- Staat
- MI
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 06.04.2021
- Beginn
- 11.10.2021
- Tage bis Beginn
- 188,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Atrial fibrillation
COVID-19
Death
Influenza virus test
Respiratory syncytial virus test
SARS-CoV-2 test positive
Symptomtext
Date of Admission: 10/11/2022 Date of Discharge:Deceased on 10/22/2022 Admission Diagnosis: COVID [U07.1] Acute hypoxemic respiratory failure [J96.01] Hospital Principal Problem (Discharge Diagnoses): Paroxysmal atrial fibrillation with RVR
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 2,0
- Labordaten
- 10/10 Covid-19, Flu, RSV by NAA SARS-CoV-2 -COVID-19 Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 94,0
- Geschlecht
- M
- Eingang
- 08.11.2022
- Impfdatum
- 02.05.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 100,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Acute respiratory failure
Alanine aminotransferase increased
Anticoagulant therapy
Aortic stenosis
Aspartate aminotransferase increased
Atrial fibrillation
Blood creatinine increased
Blood gases
Blood urea increased
Bronchial secretion retention
Bronchoalveolar lavage
COVID-19
Cardiac failure congestive
Catheter placement
Chest X-ray abnormal
Condition aggravated
Culture negative
Symptomtext
8/10/2022- Presents to ED, c/o covid + at home, headache, vomiting . Covid- test. HR-109 and RR-24. Afebrile. Spo2 99% on 6L, place on Bipap. Creatnine 1.6. EGFR-40 CXR: pulmonary infiltrates. Admit acute resp failure s/t CHF exacerbation . 8/12/2022-Increased SOB, eKg no change. Monitor. Albuteral inhaler. 8/13/2022- Alternated between 6l nc and Bipap 60%. Trop critical 1.860. Heparin Drip. PM- trop now 6.180. non-ST segment elevation MI ICU.Nitro. Covid + test. EGFR-21. 8/14/2022-Venous dopplers negative. Continue Heparin drip. Start Decadron and Doxy. Held remdesivir d/t renal function. 8/16/2022- Creatnine now 3.0 BUN-110 Continue to hold ARBs/ACEi. Unable to do cardiac cath d/t renal fucntion. ALT-396
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 16,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, CAD s/p CABG , CHF, HTN, Type 2 DM, CKD stage III.
- Andere Medikamente
- -
- Allergien
- Insulin, PCN, Tetanus and Sulfa
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 27.10.2022
- Impfdatum
- 12.01.2022
- Beginn
- 25.10.2022
- Tage bis Beginn
- 286,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Death
Symptomtext
Patient expired.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 16.02.2022
- Beginn
- 27.09.2022
- Tage bis Beginn
- 223,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cardiac arrest
Life support
Pulseless electrical activity
Supraventricular tachycardia
Syphilis
Symptomtext
Patient begin treated for CoVID 19 with Paxlovid , on day 5. suffered cardiac arrest at home
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- None: EMS ACLS procedures for PEA and pulseless s v tach. epinephrine only
- Aktuelle Erkrankungen
- treated for syphilis with 2.4 million units Bicillin august 2022- one moth prior to death - no vaccination Day 5 of treatement of CoVID -19 infection with Paxlovid at death -no vaccination
- Vorgeschichte
- hypertension - controlled endometriosis alcoholism hepatitis C- treat to cure 2017
- Andere Medikamente
- Paxlovid
- Allergien
- no known Drug or food allergies
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 01.02.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 205,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
Interchange of vaccine products
SARS-CoV-2 test positive
Symptomtext
Covid vaccine x 2. Tested positive for covid on 8/25/2022. Expired at Medical Center on 8/25/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 16.06.2022
- Impfdatum
- 21.01.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 144,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Patient expired 6/14/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- PMH includes HTN, morbid obesity, COPD
- Andere Medikamente
- Unknown
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 17.02.2022
- Beginn
- 27.02.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood lactic acid
COVID-19
Confusional state
Death
Fibrin D dimer increased
General physical health deterioration
Hypotension
Infection
Procalcitonin
SARS-CoV-2 test positive
Urine analysis abnormal
Symptomtext
a 74 y.o. male resident who was sent here for above problems. He contracted Covid-19 infection after he was sent there on 2/12 for rehab. He tested (+) on 2/21. He was severely hypotensive on arrival here and confused. He has been started on pressor agent. UA show signs of infection. D dimer 1139, lactate 9.5, procalcitonin 1.8. He is confused. Later same day, his conditioned worsened and the outcome was clear, patient was made DNR and was provided comfort care until his passing,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, HEart failure, NSTEMI, PAF with RVR, cardiomyopathy, CAD, DM,
- Andere Medikamente
- unable to ascertain
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 97,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Dyspnoea
Oedema peripheral
Productive cough
Skin warm
Symptomtext
Patient received the Moderna COVID-19 vaccine on 1/14/2022. On 1/16/2022 patient was observed to have productive cough, shortness of breath, edema and warmth to left arm. Patient expired on 1/19/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- No medical or laboratory test were conducted d/t patient plan of care and being under Hospice.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HTN, DM Type 2, CKD Stage 3, CAD, Dementia
- Andere Medikamente
- Morphine 10mg Guaifenesin 200mg Lorazepam 0.5mg
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Discomfort
Symptomtext
Discomfort (unspecified) on the day following the COVID 19 booster shot. No treatment was done. Death happened on the 2nd day after booster shot. Official date of death was listed as 1/22/22, since that was the date when discovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Vascular Disease, Diabetes
- Andere Medikamente
- Statins
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 21.12.2021
- Beginn
- 25.10.2022
- Tage bis Beginn
- 308,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Fall
Loss of consciousness
SARS-CoV-2 test positive
Syncope
Symptomtext
Pt to ED 10/21 with cc of fall/syncope with LOC. 10/24 Pt is aox3, on RA not in distress, denies pain or discomfort. 10/25 pt COVID+. 10/26 Pt is aox3, on RA not in distress, denies pain or sob. 10/16 pt discharged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- 5,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Gastroesophageal reflux disease without esophagitis Gastroesophageal reflux disease without esophagitis Current use of long term anticoagulation Carotid artery stenosis Essential hypertension Mixed hyperlipidemia Chronic pain Osteoarthritis Obesity (BMI 30-39.9) Paroxysmal atrial fibrillation (CMS/HCC) Hyperglycemia Mild cognitive impairment with memory loss Lumbar foraminal stenosis CKD (chronic kidney disease), stage II Lumbar burst fracture, sequela Syncope, unspecified syncope type Permanent atrial fibrillation (CMS/HCC) Dizzinesses Fall with injury Gross hematuria LOC (loss of consciousness) (CMS/HCC) Impaired ambulation Impaired functional mobility, balance, gait, and endurance
- Andere Medikamente
- apixaban (ELIQUIS) 5 MG PO Tab dilTIAZem CR apixaban (ELIQUIS) 5 MG PO Tab dilTIAZem CR (CARDIZEM CD) 240 MG PO CAPSULE SR 24 HR donepezil (ARICEPT) 10 MG PO Tab HYDROcodone-acetaminophen (NORCO) 5-325 MG PO Tab nystatin (MYCOSTATIN) 100000
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 95,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 03.02.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 106,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest X-ray abnormal
Dyspnoea
Lung infiltration
Respiratory distress
SARS-CoV-2 test positive
Symptomtext
Shortness of breath started around 5/20/22. ED visit report states respiratory distress is present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory distress
- Hospital-Tage
- -
- Labordaten
- Positive COVID test 5/23/22, Pulmonary infiltrates on Chest X-ray
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD, Hypertension
- Andere Medikamente
- -
- Allergien
- Cephalexin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 19.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Blood pressure normal
Dizziness
Syncope
Symptomtext
Patient experienced dizziness and fainting approximately 2 days after receiving vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Blood sugar and blood pressure normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- 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
Blood glucose normal
Head injury
Syncope
Symptomtext
With the first vaccine, patient experienced dizziness within hours of receiving the vaccine. After the second vaccine, patient experienced fainting and hit her head. She was evaluated by a physician.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Normal blood sugar and blood pressure
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Head injury
Syncope
Symptomtext
With the first vaccine, patient experienced dizziness within hours of receiving the vaccine. After the second vaccine, patient experienced fainting and hit her head. She was evaluated by a physician.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Normal blood sugar and blood pressure
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 24.04.2022
- Impfdatum
- 14.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Asthenia
CSF cell count
Cognitive disorder
Electroencephalogram
Encephalitis autoimmune
Intensive care
Laboratory test abnormal
Lumbar puncture
Magnetic resonance imaging head
Scan with contrast
Seizure
Status epilepticus
Symptomtext
21 year old otherwise healthy and no history of previous seizures, that presented with seizure/status epilepticus on January 24th, 2022, 10 days after covid vaccine booster. Presumed autoimmune encephalitis after extensive work up, leading to status epilepticus and extremely difficult to control seizures with ongoing breakthrough events. Patient with ongoing hospitalization, mostly in ICU, and suffering from debility along with likely permanent cognitive impairment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 90,0
- Labordaten
- MRI head with and without contrast 1/25/22 Continuous long-term EEG on 1/28/22 Lumbar puncture with CSF analysis on 1/26/22
- Aktuelle Erkrankungen
- No illnesses, was involved in motor vehicle collision on 1/10/2022 with lingering intermittent headaches but otherwise no residual effects
- Vorgeschichte
- Anxiety
- Andere Medikamente
- none
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 16.03.2022
- Impfdatum
- 16.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Angiogram cerebral normal
Arteriogram carotid normal
Cerebral infarction
Imaging procedure
Ischaemic stroke
Magnetic resonance imaging head abnormal
Muscular weakness
Symptomtext
Ischemic stroke Acute muscle weakness on right side Went to emergency room Felt normal three hours later Stayed in hospital two days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- 2,0
- Labordaten
- MRI of brain w/o intravenous contrast: Tiny focus of acute infarct w/in superior potserior frontal white matter CT Angiography of head & neck: No significant findings T of head w/o contrast: no siginficant findings
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Gout sleep apnea
- Andere Medikamente
- Indomethacin 50 mg PRN Vitamin C 1000 mg
- Allergien
- N/A
- Vorherige Impfungen
- Posterior vitreous detachment, 60, 08/07/2021, COVID-19 vaccine, Moderna
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- 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
Drooling
Eyelid ptosis
Facial paralysis
Headache
Lacrimation increased
Sensory loss
Symptomtext
Headache, left facial/mouth/eye droop, left eye teary, mild oral drooling, decreased left cheek sensation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, Hyperlipidemia, Major depressive disorder
- Andere Medikamente
- Yes
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Dizziness
Fall
Full blood count normal
Loss of consciousness
Malaise
Metabolic function test
Sleep disorder
Vertigo
Symptomtext
I felt fine all day after the vaccination. I went to bed around 9pm and I woke up at 1am and felt very ill. I went to get a glass of water and take some Tylenol. I remember feeling as though I needed to lay down so I don't pass out. Next thing I know I woke up on the kitchen floor. I apparently did pass out and was out for a few mins. I called out to my husband and he had to helped me back to bed. When I hit my head on the floor I think I dislodged some of the crystals in my ear and it has caused me to be more dizzy than normal. I do have vertigo. I didn't start to feel better for a couple days. I did message my doctor and he asked that I come in for some tests.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- 01/24/2022 CBC - Normal CMP - Normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Autoimmune Disease Vertigo
- Andere Medikamente
- CellCept (2) 500mg 2xday Clonazepam 0.5mg 1/2tablet 3xday Zoloft 25mg 1xday Multi Vitamin Vitamin D 2000iu per day
- Allergien
- Clindamycin Effexor
- Vorherige Impfungen
- Prevnar 23- within the last 3 months Shingrix about 3 years ago. With both vaccinations by the next day felt like I needed to la
- Staat
- PA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anaphylactic reaction
Chest discomfort
Chest pain
Chills
Confusional state
Dizziness
Dyspnoea
Fall
Flushing
Head injury
Headache
Hyperhidrosis
Syncope
Tremor
Unresponsive to stimuli
Symptomtext
Systemic: Allergic: Anaphylaxis-Mild, Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Chills-Severe, Systemic: Confusion-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Mild, Systemic: fell out of chair and hit her head on floor-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Headache-Mild, Systemic: Shakiness-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 13.02.2022
- Impfdatum
- 13.02.2022
- Beginn
- 13.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dyspnoea
Facial paralysis
Mobility decreased
Myalgia
Neuropathy peripheral
Pain
Paraesthesia oral
Pyrexia
Tremor
Symptomtext
I AM VERY HEALTHY -WORK OUT 3-4X PER WEEK. NO MEDICATIONS. I PREVIOUSLY HAVE A DOCUMENTED ADVERSE REACTION TO PFIZER. I CHOOSE MY JOB OVER THE SHOT. THIS IS SECOND TIME NOW HAVING SEVERE SYMPTOMS. 103 FEVER SHAKES PAIN UNABLE TO MOVE ARM FACIAL PARALYSIS AND NEUROPATHY SHOOTING PAIN IN RIGHT SIDE OF FACE AND MOUTH TINGLING. SHAKING/RIGORS. MUSCLE ACHES BEYOND NORMAL. SHORTNESS OF BREATHE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE I HAD COVID 6WEEKS AGO
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE; I AM A PHYSICIAN
- Allergien
- NONE; ALLERGY TO PREVIOUS PZIFER 2ND VACCINE AND DOCUMENTED
- Vorherige Impfungen
- PFIZER 2ND DOSE COVID 19 VACCINE
- Staat
- PA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Loss of consciousness
Symptomtext
PATIENT CAME INTO THE STORE AND SAID SHE PASSES OUT EVERYTIME SHE IS GIVEN A SHOT. LESS THAN A MINUTES AFTER ADMINISTERING THE SHOT HTE PATIENT PASSED OUT IN THE CHAIR THAT SHE WAS SITTING IN AT THE TIME OF ADMINISTRATION. SHE KNEW IT WAS GOING TO HAPPEN AND WARNED ME AHEAD OF TIME. I TOOK PATIENTS BLOOD PRESSURE / HEART RATE AND OFFERED PATIENT WATER AND A SNACK. SHE SAT IN CHAIR FOR AN ADDITIONAL TWENTY MINUTES BEFORE SHE FELT WELL ENOUGH TO STAND UP. I DID NOT LET HER DRIVE HERSELF AFTER THIS. HER BOYFRIEND CAME DOWN AND GAVE HER A RIDE HOME,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- BLOOD PRESSURE HEART RATE BOTH WERE WITHIN NORMAL LEVELS.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- JULEBERR BIRTH CONTROL
- Allergien
- NONE LISTED
- Vorherige Impfungen
- SHE PASSES OUT AFTER ANY INJECTION OR IMMUNIZATION
- Staat
- -
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 10.02.2022
- 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: ja
Erholt: nein
Blood glucose normal
Dizziness
Palpitations
Syncope
Thirst
Symptomtext
Client received Moderna booster vaccine at 1400 was sitting in the observation area was accompanied by mother, At 1405 pt complain of being thirsty asking where the water fountain was located. Then immediately reported feeling dizzy with palpitations. Patient states he has history of arrhythmias, and cardiac ablations x3 last one in 2019, also hx of anxiety disorder and panic attacks . Pt reported after having the 2nd dose of Moderna during the 15 minutes observation period , pt fainted and was taken to the hospital. Pt was taken to patient room and place on bed and VS taken pt was AAOx4, skin warm and dry, denies pain, and SOB, with BP of 120/68, HR 89, SPO2 of 98% room air , temp 98.1, blood sugar was 95 after drinking a 200ml of apple juice. EMS was called at 1420, arrived at 1432. Report given to EMS. clinical manager notified. Patient was evaluated and taken by EMS crew at 1437 accompanied by his mother.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Accu check -95
- Aktuelle Erkrankungen
- cardiac, anxiety, panic attacks per pt
- Vorgeschichte
- cardiac
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Confusional state
Flushing
Hyperhidrosis
Hypotension
Seizure
Syncope
Symptomtext
Systemic: Confusion-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Hypotension-Severe, Systemic: Seizure-Severe, Additional Details: Pt had a seizure and fainted, EMS was called and brought pt to hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Diarrhoea
Flushing
Hyperhidrosis
Nausea
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Diarrhea-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Nausea-Mild, Systemic: Weakness-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Loss of consciousness
Syncope
Unresponsive to stimuli
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Fainting / Unresponsive-Severe, Additional Details: Patient passed out about 7 min after getting both COVID and flu shot. He stated after passing out that he was anxious/nervous about getting the COVID vaccine/side effects. He was checked out by paramedics. He called his roommate to pick him up. He was feeling normal, apologetic, and appreciative of the time and care I provided to him.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- 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: ja
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Hyperhidrosis
Hypotension
Injection site pain
Seizure
Syncope
Unresponsive to stimuli
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Hypotension-Mild, Systemic: Seizure-Mild.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Disorientation
Eye movement disorder
Loss of consciousness
Pallor
Unresponsive to stimuli
Urinary incontinence
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Additional Details: After administering Fluzone & Moderna Booster, Patient became clammy & pale. His eyes rolled back in his head & he lost consciousness. He emptied his bladder while unconscious & was unresponsive for approximately 30 seconds. I held him up by his shoulders as he was rolling forward so he would not fall out of the chair or hit his head. I shook his shoulder several times & shouted his name to rouse him. He came to and was disoriented. EMS came and evaluated him and released him to go home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Electrocardiogram
Myocarditis
Pain
Symptomtext
mild myocharditis; dull uncomfortable gripping feeling around heart under left breast spreading to my left shoulder and rib cage.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- EKG came out normal but symptoms did not subside after beta blockers were administered.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- PCOS ADHD Panic Disorder
- Andere Medikamente
- propanolol, diazepam
- Allergien
- bactrum macrobid and dicclofinac
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Additional Details: passed out shortly after the shot. regained consciousness right after
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.10.2023
- Impfdatum
- 17.01.2021
- Beginn
- 01.10.2022
- Tage bis Beginn
- 622,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arrhythmia
COVID-19
Computerised tomogram
Diverticulum
Heart rate
Immunology test
Interstitial lung disease
Laboratory test
Symptomtext
Patient also mentioned that she had a CT scan, and was diagnosed with severe diverticular disease and had half of my colon and rectum removed in June 2023.; I was diagnosed with Interstitial Lung Disease in February 2023; Got covid again; I believe, Paxlovid caused My heart rate (arrhythmias) go to 120s; I got the sick, with the Delta variant of Covid and I was Super Super sick, and was not hospitalized; This spontaneous case was reported by a patient and describes the occurrence of INTERSTITIAL LUNG DISEASE (I was diagnosed with Interstitial Lung Disease in February 2023) and ARRHYTHMIA (I believe, Paxlovid caused My heart rate (arrhythmias) go to 120s) in an elderly female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 022J21A and 022J21A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product NIRMATRELVIR, RITONAVIR (PAXLOVID) for an unknown indication. No Medical History information was reported. On 17-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 22-Feb-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In 2023, the patient started NIRMATRELVIR, RITONAVIR (PAXLOVID) (unknown route) at an unspecified dose. In October 2022, the patient experienced COVID-19 (I got the sick, with the Delta variant of Covid and I was Super Super sick, and was not hospitalized). In January 2023, the patient experienced COVID-19 (Got covid again). In February 2023, the patient experienced INTERSTITIAL LUNG DISEASE (I was diagnosed with Interstitial Lung Disease in February 2023) (seriousness criterion medically significant). In 2023, the patient experienced ARRHYTHMIA (I believe, Paxlovid caused My heart rate (arrhythmias) go to 120s) (seriousness criterion medically significant). On an unknown date, the patient experienced DIVERTICULUM (Patient also mentioned that she had a CT scan, and was diagnosed with severe diverticular disease and had half of my colon and rectum removed in June 2023.). The patient was treated with Surgery (Had half of colon and rectum removed in June 2023) for Diverticulum. At the time of the report, INTERSTITIAL LUNG DISEASE (I was diagnosed with Interstitial Lung Disease in February 2023), ARRHYTHMIA (I believe, Paxlovid caused My heart rate (arrhythmias) go to 120s), DIVERTICULUM (Patient also mentioned that she had a CT scan, and was diagnosed with severe diverticular disease and had half of my colon and rectum removed in June 2023.), COVID-19 (I got the sick, with the Delta variant of Covid and I was Super Super sick, and was not hospitalized) and COVID-19 (Got covid again) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2023, Heart rate: 120 heart beats per minute. On an unknown date, Computerised tomogram: Diagnosed with severe diverticular disease and had half of colon and rectum removed in June 2023.. On an unknown date, Immunology test: (Negative) Did all kinds of immune testing and all results came back negative.. On an unknown date, Laboratory test: The patient also reported that tests showed she had problems with lungs and was diagnosed with Interstitial Lung Disease in February 2023, and believes that it was related to Covid.. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered ARRHYTHMIA (I believe, Paxlovid caused My heart rate (arrhythmias) go to 120s) to be not related. No further causality assessments were provided for INTERSTITIAL LUNG DISEASE (I was diagnosed with Interstitial Lung Disease in February 2023), DIVERTICULUM (Patient also mentioned that she had a CT scan, and was diagnosed with severe diverticular disease and had half of my colon and rectum removed in June 2023.), COVID-19 (I got the sick, with the Delta variant of Covid and I was Super Super sick, and was not hospitalized) and COVID-19 (Got covid again). It was reported that she got the monoclonal antibodies. Patient continued, that Jan 2023 she got covid again, and took Paxlovid. She believed that Paxlovid caused heart rate (arrhythmias) go to 120s and they put her on blood pressure medication which she continues now, if not, she would have had a heart attack by now. Patient also mentioned that she had a CT scan, and was diagnosed with severe diverticular disease and had half of my colon and rectum removed in June 2023. Patient states that she breathes fine and does not take any medication. Company Comment: This spontaneous case concerns an elderly female patient with no relevant medical history reported, who experienced the unexpected, serious (medically significant), events of interstitial lung disease and arrhythmia (AESI) and the non-serious events of COVID-19, in the context of the third dose of mRNA-1273. It was reported that 8 months after the third dose, the patient got sick with COVID-19 delta variant but was not hospitalized. She got the monoclonal antibodies. About 3 months later, she got COVID-19 again and took Paxlovid. She believed that Paxlovid caused her heart rate to increase to 120 bpm (arrhythmias) and was treated with blood pressure medication. The patient reported tests that showed lung problems and was diagnosed with Interstitial Lung Disease about 4 months after the 3rd dose and believed that it was related to COVID-19. Patient explained that her doctor did all kinds of immune tests, and all results came back negative. They were planning to repeat tests in 6 months. Patient stated she that she had no breathing problems and did not take any medication. She had a CT scan and was diagnosed with severe diverticular disease on an unknown date and half her colon and rectum was removed around 8 months after the 3rd dose. No further clinical information was provided for review. Paxlovid which was used as treatment drug for COVID-1 could be a co-suspect for arrhythmia. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. This case was linked to US-MODERNATX, INC.-MOD-2023-745156 (Linked Report).; Sender's Comments: This spontaneous case concerns an elderly female patient with no relevant medical history reported, who experienced the unexpected, serious (medically significant), events of interstitial lung disease and arrhythmia (AESI) and the non-serious events of COVID-19, in the context of the third dose of mRNA-1273. It was reported that 8 months after the third dose, the patient got sick with COVID-19 delta variant but was not hospitalized. She got the monoclonal antibodies. About 3 months later, she got COVID-19 again and took Paxlovid. She believed that Paxlovid caused her heart rate to increase to 120 bpm (arrhythmias) and was treated with blood pressure medication. The patient reported tests that showed lung problems and was diagnosed with Interstitial Lung Disease about 4 months after the 3rd dose and believed that it was related to COVID-19. Patient explained that her doctor did all kinds of immune tests, and all results came back negative. They were planning to repeat tests in 6 months. Patient stated she that she had no breathing problems and did not take any medication. She had a CT scan and was diagnosed with severe diverticular disease on an unknown date and half her colon and rectum was removed around 8 months after the 3rd dose. No further clinical information was provided for review. Paxlovid which was used as treatment drug for COVID-1 could be a co-suspect for arrhythmia. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. US-MODERNATX, INC.-MOD-2023-745156:Case for Spikevax 2023-2024 PFS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- Test Name: CT scan; Result Unstructured Data: Diagnosed with severe diverticular disease and had half of colon and rectum removed in June 2023.; Test Name: immune testing; Test Result: Negative ; Test Name: tests; Result Unstructured Data: The patient also reported that tests showed she had problems with lungs and was diagnosed with Interstitial Lung Disease in February 2023, and believes that it was related to Covid.; Test Date: 2023; Test Name: heart rate
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- PAXLOVID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 29.06.2023
- Impfdatum
- 15.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Acoustic stimulation tests abnormal
Allergy test positive
Asthenia
Autoimmune disorder
Balance disorder
Blood test
Cardiac stress test
Computerised tomogram head normal
Deafness unilateral
Dizziness
Dysstasia
Echocardiogram normal
Electrocardiogram abnormal
Electrocardiogram ambulatory
Feeling hot
Food allergy
Gait inability
Gluten sensitivity
Symptomtext
I have received 2 doses of the Moderna vaccine, first one being 1/12/22 and second being 2/15/22. My first one i instantly got a headache and felt a weird sensation from the bottom of my neck right up to the back of my head that sounded like little cracks. I then proceeded to have a heart rate of 148-150 for 7-8 days, I had called my doctors office and asked if that was okay and if i should receive my second one. They had a nurse call me back, she had stated that it was okay and COVID would do worse for my heart than the Vaccine. I then got my second one, a few hours after my heart felt very weak and a couple hours later I was in full flu like symptoms for 72 hours. I was brought to the hospital 6 days after my second shot. Date being 2/21/22, I was at work when my heart rate started to go up. I noticed it at 125 and then went to the bathroom to splash cool water on my face, I started to get really dizzy and hot and at that point my heart rate was at 143 and it went from 143 to 179 in matter of seconds. I let my co worker know it was super high and wasnt sure what to do, she had me sit and I called my boss to go home, at this point it was up at 205 and i sat with a cold cloth on my neck and my face to get it to go down. I drove home which is 2 miles down the road, I called my doctors office and let them know what was going on, they had told me to call the ambulance and see if I was steady enough to wait for a ride or if they need to take me to the hospital, The ambulance ended up taking me to the hospital, where I sat for a few hours with some iv fluid running through me. My heart rate had gone down to 90 and they released me. I was okay for a couple days after that, then I got very sick all of a sudden and I couldnt walk, eat, drink, stand up. I went to the hospital again, they had me hooked up to a portable ekg machine and my heart rate had gone up sitting in there, the nurse had me sit for a while longer and then they gave me baby aspirin and a valum and i went home. I had lost 15 pounds in less than 2 months, I went to the hospital a third time and second time by ambulance, I was having heart palpitations for longer than 6 hours, and got no sleep. My heart rate had shot up to 179 while I was in the hospital, and they came in with an ekg machine. I asked the doctor to do an echocardiogram to make sure there was no swelling. That came out fine, I was referred to a cardiologist where I was scheduled for a tilt table test where I found out that I have developed POTS. I then went to another cardiologist and they had done a stress test and had to wear an event monitor for a month and a half. I now have POTS and PVC?s. In between all the hospital visits I had seen a PT for what they thought was vertigo, I had damage to my vestibular nerve causing me to have no balance. That was corrected with exercises she had given me to do. I also had seen an ent for the ringing in my ears that is constant every single day. I had catscans done to check my sinus which came out fine. I have also gone and had an mri to make sure there wasnt damage in my brain, there was not thankfully. My ent also had allergy tests done on me, I am now allergic to gluten, peanuts and most corn products, which all started with these vaccines. I was eating all of this a day prior to my first shot. And when my primary had found this out she had told me I am developing an auto immune disease that wont be able to show up in tests for a few years once it fully presents itself. I had then gone to a hearing specialist to have a hearing test done and there is hearing loss in my right ear, assuming from the ringing. I lost about a year of my life being sick due to these vaccines. Still currently going to these doctors to help everything that has happened.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- ekgs echocardiogram tilt table stress test event monitor mri catscan blood work allergy tests hearing test
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- keflex albuteral doxycycline metoprolol
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 17.05.2023
- Impfdatum
- 05.04.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 121,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Decubitus ulcer
Hypotension
Symptomtext
I95.9 HYPOTENSION 11/5/2022 ATRIAL FIBRILLATION W RAPID VENTRICULAR RESPONSE I95.9 HYPOTENSION 11/5/2022 PRESSURE ULCER OF SACRUM, UNSPECIFIED STAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 02.05.2023
- Impfdatum
- 05.03.2021
- Beginn
- 15.05.2021
- Tage bis Beginn
- 71,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Biopsy skin abnormal
Burning sensation
Neuritis
Neuroma
Neuropathy peripheral
Pain
Pain in extremity
Paraesthesia
Therapeutic nerve ablation
Symptomtext
After the second vaccine in May 2021 I developed very acute pain in my feet. I had horrible burning and pain, The pain and burning was progressing and in November 2021 stared a series of steroid injections in my feet for pain. They didn?t help. I was diagnosed with nerve inflammation : bilateral neuromas. I started a series of alcohol injection ( ablation of the neuromas). They brought me a relief. January 2022 I got more pain and tingling in feet that spread out to ankles and hands and arms. January 2023- diagnosed with short fiber neuropathy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- January 2023 I had a skin biopsy that showed short fiber neuropathy.
- Aktuelle Erkrankungen
- Stress fracture of the 2 nd metatarsal in the left foot
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 24.03.2023
- Impfdatum
- 23.03.2022
- Beginn
- 06.01.2023
- Tage bis Beginn
- 289,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Dyspnoea
Laboratory test abnormal
Lethargy
Nasal congestion
Pyrexia
SARS-CoV-2 test negative
Wheezing
Symptomtext
I had a fever, shortness of breath, wheezing, lethargic and severe cough with nasal congestion. I was negative for COVID-19, they tested me again and found a possible pneumonia. They prescribed me albuterol, I didn't feel better until after 3 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 12JAN2023- Swab Test- Positive 12JAN2023 COVID-19- Test- Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Bronchitis; Spondylolisthesis
- Andere Medikamente
- Omeprazole; Cingular; Losartan; Nasonex
- Allergien
- Codeine; Sulfa; Quinolyl; Preservatives
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 20.03.2023
- Impfdatum
- 03.02.2022
- Beginn
- 14.03.2023
- Tage bis Beginn
- 404,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Blood culture negative
Blood pressure increased
COVID-19
Chest pain
Condition aggravated
Diarrhoea
Gastrointestinal tube insertion
Hypertension
Nausea
Nothing by mouth order
Pyrexia
SARS-CoV-2 test positive
Small intestinal obstruction
Vomiting
Symptomtext
discharge summary "Hospital Course: 68 YO female with a history of psoriatic arthritis on prednisone and methotrexate, DVT/PE on Eliquis, type 2 diabetes mellitus who presents with nausea, vomiting, diarrhea, chest/abdominal pain. Found to have small-bowel obstruction. SBO - resolved with NG tube decompression - Originally NPO. NG tube removed 03/16; pt tolerated low fiber, low residue diet, able to pass gas and stool - Home pain meds - PRN Zofran - General Surgery onboard, OK for D/C COVID-19 Patient is not displaying respiratory symptoms at this time - Symptomatic management HTN Acute pain may be contributing to elevated blood pressures - resume home amlodipine and losartan HLD 10-year ASCVD risk is 28.4%. No statin therapy recorded in Home Meds. - Initiate lipitor 40 mg T2DM - Resume home oral diabetic medications Fever, 03/15 - resolved May have been 2/2 COVID-19 - 03/15 BCx NGTD Plaque psoriasis Multiple joint pain, chronic' ?Psoriatic arthritis - Sees Dr. (Rheumatology) - Followed by Dr. (Derm) for psoriasis who recommended initiation of Stelara - Reportedly taking Methotrexate 2.5 mg (5 pills weekly) and folic acid daily - Home Tacolnex ointment not on formulary - Restart home ibuprofen, Norco, methotrexate, and prednisone Hypokalemia, resolved History of pulmonary embolism, Nov 2021 Patient on Eliquis, Continue "
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 5,0
- Labordaten
- Covid positive PCR 3/14/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- * (Principal) SBO (small bowel obstruction) Essential hypertension, benign Psoriatic arthritis History of pulmonary embolus (PE) Hyperlipidemia associated with type 2 diabetes mellitus COVID-19 Hypokalemia due to excessive gastrointestinal loss of potassium
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 09.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Dyspnoea
Gait disturbance
Malaise
Pericardial effusion
Pericardial excision
Transcatheter aortic valve implantation
Walking aid user
Symptomtext
After receiving the booster shot I start to slow up short of breath and every week it was getting worse. I could not walk at all and my heart dr. wanted to know what happened to me. He immediately sent me for test. In May of 2022 they discovered Fluid around the heart. A surgeon spoke to us, he told us about the fluid around, that I needed immediate surgery. My partner asked how come this didn?t show up prior he said we did test in Feb. 2022 and there was no fluid and no need at this point for Valve replacement maybe in a couple of years. She asked directly was it the booster shot. That within a couple of days or so after the booster I started feeling sick. He said I believe it is, I have seen many cases like this recently. May 2022, at Hospital, I had surgery a Pericardial Window they removed 1.5 liters of fluid mostly blood it was crushing my heart; 20 days later I needed a TAVR heart valve at the same hospital by Dr. Since getting the booster, I was never the same as time progressed I was getting worse and worse. I almost did not survive. In September 2022 at Heart Center, Dr. did a Mitra Valve Clip. I am now wearing oxygen 24 hours a days and I am on an inhaler everyday using a walker.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- May 2022, June 2022, August 2022at Hospital August 2022 Sept 2022 Heart Center
- Aktuelle Erkrankungen
- A-Fib, High Blood Pressure
- Vorgeschichte
- A-Fib, High Blood Pressure, Prostate issues, Melanoma Cancer Survivor
- Andere Medikamente
- Torsemide Diltiazem Hydralazine Atenlol Lisinopril Allopurinol Aspirin Potassium Terazosin Pravastatin Coumadin Vit C Multiple Vitamin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 25.01.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 38,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Electrocardiogram abnormal
Mitral valve prolapse
Palpitations
Symptomtext
My Doctor ordered an Electrocardiogram for me and I found out that I have Mitral Valve Prolapse. I was having chest pains and heart palpitations prior to my Doctor ordering the testing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- ECG testing revealed Mitral Valve Prolapse.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Atenolol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 27.01.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 294,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood cholesterol increased
Heart rate increased
Hypotension
Malaise
Symptomtext
I felt a little sick the day after receiving the vaccine. On 11/17/2022 I was at physical therapy, and they said my blood pressure was low and they recommended that I keep an eye on it. I went to see my endocrinologist and had blood work and my cholesterol was higher than normal. My fitness watch indicated my resting heart rate was elevated. At this time, I am watching what I eat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Levothyroxine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 18.01.2023
- Impfdatum
- 20.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Ageusia
Alopecia
Anosmia
Anxiety
Catatonia
Chest discomfort
Cognitive disorder
Communication disorder
Computerised tomogram
Delirium
Depression
Disability
Disturbance in attention
Electroconvulsive therapy
Electroencephalogram normal
Erectile dysfunction
Erythema
Gait inability
Symptomtext
62 yr. old male ? took no prescriptions or drugs prior, yearly received flu shots, had a high technical job, very active and healthy. 10/2021 Patient had COVID, received the 4 anti-body shots 11/21 till 3/22 experienced sever hair loss, taste and smell. Patient was a employee for Technology company and required to receive the vax. J&J was not available at the time Patient received the 1ST Moderna vax on 1/20/22; 90 days after anti-body shots as recommended by medical staff. At the time of injection, he experienced pain in left arm, 4x4 red swollen area, for about 4 days. Within a week had pain across back of the head, heaviness in chest and cognitive decline issues, lack of concentration. 2/17/22 Patient received 2nd Moderna vax. In addition to the prior symptom's, patient experienced sever insomnia, sever anxiety and depression, and erectile disfunction. 6 weeks later admitted to the hospital. After a PCP visit, patient was admitted to hospital with suicidal ideation severe anxiety. NO prior family or personal history of mental health. 4/1-4/18/2022 hospitalized and discharged with no meds or follow-up doctor or therapy appointments. 4/29/22 re-admitted to hospital, via ambulance, presenting like Parkinson, tremors, unable to walk, lack of communication, some delirium. Noted as a possible drug withdrawal from previous visit. Took off controlled substances too quickly. Diagnosed with catatonia, severe depression and anxiety. 5/13/22 transferred to another hospital, with a psych wing, for treatment and began ECT sessions. Discharged from hospital 6/8/22 with meds and future appointment with a therapist and psychiatrist and follow up OP ECT sessions for another month or so. Continued therapist and psych Dr appointments to this day. 8/2022 consult with Neurological Institute. Had MRI and EEG ? both unremarkable. Patient continues on 4 medications and under weekly therapist and 2x/month doctor's care. Some improvement, not much. Patient is currently on LTD from his job as of Sept 27/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- 60,0
- Labordaten
- BRAIN MRI 3/29/22 BRAIN MRI and EEG 09/2022 CAT SCANS 05/2022
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- LATEX
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 02.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SC / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Chest discomfort
Dyspnoea
Exercise tolerance decreased
Fibrin D dimer
Heart rate increased
Malaise
Post-acute COVID-19 syndrome
Symptomtext
Long term difficulty breathing, elevated heart rate, and chest discomfort. Inability to tolerate any exercise for 4 months, followed by 6 more months of frequent relapses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Chest X-ray and D-dimer 02/09/2022
- Aktuelle Erkrankungen
- Covid 19 positive on 01/12/2022
- Vorgeschichte
- Long Covid like symptoms with ongoing shortness of breath that lasted from the onset until November 2022. Intense chest pain/ costochondritis. The shortness of breath caused low oxygenation when I would try to walk short distances (down the hallway to the bathroom) below 90%. I was unable to work until July, then starting in July only 2 -3 days per week, with great difficulty. At the onset and for the first 2 months, my resting heart rate was elevated above 100, often as high as 135 bpm. I visited the Emergency room on 02/09/2022 for shortness of breath..
- Andere Medikamente
- None
- Allergien
- Mild bee venom reaction
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 24.01.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 315,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acetabulum fracture
Anticoagulant therapy
Arthralgia
Blood bilirubin increased
Blood creatinine increased
COVID-19
Cardiac failure
Computerised tomogram abnormal
Condition aggravated
Device breakage
Diastolic dysfunction
Echocardiogram abnormal
Fall
Gait inability
Joint dislocation
Joint dislocation postoperative
Mitral valve incompetence
Pain
Symptomtext
"Patient with history of 3 COVID vaccines who had routine COVID test for facility placement and was found to be COVID detected. Provider d/c note: ""Reason for Admission: She reports that she sustained a ground level fall earlier today and has been experiencing ongoing pain since then. She typically does have chronic pain in this hip. She has history of joint replacement several years ago. She has had signs of chronic loosening of her joint for the past couple years and she has been referred to a University. She reports that she has follow-up with the orthopedic team next month. She denies numbness, weakness, paresthesias. Did not hit her head or lose consciousness. Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) See below note for details re: this brief hospitalization. Hospital Course: No notes on file These were her acute medical issues addressed: Patient is a 56 YO female with a PMHx of sickle cell disease, chronic opioid use, right hip replacement with complications who presents with mechanical fall and right hip pain. Found to have signs of hip arthroplasty displacement and inability to ambulate. Mechanical Ground level fall Right hip replacement and revision with complications Unable to ambulate CT shows acetabular vertical displacement with fractured screws with age indeterminate fractures of acetabulum, femoral head subluxed from acetabular component. She has had signs of chronic loosening of her joint for the past couple years and she has been referred and has follow-up next month Trialed crutches in ED, still needed asisstance -Ortho consult: Transfer to a center due to complexity of her THA dislocation. -transitioned Eliquis to Argatroban in case of procedure. Last dose of Eliquis was 12/4 -PT/OT; non weight bearing right hip -cautious with pain management; avoid over sedation. Heart failure with reduced ejection fraction 45-50%, grade 2 diastolic dysfunction, moderate to severe MR, mild elevation RVSP, small pericardial effusion on echo 11/26 -continue home Demadex. -beta-blocker and ACE-inhibitor/Arb contraindicated due to cocaine use and previous hyperkalemia Recent History of DVT Heparin allergy Last dose of Eliquis 12/4:00 p.m. -transition to pharmacy to dose agatroban due to renal function and possibility of surgery Sickle cell disease with chronic pain-no evidence of sickle cell pain crisis, folic acid, hydroxyurea. Continue home methadone. Chronic obstructive pulmonary disease/asthma with chronic hypoxic respiratory failure of 3 L, pulmonary hypertension-no exacerbation. Symbicort, p.r.n. albuterol. Oxygen p.r.n. OSA-CPAP. Patient would like to go home with a hospital provided CPAP if possible. Apparently this was provided to her during her last hospitalization but she forgot it at the hospital CKD stag 4, chronic hyperkalemia- baseline Cr 2.3, stable, monitor. Continue Lokelma. Tobacco abuse-nicotine patch NM anemia, stable 12/2-schistocytes noted which is intermittent/chronic Elevated transaminases, bilirubin-chronic Right inguinal hernia with bowel Polysubstance abuse, cocaine abuse Tracheomalacia Stable patient but in pain. Patient is non ambulatory on RLE. Transfer to a center for further eval and MGT of dislocated, chronic R THA apparatus. Spoke to Hospital. Spoke to Dr the Orthopedic surgeon on call. Dr. accepted patient for transfer to their total joint team. Dr. will consult and be the lead surgeon in her case. I also spoke to Admitting Hospitalist Dr likewise accepted patient to their service."""
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 1,0
- Labordaten
- COVID Detected PCR on 12/06/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular Hyperlipidemia Severe pulmonary hypertension (HCC) Chronic systolic congestive heart failure (HCC) Essential hypertension Dilated cardiomyopathy, mild Valvular heart disease Acute on chronic combined systolic and diastolic CHF (congestive heart failure) (HCC) DVT (deep venous thrombosis) (HCC) Heart failure with reduced ejection fraction (HCC) Digestive Constipation due to opioid therapy Gastroesophageal reflux disease without esophagitis Integumentary Furuncle of pubic region Psychological Adjustment disorder with anxious mood Generalized anxiety disorder Respiratory Asthma Severe Tracheobronchomalacia OSA (obstructive sleep apnea) Chronic respiratory failure with hypoxia (HCC) Pneumonia due to infectious organism Pulmonary edema Respiratory failure requiring intubation (HCC) Chronic respiratory failure with hypoxia (HCC) Urinary AKI (acute kidney injury) (HCC) Acute kidney injury superimposed on chronic kidney disease, stage III Stage 3b chronic kidney disease (HCC) AKI (acute kidney injury) (HCC) CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min (HCC) Other Sickle cell pain crisis (HCC) Tobacco abuse Insomnia Elevated LFTs Polysubstance (including opioids) dependence, daily use (HCC) Opiate dependence (HCC) Hemochromatosis due to repeated red blood cell transfusions Noncompliance with CPAP treatment Sickle cell disease (HCC) History of alcohol abuse Chronic pain Lack of intravenous access ASCUS with positive high risk HPV Hyperkalemia Sickle-cell disease with pain (HCC) Elevated troponin Hemolytic anemia (HCC) Thrombocytopenia (HCC) Toxic encephalopathy Cocaine abuse (HCC) Subacute vaginitis Right hip pain Compression fracture of L1 vertebra (HCC) S/P kyphoplasty Persistent pain in prosthetic joint (HCC) Intractable pain History of renal impairment Chest discomfort Transaminitis Hypermagnesemia Normocytic normochromic anemia Encounter to discuss test results Costochondritis Acidosis Symptomatic anemia Nausea Frailty Acute on chronic anemia Hypercapnic acidosis Cocaine use Fall Right hip pain Inability to ambulate due to hip Sickle cell disease (HCC) Polysubstance abuse (HCC) Failure of right total hip arthroplasty (HCC)
- Andere Medikamente
- -
- Allergien
- Heparin Analogues Heparin Analogues Ibuprofen
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 11.03.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 234,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myeloid leukaemia
Blood culture negative
Blood potassium decreased
Blood sodium increased
COVID-19
COVID-19 pneumonia
Chemotherapy
Chest X-ray abnormal
Condition aggravated
Diabetes insipidus
Electrolyte substitution therapy
Fatigue
Gastrooesophageal reflux disease
Hypernatraemia
Hypertension
Hypokalaemia
Lung consolidation
Lung opacity
Symptomtext
Hypernatremia - resolved Hypokalemia - resolved Diabetes insipidus Fatigue BMP on admission shows Na 153, K 2.7 Na 144, K 4.1 11/3 Pt has documented history of diabetes insipidus- follows with Dr with endocrine, treated with DDAVP - Resume home DDAVP - Replace potassium - Trend BMP - Pt received D5W, now stopped - Encourage PO fluid intake - Endocrine consulted - suggested DI possibly related to AML but unclear etiology - Recommend outpatient follow up with endocrinology Pancytopenia due to chemotherapy AML Getting chemo, last treatment 10/10/22 Restart pancytopenia prophylaxis, acyclovir, diflucan, levaquin was held while inpt as pt was tx with zosyn, will restart levaquin upon discharge for 5 day course Venetoclax held in setting of pancytopenia, will defer to heme/onc when to restart Multifocal pneumonia COVID-19 infection Suspect pneumonia likely viral due to COVID Symptoms started 10/29, tested positive on admission, SORA CXR 10/31/22 shows ill defined consolidative opacities in right hemithorax, specifically in right upper lung zone and also subtle left retrocardiac opacity Currently on vanc and zosyn (started 10/31) MRSA probe negative and blood cultures pending Sputum cultures not collected Procal elevated ID recommended supportive care at this time for COVID-19 infection as long as SORA HTN Tachycardia-resolved Patient not on BP meds at home Patient denies pain, does not appear agitated Amlodipine 10 mg daily, coreg 6.25mg BID, hydralazine PRN while inpt Will decrease norvasc to 5mg daily, continue coreg 6.25mg BID, until pt has appointment with PCP and can manage as appropriate GERD Resume home prilosec 40mg History of MSSA bacteremia Pt was recently treated with IV vanc and discharged on abx outpatient, pt was supposed to have antibiotics last until 11/4 Blood cultures negative MRSA probe negative Pt completes course of vancomycin tomorrow
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 96,0
- Geschlecht
- M
- Eingang
- 27.10.2022
- Impfdatum
- 14.04.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 188,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bladder scan
Blood culture negative
COVID-19
COVID-19 pneumonia
Dysphagia
Gastrooesophageal reflux disease
Pneumonia
Pneumonia bacterial
Procalcitonin increased
SARS-CoV-2 test positive
Sepsis
Urine analysis normal
White blood cell disorder
Symptomtext
Discharge Provider: DO Primary Care Provider: FNP Admission Date: 10/19/2022 Discharge Date: Oct 22, 2022 PRESENTING PROBLEM: Severe sepsis [A41.9, R65.20] Sepsis due to pneumonia [J18.9, A41.9] Community acquired pneumonia, unspecified laterality [J18.9] COVID-19 [U07.1] HOSPITAL COURSE: Exceedingly pleasant 97 y/o community dwelling patient of Dr. was admitted on 10/19/2022 for bilateral community acquired pneumonia with associated severe sepsis. The patient tested positive for COVID 19. He had an elevated procalcitonin as well. He was treated for both COVID 19 pneumonia and bacterial pneumonia. He was unable to provide a sputum culture. He improved with these treatments. His sepsis resolved, and he had negative blood cultures. He was deemed medically stable for discharge on 10/22/22. He completed Remdesivir during this admission, as well as 4 days of Decadron. He will not take Decadron after discharge, because he remained on RA during his admission and passed his home oxygen evaluation. He was sent home on Ceftin 500 mg PO BID for 6 days and Doxycycline 100 mg PO BID x 6 days for a total time of 10 days of antibiotics for his pneumonia. His WBC normalized. The patient had history of a TURP and has mild LUT symptoms at home. His UA was negative for infection. His bladder scan was zero after he voided. This is a stable comorbid issue requiring no medication. The patient also had s/s of dysphagia related to GERD and was discharged home on Protonix 40 mg PO BID x 14 days followed by 40 mg daily for 30 days. The patient should follow up with is PCP if this is unhelpful for possible EGD or UGI or further evaluation. He is asked to follow up with is PCP for post-hospital follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Sepsis due to pneumonia Pneumonia due to COVID-19 virus Anemia Benign essential tremor Presbycusis BPH with obstruction/lower urinary tract symptoms
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler benzonatate (TESSALON) 100 MG capsule cefuroxime (CEFTIN) 500 MG tablet doxycycline (MONODOX) 100 MG capsule guaiFE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 24.09.2022
- Impfdatum
- 01.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Arthralgia
Back pain
Chest pain
Culture
Decreased appetite
Depressed mood
Feeding disorder
Headache
Hidradenitis
Insomnia
Pain
Pain in extremity
Testicular abscess
Weight
Weight decreased
Symptomtext
Testicular abscess; Appetite absent; Depressed mood; Generalised aching; Headache; Painful R arm; Shoulder pain; Lost weight; Chest pain; Hidradenitis suppurativa; Low back pain; Difficulty sleeping; Unable to eat; Abdominal pain; This spontaneous case was reported by a consumer and describes the occurrence of TESTICULAR ABSCESS (Testicular abscess) in a 47-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product ADALIMUMAB (HUMIRA) for Hidradenitis suppurativa. The patient's past medical history included Hidradenitis suppurativa on 06-Feb-2022. Concurrent medical conditions included Tobacco user (FOUR TO FIVE CIGARETTE STICKS PER DAY) and Abstains from alcohol. Concomitant products included DICLOFENAC for Muscle relaxant. On 10-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In January 2022, ADALIMUMAB (HUMIRA) (Subcutaneous) dosage was changed to 40 milligram. On an unknown date, the patient started ADALIMUMAB (HUMIRA) (Subcutaneous) 40 milligram. On 10-Jan-2022, the patient experienced PAIN IN EXTREMITY (Painful R arm). In January 2022, the patient experienced TESTICULAR ABSCESS (Testicular abscess) (seriousness criteria hospitalization and medically significant), WEIGHT DECREASED (Lost weight), CHEST PAIN (Chest pain), HIDRADENITIS (Hidradenitis suppurativa), BACK PAIN (Low back pain), INSOMNIA (Difficulty sleeping), FEEDING DISORDER (Unable to eat), ABDOMINAL PAIN (Abdominal pain) and ARTHRALGIA (Shoulder pain). On 09-Feb-2022, the patient experienced PAIN (Generalised aching) and HEADACHE (Headache). On an unknown date, the patient experienced DECREASED APPETITE (Appetite absent) and DEPRESSED MOOD (Depressed mood). The patient was treated with TRAMADOL at an unspecified dose and frequency; CLINDAMYCIN at an unspecified dose and frequency and Surgery (surgery to drain abscess) for Testicular abscess. On 11-Jan-2022, PAIN IN EXTREMITY (Painful R arm) had resolved. At the time of the report, TESTICULAR ABSCESS (Testicular abscess) was resolving, DECREASED APPETITE (Appetite absent), DEPRESSED MOOD (Depressed mood), HIDRADENITIS (Hidradenitis suppurativa) and HEADACHE (Headache) outcome was unknown and WEIGHT DECREASED (Lost weight), PAIN (Generalised aching), CHEST PAIN (Chest pain), BACK PAIN (Low back pain), INSOMNIA (Difficulty sleeping), FEEDING DISORDER (Unable to eat), ABDOMINAL PAIN (Abdominal pain) and ARTHRALGIA (Shoulder pain) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 05-Feb-2022, Culture: Normal. On 06-Feb-2022, Culture: Normal. On an unknown date, Weight: 15 weight loss, 15 Pounds. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. It was unknown if he was enrolled in a COVID-19 vaccine trial. The patient abstains from alcohol. Scrotal pain (testicular pain), surgery, testicular swelling and testicular pain were subsumed under testicular abscess as a symptoms The patient had some problems getting new dose of HUMIRA medicine so he was off HUMIRA for two months. He was off Humira in Dec 2021 due to insurance change then, when he got back on Humira he started to feel sick. The event of sick he meant that it was abdominal pain, stomach pain, chest pain, shoulder pain, lower back hurts and swelling of testicles. He had COVID vaccine on 10 Jan 2022 and hidradenitis suppurativa symptoms got worse. He was on unknown antibiotics. On 09 Feb 2022, he took medication and felt horrible everything hurt headache, scrotum hurt look like a ball back hurt. He was hospitalized on 05 Feb 2022 to 06 Feb 2022 because the swelling of testicles worsened and it got hurt so bad. A surgery to drain the abscess in testicles was done on 06 Feb 2022. He had follow up appointment on 08 Feb 2022 to check the surgery that was done then he had surgery again on 11 Feb 2022 to drain the abscess in testicles. He mentioned that every time he got a Humira shot, he feels sick. He clarified that Moderna COVID 19 vaccine did not make his symptoms worse. He just felt his right arm hurting for one day after COVID 19 vaccine shot. For HUMIRA, the reporter causality for the events of Surgery, Testicular swelling, Testicular abscess, Testicular pain, Appetite absent, Feeling sick, Lost weight, Scrotal pain, Feels bad, Depressed mood, Headache, Generalized aching, Chest pain, Abdominal pain, Hidradenitis suppurativa, Shoulder pain, Low back pain, Difficulty sleeping, Unable to eat, Painful R arm was not provided. This case was identified as part of a retrospective clean-up activity where certain emails received in the Moderna mailbox were missed to be booked-in. Reporter did not allow further contact. Company comment: This spontaneous case concerns a 47-year-old male patient with no relevant medical history, who experienced the unexpected, serious (hospitalization) event of testicular abscess about a month after a dose of mRNA-1273. The patient describes that he experienced testicular pain and swelling which got worse until he was hospitalized for 1 day, where surgery to drain the abscess was performed. Another surgery was performed 6 days after the initial drainage. Cultures from the first surgery came back as normal. Outcome was reported as resolving. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 47-year-old male patient with no relevant medical history, who experienced the unexpected, serious (hospitalization) event of testicular abscess about a month after a dose of mRNA-1273. The patient describes that he experienced testicular pain and swelling which got worse until he was hospitalized for 1 day, where surgery to drain the abscess was performed. Another surgery was performed 6 days after the initial drainage. Cultures from the first surgery came back as normal. Outcome was reported as resolving. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220205; Test Name: CULTURE; Result Unstructured Data: Normal; Test Date: 20220206; Test Name: CULTURE; Result Unstructured Data: Normal; Test Name: Weight loss; Result Unstructured Data: weight loss, 15 Pounds
- Aktuelle Erkrankungen
- Abstains from alcohol; Tobacco user (FOUR TO FIVE CIGARETTE STICKS PER DAY.)
- Vorgeschichte
- Medical History/Concurrent Conditions: Hidradenitis suppurativa.
- Andere Medikamente
- DICLOFENAC; HUMIRA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 26.08.2022
- Impfdatum
- 21.01.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 52,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood calcium normal
Cardiac stress test normal
Chest X-ray normal
Chest pain
Discomfort
Dyspnoea exertional
Echocardiogram normal
Gastrointestinal disorder
Laboratory test normal
Scan with contrast normal
Symptomtext
In March of 2022 I began to notice chest pains. There didn't seem to be a pattern. They come and go at random. They aren't excruciating but are uncomfortable. Sometimes I feel out of breath when climbing stairs. I contacted my transplant team who advised that I see a doctor. I went to be checked and they did some tests but advised that I go to the emergency room where more tests were done. I have been following up with my cardiologist and my primary care physician who believe it may be a G.I. issue. They still have not narrowed down a diagnosis but do not believe it is heart related. I have received a round of Evusheld injections in March 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 03/14/2022 Echo cardiogram; chest X-ray; Stress test with dye injected; calcium test, nothing abnormal found in any tests.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Liver Transplant Recipient; High Blood Pressure; Mitral Valve Prolapse;
- Andere Medikamente
- Vitamin D3; PEPCID AC; NEORAL; losartan
- Allergien
- Penicillin; erythromycin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 20.04.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 107,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
COVID positive, SOB
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 30.06.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Anion gap
Asthenia
Blood creatinine increased
Blood glucose decreased
Blood urea increased
COVID-19
Carbon dioxide decreased
Chronic kidney disease
Citrobacter test positive
Computerised tomogram head normal
Condition aggravated
Exposure to SARS-CoV-2
Haemoglobin decreased
Hydronephrosis
Hydroureter
Malaise
Metabolic acidosis
Symptomtext
Patient up to date on COVID vaccinations who admitted with COVID symptoms and COVID detected PCR. Provider D/C note: " 68-year-old female with past medical history of chronic kidney disease status post kidney transplant with solitary kidney, cadaver, on immunosuppressive therapy (tacrolimus, prednisone), hydronephrosis status post stenting, DVT, hyperlipidemia,type 2 diabetes, hypertension, who presented to the emergency department with complaints of generalized weakness with onset 3-4 days prior to admission at which time she had a positive COVID contact. In the emergency department patient's vitals are stable, Accu-Chek with significant 48 blood glucose (given D10W in ED), labs significant for 8.3 hemoglobin, creatinine and BUN elevated, CO2 11, anion gap 17. CT of head was done, unremarkable. Patient reports she was supposed to have her stent removed 2 days prior but was too weak to see the urologist. Patient was admitted to the general medicine team for further evaluation. For her acute kidney injury on CKD status post renal transplant, patient had a renal ultrasound done which was significant for hydronephrosis/ hydroureter with stent present. urology was consulted stat. UA was pending however previous UA was significant for Citrobacter freundii and meropenem was started. Antibiotics were subsequently discontinued following benign UA results. Urology deferred stent exchange and negated emergency intervention due to positive COVID status. Urology continued to follow for the duration of the admission with instructions to follow-up following completion of severe respiratory isolation. Nephrology was also consulted, patient's tacrolimus levels were maintained, patient was started on bicarbonate drip for her anion gap acidosis subsequently being transition to oral bicarbonate. Patient was maintained off of all nephrotoxic medications and started on gentle hydration. Patient's AKI improved. For her COVID + patient was started on remdesivir, did not require supplemental oxygen or any further treatment, tolerated well, symptomatic improvement. Following improvement of her AKI and per recommendations of nephrology and urology patient was ready for discharge. For her covid 19+ Patient's hospital stay was not complicated"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 9,0
- Labordaten
- COVID detected PCR 07/22/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Anxiety 5/29/2018 Bladder tumor 11/13/2021 Bronchial tumor 11/13/2021 Dyslipidemia 5/29/2018 Hypertensive nephropathy, stage 1-4 or unspecified chronic kidney disease 5/8/2019 Vitamin D deficiency 7/12/2021 Uterine cancer 1/1/1998 Type 2 diabetes mellitus 10/12/2014 Severe obesity with body mass index (BMI) of 35.0 to 39.9 with comorbidity 11/9/2019 Hypertension 5/29/2018 S/P ureteral stent placement - requires periodic stent exchange (Chronic) 4/19/2022 Recurrent deep vein thrombosis (DVT) (Chronic) 4/19/2022 Immunocompromised state 1/6/2022 Debility 4/20/2022 Severe protein-calorie malnutrition 6/7/2022 Dementia
- Andere Medikamente
- Eliquis Lipitor Pepcid Folic acid Novolog Lantus Remeron Mycostatin Zoloft Prograf
- Allergien
- Amoxicillin Iodinated Contrast media Iodine Simvastatin Sulfa Betadine
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 22.01.2022
- Beginn
- 10.04.2022
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Diarrhoea
Dyspnoea
Fatigue
Impaired work ability
Influenza
Influenza virus test negative
Malaise
Respiration abnormal
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I started feeling ill early April and it just continued. I thought I was having a bought of the flu. In middle May I went to the Doctor and they gave me the Flu and COVID-19 tests. Symptoms were shortness of breath, runny nose, coughing, diarrhea; fatigue and these lasted 2-3 weeks. They were pretty bad because I missed 5 days of work. I continue to have lingering breathing problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Flu test - negative; COVID-19 test - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Obesity; Heart condition - heart murmur
- Andere Medikamente
- Simvastatin; Hydrochlorothiazide; Alfuzosine; Celecoxib; Furosemide; Eloprironol; Potassium Citrate; Baby Aspirin; Inhaler
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 15.01.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 178,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
COVID-19
Chest discomfort
Cough
Decreased appetite
Diarrhoea
Discomfort
Feeling abnormal
Insomnia
Lymph node pain
Lymphadenopathy
Mobility decreased
Nasal congestion
Nausea
Pain
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I was in a different state, and I started with a tooth ache and decided to come home. When I was traveling home, I didn't feel good. I was in pain and felt nauseous. My throat was itchy and my mom's immunocompromised, so I tested for COVID-19 when I got home, and it was positive. I've been in bed every day since then. My lymph nodes in my neck swelled up. I had a fever. They gave me amoxicillin for my tooth and Paxlovid for my COVID-19 infection. I've been taking pain medications around the clock because my lymph nodes have been aching badly. I haven't had an appetite and had diarrhea every day. I also had anxiety because of the pressure on my neck and chest. I also had a cough starting this past Sunday. I had a stuffy nose from Tuesday up until yesterday. I took some Benadryl last night to help me sleep and today's the first day I woke up feeling decent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- At Home COVID-19 07/12/2022 - Positive; At Home COVID-19 07/17/2022 - Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- PCOS; Obesity
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 15.01.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 45,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Acoustic stimulation tests
Chills
Dizziness
Full blood count
Migraine
Pain
Photophobia
Pyrexia
Sensory disturbance
Thyroid function test
Tinnitus
Vertigo
Symptomtext
I had a fever, chills, body aches, and it was the first time in my life I had a migraine in my life that sounds and lights were triggering me. And about a month and half or 2 months later, I started getting really dizzy. I thought it was stress, and a month after I went to the doctor. My ears started ringing really bad on April 15th and has not stopped. I had a hearing exam for that and I am seeing an EMT for that now. Some of the doctors do believe this is vertigo from the vaccine due to the amount of patients they are seeing now that have the vaccine in common before they meet with them.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Ear exam; CBC and thyroid test; One doctor said my thyroid was messed up but another one said it was fine.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Thyroid and glaucoma disorder
- Andere Medikamente
- meloxicam estradiol progesterone latanoprost armour thyroid
- Allergien
- Latex; avocado; bees
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 08.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Chest discomfort
Echocardiogram normal
Electrocardiogram normal
Mobility decreased
Pain in extremity
Symptomtext
Contracted Covid 3 days after the vaccine. I got slight leg pains which was tolerable but I was getting tightness of the chest and I had energy. Like I could not find it. I didn't feel like moving. I didn't have palpitations and I was attributing to just not getting enough blood flow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- EKG, Echo, which both came out fine, but by then it started subsiding.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- Biotin; fish oil
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Computerised tomogram normal
Fatigue
Magnetic resonance imaging normal
Pain
Tremor
Symptomtext
After the vaccine I started to have pain all over my body and fatigue. I started to have bad tremors. I went to the emergency room because I was having back pain that was unbearable. I was given an injection, and prescribed a new muscle relaxer. I am still having tremors.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- MRI-normal, CT- normal
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Fibro myalgia, Mass Cell Activation disease, POTs, Polycystic ovarian disease, EBV
- Andere Medikamente
- Metformin 2000mg, Trimethoprim, Tizanidine, Hydralazine, Tramadol, Cetirizine, Levothyroxine, Unisom, Tylenol, Omeprazole, Famotidine, Montelukast, Allegra, Valacyclovir, Probiotic, Palmitoylethanolamide and Multivitamin patch.
- Allergien
- Amoxicillin, Penicillin, and Gabapentin.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 27.01.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 29,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antinuclear antibody
Arthralgia
Arthritis
Borrelia test negative
Double stranded DNA antibody
Immunology test
Loss of personal independence in daily activities
Mobility decreased
SARS-CoV-2 test negative
Sleep disorder
Symptomtext
Systemic joint inflammation and pain; unable to sleep for three weeks until prednisone Nine weeks to return to normal function and mobility
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- 4 Mar22- Lyme and Covid tests (both negative) 11 Mar 22 - autoimmune blood tests ( ANA and Double strand DNA antibody elevated markers) 4 Apr 22- autoimmune blood tests ( ANA and double strand DNA antibody elevated markers)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- B vitamins, calcium, potassium citrate, magnesium citrate
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 17.04.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Electrocardiogram
Feeling abnormal
Headache
Hypertension
Symptomtext
I was feeling kinda off a little bit. I was having severe headaches and I took my blood pressure. It was very high so I went to Urgent Care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- EKG, Physical Exam
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Nerve Damage, PTSD
- Andere Medikamente
- None
- Allergien
- Latex, Pollen, Cashews
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Headache
Nausea
Pyrexia
Symptomtext
headache, fever of 101.8, nausu on day after vaccine; fever gone next day but nauseu and headache continue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Magnesium Citrate, Alprazolam, Niacin, Triamterene/hydrochlorothiazide, Atorvastatin, Metamucil
- Allergien
- Sulfa
- Vorherige Impfungen
- nausea, 62 yo, 3/8/21, 2nd vaccine, Moderna
- Staat
- NC
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Condition aggravated
Crying
Facial pain
Fatigue
Feeling abnormal
Hypoaesthesia
Limb discomfort
Mobility decreased
Pain
Pain in extremity
Paraesthesia
Symptomtext
I started feeling funny not long after the shot. I had some pain in my eyebrow area. I was so exhausted that I started crying, and my legs and arms were very heavy and it was hard to move them. In my left hand going up all the way to my shoulder, starting with my fingers, they went numb. It tingled so bad that it hurt. Then, it started in my legs. This happened on all 3 doses, but on this dose, I also had shooting pains in my lower back area and it is still happening to this day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines, Diabetic, Diabetic Peripheral Neuropathy, Arthritis, High Blood Pressure, High Cholesterol, COPD
- Andere Medikamente
- 9Sumatriptan Succinate, Ambien, 30 Multi Vitamin-Iron Tab, 30 Atorvastatin, Calcium, Lipitor, Melatonin, Gabapentin, Paxil, Prilosec, Lisinopril, Strattera, Cetirizine, Propranolol, Methocarbamol, Buspirone, Jardiance, Glipizide, Bydureon b
- Allergien
- Metformin, Mushrooms, Corn, Lettuce, Seafood
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Paraesthesia
Symptomtext
I have had periodic numbness and tingling in my hands and feet after receiving the Covid vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- spironolactone, tretinoin, dapsone, multivitamin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Decreased appetite
Ear pain
Headache
Heavy menstrual bleeding
Injection site bruising
Menstrual disorder
Musculoskeletal stiffness
Nausea
Neck pain
Paranasal sinus discomfort
Photophobia
Rhinorrhoea
Tachycardia
Symptomtext
Head ache within 10 minutes of shot, neck pain within an hour after shot. Headache continued into the next day and lights made it worse. Injection site felt bruised, neck continued to fell stiff the next day, sinus pressure and runny nose began the next day, appetite lessend and felt nauseous after eating, tachycardia several times, ear pain, menstration abnomality- cycle lasted/bled for 19 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Zyrtec as needed
- Allergien
- Dairy intollerance
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 09.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Decreased appetite
Dyspnoea
Pyrexia
Somnolence
Visual impairment
Symptomtext
Fever , sleepery, weakness , chilling ,poor vision for 5 days, absense of appetite .Difficult breathing .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Thorethroat , bronchitides
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Metoprolol , aspirin , hydroclorotiazide
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 15.03.2022
- Impfdatum
- 31.01.2021
- Beginn
- 14.03.2022
- Tage bis Beginn
- 407,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Pt admitted for left hip pain and dyspnea. Pt was tested for COVID prior to admission to rehab facility and tested positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 03.02.2021
- Beginn
- 04.02.2022
- Tage bis Beginn
- 366,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Pneumonia
SARS-CoV-2 test positive
Symptomtext
The patient tested positive for Covid-19 on 2/4/22 and developed pneumonia. he was hospitalized on 2/4/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- 5,0
- Labordaten
- Covid -19 RNA 2/4/22- result positive Covid -19 RNA 2/5/22-result positive
- Aktuelle Erkrankungen
- COPD, Type II Diabetes, Cardiovascular disease, Chronic renal disease, hypertension
- Vorgeschichte
- COPD, Type II Diabetes, Cardiovascular disease, Chronic renal disease, hypertension
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 03.03.2022
- Impfdatum
- 29.04.2021
- Beginn
- 18.01.2022
- Tage bis Beginn
- 264,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase normal
Aspartate aminotransferase normal
Bacterial test positive
Bladder catheterisation
Blood alkaline phosphatase increased
Blood bicarbonate decreased
Blood calcium normal
Blood chloride increased
Blood creatinine increased
Blood lactic acid decreased
Blood magnesium increased
Blood potassium normal
Blood sodium normal
Blood thyroid stimulating hormone decreased
Blood urea increased
COVID-19
Chest X-ray normal
Chromaturia
Symptomtext
Chief Complaint: Fever Source of Information: Available medical record History of Present Illness: This is a 63y.o. male with past medical history significant for COPD, diabetes, hyperlipidemia, hypertension, urinary tract infection, frontotemporal dementia. He presents to Hospital on 1/18/2022 for evaluation of fever and possible sepsis. He presents via EMS. Facility reports that he has been febrile at home and notes that he has a chronic Foley with dark and "infected" urine. Per reports patient is nonverbal at baseline. History is severely limited. In the ED, Vitals on arrival of T 97.6?F, BP 149/105, HR 113, RR 18, SpO2 98% on room air Labs remarkable for white blood cell count 11.6, hemoglobin 12.9, platelets 295. Sodium 142, potassium 4.7, chloride 110, bicarb 18, BUN 60, creatinine 1.42, calcium 9.5. Alk phos 127, AST 15, ALT 11. Lipase within normal limits. Lactic acid 3.3 originally now 1.3. Procalcitonin 9.12. Magnesium 2.2. Phosphorus 4.2. TSH 0.81. Troponin 0.01x3. Flu, RSV negative. COVID-positive. Blood culture pending. Urinalysis positive for nitrites, 3+ leukocyte Estrace, 4+ bacteria. Patient received Tylenol, sepsis fluid bolus 30 mL/kg. Vancomycin and cefepime. Imaging: Chest x-ray no pneumothorax or pleural effusion. No focal consolidation. The cardiomediastinal silhouette is unremarkable. EKG consistent with sinus tachycardia, no significant ST segment changes indicative of ischemia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sinus tachycardia
- Hospital-Tage
- 8,0
- Labordaten
- NOCOVER> 1 HEALTH SYSTEM LABORATORY Chart Review Copy (63 yrs) PT CLASS: Inpatient PATIENT STATUS: Discharged GENDER: male BED: ORD DR: AUTH DR: Results Covid-19, Flu, RSV by NAA Contains abnormal data Covid-19, Flu, RSV by NAA Order: Status: Final result Visible to patient: Yes (seen) Next appt: None Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA) for laboratories certified under Agency to perform high complexity testing. This test has not been FDA cleared or approved. Specimen Collected: 01/18/22 10:21 PM Last Resulted: 01/18/22 11:14 PM
- Aktuelle Erkrankungen
- ? Arthritis left knee ? Benign prostatic hypertrophy ? Chronic obstructive pulmonary disease ? Diabetes mellitus ? Hyperlipemia ? Hypertension ? Sepsis, unspecified organism ? Urinary tract infection, site not specified
- Vorgeschichte
- ? Arthritis left knee ? Benign prostatic hypertrophy ? Chronic obstructive pulmonary disease ? Diabetes mellitus ? Hyperlipemia ? Hypertension ? Sepsis, unspecified organism ? Urinary tract infection, site not specified
- Andere Medikamente
- acetaminophen (TYLENOL) 325 MG PO Tab take 650 mg by mouth every 6 hours as needed. Unknown Unknown time amlodiPINe (NORVASC) 10 MG PO Tab take 10 mg by mouth once daily. Indications: High Blood Pressure Disorder, takes in am Unknown Unknow
- Allergien
- Erythromycin Other Stated allergic to all e-MYCINS.
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 06.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 17,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Atrial fibrillation
COVID-19
Chest X-ray normal
Chronic obstructive pulmonary disease
Chronic respiratory failure
Condition aggravated
Cough
Dyspnoea
Multimorbidity
Pyrexia
Respiratory failure
SARS-CoV-2 test positive
Symptomtext
a 61 y.o. male with COPD on home oxygen, who presented with shortness of breath. He started to have increasing dyspnea 3 days ago. Has had cough, non-productive. Had fever at home. No sick contacts. Denies chest pain. Found to be COVID-19 positive. Wears 2-3 L O2 at home." Hospital Course: The patient was admitted to the hospital and was evaluated and treated per below. * COPD with acute exacerbation Acute COPD Exacerbation - with associated COVID-19 viral infection. Continue nebs, inhalers, IV steroids and antibiotics. Patient improved gradually and was feeling back to his baseline. COVID-19 infection - CXR no infiltrates and is on his home O2 requirement of 2-3L with no increased need for oxygen supplementation. Not fully vaccinated, had one dose Moderna 2/6/22. Discussed with patient and given comborbid conditions will order remdesivir for at least 3 day course. Continued at baseline oxygen requirement. Patient was feeling back to his baseline and was offered 2 more days of treatment. He declined and felt that he is ready to go home. Was discharged accordingly on a tapering course of prednisone. Follow up outpatient with primary care provider. Chronic hypoxic respiratory failure - on home O2 2.5L. Monitor closely. Paroxysmal A fib - rate controlled. Order betapace. Not on OAC at home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PAF, HRN, CAD, GERD, chronic diarrhea, oropharyngeal dysphagia, COPD, smoker
- Andere Medikamente
- ASA. nitrostat, incruse ellipta, advair, mucinex, Proventil, duoneb, betapace, Norco, solu-medrol
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dizziness
Injection site erythema
Injection site warmth
Myalgia
Ocular discomfort
Pain in extremity
Palpitations
Peripheral swelling
Pruritus
Pyrexia
Throat tightness
Symptomtext
She got her vaccine, about 15 minutes after receiving it she started having a racing heart, which lasted for about 48 hours. She also felt like she had a pulled muscle in her chest. She felt woozy, hot behind her eyes like she had a temp but did not have one, which lasted for about 48 hours. After that she thought was good, and then her arm started to hurt and ache really bad, and when she looked at it she had a round red mark about 4" in diameter and it was hot to the touch. It was approximately 3-4" below the vaccination and ice did not improve that, this she had for 3 days. She felt like her throat was closing up and she took one of her pills which helped it. She had a slight fever that lasted for a little while which lasted for about 36 hours. She had swelling of her arm, a little warm and is itching intensely. The three days that she had the muscle pain in her arm has gone away, now just itching and the red spot is less red, but is a still a little bit warm on that spot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Chronic hives, IBS.
- Andere Medikamente
- Cetirizine, vitamin D, Vitamin C, super B complex, aspirin.
- Allergien
- Latex, red #40, yellow #5 and 6, soy, cows milk. AE to tetanus at 32 years of age.
- Vorherige Impfungen
- Tetanus vaccine in 1993, about 20 minutes after she had the vaccine they were driving home and she did not feel good, felt like
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Cough
Dyspnoea
Pyrexia
SARS-CoV-2 test negative
Urticaria
Wheezing
White blood cell count increased
Symptomtext
Allergic urticaria, wheezing, cough variant asthma, cough, elevated white blood cells. Hives are constant, all day long on every part of my body, when flared up my chest gets tight and I have a hard time breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Initial apt 1/31/22 - Took COVID test due to fever, lab test confirmed not covid. Was hesitant top say it was hives from the booster. She wanted it to be covid. However after going through my diet, and activities, (what detergent I use, what areas I have been to, any new foods, new fabric of clothing, anything that could have caused the allergic reaction. hydrOXYzine pamoate 25 mg oral capsule Electronically sent twice a day was all was given, after on 2/11 I went back in because it wasn't going away after 2 weeks. SO I was prescribes these: hydrOXYzine pamoate 50 mg oral capsule Electronically sent twice a day for 14 days fo rhives famotidine 40 mg oral tablet Electronically sent 1 tab a day, take 30 min before meal Medrol Dosepak 4 mg oral tablet Electronically sent 6 tabs day 1, 5 tabs day 2, 4 tabs day 3, 3 tabs day 4, 2 tabs day 5, 1 tabs day 6 Albuterol (Eqv-ProAir HFA) 90 mcg/inh inhalation aerosol Electronically sent 2 puff q 4 h for chest tightness
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 22.01.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 24,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19 pneumonia
Supraventricular tachycardia
Symptomtext
72 year old vaccinated female was admitted for SVT and Covid-19 pneumonia. She was treated with Remdesivir. She converted back to NSR spontaneously and did not need intervention. Cardiology signed off. She will be transferred today for rehab.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CHF, mitral regurgitation, PAD, Afib, HTN, Stroke, pulmonary HTN, DJD, asthma,
- Andere Medikamente
- micro-K, ASA, proventil, nucala, Xalatan, Restasis, Synthroid, inderal, B12, Zincate, Vitamin C, Namenda, Breo, eliquis
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Aphasia
Dyspnoea
Gait inability
Limb operation
Magnetic resonance imaging heart
Scan
Symptomtext
Severe shortness of breath. Unable to walk or talk. Had to go to "ER" via ambulance and was in hospital for 4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 4,0
- Labordaten
- Emergency surgery on right leg vein 01/22/2022. Several scans were done and also a heart MRI was done on 01/26/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Was treated for Urethral cancer during 2021. 33 radiation sessions and 4 chemotherapy infusions which ended on August 27, 2021
- Andere Medikamente
- Generic Singulair, Aspirin, herbal laxative (take this a couple times per week)
- Allergien
- Allecgic to penicillin and eggs
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Allergy test positive
Blood immunoglobulin E increased
Burning sensation
Erythema
Paraesthesia
Pruritus
Swelling
Urticaria
Symptomtext
I arrived home from work on that Saturday evening and it started with a small prickle on the right side of my neck. All of a sudden it flared to a red, hot, burning sensation around my ear. About 15 minutes later I began swelling, itching, and red hives on the scalp of my head, back of my neck and completely the right side of my body. All the way to my feet. On Monday I went to a walk-in clinic and they gave me cortisol. I went to the doctor on Tuesday she referred me to a dermatologist who I just saw today. They did a blood work panel and they just gave me some medications to help calm down the hives. They did blood work, IEG allergen panel and I tested positive for an allergy reactive for dog and cat dander, however IEG was elevated to 229. I will have another test on Tuesday with the allergist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Blood work, IEG allergen panel and I tested positive for an allergy reactive for dog and cat dander and IEG was elevated to 229.
- Aktuelle Erkrankungen
- Last week of December I had a respiratory infection but I had been over it by the time January kicked in
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Synthroid; Celexa; Buspar; Adderall
- Allergien
- Cats; dogs
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 13.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 17,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Skin warm
Symptomtext
Chest pain; hot spot on right foot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec for sinus.
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 13.02.2022
- Impfdatum
- 22.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tremor
Symptomtext
Systemic: Tremors on both hands and legs-Medium, Systemic: Shakiness-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- 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
Back pain
Chest pain
Diarrhoea
Pain
Vomiting
Symptomtext
ACHINESS, BACK PAIN, CHEST PAIN, VOMITTING, DIARRHEA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Autoscopy
Muscular weakness
Paraesthesia
Visual impairment
Symptomtext
Patient received the booster on 2-2-2022 at 5pm. On 2-3-2022 she began feeling a tingling sensation throughout her fingers and then progressed to her entire body. She felt like she was having an "out of body experience." Vision was affected (the speed of visuospatial recognition was accelerated, HR 147, b/p 147/90s. Weakness in legs bilaterally.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None. She was adjusted at the Chiropractor following this event and it ceased. No further reactions or noted affects.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hx of rupture anal sphincter with ileostomy, asthma, GAD, depression, insomnia, panic disorder without agoraphobia, stopped taking oral birth control 1 month prior.
- Andere Medikamente
- Duloxetine 90mg po q.day Adderall 30mg BID Unisom Sleep Tablets PRN
- Allergien
- Tree nuts
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anticoagulant therapy
Back pain
Chest pain
Feeling abnormal
Gastrointestinal pain
Headache
Hypersomnia
Major depression
Mobility decreased
Nausea
Pain
Pyrexia
Symptomtext
woke up with major headache, nausia, mid back and chest pain. Slight fever whole body ache. Not very functional, slept alot. Stayed in bed since my whole body felt awful. All this in middle of major blizzard. Sunday felt a little better. Still feel off
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- ended up in walk in with major gut pain. Don't know if still part of the shot. Yesterday Feb 3 woke up again with major headache, back pain. I don't know if i was having a heart situation. Today i started taking eliquis 2/4/222 feel a bit better
- Aktuelle Erkrankungen
- AFIB
- Vorgeschichte
- HBP, AFIB
- Andere Medikamente
- -
- Allergien
- chemically sensitive
- Vorherige Impfungen
- 2nd covid shot minor event
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Coordination abnormal
Dyspnoea
Facial pain
Feeling abnormal
Headache
Hyperacusis
Hyperaesthesia
Neuralgia
Pruritus
Rash
Slow speech
Urticaria
Symptomtext
After receiving vaccine the patient had progressively worsening symptoms starting approx. 12 hours post-vaccine and continuing until present (11 days later). patient reports hives, itching, and rash disseminated over neck and torso. he also report headache, brain fog, neurological-type pain on the left side of his face, increasing headache and sensitivity to touch and noise. he state he feels he is having progressive slowing of speech, difficulty with coordination, and intermittent shortness of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- patient evaluated by PCP, and has attempted a regimen of anti-inflammatory medications steroids, and OTC therapies. none have reduced or alleviated symptoms.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Injection site bruising
Injection site pain
Injection site swelling
Limb injury
Paraesthesia
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Paraesthesia
Symptomtext
Pt. C/O 5/10 sharp chest pain 13 mins after receiving her Modern Booster vaccine and tingling sensation on her right arm and leg.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- MIGRAINE W AURA ASTHMA, UNSPECIFIED BILAT LATERAL EPICONDYLITIS HYPERLIPIDEMIA RESTLESS LEGS SYNDROME HTN (HYPERTENSION) CHRONIC NECK PAIN REPETITIVE STRAIN INJURY DEQUERVAINS TENOSYNOVITIS MITRAL VALVE REGURGITATION PARESTHESIA ACUTE THYROIDITIS PRESENCE OF IUD IUD SURVEILLANCE TINEA PEDIS
- Vorgeschichte
- MIGRAINE W AURA ASTHMA, UNSPECIFIED BILAT LATERAL EPICONDYLITIS HYPERLIPIDEMIA RESTLESS LEGS SYNDROME HTN (HYPERTENSION) CHRONIC NECK PAIN REPETITIVE STRAIN INJURY DEQUERVAINS TENOSYNOVITIS MITRAL VALVE REGURGITATION PARESTHESIA ACUTE THYROIDITIS PRESENCE OF IUD IUD SURVEILLANCE TINEA PEDIS
- Andere Medikamente
- predniSONE (DELTASONE) 50 mg Oral Tab rOPINIRole (REQUIP) 0.25 mg Oral Tab Bismuth Subsalicylate (PEPTO-BISMOL) 262 mg Oral Chew Tab Lisinopril-hydroCHLOROthiazide (PRINZIDE/ZESTORETIC) 10-12.5 mg Oral Tab Amoxicillin 500 mg Oral Cap Ibupro
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Swelling face
Urticaria
Symptomtext
Extensive hives all over the body and minimal facial swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- chronic hives
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 23.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lip swelling
Paraesthesia
Peripheral swelling
Urticaria
Symptomtext
Broke out in hives on my midsection, hands and legs and my lower lip was swollen. I also have a tingling sensation from my knee to my ankle on the left leg.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Diagnosed with Covid on 12/23
- Vorgeschichte
- None
- Andere Medikamente
- Wellbutrin, Zyrtec
- Allergien
- Shellfish, bee stings
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 23.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Symptomtext
Moderate chest pain, especially when breathing. Tylenol helps mildly with the pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Dyspnoea
Feeling abnormal
Headache
Heart rate increased
Myalgia
Nausea
Symptomtext
Headache, muscle and joint aches, shortness of breath, increased heart rate, mental fog, nausea lasting 24 hrs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Digestion issues
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Headache
Tremor
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Headache-Medium, Systemic: Shakiness-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Muscular weakness
Symptomtext
Patient experience arm weakness. Cannot lift arm in forward raise position. Can do bicep curls and other exercises. He does not have pain, but just weakness. If not better by Monday, patient is going to call in primary care md
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Limb injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Migraine
Nausea
Photophobia
Vision blurred
Symptomtext
nausea within 20 minutes, lasting approx 3 hours. migraine started approx 14-15 hours later, migraine caused blurred vision, light sensitivity, and nausea. lasted approx two hours. Took Excedrin Migraine an hour after migraine started to relieve symptoms. unsure if migraine will reoccur when Excedrin wears off
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- strep 2x
- Vorgeschichte
- none
- Andere Medikamente
- wellbutrin 300mg/day penecillian
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Myalgia
Pyrexia
Symptomtext
Pt. states that after receiving the 3rd dose of Moderna 01/15/2022, started experiencing symptom of a fever and "delays". 01/16/2022 symptoms of muscle aches with pain in the left side of the chest. Symptom of chest pain and "delays" still remain. No noted Primary visit/communications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Sulfa-Drugs
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Limb injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bed rest
Chest pain
Myalgia
Pyrexia
Rhinorrhoea
Trismus
Symptomtext
Felt muscle pain on left arm, Had fever, Running nose, Frozen jaw and Felt chest pain Drank a lot of water, took fever relief pills, using cooling pad, bed rest for two days Symptoms were gone in three days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- 2nd dose of COVID-19 Moderna 011D21A at 56
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Dyspnoea
Erythema
Throat irritation
Symptomtext
patient said she felt sharp pain in her back, was having trouble breathing, throat felt funny, face was red
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- BP: 150/140
- Aktuelle Erkrankungen
- anxiety, high blood pressure
- Vorgeschichte
- aniety, high blood pressure
- Andere Medikamente
- unknown
- Allergien
- reported no allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 26.12.2023
- Impfdatum
- 24.02.2022
- Beginn
- 24.12.2023
- Tage bis Beginn
- 668,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Headache
Pain
SARS-CoV-2 test
Symptomtext
Cough, headache, body aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- IDNOW
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, hypertriglyceridemia
- Andere Medikamente
- Hydrochlorothiazide, losartan
- Allergien
- Zolpidem Tartrate
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 15.12.2023
- Impfdatum
- 28.01.2022
- Beginn
- 10.12.2023
- Tage bis Beginn
- 681,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
Anion gap increased
Asymptomatic bacteriuria
Blood potassium decreased
COVID-19
Cannabinoid hyperemesis syndrome
Culture urine negative
Hypoglycaemia
Hypophagia
Insulin therapy
Ketosis
Maternal exposure before pregnancy
Nausea
SARS-CoV-2 test positive
Starvation
Vomiting
Symptomtext
Admit date: 12/10/2023 Discharge date: 12/12/2023 Admitting Physician: MD Attending Physician at the Time of Discharge: DO Primary Care Physician: FNP Reason for Admission: Starvation ketosis, intractable nausea and vomiting Hospital Course: 20 year old G1P0 female at 14 weeks gestational age with a history of Type 1 diabetes mellitis presented to ED with complaints of intractable abdominal pain and nausea and vomiting. Patient was admitted for treatment of starvation ketosis with elevated anion gap. She was managed with an insulin drip and fluids until nausea and vomiting resolved and until patient was able to tolerate oral intake. Nausea was treated originally with Zofran, compazine with no effect, but was later treated successfully with droperidol with resolution of symptoms. Nausea and vomiting suspected to be multifactorial secondary to pregnancy as well as marijuana hyperemesis syndrome. Patient was then able to tolerate normal diet and was converted to home insulin regimen prior to discharge, although due to recurrent hypoglycemia her home insulin glargine dose is being decreased to 8 units twice daily. She was monitored during the rest of the hospital course without recurrence of symptoms. Patient was also started on antibiotics for asymptomatic bacteriuria however this was discontinued as urine culture grew normal flora. Additionally, patient tested positive for Covid, however did complain of any symptoms and was monitored in isolation during hospital course. Of note, patient's potassium level was noted to be 2.9 earlier in the day of discharge. Replacement was started prior to discharge; she is being discharged with the instructions to continue potassium supplementation 40 mEq daily for the next two days. Instructed patient to have a repeat BMP obtained at PCP's office in 4-5 days to follow up on potassium level. Patient expressed understanding and is agreeable. Discharged to home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 02.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram head
Deafness unilateral
Dizziness
Tinnitus
Symptomtext
2/3/2022 tinitus in both ears, dizziness, lost right ear hearing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Head and ear CT
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ensure, one a day, metoprolol, escitalopram,
- Allergien
- iodine, shellfish
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 17.11.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Pain
Pyrexia
Symptomtext
Within 2 hours I was in bed with a fever, chills, aches, and immense pain that can only be described as being crushed all over.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Rheumatoid arthritis, fibromyalgia, IBS, PTSD
- Andere Medikamente
- Paxil, Omeprazole, gabapentin, metoprolol, chlorzoxazone, hydrocodone, guafenasin
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 19.10.2022
- Impfdatum
- 19.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Neuropathy peripheral
Pain
Pain in extremity
Symptomtext
In late May 2022, I developed pain in my left foot with certain movements (not walking). I presented at my PCP's office and saw a ARNP who referred me to an orthopedic specialist. In August 2022, I saw the orthopedic doctor, who diagnosed it as a nerve issue (neuropathy). I've never experienced that before this year.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D, B-complex, turmeric, probiotic, Ozempic, metoprolol, atorvastatin, Nexium
- Allergien
- latex and morphine
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 21.09.2022
- Beginn
- 25.09.2022
- Tage bis Beginn
- 4,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Urticaria
Symptomtext
Hives on wrists, torso. Anywhere clothing or watch band touched skin. Very itchy. Relieved with benadryl. Cannot attribute anything else to the hives (detergent, clothing, food, lotions, etc..)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- Sinus infection 2 weeks prior
- Vorgeschichte
- Diabetes type 2
- Andere Medikamente
- NA
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 24.03.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 70,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Malaise
Nasopharyngitis
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Symptomtext
When I tested positive the first time for COVID-19 I just had a scratchy throat. I went to the urgent care and was prescribed Paxlovid. Within in three days my symptoms were gone. Then I tested positive again on September 11th in the morning. I went to the urgent care and they prescribed Paxlovid and again my symptoms lasted for 3 days. I had a lot sinus drain and nose blowing like a cold.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 test, positive, 06/02/2022, 09/11/2022
- Aktuelle Erkrankungen
- Kidney stones
- Vorgeschichte
- Recovering from colon cancer
- Andere Medikamente
- Zolota; Theralith; Iron; Vitamin D2
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 21.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Chronic spontaneous urticaria
Laboratory test normal
Symptomtext
Global Widespread daily Chronic Spontaneous Urticaria began 1 week after vaccination and continues daily still almost 8 months later. Currently taking 3 Fexofenadine (180 mg) and 3 Famotidine (20 mg) daily with no alleviation of symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chronic spontaneous urticaria
- Hospital-Tage
- -
- Labordaten
- 04/25/22 - General Practitioner appointment where I had blood drawn and tests showed no irregularities.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 01.06.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 91,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
COVID-19
Cough
Fatigue
Feeling abnormal
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Started having congestion, fatigue and coughing. Took a home COVID-19 test and tested negative. The next day I was still feeling worse with a sore throat and started having back pain possibly from a pulled muscle while coughing. Took home COVID-19 tested again and it was positive. Started having a fever of 101. Called my Dr. and was prescribed PAXLOVID, started getting a bitter taste in my mouth. Began feeling better 09/06/2022. Took home COVID-19 test - negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test - negative; Home COVID-19 test - positive. Home COVID-19 test - negative.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Prediabetes
- Andere Medikamente
- Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 26.01.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 132,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Diarrhoea
Malaise
Nausea
SARS-CoV-2 test positive
Symptomtext
I received fever; nausea; diarrhea; chills; and malaise lasting 7 days. I took a prescription called PAXLOVID and I began to feel better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- I tested positive COVID 19 on 06/07/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- ARVC; Essential trimer; asthma; Skin cancer; Autism
- Andere Medikamente
- Propranolol
- Allergien
- Environmental allergy
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 28.07.2022
- Impfdatum
- 14.01.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 189,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chills
Decreased appetite
Pyrexia
Symptomtext
Appetite change, chills and fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 20.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Rash
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: the patient experienced swelling 7 to 10 days after injection. then on 7-4-22 she got a rash and then rash on mid section. Rash went away on 7-15-22. on 7/21/22 she got her second shot and has the redness at the site only.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 13.04.2022
- Beginn
- 26.06.2022
- Tage bis Beginn
- 74,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
COVID-19
Nasal congestion
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID-19 on 6/26/22. I had a really stuffy head, stuffy nose, general congestion, and an achy back. I decided to take an at-home test and it turned up positive. I was prescribed PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 test- 6/26/22- positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Atorvastatin; losartan; ezetimibe
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exploratory operation
Injection site pain
Pain in extremity
Symptomtext
I received the Modera half dose for my booster vaccine. In the afternoon and several hours later, I had pain down my right arm, down my shoulder and fingers. I did not have any fever. It was really painful for 2-3 days. Then I went back from my regular pain from 2AM to about 6AM, and it is still a continuation from my second vaccine. My doctor advised me to get this dose because if I got COVID I would die. On 01-26-2022 I saw an orthopedic doctor and had an office appointment and that I could think about getting an injection that possibly might help. On 03-16-2022, my doctor gave me a cortisone injection and at that time my doctor he still felt it was a possible serum reaction. He also stated that he could possibly do surgery and look around and that the surgery would be long recuperation. I did not have the surgery just for them to look around. The doctor recommended for me not to get the second booster. I continued on with same right shoulder pain from 2am to 6am up until I got a good amount of coffee in me to get relief.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Cortisone Injection; 03/16/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hashimoto Disease
- Andere Medikamente
- Synthroid; Vitamin D 3
- Allergien
- Penicillin; Ciproflaxin, Monohydrate tabs
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 24.06.2022
- Impfdatum
- 11.02.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 21,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Antineutrophil cytoplasmic antibody negative
Antinuclear antibody positive
Biopsy
Complement factor normal
Eczema
Full blood count normal
Henoch-Schonlein purpura
Hepatitis viral test negative
Laboratory test normal
Oedema peripheral
Pain in extremity
Petechiae
Rheumatoid factor negative
Urine analysis normal
Symptomtext
Three weeks later patient noted petechia along posterior/medial calves and scattered along lower extremities, intermittent pain and edema of lower extremities. This worsened over the next four weeks. Ultimately diagnosed with Henoch Schonlein Purpura by Rheumatology in June. Biopsy prior to that had been nonspecific and only ANA positive noted on extensive lab workup.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- 21 APR 22: ANA: SPECKLED HOMOGENOUS 1: 160 OTHER APRIL LABS: Immunoglob panel, UA , RF, CBC, Hep Panel, Complement panel, ANCA -- NEGATIVE 16 MAY: Tissue exam -- > subacute spongiotic dermatitis, negative for fungal organisms, ortho/parakeratosis, mild spongiosis, acanthosis and superficial perivascular lymphohistiocytic inflammation with minimal extravasation of red blood cells, no evidence of vasculitis is seen, non specific and clinical correlation is recommended
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- None
- Andere Medikamente
- MULTIVITAMIN (otc), SYSTANE COMPLETE EYE DROPS
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 19.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 13,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Colitis microscopic
Colonoscopy abnormal
Diarrhoea
Pathology test
Symptomtext
Starting a week or so after receiving the vaccine, I developed severe diarrhea that persisted. I called the clinic on 04/01/2022 and they advised me to go to the ER. So, I went and they referred me to a gastroenterologist. The gastroenterologist did a colonoscopy and found Microscopic Lymphocytic Colitis. They started me on a course of steroids (budesonide) and I am still on it currently. I will be having an upper GI tract endoscopy. The nurse said sometimes this is caused by viruses and sometimes bacteria, but unsure in this case.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Pathology results from the colonoscopy: Microscopic Lymphocytic Colitis.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- History of Cancer Hx of Thyroidectomy; PTSD; Hemicolectomy
- Andere Medikamente
- Sertraline; levothyroxine; trazadone; multivitamin; vitamin D3; calcium
- Allergien
- Sulfa; penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 19.01.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 122,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Malaise
SARS-CoV-2 test positive
Symptomtext
Up to date with covid vaccination yet admitted to hospital with symptomatic covid infection PCR + 5/21/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 3,0
- Labordaten
- PCR Pos for COVID 5/21/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 24.01.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 113,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Electrolyte imbalance
Hypoxia
Nausea
Pain
Renal injury
SARS-CoV-2 test positive
Vomiting
Symptomtext
Patient received moderna vaccine on 5/16/21, 6/13/21 and 1/24/22. Presented to ER on 5/17/22 and found to be COVID 19 positive. presented to the emergency department secondary to refractory vomiting. Was also positive for COVID-19. Electrolytes and kidney injury corrected over the course of his 1st 24 hours of admission with IV fluids and p.o. was advanced as nausea and vomiting had resolved. Pain issues were addressed with Tylenol and lidocaine patch. Was monitored for hypoxia and was oxygenating normally throughout his hospital stay. Daily alcohol drinker and he was monitored closely for signs of withdrawal but did not show any. Cessation of alcohol and also nicotine encouraged sun his hospital stay. By 05/18/2022 was tolerating p.o. without difficulty and as there was an absence of COVID-19 symptoms was discharged home with advisement to quarantine for 5 more days and also with discussion as to signs and symptoms that would be of more urgent concern. Discharged on 5/18/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- 2,0
- Labordaten
- 5/17/22 COVID19: positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Alcohol abuse. Chronic hyponatremia. Psoriasis. Hypertension. COPD, not supplemental oxygen dependent. Nicotine addiction. Insomnia. Anxiety. Gout.
- Andere Medikamente
- albuterol 108 (90 Base) MCG/ACT Aers Commonly known as: ProAir HFA take 2 Puffs by inhalation every 4 hours as needed for Wheezing or Cough (shortness of breath). Cimzia Prefilled 2 X 200 MG/ML Pskt Generic drug: Certolizumab Pegol 400 mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Pain in extremity
Pyrexia
Symptomtext
Fever as high as 103 for 36 hours. Right arm sore for 24 hours. Large swollen lymph node on R collarbone. Painful for 48 hours, continues to be largely swollen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Low thyroid Herpes Simplex 2
- Andere Medikamente
- Valocyclovir, Prilosec, levothyroxine, fosamax, multi vitamin, calcium, evening primrose oil,
- Allergien
- Sulfa
- Vorherige Impfungen
- Pfizer covid vaccine
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 06.04.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 41,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Head discomfort
Headache
Malaise
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
On the evening of 5-16-2022, I started having a sore throat, a headache, fatigue, dry cough, low grade fever (not above 100.0) and head congestion. I took a home Covid test on 5-17 and it was positive. I called my doctor on the same day and went to have a follow up Covid test at Hospital and it was also positive. I asked my doctor for the monoclonal infusion. I had the infusion at 10AM today. I am still not feeling well. I am reporting my breakthru case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home Covid test on 5-17 Hospital PCR test on 5-17
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Sarcoidosis, Asthma, Osteoporosis, Mood disorder,
- Andere Medikamente
- Prozac 30mg daily, Klonopin 0.5mg as needed, Singular 10mg daily, Albuterol inhaler 90mcg 2 puffs prn, Buspirone 10mg daily, Prolia injection every 6 months (administered 6 months ago), Folic acid 1mg daily, Magnesium 200mg bid
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 03.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test negative
Gastrooesophageal reflux disease
Joint swelling
Mechanical urticaria
Rash erythematous
Rash papular
Rash pruritic
Throat tightness
Urticaria
Symptomtext
11 Days After Vaccination, Patient began developing urticaria, first in the left axillary region. This spread to the rest of the body over the following couple of days. The rash was red, raised, and itchy. The patient also noted pronounced dermatographism at that time. Three days after the rash appeared, the patient reported swelling of the joints, specifically knees and fingers. Additionally around that time patient expressed a feeling of throat tightness, although retrospectively this has been identified to be more representative of acid reflux. During the first few days, the patient took OTC Benadryl. Patient presented to urgent care on February 18 and was given a cortisone injection, an epipen prescription, and advised to start taking Zyrtec OTC. Joint swelling did resolve but rash and itching persisted. On February 28, patient presented to her primary care physician, Dr, who noted the continued diffuse, intermittent, rash which was extremely responsive to contact with the skin. At this time, idiopathic urticaria was expected and the link was not yet made to the COVID vaccine. The PCP ran a blood allergy panel, suggested patient take zyrtec twice daily and add in pepcid twice daily, prescribed montelukast, and referred to an allergist. The rash responded well to the medication regimen. The blood allergen test was unremarkable. In anticipation of the skin test with the allergist, the patient was advised to stop all antihistamines for three days prior. This cessation of medication resulted in an extreme flare up of the rash, with full body itching, including the scalp, palms, and soles. These symptoms were not tolerable and the extreme irritability of the skin was not conducive to allergy skin testing, so the patient resumed zyrtec and pepcid with much relief. The allergist, Dr, immediately identified the rash as a possible reaction to the Moderna Booster, noting that he had seen a similar reaction in many patients. He agreed with the medication regimen prescribed by the PCP and predicted that the reaction would subside naturally within three months or so. He recommended follow up at that time. Fast forward three months, on May 19, the rash persists although is much more mild. If the patient misses a dose of her twice daily medication regimen, the rash flares up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- Blood allergen testing was unremarkable.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Supraventricular Tachycardia, Irritable Bowel Syndrome
- Andere Medikamente
- Norgestimate Ethinyl Estradiol, Diltiazem, Spironolactone
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 13.04.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Musculoskeletal pain
Pain in extremity
Symptomtext
Patient complained of pain in her R arm. After one week pain moved to her shoulder blades.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 25,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Exposure to SARS-CoV-2
Malaise
Oropharyngeal pain
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I just had a scratchy sore throat with a ticking kind of cough and I thought it was just allergies but a number of people at my daughter's wedding was positive and I did a home test and tested positive and called my primary care doctor and I came in the office to do a PCR test that was also positive. I had symptoms for 6 to 7 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 Test Positive PCR COVID-19 Test Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Coronary Artery Disease Hashimoto's Disease
- Andere Medikamente
- Synthroid 112mcg Est talopram 20mg Mesalamine 10mg Vesipa 10mg Estradiol 1 mg Rovastatin 20 mg Losartan 25 mg CoQ 10 10 mg Vitamin D3 3000 IU Biotin 10000mcg
- Allergien
- Formaldehyde FRT as well Latex
- Vorherige Impfungen
- COVID-19 1st Dose 3/15/21 COVID-19 2nd Dose 4/9/21 COVID-19 3rd 10/28/21. Moderna Vaccination
- Staat
- MN
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Erythema
Fatigue
Rash pruritic
Symptomtext
Widespread erythematous, pruritic rash and joint pain/fatigue developed 5 days post injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- DM type II, hyperlipidemia, arthritis, class 1 obesity
- Andere Medikamente
- Metformin, Atorvastatin
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Alopecia
Chills
Discomfort
Fatigue
Headache
Lymphadenopathy
Onychalgia
Pain
Pyrexia
Rash
Restlessness
Symptomtext
Summary: rash, hair loss (general thinning and dime-sized distinct patch lost at front crown) extreme fatigue, hair loss and fatigue lasting over 3 months; fever, chills, body aches worse than any patient had experienced in over 10 years; reaction to shot 2 triggered flare in inflammatory bowel or endometriosis pain, inflammation around IUD requiring removal, ovarian cysts and pain. Patient recorded menstrual cycle days and received booster on day 3 of menstrual cycle (based on studies showing hormonal role in vaccine seroconversion). Patient was mandated to receive booster shot or be fired from her employment (graduate student instructor) and be unable to complete her doctoral degree (registration and enrollment hold and suspension). Patient contacted primary care and OBGYN providers, COVID-19 advisory committee, and disability compliance office with concerns about side effects from second shot (previously reported). Case was escalated to the Medical Director. Dr. stated that the Office had removed the normal medical exception option for the COVID-19 vaccination and only a very narrow list of CDC reactions could quality for exemption. Due to the failure of vaccine trials to adequately represent and record side effects common in women and people with auto-immune risk, doctors initially did not believe patient. Patient suspected COVID-19 infection in March of 2020. Patient requested nucleocapsid test to confirm seropositivity, but was denied and could not self-order test at any location (patient also contacted laboratory facilities). Please see report of reaction to 2nd Pfizer dose in E report number 780379. Given the threat to patient's livelihood and education, patient received Moderna booster after medical exemption requests were denied. Patient developed a fever (normal is 97.6) that slowly rose until patient took ibuprofen at around 101. Patient developed chills, body aches, head ache, restlessness, extreme pressure and pain in fingernails (like they were going to pop off), followed by extreme fatigue for over 3 months, left armpit lymph node swelling for over 2 weeks, rash on neck and under armpit that was unusual to patient, general hair thinning and loss of dime-sized patch of hair.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- doctors did not do any tests to the booster reaction. shot 2 reaction included gastro stool and blood testing, abdominal and pelvic CT scan with contrast, multiple transvaginal ultrasounds. no cause of extreme pain could be found other than ovarian cyst and fluid in pelvic culdesac
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Pfizer, shot 2, ep7534 on 3/21/21; Patient has never reacted to any previous vaccination beyond a mild sore arm and patient has
- Staat
- MI
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Pain
Pain in extremity
Symptomtext
Moderna vaccine expiration date 4/24/2022. Date administered 4/25/2022 was 1 day past expiration date. Arm sore and achy. No other symptoms noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 11.03.2022
- Beginn
- 10.04.2022
- Tage bis Beginn
- 30,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ear pain
Headache
Oropharyngeal pain
Paranasal sinus discomfort
Sinus congestion
Sinusitis
Symptomtext
Sinus congestion, sinus pressure, headache, earache, throat pain Diagnosed as a sinus infection. Antibiotics were ordered and are currently being taken as directed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Severe allergies, chronic sinus infections
- Andere Medikamente
- Enalapril, Allegra
- Allergien
- Benadryl, Singulair, Penicillin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Injection site pain
Pain
Symptomtext
A bad headache, site of injection soreness, overall tiredness and body aches . Took three ibuprofen went to bed, feel better on morning of April 2nd.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Rheumatoid Arthritis
- Andere Medikamente
- Premarin, Methotrexate, Metoprolol, Levothyroxine, Minocycline, multi vitamin, bone health caltrate, ibuprofen, famatidine, Pantoprazole, Loratadine, montelukast
- Allergien
- Sulfasalazine,
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- 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: nein
Dizziness
Headache
Injection site pain
Nausea
Pain
Pyrexia
Tinnitus
Vomiting
Symptomtext
Both vaccines once given I had side effects within 2-3 hours. Listed below: High fever (101-102 F) 2-3 days long Full body aches Nausea Headache Severely sore arm pain at location of shot Vomiting (first day/night) Ringing in ears Light headed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 20.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray normal
Chest discomfort
Fatigue
Influenza virus test negative
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test negative
Symptomtext
severe respiratory congestion, tightness of chest, fatigue, body aches, fever lasting up to 9 days at this point.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Influenza test negative, Covid-19 test negative, chest x-ray no acute cardiopulmonary.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- Rosuvastatin, Ezetimibe, Amlodipine, Vascepa
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 25.03.2022
- Beginn
- 26.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Injection site erythema
Injection site induration
Injection site pain
Injection site pruritus
Injection site swelling
Injection site vesicles
Malaise
Pyrexia
Symptomtext
Patient received her 2nd dose of the Moderna primary series on March 25, 2022 at approximately 1:30pm. On March 26, the patient noted feeling "ill" and with a severe constant headache with fevers. She then noted a raised, red area surrounding the injection site. She reports the redness and swelling as progressively gotten worse in terms of area increasing as well as firmness of the area and in swelling and redness. Itching and "the sensation of blisters after a burn" were also described by the patient referring to the injection site location. The patient reports taking mild analgesics and Benadryl with no relief. The patient reported her reaction to local health department staff at approximately 10:30 on March 28, after 48 hours of no relief or improvements.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Wellbutrin 300 mg Vitamin C Excedrin Migraine, daily Collagen Supplement
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 24.03.2022
- Impfdatum
- 04.03.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 296,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Fatigue
Pain
Pyrexia
Symptomtext
fever, cough, aches - lasting 2 days fatigue - lasting 3 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Losartan, Rosuvastatin, Vitamin D3, Zolpidem
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Disturbance in attention
Dizziness
Feeling abnormal
Movement disorder
Thinking abnormal
Vertigo
Symptomtext
Brain Fog, concentration problem with scattered thinking and anxiousness---still resolving. [Vertigo, dizziness and movement issues]- this section lasting for 1 day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- rheumatoid arthritis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 14.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash maculo-papular
Symptomtext
Erythematous maculopapular rash on bilateral hands and some in the areas of his popliteal fossa, some on his feet as well
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none.
- Vorgeschichte
- anxiety about health
- Andere Medikamente
- none
- Allergien
- none, does note some seasonal allergies
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Limb discomfort
Poor quality product administered
Product storage error
Vaccination site pain
Symptomtext
one vial who was been administered after 30 days on fridge; Arm Discomfort; Fatigued; Very sore arm at the injection site; Patient received vaccine 4 days after use by date; This spontaneous case was reported by a pharmacist and describes the occurrence of LIMB DISCOMFORT (Arm Discomfort), FATIGUE (Fatigued), VACCINATION SITE PAIN (Very sore arm at the injection site), POOR QUALITY PRODUCT ADMINISTERED (Patient received vaccine 4 days after use by date) and PRODUCT STORAGE ERROR (one vial who was been administered after 30 days on fridge) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. Co-suspect product included non-company product PNEUMOCOCCAL VACCINE POLYSACCH 23V (PNEUMOVAX 23) for an unknown indication. Concurrent medical conditions included Blood pressure abnormal and Penicillin allergy. Concomitant products included AMLODIPINE for Blood pressure abnormal. On 10-Feb-2022, the patient received first dose of PNEUMOCOCCAL VACCINE POLYSACCH 23V (PNEUMOVAX 23) (Intramuscular) 1 dosage form. On 10-Feb-2022 at 12:18 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 10-Feb-2022, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (Patient received vaccine 4 days after use by date). On 11-Feb-2022, the patient experienced LIMB DISCOMFORT (Arm Discomfort), FATIGUE (Fatigued) and VACCINATION SITE PAIN (Very sore arm at the injection site). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (one vial who was been administered after 30 days on fridge). On 11-Feb-2022, FATIGUE (Fatigued) had resolved. On 12-Feb-2022, LIMB DISCOMFORT (Arm Discomfort) and VACCINATION SITE PAIN (Very sore arm at the injection site) had resolved. At the time of the report, POOR QUALITY PRODUCT ADMINISTERED (Patient received vaccine 4 days after use by date) and PRODUCT STORAGE ERROR (one vial who was been administered after 30 days on fridge) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered FATIGUE (Fatigued) and VACCINATION SITE PAIN (Very sore arm at the injection site) to be related. No further causality assessments were provided for LIMB DISCOMFORT (Arm Discomfort), POOR QUALITY PRODUCT ADMINISTERED (Patient received vaccine 4 days after use by date) and PRODUCT STORAGE ERROR (one vial who was been administered after 30 days on fridge). Treatment information was not provided by the reporter. This case was linked to MOD-2022-500102 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood pressure abnormal; Penicillin allergy
- Vorgeschichte
- -
- Andere Medikamente
- AMLODIPINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 24.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site mass
Injection site pruritus
Symptomtext
Woke up the next morning after Moderna booster vaccine and noticed left arm had a little red lump where shot was given and it was itchy. The lump was gone yesterday ( 3/1/2022) when she went to see the doctor, but the redness was getting bigger. Doctor measured redness to be 10 cm long x 6 cm wide. Doctor prescribed Cetirizine. Today reports that redness has decreased since yesterday. "not all the way gone, still a little bit there."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypothyroid
- Andere Medikamente
- Levothyroxine, trazodone, desvenlafaxine, Vitamin C, Vitamin D3, Zinc, Vitamin B12, Calcium, OTC allergy pill, baby aspirin
- Allergien
- Wellbutrin
- Vorherige Impfungen
- Moderna vaccine 1st (2/19/2021) injection seen by MD and DX with Cellulitis. MD prescribed an antibiotic with this dose and Cell
- Staat
- PA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 25.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Urticaria
Symptomtext
Hives and dermatographism all over body. Coming in increments throughout the day. Occurring daily. Patches of hives lasting 30 mins then moving to other areas of body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Junel Lexapro
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Fatigue
Headache
Injection site pain
Nausea
Pain
Pyrexia
Symptomtext
Fever, chills, body aches, joint pain mostly in hips, fatigue, headaches, nausea and pain at injection site started around 6 pm 2/28 and still ongoing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Headache
Pain in extremity
SARS-CoV-2 test
Vaccination site pain
Symptomtext
Pain that expands from thighs to knees/Sored thighs; Really sored right arm; Sored knees/Sored thighs; Headache; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Pain that expands from thighs to knees/Sored thighs), VACCINATION SITE PAIN (Really sored right arm), ARTHRALGIA (Sored knees/Sored thighs) and HEADACHE (Headache) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 083J21A and 022J21A) for COVID-19 vaccination. The patient's past medical history included COVID-19 on 07-Jan-2022. Concurrent medical conditions included Blood pressure high. On 26-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Feb-2022, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 23-Feb-2022, the patient experienced PAIN IN EXTREMITY (Pain that expands from thighs to knees/Sored thighs), VACCINATION SITE PAIN (Really sored right arm), ARTHRALGIA (Sored knees/Sored thighs) and HEADACHE (Headache). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) for Pain, at an unspecified dose and frequency. At the time of the report, PAIN IN EXTREMITY (Pain that expands from thighs to knees/Sored thighs), VACCINATION SITE PAIN (Really sored right arm), ARTHRALGIA (Sored knees/Sored thighs) and HEADACHE (Headache) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 07-Jan-2022, SARS-CoV-2 test: positive (Positive) Positive. The patient was taking medication for her high blood pressure as concomitant medication. The lot number for second dose was also reported as 022J21A. It was mentioned that pain symptoms got better on 23 FEB 2022 when she took painkillers. The headache came back on the day of reporting. And she was feeling more pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220107; Test Name: COVID-19 test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Blood pressure high
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 25.02.2022
- 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: nein
Chills
Headache
Pain
Symptomtext
Narrative: 2/4/22: moderna 3rd dose covid booster. Next day Saturday started feeling a headache/chill moving up his neck into the back of his head. Also had chills, woke up with a headache at the base of his skull, acetaminophen no help, a little better with a hot shower but headache returned, though less intense. Woke up Monday again with pain at base of skull and headache, decreased to a dull pain with hot shower. No headache after Wednesday. Headache did NOT wake him from sleep, he woke up as normally then felt a headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nausea
Vomiting
Symptomtext
Nausea and vomiting within about 15 minutes of administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Bipolar disorder PTSD
- Andere Medikamente
- latuda prazosin lamictal depakote chlorpromazine conidine
- Allergien
- no know allergies
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 22.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Erythema
Impaired work ability
Rash erythematous
Swelling
Swelling face
Throat tightness
Symptomtext
Day 2 after vaccine...102 temp for 1 week. Day 3 after vaccine...red sunburn like rash on left side of face...Day 5 after vaccine...red sunburn like rash spread to whole face...accompanied with major swelling of face and nose. ...throat feeling slightly closed. Went to Urgent care and they prescribed 14 day dosage of prednisone 10 mg. Did follow up appointments with my dermatologist and my allergist. It is now 1 month later and I am still experiencing slight redness and swelling of face....missed 2 weeks of work.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure anxiety
- Andere Medikamente
- metropolol fluoxetine lisinopril
- Allergien
- lactose intolerant gluten sensitive latex
- Vorherige Impfungen
- hives and welts all over body/Moderna dose #1/1-2021/age 59
- Staat
- MO
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 12.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Pruritus
Rash
Symptomtext
Site: Redness at Injection Site-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Tunnel vision
Symptomtext
Patient experienced dizziness and has continued having dizziness including tunnel vision. This is occurring randomly. We recommend that he sees his physician to evaluate and rule out any blood pressure issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None at this time.
- Aktuelle Erkrankungen
- non
- Vorgeschichte
- none
- Andere Medikamente
- Montelukast, Omeprazole
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Blood magnesium
Chest X-ray
Chest discomfort
Diarrhoea
Dizziness
Electrocardiogram
Full blood count
Metabolic function test
Pain
Troponin
Vomiting
Symptomtext
Chest tightness, vomiting, diarrhea, body aches, dizziness, anxiety
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 02/17/22: EKG, troponin, CBC, cmp, magnesium, chest X-ray
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Omeprazole, aspirin, magnesium, krill oil, vitamin c, vitamin d, b12
- Allergien
- Azithromycim, kiwi, pomegranate, raspberries
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Rash
Symptomtext
About two weeks after the booster rash under both breast and neck treating with over the counter cream but it does not work have to schedule a doctor appointment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- 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
Arthralgia
Injection site pain
Pain
Symptomtext
At around 10pmdate of administration, patient reported starting of symptoms ( body aches, no fever, joint pain, injection site pain)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- none know
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pruritus
Rash
Urticaria
Symptomtext
Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash Generalized-Severe, Systemic: ENTIRE BODY ITCHED AND HAD HIVES-Severe, Additional Details: PATIENT CAME TO PHARMACY ABOUT 15 MINUTES AFTER INJECTION COMPLAINING OF ENTIRE BODY ITCHING. I GAVE 50MG OF BENADRYL AND SHE SAT FOR ABOUT ANOTHER 15 MINUTES WITH NO RELIEF. I TALKED WITH CLINIC NURSE SHE CAME OVER AND LOOKED AT PATEINT AND DETERMINED WE SHOULD CALL AN AMBULANCE. THEY LOOKED HER OVER IN THE STORE AND SHE WALKED OUT THE DOOR WITH THEM. DON'T KNOW IF SHE WENT WITH THEM OR NOT. I TRIED TO CALL PATIENT TO GET UPDATE BUT NO ANSWER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 30.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pruritus
Injection site swelling
Pruritus
Rash
Symptomtext
Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Allergic: Itch Generalized-Medium, Systemic: Allergic: Rash Generalized-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bone pain
Chills
Diarrhoea
Fatigue
Headache
Insomnia
Nausea
Pyrexia
Symptomtext
Fever, chills, nausea, diarrhea, headache, bone pain, sleeplessness and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bone pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Levaquin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Erythema
Pruritus
Skin test
Swelling
Urticaria
Symptomtext
itchy; red; swelling/raised; Since receiving the booster dose of the vaccine, this has been worse/Hives; This spontaneous case was reported by an other health care professional and describes the occurrence of URTICARIA (Since receiving the booster dose of the vaccine, this has been worse/Hives), PRURITUS (itchy), ERYTHEMA (red) and SWELLING (swelling/raised) in a 32-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. In January 2022, the patient experienced URTICARIA (Since receiving the booster dose of the vaccine, this has been worse/Hives). On an unknown date, the patient experienced PRURITUS (itchy), ERYTHEMA (red) and SWELLING (swelling/raised). The patient was treated with LEVOCETIRIZINE DIHYDROCHLORIDE (XYZAL) at an unspecified dose and frequency; DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at an unspecified dose and frequency; PREDNISONE at an unspecified dose and frequency and FEXOFENADINE HYDROCHLORIDE (ALLEGRA [FEXOFENADINE HYDROCHLORIDE]) at an unspecified dose and frequency. At the time of the report, URTICARIA (Since receiving the booster dose of the vaccine, this has been worse/Hives), PRURITUS (itchy), ERYTHEMA (red) and SWELLING (swelling/raised) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood test: results not provided results not provided. On an unknown date, Skin test: results not provided results not provided. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient has no history of prior allergies. The patient reported that after receiving the first 2 shots started to develop hives that have continued up until today (07-Feb-2022). In addition those occurred all over body, itchy, red, raised, and occur with swelling. The primary care doctor, and an allergist who conducted blood, and skin testing for allergies. Since receiving the booster dose of the vaccine, that had been worse and occurring every day despite the OTC medications which helped. The patient went to the emergency room for her symptoms on Saturday where they gave prednisone. The patient had an upcoming appointment with an allergist on 07-MAR-2022. No concomitant medications were reported. This case was linked to MOD-2022-474585 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood test; Result Unstructured Data: results not provided; Test Name: Skin test; Result Unstructured Data: results not provided.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 29.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Bedridden
Dizziness
Eructation
Gait disturbance
Headache
Nausea
Oropharyngeal discomfort
Oropharyngeal pain
SARS-CoV-2 test
Vaccination complication
Vaccination site pain
Symptomtext
Had reactions; Sick to her stomach; Felt like she was going to get a sore throat; It felt like something was stuck in her throat; She could barely walk back & forth to the bathroom; Had dizzy spells to the point where she could barely walk back & forth to the bathroom; Was nauseated; Head hurt; Left arm hurt really bad & it felt beat to a pulp; Had excessive air coming up & was burping; Was in bed for 4 days; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (Had reactions), BEDRIDDEN (Was in bed for 4 days), ABDOMINAL DISCOMFORT (Sick to her stomach), ERUCTATION (Had excessive air coming up & was burping) and OROPHARYNGEAL PAIN (Felt like she was going to get a sore throat) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Environmental allergy and Allergy to antibiotic (Allergic to antibiotics). On 29-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VACCINATION COMPLICATION (Had reactions), BEDRIDDEN (Was in bed for 4 days), ABDOMINAL DISCOMFORT (Sick to her stomach), ERUCTATION (Had excessive air coming up & was burping), OROPHARYNGEAL PAIN (Felt like she was going to get a sore throat), OROPHARYNGEAL DISCOMFORT (It felt like something was stuck in her throat), GAIT DISTURBANCE (She could barely walk back & forth to the bathroom), DIZZINESS (Had dizzy spells to the point where she could barely walk back & forth to the bathroom), VACCINATION SITE PAIN (Left arm hurt really bad & it felt beat to a pulp), NAUSEA (Was nauseated) and HEADACHE (Head hurt). At the time of the report, VACCINATION COMPLICATION (Had reactions), ABDOMINAL DISCOMFORT (Sick to her stomach), OROPHARYNGEAL PAIN (Felt like she was going to get a sore throat), OROPHARYNGEAL DISCOMFORT (It felt like something was stuck in her throat), GAIT DISTURBANCE (She could barely walk back & forth to the bathroom), DIZZINESS (Had dizzy spells to the point where she could barely walk back & forth to the bathroom), NAUSEA (Was nauseated) and HEADACHE (Head hurt) outcome was unknown and BEDRIDDEN (Was in bed for 4 days), ERUCTATION (Had excessive air coming up & was burping) and VACCINATION SITE PAIN (Left arm hurt really bad & it felt beat to a pulp) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: positive (Positive) Before getting the dose the patient had tested positive for Covid.. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were provided. No treatment medications were reported. This case was linked to MOD-2022-474388 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid test; Test Result: Positive ; Result Unstructured Data: Before getting the dose the patient had tested positive for Covid.
- Aktuelle Erkrankungen
- Allergy to antibiotic (Allergic to antibiotics); Environmental allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- 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: ja
Erholt: nein
Computerised tomogram
Dizziness
Electrocardiogram
Laboratory test
Urine analysis
Vertigo
X-ray
Symptomtext
After receiving the booster I started feeling dizziness and light headed and it is still going on. My doctor said that it is vertigo. It's not as bad as it was when I first got the vaccine. I talked to my doctor virtual and she told me that she didn't want to prescribe me anything and to go to the ER. They ran a round of test on me. ER doctor didn't prescribe me anything. I went to my PCP and she prescribe me, Meclizine 25 mg.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- CAT SCAN, EKG, X-RAY'S AND LAB AND UNRINE. All test was negative.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetic, Cholesterol and Thyroids.
- Andere Medikamente
- Metformin 500 mgs, Levothyroxine 112mcgs, Atorvastatin 20 mgs and Muti- Vitamin once daily.
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Symptomtext
Lymph nodes under right arm became slightly enlarged and tender starting the afternoon following the injection. On the second day after the shot, the lymph nodes just above/behind the right clavicle became slightly enlarged and tender as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ADHD, Tachycardia
- Andere Medikamente
- Adderall, Lopressor, Xyzal, Alpha Lipoic Acid, Benadryl
- Allergien
- Eggs, Wheat, Bupropion, Shellfish
- Vorherige Impfungen
- Both previous Moderna Covid-19 vaccine shots. The first one was administered on July 12, 2021 in the upper right arm.There was m
- Staat
- IL
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Angiogram pulmonary normal
COVID-19
Chest X-ray normal
Fall
Femur fracture
Fibrin D dimer increased
Pain in extremity
SARS-CoV-2 test positive
Ultrasound Doppler normal
Symptomtext
REceived moderna vaccine on 3/10/21, 4/7/21, and 1/27/22. Found to be COVID positive on 1/29/22. Presented to ER on 1/29/22. was admitted on 1/29/2022 presented with episode of fall without hitting her head/loss of consciousness. Presented with right leg pain. Imaging-right femur fracture. Orthopedic consulted. S/p right femur retrograde nail on 01/29/22 Screening COVID test positive, was vaccinated. Clinically asymptomatic. Elevated D-dimer-CT angio negative for PE, ultrasound leg negative for DVT. On room air, Waiting rehab placement when off covid isolation PT evaluation done. Patient is medically stable to be discharge Rehab. Discharged on 2/8/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- 10,0
- Labordaten
- 1/29/22 COVID19: positive 1/29/22 chest xray: Portable chest fails to demonstrate an acute abnormality.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ? Asthma ? Depression ? Hypoglycemia ? Iron deficiency ? Pernicious anemia
- Andere Medikamente
- PROzac 20 MG Caps Generic drug: FLUoxetine 60 mg, Oral, DAILY Symbicort 160-4.5 MCG/ACT Aero Generic drug: budesonide-formoterol fumarate 2 Puffs, Inhalation, 2 TIMES DAIL
- Allergien
- novocain
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Computerised tomogram
Rash
Urticaria
Eye swelling
Mouth swelling
Pruritus
Swelling face
Swollen tongue
Symptomtext
Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Allergic: Itch Generalized-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash Generalized-Severe, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cellulitis
Chills
Lymphadenopathy
Pain
Pyrexia
Symptomtext
Fever fever, chills, achy, cellulitis, lymph node swelling Narrative: WENT TO URGENT CARE AND PRESCRIBED KEFLEX/STEROIDS X 7 DAYS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Symptomtext
Severe itchiness and rashes all over body and face. Tiny bumps at the site of rashes. The symptoms come and go randomly throughout the day/night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 08.06.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 62,0
- Dosis
- UNK
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Culture stool negative
Extra dose administered
Metabolic function test
Parasite stool test negative
Red blood cell sedimentation rate normal
Stress
Urticaria
Symptomtext
I am a healthy female, Never had allergies once I took the Moderna vaccine hives started coming I?ve been to my pcp, Allergist, Dermatologist and nothing. My labs are completely good. My allergist recommended xzyal once a day I?ve been taking the hives would constantly go away and come back but the xzyal provided comfort. I took the Moderna Booster and the hives came back flaring up worst than before and this time nothing helps. I need help I cannot live like this. The feeling is stressful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- Ova parasite stool test, culture stool, esr, comp. My results were good
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Non. I am a healthy female, Never had allergies once I took the vaccine hives started coming I've been to my pcp, Allergist, Dermatologist and nothing. My labs are completely good. My allergist recommended xzyal once a day I?ve been taking the hives would constantly go away and come back but the xzyal provided comfort. I took the Moderna Booster and the hives came back flaring up worst than before and this time nothing helps. I need help I cannot live like this. The feeling is stressful.
- Andere Medikamente
- Xyzal, Allegra, Benadryl
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 17.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pruritus
Urticaria
Symptomtext
Hives all over my body. It started a week after I got the shot. I have no allergies of any types. I had to go to the ER, and it has been happening for a week and a half with no signs of getting better. The breakouts happen randomly throughout the day, and it itches a lot. Allergy pills like Allegra and Montelukast are not helping much.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- A visit to the ER on 1/26/22.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- GERD, hiatal hernia.
- Andere Medikamente
- Multivitamin, vitamin B12, Biotin, Omeprazole, Vyfemla (birth control).
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 22.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Rash pruritic
Symptomtext
I developed an itchy rash about one week after I got my 3rd dose of modern (the booster). Rash started on my chest then went to my scalp/neck and is now mostly on my neck, arms, and legs. There is no distinct pattern to this rash, just red marks in the skin if rubbed against and/or itched. Allergy medicine such as Benadryl does help to make it go away. Heat makes it worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash pruritic
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Birth Control
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Dizziness
Dizziness postural
Nausea
Vertigo
Vomiting
Symptomtext
head spinning upon awaking at 4 AM; dizzy upon standing to urinate nauseous while evacuating & drinking fluid dizziness & weakness lasted 12 hours vomited after drinking a beverage with electrolytes able to eat a few bites of toast finally able to awaken and no dizziness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dermatologic examination
Rash
Urticaria
Symptomtext
On the 24th of January I began experiencing a full body rash, and breaking out in hives anywhere something rubbed against my skin. Affected areas include scalp, face, armpits, inner thighs, both sides of torso, feet, legs, and elbows. It is now February 5th and the symptoms have not subsided. I have gone to urgent care, the emergency room, and have seen a dermatologist. I was prescribed Predizone; however, the rash is still there.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Gone to urgent care, emergency room and dermatologist all of which do not know what is causing the reaction.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Myalgia
Pyrexia
Symptomtext
Myalgia & Fever Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast mass
Breast swelling
Lymphadenopathy
Rash
Rash erythematous
Symptomtext
Swollen lymph notes in both armpits, Swollen left breast with red rash and lump
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- Levothyroxine tables, estradiol transdermal patch
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 20.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site discolouration
Injection site swelling
Injection site warmth
Symptomtext
Her mom stated that the site of injection was warm, not bumpy and the size of a baseball. There are no nodules and the center is blotchy and flesh colored. No other symptoms reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discolouration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Pain in extremity
Symptomtext
Pain left arm for 36 hours. Headache for 36 hours. Very tired for 48 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- 81 mg aspirin, vitamin pill, vitamin c
- Allergien
- None
- Vorherige Impfungen
- Covid 19 on 1/29/2021
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Hypersomnia
Nausea
Pain
Pain in extremity
Pyrexia
SARS-CoV-2 test negative
Symptomtext
Beginning at about 12am I had light soreness in my arm after my 3rd dose. When I woke up on the 26th at 10am I had fever, chills, sore everywhere, nausea, and headache. I called doctor Wednesday morning and they told me to take OTC Acetaminophen, I slept for over 16hrs. I took my temperature 100.9 late Wednesday evening. I was not allowed to return to school or work until my temperature was under 100. 12 hours into Thursday the symptoms subsided and I was fine and soreness in arm subsided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Covid-19 rapid test at my place of work was negative on Wednesday.
- Aktuelle Erkrankungen
- None. Ablation on December 2nd and kicked in around Jan 5th
- Vorgeschichte
- Bulging disk, ADHD, Depression, Anxiety
- Andere Medikamente
- 2 500mg Etodolac Daily, 10mg cyclobenzaprine, 50mg Pregabalin 3 XS daily, Birth control, 10mg Adderall
- Allergien
- Medical grade adhesive tape
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site swelling
Pain
Pyrexia
Vomiting
Symptomtext
Patient received her Moderna booster on 02/01/22. Her husband called this morning 02/02/22 to report that patient was experiencing low grade fever, body aches, mild swelling/soreness at the injection site, and one episode of vomiting. She was concerned because she only had a sore arm with the first and second doses of Moderna. After discussing her symptoms in detail, she thinks the vomiting episode was because she choked on her coffee and she is reporting no nausea. She is not reporting any itching, rash, or any sign of allergic reaction. I told her to take Tylenol and drink plenty of fluids and rest for 24 hours. I also recommended that if she does not feel any better in the next 24 hours to reach out to her physician to make sure they don't want to see her. I told her to reach out if there are any new symptoms or questions and I also told her I was going to report her symptoms to VAERS and encouraged her to use the VSAFE platform to report directly to CDC.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Fatigue
Headache
Lymphadenopathy
Myalgia
Nervous system disorder
Pyrexia
Symptomtext
Swollen left armpit for 2 weeks, Muscle pain, Chills, Fever, Headache, Tiredness, and Ongoing Nervous system issues with random sharp pain in joins
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- One A Day vitamins
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Pain
Visual impairment
Symptomtext
Systemic: Abdominal Pain-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Visual Changes/Disturbances-Medium.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 29.01.2022
- Beginn
- 30.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Product administered to patient of inappropriate age
Symptomtext
Moderna 1st shot was given to 12 years old kid at the health clinic. Patient experience some pain but no fever as off 01/30/2022. Advil 250mg was given to stop the pain for 1 dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site swelling
Rash erythematous
Skin warm
Symptomtext
Symptoms presented next day with large red rash and swelling at injection site and covering side of upper arm down to the top of elbow area and hot to the touch. Patient presented at urgent care and cephalexin was prescribed and circle was drawn around the rash to see if it would get worse. Rash seems to be getting better at time of reporting .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- psoriasis
- Andere Medikamente
- Humira
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
C-reactive protein increased
Pain in extremity
Peripheral swelling
Ultrasound scan normal
Symptomtext
Patient developed right arm pain and swelling. Started about 24 hours after vaccine. Recieved medrol dose pack, antihistamine. Pain and swelling improving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- US for DVT negative. Elevated CRP.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 23.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Headache
Influenza virus test negative
Nausea
Oropharyngeal pain
Pain
Paranasal sinus discomfort
SARS-CoV-2 test negative
Symptomtext
On Monday 01/24/2022, I woke with backache, headache and nauseas, It went away by the afternoon. The next morning the body ache started getting worse and got a low grade fever 99.5 and that continue until Wednesday as well. 12/26/2022 Sinus pressure and headaches started, as of yesterday and today I have a sore throat. I went to the clinic on 01/26/2022 to get tested for Flu and covid they both came back negative. I have been taking Dayquil and ibuprofen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Flu and COVID, results were back negative
- Aktuelle Erkrankungen
- Tested Positive for Covid-19 on 12/24/2021
- Vorgeschichte
- N/A
- Andere Medikamente
- Singular 10MG 1 daily, Birth control 1 a day.
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Erythema
Eye swelling
Feeling hot
Pruritus
Rash
Symptomtext
On the morning of Jan 26, 2022, my entire body was covered in rashes. It was very itchy. I took Claritin thinking it was just allergies. During the day, the rash got bigger. I felt it was creeping over my face. My ears felt hot and my eyes felt swollen. I went to urgent care, where I was prescribed 3 tabs of prednisone 20mg for 5 days. It was also advised to take Benadryl before I slept that night. As of date, I am on my third day of prednisone. There are a few rashes left, especially on my lower body. But, the swelling and redness are gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin C, B-complex, Vitamin D, Biotin
- Allergien
- Shellfish
- Vorherige Impfungen
- Mild fever and chills on the first night of the vaccine.
- Staat
- NV
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Abdominal pain
Asthenia
Cold sweat
Decreased appetite
Frequent bowel movements
Impaired driving ability
Injection site pain
Nausea
Somnolence
Symptomtext
First day sore arm at injection site. Less painful than previous doses. Felt fine for 2 days with little nausea, decided to go to work overnight shift. During lunch; decreased appetite and bloating, Nausea increased to moderate and severe abdominal pain. Hot and cold sweats but no fever, multiple stools. Debated leaving work early. Managed to make it home after shift, took Pepto Bismol and gas x and slept more than usual. Decreased appetite until Day 5 returned to work and felt okay but a little weak. Day 6 woke up in the middle of sleep and had severe abdominal pain and nausea. Tried to take Pepto Bismol and gas x with no relief. Debated going to the Emergency room. Could not go to work. Hot shower helped relieve the pain to go back to sleep. Unable to drink water due to nausea. Slept for 14 hours woke up feeling queasy, able to eat a little rice and chicken broth.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- elevated cholesterol
- Vorgeschichte
- Chronic Lower back pain
- Andere Medikamente
- Vitamin D3, Calcium, Folic Acid
- Allergien
- Eggs
- Vorherige Impfungen
- Both 1st and 2nd dose of Moderna in Jan/Feb 2021 sore arm, Fever>101, unable to work, cold sweat, headache, fatigue, body aches.
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site rash
Injection site reaction
Injection site swelling
Injection site vesicles
Skin weeping
Symptomtext
I experienced a raw, oozing, very painful blister about the size of a pinto bean located approximately 1 inch from the outside radius of my injection site. Regarding the injection site itself, it was about the size of a plum and became raised/bumpy with what appeared to be extremely tiny papules.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- I have a history of childhood auto-immune disease (juvenile rheumatoid arthritis) but I have not had any active arthritis for over 18 years now. I have been in full remission since my early 20's and I'm now 40 years old.
- Andere Medikamente
- None.
- Allergien
- Amoxicillin
- Vorherige Impfungen
- I experienced an allergic reaction (itching, redness, and swelling) on my right eyelid 1 week after my second dose of Moderna. I
- Staat
- MI
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Back pain
Diarrhoea
Fatigue
Headache
Symptomtext
When I got home I had a severe headache and my back was hurting. I took pain meds but the pain continued for about 3 days off and on. That evening I also started having abdominal pain and diarrhea followed by fatigue. When I got home I had a severe headache and my back was hurting. I took pain meds but the pain continued for about 3 days off and on. That evening I also started having abdominal pain and diarrhea followed by fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Feeling cold
Headache
Nausea
Pyrexia
Symptomtext
Pt woke up next day "freezing to death", nausea, headache in right temple, fever of 102F.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gait disturbance
Rash
Rash erythematous
Rash pruritic
Symptomtext
Erythematous, very itchy rash that started on right arm and spread to distal extremities. Painful palms and soles that do not itch. Hurts to walk.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- no testing done other than exam. 50-60% improved on day after treatment of oral cetirizine and topical moderate potency steroid started.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Restless legs syndrome
Symptomtext
Restless leg sensations in both legs; aching, and urge to move. Onset 4:30 pm on day 8 after booster with Moderna Covid-19 vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Strep throat.
- Vorgeschichte
- Paroxysmal tachycardia.
- Andere Medikamente
- Prenatal vitamins. Propranolol as needed (not taken within 1 month prior to vaccination or adverse event).
- Allergien
- Amoxicillin rash.
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis reactive
Bone pain
Joint swelling
Symptomtext
This same reaction has occurred before: after receiving covid vaccine, approx 12 hours later, had onset of deep bone aches, but also got a swollen, painful 4th MCP joint of left hand. This reactive arthritis lasts weeks afterwards and comes and goes. It hadn't recurred for awhile before she got her booster dose on 1-13-22 which triggered it again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none noted
- Vorgeschichte
- type 2 diabetes, hypertension, history of colon cancer, history of ulcerative colitis (history of total colectomy)
- Andere Medikamente
- Novolog, Lantus, lisinopril, omeprazole, vit D (ergo)
- Allergien
- gabapentin, hydrocodone, morphine, latex/adhesive, pertussis vaccine
- Vorherige Impfungen
- Moderna covid vaccine, 4-23-21, 5-21-21 (caused same joint swelling) Pertussis vaccine (unsure of age of reaction, caused large
- Staat
- MO
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Urticaria
Symptomtext
Hives across the chest, arm, and back. Patient had itching and redness as well. Patient took Zyrtec and was feeling better by end of day. Patient said she may follow up with an urgent care visit tomorrow if still having symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- microgestin 1/20
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Haematuria
Pain in extremity
Symptomtext
Sudden onset after usual slight arm pain, feeling tired, of intermittent gross hematuria which continued for 48 hours. No treatment. May or may not be causally related. Have had similar events 5 years and 2 years ago. Work up showed only varicosities peri prostatic. No infections at the time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- rTreated hypertension, post CABAG, Aortic valve replacement
- Andere Medikamente
- Rosuvastin, Ezetimide, Ramipril, Baby Aspirin, chlorthalidone,
- Allergien
- non
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Lymphadenopathy
Symptomtext
Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Lymph Node Swelling-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 13.10.2021
- Beginn
- 13.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pruritus
Symptomtext
Site: Itching at Injection Site-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthropod bite
Back pain
Erythema
Lymphadenopathy
Pain
Pruritus
Swelling
Urticaria
Symptomtext
Two hours after receiving booster shot had small itchy raised bump similar to mosquito bite. 12 hours later welt had grown to raised swollen red area which was sore, and had very large swollen lymph note in armpit area of right arm (shot was injected in right arm) and swollen lymph note in neck in right side. Back is very sore, and right arm is very painful to move still 24 hours later after injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Tested positive for COVID on 1-12-2022. Illness began 1-11-22. Completed 10 day isolation, received booster shot on 10th day following positive test.
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Synthroid 25 mg
- Allergien
- Allergy to pineapple, Wellbutrin, Vicks chest rub
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- 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: ja
Pruritus
Symptomtext
0908 vaccine given, 0925 patient says itchy on face, back ,neck, chest, 0930 Benadryl 50mg Im L arm given. 0950 patient states feels better, no other symptoms. 1020 symptoms gone
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- migraines, arthritis, fibromyalgia
- Andere Medikamente
- gabapentin 100g, multivitamins, Motrin, Aleve
- Allergien
- iodine, shellfish, dander, polyethylene glycol
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 23.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Injection site erythema
Symptomtext
Site: Redness at Injection Site-Mild, Additional Details: 911 took her to hospital. No evidence of allergy reaction, and most likely anxiety issue. She did indicate that she has anxiety in general.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Dizziness
Dysgeusia
Feeling abnormal
Headache
Nausea
Vaccination site pain
Vaccination site swelling
Symptomtext
injection site tender; injection site swollen; joint achiness; dull headache; a little bit of chills; a little bit of nausea; feels so crappy; funny metallic taste in her mouth; little dizzy; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (feels so crappy), DYSGEUSIA (funny metallic taste in her mouth), DIZZINESS (little dizzy), VACCINATION SITE PAIN (injection site tender) and VACCINATION SITE SWELLING (injection site swollen) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 19-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Jan-2022, the patient experienced DIZZINESS (little dizzy). On 20-Jan-2022, the patient experienced FEELING ABNORMAL (feels so crappy), DYSGEUSIA (funny metallic taste in her mouth), VACCINATION SITE PAIN (injection site tender), VACCINATION SITE SWELLING (injection site swollen), ARTHRALGIA (joint achiness), HEADACHE (dull headache), CHILLS (a little bit of chills) and NAUSEA (a little bit of nausea). At the time of the report, FEELING ABNORMAL (feels so crappy), DYSGEUSIA (funny metallic taste in her mouth), DIZZINESS (little dizzy), VACCINATION SITE PAIN (injection site tender), VACCINATION SITE SWELLING (injection site swollen), ARTHRALGIA (joint achiness), HEADACHE (dull headache), CHILLS (a little bit of chills) and NAUSEA (a little bit of nausea) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant drug details were reported. No treatment details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Patient came in today with redness and severe swelling at the site of injection. Area very sensitive to touch. She said it started when she woke up 1/23 after receiving the vaccination 1/22. No oozing or pus present. Suggested she use an oral NSAID for swelling relief and ice the area. Told her to follow up with physician if symptoms do not resolve.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unkown
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
Chills
Lethargy
Pyrexia
Symptomtext
About 9:30 PM back began to ache, about 10:05 began shivering and chilling continuing for about 2 hours. Had noticeable fever and aching in large joints rest of the night. Fever began to break about 6:30 AM. Was very lethargic the next 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Environmental allergies, hypertension
- Andere Medikamente
- Ortho-tricyclen, amlodipine, meloxicam, Claritin, calcium supplement
- Allergien
- None, all environmental
- Vorherige Impfungen
- Similar but longer lasting and more intense
- Staat
- OR
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Additional Details: Patient reported appreciable lightheadedness within 2 minutes of receiving vaccination. Provided water from emergency kit and crackers at patient request. She later reported feeling better especially after consuming water.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Additional Details: Patient returned to pharmacy 3 days after vaccine to report 1 x 2 inch red/swollen/painful area below the vaccination area. Started 1 day after vaccination administration and worst on 2nd day after, starting to improve but not resolved on day 3.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Hyperhidrosis
Nausea
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Nausea-Mild, Additional Details: Pt reports getting very anxious around needles and cautioned immunizer about history of getting dizzy/fainting with previous vaccines. About 5 minutes after vaccine was given, pt was feeling faint, dizzy and nauseous. Had patient lay on the floor and position her legs upright on a chair. She laid down for ~5 minutes and felt better. Pt did not fully lose consciousness. Did not want me to inform primary care doctor about situation because this is not a new phenomenon for her.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Symptomtext
Pt states that on her way home from the store her feet became itchy. By the time she got home it was all she could do to get up her stairs as her feet were incredibly itchy and red. States she had this kind of reaction to a different medication she was allergic to.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Breast swelling
Lymphadenopathy
Swelling
Tenderness
Symptomtext
Received shot in L deltoid muscle at 11AM on 1/17/22. About 9PM on 1/17/22, developed worsening pain in L arm pit region. By the morning of 1/18/22, developed severe swelling in arm pit, down to breast and across front of chest. It is now 1/20/22 and the swelling and pain in the L arm pit region has not improved. It continues to be very painful to move, to the touch, and swollen. There is no swelling or pain at actual injection site though.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Endometriosis
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site swelling
Lymphadenopathy
Pain
Symptomtext
Site: Swelling at Injection Site-Severe, Additional Details: Patient called to state that about 24 hours after immunization she experiencef swelling in lymph nodes in arm pit area along with stabbing pain. Patient is going to follow up with PCP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adverse event
Blood pressure abnormal
Chills
Dizziness
Symptomtext
Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Medium, Additional Details: Patient reporting having chills about 5 minutes post-booster injection. Emergency medical services (911) were dispatched. Upon arrival of the paramedics, patient's blood pressure stabilized and patient refused to be transported to the hospital. Followed up with the patient via telephone ~1 hour post-adverse event and the patient reported to be feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nausea
Vomiting
Symptomtext
Systemic: Vomiting-Medium, Additional Details: recieved vaccine about 11:50 am pt stayed here for 15 minute observation and was fine when he left he stated that he was nauseous on way home, called pharmacy at 4:30pm and stated that he had vomitted 5 or 6 times since he got home. I counseled him what to do and if needed he should contact md. Followed up with pt 1/18 and he stated that he continued to have vomiting that evening and nausea the next day. He stated that he never contacted md. and Today 1/18 he is feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
Systemic: Headache-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bed rest
Myalgia
Pyrexia
Symptomtext
Felt muscle pain on left arm. Had a low grade-fever for two days. Drank a lot of water and had bed rest for two days. Fever and muscle pain were gone on the third day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Fever and muscle pain on 2nd shot of COVID-19 Vaccine at 65 on 06/23/2021 Moderna 011D21A
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Lymphadenopathy
Symptomtext
Persistent swollen lymph nodes exerting serious pain in both armpits since the administration of the booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- none.
- Aktuelle Erkrankungen
- none.
- Vorgeschichte
- hypertension.
- Andere Medikamente
- none.
- Allergien
- none.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 22.04.2021
- Beginn
- 14.01.2022
- Tage bis Beginn
- 267,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Abdominal pain
Appendicitis
Surgery
Symptomtext
abdominal pain, ED visit that ended up as acute appendicitis surgery
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 16.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Headache
Injection site pain
Insomnia
Pain
Pyrexia
Symptomtext
This was a COVID booster. I had a terrible headache, terrible body aches, body chills and a fever, and insomnia for the entire day following the shot. I am still experiencing exhaustion and arm pain at the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Allergic to eggs.
- Vorherige Impfungen
- Flu Vaccine
- Staat
- MI
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Injection site pain
Symptomtext
PATIENT CAME TO PHARMACY ON 01/14/2021 AT 4:45PM ASKING IF SHE CAN RECEIVE A BOOSTER DOSE OF MODERNA VACCINE. PATIENT FILLED OUT THE CDC QUETIONNAIRE FORM AND IT WAS REVIEWED PRIOR TO VACCINATION, HOWEVER THE BOOSTER WAS ADMINISTERED 1 MONTH BEFORE THE RECOMMENDED INTERVAL AT 4 MONTHS RATHER THAN AT 5 MONTHS APART. PATIENT WAS REACHED OUT NEXT DAY MORNING ON 01/15/2022 UPON FINDINGS OF THE MISTAKE AND COUNSELED ON POSSIBLE SIDE EFFECTS. PATIENT STATED SHE WAS ONLY HAVING MILD SORENESS AROUND THE INJECTION SITE. NO OTHER ADVERSE REACTIONS WERE REPORTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 13.12.2023
- Impfdatum
- 27.01.2022
- Beginn
- 12.12.2023
- Tage bis Beginn
- 684,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
SARS-CoV-2 test
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- SARS-CoV-2 test
- Hospital-Tage
- -
- Labordaten
- IDNOW
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 10.08.2023
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- 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
Symptomtext
Vaccine lot number 022J21A for Moderna was expired on 04/24/2022. The vaccine was injected to the patient on 05/13/2022. We were notified on 07/03/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 13.06.2023
- Impfdatum
- 24.01.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 330,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Obstructive sleep apnoea syndrome
Symptomtext
ADULT OBSTRUCTIVE SLEEP APNEA, MODERATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Obstructive sleep apnoea syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 01.05.2023
- Impfdatum
- 28.01.2022
- Beginn
- 24.04.2023
- Tage bis Beginn
- 451,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 2 vaccines Janssen 3/30/21 Lot# 1808609; Moderna 1/28/22 Lot# 022J21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 20.04.2022
- Beginn
- 20.11.2022
- Tage bis Beginn
- 214,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Biopsy breast abnormal
Breast cancer
Mammogram abnormal
Symptomtext
I had a routine mammogram 15OCT2022 after that I got a call for a need to go have a biopsy as small calcifications was noted in my left breast. The biopsy showed cancer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy breast abnormal
- Hospital-Tage
- -
- Labordaten
- Mammogram and Biopsy diagnosis breast cancer.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seasonal allegories
- Andere Medikamente
- Levothyroxine; Losartan
- Allergien
- Adhesive
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 24.04.2023
- Impfdatum
- 16.01.2022
- Beginn
- 18.04.2023
- Tage bis Beginn
- 457,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case after 3 vaccines Moderna 1/21/21 Lot# 027L20A; Moderna 6/17/21 Lot# 036C21A; MOderna 1/16/22 Lot# 022J21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 27.03.2023
- Impfdatum
- 15.01.2022
- Beginn
- 22.03.2023
- Tage bis Beginn
- 431,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 1/26/21 Lot# 012L20A; Moderna 2/6/21 LOt# 012L20A; Moderna 1/15/22 Lot# 022J21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 27.01.2022
- Beginn
- 28.02.2023
- Tage bis Beginn
- 397,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 10.01.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 44,0
- Dosis
- 3
- Route/Site
- IM / LA
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
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.02.2023
- Impfdatum
- 02.12.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Symptomtext
No Adverse Event; This spontaneous case was reported by a consumer and describes the occurrence of NO ADVERSE EVENT (No Adverse Event) in a patient of an unknown age and gender who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 022J21A) for COVID-19 prophylaxis. Previously administered products included for Drug use for unknown indication: PFIZER BIONTECH COVID-19 VACCINE (First Booster dose) on 01-Sep-2022. Past adverse reactions to the above products included No adverse event with PFIZER BIONTECH COVID-19 VACCINE. On 02-Dec-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, NO ADVERSE EVENT (No Adverse Event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No Adverse Event) to be not related. Caller has had two Booster doses, one on 01-Sep-2022 which was Pfizer and then on 02-Dec-2022 which was Moderna. Caller said they had Moderna for the original COVID-19 boosters but then got the Pfizer's new modified version. Then they got the Bivalent booster of Moderna. Caller said they were told they can get the Moderna bivalent booster done after 2 months repeatedly. Caller said after 3 months it starts wearing off. The information they got said the vaccines starts tapering off. Dates for previous doses and monovalent boosters were not gathered to ensure given within authorized vaccine schedule. Caller declined contact information and declined consent for follow up. No concomitant medication reported. No treatment medication reported. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 09.02.2023
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 08.02.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 08.02.2023
- Impfdatum
- 18.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.02.2023
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 07.02.2023
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 06.02.2023
- Impfdatum
- 17.01.2022
- Beginn
- 02.02.2023
- Tage bis Beginn
- 381,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 1 booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- positive covid pcr 2/2/23
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- AFib CAD DM2 HFpEF BPH
- Andere Medikamente
- unknown
- Allergien
- adhesive tape, gabapentin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 19.01.2023
- Impfdatum
- 24.02.2022
- Beginn
- 19.01.2023
- Tage bis Beginn
- 329,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough case dose 1 4/26/21 017B21A Moderna dose 2 5/24/21 043B21A Moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ 1/19/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 16.01.2023
- Impfdatum
- 10.02.2021
- Beginn
- 05.01.2023
- Tage bis Beginn
- 694,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient hospitalized for 5 days following a positive COVID-19 test
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD, CHF, A-fib, GERD, hyperlipidemia, hypertension, MI, TIA, seizure disorder, a cochlear implant, a cardiac catheter, and a heart artery stent
- Andere Medikamente
- Citalopram, Hydrocodone, Lisinopril, pantoprazole, levetiracetam, levothyroxine, methocarbamol, metoprolol, tamsulosin, ipratropium, loratadine, sennosides
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 10.02.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 313,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 12/23/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 26.02.2021
- Beginn
- 10.10.2021
- Tage bis Beginn
- 226,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Influenza virus test
Iron deficiency anaemia
Lymphoma
Respiratory syncytial virus test
SARS-CoV-2 test positive
Symptomtext
Date of Admission: 10/10/2022 Date of Discharge: 10/14/2022 Admission Diagnosis: COVID-19 virus infection [U07.1] Iron deficiency anemia lymphoma Hospital Principal Problem (Discharge Diagnoses): COVID-19 virus infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- 10/10 Covid-19, Flu, RSV by NAA SARS-CoV-2 -COVID-19 Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 02.03.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 285,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 8/12/21 Lot# 033C21A; Moderna 9/17/21 Lot# 025B21A; Moderna 3/2/22 Lot# 022J21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine stored post puncture for longer period of time than recommended (28 days)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 14.11.2022
- Impfdatum
- 15.12.2021
- Beginn
- 19.09.2022
- Tage bis Beginn
- 278,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chemotherapy
Chronic lymphocytic leukaemia
SARS-CoV-2 test positive
Symptomtext
09/19/22 admitted to Oncology for "CLL, inpatient chemo". PMHx of "A-fib, Arrhythmia, Arthritis, AS, bilateral lower extremity edema, bleeding tendency, chronic renal failure, CLL, Congestive heart failure"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 09/19/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 01.11.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine stored for longer than recommended period of time post puncture
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 101,0
- Geschlecht
- M
- Eingang
- 26.10.2022
- Impfdatum
- 25.01.2022
- Beginn
- 03.09.2022
- Tage bis Beginn
- 221,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dementia Alzheimer's type
Disease complication
Symptomtext
Narrative: due to complications of Advanced Alzheimer's Disease.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dementia Alzheimer's type
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 09.03.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 226,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 10/21/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 03.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Brain neoplasm benign
Sleep disorder
Tinnitus
Symptomtext
The day after receiving my vaccine, I had a lot of loud noise in my head. It sounded like bees buzzing loudly with chirping, banging, clanging. It lasted around three weeks to that degree and was so bad that I couldn't sleep at night. Around a month ago, in September, it started to calm down a little bit. I have a benign brain tumor behind my ear, and I have experienced tinnitus in the past but never to that degree.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Brain neoplasm benign
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Atrial fibrillation; Acid reflux; Degenerative disk disorder; Arthritis
- Andere Medikamente
- Eliquis; Sotalol; Restasis; Vitamin D; Omeprazole; Potassium
- Allergien
- Wool
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 20.01.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 244,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 08.08.2022
- Impfdatum
- 19.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Alopecia areata
Biopsy skin abnormal
Symptomtext
Hair loss, in patches, then total loss of hair on scalp, eyebrows, and eyelashes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alopecia
- Hospital-Tage
- -
- Labordaten
- Skin biopsies were performed on 4/1/2022 which revealed alopecia areata without evidence of trauma or androgenetic alopecia. the clinical diagnosis is alopecia universals.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes II Hypertension Hypothyroid
- Andere Medikamente
- Metformin Levothyroxine HCTZ Talmisartan
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 23.06.2022
- Beginn
- 23.06.2022
- 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
No adverse event
Product storage error
Symptomtext
Vaccine that expired on 24-April-2022, vial was initially stored in the refrigerator on 23-Jun-2022, unused portion was put in refrigerator; No adverse event; Dose administered after manufacturer date of expiry to 11th patient; 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 to 11th patient), PRODUCT STORAGE ERROR (Vaccine that expired on 24-April-2022, vial was initially stored in the refrigerator on 23-Jun-2022, unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event) in a 20-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 23-Jun-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to 11th patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine that expired on 24-April-2022, vial was initially stored in the refrigerator on 23-Jun-2022, unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to 11th patient), PRODUCT STORAGE ERROR (Vaccine that expired on 24-April-2022, vial was initially stored in the refrigerator on 23-Jun-2022, unused portion was put in refrigerator) 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 (Dose administered after manufacturer date of expiry to 11th patient) and PRODUCT STORAGE ERROR (Vaccine that expired on 24-April-2022, vial was initially stored in the refrigerator on 23-Jun-2022, unused portion was put in refrigerator). Concomitant medication details were not reported by the reporter. Vial was initially stored in the refrigerator on 05-MAY-2022, 06-MAY-2022, 19-MAY-2022, 02-JUN-2022, 09-JUN-2022 and 23-JUN-2022. Vial did not undergo any temperature execursion. It was reported that vaccines were removed from the freezer on date of appointments to be used, and any unused portion was put in refrigerator. Treatment details were not reported by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-619547 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-619547:Same reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 19.05.2022
- Beginn
- 19.05.2022
- 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
Extra dose administered
No adverse event
Product storage error
Symptomtext
Vial expired on 24-Apr-2022 was administered on 19-May-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator; No adverse event; Dose administered after manufacturer date of expiry; patient received 2nd booster dose of expired vaccine; 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), EXTRA DOSE ADMINISTERED (patient received 2nd booster dose of expired vaccine), PRODUCT STORAGE ERROR (Vial expired on 24-Apr-2022 was administered on 19-May-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event) in an 85-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 19-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) and EXTRA DOSE ADMINISTERED (patient received 2nd booster dose of expired vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial expired on 24-Apr-2022 was administered on 19-May-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry), EXTRA DOSE ADMINISTERED (patient received 2nd booster dose of expired vaccine), PRODUCT STORAGE ERROR (Vial expired on 24-Apr-2022 was administered on 19-May-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator) 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 (Dose administered after manufacturer date of expiry), EXTRA DOSE ADMINISTERED (patient received 2nd booster dose of expired vaccine) and PRODUCT STORAGE ERROR (Vial expired on 24-Apr-2022 was administered on 19-May-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator). No concomitant medications were reported. Number of doses/vials were reported as 200 doses 20 vials. The vials were initially stored in the refrigerator on 05-May-2022, 06-May-2022,19-May-2022, 02-Jun-2022, 09-Jun-2022 and 23-Jun-2022. Office manager explained that vaccines were removed from the freezer on date of appointments to be used, and any unused portion was put in refrigerator. The vial did not undergo any temperature excursions. Reporter found out because a couple were going on a cruise, and needed to verify their vaccine information and upon entering the lot, it showed the vaccine expired 24-Apr-2022. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2022-619547 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-619547:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 06.08.2022
- Impfdatum
- 23.06.2022
- Beginn
- 23.06.2022
- 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
Product storage error
Symptomtext
Vaccine expired on 24-April-2022, vial was initially stored in the refrigerator on 23-Jun-2022 and unused portion was put in refrigerator; No adverse event; Dose administered after manufacturer date of expiry to 12 patients; 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 to 12 patients), PRODUCT STORAGE ERROR (Vaccine expired on 24-April-2022, vial was initially stored in the refrigerator on 23-Jun-2022 and unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event) in a 45-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Jun-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 23-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to 12 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 24-April-2022, vial was initially stored in the refrigerator on 23-Jun-2022 and unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to 12 patients), PRODUCT STORAGE ERROR (Vaccine expired on 24-April-2022, vial was initially stored in the refrigerator on 23-Jun-2022 and unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to 12 patients) and PRODUCT STORAGE ERROR (Vaccine expired on 24-April-2022, vial was initially stored in the refrigerator on 23-Jun-2022 and unused portion was put in refrigerator). No concomitant medications were reported. Number of doses/vials was reported as 200 doses 20 vials. The vial was initially stored in the refrigerator on 5-May-2022, 6-May-2022, 19-May-2022, 02-Jun-2022, 09-Jun-2022 and 23-June-2022. Office manager explained that vaccines were removed from the freezer on date of appointments to be used, and the unused portion was put back in refrigerator. No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2022-619547 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-619547:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 06.08.2022
- Impfdatum
- 09.06.2022
- Beginn
- 09.06.2022
- 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
Product storage error
Symptomtext
vaccines were removed from the freezer on date of appointments to be used, and any unused; No adverse event; Dose administered after manufacturer date of expiry to patient; 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 to patient), PRODUCT STORAGE ERROR (vaccines were removed from the freezer on date of appointments to be used, and any unused) and NO ADVERSE EVENT (No adverse event) in an 18-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Jun-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 09-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vaccines were removed from the freezer on date of appointments to be used, and any unused) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to patient), PRODUCT STORAGE ERROR (vaccines were removed from the freezer on date of appointments to be used, and any unused) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to patient) and PRODUCT STORAGE ERROR (vaccines were removed from the freezer on date of appointments to be used, and any unused). No concomitant drug was reported. Number of dose or vials reported as 200 doses 20 vials. The vial was initially stored in the refrigerator on 5-May-2022, 6-May-2022, 19-May-2022, 02-Jun-2022, 09-Jun-2022 and 23-June-2022. It was reported that vaccines were removed from the freezer on date of appointments to be used, and any unused portion was put in refrigerator. Vial did not undergoes 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
- TX
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 06.08.2022
- Impfdatum
- 09.06.2022
- Beginn
- 09.06.2022
- 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
No adverse event
Product storage error
Symptomtext
Vial expired on 24-Apr-2022 was administered on 9-JUN-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator; 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), PRODUCT STORAGE ERROR (Vial expired on 24-Apr-2022 was administered on 9-JUN-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 09-Jun-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial expired on 24-Apr-2022 was administered on 9-JUN-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry), PRODUCT STORAGE ERROR (Vial expired on 24-Apr-2022 was administered on 9-JUN-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator) 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 (Dose administered after manufacturer date of expiry) and PRODUCT STORAGE ERROR (Vial expired on 24-Apr-2022 was administered on 9-JUN-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator). No concomitant medications were reported. Number of doses/vials were reported as 200 doses 20 vials. The vials were initially stored in the refrigerator on 05-May-2022, 06-May-2022,19-May-2022, 02-Jun-2022, 09-Jun-2022 and 23-Jun-2022. Office manager explained that vaccines were removed from the freezer on date of appointments to be used, and any unused portion was put in refrigerator. The vial did not undergo any temperature excursions. Reporter found out because a couple were going on a cruise, and needed to verify their vaccine information and upon entering the lot, it showed the vaccine expired 24-Apr-2022. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2022-619399, US-MODERNATX, INC.-MOD-2022-619552, US-MODERNATX, INC.-MOD-2022-619354, US-MODERNATX, INC.-MOD-2022-619424, US-MODERNATX, INC.-MOD-2022-619485, US-MODERNATX, INC.-MOD-2022-619493, US-MODERNATX, INC.-MOD-2022-619520, US-MODERNATX, INC.-MOD-2022-619541, US-MODERNATX, INC.-MOD-2022-619632, US-MODERNATX, INC.-MOD-2022-619709, US-MODERNATX, INC.-MOD-2022-619474 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-619399: US-MODERNATX, INC.-MOD-2022-619552: US-MODERNATX, INC.-MOD-2022-619354: US-MODERNATX, INC.-MOD-2022-619424: US-MODERNATX, INC.-MOD-2022-619485: US-MODERNATX, INC.-MOD-2022-619493: US-MODERNATX, INC.-MOD-2022-619520: US-MODERNATX, INC.-MOD-2022-619541: US-MODERNATX, INC.-MOD-2022-619632: US-MODERNATX, INC.-MOD-2022-619709: US-MODERNATX, INC.-MOD-2022-619474:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 06.08.2022
- Impfdatum
- 02.06.2022
- Beginn
- 02.06.2022
- 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
Product storage error
Symptomtext
vaccines were removed from the freezer on date of appointments to be used,; No adverse event; Dose administered after manufacturer date of expiry to patient; 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 to patient), PRODUCT STORAGE ERROR (vaccines were removed from the freezer on date of appointments to be used,) and NO ADVERSE EVENT (No adverse event) in an 18-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Jun-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 02-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vaccines were removed from the freezer on date of appointments to be used,) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to patient), PRODUCT STORAGE ERROR (vaccines were removed from the freezer on date of appointments to be used,) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to patient) and PRODUCT STORAGE ERROR (vaccines were removed from the freezer on date of appointments to be used,). No concomitant medications were reported. Total 200 doses and 20 vials were administered. The vials were initially stored in the refrigerator on 05-May-2022, 06-May-2022, 19-May-2022, 02-Jun-2022, 09-Jun-2022 and 23-Jun-2022. Reporter explained that vaccines were removed from the freezer on date of appointments to be used, and any unused portion was put in refrigerator. The vial did not undergo any temperature excursions. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2022-619547 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-619547:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 06.08.2022
- Impfdatum
- 02.06.2022
- Beginn
- 02.06.2022
- 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
Product storage error
Symptomtext
The vaccine that expired on 24-April-2022 was administered on 2-Jun-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.; No adverse event; Dose administered after manufacturer date of expiry to 12 patients; 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 to 12 patients), PRODUCT STORAGE ERROR (The vaccine that expired on 24-April-2022 was administered on 2-Jun-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.) and NO ADVERSE EVENT (No adverse event) in a 23-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 02-Jun-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 02-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to 12 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vaccine that expired on 24-April-2022 was administered on 2-Jun-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to 12 patients), PRODUCT STORAGE ERROR (The vaccine that expired on 24-April-2022 was administered on 2-Jun-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to 12 patients) and PRODUCT STORAGE ERROR (The vaccine that expired on 24-April-2022 was administered on 2-Jun-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.). No concomitant medications were reported. A Moderna vaccine that expired on 24April2022, was given past the expiration date through the month of June to 12 patients. Office manager explained that vaccines were removed from the freezer on date of appointments to be used, and any unused portion was put in refrigerator.The vial did not undergo any temperature excursions. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2022-619547 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-619547:Same reporter/event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 06.08.2022
- Impfdatum
- 19.05.2022
- Beginn
- 19.05.2022
- 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
No adverse event
Product storage error
Symptomtext
The vaccine that expired on 24-April-2022 was administered on 19-MAY-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.; no adverse event; Dose administered after manufacturer date of expiry to the patient; 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 to the patient), PRODUCT STORAGE ERROR (The vaccine that expired on 24-April-2022 was administered on 19-MAY-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.) and NO ADVERSE EVENT (no adverse event) in a 68-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 19-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to the patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vaccine that expired on 24-April-2022 was administered on 19-MAY-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to the patient), PRODUCT STORAGE ERROR (The vaccine that expired on 24-April-2022 was administered on 19-MAY-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.) 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 (Dose administered after manufacturer date of expiry to the patient) and PRODUCT STORAGE ERROR (The vaccine that expired on 24-April-2022 was administered on 19-MAY-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.). No concomitant medications were reported. The vial was initially stored in the refrigerator on 5May2022, 6May2022,19May2022, 02Jun2022, 09Jun2022 and 23June2022. vaccines were removed from the freezer on date of appointments to be used, and any unused portion was put in refrigerator. The vial did not undergo any temperature excursions. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2022-619547 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-619547:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 06.08.2022
- Impfdatum
- 19.05.2022
- Beginn
- 19.05.2022
- 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
No adverse event
Product storage error
Symptomtext
the vial was initially stored in the refrigerator on 19-May-2022 after expiration date 24-Apr-2022; No adverse event; Dose administered after manufacturer date of expiry to patient; 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 to patient), PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator on 19-May-2022 after expiration date 24-Apr-2022) and NO ADVERSE EVENT (No adverse event) in an 81-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 19-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator on 19-May-2022 after expiration date 24-Apr-2022) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to patient), PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator on 19-May-2022 after expiration date 24-Apr-2022) 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 (Dose administered after manufacturer date of expiry to patient) and PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator on 19-May-2022 after expiration date 24-Apr-2022). No concomitant medications were reported. Number of doses/vials were reported as 200 doses 20 vials. Date the vial was initially stored in the refrigerator were reported as 05-May-2022, 06-May-2022,19-May-2022, 02-Jun-2022, 09-Jun-2022 and 23-Jun-2022. Office manager explained that vaccines were removed from the freezer on date of appointments to be used, and any unused portion was put in refrigerator. Date(s) of administration of vaccine was reported as 05-May-2022, 06-May-2022,19-May-2022, 02-Jun-2022, 09-Jun-2022 and 23-Jun-2022 to12 patients. The vial did not undergo any temperature excursions. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 06.08.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
vaccine that expired on 24April2022, vial was initially stored in the refrigerator on 5May2022, unused portion was put in refrigerator; No adverse event; Dose administered after manufacturer date of expiry to patient; 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 to patient), PRODUCT STORAGE ERROR (vaccine that expired on 24April2022, vial was initially stored in the refrigerator on 5May2022, unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event) in a 63-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 05-May-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 05-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vaccine that expired on 24April2022, vial was initially stored in the refrigerator on 5May2022, unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to patient), PRODUCT STORAGE ERROR (vaccine that expired on 24April2022, vial was initially stored in the refrigerator on 5May2022, unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to patient) and PRODUCT STORAGE ERROR (vaccine that expired on 24April2022, vial was initially stored in the refrigerator on 5May2022, unused portion was put in refrigerator). No concomitant medication were reported. Number of doses/vials: 200 doses 20 vials. The vial was initially stored in the refrigerator on 5-May-2022. It was explained that vaccines were removed from the freezer on date of appointments to be used, and the unused portion was put back in refrigerator. The vial did not undergo any temperature excursions No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 06.08.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- 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
No adverse event
Product storage error
Symptomtext
vaccine that expired on 24April2022, vial was initially stored in the refrigerator on 5May2022, unused portion was put in refrigerator; No adverse event; Dose administered after manufacturer date of expiry to 12 patients; 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 to 12 patients), PRODUCT STORAGE ERROR (vaccine that expired on 24April2022, vial was initially stored in the refrigerator on 5May2022, unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 05-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to 12 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vaccine that expired on 24April2022, vial was initially stored in the refrigerator on 5May2022, unused portion was put in refrigerator) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry to 12 patients), PRODUCT STORAGE ERROR (vaccine that expired on 24April2022, vial was initially stored in the refrigerator on 5May2022, unused portion was put in refrigerator) 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 (Dose administered after manufacturer date of expiry to 12 patients) and PRODUCT STORAGE ERROR (vaccine that expired on 24April2022, vial was initially stored in the refrigerator on 5May2022, unused portion was put in refrigerator). No concomitant medication were reported. Number of doses/vials: 200 doses 20 vials. The vial was initially stored in the refrigerator on 5-May-2022, 6-May-2022, 19-May-2022, 02-Jun-2022, 09-Jun-2022 and 23-June-2022. Office manager explained that vaccines were removed from the freezer on date of appointments to be used, and the unused portion was put back in refrigerator. The vial did not undergo any temperature excursions No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 06.08.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- 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
No adverse event
Product storage error
Symptomtext
The vaccine that expired on 24-April-2022 was administered on 5-May-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.; 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), PRODUCT STORAGE ERROR (The vaccine that expired on 24-April-2022 was administered on 5-May-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.) and NO ADVERSE EVENT (no adverse event) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 prophylaxis. No Medical History information was reported. On 05-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vaccine that expired on 24-April-2022 was administered on 5-May-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry), PRODUCT STORAGE ERROR (The vaccine that expired on 24-April-2022 was administered on 5-May-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.) 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 (Dose administered after manufacturer date of expiry) and PRODUCT STORAGE ERROR (The vaccine that expired on 24-April-2022 was administered on 5-May-2022, vial was initially stored in the refrigerator on 5-May-2022, unused portion was put in refrigerator.). No concomitant medications were reported. On 5-May-2022, the patient received a fourth dose (booster dose)(Lot: 022J21A) of Moderna vaccine. The vial were initially stored in the refrigerator on 5May2022, 6May2022,19May2022, 02Jun2022, 09Jun2022 and 23June2022. vaccines were removed from the freezer on date of appointments to be used, and any unused portion was put in refrigerator. The vial did not undergone 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
- MI
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 27.07.2022
- Impfdatum
- 18.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Coagulopathy
Heavy menstrual bleeding
Menstrual disorder
Symptomtext
A lot of Clotting during my cycle they are just dropping out and it still happening and it?s July 2023 my mental cycle are heavier and dark red bleeding and I?m bleeding every 2 week or every 18/20 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Coagulopathy
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/a
- Andere Medikamente
- Iron pills vitamin D and vitamin b12
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 27.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 106,0
- Dosis
- 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
- 34,0
- Geschlecht
- M
- Eingang
- 26.07.2022
- Impfdatum
- 20.01.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 186,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 101,0
- 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
- -
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 01.02.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 166,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
HOSPITALIZED WITH COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 24.02.2022
- Beginn
- 18.07.2022
- Tage bis Beginn
- 144,0
- Dosis
- 2
- 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
- MO
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 14.01.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 158,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested Covid+ 6/21/2022 Admitted to Hospital 6/20/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 16,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy kidney
Computerised tomogram
Haematuria
Renal artery stent placement
Scan with contrast
Symptomtext
Gross Hematuria
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy kidney
- Hospital-Tage
- 7,0
- Labordaten
- Hospitalization: 2/17/22 x 1 week, 4/18/22 x 4 days CT Scans with and without contrast Renal Biopsy 2/21/22, 4/18/22 Renal stent placement x 2 Nephrology Consult - Pending
- Aktuelle Erkrankungen
- A FIB
- Vorgeschichte
- Atrial Fibrillation
- Andere Medikamente
- METOPROLOL VITAMIN D 3 XERALTO Women's One-A-Day Multivitamin
- Allergien
- Nickle
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 10.03.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 100,0
- 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
Confirmed breakkthrough case COVID-19 (Moderna) 1 03/10/2021 local Health Dept. Moderna 044A21A COVID-19 (Moderna) 2 04/07/2021 local Health Dept. Moderna 040B21A COVID-19 (Moderna) 3 03/10/2022 HCF Moderna 022J21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive LAB COVID Test - 6/18/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 24.06.2022
- Impfdatum
- 11.04.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 70,0
- Dosis
- 5
- 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
- MA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 19.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
COVID-19
Drug ineffective
SARS-CoV-2 test
Interchange of vaccine products
Symptomtext
Did you/the patient previously receive a COVID-19 Vaccine?: Yes; Did you/the patient previously receive a COVID-19 Vaccine?: Yes; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35-year-old male patient received BNT162b2 (BNT162B2), on 18Mar2021 at 17:00 as dose 1, single (Lot number: EP6955), in left arm, on 09Apr2021 at 17:00 as dose 2, single (Lot number: EW0151), in left arm and on 19Aug2021 at 17:00 as dose 3 (booster), single (Lot number: EW0185) at the age of 34 years, in left arm for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 21Jan2022 at 17:00 as dose 4 (booster), single (Lot number: 022J21A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Crohn's Disease" (unspecified if ongoing). Concomitant medication(s) included: DEXLANSOPRAZOLE; INFLECTRA [INFLIXIMAB DYYB], start date: Jan2021. Past drug history included: Flagyl, reaction(s): "Allergy". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Did you/the patient previously receive a COVID-19 Vaccine?: Yes". The patient underwent the following laboratory tests and procedures: Body temperature: (unspecified date) 101.0 Fahrenheit; SARS-CoV-2 test: (19May2022) Positive, notes: Had a positive test on 19May, took the five day course of paxlovid starting that date; (24May2022) Negative, notes: As of 24May, I was testing negative again; (31May2022) Negative, notes: However as of 31May started to feel unwell, and mildly feverish with a cough (99) but tested negative; (01Jun2022) Positive, notes: As of this morning, I now have a proper 101.0 fever, loud cough, big headache and body aches and testing very positive, very quickly. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient had a paxlovid / COVID rebound. Had a positive test on 5/19, took the five day course of paxlovid starting that date. As of 24May, I was testing negative again and feeling asymptomatic. However as of 31May I started to feel unwell, and mildly feverish with a cough (99) but tested negative. As of this morning, I now have a proper 101.0 fever, loud cough, big headache and body aches and testing very positive, very quickly. The patient received other medication in 2 weeks, which included Dexlansoprazole (Dexlansoprazole) and Inflextra (start date: Jan/2021).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body temperature
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: Test Result:101.0 Fahrenheit; Test Date: 20220519; Test Name: COVID-19 test; Test Result: Positive ; Comments: Had a positive test on 19May, took the five day course of paxlovid starting that date.; Test Date: 20220524; Test Name: COVID-19 test; Test Result: Negative ; Comments: As of 24May, I was testing negative again; Test Date: 20220531; Test Name: COVID-19 test; Test Result: Negative ; Comments: However as of 31May started to feel unwell, and mildly feverish with a cough (99) but tested negative.; Test Date: 20220601; Test Name: COVID-19 test; Test Result: Positive ; Comments: As of this morning, I now have a proper 101.0 fever, loud cough, big headache and body aches and testing very positive, very quickly
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Crohn's disease
- Andere Medikamente
- DEXLANSOPRAZOLE; INFLECTRA [INFLIXIMAB DYYB]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 25.02.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 88,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Discomfort
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse reaction to the vaccine but contracted Covid 19 and tested positive May 24, 2022. I took ibuprofen and Mucinex for three days to alleviate the discomfort.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Rapid test in the doctor's office.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; migraines; obesity
- Andere Medikamente
- Participant declined to provide details.
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- U
- Eingang
- 28.05.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- 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
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (receiving doses after its beyond use date) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 10-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (receiving doses after its beyond use date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (receiving doses after its beyond use date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. It was reported that 3 doses from different vials were used and no temperature excursions. It was reported that the vial was initially stored in the refrigerator on 11-Jan- 2022 and beyond use date for that was 11-Feb-2022. It was reported that the vial undergo any temperature excursions reported None. No concomitant medication was reported. No treatment medication was reported. This case was linked to MOD-2022-573737 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.05.2022
- Impfdatum
- 02.03.2022
- Beginn
- 02.03.2022
- 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
Symptomtext
receiving doses after its beyond use date (11 feb2022); This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (receiving doses after its beyond use date (11 feb2022)) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 022j21a) for COVID-19 vaccination. No Medical History information was reported. On 02-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 02-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (receiving doses after its beyond use date (11 feb2022)). At the time of the report, EXPIRED PRODUCT ADMINISTERED (receiving doses after its beyond use date (11 feb2022)) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. The vial was initially stored in the refrigerator on 11-Jan-2022. Beyond use date reported as 11-Feb-2022. The vial does not undergo any temperature excursions. No treatment medications was reported. This case was linked to MOD-2022-573737 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.05.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
receiving doses after its beyond use date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (receiving doses after its beyond use date) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 022j21a) for COVID-19 vaccination. No Medical History information was reported. On 14-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 14-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (receiving doses after its beyond use date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (receiving doses after its beyond use date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported . It was reported that 3 doses from different vials were used and no temperature excursions. It was reported that the vial was initially stored in the refrigerator on 11-Jan- 2022 and beyond use date for that was 11-Feb-2022. No treatment medication was reported. This case was linked to MOD-2022-573737 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 24.05.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was expired on 24-Mar-2022 and was stored in refrigeration on 29-Mar-2022 and administered on 26-APR-2022; Adminstered vaccine past the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Adminstered vaccine past the expiration date) and PRODUCT STORAGE ERROR (Vaccine was expired on 24-Mar-2022 and was stored in refrigeration on 29-Mar-2022 and administered on 26-APR-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 26-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 26-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Adminstered vaccine past the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was expired on 24-Mar-2022 and was stored in refrigeration on 29-Mar-2022 and administered on 26-APR-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Adminstered vaccine past the expiration date) and PRODUCT STORAGE ERROR (Vaccine was expired on 24-Mar-2022 and was stored in refrigeration on 29-Mar-2022 and administered on 26-APR-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medications details were not reported by the reporter. Reportedly, by used date was mentioned as 24-Apr-2022. The vaccines were stored in the freezer and only removed as needed to thaw and then administered. It was mentioned that vials were taken out at a time and thawed as they did not thawed an entire box. Treatment details were not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 05.02.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 32,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abortion missed
Abortion spontaneous
Exposure during pregnancy
Foetal growth restriction
Pregnancy test positive
Ultrasound antenatal screen abnormal
Uterine dilation and curettage
Symptomtext
Missed miscarriage diagnosed on 4/12/2022. Timeline: last menstrual period on 1/29/2022, Covid vaccine Moderna booster on 2/5/2022, positive pregnancy test on 2/25/22, missed miscarriage date based on ultrasound was 3/9/2022 (5 weeks 4 days gestation). Ultrasound on 4/4/2022 confirmed pregnancy was only at 5 weeks and 4 days, ultrasound on 4/12/2022 confirmed no progress to pregnancy and was still measuring at 5 weeks and 4 days. Treatment selected was a D&C (Dilation and Curettage) surgery which was completed on 4/14/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abortion missed
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prenatal vitamin, Singulair
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 21.05.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 24-Apr-2022 and removed from the fridge on 27-Apr-2022; administered vaccines past the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered vaccines past the expiration date) and PRODUCT STORAGE ERROR (Vaccine expired on 24-Apr-2022 and removed from the fridge on 27-Apr-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 27-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered vaccines past the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 24-Apr-2022 and removed from the fridge on 27-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered vaccines past the expiration date) and PRODUCT STORAGE ERROR (Vaccine expired on 24-Apr-2022 and removed from the fridge on 27-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. Reportedly, the by used date was mentioned as 24-Apr-2022. The vaccines were stored in the freezer and only removed as needed to thaw and then administered. It was mentioned that vials were taken out at a time and thawed as they did not thawed an entire box. On 27-Apr-2022, the vaccine was removed from the Fridge. 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
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 21.05.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 24-Apr-2022 and removed from the fridge on 25-Apr-2022 and administred on 25-Apr-2022; administered vaccines past the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered vaccines past the expiration date) and PRODUCT STORAGE ERROR (Vaccine expired on 24-Apr-2022 and removed from the fridge on 25-Apr-2022 and administred on 25-Apr-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 25-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered vaccines past the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 24-Apr-2022 and removed from the fridge on 25-Apr-2022 and administred on 25-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered vaccines past the expiration date) and PRODUCT STORAGE ERROR (Vaccine expired on 24-Apr-2022 and removed from the fridge on 25-Apr-2022 and administred on 25-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medications details were not reported by the reporter. Reportedly, by used date was mentioned as 24-Apr-2022. The vaccines were stored in the freezer and only removed as needed to thaw and then administered. It was mentioned that vials were taken out at a time and thawed as they did not thawed an entire box. Treatment details were not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.05.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- 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
Vial was initially stored in the refrigerator possibly on 10-Jan-2022, 11-Jan-2022, or 12-Jan-2022 and administered on 10-Mar-2022; Administered 3 vaccines beyond the beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered 3 vaccines beyond the beyond use date) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator possibly on 10-Jan-2022, 11-Jan-2022, or 12-Jan-2022 and administered on 10-Mar-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 10-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered 3 vaccines beyond the beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator possibly on 10-Jan-2022, 11-Jan-2022, or 12-Jan-2022 and administered on 10-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered 3 vaccines beyond the beyond use date) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator possibly on 10-Jan-2022, 11-Jan-2022, or 12-Jan-2022 and administered on 10-Mar-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications information was not reported. Vial did not undergo any temperature excursions. No treatment medications were provided. This case was linked to MOD-2022-566621 (Patient Link). Reporter did not allow further contact Most recent FOLLOW-UP information incorporated above includes: On 12-May-2022: Follow-up contains no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.05.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
administered 3 vaccines beyond the beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered 3 vaccines beyond the beyond use date) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 14-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered 3 vaccines beyond the beyond use date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered 3 vaccines beyond the beyond use date) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that the pharmacy administered 3 vaccines beyond the beyond use date a couple of months ago. The health officials were requiring them to get this settled out before they could get some more vaccines. Date the vial was initially stored in the refrigerator was possibly 10-Jan-2202, 11-Jan-2022, or 12-Jan-2022. Vail did not undergo any temperature excursions. No treatment medications were provided. This case was linked to MOD-2022-566953, MOD-2022-566958 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 12-May-2022: Follow-up received contain no new information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.05.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- 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
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. Patients pre-existing conditions and allergy are unknown. On 26-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medication was reported No Treatment medication was reported. HCP reports on Apr-26-2022 3 patients received expired vaccine. Administrations included 2 second booster and 1 first booster of Moderna covid-19 vaccine.HCP reports no side effects regarding the individuals. patients pre-existing conditions and allergy are unknown. Patient administer 1st booster dose. This case was linked to MOD-2022-553198 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patients pre-existing conditions and allergy are unknown.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- 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
Expired product administered
No adverse event
Symptomtext
Vaccine expired on 4/24/22 no adverse symptoms noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- 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: ja
Expired product administered
Symptomtext
Patient was given Moderna-2nd Dose Booster on 4/26/2022. Vial expired on 4/24/22. Moderna and CDC-Agency notified. Advised to re-vaccinate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- migraines
- Vorgeschichte
- migraines
- Andere Medikamente
- phenergan, sumaptriptan
- Allergien
- nirtroglycerin
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- 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: ja
Expired product administered
Symptomtext
Patient was given Moderna-2nd dose Booster on 4/26/2022. Vial expired on 4/24/22. Denies adverse reaction. Moderna and CDC notified. Advised to re-vaccinate patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- see attached
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Patient given Moderna 1st dose booster on 4/26/2022. Vial expired on 04/24/2022. Denied adverse reaction. Moderna and CDC notified. Advised to re-vaccinate patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- HTN, DM type 2, COPD
- Vorgeschichte
- HTN, DM type 2, COPD, pacemaker
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 19.01.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 69,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Paranasal sinus discomfort
SARS-CoV-2 test
Symptomtext
I had a lot of sinus pressure. This lasted for about 2 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paranasal sinus discomfort
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test
- Aktuelle Erkrankungen
- I tested positive for COVID-19 12/24/2021
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- U
- Eingang
- 28.04.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- 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 initially stored in the refrigerator on 25-Mar-2022 and vaccine was administred on 25-Apr-2022; gave an expired dose of a Moderna vaccine; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (gave an expired dose of a Moderna vaccine) and PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator on 25-Mar-2022 and vaccine was administred on 25-Apr-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 25-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (gave an expired dose of a Moderna vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator on 25-Mar-2022 and vaccine was administered on 25-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (gave an expired dose of a Moderna vaccine) and PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator on 25-Mar-2022 and vaccine was administered on 25-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant mediations were not reported Dose administered after manufacturer date of expiry. The vial does not undergo any temperature excursions. Treatment information was not reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- 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
No adverse event
Symptomtext
Vaccine was administered beyond use date. Patient was monitored with proper follow up. No abnormal side effects or adverse reactions were present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Dye
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Vaccine was administered beyond the beyond use date. Patient was monitored with proper follow up. No abnormal side effects or adverse reactions were present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 02.03.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Vaccine was administered beyond use date. Patient was monitored with proper follow up. No abnormal side effects or adverse reactions were present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 20.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Rhinorrhoea
Symptomtext
04/09/2022 A few days after my vaccination I started to cough and the doctor diagnosed it as rhinorrhea, no shortness of breath but a lot of coughing that was not under control. The Doctor prescribed benzonatate for symptoms, and they have not really gone away. Symptoms are still continuing as they were with minimal tapering of symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- 20 Hour Flu last week of March
- Vorgeschichte
- High Blood Pressure; High Cholesterol
- Andere Medikamente
- Calbittelol, Amlodipine, Atorvastatin, Omeprazole
- Allergien
- Advair; Hydrocodone
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 15.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia oral
Symptomtext
Numbness starting at the tip of my tongue then it spread entire tongue, roof of my mouth and my lips. And then it reversed, appearing to be getting better and then it came back to just the tip of my tongue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia oral
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- One a day vitamin; Vitamin D 1000mg
- Allergien
- Calycin; Penicillin; Hay Fever; Clindamycin; Statin drugs
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Moderna vaccine given to patient under the age of 18. Mom notified. Pharmacist explained Moderna was not approved for 17 and younger. Patient already received 2 doses of Pfizer. Mom was aware patient received Moderna vaccine. Mom was not concerned, but appreciated being notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- 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
No adverse event
Symptomtext
no adverse outcomes at time of administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- HIV
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- 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
Symptomtext
Dose administered after more than 12 hours post punctured; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after more than 12 hours post punctured) in a 40-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. Concurrent medical conditions included Reflux gastritis since 04-Apr-2022. Concomitant products included DIPHTHERIA VACCINE TOXOID, PERTUSSIS VACCINE ACELLULAR, TETANUS VACCINE TOXOID (TDAP) for an unknown indication. On 04-Apr-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 04-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after more than 12 hours post punctured). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after more than 12 hours post punctured) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No treatment medication information provided. Hight: 6 feet 7 inch. Weight: 232 Ibs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Reflux gastritis
- Vorgeschichte
- -
- Andere Medikamente
- TDAP
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 11.01.2022
- Beginn
- 13.02.2022
- Tage bis Beginn
- 33,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Biopsy colon
Colonoscopy abnormal
Gastrointestinal disorder
Gastrointestinal haemorrhage
Gastrointestinal mucosa hyperaemia
Intestinal ulcer
Oedema mucosal
Red blood cell transfusion
Symptomtext
Patient admitted for GI bleed - he received 4 units PRBC. Colonoscopy 2/15/22 - there was marked increased erythema, swelling, friability, and ulceration associated with the floor of the cecum and along the cecal side of the ileocecal valve. Multiple biopsies were obtained from this area and sent for pathology review. Discharged to home. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy colon
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was initially stored in the refrigerator on 02-Feb-2022 and dose administered on 07-Mar-2022 beyond 30-day use; We had given Moderna COVID-19 vaccine that was beyond the 30 days use by date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We had given Moderna COVID-19 vaccine that was beyond the 30 days use by date) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 02-Feb-2022 and dose administered on 07-Mar-2022 beyond 30-day use) in a 30-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Mar-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 07-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (We had given Moderna COVID-19 vaccine that was beyond the 30 days use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 02-Feb-2022 and dose administered on 07-Mar-2022 beyond 30-day use). At the time of the report, EXPIRED PRODUCT ADMINISTERED (We had given Moderna COVID-19 vaccine that was beyond the 30 days use by date) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 02-Feb-2022 and dose administered on 07-Mar-2022 beyond 30-day use) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The patient had given Moderna COVID-19 vaccine that was beyond the 30 days use by date, The vial was initially stored in the refrigerator on 02-Feb-2022 and dose administered on 07-Mar-2022 beyond 30 day use. It was reported that the vial had not undergone any temperature excursions. The patient had no event experienced and there was no product complaint associated. No treatment medications were reported. This case was linked to MOD-2022-519582, MOD-2022-519593, MOD-2022-519602 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Member received 2nd booster dose six months after initial booster dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient received 2nd booster dose 6 months after initial booster dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- U
- Eingang
- 25.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- 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 was initially stored in the refrigerator on 02Feb2022, and dose administered on 07Mar2022 beyond 30-day use; vaccine administered beyond the 30 day use by date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine administered beyond the 30 day use by date) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02Feb2022, and dose administered on 07Mar2022 beyond 30-day use) in a 38-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine administered beyond the 30 day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02Feb2022, and dose administered on 07Mar2022 beyond 30-day use). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine administered beyond the 30 day use by date) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02Feb2022, and dose administered on 07Mar2022 beyond 30-day use) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant drug reported. The vial was initially stored in the refrigerator on 02-Feb-2022. Patient received booster 1/2 doses. No temperature excursions reported. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- U
- Eingang
- 25.03.2022
- Impfdatum
- 14.03.2022
- Beginn
- 14.03.2022
- 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 was initially stored in the refrigerator on 02-Feb-2022 and dose administered on 14-Mar-2022 beyond 30-day use; We discovered that we've given Moderna Covid-19 vaccine that was beyond the 30 day use by date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We discovered that we've given Moderna Covid-19 vaccine that was beyond the 30 day use by date.) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02-Feb-2022 and dose administered on 14-Mar-2022 beyond 30-day use) in a 19-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (We discovered that we've given Moderna Covid-19 vaccine that was beyond the 30 day use by date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02-Feb-2022 and dose administered on 14-Mar-2022 beyond 30-day use). At the time of the report, EXPIRED PRODUCT ADMINISTERED (We discovered that we've given Moderna Covid-19 vaccine that was beyond the 30 day use by date.) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02-Feb-2022 and dose administered on 14-Mar-2022 beyond 30-day use) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information provided. The vial did not undergo any temperature excursion. No treatment information provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- U
- Eingang
- 25.03.2022
- Impfdatum
- 22.03.2022
- Beginn
- 22.03.2022
- 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 was initially stored in the refrigerator on 02Feb2022, and dose administered on 22Mar2022 beyond 30-day use; We discovered that we've given Moderna Covid-19 vaccine that was beyond the 30 day use by date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We discovered that we've given Moderna Covid-19 vaccine that was beyond the 30 day use by date.) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02Feb2022, and dose administered on 22Mar2022 beyond 30-day use) in a 34-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (We discovered that we've given Moderna Covid-19 vaccine that was beyond the 30 day use by date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02Feb2022, and dose administered on 22Mar2022 beyond 30-day use). At the time of the report, EXPIRED PRODUCT ADMINISTERED (We discovered that we've given Moderna Covid-19 vaccine that was beyond the 30 day use by date.) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02Feb2022, and dose administered on 22Mar2022 beyond 30-day use) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information provided. Date the vial was initially stored in refrigerator 02-Feb-2022 The vial did not undergo any temperature excursion. No treatment information provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 23.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
For unknown reason (not documented in chart) patient received the first Moderna COVID-19 Vaccine dose on 1/27/22 and the second dose of Moderna COVID-19 Vaccine on 2/17/22 which is earlier than 28 days and outside of the 4-day grace period. There were no adverse events associated with administration of the vaccine. Per CDC guidance, doses inadvertently administered earlier than the grace period should not be repeated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- not applicable ? dose given too soon therefore no medical tests/lab results indicated
- Aktuelle Erkrankungen
- Not applicable. Dose administered too soon and other illnesses do not add to assessment
- Vorgeschichte
- Not applicable. Dose administered too soon and patient is not immunocompromised.
- Andere Medikamente
- Not applicable. Dose administered too soon and medications at time of vaccination not necessary
- Allergien
- Not applicable. Dose administered too soon and previous ADRs do not add to assessment
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- 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: unbekannt
Expired product administered
Symptomtext
Administered a Moderna Booster dose on 3/22/22 around 11:29a past the Beyond Use Date of 3/3/2022 and manufactured expiration date of 4/24/2022. Learned of error today when examining number of doses remaining.
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
- 22.03.2022
- Impfdatum
- 14.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Administered a Moderna Booster dose on 3/14/22 around 2:09pm past the Beyond Use Date of 3/3/2022 and manufactured expiration date of 4/24/2022. Learned of error today when examining number of doses remaining.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 15,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Administered a Moderna 2nd dose on 3/7/22 around 12:30a past the Beyond Use Date of 3/3/2022 and manufactured expiration date of 4/24/2022. Learned of error today when examining number of doses remaining.
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
- 22.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Administered a Moderna Booster dose on 3/7/22 around 10:24a past the Beyond Use Date of 3/3/2022 and manufactured expiration date of 4/24/2022. Learned of error today when examining number of doses remaining.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
I was contacted by my district pharmacy manager, he told me that a patient had received an infection from a Moderna COVID vaccination that was given on 01/10/2022. I do not know about adverse events, treatments, and/or outcomes. This was told to me third hand. Never talked to the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- I was contacted by my district pharmacy manager, he told me that a patient had received an infection from a Moderna COVID vaccination that was given on 01/10/2022
- Allergien
- KNDA
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 16.03.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Inadvertently administered Moderna as the second dose versus Pfizer which was given as the first dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none at the time
- Vorgeschichte
- none at this time
- Andere Medikamente
- Acetaminophen
- Allergien
- No known drug allergies
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 02.02.1922
- Beginn
- 05.02.2022
- Tage bis Beginn
- 36.528,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes virus infection
Symptomtext
Herpetic outbreak lasted for two months despite medication
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes virus infection
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Osteoarthritis,
- Andere Medikamente
- Estrogen, progesterone, tumeric, but e and bs, glucosamine, vit k, probiotics
- Allergien
- -
- Vorherige Impfungen
- Moderna
- Staat
- NV
- Alter
- 17,0
- 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: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse reaction, Patient is a 17 year 10 month old 264 pound female that received the Moderna booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No diagnosed medical problems
- Vorgeschichte
- None
- Andere Medikamente
- Iron 325 mg
- Allergien
- No Known Drug Allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
patient reports having lymph node swelling affecting neck, supraclavicular region and left axilla after vaccination. symptoms persisted for more than 6 weeks after vaccination and patient pursued medical evaluation given persistent lymph node swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- labs, chest xray and ultrasounds ordered.
- Aktuelle Erkrankungen
- none known.
- Vorgeschichte
- duane syndrome
- Andere Medikamente
- none
- Allergien
- none known.
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Patient came in with a consent form and Covid card and said she is getting Moderna. Covid Card Said Moderna so we looked at the consent and put the lot and vaccine received on card and consent form. The check in person checked the age based on the year, put Moderna and lot on the consent form so she went the vaccinator to receive the vaccine. Vaccinator asked patient what she received before and looked at everything to verify patient received Moderna before. Either the previous place where patient received the vaccine reported it wrong or the card is wrong. We spoke to mother to inform her what happened and she is aware patient is eligible to get booster in 5 months for Pfizer. Mother was confused because child also told her the first time she got the first dose of Covid vaccine she received Moderna as well. Patient was monitored for 15 minutes after receiving the vaccine. Patient was doing okay and mother is aware.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 28.01.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
administered Moderna Covid-19 vaccines beyond the 30 day use by date to 20 patients; administered Moderna Covid-19 vaccines beyond the 30 day use by date to 20 patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered Moderna Covid-19 vaccines beyond the 30 day use by date to 20 patients) and PRODUCT STORAGE ERROR (administered Moderna Covid-19 vaccines beyond the 30 day use by date to 20 patients) in a 26-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 045L21A and 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2022 at 10:07 AM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 25-Feb-2022 at 9:43 AM, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to .5 milliliter. On 25-Feb-2022 at 9:43 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered Moderna Covid-19 vaccines beyond the 30 day use by date to 20 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (administered Moderna Covid-19 vaccines beyond the 30 day use by date to 20 patients). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered Moderna Covid-19 vaccines beyond the 30 day use by date to 20 patients) and PRODUCT STORAGE ERROR (administered Moderna Covid-19 vaccines beyond the 30 day use by date to 20 patients) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. It was reported that 20 doses from 5 vials were used. The vials were initially stored in the refrigerator on 19-Jan-2022. It was reported that the vials did not underwent temperature excursions. No concomitant medications were reported. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 04-Mar-2022: Non significant follow-up information received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
Product administered to patient of inappropriate age
Symptomtext
Patient received Pfizer for her first dose, Moderna for her 2nd dose (only 17 at time of 2nd dose)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
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 in the refrigerator on25 Jan 2022/ Date of administration of vaccine 03 Mar 2022; Four patients received an expired 30-day use by date booster dose; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Four patients received an expired 30-day use by date booster dose) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator on25 Jan 2022/ Date of administration of vaccine 03 Mar 2022) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 03-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Four patients received an expired 30-day use by date booster dose). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator on25 Jan 2022/ Date of administration of vaccine 03 Mar 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Four patients received an expired 30-day use by date booster dose) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator on25 Jan 2022/ Date of administration of vaccine 03 Mar 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No relevant concomitant medications were provided. The vial was initially stored in the refrigerator on 25 Jan 2022. The vial did not undergo any temperature excursion. It was reported that the patients were not experiencing any symptoms after receiving the vaccine. No treatment information was provided. This case was linked to MOD-2022-503153, MOD-2022-503157, MOD-2022-503162 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- 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
Incorrect dose administered
Symptomtext
The patient was given a booster at the wrong interval and dosage. He received a Janssen vaccine on 1/6/22. A dose of Moderna at 0.5mL was given as a booster on 1/27/2022..
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 07.03.2022
- 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: unbekannt
Inappropriate schedule of product administration
No adverse event
Symptomtext
second dose of Moderna was given on day 21 and not day 28. Given 7 days early. Spoke to patient and he had no adverse reactions to report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 27.03.2021
- Beginn
- 03.03.2022
- Tage bis Beginn
- 341,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Event occurred after vaccination. Patient was diagnosed with Covid Tylenol Inpatient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- Covid test positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, GERD, Migraines, Chronic pain, Anxiety, Adenomyosis, BMI 45
- Andere Medikamente
- -
- Allergien
- Contrast Dye, Dilaudid, Iodine
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge / Patient received vaccine 3 days after use by date; Patient received vaccine 3 days after use by date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine 3 days after use by date) and PRODUCT STORAGE ERROR (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge / Patient received vaccine 3 days after use by date) in a 49-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022j21a) for COVID-19 vaccination. No Medical History information was reported. On 09-Feb-2022 at 4:06 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 09-Feb-2022 at 4:06 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine 3 days after use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge / Patient received vaccine 3 days after use by date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine 3 days after use by date) and PRODUCT STORAGE ERROR (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge / Patient received vaccine 3 days after use by date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant Medications were provided. There was one vial which was been administered after 30 days on fridge (30th day was on 06-Feb-2022). The patient received 1 booster and 1 primary dose. On 09-Feb-2022 the patient received the vaccine almost 3 hours after the first puncture. HCP stated that there was no temperature excursion during the administration of that vial ( the vials were in the fridge). It was reported that the patient experienced no adverse events. 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
- SC
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge; HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge) and PRODUCT STORAGE ERROR (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge) in a 25-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022j21a) for COVID-19 vaccination. No Medical History information was reported. On 10-Feb-2022 at 9:30 AM, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 10-Feb-2022 at 9:30 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge) and PRODUCT STORAGE ERROR (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. The concomitant medications on use were not provided. Patient received vaccine four days after use by date and stated that patient experienced no adverse side effects from vaccine. HCP stated that they received a box of vials on 7 Jan 2022. There was one vial which was used after 30 days being in the fridge (30 days were on 6 Feb 2022) and they administered Moderna COVID-19 vaccine to five patients. The vaccines were administered in the pharmacy. On 10 Feb 2022 the patients received the vaccine one hours after first puncture. HCP stated that there was no temperature excursion during the administration of that vial (the vials were in the fridge). No treatment information was provided. This case was linked to MOD-2022-480636.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge, 3 patients on 10FEB2022 (1 Booster dose and 2 primary doses); This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge, 3 patients on 10FEB2022 (1 Booster dose and 2 primary doses)) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Feb-2022 at 9:42 AM, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 10-Feb-2022 at 9:42 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge, 3 patients on 10FEB2022 (1 Booster dose and 2 primary doses)). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge, 3 patients on 10FEB2022 (1 Booster dose and 2 primary doses)) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication and treatment information was reported. HCP stated that they received a box of vials on 7-Jan-2022. There was one vial which was used after 30 days being in the fridge (30 days were on 6-Feb-2022) and they administered Moderna COVID-19 vaccine to 5 patients. HCP stated that she does not have the personal information of those patients. The vaccines were administered in the pharmacy: 3 patients on 10-Feb-2022 (1 Booster dose and 2 primary doses) and 2 patients on 9-Feb-2022 (1 booster and 1 primary dose ). On 10-Feb-2022 the patients received the vaccine one hours after first puncture and on 9-Feb-2022 the patients received the vaccine almost 3 hours since the first punctured. HCP stated that there is no temperature excursion during the administration of that vial (the vials were in the fridge). Patient had no allergy to medications, food and other products. Patient received vaccine 4 days after use by date, and stated that patient experienced no adverse side effects from vaccine. This case was linked to MOD-2022-480648 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 11-Feb-2022: Follow up received on 11-FEB-2022 Contains non Significant information On 01-Mar-2022: Significant follow up appended- reporter added, patient details added, Product details added,Narrative updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- -
- Geschlecht
- M
- Eingang
- 05.03.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge, 2 patients on 9FEB2022 ( 1 booster and 1 primary dose )./ vaccine 3 days after use by date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge, 2 patients on 9FEB2022 ( 1 booster and 1 primary dose )./ vaccine 3 days after use by date) in a 36-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Feb-2022 at 3:06 PM, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 09-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge, 2 patients on 9FEB2022 ( 1 booster and 1 primary dose )./ vaccine 3 days after use by date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP administered to 5 patients vaccines after 30 days the vaccines were on the fridge, 2 patients on 9FEB2022 ( 1 booster and 1 primary dose )./ vaccine 3 days after use by date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment medication was provided. HCP called to ask about a box of vials that they received on 7JAN2022. There is one vial who was been administered after 30 days on fridge (30 days were on 6FEB2022). The LOT NUMBER of that vial was 022J21A and they administered a Moderna COVID-19 vaccine to 5 patients. HCP stated that she don?t have the Personal information of those patients. The vaccines were administered in the pharmacy: 3 patients on 10FEB2022 (1 Booster dose and 2 primary doses) and 2 patients on 9FEB2022 ( 1 booster and 1 primary dose ). The expiration date of the vial affected is 24APR2022. On 10FEB2022 the patients received the vaccine one hours after first puncture and on 9FEB2022 the patients received the vaccine almost 3 hours since the first punctured. HCP stated that there is no temperature excursion during the administration of that vial ( the vials were in the fridge). This case was linked to MOD-2022-480636 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 11-Feb-2022: Follow up received contains Non significant information. Fax no. updated. On 01-Mar-2022: Report type changed from invalid to spontaneous, drug start date and details, patient and reporter details and event start date updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 04.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient came to drop off window stating he had completed his primary series and had received a booster but now wanted his additional dose because he has cancer, is receiving treatment for cancer and is immunocompromised. We processed the additional dose for the patient. After the shot was administered (full additional dose) I made the patient a new vaccine record card. Upon reviewing patient's clinical services history, the patient had received the primary series and had already received the additional dose and was due for a booster. But patient received a 4th (full dose) instead of booster (half dose). All 4 covid vaccines given were Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Cancer
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 03.03.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
pt vaccinated too early for 2nd dose. no issues with pt at this time
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 02.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- 27.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
I have spoke to patient's father, and he has stated that the child has not has any known adverse reactions
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vital functions abnormal
Symptomtext
absent of vital signs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vital functions abnormal
- Hospital-Tage
- -
- Labordaten
- not applicable
- Aktuelle Erkrankungen
- right tibial fracture
- Vorgeschichte
- COPd, DM type 2, chronic kidney disease
- Andere Medikamente
- norvasc, aspirin, lipitor, colace, insulin glargine, remeron, daily multivitamin, zoloft, aldactone, eliquis, coreg, lasix, tramadol
- Allergien
- Iodine, Penicillin, robaxin, contrast dye
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 02.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- 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
this person requested a home visit and lived in an independent facility. Per he was due for this second dose. when the Rn arrived she had also reviewed system and confirmed he was due for his second dose of moderna. she brought 0.5ml and spoke with the gentleman. he was adamant he was due for his booster dose. he noted he had been given a vaccine second dose while hospitalized. he did not have his vaccine card abut was very clear that if it was not noted in system it was an omission in recording. The RN proceeded to only administer 0.25mg which is the booster dose. The following day while double checking system it was questioned why only 0.25 was administered. The nurse explained the gap in recording. the team did more review and reached out to the hospital who reviewed their system. They noted that no Covid vaccine was given but another vaccine was given while in the hospital. we consulted the CDC website for guidance. Since this was noted not on the same clinical day as the second dose the recommendation was to repeat a full second dose. The RN attempted to reach the person but was unable. she finally made a stop at his residence and administered as recommended by the CDC a full 0.5mg of Moderna on March 1,2022. it was all recorded in system. Nurse observed patient for thirty minutes and gave him proper instructions. All of this was done with his approval
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- COPD and ulcers of his legs obesity living in an independent care facility
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 01.03.2022
- 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
No adverse event
Product storage error
Symptomtext
No adverse reaction noted shot given @ 0730 2/22/22. Vial opened @ 0900 2/21/22 vial was used 1st time 2/21/22 0900 & second time 2/22/22 0730. Refrigerated all the time. 2/28/22 Spoke with employee. No adverse effect after vaccine 2/22/22 Tx for achyness @ night. Spoke with MD director and she suggested following up with employee one month after this 2nd dose. Spoke with employee and will come later this month for booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- 1st COVID shot 1/24/22 Moderna
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 27.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eczema
Feeding disorder
Mouth haemorrhage
Scab
Symptomtext
Crusty, bleeding slits, in corner of mouth. Could not eat. Eczema.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eczema
- Hospital-Tage
- -
- Labordaten
- Went to doctor got prescribed creme. Never had Eczema.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Leukemia
- Andere Medikamente
- Nuvaring, Vitamin B2, Magnesium Oxide, Turmeric, CoQ10
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.02.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
This spontaneous case reported by a pharmacist, describes the occurrence of administered expired product (administered a dose after the 30 days use-by date in the refrigerator) in a patient, of an unknown age and gender, who received mRNA-1273 (Moderna COVID-19 vaccine, batch/lot# 022J21A) for COVID-19 immunization. No medical history reported. On Feb 22, 2022, patient received a dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On Feb 22, 2022, patient administered expired product (administered a dose after the 30 days use-by date in the refrigerator). At the time of the report, administered expired product (administered a dose after the 30 days use-by date in the refrigerator) outcome: unknown. The vial initially stored in the refrigerator on Jan 20, 2022. The reporter did not provide any causality assessments, concomitant medication or treatment information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
SARS-CoV-2 test
Symptomtext
Administered a second dose of the Moderna Covid 19 vaccine from a vial that had been first punctured 22 hours ago; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered a second dose of the Moderna Covid 19 vaccine from a vial that had been first punctured 22 hours ago) in a 20-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 022J21A and 022J21A) for COVID-19 vaccination. The patient's past medical history included COVID-19 (Had twice before receiving the first dose). On 24-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Feb-2022 at 7:30 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 22-Feb-2022 at 7:30 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered a second dose of the Moderna Covid 19 vaccine from a vial that had been first punctured 22 hours ago). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered a second dose of the Moderna Covid 19 vaccine from a vial that had been first punctured 22 hours ago) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: positive (Positive) Twice before receiving the first dose. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient had not reported any symptom after receiving the vaccine. The patient did not take concomitant medication. The vial was initially stored in the refrigerator was on 21 Feb 2022 and punctured on 21 Feb 2022 at 9.00 AM. The vial was exposed to room temperature range for 3 minutes.No temperature excursions reported. No treatment medications reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID Test; Test Result: Positive ; Result Unstructured Data: Twice before receiving the first dose
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (Had twice before receiving the first dose)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 16,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
vaccine given past 30 days of being thawed and stored in refrigerator
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 18,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
vaccine given past 30 days of being thawed and stored in refrigerator
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 18,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
vaccine given past 30 days of being thawed and stored in refrigerator
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 18,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
vaccine given past 30 days of being thawed and stored in refrigerator
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 18,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
vaccine given past 30 days of being thawed and stored in refrigerator
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 25.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 18,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
vaccine given past 30 days of being thawed and stored in refrigerator
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient was given Moderna booster dose. Child is 15 years old. No adverse reactions noted during waiting period.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- 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: nein
Inappropriate schedule of product administration
Symptomtext
Error: Booster given too early.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 24.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
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
- 67,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
covid-19 illness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 21,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient was given booster of Moderna 1 month too soon,patient did not have adverse reactions. patient is aware the booster was given 1 mo early.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no adverse reaction. was given 30 days too early
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 8,0
- Dosis
- UNK
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antinuclear antibody positive
Symptomtext
ANA blood test February 1, 2022 was. Positive 1:160
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Antinuclear antibody positive
- Hospital-Tage
- -
- Labordaten
- ANA Blood Panel February 2, 2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- BPH CKD stage 3a Controlled hypertension Controlled obstructive sleep apnea Kidney stones Peripheral Neuropathy
- Andere Medikamente
- Allopurinol Atorvastatin Dutasteride Tamsulosin Aspirin 81 mg Azelestine Telmisartan
- Allergien
- Fire Ant Venom
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
No adverse event
Symptomtext
no adverse event reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Immunocompromised patient presented for 4th vaccination injection. Patient received full vaccine dose instead of booster dose (.25ml)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- obesity, type 2 diabetes mellitus, hyperlipidemia, ductal carcinoma in situ of left breast
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 12.02.2021
- Beginn
- 14.02.2022
- Tage bis Beginn
- 367,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Maternal exposure during pregnancy
Product temperature excursion issue
SARS-CoV-2 test
Symptomtext
Maternal exposure during pregnancy; Administered with vaccine that has been outside the refrigeration for more than 24 hours; temperature excursion; This spontaneous prospective pregnancy case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered with vaccine that has been outside the refrigeration for more than 24 hours), MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy) and PRODUCT TEMPERATURE EXCURSION ISSUE (temperature excursion) in a 36-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for COVID-19 vaccination. The patient's past medical history included COVID-19. On 12-Feb-2021, the patient received first dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On 03-Mar-2021, received second dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) dosage was changed to 1 dosage form. On 15-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 14-Feb-2022 at 12:30 PM, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (temperature excursion). On 15-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered with vaccine that has been outside the refrigeration for more than 24 hours). On an unknown date, the patient experienced MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy). On 15-Feb-2022 at 4:30 AM, PRODUCT TEMPERATURE EXCURSION ISSUE (temperature excursion) outcome was unknown. At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered with vaccine that has been outside the refrigeration for more than 24 hours) and MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: positive (Positive) Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that about 5.5ml vial that was left outside the refrigerator for more than 24hours (14Feb2022 at 12:30 to 15Feb2022 at 4:30pm) and administered to patient on 15Feb2022. Patient was fine and there is no show of any sign and symptoms. Storage condition at the time of the excursion - Ambient temperature. It was reported maximum or minimum temperatures reached (specified temp is in C or F)- 65 degrees Fahrenheit Excursion duration was 24 hours Vial(s) moved from freezer to refrigerator on 13Feb2022 at 4:00pm Vial was Discarded On Visual inspection noting any vaccine state change Vial was Thawed / in Liquid form Proposed desired Use by Date - Vial used on 15Feb2022 Number of vials/doses impacted-1 (5.5ml) It was reported vials were not punctured before the excursion No concomitant and treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 virus test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- 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: ja
Extra dose administered
Interchange of vaccine products
Symptomtext
08/31/21 Janssen COIVD vaccine given. 01/06/22 Moderna COVID booster, vaccine given. (.25ml) 02/11/22 Moderna COVID vaccine given. (0.5ml) per providers insructions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- Asthma Hepatitis C
- Vorgeschichte
- Asthma, Hepatitis C, Nicotine dependence, allergic rhinitis, overactive bladder.
- Andere Medikamente
- Refresh Tears 0.5 % eye drops Instill 1 drop 4 times a day in both eyes. acetaminophen 325 mg tablet take 2 tablet by oral route every 6 hours as needed for pain or fever. Flonase Allergy Relief 50 mcg/actuation nasal spray,suspension spray
- Allergien
- Tomatoes Penicillin Venom-honey bee
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 17.02.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- 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
Patient was given Moderna vaccine as his 1st dose of COVID-19 vaccine. Patient is fine, and parents are aware and will continue to monitor. Parent also aware that child will receive Pfizer vaccine 28 days after today's vaccine.
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
- Straterra 18 mg, Melatonin 6 mg, Guanfacine 3 mg
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
THERE WERE NO ADVERSE EVENTS TO REPORT. THIS REPORT IS BEING FILED BEACUSE THE PATIENT WAS ADMINISTERED A BOOSTER DOSE FROM A VIAL OF MODERNA VACCINE THAT HAD BEEN OUT OF THE REFRIGERATOR FOR MORE THAN 12 HOURS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Mentally unstable patient who came into the clinic on 02/09/22 requesting for a booster dose. On the clinic record he only had Johnson and Johnson which was administered in september, Unknown to the nurse he had taken pfizer in a different clinic which he talked about after the booster was administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Neuropathy Anosognosia
- Vorgeschichte
- chronic mental illness
- Andere Medikamente
- NO
- Allergien
- Atypical antipsychotics-sedation left numbness
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 15.02.2022
- 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: ja
Product administered to patient of inappropriate age
Symptomtext
The patient, who is a resident of another state came in and requested to receive a Moderna booster dose to his first two Moderna doses that he received on 04/22/2021 and 05/19/2021 at clinic. The patient presented his card showing his previous two Moderna doses. I administered the booster dose. Later that day, I was filing paperwork from that day's vaccines and realized that the patient was 17 at the time that he received all three of his Moderna vaccines. I called the patient, who was fine. I then contacted the clinic where he received the previous two vaccines to confirm his age and that he had received Moderna. The clinic confirmed both and said that they would submit VAERS reports.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- 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
No adverse event
Symptomtext
Booster dose of Modern a given at 3 months and 2 weeks. No adverse medical event experienced by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 15.02.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Interchange of vaccine products
No adverse event
Symptomtext
At work-based community clinic, patient received two doses of vaccine on the same day (different brands). After receiving first dose, patient got back in line for a different dose. No adverse effects reported or noted during waiting period for either.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 13.02.2022
- Impfdatum
- 28.01.2020
- Beginn
- 30.01.2020
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram T wave inversion
Symptomtext
Giant T-Wave on EKG
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram T wave inversion
- Hospital-Tage
- -
- Labordaten
- 12lead EKG with cardiologist
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetic
- Andere Medikamente
- Insulin (Novalog, Basaglar) Vit D Multivitamin Fish oil
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gait inability
Symptomtext
Patient says he is not able to walk after getting the shot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gait inability
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Back pain and nerve pain in lower extremities
- Vorgeschichte
- heart disease
- Andere Medikamente
- Zetia, Coreg, Prednisone, Trelegy, Crestor, Ventolin, Nexium, Repatha, Lasix, Robaxin, plavix, Lisinopril
- Allergien
- Prilosec
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 6,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient is 6 years old and the Moderna vaccine is not approved for him. No adverse events have been reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exposure during pregnancy
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Moderna Covid-19 vaccine administered to unauthorized age group. Patient was only 17 years of age. No reactions or symptoms to report. No pregnancy complications to report at th is time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure during pregnancy
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Pyridoxine, Prenatal Plus
- Allergien
- Delsuym
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
Expired dose given to patient; It was taken out of the freezer and placed in the refrigerator on 29-Jan-2022. The vial was punctured on 02-Feb-2022 at 10:00 AM; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose given to patient) and PRODUCT STORAGE ERROR (It was taken out of the freezer and placed in the refrigerator on 29-Jan-2022. The vial was punctured on 02-Feb-2022 at 10:00 AM ) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Feb-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose given to patient) and PRODUCT STORAGE ERROR (It was taken out of the freezer and placed in the refrigerator on 29-Jan-2022. The vial was punctured on 02-Feb-2022 at 10:00 AM ). On 03-Feb-2022, EXPIRED PRODUCT ADMINISTERED (Expired dose given to patient) and PRODUCT STORAGE ERROR (It was taken out of the freezer and placed in the refrigerator on 29-Jan-2022. The vial was punctured on 02-Feb-2022 at 10:00 AM ) had resolved. 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 an excursion where product was administered 27 hours after the vial was punctured. The Moderna vial, Lot # 022J21A , was taken out of the freezer and placed in the refrigerator on 29-Jan-2022. The vial was punctured on 02-Feb-2022 at 10:00 AM and a doses was administered on 03-Feb-2022 between 10 am and 1pm. The punctured vial remained at room temperature. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 50,0
- 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: ja
Expired product administered
No adverse event
Symptomtext
VACCINE ADMINISTERED (02/07/2022) AFTER BEYOND USE DATE(02/06/2022).CUSTOMER IS FINE AND NO ADVERSE EFFECTS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 19,0
- 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: ja
Expired product administered
Symptomtext
VACCINE ADMINISTERED (02/07/2022), THE DAY AFTER BEYOND USE DATE (02/06/2022).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Genital lesion
Herpes simplex
Symptomtext
5 days after receiving the COVID booster patient had reactivation of HSV1 viral lesions in the genital area. Last and only outbreak was 6 years ago. Multiple lesions (4). No other side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Genital lesion
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Reports that at the age 16 she received 2 vaccines (she thinks one was the second dose of HPV and attributes it to this). Shortl
- Staat
- WI
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- 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: nein
Product storage error
Symptomtext
Moderna vial was first punctured on 2/3/22 6 pm (room temp) and was to expire at 6 am on 2/4/22. Patient recevied an adminstration of booster dose from this vial at noon on 2/4/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
No adverse event
Symptomtext
On 09/27/2021, pt entered our facility and reported receiving unknown COVID vaccine. Per P&P, Intake RN placed an order to "review for COVID 19 Vaccination." On 10/16/2021, staff RN completed the order prior to confirming vaccination information. On 01/28/2022, pt. placed a sick call slip "requesting to get a COVID shot." Staff RN placed an order to "Administer COVID 19 Vaccine Order" per our P&P. On 02/02/2022, pt received Moderna 0.5 dose to left arm, monitored for 15 minutes with no adverse reaction. It was later identified that the patient had already received 1st and 2nd doses of vaccines while in the process of inputting COVID-19 vaccination information in the system. Immediately, pt. was re-evaluated with no s/s of adverse effects r/t to the vaccine and confirmation received that his intention was to receive a booster. Action Plan: To review all patients COVID vaccination history/status in the system prior to placing order/administering COVID-19 vaccines. We will update our current COVID-19 vaccination consent to include the question, "Have you received a COVID-19 vaccination."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HYPERTENSION
- Andere Medikamente
- Amlodipine 5 mg po @ 9:02 AM
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
Patient received second dose of the moderna Covid-19 vaccine 7days early. Patient was observed for 15 minutes after receiving the dose. No adverse reactions occurred during that time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Patient came to the clinic for her booster dose of the COVID vaccine, with her mother. The front desk gave them the forms to fill out and then brought the completed forms to this RN. The MA then took the forms and gave the patient the Moderna booster vaccine. The MA noticed the patients age after the vaccine was given when she was putting the encounter in the chart. This RN called the patient's mother and advised her of the situation, provided information on what happened and what side effects to be aware of. Mother verbalized understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Confusional state
Lethargy
Symptomtext
patient extremely confused & lethargic. Patient was taken to the emergency room and admitted to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Confusional state
- Hospital-Tage
- 11,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 29.01.2022
- Beginn
- 30.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
1st shot Covid Moderna was given to kid younger than 18 years old at the health clinic by error.
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
- nka
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient administered Moderna vaccine rather than the pediatric approved Pfizer dose.
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
- NKDA/NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Oedema peripheral
Swelling
Symptomtext
Edema to left arm and hand- resident stated that the swelling was noted overnight, CRNP notified-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oedema peripheral
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Hydro nephrosis, Urinary retention
- Vorgeschichte
- GERD, HTN, Hypothyroidism, Anxiety, Type 2 DM, CKD, Hypotonic, bladder, Hyperlipidemia
- Andere Medikamente
- Acetaminophen, Clonazepam, Insulin, Tamsulosin, Pregabalin, Senna, Pramipexole, Miralax, Potassium Chloride, Metoprolol, Isosorbide , Synthroid, Ezetimibe, Clopidogrel, Duloxetine, Calcium Carbonate, Buspirone, Atorvastatin
- Allergien
- Tape
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Patient administered Moderna vaccine that has been at room temperature greater than 12 hrs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Symptomtext
No adverse event known at time of reporting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- diabetes, hx of kidney ca
- Andere Medikamente
- metformin, creon
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Skin warm
Tenderness
Symptomtext
Patient called ADR line complaining of warm, tender spot above ankle 2 days after receiving Moderna COVID vaccine (2nd dose). Patient instructed to seek immediate medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Skin warm
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Dose administered after discard time No adverse effect
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Patient was administered a dose of Moderna that was at room temperature greater than 12hrs after first puncture. No known adverse events at time of report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies.
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Product storage error
Symptomtext
Patient was administered a dose of Moderna that had been at room temperature for greater than 12 hrs after first puncture. Patient was due for a booster dose and was give 0.5mL dose -per chart review. No known adverse reaction at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.01.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Moderna vaccine given 12 hours after opening; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna vaccine given 12 hours after opening) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna vaccine given 12 hours after opening). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna vaccine given 12 hours after opening) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication details was reported. No treatment medication details was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immunodeficiency
Incorrect dose administered
No adverse event
Symptomtext
Patient is immunocompromised having recently completed chemotherapy at the end of December 2021. He came to the pharmacy for his 3rd dose of Moderna vaccine which should have been the full dose of 0.5ml. He was mistakenly given what a non-immunocompromised individual would get as a booster dose of 0.25ml of Moderna vaccine. No symptoms or issues reported by the patient or caregiver. Patient is coming in later to receive proper dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunodeficiency
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cancer patient; completed chemotherapy near the end of December 2021.
- Vorgeschichte
- Cancer
- Andere Medikamente
- -
- Allergien
- No known drug allergies.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
15 year old inadvertently was administered Moderna 0.50 mL as her first dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- -
- Geschlecht
- U
- Eingang
- 25.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
administered with vaccine from a vial punctured for more than 12 hours; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with vaccine from a vial punctured for more than 12 hours) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 21-Jan-2022 at 8:40 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with vaccine from a vial punctured for more than 12 hours). On 21-Jan-2022, EXPIRED PRODUCT ADMINISTERED (administered with vaccine from a vial punctured for more than 12 hours) had resolved. 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. No concomitant and treatment Drug details were reported. The vial was 1st punctured on 20Jan2022 at 11:53am. The 1st dose vial was exposed to room temperature for greater than 24 hours-21 hrs. This case was linked to MOD-2022-458007 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- -
- Geschlecht
- U
- Eingang
- 25.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- 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
administered with a vaccine from a vial which has been punctured for more than 12 hours; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with a vaccine from a vial which has been punctured for more than 12 hours) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022J21A) for COVID-19 vaccination. No Medical History information was reported. On 21-Jan-2022 at 10:00 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Jan-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with a vaccine from a vial which has been punctured for more than 12 hours). On 21-Jan-2022, EXPIRED PRODUCT ADMINISTERED (administered with a vaccine from a vial which has been punctured for more than 12 hours) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The vial was first punctured on 20-Jan-2022 at 11:53 AM. Concomitant medication was not provided. Treatment information was not provided. This case was linked to MOD-2022-458066 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Incorrect dose administered
Symptomtext
Pt had received booster dose from us at Pharmacy on 12/02/2021 at the 0.25 ml dose after having received a J&J vaccine earlier in 2021. Pt's mother signed up pt for an additional Moderna vaccine believing that she needed a second dose and an additional dose was administer on 01/24/2022 as though it was a second dose for the pt at the dose of 0.5 ml.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- 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 partially 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
- OH
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Heart rate increased
Symptomtext
RAPID HEART RATE UP TO 160
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate increased
- Hospital-Tage
- -
- Labordaten
- I HAD THIS HAPPEN BEFORE BUT IT HAS BEEN A LONG TIME. I WAS WORKED UP BUT NO CAUSE FOUND. LATER I WAS DIAGNOSED WITH HEREDITARY HEMOCHROMATOSIS SO I FIGURED IT WAS RELATED TO THAT. I HAD 25MG METOPROLOL ON HAND AND I TOOK IT. IT RESOLVED WHEN THE MEDICATION TOOK AFFECT.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- ASTHMA NORMAL TENSION GLUACOMA HEREDITARY HEMOCHROMATOSIS
- Andere Medikamente
- WILL FILL IN LATER
- Allergien
- COUGHING WITH PROPOFOL DURING COLONOSCOPY 2011
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Blood pressure decreased
Heart rate decreased
Peripheral coldness
Symptomtext
Patient explained past history of syncopal episodes after injections. At 1103 AM on 01/17/2022 she got Moderna booster vaccine dose 0.25 ml. (Lot 22j21a) and immediately said she wanted to lie down. Provider laid patient on the floor and at 1106 AM her Pulse was 55 BP was 85/55 Her hands were cold. She remained alert oriented as said she did not want 911 to be called. There was no wheezing no itching no shortness of breath. No swelling, no redness of face or tongue, or any other allergic type reactions. Her Vitals at 1110 were pulse were last recorded at 11:25am of 102/69 and 61 respectively. She was given juice and[INVALID]s and was able to eat without problems and she sat for an addition half hour until she felt good enough to go home. Faint with needle injections.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Error: Booster Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Error: Booster Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Error: Booster Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Product administration error
Symptomtext
Error: Booster Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Menstruation irregular
Symptomtext
Menstrual Period Irregularity, i.e., patient taking Yasmin drospirenone and ethinyl estradiol active hormonal pills began menses
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstruation irregular
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
GAVE PATIENT A FULL 0.5 ML DOSE OF MODERNA INSTEAD OF 0.25 ML PER CDC GUIDELINES FOR PATIENTS WHO ARE IMMUNOCOMPROMISED. PATIENT AND PATIENT'S DOCTOR REQUESTED THE 0.5 ML DOSE. NO CURRENT SIDE EFFECTS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -