- Staat
- -
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 14.04.2023
- Impfdatum
- 19.02.2021
- Beginn
- 01.10.2022
- Tage bis Beginn
- 589,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Acetabulum fracture
Asthenia
Blood creatinine abnormal
COVID-19
Death
Fall
Fatigue
SARS-CoV-2 test positive
Stoma prolapse
Symptomtext
10/8/22 Pt admitted to the hospital with generalized weakness and fatigue; found to be positive for COVID; desired hospice; hospice process began; 10/14/22 pt had a prolapsed ostomy, still functioning, no intervention needed; also pt fell and fractured right acetabulum; orthopedics recommended wheelchair x 4-6 wks; 10/16/22 creatinine worsened; pt aware the outcome is not good; transitioned his status to DNR comfort measures; 10/17/22 hospice in hospital took over and pt passed away in the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 10,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- colon CA, metastatic
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 12.02.2021
- Beginn
- 22.02.2022
- Tage bis Beginn
- 375,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Death
Symptomtext
Narrative: PATIENT PASSED AWAY DUE TO COVID-19. HE WAS HOSPITALIZED AND HAD RECEIVED THREE COVID-19 VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 74,0
- Dosis
- 4
- Route/Site
- - / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Back pain
COVID-19
Computerised tomogram
Echocardiogram
Electrocardiogram
Musculoskeletal chest pain
Pulmonary embolism
Pulmonary infarction
Thrombosis
Ultrasound Doppler
Vaccine breakthrough infection
Symptomtext
I may have experienced a breakthrough case of COVID-19. After about a week of Covid I started having pains in my ribs and back. I called a Doctor Who told me to go get seen in the emergency room. The emergency room staff told me I had bilateral pulmonary embolism with infarction. I spent three days in the hospital. I am now on blood thinners. I wish I knew the status of the blood clots at this point, but I do not. I definitely feel much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 3,0
- Labordaten
- On June 26 I had a EKG, ultrasound of my heart and both legs, a CT scan. I think the CT scan came before the heart and leg ultrasound.
- Aktuelle Erkrankungen
- Unfortunately I don?t keep a journal of things like that. I don?t remember.
- Vorgeschichte
- I am a bit obese.
- Andere Medikamente
- No prescriptions, I don?t seem to remember taking any dietary supplements or herbal remedies.
- Allergien
- I am allergic to amoxicillin.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 26.03.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 61,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Death
Heart transplant
Liver transplant
Symptomtext
Hospitalized 3/20 , heart and liver transplant on 4/20/22, of death on 5/27/2022,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 68,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Heart and liver transplant on 4/20/2022, immunosuppression, asthma, cardiomyopathy, CHF, HTN
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac arrest
Death
Symptomtext
Cardiac arrest and death
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COPD exacerbation
- Vorgeschichte
- COPD, Alcohol dependence, Dementia, Hypertension, Tobacco use
- Andere Medikamente
- Albuterol, Advair, Duoneb,
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Foetal exposure during pregnancy
Foetal heart rate
Premature baby death
Symptomtext
The baby died after birth 5 days after first vaccine; Foetal exposure during pregnancy; This spontaneous case was reported by a consumer and describes the occurrence of PREMATURE BABY DEATH (The baby died after birth 5 days after first vaccine) in a male neonate of an unknown age exposed to mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) , while the mother received the product for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. MEDICAL HISTORY (Parent): On an unknown date patient had performed following tests. There was a vaginal bleeding. Patient blood pressure 117/76, pulse 80, respiration 18, oxygen saturation 99%, temperature 98.6 degree Fahrenheit. multiple sonographic images of the fetus and uterus were obtained using transabdominal technique, single viable intrauterine pregnancy was visualized. Treatment medication included metronidazole (Flagyl) 500 mg oral tablet and nitrofurantoin (Macrodantin) 100 mg oral capsule. The mother's past medical history included Maternal exposure during pregnancy. No Medical History information was reported. On 31-Jan-2022, the mother received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. The mother's last menstrual period was on an unknown date and the estimated date of delivery was 27-Jun-2022. On 31-Jan-2022, the neonate was diagnosed with FOETAL EXPOSURE DURING PREGNANCY (Foetal exposure during pregnancy). The neonate was diagnosed with PREMATURE BABY DEATH (The baby died after birth 5 days after first vaccine). The Neonate was exposed to mRNA-1273 (Moderna COVID-19 Vaccine) during pregnancy. The delivery occurred, which was reported as Premature. For neonate 1, The outcome was reported as Pre-Term Birth NOS. The placenta is fundal, and evaluation is limited due to lack of amniotic fluid. No detectable amniotic fluid. The cervix contains a small amount of fluid, with a length of 6.6 cm. Fetal measurements: Biparietal diameter: 4.3 cm cm / 19 weeks 0 days. Abdominal circumference: 14.3 cm / 19 weeks 4 days. Femur length: 3 cm / 19 weeks 1 day. Composite gestational age: 19 weeks 1 day. On 31-Jan-2022, FOETAL EXPOSURE DURING PREGNANCY (Foetal exposure during pregnancy) had resolved. The neonate died on an unknown date. It is unknown if an autopsy was performed. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 01-Feb-2022, Foetal heart rate: 161 beats per minute 161beats per minute. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Transplacental) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Transplacental), the reporter did not provide any causality assessments. No concomitant and treatment medication details were provided. Delivery occurred at 20 weeks gestation 5 days after first shot. Company comment: This is a spontaneous case of fetal exposure during pregnancy at 19 weeks of gestation, for a male neonate who experienced serious unexpected event of premature baby death after mother?s vaccination with the first dose of mRNA-1273. Patient?s mother experienced diarrhea, leaking amniotic fluids and vaginal bleeding the same day after first dose of mRNA-1273. She visited the ER, an ultrasound was performed; single viable intrauterine gestation, marked oligohydramnios, trace fluid was seen within the cervical canal. The mother was diagnosed with Acute cystitis with hematuria and premature rupture of membranes. Five days later, she had contractions, went to the emergency room and had a premature delivery. The baby died on an unknown date with no further information available. Mother?s acute cystitis and premature rupture of membrane could be confounders. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. This case was linked to MOD-2022-486635 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 17-Feb-2022: Significant Followup was received on 17-FEB-2022, and includes patient details and parent delivery notes information.; Sender's Comments: This is a spontaneous case of fetal exposure during pregnancy at 19 weeks of gestation, for a male neonate who experienced serious unexpected event of premature baby death after mother?s vaccination with the first dose of mRNA-1273. Patient?s mother experienced diarrhea, leaking amniotic fluids and vaginal bleeding the same day after first dose of mRNA-1273. She visited the ER, an ultrasound was performed; single viable intrauterine gestation, marked oligohydramnios, trace fluid was seen within the cervical canal. The mother was diagnosed with Acute cystitis with hematuria and premature rupture of membranes. Five days later, she had contractions, went to the emergency room and had a premature delivery. The baby died on an unknown date with no further information available. Mother?s acute cystitis and premature rupture of membrane could be confounders. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Premature baby death
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220201; Test Name: fetal heart rate; Result Unstructured Data: 161beats per minute
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 02.04.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 100,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Balance test
Chills
Fatigue
Headache
Influenza like illness
Intracranial mass
Labyrinthitis
Magnetic resonance imaging head abnormal
Nystagmus
Pain
Presyncope
Rash
Rash erythematous
Vertigo positional
X-ray dental
Symptomtext
About 12 hours after vaccination I started feeling headache and body ache. It continued throughout the night. I did not feel feverish but I had chills and extreme fatigue. Just very extreme flu like symptoms. After those symptoms cleared up I had a red lacey rash across my entire torso front and back. That cleared up after a few days. I didn't have any problems until July when I was exercising I happened to move my head quickly and almost blacked out. I thought it would go away but it continued throughout the night. I went to urgent care the next day. They told they thought I had an inner ear infection in the right ear and they sent me home to wait for it to resolve. It did not so I called my primary physician to be seen as a follow up. She examined me and she stated she didn't see signs of an ear infection. She saw an Nystagmus. She had me to do movement and balance tests. She thought I had Benign paroxysmal positional vertigo, BPPV. She recommended I go to physical therapy. I made the appointment and by the time I went I felt a little bit better but it might have been the, Meclizine medication that as prescribed. I went to the physical therapist and he did some tests and did not see any Nystagmus. He asked me if I saw an ENT. I went to see the ENT and she was very dismissive to my symptoms. She told me that it might be TMJ and that I should see a dentist. During this time the vertigo has not gone away and I didn't have any other neurological issues. The dentist said that I should go to a oral surgeon. The oral surgeon said that I should see a specialist but I couldn't due financial reasons. At this point it had been a couple of months. In September I went to see my primary again because it wasn't going away. She said that I should have an MRI of inner auditory canal. The MRI showed a 1.7 centimeter extra axial mass in the right frontal lobe, above my right eye. I have another MRI with contrast of my brain tomorrow night. They couldn't see if it was malignant so this MRI is to determine that.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- Two MRI; Balance and Movement tests; Panoramic x-ray
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Depression; Anxiety
- Andere Medikamente
- Fluoxetine; Wellbutrin; Progesterone; Iron supplement; Multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Cardiac monitoring
Chest X-ray
Computerised tomogram head
Electrocardiogram
Pain
Syncope
Ultrasound Doppler
Symptomtext
Aches (full body) and fainted. Admitted to emergency room at a local medical center (stayed 1 day) then transferred to a second medical center.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 1,0
- Labordaten
- EKG, heart monitor, blood test, brain Ct, carotid doppler, and chest x-ray (06/02-06/03).
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Hydrochlorothiazide; nifedipine; CALTRATE.
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 02.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphasia
Bradyphrenia
Cardiac monitoring
Cognitive disorder
Dizziness
Echocardiogram normal
Electrocardiogram normal
Feeling abnormal
Feeling drunk
Heart rate increased
Laboratory test normal
Presyncope
Vision blurred
Symptomtext
Following a band performance on the evening of 3/19/22 while packing up, overcome with lightheadedness and almost fainted. Symptoms increased to a few times weekly, then daily. Dizzyness, lightheaded, rapid heart rate. 4/25/22 Blurry vision for an hour and a half in the afternoon Cognitive brain fog, slower processing, unable to recall words 4/26-4/28/22 felt "drunk", dizziness continued, five sick days overall resulting from inability to function
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- Sought treatment on 4/21/22, labwork done all normal Telemed appointment on 4/29/22 and tests ordered EKG on 4/02/22 within normal Physical Therapist to rule out vertigo on 4/03/22 Zio Heart monitor adhered from 5/07/22-5/14/22 Echocardiogram on 5/12/22 within normal
- Aktuelle Erkrankungen
- Covid-19 symptom onset 01/03/22
- Vorgeschichte
- None
- Andere Medikamente
- 'Smarty Pants' Women's Formula multivitamin
- Allergien
- Sulpha
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 05.06.2022
- Impfdatum
- 01.03.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 94,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Agitation
Computerised tomogram head normal
Endotracheal intubation
Respiratory distress
Seizure
Unresponsive to stimuli
Symptomtext
Patient was staring off at Skilled Nursing Facility, patient then had a seizure in ER - requiring intubated for respiratory distress. Patient's cause of seizure is of unclear etiology per Neuro Critical Care Physician Note. MRI pending, patient still intubated, not following commands and not answering orientation questions despite being all small dose of sedation for agitation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory distress
- Hospital-Tage
- 2,0
- Labordaten
- CT head 6/3/2022 - Showed no new findings other than old CVA territory. MRI pending 6/5
- Aktuelle Erkrankungen
- Diabetes Type 2, Parkinson's Disease, COPD (on home O2)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Pencillin and Blue Dye
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Urinary incontinence
Symptomtext
PATIENT FELT DIZZY AND SAID HE LOST CONSCIOUS FOR FEW MINUTES AND THEN WOKE UP . WHEN I SAW THE PATIENT HE WAS AWAKE BUT FELT LIGHT HEADED. I LAID HIM ON THE FLOOR AND ELEVEATED HIS LEGS ON A CHAIR. I CHECKED HIS BLOOD PRESSURE 4 TIMES WITH 2 DIFFERENT MONITORS AND IT WAS BETWEEN 130/90 . I GOT HIM WATER AND HE DRANK HALF OF A BOTTLE ,. HE STAYED ON THE FLOOR FOR 10 MINUTES AND THEN WAS ABLE TO GET UP AND WENT HOM WITH HIS MOTHER. I CALLED AND CHECKED ON HIM AFTE 1 AND THEN 3 HOURS AND HE SAID HE WAS FEELING NORMAL . PATIENT ALSO SAID HE LOST CONTROL OF HIS BLADDER WHEN HE WAS SITTING ON THE CHAIR.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anaphylactic reaction
Symptomtext
Anaphylaxis requiring two, six-hour ER visits. Treatment included multiple epinephrine injections.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- CLL
- Vorgeschichte
- None
- Andere Medikamente
- Calquence 100mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anxiety
Dizziness
Flushing
Presyncope
Symptomtext
After receiving vaccine went to lobby to wait 15 minutes, within 10minutes got lightheaded and near passed out. Husband got nurse. Nurse found patient sitting in chair with head between knees face flushed. Lowered patient to ground on back and raised legs. Gave juice and water. Patient states gets anxiety and did not taker her medications this am. B/P 67/40. EMS activated and took to ER B/P at this time has gone to 124/76
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- anxiety
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- passing out
- Staat
- NC
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Impaired work ability
Syncope
Symptomtext
patient had syncopal episode at work the day after recieveing Moderna booster covid-19 vaccine. patient rested and took day off work and now has no symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 25.03.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood glucose decreased
Loss of consciousness
Symptomtext
After patient's wait time post vaccine, he passed out in the parking lot. Ambulance was called and taken to hospital where he came to. Stated that his blood sugar was extremely low, in the 20s. Was in the hospital for 4-5 days because they could not get his sugar under control.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes, Seizures (states related to poorly managed blood sugar)
- Andere Medikamente
- Lantus, Keppra, Ramipril, Irbesartan, Atorvastatin, Trazodone, Gabapentin
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- 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
Abdominal pain upper
Body temperature increased
Chills
Dizziness
Euphoric mood
Headache
Hypoaesthesia
Impaired work ability
Pain in extremity
Paraesthesia
Syncope
Symptomtext
Patient received a Moderna booster 3/15/22 around 1600. Calls 3/17/22 reporting many side effects: 3/15/22 arm pain 5-6 times worse than first dose; 3 hours after shot numbness and tingling in hands, felt a "happiness" in head for about 30 minutes 3/16/22 0300- woke up with chills; temp 100.4 at 0600 with terrible HA, arm pain and stomach ache; stayed home from work; at about 1130 he felt dizzy and the next thing he saw was his father was standing over him as he had fainted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None known
- Andere Medikamente
- None
- Allergien
- Penicillin Robaxin
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- 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
Loss of consciousness
Symptomtext
Patient passed out for a few seconds.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- unknown.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Loss of consciousness
Symptomtext
Vaccine was administered and patient became unconscious within seconds.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- HPV- passed out
- Staat
- FL
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 19.02.2022
- 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: ja
Erholt: nein
Accident
Dizziness
Hypoaesthesia
Loss of consciousness
Fatigue
Laboratory test normal
Nausea
Road traffic accident
Syncope
Vomiting
Symptomtext
Waited 15 minutes at store after vaccine, it was recommended by pharmacist to walk the store so he did. Left facility with our vehicle and about a mile down the road he felt numb from head to toe and fainted within 3 seconds, approximately 18 minutes after received vaccine. Ended up wrecking the vehicle and came to about 4-5 minutes later getting pulled from vehicle, not remembering anything. About 2-3 times daily Since then he gets waves of tiredness, fussiness, dizziness and nausea. Vomited 2 days after incident without reason (wasn?t feeling sick, just vomited at work desk, didn?t feel it coming).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Lab work at ER, was told it was normal. Radiographs were normal.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Allergic to peaches.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Discomfort
Disorientation
Fall
Immediate post-injection reaction
Loss of consciousness
Sensory disturbance
Somnolence
Syncope
Symptomtext
Patient came in for a COVID vaccine appointment. She mentioned to me she had her period and was cramping. She said this is her third time and that each time she got the vaccine she was having her period and that even when she caught COVID she had her period. After proper screening and confirmation she was here to get the Moderna booster, I told her to stay in the store for 15 minutes after getting the vaccine. Immediately after I gave her the vaccine she told me she felt heavy and she seemed to faint or lose consciousness over the next minute. She slumped backward and I caught her with her upper arm and slowly let her lie down on the ground. I called over to my coworker to call emergency as I tried to wake her and find her pulse and take her blood pressure. She then woke up within 2 minutes and I took her pulse which was 54beats per minute and her blood pressure 115/80. She told me she felt heavy and had a metallic feeling. She said when she woke up she felt like she was sleeping and confused as to why she woke up in the area she was in but then quickly oriented her self and knew she had come in for a vaccine. At 3:25pm she said she doesn't want us to call paramedics and she is starting to feel better. She mentioned she also biked here. She also said her period was giving her cramps and a nausea feeling. She mentioned afterward that she has had a fear of needles in the past and has fainted from blood draws but that was over 10 years ago. We recommended she follow up and report to her doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Hypersomnia
Syncope
Symptomtext
PT COMPLAINED OF SLEEPING FOR 36 HOURS. THEN DIZZINESS AFTER AWAKENING. THEN SYNCOPE ON 2/12/22. 911 WAS CALLED. PT HAS RECOVERED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Loss of consciousness
Pallor
Vomiting
Symptomtext
Patient went pale, blacked out for ~20 seconds, but did not fall. He said he felt terrible and threw up. EMS was called; however, patient recovered and decided to not go to the hospital. Then the proceeded to go home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 20.11.2023
- Impfdatum
- 07.04.2022
- Beginn
- 19.11.2023
- Tage bis Beginn
- 591,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Chills
Cough
Dyspnoea
Pyrexia
COVID-19
SARS-CoV-2 test positive
Symptomtext
Shortness of breath, weakness, subjective fevers/chills, and cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 12.10.2023
- Impfdatum
- 11.02.2022
- Beginn
- 01.03.2023
- Tage bis Beginn
- 383,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Chest pain
Symptomtext
I have been having severe burning in my chest. It has never happen before. I went to the er sometime in March 2023. They did some blood test.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Blood tests.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 03.05.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea exertional
Electrocardiogram
Erythema
Fatigue
Magnetic resonance imaging heart
Pain in extremity
Peripheral swelling
Stress echocardiogram
X-ray limb
Symptomtext
1) Profound fatigue - onset 6 hours -> Resolved in 5 days. 2) Left chest base, area of apex of heart - onset 3 days -> resolved in 3 months. 3) Dyspnea with exertion - onset 3 days -> improved after 3 1/2 months but still with symptoms 4) Left index finger redness, swelling and pain at MCP jt. - onset 1 week -> resolved in 2 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- 5/10/22 - Left hand x-ray 7/6/22 & 7/11/22 - ECG 7/20/22 - Cardiac Stress ECHO 8/20/22 - Cardiac MRI Appt. pending for LT angiogram
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -Hypertension -Disseminated Superficial Porokeratosis
- Andere Medikamente
- Lisinopril 20mg., Vit B complex, C, D, calcium
- Allergien
- Nickel
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 10.04.2023
- Impfdatum
- 06.04.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 133,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Autoimmune disorder
Back pain
Chest X-ray abnormal
Computerised tomogram thorax abnormal
Cough
Dyspnoea
Ear infection
Eustachian tube dysfunction
Flank pain
Full blood count normal
Lichen planus
Lung disorder
Lung infiltration
Malaise
Nasopharyngitis
Oropharyngeal pain
Pneumonitis
Pyrexia
Symptomtext
In August 2022, I got what I believed to be a urinary tract infection. I had a pain in right side and back. I had mild cold symptoms. I had one day of fever. It got worse through the week. I went to the emergency department. They did an abdominal CT. I did not have an infection. They gave me steroids. I had a sinus infection. At the time, I was diagnosed with auto immune flare up lichen planus and eustachian tube dysfunction and urticaria. I was seen on 8/22, 8/29 and 9/9. I was given antibiotics, but I was sick for 8 weeks. I did not feel better until the end of October. In January 2023 I had another sinus infection which went away. In early February, I had a sinus infection and double ear infection and began to have an upper respiratory infection. I had a fever and sore throat for one day. I began to cough a lot and short of breath. Friday, February 24, 2023, I had a doctor appointment. I had taken an antibiotic for one week, then another week. I then had an X-Ray. It showed infiltrates in my lungs. I had a CT scan on April 6th which showed pneumonitis, infiltrates, upper airway issues and some swirling effects. I continue to be short of breath, but my oxygen levels are normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- X-Ray, abnormal, 02/2023; CT scan, abnormal, 04/2023; CBC, normal, 04/2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- AFIB but ablated
- Andere Medikamente
- ELIQUIS
- Allergien
- Shellfish; AUGMENTIN; clindamycin; doxycycline
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 13.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bursitis
Injected limb mobility decreased
Injection site pain
Insomnia
Magnetic resonance imaging
X-ray limb
Symptomtext
10/11/2022 patient verbal report given to local Health Department: - Patient reported that pain in area of COVID vaccination (left deltoid and/or shoulder joint) began approximately 24 hours post vaccination - Pain level was reported as being 7/10 on 1-10 pain scale - Symptoms reported included limited range of motion due to pain in area and trouble sleeping - Patient reported then waiting "a couple of months" before deciding to seek diagnosis/treatment for the pain - At this time (June/July 2022) the patient requested her PCP to order an X-ray of her left shoulder area - July 2022, X-rays taken of left shoulder region at local Hospital; images analyzed by a radiologist, no diagnosis reported by patient - At this time (July 2022) cortisone injections were prescribed as treatment; patient reported limited pain relief - July 2022, MRI of area was taken, appointment made with orthopedic surgeon. - Dr. consulted, met with patient, and subsequently diagnosed patient with bursitis in left shoulder joint region - Physical therapy and additional cortisone injections ordered as treatment and continued through the taking of this report Oct 2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- (see #18)
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- NONE REPORTED
- Andere Medikamente
- NONE REPORTED
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 08.08.2022
- Impfdatum
- 13.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Hypoaesthesia
Injected limb mobility decreased
Injection site hypoaesthesia
Pain in extremity
Symptomtext
Pt received 2nd dose Moderna on 6/13/22. Pt states having arm soreness for 1 day. After the soreness disappeared, pt noticed numbness in the left arm at the site of injection. The numbness radiated up near the neck and down the arm. the pt had been rubbing/ massing the arm and taking IBU. But still no relief. Pt has been seen by MD in June & July to rule out stroke. She has been cleared by her MD. Pt states having decreased arm function and ability to carry items. Reported arm numbness issue to pharmacy on 8/1/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- Unsure what tests were done to rule out stroke by MD.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HYPOTHYROIDISM, ASTHMA, ANEURYSM (2008), PAIN-CHRONIC PAIN SYNDROME; UNSPECIFIED THORACIC, THORACOLUMBAR AND LUMBOSACRAL INTERVERTEBRAL DISC DISORDER
- Andere Medikamente
- VITAMIN D, VITAMIN C, BIOTIN-THESE WERE TAKEN ON DAYS BEFORE AND AFTER VACCINATION. NOT TAKEN ON DAY OF VACCINE.
- Allergien
- IODINE-HIVES ERYHTORMYCIN-NAUSEA/VOMITING
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Gait disturbance
Lung consolidation
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
04/22/2022 vaccination. 06/22/2022 I woke up feeling congested, solid consolidation in my chest. Short of breath and hard to walk to bathroom. The fever stayed below 103 but in the 100's. I contacted my physician. My family had to drive over from another city to deliver the medication which I took the next morning. I had a pulse ox, as well. I was prescribed PAXLOVID a half dose. That last dosage, I feel asleep so much I had to take the last dose the following day, on the 6th.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Cleft pallet; Back Injury; GERD; Seasonal Allergies; Heart Murmur
- Andere Medikamente
- ZYRTEC; MUCINEX; TYLENOL; acid reflux
- Allergien
- Aspirin; NSAIDS; cisplatin; DEMEROL
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 104,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anaemia
Blood iron decreased
Blood test abnormal
Condition aggravated
Fatigue
Haemoglobin decreased
Symptomtext
I went in for my regular Diabetes blood test, and that is when they told me I had Anemia. And then I went in to the doctor that and it was iron related. They stated my hemoglobin (red blood cells) were low. I had another blood test, and still the anemia was low. Last Thursday I went into the hematologist they did blood test and he told me that my iron was low and my hemoglobin was low and that he thought I was low iron that was effecting this. And he stated that their could be other facts but he was pretty well in feeling that the iron was the man cause. I was feelin fatigued for 2 months or so.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Blood test, hemoglobin (red blood cells) were low, low iron.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes; Anemia
- Andere Medikamente
- JANUVIA; ACTOPLUS; LOTREL; DIOVAN; CRESTOR; aspirin; iron supplement; vitamin D3
- Allergien
- CECLOR; CLEOCIN
- Vorherige Impfungen
- All doses of COVID-19 felt fatigue.
- Staat
- MD
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 21.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Extra dose administered
Hyperacusis
Tinnitus
Symptomtext
I had Tinnitus previously but it initially became worse after dose 2 as detailed in VAERS report (1773157). After my 4th Moderna dose, I noticed a day or so later that my Tinnitus was worse than usual. I remember watching TV and the sounds becoming really annoying, louder than usual. After the second dose when it became worse I did go to see an ENT and they tested my hearing, which came back fine, but after this 4th dose I did not consult anybody but did mention it several times to my Therapist. The Tinnitus remains the same and has not gotten better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure; Tinnitus (from previous vaccination)
- Andere Medikamente
- Losartan; Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- worsening tinnitus following 2nd Moderna vaccination (VAERS 1773157)
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 07.04.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 74,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
COVID-19
Chest X-ray normal
Chest pain
Cough
Dyspnoea
Electrocardiogram normal
Fatigue
Feeling hot
Headache
Inflammatory marker increased
Oropharyngeal pain
Pain
Pain in extremity
SARS-CoV-2 test positive
Sneezing
Ultrasound scan normal
Symptomtext
When he caught COVID-19 he started feeling really achy and tired He had a sore throat and was warm but had no fever. He was sneezing and coughing. He had pain in his lower back and a headache. On June 22, 2022 he was feeling worse. His blood pressure was fine, but then all of a sudden he felt like he was having a hard time taking in air. His pulse was around 92 beats per minute. He was having pain in his right leg as well. We called his physician. The advice nurse called us back and said that he should go to the ER. He had pain in his sternum as well and the nurse thought it could have something to do with his heart. When we went to the ER the physician checked him out. They gave him Remdesivir. He was admitted and stayed at the hospital. They ended up giving him 3 doses of the Remdesivir, an albuterol inhaler, and cough medicine. He continued taking his vitamins. He was hospitalized for 2 nights and 3 days. His symptoms are not present anymore.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 3,0
- Labordaten
- 6/21/2022- Rapid COVID-19 Test-Positive; 6/22/2022- PCR COVID-19 test- Positive; 6/22/2022- EKG- Normal; 6/22/2022- Chest X-ray- Normal; 6/22/2022, 6/23/2022, 6/24/2022- Lab work- Inflammatory markers were slightly elevated; 6/23/2022- Ultrasound of lower extremities- No blood clots were found
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obese; Diabetes; Chronic Kidney Disease
- Andere Medikamente
- Simvastatin; Glipizide; Valsartan; Alopurinol; Trazadone; NPH Insulin; Vitamin D; Vitamin C; Multivitamin; Tylenol
- Allergien
- Lisinopril; Losartan; Blood Pressure Medications
- Vorherige Impfungen
- He received the Moderna COVID-19 Vaccine 2nd dose on 4/6/2021. He felt like he was ran over by a bus. He had a sore arm. He wasn
- Staat
- NC
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 20,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diaphragmatic disorder
Dizziness
Dyspnoea
Electrocardiogram normal
Limb discomfort
Symptomtext
For the last few weeks I have been having shortness of breath and it feels like I have a hole in my diaphragm. It feels like air is leaking out of my diaphragm when I take a breath. I have been getting really dizzy as well. It feels like my internal cavities of my body don't have the right pressure. My legs feel like led as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- EKG- Normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Seasonal Allergies; Acid Reflux
- Andere Medikamente
- Omeprazole; Dicyclomine; Stool Softener; HCTZ; Flonase; Multivitamin; Magnesium, Vitamin B, D3; Turmeric
- Allergien
- Penicillin; All Statins; Levaquin; There are very few antibiotics that I can take; I can't eat corn; Lectin
- Vorherige Impfungen
- I haven't taken a Flu vaccine since 2006 because I got really sick.
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 04.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Cardiac monitoring
Dizziness
Fatigue
Heart rate irregular
Nausea
Palpitations
Symptomtext
It been off and on that I have been profoundly fatigued and then I have times when I have irregular heartbeat. Upon exertion, i feel faint and have my heart racing along with nausea. I saw a cardiologist yesterday and I am currently wearing a heart monitor. Next week I am scheduled for a stress test on June 24th. I will be wearing the monitor for 2 weeks. I had a routine bloodwork which was normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Heart Monitoring-In Process-06-16-2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure Asthma IBSD
- Andere Medikamente
- Singulair, Lisinopril HCTZ, Lyrica, Topamax, Amitriptyline, Osphena, Propranolol, Clonazepam, Cranberry Juice Capsule, Potassium, Vitamin D3, Vitamin C, Probiotic, Dynamic Health Drink,
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 07.06.2022
- Impfdatum
- 07.03.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 91,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Dyspnoea
Positive airway pressure therapy
Tachycardia
Symptomtext
Hospitalized with dyspnea and tachycardia treated BiPAP with O2, refused intubation. also treated with dexamethasone and remdesivir
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Locally metastatic squamous cell carcinoma of esophagus on chemotherapy for this currently. Interpreter needed.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 03.06.2022
- Impfdatum
- 25.03.2021
- Beginn
- 01.06.2022
- Tage bis Beginn
- 433,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest X-ray abnormal
Cough
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
72-year-old male who presents emergency room complaining increased shortness of breath. He also has had increasing cough. He reports that his symptoms started yesterday afternoon. Patient states he has not had any fever at home. He did have a temperature of 99.6? on presentation to the emergency room. Patient has a history of severe COPD and is on 4 liters/minute of oxygen continuous at home. His pulse ox on presentation to the emergency room was 87% and his oxygen was increased to 6 L. patient takes an aspirin daily 81 mg. He also is on prednisone 20 mg daily and states that he has been on this for the past 6 weeks. His pulmonologist is Dr. He also is followed by Dr. Cardiology. Will his chest x-ray tonight shows some by basilar stranding but overall does not appear much different than his previous chest x-rays. The patient has had his initial COVID shots and has had 2 boosters. He reports that he when out to eat at a restaurant approximately 1 week ago. His COVID swab tonight is positive. I have been asked to admit the patient due to an increased oxygen requirement. On the patient is a retired respiratory therapist who worked at this facility. PT IS CURRENTLY INPATIENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Feeling abnormal
Irritability
Mobility decreased
Myalgia
Nervousness
Pain
Pain in extremity
Symptomtext
I developed a sore arm. The next day I was very sore, extreme fatigue, muscle aches and feeling "out of it". Emotionally I felt very jumpy and irritable which is very much not like me. For two weeks I stayed in bed. I did not take anything to help elevate my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Soft tissue arthritis
- Andere Medikamente
- Yes and participant declined to provide information.
- Allergien
- Strawberries; gluten; AUGMENTIN; CIPRO
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 8,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Audiogram abnormal
Biopsy breast
Condition aggravated
Conductive deafness
Confusional state
Deafness unilateral
Disorientation
Ear discomfort
Electrocardiogram
Fear
Head discomfort
Headache
Hearing aid therapy
Hypoacusis
Magnetic resonance imaging
Mixed deafness
Ophthalmic migraine
Speech disorder
Symptomtext
On the evening of the 28th I felt like there was a fullness in right ear and that side of my head and I noticed I couldn't hear well. I put in my hearing aid and that did not help. That morning I had been at the dentist and had a filling but did not think that was related but it was on the upper right side of my mouth. The next day thinking it may be allergies I took some medication to maybe try and help that. I started with Mucinex, Store brand Severe cold and Flu multi-symptom with acetaminophen, then I tired the Mucinex with Sudafed. None of that helped so I had done a Neti pot, a dehumidifier, and nothing helped. Finally I tried a Benadryl which I realized later was expired. I went to the ER on the 29th because nothing was helping and I still could not hear. The ER gave me Flonase- they did not run any tests or labs. I then realized I had conductive loss in my head and that scared me- I do have a history of Otosclerosis but it has not been progressing recently- my hearing has been stable. I have had bilateral stapedectomy and have now have titanium bilateral stapes. Monday I made contact with the doctor's office. On May 2nd I had right breast biopsy's and the following day I had an ocular migraine that made me go to Urgent Care-I had a mild headache that occurred after but I did have the visual disturbance with fogging and jagged rings along with a lot of confusion and disorientation. This made me feel like my brain was having a difficult time processing and was having a hard time verbalizing anything. The Urgent care said I should see an eye specialist. On May 4th I saw a doctor and we did an Audiogram and there was a 90% hearing loss and it was profound hearing loss on the right side-further explained it was a mixed and conductive hearing loss meaning middle and inner ear. He gave me an prescription for Prednisone 10mg. I started the med on the afternoon of the fourth, and stopped the Flonase, I was on the Prednisone for 16 days and titrated the dose down over the those 16 days. I also saw an Audiologist that day and she looked in my ear and it all looked normal to her other than a small dry patch but it was all normal. On May 5th I was evaluated for a stroke because of the confusion I had experienced with the ocular migraine. The next day I saw an OD he and a student both evaluated me that day and he stated that my eye looked normal and encouraged more cardiac care and Imaging with my PCP. I had an MRI on May 9th to look into my ears more. I asked my PCP to add a scan for a TIA but it was incomplete. May 11th I went back to the doctor and we did another Audiogram there was a little improvement in some areas of my hearing about 50-55 decimoles but I also lost some hearing in other areas. He kept me on the Prednisone and referred me back to my PCP. I am trying to work with a new Audiologist to calibrate my new hearing aids to this new hearing loss and follow up Thursday June 9th. I do not hear normally, there is an echo and sometimes it sounds like I am in a tin can. I try and pop my ear like when you are on an airplane and your ear pops it feels like I need to do that on the right ear. Sometimes things sound normal other times there is major distortion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Audiogram; MRI; ECG; EKG
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seasonal Allergies
- Andere Medikamente
- Valacyclovir 500mg once a day, Naltrexone 3mg once a day, Source Naturals- Mag 200mg twice a day, Ester-C 250mg, Natural Factors DGL Licorice Extract 2-4 tabs a day PRN, Kirkland Vitamin D 2000mg, Country Life Coqueton 200mg twice a day, Vi
- Allergien
- BACTRIM
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Blood lactic acid
Blood test
Chest X-ray
Coronavirus infection
Dyspnoea
Frequent bowel movements
Oxygen saturation decreased
Rhinorrhoea
White blood cell count
Symptomtext
It started with a runny nose and then the next day it was running more and by Tuesday morning, I was having a hard time breathing. I went to my PC and he sent me to the ER because I was so low on oxygen. They kept me there for about 6 hours to get the oxygen level to rise back up. My level went up so they sent me home. That night I had some afib with my heart and so the next morning when I woke up I was struggling to breath so that time they admitted. I was given oxygen. When the results for the blood panel and chest x-ray came back. I was given a different type of nose swab to detect more lung infections. I was diagnosed with Corona HD43. They placed me in isolation and started treatment. Due to the lactic acid, they gave me a medication to flush it out which made me go to the bathroom 60 times throughout the course of the night. My heart was still in afib. I was treated with antibiotics. I was in the hospital for 6 days. I was also treated with prednisone. I was discharged on 05-16. I am still currently in oxygen. I have not yet fully recovered, I am scheduled to see a pulmonologist and my primary care physician on Monday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 6,0
- Labordaten
- blood panel-WBC up and lactic acid building up-05-10-2022 and 05-11-2022, chest xray-05-10-2022 and 05-11-2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- chronic headache, chronic muscle ache in right shoulder and right lower back, Back injury
- Andere Medikamente
- bupropion 150 mg -1xDaily, Cpap, cyclobenzaprine 10mg 3xdaily as needed , Diltiazem 240 mg 2xdaily, esomeprazole 40mg 1xnightly, levothyroxine 125mcg 1xin the morning , Multi vitamin simvastatin 10mg, tramadol as needed, warfarin
- Allergien
- morphine
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 09.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Adverse drug reaction
Blood electrolytes normal
Blood test
Decreased appetite
Diarrhoea
Fatigue
Fluid intake reduced
Full blood count normal
Hypophagia
Nervous system disorder
Paraesthesia oral
Red blood cell sedimentation rate normal
Thyroid function test normal
Urticaria
Viral infection
Vomiting
Weight decreased
White blood cell count decreased
Symptomtext
Patient presented on 5/16 and informed pharmacist that she has been dealing with side effects of her booster dose that was administered in Feb. The patient states that 2 days after getting her booster shot, she started having a lack of appetite, general tiredness, and diarrhea and vomiting. She could not eat or drink much of anything without it experiencing the diarrhea or vomiting. She went to urgent care, and they did blood tests, with the determination that it was a virus and there was not much else that could be done than to let it run its course. The patient has lost approx. 30 pounds of weight since the vaccination, and is just now starting to recover from the side effects. She has also had welts on her tongue, and has had some nerve issues with her tongue (feels like there is something on the end of her tongue, but nothing is on there)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- 3/16/22: Thyroid normal, sed rate normal- no inflammatory response, electrolytes good, blood count fine- WBC slightly low could be a sign of congruent viral infection or effects of vaccine. Nothing acute we would have to take care of, follow up with PCP
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, seasonal allergies, hyperlipidemia, GERD, Arthritis
- Andere Medikamente
- Metoprolol 50mg ER daily Atorvastatin 40mg daily Omeprazole 40mg daily
- Allergien
- Amoxicillin, Sulfa
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 09.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Bursitis
Condition aggravated
Gait disturbance
Hypoaesthesia
Mobility decreased
Neuralgia
Pain in extremity
Tendonitis
X-ray abnormal
Symptomtext
Two weeks after dose 3, I experienced a flare up of my arthritis, pain and numbness in my left leg that progressed up my leg from below my knee to above my hip, and I could not stand any pressure on it and was bedridden. I went from being very active to being bedbound unable to walk due the pain. I was bedridden for about 10 days until I could see an orthopedic specialist. I was diagnosed with trochanteric tendonitis and bursitis and I was experiencing nerve pain as well. I have received a cortisone injection to my hip on 5/5/2022, was x-rayed to confirm diagnosis and given exercises to perform at home. This has also effected the way I walk, and I feel that I am a fall risk.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- x-rays to confirm trochanteric tendonitis and bursitis
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- hypertension, type II diabetic, osteoarthritis.
- Andere Medikamente
- Novolin 70/30 insulin twice daily, levothyroxine, meclizine, glimepiride, omeprazole, aspirin, gabapentin, benazepril, Chlorpheniramine, Ativan, ibuprofen, pravastatin
- Allergien
- all muscle relaxants, codeine, Lipitor, neupro patch, Trulicity, tramadol, sulfa, Belsomra, trazadone, flexeril
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 8,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Canalith repositioning procedure
Contusion
Ear infection
Fatigue
Gait disturbance
Impaired driving ability
Impaired work ability
Injection site pain
Mobility decreased
Nasopharyngitis
Vertigo
Viral infection
Symptomtext
-Painful injection site, huge bruise for almost 2 weeks, minor cold symptoms & fatigue for 2 days - 4/16, woke up & started to get out of bed, had major vertigo - I have NO idea if this is related to the vaccine; had to stay in bed most of the day, unable to walk without assistance - a nurse recommended meclizine 25mg, started taking otc dissolvable meclizine on Sunday, along with benadryl, started doing Epley maneuver daily - gradually started getting better, but needed to stay home from work all week; was able to work from home, but didn't drive at all 4/21- Was able to speak to a telehealth doctor, she prescribed oral meclizine, 25mg, 3x a day, plus a prednisone steroid pack. started Meclizine on 4/21, started prednizone on 4/22. started seeing results by 4/24 4/25 saw Dr., he examined me, suggested it may have been a minor viral infection in my left ear, should go away by itself. Did Epley 2X in office 5/3 still having minor episodes of vertigo, but not disabling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- no tests, just the doctor visit
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- methimazole 5mg, 3x/week tylenol chlorpheniramine maleate + phenylephrine hydrochloride - otc allergy medication
- Allergien
- no medication allergies known allergic to strawberries & chocolate latex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 10.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dyspnoea
Headache
Heart rate increased
Hypoaesthesia
Palpitations
Symptomtext
Client presented to clinic on 4/13/2022 for 2nd dose of Moderna COVID-19 Vaccine. She stated that the day after she received her first dose on 3/10/2022, she felt chest pain and shortness of breath for about a week, and stated that it "comes and goes." She described feeling palpitations, and felt her pulse increase. Client described having a headache since receiving her first dose. On 4/13/2022 she presented with a headache and when assessed, a blood pressure of 154/100. Client received 1st dose of vaccine in the right arm but felt a numbing sensation on the left arm. Client was not vaccinated with her 2nd dose of Moderna and was referred to her Primary Care Physician.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Breast pain
Injection site pain
Paraesthesia
Symptomtext
Pins and needles pains to left breast area that spreads to left inner axillary and to left shoulder
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- DM, High cholesterol
- Vorgeschichte
- DM Asthma
- Andere Medikamente
- -
- Allergien
- Atorvastatin and Metformin
- Vorherige Impfungen
- 4/30/21
- Staat
- NJ
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 15.04.2022
- Impfdatum
- 10.03.2022
- Beginn
- 12.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Dizziness postural
Head discomfort
Laboratory test normal
Migraine
Ocular discomfort
Photophobia
Skin discolouration
Symptomtext
2 DAYS AFER GETTING MY FIRST VACCINE I GOT MAJOR DISCOLORATION ON BOTH MY LEFT AND RIGHT HANDS. I HAVE SEEN MY LUPUS DR AND DERMATOLOGIST AND THEY BOTH HAVE SAID THEY DONT KNOW WHAT CAUSED THIS AND CAN NOT TREAT IT. I HAVE ALSO HAD PRESSURE IN MY HEAD LIKE A MIGRAINE , LIGHT SENSITIVITY, CANT TURN MY HEAD QUICKLY OR I GET DIZZY AND PRESSURE BEHIND MY EYES AND TOP OF NOSE. I DO NOT SUFFER FROM MIGRAINES AND NEVER GET HEADACHES. ALL OF THESE SYMPTOMS STARTED 2 DAYS AFTER MY VACCINE AND HAVE NOT GONE AWAY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- I HAVE HAD RECENT LABS WITH MY RHEUMATOLOGIST. THEY CAME BACK NORMAL.
- Aktuelle Erkrankungen
- LUPUS SINCE 2013
- Vorgeschichte
- LUPUS SINCE 2013
- Andere Medikamente
- multivitamin 81mg aspirin daily Plaquenel 200mg bid for LUPUS
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 08.03.2022
- Beginn
- 13.03.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Dysarthria
Extra dose administered
Glossodynia
Tongue disorder
Tongue erythema
Symptomtext
PT REPORTED TONGUE SORENESS, REDNESS, AND SLURRED SPEECH STARTING ON DAY 6. ON ABOUT DAY 14, SHE ALSO REPORTS "PIMPLES" THAT SHOWED UP ON HER TONGUE. AFTER SPEAKING WITH A PHYSCIAN, SHE WAS ADVISED TO TAKE AN ANTIHISTAMINE AS WELL AS AN UNKNOWN ANTIFUNGAL THAT HAS HELPED "60 - 70%," BUT SHE IS STILL REPORTING RESIDUAL SORENESS AND SLURRED SPEECH AFTER 1 MONTH. SHE SAYS THAT THIS HAPPEND WITH HER PREVIOUS SHOT (DOSE 3) AS WELL AND LASTED A TOTAL OF 4 MONTHS. SHORTLY AFTER HER PREVIOUS DOSE, IT WAS FOUND THAT SHE HAD A DENTAL INFECTION REQUIRING ROOT CANAL WITH A SUBSEQUENT THRUSH INFECTION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- MODERNA COVID-19 VACCINE ADMINISTERED 09/2021, LOT 014F21A; SAME ADVERSE EVENT DESCRIBED HERE (TONGUE REDNESS, SORENESS, SLURRED
- Staat
- WY
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 17.03.2022
- Beginn
- 20.03.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Condition aggravated
Erythema
Inflammation
Rash
Swelling
Throat irritation
Urticaria
Symptomtext
Developed hives three days after the vaccine. "Not very swollen or inflamed-over whole body". Not itchy. A little less red now but still present. Also had an itchy throat recently. Lymphoma now out of remission (had stem cell transplant). Had been in remission the last 7 years. Nothing going on at the time of the shot. Changed laundry detergent etc. after developiing the rash. Had a hostory of a rash with initial mantel cell lymphoma. Going to start Car T transplant in a week. Oncology team reccomended the booster dose and is aware of the rash. Has taken pictures. Has not notified primary MD. Encouraged to notify and discuss if another dose is eligible to consider close observation for anaphlaxis Cont. or not receving the same type of COVID vaccine. States "I don't think I will be getting another one". Wanted to report the rash in case others need to know that it could be a side effect.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Lymphoma
- Vorgeschichte
- Lymphoma
- Andere Medikamente
- None
- Allergien
- Hives from food in the past
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 22.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Breast pain
Breast tenderness
Injection site pain
Injection site rash
Injection site reaction
Injection site swelling
Injection site urticaria
Injection site warmth
Musculoskeletal chest pain
Musculoskeletal pain
Pain
Rash erythematous
Rash maculo-papular
Rash papular
Rash pruritic
Skin lesion
Tenderness
Symptomtext
Maculopapular, pruritic rash in multiple areas surrounding injection site starting on date of injection (posterior axilla, shoulder, and left arm distal to left deltoid from Moderna injection site). Red, raised, hive-like lesion to injection site at left deltoid starting the following morning 3/23/22. Left deltoid is slight swollen, hot, and tender to palpation. Tenderness and aching radiating into left breast, left chest wall mid-axillary line, and left scapula still present on 3/24/22. Rash resolved on 3/23/22, but hive on injection site still present today 3/24/22. OTC benadryl and ibuprofen used at home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Eczema
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Chills
Condition aggravated
Diplopia
Headache
Migraine
Nausea
Neuropathy peripheral
Pain
Pain in extremity
Symptomtext
Six hours after injection, arm very sore, elevated temp ranging between 100-103, nausea, migraine type, throbbing headache, body aches, body chills, symptoms lasting 3 days. Since the vaccine, neuropathy in legs and feet worsen, medication for neuropathy and restless leg syndrome not helping, off and on again migraine headaches, occasional double vision.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Neuropathy in legs and feet, right worse than left; restless leg syndrome
- Andere Medikamente
- Gabapentin Ropinirole Seroquel Clonazepam
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Pain in extremity
Peripheral swelling
Symptomtext
Patient says that her arm has been sore (barely able to lift up) and swollen, since she had gotten the shot and still is today 3/17/22, so it has been over a month.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Condition aggravated
Cystitis
Insomnia
Musculoskeletal stiffness
Neck pain
Palpitations
Raynaud's phenomenon
Symptomtext
Approximately 6 to 7 hours after receiving the COVID-19 booster shot, patient experienced chest pain in the left side of the chest near the heart. Pain persisted throughout the night along with insomnia and heart palpitations (strong heartbeat, heart rhythm felt normal to patient). Pain was persistent and diminished morning of 10Mar2022. Flare up of Raynaud's syndrome and cystitis morning of 10Mar2022 along with neck pain and stiffness (worse than usual).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hashimoto's thyroiditis Raynaud's syndrome (idiopathic) recent onset cystitis (diagnosed ~Sept 2021) asthma
- Andere Medikamente
- loratidine (10 mg dose once daily) magnesium glycinate (45% RDA) kelp (for iodine intake)
- Allergien
- acetaminophen anaphylactic reaction to Gadolinium contrast dye
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Confusional state
Dizziness
Fatigue
Headache
Hypoaesthesia
Injection site pain
Myalgia
Paraesthesia
Pyrexia
Swelling face
Symptomtext
First dose was given on 1/04/2022 at the hospital where she delivered baby. Second dose was given at 4:49pm on 3/3/2022. In the evening of 3/3/22 she felt overly tired. Her symptoms got worse on the morning of 3/4/22 including throbbing headache, fever of 102, severe full body muscle pain, injection site pain. She also reported her face got swollen (facial skin got tighter) and severe numbness arms and hands and tingling of fingers. Also, she is very dizzy and confused.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- NO
- Allergien
- Iodine Presevative
- Vorherige Impfungen
- Tdap
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 03.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Blood lactic acid
Chills
Condition aggravated
Fatigue
Myalgia
Tooth infection
Vaccination complication
Symptomtext
Chills, fatigue, mild myalgia starting 3/1/22, received third dose Moderna vaccine 2/28/22 day before, history of dental infection recently and on po antibiodics for, seen ER Dr initially and finished on 3/1/22, Dr discharged on 3/1/22 with diagnoisis of Adverse effect of COVID-19 vaccine, suspected combinatio nof ongoing dental infection and recent COVID vaccine, IVF's and PO tylenol given in ER, Lactate initally elevated at 2.5 but after IVF's repeated and down to 1.3, temp. 100.2 in ER, pt. discharged home and to follow up in 3 days with primary Dr.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse reaction
Blood test
Diarrhoea
Dizziness
Dyspnoea
Electrocardiogram
Gastroenteritis viral
Mobility decreased
Muscular weakness
Nausea
Neurological examination
Pain in extremity
Vaccination site reaction
Symptomtext
On 2/26 morning, I couldn't really use my arm due to arm weakness on top of pain. Around new I began experiencing nausea and diarrhea. That afternoon I began experiencing dizziness and shortness of breath and went to the ER. They gave me Zofran and Tylenol. They told me that I have COVID arm and a stomach virus which they said I probably had it before the vaccine. I went to my PcP on 2/28, and she determined that it was an adverse reaction and prescribed a prednisone inhaler.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- EKG, blood test, metabolic panel, series of neurochecks.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, Lung tumors, Kidney disease
- Andere Medikamente
- Sertraline
- Allergien
- Raw onions, Penicillin-based medications, Amoxicillin, Clindamycin, Mantu
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest discomfort
Dyspnoea
Muscle spasms
Symptomtext
Chest tightness, SOB and leg spasms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- BP 189/100.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Famotidine, Tizanidine
- Allergien
- Penicillin, Fluoroquinolone, Codeine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pharyngeal paraesthesia
Somnolence
Symptomtext
RN received call from immunizations dept regarding possible adverse reaction to moderna vaccine. Patient is also an employee of organization where vaccine administered. Patient was reporting tingling feeling in throat, possible swelling. Assessed patient, vital signs were BP 135/87 HR 55, o2 sat 97%, R 15, Temp 97.5. Patient was able to speak and communicate effectively. Patient appeared sleepy. No swelling present on face, inside of mouth, tongue. No wheezing present. Patient reported she has experienced similar symptoms with second dose of moderna vaccine. Provided report to Dr. Patient kept in patient room for observation. Patient reported their symptoms were improving. Following 30 minutes, patient allowed to return to work station. Vital signs upon exit from clinic were BP 132/85, HR 65, o2 sat 97% T: 97.5 Resp 16
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pharyngeal paraesthesia
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- oxycodone
- Vorherige Impfungen
- Moderna covid vaccine 09/02/21, per patient, tingling in throat, cardiac complications.
- Staat
- NM
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 13.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Lymphadenopathy
Migraine
Night sweats
Symptomtext
Pt. states that after receiving the 3rd dose of Moderna 02/09/2022, started experiencing symptoms 02/13/2022 of swelling of the lymphnoids, night sweats, migraines, and headaches. Migraines and headaches are continuous, No noted Primary visit/communications. (Covid + 11/2021 similar symptoms with previous swelling and night sweats) (Previous 1st and 2nd doses were Phizer)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chest pain
Chills
Headache
Hyperhidrosis
Myalgia
Pruritus
Taste disorder
Symptomtext
Chills, sweats, joint/muscle aches, itching over entire body. Itching subsided the next day on 02/08, change in taste buds, chest pain and headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure, thyroid.
- Andere Medikamente
- Daily meds. (morning time)
- Allergien
- Penicillin.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Dyspnoea
Pruritus
Pyrexia
Rash
Symptomtext
Patient had rash, itching, chest pain, shortness of breath, and fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- -
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Abdominal rigidity
Arthralgia
Chromaturia
Dysstasia
Injection site pain
Mobility decreased
Myalgia
Pain
Pyrexia
Symptomtext
about 10 hours after administration. I spiked a fever of 102.4. it would not change. down below 101 for 12 hours with acetaminophen. I had body pain, severe joint pain , Every muscle and joint hurt. It was to the point, that I could not get up on my own. This gradually improved, but would flare up if my temp went above 101, severe abdominal pain,intense for about 24 hours. It began gradually approximately 10 hours after getting the injection. It felt more like spasms as compared to gastrointestinal pain. My arm...where I had the injection was so painful, I could not raise it. I had and continue the have painful joints. very dark urine for about 36 hours despite drinking lots of fluids I also have bra
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Asthma endometriosis
- Vorgeschichte
- Asthma Breast cancer
- Andere Medikamente
- see list
- Allergien
- multiple see list
- Vorherige Impfungen
- aNAPHLAXIS TO FLU SHOT IN youth and large local reaction to 2021 flu shot
- Staat
- WI
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Body temperature increased
Chest X-ray
Chest pain
Computerised tomogram thorax
Condition aggravated
Dizziness
Dyspnoea
Electrocardiogram
Hyperhidrosis
Nausea
Pain
Pain in extremity
Palpitations
Troponin
Vaccination complication
Symptomtext
Approximately 19-20 hrs. post booster I began with chest pain and palpitations. As the day progressed the chest pain became more intense with radiation to both upper arms and associated SOB, lightheadedness, and nausea. This lasted through out day/night. I awoke from a sound sleep at 5AM 2/6 with severe substernal CP, profound diaphoresis, SOB, nausea and lightheadedness. Temp was 101. Presented to local ER for evaluation. CXR, labs (to include troponin x2), ECG, chest CT were completed. Received IVF bolus. Diagnosis was a reaction to COVID 19 Booster. Discharged to home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- See above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- DMII, asthma, hepatic steatosis
- Andere Medikamente
- Metformin, Omeprazole, Zyrtec, melatonin, Pulmicort MDI, Imitrex PRN, Albuterol MDI PRN, liver health supplements.
- Allergien
- NKDA
- Vorherige Impfungen
- Palpitations, sinus tachycardia after Moderna dose 2 on 1/26/21.
- Staat
- OR
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Chills
Dyspnoea
Headache
Pain in extremity
Restlessness
Symptomtext
Headache, sore arm and chills (all expected) set in around midnight (about 12 hours after the booster shot). Restless sleep. Throughout the night I noticed a lot of chest tightness, soreness and aching just to the left of center of my chest, as well as, it being harder for me to breathe deeply. The whole next day was very much the same. Now (two days later), I have shed most all of the original symptoms. The chest pain has subsided, but is still there a tiny bit. I'd say about 10% of what it was yesterday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 18.12.2023
- Impfdatum
- 28.07.2022
- Beginn
- 15.12.2023
- Tage bis Beginn
- 505,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Pyrexia
SARS-CoV-2 test
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- IDNOW
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hyperlipidemia, CAD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 25.04.2022
- Beginn
- 17.04.2023
- Tage bis Beginn
- 357,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cough
Oropharyngeal pain
Pyrexia
Rhinorrhoea
Sinus congestion
Symptomtext
About April 17th I woke up with my right sinus plugged up with nasal drip and sore throat. I had a fever of 102. The next day it had affected both sides. I went to the urgent care. I have had a bit of a cough and was given a prescription for my cough. As of today I am feeling much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Epilepsy; Kidney Disease; High Cholesterol
- Andere Medikamente
- Levothyroxine; Levetiraceta; Atorvastatin; Omeprazole; Lisinopril; Mycophemolate
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 20.04.2023
- Impfdatum
- 13.04.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 184,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Musculoskeletal stiffness
Oropharyngeal pain
SARS-CoV-2 test positive
Streptococcus test negative
Symptomtext
My symptoms started around the morning of October 14, 2022. I had a slight sore throat, and my neck was stiff. I tested myself for COVID-19 that afternoon. The result was negative. The following day, I had the same symptoms. I tested myself for COVID-19 again. The result was also negative. The third day, the symptoms persisted. I thought I might have Strep Throat. I visited the outpatient clinic at the hospital. I told them about my symptoms and about my negative COVID-19 test results. They cultured my throat which was negative for Strep. They performed a COVID-19 test. The result came back positive. They prescribed Paxlovid 150mg. I filled it the same day. I took the required dosages. I started feeling better after 24 hours, but I continued taking the medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 10/14/2022 At Home COVID-19 Test - Negative; 10/15/2022 At Home COVID-19 Test - Negative; 10/16/2022 COVID-19 Test - Positive; 10/16/2022 Strep Test - Negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D3; Vitamin B12; Probiotic
- Allergien
- Seasonal
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 05.04.2023
- Impfdatum
- 09.12.2022
- Beginn
- 10.02.2023
- Tage bis Beginn
- 63,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Brain fog
COVID-19
Cough
Fatigue
Headache
Malaise
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
Got COVID around 2/10/23 cough, headache, fatigue, body aches. Too Paxlovid tight away with zinc, vita c and a cough suppressant, advil. Much improved in 1 week, then spiked a fever again on 2/19/23 with snot everywhere, sneezing, headache, horrible body aches an severe fatigue. I was really sick all week. Returned to work on 2t27/23 and struggled with exhaustion and brain fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Just 3 positive covid tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression GERDS
- Andere Medikamente
- Protonix 40 MG Prozac 40 MG Wellbutrin 150 MG Magnesium Turmeric Vita D
- Allergien
- Morphine Demoral
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 30.03.2023
- Impfdatum
- 22.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Biopsy thyroid gland
Oropharyngeal pain
Sensation of foreign body
Thyroid mass
Ultrasound thyroid abnormal
Symptomtext
I had chronic sore throat. I ignored it but it never seemed to go away. Then I started to have trouble feeling things while swallowing like a lump in my throat. The symptoms kind of built up after this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 26AUG2022 - Ultrasound - large nodule in right thyroid 2.4cm x 2.2cm x 2.2cm; 03OCT2022 - Ultrasound - confirmed the large nodule in right thyroid; 02NOV2022 - Biopsy - 3 samples taken - no cancer and told to have checked annually.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Flonase
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 06.03.2023
- Impfdatum
- 03.03.2022
- Beginn
- 27.02.2023
- Tage bis Beginn
- 361,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Dysphonia
Oropharyngeal pain
Paranasal sinus discomfort
Paranasal sinus hypersecretion
Pyrexia
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
I started with a sore throat and raspy voice. As the day progressed my head filled up with sinus pressure, drainage and congestion. I went to urgent care and completed a COVID-19 PCR test, and it was negative on February 27, 2023. I had to wait until March 01, 2023, and went back because my home COVID-19 test was positive. I went back to urgent care and also received a positive COVID-19 test. I began taking Paxlovid the same day. I didn't have any fever until March 03, 2023, but I am no longer having that. I still have a cough and sinus drainage, so I am still recovering.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Test-Positive-March 01, 2023 COVID-19 PCR-Positive-March 01, 2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- N/A
- Allergien
- Tamiflu
- Vorherige Impfungen
- Pfizer dose 1-2. Moderna-I experienced sinus drainage and congestion for about 2 weeks.
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 03.01.2023
- Impfdatum
- 06.04.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 110,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Decreased appetite
Pain
Pruritus
Pyrexia
SARS-CoV-2 test positive
Skin burning sensation
Skin lesion
Symptomtext
I received my 4th dose of Moderna COVIFD-19 vaccine on 04/06/2022. My COVID-19 symptoms started on 07/25/2022 in the morning around 08:00AM. I had fever, body aches, chills, and loss of appetite. I called the clinic the day I tested positive for COVID-19 which was on July 25. They told me since I had no long standing health conditions I wasn't qualified for any medications. I called back again to the same clinic on 07/30/2022 since my symptoms got worst. They prescribed me with Paxlovid for 5 days. On July 30th after COVID-19 infection I got lesions on my scalp. It was burring and itchy. I went to the urgent care they thought it was shingles or ring worms. They didn't do anything to verify it. They prescribed Anti fungal medications for my scalp. It didn't help at all. On December I called the Clinic back again and they prescribed me with 2 weeks of Antibiotics. On 12/28/2022 they prescribed me with Temovate Cream 2 times daily external solution for my scalp. I am still using it. From September- November I was experiencing brain fog so I went to my Homeopathic doctor on 11/10/2022. She prescribed me Catclaw, Feverfew, and Ginkgo Biloba. This really helped to clear the brain fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 03JAN2023 COVID-19 Test- Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zoloft; Wellbutrin; Atorvastatin; Zyrtec; Multivitamins
- Allergien
- Morphine; Lithium; Latex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 14.11.2022
- Impfdatum
- 05.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Foreign travel
Injection site rash
Rash erythematous
Rash pruritic
Rash pustular
Scab
Skin discolouration
Skin fissures
Skin weeping
Symptomtext
I received my second Moderna booster for COVID-19 on 4/5/2022. About 10-15 days later, I developed a rash on my left arm. It oozed, wept, cracked, and became scabby. It started with satellite bumps around the injection site. While I slept, it would ooze through my pajama top. It itched like crazy and began to spread all over my body. The pus-filled bumps looked like cigarette burns and popped up on my legs, feet, neck, torso, hands, and back. My dermatologist told me that my immune system would essentially overrespond to everything. If I had a minor scratch or an insect bite, I would see little pus-filled bumps pop up around them. I went on a trip overseas (4/27/2022-5/25/2022) and saw a doctor twice while I was there. In the country I visited, it's unheard of for people to get 4 shots for COVID-19. The doctors had never seen anything like it, and they even sent pictures of my condition to their colleagues. The second doctor I saw in the country I visited prescribed me antihistamines and a steroid cream. Prior to that, I had seen another doctor in the same country, and she had prescribed me antibiotics, antihistamines, and steroid cream. The antihistamines helped with the itching while was intense, but I used them sparingly. The steroid cream also helped, but you're only supposed to use it in moderation, so I was reluctant it to use too much or too long. When I got back home, I saw a dermatologist, who recommended a steroid cream and antihistamines as needed. At the time of this writing, I still have spots at the injection site and on my forearms, plus a few on my hands, my back, and my foot. The spots start itching whenever I take a hot shower. They are discolored and range from red to purple. I have to be careful when I scratch the sores, because if I break the skin, it will begin oozing. I hardly ever take any antihistamines anymore, though they did help when the itching was severe in April, May, and June 2022. I sometimes also apply ice packs to the sores, and this helps for about an hour. The dermatologist at home told me that he has seen many similar cases in vaccine recipients and informed me that I was "somewhere in the middle of the scale" in terms of severity.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- CENTRUM silver multivitamin.
- Allergien
- Penicillin; LEVAQUIN.
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 02.05.2022
- Beginn
- 27.09.2022
- Tage bis Beginn
- 148,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Fatigue
Nasopharyngitis
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I had extremely mild, no aches, and cold like symptoms. I had fatigue, little so throat, and a little cough. I went to a wedding, they were testing for COVID-19 and my test came up positive. I went urgent care and tested positive there again. They prescribed me PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 10/09/2022, positive, COVID-19
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Intermittent Asthma
- Andere Medikamente
- Levothyroxine; vitamin D; vitamin supplement
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 03.09.2022
- Impfdatum
- 14.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse reaction
Asthenia
Axillary mass
Balance disorder
Dark circles under eyes
Dizziness
Dizziness postural
Gait disturbance
Hyperacusis
Nausea
Sensory disturbance
Vertigo
Symptomtext
Woke up with vertigo while lying in bed. Strong sensation of fast movement, I felt bed close to the bed. More vertigo when walking to bathroom, I felt myself go sideways a bit, as if I was bumped off track. Lots of nausea and dizziness during the following week. I now experience dizziness when looking up from a standing and sitting position. Very low energy. Dark circles under my eyes. Lump under my L arm pit appeared the day after injection. Lack of energy tough. Sensitivity to noise,I continue to experience walking off track, I ljust go sideways sometimes, feels like I?m off balance suddenly. I basically felt as if I had experienced a concussion, aside from the vertigo, the morning after I received the covid booster. I did not have a concussion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- I am currently completing paperwork to be a patient I have not yet been seen by a medical professional regarding this adverse vaccine reaction .
- Aktuelle Erkrankungen
- I had covid in January of 2022.
- Vorgeschichte
- -
- Andere Medikamente
- Probiotics Vit C
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 18.08.2022
- Impfdatum
- 16.02.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 160,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse reaction to the vaccine. I tested positive for COVID-19 on 07/26/2022 with a home test. I had congestion, achiness and fever. I was on travel and contacted my doctor and he prescribed PAXLOVID which I was able to get. When I started taking PAXLOVID, I felt better within 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Home test was positive for COVID-19 on 07/26/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic hives
- Andere Medikamente
- ZYRTEC
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 15.08.2022
- Impfdatum
- 13.05.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 75,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I CAME DOWN WITH A SLIGHT CASE OF COVID-19, SORE THROAT AND COUGHING, TOOK PAXLOVID FOR 4 DAYS (UNTIL I SHOWED SIGNS OF AN ALLERGIC REACTION TO PAXLOVID), AND HAVE BEEN SLOWLY IMPROVING SINCE THE ONSET OF THE DISEASE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 5 DIFFERENT HOME COVID TESTS, 2 OF WHICH SHOWED POSITIVE, THE LAST 2 OF WHICH SHOWED NEGATIVE.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- RHEUMATOID ARTHRITIS
- Andere Medikamente
- LISINOPRIL, METHOTREXATE
- Allergien
- ALLERGIC TO SULFA DRUGS
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 29.07.2022
- Impfdatum
- 28.04.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 89,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Feeling of body temperature change
Headache
Hyperhidrosis
Nasal congestion
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
I still have COVID-19 right now. It started with a lot of sneezing, coughing, sweating, hot and cold chills. I took a COVID-19 test at home, which was positive. I had an awful headache. Today is the 3rd or 4th day, and I am still sweating and coughing. Stuffy nose and congestion, mild fever today. I stopped sneezing, though. I am taking TYLENOL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- At home test positive. PCR positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Vitamins; calcium
- Allergien
- NSAIDS
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 14.04.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 74,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Feeling abnormal
Nasopharyngitis
Pain in extremity
SARS-CoV-2 test positive
Symptomtext
I had a sore arm and tired for one day. I started to feel bad on 06/24/22 feeling like a bad cold. I tested positive on 06/27/2022 for COVID-19 with a PCR test. The home test I took was negative. I took Mucinex, Tylenol and Night Quil to help with my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- PCR test for COVID-19 was positive and home test was negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis; kidney disease
- Andere Medikamente
- Yes
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 19.04.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 50,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Malaise
Respiratory tract infection
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
04/19/2022 Vaccination. 06/28/2022 I woke up with a headache and I was coughing but I do normally due to asthma. I thought bad allergies. Runny nose. I was sneezing a lot. After a few days, I was so fatigued I couldn't stay awake. I was traveling with my son. I took a home test and it was COVID positive. The symptoms appeared 5 days after I got to where I was traveling to so I am unsure if I got it there or who I was expose to. I was prescribed antibiotic what I thought was a bladder infection. My asthma is a little worse but it usually happens after I have anything respiratory in regards to infections and I thought COVID had set it off.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Positive
- Aktuelle Erkrankungen
- Asthma Flare-up
- Vorgeschichte
- Hypertension; Asthma; Spinal Stenosis in Neck
- Andere Medikamente
- Allegra; Mucinex; Singular; HCTZ; Vitamin D3; Albuterol Inhaler
- Allergien
- Codeine; Antiseptic Epinephrine; Sulfa; Milk; Oats; Mold; Adhesive Bandages; Cedar; Grass; Dust
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 20.04.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 69,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
On June 28 2022 I started with some mild sniffles and occasional cough. The next day it was slightly more congestion and cough. On June 29, 2022 I took a COVID-19 test and it was negative. The next few days I got a little more congestion and cough. I do not think I ran a fever, just a little more tired than usual. I rechecked about 3-4 days later and I was still positive. On July 6, 2022 I tested negative and have negative ever since. I contacted my physician and they sent out Paxlovid. I took the medication twice a day for five days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Hypothyroid
- Andere Medikamente
- Triamterene/HCTZ; Amlodipine; Levothyroxine; Zinc; B12; Vitamin D; Vitamin C; Omega 3
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 31.05.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Asthenia
COVID-19
Diarrhoea
Energy increased
Malaise
Nausea
Pain
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I went to a conference, I had a scratchy throat that came and went but I decided to come home a day early. I started feeling unwell on June 29, 2022, my energy would go up and down, I would feel nauseous, I had diarrhea, very achy my joints hurt. I used a home COVID-19 test on Sunday July 3, 2022 but it was very faint. Two days later I took another home COVID-19 test that came back positive very fast. I called my doctor who called my back and prescribed PAXLOVID and supplements he recommended I take. By Saturday I started to feel better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- CYMBALTA; vitamin D; coQ10; omegas; vitamin C
- Allergien
- Gluten sensitivity
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 86,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Drainage
Exposure to SARS-CoV-2
Fatigue
Insomnia
Loss of personal independence in daily activities
Nasopharyngitis
Pain
Quarantine
SARS-CoV-2 test positive
Throat clearing
Throat irritation
Symptomtext
It started a week ago. July 6, 2022. At first, I thought it was just a bad cold. I had gotten all 4 of the shots, so I was pretty confident that I wasn't at too much risk. We had attended a wedding that turned out to be a spreader event. My grandson and son who both live with me both came down with COVID-19. My first evidence that I had it was a scratchy throat. I tried to clear that but I wasn't able to. That turned into what I thought was a normal cold. Sleeping that night was very difficult. I had a lot of drainage and was really achy. I was also tired and fatigued. I got up the next day and it felt like a bad cold to me. With all the other incidences around me, I took a home test and it was positive right away. That's when we tested my son if he was sick as well. We knew my grandson had COVID-19 and my son had symptoms and he tested positive as well. On Friday, I called the doctor's office and wanted to ask what I should do. I asked if I should get treatment and asked about isolation. I had a telehealth visit and we talked it through, and he mentioned that there was a lot of interactions with medication. By that Friday though, I actually was feeling better, particularly that night as well because I felt like I was on the mend. We decided to let it go for a little bit and it did continue to get better. Today is the first day I've been off quarantine. My body is fatigued and tired. I can't do much without having to sit down and take a rest. Other than that, I feel pretty good. Tomorrow would be a full week since this started.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 07/08/2022 at home COVID-19 test - positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- History of 3 Heart Attacks; Type 2 Diabetes; Hypertension
- Andere Medikamente
- Metformin; atorvastatin; glipizide; beta blocker unknown; amlodipine; hydrochlorothiazide, JARDIANCE; low dose aspirin
- Allergien
- Lisinopril
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 11.07.2022
- Impfdatum
- 28.01.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 129,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dizziness
SARS-CoV-2 test positive
Symptomtext
Patient had episodes of dizziness prompting him to be seen. Was admitted and found to be COVID positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD, hypertension, aortic aneurysm
- Andere Medikamente
- advair, carvedilol, plavix
- Allergien
- penicillin, aspirin, clindamycin
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 30.06.2022
- Impfdatum
- 30.03.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 82,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Fatigue
Malaise
Oropharyngeal pain
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
COVID-19 symptoms started on 06/20/22; tested positive on 06/22/22. I had chills, sore throat, fatigue, and when I tested positive I was seen by my clinician and was prescribed Paxlovid. I took the first dose that night at 830PM. Symptoms lasted probably 4-5 days. My condition didn't degrade any further and took pulse ox readings every few hours and had no issues and it all stayed within normal ranges and then I took the Paxlovid doses as prescribed-all ten doses- around 830PM and 830AM next day. I tested negative with rapid antigen test on 06/27/22 and today 06/30/22 it was negative as well and I am not experiencing any symptoms at this point.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 Positive 06/22/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 01.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Computerised tomogram
Dizziness
Dysarthria
Fall
Magnetic resonance imaging
Symptomtext
very dizzy and fell ... speaking slurred, had to go to ER room
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- 3,0
- Labordaten
- CT scan, blood tests, MRI
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- spinal stenosis, hip replacement,high cholesterol
- Andere Medikamente
- Crestor 10mg, Vitamin c, Magnesium, aspirin 81mg, ibuprofen , tramadol
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 11.04.2022
- Beginn
- 17.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None, I have not seen a doctor for this apparent side-effect. I have been taking Allegra (180mg) daily.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None.
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain lower
Arthralgia
Asthenia
Decreased appetite
Discomfort
Fatigue
Headache
Nasal congestion
Pain
Pain in extremity
Renal pain
Symptomtext
Headache. It's a stuffy heavy feeling. Great lack of energy. Tiredness. Body aches. Joint Aches. My hands have hurt. I have had very, very intense pain in the kidney area of my back and also the lower abdomen area in the front of my body. I'm not eating a lot. I just don't want to eat. I'm hungry, but I just don't want to eat. I want this to be over with...the whole feeling here.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain lower
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- High Blood Pressure, Glaucoma, Diabetes -no meds or insulin, High Cholesterol, Gastroesophageal Reflux
- Andere Medikamente
- Timolol 0.5% 1 drop per eye per day, Atorvastatin 80mg per day, Pantoprazole 40mg per day, Meloxicam 15mg per day, Losartan 100mg per day, Metoprolol 100mg per day, 1500mg Krill Oil, Probiotic
- Allergien
- Narcotics
- Vorherige Impfungen
- All of them, I had shoulder pain.
- Staat
- WA
- Alter
- 70,0
- Geschlecht
- U
- Eingang
- 20.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Lymphadenopathy
Pain
Pyrexia
Symptomtext
102.0 fever, body aches, fatigue, enlarged lymph nodes, These lasted 48 hours, though enlarged lymph nodes continues at time of report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure, GERD, vestibular migraine
- Andere Medikamente
- Omeprazole, metoprolol, multivitamin
- Allergien
- Effexor, Hydrochlorothiazide, codeine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 14.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood urine present
Joint swelling
Malaise
Symptomtext
Patient came to the pharmacy to state that he had blood in his urine for 2 days following vaccination with his first booster dose of Moderna. Pt also stated that his knees were swollen. Symptoms did improve, but he stated that he felt very ill after his booster dose. Pt had no problems from his first 2 shots of Moderna. Pt does have IGA vasculitis and it is possible he had a flare-up after vaccination. He was told to look for blood in his urine, as this is a sign that his kidneys are affected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Psoriasis, IGA vasculitis, Urostomy due to bladder removal due to cancer
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 19,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dizziness
Fatigue
Headache
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case of COVID, I felt really tired and aching, then I got the worse sore throat of my life, headache, body aches and dry couch. The dr. prescribed Paxlovid, and it is helping with the sore throat, but I still have dry cough and really tired and get lightheaded when I am standing up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- COVID test.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Triamterene-HCTZ; multivitamin; probiotic.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 18,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Herpes zoster
Pruritus
Pustule
Swelling
Symptomtext
On 5/9 I noticed I had two small red bumps on my left side. They did not itch, there was no pain or discomfort. I assumed it was a bug bite from yard work earlier in the day. The next day I noticed there was one more larger spot close to the first two. I put clobetasol on that as well. By Tuesday evening I noticed that I had a couple more little spots. The following day I had another large spot. I noticed they had little pustules under, they were kind of raised. There was still little to no itching. On Thursday there was more itching and the spots continued in a linear fashion. I thought it was shingles but there was not discomfort. I went to see my primary care and she thought it was shingles as well. It now uncomfortable with pressure but minimal to no itching. She prescribed me a antiviral, valacyclovir.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoarthritis; Type II diabetic; Kidney Stones; Benign Essential Blepharospasm
- Andere Medikamente
- Urocit-K; Puranol; Adderall; hydrochlorothiazide; metformin; Aleve; Pepcid; Claritin
- Allergien
- Betadine; thiomersal; fluconazole; Levaquin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 19.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Erythema
Insomnia
Mechanical urticaria
Mental disorder
Pruritus
Rash papular
Skin warm
Urticaria
Symptomtext
I started to experience really gradual itching all over my body so I started to take Zyrtec. As the days went on it started to progress and now I have welts and raised areas all over the body that are hot to touch. On 05/05/2022 I went to the dermatologist and was diagnosed with Dermatographia and was told that it was related to the booster vaccine. I was prescribed prednisone and told to continue to take the Zyrtec. It is slowly getting better, but it has not gone away my ears are hot and red. I use lotion to help relieve some of the itch and the heat of my skin. Sometimes I cant even get in a comfortable sleeping position due to the itching and that has really caused me to have sleepless nights. I have psychological problems do to the way I look with the welts and the redness. I wonder if it can do this to my skin is it affecting my organs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Veratamil 180mg once daily
- Allergien
- Latex, Demerol, Sertraline
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 10.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Rash
Symptomtext
I had the shot and 2 days later I had itching and a rash. I tried hydrocortisone cream and it cleared up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Cancer Survivor Chronic A fib Urticaria
- Andere Medikamente
- Eloquist Flecainide Vitamin D3 Vitamin B12 Calcium Fish Oil Vitamin C Collase Miralax Zyrtec
- Allergien
- Sulfa Talwin Preparation H
- Vorherige Impfungen
- Shingles-severe arm pain and fatigue.
- Staat
- MS
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Pruritus
Rash
Urine analysis
Vulvovaginal discomfort
Symptomtext
One week after the vaccine I noticed a deep down under skin in the flesh a itch. I also had little bumps starting on right arm then went to stomach and went to vagina to knee then back up to neck and back. Symptoms are on going. Doctor prescribed hydroxyzine HCL 25 mil and Mometasone furoate 0.1 percent 45 ml.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Bloodwork, Urine
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetic, Heart, Anemia, High blood pressure
- Andere Medikamente
- Janumet XL 100-1000, Lisinopril-HCT, Ezetimibe, Potassium chloride, Baby aspirin, Loratadine 10 mil
- Allergien
- None
- Vorherige Impfungen
- All COVID-19 vaccine I had an reaction
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Symptomtext
Approximately a few days after my 2nd booster (Dose 4) I experienced the following symptoms: Hip pain (Left hip). I called a doctor for consultation and was prescribed with a muscle relaxant and prednisone. It marginally helped with my condition but not as much. As of today 04/27/22 I still have the same symptoms but have not fully recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 14.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Pyrexia
Swelling face
Symptomtext
low grade fever (99.5 - 99.8), cough, and intermittent swelling under right jaw 10 days after vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension, hyperlipidemia, coronary atherosclerotic heart disease, chronic anxiety, chronic depression
- Andere Medikamente
- ASA 81 mg, atenolol 50mg-chlorthalidone 25 mg, mirtazapine 15 mg, simvastatin 40 mg, venlafaxine ER 75mg
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Injection site pain
Myalgia
Symptomtext
injection site soreness, mild headache, muscle ache, chills
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- seasonal allergies to pollen
- Vorgeschichte
- None
- Andere Medikamente
- Loratadine, Vit D, Vit B12
- Allergien
- None
- Vorherige Impfungen
- Moderna, Booster, #1
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 21.03.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 18,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Feeling abnormal
Gout
Malaise
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Woke up with sore throat and a runny nose. I used a home test about 12 hours after those symptoms and the test was negative. I tested again due to still feeling poorly so I tested again about 12 hours after the first test and that was positive. Saturday afternoon I did have a virtual visit with urgent care due to not having a spleen and I was worried. I had also recently had been treated for Gout with Prednisone and I was worried that I was going to have a harsh response to having Covid so I wanted to get be on Paxlovid to treat the Covid symptoms. I do think had I not been on the prednisone I would have not had any Corvid symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Home Covid test, took Paxlovid for treatment
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Polycystic Kidney Disease, Spleen Removal
- Andere Medikamente
- Estrogen, Vitamin D3
- Allergien
- Penicillin, Bee Venom, Eye Drop- Allergan
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Nausea
Vaccination site bruising
Vaccination site erythema
Vaccination site pruritus
Vaccination site swelling
Vaccination site warmth
Symptomtext
Patient received 2nd Moderna booster on 4/19/22. Patient first noticed itching, redness, swelling and warmth at vaccine site on left arm on 4/21/22. She returned to the local County Health Department at 0830 on 4/22/22 to report the event. Patient states "that her arm looks better today than it did yesterday." Patient also states she put an ice pack on her arm yesterday. 10-15 mm redness/swelling noted to left upper arm. Warm to touch. Small bruise noted in lower area of redness. No red streaks or drainage. Patient complains of feeling nauseous. Nurse supervisor examined patient as well. Advised to apply warm compresses today and to follow up with primary care physician if symptoms change or worsen. Reported to Nurse/Supervisor on 4/22/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None known
- Andere Medikamente
- Blood thinner
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Symptomtext
This event occurred in the patient's home. At 15 minutes post vaccination, the patient reported dizziness. At this point, we had the patient drink some juice, water, and eat a banana, then lay down with legs elevated above heart. Patient had not eaten anything prior to receiving the vaccine. After about 5 minutes, the patient reported no improvement in dizziness and starting have chills. Vital signs (blood pressure and pulse) were stable throughout. No thermometer was present to check temperature. After another 15 minutes with no improvement, patient had more juice. Around 45 minutes post vaccination, the patient began to experience improvement in his dizziness and after 60 minutes, the dizziness resolved with only mild chills remaining.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None at time of vaccination
- Vorgeschichte
- None reported by patient
- Andere Medikamente
- Patient reported taking no medications.
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 15.04.2022
- Impfdatum
- 11.03.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- 21,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Alanine aminotransferase increased
Anosmia
Anti-transglutaminase antibody negative
Antinuclear antibody negative
Blood cortisol
Blood glucose increased
Blood immunoglobulin A
Blood immunoglobulin G
Blood iron
Blood thyroid stimulating hormone normal
C-reactive protein normal
Diarrhoea
Dyspepsia
Epstein-Barr virus antibody negative
Epstein-Barr virus antibody positive
Fatigue
Full blood count abnormal
Symptomtext
fatigue, muscle aches (arms, hands, back), indigestion, diarrhea, almost complete loss of smell and taste. Occurred after first series of 2 and finally resolved after 9 months. then had booster dose adn sx all returned again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 2/24/22 - IgA, T3, CRP, ThgA, TTG, Gliadin IgG and IgA, TSH, T4, ANA - all normal - CMP with mildly elev ALT and glucose, not likely clin significant - CBC with % lymph very slightly low at 17.5, otherwise completely normal - EBV IgG capsid positive, EBV, IgM, negative, EBV, IgG early, positive, EBV IgG Nuclear negative - SARS-CoV-2 Ab IgG positive pending labs ordered 4/15/22 - fasting cortisol, lipid panel, ferritin, iron and iron binding capacity, B12, MMA
- Aktuelle Erkrankungen
- OSA, HTN (untreated)
- Vorgeschichte
- OSA, HTN
- Andere Medikamente
- Multivitamin, eyedrops
- Allergien
- Aspirin, Ibuprofen, Tree nuts
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 09.04.2022
- Impfdatum
- 10.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- UN / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Rash
Rash papular
Rash pruritic
Symptomtext
Over a week after receiving my second COVID-19 booster, I started getting rashes on my skin on different part of my body; below waist, hand, inner side wrist, foot, over groin, under the breast. It was itching and burning. Occasionally I could see and feel very thin elongated bump strips on the rash area. I had also itched on my head under the hair. The largest rash size was about 4"x3". The rash ?attack' would build up in few minutes and last close to an hour. I have been having rashes every day till the present day. In recent days the rash frequency has been coming down and the rash area is now smaller and less intensive in terms of itching and burning. I have never experienced such rashes in my life. (All my 3 previous COVID-19 vaccination were Moderna after which there were no rashes.) I would like to point out that my husband received his second booster on 3/11/2022 at the same pharmacy, Moderna lot 045L21A (same as my lot). However, my husband till the present day did not experience any rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- rosuvastatin, baby aspirin, vitamin D, calcium multi-vitamin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 19.03.2022
- Beginn
- 27.03.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Flushing
Urticaria
Symptomtext
Severe, full body hives and flushing for at least 8 days at the time of filling out this form.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- Diagnosis by dermatologist on 03/29/2022.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- birth control
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Injection site pain
Product administered to patient of inappropriate age
Symptomtext
A 12-year-old patient was accidentally given 0.25 ml of the Moderna COVID 19 vaccine, which is not FDA-approved for those under 18 years of age. Follow-up monitoring was completed 24 and 72 hours after injection. The patient experienced fatigue and mild injection site pain. No fever or other adverse effects were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 03.04.2022
- Impfdatum
- 02.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chronic spontaneous urticaria
Rash
Rash pruritic
Urticaria
Symptomtext
Chronic spontaneous urticaria Hives and itchy rashes all over body that come and go
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chronic spontaneous urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Covid
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Malaise
Pyrexia
Symptomtext
Starting the day after the shot, patient was sick for 5 days with chills, fever, felt ill.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- 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: ja
Erholt: unbekannt
Pruritus
Symptomtext
Patient called pharmacy and reported itching on face and neck, around 1 hours and 45 minutes after vaccination. Patient stated she would seek medical attention at place of employment ( Hospital/ Clinic)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 12.02.2022
- Beginn
- 12.03.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chills
Erythema
Headache
Myalgia
Pyrexia
Swelling
Symptomtext
headache; chills; fever/temperature of 103.2; body aches; big huge red knot; about the size of a golf ball that stuck up about 2 cm; This spontaneous case was reported by an other health care professional and describes the occurrence of ERYTHEMA (big huge red knot), SWELLING (about the size of a golf ball that stuck up about 2 cm), CHILLS (chills), PYREXIA (fever/temperature of 103.2) and MYALGIA (body aches) in a 57-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 076L21D and 045L21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 12-Feb-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 12-Mar-2022, received second dose of mRNA-1273 (Spikevax) (Intramuscular) dosage was changed to 1 dosage form. On 12-Mar-2022, the patient experienced ERYTHEMA (big huge red knot) and SWELLING (about the size of a golf ball that stuck up about 2 cm). On 13-Mar-2022, the patient experienced CHILLS (chills), PYREXIA (fever/temperature of 103.2) and MYALGIA (body aches). On 14-Mar-2022, the patient experienced HEADACHE (headache). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) at a dose of Tylenol about every 2 hours and IBUPROFEN (MOTRIN [IBUPROFEN]) at a dose of Motrin about every 2 hours. At the time of the report, ERYTHEMA (big huge red knot) and SWELLING (about the size of a golf ball that stuck up about 2 cm) outcome was unknown, CHILLS (chills) and PYREXIA (fever/temperature of 103.2) had resolved with sequelae and MYALGIA (body aches) and HEADACHE (headache) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 13-Mar-2022, Body temperature: 103.2 (High) fever/temperature of 103.2. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications was not provided by the reporter. Patient experienced symptoms saturday evening after receiving the second dose of the vaccine. Patient asked her HCP for Decadron or steroids, who denied her request.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220313; Test Name: temperature of 103.2; Result Unstructured Data: fever/temperature of 103.2
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Skin discolouration
Symptomtext
At approximately 11:31 am, patient complaint of "bumps" at right arm (9 minutes post Moderna booster vaccination). This RN assessed patient and noted slight pinkness to right arm, patient denied pruritus, no complaints of difficulty breathing or shortness of breath noted and patient appeared to be in no apparent distress. Respirations 18, pulse rate of 76, 99% spo2 on room, respirations even and unlabored. Benadryl 25 mg oral tablet was given prophylactically at 11:35 am and advised patient to remain an additional 15 minutes for observation. At approximately 11:48 am patient condition improved, she denied any pain and was in no apparent distress. Respirations, pulse rate and oxygen saturation remain stable at 18, 78, and 99% respectively. Patient was discharged home with husband at 11:54 am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Myalgia
Symptomtext
Headache, Myalgia, Fatigue Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Fatigue and HA
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 18.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Disturbance in attention
Dizziness
Extrasystoles
Fatigue
Feeling abnormal
Headache
Heart rate irregular
Lymphadenopathy
Lymphoedema
Symptomtext
Headache, lymphedema between clavicle and shoulder on right side, swollen lymph nodes on right side of body in neck, under arm and groin. Dizziness, generalized fatigue and head feeling ?foggy? or ?spacey?. Hard time concentrating and irregular heartbeat, feels like heart is skipping a beat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Muscle spasms
Neck pain
Vaccine positive rechallenge
Symptomtext
On Tuesday, 3/8/22, The patient (DOB: (Privacy)) came to the Covid-19 Vaccination Site for her Moderna Covid-19 booster vaccine and flu vaccine. Client's medical history includes low vitamin D and iron, a penicillin and latex allergy, on no medications and was to be a 30 minute wait. At 10:49 AM, client was vaccinated with Moderna Covid-19 booster dose (LOT #: 045L21A) in her left deltoid. Client was vaccinated with Flucelvax vaccine (LOT #: 308496) in her right deltoid. At 11:22 AM, while waiting in the Observation Area, client stated to EMT her fingers in her left hand and back of her neck felt "numb and crampy" an "8 out of 10" pain. At 11:22 AM, vitals were started: BP: 138/78, HR: 93, O2 sat: 100%, RR: 16. Client was offered water by EMT that she drank. At 11:32 AM, BP: 142/80, HR: 88, O2 sat: 100%, RR 16. Client states her hand and neck pain is now a "1 out of 10" and she recalls feeling a similar sensation after her first Moderna Covid-19 dose but not her second Moderna Covid-19 dose. At 11:40 AM, client states she feels much better and felt stable enough to go home. No further interventions needed. Client was educated by EMT on signs and symptoms of adverse reactions and when to go to the ED/call MD. Client was also encouraged to sign-up on smartphone-based tool. Client left vaccination site with a steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- low vitamin D and iron
- Andere Medikamente
- n/a
- Allergien
- penicillin, latex allergy
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 04.03.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse reaction
Arthralgia
Back pain
Fluid retention
Pain
Spinal pain
Symptomtext
Acute aching in all joints for 48 hours. Fluid retention in right knee started sometime during those 48 hours. Continual pain/acing in my whole back that radiates out from spinal column.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None. Medical exam at local clinic on 3/4/2022. Treatment of knee was advised and awareness of conditions that warrant an ER visit. Also, recommendation from clinician to report adverse reaction.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 03.03.2022
- Impfdatum
- 13.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Gait disturbance
Pruritus
Vertigo
Vomiting
Symptomtext
Patient received their Moderna booster. Upon receipt their arm itched slightly, but no rash. this cleared up and patient was fine for approximately 9 days. On the 10th day the patient developed extreme dizziness and vomiting. Urgent care diagnosed vertigo. The patient took Meclizine and Sudafed with no relief. She worsened and was unable to walk due to the dizziness. She then went to ER. They also thought it was vertigo and gave valium with no relief. They referred her to Neurologist. Today the patient went to neurology apt and the doctor thinks it is Neuritis. They did exercises and red light therapy with patient that gave some relief. They are following up with patient Monday. Patient came in today to get supplements rec by neurologist. Pt in good spirits and I talked to her for a long period. Will follow up closely
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Unknown. but neurologist did several tests
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- 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
Fatigue
Injection site pain
Nausea
Orbital swelling
Symptomtext
24 hrs. after receiving vaccine I developed orbital swelling. I currently still have the swelling despite antihistamines 4 days later. I also had fatigue, nausea, and site soreness that lasted 1 day after injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Symptomtext
Patient called today to report hives and itching on arms, chest and back. It started today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Sluggishness
Symptomtext
fatigue, sluggish, headache, rundown
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Symptomtext
10 Days post Moderna Covid-19 booster shot, patient presented with severe itching and hives on hands, forearms, palms, armpits, back, scalp, front of neck, and back of neck. No other lifestyle changes took place, only the addition of the 3rd dose of the vaccine. This vaccination has definite side effects and should not be required to be or simply administered knowing it will have adverse outcomes for patients. Symptoms were attempted to be managed by over the counter anti-allergy medication, but the symptoms still persist without relief.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Visible observation of rash and hives.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin Family
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- F
- 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: ja
Erythema
Feeling hot
Pruritus
Urticaria
Symptomtext
Patient reported feeling hot and began to break out in hives that spread over her chest. Her chest was visibly red and patient was observed scratching the area. Symptoms began around 2:35 pm post injection. Patient was given 50 mg of Benadryl and stayed in the clinic for the remaining 30 minute observation period. Patient reported before leaving the clinic that she that symptoms were improving, she felt better and would take additional Benadryl as needed at home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Benadryl (Diphenhydramine) 50 mg (2x25mg tablets)
- Allergien
- Patient said she had previous reaction to Covid vaccine including difficulty breathing, fever and hives.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Abortion threatened
Alanine aminotransferase
Albumin globulin ratio
Amniorrhoea
Anion gap
Aspartate aminotransferase
Bacterial test
Basophil count
Bilirubin urine
Blood albumin
Blood alkaline phosphatase
Blood bilirubin
Blood calcium
Blood chloride
Blood creatinine
Blood glucose
Blood potassium
Blood pressure measurement
Symptomtext
premature delivery; Contractions 5 days after first shot; hemorrhage in early pregnancy; Leaking amniotic fluids after first shot; Ruptured,membranes,premature; Acute cystitis with hematuria; Threatened miscarriage; hemorrhage in early pregnancy; Oligohydramnios; Severe diarrhea 7 hours after first shot; 19 weeks pregnant received first dose; This spontaneous retrospective pregnancy case was reported by a consumer and describes the occurrence of PREMATURE LABOUR (Contractions 5 days after first shot), the first episode of HAEMORRHAGE IN PREGNANCY (hemorrhage in early pregnancy), AMNIORRHOEA (Leaking amniotic fluids after first shot), PREMATURE RUPTURE OF MEMBRANES (Ruptured,membranes,premature), CYSTITIS (Acute cystitis with hematuria), ABORTION THREATENED (Threatened miscarriage), OLIGOHYDRAMNIOS (Oligohydramnios), the second episode of HAEMORRHAGE IN PREGNANCY (hemorrhage in early pregnancy) and PREMATURE DELIVERY (premature delivery) in a 24-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 31-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. The patient's last menstrual period was on an unknown date and the estimated date of delivery was 27-Jun-2022. On 31-Jan-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced the first episode of HAEMORRHAGE IN PREGNANCY (hemorrhage in early pregnancy) (seriousness criteria hospitalization and medically significant), AMNIORRHOEA (Leaking amniotic fluids after first shot) (seriousness criterion hospitalization), DIARRHOEA (Severe diarrhea 7 hours after first shot) and MATERNAL EXPOSURE DURING PREGNANCY (19 weeks pregnant received first dose). On 04-Feb-2022, the patient experienced PREMATURE LABOUR (Contractions 5 days after first shot) (seriousness criterion hospitalization prolonged). On 05-Feb-2022, the patient experienced PREMATURE DELIVERY (premature delivery) (seriousness criterion hospitalization). On an unknown date, the patient experienced PREMATURE RUPTURE OF MEMBRANES (Ruptured,membranes,premature) (seriousness criterion hospitalization), CYSTITIS (Acute cystitis with hematuria) (seriousness criterion hospitalization), ABORTION THREATENED (Threatened miscarriage) (seriousness criterion hospitalization), OLIGOHYDRAMNIOS (Oligohydramnios) (seriousness criterion medically significant) and the second episode of HAEMORRHAGE IN PREGNANCY (hemorrhage in early pregnancy) (seriousness criterion hospitalization). The patient was hospitalized from 04-Feb-2022 to 06-Feb-2022 due to ABORTION THREATENED, CYSTITIS, HAEMORRHAGE IN PREGNANCY and PREMATURE RUPTURE OF MEMBRANES. The delivery occurred on 04-Feb-2022, which was reported as Spontaneous Abortion. For foetus 1, The outcome was reported as Spontaneous Abortion w Cong Anomaly. The patient was treated with NITROFURANTOIN (oral) for Adverse event, at a dose of 100 milligram. On 31-Jan-2022, MATERNAL EXPOSURE DURING PREGNANCY (19 weeks pregnant received first dose) had resolved. On 04-Feb-2022, PREMATURE LABOUR (Contractions 5 days after first shot), AMNIORRHOEA (Leaking amniotic fluids after first shot) and DIARRHOEA (Severe diarrhea 7 hours after first shot) had resolved. On 05-Feb-2022, PREMATURE DELIVERY (premature delivery) had resolved. At the time of the report, PREMATURE RUPTURE OF MEMBRANES (Ruptured,membranes,premature), CYSTITIS (Acute cystitis with hematuria), ABORTION THREATENED (Threatened miscarriage), OLIGOHYDRAMNIOS (Oligohydramnios) and the last episode of HAEMORRHAGE IN PREGNANCY (hemorrhage in early pregnancy) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 01-Feb-2022, Alanine aminotransferase (13-56): 30 u/l (normal) 30 U/L. On 01-Feb-2022, Albumin globulin ratio (1.1-2.2): 0.8 (Low) 0.8. On 01-Feb-2022, Anion gap (6-16): 4meq/l (Low) 4meq/L. On 01-Feb-2022, Aspartate aminotransferase (15-37): 10 u/l (Low) 10 U/L. On 01-Feb-2022, Bacterial test: light (abnormal) Light. On 01-Feb-2022, Basophil count (0.00-0.22): 0 k/ul (normal) 0 k/uL and 0 percent 0 Percent. On 01-Feb-2022, Bilirubin urine: pos 3+ (abnormal) Pos 3+. On 01-Feb-2022, Blood albumin (3.4-5.0): 3.0 g/dl (Low) 3.0 g/dl. On 01-Feb-2022, Blood alkaline phosphatase (45-117): 67 u/l (normal) 67 U/L. On 01-Feb-2022, Blood bilirubin (0.2-1.0): 0.1 mg/dl (Low) 0.1 mg/dl. On 01-Feb-2022, Blood calcium (8.5-10.1): 8.7 mg/dl (normal) 8.7 mg/dl. On 01-Feb-2022, Blood chloride (98-107): 110 meq/l (High) 110 meq/L. On 01-Feb-2022, Blood creatinine (0.55-1.01): 0.60 mg/dl (normal) 0.60 mg/dl. On 01-Feb-2022, Blood glucose (70-99): 105 mg/dl (High) 105 mg/dl. On 01-Feb-2022, Blood potassium (3.5-5.1): 3.6 meq/l (normal) 3.6 meq/L. On 01-Feb-2022, Blood sodium (136-145): 138 meq/l (normal) 138 meq/L. On 01-Feb-2022, Blood urea (7-18): 7 mg/dl (normal) 7 mg/dl. On 01-Feb-2022, Blood urea nitrogen/creatinine ratio (07-25): 12 (normal) 12. On 01-Feb-2022, Carbon dioxide (21-32): 24 meq/l (normal) 24 meq/L. On 01-Feb-2022, Chromaturia: red (abnormal) Red. On 01-Feb-2022, Crystal urine: present (abnormal) Present. On 01-Feb-2022, Differential white blood cell count: auto diff Auto diff. On 01-Feb-2022, Eosinophil count (0.00-0.55): 0.15 k/ul (normal) 0.15 K/uL and 1 percent 1 percent. On 01-Feb-2022, Globulin (2.4-3.5): 3.9 g/dl (High) 3.9 g/dl. On 01-Feb-2022, Glomerular filtration rate: >120 ml/min/1.73m2 (normal) >120 mL/min/1.73m2 and >120 ml/min/1.73m2 (normal) >120 mL/min/1.73m2. On 01-Feb-2022, Glucose urine: negative (Negative) Negative. On 01-Feb-2022, Haematocrit (36-47): 34.9 percent (Low) 34.9 percent. On 01-Feb-2022, Haemoglobin (12-16): 11.8 g/dl (Low) 11.8 g/dl. On 01-Feb-2022, Human chorionic gonadotropin (0-4): 19,632 miu/ml (High) 19,632 mIU/mL and positive (Positive) Positive, Pregnancy urine positive. On 01-Feb-2022, Immature granulocyte count: 1 percent 1 Percent. On 01-Feb-2022, Lymphocyte count (0.90-4.95): 2.04 k/ul (normal) 2.04 k/uL and 14 percent 14 percent. On 01-Feb-2022, Mean cell haemoglobin (27-33): 31.1 pg (normal) 31.1 pg. On 01-Feb-2022, Mean cell haemoglobin concentration (32-36.5): 33.8 percent (normal) 33.8 percent. On 01-Feb-2022, Mean cell volume (80-99): 91.8 fl (normal) 91.8 fL. On 01-Feb-2022, Mean platelet volume (8.5-12.0): 9.7 fl (normal) 9.7 fL. On 01-Feb-2022, Monocyte count: 5 percent 5 percent and 0.73 k/ul (normal) 0.73 k/uL. On 01-Feb-2022, Neutrophil count (2.07-8.08): 11.53 k/ul (High) 11.53 k/uL, 79 percent (normal) 79 percent and 11.53 k/ul (High) 11.53 k/uL. On 01-Feb-2022, Nitrite urine: negative (Negative) Negative. On 01-Feb-2022, Platelet count (140-440): 327 k/ul (normal) 327 k/uL. On 01-Feb-2022, Protein total (6.4-8.2): 6.9 g/dl (normal) 6.9 g/dl. On 01-Feb-2022, Protein urine: pos 2+ (abnormal) Pos 2+. On 01-Feb-2022, Red blood cell count (4-5.40): 3.80 m/ul (Low) 3.80 M/uL. On 01-Feb-2022, Red blood cells urine (0-3): 100/hpf (abnormal) 100/hpf. On 01-Feb-2022, Red cell distribution width (10-14.5): 12.4 percent (normal) 12.4 percent and 41.1/fl (normal) 41.1/fL. On 01-Feb-2022, Specific gravity urine (1.005-1.030): 1.010 (normal) 1.010. On 01-Feb-2022, Ultrasound antenatal screen: single viable intrauterine pregnancy is visualized Single viable intrauterine pregnancy is visualized. On 01-Feb-2022, Urinary sediment present: few/lpf (normal) Few/lpf and absent Absent. On 01-Feb-2022, Urine analysis: present (abnormal) Present and sl cloudy (abnormal) Sl cloudy. On 01-Feb-2022, Urine ketone body: negative (Negative) Negative. On 01-Feb-2022, Urine leukocyte esterase: negative (Negative) Negative. On 01-Feb-2022, Urobilinogen urine (0.2-1.0): 0.2 ehrilch/dl (normal) 0.2 Ehrilch/dL. On 01-Feb-2022, White blood cell count (4.5-11.0): 14.6 k/?l (High) 14.6 k/?l. On 01-Feb-2022, White blood cells urine (0-5): 6-10/hpf (abnormal) 6-10/hpf. On 01-Feb-2022, pH urine (5.0-8.0): 7.0 (normal) 7.0. On an unknown date, Blood pressure measurement: 117/76 117/76. On an unknown date, Body temperature: 98.6 degree fahrenheit 98.6 degree Fahrenheit. On an unknown date, Heart rate: 80 80. On an unknown date, Oxygen saturation: 99 percent 99 percent. On an unknown date, Respiratory rate: 18 18. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that 7 hours after vaccination patient had severe diarrhea. Eventually patient was leaking amniotic fluids and had vaginal bleeding. Patient's water broke. Patient visited an emergency room (First Hospital contact info). 5 days later, on 04FEB2022 patient had contractions and visited the emergency room (2nd Hospital contact information). patient delivered the baby at 20 weeks gestation, and the baby died. Company comment: This spontaneous case concerns a 24-year-old pregnant female patient with no LMP of EDC reported with no relevant medical history who experienced the serious (hospitalization) events of hemorrhage in early pregnancy (IME), amniorrhea, oligohydramnios (IME), cystitis and threatened abortion the day of; premature rupture of membranes, premature labor, hemorrhage in early pregnancy and premature delivery 5 days after, the first dose of mRNA-1273. Testing involved a fetal ultrasound that showed a live fetus at an estimated 19 weeks 1 day gestation on 31JAN2022 and lack of amniotic fluid, a metabolic panel with no significant findings and a urinalysis with evidence of cystitis. The possible cystitis is a confounder as it can be related to PTL. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. Ultrasound findings-The cervix contains small amount of fluid with a length of 6.6 cm. Marked oligohydramnios. Placenta is fundal. No detectable amniotic fluid. Fetal measurements -Biparietal diameter-4.3 cm/19 weeks 0 days, abdominal circumference-14.3 cm /19 weeks 4 days, femur length -9 cm /19 weeks 1 day. Fetal heart rate -161 bpm. Patient was asked to stop metronidazole 500 mg ORAL Tablet(FLAGYL) No concomitant medications were reported. This case was linked to MOD-2022-486841 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 17-Feb-2022: Significant follow-up document was received on 17-FEB-2022. New reporters, lab data, treatment, concomitnt medications, new events were added.; Sender's Comments: This spontaneous case concerns a 24-year-old pregnant female patient with no LMP of EDC reported with no relevant medical history who experienced the serious (hospitalization) events of hemorrhage in early pregnancy (IME), amniorrhea, oligohydramnios (IME), cystitis and threatened abortion the day of; premature rupture of membranes, premature labor, hemorrhage in early pregnancy and premature delivery 5 days after, the first dose of mRNA-1273. Testing involved a fetal ultrasound that showed a live fetus at an estimated 19 weeks 1 day gestation on 31JAN2022 and lack of amniotic fluid, a metabolic panel with no significant findings and a urinalysis with evidence of cystitis. The possible cystitis is a confounder as it can be related to PTL. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220201; Test Name: SGPT(ALT); Result Unstructured Data: 30 U/L; Test Date: 20220201; Test Name: A/G RATIO; Result Unstructured Data: 0.8; Test Date: 20220201; Test Name: ANION GAP; Result Unstructured Data: 4meq/L; Test Date: 20220201; Test Name: SGOT(AST); Result Unstructured Data: 10 U/L; Test Date: 20220201; Test Name: BACTERIA,UA; Result Unstructured Data: Light; Test Date: 20220201; Test Name: BASOPHIL ABS; Result Unstructured Data: 0 k/uL; Test Date: 20220201; Test Name: BASOPHILS; Result Unstructured Data: 0 Percent; Test Date: 20220201; Test Name: BILIRUBINE,UA; Result Unstructured Data: Pos 3+; Test Date: 20220201; Test Name: ALBUMIN; Result Unstructured Data: 3.0 g/dl; Test Date: 20220201; Test Name: ALKALINE PHOSPHATASE; Result Unstructured Data: 67 U/L; Test Date: 20220201; Test Name: BILIRUBIN TOTAL; Result Unstructured Data: 0.1 mg/dl; Test Date: 20220201; Test Name: CALCIUM; Result Unstructured Data: 8.7 mg/dl; Test Date: 20220201; Test Name: CHLORIDE; Result Unstructured Data: 110 meq/L; Test Date: 20220201; Test Name: CREATININE; Result Unstructured Data: 0.60 mg/dl; Test Date: 20220201; Test Name: GLUCOSE; Result Unstructured Data: 105 mg/dl; Test Date: 20220201; Test Name: POTASSIUM; Result Unstructured Data: 3.6 meq/L; Test Name: BLOOD PRESSURE; Result Unstructured Data: 117/76; Test Date: 20220201; Test Name: SODIUM; Result Unstructured Data: 138 meq/L; Test Date: 20220201; Test Name: BUN; Result Unstructured Data: 7 mg/dl; Test Date: 20220201; Test Name: BUN/CREAT RATIO; Result Unstructured Data: 12; Test Name: Body temperature; Result Unstructured Data: 98.6 degree Fahrenheit; Test Date: 20220201; Test Name: CARBON DIOXIDE; Result Unstructured Data: 24 meq/L; Test Date: 20220201; Test Name: COLOR,UA; Result Unstructured Data: Red; Test Date: 20220201; Test Name: AMORPHOUS CRYSTALS; Result Unstructured Data: Present; Test Date: 20220201; Test Name: MANUAL DIFFERENTIAL; Result Unstructured Data: Auto diff; Test Date: 20220201; Test Name: EOSINO ABS; Result Unstructured Data: 0.15 K/uL; Test Date: 20220201; Test Name: EOSINOPHILS; Result Unstructured Data: 1 percent; Test Date: 20220201; Test Name: GLOBULIN; Result Unstructured Data: 3.9 g/dl; Test Date: 20220201; Test Name: AFR.AMER.EGFR; Result Unstructured Data: >120 mL/min/1.73m2; Test Date: 20220201; Test Name: NON-AFR.AMER.eGFR; Result Unstructured Data: >120 mL/min/1.73m2; Test Date: 20220201; Test Name: GLUCOSE,UA; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220201; Test Name: HEMATOCRIT; Result Unstructured Data: 34.9 percent; Test Date: 20220201; Test Name: Hemoglobin; Result Unstructured Data: 11.8 g/dl; Test Name: Pulse; Result Unstructured Data: 80; Test Date: 20220201; Test Name: HCG QUANTITATIVE; Result Unstructured Data: 19,632 mIU/mL; Test Date: 20220201; Test Name: HCG, QUALITATIVE,URINE; Test Result: Positive ; Result Unstructured Data: Positive, Pregnancy urine positive; Test Date: 20220201; Test Name: IMMATURE GRANULOCYTES; Result Unstructured Data: 1 Percent; Test Date: 20220201; Test Name: LYMPHOCYTE ABS; Result Unstructured Data: 2.04 k/uL; Test Date: 20220201; Test Name: LYMPHOCYTES; Result Unstructured Data: 14 percent; Test Date: 20220201; Test Name: MCH; Result Unstructured Data: 31.1 pg; Test Date: 20220201; Test Name: MCHC; Result Unstructured Data: 33.8 percent; Test Date: 20220201; Test Name: MCV; Result Unstructured Data: 91.8 fL; Test Date: 20220201; Test Name: MPV; Result Unstructured Data: 9.7 fL; Test Date: 20220201; Test Name: MONOCYTES; Result Unstructured Data: 5 percent; Test Date: 20220201; Test Name: MONOCYTES ABS; Result Unstructured Data: 0.73 k/uL; Test Date: 20220201; Test Name: ANC; Result Unstructured Data: 11.53 k/uL; Test Date: 20220201; Test Name: SEGMENTED NEUTROPHILS; Result Unstructured Data: 79 percent; Test Date: 20220201; Test Name: SEGS-ABS; Result Unstructured Data: 11.53 k/uL; Test Date: 20220201; Test Name: NITRITE; Test Result: Negative ; Result Unstructured Data: Negative; Test Name: OXYGEN SATURATION; Result Unstructured Data: 99 percent; Test Date: 20220201; Test Name: PH,Urine; Result Unstructured Data: 7.0; Test Date: 20220201; Test Name: PlLATELET COUNT; Result Unstructured Data: 327 k/uL; Test Date: 20220201; Test Name: Protein; Result Unstructured Data: 6.9 g/dl; Test Date: 20220201; Test Name: PROTEIN,UA; Result Unstructured Data: Pos 2+; Test Date: 20220201; Test Name: RBC; Result Unstructured Data: 3.80 M/uL; Test Date: 20220201; Test Name: RBC,URINE; Result Unstructured Data: 100/hpf; Test Date: 20220201; Test Name: RDW-CV; Result Unstructured Data: 12.4 percent; Test Date: 20220201; Test Name: RDW-SD; Result Unstructured Data: 41.1/fL; Test Name: Respiration; Result Unstructured Data: 18; Test Date: 20220201; Test Name: SPECIFIC GRAVITY; Result Unstructured Data: 1.010; Test Date: 20220201; Test Name: US OB LIMITED ONE OR MORE FETUSES; Result Unstructured Data: Single viable intrauterine pregnancy is visualized; Test Date: 20220201; Test Name: EPITHELIAL CELLS; Result Unstructured Data: Few/lpf; Test Date: 20220201; Test Name: RENAL EPITHELIALS; Result Unstructured Data: Absent; Test Date: 20220201; Test Name: MUCUS UA; Result Unstructured Data: Present; Test Date: 20220201; Test Name: TURBIDITY; Result Unstructured Data: Sl cloudy; Test Date: 20220201; Test Name: KETONES,UA; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220201; Test Name: LEUKOCYTES EATERASE; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220201; Test Name: UROBILINOGEN; Result Unstructured Data: 0.2 Ehrilch/dL; Test Date: 20220201; Test Name: WBC; Result Unstructured Data: 14.6 k/?l; Test Date: 20220201; Test Name: WBC,URINE; Result Unstructured Data: 6-10/hpf
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Injection site swelling
Neck pain
Pain
Pain in extremity
Symptomtext
Local tenderness and localized swelling at time of injection. The injection site swelling gone in 12 hours. The localized pain remained and became worse. 16 days later, minimal pain (all the time), which increases substantially with movement. The pain moved up my arm into shoulder and neck. Reported to doctor on 2/23/2022 and to pharmacist on 2/26/2022. Doctor suggested heat. Pharmacist suggested ibuprofen. Neither seems to relieve the pain. I allow the pain to limit my activities. If the pain increases with a certain movement or activity, I stop what I'm doing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Migraines
- Andere Medikamente
- Zomig 5mg PRN, Ubrelvy 100mg PRN, Levothyroxine 25mcg QAM, Amitriptyline 40mg HS, Omeprazole 40 QD, Bethanechol 25mg QID
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Heart rate increased
Pruritus
Rash erythematous
Symptomtext
Patient stated they were itching all over their body. They had red bumps on arms and on chest. They were given 50mg of diphenhydramine and monitored. Blood pressure and heart rate were elevated. No other adverse effects noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Blood Pressure: 140/90 Heart Rate: 97 bpm
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asplenic
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Same adverse effects from previous Moderna shot
- Staat
- AZ
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Fatigue
Pain
Pyrexia
Vomiting
Symptomtext
Systemic: Body Aches Generalized-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium, Systemic: Vomiting-Medium, Systemic: Weakness-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Rash
Symptomtext
patient had joint aches for 4 days. also rash on legs and inside the elbow that started 4 days after vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- 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
Immediate post-injection reaction
Injection site haemorrhage
Injection site inflammation
Symptomtext
excessive bleeding and inflammation around the injection site immediately after injection...bleeding stopped after 1 minute and applied ice pack for 15 minutes until inflammation completely resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site haemorrhage
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Product administered at inappropriate site
Pyrexia
Symptomtext
Felt like he had a fever/temperature was 100.2 F, 100.0 F; second dose like 4 inches lower on my arm than the last dose; This spontaneous case was reported by a consumer and describes the occurrence of PYREXIA (Felt like he had a fever/temperature was 100.2 F, 100.0 F) and PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (second dose like 4 inches lower on my arm than the last dose) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. The patient's past medical history included Headache and Pain neck. Concurrent medical conditions included Sinusitis. On 03-Feb-2022, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Feb-2022, the patient experienced PYREXIA (Felt like he had a fever/temperature was 100.2 F, 100.0 F) and PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (second dose like 4 inches lower on my arm than the last dose). On 03-Feb-2022, PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (second dose like 4 inches lower on my arm than the last dose) had resolved. At the time of the report, PYREXIA (Felt like he had a fever/temperature was 100.2 F, 100.0 F) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: 100.2 (High) 100.2 F and 100.0 (High) 100.0 F. The patient reported that second dose was closer to his bicep. No concomitant product information was provided. No treatment medication information was provided. This case was linked to MOD-2022-473681 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: 100.2 F; Test Name: Body temperature; Result Unstructured Data: 100.0 F
- Aktuelle Erkrankungen
- Sinusitis
- Vorgeschichte
- Medical History/Concurrent Conditions: Headache; Pain neck
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Rash erythematous
Rash papular
Rash pruritic
Symptomtext
Patient discovered a raised, rectangular, pruritic, red rash at injection site the night of vaccination, approximately 12 hours later. Approximately 2 inches in diameter. No other symptoms. Has been improving since but is still present 5 days later. Reported to pharmacy today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Macrolides, tetracyclines
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Swelling
Symptomtext
arm pain as well as swelling all through neck, possibly lymph nodes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Amniorrhoea
Diarrhoea
Exposure during pregnancy
Live birth
Premature delivery
Premature labour
Premature rupture of membranes
Preterm premature rupture of membranes
Ultrasound foetal abnormal
Vaginal haemorrhage
Symptomtext
Preterm Premature Rupture of Membranes following diarrhea- presenting as patient passing large clots of tissue and excessive amounts of blood. Event occurred roughly 7 HOURS following dose of vaccine on 01/31/2022. Patient was 19 weeks + 5 days pregnant. Patient was taken to hospital where membrane rupture and complete loss of amniotic fluid were confirmed via ultrasound. PPROM was re-confirmed on 02/01/2022 by MD. Patient was monitored for infection and placed on oral antibiotics until she started having contractions on 02/03/2022 around 7:30pm. Patient continued having contractions overnight and was checked into hospital the following day around 2:30pm, where she received more an epidural, intravenous antibiotics and fluid. Patient gave birth to a baby boy at only 20 wks +3 days pregnant. Baby weighed 9 oz and was 9.25 inches in length. There were no pregnancy complications nor concerns prior to this event. There were no observed abnormalities in the baby upon birth. This was a live birth. Estimated due date was 06/27/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Mild scoliosis; Mild arthritis of the hips; Migraine; Asthma (non-problematic)
- Andere Medikamente
- Prenatal Multi + 200mg DHA; Vitamin D3 2,000 IU; Acetaminophen 650mg (as needed); Caffeine 200mg (as needed only for migraine); Digest Gold Digestive Enzymes (occasionally); Famotidine 25mg (prn)
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Injection site warmth
Symptomtext
Patient received second Moderna vaccine on 1/31/22. Noticed tenderness at injection site on 2/1/22. Contacted pharmacy on 2/2/22 as she noted the injection site was red/swollen and warm to touch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Pain
Symptomtext
Chills, body aches and headaches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Type 2 diabetes
- Vorgeschichte
- -
- Andere Medikamente
- Metformin 500mg, Amlodipine 10mg, Atorvastatin 20mg, Sertraline 25mg
- Allergien
- Codeine
- Vorherige Impfungen
- 05/06/2021.
- Staat
- PA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Headache
Nausea
Pain
Vaccine positive rechallenge
Symptomtext
Pt. states that after receiving the 3rd Booster of Moderna 11/03/2021, started experiencing symptoms of dizziness, headache, body aches, and slight nausea. No noted Primary visit/communications. Symptoms have subsided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetic
- Andere Medikamente
- Tylenol, Victoza, Previstatin, Losartan, Protonix, Hydrochlorothiazide
- Allergien
- Levaquin, Azithromycin
- Vorherige Impfungen
- 2nd Moderna 01/28/2021 (nausea, dizziness, headache, body aches lasting 24hrs)
- Staat
- IA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 17.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Cough
Fatigue
Headache
Myalgia
Pyrexia
Sneezing
Symptomtext
Got chills, very fatigue had a fever of 100.0, sneezing, headache and coughing also experiencing weakness and muscle pains
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- cellcept, mirofinalate, calcium w/vit d
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 26.12.2023
- Impfdatum
- 16.03.2022
- Beginn
- 22.12.2023
- Tage bis Beginn
- 646,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Respiratory tract congestion
SARS-CoV-2 test
Sinus congestion
Symptomtext
Chest congestion, sinus congestion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- IDNOW
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Codeine, hydrocodone, levofloxacin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 03.02.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 27,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- 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: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- 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
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- 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: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 91,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- 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
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 02.03.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- 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
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 02.03.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- 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: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- 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: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 14.03.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 14.03.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product administration duration
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product administration duration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- 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: ja
Incorrect product administration duration
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product administration duration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product administration duration
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product administration duration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product administration duration
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product administration duration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- 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
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 02.03.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- 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
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 11.10.2023
- Impfdatum
- 22.09.2022
- Beginn
- 10.10.2023
- Tage bis Beginn
- 383,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 25.09.2023
- Impfdatum
- 09.11.2022
- Beginn
- 21.09.2023
- Tage bis Beginn
- 316,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 25.09.2023
- Impfdatum
- 09.11.2022
- Beginn
- 21.09.2023
- Tage bis Beginn
- 316,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 11.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE; no adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (no adverse event) in a female patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular use) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular use), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE). Concomitant product use was not provided by the reporter. It is unknown if the patient experienced any additional symptoms/events. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 93,0
- Geschlecht
- M
- Eingang
- 24.08.2023
- Impfdatum
- 09.02.2022
- Beginn
- 04.01.2023
- Tage bis Beginn
- 329,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breakthrough COVID-19
Symptomtext
Covid-19 Breakthrough Infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- AFIB, Basal Cell Carcinoma, COPD, Myasthenia Gravis, Hypothyroidism, Cataracts.
- Andere Medikamente
- Vit. D3, Levothyroxine, Tamsulosin, Acetaminophen, Albuterol, Ferrous Sulfate, Atorvastatin, Xarelto, Spiriva, Hydroxyzine, Pantoprazole, Pyridostigmine Bromide, Risperidone.
- Allergien
- Demerol, Keflex, PCN.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 10.08.2023
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 05.05.2023
- Impfdatum
- 27.10.2022
- Beginn
- 04.05.2023
- Tage bis Beginn
- 189,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 17.04.2023
- Impfdatum
- 07.04.2022
- Beginn
- 14.04.2023
- Tage bis Beginn
- 372,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 08.04.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 189,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray abnormal
Computerised tomogram thorax abnormal
Cough
Pneumonitis
Pulmonary mass
Sensation of foreign body
Symptomtext
I had a feeling that something was in my throat, and it would make me cough. It continued for a while and was very persistent, I decided to make an appointment with my doctor to find out what could possibly be causing this cough to go on for so long. The doctor ordered a chest x-ray that showed I had nodules in my lungs. He then ordered a CT scan that I had on October 19, 2022, that showed I had clusters of nodules with inflammation. I had two more CT scans that also showed that I have the nodules with inflammation. Each CT scan shows the clusters as either bigger or smaller clusters they are never gone just the size is different.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest X-ray abnormal
- Hospital-Tage
- -
- Labordaten
- 14OCT2022 - Chest X-ray - positive for lung nodules and inflammation; 19OCT2022 CT scan -positive for lung nodules and inflammation; 06FEB2023 positive for lung nodules and inflammation; 16MAR2023 positive for lung nodules and inflammation
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension; Hyperlipidemia: Neuropathy; Heart Stent; Pre-Diabetes
- Andere Medikamente
- Protonix; Lipitor; Metoprolol Tartrate: Baby Aspirin; Vitamin C; Calcium; Joint Health Supplement; Multivitamin; Vitamin D3; Krill Oil; Probiotic; Biotin; Turmeric; CoQ10
- Allergien
- Tetanus; Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 14.02.2023
- Impfdatum
- 06.10.2022
- Beginn
- 13.02.2023
- Tage bis Beginn
- 130,0
- 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
- MN
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 14.04.2022
- Beginn
- 27.01.2023
- Tage bis Beginn
- 288,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 17.09.2022
- Beginn
- 11.01.2023
- Tage bis Beginn
- 116,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 1/11/2023 - 1/16/2023 (5 days) Presentation to the ED: COVID + date: 1/11/2023 Treatment: no indication for therapy. Discharge to: Home. Moderna 029L20A 1/21/2021 Moderna 001A21A 2/22/2021 Moderna 053E21A 8/18/2021 Moderna 045L21A 2/17/2022 Pfizer Bivalent GJ2524 9/17/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, HLD, hypothyroidism, CAD, renal transplant, immunocompromised.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 19.01.2023
- Impfdatum
- 28.10.2022
- Beginn
- 18.01.2023
- Tage bis Beginn
- 82,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 18.01.2023
- Impfdatum
- 01.04.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 180,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Foreign body sensation in eyes
Surgery
Symptomtext
I did not have any issues after receiving the vaccine. I started having symptoms on 09/28 as I thought I had something in my eye and removed my contact. I immediately knew something was wrong with the implant. I saw my doctor on 10/06/2022, it was determined I needed another surgery to correct the issue. I have since had the surgery but now I'm having trouble with my other eye and will probably require surgery.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Foreign body sensation in eyes
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Hypertension
- Andere Medikamente
- Aspirin; zinc; METAMUCIL; calcium; centurion
- Allergien
- Thimerosal
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 17.01.2023
- Impfdatum
- 27.09.2022
- Beginn
- 16.01.2023
- Tage bis Beginn
- 111,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 03.01.2023
- Impfdatum
- 03.11.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 57,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 03.11.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 53,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 06.02.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 302,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
HOSPITALIZED WITH COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 20.12.2022
- Impfdatum
- 21.04.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 242,0
- 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
- MN
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 19.12.2022
- Impfdatum
- 21.04.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 239,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 15.09.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 82,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully Vaccinated. COVID infection breakthrough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 09.11.2022
- Impfdatum
- 14.04.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 208,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 14.04.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 207,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 27.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 24.09.2022
- Tage bis Beginn
- 2,0
- 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 COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anorectal disorder
Hypersensitivity
Symptomtext
I experienced a rectal dysfunction and allergies which I have never had in my life.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anorectal disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Lexapro; Losartan
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 06.09.2022
- 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: ja
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 07.04.2022
- Beginn
- 06.09.2022
- Tage bis Beginn
- 152,0
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Renal transplant
Vaccine breakthrough infection
Symptomtext
Fully vaccinated and boosted twice. Renal transplant. COVID breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 21.04.2022
- Beginn
- 18.08.2022
- Tage bis Beginn
- 119,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against 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
- 46,0
- Geschlecht
- M
- Eingang
- 11.08.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Incorrect dose administered
No adverse event
Symptomtext
No adverse event; Moderna dose administered to patient after expiration; Patient received a 0.30 mL dose; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patient after expiration), INCORRECT DOSE ADMINISTERED (Patient received a 0.30 mL dose) and NO ADVERSE EVENT (No adverse event) in a 46-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 19-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .3 milliliter. On 19-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patient after expiration) and INCORRECT DOSE ADMINISTERED (Patient received a 0.30 mL dose). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patient after expiration), INCORRECT DOSE ADMINISTERED (Patient received a 0.30 mL dose) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patient after expiration) and INCORRECT DOSE ADMINISTERED (Patient received a 0.30 mL dose). No concomitant information was reported. The patient received the second booster dose. No adverse reactions had been reported for the patient. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 11.08.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Moderna dose administered to patients after expiration; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patients after expiration) and NO ADVERSE EVENT (No adverse event) in a 53-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 19-Jul-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 19-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patients after expiration). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patients after expiration) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patients after expiration). No concomitant medication reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- U
- Eingang
- 10.08.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patients after expiration) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 19-Jul-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 19-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patients after expiration). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patients after expiration) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patients after expiration). No concomitant medications were reported. Reporter declined to provide patient identifiers for the 4th patient, stating that she already had a follow up form for them. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 10.08.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Moderna dose administered to patient after expiration; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patient after expiration) and NO ADVERSE EVENT (No adverse event) in a 41-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 19-Jul-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 19-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patient after expiration). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patient after expiration) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Moderna dose administered to patient after expiration). It was reported that patient received second booster. Concomitant drugs were not reported. Treatment medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 31.03.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 127,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 14.04.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 112,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 05.08.2022
- Impfdatum
- 14.04.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 112,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 04.08.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Patient received 1st booster dose of the Moderna Covid 19 vaccine after its expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received 1st booster dose of the Moderna Covid 19 vaccine after its expiration date) and NO ADVERSE EVENT (No adverse event) in a 45-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received 1st booster dose of the Moderna Covid 19 vaccine after its expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received 1st booster dose of the Moderna Covid 19 vaccine after its expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient received 1st booster dose of the Moderna Covid 19 vaccine after its expiration date). No concomitant medication was reported. Date the vial was initially stored in the refrigerator: 19-Jul-2022. On 19-Jul-2022, the patient received the first booster dose. The vial did not undergo any temperature excursions. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 51,0
- Geschlecht
- U
- Eingang
- 02.08.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (gave dose of Moderna Covid-19 vaccine after the expiration date.) and NO ADVERSE EVENT (No adverse event) in a 51-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Jul-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 22-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (gave dose of Moderna Covid-19 vaccine after the expiration date.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (gave dose of Moderna Covid-19 vaccine after the expiration date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medications was not provided by the reporter. On unknown date, the vial was initially stored in the refrigerator. The vial did not undergo any temperature excursions. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 36,0
- Geschlecht
- U
- Eingang
- 02.08.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Gave Moderna COVID-19 vaccine after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Gave Moderna COVID-19 vaccine after the expiration date) and NO ADVERSE EVENT (No adverse event) in a 36-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. It was unknown if the patient had allergies to medications, food and other products. It was unknown if the patient ever had COVID positive test or diagnosis. It was unknown if the patient had acute and chronic illnesses at the time of vaccination. On 22-Jul-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 22-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Gave Moderna COVID-19 vaccine after the expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Gave Moderna COVID-19 vaccine after the expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Gave Moderna COVID-19 vaccine after the expiration date). No concomitant medication was reported by reporter. A total of 7 doses were used post expiration date. Vial did not undergo any temperature excursion. It was also unknown whether patient seek medical care. No treatment medication was reported by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if the patient had allergies to medications, food and other products. It was unknown if the patient ever had COVID positive test or diagnosis. It was unknown if the patient had acute and chronic illnesses at the time of vaccination.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 33,0
- Geschlecht
- U
- Eingang
- 02.08.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Dose administered on 22-Jul-2022, after the expiration date 05-Jul-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered on 22-Jul-2022, after the expiration date 05-Jul-2022) in a 33-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Jul-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 22-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered on 22-Jul-2022, after the expiration date 05-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered on 22-Jul-2022, after the expiration date 05-Jul-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Date the vial was initially stored in the refrigerator was unknown. The vial did not undergo any temperature excursions. No treatment information were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 29,0
- Geschlecht
- U
- Eingang
- 02.08.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- 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
No adverse event
Symptomtext
No adverse event; Patient received vaccine after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after the expiration date) and NO ADVERSE EVENT (No adverse event) in a 29-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. It was unknown if the patient had allergies to medications, food and other products. It was unknown if the patient ever had COVID positive test or diagnosis. It was unknown if the patient had acute and chronic illnesses at the time of vaccination. On 22-Jul-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 22-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after the expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after the expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. The date the vial was initially stored in the refrigerator was unknown. The vial did not undergo any temperature excursions. Treatment information was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if the patient had allergies to medications, food and other products. It was unknown if the patient ever had COVID positive test or diagnosis. It was unknown if the patient had acute and chronic illnesses at the time of vaccination.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 45,0
- Geschlecht
- U
- Eingang
- 02.08.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after date of expiry) and NO ADVERSE EVENT (no adverse event) in a 45-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 prophylaxis. The patient ever had COVID + test or diagnosis was unknown. The AE and both Acute and Chronic illnesses at the time of vaccination was unknown. The Allergies including medications, food, and other products was unknown. On 22-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 22-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after date of expiry). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after date of expiry) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Dose administered after date of expiry). No concomitant medications reported. It was reported that 7 doses of Moderna Covid-19 vaccine after the expiration date were administered. The date the vial was initially stored in the refrigerator was unknown. The vial did not undergo any temperature excursions. Other vaccines given within 1 month prior to Moderna COVID-19 vaccine was unknown. The AE cause patient to seek medical care that is office visit, Urgent care, ER, hospitalized was unknown. It was unknown if patient experienced a similar event in the past. The cause of death and was autopsy done was unknown. It was unknown if the symptoms improved or worsened.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient ever had COVID + test or diagnosis was unknown. The AE and both Acute and Chronic illnesses at the time of vaccination was unknown. The Allergies including medications, food, and other products was unknown.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 36,0
- Geschlecht
- U
- Eingang
- 02.08.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Dose administered after manufacturer date of expiry; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) and NO ADVERSE EVENT (No adverse event) in a 36-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 prophylaxis. It was unknown if patient had any allergies, medical history or if received any other vaccine within 1 month prior to Moderna COVID-19 vaccine. Unknown if patient ever had COVID test or diagnosis. On 22-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 22-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry). It was reported that patient received 1st booster. Concomitant drugs were not reported. It was reported that patient received various doses. It was also reported that it was unknown if patient had patient experienced a similar event in the past, unknown if patient was hospitalized. It was also unknown if events improved or worsened. It was reported that 7 doses were administered. It was unknown if vial was initially stored in the refrigerator. The vial did not undergo any temperature excursions. Treatment medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient had any allergies, medical history or if received any other vaccine within 1 month prior to Moderna COVID-19 vaccine. Unknown if patient ever had COVID test or diagnosis.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 44,0
- Geschlecht
- U
- Eingang
- 02.08.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Dose administered after the expiration date 05-Jul-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after the expiration date 05-Jul-2022) in a 44-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 prophylaxis. Allergies (medications, food, and other products) were reported as unknown. It is unknown that patient ever had COVID positive test or diagnosis. Medical History was reported as unknown. Other vaccines given within 1 month prior to Moderna COVID-19 vaccine (type, brand, lot, route, dose number) was unknown. On 22-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 22-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after the expiration date 05-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after the expiration date 05-Jul-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient was administered with 1st booster dose. No concomitant medications were reported. Date the vial was initially stored in the refrigerator was unknown. The vial did not undergo any temperature excursions. AE caused patient to seek medical care (office visit, Urgent care, ER, hospitalized) was unknown. The patient experienced a similar event in the past was unknown. AE Outcome (recovered, residual effects, ongoing, unknown) was unknown. Symptoms improved or worsened was unknown. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Allergies (medications, food, and other products) were reported as unknown. It is unknown that patient ever had COVID positive test or diagnosis. Medical History was reported as unknown. Other vaccines given within 1 month prior to Moderna COVID-19 vaccine (type, brand, lot, route, dose number) was unknown.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 29.04.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 83,0
- 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
On July 21, 2022 I tested positive for COVID-19 at my doctor office. I tested twice, the rapid test came back negative and the PCR test came back positive. My Dr. prescribe me Paxlovid on the same day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Tested positive for COVID-19 July 21, 2022 Prescribe Paxlovid on July 21, 2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 diabetes Asthma Allergies High Blood Pressure High Cholesterol
- Andere Medikamente
- Metformin Celexa Amdllpine Toprol Allergy medicine Protoniz
- Allergien
- Bactrim ds Trazdone Lisinpril
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 29.07.2022
- Impfdatum
- 10.02.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 166,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- -
- Geschlecht
- F
- Eingang
- 29.07.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Dose administered after 30 day beyond use date/administered an expired vaccine; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30 day beyond use date/administered an expired vaccine) in an adult female patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. Concurrent medical conditions included Hypertension, Nervous system disorder NOS (Nerve condition) and Drug allergy (Aspirin). Concomitant products included HYDROCHLOROTHIAZIDE, LOSARTAN POTASSIUM (HYZAAR) for Hypertension, GABAPENTIN for Nervous system disorder NOS. On an unknown date, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after 30 day beyond use date/administered an expired vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30 day beyond use date/administered an expired vaccine) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Height and weight was unknown. It was reported that they put on the ready to use sticker and had to go back from 01-Jul-2022 through 05-Jul-2022 and found one more patient to add to their case apart from the initial 2 patients. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy (Aspirin); Hypertension; Nervous system disorder NOS (Nerve condition)
- Vorgeschichte
- -
- Andere Medikamente
- HYZAAR; GABAPENTIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 28.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Dose administered after 30-day Use By Date or after manufacturer date of expiry; HCP administer the vaccine to patient, after the expiration on the 5Jul2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP administer the vaccine to patient, after the expiration on the 5Jul2022) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) in an 81-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. The patient had no allergies (medications,food and other products). The patient had no history relating to mentioned AE and both Acute and Chronic illnesses at the time of vaccination and never had COVID-19 positive test or diagnosis. The patient had no other vaccines given within 1 month prior to Moderna COVID-19 vaccine. On 15-Jul-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 15-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP administer the vaccine to patient, after the expiration on the 5Jul2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP administer the vaccine to patient, after the expiration on the 5Jul2022) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The adverse effect did not cause patient to seek medical care (office visit, Urgent care, ER, hospitalization). The patient did not experience a similar event in the past. On 31-May-2022, the vial was initially stored in the refrigerator. The vial did not undergo any temperature excursions. Treatment information was unknown. This case was linked to MOD-2022-613364 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no allergies (medications,food and other products). The patient had no history relating to mentioned AE and both Acute and Chronic illnesses at the time of vaccination and never had COVID-19 positive test or diagnosis. The patient had no other vaccines given within 1 month prior to Moderna COVID-19 vaccine.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 28.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Dose administered after 30-day Use By Date or the vaccine was store after manufacturer date of expiry; HCP administer the vaccine to patient, after the expiration on the 5Jul2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP administer the vaccine to patient, after the expiration on the 5Jul2022) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or the vaccine was store after manufacturer date of expiry) in a 26-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 13-Jul-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 13-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP administer the vaccine to patient, after the expiration on the 5Jul2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or the vaccine was store after manufacturer date of expiry). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP administer the vaccine to patient, after the expiration on the 5Jul2022) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or the vaccine was store after manufacturer date of expiry) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Patient was never tested positive for COVID. No medical history reported, related to mentioned AE both Acute and Chronic illnesses at the time of vaccination. Information about other vaccines given within 1 month prior to Moderna COVID-19 vaccine was unknown. Patient did not experienced a similar event in the past. Date the vial was initially stored in the refrigerator on 31-May-2022. The vial did not undergo any temperature excursions. No treatment information was reported. This case was linked to MODERNATX, INC.-MOD-2022-613384 (E2B Linked Report). Sender's Comments: MODERNATX, INC.-MOD-2022-613384:(same reporter)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none noted
- Vorgeschichte
- Per her chart Essential Hypertension and Idiopathic peripheral autonomic neuropathy
- Andere Medikamente
- Per chart gabapentin and hyzaar
- Allergien
- Aspirin
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
Patient completed monitoring period and no adverse reaction noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None noted
- Vorgeschichte
- Per chart disorder of bladder, joint pain, weight loss, and vitamin D deficiency
- Andere Medikamente
- Per chart amitiza, Aspirin, citalopram, diazepam, escitalopram, fluticasone, rosuvastatin, lactulose, losartan, and meclizine
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
Patient completed Monitoring Period and No adverse reactions noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None noted
- Vorgeschichte
- Vaginitis and Vulvovaginitis per chart
- Andere Medikamente
- None noted
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 61,0
- Geschlecht
- U
- Eingang
- 24.07.2022
- Impfdatum
- 16.07.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
One of our Medical Assistants gave a dose of expired Moderna Covid-19 vaccine.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (One of our Medical Assistants gave a dose of expired Moderna Covid-19 vaccine.) in a 61-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 16-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (One of our Medical Assistants gave a dose of expired Moderna Covid-19 vaccine.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (One of our Medical Assistants gave a dose of expired Moderna Covid-19 vaccine.) 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 received second booster dose on 16-Jul-2022. Number of doses/vials were reported as 1 dose. The vial did not undergo any temperature excursions. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.07.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Circumstance or information capable of leading to medication error
Symptomtext
possible doses administered after expiration date of Moderna vial; This spontaneous case was reported by an other health care professional and describes the occurrence of CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (possible doses administered after expiration date of Moderna vial) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (possible doses administered after expiration date of Moderna vial). At the time of the report, CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (possible doses administered after expiration date of Moderna vial) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. No treatment medications was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
We had a dose of Moderna Covid-19 that was given after it expired; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We had a dose of Moderna Covid-19 that was given after it expired) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Jul-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 15-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (We had a dose of Moderna Covid-19 that was given after it expired). At the time of the report, EXPIRED PRODUCT ADMINISTERED (We had a dose of Moderna Covid-19 that was given after it expired) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. It was reported that vial was initially stored in the refrigerator on 27 Jun 2022 and vial did not undergo any temperature excursions. It was unknown whether patient had Allergies and ever had COVID positive test or diagnosis. It was unknown whether patient was given other vaccines given within 1 month prior to Moderna COVID-19 vaccine. It was unknown AE cause patient to seek medical care. It was unknown whether the patient experienced a similar event in the past. 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
- CA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 23.07.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.07.2022
- Tage bis Beginn
- 122,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Extra dose administered
Product administered to patient of inappropriate age
Symptomtext
Dose administered after 30-day Use By Date or after manufacturer date of expiry,expired vial was punctured and used on a patient; Second booster dose administered to 45 year old patient; Second booster dose administered to 45 year old patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date or after manufacturer date of expiry,expired vial was punctured and used on a patient), EXTRA DOSE ADMINISTERED (Second booster dose administered to 45 year old patient) and PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (Second booster dose administered to 45 year old patient) in a 45-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 045L21A and 045L21A) for COVID-19 vaccination. It was reported that patient had no allergies. It was reported that patient never had COVID positive test or diagnosis. It was also reported that patient did not receive other vaccines within 1 month prior to Moderna COVID-19 vaccine. On 18-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 18-Jul-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 18-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date or after manufacturer date of expiry,expired vial was punctured and used on a patient), EXTRA DOSE ADMINISTERED (Second booster dose administered to 45 year old patient) and PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (Second booster dose administered to 45 year old patient). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date or after manufacturer date of expiry,expired vial was punctured and used on a patient), EXTRA DOSE ADMINISTERED (Second booster dose administered to 45 year old patient) and PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (Second booster dose administered to 45 year old patient) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. It was reported that patient received first booster and second booster dose of Moderna COVID-19 vaccine. It was reported that the vial did not undergo any temperature excursions. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was reported that patient had no allergies. It was reported that patient never had COVID positive test or diagnosis. It was also reported that patient did not receive other vaccines within 1 month prior to Moderna COVID-19 vaccine.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 21.07.2022
- Impfdatum
- 20.04.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 62,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Nasal congestion
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 06/21/2022 with symptoms of mild nasal congestion, and mild cough. I was advised to treat my symptoms with Nyquil, Dayquil, and ibuprofen. I was ill for 2 days before my symptoms began to resolve. I fully recovered with no lingering symptoms. I continued to test positive until 07/03/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab home test was positive on 06/22/2022;
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Multivitamin; Vitamin D; Probiotic; Melatonin
- Allergien
- Lisinopril
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 08.07.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial was initially stored in the refrigerator on 08 JUL 2022 after expiration date on 05 JUL 2022; Received expired first booster dose beyond manufacturer date of expiry; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired first booster dose beyond manufacturer date of expiry) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 08 JUL 2022 after expiration date on 05 JUL 2022) in a 32-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired first booster dose beyond manufacturer date of expiry). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 08 JUL 2022 after expiration date on 05 JUL 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received expired first booster dose beyond manufacturer date of expiry) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 08 JUL 2022 after expiration date on 05 JUL 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant products were reported. Patient received first booster dose of Moderna COVID-19 vaccine about 2 PM. The manufacturer expiration Date reported as 05 JUL 2022. Number of doses/vials reported was 1 dose / 1 Vial. The vial did not undergo any temperature excursions. The vial was initially stored in the refrigerator on 08 JUL 2022 9 AM. No treatment drugs were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 14.04.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 90,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 14.03.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 115,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Inappropriate schedule of product administration
Product storage error
Symptomtext
received the second primary dose of the Moderna COVID-19 vaccine from a pre-dawn syringe that was left at room temperature for 27 hours; 1st primary dose: Moderna, administered on 14Mar2022 and 2nd primary dose: Moderna, administered on 07Jul2022; vial was first punctured*: 06Jul2022 at 10:03 AM and administration of vaccine*: 07Jul2022 at 1:52 PM; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT STORAGE ERROR (received the second primary dose of the Moderna COVID-19 vaccine from a pre-dawn syringe that was left at room temperature for 27 hours), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st primary dose: Moderna, administered on 14Mar2022 and 2nd primary dose: Moderna, administered on 07Jul2022) and EXPIRED PRODUCT ADMINISTERED (vial was first punctured*: 06Jul2022 at 10:03 AM and administration of vaccine*: 07Jul2022 at 1:52 PM) in a 35-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 060A22A and 045L21A) for COVID-19 prophylaxis. It was unknown that patient had ever COVID+ test or diagnosis in the past but did not get COVID-19 within past 90 days. Previously administered products included for Product used for unknown indication: Gardasil (1 dose) on 14-Mar-2022 and Gardasil (1 more dose) on 07-Jul-2022. Past adverse reactions to the above products included No adverse event with Gardasil and Gardasil. Concurrent medical conditions included Latex allergy. Concomitant products included AMFETAMINE ASPARTATE, AMFETAMINE SULFATE, DEXAMFETAMINE SACCHARATE, DEXAMFETAMINE SULFATE (ADDERALL) and LEVOTHYROXINE SODIUM (SYNTHROID) for an unknown indication. On 14-Mar-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 07-Jul-2022 at 1:52 PM, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 07-Jul-2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st primary dose: Moderna, administered on 14Mar2022 and 2nd primary dose: Moderna, administered on 07Jul2022) and EXPIRED PRODUCT ADMINISTERED (vial was first punctured*: 06Jul2022 at 10:03 AM and administration of vaccine*: 07Jul2022 at 1:52 PM). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (received the second primary dose of the Moderna COVID-19 vaccine from a pre-dawn syringe that was left at room temperature for 27 hours). At the time of the report, PRODUCT STORAGE ERROR (received the second primary dose of the Moderna COVID-19 vaccine from a pre-dawn syringe that was left at room temperature for 27 hours), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st primary dose: Moderna, administered on 14Mar2022 and 2nd primary dose: Moderna, administered on 07Jul2022) and EXPIRED PRODUCT ADMINISTERED (vial was first punctured*: 06Jul2022 at 10:03 AM and administration of vaccine*: 07Jul2022 at 1:52 PM) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. The vial was initially stored in the refrigerator on 20-Jun-2022. The vial was first punctured on 06-Jul-2022 at 10:03 AM. The vial was stored in room temperature post puncture. The vial did not undergo any temperature excursions. The Total amount of time the vial was exposed to room temperature range was 27 hours. The AE did not cause patient to seek medical care. The patient did not experience similar event in the past.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Latex allergy
- Vorgeschichte
- Comments: It was unknown that patient had ever COVID+ test or diagnosis in the past but did not get COVID-19 within past 90 days.
- Andere Medikamente
- ADDERALL; SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- -
- Geschlecht
- U
- Eingang
- 12.07.2022
- Impfdatum
- 06.07.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
administered doses past it's expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered doses past it's expiration date) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 06-Jul-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 06-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered doses past it's expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered doses past it's expiration date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The Moderna COVID-19 vial expired on 05Jul2022 and administered in 06Jul2022. Number of doses/vials present was 1. The vial was initially stored in the refrigerator on 06-Jul-2022. It did not undergo any temperature excursions. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 79,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Influenza virus test positive
Lethargy
SARS-CoV-2 test positive
Streptococcus test negative
Symptomtext
Two months after dose 4 of the Moderna Vaccine, I started feeling lethargic on 6/20/2022, so I took a Home Covid test and tested positive. Went to my Dr the next day and was tested for Strep, Covid and for the Flu, I only tested positive for Covid. My Dr. gave me a choice of taking a pill (antiviral) or using an IV in the hospital. Since I have a problem with pills, I chose using the IV, however it would've be 4 more days until I could get in to the hospital to have it done. I started feeling a little better, so I decided now to have it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Strep test - Negative, Covid test - positive, Flu test - positive
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- Thyroid; High Blood Pressure, Afib
- Andere Medikamente
- Synthroid, Folbee; Diltialazam; Esiquis; Estrodiol; Multivitamin; Calcium
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 06.07.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Nasopharyngitis
SARS-CoV-2 test positive
Symptomtext
June18 12:00pm I just felt like I had a bad cold June 19 I tested positive for COVID-19 with a home test and then I went to the pharmacy and tested and received results on June 20th. June 20th Test results from the pharmacy were positive Called my PCP and left a message and he called in a prescription for Paxlovid. I took as prescribed. A few days later I started to feel better not that I felt horrible just symptoms of a cold.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 At Home Test
- Aktuelle Erkrankungen
- Tonsils Cancer
- Vorgeschichte
- NA
- Andere Medikamente
- Irbesartan; Rosuvastatin; Amlodipine; Baby Aspirin
- Allergien
- Nacine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 02.04.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 67,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Extra dose administered
SARS-CoV-2 test positive
Symptomtext
2nd booster in April. Got Covid 6/8/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home antigen positive 6/8/2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none at time of vaccination in April. At time of Covid infection in June, I took Aleve, Delsym and Paxlovid x 5 days 6/8-6/12/2022
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 06.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 82,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Extra dose administered
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Received dose 4 of Moderna COVID-19 vaccine on 4/4/2022, then tested positive with a home test with positive results. Then went to a medical canter and was tested again. Was prescribed the antiviral molnupiravir 200mg capsules, took 4 tablets twice a day for 5 days. Breakthrough case.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Diltiazem; buspirone; baby aspirin; MIRALAX; vitamin B-complex; multivitamin; melatonin; stool softener; TYLENOL PM
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 21.04.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 68,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- 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
no adverse event- underage
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
UNDERAGE NO ADVERSE EVENTS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 18.05.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 19,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
Interchange of vaccine products
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Upper-airway cough syndrome
Symptomtext
05/18/2022 vaccination. 06/06/2022 were exposed to COVID. My partner was away and was exposed. When he arrived that night, he had a bit of a sniffle. 06/08/2022 found out he was exposed. 06/09/2022 I tested positive and contacted my Dr. It took a week for Dr. to contact me back. I was 'ok' they didn't contact me back as I wasn't feeling too poorly. I had some post-nasal gunk, sneezing. I had talked with a nurse and somehow the communication got dropped. 06/16/2022 Spoke to Dr. I thought I was 'fine'. I had gone to the hotel room to see my partner. Somehow I ended up having a relapse. 06/17/2022 I was still testing positive. I continued isolation. Sniffles, post nasal drip, sneezing. 06/21/2022 I tested COVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- 01/2022 broke 5th metatarsal
- Vorgeschichte
- ADHD; depression; obesity; mild asthma; membrane dystrophy; corneal abrasion; sensitive ears; HX vertigo
- Andere Medikamente
- Concerta; VALTREX; valacyclovir; LEXAPRO; moxifloxacin; multivitamin; B-12; acidophilus; cranberry extract; BENADRYL; fish oil
- Allergien
- DEMEROL; sulfa; dust (I take allergy shots for dust); possible soy
- Vorherige Impfungen
- COVID vaccinations; vertigo (esp. after the JJ shot).
- Staat
- FL
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 20.06.2022
- Impfdatum
- 19.02.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 119,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
patient hospitalized
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 120,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
NOTHING REPORTED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- LONG TERM STEROID USE
- Andere Medikamente
- TRAVOPROST 0.004% EYE DROPS
- Allergien
- ALLOPURINOL
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 10.06.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient was given Moderna COVID vaccine. Patient was 15 year old at time of injection. Moderna is not indicated for persons under the age of 18 at this time. No current symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Acne Vulgaris
- Andere Medikamente
- Doxycycline Hyclate 100 Mg Capsule Benzoyl Peroxide 5% Cleanser
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- 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 initially stored on 31-JAN-2022 and then administered on 14-APR-2022; The patient received dose after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 14-APR-2022) in a 49-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Apr-2022 at 1:11 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 14-Apr-2022 at 1:11 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 14-APR-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 14-APR-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product use was reported. It was reported that HCP did not know that the vials should not be used past 30 days from thawing the vials. The vials were initially stored on 31-Jan-2022 and the thaw expiration date was 02-Mar-2022. It was also reported that the vial did not undergo any temperature excursions and the total doses given were 20 doses of 15 vials used. The patient received first booster dose. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- 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 intially stored on 31-Jan-2022 and thaw expired on 02-Mar-2022; Patient received dose after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial intially stored on 31-Jan-2022 and thaw expired on 02-Mar-2022) in a 46-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 12-May-2022 at 11:51 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 12-May-2022 at 11:51 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received dose after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial intially stored on 31-Jan-2022 and thaw expired on 02-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial intially stored on 31-Jan-2022 and thaw expired on 02-Mar-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant products were not provided. It was reported that the affected Lot 045L21A was initially stored on 31-Jan-2022 and the thaw expired on 02-Mar-2022. Total doses administered was reported as 20 doses and number of vials used was 15. The vial did not undergo any temperature excursion. Treatment medications were not reported. This case was linked to MOD-2022-583132 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- 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
Date the vial was initially stored was on 31 Jan 2022 and patient administered vaccine on 8 Mar 2022; Receiving doses after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Receiving doses after the beyond use date) and PRODUCT STORAGE ERROR (Date the vial was initially stored was on 31 Jan 2022 and patient administered vaccine on 8 Mar 2022) in a 49-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Mar-2022 at 8:31 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 08-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Receiving doses after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored was on 31 Jan 2022 and patient administered vaccine on 8 Mar 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Receiving doses after the beyond use date) and PRODUCT STORAGE ERROR (Date the vial was initially stored was on 31 Jan 2022 and patient administered vaccine on 8 Mar 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. It was reported that HCP provided doses of the Moderna COVID19 vaccine after the beyond use date as the HCP did not know that the vials should not be used past 30 days from thawing the vials. Vial did not undergo any temperature excursions. Date vials initially stored: 31-Jan-2022. No treatment drug details was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 17.03.2022
- Beginn
- 17.03.2022
- 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
Vial initially stored on 31-JAN-2022 and then administered on 17-MAR-2022; received dose after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 17-MAR-2022) in a 28-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Mar-2022 at 7:51 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 17-Mar-2022 at 7:51 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (received dose after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 17-MAR-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 17-MAR-2022) 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. Patient had received first booster dose. Reporter provided doses of moderna COVID 19 vaccine after the beyond use date as reporter did not know that the vials should not be used past 30 days from thawing the vials. Date vials were initially stored was reported as 31-Jan-2022. Thaw expiration date was reported as 2-Mar-2022. Total twenty doses were given. Total fifteen vials were used. Vial did not undergo any temperature excursion. No treatment medication were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Date the vial was initially stored was on 31 Jan 2022 and patient administered vaccine on 07 Apr 2022; Patient administered vaccine on 07 Apr 2022 and thaw expiration date was on 02 Mar 2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 07 Apr 2022 and thaw expiration date was on 02 Mar 2022) and PRODUCT STORAGE ERROR (Date the vial was initially stored was on 31 Jan 2022 and patient administered vaccine on 07 Apr 2022) in a 31-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 07-Apr-2022 at 9:16 AM, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to .5 milliliter. On an unknown date, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 07-Apr-2022 at 9:16 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 07 Apr 2022 and thaw expiration date was on 02 Mar 2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored was on 31 Jan 2022 and patient administered vaccine on 07 Apr 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 07 Apr 2022 and thaw expiration date was on 02 Mar 2022) and PRODUCT STORAGE ERROR (Date the vial was initially stored was on 31 Jan 2022 and patient administered vaccine on 07 Apr 2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. It was reported that patient received doses after the beyond use date.Date vials were initially stored in refrigerator was reported as 31 Jan 2022. It was reported that the thaw expiration date was on 02 Mar 2022, and the total doses given were 20 doses of 15 vials used. It was reported that the vials had not undergone any temperature excursion. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- 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
Symptomtext
Receiving doses after the beyond use date/ Thaw expiration date was 3/2/2022, date administrered was on 5/5/2022 8:16 PM; Receiving doses after the beyond use date/ Thaw expiration date was 3/2/2022, date administrered was on 5/5/2022 8:16 PM; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Receiving doses after the beyond use date/ Thaw expiration date was 3/2/2022, date administrered was on 5/5/2022 8:16 PM) and PRODUCT STORAGE ERROR (Receiving doses after the beyond use date/ Thaw expiration date was 3/2/2022, date administrered was on 5/5/2022 8:16 PM) in a 24-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 05-May-2022 at 8:16 PM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 05-May-2022 at 8:16 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Receiving doses after the beyond use date/ Thaw expiration date was 3/2/2022, date administrered was on 5/5/2022 8:16 PM). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Receiving doses after the beyond use date/ Thaw expiration date was 3/2/2022, date administrered was on 5/5/2022 8:16 PM). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Receiving doses after the beyond use date/ Thaw expiration date was 3/2/2022, date administrered was on 5/5/2022 8:16 PM) and PRODUCT STORAGE ERROR (Receiving doses after the beyond use date/ Thaw expiration date was 3/2/2022, date administrered was on 5/5/2022 8:16 PM) 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 the HCP administered the vaccine after the beyond use date, as the HCP didn't know that the vials shouldn't be used past 30 days from thawing the vials. Vials were initially stored on 31-Jan-2022. Thaw expiration date was 02-Mar-2022. The vial did not undergo any temperature excursion. 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
- SC
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- 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
Symptomtext
the vial was initially stored on 31-Jan-2022 and the vaccine was administered on 26-MAY-2022; Dose of the Moderna COVID-19 vaccine was administered after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose of the Moderna COVID-19 vaccine was administered after the beyond use date) and PRODUCT STORAGE ERROR (the vial was initially stored on 31-Jan-2022 and the vaccine was administered on 26-MAY-2022) in a 63-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 26-May-2022 at 1:00 AM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 26-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose of the Moderna COVID-19 vaccine was administered after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (the vial was initially stored on 31-Jan-2022 and the vaccine was administered on 26-MAY-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose of the Moderna COVID-19 vaccine was administered after the beyond use date) and PRODUCT STORAGE ERROR (the vial was initially stored on 31-Jan-2022 and the vaccine was administered on 26-MAY-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The vial did not undergo any temperature excursions. No treatment information was reported. This case was linked to MOD-2022-583132 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 19.05.2022
- Beginn
- 19.05.2022
- 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
Symptomtext
The vials initially stored on 31-JAN-2022, thawed expiration date was 2-MAR-2022 and vaccine was administered on 10-MAY-2022; provided doses of Moderna COVID-19 vaccine after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (provided doses of Moderna COVID-19 vaccine after the beyond use date) and PRODUCT STORAGE ERROR (The vials initially stored on 31-JAN-2022, thawed expiration date was 2-MAR-2022 and vaccine was administered on 10-MAY-2022) in a 26-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 19-May-2022 at 7:30 AM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 19-May-2022 at 7:30 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (provided doses of Moderna COVID-19 vaccine after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vials initially stored on 31-JAN-2022, thawed expiration date was 2-MAR-2022 and vaccine was administered on 10-MAY-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (provided doses of Moderna COVID-19 vaccine after the beyond use date) and PRODUCT STORAGE ERROR (The vials initially stored on 31-JAN-2022, thawed expiration date was 2-MAR-2022 and vaccine was administered on 10-MAY-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. The vials initially stored on 31 Jan 2022, and thawed expiration date was 2 Mar 2022. The vial did not undergo any temperature excursions. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- 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
Symptomtext
Date the vial was initially stored : 31-Jan-2022., Date(s) of administration of vaccine :17-MAY-2022; patients received expired Moderna COVID-19 vaccine beyond the 30 day refrigerator shelf life; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patients received expired Moderna COVID-19 vaccine beyond the 30 day refrigerator shelf life) and PRODUCT STORAGE ERROR (Date the vial was initially stored : 31-Jan-2022., Date(s) of administration of vaccine :17-MAY-2022) in a 21-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 17-May-2022 at 5:37 AM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 17-May-2022 at 5:37 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (patients received expired Moderna COVID-19 vaccine beyond the 30 day refrigerator shelf life). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored : 31-Jan-2022., Date(s) of administration of vaccine :17-MAY-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patients received expired Moderna COVID-19 vaccine beyond the 30 day refrigerator shelf life) and PRODUCT STORAGE ERROR (Date the vial was initially stored : 31-Jan-2022., Date(s) of administration of vaccine :17-MAY-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant drug was reported. The vial was initially stored on 31-Jan-2022. It was reported that vial did not undergo temperature excursion. Thaw expiration date was reported as 02-Mar-2022. It was reported that HCP did not know that vails should not be used past 30 days from thawing the vials. Total Doses given: 20 doses, 15 vials have been used. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- 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
the vial was initially stored on 31-Jan-2022 and the vaccine was administered on 15-Mar-2022; dose of the Moderna COVID-19 vaccine was administered after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (dose of the Moderna COVID-19 vaccine was administered after the beyond use date) and PRODUCT STORAGE ERROR (the vial was initially stored on 31-Jan-2022 and the vaccine was administered on 15-Mar-2022) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Mar-2022 at 1:10 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 15-Mar-2022 at 1:10 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (dose of the Moderna COVID-19 vaccine was administered after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (the vial was initially stored on 31-Jan-2022 and the vaccine was administered on 15-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (dose of the Moderna COVID-19 vaccine was administered after the beyond use date) and PRODUCT STORAGE ERROR (the vial was initially stored on 31-Jan-2022 and the vaccine was administered on 15-Mar-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Thaw expiration date was reported as 02-Mar-2022. It was reported that the HCP did not know that the vial should not be used past 30 days from thawing the vial. The vial did not undergo any temperature excursions. No treatment information was provided by the reporter. This case was linked to MOD-2022-583132 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial initially stored on 31-JAN-2022 and then administered on 26-May-2022; The patient received dose after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 26-May-2022) in a 58-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 26-May-2022 at 12:30 PM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 26-May-2022 at 12:30 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 26-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 26-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. Patient had received 1 booster dose. It was reported that the HCP administered the vaccine after the beyond use date, as the HCP didn't know that the vials shouldn't be used past 30 days from thawing the vials. Vials were initially stored on 31-Jan-2022. Thaw expiration date was 02-Mar-2022. The vial did not undergo any temperature excursion. 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
- SC
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- 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 initially stored on 31-JAN-2022 and then administered on 12-May-2022; receiving doses after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (receiving doses after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 12-May-2022) in a 32-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 12-May-2022 at 12:30 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 12-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (receiving doses after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 12-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (receiving doses after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 12-May-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant were reported. The vials initially stored on 31-Jan-2022. Thaw expiration date was 02-Mar-2022. It was reported that 15 vials were used. No treatment were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- 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
Receiving doses after the beyond use date/ Thaw expiration date was 3/2/2022, date administered was on 10-May-2022 11:43 AM; Receiving doses after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Receiving doses after the beyond use date) and PRODUCT STORAGE ERROR (Receiving doses after the beyond use date/ Thaw expiration date was 3/2/2022, date administered was on 10-May-2022 11:43 AM) in a 27-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 10-May-2022 at 11:43 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 10-May-2022 at 11:43 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Receiving doses after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Receiving doses after the beyond use date/ Thaw expiration date was 3/2/2022, date administered was on 10-May-2022 11:43 AM). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Receiving doses after the beyond use date) and PRODUCT STORAGE ERROR (Receiving doses after the beyond use date/ Thaw expiration date was 3/2/2022, date administered was on 10-May-2022 11:43 AM) 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 HCP administered the vaccine after the beyond use date, as the HCP didn't know that the vials shouldn't be used past 30 days from thawing the vials. Vials were initially stored on 31-Jan-2022. Thaw expiration date was 02-Mar-2022. The vial did not undergo any temperature excursion. 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
- SC
- Alter
- 37,0
- Geschlecht
- U
- Eingang
- 09.06.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Date the vial was initially stored was on 31 Jan 2022 and patient administered vaccine on 31 Mar 2022; Patient administered vaccine on 31 Mar 2022 and thaw expiration date was on 02 Mar 2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 31 Mar 2022 and thaw expiration date was on 02 Mar 2022) and PRODUCT STORAGE ERROR (Date the vial was initially stored was on 31 Jan 2022 and patient administered vaccine on 31 Mar 2022) in a 37-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 31-Mar-2022 at 10:18 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 31-Mar-2022 at 10:18 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 31 Mar 2022 and thaw expiration date was on 02 Mar 2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored was on 31 Jan 2022 and patient administered vaccine on 31 Mar 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 31 Mar 2022 and thaw expiration date was on 02 Mar 2022) and PRODUCT STORAGE ERROR (Date the vial was initially stored was on 31 Jan 2022 and patient administered vaccine on 31 Mar 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. It was reported that patient received doses after the beyond use date.Date vials were initially stored in refrigerator was reported as 31 Jan 2022. It was reported that the thaw expiration date was on 02 Mar 2022, and the total doses given were 20 doses of 15 vials used. It was reported that the vials had not undergone any temperature excursion. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- 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
Date vials initially stored was 31-Jan-2022, Thaw expiration date: 02-Mar-2022, vaccine administered on 03-Mar-2022; Receiving doses after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Receiving doses after the beyond use date) and PRODUCT STORAGE ERROR (Date vials initially stored was 31-Jan-2022, Thaw expiration date: 02-Mar-2022, vaccine administered on 03-Mar-2022) in a 60-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Mar-2022 at 8:19 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 03-Mar-2022 at 8:19 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Receiving doses after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date vials initially stored was 31-Jan-2022, Thaw expiration date: 02-Mar-2022, vaccine administered on 03-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Receiving doses after the beyond use date) and PRODUCT STORAGE ERROR (Date vials initially stored was 31-Jan-2022, Thaw expiration date: 02-Mar-2022, vaccine administered on 03-Mar-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. It was reported that the vials were initially stored on 31-Jan-2022 and the thaw expiration date was 02-Mar-2022. It was also reported that the vial didn't undergo any temperature excursions. The patient received their first booster dose. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- 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
the vial was initially stored on 31-Jan-2022 and the vaccine was administered on 03-Mar-2022; dose of the Moderna COVID-19 vaccine was administered after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (dose of the Moderna COVID-19 vaccine was administered after the beyond use date) and PRODUCT STORAGE ERROR (the vial was initially stored on 31-Jan-2022 and the vaccine was administered on 03-Mar-2022) in a 28-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Mar-2022 at 8:15 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 03-Mar-2022 at 8:15 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (dose of the Moderna COVID-19 vaccine was administered after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (the vial was initially stored on 31-Jan-2022 and the vaccine was administered on 03-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (dose of the Moderna COVID-19 vaccine was administered after the beyond use date) and PRODUCT STORAGE ERROR (the vial was initially stored on 31-Jan-2022 and the vaccine was administered on 03-Mar-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Thaw expiration date was 02-Mar-2022. It was reported that the HCP did not know that the vial should not be used past 30 days from thawing the vial. The vial did not undergo any temperature excursions. No treatment information was provided by the reporter. This case was linked to MOD-2022-583132 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 03.03.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The patient received dose after the beyond use date; Vial initially stored on 31-JAN-2022 and then administered on 03-MAR-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 03-MAR-2022) in a 56-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Mar-2022 at 8:12 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 31-Jan-2022, the patient experienced PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 03-MAR-2022). On 03-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 03-MAR-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication reported. It was reported that HCP provided doses of the Moderna COVID19 vaccine after the beyond use date as the HCP didn't know that the vials shouldn't be used past 30 days from thawing the vials Vial did not undergo any temperature excursions. Total 20 doses were administered. Total 15 vials were used. Thaw expiration date was reported as 02-Mar-2022. 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
- SC
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- 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
Vial initially stored on 31-JAN-2022 and then administered on 10-MAR-2022; The patient received dose after the beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 10-MAR-2022) in a 63-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Mar-2022 at 8:41 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 10-Mar-2022 at 8:41 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 10-MAR-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 10-MAR-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. It was reported that the vials were initially stored on 31-Jan-2022 and the thaw expiration date was 02-Mar-2022. It was also reported that the vial didn't undergo any temperature excursions. The patient received their first booster dose. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 10.03.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The patient received dose after the beyond use date; Vial initially stored on 31-JAN-2022 and then administered on 10-MAR-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 10-MAR-2022) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Mar-2022 at 8:37 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 31-Jan-2022, the patient experienced PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 10-MAR-2022). On 10-Mar-2022 at 8:37 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The patient received dose after the beyond use date) and PRODUCT STORAGE ERROR (Vial initially stored on 31-JAN-2022 and then administered on 10-MAR-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant drug was reported. It was reported that HCP provided doses of the Moderna COVID19 vaccine after the beyond use date as the HCP didn't know that the vials shouldn't be used past 30 days from thawing the vials Vial did not undergo any temperature excursions. Total 20 doses were administered. Total 15 vials were used. Thaw expiration date was reported as 02-Mar-2022. No treatment medications were reported This case was linked to MOD-2022-583498, MOD-2022-583519 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 06-Jun-2022: Follow up received contains patient information , reporter email and suspect product information and additional event of product storage error was added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 08.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Client was injected with Moderna 0.5ml LD. Incorrect dose was given. Based on client's medical condition, client was thought to be immunocompromised. Based on CDC Guidance for immunocompromised, client did not meet criteria and should have received Moderna 0.25ml as a 1st booster dose. Instead client received an Additional Dose (primary 3rd dose). At this time client has not reported any adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- See Medication List
- Vorgeschichte
- Dysthymic disorder Convulsions Esophageal Reflux Environmental Seasonal Allergies Elevated Serum Creatine
- Andere Medikamente
- Genvova 150-200-10mg tab doxycycline monohydrate (MONODOX) 100mg capsule
- Allergien
- Banana Iodine Kiwi (Actinidia Chinensis) Tomato Fish Containing products Shellfish Derived
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 05.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tinnitus, no treatment available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Stomach upset.
- Vorgeschichte
- Depression.
- Andere Medikamente
- Sertraline; Remifemin.
- Allergien
- Sulfa drugs.
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 04.06.2022
- Impfdatum
- 04.06.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- 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
Product temperature excursion issue
Symptomtext
the vial underwent temperature excursions; vial was moved from freezer to refrigerator and expired on 20-Jan-2022; received an expired vaccine for a booster dose; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received an expired vaccine for a booster dose), PRODUCT TEMPERATURE EXCURSION ISSUE (the vial underwent temperature excursions) and PRODUCT STORAGE ERROR (vial was moved from freezer to refrigerator and expired on 20-Jan-2022) in a 20-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer and Pfizer. Past adverse reactions to the above products included No adverse event with Pfizer and Pfizer. On 22-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (received an expired vaccine for a booster dose). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (the vial underwent temperature excursions) and PRODUCT STORAGE ERROR (vial was moved from freezer to refrigerator and expired on 20-Jan-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (received an expired vaccine for a booster dose), PRODUCT TEMPERATURE EXCURSION ISSUE (the vial underwent temperature excursions) and PRODUCT STORAGE ERROR (vial was moved from freezer to refrigerator and expired on 20-Jan-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. Patient received first booster on 22-Apr-2022. The date the vial was initially stored in the refrigerator on 20-Jan-2022 Storage condition at the time of the excursion: refrigerated storage Maximum or minimum temperatures reached, as applicable : Maximum 44.6?F minimum 38.8?F Excursion duration was reported as 3 months No treatment drug details was reported. This case was linked to MOD-2022-572778 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Product temperature excursion issue
Symptomtext
the vial undergo temperature excursions; Vaccine initially stored in the refrigerator on 20 Jan 2022, Administered on 29 Mar 2022; 13 patients received an expired vaccine for a booster dose; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (13 patients received an expired vaccine for a booster dose), PRODUCT TEMPERATURE EXCURSION ISSUE (the vial undergo temperature excursions) and PRODUCT STORAGE ERROR (Vaccine initially stored in the refrigerator on 20 Jan 2022, Administered on 29 Mar 2022) in a 38-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. The patient had no allergies. It was unknown whether the patient was ever had COVID-19 test or diagnosis. 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 (13 patients received an expired vaccine for a booster dose). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (the vial undergo temperature excursions) and PRODUCT STORAGE ERROR (Vaccine initially stored in the refrigerator on 20 Jan 2022, Administered on 29 Mar 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (13 patients received an expired vaccine for a booster dose), PRODUCT TEMPERATURE EXCURSION ISSUE (the vial undergo temperature excursions) and PRODUCT STORAGE ERROR (Vaccine initially stored in the refrigerator on 20 Jan 2022, Administered on 29 Mar 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. The height of the patient is 172.72 cm. They administered vaccine from 23-Feb-2022 until the 12-may-2022 to 13 patients, all booster dosages, after vaccines were expired. The vial was moved from freezer and was initially stored in the refrigerator on 20-Jan-2022. The vial underwent temperature excursions for 3 months. The vial was in refrigerated storage condition at the time of the excursion. Maximum or minimum temperatures reached were Maximum 44.6?F and minimum 38.8?F. The Visual inspection did not note any vaccine state change and they were in seal boxes. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no allergies. It was unknown whether the patient was ever had COVID-19 test or diagnosis.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 30.05.2022
- 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 temperature excursion issue
Symptomtext
Dosages expired on the 20Jan2022, initially stored in the refrigerator on 20Jan2022, The vial unerwent temperature excursions; Received dosages in January with the same lot number, 045L21A that expired on the 20Jan2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received dosages in January with the same lot number, 045L21A that expired on the 20Jan2022) and PRODUCT TEMPERATURE EXCURSION ISSUE (Dosages expired on the 20Jan2022, initially stored in the refrigerator on 20Jan2022, The vial unerwent temperature excursions) in a 22-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer (Dose 2) and Pfizer (Dose 1). Past adverse reactions to the above products included No adverse event with Pfizer and Pfizer. 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 (Received dosages in January with the same lot number, 045L21A that expired on the 20Jan2022). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Dosages expired on the 20Jan2022, initially stored in the refrigerator on 20Jan2022, The vial unerwent temperature excursions). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received dosages in January with the same lot number, 045L21A that expired on the 20Jan2022) and PRODUCT TEMPERATURE EXCURSION ISSUE (Dosages expired on the 20Jan2022, initially stored in the refrigerator on 20Jan2022, The vial unerwent temperature excursions) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient had no allergies. It was unknown if patient ever had COVID positive test or diagnosis. Patient had no Acute and Chronic illnesses at the time of vaccination. No concomitant drug was reported. The reporter stated that she received dosages in January with the same lot number, 045L21A that expired on the 20-Jan-2022 and they were put in the freezer and from 23-Feb-2022 until the 12-May-2022 they administered them to 13 patients, all booster dosages, after they expired. Date the vial was initially stored in the refrigerator: 20-Jan-2022. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 30.05.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- 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
Product temperature excursion issue
Symptomtext
Vials were undergone temperature excursion by maximum 44.6 degree F and minimum by 38.8 degree F; Vaccine expired on the 20jan2022 were put in the freezer and from 23feb2022 until the12may2022 administerto patient; patient received an expired vaccine for a booster dose; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received an expired vaccine for a booster dose), PRODUCT TEMPERATURE EXCURSION ISSUE (Vials were undergone temperature excursion by maximum 44.6 degree F and minimum by 38.8 degree F) and PRODUCT STORAGE ERROR (Vaccine expired on the 20jan2022 were put in the freezer and from 23feb2022 until the12may2022 administerto patient) in a 19-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No allergies to food and other products. On 08-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received an expired vaccine for a booster dose). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vials were undergone temperature excursion by maximum 44.6 degree F and minimum by 38.8 degree F) and PRODUCT STORAGE ERROR (Vaccine expired on the 20jan2022 were put in the freezer and from 23feb2022 until the12may2022 administerto patient). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received an expired vaccine for a booster dose), PRODUCT TEMPERATURE EXCURSION ISSUE (Vials were undergone temperature excursion by maximum 44.6 degree F and minimum by 38.8 degree F) and PRODUCT STORAGE ERROR (Vaccine expired on the 20jan2022 were put in the freezer and from 23feb2022 until the12may2022 administerto patient) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications was not provided by the reporter. Unknown whether the patient ever had COVID + test or diagnosis. On 20JAN2022, the vial was initially stored in the refrigerator. The vial undergone temperature excursions. Excursion duration: 3 months. Patient did not seek medical care for the AE. Unkown if the patient symptoms improved or worsened. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No allergies to food and other products.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 30.05.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- 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
Product temperature excursion issue
Symptomtext
Vial that expired on the 20Jan2022 were put in the freezer underwent excursion for 3 months; vial that expired on the 20Jan2022 were put in the freezer underwent excursion for 3 months; Patient received an expired vaccine for a booster dose; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received an expired vaccine for a booster dose), PRODUCT STORAGE ERROR (Vial that expired on the 20Jan2022 were put in the freezer underwent excursion for 3 months) and PRODUCT TEMPERATURE EXCURSION ISSUE (vial that expired on the 20Jan2022 were put in the freezer underwent excursion for 3 months) in a 20-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. Patient had no allergies and no history relating to mentioned AE both Acute and Chronic illnesses at the time of vaccination. No other vaccine given within 1 month prior to Moderna COVID-19 vaccine. It was unknown if patient ever had COVID test or diagnosis. Previously administered products included for Product used for unknown indication: Janssen (Jansen for primary series). Past adverse reactions to the above products included No adverse event with Janssen. On 27-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received an expired vaccine for a booster dose). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial that expired on the 20Jan2022 were put in the freezer underwent excursion for 3 months) and PRODUCT TEMPERATURE EXCURSION ISSUE (vial that expired on the 20Jan2022 were put in the freezer underwent excursion for 3 months). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received an expired vaccine for a booster dose), PRODUCT STORAGE ERROR (Vial that expired on the 20Jan2022 were put in the freezer underwent excursion for 3 months) and PRODUCT TEMPERATURE EXCURSION ISSUE (vial that expired on the 20Jan2022 were put in the freezer underwent excursion for 3 months) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant drugs were not reported. It was reported that patient did not seek any medical attention. It was reported that the vial which expired was initially stored in refrigerator on 20-Jan-2022 and later were put in the freezer and from 23-Feb-2022 until the 12-May-2022 it was administered to 13 patients, all booster dosages, after the expiry. It was also reported that the vials underwent maximum 44.6 degree F and minimum 38.8 degree F of temperature excursion for 3 months. No visual inspection noting any vaccine state change as vials were in seal boxes. Number of vials/doses impacted: 660 doses, and they have now 520. This case was linked to MOD-2022-572778 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient had no allergies and no history relating to mentioned AE both Acute and Chronic illnesses at the time of vaccination. No other vaccine given within 1 month prior to Moderna COVID-19 vaccine. It was unknown if patient ever had COVID test or diagnosis.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 30.05.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- 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
Product temperature excursion issue
Symptomtext
The vial was moved from freezer to refrigerator and expired on 20-Jan-2022; Maximum or minimum temperatures reached, as applicable Maximum 44.6?F minimum 38.8?F; Patient received an expired vaccine for a booster dose on 01-Mar-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received an expired vaccine for a booster dose on 01-Mar-2022), PRODUCT STORAGE ERROR (The vial was moved from freezer to refrigerator and expired on 20-Jan-2022) and PRODUCT TEMPERATURE EXCURSION ISSUE (Maximum or minimum temperatures reached, as applicable Maximum 44.6?F minimum 38.8?F) in a 19-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Moderna Vaccine (First dose with lot number 014B21A) on 02-May-2021 and MODERNA COVID-19 VACCINE (Second dose with lot number 037C21A) on 30-May-2021. Past adverse reactions to the above products included No adverse event with MODERNA COVID-19 VACCINE and Moderna Vaccine. Concurrent medical conditions included Allergy to venom (Bee venom) and Sulfonamide allergy (Sulfa antibiotics). On 01-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received an expired vaccine for a booster dose on 01-Mar-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was moved from freezer to refrigerator and expired on 20-Jan-2022) and PRODUCT TEMPERATURE EXCURSION ISSUE (Maximum or minimum temperatures reached, as applicable Maximum 44.6?F minimum 38.8?F). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received an expired vaccine for a booster dose on 01-Mar-2022), PRODUCT STORAGE ERROR (The vial was moved from freezer to refrigerator and expired on 20-Jan-2022) and PRODUCT TEMPERATURE EXCURSION ISSUE (Maximum or minimum temperatures reached, as applicable Maximum 44.6?F minimum 38.8?F) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product use was provided. The date the vial was initially stored in the refrigerator on 20-Jan-2022. The vial undergo any temperature excursions: yes Storage condition at the time of the excursion: refrigerated storage Maximum or minimum temperatures reached, as applicable : Maximum 44.6?F minimum 38.8?F Excursion duration: 3 months No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to venom (Bee venom); Sulfonamide allergy (Sulfa antibiotics)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 30.05.2022
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product temperature excursion issue
Symptomtext
The vial undergo temperature excursions; 13 patients received an expired vaccine for a booster dose; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (13 patients received an expired vaccine for a booster dose) and PRODUCT TEMPERATURE EXCURSION ISSUE (The vial undergo temperature excursions) in a 21-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. no Allergies were reported. Previously administered products included for Product used for unknown indication: pfizer (As primary series). Past adverse reactions to the above products included No adverse reaction with pfizer. On 28-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (13 patients received an expired vaccine for a booster dose). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (The vial undergo temperature excursions). At the time of the report, EXPIRED PRODUCT ADMINISTERED (13 patients received an expired vaccine for a booster dose) and PRODUCT TEMPERATURE EXCURSION ISSUE (The vial undergo temperature excursions) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication reported. It was reported that no other vaccines given within 1 month prior to Moderna COVID-19 vaccine It was reported that dosages received in January with the same lot number, 045L21A. They were put in the freezer and from 23-Feb-2022 until the 12-May-2022 they administer them to 13 patients, all booster dosages, after they expired. Maximum and minimum temperatures reached were 44.6 degree F and 38.8 degree F. Excursion duration were reported as 3 months. Vials were moved from freezer to refrigerator on 20-JAn-2022. The vial undergo any temperature excursions. Number of vials/doses impacted: 660 doses, and they have now 520. No treatment medication reported. This case was linked to MOD-2022-572778 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: no Allergies were reported.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 30.05.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- 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
Product temperature excursion issue
Symptomtext
13 patients received an expired vaccine for a booster dose; Vaccine was stored in the refrigerated after 30-day Use By Date, therefore product storage error was captured.; 13 patients received an expired vaccine for a booster dose; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (13 patients received an expired vaccine for a booster dose), PRODUCT TEMPERATURE EXCURSION ISSUE (13 patients received an expired vaccine for a booster dose) and PRODUCT STORAGE ERROR (Vaccine was stored in the refrigerated after 30-day Use By Date, therefore product storage error was captured.) in a 20-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (13 patients received an expired vaccine for a booster dose). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (13 patients received an expired vaccine for a booster dose) and PRODUCT STORAGE ERROR (Vaccine was stored in the refrigerated after 30-day Use By Date, therefore product storage error was captured.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (13 patients received an expired vaccine for a booster dose), PRODUCT TEMPERATURE EXCURSION ISSUE (13 patients received an expired vaccine for a booster dose) and PRODUCT STORAGE ERROR (Vaccine was stored in the refrigerated after 30-day Use By Date, therefore product storage error was captured.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. She stated that she received dosages in January with the same lot number, 045L21A that expired on the 20-Jan-2022 and they were put in the freezer and from 23-Feb-2022 until the 12-May-2022 they administer them to 13 patients, all booster dosages, after they expired. Gave consent to be follow by safety Number of doses/vials was13 doses out of 12 vials. The vial was initially stored in the refrigerator on 20-Jan-2022. Vaccine was administered from 23-Feb-2022 until the 12-May-2022. Vial was underwent temperature excursions Vial was refrigerated condition at the time of the excursion. Lot number and Expiration Date*: 045L21A5, Jul-2022 Vial temperatures Maximum 44.6?F minimum 38.8?F reached. Vial Excursion duration was 3 months. No,Visual inspection noting any vaccine state change, they are in seal boxes. Number of vials/doses impacted: 660 doses, and they have now 520 No any previous excursions with the impacted vial(s). Patient had no allergy medications, food and other products. Patient ever had COVID + test or diagnosis was reported as unknown. Vial was underwent temperature excursions. No other vaccines given within 1 month prior to Moderna COVID-19 vaccine (type, brand, lot, route,Dose). No concomitant medication were reported. No treatment drug were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- 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 temperature excursion issue
Symptomtext
The vial undergo temperature excursions; 13 patients received an expired vaccine for a booster dose; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (13 patients received an expired vaccine for a booster dose) and PRODUCT TEMPERATURE EXCURSION ISSUE (The vial undergo temperature excursions) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer COVID-19 Vaccine (Primary series). Past adverse reactions to the above products included No adverse event with Pfizer COVID-19 Vaccine. Concurrent medical conditions included Food allergy and Allergy to antibiotic (Allergic to Sulfa Antibiotics.). On 01-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (13 patients received an expired vaccine for a booster dose). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (The vial undergo temperature excursions). At the time of the report, EXPIRED PRODUCT ADMINISTERED (13 patients received an expired vaccine for a booster dose) and PRODUCT TEMPERATURE EXCURSION ISSUE (The vial undergo temperature excursions) 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. Treatment details was not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to antibiotic (Allergic to Sulfa Antibiotics.); Food allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- 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
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- 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
- 49,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
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
- 24.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- 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
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
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
- 24.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- 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
- 76,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 16,0
- Geschlecht
- U
- Eingang
- 24.05.2022
- Impfdatum
- 28.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Product administered to patient of inappropriate age
Symptomtext
3 incidents in clinic where 3 minors were given Moderna Covid-19 vaccine booster doses (0.25mL).; They each received doses 1 & 2 of Pfizer Covid-19 vaccine prior to receipt of Moderna booster; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (3 incidents in clinic where 3 minors were given Moderna Covid-19 vaccine booster doses (0.25mL).) and INTERCHANGE OF VACCINE PRODUCTS (They each received doses 1 & 2 of Pfizer Covid-19 vaccine prior to receipt of Moderna booster) in a 16-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. Previously administered products included for Drug use for unknown indication: PFIZER BIONTECH COVID-19 VACCINE (2nd dose) and PFIZER BIONTECH COVID-19 VACCINE (1st dose). Past adverse reactions to the above products included No adverse event with PFIZER BIONTECH COVID-19 VACCINE and PFIZER BIONTECH COVID-19 VACCINE. On 28-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On an unknown date, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (3 incidents in clinic where 3 minors were given Moderna Covid-19 vaccine booster doses (0.25mL).) and INTERCHANGE OF VACCINE PRODUCTS (They each received doses 1 & 2 of Pfizer Covid-19 vaccine prior to receipt of Moderna booster). At the time of the report, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (3 incidents in clinic where 3 minors were given Moderna Covid-19 vaccine booster doses (0.25mL).) and INTERCHANGE OF VACCINE PRODUCTS (They each received doses 1 & 2 of Pfizer Covid-19 vaccine prior to receipt of Moderna booster) 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.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- 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
Product storage error
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 22.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine given after it had been stored in the refrigerator for >30 days, outside of the window of time provided by manufacturer. No adverse events reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient was given Moderna Vaccine for 3rd dose. Patient does not fall under the approved Moderna age group.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Anxiety F41.9 Low 6/25/2021 - Present Bronchospasm J98.01 Low 12/31/2020 - Present ADD (attention deficit disorder) F98.8 Low 4/18/2016 - Present
- Andere Medikamente
- amphetamine-dextroamphetamine (Adderall XR) 20 MG 24 hr capsule Take 1 capsule by mouth daily. drospirenone-ethinyl estradiol (YAZ) 3-0.02 MG per tablet Take 1 tablet by mouth daily. Cholecalciferol (DIALYVITE VITAMIN D 5000 PO) albuterol
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
This patient presented on 2.1.22 requesting COVID-19 1st dose vaccine. Pt was provided 0.5 ml IM R Deltoid. Staff later realized patient would not be 18 years old until 3.4.22. No adverse reactions were reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None Reported
- Vorgeschichte
- None Reported
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 14.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
After vial was needle punctured it was immediately returned to fridge; Dose administered >12 hours post puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered >12(hours post puncture) and PRODUCT STORAGE ERROR (After vial was needle punctured it was immediately returned to fridge) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 10-May-2022 at 12:30 PM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-May-2022 at 12:30 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered >12 hours post puncture). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (After vial was needle punctured it was immediately returned to fridge). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered >12 hours post puncture) and PRODUCT STORAGE ERROR (After vial was needle punctured it was immediately returned to fridge) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication were reported. It was reported that the vial was initially stored in the refrigerator on 05 May 2022. It was reported that the vial was first punctured 09 May 2022 at 5:00 P.M It was reported that the vial was exposed to room temperature range 8? to 25?C= 46? to 77?F a few seconds after vial was needle punctured and it was immediately returned to fridge. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 09.05.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient and family verbally vetted as all over 18. Shot given. Upon entering, discovered as 15.5 years old
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- noe
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 15.03.2021
- Beginn
- 05.05.2022
- Tage bis Beginn
- 416,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest X-ray
SARS-CoV-2 test positive
Symptomtext
EN route to the hospital his COVID-19 PCR returned positive. He has received his first dose of remdesivir and dexamethasone per protocol. Follow-up chest x-ray this morning was reassuring. He is requiring 2 L nasal cannula. Transplant Infectious Disease has been consulted. On-call critical care consultant is also aware of the situation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 18.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Monoplegia
Symptomtext
arm paralyzed, weak
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
Patient was given 0.5ml booster dose instead of 0.25ml booster dose. Patient was informed, did not report any adverse reactions and had no further concerns at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Product administered to patient of inappropriate age
Symptomtext
pt was given 4th moderna dose when they are not yet eligible.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Booster given too early.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Anxiety; ADHD
- Andere Medikamente
- Adderall; Wellbutrin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient was given the Covid 19 Moderna vaccine x2 at age 14. No adverse symptoms have been reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- 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
Patient was given the Covid 19 Moderna vaccine x2 at age 14. No adverse symptoms have been reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Product storage error
Symptomtext
VACCINE WAS NOT DISPOSED OF DURING THE PREVIOUS NIGHT. MORNING SCHEDULE WAS HECTIC WITH MANY PATIENTS EARLY FOR VACCINE APPOINTMENTS AND REQUIRING TRANSLATORS. INTERN PHARMACIST CAME INTO ADMINISTER VACCINES AND DID NOT DOUBLE CHECK IF THE VACCINES WERE JUST OPENED AND DREW VACCINE THAT WERE OPENED THE DAY PRIOR. VACCINES WAS 4 HOURS POST 12 HOURS PUNCTURE EXPIRATION. PATIENT WHERE GIVEN MODERNA AS 2ND BOOSTER. PATIENT WAS CONTACTED AND REPORTED NO ADVERSE EVENT FROM THE VACCINE .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
VACCINE WAS NOT DISPOSED OF DURING THE PREVIOUS NIGHT. MORNING SCHEDULE WAS HECTIC WITH MANY PATIENTS EARLY FOR VACCINE APPOINMENTS AND REQUIRING TRANSLATORS. PHARMACIST CAME INTO ADMINISTER VACCINES AND DID NOT DOUBLE CHECK IF THE VACCINES WERE JUST OPENED AND DREW VACCINE THAT WERE OPENED THE DAY PRIOR. VACCINE WAS 4 HOURS POST 12 HOURS PUNCTURE EXPIRATION. PATIENT WERE GIVEN MODERNA AS 2ND BOOSTER. PATIENT WAS CONTACTED AND REPORTED NO ADVERSE EVENT FROM THE VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Product storage error
Symptomtext
VACCINE WAS NOT DISPOSED OF DURING THE PREVIOUS NIGHT. MORNING SCHEDULE WAS HECTIC WITH MANY PATIENTS EARLY FOR VACCINE APPOINTMENTS AND REQUIRING TRANSLATORS. INTERN PHARMACIST CAME INTO ADMINISTER VACCINES AND DID NOT DOUBLE CHECK IF THE VACCINES WERE JUST OPENED AND DREW VACCINE THAT WERE OPENED THE DAY PRIOR. VACCINES WAS 4 HOURS POST 12 HOURS PUNCTURE EXPIRATION. PATIENT WHERE GIVEN MODERNA AS 2ND BOOSTER. PATIENT WAS CONTACTED AND REPORTED NO ADVERSE EVENT FROM THE VACCINE .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
VACCINE WAS NOT DISPOSED OF DURING THE PREVIOUS NIGHT. MORNING SCHEDULE WAS HECTIC WITH MANY PATIENTS EARLY FOR VACCINE APPOINMENTS AND REQUIRING TRANSLATORS. INTERN PHARMACIST CAME INTO ADMINISTER VACCINES AND DID NOT DOUBLE CHECK IF THE VACCINES WERE JUST OPENED AND DREW VACCINE THAT WERE OPENED THE DAY PRIOR. VACCINE WAS 4 HOURS POST 12 HOURS PUNCTURE EXPIRATION. PATIENT WERE GIVEN MODERNA AS 2ND BOOSTER. PATIENT WAS CONTACTED AND REPORTED NO ADVERSE EVENT FROM THE VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 22.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
Vaccine not disposed of during the previous night. Morning schedule was hectic with many patients early for vaccine appointments. Intern pharmacist came to administer vaccines and did not double-check if the vaccines were just opened; drew vaccine that were opened the day prior. Vaccine was 4 hours post 12 hours puncture expiration. Patient given Moderna as 2nd booster. Patient contacted. No reported adverse event from the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 22.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
VACCINE WAS NOT DISPOSED OF DURING THE PREVIOUS NIGHT. MORNING SCHEDULE WAS HECTIC WITH MANY PATIENTS EARLY FOR VACCINE APPOINMENTS AND REQUIRING TRANSLATORS. INTERN PHARMACIST CAME INTO ADMINISTER VACCINES AND DID NOT DOUBLE CHECK IF THE VACCINES WERE JUST OPENED AND DREW VACCINE THAT WERE OPENED THE DAY PRIOR. VACCINE WAS 4 HOURS POST 12 HOURS PUNCTURE EXPIRATION. PATIENT WERE GIVEN MODERNA AS 2ND BOOSTER. PATIENT WAS CONTACTED AND REPORTED NO ADVERSE EVENT FROM THE VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Epistaxis
Symptomtext
Nose bleeds without any direct irritation. Occurred approximately 6 times over the course of 2 weeks, specifically while driving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Epistaxis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, obesity
- Andere Medikamente
- Metoprolol, Losartan, Allopurinol, Vitamin C, Vitamin D, Fish Oil, Probiotic, Apple cider vinegar
- Allergien
- Sulfa, Lisinopril
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
The patient was administered a Moderna COVID-19 vaccine booster dose that had surpassed the refrigeration expiration date by one day. Per our pharmacy, this Moderna COVID-19 vaccine (LOT #045L21A) expired on 4/6/2022 at 15:11. The patient received a booster dose on 4/7/2022 at 10:51 AM. No adverse reactions were documented after the patient was administered this vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Nitrous Oxide
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 18.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
The patient was administered a Moderna COVID-19 booster dose that had surpassed the refrigeration expiration date by two days. Per our pharmacy, this Moderna COVID-19 vaccine (LOT #045L21A) expired on 4/6/2022 at 15:11. The patient received a booster dose on 4/8/2022 at 9:34 AM. No adverse reactions were documented after the patient was administered this vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
The patient was administered a Moderna COVID-19 booster dose that had surpassed the refridgeration experation date by one day. Per our pharmacy, this Moderna COVID-19 vaccine (LOT #045L21A) expired on 4/6/2022 at 15:11. The patient received a booster dose on 4/7/2022 at 8:31 AM. No adverse reactions were documented after the patient was administered this vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 16.04.2022
- 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
The vial was initially stored in the refrigerator on 07-Mar-2022, expired on 06-Apr-2022 and the dose was administered on 08-Apr-2022; Patient potentially administered with expired vaccine (beyond 30 days use by date)/Expired booster vaccine dose administered after 30-day use by date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient potentially administered with expired vaccine (beyond 30 days use by date)/Expired booster vaccine dose administered after 30-day use by date) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 07-Mar-2022, expired on 06-Apr-2022 and the dose was administered on 08-Apr-2022) in a 77-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. Concurrent medical conditions included Immunocompromised. 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 (Patient potentially administered with expired vaccine (beyond 30 days use by date)/Expired booster vaccine dose administered after 30-day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 07-Mar-2022, expired on 06-Apr-2022 and the dose was administered on 08-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient potentially administered with expired vaccine (beyond 30 days use by date)/Expired booster vaccine dose administered after 30-day use by date) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 07-Mar-2022, expired on 06-Apr-2022 and the dose was administered on 08-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. It was reported by health care professional that there was an error in documentation that occurred in their facility. The 30 days use by date was written inadvertently as 16-Apr and they found out that it was supposed to be 06-Apr-2022. Some patients were potentially given these vaccines on 07-Apr-2022 to 08-Apr-2022. The vial was initially stored in the refrigerator on 07-Mar-2022. The vial had not undergone any temperature excursions. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 12-Apr-2022: Follow up received includes significant information: suspect vaccine information was added. On 12-Apr-2022: Follow up received includes significant information: Live FU received, significant checkbox ticked because the case was valid in FU 2 version (received patient details). Added patient details and historical condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Immunocompromised
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 16.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was first punctured on 04-Apr-2022, was stored in refrigerator post puncture and expired vaccine administered on 05-Apr-2022, past 12 hours puncture time.; expired Moderna vaccine administered past 12 hours puncture time; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time) and PRODUCT STORAGE ERROR (The vial was first punctured on 04-Apr-2022, was stored in refrigerator post puncture and expired vaccine administered on 05-Apr-2022, past 12 hours puncture time.) in a 64-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Apr-2022 at 9:00 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Apr-2022 at 9:00 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was first punctured on 04-Apr-2022, was stored in refrigerator post puncture and expired vaccine administered on 05-Apr-2022, past 12 hours puncture time.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time) and PRODUCT STORAGE ERROR (The vial was first punctured on 04-Apr-2022, was stored in refrigerator post puncture and expired vaccine administered on 05-Apr-2022, past 12 hours puncture time.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient received the second booster dose of Moderna Covid-19 vaccine on 05-Apr-2022 (lot number : 045L21A, expiry date : 05-Jul-2022). No concomitant drug was reported. It was reported that the vial was initially stored in the refrigerator on 04-Apr-2022. The vial was first punctured on 04-Apr-2022 at 1:55 PM and administration of vaccine on 05-Apr-2022 at 9:00 AM . The vial was stored in refrigerator post puncture. Total amount of time the vial was exposed to room temperature range was reported as unknown, the vial was not exposed to room temperature for more than 24 hours. The vial did not undergo any temperature excursions. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- -
- Beginn
- 05.04.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
expired Moderna vaccine administered past 12 hours puncture time; expired Moderna vaccine administered past 12 hours puncture time; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time) and PRODUCT STORAGE ERROR (expired Moderna vaccine administered past 12 hours puncture time) in an 83-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (expired Moderna vaccine administered past 12 hours puncture time). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time) and PRODUCT STORAGE ERROR (expired Moderna vaccine administered past 12 hours puncture time) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that the patient took 1st booster vaccine. It was reported that the vial was initially stored in the refrigerator on 04-Apr-2022. The vial was first punctured on 04-Apr-2022 at 1:55 PM and administration of vaccine on 05-Apr-2022 at 9:00 AM - 1:40 PM. The vial was stored in refrigerator post puncture. Total amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) was reported as unknown, the vial was not exposed to room temperature for >24 hours. The vial did not undergo any temperature excursions. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 16.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product storage error
Symptomtext
Moderna COVID-19 vaccine was administered to the patient with more than 12 hours after the vial was first punctured; The vial was first punctured on 04-Apr-2022 and administered on 05-Apr-2022. The vial was stored in refrigerator post puncture; This spontaneous case was reported by a nurse and describes the occurrence of POOR QUALITY PRODUCT ADMINISTERED (Moderna COVID-19 vaccine was administered to the patient with more than 12 hours after the vial was first punctured) and PRODUCT STORAGE ERROR (The vial was first punctured on 04-Apr-2022 and administered on 05-Apr-2022. The vial was stored in refrigerator post puncture) in a 61-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: JANSSEN COVID-19 VACCINE (Primary series J and J Vaccine). Past adverse reactions to the above products included No adverse event with JANSSEN COVID-19 VACCINE. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Apr-2022, the patient experienced PRODUCT STORAGE ERROR (The vial was first punctured on 04-Apr-2022 and administered on 05-Apr-2022. The vial was stored in refrigerator post puncture). On 05-Apr-2022, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (Moderna COVID-19 vaccine was administered to the patient with more than 12 hours after the vial was first punctured). At the time of the report, POOR QUALITY PRODUCT ADMINISTERED (Moderna COVID-19 vaccine was administered to the patient with more than 12 hours after the vial was first punctured) and PRODUCT STORAGE ERROR (The vial was first punctured on 04-Apr-2022 and administered on 05-Apr-2022. The vial was stored in refrigerator post puncture) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The patient took the 1st booster vaccine. It was reported that first booster dose of Moderna COVID-19 vaccine was administered to the patient with more than 12 hours after the vial was first punctured. The vial was initially stored in the refrigerator on 04-Apr-2022. The vial was first punctured on 04-Apr-2022 at 1:55 PM and vaccine was administered on 05-Apr-2022 at 9:00 AM - 1:40 PM EST. The vial was stored in refrigerator post puncture. Total amount of time the vial was exposed to room temperature range was reported as unknown, the vial was not exposed to room temperature for >24 hours. The vial did not undergo any temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
expired Moderna vaccine administered past 12 hours puncture time; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Date the vial was initially stored in the refrigerator: 4APR2022. Date(s) and time(S) vial was first punctured: 4APR2022 at 1:55 PM. Vial did not undergo any temperature excursions. It was reported that 7 doses of the Moderna COVID-19 vaccine were administered to patients more than 12 hours after the vial was first punctured. HCP stated that she would like to get information on stability of the Moderna vaccine that was administered to patients past 12 hours puncture time. No treatment information was provided by the reporter. No concomitant medications were provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
expired Moderna vaccine administered past 12 hours puncture time; expired Moderna vaccine administered past 12 hours puncture time; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time) and PRODUCT STORAGE ERROR (expired Moderna vaccine administered past 12 hours puncture time) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (expired Moderna vaccine administered past 12 hours puncture time). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time) and PRODUCT STORAGE ERROR (expired Moderna vaccine administered past 12 hours puncture time) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant information was provided. Patient received 2nd booster dose. Date the vial was initially stored in the refrigerator was reported as 4-APR-2022 Date(s) and time(S) vial was first punctured reported as 4-APR-2022 at 1:55 PM Date(s) and time(s) of administration of vaccine was 5-APR-2022 at 9:00 AM - 1:40 PM The vial was stored in Refrigerator after post puncture. It was reported that the vial doesn't undergone any temperature excursions and total amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) was Unknown. it was reported that not more than 24hours the vial was exposed. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
expired Moderna vaccine administered past 12 hours puncture time; expired Moderna vaccine administered past 12 hours puncture time; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time) and PRODUCT STORAGE ERROR (expired Moderna vaccine administered past 12 hours puncture time) in a 56-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (expired Moderna vaccine administered past 12 hours puncture time). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time) and PRODUCT STORAGE ERROR (expired Moderna vaccine administered past 12 hours puncture time) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient received 2nd booster dose. It was reported that first booster dose of Moderna COVID-19 vaccine was administered to the patient with more than 12 hours after the vial was first punctured. The vial was initially stored in the refrigerator on 04-Apr-2022. The vial was first punctured on 04-Apr-2022 at 1:55 PM and vaccine was administered on 05-Apr-2022 at 9:00 AM - 1:40 PM EST. The vial was stored in refrigerator post puncture. Total amount of time the vial was exposed to room temperature range was reported as unknown, the vial was not exposed to room temperature for >24 hours. The vial did not undergo any temperature excursions. No concomitant medications was provided. No treatment medications was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 16.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
expired Moderna vaccine administered past 12 hours puncture time; expired Moderna vaccine administered past 12 hours puncture time; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time) and PRODUCT STORAGE ERROR (expired Moderna vaccine administered past 12 hours puncture time) in a 60-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (expired Moderna vaccine administered past 12 hours puncture time). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired Moderna vaccine administered past 12 hours puncture time) and PRODUCT STORAGE ERROR (expired Moderna vaccine administered past 12 hours puncture time) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient received 2nd booster dose. Date the vial was initially stored in the refrigerator: 4-APR-2022 Date(s) and time(S) vial was first punctured: 4-APR-2022 at 1:55 PM Date(s) and time(s) of administration of vaccine: 5-APR-2022 at 9:00 AM - 1:40 PM EST How was the vial stored post puncture RT/fridge: Refrigerator Did the vial undergo any temperature excursions: No No concomitant medications was provided. No treatment medications was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 14.04.2022
- Impfdatum
- 29.06.2021
- Beginn
- 01.04.2022
- Tage bis Beginn
- 276,0
- 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
Event occurred after third vaccine; breakthrough case admission
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID + 4/1/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 14.04.2022
- Impfdatum
- 28.02.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 44,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
The patient is immunocompromised and instead of receiving 0.25 ml for the second booster dose received 0.5 ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- GERD,HBP Heart
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immunosuppression
Incorrect dose administered
Symptomtext
The patient is immunosuppressed and received the second booster, received 0.5 ml instead of 0.25 ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunosuppression
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High Blood Pressure, Cancer, Cholesterol
- Andere Medikamente
- -
- Allergien
- seafood
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 14.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
The patient received 0.5 ml of the vaccine instead of 0.25 ml for the second booster dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 14.04.2022
- Impfdatum
- 14.11.1947
- Beginn
- 13.04.2022
- Tage bis Beginn
- 27.179,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
The patient received 0.5 ml of the vaccine instead of 0.25 ml as the Second Booster requires
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
The patient received 0.5 ml instead of 0.25 ml of the Moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 13.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Patient was mistakenly given 1mL for their primary dose. The provider themselves prepared the vaccine and thought that 1ml was the dosage for the primary vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 13.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Patient was given a second booster based on updated recommendations. However, the provider misinterpreted the current recommendations and rather than giving the 0.25mL for the booster doses she administered 0.5mL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / 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's parent requested Moderna vaccine for patient's booster. Patient was asked to wait 15 minutes after shot, both parent and patient stated that patient did not have any adverse reaction after waiting 15 minutes. Realized after administration of vaccine that Moderna is not approved as a booster dose for individuals under 18 years of age.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blindness
Corneal disorder
Visual impairment
Symptomtext
Systemic: Visual Changes/Disturbances-Severe, Additional Details: patient stated that she could not see out of her left eye and that her eye doctor told her that her cornea was completely dried out
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blindness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Interchange of vaccine products
No adverse event
Symptomtext
First Covid-19 vaccine was Pfizer given 8/14/2021. Inadvertent administration of other mRNA vaccine. Pt made aware, remained in clinic for approx 20 min post administration. no adverse reactions reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Administered 2nd Moderna booster from vial that was past its 12 hour expiration time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 02.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest X-ray
Intermenstrual bleeding
Lymphadenopathy
Menstrual disorder
Ultrasound scan
Symptomtext
Extremely swollen lymph nodes along left side of neck Abnormal Period, missed one completely and then spotted for a month.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest X-ray
- Hospital-Tage
- -
- Labordaten
- 2-7 Chest x ray 2-17 neck ultrasound
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 14.03.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
On 3/14/22 Patient was administered 3rd dose of covid vaccine after he verbally stated not receiving any prior covid vaccines during registration process. He was administered full dose moderna covid vaccine, after 15 minutes of monitoring he left clinic feeling well and with no adverse reaction . Patient stated no hx of allergies, health risks, or being immunocompromised.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 04.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Interchange of vaccine products
No adverse event
Symptomtext
This patient received one Johnson and Johnson dose and two Moderna doses. He then received an additional half dose of Moderna today (4//4/22). He was not yet due for an additional dose today. No adverse reactions noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No allergies
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 62,0
- Geschlecht
- U
- Eingang
- 02.04.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (A patient was vaccinated with a booster dose (0.25mL) of Moderna Covid-19 vaccine from a vial that had been out in room temperature beyond 12 hrs.) and PRODUCT STORAGE ERROR (Vials were initially stored in the refrigerator on 25-Mar-22 and administered on 29-Mar-22 from a vial that had been out in room temperature beyond 12 hours) in a 62-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Mar-2022 at 3:30 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 29-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (A patient was vaccinated with a booster dose (0.25mL) of Moderna Covid-19 vaccine from a vial that had been out in room temperature beyond 12 hrs.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vials were initially stored in the refrigerator on 25-Mar-22 and administered on 29-Mar-22 from a vial that had been out in room temperature beyond 12 hours.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (A patient was vaccinated with a booster dose (0.25mL) of Moderna Covid-19 vaccine from a vial that had been out in room temperature beyond 12 hrs.) and PRODUCT STORAGE ERROR (Vials were initially stored in the refrigerator on 25-Mar-22 and administered on 29-Mar-22 from a vial that had been out in room temperature beyond 12 hours) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was unknown whether patient had experienced a similar event in the past, any allergies (medications, food and other products), had ever COVID positive test or diagnosis. No concomitant medications were reported. It was unknown if the Adverse event caused patient to seek medical care (office visit, Urgent care, ER) and if other vaccines given within 1 month prior to Moderna COVID-19 vaccine. The vial was initially stored in the refrigerator was on 25 March 2022, date on which vial was first punctured was 28 March 2022 at 10:30 am the date of administration of vaccine was on 29 march 2022 at 3:30 pm. The vail was stored at room temperature post puncture. The vial did not undergo any temperature excursion. Total amount of time the vial was exposed to room temperature range (8 degree Celsius to 25 degree Celsius equals to 46 degree Celsius to 77 degree farad) was 30.5 hrs. 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
- ID
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- 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
they gave a booster dose of the Moderna Covid-19 Vaccine to a patient today (30Mar2022) at 1:37pm from a vial that was first punctured yesterday (29Mar2022) at 1:48 pm; they gave a booster dose of the Moderna Covid-19 Vaccine to a patient today (30Mar2022) at 1:37pm from a vial that was first punctured yesterday (29Mar2022) at 1:48 pm; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (they gave a booster dose of the Moderna Covid-19 Vaccine to a patient today (30Mar2022) at 1:37pm from a vial that was first punctured yesterday (29Mar2022) at 1:48 pm) and PRODUCT STORAGE ERROR (they gave a booster dose of the Moderna Covid-19 Vaccine to a patient today (30Mar2022) at 1:37pm from a vial that was first punctured yesterday (29Mar2022) at 1:48 pm) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 30-Mar-2022 at 1:37 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Mar-2022 at 1:37 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (they gave a booster dose of the Moderna Covid-19 Vaccine to a patient today (30Mar2022) at 1:37pm from a vial that was first punctured yesterday (29Mar2022) at 1:48 pm). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (they gave a booster dose of the Moderna Covid-19 Vaccine to a patient today (30Mar2022) at 1:37pm from a vial that was first punctured yesterday (29Mar2022) at 1:48 pm). At the time of the report, EXPIRED PRODUCT ADMINISTERED (they gave a booster dose of the Moderna Covid-19 Vaccine to a patient today (30Mar2022) at 1:37pm from a vial that was first punctured yesterday (29Mar2022) at 1:48 pm) and PRODUCT STORAGE ERROR (they gave a booster dose of the Moderna Covid-19 Vaccine to a patient today (30Mar2022) at 1:37pm from a vial that was first punctured yesterday (29Mar2022) at 1:48 pm) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product use was reported. On 29-Mar-2022, the vial was initially stored in the refrigerator. On same day at 01:48 pm vial was first punctured. On 30-Mar-2022 at 1:37 pm, dose administered more than 12 hours post puncture. The vial did not undergo any temperature excursions. Total amount of time the vial was exposed to room temperature was reported as for 6 minutes. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
full dose was given for 4th shot instead of half dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- 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
Incorrect dose administered
Symptomtext
full dose was given for 4th shot instead of half dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Patient was given full dose for 2nd booster instead of half dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 02.02.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 41,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Sepsis
Symptomtext
Patient presented to the ED and was subsequently hospitalized for sepsis within 6 weeks of receiving covid vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sepsis
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Moderna given outside of the window for when the vial was punctured, punctured at 148pm on 03/29/2022, administered at 137pm on 03/30/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heavy menstrual bleeding
Menstruation delayed
Symptomtext
Delay in menstrual cycle. When cycle began, it lasted abnormally long. Bleeding occurred for more than 19 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heavy menstrual bleeding
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Sinuses
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
pt is under age 18 and received a half dose moderna vaccine. no adverse reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Sprintec
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 25.03.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
Patient present with his aunt requesting for COVID Vaccine booster without vaccine card. Both patient and aunt insist that they are needing their COVID booster vaccine. Nurse verified Electronic medical record and State registry for vaccine. Both showed only 2 previous administrations on 3/9/2021 and 3/31/2021. Nurse inquired multiple times for vaccine card and immunization history. Patient responded that he do not have a card and only received 2 COVID vaccines in the past. Nurse proceeded to obtain consent and administer booster dose of Moderna Vaccine. Patient was allowed to wait for 15 minutes after the vaccine. After the visit, patient returned to the nurse's station with his previous vaccine card, which shows 3 COVID Vaccine administration with last dose administered in November 2021. Patient and provider were notified. Patient is stable and no further orders given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Schizophrenia, Emphysema/COPD
- Vorgeschichte
- Schizophrenia, Emphysema/COPD,
- Andere Medikamente
- Invega 156 mg, Seroquel 25 mg, Cogentin 0.5 mg, Losartan 25 mg, Symbicort 80-4.5 mcg, Albuterol 90 mcg, Hydrochlorothiazide 25 mg
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received a Moderna Covid-19 vaccine vial on 31 Jan 2021 and the placed it in the refrigerator on the same day and administered on 10 Mar 2022; Administered with the vaccine beyond the 30 day use by date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Received a Moderna Covid-19 vaccine vial on 31 Jan 2021 and the placed it in the refrigerator on the same day and administered on 10 Mar 2022) in a 19-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Mar-2022 at 4:59 PM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 10-Mar-2022 at 4:59 PM, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine beyond the 30 day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received a Moderna Covid-19 vaccine vial on 31 Jan 2021 and the placed it in the refrigerator on the same day and administered on 10 Mar 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered with the vaccine beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Received a Moderna Covid-19 vaccine vial on 31 Jan 2021 and the placed it in the refrigerator on the same day and administered on 10 Mar 2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. A nurse practitioner reported a vaccine administration error. They stated that they received a Moderna Covid-19 vaccine vial on 31 Jan 2021 and placed it in the refrigerator on the same day ,specific time was unknown. They administered the vaccine to patient beyond the 30 days use by date. The patient did not reported any adverse events. Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 24.03.2022
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Administered with the vaccine beyond the 30 day use by date; administered with the vaccine beyond the 30 day use by date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with the vaccine beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Administered with the vaccine beyond the 30 day use by date) in a 25-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Mar-2022 at 9:21 AM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 09-Mar-2022 at 9:21 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with the vaccine beyond the 30 day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Administered with the vaccine beyond the 30 day use by date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered with the vaccine beyond the 30 day use by date) and PRODUCT STORAGE ERROR (Administered with the vaccine beyond the 30 day use by date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant products were reported. No treatment drugs were reported A nurse practitioner reports a vaccine administration error. They state that they received a Moderna Covid-19 vaccine vial on 31Jan2021 and the placed it in the refrigerator on the same day (specific time unknown).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
5 doses were given from a vial exposed to several temperature excursions; 5 doses were given from a vial exposed to several temperature excursions; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (5 doses were given from a vial exposed to several temperature excursions) and POOR QUALITY PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several temperature excursions) in an 87-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Mar-2022, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several temperature excursions). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (5 doses were given from a vial exposed to several temperature excursions). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (5 doses were given from a vial exposed to several temperature excursions) and POOR QUALITY PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several temperature excursions) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment drug information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
5 doses were given from a vial exposed to several tempereature excursions; 5 doses were given from a vial exposed to several tempereature excursions; This spontaneous case was reported by a health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (5 doses were given from a vial exposed to several tempereature excursions) and POOR QUALITY PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several tempereature excursions) in an 81-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Mar-2022, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several tempereature excursions). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (5 doses were given from a vial exposed to several tempereature excursions). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (5 doses were given from a vial exposed to several tempereature excursions) and POOR QUALITY PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several tempereature excursions) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. The vial was exposed at minimum temperature of 199.9 degree Celsius for 30 minutes. Storage condition at the time of the excursion was refrigerated storage. No concomitant and treatment medications were reported by the reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
5 doses were given from a vial exposed to several tempereature excursions; 5 doses were given from a vial exposed to several tempereature excursions; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (5 doses were given from a vial exposed to several tempereature excursions) and POOR QUALITY PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several tempereature excursions) in a 72-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Mar-2022, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several tempereature excursions). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (5 doses were given from a vial exposed to several tempereature excursions). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (5 doses were given from a vial exposed to several tempereature excursions) and POOR QUALITY PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several tempereature excursions) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications information was reported. It was reported that vaccines exposed to temperature out of range. Too warm Too cold On 28-Jan-22 at 1.8 Degrees Celsius for 1 hour On 27-Jan-22 at 8.7 Degrees Celsius for 30 mins On 03-Feb-22 at 12.3 Degrees Celsius for 1 hour On 09-Feb-22 at 11.4 Degrees Celsius for 30 mins On 10-Feb-22 at 8.2 Degrees Celsius for 30 mins On 09-Feb-22 at 11.4 Degrees Celsius for 30 mins On 28-Feb-22 at 8.7 Degrees Celsius for 30 mins On 03-Mar-22 at 11.7 Degrees Celsius for 30 mins On 08-Mar-22 at -199.9 Degrees Celsius for 30 mins which was the minimum temperature On 13-Mar-22 at 1.9 Degrees Celsius for 1 hour Hours accumulated 3.5 2.5 It was reported that the storage condition at the time of the excursion was refrigerated storage and total 5 vials were involved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Pt presented to vaccination site and requested Moderna COVID vaccine 2nd additional dose. Patient received Moderna 1st dose on 3/16/21, Moderna 2nd dose on 4/13/21, Moderna additional dose 10/13/21. RN 1 submitted a medical consult via withheld to Clinical Project Coordinators requesting to proceed with Moderna COVID vaccine 2nd additional dose. Clinical Project Coordinator RN 2 elevated request to medical consult team. MD 1 from medical consult team approved request for Moderna COVID vaccine 2nd additional dose. On 3/21/22, patient received Moderna COVID vaccine (LOT# 045L21A) 2nd additional dose at 1607. EMT 1 educated patient on signs and symptoms of adverse reactions, when to seek emergency care, and to register on V-Safe. At approximately 1625, patient left facility with unlabored respirations and steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (5 doses were given from a vial exposed to several temperature excursions) and POOR QUALITY PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several temperature excursions) in a 41-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Mar-2022, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several temperature excursions). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (5 doses were given from a vial exposed to several temperature excursions). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (5 doses were given from a vial exposed to several temperature excursions) and POOR QUALITY PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several temperature excursions) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. The concomitant medications on use were not provided. The vial was exposed at minimum temperature of 199.9 degree Celsius for 30 minutes. Storage condition at the time of the excursion was refrigerated storage. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 17.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Booster dose received < 5 months from 2nd dose/Patient received booster dose a month or 2 early per HCP/Booster dose administered early; This spontaneous case was reported by a nurse and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Booster dose received < 5 months from 2nd dose/Patient received booster dose a month or 2 early per HCP/Booster dose administered early) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-Mar-2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Booster dose received < 5 months from 2nd dose/Patient received booster dose a month or 2 early per HCP/Booster dose administered early). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Booster dose received < 5 months from 2nd dose/Patient received booster dose a month or 2 early per HCP/Booster dose administered early) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications was not provided by the reporter. The hcp who stated that a patient had received primary series but received their booster dose a month or 2 early from their 2nd primary series dose which was on 19Nov2021 per the HCP. The HCP stated that she is aware that booster dose should be at least 5 months later after the 2nd dose and asked if they should be looked for any adverse reactions. Treatment information was not provided. This case was linked to MOD-2022-515204 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- -
- Geschlecht
- U
- Eingang
- 22.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
5 doses were given from a vial exposed to several temperature excursions; 5 doses were given from a vial exposed to several temperature excursions; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several temperature excursions) and PRODUCT STORAGE ERROR (5 doses were given from a vial exposed to several temperature excursions) in an adult patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Mar-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several temperature excursions). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (5 doses were given from a vial exposed to several temperature excursions). At the time of the report, EXPIRED PRODUCT ADMINISTERED (5 doses were given from a vial exposed to several temperature excursions) and PRODUCT STORAGE ERROR (5 doses were given from a vial exposed to several temperature excursions) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 17.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient was given a moderna booster instead of a pfizer booster. She was too young for moderna booster, as she was only 16 at time of vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 16.03.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient received Moderna vaccine when under the age of 18
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Prozac
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient received the second booster, but she claimed she hasn't received the first booster. She did not fill out the consent form truthfully. So she received the fourth dose which she was not suppose to .When processing the form, the error was found.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- seafood, fish, codine
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
A patient was inadvertently administered from an expired vaccine; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (A patient was inadvertently administered from an expired vaccine) in a 33-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (A patient was inadvertently administered from an expired vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (A patient was inadvertently administered from an expired vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication were provided. 2 patients had administered from expired vaccines (beyond use by date). HCP does not have that information but states the Use by date was on 07 Mar 2022. Date(s) of administration of vaccine, 1st patient on 07 Mar 2022 at 2:30 pm and 2nd patient on 09 Mar 2022 at 11:30 am. The vial did not undergo any temperature excursions. No treatment details were provided. This case was linked to MOD-2022-508368 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 15.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Vaccine booster received too soon. 2nd dose received 2/10/22, 3rd dose received 3/11/22. Interval is 5 months for general population. No further adverse reaction/event noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- 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: nein
Product storage error
Symptomtext
Patient received booster dose of Moderna vaccine on 3/7/2022 at 1439 using an expired dose with beyond use date of 3/7/2022 at 0430. No harm to patient or monitoring provided. Per CDC guidelines, Moderna manufacturer has been contacted for information on the stability of the vaccine and whether the dose needs to be repeated. The patient will be contacted for follow-up once this information is available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
Patient received booster dose of Moderna on 3/9/2022 at 1153 using an expired dose with beyond use date of 3/7/2022 at 0430. No harm to patient or monitoring provided. Per CDC guidelines, Moderna manufacturer has been contacted for information on the stability of the vaccine and whether the dose needs to be repeated. The patient will be contacted for follow-up once this information is available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 12.03.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
A female patient was administered an expired vaccine.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (A female patient was administered an expired vaccine.) in a 33-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. Concurrent medical conditions included Penicillin allergy. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (A female patient was administered an expired vaccine.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (A female patient was administered an expired vaccine.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. It was unknown if the patient ever had tested COVID positive or diagnosis. No concomitant medications were reported. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Penicillin allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Symptomtext
At approximately 14:45 (10 minutes post Moderna vaccine booster), patient complaint of "chest tightness." This RN immediately assessed patient who denied difficulty breathing, shortness of breath, and no evidence of hives/rash noted. Vital signs taken - pulse 86, 21 respirations, 150/94, 100% spo2 on room air. Patient was brought to gurney and had complaint of worsening "chest tightness." RN STAT was called, STAT team arrived at 14:49. RN team encouraged deep breathing, vital signs were immediately taken at 14:50 - pulse rate of 76, 22 respirations, 166/107 blood pressure, 100% spo2 on room air. At approximately 14:55, patient verbalized improvement in chest tightness. Vital signs reassessed at 15:00 - pulse rate 82, 19 respirations, 158/81 blood pressure, 100% spo2 on room air, continues to deny shortness of breath or difficulty breathing, no hives or rash noted, respirations even and unlabored. Patient was scheduled with Dr. in family medicine for further evaluation. Patient escorted by RN STAT team via wheelchair to Dr. for further assessment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest discomfort
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 11.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
VACCINE GIVE EARLY BY 16 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
- VA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 11.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
vaccine given 44 days earlier due to language barrier and lack of documentation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 15.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Vision blurred
Symptomtext
blurred vision within 24 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vision blurred
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 11.03.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Pt was given booster shot ahead of time. Pt was to receive booster shot in June 2022. Pt didn't present adverse reaction to the vaccine 30 minutes after administration. Case was discussed with Dr. with no action needed at this time. Pt oriented to return to the clinic if symptoms occurs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hepatitis C, HBP, Hyperthyrodism
- Andere Medikamente
- Amiodarone, Empaglifozin, Sacubitril/Valsartan, Atorvastatin, Metoprolol, Warfarin, Finasteride, Folic Acid, Gabapentin, Tamsulosin, Buprenorphine/Naloxone, ASA, Thiamine, Nutritional Supplement
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Patients date of birth was miscalculated. Moderna was selected and given as a booster shot to the patient who was at the age of 17 years and 10 months old at the time of vaccination.
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
- 77,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 03.03.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product storage error
Symptomtext
administered Moderna Covid-19 vaccines beyond the 30 day use by date to 20 patients; Vaccines initially stored in the refrigerator on 19-Jan-2022 but was given beyond 30 days use by date; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (Vaccines initially stored in the refrigerator on 19-Jan-2022 but was given beyond 30 days use by date) and POOR QUALITY PRODUCT ADMINISTERED (administered Moderna Covid-19 vaccines beyond the 30 day use by date to 20 patients) in a 77-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Mar-2022 at 9:16 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In February 2022, the patient experienced PRODUCT STORAGE ERROR (Vaccines initially stored in the refrigerator on 19-Jan-2022 but was given beyond 30 days use by date). On 03-Mar-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced POOR QUALITY PRODUCT ADMINISTERED (administered Moderna Covid-19 vaccines beyond the 30 day use by date to 20 patients). At the time of the report, PRODUCT STORAGE ERROR (Vaccines initially stored in the refrigerator on 19-Jan-2022 but was given beyond 30 days use by date) and POOR QUALITY PRODUCT ADMINISTERED (administered Moderna Covid-19 vaccines beyond the 30 day use by date to 20 patients) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that patient took 1st dose on 26-Feb-2021 and second dose on 26-Mar-2021. No treatments were reported. Most recent FOLLOW-UP information incorporated above includes: On 04-Mar-2022: Follow-up received updated Non-significant information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 09.03.2022
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
PT WAS GIVEN FULL DOSE MODERNA FOR HIS BOOSTER DOSE. NO C/O ANY S/E AT THIS TIME
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 14.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- 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
Pediatric patient was given the Moderna Covid-19 vaccine and should have received Pfizer. No adverse reaction noted after receiving the vaccine. Per CDC guidelines patient is scheduled to receive her 2nd vaccine (Pfizer) on 3-15-2022. Per CDC "If Moderna Covid-19 Vaccine administered: As the first doe, administer the age-appropriate Pfizer-BioNTech Covid-19 Vaccine as the second dose at least 28 days after the Moderna Vaccine dose. Administer a Pfizer-BioNTech booster dose at least 5 months later."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- Not applicable. No adverse reaction occurred during this incident.
- Aktuelle Erkrankungen
- Post partum anemia, constipation.
- Vorgeschichte
- None
- Andere Medikamente
- Colace 100 mg, Iron 325 mg, Pre-Natal Multivitamin, Pepcid 40 mg.
- Allergien
- No known allergies.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
"The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
"The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
The vaccine received, determined to have a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the manufacturer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
"The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
"The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
"The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
"The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 07.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer. At facility, I served as a Operator, who is responsible for transporting COVID-19 and flu vaccines to sites. Standards for transporting these vaccines include keeping said products between 2C-8C. In order to maintain such cold temperatures requires the use of: cooler bag, 3 fridge plates, 1 frozen plate, and 2 sheets of bubble wrap. The bubble wrap serves to protect the vaccines from having direct contact with any of the cold plates. Somewhere during the transportation process, one of the sides of the bubble wrap got pushed down, causing potential exposure of the vaccines to the cold plates, which are most likely below 2C. Due to insufficient data to support the idea that the vaccines were considered active, we must assume that the 4 Moderna vaccines provided during our shift on 3/7/2022 are possibly invalid. We arrived to their sites around 9:00 AM on 3/7/2022. We provided our vaccination services to our patient, and followed standard procedure. After observing the patient for over 15 minutes, having the patient report no adverse symptoms, we allowed them to go back to their sites.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 07.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer. At HCF, I served as a Cold Chain Operator (CCO), who is responsible for transporting COVID-19 and flu vaccines to encampment sites. Standards for transporting these vaccines include keeping said products between 2C-8C. In order to maintain such cold temperatures requires the use of: cooler bag, 3 fridge plates, 1 frozen plate, and 2 sheets of bubble wrap. The bubble wrap serves to protect the vaccines from having direct contact with any of the cold plates. Somewhere during the transportation process, one of the sides of the bubble wrap got pushed down, causing potential exposure of the vaccines to the cold plates, which are most likely below 2C. Due to insufficient data to support the idea that the vaccines were considered active, we must assume that the 4 Moderna vaccines provided during our shift on 3/7/2022 are possibly invalid. We arrived to their encampment around 9:00 AM on 3/7/2022. We provided our vaccination services to our patient, and followed standard procedure. After observing the patient for over 15 minutes, having the patient report no adverse symptoms, we allowed them to go back to their encampment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 07.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
At HCF, I served as a Cold Chain Operator (CCO), who is responsible for transporting COVID-19 and flu vaccines to encampment sites. Standards for transporting these vaccines include keeping said products between 2C-8C. In order to maintain such cold temperatures requires the use of: cooler bag, 3 fridge plates, 1 frozen plate, and 2 sheets of bubble wrap. The bubble wrap serves to protect the vaccines from having direct contact with any of the cold plates. Somewhere during the transportation process, one of the sides of the bubble wrap got pushed down, causing potential exposure of the vaccines to the cold plates, which are most likely below 2C. Due to insufficient data to support the idea that the vaccines were considered active, we must assume that the 4 Moderna vaccines provided during our shift on 3/7/2022 are possibly invalid. We arrived to their encampment around 9:00 AM on 3/7/2022. We provided our vaccination services to our patient, and followed standard procedure. After observing the patient for over 15 minutes, having the patient report no adverse symptoms, we allowed them to go back to their encampment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 07.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
At health employer, I served as a Operator (CCO), who is responsible for transporting COVID-19 and flu vaccines to encampment sites. Standards for transporting these vaccines include keeping said products between 2C-8C. In order to maintain such cold temperatures requires the use of: cooler bag, 3 fridge plates, 1 frozen plate, and 2 sheets of bubble wrap. The bubble wrap serves to protect the vaccines from having direct contact with any of the cold plates. Somewhere during the transportation process, one of the sides of the bubble wrap got pushed down, causing potential exposure of the vaccines to the cold plates, which are most likely below 2C. Due to insufficient data to support the idea that the vaccines were considered active, we must assume that the 4 Moderna vaccines provided during our shift on 3/7/2022 are possibly invalid. We arrived to their encampment around 9:00 AM on 3/7/2022. We provided our vaccination services to our patient, and followed standard procedure. Patient received his 2nd dose of Moderna at 9:20AM with us. After observing the patient for over 15 minutes, having the patient report no adverse symptoms, we allowed them to go back to their encampment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 05.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no recommendation to repeat the dose from the vaccine manufacturer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 05.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no recommendation to repeat the dose from the vaccine manufacturer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 04.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
"The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 04.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
"The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 04.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
"The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 03.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
"The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 03.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
"The vaccine this patient received was determined to have had a temperature excursion below the recommended storage temperature prior to administration. There was no guidance to repeat the dose from the vaccine manufacturer."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Immunodeficiency
Incorrect dose administered
Symptomtext
IMMUNOCOMPROMISED PATIENT WAS GIVEN 0.5ML DOSE FOR 4TH COVID SHOT INSTEAD OF 0.25ML PATIENT HAS NOT EXPERIENCED ANY PROBLEMS AND NO TREATMENT WAS NEEDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunodeficiency
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Patient received booster before the 5 month mark
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Underdose
Symptomtext
Patient came in for 2nd dose of Moderna vaccine which should have been 0.5mL. Patient was only given 0.25mL. Dr notified ordered to administer additional 0.25mL of Moderna vaccine ass soon as possible same day for a total of 0.5mL to complete second dose requirement. No adverse reactions noted. Pt advised to return in 5 months for booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient received 0.5mL, but the dose should have been 0.25mL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- 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 was given second dose three weeks early, first dose on vaccine card 2/09/2022 (this info was not in database). Patient is homeless and no contact number or address to follow up with patient.
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
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 27.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Hypoaesthesia oral
Symptomtext
45 minutes after receiving injection, my face, from my nose, across my cheeks, and downward, went numb. This feeling lasted 24 hours. 72 hours later bottom lip still numb.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D3 and C, zinc, quercetin
- Allergien
- N/A
- Vorherige Impfungen
- Facial numbness, age 60, Jan 13 and Feb 13 2021. Covid vaccine, Moderna.
- Staat
- MD
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 27.02.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
On January 29th 2022 patient came to pharmacy asking to receive her first covid vaccine. She chose to receive Moderna, but failed to indicate that she has received the Janssen Covid -19 vaccine previously in April 2021 at a different location. during my conversation prior to administering the vaccine I inquired as to why the patient had chosen to wait so long to receive her first vaccine. During that conversation, She disclosed to me that she was not comfortable with the vaccines since these are novel vaccines. A little later, and I had administered the vaccine. On 02/26/2022, patient returned to receive her second dose of Moderna Vaccine (0.5ml), soon after I administered her second dose, She revealed that she had actually received a dose of Janssen vaccine the year before. I do not know if patient is or has been experiencing any adverse events from this vaccine. I have made several attempts to reach her by phone and have not been able to get a hold of her. She left soon after getting the vaccines not heeding my advice to remain seated for 15 minutes after the receiving the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 27.02.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
PT comes into clinic to receive second dose of moderna. PT previously received first dose of moderna on 1/5/22 at the age of 17. PT did not have any visual signs of being symptomatic before or after the vaccine administration. PT and family were notified of medical error. PT was advised that only pfizer should have been given as she is a minor. PT was advised that if she had any reaction or concerns about the vaccine, she can contact her PCP or ED dept., if necessary. PT said she was feeling okay upon exiting the clinic and did not have any further questions or concerns.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- unknown
- Allergien
- no, according to written and verbal questions asked
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- 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
The vial was initially stored in the refrigerator on 20-Jan-2022 and was administered more than 30 days after; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vial was initially stored in the refrigerator on 20-Jan-2022 and was administered more than 30 days after) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Johnson & Johnson vaccine (Patient has received a primary Johnson & Johnson vaccine) on 08-Jul-2021. Past adverse reactions to the above products included No adverse event with Johnson & Johnson vaccine. On 22-Feb-2022 at 11:45 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Feb-2022 at 11:45 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vial was initially stored in the refrigerator on 20-Jan-2022 and was administered more than 30 days after). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vial was initially stored in the refrigerator on 20-Jan-2022 and was administered more than 30 days after) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. Patient received the booster dose. Vial didn't undergo any temperature excursions. No symptoms were reported. No medications, treatments, or additional doses had been administered at the time of this report. This case was linked to MOD-2021-054280, MOD-2021-042747, MOD-2021-060758 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 25.02.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
Patient provided different names, as a result vaccinated several times. 2/9/2021 - Moderna. 3/9/2021 - Moderna. 5/26/2021 - J&J. 11/8/2021 - Moderna. 2/23/2022 - Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- 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
- Long-haul COVID-19, elevated LFTs
- Vorgeschichte
- Long-haul COVID-19, elevated LFTs
- Andere Medikamente
- Albuterol, Armodafinil, Escitalopram, Breo, Metformin, Zofran, Oxygen, ParaGard IUD, Spironolactone
- Allergien
- Tamiflu, Ferric carboxymaltose, Penicillin G, Progesterone, eggs, flu vaccine
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Thrombocytopenic purpura
Vaccination complication
Symptomtext
Vaccine induced thrombocytopenic purpura
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombocytopenic purpura
- Hospital-Tage
- 20,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes, obesity, hyperlipidemia
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient did not have any adverse events. The immunization was given outside of suggested age range. Patient was 17 years and 8 months at time of immunization.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 39,0
- 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
Underdose
Symptomtext
0.25ml booster Moderna shot was given instead of the second dose 0.50ml that the client actually needed. The client was contacted and informed of error. Information on this was emailed and the recommendation was if another 0.25 could be given today, it would be ok to count as 0.50 2nd dose. If not able to be given today then 0.50 would have to be given. The client was notified and agreed to get another 0.25ml which was done at her convenience at her home at appx 1pm 0.25ml Mderna was administered at the client's home on the same arm as her request. The vaccine was drawn from the same vial as the previous vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None Known
- Andere Medikamente
- Not known
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 18.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Syringe issue
Underdose
Symptomtext
Patient was injected by MA for his booster dose. His first dose was Janssen on 06/18/2021. Today, he requested Moderna for his booster dose. MA injected the Moderna 0.25 mls booster to patient's left arm, with another MA witnessing. Per MA, there was a leak on the syringe while she was injecting, and there was nothing administered to the patient. Patient was informed, and he agreed for another injection on the same arm, this time given by MA. Patient tolerated the procedure well and was observed for 15 minutes with no reaction to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 17.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- 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
Incorrect dose administered
Symptomtext
Pt reported needing a booster. he was given 0.25ml of moderna vaccine, but upon reconciliation, it was determined that he had only had 1 dose of Moderna, meaning he needed a second 0.25ml to receive the second vaccine. Upon further review, the patient was given these doses too closely to his initial dose of Moderna and will need to complete a full second dose in several weeks to get back on track with his vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HLD, DM2
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
Patient came in to office stating they needed Moderna booster. Booster was administered. While documenting vaccine, staff member noticed that patient had already received booster on 11/08/2021. Dose administered today, 02/16/2022, was patient's fourth dose of Moderna (0.25 mL). Patient was monitored after vaccine, no adverse reaction noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None performed.
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- Hypertension, Coronary artery disease, Diabetes mellitus type 2, Hyperlipidemia, Hypothyroidism, Left eye blindness
- Andere Medikamente
- Novolog, Clonidine, Simvastatin, Hydralazine, Clopidogrel, Quinapril, Isosorbide Mononitrate
- Allergien
- Allergic to Lipitor and Lisinopril.
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Vaccine was given too early. 1st dose- 10/28/2021 & 2nd dose- 11/29/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- none
- Allergien
- Bacitracin and SULFAMETHIZOLE
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 06.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
swollen neck lymph node on left side the size of a golfball, swollen lymph node under the left arm the size of a peach
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- none
- Andere Medikamente
- amoxil 500mg 4 caps 1 hr prior to dental appointments
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Swelling of eyelid
Symptomtext
Received call from patient stating her eyes were almost swollen shut, she also stated had gotten tightness in throat after receiving first dose of vaccine but she did not seek medical care. Advised patient to call emergency
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Swelling of eyelid
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Patient reports felt tightness in throat after first dose of COVID-19 vaccine
- Staat
- CO
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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
Given full dose versus booster in 4th dose. Had an old Booster vs. Additional Dose Workflow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- CKD STAGE 4 (GFR 15-29) LUNG CANCER, LEFT UPPER LOBE HYPERLIPIDEMIA ADULT OBSTRUCTIVE SLEEP APNEA CHRONIC HYPOXEMIC RESPIRATORY FAILURE DM 2 SECONDARY HYPERPARATHYROIDISM, RENAL ORIGIN CHRONIC PANCREATITIS PRESENCE OF UROSTOMY ATHEROSCLEROSIS OF AORTA HX OF KIDNEY TRANSPLANT ESSENTIAL HTN HX OF PROSTATE CANCER HX OF URINARY BLADDER CANCER HX OF RADICAL CYSTECTOMY VITAMIN D DEFICIENCY RIGHT BUNDLE BRANCH BLOCK ANEMIA
- Andere Medikamente
- predniSONE (DELTASONE) amlodipine (NORVASC) Omeprazole (PRILOSEC) Atorvastatin (LIPITOR) Carvedilol (COREG) Lisinopril (PRINIVIL/ZESTRIL) Tacrolimus (PROGRAF) HUMALOG KWIKPEN INSULIN K-PHOS ORIGINAL LANTUS U-100 INSULIN Ethacrynic
- Allergien
- Furosemide Morphine Nifedipine
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Interchange of vaccine products
Symptomtext
Overvaccinated instance: Jansen - Jansen - Moderna. Above patient presented to our clinic stating they are here for their booster dose and requested Moderna vaccine. They stated they previously had received Jansen. They did not produce a CDC vaccine card indicating previous vaccines. Its unknown if our administrative staff checked the Immunization Registry to check their previous vaccines. Only vaccines administered are in this registry. When the patient presented to RN, she says he did not present or have any vaccination card and also indicated he was here for his booster vaccine after previously receiving a Jansen vaccine. The vaccine was administered. Our observation audit team later discovered this patient had received two previous Jansen vaccines on 03/17/2021 (Lot #1805031) and 10/22/2021 (Lot #1822811).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Pt was inadvertently given a booster dosing for their first moderna vaccination. After which, a second dosing of 2.5ccs was given into the same arm to equate to a 5cc total dosing for their first shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Novolin N
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 10.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse event occurred but the patient was only 17 at the time of vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysstasia
Muscular weakness
Symptomtext
Pharmacist received phone call from patient around noon on 2/8/22. She reported extreme weakness in arms and legs. Patient reports not being able to stand and having to pull self across floor, while also suffering from arm weakness. She reports symptoms starting around 8pm on 2/7/22 and persisting until approximately 10:30am on 2/8/22. Treatments: Patient did not report any. Outcome: Patient reports symptoms subsiding the morning of 2/8/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysstasia
- Hospital-Tage
- -
- Labordaten
- None reported.
- Aktuelle Erkrankungen
- None reported.
- Vorgeschichte
- Depression, Anxiety, Chronic Back Pain, Fibromyalgia, GERD, "Tachycardia(unspecified) w/New Persistent Headache."
- Andere Medikamente
- -
- Allergien
- No known allergies.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- -
- Geschlecht
- F
- Eingang
- 10.02.2022
- 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
Dyspepsia
Symptomtext
Woman experienced heart burn like pain in her chest. no shortness of breath
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspepsia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Zoloft
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- 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
Received 2nd dose at 3 weeks not 4 weeks, called cdc. informed pt to get another shot after 28 days, pt refused. Informed pt to call pharmacy if notice any adverse reactions and given vaers website to report. previous pharmacist wrote the follow up date wrong at 3 weeks, and pt went off on that. did not process through insurance
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown/na
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- 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
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient is under the age of 18 but they requested to get Moderna booster and that is what was administered to them. At this time they have not had any reactions to the dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Sertraline and Vitamind D.
- Allergien
- None that we are aware of.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- 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
Device connection issue
Underdose
Symptomtext
During the administration of the patient's 2nd dose of Modena vaccine, the needle detached from the syringe. This caused the patient to not receive the full dosage of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Device connection issue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 06.02.2022
- Impfdatum
- 06.02.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
The only adverse event is that the 4th dose on this immunocompromised patient was 0.5 ml vs recent CDC guideline of 0.25 ml. Patient reported absolutely no issues about 7 hours after administration and had no reaction, not even sore arm, after first 3 doses. This is purely and administration error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Cron's disease (infusions every 8 weeks with Remicade)
- Vorgeschichte
- same as item 11
- Andere Medikamente
- n/a
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Gave booster at 4 months instead of 5. Upon follow-up 5 hours later, patient reported she felt fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
Medication error
No adverse event
Symptomtext
This is a report of a medication error only. Patient administered a fourth dose of Moderna COVID-19 vaccine in error. He presented to clinic on 1/28/2022 for booster. Staff verified afterward, he already received his Moderna booster on 12/15/2021. Patient had no adverse outcomes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- Barrett's esophagus, depression, dysphagia, diabetes mellitus, hypertension
- Andere Medikamente
- Aspirin 81mg, Fluconazole 150mg, Lisinopril 2.5mg, Metformin 1000mg, Omeprazole 40mg
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Received expired booster vaccine >12 hours post puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired booster vaccine >12 hours post puncture) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045L21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Jan-2022 at 11:00 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired booster vaccine >12 hours post puncture). On 27-Jan-2022, EXPIRED PRODUCT ADMINISTERED (Received expired booster vaccine >12 hours post puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. No treatment details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient arrived to clinic for Moderna booster. Booster was administered 29 days before the 5 month interval had elapsed. Patient was made aware of the administration error and informed what symptoms she may experience. At this time, patient is experiencing no symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Type 2 Diabetes
- Vorgeschichte
- Type 2 Diabetes
- Andere Medikamente
- Metformin 1,000 mg Ibuprofen 600 mg
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient received Moderna instead of Pfizer based on age, no problems reported as far as we know as of 1/27/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
The patient requested the third dose of Pfizer. Pfizer was processed, but 0.25ml Moderna was administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Patient came by to request the third those of Pfizer, Pfizer was processed but a Moderna 0.25ml was administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
The patient came for the third dose pfizer booster. the patient is 12 years old, The patient was process the pfizer vaccine but it was Moderna 0.25ml that was administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- None at the moment
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 11.07.2021
- Impfdatum
- 11.07.2021
- Beginn
- 11.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysgeusia
Immediate post-injection reaction
Symptomtext
Metallic taste crept up throat into mouth immediately upon receiving the first dose of the vaccine. I let the pharmacy know, and they said that was a first. It was instantaneous and happened before I even made it to the 15 minute waiting chair.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysgeusia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Scoliosis, nerve disorder, minor arthritis,
- Andere Medikamente
- Medical marijuana patient
- Allergien
- Allergic to hydrocodone
- Vorherige Impfungen
- -