vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications information was not reported. It was reported that the vials were not stored in the refrigerator, they directly thaw them from the freezer before administration. Vial 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
- NJ
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- 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
They do not store them in the refrigerator, they directly thaw them from the freezer before administration; administered with expired vaccine on 29 Apr 2022 - 5 doses; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine on 29 Apr 2022 - 5 doses) and PRODUCT STORAGE ERROR (They do not store them in the refrigerator, they directly thaw them from the freezer before administration) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. Previously administered products included for Drug use for unknown indication: Pfizer (Received 3 doses). Past adverse reactions to the above products included No adverse event with Pfizer. On 29-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine on 29 Apr 2022 - 5 doses). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They do not store them in the refrigerator, they directly thaw them from the freezer before administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine on 29 Apr 2022 - 5 doses) and PRODUCT STORAGE ERROR (They do not store them in the refrigerator, they directly thaw them from the freezer before administration) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. A medical assistant reports that they administered an expired dose of the Moderna Covid-19 vaccine to 11 patients on different dates (15-Apr-2022 - 2 doses; 29-Apr-2022- 5 doses; 13-May-2022 - 4 doses). Lot number 066H21A; expiration date 04-Apr-2022. No patient adminstered with the vaccine had reported any event at the time of the call. Number of doses/vials: - 11 doses; probably 3 vials. The vial did not undergo any temperature excursions. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- 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 preparation error
Symptomtext
Vial was not stored in the refrigerator, It was directly thawed from the freezer before administration; administered expired vaccine; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered expired vaccine) and PRODUCT PREPARATION ERROR (Vial was not stored in the refrigerator, It was directly thawed from the freezer before administration) in a 79-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered expired vaccine). On an unknown date, the patient experienced PRODUCT PREPARATION ERROR (Vial was not stored in the refrigerator, It was directly thawed from the freezer before administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered expired vaccine) and PRODUCT PREPARATION ERROR (Vial was not stored in the refrigerator, It was directly thawed from the freezer before administration) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was reported. The vial did not undergo any temperature excursions. No adverse events were reported by the patient. The vial was initially not stored in the refrigerator they directly thaw them from the freezer before administration. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- 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
Symptomtext
Administered with expired vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered with expired vaccine) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered with expired vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered with expired vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient received 4th booster dose. No concomitant medications was provided by the reporter. No treatment medications was provided by the reporter. Vial did not undergo any temperature excursions. The Vial was not stored in the refrigerator, they were directly thaw from the freezer before administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- 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
Symptomtext
Patient received a vaccine on 15-Apr-2022, which had got expired on 04-Apr-2022.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received a vaccine on 15-Apr-2022, which had got expired on 04-Apr-2022.) in a 57-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received a vaccine on 15-Apr-2022, which had got expired on 04-Apr-2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received a vaccine on 15-Apr-2022, which had got expired on 04-Apr-2022.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The vial did not undergo any temperature excursions. Concomitant drugs were not reported. Treatment details were not given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- 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
Symptomtext
administered with expired vaccine 13May2022 - 4 doses administered with expiry date 04 Apr 2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine 13May2022 - 4 doses administered with expiry date 04 Apr 2022) in a 66-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine 13May2022 - 4 doses administered with expiry date 04 Apr 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine 13May2022 - 4 doses administered with expiry date 04 Apr 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information provided. No treatment medication information provided. The vial was not stored in the refrigerator, directly it was thawed from the freezer before administration. The vial did not undergo any temperature excursions. Most recent FOLLOW-UP information incorporated above includes: On 16-May-2022: Follow up received and patient demographic details added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- 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
Symptomtext
administered with expired vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported The vials were not stored in the refrigerator and directly thawed them from the freezer before administration. The vial did not undergo any temperature excursions. 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
- NJ
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- 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
Symptomtext
Patients were administered with expired vaccine on 29-Apr-2022- 5 doses; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients were administered with expired vaccine on 29-Apr-2022- 5 doses) in a 72-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients were administered with expired vaccine on 29-Apr-2022- 5 doses). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients were administered with expired vaccine on 29-Apr-2022- 5 doses) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. The vial did not undergo any temperature excursions. The vial was initially not stored in the refrigerator they directly thaw them from the freezer before administration. No treatment medication were provided. Most recent FOLLOW-UP information incorporated above includes: On 16-May-2022: Follow up received and contains significant information included patient demographics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product preparation error
Symptomtext
Vial was not stored in the refrigerator, It was directly thawed from the freezer before administration; administered with expired vaccine 15-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine 15-Apr-2022) and PRODUCT PREPARATION ERROR (Vial was not stored in the refrigerator, It was directly thawed from the freezer before administration) in an 87-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine 15-Apr-2022). On an unknown date, the patient experienced PRODUCT PREPARATION ERROR (Vial was not stored in the refrigerator, It was directly thawed from the freezer before administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine 15-Apr-2022) and PRODUCT PREPARATION ERROR (Vial was not stored in the refrigerator, It was directly thawed from the freezer before administration) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. Number of doses administered were 11 doses, probably 3 vials. The vials were not stored in the refrigerator, they were directly thawed from the freezer before administration. No temperature excursions were reported. No patient administered with the vaccine has reported any event at the time of the call. No treatment medication was provided. Most recent FOLLOW-UP information incorporated above includes: On 16-May-2022: Follow-up received includes patient details and dose details added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 28.01.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 103,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Influenza A virus test positive
Influenza B virus test positive
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive SARS-CoV-2 (COVID-19) and Influenza AB by Nucleic Acid Amplification on 5/11/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, diabetes mellitus
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 29.12.2021
- Beginn
- 11.05.2022
- Tage bis Beginn
- 133,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 5/11/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered a booster dose of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered a second booster dose of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered a booster dose of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered a booster dose of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered a booster dose of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered a second dose of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
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
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered a booster dose of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered a second booster dose of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
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
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered a second booster dose of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered a booster dose of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered a booster dose of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered a booster dose of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered the second booster of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
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
- 10.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- 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 was administered the second booster of Moderna on 4/5/22 but the vial had expired on 4/4/22. Incident was reported to Moderna and a lot analysis was completed. Results showed the vaccine "maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 12.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 Celsius thaw state on or about 20-Dec-2021 and administered on 12-Feb-2022; Covid-19 vaccine that were given beyond the 30 day use by date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 20-Dec-2021 and administered on 12-Feb-2022) in a 30-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. It was reported Acute illness at the time of vaccination and up to one month before and Chronic or long-standing health conditions were unknown. On 12-Feb-2022 at 12:50 PM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 12-Feb-2022 at 12:50 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 20-Dec-2021 and administered on 12-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 20-Dec-2021 and administered on 12-Feb-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Prescriptions, over the counter medications, dietary supplements or herbal remedies being taken at time of vaccination and/or at the time of adverse event were unknown. Other vaccine given on the same day as that of Moderna vaccine was unknown. Other vaccines received within one month prior to any dose of Moderna COVID-19 vaccine was unknown. Patient was administered vaccine past its 30 days expiry date vaccine went into 2 to 8 Celsius thaw state on or about to 20-Dec-2021, this vaccine was administered until its manufacturing (Mfg) expiration date of 04-Apr-2022. No treatment medication information provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was reported Acute illness at the time of vaccination and up to one month before and Chronic or long-standing health conditions were unknown.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022 at 17:36:48; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022 at 17:36:48; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022 at 17:36:48) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022 at 17:36:48) in a 34-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Feb-2022 at 5:36 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Feb-2022 at 5:36 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022 at 17:36:48). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022 at 17:36:48). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022 at 17:36:48) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022 at 17:36:48) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported by reporter. The patient's ethnicity was reported. It was unknown if the patient had acute illness at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long lasting health conditions. Concomitant product use was not provided by the reporter. It was unknown if the patient received any prescriptions, over the counter medications, dietary supplements or herbal remedies at the time of vaccination and or at the time of adverse event. It was unknown if the patient received other vaccines given on the same day and it was also unknown if the patient received other vaccines within one month prior to any dose of Moderna vaccine. It was unknown if the patient experienced any adverse events or not. The patient received Moderna vaccine past its 30 day of expiry date. It went into 2-to-8-degree Celsius thaw state on or about 24-Dec-2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. No treatment information was provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 09-Feb-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 09-Feb-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 09-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 09-Feb-2022) in a 48-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Feb-2022 at 2:58 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 09-Feb-2022 at 2:58 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 09-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 09-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 09-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 09-Feb-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. Census Ethnicity of the patient was reported. The patient received booster dose. 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
- MA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022) and EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022) in a 35-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Feb-2022 at 9:34 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 10-Feb-2022 at 9:34 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022). At the time of the report, PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022) and EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The ethnicity was reported. The patient had received the booster dose. It was reported that a series of approximately 540 patients had received lot 066H21A past its 30 days of an expiry date. The vaccine was administered up until its manufactured expiry date of 04-Apr-2022 and lot number was no longer possessed. No treatment medications were reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- 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 went into 2?8-degree Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 15:27; Vaccine went into 2?8-degree Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 15:27; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2?8-degree Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 15:27) and PRODUCT STORAGE ERROR (Vaccine went into 2?8-degree Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 15:27) in a 23-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Mar-2022 at 3:27 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 11-Mar-2022 at 3:27 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2?8-degree Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 15:27). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2?8-degree Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 15:27). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2?8-degree Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 15:27) and PRODUCT STORAGE ERROR (Vaccine went into 2?8-degree Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 15:27) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Reportedly patient ethnicity was given. Concomitant medications details were not reported by the reporter. Booster vaccine administration time reported as 15:27:29. Treatment details was not reported by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 12.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022; Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Feb-2022 at 11:54 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 12-Feb-2022 at 11:54 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021, this vaccine was administered up until its manufacturing expiry date of 4 April 2022. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- 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
Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 07-Feb-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 07-Feb-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 07-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 07-Feb-2022) in a 28-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Feb-2022 at 4:02 PM, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 07-Feb-2022 at 4:02 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 07-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 07-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 07-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 07-Feb-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine administration time was given as 16:02:08. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- 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
Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 03-Mar-2022; Received vaccine past its 30-days Exp date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 03-Mar-2022) in a 72-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. It was unknown if patient had any acute illnesses at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long-standing health conditions. On 03-Mar-2022 at 11:24 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 03-Mar-2022 at 11:24 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 03-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 03-Mar-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications information was reported. It was unknown if any prescriptions, over-the-counter-medications, dietary supplements, or herbal remedies were being taken by the patient at the time of vaccination and/or at the time of the adverse event. It was unknown if other vaccines were given on the same day or within one month prior to any dose of Moderna COVID-19 Vaccine to the patient. Patient received the booster dose. It was reported that vaccines went into 2-8 C thaw state on or above 24-Dec-2021 and were administered up until the expiry date of 04-Apr-2022. No treatment medications were provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient had any acute illnesses at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long-standing health conditions.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- 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
Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-JAN-2022.; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-JAN-2022.; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-JAN-2022.) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-JAN-2022.) in a 42-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 31-Jan-2022 at 3:39 PM, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 31-Jan-2022 at 3:39 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-JAN-2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-JAN-2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-JAN-2022.) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-JAN-2022.) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. The patient ethnicity was reported. On 31-Jan-2022 at 15:39:19, Patient administered second dose. It was reported that patient received lot its 30 day expiry date. No treatment information was reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 41-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Feb-2022 at 4:59 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 03-Feb-2022 at 4:59 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that patient ethnicity. The patient received Moderna vaccine on 03-Feb-2022 16:59:33, past its 30 day of expiry date. Vaccine went into 2 to 8 degree Celsius thaw state on or about 24-Dec-2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. No treatment medications were provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 12.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in an 18-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Feb-2022 at 11:20 AM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 12-Feb-2022 at 11:20 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was reported. Patient received vaccine past its 30 day expiry date. Vaccine went into 2 to 8 degree celsius thaw state on or about 24-Dec-2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. Reporter no longer possessed this lot number. No treatment medication was provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 13.03.2022
- Beginn
- 13.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 13-MAR-2022 at 15:46:32; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 13-MAR-2022 at 15:46:32; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 13-MAR-2022 at 15:46:32) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 13-MAR-2022 at 15:46:32) in a 20-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Mar-2022 at 3:46 PM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 13-Mar-2022 at 3:46 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 13-MAR-2022 at 15:46:32). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 13-MAR-2022 at 15:46:32). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 13-MAR-2022 at 15:46:32) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 13-MAR-2022 at 15:46:32) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. The patient's ethnicity was reported as white. It was unknown if the patient had acute illness at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long lasting health conditions. Concomitant product use was not provided by the reporter. It was unknown if the patient received any prescriptions, over the counter medications, dietary supplements or herbal remedies at the time of vaccination. It was unknown if the patient received other vaccines given on the same day and it was also unknown if the patient received other vaccines within one month prior to any dose of Moderna vaccine. It was unknown if the patient experienced any adverse events or not. The patient received Moderna vaccine past its 30 day of expiry date. Vaccine was administered on 13-Mar-2022 at 15:46:32. It went into 2-to-8-degree Celsius thaw state on or about 24-Dec-2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. No treatment information was provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 09-FEB-2022; Patient received vaccine past its 30-days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30-days expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 09-FEB-2022) in a 38-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Feb-2022 at 3:00 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 09-Feb-2022 at 3:00 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30-days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 09-FEB-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30-days expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 09-FEB-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient ethnicity was reported as White. No concomitant medications were provided by reporter. No treatment medications were provided by reporter. On 09-FEB-2022 at 15:00:57, patient received an expired booster dose. It was reported that vaccines went into 2-8 C thaw state on or above 24-Dec-2021 and were administered up until the MFG expiry date of 04-Apr-2022. Prescriptions, over the counter medications, dietary supplements or herbal remedies being taken at time of vaccination or at the time of the adverse event were reported as unknown. Other vaccines given on the same day as Moderna COVID-19 vaccine and other vaccines received within one month prior to any dose of Moderna COVID-19 vaccine were reported as unknown. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- 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 an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 18-Feb-2022) in a 46-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Feb-2022 at 12:39 PM, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 18-Feb-2022 at 12:39 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 18-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 18-Feb-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. The patient ethnicity was reported as white. Concomitant medication was not reported. Treatment medication was not reported. Patient received vaccine past its 30 day expiry date. Vaccine went into 2 to 8 degree Celsius thaw state on or about 24-Dec-2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. Reporter no longer possess this lot number. On 18-Feb-2022 at 12:39:51 the patient was administered with second dose. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Received vaccine past its 30-days Exp date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 46-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2022 at 2:23 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Jan-2022 at 2:23 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Patient took Moderna booster dose. Vaccine administration time reported as 14:23:26. The patient was administered booster dose that went into 2 to 8 Celsius thaw state on or above 24-Dec -2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; This spontaneous case was reported by an emergency medical technician and describes the occurrence of PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 48-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2022 at 1:19 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Jan-2022 at 1:19 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient ethnicity was reported. No concomitant medication information was provided. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. No treatment medication information was given. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022) in a 20-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Feb-2022 at 4:59 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Feb-2022 at 4:59 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Ethnicity of the patient was reported. Concomitant medication of the patient was not reported. The patient was administered vaccine past its 30 days expiry date. Vaccine administration time was given as 16:59:16. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Covid-19 vaccine that were given beyond the 30 day use by date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Feb-2022 at 2:54 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 11-Feb-2022 at 2:54 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Us Census Ethnicity of patient was reported as Hispanic or Latino of any race. No concomitant medication information provided. It was reported that, vaccine was administered on 11-Feb-2022 at 14:54:00 and it was booster dose. Its 30 days expiry date vaccine went into 2 to 8 ?C thaw state on or about to 20-Dec-2021, this vaccine administered until its Mfg date of 04-Apr-2022 No treatment information provided. This case was linked to MOD-2022-542869.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 06.02.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021; vaccine administered past its 30-days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Feb-2022 at 4:07 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Feb-2022 at 4:07 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that, vaccine was administered on 06-Feb-2022 at 16:07:47. Vaccine dose reported was booster. No treatment details were reported. Ethnicity was given. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- 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
Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022; Received vaccine past its 30-days Exp date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022) in a 25-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066h21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Feb-2022 at 1:28 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 20-Feb-2022 at 1:28 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications information was reported. Patient received the booster dose. It was reported that vaccines went into 2-8 C thaw state on or above 24-Dec-2021 and were administered up until the MFG expiry date of 04-Apr-2022. No treatment medications were provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 25-Mar-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 25-Mar-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 25-Mar-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 25-Mar-2022) in an 84-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Mar-2022 at 12:24 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 25-Mar-2022 at 12:24 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 25-Mar-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 25-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 25-Mar-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 25-Mar-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. Treatment medications were not reported. Patient received booster vaccine past its 30-day expiry date. Vaccine went into 2-to-8-degree Celsius thaw state on or about 24-Dec-2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. Reporter no longer possess this lot number. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Apr-2022 at 11:15 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Apr-2022 at 11:15 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. Treatment medications were not reported. Patient received additional vaccine past its 30-day expiry date. Vaccine went into 2-to-8-degree Celsius thaw state on or about 24-Dec-2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. Reporter no longer possess this lot number. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 12.02.2022
- Beginn
- 12.02.2022
- 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
This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022) in a 39-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Feb-2022 at 11:45 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 12-Feb-2022 at 11:45 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant information was reported. The patient's Ethnicity reported as Black or African American. Patient allergies to medications, food and other products was unknown. Vaccination date was reported as 12 Feb 2022 11:45:19.The patient received booster dose. Its 30 days Expiry date vaccine went into 2 to 8 degree C thaw state on or about to 20-Dec-2021, this vaccine administered until its Mfg. expiry date of 04-Apr-2022. No treatment information was reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 12.02.2022
- Beginn
- 12.02.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066h21a) for COVID-19 vaccination. No Medical History information was reported. On 12-Feb-2022 at 4:54 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 12-Feb-2022 at 4:54 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 12-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant information was reported. Patient allergies to medications, food and other products was unknown. Vaccination date was reported as 12 Feb 2022 16:54:37.The patient received booster dose. Its 30 days Expiry date vaccine went into 2 to 8 degree C thaw state on or about to 20-Dec-2021, this vaccine administered until its Mfg exp. date of 04-Apr-2022. No treatment information was reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- 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
Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Received vaccine past its 30-days Exp date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 31-Jan-2022 at 6:26 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 31-Jan-2022 at 6:26 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The Ethnicity was reported. No concomitant medications were reported. The patient received Moderna vaccine past it's 30 day of expiry date. Vaccine went into 2 to 8 degree celsius thaw state on or about 24-Dec-2021. This vaccine was administered up until it's manufacturing expiry date of 04-Apr-2022. No treatment medications were provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- 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
Received vaccine past its 30-days Exp date, Vaccines went into 2-8?C thaw state on or about 24-Dec-2021.; Patient received vaccine past its 30 days expiry date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date, Vaccines went into 2-8?C thaw state on or about 24-Dec-2021.) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Feb-2022 at 4:50 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 03-Feb-2022 at 4:50 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date, Vaccines went into 2-8?C thaw state on or about 24-Dec-2021.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date, Vaccines went into 2-8?C thaw state on or about 24-Dec-2021.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. patient's ethnicity was reported. It was reported that this vaccine was administered up until its Mfg Exp date of 04-Apr-2022. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Received vaccine past its 30-days; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 32-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Feb-2022 at 11:04 AM, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 14-Feb-2022 at 11:04 AM, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The patient received vaccine past its 30 day expiry date on 14-Feb-2022 at 11:04:17 AM. Vaccine went into 2 to 8 degree Celsius thaw state on about 24-Dec-2021. The vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. No treatment information was reported. This case was linked to MOD-2022-542869.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- 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 went into 2-8 degree Celsius thaw state on or about 24-Dec-2021 and administered on 27-JAN-2022 14:36:33; Vaccine went into 2-8 degree Celsius thaw state on or about 24-Dec-2021 and administered on 27-JAN-2022 14:36:33; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 degree Celsius thaw state on or about 24-Dec-2021 and administered on 27-JAN-2022 14:36:33) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 degree Celsius thaw state on or about 24-Dec-2021 and administered on 27-JAN-2022 14:36:33) in a 34-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. It was unknown if patient had any acute illnesses at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long-standing health conditions. On 27-Jan-2022 at 2:36 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 27-Jan-2022 at 2:36 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 degree Celsius thaw state on or about 24-Dec-2021 and administered on 27-JAN-2022 14:36:33). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 degree Celsius thaw state on or about 24-Dec-2021 and administered on 27-JAN-2022 14:36:33). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 degree Celsius thaw state on or about 24-Dec-2021 and administered on 27-JAN-2022 14:36:33) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 degree Celsius thaw state on or about 24-Dec-2021 and administered on 27-JAN-2022 14:36:33) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was unknown if any prescriptions, over-the-counter-medications, dietary supplements, or herbal remedies were being taken by the patient at the time of vaccination and/or at the time of the adverse event. It was unknown if other vaccines were given on the same day as Moderna COVID-19 Vaccine to the patient. It was unknown if patient received other vaccines within one month prior to any dose of Moderna COVID-19 Vaccine. On 27-JAN-2022 14:36:33, the patient received a booster dose (Lot: 066H21A and expiry date 04-APR-2022) of Moderna vaccine. Reported that patient received Vaccine past its 30-day expiry date, vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021. No treatment drug information was reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient had any acute illnesses at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long-standing health conditions.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022; Patient received vaccine past its 30 days expiry date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022) in a 34-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 31-Jan-2022 at 1:33 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 31-Jan-2022 at 1:33 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient ethnicity reported. Concomitant products were not provided. Patient received booster dose vaccination time was reported as 13:33:16. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. Treatment medications were not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and was administered on 28-Jan-2022; Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and was administered on 28-Jan-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and was administered on 28-Jan-2022) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and was administered on 28-Jan-2022) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. It was unknown if the patient had been diagnosed or tested positive for COVID-19. It was unknown if the patient had any acute illness at the time of vaccination and up to 1 month before. Other vaccines received on the same day as of Moderna or other vaccines received one month prior to any dose of Moderna was unknown. On 28-Jan-2022 at 1:06 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Jan-2022 at 1:06 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and was administered on 28-Jan-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and was administered on 28-Jan-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and was administered on 28-Jan-2022) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and was administered on 28-Jan-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The ethnicity of the patient was reported. No Concomitant product use was reported. The patient received vaccine past its 30 day expiry date The vaccine went into 2-8 degree Celsius thaw state on or about 24-Dec-2021. The vaccine was administered up until it manufactured expiry date of 04-Apr-2022. The patient received booster dose. It was unknown if any prescriptions, over-the-counter-medications, dietary supplements, or herbal remedies were being taken by the patient at the time of vaccination and/or at the time of the adverse event. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if the patient had been diagnosed or tested positive for COVID-19.It was unknown if the patient had any acute illness at the time of vaccination and up to 1 month before.Other vaccines received on the same day as of Moderna or other vaccines received one month prior to any dose of Moderna was unknown.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- 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
This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and administered on 28MAR2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-MAR-2022) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Mar-2022 at 12:48 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Mar-2022 at 12:48 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and administered on 28MAR2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-MAR-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and administered on 28MAR2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-MAR-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications reported by reporter. Treatment medication not reported. The patient took booster dose on 28-Mar-2022 at 12:48:41. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.) in a 72-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2022 at 12:09 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Jan-2022 at 12:09 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The ethnicity of the patient was reported. No Concomitant product use was reported. The patient received vaccine past its 30 day expiry date The vaccine went into 2-8 degree Celsius thaw state on or about 24-Dec-2021. The vaccine was administered up until it manufactured expiry date of 04-Apr-2022. The patient received booster dose. 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
- MA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Feb-2022 at 12:14 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 20-Feb-2022 at 12:14 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 20-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The patient had received the booster dose. It was reported that a series of approximately 540 patients had received lot 066H21A past its 30 days of an expiry date. The vaccine was administered up until its manufactured expiry date of 04-Apr-2022 and lot number was no longer possessed. No treatment medications were reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2022 at 12:09 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Jan-2022 at 12:09 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported Vaccines went into 28 degree Celsius thaw state on or about 24 Dec 2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022) in a 51-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 31-Jan-2022 at 3:30 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 31-Jan-2022 at 3:30 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information provided. A patient was administered vaccine past its 30 days expiry date vaccine went into 2 to 8 Celsius thaw state on or about to 24-Dec-2021, this vaccine administered was until its manufacturing (Mfg) expiration date of 04-Apr-2022. No treatment medication information provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- 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 went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022; Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022) in a 60-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Apr-2022 at 11:16 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Apr-2022 at 11:16 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant Medications were provided by the Reporter. Its 30 days Expiry date vaccine went into 2 to 8 ?C thaw state on or about to 24-Dec-2021, this vaccine administered until its Mfg date of 04-Apr-2022 No Treatment Medications were provided by the Reporter This case was linked to MOD-2022-542869.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2022 at 2:41 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Jan-2022 at 2:41 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient ethnicity reported . Concomitant products were not provided. Treatment medications were not reported. Patient received booster dose vaccination time was reported as 14:41:17. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- 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
Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and was administered on 18-Mar-2022; Patient received vaccine 30-days Expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine 30-days Expiry date) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and was administered on 18-Mar-2022) in a 41-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Mar-2022 at 2:17 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 18-Mar-2022 at 2:17 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine 30-days Expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and was administered on 18-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine 30-days Expiry date) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021 and was administered on 18-Mar-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient was given booster dose on 18-MAr-2022, 14:17:58. Prescriptions, over the counter medications, dietary supplements or herbal medicines being taken at the time of vaccination and or at the time of adverse event was unknown. Treatment and concomitant information was not provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- 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
This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp. date) and PRODUCT STORAGE ERROR (Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and was administered on 18MAR2022) in a 21-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Mar-2022 at 2:16 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 18-Mar-2022 at 2:16 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp. date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and was administered on 18MAR2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp. date) and PRODUCT STORAGE ERROR (Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and was administered on 18MAR2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022) in a 33-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Feb-2022 at 12:19 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 11-Feb-2022 at 12:19 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine administration time was given as 12:19:38. . No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022) in a 43-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2022 at 12:10 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Jan-2022 at 12:10 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-Jan-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Ethnicity of the patient was reported as private. Concomitant medication of the patient was not reported. The patient was administered vaccine past its 30 days expiry date. Vaccine administration time was given as 12:10:08. . No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; This spontaneous case was reported by an emergency medical technician and describes the occurrence of PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 52-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Jan-2022 at 6:40 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 25-Jan-2022 at 6:40 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. No treatment medication information was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 06.02.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 06-Feb-2022; Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 06-Feb-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 06-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 06-Feb-2022) in a 32-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Feb-2022 at 10:51 AM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 06-Feb-2022 at 10:51 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 06-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 06-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 06-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 celsius thaw state on or about 24-Dec-2021 and administered on 06-Feb-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Patient has Ethnicity as private Its 30 days Expiry date vaccine went into 2 to 8 ?C thaw state on or about to 24-Dec-2021, this vaccine administered until its Mfg date of 04-Apr-2022 No Concomitant Medications were provided by the Reporter No Treatment Medications were provided by the Reporter This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Received vaccine past its 30-days Exp date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 31-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Mar-2022 at 12:24 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 11-Mar-2022 at 12:24 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The patient received Moderna vaccine past its 30 day of expiry date. Vaccine went into 2-to-8-degree Celsius thaw state on or about 24-Dec-2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. No treatment medications were provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 06.02.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 06-Feb-2022; Patient received vaccine past its 30 days expiry date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 06-Feb-2022) in a 64-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Feb-2022 at 9:49 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Feb-2022 at 9:49 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 06-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 C thaw state on or about 24-Dec-2021 and administered on 06-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant products were not provided. Patient received booster dose vaccination time was reported as 09:49:26. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. Treatment medications were not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 19.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 19-Feb-2022; Patient received vaccine past its 30 days expiry date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 19-Feb-2022) in a 54-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. The patient's acute illness at the time of vaccination and up to 1 month before and chronic or long standing health conditions was unknown. Other vaccines received on the same day as of Moderna or other vaccines received one month prior to any dose of Moderna was unknown. On 19-Feb-2022 at 11:01 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 19-Feb-2022 at 11:01 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 19-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 19-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Ethnicity was given as private. The patient was given booster dose on 19-Feb-2022 at 11:01:54. The manufacturer expiry date was on 04-Apr-2022. Prescriptions, over the counter medications, dietary supplements or herbal medicines being taken at the time of vaccination and or at the time of adverse event was unknown. Treatment information was not provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient's acute illness at the time of vaccination and up to 1 month before and chronic or long standing health conditions was unknown. Other vaccines received on the same day as of Moderna or other vaccines received one month prior to any dose of Moderna was unknown.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and was administered on 09FEB2022; Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and was administered on 09FEB2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and was administered on 09FEB2022) and PRODUCT STORAGE ERROR (Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and was administered on 09FEB2022) in a 45-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Feb-2022 at 7:46 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 09-Feb-2022 at 7:46 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and was administered on 09FEB2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and was administered on 09FEB2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and was administered on 09FEB2022) and PRODUCT STORAGE ERROR (Vaccine went into 2 to 8 degree Celsius thaw state on or about 20DEC2021 and was administered on 09FEB2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. 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
- MA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product storage error
Symptomtext
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; This spontaneous case was reported by an emergency medical technician and describes the occurrence of POOR QUALITY PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 79-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Apr-2022 at 10:54 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On an unknown date, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, POOR QUALITY PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Patient received the second booster dose. Vaccines went into 2-8 degree Celsius thaw state on or about 24 Dec 2021. No treatment medications were reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 19.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- 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 an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 19-Mar-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 19-Mar-2022) in a 27-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. It was reported Acute illness at the time of vaccination and up to one month before and Chronic or long-standing health conditions were none. Prescriptions, over the counter medications, dietary supplements or herbal remedies being taken at time of vaccination and/or at the time of adverse event were none. Other vaccine given on the same day as that of Moderna vaccine was unknown. Other vaccines received within one month prior to any dose of Moderna COVID-19 vaccine was unknown. On 19-Mar-2022 at 11:37 AM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milligram. On 19-Mar-2022 at 11:37 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 19-Mar-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 19-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 19-Mar-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 19-Mar-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information provided. A patient was administered vaccine past its 30 days expiry date vaccine went into 2 to 8 Celsius thaw state on or about to 24-Dec-2021, this vaccine administered was until its manufacturing (Mfg.) expiration date of 04-Apr-2022. No treatment medication information provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was reported Acute illness at the time of vaccination and up to one month before and Chronic or long-standing health conditions were none. Prescriptions, over the counter medications, dietary supplements or herbal remedies being taken at time of vaccination and/or at the time of adverse event were none. Other vaccine given on the same day as that of Moderna vaccine was unknown. Other vaccines received within one month prior to any dose of Moderna COVID-19 vaccine was unknown.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 26.03.2022
- Beginn
- 26.03.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 36-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 26-Mar-2022 at 1:33 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 26-Mar-2022 at 1:33 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) and EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. No treatment medication information was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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 went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 28 Jan 2022; Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 28 Jan 2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 28 Jan 2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 28 Jan 2022) in a 46-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2022 at 2:29 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Jan-2022 at 2:29 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 28 Jan 2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 28 Jan 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 28 Jan 2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 28 Jan 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was unknown if the patient received any prescriptions, over the counter medications, dietary supplements or herbal remedies at the time of vaccination. It was unknown if the patient received other vaccines given on the same day and it was also unknown if the patient received other vaccines within one month prior to Moderna vaccine. The patient received booster dose and vaccination time reported as at 14.29.38. It was reported that, the vaccines went in to 2-8 Celsius thaw state on or about 24 Dec 2021.This vaccine was administered up until its manufacturing expiry date of 04 Apr 2022. It was unknown if the patient experienced any adverse events or not. No treatment medications were reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 06.02.2022
- Beginn
- 06.02.2022
- 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 went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 06 Feb 2022; Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 06 Feb 2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 06 Feb 2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 06 Feb 2022) in a 39-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Feb-2022 at 1:09 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Feb-2022 at 1:09 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 06 Feb 2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 06 Feb 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 06 Feb 2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24 Dec 2021 and administered on 06 Feb 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient ethnicity reported. Concomitant medication of the patient was not reported. Vaccine administration time was given as 06 Feb 2022 at 13.09.22. The patient received booster dose. Vaccine received past its 30 days expiry date.Vaccine went into 2 to 8 Celsius thaw state on or about 24 Dec 2021. This vaccine was administered up until its manufacturing expiry date of 04 Apr 2022. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 05.03.2022
- Beginn
- 01.12.2021
- 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
Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on vaccine administration date.; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on vaccine administration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on vaccine administration date.) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on vaccine administration date.) in a 46-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Mar-2022 at 1:56 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. In December 2021, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on vaccine administration date.). On 05-Mar-2022 at 1:56 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on vaccine administration date.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on vaccine administration date.) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on vaccine administration date.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. Patient received booster dose. This vaccine was administered up until its manufacturer expiry date of 04-Apr-2022. 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
- MA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Vaccine received post its 30 days Expiry date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 77-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Feb-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 05-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine administration time was given as 05-Feb-2022 at 13:13:51. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022.; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022.; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022.) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022.) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Mar-2022 at 1:11 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 11-Mar-2022 at 1:11 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022.) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine administration time was given as 11-MAR-2022 at 13:11:07 No treatment information was provided by the reporter. This case was linked to MOD-2022-542869.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022. This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.) in a 52-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2022 at 6:59 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Jan-2022 at 6:59 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 28-JAN-2022.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient ethnicity was reported. No concomitant medication information provided. It was reported that, vaccine was administered on 28-Jan-2022 at 18:59:19 It was reported that, vaccine went into 2 to 8 ?C thaw state on or about to 24-Dec-2021, this vaccine administered until its Mfg date of 04-Apr-2022 No treatment information provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- 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
This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Feb-2022 at 10:00 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 15-Feb-2022 at 10:00 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that, vaccine was administered on 15-Feb-2022 at 10:00:10. Dose number reported was booster. No treatment details were reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- 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
patient received vaccine past its 30 days expiry date/ vaccine went in to 2-8C thaw state; patient received vaccine past its 30 days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (patient received vaccine past its 30 days expiry date/ vaccine went in to 2-8C thaw state) in a 31-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Feb-2022 at 3:28 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 03-Feb-2022 at 3:28 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (patient received vaccine past its 30 days expiry date/ vaccine went in to 2-8C thaw state). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (patient received vaccine past its 30 days expiry date/ vaccine went in to 2-8C thaw state) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The patient's ethnicity was reported as private of any race. It was reported that, the vaccines went in to 2-8 C thaw state on or about 24-Dec-2021. No treatment medications were reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 11-Mar-2022; Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 11-Mar-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 11-Mar-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 11-Mar-2022) in a 41-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Mar-2022 at 1:03 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 11-Mar-2022 at 1:03 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 11-Mar-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 11-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 11-Mar-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 11-Mar-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021, this vaccine was administered up until its manufacturing expiry date of 4 April 2022. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 'vaccine administration date'; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 'vaccine administration date'; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 'vaccine administration date') and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 'vaccine administration date') in a 33-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066h21a) for COVID-19 vaccination. No Medical History information was reported. On 25-Mar-2022 at 3:46 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 25-Mar-2022 at 3:46 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 'vaccine administration date'). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 'vaccine administration date'). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 'vaccine administration date') and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 'vaccine administration date') outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. The patient received vaccine past its 30 day expiry date on 25-Mar-2022 at 15:46:56 , booster dose. Vaccine went into 2 to 8 degree Celsius thaw state on about 24-Dec-2021. The vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- 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 an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Feb-2022 at 11:01 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 05-Feb-2022 at 11:01 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Ethnicity was reported as white. Vaccine went into 2-8 ?C thaw state on or about 24-Dec-2021, this vaccine was administered up until its manufacturing expiry date of 4 April 2022. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- 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
Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021; Patient received vaccine past its 30 days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) in an 81-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Apr-2022 at 10:46 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Apr-2022 at 10:46 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine administration time was given as 02-Apr-2022 at 10:46:21 No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Covid-19 vaccine that were given beyond the 30 day use by date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 29-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2022 at 4:57 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Jan-2022 at 4:57 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information provided. Patient's Census Ethnicity was reported. Patient received booster dose of Moderna. It was reported that, vaccine was administered on 28-Jan-2022 at 16:57:41. Its 30 days expiry date vaccine went into 2 to 8 degree Celsius thaw state on or about to 20-Dec-2021, this vaccine administered until its Mfg date of 04-Apr-2022. No treatment information provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- 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
Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021; vaccine administered past its 30-days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) in a 61-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Mar-2022 at 12:57 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Mar-2022 at 12:57 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that, vaccine was administered on 02-Apr-2022 at 12:57:27. Vaccine dose reported was booster. 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
- MA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Vaccine received post its 30 days Expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Apr-2022 at 11:59 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Apr-2022 at 11:59 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Patient's ethnicity was reported. Vaccine administration time was given as 02-Apr-2022 at 11:59:54 No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Vaccine received post its 30 days Expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in an 81-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Apr-2022 at 9:57 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Apr-2022 at 9:57 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine administration time was given as 02-Apr-2022 at 09:57:19. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 19.02.2022
- Beginn
- 19.02.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Vaccine received post its 30 days Expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 38-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Feb-2022 at 4:34 PM, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 19-Feb-2022 at 4:34 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine administration time was given as 19 Feb 2022 at 16:34:31. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021; Patient received vaccine past its 30 days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) in a 56-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 26-Feb-2022 at 11:23 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 26-Feb-2022 at 11:23 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Vaccine administration time 11:23:12. The patient was administered booster dose that went into 2-8c thaw state on or above 24-Dec -2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. It was unknown if the patient had acute illness at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long lasting health conditions. No treatment medications were reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- 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
This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp. date. Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 36-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Mar-2022 at 11:52 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 11-Mar-2022 at 11:52 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp. date. Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp. date. Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information provided. The patient had received the vaccine dose number as booster with 0.5 ml. It was reported that, vaccine was administered on 11 Mar -2022 at 11:52:29. Its 30 days expiry date vaccine went into 2 to 8 ?C thaw state on or about to 20-Dec-2021, this vaccine administered until its Mfg. date of 04 Apr 2022. No treatment information provided. The Us Census Ethnicity reported as White. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- 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
Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021; vaccine administered past its 30-days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Apr-2022 at 10:58 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Apr-2022 at 10:58 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Vaccine administration time 10:58:21. The patient was administered booster dose that went into 2-8c thaw state on or above 24-Dec-2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. It was unknown if the patient had acute illness at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long lasting health conditions. 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
- MA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 18-Feb-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 18-Feb-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 18-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 18-Feb-2022) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Feb-2022 at 1:20 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 18-Feb-2022 at 1:20 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 18-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 18-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 18-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 18-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Census Ethnicity of the patient was reported. Concomitant medication of the patient was not reported. Vaccine administration time was given as 13:20:05. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- 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
This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 30-MAR-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 30-MAR-2022) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 30-Mar-2022 at 3:06 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 30-Mar-2022 at 3:06 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 30-MAR-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 30-MAR-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 30-MAR-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 30-MAR-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. On 30-Mar-2022 at 15:06:50, Patient administered booster dose. It was reported that patient received lot its 30 day expiry date. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Vaccine received post its 30 days Expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 37-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 31-Mar-2022 at 9:03 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 31-Mar-2022 at 9:03 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine administration time was given as 31-Mar-2022 09:03:13. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022) in an 84-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Apr-2022 at 10:47 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Apr-2022 at 10:47 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 02-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Census Ethnicity of the patient was reported. Concomitant medication of the patient was not reported. The patient received second booster dose and vaccine administration time was given as 10:47:30. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 04-MAR-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 04-MAR-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 04-MAR-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 04-MAR-2022) in a 19-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Mar-2022 at 12:36 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-Mar-2022 at 12:36 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 04-MAR-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 04-MAR-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 04-MAR-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 04-MAR-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. On 04-Mar-2022 at 12:36:33, Patient administered booster dose. It was reported that patient received lot its 30 day expiry date. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Covid-19 vaccine that were given beyond the 30 day use by date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 55-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Mar-2022 at 12:08 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 29-Mar-2022 at 12:08 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information provided. It was reported that, vaccine was administered on 29-Mar-2022 at 12:08:55 Its 30 days expiry date vaccine went into 2 to 8 ?C thaw state on or about to 20-Dec-2021, this vaccine administered until its Mfg date of 04-Apr-2022 No treatment information provided. This case was linked to MOD-2022-542869.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccines went into 2-8 C thaw state on or about 20-Dec-2021; Received vaccine past its 30-days Exp date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 20-Dec-2021) in a 35-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2022 at 4:56 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 28-Jan-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 20-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received vaccine past its 30-days Exp date) and PRODUCT STORAGE ERROR (Vaccines went into 2-8 C thaw state on or about 20-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; patient received vaccine past its 30 days expiry date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Feb-2022 at 4:12 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 14-Feb-2022 at 4:12 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported by reporter. No treatment medication was reported by reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022; Patient received vaccine past its 30 day expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 day expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022) in a 39-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. It was reported Acute illness at the time of vaccination and up to one month before and Chronic or long-standing health conditions were unknown. On 31-Jan-2022 at 1:32 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 31-Jan-2022 at 1:32 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 day expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 day expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 31-Jan-2022) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Prescriptions, over the counter medications, dietary supplements or herbal remedies being taken at time of vaccination and/or at the time of adverse event were unknown. Other vaccine given on the same day as that of Moderna vaccine was unknown. Other vaccines received within one month prior to any dose of Moderna COVID-19 vaccine was unknown. A patient was administered vaccine past its 30 days expiry date vaccine went into 2 to 8 Celsius thaw state on or about to 24-Dec-2021, this vaccine administered was until its manufacturing (Mfg) expiration date of 04-Apr-2022. Patient received the booster dose of vaccine on 31-Jan-2022, with manufacturer expiry date 04-Apr-2022. No treatment medication information provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was reported Acute illness at the time of vaccination and up to one month before and Chronic or long-standing health conditions were unknown.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- 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
Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021; vaccine administered past its 30-days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) in a 57-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Apr-2022 at 11:47 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Apr-2022 at 11:47 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that, vaccine was administered on 02-Apr-2022 at 11:47:25. 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
- MA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 12:11:27; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 12:11:27; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 12:11:27) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 12:11:27 ) in a 29-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Mar-2022 at 12:11 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 11-Mar-2022 at 12:11 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 12:11:27). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 12:11:27 ). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 12:11:27) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-MAR-2022 12:11:27 ) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient's ethnicity was reported . It was unknown if the patient had acute illness at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long lasting health conditions. Concomitant product use was not provided by the reporter. It was unknown if the patient received any prescriptions, over the counter medications, dietary supplements or herbal remedies at the time of vaccination. It was unknown if the patient received other vaccines given on the same day and it was also unknown if the patient received other vaccines within one month prior to any dose of Moderna vaccine. It was unknown if the patient experienced any adverse events or not. The patient received Moderna vaccine past its 30 day of expiry date. Vaccine was administered on 11-Mar-2022 at 12:11:27. It went into 2-to-8-degree Celsius thaw state on or about 24-Dec-2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. No treatment information was provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Vaccine received post its 30 days Expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2022 at 12:13 PM, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 28-Jan-2022 at 12:13 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient ethnicity was reported. Concomitant medication of the patient was not reported. Vaccine administration time was given as 28-Jan-2022 at 12:13:58 No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 12.02.2022
- Beginn
- 12.02.2022
- 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
Vaccine went into 2-8 Celsius thawstate on or about 24-Dec-2021 and administered on 12-FEB-2022 at 12:12:58; Vaccine went into 2-8 Celsius thawstate on or about 24-Dec-2021 and administered on 12-FEB-2022 at 12:12:58; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thawstate on or about 24-Dec-2021 and administered on 12-FEB-2022 at 12:12:58) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thawstate on or about 24-Dec-2021 and administered on 12-FEB-2022 at 12:12:58) in a 35-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Feb-2022 at 12:12 PM, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 12-Feb-2022 at 12:12 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thawstate on or about 24-Dec-2021 and administered on 12-FEB-2022 at 12:12:58). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thawstate on or about 24-Dec-2021 and administered on 12-FEB-2022 at 12:12:58). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thawstate on or about 24-Dec-2021 and administered on 12-FEB-2022 at 12:12:58) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thawstate on or about 24-Dec-2021 and administered on 12-FEB-2022 at 12:12:58) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. The patient received Moderna vaccine past its 30 day of expiry date. Vaccine was administered on 12-Feb-2022 at 12:12:58. It went into 2-to-8-degree Celsius thaw state on or about 24-Dec-2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. No treatment information was provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Vaccine received post its 30 days Expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 25-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Feb-2022 at 3:05 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 03-Feb-2022 at 3:05 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine administration time was given as 03-Feb-2022 at 15:05:02. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 12.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021; Patient received vaccine past its 30 days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) in a 43-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Feb-2022 at 2:53 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 12-Feb-2022 at 2:53 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient ethnicity was reported. Concomitant medication of the patient was not reported. Vaccine administration time was given as 12-Feb-2022 at 14:53:45 No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Covid-19 vaccine that were given beyond the 30 day use by date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Apr-2022 at 2:59 PM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-Apr-2022 at 2:59 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Covid-19 vaccine that were given beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. of the patient was reported . No concomitant medication information was provided. It was reported that, vaccine was administered on 04-Apr-2022 at 14:59:04 Its 30 days expiry date vaccine went into 2 to 8 ?C thaw state on or about to 20-Dec-2021, this vaccine administered until its Mfg date of 04-Apr-2022 No treatment information was provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021; vaccine administered past its 30-days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) in a 37-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Feb-2022 at 5:59 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 11-Feb-2022 at 5:59 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine administered past its 30-days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. It was reported that, booster dose of vaccine was administered on 11-Feb-2022 at 17:59:31. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- 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
patient received vaccine past its 30 days expiry date/ vaccine went in to 2-8C thaw state; patient received vaccine past its 30 days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (patient received vaccine past its 30 days expiry date/ vaccine went in to 2-8C thaw state) in a 69-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. It was unknown if the patient had acute illness at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long lasting health conditions. On 02-Apr-2022 at 10:55 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Apr-2022 at 10:55 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (patient received vaccine past its 30 days expiry date/ vaccine went in to 2-8C thaw state). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (patient received vaccine past its 30 days expiry date/ vaccine went in to 2-8C thaw state) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. ethnicity of the patinet was reported. It was unknown if the patient received any prescriptions, over the counter medications, dietary supplements or herbal remedies at the time of vaccination. It was unknown if the patient received other vaccines given on the same day and it was also unknown if the patient received other vaccines within one month prior to Moderna vaccine. It was reported that, the vaccines went in to 2-8 C thaw state on or about 24-Dec-2021. It was unknown if the patient experienced any adverse events or not. No treatment medications were reported. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if the patient had acute illness at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long lasting health conditions.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Vaccine received past its 30 days Expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine received past its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Feb-2022 at 2:20 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 11-Feb-2022 at 2:20 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine received past its 30 days Expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine received past its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient census ethnicity reported. Concomitant medication of the patient was not reported. On 11-Feb-2022 patient received Moderna booster dose. Vaccine administration time was given as 11-Feb-2022 at 14:20:53. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 04-APR-2022; Vaccine received post its 30 days Expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 04-APR-2022) in a 70-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Apr-2022 at 5:29 PM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-Apr-2022 at 5:29 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 04-APR-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 04-APR-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine administration time was given as 04-Apr-2022 17:29:33. Patient was administered a second booster dose. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021; Vaccine received post its 30 days Expiry date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) in a 36-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Feb-2022 at 3:45 PM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 01-Feb-2022 at 3:45 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine received post its 30 days Expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days Exp date Vaccines went into 2-8 C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine administration time was given as 01-Feb-2022 at 15:45:11. No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021; Patient received vaccine past its 30 days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) in a 31-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Mar-2022 at 11:50 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 29-Mar-2022 at 11:50 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (Received vaccine past its 30-days expiry date vaccines went into 2-8 degree C thaw state on or about 24-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Vaccine administration time was given as 29-Mar-2022 at 11:50:23 No treatment information was provided by the reporter. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- 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
Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022) in a 23-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Feb-2022 at 2:13 PM, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 05-Feb-2022 at 2:13 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 05-Feb-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. Treatment medications were not reported. Patient received vaccine past its 30 day expiry date. Vaccine went into 2 to 8 degree Celsius thaw state on or about 24-Dec-2021. This vaccine was administered up until its manufacturing expiry date of 04-Apr-2022. Reporter no longer possess this lot number. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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 went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022; Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022) in a 29-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Feb-2022 at 5:56 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 11-Feb-2022 at 5:56 PM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022) and PRODUCT STORAGE ERROR (Vaccine went into 2-8 Celsius thaw state on or about 24-Dec-2021 and administered on 11-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that, vaccine was administered on 11-Feb-2022 at 17:56:27. 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
- MA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- 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
patient received vaccine past its 30 days expiry date/ vaccine went in to 2-8C thaw state; patient received vaccine past its 30 days expiry date; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (patient received vaccine past its 30 days expiry date/ vaccine went in to 2-8C thaw state) in a 23-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066H21A) for COVID-19 vaccination. It was unknown if the patient had acute illness at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long lasting health conditions. On 02-Apr-2022 at 11:03 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Apr-2022 at 11:03 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received vaccine past its 30 days expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (patient received vaccine past its 30 days expiry date/ vaccine went in to 2-8C thaw state). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received vaccine past its 30 days expiry date) and PRODUCT STORAGE ERROR (patient received vaccine past its 30 days expiry date/ vaccine went in to 2-8C thaw state) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient's Us Census ethnicity was reported as Black or African American. It was unknown if the patient received any prescriptions, over the counter medications, dietary supplements or herbal remedies at the time of vaccination. It was unknown if the patient received other vaccines given on the same day and it was also unknown if the patient received other vaccines within one month prior to Moderna vaccine. It was reported that, the vaccines went in to 2-8 C thaw state on or about 24-Dec-2021. It was unknown if the patient experienced any adverse events or not. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if the patient had acute illness at the time of vaccination and up to one month before. It was unknown if the patient had chronic or long lasting health conditions.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -