- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 06.10.2023
- Impfdatum
- 10.03.2022
- Beginn
- 11.09.2023
- Tage bis Beginn
- 550,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Chest X-ray normal
Chest pain
Chills
Cough
Dyspnoea
Obesity
Prone position
Pyrexia
SARS-CoV-2 test positive
Upper respiratory tract congestion
Symptomtext
Patient is a 70 y.o. male patient of, MD with history of remote stroke with residual left-sided deficits, hypertension, and hyperlipidemia, now presented to Hospital with acute hypoxemic restaurant failure secondary to COVID-19. Acute hypoxemic respiratory failure secondary to COVID-19 pneumonia Place patient on supplemental oxygen in ED Date of onset of symptoms: 9/11/2023. Symptoms present on admission: Chest pain, shortness of breath, fevers, chills, dry cough, upper respiratory congestion. Date of covid positive test: 9/11/2023. Vaccination status: vaccinated Chest x-ray clear Temperature peaked at 103.1-resolved. Tylenol as needed. Patient weaned from 2L NC 9/13. Now on room air. Received remdesivir while inpatient Encourage IS, mucinex, decadron, and albuterol inhaler. Prone positioning as tolerated. History of remote stroke Hypertension Hyperlipidemia SBP 130-170's, home meds resumed PT/OT Obesity Outpatient diet and exercise regimen. Evaluation for OSA and/or continuation of home CPAP. BMI: 35.91.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 19.06.2023
- Impfdatum
- 04.02.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 279,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cerebrovascular accident
Symptomtext
ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 13.06.2023
- Impfdatum
- 04.03.2022
- Beginn
- 23.12.2022
- Tage bis Beginn
- 294,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cerebrovascular accident
Obstructive sleep apnoea syndrome
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE OBSTRUCTIVE SLEEP APNEA ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 04.04.2022
- Beginn
- 23.04.2022
- Tage bis Beginn
- 19,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Atrial fibrillation
Urinary tract infection
Symptomtext
ACUTE RESPIRATORY FAILURE 5/30/2022 ATRIAL FIBRILLATION, PAROXYSMAL ACUTE RESPIRATORY FAILURE 5/30/2022 UTI (URINARY TRACT INFECTION)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 21.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Angiogram cerebral normal
Basal ganglia haemorrhage
Cerebral haemorrhage
Computerised tomogram head abnormal
Hemiplegia
Imaging procedure
Symptomtext
Patient presented to ED on 2/26/22 with right hemiplegia, CT head found a left basal ganglia hemorrhage. Follow-up imaging studies and a recent cerebral angio performed on 9/22/22, failed to reveal evidence of any aneurysm, early venous drainage, nidus, dissection, vasculitis, vasospasm or tumor blush was identified which would explain her spontaneous ICH.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebral haemorrhage
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- covid infection 1 month prior to AE
- Vorgeschichte
- depression
- Andere Medikamente
- zoloft 100mg daily, adderall prn
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 15.04.2021
- Beginn
- 12.09.2022
- Tage bis Beginn
- 515,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Chest pain
Cough
Symptomtext
Patient admitted to hospital 9/12/22 with c/o chest pain with non-STEMI and cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- History of CVA, Hypothyroidism, Hypertension, Type 2 Diabetes
- Andere Medikamente
- Felodipine ER 10mg po daily Indapamide 2.5mg po daily Potassium Chloride ER 20 MEQ po daily Metformin ER 1000mg po BID Atorvastatin 80mg po daily Magnesium 400mg po daily Aspirin 81mg po daily Pantoprazole 40mg po daily PreserVision 1 capsu
- Allergien
- Codeine, Penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 93,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anticoagulant therapy
COVID-19
Computerised tomogram thorax abnormal
Dyspnoea
Hypoxia
Pulmonary embolism
SARS-CoV-2 test positive
Symptomtext
Provider summary "the patient presented with dyspnea found to be COVID positive and have multifocal pulmonary embolism without right heart strain. Required oxygen, weaned during stay to room air without issue. Treated with lovenox while hospitalized -- > eliquis on discharge. Provoked so needs 3-6 months therapy, with consideration for life long given his having cancer. Stay complicated by AMS due to decadron, which was stopped and not provided for covid hypoxia. CT actually showed minimal parenchymal injury to lungs so hypoxia really just was from pulmonary embolism"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 5,0
- Labordaten
- Positive COVID PCR 6/17/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Prostate cancer (HCC) (Chronic) 1/4/2012 Normocytic normochromic anemia 9/24/2014 Pneumonia due to infectious organism 5/5/2017 Long term current use of immunosuppressive drug (Chronic) 12/6/2018 Essential hypertension 12/6/2018 Hypoxia 11/14/2019 Elevated troponin 9/10/2020 Stenosis of right vertebral artery (Chronic) 9/10/2020 Impaired hearing (Chronic) 9/10/2020 Acute respiratory failure with hypoxia 1/9/2021 Generalized weakness 1/9/2021
- Andere Medikamente
- abiraterone acetate 250 mg TAKE 4 TABLETS BY MOUTH ONCE DAILY AS DIRECTED. TAKE 1 HOUR BEFORE OR 2 HOURS AFTER A MEAL amlodipine besylate 5 mg Oral Daily apixaban 5 mg Take 10mg twice a day for 7 days then take 5mg twice a day thereafter
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 02.03.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 235,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Acute respiratory failure
Atrial fibrillation
COVID-19 pneumonia
Chronic obstructive pulmonary disease
Computerised tomogram
Gastrointestinal haemorrhage
Laboratory test
Obesity
Pulmonary mass
Type 2 diabetes mellitus
Symptomtext
Moderna COVID vaccines received on 02/02/2021 and 03/02/2021 Hospitalized at Hospital on 10/23/2021 Diagnosis of Acute Respiratory Failure, Acute GI bleed, COPD, Atrial Fibrillation with rapid ventricular response, COVID 19 pneumonia, DM II in Obesity, Pulmonary nodule Treatment included: Supplemental Oxygen, CT scan, Labs, Decadron, ceftriaxone, azithromycin, hospitalization Moderna Booster received on 12/7/2021 after the adverse event of 10/23/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 21.05.2021
- Beginn
- 04.08.2021
- Tage bis Beginn
- 75,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Acute myocardial infarction
Asthenia
Cardiac failure congestive
Inappropriate schedule of product administration
Symptomtext
Moderna vaccine received on 5/21/2021 before adverse event then received Moderna vaccines on 8/27/2021 and 2/16/2022 after the event Hospitalized with Non-STEMI and congestive heart failure at Hospital in July 2021 Hospitalized with weakness on 8/4/2021 at Hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 11.02.2021
- Beginn
- 11.02.2022
- Tage bis Beginn
- 365,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Cerebrovascular accident
Dysgraphia
Facial paralysis
Feeling abnormal
Gait disturbance
Hyperhidrosis
Hypertension
Hypoaesthesia
Impaired driving ability
Impaired work ability
Motor dysfunction
Nausea
Speech disorder
Symptomtext
10 minutes after receiving the moderna shot, patient states she felt funny (unsteady in her walking). She went into the produce department and started to sweat. She walked outside to her car and felt sick to her stomach. She got into her car, backed out of the parking space. But then she only drove a few minutes and parked the car again because she couldn't feel the brakes of her car with her feet. She also felt numbness in her hands. Her friend came, and told her that her mouth looked twisted. The paramedics were called. They did some tests and told her they were transporting her to the hospital as a stroke victim. The outcome is that her doctor told her she had a stroke, and that the doctor informed her they didnt know if the stroke was a result of the vaccine. After one week she regained feeling in her fingers, and she has been attending speech therapy since February 2022. She was cleared to drive February 28 and will be heading back to work shortly. She still has to do some occupational therapy to do because she can't write yet. Her neurologist said she was mostly affected in the motor part of her brain. She states she has high blood pressure but that it is controlled.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- Patient had surgery on her foot
- Vorgeschichte
- None
- Andere Medikamente
- Patient reports not taking any other medicines at the time
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 12.10.2023
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Paralysis
Symptomtext
Temporary paralysis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi vitamin, vitamin d, calcium, bioflex, vitamin e, vitamin c, fish oil
- Allergien
- Sensitivity to latex, aspirins, caffeine and other unknown medications, sausage, milk
- Vorherige Impfungen
- 2nd dose shingles, milder paralysis, shingix,60-61
- Staat
- AR
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 02.02.2023
- Impfdatum
- 13.05.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 160,0
- Dosis
- UNK
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Cerebral haematoma
Haemorrhagic stroke
Laboratory test
Symptomtext
I had a hemorrhagic stroke beginning on 10/20/2022. I also had a hematoma in my brain that was discovered early 2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Haemorrhagic stroke
- Hospital-Tage
- 56,0
- Labordaten
- I had hundreds of tests and labs done starting 10/20/2022 at the Hospital until I left in mid January, 2023. I was admitted into the hospital 3 times between 10/20/2022 and med Jan. 2023.
- Aktuelle Erkrankungen
- Raynaud?s Disease Hypothyroidism Overactive Bladder Sleep Apnea Depression Anxiety
- Vorgeschichte
- Raynaud?s Disease Hypothyroidism Overactive Bladder Sleep Apnea Depression Anxiety
- Andere Medikamente
- Trintellix Buspirone Levothyroxine Linzess Simvastatin L-5-MTHF (folate) Magnesium Vitamin D Multivitamin VESIcare
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 27.09.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alopecia
Angiogram
Anxiety
Balance disorder
Chest X-ray
Blood glucose normal
Blood pressure increased
Dizziness
Flushing
Hypopnoea
Chest pain
Echocardiogram
Feeling abnormal
Hypertension
Impaired work ability
Laboratory test
Magnetic resonance imaging head
Magnetic resonance imaging spinal
Symptomtext
Thirty minutes after receiving the booster I had an abrupt full body flushing with presyncope, accelerated hypertension (BP 175/110), tachycardia ) HR 110. My blood pressure and heart rate has never returned to normal. I now have POTS and hypertension and am barely responding to beta blockers and calcium channel blockers. I have had persistent chest pain, out of the blue anxiety, hair loss, brain fog, right ear tinnitus, and imbalance and dizziness ever since receiving the booster. I didn't have any of these issue before receiving the vaccine. I had three months of limb weakness and difficulty using my fingers for about 2 months, which has since improved. I am currently now out of work after working in the health care setting for 27 years, I am about to lose my health insurance if I can't go back to work. I had none of the symptoms until receiving the moderna booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- 4,0
- Labordaten
- 3 ER visits, 1 unrgent care visit, 2 hospitalizations, 3 ENT visits, cardiology, neurology and physical therapy visits. Brain MRI, Cervical MRI, CTA head and neck, CXR, labs, ECHO cardiogram, vestibular therapy, ophthalmology neurology. Many prescriptions to help control symptoms.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Unspecified connective tissue disease
- Andere Medikamente
- Vitamin D 3, omega 3 fatty acid, Elavil, plaquenil
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 26.08.2022
- Impfdatum
- 19.02.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 181,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anticoagulant therapy
Antiplatelet therapy
COVID-19
Catheterisation cardiac abnormal
Cerebral venous sinus thrombosis
Coronary arterial stent insertion
Echocardiogram abnormal
Electroencephalogram normal
Infarction
Magnetic resonance imaging normal
SARS-CoV-2 test positive
Seizure
Symptomtext
PRESENTING PROBLEM: Stroke-like symptoms [R29.90] Stroke determined by clinical assessment (HCC) [I63.9] COVID-19 [U07.1] HOSPITAL COURSE: Recrudescence of Prior Left MCA Infarct in Light of + COVID-19 48 y.o. female w/PMH of HLD, Obesity (BMI 44.29), T2DM, Esophageal spasm, Constipation, and COVID-19 (+) 06-2022 (is Vaccinated w/Medorna w/booster), who was hospitalized in 06-2022 w/Chronic Non-Occlusive dural sinus thrombosis (MRV) w/late subacute venous infarcts Echo had showed Left Apical Thrombus s/p Eliquis 5 mg BID, pt also had undergone heart cath w/Stent placement s/p Plavix, during that hospitalization pt also had one reported witnessed seizure at home but negative EEG thus, started on Vimpat 100 mg BID, pt follows cardiology. This pt presented again on 8/19/2022 w/20 Hour R. U/L Ex and R. Face paresthesia which then resolved. Advanced imaging including MRI were negative for any acute new findings. Pt was (+) again for COVID-19 but without symptoms, is in room air and denies SOB, chest pain. Pt states she is back to her baseline and would like to go home. Pt's home pantoprazole was discontinued due to pt being on Plavix. Famotidine was ordered instead.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebral venous sinus thrombosis
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Recrudescence of Prior Left MCA Infarct in Light of + COVID-19 Type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin (HCC) Morbid obesity with BMI of 45.0-49.9, adult (HCC) Hyperlipidemia associated with type 2 diabetes mellitus (HCC) Hypertension associated with diabetes (HCC) Recurrent genital HSV (herpes simplex virus) infection Anxiety Dysmenorrhea Other chest pain Adenomatous colon polyp COVID-19 Seizure (HCC) Left ventricular apical thrombus LV (left ventricular) mural thrombus Coronary artery disease involving native coronary artery of native heart without angina pectoris Leg edema Moderate episode of recurrent major depressive disorder (HCC)
- Andere Medikamente
- acyclovir (ZOVIRAX) 200 MG capsule apixaban (ELIQUIS) 5 MG tablet atorvastatin (LIPITOR) 80 MG tablet clopidogrel (PLAVIX) 75 MG tablet famotidine (PEPCID) 20 MG tablet guaifenesin (HUMIBID E) 400 MG TABS hydroCHLOROthiazide (HYDRODIURIL) 2
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 09.04.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 42,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Chest X-ray
Computerised tomogram thorax abnormal
Cough
Dyspnoea
Echocardiogram
Influenza virus test negative
Intensive care
Pneumonia
Pulmonary thrombosis
SARS-CoV-2 test negative
Symptomtext
5/21/2022 I began with a slight cough that progressed throughout the day. on 5-22-2022 I woke with Shortness of breath. It got progressive worse Went to ER and was diagnosed with multi blood clots in both lungs and pneumonia in my left lung. Was admitted to ICU for 1 day and released from the hospital after 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 3,0
- Labordaten
- Multiple blood tests, chest xray, echocardiogram, CT of lungs. Tested for flu and covid. Both were negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetic High blood pressure
- Andere Medikamente
- multivitamin vitamin D vitaminB1 Vitmin B complex Vitamin C Biotin Glimpiride Simvastin Losartan Sertraline
- Allergien
- Penicillin Lisinopril
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 03.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Syncope
Symptomtext
Pt experienced a fainting episode in the early morning of 4/3/22. She then checked her blood pressure and saw that it was 90/60. She has been feeling faint since but not bad enough to seek medical care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Atrial tachycardia, long-COVID symptoms (March 2020 illness)
- Andere Medikamente
- D-Ribose, multivitamin, black cohosh, diltiazem 15 mg TID
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 26.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Seizure
Symptomtext
The patient had a seizure about 12 hours after receiving the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- Not known.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
Electric shock sensation
Mobility decreased
Neck pain
Symptomtext
Starting the evening patient received vaccine, he experienced some shoulder pain and felt like electrical charges were going across back of neck from shoulder to shoulder. He woke up the next morning and didn't have full range of motion in neck, hard to move side to side. He went to chiropractor next day and got an adjustment and manipulations and feel much better. His chiropractor was the one to suggest patient report this to vaers. Patient said pain dimished alot once the chiropractor adjusted him. He had minimal pain/soreness in his neck lasting about 2-3 days after vaccination was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- steroid shots every month for knees
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 02.03.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Head injury
Loss of consciousness
Malaise
Symptomtext
After receiving vaccine pt sat down in a chair and about 2-3 minutes later pt yelled "I don't feel good." I ran over to pt as she slowly lost consciousness and fell off of chair onto the floor face down. I sat on the floor with pt and monitored her breathing, she never stopped breathing and woke up after about 1 minute. Someone had already called 911 and they were on their way. When she woke up she sat upright on the floor. She was alert and speaking normally, we gave her Gatorade, water, and crackers. She stated she only had eaten a banana all day and she has a history of fainting when donating blood. I asked her if her head hurt because I was not sure how hard she hit her head, she stated it did not hurt. Two police officers arrived and we explained the story, then a medic arrived and we explained the story to him. I told him that she did fall and was face down and hit her head but I wasn't sure how hard she hit her head. He said he would check the pt out, he took vitals and told her that her blood pressure was still a little low and offered to take her to the hospital if she wanted. She stated that she felt ok and declined a trip to the hospital. Her son arrived at the store to drive her home so she wouldn't be driving herself. Her and her son remained in the store for a few more minutes and she said she felt ready to stand up. Her and her son walked out of the store together.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown.
- Vorgeschichte
- pt stated they have no chronic conditions.
- Andere Medikamente
- unknown
- Allergien
- pt stated none.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Seizure
Symptomtext
PATIENT PASSED OUT & THEN HAD A SEIZURE TOTAL TIME LASTED LESS THAN 2 MINUTES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ZOLOFT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Dyspnoea
Eye movement disorder
Feeling hot
Head injury
Loss of consciousness
Syncope
Thirst
Wheezing
Symptomtext
Vaccine attendant properly and appropriately administered the Moderna COVID vaccine to patient in her left deltoid. Within 5 minutes of receiving the vaccine, patient became unconscious. She was sitting in a chair next to a table in the clinic atrium (just outside the pharmacy) and suddenly slumped into her chair and hit her head quite loudly on the table, which triggered me to respond. When I approached her, her head was tilted backward, she was wheezing/gasping for air and her eyes were rolling back into her head. EMS was immediately notified and remained on the line with us. While retrieving the epinephrine (not administered) she regained consciousness and immediately began using her phone. (As if she didn't realize anything had happened). She reported feeling thirsty and hot, however was directed not to eat or drink anything until she was seen by EMS. She was escorted to the ambulance by EMT for observation and evaluation. EMT returned her to the building following brief evaluation (5-10 minute) and commented that it was believed to be a syncopal episode. She remained in the same chair in the clinic atrium for an additional 15-20 minutes and was provided with water and a small snack. She called her boyfriend to pick her up. I asked her several times if she was feeling ok and asked her boyfriend to call me if she has any status changes. She reported that she has fainted when having venipuncture, but never with a vaccine. I advised her that going forward, she let future vaccinators know that she may need to be more closely monitored during her observation period. Patient does not have a PCP listed in her chart. Of note, it did not look to be a syncopal episode to me, which is why we called 911.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- NONE KNOWN.
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Dyspnoea
Flushing
Hyperhidrosis
Syncope
Symptomtext
Patient is a pregnant female (17 weeks with twins) came in to get her booster shot for Moderna. After getting the vaccine she started to feel light headed during her 15 minute wait time. Once back seated the patient fainted for 60 seconds. I tried to get patient to respond. Once the patient came back to. She was flush, sweaty and dizziness. BP was 118/82 seated. She was having trouble breathing so she removed her mask. The patient had received both doses of Moderna prior to this with no incident. 911 was called and the patient left with them. She was taken to Medical Center.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- BP: 118/82 seated adult cuff used
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Head injury
Loss of consciousness
Seizure
Symptomtext
Patient loss consciousness and fell onto floor. During fall, patient hit his head on the ground and had a seizure. EMS was called and patient received medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None per patient
- Vorgeschichte
- None per patient
- Andere Medikamente
- None per patient
- Allergien
- KNDA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 08.05.2023
- Impfdatum
- 06.02.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Bone pain
Cardiac discomfort
Cardiac disorder
Cataract
Chest discomfort
Chest pain
Condition aggravated
Diplopia
Dysgeusia
Dyspnoea
Eye disorder
Eyeglasses therapy
Fatigue
Hyperhidrosis
Myalgia
Nipple pain
Pain
Symptomtext
He got his vaccine, he had a sore arm, like somebody hit him with a sledge hammer and a metallic taste that day, he just wanted to sleep. Within a couple of days his vision started getting double and very very bad . His heart just felt like he could not get enough air, had some weird heart palpitations, near the center of his chest. He would get shooting pains in his arms and joints and feeling and tingling like his arms were going to sleep. He would get pains in his joints, especially previous broken bones. He could not sleep flat anymore because he could not get enough oxygen and now has to sleep sitting up in a recliner. This was about 2 1/2 weeks after that shot. He did not have this problem prior and used to sleep on his stomach or back before the vaccine. His eyesight has gone progressively worse, he can see with his glasses and a magnifying glass, but as the day progress his eyes get bugged out, blurred and having double vision. He has gone to the eye doctor and has had glass prescriptions changed 3 times in one year, and was told he had bad cataracts. Unless he takes certain supplements in the morning he ends up defecating about 3 times. If he lays down and gets up real quick there is a significant change in his heart. If he is kneeling and gets up it feels like an elevator in his chest and shortness of breath. Taking his garbage to the curb, 78' wears him out and he sweats profusely from that. He has 0 tolerance with heat when it was in the 70s he tried to take his dog for a walk, and just walking about 8th of a mile would start seating profusely. The heat bothers him really bad now. He did not have this problem before. He formerly ran a bucket utility truck in the sun and it lever bothered him, and now he cannot tolerate the heat at all. He did not have vision issues prior to the vaccine other than needing readers. No family members have a history of cataracts. The eye doctor said she had never seen eye issues that progressed so rapidly. He has had shakes that has developed and his body shakes, which started about a month after the 2nd shot and has gotten worse since the 3rd vaccine. He cannot have a full cup of coffee to drink or it will spill. He gets stabbing pains, 3 fingers in and just drives his heart one 5:00 from nipple area, 3:00 and in between 10-11:00 on his left pec which is larger than his right. He is going to the ER today. After his 2nd vaccine he felt like he had a sledge hammer hit him in the left arm, and wanted to sleep again. He did not feel too good, but after 2-3 days that disappeared.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Eyes,
- Aktuelle Erkrankungen
- Cold at end of January, COVID test negative.
- Vorgeschichte
- A-fib, history of substance abuse.
- Andere Medikamente
- Suboxone, Xanax, Zyrtec, Tylenol/Ibuprofen.
- Allergien
- None.
- Vorherige Impfungen
- metallic taste and sledge hammer feeling and shakes.
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 30.03.2022
- Beginn
- 19.01.2023
- Tage bis Beginn
- 295,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Mobility decreased
Pain
Pyrexia
Symptomtext
I had fever, chills, and ache all over. I was in the bed a couple of days and could get up. My doctor prescribed PAXLOVID and steroids', which we lost our appetite.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Breast cancer 1998; Nerve pain in right leg
- Andere Medikamente
- Hydrochlorothiazide; pantoprazole; rosuvastatin; gabapentin
- Allergien
- None
- Vorherige Impfungen
- Every vaccine I would have ache and chills.
- Staat
- OR
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 27.02.2023
- Impfdatum
- 22.02.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 129,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
Blood test
Electrocardiogram
Electrocardiogram ambulatory
Palpitations
Symptomtext
I had vaccination on 02/22/2022. I started to experience with heart palpitations and atrial fibrillation in 07/2022 and monitored vitals with watch. I contacted my primary doctor who referred me to a cardiologist. I went to the emergency room on 10/17/2022 for atrial fibrillation. I wore a Holter monitor for two weeks and was seen by cardiology 02/7/2023. I have a follow up appointment on March 7th 2023 for possible pacemaker.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- 11/04/2022-11/18/2022 Holter monitor 07/2022 EKG, blood panel, vitals
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 10.11.2022
- Impfdatum
- 27.07.2021
- Beginn
- 13.09.2022
- Tage bis Beginn
- 413,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest pain
SARS-CoV-2 test positive
Symptomtext
08/13/22 presents to ED for "chest pain". PMHx of "cigarette smoking, otherwise no medical problems"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 09/13/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 05.10.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 28,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthma
COVID-19
Condition aggravated
Dyspnoea
Symptomtext
Pt has been short of breath for one week. Pt has chronic asthma and is on 3L home oxygen. Pt admitted for COVID-19 and asthma exacerbation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 10.09.2022
- Impfdatum
- 17.03.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 166,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Adenocarcinoma metastatic
Asthma
Asymptomatic COVID-19
Biopsy
Biopsy bone abnormal
Blood creatinine
Blood culture negative
Chronic kidney disease
Discharge
Dry gangrene
Essential hypertension
Ex-tobacco user
Osteomyelitis
Renal cell carcinoma
SARS-CoV-2 test positive
Sepsis
Thromboangiitis obliterans
Toe amputation
Symptomtext
Physician Discharge Summary Patient ID: Age: 74 y.o. Admit Date: 8/30/2022 1:01 PM Discharge Date: 9/3/2022 Admitting Physician: Discharge Physician: MD Discharge Diagnosis: Principal Problem: Gangrene of both feet Active Problems: Mild intermittent asthma without complication Stage 3b chronic kidney disease Thromboangiitis obliterans (Buerger's disease) Renal cell carcinoma of left kidney Sepsis COVID-19 Essential hypertension Type 2 diabetes mellitus without complication, without long-term current use of insulin HPI: Patient is a 74 y.o. female who presents to ED from Vascular office due to worsening R foot infection. Has h/o Buerger's disease and has been seen here at at medical facility. Mostly dry gangrene and R 5th toe auto amputated recently. Has foul smelling drainage to R foot. Dry gangrene to L foot and scatt fingers that do not appear acutely infection. She is at a nursing home and states she had COVID 2 weeks ago, is positive today, denies any respiratory symptoms. Also has h/o renal cell carcinoma, states she has not had treatment due to uncontrolled Buerger's. Was sent here for admission for R foot amputation and IV antibiotics. Hospital Course: Patient was seen by vascular surgeon, who recommended R toe 1-4 amputations, L toe 1-3 amputations. Patient underwent toe amputations with bone shears and a rongeur was used to remove the residual phalanx and the metatarsal head was resected back to healthy appearing bone. Plastic surgery was consulted for the Bilateral hand digital dry gangrenous changes without acute ascending cellulitis or tenosynovitis involving left index; right index, middle, and ring fingers to the distal proximal phalanges. Plastic surgery recommended that her gangrenous fingers which appear to be stable dry gangrene progressing to autoamputation over the right ring finger. No acute surgical intervention at this time and continue Betadine paint twice per day. Infectious disease was consulted, patient was on broad spectrum abx vancomycin, cefepime and metronidazole. After the surgery, the infected bone was removed, patient transitioned to oral meds augmentin and doxycyxline at discharge. Patient discharged back to her nursing home. * Gangrene of both feet 1. Gangrene of bilateral toes in a patient with h/o Buerger's disease. Imaging finding of osteomyelitis in the right foot toes 2. Right 3rd, 4th, and 5th toe osteomyelitis s/p amputation of the Right 1st, 2nd, 3rd and 4th toes and Left 1st, 2nd and 3rd toes. 3. Sepsis likely 2/2 toe osteomyelitis, POA, resolved 4. Dry gangrene of the fingers likely 2/2 Buerger's disease Vascular surgery completed amputations, Infected bone removed. F/up at discharge Plastic surgery recommend continue painting digits with betadine. F/up at discharge Oral Augmentin and Doxycycline for 7 days per ID recommendations Blood culture, no growth at 48 hours. Continue home pain medications morphine and percocet q4h prn for pain control. COVID-19 Reports testing positive for COVID 2 weeks ago at nursing home. Patient asymptomatic, no indications for Remdesivir/Dexamethasone. Stage 3b chronic kidney disease Creatinine at baseline. Monitor input and output. Encourage po intake. Renal cell carcinoma of left kidney CT guided biopsy of the left iliac crest on 6/22/2022. Pathology showed: Metastatic adenocarcinoma, suspicious for renal cell origin. Patient following oncologist at medical facility. Patient to follow up after discharge. Thromboangiitis obliterans (Buerger's disease) Continue Asprin 325 mg daily, Plavix, Imdur 60 mg twice daily. Continue smoking cessation. Mild intermittent asthma without complication Resume home inhaler symbicort at discharge Type 2 diabetes mellitus without complication, without long-term current use of insulin Resume home anti diabetes medications Essential hypertension Resume home antihypertensives at discharge. Physical Exam on the Date of Discharge: Physical Exam Vitals reviewed. Constitutional: General: She is not in acute distress. Appearance: She is not ill-appearing. HENT: Mouth/Throat: Mouth: Mucous membranes are moist. Eyes: Extraocular Movements: Extraocular movements intact. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulses: Normal pulses. Heart sounds: No murmur heard. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: No wheezing. Abdominal: Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: Cervical back: Normal range of motion. Right Lower Extremity: (toe amputations and dressing in place) Left Lower Extremity: (toe amputations and dressing in place) Neurological: General: No focal deficit present. Mental Status: She is alert and oriented to person, place, and time. Psychiatric: Mood and Affect: Mood normal. Consults: IP CONSULT TO PLASTIC SURGERY IP CONSULT TO VASCULAR SURGERY IP CONSULT TO SOCIAL WORK IP CONSULT TO INFECTIOUS DISEASES Significant Diagnostic Studies: Xray foot Disposition: SNF Discharge Condition: good
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Essential hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 22.08.2022
- Impfdatum
- 26.05.2021
- Beginn
- 18.08.2022
- Tage bis Beginn
- 449,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Chronic obstructive pulmonary disease
Cough
Diabetes mellitus inadequate control
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Pt complained of worsening cough, weakness and shortness of breath over the last 10 days. Pt has uncontrolled diabetes mellitus and COPD with a history of renal cell cancer. Pt was found to be COVID positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 28.03.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Cardiac stress test
Chest X-ray
Computerised tomogram
Echocardiogram
Electrocardiogram
Electrocardiogram ambulatory
Palpitations
Scan
Tachycardia
Symptomtext
5 Days following second vaccine I experienced heart palpitations and tachycardia that sent me to the ER. I am still dealing with these palpitations every single day. I?ve had a bunch of tests done and they can?t figure out what?s wrong. I?ve never had heart palpitations in my life until I got the second shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- 2,0
- Labordaten
- Echocardiogram, EKG, Stress Test, Halter Monitor, Cat scan, Chest X-ray, Nuclear Scan, Blood tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 17.05.2022
- Impfdatum
- 02.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dehydration
Heart rate increased
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Upper-airway cough syndrome
Symptomtext
Starting 05/12/2022, I had a mild post nasal drip. On 05/13/2022 I tested positive for COVID (faint line) and that evening I had a very mild low grade fever. I called my doctor on Friday and got an rx for Paxlovid. The next day, on Saturday, I started the Paxlovid and I had a mild fever of 99.0-99.5. This same day I tested for COVID again and it was a bright line this time. Sunday my temp lowered to the range of 98-99. I had a mild cough but nothing bad and a slight runny nose. Yesterday the cough was better and I had a mild runny nose. Today I am feeling I'm almost completely better, no fever and rare cough and runny nose. Per my smart watch, my SpO2 was normal the entire episode and my HR may have gone up slightly but I am sure its due to being dehydrated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- 2 weeks prior: runny nose; tested for Covid 3 times but all negative
- Vorgeschichte
- Heart Condition
- Andere Medikamente
- Atorvastatin 40mg daily; metoprolol succinate 12.5mg daily; baby aspirin 81mg daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arrhythmia
Heart rate increased
Incorrect dose administered
Symptomtext
I had a heart rhythm that was abnormal along with a high heart rate, I requested the booster half dose of Moderna and just found out that they gave me a full dose. I only had approval to get half a dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Rheumatoid Arthritis
- Andere Medikamente
- Humira, Prednisone, B12, Folic Acid
- Allergien
- Multi
- Vorherige Impfungen
- 1/14/21, Moderna- shortness of breath, hives
- Staat
- -
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Burning sensation
Chills
Cyanosis
Dermatitis
Diarrhoea
Feeling of body temperature change
Headache
Hyperhidrosis
Immediate post-injection reaction
Injected limb mobility decreased
Limb discomfort
Migraine
Mobility decreased
Musculoskeletal chest pain
Neuralgia
Pain
Pain in extremity
Symptomtext
Following is the exact timeline of events: * first day * right arm got heavy the moment I was vaccinated * arm got even heavier throughout the day * in the evening arm barely could be moved anymore and hurt * right leg revealed huge blue spot like I was hit * my body turned ice cold and fingers started to tickle * then I turned hot with chills * every 5 minutes ice cold to hot with chills * during the night, I got a fever of 41.6?C and I didn't have a fever in 20-25 years - not even when I had covid *next day *headaches and migraines started * my left skull skin started to hurt like burning / inflammation feeling *PMS cramps for no reason * feet started to swell * next day * diarrhea started * started to sweat for no reason, thermometer said temperature was low * next day * arm was still hurting but less than first three days * back left rib cage started to hurt, lumbago like, nerves shooting through both legs, bending down was almost impossible - Migraines stopped after about 2,5 weeks, some days were really bad, never had it before, sometimes still light headaches, triggers easily, I never really had a problem with migraines/ headaches before - just had an headache once in a while.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- bilateral ear Infection in both ears; antibiotic treatment started march 19th 2022, which is longer than one month prior
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 12.04.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 24,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal discomfort
Blood test normal
Cholecystectomy
Cholelithiasis
Condition aggravated
Hypertension
Incision site pain
Ultrasound abdomen abnormal
Vomiting
Symptomtext
05/06/2022 I had stomach distress, vomiting for 12 hours. My blood pressure was high off and on. I went to the ER the next day and had my gall bladder removed. Stayed overnight in the hospital. I was diagnosed 30 years ago with gall stones, but they did they did not want to take it out then. It hasn't bothered me until 05/06/2022. I feel good now, just a little sore at the incision site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Ultra sound, saw gall stones requiring surgery, Bloodwork, normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hiatal Hernia
- Andere Medikamente
- Ferrous Sulfate Iron 65mg
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 05.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Arthralgia
Back pain
Depression
Heart rate
Heart rate increased
Hypokinesia
Neck pain
Nerve injury
Nervousness
Pain in extremity
Swelling
Tremor
Symptomtext
swelling; pain in the left shoulder/pain almost to the elbow; like some nerves were damaged; arm started to shake real bad; pain in the left side of the neck; a little bit of pain in the low back; rapid heart beats; Anxiety; nervousness; depressed; sore left arm; could hardly pick up her arm, and could not lie on it; This spontaneous case was reported by a consumer and describes the occurrence of TREMOR (arm started to shake real bad), NECK PAIN (pain in the left side of the neck), BACK PAIN (a little bit of pain in the low back), HEART RATE INCREASED (rapid heart beats) and ANXIETY (Anxiety) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Mitral valve prolapse (rapid heart beats, pounding heart, anxiety attacks), Blood pressure high (35 years ago), Cholesterol, Allergy, Anxiety, Penicillin allergy and Contrast media allergy. Concomitant products included CETIRIZINE HYDROCHLORIDE (ZYRTEC ALLERGY) and MONTELUKAST SODIUM (SINGULAIR) for Allergy, DIAZEPAM (VALIUM) for Anxiety, SIMVASTATIN for Cholesterol, DILTIAZEM for Mitral valve prolapse, VALPROATE SEMISODIUM (DEPAKOTE) for an unknown indication. On 05-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 05-Mar-2022, the patient experienced PAIN IN EXTREMITY (sore left arm). On 12-Mar-2022, the patient experienced TREMOR (arm started to shake real bad), NECK PAIN (pain in the left side of the neck), BACK PAIN (a little bit of pain in the low back), HEART RATE INCREASED (rapid heart beats), ANXIETY (Anxiety), NERVOUSNESS (nervousness), DEPRESSION (depressed) and ARTHRALGIA (pain in the left shoulder/pain almost to the elbow). 12-Mar-2022, the patient experienced NERVE INJURY (like some nerves were damaged). In March 2022, the patient experienced HYPOKINESIA (could hardly pick up her arm, and could not lie on it). On an unknown date, the patient experienced SWELLING (swelling). The patient was treated with HYDROCODONE BITARTRATE, PARACETAMOL (NORCO) for Pain, at a dose of 1 tablet 7.5 mg. At the time of the report, TREMOR (arm started to shake real bad), NECK PAIN (pain in the left side of the neck), BACK PAIN (a little bit of pain in the low back), HEART RATE INCREASED (rapid heart beats), ANXIETY (Anxiety), NERVOUSNESS (nervousness), DEPRESSION (depressed), HYPOKINESIA (could hardly pick up her arm, and could not lie on it), NERVE INJURY (like some nerves were damaged), SWELLING (swelling), ARTHRALGIA (pain in the left shoulder/pain almost to the elbow) and PAIN IN EXTREMITY (sore left arm) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 12-Mar-2022, Heart rate: rapid Rapid. Patient appointment to visit her doctor on 2-May-2022. Patient experienced symptoms like that before receiving the Moderna COVID-19 vaccine but not like that. This case was linked to MOD-2022-536167, MOD-2022-536174 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220312; Test Name: heart beats; Result Unstructured Data: Rapid
- Aktuelle Erkrankungen
- Allergy; Anxiety; Blood pressure high (35 years ago); Cholesterol; Contrast media allergy; Mitral valve prolapse (rapid heart beats, pounding heart, anxiety attacks); Penicillin allergy
- Vorgeschichte
- -
- Andere Medikamente
- DEPAKOTE; SIMVASTATIN; DILTIAZEM; ZYRTEC ALLERGY; SINGULAIR; VALIUM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 13.04.2022
- Impfdatum
- 12.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthma
Condition aggravated
Erythema
Pain in extremity
Peripheral swelling
Pruritus
Rash
Skin discolouration
Urticaria
Symptomtext
Starting the night of 3/24 I began experiencing whole body itchiness. The next morning, my hands were swollen and red and painful. Throughout the day it began to turn purple. I went to urgent care and they put me on prednisone. Over the next 5 days I began getting random rashes and hives over my body. I also felt that my asthma was getting worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Albuterol Inhaler, Advair
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Mobility decreased
Pain
Peripheral swelling
Pruritus
Skin warm
Symptomtext
swollen arm, itchiness, pain, redness, hot to touch, mobility restricted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- estradiol, levothyroxin, furosemide
- Allergien
- methotrexate, remicade, colyte, imodium. box elder, wasp stings
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 24.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Bursitis
Immediate post-injection reaction
Incorrect route of product administration
Injection
Joint range of motion decreased
Mobility decreased
Pain in extremity
Rotator cuff syndrome
Swelling
Tenderness
Ultrasound scan abnormal
X-ray
Symptomtext
Patient got immediate pain when vaccine was administered too high on the arm. Pain continued to arm immobility including swelling and tenderness with shoulder and joint pain. She also had numbing in the thumb. Patient too 325 mg on tylenol thursday evening for the pain and it did not help.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- 3/25 urgent care - they wanted to go to ortho and did an x-ray to make sure there was not needle. Suspected injury to rotator cuff because of no range of movement. 3/28 ortho urgent care-subchromial bustitus and secondary cerva. They did an ultrasound and a cortisone injection. Both indication injection site was too high
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- RA diagnosis
- Andere Medikamente
- n/a
- Allergien
- pcn, advil
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 25.03.2022
- Impfdatum
- 05.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Cardiac flutter
Heart rate increased
Hypertension
Myalgia
Urine analysis normal
Symptomtext
I had super high heart rates and high blood pressure after getting the vaccine and still do, my heart rate now sits around 130 BPM and when I went to the ER it was because I check my BP at home and it was 170/116 and I had no problems with blood pressure before the vaccine, I?m only 19 years old. now I can feel my heart flutter and times and I get really bad muscle pains like I have the flu at random times and I?m scared to get the 2nd dosage
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Blood and urine sample came back fine I believe
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Right bundle branch block Depression ADHD Anxiety
- Andere Medikamente
- Vyvanse Doxipin Effexor
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 14.03.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain
Diarrhoea
Dizziness
Hypoaesthesia
Hypoaesthesia oral
Paraesthesia oral
Retching
Sensation of foreign body
Symptomtext
Pt was doing just fine about 15 minutes into 30 minute observation period pt expressed experiencing the following: numbness on bilateral cheeks and jaw, tingling on tongue, feeling of something in her throat. At the time pt was breathing fine and was listening to calming music and focus on her breathing. At the 30 min mark pt was still having numbness in the face and mouth as well as dry heaving, dizziness, kneeling on floor, sharp/significant left abdominal pain. Pt was not SOB and had no facial/tongue swelling. Provider determined epi-pen not needed at this time. Pt was then wheeled down to ER where she started to have what she reported as watery diarrhea x 10 minutes w/ abdominal pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- no labs drawn in ED since they couldn't start IV. no imaging done. Pt was given Zofran and sent home.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Morbid obesity, PTSD, Anxiety, Depression, Chronic migraines, hiatal hernia,
- Andere Medikamente
- triamcinolone 0.025%, topiramate 50mg, topiramate 25mg, phenylephrine 0.25%, oxybutynin 5 mg, ondansetron 8 mg, Prenatal multivitamin, lorazepam 1 mg, citalopram 40 mg, buspirone 10 mg, bupropion 150 mg, budesonide-formoterol 80mcg-4.5mcg,
- Allergien
- egg containing compounds, ibuprofen, Imitrex, flu vaccine, LaMiCtal
- Vorherige Impfungen
- Reaction to first Moderna COVID -19 vaccine. Sx similar to this reaction. At the time pt was given epi and taken to ER where she
- Staat
- CO
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 33,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arrhythmia
Condition aggravated
Hypertension
Symptomtext
patient presented with hypertension and arrythmias post covid vaccine and went to dr. office
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- chronic pain, sinus tachycardia, Hypertension, muscle spasms
- Andere Medikamente
- no
- Allergien
- pcns, Seroquel, butrans, vicodin
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Diarrhoea
Dyspnoea
Fatigue
Migraine
Tremor
Symptomtext
Shortness of breath, chills, diarrhea, shaking, migraines, fatigue, exhaustion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Omeprazole 40mg, Topiramate 25mg, Montelukast sod 10mg, Maltrexone-cmpd 3mg, Amitriptyline 50mg, Promethazine 25mg, Zanadine 25mg, Sildenafil 20mg, Alertec, Flonase nasal spray, Albuterol inhaler, Fluticasone maintenance inhaler, Propionate
- Allergien
- Morphine, Sulfa, Oxybutane, Tree nut, Coconut
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 15.03.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dizziness
Fatigue
Hypoaesthesia
Injection site erythema
Injection site inflammation
Myalgia
Nausea
Paraesthesia
Symptomtext
Increased fatigue, nausea, redness and inflammation at injection site. Numbness and tingling in hands . Muscle aches . Dizziness , generalized weakness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Nine
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Clindamycin, transfix
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Headache
Impaired driving ability
Tinnitus
Vertigo
Vertigo positional
Symptomtext
The same night I received the booster I developed a severe headache (same as with previous second dose) and took Tylenol. I woke up in the middle of the night (maybe 3 or 4 am) with severe vertigo, headache and ringing in my ears. The vertigo symptoms became less severe on March 5th that I could at least drive again. I still have positional episodes. The ringing in my b/l ears has not lessened. I have a continuous low volume ringing with period of loud ringing in one or both ears (varies). My headaches are better than at onset but continue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- I?ve seen my primary physician today. I am going to consult with an ENT as soon as I can get an appointment.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 13.03.2022
- Impfdatum
- 18.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal discomfort
Biopsy skin
Blood test abnormal
Chest X-ray
Chest pain
Deafness unilateral
Dyspnoea
Electrocardiogram
Eye pruritus
Headache
Hypersensitivity
Pruritus
Skin burning sensation
Urticaria
Vision blurred
Symptomtext
headache, upset stomach, blurred vision and itchy eyes, trouble hearing in left ear, chronic hives, difficulty breathing, chest pain, burning and itching skin all over the upper half of the body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- ekg, chest x-ray, biopsy of the hive and blood work. Blood work came back as "A severe allergic reaction"
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 01.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Electrocardiogram
Hypotension
Visual impairment
Symptomtext
Hypotension, Almost blacking out, seeing stars.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- EKG run day after.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Acetaminophen, aspirin, tolfnate, clomitrizole.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dyspnoea exertional
Headache
Malaise
Symptomtext
Patient has she has been feeling extremely unwell, had a terrible headache, and had trouble breathing when moving around.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Breast swelling
Chills
Decreased appetite
Fatigue
Headache
Hyperhidrosis
Hypoaesthesia
Induration
Inflammation
Injection site induration
Injection site pain
Injection site reaction
Insomnia
Lymphadenopathy
Mobility decreased
Muscle spasms
Oropharyngeal pain
Symptomtext
1. Insomnia beginning 8 hours after injection, I was exhausted but could not sleep more than 20 minutes at a time, this went on for 48 hours. 2. Pain and hard disc of muscle at injection site, remained for 9 days, began 2/12. 3. Neck and trapezius muscles were hard for 7 days, began 2/12. 4. Stabbing pain under right shoulder blade for 9 days, began 2/12. 5. Right armpit lymph node swelling for 9 days, began 2/12. 6. Right breast tissue and adjacent lymph node swelling for 9 days, began 2/12. 7. Right armpit felt like sandpaper had taken off the skin, began 2/18 and still ongoing. 8. Could not raise right arm due to excessive pain for 8 days, began 2/12. 9. Shooting pain from shoulder to palm for 8 days, began 2/13. 10. Shooting pain from right elbow to palm became worse and more frequent 2/15 and lasted until 2/20. Intermittent periods of arm numbness and tingling. Could not use arm normally for 9 days. 11. Dull ache and throbbing from right elbow to palm began 2/20 and is still on going. 12. Right palm cramps and spasms began 2/13, ended 2/20. Dull ache in palm is still on going. 13. Chills beginning 2/12 and lasting for 48 hours with periods of intermittent sweating. 14. Excessive fatigue due to inability to sleep for 48 hours. 15. Headache beginning 2/12 and lasting 5 days. 16. Sore throat beginning 2/13 for 48 hours. 17. Lack of appetite beginning 2/12 and lasting for 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Doctor recommended going to the Emergency Room and undergoing an MRI to discover extent of nerve inflammation. Patient did not go due to local inclement weather conditions.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Sprintec
- Allergien
- cefzil, cats, local pollen
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Complex regional pain syndrome
Condition aggravated
Neuralgia
Pain
Screaming
Symptomtext
Exactly 12 hours after injection of the booster I woke up in severe pain. I have CRPS and have had it for over 30 years. When injecting into the muscle, it caused my CRPS to worsen to the worst degree yet. I have it all over my body. The pain made me scream in agony and still does. After going for a walk yesterday (I have to move), my body got even worse nerve pain because of the booster. Waking up today was horrible in that my pain was off the charts. It takes hours for the pain to settle. It has not EVER gotten as settled as it was before the booster. The booster caused excruciating pain and continues to this day. NO one who has a nerve condition should EVER be vaccinated/boosted when it goes into the muscle!!!!!!! Please develop vaccines and boosters that just go under the skin. Otherwise, you are changing the life expectancies to all of us who are unable to be vaccinated/boosted. Please.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- No tests for CRPS reaction. No research has been done to help us!!!!!!!!!!! Research is NEEDED on this horrible disease. Research to take care of those who have had it for over 10 years. 30 years ago there was hardly word on this condition. Most doctors had no idea what it was. I saw a specialist who opened my compartments which caused CRPS. Taking care of oneself shouldn't cause another medication condition that worsens one's life. Living in heck isn't easy. Thank you!
- Aktuelle Erkrankungen
- COVID-19
- Vorgeschichte
- CRPS
- Andere Medikamente
- Fluoxetine, Lorazepam, Trazadone, Melatonin, Claritin, Lyrica, Senna, Miralax, Morphine, Claritin, Aspirin 81 mg, Plavix, Tylenol prn
- Allergien
- stomach cannot tolerate several medications. Pennicilin reacted with a rash.
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site swelling
Injection site warmth
Mobility decreased
Pain in extremity
Symptomtext
Arm swollen and warm to touch at injection site. Pain in arm; unable to lift arm properly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure, arthritis.
- Andere Medikamente
- Vitamin, Tylenol.
- Allergien
- Erythromycin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dystonia
Hypoaesthesia
Paraesthesia
Symptomtext
Patient stated later in the day of 2/18/2022 (after immunization), her left arm was numb and tingly. She reported up to 6 episodes of dystonia within 48 hours post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 17.04.2023
- Impfdatum
- 14.04.2022
- Beginn
- 23.12.2022
- Tage bis Beginn
- 253,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acoustic stimulation tests abnormal
COVID-19
Cough
Deafness unilateral
Ear discomfort
Ear disorder
Feeling abnormal
Headache
Hyperhidrosis
Influenza A virus test negative
Influenza B virus test
Middle ear effusion
Pyrexia
Respiratory syncytial virus test negative
SARS-CoV-2 test positive
Symptomtext
I got home from work at 4:30 PM, and I started feeling bad. I had a terrible headache, a temperature of 102.5, and a dry, unproductive cough. I took Tylenol PM, but it didn't help. The following morning, I showed up for work, and I was sent to the workplace clinic at 7:30 AM. I underwent a PCR test and got a positive result for COVID-19. I was also tested for RSV, influenza A, and influenza B, and the results on those were negative. I was then sent home to isolate for ten days. I was given Tessalon Perles, Tylenol, Motrin, and Paxlovid. It took four days for the fever to break. During my fever, I sweated profusely. I often had to change my bedclothes and the clothes I was wearing. After the fourth and fifth day, I started having issues with my right ear. Whenever I went to bed, it was clogged, but it was clear whenever I woke up the following morning. My problem with my right ear persists to this day, and it has affected my hearing to the point that I can't really gauge the volume of my own voice, so I often sound like I'm yelling. I went to an audiologist on 2/27/2023. My hearing in the left ear was fine, but when the audiologist administered the audiograph to the right ear, it flatlined. I couldn't hear anything out of that ear. She then checked my right ear with the otoscope and noted that there was a lot of fluid buildup. I get my healthcare through the agency, and I have been waiting ever since to see an ENT specialist. I was told that it would probably take three months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 23DEC2022 - PCR Test - Positive for COVID-19, Negative for RSV, Influenza A, and Influenza B; 27FEB2023 - Hearing Test - Normal Hearing Detected in Left Ear, Obstructed Hearing and Fluid Buildup Detected in Right Ear
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression; Post-Traumatic Stress Disorder; Anxiety; Fluid in Right Ear with Difficulty Hearing
- Andere Medikamente
- Quetiapine; Duloxetine; Ensure Nutritional Shake
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 04.04.2023
- Impfdatum
- 21.09.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 71,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Malaise
Nasopharyngitis
SARS-CoV-2 test positive
Symptomtext
Began not feeling well at end of December. Began having cough and cold like symptoms. Went in to PCP and was prescribed Paxlovid and symptoms began to resolve and around day 4 or 5 began to feel better
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- NOne
- Andere Medikamente
- Zetia, Fosamax
- Allergien
- Mold, dust, codeine
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 13.03.2023
- Impfdatum
- 01.03.2022
- Beginn
- 25.12.2022
- Tage bis Beginn
- 299,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Covid-19 I tested positive for Covid 19 on December 26, 2022 I experienced fatigue and a fever. I was prescribed PAXLOVID for my symptoms. I started to feel better on January 3, 2023. I tested negative on January 4, 2023 and I tested positive again on January 6, 2023 I then retested and tested negative on January 12, 2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- MUGS
- Andere Medikamente
- Losartan; CIALIS; atorvastatin; aspirin; multivitamin; cabergoline
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 13.03.2023
- Impfdatum
- 09.03.2022
- Beginn
- 03.09.2022
- Tage bis Beginn
- 178,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
Nasopharyngitis
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Started having a sore throat and cold symptoms. Took a COVID-19 test and was positive. Doctor prescribed Paxlovid. Took full course of Paxlovid and then a week later started having COVID-19 symptoms again. Tested positive again for COVID-19 and was sick for about a month.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- 2022MAR09 Home COVID-19 test - Positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- COPD; Hypothyroidism; Macular Degeneration; Lung Cancer in remission; Triple Bypass; Neuropathy; Lupus; Sjorgrens; Arthritis.
- Andere Medikamente
- Calcium Magnesium Zinc Supplement; Lipitor; Spiriva Inhaler; Vitamin D3; Miralax; Zetia; Breo Inhaler; Moprolol Tartrate; Plaquenil; Lunesta; Lasix; Gabapentin; Montelukast Sodium; Citalopram; Eye Preservatives; Levothyroxine Sodium; Cellce
- Allergien
- Neulasta; Iron pills; Crestor.
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 20.02.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 253,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
I took an administered COVID-19 on 10/29/2022 for a cruise I was going on. That came back negative. I then tested positive for COVID-19 on 11/01/2022. It started with a very runny nose and some sneezing and a little chest congestion on 10/31/2022. Then what I was most troubled by was a very sore throat in the morning and that lasted for about 3 days. I simply treated it with throat lozenges. Luckily the symptoms were mild. After 5 days, I was fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 29OCT2022 COVID-19 test negative; 01NOV2022 COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Kidney Disease; Crohn's Disease; Slight Elevated Blood Pressure; Asthma
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 20.09.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 100,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Pyrexia
SARS-CoV-2 test positive
Symptomtext
12/29/22 presents to ED for "fever" "corona virus concern". PMHx of "multiple myeloma on chemo and PE on anticoagulation"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- 12/29/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 27,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Cough
Fall
Oropharyngeal pain
Pyrexia
Rhinorrhoea
Symptomtext
Pt presented to the ED after falling in the bathroom. He had developed a runny nose and a cough with sore throat. He also had a fever yesterday. Pt was admitted for COVID and generalized weakness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 05.04.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 164,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Fever, body aches, fatigue the day following return from out-of-state conference. Covid home test positive. Contacted PCP who advised clinic visit for testing, which was also positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 09/16/2022 COVID home test positive 09/16/2022 PCR test positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 04.04.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 109,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
SARS-CoV-2 test negative
Symptomtext
I received my Covid- 19 vaccine on 04/04/2022. On 07/22/2022 I was diagnosed with covid. I was fatigued for three days in a row. I was prescribed Paxlovid. On the 5th day I tested negative for Covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 04.10.2022
- Impfdatum
- 30.03.2022
- Beginn
- 20.09.2022
- Tage bis Beginn
- 174,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Pyrexia
SARS-CoV-2 test
Symptomtext
Sore arm, slight fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- COVID, throat swab
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Pre-Diabetic, elevated blood pressure, cataracts
- Andere Medikamente
- Nizoral, Cozaar, Lasix, Calcium, Cosopt, Allegra, Lipitor, Xalatan, Flonase, Aspirin, Colace, Metformin, Turmeric, Cinnamon Extract
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 26.09.2022
- Impfdatum
- 21.03.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 123,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood sodium decreased
Blood test abnormal
COVID-19
Fatigue
Headache
Nausea
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
2 days before testing positive for COVID-19 I had a slight sore throat while I was on vacation. On July 26th I got up from bed and was nauseated, fatigue, and had a splitting headache. I went to a hospital because it was that bad. The gave me antibodies and they tested my blood. They said I had a dangerously low sodium level and sent me to a bigger hospital in a ambulance. The next day they tested me for COVID-19 and I tested positive. I just started to feel better 2 weeks ago
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- 5,0
- Labordaten
- COVID-19; 07/24/2022;07/27/2022; Positive; Blood test- Low Sodium
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Restasis; Lyrica; Vitamin D; Calcium plus D3; Ibandronate; Florajen; Melatonin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 31.08.2022
- Impfdatum
- 20.02.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 186,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Arthralgia
Fatigue
Pyrexia
Respiratory tract congestion
Symptomtext
fatigue, fever, congestion, cough, arthralgias
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 22.02.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 38,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Dry skin
Vaccination site pruritus
Symptomtext
On 02/22/2022 I had my 4th vaccination with Moderna. About 6-8 weeks after, I noticed it was itchy at the vaccination site. I thought possible mosquito bit. It got worse and worse as time went on going from half dollar to now the size of my palm. It is rough feeling to the touch. Treatment included triamcinolone acetamide but it didn't work. I use CALADRYL that seems to work. It is still present on my arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pruritus
- Hospital-Tage
- -
- Labordaten
- Blood panel was performed on 05/22/2022 and everything was fine.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Mixed connective tissue disease; Hashimoto; Breast CA 2013
- Andere Medikamente
- Hydroxychloroquine; amlodipine; metoprolol; ADDERALL; vitamin D
- Allergien
- Fluoride; lisinopril
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 14.08.2022
- Impfdatum
- 26.04.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 70,0
- Dosis
- 4
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Symptomtext
some soreness at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma High cholesterol high blood pressure anxiety
- Andere Medikamente
- lodine,valsartan,loratadine,wellbutrin, prozac, pravastatin, nexium, advair, doxipin, cholestyramine vit D3 magnesium
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 12.08.2022
- Impfdatum
- 20.02.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 129,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Laboratory test abnormal
Pyrexia
Urinary tract infection
Symptomtext
Hospitalization for fever post-treatment for UTI and tested positive upon admission on dates 6/29/22-7/5/22. Treated with dexamethasone, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Not recorded; previous adverse reaction to hydrocodone
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 15.04.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 62,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anosmia
COVID-19
Cough
Fatigue
Headache
Pain
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I was on a cruise ship. Everyone was vaccinated. Five present was in isolation due to COVID-19. I developed a scratchy throat then took a COVID-19 test that was positive. I also received a positive PCR COVID-19 test. I was put in isolation. Two days later, I got really tired with fatigue, with a headache and achy that lasted two days. I also had a dry cough and lost my sense of smell. I was still positive on day 10 which was the protocol to get out. I went home and then on day 15, I finally tested negative. I did see nurses that on the ship that took care of me and was under supervision of a doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test - positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Sleep apnea
- Andere Medikamente
- Fluoxetine; Multivitamins; Zinc; Vitamin D; Vitamin B Complex; Omega 3
- Allergien
- Thimerosal
- Vorherige Impfungen
- Moderna 1st dose - rash about 2 weeks after vaccine
- Staat
- TN
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 09.04.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 68,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Lethargy
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Skin lesion
Symptomtext
Did a home test on 06/16/2022, it was positive, went to my doctor 06/17/2022, tested positive, was given the anti-virals, on 4th day developed a sore spot on my ankle like I get when I take Sulfa drugs. The spot went away after I stopped the anti-viral. COVID_19 symptoms of fever, lethargy, sore throat, achy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 06/16/2022 - COVID-19 home test- positive 06/17/2022 - COVID-19 antigen test- positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Loratadine
- Allergien
- Penicillin; Sulfa
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 07.04.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 63,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Headache
Malaise
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Vomiting
Symptomtext
I contracted COVID-19 on 06/09/2022 with symptoms of dry cough, sneezing, runny nose, congestion, low grade fever, vomiting, and slight headache. I was prescribed Paxlovid on 06/12/2022. I was ill for 5 days before my symptoms began to resolve. I have fully recovered with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab home test was positive on 06/12/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; High Cholesterol
- Andere Medikamente
- Amlodipine; Atorvastatin; Multivitamin; Caltrate; Aspirin
- Allergien
- Sulfa; Keflex
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 76,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Cough
Fatigue
Muscle fatigue
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Symptoms were basic, I had a very sore throat which lasted 3 days 24-26th. Nasal congestion and a slight cough. I had some fatigue and muscle fatigue but I'm not sure if it was related to COVID-19 or Paxlovid. I had muscle aches which were related to Paxlovid. I had chills 1 evening but no fever. I ran 97.7 body temperature.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 bannex now at home test - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Cardiovascular disease; Chronic kidney disease; Hypertension
- Andere Medikamente
- Lipitor; Low dose Aspirin; Multivitamin; Vitamin D; Vitamin C; COQ10; Fish Oil; Iron
- Allergien
- Amoxicillin in combination Clavulanic Acid
- Vorherige Impfungen
- 1st dose moderna I was just tired, sleepy and achy.
- Staat
- FL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 14.02.2022
- Beginn
- 03.07.2022
- Tage bis Beginn
- 139,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
COVID-19
Diarrhoea
Muscle spasms
Nausea
SARS-CoV-2 test positive
Vomiting
Symptomtext
Pt presented with abdominal pain and cramping along with nausea vomitiing and diarrhea. Pt also tested positive for covid. Pt discharged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Liver Transplant diabeties, HLD, Heart failure, CKD osteopenia hypothyroidism
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 12.06.2022
- Tage bis Beginn
- 62,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse reaction to the vaccine. I became systematic on 06/12/22 and tested negative for COVID-19. I tested positive for COVID-19 06/13/2022. I was prescribed Paxlovid which helped with my symptoms of sore throat, runny nose and congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Home test for COVID-19 positive on 06/13/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; pericarditis and seasonal allergies
- Andere Medikamente
- Yes: declined to provide details
- Allergien
- Pertisis vaccine; doxycycline
- Vorherige Impfungen
- Pertisis vaccine in 1960. I went into anyphalatic shock.
- Staat
- MA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 73,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Malaise
Nausea
Oropharyngeal discomfort
Oropharyngeal pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Vomiting
Symptomtext
I contracted COVID-19 on 06/20/2022 with symptoms of nausea, vomiting, sore throat, cough, runny nose, and low grade fever of 100.5. I was not prescribed any medications. I was ill for 3 days before my symptoms began to resolve. I have had a lingering symptoms of tickle in the back of my throat and occasional cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 PCR test was positive on 06/22/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D; atorvastatin; omeprazole; FLOMAX
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 02.04.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 66,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Cough
Discomfort
Influenza like illness
Pain
Polymerase chain reaction positive
Throat irritation
Symptomtext
I actually had a slight cough and irritation in my throat and didn't think much of it. My husband was more sick than me, and he wanted to go to urgent care. I started to have the same symptoms as he did so I knew something was up. I felt flu-like symptoms and was very uncomfortable. I had body aches, chills. I took Tylenol. This lasted about 3 days. It was mild for me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- PCR- positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Blood pressure medication; Calcium
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 15.04.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 68,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anosmia
COVID-19
Headache
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
positive covid 19 home test on June 24, 2022. Symptoms included sore throat, fever, headache, head congestion. Loss of sense of smell on June 28, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- covid 19 home test on June 24 2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- arthritis, pre-diabetes
- Andere Medikamente
- Alendronate sodium, calcium
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 02.07.2022
- Impfdatum
- 01.03.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 88,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
SARS-CoV-2 test positive
Upper-airway cough syndrome
Symptomtext
I want to clarify above. I had 3 total. vaccines: 1) J&J in April of 2021. 2) Moderna in Oct of 2021. 3) Moderna in March of 2022. My ?adverse event? was: I had symptoms of what I thought were spring allergies - post nasal drip and coughing. The coughing kept getting worse to the point where I tested myself for Covid 19 and found that I was positive. I also experienced some fatigue. I?d say the symptoms lasted maybe 5 days. I talked to a nurse at my clinic over the phone. I never needed to be seen by a doctor. I recovered easily at home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- I took a Covid test that we received through the mail from the Government. Over the course of 2 days I took 2 of the tests. Both were positive.
- Aktuelle Erkrankungen
- None that I recall
- Vorgeschichte
- osteo arthritis,
- Andere Medikamente
- For sure: Fish oil 1280 mg/day, potassium 1100 mg /day, probiotic with DE111 - 1 capsule per day. I can?t recall if I was taking B9 and B12 at the time. I also commonly take Metamucil and intermittently Benefiber (don?t think those
- Allergien
- I have environmental allergies - cats, dogs, evergreen trees,
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 18.04.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 36,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
Positive Covid Test on May 25, 2022. On May 23. Had what I thought was mild allergies. Slight headache, mild sore throat. Sore throat only lasted 1 day. Mild headache persisted for 4 days. Start sneezing a lot on the 25th....unusual for me. Did Covid Test-positive. Called doc. Prescribed Molnupiravir 200 mg, 4 capsules, 2x daily, for 5 days. Self isolated. sneezing stopped but congested cough started. Tired for 3 days. 5th day was much better. Following Tuesday returned to work (with mask). Cough was much less but continued. Would start about 4 hours after rising and continue until mid day. This lasted until about June 8th. No other symptoms except cough. Not tired. No brain fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home Covid Test May 25th, 2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure, seasonal allergies, no thyroid
- Andere Medikamente
- Tirosent, Amolydipine Bysalet, Vitamin A,D and K, Magnesium, Biotin, Zyrtex,
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 16.06.2022
- Impfdatum
- 25.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Formication
Insomnia
Pruritus
Rash
Skin discolouration
Symptomtext
It started out with a burn feeling and itches. It spread all over my body. When they dry out the leave black marks. I still have the spots on my body. I felt like something is crawling on me. Next day my skin look like someone burnt me. I went to the doctor and they prescribe me some cream and Z-Pak. It difficult to sleep at night. The marks look like ring worms.
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
- 36,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 01.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Pruritus
Urticaria
Symptomtext
Severe itching behinning on scalp, ears and base of neck. Next morning proceeded to chest, trunk and arms, as well as developing severe hives covering entire body. Recieved a steroid for 2 weeks and told to take antihistamine 3x a day. After week/week and a half turned into dermatographia. Have been on antihistamines since 2x a day to 4x a day as well as montelukast for the past 3 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- Scratch in office
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Gluten
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 20.03.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Symptomtext
Acute urticaria from the Moderna COVID-19 booster. It caused persistent hives and itchiness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Minimal Change Nephrotic Syndrome
- Andere Medikamente
- NuvaRing Vitamin C Women's MultiVitamin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 19.02.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
Fatigue
Impaired work ability
SARS-CoV-2 test positive
Symptomtext
My husband who is also fully vaccinated, tested positive on 5/2 and I then tested positive 6 days later on 5/8 through an at home Covid test although I had no noticeable symptoms. I called my healthcare provider's office and spoke with the on call doctor who prescribed Plaxovid which I began that same day on 5/8. The only symptom that I think I had was moderate fatigue for two days but not even to the point that I had to miss a full day of work. After the 5 day Plaxovid regimen, I have been testing my self regularly with at home tests and they have all been negative. Yay science and yay Plaxovid and yay vaccines!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home covid test-positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mild High Blood pressure
- Andere Medikamente
- Lisinopril Multivitamin Antacid
- Allergien
- Hydroxyzine
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 17.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Choking
Dizziness
Impaired driving ability
Injection site pain
Injection site swelling
Insomnia
Nausea
Pyrexia
Sleep apnoea syndrome
Sleep study abnormal
Swelling
Symptomtext
Every night I was having difficulty sleeping waking up choking. And when I was sleeping I was awake. I was having such difficultly sleeping that I was nodding off while driving. And doctor ordered a sleep study. I was diagnosed with sleep apnea. I had no symptoms the month prior to having COVID and then started having difficulty sleeping. I let it go on for a while before going to the doctor. I also had adverse reaction to the injection site being painful and the swelling went under my arm to my breast muscle and I couldn't lift it for 2 days. I had a 101-103 fever for 2 days. The 3rd morning I was regular temperature. Besides the nausea and dizziness that was about all the reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Sleep study - sleep apnea; bloodwork - normal
- Aktuelle Erkrankungen
- Sick with COVID
- Vorgeschichte
- Asthma from birth
- Andere Medikamente
- Albuterol sulfate as needed
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 18.05.2022
- Impfdatum
- 05.02.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- 55,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Skin test
Symptomtext
Rash and severe itching, primarily on chest and back. Also intermittent itching on palms of hands and inside of ears
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Dermatology sent a skin sample to lab for analysis. Results indicated a reaction to medication of some type. At first condition was treated with oral steroids, which eliminated the symptoms but within two weeks, conditions returned. Now treating with topical steroid cream, which relieves symptoms. Additional notes: I have received two Moderna booster vaccinations (9/29/2021 and 4/26/2022) subsequent to this vaccination on 2/5/2021. We have been unable to determine the definitive cause of this condition, but suspect it could be related to the COVID vaccine.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High cholestoral, seizures (2 - 2019/2020), PVCs, kedney stones, ED
- Andere Medikamente
- Levetiracetam. Atorvastatin, Nadolol, Potassium Citrate, Tadalafil
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 24,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dizziness
Exposure to SARS-CoV-2
Fatigue
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I was exposed to COVID-19 on 05/05/2022 by someone visiting my office. The following Monday I started experiencing symptoms. I was feeling lightheaded and woozy and by midday I had a fever, so I took a home test. That test was positive. I saw my doctor the next day and started taking antivirals. By the next day I was feeling much better. Today, I am basically feeling fine except for some fatigue that could be allergies. I am doing my normal daily activities and going to work. However, I am continuing to test positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- COVID-19 test 05/09/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Allergies Tinnitus
- Andere Medikamente
- Claritin Flonase Calcium Multivitamin Vitamin B2
- Allergien
- Dust Pollen Grass Weeds
- Vorherige Impfungen
- 2nd Moderna vaccine (03/06/2021). My blood pressure went so low that I passed out, hit my head, and ended up in the emergency ro
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Muscle spasms
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I had a runny nose & a sore throat & then I started having chest coughs & then I had to go to ER my muscles were having spasms & i had to go to ER twice because I tested positive for Covid-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Atorvastatin, Primidone, Flomax, Amlodipine, Valacyclovir
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 07.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blister
Ear swelling
Erythema
Eye contusion
Eye swelling
Facial pain
Headache
Lymphadenopathy
Ocular hyperaemia
Pain
Pain of skin
Pruritus
Pustule
Scab
Scar
Swelling face
Symptomtext
03/08 SWELLING THE SIZE OF LEMONS UNDER LEFT ARMPIT AND SIDE IN GLANDS AND PAIN. 03/09 SPOT ON RIGHT TEMPLE LARGER THAN A QUARTER, BLISTERED RED & PAINFUL, SWELLING ALONG RIGHT SIDE OF FACE, IN JAW AND BEHIND EAR. 03/10 ITCHING AND PAIN IN SCALP, FOREHEAD, FACE, AND SAME SYMPTOMS AS DAY BEFORE. 03/11 UPON WAKING IN MORNING RIGHT EYE SWELLED UP AND BRUISED AND EYEBALL BRIGHT RED. PLUS SAME SYMPTOMS AS DAYS BEFORE. TOOK 4 WEEKS TO RECOVER FROM SORE AS IT HAD PUSS UNDER THE SCAB DAILY THAT HAD TO BE CLEANED. LEFT DEEP SCAR.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial pain
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DIABETIC TYPE 2; HIGH BLOOD PRESSURE; ACID RE-FLUX; MORBID OBESE
- Andere Medikamente
- METOPROLOL TART 50MG 2XDAY; HYDROCHLORO
- Allergien
- NUBAIN, SPRING AND FALL ALLERGIES
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 30.04.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear swelling
Pharyngeal swelling
Pruritus
Swollen tongue
Urticaria
Symptomtext
Per patient, states received Moderna vaccine on 4/30/22 and started experiencing itching and hives on legs and experiencing swelling in throat, tongue and ears.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- unknown.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- Unknown
- Allergien
- Per Chart no known drug allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 34,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Asthenia
COVID-19
SARS-CoV-2 test positive
Vomiting
Symptomtext
weakness, vomiting, COVID positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 17.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Urticaria
Symptomtext
I now suffer from chronic hives throughout my entire body. From neck to genitalia to feet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- I had to go to urgent care at a HCF and they put me on a steroid to help subside the hives. I still suffer from chronic hives and I am now take loratadine regularly.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- G6PD
- Andere Medikamente
- Fish oil, whole food protein, magnesium, and D3
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
URTICARIAL REACTION PERSISTANT SINCE FRIDAY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HTN, Dislipidemia
- Andere Medikamente
- losartan, crestor
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash erythematous
Rash papular
Rash pruritic
Symptomtext
Itchy rash; bumpy rash; Red rash This spontaneous case was reported by a consumer and describes the occurrence of RASH PRURITIC (Itchy rash), RASH PAPULAR (bumpy rash) and RASH ERYTHEMATOUS (Red rash) in a 61-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 083J21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: flu vaccine (Patient receives the flu vaccine regularly). Past adverse reactions to the above products included No adverse event with flu vaccine. On 08-Apr-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 09-Apr-2022, the patient experienced RASH PRURITIC (Itchy rash), RASH PAPULAR (bumpy rash) and RASH ERYTHEMATOUS (Red rash). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for Itching, at an unspecified dose and frequency and CORTISONE for Itching, at an unspecified dose and frequency. At the time of the report, RASH PRURITIC (Itchy rash), RASH PAPULAR (bumpy rash) and RASH ERYTHEMATOUS (Red rash) had not resolved. The action taken with mRNA-1273 (Spikevax) (Intramuscular) was unknown. No concomitant medications was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Extra dose administered
Fatigue
Influenza like illness
Injection site pain
Injection site rash
Pyrexia
Symptomtext
Fever, joint aches, very flu type feelings of needing to lay down and sleep and of course sore and and a rash where shot went in and below that point of my left arm. Took Tylenol and went to bed as soon as I got home from work Friday around 5:00 pm and slept for 3-4 hours. Went back to bed and slept until around 8:00 Saturday morning. Felt very tired all day Saturday and then on Sunday started coming around a little bit. So it started severely at 2:00 pm at work on Friday almost 24 hours after I received my vaccine booster and finally started feeling better by Sunday when I woke up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 09.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Extra dose administered
Pain in extremity
Vaccine positive rechallenge
Symptomtext
REACTION STARTED THE NIGHT OF THE ADMINISTRATION. PATIENT HAD SEVERE REDNESS OF UPPER ARM. REDNESS WAS FROM SHOULDER TO ELBOW. RED AND PAINFUL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A THIS SAME EVENT HAPPENED DURING 3RD VACCINE
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- COVID BOOSTER #3
- Staat
- TX
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Induration
Pruritus
Symptomtext
Itching, redness, hard, about 3 inches horizontal and 2 inches vertical
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Recently diagnosed diabetes (09/01/2021
- Andere Medikamente
- Metformin, Rosuvastatin, Prilosec, Allegra, Vitamin C and D, Trazodone, Celebrex, Tylenol
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 15.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Allergy test negative
Antibody test abnormal
Antinuclear antibody
Blood immunoglobulin E
Blood test normal
Blood thyroid stimulating hormone normal
C-reactive protein normal
Complement factor normal
Compression fracture
Full blood count normal
Mechanical urticaria
Red blood cell sedimentation rate normal
Tryptase
Symptomtext
Symptoms: diffuse dermatographic urticaria Treatments: 40 mg PO prednisone x5 days, 62.5 mg IM solumedrol x2 doses, 50 mg PO diphenhydramine in evenings, 10 mg PO certrizine in mornings (later switched to 60 mg fexofenadine daily)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- Blood tests drawn 3/31 show normal CBC (w/diff), CMP, sed rate, CRP (w/ C3+C4), TSH, and thyroid antibodies. Allergen panel is within normal limits, aside from elevated antibodies to dermatophagoides. Tryptase, ANA screen, and IgE antibody levels still pending.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Depression, Anxiety, ADHD
- Andere Medikamente
- 20 mg vilazodone 10 mg Adderall
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Symptomtext
lightheaded, dizzy, nausea approximately 5 minutes after administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site induration
Injection site nodule
Injection site pain
Injection site swelling
Injection site warmth
Symptomtext
Pain, redness, swelling and heat at injection site. Localized to left deltoid, there is a patch approximately 1" X 2" with a hard knot of tissue mass under skin patient stated that there were no other symptoms systemic. She said symptoms began about 2 hours after vaccination and progressively got worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- multivitamin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 22.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Atrial fibrillation
Blood test normal
Chest X-ray normal
Cough
Electrocardiogram abnormal
Fatigue
Feeling abnormal
Headache
Symptomtext
02/23/2022 A Day after my vaccine, I noticed brain fog, weakness, and fatigue like no energy at all. Coughing along with a headache as well. The entire time I have never had this amount of fatigue before and it has continued since. Headaches were very intermittent and coughing is still currently going on. 03/16/2022 I went to the ER, where the doctors established, I was in A-Fib. I then went to my doctor and had a heart monitor ordered and am currently wearing the heart monitor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- EKG diagnosed A-fib; Bloodwork: Stated everything was normal; Chest X-Ray looked good too.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multivitamins; B-12; D3; Calcium
- Allergien
- Penicillin; Azithromycin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site swelling
Injection site warmth
Symptomtext
Patient got covid moderna Booster vaccine 0.25 ml expiration ( 05/03/2022) on 03/15/2022 IM route deltoid muscle at 06:45 pm. on 03/16/2022 , the patient said that she had in the area of injection was swallowing and it was warm to the touch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, several liver disease untreated.
- Andere Medikamente
- Tylenol 500mg
- Allergien
- Not allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gait disturbance
Impaired work ability
Pain in extremity
Peripheral swelling
Symptomtext
SHE HAS A WOLLEN LEFT FOOT FOR 3 DAYS WITH VERY PAIN. SHE CALLED THIS MORNING AND AFTERNOON. SAYING SHE CAN NOT WALK ON LEFT FOOT. SHE MISSED WORKING, SELFOWNED BUSINESS. I SUGGEST HER TO GO TO NEAREST URGENT CARE OR EMERGENCY ROOM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- HYPERTENSION,
- Vorgeschichte
- NOT KNOWN
- Andere Medikamente
- NONE
- Allergien
- PENICILLIN, AND OTHERS
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 15.03.2022
- Impfdatum
- 13.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Erythema
Inflammation
Pruritus
Rash
Skin warm
Swelling
Urticaria
Symptomtext
Full body rash. Hives present as wheals, lumps, red inflamed lines. Presents intermittently over entire body. Hives are hot, swollen, and itchy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COVID 19 12/28/2020
- Vorgeschichte
- Eosinophilic Esophagitis Post-COVID Chronic Palpitations Postural Orthostatic Tachycardia Syndrome GERD
- Andere Medikamente
- Esomeprazole 20mg PO Daily Florinef 0.1mg PO BID
- Allergien
- Yellow Dye #5 and #6 Series of Environmental allergies Quaternion 15 Formaldehyde Mold Extracts Latex
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 09.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Pain
Pyrexia
Symptomtext
Fever, body aches and tiredness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site erythema
Injection site swelling
Injection site warmth
Pain in extremity
Symptomtext
Swelling and redness 10 inches around injection site, warm to the touch, painful arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Eczema
- Andere Medikamente
- Celebrex 200 mg BID
- Allergien
- Chlorhexidine gluconate, methylisothiazolinone
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 06.03.2022
- Impfdatum
- 03.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Dizziness
Hyperhidrosis
Illness
Injection site pain
Injection site swelling
Pain
Symptomtext
I had the same reaction for both doses: I was sick for two days, I had extreme sweating all night for two days, I had extreme body pain for two days, I felt dizzy/confused, and I had extreme injection site pain and swelling for three days. The reaction from this shot was worse than when I had COVID-19, twice. There were nights after the first dose but before the second dose that I woke up sweating. I still feel confused at times.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- There were none because you said it is normal.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High Blood Pressure, obesity
- Andere Medikamente
- Amlodapine/Benazapril 5/10, zyrtec, flonase, multivitamin, D3.
- Allergien
- X-ray contrast dye.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Erythema
Injection site pain
Injection site reaction
Pruritus
Swelling
Symptomtext
PT REPORTED PAIN AT INJECTION SITE STARTING THE NIGHT OF VACCINATION AND INJECTION SITE REACTION HAS GOTTEN WORSE IN THE PAST 2 DAYS (REDNESS, SWELLING AND ITCHING)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Fall
Headache
Tinnitus
Symptomtext
Loss of balance, Headaches, Ringing of the ears, Experienced loss of balance and fell during a walk.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Muscle test for reflex.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Allergies, Irregular Heartrate
- Andere Medikamente
- Nadolol (Beta blocker) 20mg 1x day, Loratadine 10mgs 1xday
- Allergien
- Aspirin, Advil, Augmentin
- Vorherige Impfungen
- Experienced Allergic reaction to the Influenza Vaccine, required treatments with Antibiotics and Steroids for multiple months.
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Nausea
Symptomtext
The patient's face felt numb all over including the forehead; Felt nauseous; This spontaneous case was reported by a consumer and describes the occurrence of HYPOAESTHESIA (The patient's face felt numb all over including the forehead) and NAUSEA (Felt nauseous) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 vaccination. Concurrent medical conditions included Asthma (patient has a history of mild asthma). Concomitant products included BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE (SUBOXONE) for an unknown indication. On 24-Feb-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 24-Feb-2022, the patient experienced HYPOAESTHESIA (The patient's face felt numb all over including the forehead) and NAUSEA (Felt nauseous). At the time of the report, HYPOAESTHESIA (The patient's face felt numb all over including the forehead) and NAUSEA (Felt nauseous) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No treatment medications were reported. After 15 minutes from vaccination, while the patient was walking out of the facility, the patient experienced the adverse events. The patient wanted to know whether those symptoms were normal or not.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma (patient has a history of mild asthma)
- Vorgeschichte
- -
- Andere Medikamente
- SUBOXONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 25.02.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Patient felt faint shortly after getting vaccination. I instructed the patient to put his head between his knees. He still felt like he was going to pass out so I had him lay on the ground with his feet on a chair. After a few minutes the patient was feeling better. He drank some water and was able to sit in the chair after about 10 minutes, then left the store.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 21.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Hypoaesthesia oral
Lymphadenopathy
Neck pain
Pain in extremity
Swollen tongue
Symptomtext
Swollen lymph node in Left clavicle area. Neck and Left arm pain. Tongue numbness or swelling. Bilateral hip pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- lyrica, mvi
- Allergien
- nickel
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Headache
Pyrexia
Urticaria
Symptomtext
Within hours of injection she was in bed 24 hours a day for 3 nights. Stabbing headaches, fever, chills and aches & pains in joints, urticaria
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 20.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose increased
Chills
Decreased appetite
Dizziness
Fatigue
Headache
Injection site erythema
Injection site pain
Pyrexia
Symptomtext
Redness/pain at site of injection, fever, chills, loss of appetite, dizziness, extreme tiredness, headache, and high blood sugar.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetes, asthma, high blood pressure, chronic back and knee pain
- Andere Medikamente
- celecoxib, lisinopril, dulaglutide, montelukast, paroxetine, simvastatin, Advair Diskus, glyburide, cyclobenzaprine, diclofenac, gabapentin, morphine 15 MG 12 hr. tablet, hydromorphone 2 MG
- Allergien
- Sulfamethoxazole-Trimethoprim, Clindamycin
- Vorherige Impfungen
- Covid-19 Moderna, both previous shots but symptoms not as severe.
- Staat
- MA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 11.02.2021
- Beginn
- 12.02.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
COVID-19
Cardiac murmur
Dizziness
Headache
Pyrexia
Symptomtext
I had a fever for 2 days, headache, and stomach ache. For 2 days a week I had dizzy spells. After a couple of days I reach out to my doctor to get some help. My doctor prescribe me some medicine that I take every other day. I just found out I had COVID. I did found out I had an heart murmur.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Irritable bowel syndrome Vertigo
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 18.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Pain
Pyrexia
Skin warm
Symptomtext
LUE red, warm 1 week after injection; erythema getting worse; pain. Reported fever/chills few days ago
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Reports Hx asthma and seizures, SUD, Hx gastric ulcers/GI bleed
- Andere Medikamente
- TUMS prn, lithium 600mg, Zyprexa 5mg, trazadone 100mg, Tylenol 650mg
- Allergien
- Pollen
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- U
- Eingang
- 17.02.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Peripheral swelling
Symptomtext
Left arm pain and swelling that occurred down the arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Erythema
Inappropriate schedule of product administration
Pain in extremity
Skin warm
Urticaria
Symptomtext
Pt said left arm was just sore Fri & Sat. Sunday Pt states she developed redness/welt on Sunday night. It was warm to the touch. Monday she noticed bruising on arm. Pt did state she on that side and doesnt know that contributed to brusisng. Pt stated today (Tuesday 2/15) that redness is going down & it is still warm to the touch but a lot better Pt states she takes Tylenol & Ibuprofen daily
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- 1st dose 3/11/21 2nd dose 4/12/21 3rd dose 9/10/21
- Aktuelle Erkrankungen
- Immune system problem
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Symptomtext
pt came on friday 2/11 with rash on her left arm saying that she got it after the shot, she tried benadryl and did not help, i called the office of her dr and left a msg for him to call us back to discuss the issue, i also recomended cortisone 10 cream to be applied, when i came back to work on2/15 i called her to follow up she said she is improving and she stopped the cortisone cream after 2 days, and never heard from the dr office, at the pharmacy the dr did not call back either, i told her to continue on the cream i asked her if something new has happened after this 3rd moderna booster shot since it is the 3rd dose and unlikely to get side effect specially she did not report anything after the 1st and 2nd dose that she took somewhere else, only today she told us the she got reactions after the second dose back in 4/9/2021 and went to urgent care and told her that this is normal side effects that is why she did not think to mention to us
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- diabetus,
- Andere Medikamente
- diabetic med
- Allergien
- no
- Vorherige Impfungen
- moderna 4/9/2021
- Staat
- NH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Symptomtext
Late on Feb 8th I started to get a tickle in my throat, the following day, by 8pm I had a 102 F. fever. I took 2 at home tests and both were positive. I called my Transplant team and they scheduled Monoclonal Antibodies for the following day 2/10/22 at 2pm. My fever broke over night and all symptoms worked there way out by 2/14/22. I AM IMMUNOCOMPROMISED. I got my 4th vaccine right on the 4 month mark per Dr. guidelines. I am very certain that I caught this at the grocery store the morning of 2/7/22 when I accidentally ran into someone coughing severely in the parking lot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- 2/9/22: 2 at home tests - both positive.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Liver Transplant in 04/06/2021.
- Andere Medikamente
- mycophenolate mofetil 250 mg capsule 2x day, pantoprazole DR 20 mg tablet 1x day, Senna 8.6mg tablet 1x day, sulfamethoxazole-trimethoprim 400-80 mg tablet 3x week, tacrolimus 1mg capsule 5x day, ursodiol 300 mg capsule 3x day, trazodone 10
- Allergien
- Tetanus Shot
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 12.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Nausea
Pyrexia
Vomiting
Symptomtext
ON SATURDAY EVENING, STARTED WITH CHILLS AND FEVER. BY SUNDAY MORNING, HE WAS THOSE 2 THINGS PLUS NAUSEA/VOMITING AND A MAJOR HEADACHE. HE SAID HE TOOK 3 BAYER ASPIRIN BACK AND BODY TABLETS AND STAYED IN BED ALL DAY. HE ALSO TOOK 1 REGLAN 10MG TABLET TO CALM HIS STOMACH. BY MONDAY HE WAS FEELING MUCH BETTER, JUST TIRED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Burning sensation
Joint stiffness
Pain
Symptomtext
Patient described about an hour after vaccination, her arm "felt on fire; burning sensation." She stated her elbow felt stiff. She reported no swelling or redness. No anaphylactic symptoms. Her PCP recommended she take Benadryl and ice her arm. Followed-up with patient next day. Her arm is sore, but no longer "burning." She is experiencing body aches, which is to be expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None required.
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- Arthritis, diabetes, migraine, insomnia
- Andere Medikamente
- Aspirin 81mg chew, Clopidogrel 75mg, Duloxetine 30mg, Furosemide 40mg, Gabapentin 800mg, Hydroxyzine pamoate 25mg, Lantus ? SoloSTAR, Metformin 500mg, Vitamin D3 50,000IU
- Allergien
- Lamictal, Lyrica, Plaquenil, Sulfa antibiotics, Topamax, Vancomycin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 10.02.2022
- 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: nein
Arthralgia
Chills
Dizziness
Headache
Insomnia
Lymph node pain
Lymphadenopathy
Myalgia
Pyrexia
Vomiting
Symptomtext
Vomiting, extreme dizziness, headache, severe muscle pain, severe joint pain, involuntary convulsions, fever, chills, insomnia, enlarged painful lymph nodes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 29.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Peripheral swelling
Vertigo
Symptomtext
The evening she received her vaccine, the patient experience arm swelling and red spots around the injection site. The following morning she developed vertigo. Her symptoms resolved within 7 days. The patient did experience the same side effects with doses #1 and #2, patient reports symptoms lasted about 8 weeks at that time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Similar reaction to doses 1 and 2
- Staat
- NC
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dizziness
Erythema
Injection site erythema
Injection site swelling
Injection site warmth
Nausea
Symptomtext
Injection site red, raised, extremely swollen, hot to touch. Redness is beginning to travel down. It is just above elbow and working around to the posterior side of arm. Dizziness accompanied with generalized weakness and nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Levothyroxine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Patient reports hives on both arms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- HIGH BLOOD PRESSURE, DIABETES, HIGH CHOLESTEROL
- Vorgeschichte
- DIABETES, HIGH BLOOD PRESSURE
- Andere Medikamente
- METFORMIN, LOSARTAN, SIMVASTATIN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 09.05.2023
- Impfdatum
- 15.02.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 16,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoxia
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOXIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoxia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 18.04.2023
- Impfdatum
- 06.04.2022
- Beginn
- 07.04.2023
- Tage bis Beginn
- 366,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated (J&J) with 1 booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 6,0
- Labordaten
- positive covid pcr 4/10/23
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Cancer (lung cancer s/p resection (>10 years ago); adenocarcinoma of the cecum ), CVA (with chronic dysphagia with aspiration with all consistencies per video fluoroscopy July 2019. ), Hyperlipidemia, Hypertension and Other (anxiety, depression, atrial fibrillation. )
- Andere Medikamente
- unknown
- Allergien
- morphine
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 17.04.2023
- Impfdatum
- 06.04.2022
- Beginn
- 03.01.2023
- Tage bis Beginn
- 272,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
I caught COVID-19 from a close friend. I had a very mild case but was prescribed PAXLOVID. After finishing the prescription, I caught COVID-19 again but it was a mild case again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Beclomethasone dipropionate
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 27.03.2023
- Impfdatum
- 30.12.2022
- Beginn
- 20.03.2023
- Tage bis Beginn
- 80,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 2 vaccines Moderna 3/1/22 Lot# 083J21A; Moderna 3/30/22 Lot# 083J21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 27.02.2023
- Impfdatum
- 17.02.2022
- Beginn
- 24.02.2023
- Tage bis Beginn
- 372,0
- 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 3/13/21 Lot# 038A21A; MOderna 4/10/21 Lot# 037B21A; Moderna 2/17/22 Lot# 083J21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 27.03.2021
- Beginn
- 15.09.2022
- Tage bis Beginn
- 537,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
COVID-19 immunisation
SARS-CoV-2 test
Vaccination failure
Symptomtext
CONFIRMED CLINICAL VACCINE FAILURE; CONFIRMED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient via other manufacturer (Pfizer) and concerned a 51 year old male. Initial information was processed along with additional information received on 26-DEC-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: drug allergy (Drug name not reported), restless leg, and asthma and other pre-existing medical conditions included: The patient was taking any other medication or products within 2 weeks of starting covid-19 treatment (Paxlovid). The patient received first dose covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1808978 expiry: UNKNOWN) 1 total, dose was not reported, administered on 27-MAR-2021 into left arm for covid-19 prophylaxis. Age at time of vaccination 49 years old. Concomitant medications included ropinirole. The patient received second dose of non-company suspect vaccine included: elasomeran (moderna covid-19 vaccine) (dose number in series 2) (form of admin, route of admin and were not reported, batch number: 026D21A expiry: UNKNOWN) dose was not reported, administered on 04-OCT-2021 into left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with elasomeran. The patient received third dose of non-company suspect vaccine included: elasomeran (dose number in series 2) (moderna covid-19 vaccine) (form of admin, route of admin and were not reported, batch number: 003F21A expiry: UNKNOWN) dose was not reported, administered on 01-NOV-2021 into left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with elasomeran (dose number in series 2). The patient received fourth dose of non-company suspect vaccine included: elasomeran (dose number in series 2) (moderna covid-19 vaccine) (form of admin, route of admin and were not reported, batch number: 083J21A expiry: UNKNOWN) and dose was not reported, administered on 25-APR-2022 into left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with elasomeran (dose number in series 2). The patient received fifth dose of non-company suspect vaccine included: elasomeran (dose number in series 3) (moderna covid-19 vaccine) (form of admin, route of admin, and batch number were not reported) dose was not reported, administered on 15-SEP-2022 at 12:00 into left arm for covid-19 prophylaxis which was a revaccination with different covid-19 vaccine (dose number in series 3). On an unspecified date in DEC-2022, the patient experienced covid-19 and had symptoms along with extreme fatigue which led to confirmed covid-19 infection (dose number in series 3) and confirmed clinical vaccine failure (dose number in series 1). On 04-DEC-2022, the patient had treated with non-company suspect drug Paxlovid (route of administration, batch number and expiry were not reported) dose and frequency were not reported until 09-DEC-2022 as treatment for covid-19. On 10-DEC-2022, the patient was tested negative. On 11-DEC-2022, the patient was tested positive and on 12-DEC-2022 tested positive more strongly. Patient's mild symptoms also had reappeared (mild chest congestion). At the time of report, the patient had not experienced a resurgence of the extreme fatigue which was felt during the first week of COVID-19. The action taken with covid-19 vaccine ad26.cov2.s, and elasomeran was not applicable. The patient had not recovered from confirmed covid-19 infection, and the outcome of confirmed clinical vaccine failure and revaccination with different covid-19 vaccine was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint: 90000264627.; Sender's Comments: V0: 20221251654- confirmed clinical vaccine failure. The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event. Specifically: SPECIAL SITUATIONS. Therefore, this event is considered inconsistent with vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221210; Test Name: COVID-19 VIRUS TEST; Test Result: Negative ; Test Date: 20221211; Test Name: COVID-19 VIRUS TEST; Test Result: Positive ; Test Date: 20221212; Test Name: COVID-19 VIRUS TEST; Test Result: Positive
- Aktuelle Erkrankungen
- Asthma; Drug allergy (Drug name not reported.); Legs restless
- Vorgeschichte
- Comments: The patient was taking any other medication or products within 2 weeks of starting covid-19 treatment (Paxlovid).
- Andere Medikamente
- ROPINIROLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 27.04.2022
- Beginn
- 25.11.2022
- Tage bis Beginn
- 212,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Ankle fracture
Ankle operation
Fall
Walking aid user
X-ray limb abnormal
Symptomtext
She got her 4th vaccine, did not have any reactions. She is associating her broken ankle as you can develop osteoporosis and her body is breaking without doing anything. On 11/25/22, that morning she took a bath and got up, and she weighed herself and weighed 153#. She went back into the bathroom she heard a loud cracking sound and she fell, and noticed that her ankle was broken and twisted. She crawled to get to her cell phone and called her son, and he came to the house. She managed to get to the front door to let him in and he more or less picked her up and carried her to the car. He took her to an ER clinic and they took her right in, said it was broken bad and needed surgery. She called Dr.'s office and they were not to be in the office until Monday. She was given some pain medicine from the ER and she took those. On Monday morning she called the office and they told her to get there as quick as she could and had to get a ride. At 9:00 AM she was at the clinic and at that point they took her back, she had her x-rays and they told her that she would have surgery the following Monday. She had her daughter take her to the surgery. She was told that she had multiple breaks and that it was super bad. In the last week she has not been in pain 24/7 and she is now using a walker and not well enough for her to go to therapy. Her next APT is on 1/12/23 at 11:00 AM for FU on the ankle. She thinks they are doing a disservice making people to get the shots.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ankle fracture
- Hospital-Tage
- -
- Labordaten
- X-rays and surgery.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Asthma as a child, diabetes.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.11.2022
- Impfdatum
- 30.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Feeling abnormal
Hypothyroidism
Symptomtext
low thyroid numbers; balance/equilibrium problem; felt like falling over; This spontaneous case was reported by a patient and describes the occurrence of HYPOTHYROIDISM (low thyroid numbers) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for an unknown indication. Concurrent medical conditions included Type 2 diabetes mellitus, Blood pressure high and Thyroid disorder. Concomitant products included METFORMIN and BISOPROLOL FUMARATE for an unknown indication. On 30-Mar-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Sep-2022, the patient received dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On an unknown date, the patient experienced HYPOTHYROIDISM (low thyroid numbers) (seriousness criterion medically significant), BALANCE DISORDER (balance/equilibrium problem) and FEELING ABNORMAL (felt like falling over). The patient was treated with LEVOTHYROXINE ongoing since an unknown date for Thyroid disorder, at a dose of 25 milligram(once). At the time of the report, HYPOTHYROIDISM (low thyroid numbers), BALANCE DISORDER (balance/equilibrium problem) and FEELING ABNORMAL (felt like falling over) was resolving. Patient had no allergies. Patient did not had COVID positive test or diagnosis. No treatment information was provided. Patient took the Pfizer for the bivalent booster as 3rd booster dose on 19Sep2022, lot number W25J2524 and did not have any problems, also had flu vaccine in Sep2022 but not the same day as the Covid-19 vaccine. Company comment: This spontaneous case concerns a patient of unknown age and gender, with no relevant medical history reported, who experienced the serious (medically significant) unexpected event of hypothyroidism on an unknown date after receiving a fourth dose of mRNA-1273. Patient states that on the last medical checkup, thyroid numbers were low, and levothyroxine was prescribed. No further information was available for medical reviewing. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. This case was linked to MOD-2022-667381 (Patient Link). Reporter did not allow further contact; Sender's Comments: This spontaneous case concerns a patient of unknown age and gender, with no relevant medical history reported, who experienced the serious (medically significant) unexpected event of hypothyroidism on an unknown date after receiving a fourth dose of mRNA-1273. Patient states that on the last medical checkup, thyroid numbers were low, and levothyroxine was prescribed. No further information was available for medical reviewing. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Balance disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood pressure high; Thyroid disorder; Type 2 diabetes mellitus
- Vorgeschichte
- -
- Andere Medikamente
- METFORMIN; BISOPROLOL FUMARATE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 27.10.2022
- Impfdatum
- 31.03.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 209,0
- 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 three vaccines Moderna 6/5/21 Lot# 022B21A; Moderna 7/3/21 Lot# 033C21A; Moderna 3/31/22 Lot# 083J21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 27.10.2022
- Impfdatum
- 09.04.2022
- Beginn
- 25.10.2022
- Tage bis Beginn
- 199,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Moderna 3/11/21 Lot# 023M20A; Moderna 4/11/21 Lot# 018B21A; Moderna 12/3/21 Lot# 013F21A; Moderna 4/9/22 Lot# 083J21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 19.10.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Symptomtext
First Outbreak of shingles.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 10.03.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 215,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 11.08.2022
- Impfdatum
- 09.02.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 177,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested positive for Covid, on PAXLOVID medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; factor five leiden
- Andere Medikamente
- Omeprazole; azelastine HCI; TRELEGY ELLIPTA; NASACORT; fish oil; iron; probiotics; multivitamin; vitamin D3; vitamin B12; calcium; biotin; diclofenac sodium; montelukast; red yeast rice; vitamin C; vitamin A; zinc; famotidine; magnesium; as
- Allergien
- Pineapple; kiwi; avocado; mushrooms
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 08.08.2022
- Impfdatum
- 06.02.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 164,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Nasal herpes
Skin lesion
Swelling face
Symptomtext
I experienced a sore inside my left nostril, my entire nose got swollen and red on the outside and they described the sore in my nose as herpes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Lupus
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 02.05.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 65,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
COVID-19 I tested positive for COVID-19 on July 6, 2022 only symptom I experienced was a runny nose. I was prescribed molnupiravir 200mg for 5 days. I started to feel better. I tested again on July 12, 2022 and the results were negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid testing
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamins; fish oil; melatonin; trazadone; cyclosporine;
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 10.03.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 141,0
- 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
hospitalization with covid; fully vaccinated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 1,0
- Labordaten
- positive covid pcr 7/29/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- CAD s/p recent PCI of LAD paroxysmal Afib s/p PM HLD Hypothyroidism chronic hypoxemic respiratory failure on 2L O2 NC
- Andere Medikamente
- unknown
- Allergien
- aspirin, morphine, IV dye
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 04.03.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 124,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Extra dose administered
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Confirmed breakthrough case: COVID-19 (Moderna) 1 02/16/2021 Moderna 007M20A COVID-19 (Moderna) 2 03/16/2021 Moderna 010A21A COVID-19 (Moderna) 3 08/25/2021 Moderna 09D21A COVID-19 (Moderna) 4 03/04/2022 Moderna 083J21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID Lab - Test 7/6/2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 81,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
COVID-19
Electrocardiogram abnormal
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
See above. Reporting break through COVID (per VAERS phone instructions) after 2 vaccines and 2 boosters. Adverse reaction positive COVID test and A-Fib.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- 7-1-22 EKG confirming A-Fib.
- Aktuelle Erkrankungen
- Trying to report break through COVID infection per instructions via phone from VAERS on 7/11/22. Moderna Vaccines 1/11/21, 2/8/21, Moderna Boosters 11/27/21, 4/8/22. POSITIVE COVID test 6/28/22., and subsequent ER visit due to A-Fib (new diagnosis) 6/30/22., believed to be caused by COVID infection.
- Vorgeschichte
- IBS, Pancreatic Insufficiency
- Andere Medikamente
- Tylenol 500 mg on day of ER visit (6/30/22)
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 58,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient received booster 1 month after primary; This spontaneous case was reported by a pharmacist and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received booster 1 month after primary) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 004M21A, 083J21A and 083J21A) for COVID-19 vaccination. Patient did not have allergies to medications, food and other products. On 06-Apr-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 03-May-2022, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .5 milliliter. On 03-Jun-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .25 milliliter. On 03-Jun-2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received booster 1 month after primary). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received booster 1 month after primary) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient was not taking other medication. It was reported that Patient did not report having side effects. The expiration dates were not provided. Patient HCP is unaware patient received the 1st booster a month after primary. No treatment information reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient did not have allergies to medications, food and other products.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 05.07.2022
- Impfdatum
- 23.02.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 125,0
- 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 three doses Moderna 2/8/212 Lot# 027L20; Moderna 3/8/21 Lot# 010M20A; Moderna 2/23/22 Lot# 083J21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product use issue
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine dose deemed effective, no re-vaccination needed. Moderna Case ID Unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product use issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine dose deemed effective, no re-vaccination needed. Moderna Case ID Unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine dose deemed effective, no re-vaccination needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine dose deemed effective, no re-vaccination needed. Moderna Case ID Unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine dose deemed effective, no re-vaccination needed. Moderna Case ID Unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine dose deemed effective, no re-vaccination needed. Moderna Case ID Unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine dose deemed effective, no re-vaccination needed. Moderna Case ID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine dose deemed effective, no re-vaccination needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine dose deemed effective, no re-vaccination needed. Moderna Case ID Unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine dose deemed effective, no re-vaccination needed. Moderna Case ID Unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine deemed effective and no re-vaccination needed Moderna Case Unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine deemed effective and no re-vaccination needed Moderna Case ID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna, and vaccine deemed effective and no re-vaccination needed. Moderna Case ID Unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine deemed effective and no re-vaccination needed Moderna Case ID Unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine deemed effective and no re-vaccination needed Moderna Case ID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Moderna and vaccine deemed effective and no re-vaccination needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after use by date. Efficacy study done by Modera and vaccine deemed effective and no re-vaccination needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 83,0
- Geschlecht
- U
- Eingang
- 15.06.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- 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 storage error
Symptomtext
vaccine was in refrigerator on 07-FEB-2022 and administered on 20-APR-2022; Vaccine was administered beyond the use date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered beyond the use date) and PRODUCT STORAGE ERROR (vaccine was in refrigerator on 07-FEB-2022 and administered on 20-APR-2022) in an 83-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 20-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered beyond the use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vaccine was in refrigerator on 07-FEB-2022 and administered on 20-APR-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered beyond the use date) and PRODUCT STORAGE ERROR (vaccine was in refrigerator on 07-FEB-2022 and administered on 20-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 reported Patient had received total three doses. This dose was a booster. It was reported that as per Moderna lot analysis regarding doses administered on 20-APR-2022 from lot number 083J21A, Moderna cannot guarantee patients received full protection against the Covid-19 virus. No treatment medications were reported Most recent FOLLOW-UP information incorporated above includes: On 09-Jun-2022: Follow-up received contains non significant Information. Narrative updated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 87,0
- Geschlecht
- U
- Eingang
- 14.06.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- 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 put in the fridge on 07Feb2022 and doses were administered on 20APR2022; expired doses of Moderna COVID-19 were administered beyond the beyond use date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired doses of Moderna COVID-19 were administered beyond the beyond use date) and PRODUCT STORAGE ERROR (Vaccine put in the fridge on 07Feb2022 and doses were administered on 20APR2022) in an 87-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. 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 (expired doses of Moderna COVID-19 were administered beyond the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine put in the fridge on 07Feb2022 and doses were administered on 20APR2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired doses of Moderna COVID-19 were administered beyond the beyond use date) and PRODUCT STORAGE ERROR (Vaccine put in the fridge on 07Feb2022 and doses were administered on 20APR2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. As per report Patient received 2nd booster dose No concomitant medications were provided. For LOT 083J21A the vials were initially stored in the refrigerator On 07 FEB 2022 ,. The vial did not undergo any 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
- NV
- Alter
- 68,0
- Geschlecht
- U
- Eingang
- 14.06.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- 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 was put in the fridge on 07-Feb-2022 and doses were administered on 12-Apr-2022; Expired doses of Moderna COVID-19 were administered beyond the beyond use date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date) and PRODUCT STORAGE ERROR (Vaccine was put in the fridge on 07-Feb-2022 and doses were administered on 12-Apr-2022) in a 68-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was put in the fridge on 07-Feb-2022 and doses were administered on 12-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date) and PRODUCT STORAGE ERROR (Vaccine was put in the fridge on 07-Feb-2022 and doses were administered on 12-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. It was reported that, the patient received total 4 doses, and this was 2nd booster dose. On 07-Feb-2022, the vials were initially stored in the refrigerator. The vial did not undergo any temperature excursions. No treatment medications were provided. Most recent FOLLOW-UP information incorporated above includes: On 09-Jun-2022: Follow-up received contains no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 70,0
- Geschlecht
- U
- Eingang
- 14.06.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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 storage error
Symptomtext
Vial was stored in refrigerator on 07-Feb-2022 and administered on 01-Apr-2022; Expired dose administered/Vaccine was administered beyond the beyond use date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered/Vaccine was administered beyond the beyond use date) and PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 07-Feb-2022 and administered on 01-Apr-2022) in a 70-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 01-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered/Vaccine was administered beyond the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 07-Feb-2022 and administered on 01-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered/Vaccine was administered beyond the beyond use date) and PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 07-Feb-2022 and administered on 01-Apr-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 not reported. It was reported that, patient received total 3 doses and this was booster dose. Vial did not undergo any temperature excursion. No treatment medications were provided. Most recent FOLLOW-UP information incorporated above includes: On 09-Jun-2022: Live Follow up received contains non significant information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 62,0
- Geschlecht
- U
- Eingang
- 14.06.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- 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
For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022; Expired doses of Moderna COVID-19 were administered beyond the beyond use date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date.) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022) in a 62-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date.) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022) 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. It was reported that patient received total 4 doses, Vial did not undergo any temperature excursion. No treatment medication was reported by reporter. Most recent FOLLOW-UP information incorporated above includes: On 09-Jun-2022: Follow up received contain Non significant information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 70,0
- Geschlecht
- U
- Eingang
- 14.06.2022
- 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 was initially stored in the refrigerator on 07-Feb-2022 and administered on 11-Mar-2022; Expired doses administered; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses administered) and PRODUCT STORAGE ERROR (Vaccine was initially stored in the refrigerator on 07-Feb-2022 and administered on 11-Mar-2022) in a 70-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 11-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was initially stored in the refrigerator on 07-Feb-2022 and administered on 11-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses administered) and PRODUCT STORAGE ERROR (Vaccine was initially stored in the refrigerator on 07-Feb-2022 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. No concomitant medications were reported. It was reported that, the vaccine was administered beyond the beyond use date. The vial was initially stored in the refrigerator on 07-Feb-2022. The vial did not undergo any temperature excursions. No treatment medications were provided. Most recent FOLLOW-UP information incorporated above includes: On 09-Jun-2022: Live Follow-up received contain Non significant information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 59,0
- Geschlecht
- U
- Eingang
- 14.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- 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 storage error
Symptomtext
For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 06-Apr-2022; Vaccines were administered beyond use date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccines were administered beyond use date) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 06-Apr-2022) in a 59-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccines were administered beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 06-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccines were administered beyond use date) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 06-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications details were not reported by the reporter. Patient took booster of Moderna and took total 3 doses. Lot number 083J21A was refrigerated on 7-Feb-2022. Vial did not undergo any temperature excursion It was reported that as per Moderna lot analysis regarding doses administered on March 11, 2022 and March 16, 2022 from lot number 033H21A, and doses administered on April 20, 2022 from lot number 083J21A, Moderna cannot guarantee patients received full protection against the Covid-19 virus. Treatment details was not reported by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 09-Jun-2022: Follow up received contains No new information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 68,0
- Geschlecht
- U
- Eingang
- 14.06.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- 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
Kept in fridge on 07-Feb-2022 and administered on 08-Apr-2022; expired doses of Moderna COVID-19 were administered beyond the beyond use date; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT STORAGE ERROR (Kept in fridge on 07-Feb-2022 and administered on 08-Apr-2022) and EXPIRED PRODUCT ADMINISTERED (expired doses of Moderna COVID-19 were administered beyond the beyond use date) in a 68-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired doses of Moderna COVID-19 were administered beyond the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Kept in fridge on 07-Feb-2022 and administered on 08-Apr-2022). At the time of the report, PRODUCT STORAGE ERROR (Kept in fridge on 07-Feb-2022 and administered on 08-Apr-2022) and EXPIRED PRODUCT ADMINISTERED (expired doses of Moderna COVID-19 were administered beyond the beyond use date) 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. It was reported that the patient received total 4 doses and the dose received on 8-Apr-2022 was the second booster. The vials were kept in refrigerator on 07-Feb-2022 and administered on 8-Apr-2022. The vial did not undergo any temperature excursions 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
- NV
- Alter
- 86,0
- Geschlecht
- U
- Eingang
- 13.06.2022
- Impfdatum
- 18.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Expired doses administered; Vaccine put in the fridge on 07Feb2022 and doses were administered on 18Apr2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses administered) and PRODUCT STORAGE ERROR (Vaccine put in the fridge on 07Feb2022 and doses were administered on 18Apr2022) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 18-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses administered) and PRODUCT STORAGE ERROR (Vaccine put in the fridge on 07Feb2022 and doses were administered on 18Apr2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses administered) and PRODUCT STORAGE ERROR (Vaccine put in the fridge on 07Feb2022 and doses were administered on 18Apr2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication reported. No treatment medication reported. On 07-Feb-2022 this vial was put in refrigerator and was administered on 18-Apr-2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 77,0
- Geschlecht
- U
- Eingang
- 13.06.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- 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
For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022; Expired doses of Moderna COVID-19 were administered beyond the beyond use date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022) in a 77-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 11-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022) 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 Patient took 2nd booster dose of Moderna and took total 4 doses. Lot number 083J21A was refrigerated on 7-Feb-2022. Vial did not undergo any temperature excursion No treatment medication was reported by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 76,0
- Geschlecht
- U
- Eingang
- 13.06.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- 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
For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022; Expired doses of Moderna COVID-19 were administered beyond the beyond use date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date.) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022) in a 76-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date.) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Patient took total 4 doses. Took booster 2 dose of Moderna on 12-Apr-2022. Patient received vaccine on 07-Feb-2022., Lot number 083J21A was refrigerated on 7-Feb-2022. Vial did not undergo any temperature excursion. Treatment information was not provided. This case was linked to MOD-2022-584673, MOD-2022-584679 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 64,0
- Geschlecht
- U
- Eingang
- 13.06.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- 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 storage error
Symptomtext
For lot 083J21A refrigeration was on 07-Feb-2022, and date of administration on 01-Apr-2022; Expired doses administered beyond the BUD; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses administered beyond the BUD) and PRODUCT STORAGE ERROR (For lot 083J21A refrigeration was on 07-Feb-2022, and date of administration on 01-Apr-2022) in a 64-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 01-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses administered beyond the BUD). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (For lot 083J21A refrigeration was on 07-Feb-2022, and date of administration on 01-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses administered beyond the BUD) and PRODUCT STORAGE ERROR (For lot 083J21A refrigeration was on 07-Feb-2022, and date of administration on 01-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Patient took booster of Moderna and took total 3 doses. Lot number 083J21A was refrigerated on 7-Feb-2022. Vial did not undergo any temperature excursion. 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
- NV
- Alter
- 48,0
- Geschlecht
- U
- Eingang
- 13.06.2022
- 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
Symptomtext
Expired doses administered; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses administered) in a 48-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 29-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided by the reporter No temperature excursion was reported. No treatment medication was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 71,0
- Geschlecht
- U
- Eingang
- 13.06.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- 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
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses administered) and PRODUCT STORAGE ERROR (Initially vaccine was stored in fridge on 07-Feb-2022and was administered on 08-APR-2022 after more than 30 days) in a 71-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Initially vaccine was stored in fridge on 07-Feb-2022and was administered on 08-APR-2022 after more than 30 days). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses administered) and PRODUCT STORAGE ERROR (Initially vaccine was stored in fridge on 07-Feb-2022and was administered on 08-APR-2022 after more than 30 days) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. It was reported that, the patient received total 4 doses and this was second booster dose. On 07-Feb-2022, the vials were initially stored in the refrigerator. The vial did not undergo any temperature excursions. Treatment information was not provided. This case was linked to MOD-2022-584673 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 24,0
- Geschlecht
- U
- Eingang
- 11.06.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
This spontaneous case reported by an other healthcare professional, describes the occurrence of administered expired product (administered expired dose) and product storage error (vial refrigerated Feb 7, 2022; administered Mar 29, 2022) in a 24-year-old patient, of an unknown gender, who received mRNA-1273 (Moderna COVID-19 vaccine, batch/lot# 083J21A) for COVID-19 immunization. No medical history reported. On Mar 29, 2022, patient received the first dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On Mar 29, 2022, patient administered expired product (administered expired dose). On an unknown date, patient experienced product storage error (vial refrigerated Feb 7, 2022; administered Mar 29, 2022). At the time of the report, administered expired product (administered expired dose) and product storage error (vial refrigerated Feb 7, 2022; administered Mar 29, 2022) outcome: unknown. The reporter did not provide any causality assessments, concomitant medication or treatment information. Vial initially stored in refrigerator Feb 7, 2022, did not undergo any temperature excursions. This case linked to MOD-2022-584679 (patient link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 63,0
- Geschlecht
- U
- Eingang
- 11.06.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- 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 storage error
Symptomtext
For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022; Expired doses of Moderna COVID-19 were administered beyond the beyond use date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date.) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022) in a 63-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 13-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date.) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022) 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. Patient took booster dose of Moderna and took total 3 doses.Patient received vaccine on 07 Feb 2022. Lot number 083J21A was refrigerated on 7-Feb-2022. Vial did not undergo any temperature excursion. No treatment medication was reported by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 65,0
- Geschlecht
- U
- Eingang
- 11.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- 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 storage error
Symptomtext
Lot 083J21A put in the fridge on 07-Feb-2022 and was administered on 06-Apr-2022; Expired dose of Moderna COVID-19 was adminsitered beyond the beyond use date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose of Moderna COVID-19 was adminsitered beyond the beyond use date) and PRODUCT STORAGE ERROR (Lot 083J21A put in the fridge on 07-Feb-2022 and was administered on 06-Apr-2022) in a 65-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 06-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose of Moderna COVID-19 was adminsitered beyond the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Lot 083J21A put in the fridge on 07-Feb-2022 and was administered on 06-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose of Moderna COVID-19 was adminsitered beyond the beyond use date) and PRODUCT STORAGE ERROR (Lot 083J21A put in the fridge on 07-Feb-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. Concomitant medication of the patient was not reported. The vial did not undergo any temperature excursion. No treatment information was provided by the reporter. This case was linked to MOD-2022-584673 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 70,0
- Geschlecht
- U
- Eingang
- 11.06.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- 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
Vials put in fridge on 07Feb2022 and administered on 13 Apr 2022; expired doses of Moderna COVID-19 administered beyond the beyond use date; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT STORAGE ERROR (Vials put in fridge on 07Feb2022 and administered on 13 Apr 2022) and EXPIRED PRODUCT ADMINISTERED (expired doses of Moderna COVID-19 administered beyond the beyond use date) in a 70-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) 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 (expired doses of Moderna COVID-19 administered beyond the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vials put in fridge on 07Feb2022 and administered on 13 Apr 2022). At the time of the report, PRODUCT STORAGE ERROR (Vials put in fridge on 07Feb2022 and administered on 13 Apr 2022) and EXPIRED PRODUCT ADMINISTERED (expired doses of Moderna COVID-19 administered beyond the beyond use date) outcome was unknown. 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 total 4 doses. Total, 22 doses were administered from a few different vials. The vial did not undergo any temperature excursions. 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
- NV
- Alter
- 91,0
- Geschlecht
- U
- Eingang
- 11.06.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- 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
For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022; Expired doses administered beyond the BUD; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses administered beyond the BUD) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022) in a 91-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses administered beyond the BUD). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses administered beyond the BUD) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Patient took 2nd booster of Moderna and took total 4 doses. Lot number 083J21A was refrigerated on 7-Feb-2022. Vial did not undergo any temperature excursion. 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
- NV
- Alter
- 86,0
- Geschlecht
- U
- Eingang
- 11.06.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
This spontaneous case reported by an other healthcare professional, describes the occurrence of administered expired product (expired dose administered beyond-use-date) and product storage error (vial refrigerated Feb 7, 2022; administered Apr 18, 2022) in an 86-year-old patient, of an unknown gender, who received mRNA-1273 (Moderna COVID-19 vaccine, batch/lot# 083J21A) for COVID-19 immunization. No medical history reported. On Apr 18, 2022, patient received the fourth dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On Apr 18, 2022, patient administered expired product (expired dose administered beyond-use-date). On an unknown date, patient experienced product storage error (vial refrigerated Feb 7, 2022; administered Apr 18, 2022). At the time of the report, administered expired product (expired dose administered beyond-use-date) and product storage error (vial refrigerated Feb 7, 2022; administered Apr 18, 2022) outcome: unknown. The reporter did not provide any causality assessments, concomitant medication or treatment information. The patient received a total of 4 doses (second booster). The vial initially stored in the refrigerator Feb 7, 2022, did not undergo temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 69,0
- Geschlecht
- U
- Eingang
- 11.06.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- 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
For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022; Expired doses administered beyond the BUD; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses administered beyond the BUD) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022) in a 69-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses administered beyond the BUD). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses administered beyond the BUD) and PRODUCT STORAGE ERROR (For lot 083J21A put in the fridge on 07Feb2022, and date of administration on 12-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Patient took 2nd booster of Moderna and took total 4 doses. Lot number 083J21A was refrigerated on 7-Feb-2022. Vial did not undergo any temperature excursion. 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
- NV
- Alter
- 53,0
- Geschlecht
- U
- Eingang
- 11.06.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- 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 storage error
Symptomtext
Initially vaccine was stored in fridge on 07 Feb 2022and was administered on 20 APR 2022 after more than 30 days; Expired doses of Moderna COVID-19 were administered beyond the beyond use date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date.) and PRODUCT STORAGE ERROR (Initially vaccine was stored in fridge on 07 Feb 2022and was administered on 20 APR 2022 after more than 30 days) in a 53-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 20-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Initially vaccine was stored in fridge on 07 Feb 2022and was administered on 20 APR 2022 after more than 30 days). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired doses of Moderna COVID-19 were administered beyond the beyond use date.) and PRODUCT STORAGE ERROR (Initially vaccine was stored in fridge on 07 Feb 2022and was administered on 20 APR 2022 after more than 30 days) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medications were provided. It was reported that, the patient received total 3 doses and this was booster dose. Vial did not undergo any temperature excursions. No treatment medications were provided. This case was linked to MOD-2022-584679, MOD-2022-584673 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 08-Jun-2022: Follow-up information was received includes patient demographics, event product storage error added and reporter details updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 23,0
- Geschlecht
- U
- Eingang
- 09.06.2022
- Impfdatum
- 19.04.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Expired product administered
Product storage error
SARS-CoV-2 test
Symptomtext
Covid-19; Vaccine was expired 2 weeks before the administration date and was stored and refrigerator on 17-May-2022; Vaccine was administered on 17-May-2022 and found out that the vaccine had been expired 2 weeks ago; This spontaneous case was reported by a nurse and describes the occurrence of COVID-19 (Covid-19), PRODUCT STORAGE ERROR (Vaccine was expired 2 weeks before the administration date and was stored and refrigerator on 17-May-2022) and EXPIRED PRODUCT ADMINISTERED (Vaccine was administered on 17-May-2022 and found out that the vaccine had been expired 2 weeks ago) in a 23-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch nos. 083J21A and 083J21A) for COVID-19 vaccination. Patient had no known drug allergies (NKDA). On 19-Apr-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 17-May-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 17-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered on 17-May-2022 and found out that the vaccine had been expired 2 weeks ago). On an unknown date, the patient experienced COVID-19 (Covid-19) and PRODUCT STORAGE ERROR (Vaccine was expired 2 weeks before the administration date and was stored and refrigerator on 17-May-2022). At the time of the report, COVID-19 (Covid-19), PRODUCT STORAGE ERROR (Vaccine was expired 2 weeks before the administration date and was stored and refrigerator on 17-May-2022) and EXPIRED PRODUCT ADMINISTERED (Vaccine was administered on 17-May-2022 and found out that the vaccine had been expired 2 weeks ago) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: positive (Positive) Positive. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Number of doses/vials: 26 doses some were primary doses and some boosters. On 17-May-2022, the vial was stored in fridge. The vial did not undergo any temperature excursions. Reporter stated that none of patient had reported side effects. No treatment information was reported. Company Comment: This spontaneous case concerns a 23-year-old patient of unknown gender with no medical history reported who experienced the unexpected, non-serious adverse event of special interest of COVID-19 which occurred on unspecified interval after receiving the second dose of mRNA-1273 vaccine. Product storage error and Expired product administered were reported as additional events. Patient received the first dose of mRNA-1273 vaccine within the recommended dosing interval of 28 days. The onset date of COVID-19, clinical course, diagnostic investigations, and treatment details were not reported. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 23-year-old patient of unknown gender with no medical history reported who experienced the unexpected, non-serious adverse event of special interest of COVID-19 which occurred on unspecified interval after receiving the second dose of mRNA-1273 vaccine. Product storage error and Expired product administered were reported as additional events. Patient received the first dose of mRNA-1273 vaccine within the recommended dosing interval of 28 days. The onset date of COVID-19, clinical course, diagnostic investigations, and treatment details were not reported. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient had no known drug allergies (NKDA).
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Clinic accidently administered the Moderna COVID-19 vaccine to a 14 year old patient for their initial dose of their primary series on 21APR2022. Due to the patient's age (under 18 years) they were not eligible to receive this type of COVID-19 vaccine per CDC and Agency guidelines. This vaccination error was discovered on 01JUN2022 by immunizations team when the mother of patient came into to get the second dose shot of the their primary series. The mother of the patient was informed about the error and a Agency and VAERS report submitted. The Agency was contacted on 01JUN2022 to get further guidance and recommendations. The mother of the patient stated that her 14 year old daughter did not experience any adverse reactions to the initial Moderna COVID-19 vaccination that was administered on 21APR2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 22.03.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 77,0
- Dosis
- 2
- 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
- OH
- Alter
- 38,0
- Geschlecht
- U
- Eingang
- 08.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- 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
Patient received Moderna vaccine that had been expired for 2 weeks; Patient received Moderna vaccine that had been expired for 2 weeks; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received Moderna vaccine that had been expired for 2 weeks) and PRODUCT STORAGE ERROR (Patient received Moderna vaccine that had been expired for 2 weeks) in a 37-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch nos. 083J21A and 083J21A) for COVID-19 vaccination. The patient had no known drug allergy (NKDA). The patient was not had positive for COVID-19. On 17-May-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 17-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received Moderna vaccine that had been expired for 2 weeks). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Patient received Moderna vaccine that had been expired for 2 weeks). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received Moderna vaccine that had been expired for 2 weeks) and PRODUCT STORAGE ERROR (Patient received Moderna vaccine that had been expired for 2 weeks) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported It was reported that since the expiration date was not written on the vial, thus it was not noticed it had already expired. On an unknown date the vial was initially stored in the refrigerator. The vial did not undergo any temperature excursions. The vaccine stored in fridge on 17-May-2022. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no known drug allergy (NKDA). The patient was not had positive for COVID-19.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 45,0
- Geschlecht
- U
- Eingang
- 08.06.2022
- Impfdatum
- 19.04.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
SARS-CoV-2 test
Symptomtext
Expired vaccine was stored in refrigerator on 17-May-2022; administered the Moderna COVID-19 vaccine and found out that the vaccine had been expired for 2 weeks; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered the Moderna COVID-19 vaccine and found out that the vaccine had been expired for 2 weeks) and PRODUCT STORAGE ERROR (Expired vaccine was stored in refrigerator on 17-May-2022) in a 45-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch nos. 083J21A and 083J21A) for COVID-19 vaccination. The patient's past medical history included COVID-19. Concurrent medical conditions included Allergy to antibiotic (Sulfa). On 19-Apr-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 17-May-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 17-May-2022, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (administered the Moderna COVID-19 vaccine and found out that the vaccine had been expired for 2 weeks). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Expired vaccine was stored in refrigerator on 17-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered the Moderna COVID-19 vaccine and found out that the vaccine had been expired for 2 weeks) and PRODUCT STORAGE ERROR (Expired vaccine was stored in refrigerator on 17-May-2022) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: positive (Positive) Positive. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. The reporter reported that since the expiration date was not written on the vial they did not noticed that the vaccine had already expired. The vial did not undergo any temperature excursions. The patient did not report any side effects. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Virus test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Allergy to antibiotic (Sulfa)
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 25,0
- Geschlecht
- U
- Eingang
- 08.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- 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
SARS-CoV-2 test
Symptomtext
Received the Moderna COVID 19 vaccine after manufacturer date of expiry; Vaccine had been expired for 2 weeks and stored in fridge on 17 May 2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received the Moderna COVID 19 vaccine after manufacturer date of expiry) and PRODUCT STORAGE ERROR (Vaccine had been expired for 2 weeks and stored in fridge on 17 May 2022) in a 25-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 083J21A) for COVID-19 vaccination. Patient had no known drug allergies. On 17-May-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 17-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received the Moderna COVID 19 vaccine after manufacturer date of expiry) and PRODUCT STORAGE ERROR (Vaccine had been expired for 2 weeks and stored in fridge on 17 May 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received the Moderna COVID 19 vaccine after manufacturer date of expiry) and PRODUCT STORAGE ERROR (Vaccine had been expired for 2 weeks and stored in fridge on 17 May 2022) outcome was unknown. 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. Concomitant product use was not provided by the reporter. The health care professional (HCP) stated that they administered the Moderna COVID 19 vaccine on 17-May-2022 and found out that the vaccine had expired for 2 weeks. The HCP explained that since the expiration date was not written on the vial, they did not notice that it had already expired. On 17-May-2022, the vial was initially stored in the refrigerator and the vial did not undergo any temperature excursions. The patient did not report any side effects. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient had no known drug allergies.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 24.04.2022
- Beginn
- 24.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Under age for the Modera Vaccine-patient had no adverse reactions to vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- 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
Symptomtext
A patient received an expired dose of the Moderna COVID-19 vaccine; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (A patient received an expired dose of the Moderna COVID-19 vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 083J21A) for COVID-19 vaccination. No Medical History information was reported. On 10-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 10-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (A patient received an expired dose of the Moderna COVID-19 vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (A patient received an expired dose of the Moderna COVID-19 vaccine) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant drug was reported. Number of doses or vials reported as 1 dose but there may be more. Date the vial was initially stored in the refrigerator was unknown by the hcp. Vial did not undergoes 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
- WI
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- 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
No adverse event
Product administered to patient of inappropriate age
Symptomtext
The Moderna covid vaccination was given to an underage patient. Patient was 13 years old at time of vaccination. No adverse reaction noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Generalized anxiety disorder Social Anxiety disorder
- Andere Medikamente
- Lamotrigine, Propranolol and Trazodone
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 11.05.2022
- Beginn
- 11.05.2022
- 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
No adverse event
Symptomtext
No adverse reaction to the injection at given time. Administrator realized vaccine was expired after administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Seizure Disorder, Mild Intermittent Asthma without complications, constipation and seasonal allergies.
- Andere Medikamente
- Fish Oil 500 mg, Amitza 8 mcg, Clonazepam .05 mg, Lactulose 10 mg
- Allergien
- Morphine, Augmentin and Diflucan
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 11.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- 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
Symptomtext
Patient received a booster dose of the Moderna Covid-19 vaccine on 04-May-2022 lot number which was expired on 03-May-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received a booster dose of the Moderna Covid-19 vaccine on 04-May-2022 lot number which was expired on 03-May-2022) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received a booster dose of the Moderna Covid-19 vaccine on 04-May-2022 lot number which was expired on 03-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received a booster dose of the Moderna Covid-19 vaccine on 04-May-2022 lot number which was expired on 03-May-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. Information on first two doses was unknown. Patient received a booster dose of the expired Moderna Covid-19 vaccine. It was not known which booster dose the patient received and also not known which arm the injection was received in. No other side effects or adverse events were known. No treatment medications were reported. This case was linked to MOD-2022-561462, MOD-2022-560262, MOD-2022-561464, MOD-2022-560259 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- 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
Dose of vaccine give 2 days after the expiration date on qr code of vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- 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
Dose given 2 days after vaccine expiration date on code
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- 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
Gave vaccine 2 days after expiration date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- 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 given vaccine 2 days after expiration date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- 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
Vaccine administered 2 days after the expiration date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- 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
Date given 2 days after expiration date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- 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
No adverse event
Symptomtext
The vial used to give the vaccine expired yesterday (5/3/2022). It was kept under appropriate conditions, and the patient has had no untoward effects thus far.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 100,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 23.03.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 35,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental underdose
Inappropriate schedule of product administration
Symptomtext
2nd dose administered as half dose (0.25ml) instead of full dose (0.5ml); 1st dose: 23Mar2022 ,2nd dose: 27Apr2022 .36 days; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL UNDERDOSE (2nd dose administered as half dose (0.25ml) instead of full dose (0.5ml)) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st dose: 23Mar2022 ,2nd dose: 27Apr2022 .36 days) in a 100-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 027L21A and 083J21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Mar-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 27-Apr-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to .25 milliliter. On 27-Apr-2022, the patient experienced ACCIDENTAL UNDERDOSE (2nd dose administered as half dose (0.25ml) instead of full dose (0.5ml)) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st dose: 23Mar2022 ,2nd dose: 27Apr2022 .36 days). At the time of the report, ACCIDENTAL UNDERDOSE (2nd dose administered as half dose (0.25ml) instead of full dose (0.5ml)) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st dose: 23Mar2022 ,2nd dose: 27Apr2022 .36 days) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
employee forgot her vaccination card and 2nd booster was administered prior to her 4 months from booster shot back in 01/20/22. No reactions to report
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
Patient attended the Covid clinic and requested a Moderna vaccine. The majority of the patients were receiving Pfizer. In order to prevent the wrong vaccine from being administered the consent form was marked in big letters Moderna. I assumed the paperwork had been checked, asked patient about allergies and previous reactions and she noted no reactions or side effects. I gave the injection and when recording the date on her Vaccine card it was noted that her last vaccine booster was administered on 2/1/22. No adverse events have been noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- No adverse events have been noted.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 16.03.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
After the BUD /the dose administered this morning spent more than 12 hours punctured prior to administration; After the BUD /the dose administered this morning spent more than 12 hours punctured prior to administration; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (After the BUD /the dose administered this morning spent more than 12 hours punctured prior to administration) and PRODUCT STORAGE ERROR (After the BUD /the dose administered this morning spent more than 12 hours punctured prior to administration) in a 70-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 027L21A and 083J21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Mar-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 14-Apr-2022, received second dose of mRNA-1273 (Spikevax) (Intramuscular) dosage was changed to 1 dosage form. On 14-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (After the BUD /the dose administered this morning spent more than 12 hours punctured prior to administration). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (After the BUD /the dose administered this morning spent more than 12 hours punctured prior to administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (After the BUD /the dose administered this morning spent more than 12 hours punctured prior to administration) and PRODUCT STORAGE ERROR (After the BUD /the dose administered this morning spent more than 12 hours punctured prior to administration) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. It was reported that, Date the vial was initially stored in the refrigerator was 12-Apr-2022. Date and time vial was first punctured was 13-Apr-2022 at 7:00 AM. Date and time of administration of vaccine was 14-Apr-2022 (this morning, probably prior to 9:00 AM). The vial was stored post puncture at Room temperature, drawn up into syringes.The vial did not undergo any temperature excursions. Total amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) was 16 hours. 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
- PA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 10.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 14.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
WRONG DOSE 0.5 VS. 0.25 ML
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 11.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fall
Immunisation reaction
Symptomtext
Patient stated that he began falling multiple times daily. His wife took him to hospital and the patient stated the staff said that the vaccine might have caused the adverse reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fall
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 11.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Patient received the 2nd booster dose; 0.50mL administered rather than 0.25mL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 17.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Administration Error of COVID Moderna vaccine to person under 18, No adverse effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- 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
Product administration error
Symptomtext
Administration Error of COVID Moderna vaccine to person under 18, No adverse effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 17.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Product administration error
Symptomtext
Administration Error of COVID Moderna vaccine to person under 18, No adverse effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- 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
Product administration error
Symptomtext
Administration Error of COVID Moderna vaccine to person under 18, No adverse effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 17.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Product administration error
Symptomtext
Administration Error of COVID Moderna vaccine to person under 18, No adverse effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- 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
Administration Error of COVID Moderna vaccine to person under 18, No adverse effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 17.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Product administration error
Symptomtext
Administration Error of COVID Vaccine, Moderna administered to patient under 18
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- 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
Product administration error
Symptomtext
Administration Error of Moderna vaccine to patient under 18. No adverse effects noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Photopsia
Visual impairment
Symptomtext
no issues during administration. patient called at 12:25 reporting that she had developed vision issues 15 minutes prior that had not gone away. patient reports a sparkling in right part of right eye. patient reports not being able to clearly read literature online as she looked up this issue via internet. she reported no pain at the time. patient was recommended to monitor and if problem continues or progresses to seek medical help immediately. patient reported having tiredness after previous shots and stated she would take a nap and see how she was when she woke up. I requested she follow up with us regarding conditition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Photopsia
- Hospital-Tage
- -
- Labordaten
- patient to contact ophthalmologist if condition continues
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 18.02.2022
- Beginn
- 20.03.2022
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Duodenal ulcer
Gastrooesophageal reflux disease
Iron deficiency anaemia
Oesophagogastroduodenoscopy abnormal
Vascular cauterisation
Symptomtext
Iron deficiency anemia due to chronic blood loss - He was given 80 mg IV protonix, Zofran, 2 g IV magnesium in ED. On admission, GI was consulted. Underwent EGD on 3/21 which showed reflux esophagitis, and a deeply cratered non-bleeding duodenal ulcer with visible vessel. Vessel treated with bipolar cautery. Discharged home. ED visit to hospital admission within 6 weeks of receiving hte COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Duodenal ulcer
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 04.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Patient who is 13 years old inadvertently administered COVID Moderna Vaccine on the left deltoid at 3:50 pm on 04/04/22. This was patient first COVID Vaccine. Patient informed as well as the PCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 04.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
A full dose of Moderna 0.5 mL was given when a booster should have been given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 30.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 24.02.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 11,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Unevaluable event
Symptomtext
Patient had an ED visit and/or hospitalization within 6 weeks of receiving COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 28.03.2022
- Impfdatum
- 02.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 21,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Sepsis
Symptomtext
Severe sepsis without septic shock. He completed 5 days of broad-spectrum antibiotics and was stable for discharge to home. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sepsis
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Employee received Moderna booster, employee is only 17 years old
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypotonia
Resuscitation
Skin discolouration
Unresponsive to stimuli
Symptomtext
Resident became unresponsive in the dining room. Resident was flaccid and gray in color. Nursing staff initiated CPR and resident was transferred to the hopsital via 911.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- The resident recently admitted to the long-term care facility following falls at home and a stroke. Following admission resident had a fall and episode of hypoglycemia following increase in insulin.
- Vorgeschichte
- Diabetes, hypertension, hyperlipidemia, coronary artery disease, chronic systolic heart failure, history of falls.
- Andere Medikamente
- Clopidogrel Bisulfate Tablet 75 mg, Lisinopril Tablet 20 mg, Rosuvastatin Calcium Tablet 40 mg, Carvedilol Tablet 6.25 mg, Sennosides Tablet 8.6mg, Cholecalciferol Tablet 1000 units, Omeprazole Tablet Delayed Release 20 mg, Nitroglycerin
- Allergien
- Avocado, Shellfish
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 16.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse effects, administered Moderna vaccine to employee that is <18 years old
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 12.03.2022
- Beginn
- 12.03.2022
- 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
Received a Moderna Covid-19 vaccine Booster dose more than 12 hours post punctured; This spontaneous case was reported by a consumer and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received a Moderna Covid-19 vaccine Booster dose more than 12 hours post punctured) in a 76-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 vaccination. Concurrent medical conditions included Immunocompromised. On 12-Mar-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 12-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received a Moderna Covid-19 vaccine Booster dose more than 12 hours post punctured). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received a Moderna Covid-19 vaccine Booster dose more than 12 hours post punctured) outcome was unknown. Patient took Moderna vaccine on deltoid muscle. No concomitant and treatment medication was reported by the reporter. This case was linked to MOD-2022-512457 (Patient Link). Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Immunocompromised
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 12.03.2022
- Beginn
- 12.03.2022
- 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
received a Moderna COVID-19 vaccine Booster dose after 12 hours post punctured; This spontaneous case was reported by a consumer and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received a Moderna COVID-19 vaccine Booster dose after 12 hours post punctured) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 vaccination. Concurrent medical conditions included Immunocompromised. On 12-Mar-2022 at 1:30 PM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 12-Mar-2022 at 1:30 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (received a Moderna COVID-19 vaccine Booster dose after 12 hours post punctured). At the time of the report, EXPIRED PRODUCT ADMINISTERED (received a Moderna COVID-19 vaccine Booster dose after 12 hours post punctured) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The reporter did not know if the patient had any allergies or tested positive for COVID-19 or received any other vaccine within 1 month prior to Moderna. The reporter did not know if the patient had any acute or chronic illnesses. The reporter did not know if the patient was taking any concomitant medication. The reporter did not have any information about the first 3 doses or manufacturer of the COVID-19 vaccine for the patient. The vial was initially stored in the refrigerator was on 09-Mar-2022. The vial was first punctured on 11-Mar-2022 on 15:13 pm. The vial was stored in room temperature post puncture and the vial did not undergo any temperature excursions. Total amount of time the vial was exposed to room temperature range (8 degree to 25 degree Celsius = 46 degree to 77-degree Fahrenheit) was 22 hours. The reporter confirmed that the patient received the booster dose in her deltoid muscle and also the reporter did not know if the patient was experiencing any symptoms. No treatment information was provided by the reporter. This case was linked to MOD-2022-512464 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Immunocompromised.
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 12.03.2022
- Beginn
- 12.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
No adverse event
Symptomtext
Patient walked in for vaccination. Moderna Covid-19 vaccine dose number 2 was processed for patient. After receiving vaccination, patient stated that this was his 4th dose of Moderna vaccine. He actually wanted to receive a different vaccine. Patient did not have any side effects/symptoms. Pharmacy staff followed up with him 3 days later and he was good with no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 16.03.2022
- Impfdatum
- 29.04.2021
- Beginn
- 04.02.2022
- Tage bis Beginn
- 281,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
ADMITTED TO HOSPITAL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 10,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 16.03.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Extra dose administered
Product storage error
Product temperature excursion issue
Symptomtext
09Mar2022 stored in the refrigerator, first punctured on 09Mar2022, vial stored room temperature for about 24 hours, on 10Mar2022 administration of vaccine; 09Mar2022 stored in the refrigerator, first punctured on 09Mar2022, vial stored room temperature for about 24 hours, on 10Mar2022 administration of vaccine; Patient received a 4th dose; Dose was administered 12 hours post puncture to the patient/Dose was administered about 24 hours post puncture being at RT; This spontaneous case was reported by a pharmacist and describes the occurrence of EXTRA DOSE ADMINISTERED (Patient received a 4th dose), EXPIRED PRODUCT ADMINISTERED (Dose was administered 12 hours post puncture to the patient/Dose was administered about 24 hours post puncture being at RT), PRODUCT STORAGE ERROR (09Mar2022 stored in the refrigerator, first punctured on 09Mar2022, vial stored room temperature for about 24 hours, on 10Mar2022 administration of vaccine) and PRODUCT TEMPERATURE EXCURSION ISSUE (09Mar2022 stored in the refrigerator, first punctured on 09Mar2022, vial stored room temperature for about 24 hours, on 10Mar2022 administration of vaccine) in an 81-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Mar-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Mar-2022, the patient experienced EXTRA DOSE ADMINISTERED (Patient received a 4th dose) and EXPIRED PRODUCT ADMINISTERED (Dose was administered 12 hours post puncture to the patient/Dose was administered about 24 hours post puncture being at RT). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (09Mar2022 stored in the refrigerator, first punctured on 09Mar2022, vial stored room temperature for about 24 hours, on 10Mar2022 administration of vaccine) and PRODUCT TEMPERATURE EXCURSION ISSUE (09Mar2022 stored in the refrigerator, first punctured on 09Mar2022, vial stored room temperature for about 24 hours, on 10Mar2022 administration of vaccine). At the time of the report, EXTRA DOSE ADMINISTERED (Patient received a 4th dose), EXPIRED PRODUCT ADMINISTERED (Dose was administered 12 hours post puncture to the patient/Dose was administered about 24 hours post puncture being at RT), PRODUCT STORAGE ERROR (09Mar2022 stored in the refrigerator, first punctured on 09Mar2022, vial stored room temperature for about 24 hours, on 10Mar2022 administration of vaccine) and PRODUCT TEMPERATURE EXCURSION ISSUE (09Mar2022 stored in the refrigerator, first punctured on 09Mar2022, vial stored room temperature for about 24 hours, on 10Mar2022 administration of vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications were not reported. Treatment medications were not reported. The vial was first punctured on 09-Mar-2022. The vial was stored post puncture for about 24 hours. The vial was exposed to room temperature of maximum 70 degree Fahrenheit, minimum of 68 degree Fahrenheit for about 24 hours. The temperature excursion duration was 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 15.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Pt was given booster, .25cc of Moderna, and he is 13 years of age. Pt was monitored for 30 minutes. Pt did not experince any adverse event or reaction from receiving the vaccine. Pt's Mother was informed of the error. Pt was monitored for 30 mintuse
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient was administered an expired vaccine. Vaccine expired on 3/5/2022 after 30 days at refrigerated temperature. Vaccine was administered on 3/7/2022. Patient informed of event and need to receive a repeat dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- 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
Symptomtext
Administered with vaccine refrigerated for 33 days; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered with vaccine refrigerated for 33 days) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 083J21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered with vaccine refrigerated for 33 days). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered with vaccine refrigerated for 33 days) 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 the reporter. The vial was initially stored in the refrigerator from 23-Jan-2022. The vial did not undergo any temperature excursions. No treatment medication was reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 04.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
The patient presented for COVID-19 booster, therefore nurse gave him a Moderna booster. Patient reported no adverse side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 03.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oedema peripheral
Tenderness
Symptomtext
Very swollen underarm that is sensitive to touch and has not gone down after days- even with warm compress
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oedema peripheral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Disturbance in attention
Insomnia
Otorrhoea
Tinnitus
Symptomtext
On same day of vaccination, I experienced severe and almost unbearable ringing in both ears. On same night, I experienced a watery discharge from my right ear which fortunately, alleviated the symptoms after several hours. The closest ENT appointment was given for March 8. Currently, I am still experiencing the noise from my left ear which is traumatizing. Difficulty sleeping and concentrating.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Disturbance in attention
- Hospital-Tage
- -
- Labordaten
- Upcoming appointment.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- -
- Vorherige Impfungen
- In both Moderna Vaccine shots, I experienced vertigo.
- Staat
- FL
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 22.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Heart rate
Oxygen saturation
Symptomtext
Patient had pluse ox readings in the 80's and heart rate of 100-130.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
due to patient age, not eligible for vaccination with Moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 30.04.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 210,0
- 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
Event occurred after 2nd vaccine; breakthrough case admission
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 11/26/21 COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
PT WAS ADMINSTERED 0.5 ML INSTEAD OF 0.25ML FOR 4TH BOOSTER DOSE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- AUTOIMMUNE DISEASE
- Andere Medikamente
- CIMZIA
- Allergien
- SULPHA, GENTAMICIN, PENICILLIN, SULFA, ERYTHROMYCIN, LEVONOX
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Vaccine given 21 days after. Dosage requirement at 28 days .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- N/a
- Andere Medikamente
- N/A
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient is a 17-year-old who received a booster with the Moderna vaccine (0.25mL) when Moderna is currently only approved for 18 years and older. Patient was made aware of the event and reported having no adverse effects from the vaccine at the time of the call.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dystonia
Symptomtext
Full body. Grade 4 Dystonia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dystonia
- Hospital-Tage
- -
- Labordaten
- 2/19/22 CBC w dif CMP Magnesium T4, free TSH at emergency department All within normal limits.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Generalized seizure trait
- Andere Medikamente
- Famotidine Buspirone Clonazepam Lamotrigine Spironolactone
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Distractibility
Tinnitus
Symptomtext
Approx close to midnite on Feb 14th I started getting a highpitched buzzing/whistling noise in my ears. Sounded like inside head, not an exterior type of noise. It has not stopped. Today is the 6th day, it is very distracting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Distractibility
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- irregular heartbeat and palpitations
- Andere Medikamente
- I take thyroid pill on a daily basis, I did not take one that morning, nor on 2/15/2022
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 18.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Vaccine was administered too early in the series - given after 14 days rather the full 28 day interval. Patient did not report any adverse effects. Patient is scheduled to receive an additional dose to account for the early dose 28 days following the dose administered early.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 18.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Vaccination administered too early in series - administered after a 2 week interval rather than 28 days. No adverse effects or symptoms reported by patient. Patient is scheduled to receive an additional dose to replace the early dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 18.02.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient received first dose on January 27th 2022 then received second dose on February 17th, 2022. Recieved second dose 22 days after first dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 15.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
A 0.5mL 4th dose was given to an immunocompromised patient. When the dose was verified, I asked if this was the correct dose for an immunocompromised individual. The RPh who verified it said 0.5mL is the correct dose. I proceeded with the shot. I am sure they looked up something and perhaps misinterpreted the findings when it comes to the dose to be given as a fourth dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 15.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient presented for Nurse Visit with Cousin for 2nd dose Moderna Vaccine. Patient checked in at front desk with cousin was told he could not get vaccine without parent present. Front desk called mother and received verbal consent for Patient to get 2nd dose of Moderna 0.5mL Covid vaccine. Consent scanned in patient chart under health records. Patient received first dose of Moderna 0.5mL Covid vaccine on 01/12/22 at visit with provider. Vaccine was not documented at 01/12/22 office visit by nurse but note stated that Patient was scheduled for 2nd dose in 4 weeks. Patient presented vaccination card as proof of vaccine. Vaccination card stated first dose Moderna with lot# given on 01/12/22 at facility. Based on vaccination card and 01/12/22 master IM note, Moderna 0.5mL 2nd dose was administered on 02/15/22 to Patient. Due to Patient age at 17 with birthdate, patient should have received Pfizer 0.3mL vaccine for Children under the age of 18. Parent contacted per CDC guidelines and no further medical treatment is needed unless reaction occurs. Patient/parent encouraged to seek immediate medical attention if allergic reaction symptoms occurs such as trouble breathing, rapid heartbeat, swelling/rash at inj. site, etc.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- Kept patient for CDC recommended 15 minute window to observe for possible allergic reaction to vaccination. Paient stated when ask post vaccine, he was feeling fine and having no reactions to vaccine administered. Per CDC recommendation for error no further treatment needed at this time unless reaction occurs. Contacted parent to educate on vaccination error that was made. Parent asked the difference between the Pfizer and Moderna informed that moderna is not approved for ages 18 and under. Pfizer is approved for ages 5 and older. Informed that child is vaccinated against Covid and does not need to repeat vaccination. Mother states child is doing fine no adverse reactions. Encouraged to seek medical attention if adverse reactions occur.
- Aktuelle Erkrankungen
- None noted
- Vorgeschichte
- None noted
- Andere Medikamente
- No active medications
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wound
Symptomtext
Patient called 2-13-22 saying that after the vaccine she developed a fluid filled sore in her armpit which has no pain but she was concerned it was from the vaccine. The pharmacist assured the patient it was probably coincidental
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wound
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 06.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
Patient got a 0.5ml dose of Moderna's COVID19 vaccine 21 days after receiving the booster dose (0.25ml) of Moderna. Patient did not experience any adverse events as of 02/06/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD, sleep apnea
- Andere Medikamente
- Lisinopril 5mg, Pantoprazole 20mg, Pregabalin 225mg, Breo ellipta 200/25mcg, Fenofibrate 145mg, Metoprolol ER succinate 50mg, Bupropion XL 300mg,
- Allergien
- NKDA
- Vorherige Impfungen
- -