- Staat
- -
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 11.07.2023
- Impfdatum
- 20.04.2022
- Beginn
- 20.03.2023
- Tage bis Beginn
- 334,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Biopsy kidney
Blood creatinine increased
Blood glucose normal
Computerised tomogram thorax abnormal
Dyspnoea
Fatigue
Haemodialysis
Hypoglycaemia
COVID-19
COVID-19 pneumonia
Catheter placement
Chest X-ray abnormal
Computerised tomogram abdomen normal
Lung infiltration
Lung opacity
Metabolic acidosis
Symptomtext
Patient is a 76 y.o. male patient of DO with history of type 2 diabetes with previous diabetic foot wound, paroxysmal atrial fibrillation, OSA intolerant to CPAP presented to Hospital with acute shortness of breath. Acute respiratory failure with hypoxia secondary to COVID-19 pneumonia Acute renal failure, possibly due to COVID-19 Metabolic acidosis, likely due to renal failure, resolved OSA, untreated Patient presented after developing shortness of breath and generalized fatigue yesterday On presentation oxygen was in the 60s and did respond well to nonrebreather Chest x-ray reviewed that shows diffuse bilateral interstitial infiltrate CT of the chest abdomen pelvis showed multifocal patchy opacities within the chest bilaterally concerning for viral pneumonia, no hydronephrosis or other abnormality noted within the abdomen or pelvis Positive for COVID-19 on admission Continue dexamethasone 6 mg daily Completed course of Remdesivir Continue supplemental oxygen to maintain oxygen saturation greater than 88%, will use BiPAP if necessary on 3L O2. Continue to wean off as tolerated Acute renal failure requiring hemodialysis Unclear etiology of acute renal failure CT of the abdomen pelvis not show evidence of hydronephrosis Creatinine significantly elevated at 7.65 on presentation UA unremarkable S/p tunneled catheter placement and kidney biopsy per IR 3/27 Undergoing hemodialysis per nephrology FU pathology report Type 2 diabetes with diabetic foot wound and long-term insulin use History of osteomyelitis of the foot currently on outpatient IV antibiotics Known history of type 2 diabetes with most recent A1c of 7.7 Blood sugars have been under adequate control at home Was hypoglycemic on arrival so we held basal insulin and started sliding scale insulin Basal insulin increased to 40 units last night Blood sugar at goal Continue sliding scale insulin Continue to monitor blood sugars and adjust regimen as necessary He is currently on cefepime and vancomycin for recent diabetic foot wound No evidence of worsening infection, appreciate ID recommendations, completed cefepime 3/24. Continue wound care and wound VAC management but budipine. Outpatient follow-up with primary podiatrist Paroxysmal atrial fibrillation Patient has history of paroxysmal atrial fibrillation, likely stress-induced Currently in normal sinus rhythm with rate controlled Not currently on anticoagulation as it was a one-time episode OSA Known history of OSA and has been able to tolerate CPAP so he is not on CPAP at home Is having acute respiratory failure with concerns for COVID-pneumonia as discussed above Continue supplemental oxygen to maintain oxygen saturation greater than 88% but if unable to maintain saturation he may require BiPAP given his acute respiratory failure and COVID-pneumonia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 15,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Cerebral haemorrhage
Cerebrovascular accident
Symptomtext
APPROXIMATELY 9PM ON 9/22/22 IN THE EVENING AFTER COVID 19 BOOSTER SHOT, PATIENT, SUFFERED A BRAIN BLEED (STROKE). SUBSEQUENT TO HOSPITALIZATION, PATIENT TRANSFERRED TO REHABILITATION FOR 32 DAYS THEN HOME CARE FOR 10 DAYS, NOW IN OUTPATIENT PHYSICAL, SPEECH, AND OCCUPATIONAL THERAPY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebral haemorrhage
- Hospital-Tage
- 15,0
- Labordaten
- FIFTEEN DAY AT HOSPITAL, 32 DAYS AT REHAB
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- DIABETES, TYPE 2 HEART MURMER
- Andere Medikamente
- Metformin Simvastatin Lisinopril Methylphenidate HCl Vitamin D3 Ferrous-sulphate Sertraline amLODIPine Pantoprazole
- Allergien
- APPLES
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 04.11.2022
- Impfdatum
- 28.03.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 221,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Patient expired 11/4/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Stage IV metastatic cecal adenocarcinoma
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 26.09.2022
- Impfdatum
- 08.04.2022
- Beginn
- 18.09.2022
- Tage bis Beginn
- 163,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Diarrhoea
Hypovolaemic shock
Norovirus infection
SARS-CoV-2 test positive
Septic shock
Symptomtext
Patient up to date on COVID vaccines who admitted with COVID detected PCR and possible complications from COVID. No hypoxia during stay. Provider d/c note: "73 YO male with CKD, CAD, cardiomyopathy and COPD. Came in with weakness and was found to be in shock. Likely a combination of septic shock and hypovolemic shock. He required a very short course of pressors in the ER but recovered quickly. The patient was noted to have COVID and Norovirus infection. No bacterial infection was found. The patient was treated with supportive care. Patient didn't require any oxygen or have any respiratory symptoms. His diarrhea resolved and he was discharged home in a stable condition."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Septic shock
- Hospital-Tage
- 3,0
- Labordaten
- COVID Detected PCR on 9/18/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular Cardiomyopathy (*) Chronic systolic congestive heart failure (*) Coronary artery disease involving native coronary artery of native heart without angina pectoris Essential hypertension, benign Mixed hyperlipidemia Generalized ischemic myocardial dysfunction Hypertension Digestive GERD (gastroesophageal reflux disease) Norovirus Endocrine Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (*) Diabetic ulcer of toe of right foot associated with type 2 diabetes mellitus, with fat layer exposed (*) Diabetic ulcer of toe of right foot associated with type 2 diabetes mellitus, with fat layer exposed (*) Psychological MDD (major depressive disorder), recurrent episode, moderate (*) Severe episode of recurrent major depressive disorder, without psychotic features (*) ADD (attention deficit disorder) Respiratory Chronic maxillary sinusitis COPD (chronic obstructive pulmonary disease) (*) Obstructive sleep apnea syndrome Urinary Stage 3a chronic kidney disease Other Cardiac defibrillator in place Gout Other chronic pain Benign prostatic hyperplasia
- Andere Medikamente
- -
- Allergien
- Atorvastatin, Metformin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 02.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Amnesia
Asthenia
Balance disorder
Cerebrovascular accident
Computerised tomogram head abnormal
Transient global amnesia
Visual field defect
Symptomtext
He got his vaccine, he woke up 2 days after with no energy whatsoever, and very poor equilibrium and very poor peripheral vision in his right eye. It stayed about the same, and did not think too much about it at the time, but went to the doctor in August. From there he also went to an eye surgeon and had a CT scan done and the prognosis was that he had a occipital stroke that affected his equilibrium and lost 30% of the peripheral vision in the right eye. He did not have any problems with his vision prior to the vaccine. He went to the ER on 8/28/22 where he had a sudden complete loss of memory and was diagnosed as transient global amnesia. This lasted for about 15 hours which cleared on it's own. He was admitted over night to the hospital. Since his diagnosis he has gone for another CT scan and has seen a neurologist who has scheduled an EEG which he is going to have on Thursday and had the CT yesterday. His name is Dr. at Hospital. He saw her for the first time on 9/6/22. She added a baby aspirin to his regimen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 1,0
- Labordaten
- CT scans and EEG.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Pantoprazole, Atorvastatin.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 07.01.2021
- Beginn
- 09.08.2022
- Tage bis Beginn
- 579,0
- Dosis
- 4
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anisocoria
Atrial fibrillation
Blood pressure abnormal
Bradycardia
COVID-19
Condition aggravated
Death
Dyspnoea
Echocardiogram abnormal
Ejection fraction decreased
Endotracheal intubation
Haemodynamic instability
Pulseless electrical activity
Resuscitation
SARS-CoV-2 test positive
Whole body scan
Symptomtext
74y.o. male patient with PMH of COPD/asthma, A. fib not on AC, and possible CHF who presented with SOB and A. fib with RVR with rates to 180 and SBP in 70s. In the ED the patient received IV fluids with a recovery of his blood pressure. 5 mg IV metoprolol was given for rate control in addition to home metoprolol. The patient quickly became bradycardic and went into PEA. CPR was started and ROSC was achieved after 3 rounds of epi. The patient was intubated and sedated and started on 4 pressors, broad-spectrum antibiotics. Echo revealed EF 15%, pan scan demonstrating findings concerning for pneumonia, cholecystitis, shock bowel, small punctate hemorrhage versus calcification in the periventricular white matter. General surgery, cardiology, neurosurgery were consulted. The patient had anisocoria on 8/10 prompting stat neurosurgery consult. A CT scan was ordered but given the patient's hemodynamic instability, the patient was not transferred for completion of the scan. Family was called and the situation was explained. Family expressed that patient would not have wanted to be on life support and changed the patient's CODE STATUS to DNR/DNI. The family then came to the hospital for compassionate extubation, which was performed on 8/10 at 1400. The patient expired with family at the bedside.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- 8/9 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angiopathy
Atrial fibrillation
Balance disorder
Blood electrolytes normal
Blood glucose normal
Brain natriuretic peptide increased
Bundle branch block right
Cardiomegaly
Cerebrovascular accident
Chest X-ray abnormal
Chromaturia
Computerised tomogram head abnormal
Dysstasia
Electrocardiogram abnormal
Fall
Full blood count normal
Liver function test normal
Magnetic resonance imaging head abnormal
Symptomtext
5/4/22-Patient brought to Emergency Department by EMS secondary to bilateral leg weakness leading to a fall. Reported legs feeling weak for past week, hard time getting up or standing, veering to R when walking. No headache focal weakness or problems with speech. Balance problems persisted and resulted in fall. Able to get herself up. MRI and head CT interpreted by Neurology per H&P "...stroke had happened probably a week, and there is evidence of bleeding but more petechial hemorrhage but probably from an underlying ischemic stroke."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- 5/4/22 - MRI and CT of head. EKG - atrial fib with slow ventricular response, right bundle branch block CXR - moderate cardiomegaly with atypical vascular congestion. blood glucose 123 UA was yellow, clear, specific gravity 1.025, trace leukocyte, WBC 11-50. BNP - 1730, troponin < 0.0.4 electrolytes, renal & hepatic, CBC - wnl
- Aktuelle Erkrankungen
- 5/2/22-urinary tract infection
- Vorgeschichte
- CAD s/p CABG Hx of breast cancer iron deficiency anemia Sjorgen disease of eye hyperlipidemia Hypertension diverticulitis post colectomy fibromyalgia major depression, anxiety bronchial asthma chronic atrial fibrillation post AtriClip - no anticoagulation
- Andere Medikamente
- metoprolol diazepam lamotrigine zolpidem pantoprazole atorvastatin olanzapine
- Allergien
- oxycodone (Itching) codeine (Hives) morphine (hives)
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Nausea
Nocturia
Symptomtext
Patient reported feeling nauseated the morning 4/13/22; vaccine administered 4/13/22 at 1539. Patient was up several times throughout noc to bathroom. Last observed well at 0530 on 4/14/22. Patient was noted deceased just prior to 0800 on 4/14/22 when CNA went to wake for bath. No signs of localized reaction from injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- COPD; Alzheimers; Restless Legs syndrome; essential hypertension; Type 2 diabetes; major depressive disorder; insomnia; hypothyroidism; gastro-esophageal reflux disease; macular degeneration (bilateral); chronic systolic heart disease; slow transit constipation; cognitive communication deficit; venous insufficiency.
- Andere Medikamente
- Acetaminophen ER 650 mg PO daily; Amlodipine 10 mg PO daily; Clonazepam 0.5 mg PO QHS; Desvenlafaxine Succinate ER 50mg PO Daily; Enulose 10g/15ml, 30 ml PO BID; Furosemide 20 mg PO daily; Ibuprofen 400 mg PO Daily; Irbesartan 300 mg PO
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Malaise
Symptomtext
Woke up sick on tuesday april 5th, found dead in his apartment on wednesday april 6th.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Gluacoma
- Andere Medikamente
- Latonaprost,Timolol
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 05.04.2023
- Impfdatum
- 02.04.2022
- Beginn
- 11.09.2022
- Tage bis Beginn
- 162,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Bell's palsy
Blood test normal
COVID-19
Computerised tomogram normal
Feeling abnormal
Insomnia
Productive cough
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I woke up with a scratchy throat and didn't feel right. The next day, I woke up and tested myself for COVID-19. The result was positive. I called my doctor's office to get medication. I don't remember the name of it. We picked up the prescription. I took it for the prescribed course. I tested positive for COVID-19 during that time. I had a hard time sleeping. I had a lot of phlegm. Otherwise, it wasn't that bad. Towards the end of 10 days, I tested negative for COVID-19, but I still felt very weak. After a few days, I tested positive for COVID-19 again. I called my doctor back. They told me to quarantine again. After 10 days, I tested negative again. A few days after that, I came down with Bell?s Palsy. I went to the hospital to confirm whether it was Bell?s Palsy or a stroke. They ran tests and prescribed more medications. It took several weeks to get over it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- 09/12/2022 At Home COVID-19 Test - Positive; 10/2022 CT Scan - Normal; 10/2022 Blood Work - Normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic Pain; Chronic Migraines; Osteoporosis; Barrett's Esophagus; Asthma
- Andere Medikamente
- Topiramate; Betamethasone; Breo Ellipta Inhaler; Gabapentin; Metoprolol; Pantoprazole; Ventolin Inhaler; Fluticasone; Simvastatin; Myrbetriq; Celecoxib; Montelukast; Reclast Infusion; Calcium Citrate; Ultravitamin; Vitamin C; Zinc; Magnesiu
- Allergien
- Bees; Tree Nuts; Garlic; Keflex
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 14.10.2022
- Impfdatum
- 02.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 19,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angiocardiogram
Atrial fibrillation
Atrial flutter
Cardiac stress test
Dizziness
Dyspnoea
Echocardiogram
Electrocardiogram abnormal
Electrocardiogram ambulatory
Magnetic resonance imaging heart
Presyncope
Supraventricular tachycardia
Tachycardia
Symptomtext
Tachycardia, SOB and light-headedness with near syncope with exertion noted 04/21/2022. During visit with primary care on 06/23/2022, abn ECG noted. Follow up with cardiologist on 08/25/2022 with diagnosis of supraventricular tachycardia, atrial flutter, paroxysmal atrial fibrillation and possible Wolff Parkinson White syndrome and possible hypertrophic cardiomyopathy. Tests included 48-hour Holter monitor August 8-11, 2022; Transthoracic resting echocardiogram August 30, 2022; Exercise stress test 09/21/2022; cardiac MRI/MRA October 6, 2022. A catheter ablation procedure is scheduled on November 30, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- Tests included 48-hour Holter monitor August 8-11, 2022; Transthoracic resting echocardiogram August 30, 2022; Exercise stress test 09/21/2022; cardiac MRI/MRA October 6, 2022.
- Aktuelle Erkrankungen
- Essential hypertension
- Vorgeschichte
- Scoliosis and kyphosis with chronic neck and back pain
- Andere Medikamente
- Hydrochlorothiazide 12.5 mg daily
- Allergien
- penicillin; sulpha; cefpodoxime
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 03.09.2022
- Impfdatum
- 13.04.2022
- Beginn
- 31.07.2022
- Tage bis Beginn
- 109,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Cerebellar infarction
Cerebellar stroke
Condition aggravated
Hypertension
Magnetic resonance imaging head abnormal
Malaise
Muscular weakness
Nausea
Oedema
Pain in extremity
SARS-CoV-2 test positive
Synovial cyst
Ultrasound Doppler
Ultrasound Doppler abnormal
Vertigo
Vomiting
Symptomtext
Age: 88 y.o. Admit Date: 7/31/2022 9:54 AM Discharge Date: 8/6/2022 Admitting Physician: Discharge Physician: Discharge Diagnosis: Principal Problem: Cerebellar stroke Active Problems: Internal carotid artery stenosis, left Primary hypertension Vertigo DM type 2 (diabetes mellitus, type 2) HPI: Patient is a 88 y.o. male with a history below admitted for Vertigo. Pt came in with complaints of nausea, vomiting, starting 5am. Noticed room appeared to be spinning. Worse with movement. Vomitus was bilious. No abdominal pain / tenderness. Recent covid infection, but no longer symptomatic and only had mild course. No suspicious foods or recent sick contacts. No fever / chills, no diarrhea / constipation. Discussed with er. Will admit Hospital Course: No notes on file He was initially admitted to the coverage unit after he tested positive for COV ID?19 infection. He was initially diagnosed with this medical condition last July 8. Osseous already completed his quadrant. He was transferred to neurology floor. He had MRI of the head that shows an acute infarct in the right cerebellum measuring 1.5 cm. Carotid ultrasound was done and it showed a possible greater than 70% stenosis of the left ICA. Permissive hypertension was observed. He was seen by PT, OT, ST. He was started on aspirin. He was seen by neurology. His condition improved he was also seen by possible surgery and further review of the don't think patient has significant stenosis. He is currently doing better. He'll be discharged to rehabilitation center today. He will follow up with vascular surgery in 6 months. Discharge was held for a day as he was complaining with leg pain. Venous doppler did not show DVT and there was popliteal cyst. He is doing better and will be discharged to rehab today. Physical Exam on the Date of Discharge: Physical exam: General Appearance: alert, NAD Neck: no JVD, no LN enlargement Lungs: clear, no wheezing Heart: RRR, S1 S2 heard Abdomen / GI: soft, non-tender, no ascites Extremities / musculoskeletal: edema, no synovitis Skin: no rash, dry skin Neuro: follows commands, moves extremities with right leg weakness Consults: IP CONSULT TO SOCIAL WORK IP CONSULT TO VASCULAR SURGERY IP CONSULT TO NEUROLOGY Significant Diagnostic Studies: Mri head as above Disposition: SNF Discharge Condition: good
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebellar stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 17.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Cardiac imaging procedure abnormal
Cardiac valve disease
Chills
Chordae tendinae rupture
Computerised tomogram
Condition aggravated
Dyspnoea
Echocardiogram
Electrocardiogram
Fatigue
Feeling abnormal
Headache
Heart rate abnormal
Myocardial necrosis marker increased
Pain
Poor quality sleep
Pulmonary oedema
Symptomtext
I am a 62 year old man with congenital heart disease. I had my second open-heart surgery at age 16 to close a ventricular septal defect. For the most part since then, except for some ablations, I have been healthy and well. All of my COVID-19 shots have been from MODERNA. I have not been infected by COVD-19 thus far. Back on April 6, 2022 at 5pm, I received my second booster. I did not sleep well that night and felt poorly upon waking up. I had a headache, body aches, fatigue, chills and slight fever. Later that day I started to have shortness of breath and an abnormal heart rhythm. The next day I continued to get worse and I went to the hospita l thinking I had the virus. After some tests it was confirmed that I did not have COVID-19, but I did have fluid in my lungs and an enhanced heart enzyme level. Over the next few nights I visited 3 emergency rooms and ended up with an MRI on my heart. The report indicated that 2 of the chorae connecting my mitral valve had broken off. I know there is little research about the impact your COVID-19 vaccine on the heart, but I believe there is some connection here. It is too much of a coincidence to have the vaccine and feel the way I did soon afterwards. Please know that my cardiologists have noted a problem with my mitral valve for over 10 years. Did the shot adversely affect my heart, so that the chordae broke off? I am unsure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary oedema
- Hospital-Tage
- 17,0
- Labordaten
- CAT SCAN, MRI, ECHOCARDIGRAM,EKG, BLOOD WORK
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Congential Heart Disease. VSD repair at ages 3 and 16.
- Andere Medikamente
- Lisinipril, Metotoporal, Furesomide
- Allergien
- Peniclllin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 29.03.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Cardiac monitoring
Chest pain
Decreased appetite
Dyspnoea
Echocardiogram abnormal
Electrocardiogram
Exercise tolerance decreased
Fatigue
Fear
Influenza like illness
Injection site pain
Injection site swelling
Pericardial effusion
Pericarditis
Symptomtext
I experienced general arm pain and swelling at the site of the injection fairly immediately and typical flu like symptoms beginning approximately 24 hours after my 2nd Moderna Booster. The flu-like symptoms laster approximately 36 hours and after recovering I was left with a lingering fatigue. On Sunday 4/3/22 I experienced mild, brief chest pain at approximately ten AM - it left quickly and I felt unconcerned as it left within 15 or so minutes on its own. I went to the gym at 3 PM the same day planning to jog on the treadmill for 30 minutes as I often do. I felt fatigued so started at a 2.0 MPH walking speed. Within ten minutes I was struggling as if I was walking up a steep hill (treadmill was completely flat). I continued for another ten minutes and became quite distressed as I was having tremendous difficulty catching my breath. I laid down on a bench for about 20 minutes until a friend drove me home. I recovered except for still experiencing lingering fatigue and I had little appetite. At ten PM i was sitting in bed and realized I was once again having chest pain - it was stronger than before and I was quite concerned, so I checked my blood pressure using a home monitor - it was 176/110. I phoned a friend to take me to my local ER Health Hospital as I feared I was having a heart attack! I was evaluated and kept in the ER for 17 hours before being placed on a floor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- While hospitalized I had my vitals and heart monitored the entire duration of my stay, I had several blood tests, an EKG, and an echocardiogram. I was discharged on 4/5/2022: "Patient was cleared for discharge with clinical presentation, motely related to pericarditis or pleuritic finding after a booster shot for COVID she took". My cardiologist personally looked at the Echo and observed fluid on my pericardium and diagnosed me with Pericardial Effusion and I am being treated for that presently.
- Aktuelle Erkrankungen
- Ear Shingles
- Vorgeschichte
- COPD/Asthma (no medication after completing a course of acupuncture several years ago)
- Andere Medikamente
- Acyclovir 400 mg tablets & cream PRN
- Allergien
- Gluten
- Vorherige Impfungen
- After my first Moderna vaccine I experienced high blood pressure for the first time in my life. I had a thorough cardiac checku
- Staat
- NY
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 13.05.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Symptomtext
Systemic: Bell's Palsy-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 15.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Chills
Computerised tomogram
Cough
Hernia
Loss of consciousness
Pneumothorax
Positron emission tomogram
Pulmonary mass
X-ray
Symptomtext
Chill all night leading to cough to the extreme of passing out Hospital found lung colapsed, mass in lung, torn herniaon rt side from coughing lower rt lung collapse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- CAt Scan PET scan xray
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Controlled blood pressure and colesteral
- Andere Medikamente
- All once a day Hydrochlorothiazide 25mg Atorvastatin 10mg Aspirin 81 mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 06.04.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 27,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Ageusia
Anosmia
COVID-19
Chest X-ray
Chest discomfort
Chills
Cough
Deep vein thrombosis
Dyspnoea
Fatigue
Headache
Myalgia
Pain in extremity
Peripheral swelling
Photophobia
Pyrexia
Rash
Symptomtext
I contracted COVID-19 on 5/3/2022 with symptoms of cough, congestion, fever, chills, rashes, ear ringing, myalgia, extreme fatigue, chest tightness, shortness of breath, loss of smell and taste, abdominal pain, severe headache, and light sensitivity. I was prescribed Guaiatussin Apfy, and began taking it on 5/8/2022. I have been using my Neti Pot once daily and Fluticasone. My symptoms have not resolved as of yet. I experienced Deep Vein Thrombosis and swelling/pain in my arm and leg above the knee since my Dose 4 of the Vaccine and it has not resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- COVID-19 PCR test 5/8/2022 was positive Chest x-rays to screen for COVID-19 Pneumonia
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Chronic Fatigue Fibromyalgia Me System Sensitivity Allergy Triggered Asthma
- Andere Medikamente
- Vitamin D Gummies Magnesium 100mg Metphormin 125mcg Daily Propranolol 2.5mg Daily Torsamide 10mg Daily Zyrtec Generic Gabapentin 300mg Nightly Zulpadem/Ambien 2.5mg Nightly
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test normal
Chest X-ray normal
Computerised tomogram normal
Electrocardiogram normal
Feeling abnormal
Headache
Heart rate decreased
Heart rate increased
Hypotension
Loss of consciousness
Nausea
Oxygen saturation decreased
Pain
Symptomtext
I started feeling the normal achy nausea headache. Got aspirin. Went back to sleep. About 9am went to kitchen and felt nauseous. Made tea and toast and then passed out. My husband came to help me up. I regained consciousness but everything was foggy. I needed to vomit after drinking water. I went back to bed. Husband called ambulance. EMTs came and my blood pressure was low. They took me to the local hospital. I went through testing and monitoring. My pulse and oxygen went up and down. I stayed at hospital for about 5 hours and was released. I did not pass out again but still had a headache. Within one more day I was fine, symptom free.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- CT scan normal. EKG normal. Lung x-ray normal. Blood panel normal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Caltrate; Vitamin D; Gabapentin; Lovastatin; Meloxicam; Multivitamin; Pantoprazole; Zinc
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blood magnesium
Blood thyroid stimulating hormone
Computerised tomogram head
Dizziness
Dyskinesia
Fall
Feeling hot
Fibrin D dimer
Flushing
Full blood count
Gait disturbance
Head injury
Hyperhidrosis
Laboratory test
Lipids
Metabolic function test
Nausea
Symptomtext
Woke up at 5am, prepared coffee, and event happened at 5:30 am Felt hot, flushed, sweat pouring down face, weak, dizzy tunnel vision, nausea, fainted and fell hitting my head and left hand on the kitchen counter. No cuts on my head but my left hand was scraped skin. I was out for what seemed like 30 seconds after falling. When I came to my husband helped me to the bathroom because I thought I was going to vomit (I didn't) but I had to hold onto the wall as I experienced jerky movements. He took me to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 1,0
- Labordaten
- April 1, 2022: CBC W-PLT Auto Compd (LOINC: 57021-8), COMP METAB PANEL (LOINC: 24323-8), UA AUTO W-O SCOPT (LOINC 50556-0), D-DIMER QUANT (LOINC: 7799-0), Magnesium (LOINC-19123-9), TROPONIN I High Sensitivity (LOINC: 19123-9), Thyroid STIM TSH (LOINC: 11580-8), Lipid Panel (LOINC: 59062-0), Basic METABO CA TOTA (LOINC: 24321-2), CH-Chest 1V (LOINC: 36554-4), CT-Head WO Contrast (LOINC: 30799-1), UE-Hand 3V (LOINC: 24722-1, US-Carotid DPLX Scan (LOINC: 43765-7)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Metoprolol Succinate Extended-Release tablet, 25mg
- Allergien
- Phenergan/Promethazine Latex
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest X-ray
Chest discomfort
Fibrin D dimer
Oropharyngeal pain
Pain
Pericarditis
Symptomtext
The following day I had the aches associated with the shot. The following day it was better but on Wednesday I woke with a sore throat and a tightness in my chest. I went to a walk-in clinic for assessment but referred me to the ER. They gave me a shot to reduce any inflammation around my heart.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- D-dimer test; chest x-ray
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- CHF
- Andere Medikamente
- Crestor 10mg, Pregavalin 50mg and Various Supplements and Vitamins (Opted to not list supplements)
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 16.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hypotension
Nausea
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Mild, Systemic: Hypotension-Severe, Systemic: Nausea-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Blood test
Computerised tomogram
Electrocardiogram
Loss of consciousness
Nausea
Symptomtext
weakness, nausea, black out within in a few minutes of waking up in morning
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- 1,0
- Labordaten
- CTSCAN. ekg and blood work
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- atorvastatin, levothyroxine, low dose aspirin, vitamin C, multivitamin, OPC-3, calcium plus, activated b-complex, turmeric with curcumin
- Allergien
- Risedronate
- Vorherige Impfungen
- tired and achy
- Staat
- CT
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 09.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Mild, Systemic: Weakness-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 26.03.2022
- Beginn
- 27.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fatigue
Impaired work ability
Insomnia
SARS-CoV-2 antibody test
Seizure
Tremor
Symptomtext
tremors while awake & sleeping; not being able to sleep good at night; after medication feeling extremely tired and unable to work; after medication feeling extremely tired and unable to work; seizures/seizures behaviors/multiple seizures while awake & sleeping; This spontaneous case was reported by a consumer and describes the occurrence of SEIZURE (seizures/seizures behaviors/multiple seizures while awake & sleeping) in a 48-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 048l21a) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Seizure and Neurological symptoms NOS. Concurrent medical conditions included Autoimmune disorder (preexisting clinical condition Voltage-Gated Potassium Channel Antibody Disorder, extremely rare that was diagnosed when patient was going through breast cancer and when patient also had a seizure at that time "similar to what she was experiencing"), Breast cancer female (she had treatment and surgery) since January 2015 and Allergy to antibiotic (amoxicillin). Concomitant products included LEVOTHYROXINE SODIUM (SYNTHROID) and HYDROCHLOROTHIAZIDE, LISINOPRIL (LISINOPRIL AND HYDROCHLOROTHIAZIDE) for an unknown indication. On 26-Mar-2022 at 3:00 PM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 27-Mar-2022 at 10:00 PM, the patient experienced SEIZURE (seizures/seizures behaviors/multiple seizures while awake & sleeping) (seriousness criterion medically significant). On an unknown date, the patient experienced TREMOR (tremors while awake & sleeping), INSOMNIA (not being able to sleep good at night), IMPAIRED WORK ABILITY (after medication feeling extremely tired and unable to work) and FATIGUE (after medication feeling extremely tired and unable to work). The patient was treated with LEVETIRACETAM DIHYDROCHLORIDE (KEPPRA [LEVETIRACETAM DIHYDROCHLORIDE]) for Seizures, at a dose of 1000 milligram twice a day and LORAZEPAM for Seizures, at a dose of .5 milligram twice a day. At the time of the report, SEIZURE (seizures/seizures behaviors/multiple seizures while awake & sleeping) was resolving and TREMOR (tremors while awake & sleeping), INSOMNIA (not being able to sleep good at night), IMPAIRED WORK ABILITY (after medication feeling extremely tired and unable to work) and FATIGUE (after medication feeling extremely tired and unable to work) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In December 2021, SARS-CoV-2 antibody test: positive (Positive) positive, right after Christmas. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. Following vaccination, the next day at 10 pm patient started to experience seizures, went to ER, seizures behaviors, in ER received 2 seizures meds but then was released to come home after 6 hours as the facility did not had the structure to admit patient for longer treatment, multiple seizures and tremors while awake and sleeping, not being able to sleep good at night, after medication feeling extremely tired and unable to work. HCP told that it was patient's body way to react to the vaccination in combination with patients preexisting clinical condition VGKC antibody disorder. Treatment medication reported as Potassium HCL 20mcg twice daily. The symptoms improved with administration with medication "much lessen with lorazepam". It was reported that medication had helped but symptoms were still there and if they retire the medication symptoms would come back. Patient did not receive any other vaccines, it was patients first vaccine she received since cancer. On 30-Jun-2022, patient had schedule an appointment for in house visit. Company Comment: This is a Spontaneous case concerning a 48-year-old female patient, with relevant medical history of seizure, neurological symptoms, autoimmune disorder, and breast cancer, who experienced the unexpected, serious (medically significant), and AESI of Seizure. The event occurred 1 day after the first dose of mRNA-1273 vaccine. Patient was admitted to ER for 6 hours due to seizures. She received treatment with levetiracetam and lorazepam and then was released, as ER didn?t have the structure to admit her for longer treatment. Patient experienced multiple seizures and tremors, not being able to sleep good at night. After medication she felt extremely tired and unable to work. Medical history of seizure, neurological symptoms, autoimmune disorder, and breast cancer, remain confounders for the events. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This is a Spontaneous case concerning a 48-year-old female patient, with relevant medical history of seizure, neurological symptoms, autoimmune disorder, and breast cancer, who experienced the unexpected, serious (medically significant), and AESI of Seizure. The event occurred 1 day after the first dose of mRNA-1273 vaccine. Patient was admitted to ER for 6 hours due to seizures. She received treatment with levetiracetam and lorazepam and then was released, as ER didn?t have the structure to admit her for longer treatment. Patient experienced multiple seizures and tremors, not being able to sleep good at night. After medication she felt extremely tired and unable to work. Medical history of seizure, neurological symptoms, autoimmune disorder, and breast cancer, remain confounders for the events. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- Test Date: 202112; Test Name: COVID positive test; Test Result: Positive ; Result Unstructured Data: positive, right after Christmas
- Aktuelle Erkrankungen
- Allergy to antibiotic (amoxicillin); Autoimmune disorder (preexisting clinical condition Voltage-Gated Potassium Channel Antibody Disorder, extremely rare that was diagnosed when patient was going through breast cancer and when patient also had a seizure at that time "similar to what she was experiencing"); Breast cancer female (she had treatment and surgery)
- Vorgeschichte
- Medical History/Concurrent Conditions: Neurological symptoms NOS; Seizure
- Andere Medikamente
- SYNTHROID; LISINOPRIL AND HYDROCHLOROTHIAZIDE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 26.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discomfort
Electric shock sensation
Lymphadenopathy
Neuralgia
Pain
Pain in extremity
Symptomtext
Electroshocks in my hands spiking from my shoulder blades down to the finger tips. It was more than a tingly feeling; felt like needles pinching my nerves and feeling pain at the tip of my hands. The strongest pain was on the left, on the side of the vaccine. I also had a large bump under my left armpit which I read is a normal thing from my lymph nodes reacting. However, the electroshock feeling was very new and uncomfortable. It would happen sporadically throughout the day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Heart Murmur
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back injury
Blood test
Computerised tomogram head
Computerised tomogram thorax
Echocardiogram
Electrolyte imbalance
Fall
Feeling abnormal
Feeling hot
Headache
Hypertension
Impaired driving ability
Influenza
Loss of consciousness
Pyrexia
Road traffic accident
SARS-CoV-2 test negative
Syncope
Symptomtext
He got his 4th vaccine, that night after about a few hours starting to get a high fever, got really hot and told his wife he thought he had a fever. She had a splitting headache between his temples. He took 1000 mg of Tylenol as he cannot take any other kind of pain reliever. It then came back again and kept taking it to get rid of the headaches. He did not measure his temperature and knew that he had a fever. Felt like he had a virus or the flu. He did a COVID test and that was negative, but just felt bad. He thinks that his immune system was kicking in 100%. These symptoms lasted on and off for the last few days. A few days after the vaccine, he was going to the bank an ATM and was driving down the highway, was OK, 40 miles until he got to where he was going. He got into the parking lot where the bank was and coming up to the machine and everything went black, passed out going into the bank and drove through the side window of the bank, storage room. Somebody came around right away who witnessed the event and called 911. Glass was falling into his car, tried to get out of the car and fell on the road onto his back in the parking lot. The ambulance took him to the hospital and asked if he was wearing a seatbelt which he was. The doctor in the ER said that he had syncope. They informed him that his electrolytes were messed up and gave him magnesium, potassium and other medicine through IV's. He stayed in observation over night. They did CAT scans of his brain and also did one of his heart checking for a blood clot or heart attack. His BP was high when the paramedics came and it was 200/100 something. He cannot drive until he goes back to his PCP and is given the clearing to do so. He now has a home health nurse coming 2 times a week to check his VS to see if he is OK. He has never had an events after the vaccines. The last one had a slight fever, but nothing too bad.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- 1,0
- Labordaten
- Blood work, CAT scan and US of his heart.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure, high cholesterol, low thyroid, borderline diabetes.
- Andere Medikamente
- Multivitamin, Tylenol, Atenolol 25 mg, once a day, Irbesartan/Hydroxyzine 300/12.5, Rosuvastatin 20 mg, Synthroid 125 mcg, Metformin 500 every 24 hours,
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 26.03.2022
- Beginn
- 26.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Computerised tomogram
Fatigue
Headache
Hypersomnia
Malaise
Memory impairment
Myalgia
Nausea
Seizure
Tremor
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 7+
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Loss of consciousness
Symptomtext
patient passed out
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none to knowledge
- Vorgeschichte
- no
- Andere Medikamente
- not sure
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 24.03.2022
- Impfdatum
- 19.03.2022
- Beginn
- 20.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Dyspnoea
Echocardiogram normal
Electrocardiogram normal
Hyperhidrosis
Myocarditis
Troponin increased
Nausea
Palpitations
Symptomtext
Myocarditis. Presented to ED with 3 days of progressive substernal chest pain starting the day after he received the second vaccine. Chest pain episodes were intermittent, happening at times of rest, would last 1.5-3 hours, resolving spontaneously. Chest pain episodes associated with shortness of breath, mild nausea, diaphoresis and feelings of racing heart. Admitted for observation and treated with as needed NSAIDs and a dose of corticosteroid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Markedly elevated high sensitivity troponin on 3/22. No ekg changes. Echo normal on 3/23.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 24.04.2023
- Impfdatum
- 21.04.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 224,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Neuropathy peripheral
Orthosis user
Paraesthesia
Symptomtext
I did not have an adverse reaction to the vaccine. In December, I noticed burning or tingling in my left and right hands, legs and feet. I have been to my doctor and was diagnosed neuropathy. I wear braces on my legs to help with my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HIV
- Andere Medikamente
- N/A
- Allergien
- Penicillin; sulfa
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 14.04.2023
- Impfdatum
- 13.04.2022
- Beginn
- 29.03.2023
- Tage bis Beginn
- 350,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Breakthrough COVID-19
Chest pain
Chills
Fatigue
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I experienced a breakthrough case of COVID-19 with chest pain, very sore throat, severe fatigue and chills.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 31March2023 - COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Citalopram; Atorvastatin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 05.04.2023
- Impfdatum
- 04.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 27,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure increased
Blood test normal
Cardiac stress test normal
Condition aggravated
Hypertensive crisis
Magnetic resonance imaging normal
Ophthalmic migraine
Papilloedema
Symptomtext
5/1/22 I started having increased blood pressure issues and increased ocular migraines. On 7/1/22, I wound up in the ER with hypertensive crisis. It took 11 hours to get it under control and I was sent home with a change in medication, Amlodipine. I was back in the Emergency Room on 7/4/22. It took about 5 hours to resolve the high blood pressure and I was sent back home with an increase in Amlodipine. Through all of this my ocular migraines were still being troublesome to the extent I had never had before. Since July it has been a round robin of medications to get my blood pressure in control. On 3/28/23 I had an MRI which for the migraines which showed an injury from when I was a child, nothing new. Yesterday at the optometrist they discovered a swelling on my left retina nerve that could be affecting my vision and linked to my high blood pressure and ocular migraines. This morning my Lisinopril was decreased trying to straighten things out. I have a follow up with my doctor and neurologist trying to get the ocular migraines and blood pressure under control.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 1JUL22- Bloodwork- Normal; 1SEP22- Stress Test-Normal; 4JUL22- Bloodwork-Normal; 4JUL23- Stress Test-Normal; 28MAR23-MRI-Showed injury from childhood, otherwise Normal; Constant bloodwork, unknown dates in 2023- Mostly Normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Enalapril/Hydrochlorothiazide , Premarin Cream, Calcium Chew, Krill Oil, Vitamin D, Magnesium
- Allergien
- Sulfa Drugs, Reacative allergy to mold and pollens
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 04.11.2022
- Impfdatum
- 22.03.2022
- Beginn
- 25.10.2022
- Tage bis Beginn
- 217,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram pulmonary abnormal
Atelectasis
COVID-19
Chest discomfort
Chronic obstructive pulmonary disease
Computerised tomogram thorax
Condition aggravated
Dementia
Electrocardiogram normal
Fibrin D dimer increased
Hyperglycaemia
Metabolic function test normal
Pneumonia
Positive airway pressure therapy
Respiratory failure
Troponin increased
Wheezing
Symptomtext
Discharge Provider: MD Primary Care Provider: NP Admission Date: 10/25/2022 Discharge Date: 10/27/2022 Discharge Diagnoses: Acute Exacerbation of COPD Chronic Hypoxic Respiratory Failure COVID-19 Hyperglycemia Dementia History of CVA Hypertension GERD Restless leg syndrome Hospital Course: Pt is a 73 y.o. female w/ a pertinent PMHx of COPD, Dementia, and CVA who is admitted to Hospital on 10/25/2022 for Acute exacerbation of COPD and COVID-19 infection. In the ED, she was hypoxic requiring BiPAP. She was given IV steroids in the ED along with DuoNeb. In the hospital, she was quickly weaned down to her home O2 of 2L NC. She was transitioned to PO prednisone. She continued to do well with ambulation. She was then discharged with a 12 day steroid taper and follow up with PCP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- ED visit on 10/1/2022 at Hospital Patient presented with acute onset right-sided chest discomfort. CT of the right upper part of her chest. Hard to know with X better or worse. Sometimes has reproducible sometimes worse with coughing or breathing. She denies any known fevers, chills, sweats, sick contacts. She does have a history of chronic obstructive pulmonary disease she is under T dizzy nasal cannula. She does have some wheezing on examination. Her electrocardiogram is completely normal. Her D-dimer is elevated troponins are flat. They are both elevated but in the indeterminate range and similar to her prior evaluations. Her BMP is normal COVID testing is negative also. Because of her symptoms a CT angiogram was ordered for this patient. This was negative for any pulmonary embolism or concerning pathology. However did show evidence of possible pneumonia versus atelectasis. She will be given a course of doxycycline and steroids. States she has all her nebulizers and treatments at home. [EC] She feels comfortable and desires discharge back home. Does not stay in the emergency department much longer. She is contacting her son for transport. [EC]
- Vorgeschichte
- Dyspnea Chronic respiratory failure with hypoxia (HCC) Asthma Chronic obstructive pulmonary disease (COPD) (HCC) Pulmonary nodule COPD with acute exacerbation (HCC) COPD exacerbation (HCC) Sinus tachycardia Hypertension CVA (cerebrovascular accident) (HCC) Cerebral vascular disease GERD (gastroesophageal reflux disease) Thrombocytosis Tremor, essential Dementia (HCC) Rib pain Dyslipidemia Health care maintenance Generalized anxiety disorder Osteopenia History of tobacco abuse 60 pack year history quit 2011 Insomnia Restless legs syndrome Weakness Depression Anxiety
- Andere Medikamente
- alendronate (FOSAMAX) 35 MG tablet atorvastatin (LIPITOR) 80 MG tablet clopidogrel (PLAVIX) 75 MG tablet dilTIAZem (CARDIZEM CD) 240 MG 24 hr capsule Fluticasone-Umeclidin-Vilant (TRELEGY ELLIPTA) 100-62.5-25 MCG/INH inhaler furosemide (LAS
- Allergien
- Aspirin Cymbalta [Duloxetine Hcl] Lidocaine Zinc Zinc [Acetic Acid]
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 07.10.2022
- Impfdatum
- 13.02.2021
- Beginn
- 03.10.2022
- Tage bis Beginn
- 597,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain
COVID-19
Endoscopic retrograde cholangiopancreatography
Hypotension
Nausea
SARS-CoV-2 test positive
Vomiting
Symptomtext
Pt to ED 10/3 for c/o persistent abd pain with n/v. RRT called for hypotension. Pt COVID+ 10/3. 10/4 Pt is A&Ox4 ,airway is patent, speech is clear, respirations are even and unlabored. 10/4 to OR for ERCP. 10/5 pt is aox4,on RA not in distress,ambulatory, denies pain or sob. 10/6 pt discharged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- 3,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diaphragmatic hernia Diaphragmatic hernia Digestive Gastroesophageal reflux disease without esophagitis Cholangitis cute cholangitis Mixed hyperlipidemia Primary hypertension Rheumatoid arthritis History of spinal fracture AK (actinic keratosis) Urinary hesitancy Intracranial arachnoid cyst Cerebral infarction, chronic Encounter for abdominal aortic aneurysm (AAA) screening Macrocytic anemia High gradeB-cell lymphoma Lung nodule Screning for colon cancer History of lymphoma History of aspergillosis Chonic diastolic congestive heart failure Abdominal pain, RUQ (right upper quadrant) S/P endoscopy COVID Arthritis Long term systemic steroid user
- Andere Medikamente
- amoxicillin-potassium clavulanate (AUGMENTIN) atorvastatin (LIPITOR) 20 MG PO Tab Cholecalciferol (Vitamin D3) 50 MCG (2000 UT) PO Cap ibuprofen (MOTRIN) 600 MG PO Tab ketoconazole (NIZORAL) 2 % EXTERNAL Cream leflunomide (ARAVA) 20 MG PO T
- Allergien
- Zofran
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 06.10.2022
- Impfdatum
- 04.04.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 163,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Computerised tomogram
Dysarthria
Dyskinesia
Hypertension
Magnetic resonance imaging head abnormal
Transient ischaemic attack
Wheezing
Symptomtext
I was sitting down; I was talking to my daughter, and I was slurring your words and looked like I was having a stroke. She gave you water and could not take it in because I couldn?t control the left of your mouth and called 911 and went to the hospital by ambulance. In the stroke ward. Afib was escalating and got a intravenous drip Diltiazem. They determined a mini stroke with no lasting damage. I was there from 14 to 16 Sep22. I do have a whizzing in my chest as I slept three after I came home from the hospital. High Blood Pressure has been up and down for several.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- 2,0
- Labordaten
- MRI : Mini Stroke; Cat scans
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Heart Disease; Arteritis
- Andere Medikamente
- Amlodipine; Amitriptyline; Bisoprolol ; Eliquis; Hydrochlorothiazide; Nexium ; Plavix; Doxazosin; Lidocaine patches; Cardizem; Tylenol; Omega Fish Oil Liquid; Vitamin D; Vitamin C; Zinc; Vitamin B Complex; Turmeric; Lutein; Biotin
- Allergien
- Aspirin; Ace inhibitors; Ciprofloxacin; Tetracycline; Levaquin; Peanuts
- Vorherige Impfungen
- Flu - I don't recall . I got more sick and faint, headache & shaky
- Staat
- MN
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 20.09.2022
- Impfdatum
- 02.02.2021
- Beginn
- 05.09.2022
- Tage bis Beginn
- 580,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
SOB AND COUGH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- POSITIVE COVID TEST 02/12/21
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ? Acute blood loss anemia 10/7/2016 ? Anemia 10/7/2016 ? Back pain due to mass pressing against the ribs ? Cancer (HCC) skin ca forehead removed ? Cancer of lung (HCC) 2016 right lower lobe ? Deep vein thrombosis (DVT) (HCC) 2016 L. leg/ after lung surgery ? Essential hypertension 10/7/2016 ? HLD (hyperlipidemia) 10/7/2016 ? HTN (hypertension) ? Hypercholesteremia ? Lung mass ? Pyelonephritis ? Renal disease ? Sleep apnea mild - not using CPAP due to back pain from mass ? Status post partial lobectomy of lung 10/7/2016
- Andere Medikamente
- calcium carbonate/vitamin D3 (CALTRATE-600 PLUS VITAMIN D3 ORAL) Cholecalciferol, Vitamin D3, 50 mcg (2,000 unit) oral tablet lisinopril (PRINIVIL;ZESTRIL) 10 mg oral tablet simvastatin (ZOCOR) 20 mg Oral Tab
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 14.09.2022
- Impfdatum
- 30.03.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 154,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Asthenia
COVID-19
Condition aggravated
Dehydration
Fractured sacrum
Hypotension
Muscle disorder
Pain
Polyuria
Renal failure
Renal function test normal
Weight increased
Symptomtext
Admission Date: 8/31/2022 Discharge Date: 9/5/2022 PRESENTING PROBLEM: Dehydration [E86.0] General weakness [R53.1] Muscular deconditioning [R29.898] AKI (acute kidney injury) (HCC) [N17.9] COVID-19 virus infection [U07.1] HOSPITAL COURSE: Patient is a very pleasant 93-year-old male presenting with generalized weakness uncontrolled pain related his sacral fraction and hypotension. Patient was admitted patient's diuretics were held patient was hydrated patient empirically treated Decadron for his COVID-19. Patient's renal insufficiency improved with hydration patient's blood pressure improved with treatment patient was empirically covered with doxycycline and Rocephin during hospitalization. Patient's pain improved was able low work with PT and OT with recommendations for subacute rehab. The patient stable normal renal function good saturation hypotension resolved. Patient is back on his home medications with exception of Lasix which will be dosed daily for a greater than or equal to 2 lb weight gain along with his potassium chloride patient need labs within a week to re-evaluate his blood count and his kidney function electrolytes. Patient in stable condition for discharge to subacute rehab
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- 3/9/22- Office Visit to PCP office for bilateral leg edema
- Vorgeschichte
- CAD (coronary artery disease) Paroxysmal atrial fibrillation (HCC) Open fracture of nasal bone Stroke (HCC) Hypercholesterolemia Hypertension Aortic stenosis Postural dizziness with presyncope Unspecified severe protein-calorie malnutrition (HCC) Pancytopenia (HCC) Stage 3 chronic kidney disease (HCC) Chronic anticoagulation with warfarin Acute on chronic combined systolic and diastolic congestive heart failure (HCC) Cardiomyopathy, ischemic RBBB Severe aortic stenosis Thrombocytopenia (HCC) Atrial fibrillation, persistent (HCC) S/P TAVR (transcatheter aortic valve replacement), 01/16/2020 Bronchopneumonia due to human metapneumovirus (hMPV) Warfarin-induced coagulopathy (HCC) Chronic diastolic congestive heart failure (HCC) Coronary artery disease without angina pectoris Mild left ventricular systolic dysfunction (EF 0.50) Status post balloon aortic valvuloplasty, 12/02/2019 S/P CABG x 3 Status post insertion of drug eluting stent to distal left main and proximal circumflex, 12/02/2019 Cardiomyopathy (HCC) PVC (premature ventricular contraction) Severe tricuspid regurgitation by prior echocardiogram Epistaxis due to trauma Hypotension Arthralgia of right upper arm Nonrheumatic aortic valve insufficiency Nonrheumatic mitral valve regurgitation Tremor Bradycardia Essential tremor Hypothyroidism, unspecified type Chronic bronchitis, unspecified chronic bronchitis type (HCC) Atherosclerosis of aorta (HCC) Pneumonia Sacral insufficiency fracture Elevated transaminase level General weakness Physical deconditioning
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet amiodarone (PACERONE) 200 MG tablet apixaban (ELIQUIS) 5 MG tablet ascorbic acid (VITAMIN C) 500 MG tablet aspirin 81 MG chewable tablet Cholecalciferol (D3 PO) cyanocobalamin 100 MCG tablet doxycycline
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 19.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fear
Feeling cold
Injection site erythema
Injection site swelling
Lymphadenopathy
Tremor
Symptomtext
After receiving the shot, I expected some mild effects. What I got was frightening. It began with swelling at the injection sight about 8" of redness and swelling, lymph nodes swelled too. Roughly 36 hours later, I was in bed and awoke because I was FREEZING COLD. I was SHIVERING AND SHAKING all over and my TEETH WERE CHATTERING. I was alone. I was afraid I would die. No phone within reach. This lasted for several hours. VERY SCARY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Blood pressure medication
- Allergien
- none
- Vorherige Impfungen
- Mild swelling at injection site, mild fever and fatigue.
- Staat
- KY
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 122,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Anxiety
Aortic valve sclerosis
Arrhythmia
COVID-19
Cardiac stress test abnormal
Cardiovascular symptom
Chest X-ray abnormal
Chest pain
Condition aggravated
Echocardiogram
Echocardiogram abnormal
Ejection fraction
Ejection fraction normal
Essential hypertension
Extrasystoles
Hyperlipidaemia
Insulin-requiring type 2 diabetes mellitus
Left ventricular hypertrophy
Symptomtext
ED to Hosp-Admission Discharged 8/12/2022 - 8/13/2022 (27 hours) HOSPITAL MD Last attending ? Treatment team Atypical chest pain Principal problem Discharge Summary RN (Registered Nurse) Pt D/C per orders, new medication education provided by this nurse and verbalized understanding. PT left floor walking with no acute distress noted. Discharge Summary MD (Physician) ? ? Hospitalist Discharge Summary Age: 70 y.o. Admit Date: 8/12/2022 11:18 AM Discharge Date: 08/13/22 Hospitalist Physician: DO Discharge Diagnosis: Principal Problem: Atypical chest pain Active Problems: Type 2 diabetes mellitus without complication, with long-term current use of insulin Hyperlipidemia associated with type 2 diabetes mellitus NSVT (nonsustained ventricular tachycardia) COVID-19 Essential hypertension Consults: IP CONSULT TO CARDIOLOGY Subjective (08/13/22): Pt feeling better this AM. Anxious about stress test results. States he would like to be able to make his daughter's birthday dinner today. Denied CP/Palpiations/SOB/N/V/D Hospital Course: (8/12/2022-08/13/22) Patient admitted for atypical chest pain workup. Patient has history of palpitations/lightheadedness secondary to nonsustained ventricular tachycardia. Home medications including flecainide and atenolol 12.5 mg. Troponin is negative ?2. TTE showed left ventricular ejection fraction of 59% with normal ventricular wall motion. Normal left ventricular diastolic function was also noted. Patient underwent a cardiac stress test as well which show ejection fraction of 52% with no signs of ischemia. This was a normal study. Patient's home atenolol will be increased to 25 mg daily for his nonsustained ventricular tachycardia which thought to be contributing to his palpitations and symptoms. He is to follow-up with his primary care provider and cardiologist. He is now stable for discharge with close follow-up. Physical Exam (08/13/22): General: Alert; NAD; pleasant HEENT: NCAT CVS: Regular rate; irregular rhythm; no pathological murmurs noted RESP: CTA b/l; No wheezes, rhonci, or rales ABD: Soft, Nontender, Nondistended SKIN: No jaundice EXT: No pitting edema MSK: No deformity NEURO: Alert; No focal deficits PSYCH: Cooperative; appropriate mood and affect Diagnostic Studies: Transthoracic Echocardiogram Result Date: 8/13/2022 Aortic Valve The aortic valve has mild sclerosis. The aortic valve opens well. No aortic regurgitation is present. No aortic stenosis Atria The left atrial volume index is 'normal (16-34 ml/m2).'. Right atrial size is normal. The interatrial septum is intact with no evidence for an atrial septal defect. Diastology Spectral Doppler of the mitral valve shows a normal E/A wave ratio. A variety of Doppler measurements indicate normal left ventricular diastolic function. Great Vessels The aortic root is normal size. The aorta at the Sinuses of Valsalva is '3.2' cm in diameter. The ascending aorta is '3.4' cm in diameter, at the maximal visualized area. The inferior vena cava appeared normal (<2.1 cm) and decreased > 50% with respiration (RAP 0-5 mmHg). Estimated RAP of 3 mmHg. Left Ventricle The left ventricular end-diastolic dimension is 'normal for men (4.2-5.8cm).'. The relative wall thickness is >0.42 (increased). There is borderline concentric left ventricular hypertrophy. Left ventricular ejection fraction is '55%-60%' based on biplane method. Left ventricular ejection fraction derived by 3DE '59' %. The left ventricular wall motion is normal. Mitral Valve The mitral valve is grossly normal. There is no mitral valve stenosis. There is trace mitral regurgitation. Pericardium/Pleural There is no pericardial effusion. There is no pleural effusion. Procedure The exam was of adequate technical quality. Complete 2D MMode echocardiogram. Complete spectral Doppler interrogation Color flow velocity mapping. Exam was performed on 'EPIQ' Examination was completed in the patients room. Pulmonic Valve The pulmonic valve is not well visualized. The pulmonic valve is not well seen, but is grossly normal. There is no pulmonic valvular stenosis. Trace pulmonic valvular regurgitation. Right Ventricle The right ventricle is normal size. The right ventricular systolic function is normal. The estimated global right ventricular systolic function based upon the tricuspid annular plane of systolic exursion (TAPSE) is 'normal >17mm.' The estimated global right ventricular systolic function based upon the TDE maximal myocardial systolic velocity S' is 'normal >10 cm/s.' Tricuspid Valve The tricuspid valve is grossly normal. There is no tricuspid stenosis. There is trace tricuspid regurgitation. MMode 2D Measurements & Calculations Doppler Measurements & Calculations Z-Scores(Vital Signs) Classic Z-Scores(Vital Signs) Z-Scores(Vital Signs) Other Measurements & Calculations Conclusion Left ventricular ejection fraction derived by 3DE '59' %. The left ventricular wall motion is normal. There is trace tricuspid regurgitation. Trace pulmonic valvular regurgitation. A variety of Doppler measurements indicate normal left ventricular diastolic function. There is trace mitral regurgitation. Stress Test, Pharmacological,w/Myoview (Lexiscan 0.4 mg IV x 1) Result Date: 8/13/2022 ECG SB, NSSTTWC Non-diagnostic Lexiscan stress test. Left Ventricle The LV EF is calculated at 52% Procedure The patient was given 0.4 mg IV of Lexiscan per protocol. There are no significant ST segment changes throughout the injection or recovery period. The patient tolerated the procedure well lexiscan myoview 1 day Lexiscan Nuclear Stress Test Rest Injection Patient was injected with 9.99mCi of tetrofosmin IV at rest Risk Factors DM, HTN, HLD Stress Findings VENTRICULAR PREMATURE BEATS ISOLATED No ischemic ST changes during the stress test. Stress Injection An additional 29.99 mCi of tetrofosmin IV was injected at peak exercise Stress Supervision Provider: APRN MMode 2D Measurements & Calculations Boston Z-Scores(Vital Signs) Other Measurements & Calculations Conclusion The LV EF is calculated at 52% normal study XR Portable Chest Result Date: 8/12/2022 Medical Center Radiology PATIENT NAME: MR#: PROCEDURE DATE: 08/12/2022 ACCOUNT#: ACCESSION #: ROOM#: ORDERING PHYS: MD Chest pain Chest one-view Findings: Less than optimally inflated lungs without infiltrate or effusion. Cardiac size within normal. IMPRESSION: No acute cardiopulmonary finding. THIS IS AN ELECTRONICALLY VERIFIED REPORT 8/12/2022 12:23 PM: MD, MD: 08/12/2022: 08/12/2022 JOB #: Radiology Page 1 of 1 COPY ED to Hosp-Admission Discharged 8/12/2022 - 8/13/2022 (27 hours) HOSPITAL MD Last attending ? Treatment team Atypical chest pain Principal problem Discharge Summary RN (Registered Nurse) Pt D/C per orders, new medication education provided by this nurse and verbalized understanding. PT left floor walking with no acute distress noted. Discharge Summary MD (Physician) ? ? Hospitalist Discharge Summary Patient ID: MRN: Name: Age: 70 y.o. Birthday: Admit Date: 8/12/2022 11:18 AM Discharge Date: 08/13/22 Unit: Hospitalist Physician: DO Discharge Diagnosis: Principal Problem: Atypical chest pain Active Problems: Type 2 diabetes mellitus without complication, with long-term current use of insulin Hyperlipidemia associated with type 2 diabetes mellitus NSVT (nonsustained ventricular tachycardia) COVID-19 Essential hypertension Consults: IP CONSULT TO CARDIOLOGY Subjective (08/13/22): Pt feeling better this AM. Anxious about stress test results. States he would like to be able to make his daughter's birthday dinner today. Denied CP/Palpiations/SOB/N/V/D Hospital Course: (8/12/2022-08/13/22) Patient admitted for atypical chest pain workup. Patient has history of palpitations/lightheadedness secondary to nonsustained ventricular tachycardia. Home medications including flecainide and atenolol 12.5 mg. Troponin is negative ?2. TTE showed left ventricular ejection fraction of 59% with normal ventricular wall motion. Normal left ventricular diastolic function was also noted. Patient underwent a cardiac stress test as well which show ejection fraction of 52% with no signs of ischemia. This was a normal study. Patient's home atenolol will be increased to 25 mg daily for his nonsustained ventricular tachycardia which thought to be contributing to his palpitations and symptoms. He is to follow-up with his primary care provider and cardiologist. He is now stable for discharge with close follow-up. Physical Exam (08/13/22): General: Alert; NAD; pleasant HEENT: NCAT CVS: Regular rate; irregular rhythm; no pathological murmurs noted RESP: CTA b/l; No wheezes, rhonci, or rales ABD: Soft, Nontender, Nondistended SKIN: No jaundice EXT: No pitting edema MSK: No deformity NEURO: Alert; No focal deficits PSYCH: Cooperative; appropriate mood and affect Diagnostic Studies: Transthoracic Echocardiogram Result Date: 8/13/2022 Aortic Valve The aortic valve has mild sclerosis. The aortic valve opens well. No aortic regurgitation is present. No aortic stenosis Atria The left atrial volume index is 'normal (16-34 ml/m2).'. Right atrial size is normal. The interatrial septum is intact with no evidence for an atrial septal defect. Diastology Spectral Doppler of the mitral valve shows a normal E/A wave ratio. A variety of Doppler measurements indicate normal left ventricular diastolic function. Great Vessels The aortic root is normal size. The aorta at the Sinuses of Valsalva is '3.2' cm in diameter. The ascending aorta is '3.4' cm in diameter, at the maximal visualized area. The inferior vena cava appeared normal (<2.1 cm) and decreased > 50% with respiration (RAP 0-5 mmHg). Estimated RAP of 3 mmHg. Left Ventricle The left ventricular end-diastolic dimension is 'normal for men (4.2-5.8cm).'. The relative wall thickness is >0.42 (increased). There is borderline concentric left ventricular hypertrophy. Left ventricular ejection fraction is '55%-60%' based on biplane method. Left ventricular ejection fraction derived by 3DE '59' %. The left ventricular wall motion is normal. Mitral Valve The mitral valve is grossly normal. There is no mitral valve stenosis. There is trace mitral regurgitation. Pericardium/Pleural There is no pericardial effusion. There is no pleural effusion. Procedure The exam was of adequate technical quality. Complete 2D MMode echocardiogram. Complete spectral Doppler interrogation Color flow velocity mapping. Exam was performed on 'EPIQ' Examination was completed in the patients room. Pulmonic Valve The pulmonic valve is not well visualized. The pulmonic valve is not well seen, but is grossly normal. There is no pulmonic valvular stenosis. Trace pulmonic valvular regurgitation. Right Ventricle The right ventricle is normal size. The right ventricular systolic function is normal. The estimated global right ventricular systolic function based upon the tricuspid annular plane of systolic exursion (TAPSE) is 'normal >17mm.' The estimated global right ventricular systolic function based upon the TDE maximal myocardial systolic velocity S' is 'normal >10 cm/s.' Tricuspid Valve The tricuspid valve is grossly normal. There is no tricuspid stenosis. There is trace tricuspid regurgitation. MMode 2D Measurements & Calculations Doppler Measurements & Calculations Z-Scores(Vital Signs) Classic Z-Scores(Vital Signs) Z-Scores(Vital Signs) Other Measurements & Calculations Conclusion Left ventricular ejection fraction derived by 3DE '59' %. The left ventricular wall motion is normal. There is trace tricuspid regurgitation. Trace pulmonic valvular regurgitation. A variety of Doppler measurements indicate normal left ventricular diastolic function. There is trace mitral regurgitation. Stress Test, Pharmacological,w/Myoview (Lexiscan 0.4 mg IV x 1) Result Date: 8/13/2022 ECG SB, NSSTTWC Non-diagnostic Lexiscan stress test. Left Ventricle The LV EF is calculated at 52% Procedure The patient was given 0.4 mg IV of Lexiscan per protocol. There are no significant ST segment changes throughout the injection or recovery period. The patient tolerated the procedure well lexiscan myoview 1 day Lexiscan Nuclear Stress Test Rest Injection Patient was injected with 9.99mCi of tetrofosmin IV at rest Risk Factors DM, HTN, HLD Stress Findings VENTRICULAR PREMATURE BEATS ISOLATED No ischemic ST changes during the stress test. Stress Injection An additional 29.99 mCi of tetrofosmin IV was injected at peak exercise Stress Supervision Provider: APRN MMode 2D Measurements & Calculations Boston Z-Scores(Vital Signs) Other Measurements & Calculations Conclusion The LV EF is calculated at 52% normal study XR Portable Chest Result Date: 8/12/2022 Medical Center Radiology PATIENT NAME: MR#: PROCEDURE DATE: 08/12/2022 ACCOUNT#: ACCESSION #: ROOM#: ORDERING PHYS: MD Chest pain Chest one-view Findings: Less than optimally inflated lungs without infiltrate or effusion. Cardiac size within normal. IMPRESSION: No acute cardiopulmonary finding. THIS IS AN ELECTRONICALLY VERIFIED REPORT 8/12/2022 12:23 PM: MD, MD: 08/12/2022: 08/12/2022 JOB #: Radiology Page 1 of 1 COPY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 60,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Blindness unilateral
Cough
Dyspnoea
Full blood count normal
Nasal congestion
Ophthalmological examination abnormal
Optic ischaemic neuropathy
Oropharyngeal pain
Papilloedema
Retinogram abnormal
Sleep apnoea syndrome
Sleep study abnormal
Symptomtext
I have been diagnosed with Anterior Ischemic Optic Neuropathy commonly known as an eye stroke. It was a gradual onset. There is probable permanent loss of vision in my left eye. It was treated with one week of Prednisone at 30mg per day with 2 days of weaning off the medication. I'm still under treatment to prevent potential neurological events in the future like brain or eye stroke. It's greatly impacted my vision. At the same time that I was losing vision, I developed a cough, some nasal congestion, and a sore throat. It got worse, better, and then perceptibly worse over the course of three to four days. It prompted a visit to urgent care on the 5th day due to difficulty breathing. At that time, I was advised to follow up with an Ophthalmologist due to the loss of vision.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 06/20/2022 Retinal Imaging - Optic Nerve Edema; 06/30/2022 Complete Eye Exam - Anterior Ischemic Optic Neuropathy; 06/30/2022 Complete Blood Panel - Normal; 07/13/2022 Sleep Study - Mild Sleep Apnea
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Losartan; Hydrochlorothiazide; B Complex; Vitamin C; Vitamin D; Vitamin E; Calcium; Chondroitin/Glucosamine; Loratadine; Lutein; Probiotics
- Allergien
- Seasonal Allergies; Latex sensitivity
- Vorherige Impfungen
- 02/11/2021, Moderna COVID-19 Vaccine, Dose 1, Age: 69 - Moderate to severe pain and inflammation at injection site and, extreme
- Staat
- GA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 20.04.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 64,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Deafness unilateral
Diarrhoea
Dyspnoea
Fatigue
Headache
Malaise
Pain
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I contracted COVID-19 on 06/23/2022 with symptoms of scratch throat, headache, body aches, fever of 100, diarrhea, shortness of breathe, loss of hearing in right ear for one day, and fatigue. I was prescribed an antiviral, but did not take it due to learning of the vast amount of rebound infections. I was ill for 10 days before my symptoms began to resolve. I am fully recovered with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab home test was positive on 06/23/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Osteoporosis
- Andere Medikamente
- Levothyroxine
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 10.04.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 56,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Fatigue
Feeling abnormal
Headache
Impaired work ability
Loss of personal independence in daily activities
Malaise
Mobility decreased
Pain
Pyrexia
SARS-CoV-2 test positive
Sinus pain
Tremor
Vaccine breakthrough infection
Symptomtext
Breakthrough case of COVID-19. The first day that I knew that I was sick I had a lot of sinus pain and a headache and fatigue, I had a fever and was shaking really hard, fever was up to 101, I had chills very bad. The next day the chills were gone but I was pretty achy. The symptoms were only for a couple of days. I was so tired that I could not even move, I could not do basic chores, I had a really bad headache. By the third day, it was just hard to get up and I had a very bad chesty cough, and a fever late in the day. The fourth day I was able to get the PAXLOVID. I was still very tired but I was no longer getting a fever or as achy, I was still coughing but not as bad. After taking the PAXLOVID I felt much better. However I still feel crummy and tired and this is still going on now. I feel fine and then try to do some house chores and that would just wipe me out for the day. After about 10 days I went outside for a walk and then the next day I was back to laying down and not being able to do much after that. I have good days and bad days now, I am back to work but I still have days where I cannot function at all.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid test positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism; Kidney disease
- Andere Medikamente
- SYNTHROID; vitamin D3; calcium; ascorbic acid; black cohosh; melatonin; fexofenadine; magnesium.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 10.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac monitoring
Cardiac stress test
Chest X-ray
Computerised tomogram
Echocardiogram
Electrocardiogram
Heart rate increased
Hypertension
Hypoaesthesia
Laboratory test normal
Magnetic resonance imaging
Palpitations
Paraesthesia
Ultrasound scan
Ultrasound thyroid
Symptomtext
I started noticing heart palpitations when I would get in bed at night. My heart would pound very hard. I have a finger pulse reader and it was showing that it was in the low 40s. It would stop and then happen sporadically for a span of two weeks. I only had them at night. I had high blood pressure occasionally when I would check. I went to the ER and they did an EKG and admitted me. I had an ECHO, stress test. They ended up letting me go home and gave me a 30 day monitor for my heart. I did see the cardiologist then because my heart rate was really high and he put me on a beta blocker, metoprolol, and told me to take a baby aspirin. Then I started having tingling in my toes and lower legs on April 21st. Two nights before that the numbness and tingling started to go up my left side up into my face. I went to the same ER and they admitted me and did different test to rule out brain bleeds and clots in my lungs. When I left I was referred to a neurologist that I won't be able to see until September. Everyday since my second hospital visit I have had some numbness on some part of my left side.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- 4,0
- Labordaten
- ECHO; Stress Test; CT Scan; Chest x-ray; MRI; Ultra scan of arteries and thyroid.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Medical grade tape; Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 02.04.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 57,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Arthralgia
COVID-19
Discomfort
Fatigue
Headache
Mobility decreased
Myalgia
Pain
SARS-CoV-2 test positive
Somnolence
Symptomtext
I felt so tired that I could not stay awake. I had really severe muscle and joint aches with overall achiness. Moving felt uncomfortable. I also had a really bad headache. I took a COVID-19 Home Test and it was positive. We all quarantined together and my additional family members also tested positive. I took a PCR COVID-19 Test at an urgent care center upon my return.It took 11 days to test negative. I rested and stayed in bed. I took Nyquil at night and Dayquil during the day as I did not qualify for Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- COVID 19 Home Test-May 29, 2022-Positive COVID-19 PCR-June 3rd-Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Sleep Apnea
- Andere Medikamente
- Aspirin; Calcium; Magnesium
- Allergien
- Cipro
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac discomfort
Chest discomfort
Dyspnoea
Full blood count
Ventricular extrasystoles
Symptomtext
Approximately 1 week after my 4th dose vaccination I experienced the following symptoms: Occasional PDC and it became frequent as weeks have come by and I had some shortness of breath and chest tightness. My heart felt swollen and inflamed. I saw my nurse practitioner and was prescribed with atenolol 25mg/1x day and it did settle down my PDC. I will be seeing a cardiologist on 07/15/22 for a follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- CBC
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Multivitamins; SYNTHROID; COLACE; fish oil; azelastine nasal spray; doxycycline
- Allergien
- BACTRIM; latex; bee stings
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 30.03.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 47,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
COVID-19
Chest X-ray normal
Computerised tomogram normal
Ear discomfort
Headache
Migraine
Nausea
Paranasal sinus discomfort
Photophobia
SARS-CoV-2 test positive
Sinus headache
Vertigo
Symptomtext
I thought that I had allergies due to extreme sinus headache, sinus pressure and my right ear felt like it would burst. I was also tired. This went on for 3 days and I called my doctor on the 4th day to check my ear. Her assistant came out to the car and gave me a PCR COVID-19 Test which I tested positive for. They had me go home and isolate. I took Tylenol Cold and Sinus and isolated at home for the next 5 days and wore a mask for 5 days. The symptoms went away temporarily but I then developed Vertigo with Migraines. The most recent occurrence was this morning. I was prescribed medication for Vertigo but once the spinning is over I develop a migraine headache with extreme sensitivity to light. The doctor is having me chart how often it happens to determine whether I need to be on an additional medication to treat the migraines. I was driving when the Vertigo hit in the middle of a thunder storm. I had to drive 27 miles. I went to the hospital and had a CT Scan, Chest X-Ray, and a blood panel. I was given medications for the vertigo and nausea and headache. This has happened at least 3 times in the last 7 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- COVID-19 PCR Test-May 19, 2022-Positive CT Scan-Normal-06-10-2022 Chest X-Ray-Normal-06-10-2022 Blood Panel-Normal-06-10-2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Bioidentical Estrogen Progesterone Compound Medication; Armor Thyroid; Calcium; Magnesium; D3; Probiotic; Multi Vitamin with Iron
- Allergien
- Penicillin; Sulfa Drugs
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 28.03.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 65,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dyspnoea
Feeling abnormal
SARS-CoV-2 test positive
Symptomtext
I had a little cough that I did not think much of because I have asthma. I went out of town on the 9th and I still had the cough. The next day I was feeling out of breath and out of sorts. The next morning on the 11th, I still wasn't feeling right so we decided to take the home COVID-19 which was positive. We came and called my doctor and she prescribed PAXLOVID. I took the first dose that evening. My symptoms were mild. I never had a fever. I can't say that the PAXLOVID helped since I really was not that sick. My symptoms did not get worse though. I do still have a slight cough but it could be seasonal allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID 19-home test-06-11-2022 positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Asthma; Thyroid Disease; Macular Degeneration
- Andere Medikamente
- Levothyroxine; amlodipine; valsartan; amitriptyline; albuterol; BREO ELLIPTA inhaler, PRED FORTE; various allergy eyedrops: PRESERVISION
- Allergien
- Azithromycin; polemician; environmental allergies
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 09.04.2022
- Beginn
- 10.04.2022
- 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 nodule
Mobility decreased
Pain in extremity
Peripheral swelling
Symptomtext
arm swelling and large nodule at injection site. Swelling still present 2+ months after injection when patient presented in June 2022. She could not lift her arm above her head by early June. I had her take ibuprofen q8H for 4-5 days and swelling did reduce but nodule is still present as well as arm pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Patient visited her dr regarding arm pain in early June 2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 07.06.2022
- Impfdatum
- 21.04.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 42,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test normal
Chest pain
Electrocardiogram normal
Symptomtext
Stabbing chest pains on the upper left side. Hurt a lot and went on and on
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG showed no acute symptoms. Blood work showed no markers for heart attack.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- Combivent Respimat (Inhalation spray treatment)
- Allergien
- dust, pollen, mold
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 07.04.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 58,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Aspiration pleural cavity
COVID-19
Confusional state
Dyspnoea
Extra dose administered
Hypercapnia
Hypoxia
Interchange of vaccine products
Pleural effusion
SARS-CoV-2 test positive
Use of accessory respiratory muscles
Symptomtext
71-year-old male with chronic COPD and CHF presents to the emergency room with worsening shortness of breath. This is his fifth admission to the hospital for similar issues this past year. Has been having increasing shortness of breath and accessory muscle use. Started to have some increased confusion and family brought him into the emergency room. Noted to be hypoxic with hypercapnia. Received bronchodilator in the emergency room and placed on NIPPV. Had COVID back in March and incidentally tests positive again here today. No fevers, chills or purulent sputum at home. He has a history of mechanical aortic valve replacement. He was treated with Decadron and Remdesivir during hospital admission in March 2022 for COVID-19. He required thoracentesis for bilateral pleural effusions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 25.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ageusia
Arthralgia
Asthenia
Blood test normal
Constipation
Decreased appetite
Fatigue
Headache
Malaise
Mobility decreased
Pruritus
Pyrexia
Symptomtext
She got her vaccine on Monday, she was OK after that. By Tuesday she could not get out of bed, was sick. Has sick on and off, weak, fatigue, no appetite, her joints hurt. She started itching where she had surgery where she had her breast surgery due to cancer which was 10 years ago. This area has never bothered her until now. Also having fever and headache which subsided after taking Tylenol. Her appetite continues to be bad, she has no taste, and she is weak which is more than anything else. She saw her doctor and went to the UC where she had the vaccine, and they informed her it was a AE of the booster vaccine. This has been a while now, today makes 7 weeks and she is still having the weakness and loss of appetite as well. She can barely drink a little tea, is very constipated and can barely get out of the bed today. She has had the constipation after each vaccine, and goes back to normal and with each additional vaccine her constipation has worsened.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Her PCP did blood work which did not show any abnormalities.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure, breast cancer in 2012.
- Andere Medikamente
- Olmesartan 40 mg, Metoprolol 100 mg., Omeprazole 40 mg
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 05.06.2022
- Impfdatum
- 08.04.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 28,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Diagnosed with Lupus 30+ years ago. Been symptom free for 20+ years except rare occations during severe stress. Symptoms when tired/stressed are fatigue and fever blisters on the lips.
- Andere Medikamente
- Daily multi vitamins; B12, K1, fish oil, memory improvement supplement; Testosterone; Pregnenolone; Progestrone/estradiol.
- Allergien
- Contrast dye.
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Nausea
Pain
Palpitations
Pyrexia
Similar reaction on previous exposure to drug
Stomatitis
Vomiting
Symptomtext
Client called and reported that she is still having reactions to her vaccine 72 hours since vaccinated, and still has not let up in reaction. She reported vomiting/nausea, sores inside of her mouth, fever, headaches all over body aches, tiredness, racing heart. Client stated that it is worse and more sever than her other doses. Client stated that she was gong to call her cardiologist and follow up with him.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- pace-maker
- Andere Medikamente
- unknown
- Allergien
- -
- Vorherige Impfungen
- Moderna vaccine all of her other doses, similar reactions.
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Joint 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
- IL
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest X-ray
Cough
Dyspnoea
Fatigue
Influenza virus test negative
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Fatigue, congestion, coughing and shortness of breath. Tested negative for Covid and flu at healthcare facility. On May 12, tested positive for Covid using at-home test after attending holiday family gathering.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- PCR test and chest x-ray
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Enlarged prostate
- Andere Medikamente
- Vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 03.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Blood sodium decreased
Blood test abnormal
Cardiac monitoring
Extra dose administered
Laboratory test normal
Palpitations
Ventricular extrasystoles
Symptomtext
I began having heart palpitations on 4/7/2022, which was 4 days after I received my second Moderna booster. I saw my PCP on 4/19/2022. The PCP confirmed that she had detected premature ventricular contractions (PVCs), and she ordered bloodwork and an echocardiogram. She also instructed me to wear a heart monitor for three days. I did not receive the heart monitor until 4/27/2022, and I mailed it back on 4/30/2022. I never got the echocardiogram, because it wouldn't be possible to get an appointment until June. Regarding the bloodwork, my sodium was low, so my PCP had me restrict my fluid intake. The PVCs continued, and on the weekend of May 13-15, I felt like I was having angina pains. On 5/16/2022, I went to the emergency room. I was evaluated, and all the test results were either normal or stable. Even though I was still having PVCs, the doctor thought that my condition was stable and referred me to a cardiologist for further evaluation. My appointment with the cardiologist is on 5/25/2022. At the time of this writing, I continue to have PVCs intermittently on a daily basis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; GERD
- Andere Medikamente
- Bupropion HCl, baby aspirin, hydrochlorothiazide, telmisartan, amlodipine, isosorbide, pravastatin, omeprazole, famotidine, Flovent HFA, albuterol (PRN), azelastine, fluticasone propionate, Ambien, Fiorinal, lorazepam, fish oil supplement.
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypophagia
Immediate post-injection reaction
Influenza like illness
Injection site pain
Malaise
Mobility decreased
Muscle spasms
Nausea
Pain
Pain in extremity
Symptomtext
She got her vaccine, this was the worst person that gave her the shot that she ever had as she darted it in and then pushed it in and had immediately pain. She felt sore all over, felt like she had the flu. She went to bed and then didn't not move until today. She literally was sore all over. In her thighs was probably the worse and the arm where she put it in. She felt kind of crampy, little nauseated, did not eat much yesterday, did not feel good until today. Today she is better, feels that she is going to get over it, but feels is it worth it. They had COVID in February of this year and said that if you had COVID (Omicron), you may have a worse reaction to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Multivitamin, Lexapro, Propranolol, progesterone.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 30.04.2022
- Impfdatum
- 23.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Chills
Fatigue
Migraine
Nausea
Oropharyngeal pain
Pyrexia
Symptomtext
100.4 fever by evening of first day, chills, abdominal pain, nausea, migraine, sore throat on one side, fatigue. Fever broke overnight; all symptoms seemed to resolve by the end of the second day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- osteoporosis, arthritis, back issues (degenerative discs, foraminal stenosis)
- Andere Medikamente
- Levothyroxine, Metoprolol, Rosuvastatin, glucosamine/chondroitin/MSM, turmeric, NAC, Resveratrol, magnesium glycinate, multivitamin, baby aspirin every other day.
- Allergien
- sulfa, INH, Symbicort, latex
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 30.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Insomnia
Transient acantholytic dermatosis
Symptomtext
most intense beating of Grover's / It's really really bad case of Grover's disease/Scratching to point where I am bleeding; Can't sleep and relax; Grover's condition aggravated; This spontaneous case was reported by a consumer and describes the occurrence of TRANSIENT ACANTHOLYTIC DERMATOSIS (most intense beating of Grover's / It's really really bad case of Grover's disease/Scratching to point where I am bleeding), INSOMNIA (Can't sleep and relax) and CONDITION AGGRAVATED (Grover's condition aggravated) in a 70-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. The patient's past medical history included Tinnitus (drug induced), Pneumonia (he was overdosed with antibiotics and had Pneumonia 5 times in last 10 years), Drug overdose (Antibiotics), Drug overdose (Pharmaceutical product) and Prostate surgery. Concurrent medical conditions included Gout, Blood pressure high, Immunocompromised and Grover's disease. Concomitant products included LOSARTAN and AMLODIPINE for Blood pressure high, FEBUXOSTAT (ULORIC) for Gout, MORNIFLUMATE (FLOMAX [MORNIFLUMATE]) for Prostate surgery. On 12-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced TRANSIENT ACANTHOLYTIC DERMATOSIS (most intense beating of Grover's / It's really really bad case of Grover's disease/Scratching to point where I am bleeding), INSOMNIA (Can't sleep and relax) and CONDITION AGGRAVATED (Grover's condition aggravated). At the time of the report, TRANSIENT ACANTHOLYTIC DERMATOSIS (most intense beating of Grover's / It's really really bad case of Grover's disease/Scratching to point where I am bleeding), INSOMNIA (Can't sleep and relax) and CONDITION AGGRAVATED (Grover's condition aggravated) outcome was unknown. Patient was diagnosed with Grover's diseases few years ago. And also after the booster shot, for 5-6 days he has had the most intense beating of Grover's. Symptoms were mentioned as whole body was itching and hurting. All over the body, head, armpit, chest, arms, crotch, hands, legs, and feet. No treatment medications reported. Company Comment: This spontaneous case concerns a 70-year-old male immunocompromised patient, with relevant medical history of Grover's disease, who experienced the unexpected events of Transient acantholytic dermatosis, Condition aggravated and Insomnia. The events occurred on an unknown date after receiving the fourth dose of mRNA-1273 Vaccine. Symptoms were mentioned as whole body was itching and hurting. No treatment medications reported. The outcome of the events was reported as unknown. The patient's medical history of being immunocompromised and having Grover's disease, remain as confounders for the occurrence of the events. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. This case was linked to MOD-2022-550528 (Patient Link).; Sender's Comments: This spontaneous case concerns a 70-year-old male immunocompromised patient, with relevant medical history of Grover's disease, who experienced the unexpected events of Transient acantholytic dermatosis, Condition aggravated and Insomnia. The events occurred on an unknown date after receiving the fourth dose of mRNA-1273 Vaccine. Symptoms were mentioned as whole body was itching and hurting. No treatment medications reported. The outcome of the events was reported as unknown. The patient's medical history of being immunocompromised and having Grover's disease, remain as confounders for the occurrence of the events. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood pressure high; Gout; Grover's disease; Immunocompromised
- Vorgeschichte
- Medical History/Concurrent Conditions: Drug overdose (Pharmaceutical product); Drug overdose (Antibiotics); Pneumonia (he was overdosed with antibiotics and had Pneumonia 5 times in last 10 years); Prostate surgery; Tinnitus (drug induced)
- Andere Medikamente
- LOSARTAN; AMLODIPINE; FLOMAX [MORNIFLUMATE]; ULORIC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 16,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthritis
Extra dose administered
Injected limb mobility decreased
Injection site pain
Pain in extremity
X-ray abnormal
Symptomtext
Severe pain in my left arm and shoulder. Could hardly move it and used a heating pad. The doctor could not see me till 4/27/22. My orthopedic doctor gave me a cortezone shot. He also took an xray. He saw minor arthritis. He said he could not get further info unless he did an MRI. I cannot get and MRI because of my Artificial Aortic Heart Valve. It is still aching. Not quite as bad. I am dealing with the pain by taking Tylenol Arthitis 650 mg/6 a day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- xray 4/27/22 See above
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- arthritis
- Andere Medikamente
- -
- Allergien
- vancomycin
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 10.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Tinnitus
Symptomtext
Starting 04/10/2022, I developed really loud Tinnitus and it has continued to this day. I have had this condition since before the vaccine but it has become much worse and intolerable. I will be seeing my PCP soon in regards to it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Prostate Cancer in remission
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 24.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dyspnoea
Exercise tolerance decreased
Feeling cold
Lip dry
Loss of personal independence in daily activities
Malaise
Mobility decreased
Nausea
Pain
Positive airway pressure therapy
Pyrexia
Symptomtext
So, I got the vaccine on Sunday about 03:30PM, I was okay, I went to bed and was okay. I got up at 05:00 AM in the morning, I felt the need to use the bathroom, I felt very nauseous. I did not go back to bed, I laid on the floor in the bathroom in case I threw up. Just very nauseous but never threw up. I started to get chills and body aches where I felt I could not get up. I had my husband cover me up with robes and blankets on the floor. I had my husband get me some water. My lips were really dried out so I got some chap stick. I laid on the floor until about 08:00 AM, then my husband helped me to bed. I had chills and fever. At about 11:00AM when I woke up, I realized I was not well. The nurse I called suggested I stay hydrated and take Motrin. We did not have Motrin, but I took Ibuprofen. My fever was high at 102.8 at 05:00PM on Monday. My husband put a cool cloth on my forehead and the temp came down to 101.4 at 06:00PM. I basically had noodle soup and Jello. I was still nauseous. I had some toast and white rice, that BRAT Diet. Monday night I was having a hard time breathing. I have a CPAP and decided to use it to get more oxygen. I moved to the recliner in the front room and brought the CPAP with me. Just as it started at 05:00 AM on Monday, I began to feel better at 05:00AM on Tuesday. I still feel phewy, I am taking it easy and have not gone outside. Still eating the BRAT diet and I cancelled all of my appointments I had on Monday & Tuesday. I have nothing today so I am just taking it easy. Today id Wednesday. I am better, but certainly not back to where I was before this, I do not feel like doing any strenuous exercise. I feel walking is what will be best. I typically go to the gym and work out with a trainer, but I do not have the desire to do that. I feel that I am only able to do some walking.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- CLL Chronic Lymphatic Leukemia - in a monitoring stage, issues with lymphatic system, chronic Mono
- Andere Medikamente
- Vitamin D Drops; Vitamin A drops; Thymus PMG 2 tabs; Vitamin C; Zinc-Zyme; Cap G; Magnesium Striate; Ashwagandha; Pre- Biotic
- Allergien
- Levaquin
- Vorherige Impfungen
- All the Pfizer vaccines, mild flu like symptoms, lasted a day. (typical symptoms) and swollen glands. Shingles Vaccine - at the
- Staat
- CT
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 25.04.2022
- 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: nein
Hypoaesthesia
Injection site pain
Injection site swelling
Paraesthesia
Symptomtext
Site: Pain at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Additional Details: patient came in post administration and said his arm was sore at the injection site and had some pins and needles feeling in him arm since the injection, however , he said it was slowly improving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 29.03.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Atrial fibrillation
Cardiac function test
Condition aggravated
Full blood count
Heart rate increased
Liver function test
Renal function test
Similar reaction on previous exposure to drug
Urine analysis
Symptomtext
Two weeks after the injection, I went into atrial fibrillation with rapid ventricular response. My heart rate was over 140. It began at 8 AM Pacific time, by 9:30 I was in the local emergency room. After they spoke with my doctors in hospital, they admitted me. I was in A-fib until 6:30 PM. At around 10:30 AM they put me on an I.V. with medication to slow down my heart rhythm. But the medication did lower my blood pressure so I had to stay at the hospital for 24 hours. This same basic chain of events occurred two weeks after my 3rd dose of my COVID-19 vaccine and then again at 4 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 1,0
- Labordaten
- Complete blood count; Metabolite test for kidney and liver function; Urinalysis; Test for heart attack. Have requested more specific medical records but have not yet received them.
- Aktuelle Erkrankungen
- 3/9-fever; 3/14-biliary colic/elevated liver enzymes (possible passing of gallstone)
- Vorgeschichte
- Cerebral Cavernous Mouth Formations; Labial Hypertension; Atrial Fibrillation with Rapid Ventricular Response; Osteoarthritis; Low Platelet Count
- Andere Medikamente
- Sotalol; Spironolactone; Norvasc; Levetiracetam; Lipitor; Synthroid; Zyrtec
- Allergien
- Poor reaction to Narcotics
- Vorherige Impfungen
- similar of events occurred after 3rd dose of Pfizer vaccine
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 19.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Fatigue
Malaise
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
On 4/5/2022, I received my second Moderna booster. On maybe 4/9/2022, I attended a "super spreader event," which was a wedding. On the afternoon of 4/11/2022, I began to not feel well. I felt a bit tired and had a slight runny nose, a sore throat, and sniffles. I took an at-home test for COVID and got a positive result. I sent an email to my doctor and informed her of my situation. A few hours later, I got a video call from a HCF, in which I spoke to a nurse practitioner. A PCR test was scheduled; I took it and got a positive. I was also scheduled to receive a monoclonal antibody infusion around 1 PM on 4/15/2022, which I did receive. After about 4 hours, I felt great. My sniffles were gone, and I could breathe normally. The next day, I felt even better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Slight Heart Murmur; High Cholesterol.
- Andere Medikamente
- Simvastatin; Tamsulosin; Mirtazapine; Vitamin D; Zinc (occasional); Turmeric Extract (occasional).
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 19.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Burning sensation
Fatigue
Injection site induration
Myalgia
Pneumonia
Sleep disorder
Symptomtext
ABOUT 5 PM GOT TIRED, SHOT SITE GOT FIRM, ALL MUSCLES BURNED AND THEN TIRED. FELL ASLEEP. WOKE UP AT 2 :30 AM WITH BURNING LUNGS, CALLED 911. WAS TAKEN TO HOSPITAL WHERE THEY STATED I HAD PNEUMONIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- PRASUGREL, OMEPRAZOLE, LIPITOR
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Chapped lips
Feeling hot
Insomnia
Lip haemorrhage
Lip swelling
Mouth swelling
Oral mucosal blistering
Oral pain
Paraesthesia
Pharyngeal swelling
Pruritus
Skin burning sensation
Urticaria
Symptomtext
A few days after my covid vaccine while I was watching tv I felt my face was tingling , I went to the bathroom to look in the mirror and I can see my lip swelling and cracking and it started bleeding. Blisters inside my mouth, from one side of my mouth to the other side of my mouth and pink. My mouth and throat felt swollen. My chin was blistered and my neck. At the top of my chest I broke out with large whelps and they burn and itch. I haven't slept in 2 days. It really bothers me. My mouth hurts. My head felt hot but didn't take my temp. All lasting a week. Treatment: None still have stuff on the top of my chest, like whelps and my mouth, bottom lip still broken and cracked.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- NO
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- Breast caner, lung cancer, licky mitral valve
- Andere Medikamente
- Levothyroxine, Atenolol
- Allergien
- Oysters, Nyquil
- Vorherige Impfungen
- Side effects to all 4 COVID/booster vaccines
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 19.02.2021
- Beginn
- 14.04.2022
- Tage bis Beginn
- 419,0
- Dosis
- 4
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Sepsis
Urinary tract infection
Symptomtext
Pt was a direct admit from Hospital and was admitted for shortness of breath and found to have a UTI with sepsis. She was tested for COVID prior to transfer and found to be COVID positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Deafness
Dizziness
Ear discomfort
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: loss of hearing (which has subsided now), clogged feeling in ears (pt had hearing loss prior to vaccine but thinks this temporarily made it worse)-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 14.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Extra dose administered
Heart rate increased
Heart rate irregular
Injection site pain
Malaise
Paraesthesia
Symptomtext
Approximately 20 minutes after receiving the 4th dose (2nd booster), I felt unwell. Flushed face, but no temperature. Although I had a feeling of unwellness after my first 3 shots, that feeling did not come until the next day after I woke up. Since April 3, my main complaints are as follows: (1) an elevated blood pressure and heart rate reading on my at-home blood pressure monitor; (2) an "irregular heartbeat" indicator coming on after multiple, but not every reading ;(3) an occasional tingling/pins and needle feeling in my mid-back on the right side; (3) occasional pain in my right bicept, near the site of the injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None yet, except for the elevated blood pressure, heart rate and "irregular heartbeat" indicator on my at-home blood pressure monitor.
- Aktuelle Erkrankungen
- Unknown- possible asymptomatic Covid Infection.
- Vorgeschichte
- None, except for low thyroid levels and elevated cholesterol.
- Andere Medikamente
- Levothyroxine; Atorvastatin
- Allergien
- None known.
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 09.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Hyperaesthesia
Hyperhidrosis
Ophthalmic migraine
Symptomtext
Skin sensitivity Diaphoresis Diarrhea Visual migraine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ophthalmic migraine
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High cholesterol Diabetes
- Andere Medikamente
- Tamsulosin. Vitamin D 125 Vitamin D. Lisinopril 5 mg One a day multivitamin Fish oil, 2000 mg omega 3 Metformin. 500 mg 2 daily
- Allergien
- No
- Vorherige Impfungen
- Fever,aches,chills, 10/21, 3/21, 2/21
- Staat
- MI
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Tracheitis
X-ray
Symptomtext
Patient received her 2nd Moderna vaccine @ pharmacy around 1030a. She then became short of breath & struggling to breath. She called our office as was told ER but wanted to come here. Provider seen her gave Duoneb which did help symptoms, XRAY, 50 mg Benadryl Provider feels Tracheitis & observed in office 2 hors was given Rx for duoneb and Benadryl. Patient was brought in by mom and both were informed not to leave patient alone. Stay hydrated and to go directly to ER if Recurrence, rash, S.O.B, difficulty swallowing or drooling, or any other Allergic Response.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Effexor, Sulfa, Mafenide
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Peripheral swelling
Swelling face
Symptomtext
Patient has swelling in both hands bad enough that she can't make fists as well as facial swelling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- eliquis
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- 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
Extra dose administered
Fatigue
Headache
Injection site reaction
Nausea
Pain
Pain in extremity
Rash macular
Respiratory tract congestion
Symptomtext
Day 2: sore arm, blotchy rash at and below injection site, body aches, fatigue Days 3-6: head ache, body aches, fatigue, congestion, nausea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- T2 Diabetes Allergy-generated asthma
- Andere Medikamente
- Metformin Glipizide Anti-oxidant
- Allergien
- Penicillin Sulfa Butazolidine Kiwi Mango Pineapple Bee stings
- Vorherige Impfungen
- Same reactions for all other Covid vaccinations and after first Covid injection also tongue tingling and dizziness
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 08.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Chest X-ray normal
Dyspnoea exertional
Dysstasia
Electrocardiogram normal
Exercise tolerance decreased
Fatigue
Headache
Loss of personal independence in daily activities
Pain
Tinnitus
Symptomtext
difficulty breathing with any exertion, unrelenting ringing/hissing in both ears, inability to exercise, fatigue, inability to do daily activities not necessary for hygiene and food headache, sharp intermittent pains (like wasp sting) on right side of body primarily Inability to exercise at pre-booster levels continues with slow improvement over the last month. 3/7/22 did weight training all muscle groups and could manage easily 2 miles on treadmill in 27 minutes at a 4.5 incline, reaching at peak a 140 heart beat. After booster increasingly difficult to climb one flight of stairs, stand long enough to brush teeth. 3 weeks post booster mild exercise possible
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- EKG and chest exray showed no abnormalities Albuterol prescribed to ease breathing
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- migraine
- Andere Medikamente
- magnesium, b-12, D3, multi
- Allergien
- none
- Vorherige Impfungen
- Covid initial and 2nd dose (similar to booster)
- Staat
- CT
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 03.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Feeling abnormal
Headache
Injection site pain
Interchange of vaccine products
Malaise
Mobility decreased
Myalgia
Nausea
Symptomtext
Injection site pain, Fatigue, Chills, Nausea, Headache, Muscle pain, Malaise , I am currently in bed. I feel terrible., I took Tylenol and Ibuprofen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- I will be seeing the doctor on 04/07/2022.
- Aktuelle Erkrankungen
- Strep C infection
- Vorgeschichte
- Neuro-sarcoidosis, Asthma
- Andere Medikamente
- Tylenol, Ibuprofen, Humira 40mL once a week (four hours after taking the 3rd dose)
- Allergien
- Penicillin, Shellfish
- Vorherige Impfungen
- 2nd dose of Pfizer
- Staat
- MN
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling cold
Headache
Injection site erythema
Injection site hypoaesthesia
Injection site induration
Injection site pain
Injection site reaction
Injection site swelling
Lymphadenopathy
Tremor
Withdrawal syndrome
Symptomtext
Day after had red sore at injection site size of dime. Also experienced what was like withdrawal symptoms like the shacks and freezing. The next morning (2 days after shot) injection site grew to the size of a 50? coin. Within 8 hours grew to the size of my palm. I've taken Tylenol for that along with the headaches and the swollen armpit lymph nodes. Its painful, red, hard to the touch, and when others gently touch it I can't feel it. This is the same reaction i had to the influenza, varicella, and second dose of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None yet if it keeps growing will go in on 5/04/2022
- Aktuelle Erkrankungen
- A cold 3 weeks prior
- Vorgeschichte
- depression Anxiety Insomnia
- Andere Medikamente
- LamoTRIgine
- Allergien
- influenza virus vaccines Varicella virus Vacc live (pf) Second dose of moderna
- Vorherige Impfungen
- Swelling of injection site within 24 hours same as booster. 8 years old, varicella virus vacc live (pf), 8/3/2010, live, merck&c
- Staat
- AZ
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- 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: nein
Blood pressure increased
Erythema
Heart rate increased
Migraine
Nausea
Photophobia
Skin swelling
Symptomtext
Sudden fever 100 degrees, 26 hours post vaccine Eyes sensitive to light Migraine Raised red area, 3? oval, appeared 24 hours post vaccine Nausea Rapid heart beat, elevated blood pressure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Fever 100 degrees, Took two Tylenol, extra strength at 5:30 PM , 4/1/2022 BP 149/78. Pulse 80. At 6:00 PM, 4/1/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 30.03.2022
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Mobility decreased
Musculoskeletal stiffness
Pain in extremity
Symptomtext
Patient says that he got severe arm pain about 4 hours after getting the vaccine, which has lead to his arm to be stiff and can barely move it. Patient also said he felt some arm pain when got injected and has never experienced that before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- nothing listed in patient profile
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Erythema
Tremor
Symptomtext
Patient got dizzy and started shaking. Face turned red. Patient calmed down shortly. Parent then admitted patient had anxiety over needles and required special attention at doctor's office for vaccinations
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- 911 was called. Patent did not want emergency services to come out. They refused.
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- none
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Diarrhoea
Insomnia
Nausea
Oxygen therapy
Palpitations
Symptomtext
Pt stated having common side effects of chills, nausea, diarrhea on the same day for approx 7 hours but on 3/23/22, started having a racing heart rate, not being able to sleep, and had to use her home oxygen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma, restrictive and obstructive lung disease
- Andere Medikamente
- unknown
- Allergien
- sulfa meds, sea food, hydrocodone
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 28,0
- 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: ja
Eye movement disorder
Feeling hot
Muscle twitching
Tremor
Symptomtext
Patient received her COVID Moderna booster vaccine. Per the technician giving the vaccine, she was reportedly feeling anxious and nervous prior to the dose because she does not like needles. Patient reported feeling warm but was able to walk out of the vaccine room without issues. About 5 minutes after, other techs heard her mom ask if she was okay and she was reportedly twitching/shaking and her eyes were going back and forth. Pharmacist on duty checked her blood pressure and it was normal. Mom requested to call 911 and paramedics arrived. She was given water and ice. Ultimately, she did not leave with the paramedics and was okay to go home with her parents.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 09.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Paraesthesia
Pruritus
Urticaria
Symptomtext
Hives / itchy skin on body, tingling on head...Meds taken, Prednisone 50mg, Benadryl 25mg, Pepcid 40mg
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/a
- Andere Medikamente
- B12, omega 369, biotin
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 13.12.2023
- Impfdatum
- 03.10.2022
- Beginn
- 12.12.2023
- Tage bis Beginn
- 435,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Fatigue
Pyrexia
SARS-CoV-2 test
Symptomtext
Cough, fevers, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- IDNOW
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, hyperlipidemia
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 05.05.2023
- Impfdatum
- 04.05.2022
- Beginn
- 19.09.2022
- Tage bis Beginn
- 138,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Antinuclear antibody positive
Arthralgia
Arthritis
Immunology test normal
Inflammation
Pain
Pain in extremity
Rash
Symptomtext
9/19/22 I woke up and all my joints from my neck to my toes ached. It was a strong ache. It lasted about a week or week and a half. It subsided except for my hands which got worse. It has never gone away. I now have arthritis in my thumb and take turmeric, ginger and ADVIL for the pain. I developed a rash on the bottom part of my shin that has never gone away. I have been tested and sent to a Rheumatologist and was tested for auto immune diseases and all came back negative except the ANA test which showed inflammation in my body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- 21NOV22 Auto Immune tests negative; 21NOV23 ANA test inflammation
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Bupropion; LO LOESTRIN; multivitamin
- Allergien
- None
- Vorherige Impfungen
- 1st Moderna vaccine, 54 years old, vaccine rash.
- Staat
- NH
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 04.05.2023
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acupuncture
Arthralgia
Bursitis
Pain in extremity
Symptomtext
Patient states that she developed severe pain in the shoulder after the vaccination. She didn't notify us back then and she mentioned it today when she came to get a bivalent shot. She went to the MD right after receiving the vaccination as the pain was not going away and the MD said it was Bursitis possibly caused by the vaccination. She tried different things and nothing helped the pain relief. She ended up going to an accupuncturist and after getting several months of accupuncture therapy, took a herbal pill per accupuncturist recommendation. She thinks the pill had helped her after taking for 2 months. She is fine now except she has a slight achy feeling in her arm all the time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 21.04.2023
- Impfdatum
- 06.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Rash
Rash pruritic
Symptomtext
The rash is on his back, chest scalp, some on the limbs, patches of rash. It is worse around the waist or anywhere that there is tight clothing or a belt. Some patches come and go anywhere around his body.; My husband has a rash that itches all over his body that has not gone away; The patient was a little tired on the first day or two.; This spontaneous case was reported by a patient family member or friend and describes the occurrence of RASH (The rash is on his back, chest scalp, some on the limbs, patches of rash. It is worse around the waist or anywhere that there is tight clothing or a belt. Some patches come and go anywhere around his body.), RASH PRURITIC (My husband has a rash that itches all over his body that has not gone away) and FATIGUE (The patient was a little tired on the first day or two.) in a 56-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 prophylaxis. Patients wife reported patient had no chronic medical conditions. The patient received no other vaccines in the 4 weeks around either of his Moderna Covid-19 vaccines. Previously administered products included for Product used for unknown indication: PFIZER BIONTECH COVID-19 VACCINE (first booster dose), PFIZER BIONTECH COVID-19 VACCINE (Primary Series, Dose 2), PFIZER BIONTECH COVID-19 VACCINE (Primary Series and Dose 1). Past adverse reactions to the above products included No adverse event with PFIZER BIONTECH COVID-19 VACCINE, PFIZER BIONTECH COVID-19 VACCINE and PFIZER BIONTECH COVID-19 VACCINE. Concomitant products included ACYCLOVIR [ACICLOVIR], FINASTERIDE, VALSARTAN, ROSUVASTATIN and TADALAFIL for an unknown indication. On 06-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced RASH (The rash is on his back, chest scalp, some on the limbs, patches of rash. It is worse around the waist or anywhere that there is tight clothing or a belt. Some patches come and go anywhere around his body.), RASH PRURITIC (My husband has a rash that itches all over his body that has not gone away) and FATIGUE (The patient was a little tired on the first day or two.). The patient was treated with PREDNISONE for Rash, at an unspecified dose and frequency; LORATADINE at an unspecified dose and frequency; DIPHENHYDRAMINE at an unspecified dose and frequency; HYDROCORTISONE at an unspecified dose and frequency and TRIAMCINOLONE ACETONIDE at an unspecified dose and frequency. At the time of the report, RASH (The rash is on his back, chest scalp, some on the limbs, patches of rash. It is worse around the waist or anywhere that there is tight clothing or a belt. Some patches come and go anywhere around his body.) and RASH PRURITIC (My husband has a rash that itches all over his body that has not gone away) had not resolved and FATIGUE (The patient was a little tired on the first day or two.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that the rash was not on patient face. The patient saw a dermatologist and was prescribed Prednisone. The Prednisone calms the rash down however the rash does not completely go away. The patient was also on Loratadine, Diphenhydramine, hydrocortisone cream, triamcinolone acetonide cream. This case was linked to US-MODERNATX, INC.-MOD-2023-720381 (E2B Linked Report). This case was linked to MOD-2023-720365 (Patient Link).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-720381:Same reporter case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patients wife reported patient had no chronic medical conditions. The patient received no other vaccines in the 4 weeks around either of his Moderna Covid-19 vaccines.
- Andere Medikamente
- ACYCLOVIR [ACICLOVIR]; FINASTERIDE; VALSARTAN; ROSUVASTATIN; TADALAFIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 11.04.2022
- Beginn
- 25.03.2023
- Tage bis Beginn
- 348,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Chills
Fatigue
Pain of skin
SARS-CoV-2 test positive
Sinusitis
Symptomtext
It felt like I had a sinus infection, my face hurt to touch, I was exhausted, I had chills. I took a home COVID-19 test that came positive. I called to have a telehealth visit with my primary care physician, we discussed my symptoms. I was given a prescription for Paxlovid that I started immediately, in a couple of days my symptoms were gone and my energy returned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 25MAR2023 Home COVID-19 test - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Crestor; Hydrochlorothiazide; Carvedilol; Adult Multivitamin; Turmeric: Luetin Xanthin; Biotin; Fish Oil; CoQ10; Vitamin D
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 15.04.2023
- Impfdatum
- 31.03.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 96,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy skin
Rash
Rash pruritic
Symptomtext
Skin rashes over arms around elbow/hands, legs mostly over knees and low thighs, buttocks, flanks. Started since July 2022 and still appearing, each lasting weeks. Very itch. It looks like Pityriasis Rosea as reported in an article
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Skin biopsy of rashes. Nov.2, 2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteopororsis, Hypothyroidism
- Andere Medikamente
- Prolia, Levothyroxine, Vit C, multivitamines, Calcium,
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 14.04.2023
- Impfdatum
- 12.04.2022
- Beginn
- 29.03.2023
- Tage bis Beginn
- 351,0
- Dosis
- 5
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Headache
Malaise
Nasal congestion
SARS-CoV-2 test positive
Symptomtext
My COVID-19 symptoms started on 03/29/2023 in the afternoon. I had fatigue, headaches, and nasal congestions. On the 03/30/2023 before going to work I tested myself and it was positive. I did a telehealth with my doctor who then prescribed me PAXLOVID for 5 days. On 04/05/2023 I tested negative. As of today I still have fatigue, runny nose and sinus/nasal symptoms but I tested negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 30MAR2023 COVID-19 test positive; 05APR2023 COVID-19 test negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- N/A
- Allergien
- LEVAQUIN
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 12.04.2023
- Impfdatum
- 11.04.2022
- Beginn
- 28.01.2023
- Tage bis Beginn
- 292,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Facial pain
Herpes zoster
Hypoaesthesia
Paranasal sinus discomfort
Post herpetic neuralgia
Sneezing
Urinary tract infection
Vaccination site erythema
Vaccination site urticaria
Symptomtext
In January 2022, I had a cough, sneezing, and sinus pressure. The cough lasted but 6 weeks. Then, I got Shingles in 3/23. I contacted my doctor and was prescribed methylprednisolone and acyclovir. I did this for a week and my face started to go numb. Now it is numb and hurting. I went to the doctor, and he told me I have Postherpetic Neuralgia. I was prescribed gabapentin for this. I also have UTI. My doctor has also changed my medication for Migraines. I am taking TOPAMAX, EMGALITY, and CIPRO. I am still dealing with this at this time. I also had a red welt around the vaccination site for about 2 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Fibromyalgia; Non-Alcoholic Fatty Liver Disease; Sleep Apnea; Hypothyroidism; Asthma
- Andere Medikamente
- Duloxetine; CELEBREX; hydroxyzine; clotiapine; baclofen; gabapentin; vitamin B12; fish oil; multivitamin; turmeric; magnesium; calcium; vitamin D; levothyroxine; rizatriptan; TYLENOL
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 04.04.2023
- Impfdatum
- 31.03.2022
- Beginn
- 25.03.2023
- Tage bis Beginn
- 359,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Headache
Pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
It started with a runny nose, a headache, and a cough. I did not run a fever. I had body aches. I test myself for COVID-19 and it was positive. I went to the doctor and they did a PCR test and it was positive. I took PAXLOVID for 5 days. Now I have a rebound case of COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 25MAR2023 COVID-19 at home test positive; 25MAR2023 COVID-19 PCR test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Valsartan
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 04.04.2023
- Impfdatum
- 30.03.2022
- Beginn
- 10.02.2023
- Tage bis Beginn
- 317,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
COVID-19
Fatigue
Feeling abnormal
Headache
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Started feeling poorly and tired. I did run fever for 6 days, lost my sense of smell, headache. The highest fever was 102.0 but it did vary throughout the day and night. I did go to the local clinic and was prescribed PAXLOVID for 3 days because of the horrible side effects. I started feeling better in about a week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 2023FEB11 home COVID-19 test positive, 2023FEB12 rapid COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin; vitamin D3+; probiotic
- Allergien
- None
- Vorherige Impfungen
- Influenza, years ago
- Staat
- WY
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 03.04.2023
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Pain
Pyrexia
Symptomtext
My symptoms were tiredness, body aches, fever , I was Ibuprofen for my symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- Losartan; Symbicort;
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 24.03.2023
- Impfdatum
- 23.03.2022
- Beginn
- 28.02.2023
- Tage bis Beginn
- 342,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Ageusia
Anosmia
COVID-19
Dyspepsia
Fatigue
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
I experienced a breakthrough case of COVID-19 and it felt like I had a cold at first, my nose was very runny but I knew it was more than a cold when I lost my sense of taste/smell. I tested positive for COVID-19 with slight fever, fatigue, loss of smell and taste, runny nose, upset stomach and heartburn. It seemed like COVID-19 made my heartburn even worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 positive 02/28/2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Cancer
- Andere Medikamente
- N/A
- Allergien
- Penicillin; codeine
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 20.03.2023
- Impfdatum
- 18.03.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 105,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heavy menstrual bleeding
Pain
Ultrasound uterus abnormal
Uterine mass
Symptomtext
Starting in July of 2022 I started having excessive menstrual bleeding that could not be controlled by medication. As of March 13, 2023, they located a baseball size in my uterus. I was also having pain that would not stop. The doctor tried 3 birth control medication which did not help. I have a follow up MRI on April 10, 2023. I am also scheduled to have a hysterectomy on April 28, 2023. My Ob-Gyn discovered the mass. I am still having the issue and awaiting surgery. I had dose 6 of the Pfizer Bivalent vaccine on November 4, 2022. This did not change the issue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Ultrasound March 13, 2023, baseball size mass discovered in uterus. Inter Uterine Ultrasound 09/27/2022 normal, no mass found.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Multiple Sclerosis
- Andere Medikamente
- NURTEC; ADDERALL; BOTOX; bupropion; FIORICET; clonazepam; B12 injections; FLORASTOR; folic acid; furosemide; gabapentin; guaifenesin; INJECTAFER; LEMTRADA; levothyroxine; lorazepam; methocarbamol; montelukast; NEXPLANON; omeprazole; oxycodo
- Allergien
- Latex; laundry detergent (except TIDE)
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 14.12.2022
- Impfdatum
- 13.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Symptomtext
itchiness, and sometimes redness, that shows up in different parts of the body. It is still going on, 8 months later. Dr. prescribed Prednisone 2x20mg/d for 5 days. + Hydroxyzine 14 daysx1 25mg
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- May 19, 2022 visited Dr.
- Aktuelle Erkrankungen
- non
- Vorgeschichte
- non
- Andere Medikamente
- non
- Allergien
- non
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 25.03.2021
- Beginn
- 29.03.2021
- Tage bis Beginn
- 4,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Gait disturbance
Pain in extremity
Peripheral swelling
Symptomtext
Prior of receiving my 1st dose of the full COVID-19 Moderna the COVIDF vaccine. I ask my primary care Dr. if there is any side effect from this COVID vaccine, Dr. informed me that there is NO side effect from this COVID-19 vaccine. Well I signed up and got my 1st full dose of Moderna the COVID vaccine on 3/25/2021, couple days later my left leg calf swelled up so bad that I had a very hard time walking, and that I thought I develop a blood clot from the vaccine. I went out to Hospital. This is when the emergency room was experiences lots of people coming in with the same issues that I was having. An Ultra sound was done to see if there was a blood clot in my left leg. This is when the doctor came into the room and informed me that they are seeing lots of patients that received the 1st full dose vaccine as a side effect causing their leg to swelled up. The next day I email my primary care CDr., about this. It took a while for the swelling to go down in the left leg. Then 2nd full dose of vaccine of Moderna on 04/22/2101, the same thing happened a couple days later left leg calf swelled up again. I email Dr. about this. When they came out with the booster shots, I informed Dr. that I am NOT going through this and NO more of these COVID vaccine/boosters. Dr. said the booster is half the dose over the full dose vaccine and will not have the side effect. He advised me in getting the 1sst booster, received 1st booster on 11/03/2021 at pharmacy, and BINGO once again the left calf swelled up. I informed Dr. this is it for me I'm NOT getting any more COVID vaccine/booster. Well Dr. and Dr. (podiatric), told me to get the 2nd Booster since I was going in as outpatient for surgery on my right foot since COVID counts was so HIGH once again. So, I went and got the 2nd Moderna booster on 06/20/2022, at Pharmacy. BINGO once again left leg calf swelled up. After this 4th COVID shot my left leg calf is still swallow and it has not gone down at all now the leg hurts.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Left leg long - Time swelling & Pain
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- Swelling of left leg calf and now pain
- Staat
- CO
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 17.11.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
C-reactive protein increased
Dizziness
Fatigue
Magnetic resonance imaging
Muscular weakness
Pain in extremity
Radiculitis brachial
Symptomtext
Pt. developed arthralgias in upper and lower extremities, fatigue, and dizziness the day following the covid vaccine. Due to intensity of symptoms and elevated crp (24)/esr(64). Pt was treated with Predinisone toper for several months. The joint pain improved over a few weeks but had persistant pain and weakness in right arm and dx with brachial neuritis based in exam/history and MRI. Pt improved over 8 months with steroids, PT, and hyperbaric oxygen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Livalo, lysine, vit d
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 10.11.2022
- Impfdatum
- 18.03.2021
- Beginn
- 11.09.2022
- Tage bis Beginn
- 542,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Pelvic pain
SARS-CoV-2 test positive
Symptomtext
09/11/22 presents to ED for "pelvic pain". PMHx of"mitral valve disorder, depression, neobladder, fibromyalgia, anxiety, COPD"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pelvic pain
- Hospital-Tage
- -
- Labordaten
- 09/11/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 27.10.2022
- Impfdatum
- 01.04.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 74,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test abnormal
Fatigue
Glycosylated haemoglobin increased
Hepatic enzyme increased
Pyrexia
Renal function test abnormal
Symptomtext
The day after I received the vaccine, I felt feverish and fatigue. It knocked me out. The symptoms were certainly gone within 24 to 48 hours. On 6/14/2022 I had blood work done. My liver enzymes were high, my A1C was up, and my kidney numbers were high. My endocrinologist suggested I go to a gastroenterologist, liver specialist, to check my liver enzyme. I had blood work done by that specialist and the results were fine. The enzymes had gone back to normal at that point. My kidney functions, I just saw my nephrologist, and he tell me that my kidneys seem to be stable. High but stable. next week I will go see my endocrinologist for my sugar, but that is to be determined. At the beginning of 11/3/2022. I will be going to my urologist, and he will let me know if I need a biopsy. I had bladder cancerous tumor removed 25 years ago in 5/2001 and in 12/2001, I had a second bladder tumor removed. Since then, I had no problems with my bladder. This was the first time the urologist looked inside my bladder and was unsure what he saw. I decided to wait 90 days check it again. As of a week ago, my liver enzymes and my kidney numbers were getting back to a better level. Next week, I will find out if my sugar levels are at a better level.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 06/14/2022- blood work- liver enzymes; glucose test; kidney test - my levels were high
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes; Chronic kidney disease
- Andere Medikamente
- Metformin; Vitamin D3; Glipizide; Tradjenta; Nebivolol; Amlodipine; Vitamin B12; Baby Aspirin; Simvastatin
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 20.04.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 135,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Ear infection
Fatigue
Feeling abnormal
Malaise
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Sinusitis
Sleep disorder
Symptomtext
I tested positive on the 2nd even though I was symptomatic on the 1st. Body ache, fever, congestion. I took PAXLOVID from the 2nd. I tested negative on the 21st. I had severe symptoms in the beginning and around the 11/12. I was sleeping less than 16 hours a day, was less fatigues. On the 14th I had a ear and sinus infection and was put on medication. I was still extremely tired up to a week ago. Now today I don't have the fog and not sleeping up to 16 hours a day anymore. On the 21st I tested negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test on the 2nd positive; on the 21st negative.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Sjogren's syndrome; High blood pressure; Gastric reflux; Osteoporosis
- Andere Medikamente
- Multivitamin; vitamin D; C; probiotic; PROLIA injection
- Allergien
- Lactose intolerant
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 14.10.2022
- Impfdatum
- 14.04.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 110,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Injection site erythema
Injection site pain
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
A little red spot and sore arm at the injection site for a day. I tested positive for COVID-19 with a home test on 08/02/2022. I had a low fever, runny nose, congestion and fatigue. I contacted my doctor the evening of 08/02/2022 and was given the prescription PAXLOVID. After 7 or 8 days I felt much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home test for COVID-19 was positive on 08/02/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Sleep Apnea; High Blood Pressure; Pacemaker; Osteoarthritis
- Andere Medikamente
- Hydrochlorothiazide; potassium extended release; atorvastatin; magnesium; multivitamin
- Allergien
- Aspirin; NSAID
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 14.10.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 91,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest X-ray
Cough
Fatigue
Headache
Myalgia
Pain
Pyrexia
SARS-CoV-2 test negative
Symptomtext
I started running a 101-102F fever; when I woke up that morning of 07/13/2022, I had that terrible fever that lasted for about 3 days. I had a really dry cough, headache, body and muscle aches, and that fever. I took an at-home COVID-19 test that came back negative. So I went to the local pharmacy to take a PCR test, but that one also came back negative. So I waited until my symptoms subsided to visit my physician. He took a chest x-ray and monitored my breathing and noted that I may have had COVID-19, but I'm doing better. As of now, I still have some minor fatigue since recovering.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test: 07/23/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Bechet's Disease; Basal & Squamous-Melanoma
- Andere Medikamente
- Multivitamin supplement; CRESTOR; hydrochlorothiazide; pantoprazole; FLONASE; ZYRTEC; vitamin D
- Allergien
- LEVAQUIN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 11.10.2022
- Impfdatum
- 11.04.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 175,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
COVID-19
Feeling abnormal
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Symptomtext
I received my second Moderna booster for COVID-19 on 4/11/2022. On the evening of 10/3/2022, I started to feel off. I felt kind of achy, so I took a home test for COVID-19 and got a positive result. I contacted my doctor on 10/4/2022 and requested PAXLOVID, which she prescribed to me. I took the PAXLOVID for the entire 5-day course. During my illness, my symptoms were mostly mild. I had a little bit of a sore throat, a temperature that never reached above 100, and a minor upset stomach. By 10/6/2022, I began to turn the corner and feel a lot better. Ever since then, I've been doing fine. I tested negative on 10/11/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test 10/3/2022 positive result; home COVID-19 test negative result.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Breast Cancer Survivor.
- Andere Medikamente
- Raloxifene; vitamin D.
- Allergien
- TIDE detergent.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 07.10.2022
- Impfdatum
- 02.04.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 150,0
- Dosis
- 4
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dizziness
Epistaxis
Exposure to SARS-CoV-2
Fatigue
Oropharyngeal pain
Pyrexia
Rebound effect
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
Late night sneezing and runny nose on August 30. Positive home antigen COVID test the next morning. My wife had a positive test and a visit to hospital two days earlier. I called my doctor on August 31 and she prescribed Paxlovid. I started taking it that day. Symptoms were a sore throat, fatigue and a 99.4 degree fever on 9/1. Started acetaminophen. No fever thereafter, but I did have nose bleeds for a few days. I tested negative on 9/6. Rebound begins on 9/10. Sneezing and runny nose on 9/10, positive test on 9/10. Some dizziness in the morning of 9/11 and a temp of 99. My notes don't say when I tested negative but I moved out of the guest room and back into our own bed on 9/15.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Antigen tests. See above.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Heart disease (CABG in 1997); stage 2 CKD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 06.10.2022
- Impfdatum
- 06.04.2022
- Beginn
- 14.08.2022
- Tage bis Beginn
- 130,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Head discomfort
Malaise
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Covid symptoms started on 08/14/2022; tested positive on 08/15/2022. I started running a fever of 100.5 and I went to urgent care. I also had congestion in my head. Symptoms lasted through that Saturday 08/20/2022. I checked to see if I was still positive a week later and I was but didn't feel sick at all. I went for an infusion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 Positive 08/15/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- high blood pressure; arthritis; diabetes type 2; PVCs; high cholesterol; spinal stenosis, acid reflux; rapid heart beat.
- Andere Medikamente
- Gabapentin; rosuvastatin; metoprolol; losartan; general allergy levlofexidine; generic for singulair, Celebrex, Prilosec, aspirin, calcium, vitamin b complex, multivitamin 50+, lutein, biotin, zinc, vitamin c, vitamin b3.
- Allergien
- Metaxalone; adhesives
- Vorherige Impfungen
- Smallpox- Rash on back. 60+ years ago.
- Staat
- NJ
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 02.04.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 139,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Audiogram abnormal
Balance disorder
Balance test
Blood folate normal
Blood test normal
Blood thyroid stimulating hormone normal
Deafness
Dizziness
Full blood count normal
Glycosylated haemoglobin normal
Lipids normal
Magnetic resonance imaging head normal
Metabolic function test normal
Thyroxine free normal
Urine analysis
Vertigo
Vitamin B12 normal
Symptomtext
I began experiencing vertigo, dizziness and balance issues. This did not occur until significantly after vaccination I have seen my PCP, had a balance test, blood work, sinus scan, brain MRI and PT. No testing showed a reason for the issue. It has improved somewhat over time and with PT continuing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- MRI brain - normal Vitamin B12/folate serum panel TSH w/reflection FT4 CBC, Lipid panel Comprehensive metabolic panel Urinalysis complete HemoglobinA1C All bloodwork was normal Balance testing- no significant result Audio gram - slight hearing loss
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Connective tissue disorder Osteoarthritis
- Andere Medikamente
- Flonase nasal spray Colestipol Esomeprazole magnesium Estradiol cream fluocinonide topical gel Gabapentin Hydroxychloroquine Meloxicam Mupirocin ointment Rest as is Calcium VitaminC Fish oil Probiotic
- Allergien
- Barbiturates Vancomycin Daptomycin Macrobid
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 01.04.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 164,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Malaise
Myalgia
Nasopharyngitis
Respiratory tract congestion
SARS-CoV-2 test positive
Symptom recurrence
Symptomtext
The first time I reported it to my Doctor and got Plaxovid and my symptoms lasted 5 days. By the time I finished the Plaxovid it was gone. I had tiredness, muscle aches, congestion. My symptoms were like a severe cold. On the night of sept 22nd I felt the symptoms come back, and I did a at home test and it was positive. The symptoms were about the same as before, again not horrible and not as bad but they lasted longer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 at home - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetic type 2
- Andere Medikamente
- Metformin; Alfonsine; Atorvastine; Metoprolol; Gabapentin; Levothyroxine; Finasteride; Cospot eyedrop; Lumagen eyedrop
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 04.10.2022
- Impfdatum
- 01.04.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 118,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
07/28/2022 Very bad sinus congestion runny nose and I had a slight fever. Talked to a dr and was given augmented and prozone because because we thought it was a sinus infection because I took a COVID-19 Test and it was negative. Sunday, It got worse so I took another test which was positive and I was given Paxlovid from my Primary doctor. I took one dose and had an allergic reaction, so I stopped taking it. I was then told to go back on the previous medication, and I had no sore throat. After about 5 days I saw improvement, but I was still positive 10 days later. Throughout this entire ordeal I took Tylenol and Motrin for the fever and pain. It started to resolve itself, but I was positive for about 30 days and I was extremely tired during this time. 9/10/22 I had to be treated with the same medication again because I had sinus issues and it didn?t completely resolve until mid September.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test (at home)
- Aktuelle Erkrankungen
- Sinus Infection
- Vorgeschichte
- High Blood Pressure. High Cholesterol, Sleep apnea
- Andere Medikamente
- Decline
- Allergien
- Tetratycline
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 04.10.2022
- Impfdatum
- 02.04.2022
- Beginn
- 19.09.2022
- Tage bis Beginn
- 170,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aphonia
COVID-19
Cough
Dry mouth
Injection site pain
Malaise
Oropharyngeal pain
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Tongue discolouration
Symptomtext
I had a sore arm at injection site that lasted for a day. I started not feeling well on 09/19/2022 with a severe sore throat, lost my voice, achy all over, congestion, coughing and my tongue was white. I tested positive for COVID-19 on 09/20/2022 via a home test. I contacted my doctor and was prescribed PAXLOVID. Today, I have a little cough that is lingering and dry mouth.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Home test was positive for COVID-19 on 09/20/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mild asthma
- Andere Medikamente
- None
- Allergien
- Dogs
- Vorherige Impfungen
- Shingles vaccine made me feel like I had the flu.
- Staat
- VT
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 30.03.2022
- Beginn
- 31.07.2022
- Tage bis Beginn
- 123,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anosmia
COVID-19
Fatigue
Nasal congestion
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
It started with fatigue, nasal congestion, fever for a couple of days of 101, and very mild sore throat for a couple days. I took an at home test and tested positive. The fatigue lasted for a couple of weeks. I also loss my sense of smell. I talked to my doctor and I decided not to take PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19, 08/01/2022, positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- LIPITOR; SYNTHROID; FLONASE; IMITREX; NEXIUM; multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 16.09.2022
- Impfdatum
- 03.03.2021
- Beginn
- 28.08.2022
- Tage bis Beginn
- 543,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
COVID-19
Chills
Confusional state
Cough
Dizziness
Faeces discoloured
Fatigue
Headache
Hyperhidrosis
Oesophagogastroduodenoscopy
SARS-CoV-2 test positive
Symptomtext
Patient to ED 9/1 CC of Black stools x4-5 days. Patient COVID+ prior to admission 8/28. Patient with chills and appeared fatigue/weak, profusely sweating and was more confused. 9/2 Patient to OR for EGD, calmed down with the coughing, vitals remain stable. 9/3 Patient is A&Ox4 and showing no s/s of distress. 9/4 Patient reports some improvement in fatigue and states is no longer experiencing dizziness. 9/5 Patient AO x 4. No c/o pain, no respiratory distress. 9/6 Patient c/o headache. 9/7 Patient discharged in stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- 7,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Benign neoplasm of rectum, Gastrointestinal hemorrhage, unspecified gastrointestinal hemorrhage type, Screening for colon cancer, Diverticulosis of large intestine without hemorrhage
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG PO Tab, cyclobenzaprine (FLEXERIL) 10 MG PO Tab, furosemide (Lasix) 20 MG PO Tab, omeprazole (PriLOSEC) 20 MG PO CAPSULE DELAYED RELEASE
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 14.09.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphasia
Headache
Memory impairment
Muscle spasms
Symptomtext
I starting cramping in the ball of my feet immediately after the vaccine. The cramping moved up to my ankles and calves. I'm also having memory issues. Mainly coming up with words is the issue and is frustrating. I was able to take calcium daily until after the vaccine and it made me so sick on my stomach. I started taking the calcium again recently to help with the cramping in my feet and legs. I also had severe headaches for a week after the vaccine too. I did see my doctor but they where unable to help me. I took a generic version of MOTRIN on occasion to help with my headaches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Thrombocythemia; Leukemia
- Andere Medikamente
- Calcium; ZYRTEC; iron
- Allergien
- Papaya; mango
- Vorherige Impfungen
- The last flu vaccine I had a headache which was unusual for me.
- Staat
- NJ
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 153,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
I felt tired after the vaccine for that afternoon but that was all. I tested positive via a home test for COVID-19 on 08/10/2022. I had coughing, sneezing and congestion. I contacted my doctor and they prescribed an antibody (don't remember the name). After taking it for two days, my symptoms went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home test for COVID-19 positive 08/10/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure; elevated cholesterol
- Andere Medikamente
- Lisinopril; Atorvastatin
- Allergien
- Demerol; Codeine; latex
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 05.05.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 82,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Asthenia
Body temperature increased
COVID-19
Chills
Cough
Diarrhoea
Dyspepsia
Fatigue
Feeling abnormal
Headache
Malaise
Myalgia
Oropharyngeal pain
Paranasal sinus discomfort
Respiratory tract congestion
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
On Tuesday morning, I woke up with a sore throat and sinus congestion and pressure. I went to a local clinic. They did a rapid COVID-19 test and a PCR COVID-19 test. They both came back negative. That day, I felt worse and worse as the day progressed. I had more coughing and more congestion. On Wednesday, I retested with an at home COVID-19 test. It was positive. It was late in the day so I couldn't call a doctor to see if we could get the antiviral. I called the doctor on Thursday morning and had a telehealth visit with him. He prescribed an antiviral. We had to drive 45 miles to get it. It was prescribed to be taken every 12 hours for 5 days with four pills total. I started feeling so ill, I started my first dose at 6pm that night. My temperature got up to about 101 degrees. I had a persistent barking cough that made my diaphragm muscles sore. I had a dull headache and sinus pain. I also had chills periodically. By the next day, after the second dose, I noticed I wasn't feeling as sick, but I was still very fatigued. Each day after, I felt better. My fever broke, and the cough decreased. By day 3, the cough was minimal. I was up moving around and doing chores. I had some stomach upset from the antiviral. It was mostly indigestion. I also had a little bit of loose bowel movements. As of yesterday, I felt well enough to clean my kitchen, but I had to rest to get my energy back. I took another COVID-19 test today and it was negative. I still have some sinus pressure and feel more tired than normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 07/26/2022 Rapid COVID 19 negative; 07/26/2022 PCR COVID-19 test negative; 07/27/2022 at home COVID-19 test positive; 08/05/2022 at home COVID-19 test negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 Diabetes; Mild Hypertension
- Andere Medikamente
- Lisinopril; GLUCOPHAGE XR; pravastatin; zinc gluconate; magnesium glycinate; vitamin D3; super K; CLARITIN; probiotic
- Allergien
- Seasonal; penicillin; topical betadine; milk proteins
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 01.08.2022
- Impfdatum
- 29.04.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 57,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Lethargy
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I had started coughing and that lasted for about two days and the second day I had low grade fever with lethargy. That all got worse and I ended up going into the Doctor and had COVID-19 PCR test which came back as positive. I was given Paxlovid which I started taking on the 28th in the afternoon and by the time I went to bed the symptoms had improved. I did the isolation period of the ten days and I tested negative on the 6th of July. On the 9th I tested positive again and the symptoms had started again which was coughing and a fever. This time my symptoms were more mild than the first time around. I did another ten days of isolating and then tested negative again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19 PCR Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Cholesterol
- Andere Medikamente
- Crestor; Trazadone; Multivitamin; Probiotic; Vitamin C; Vitamin D12; Vitamin D3; Alpha Lipoic Acid; Nexium
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 25.04.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 56,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
COVID-19
Cough
Fatigue
Pain of skin
Pulmonary congestion
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I tested positive for Covid on 06/20/2022. Symptoms included all -over body, joint and skin aches; chest and head congestion; cough; feverish; fatigue. Symptoms lasted 6 days. 12 days until a negative Covid home test.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Home Covid Test - 06/20/2022 Various home testing after 06/27/2022 until 07/04/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- GERD Cronic Nerve Pain
- Andere Medikamente
- 300mg BUPROPION 2/daily 40 mg PANTOPRAZOLE 1/daily 60mg DULOXETINE 1/daily 15 mg MELOXICAM 1/daily Calcium + D Vitamin B Complex L-Lysine Omega-3 Fish Oil Glucosemine & Condroitin
- Allergien
- Augmentin Demerol Bupinex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 21.04.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 43,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Ear discomfort
Fatigue
Productive cough
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sinus disorder
Symptomtext
The last Saturday in June, I was at the home of a client who had just returned from a trip. The husband was sick and he stayed out of the home while I was there all day although he had not been tested for COVID-19. My sinuses began to become irritated worse and worse and I noticed that I had a runny nose which isn't common for my normal sinus issues. I used some nasal spray which helped a lot because I had been congested and my ears were stuffy and I had a wet productive cough. I was also noticing some fatigue at that time and my husband started to feel unwell as well. I took an at home COVID-19 test which was positive. I called my doctor as soon as I tested positive. They did not advise the anti viral medication at that time and just suggested that I continue to monitor my symptoms and get back in touch if my symptoms worsened. My symptoms lasted around 5 days at most and now I feel better than I did before I contracted COVID-19 with the exception of some fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test-07/06/2022-positive
- Aktuelle Erkrankungen
- Migraine; Asthma attacks; joint pain.
- Vorgeschichte
- Asthma; Migraine; Ulcerative Colitis (in remission); Hypothyroidism. Peripheral Neuropathy.
- Andere Medikamente
- Synthroid; Montelukast; Ibuprofen as needed.
- Allergien
- Lidocaine; Novocain; Walnut; Melon; Avocado; Tomato; Cats.
- Vorherige Impfungen
- High fever and chills lasting 2-3 days after each COVID-19 vaccine.
- Staat
- PA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 22.04.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 68,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Head discomfort
Headache
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
On 6-27-2022, I started having body aches and a headache. The following day, I started having head congestion, a cough and sore throat. On 6-29, I had a low grade fever of 98.2 which is high for me. I took a Covid19 home test with positive results. On 6-30, I had a virtual telehealth visit with my PCP and he ordered the Monoclonal antibodies. I was taking mucinex and stopped taking ibuprofen and switched to tylenol. . I went to Hospital on 7-1 and had the antibodies. Four days after the antibodies, I started feeling alot better. I am reporting a breakthru case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 6-29-2022/7-2-2022/7-4-2022 Covid19 at home test with positive results 7-9-2022 Covid19 at home test with negative results
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Myasthenia Gravis; GERD; Osteoarthritis; Prediabetes
- Andere Medikamente
- Crestor; Zyrtec; Aspirin; Multivitamin; Calcium with Vit D; Nexium; Quinapril; Hydrochlorothiazide; Fish Oil; Pyridostigmine Bromide; Prednisone; Ibuprofen; Alphagan .1%; Mycophenolate Mofetil;
- Allergien
- Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 19.04.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Myalgia
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I developed a sore throat, runny nose, cough and muscle aches on 07/07/2022. I tested positive on 7/7 and reach out to my doctor the same day and received Paxlovid. I finished the 5 day dosage of medication. I started feeling better by day 4 of the medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypo-thyroidism
- Andere Medikamente
- Synthroid; Calcium; Vitamin D3; Vitamin C; Vitamin E
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 21.04.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 76,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Facial pain
Fatigue
Headache
Malaise
SARS-CoV-2 test positive
Symptomtext
Tested positive for COVID-19 07/09/2022 I received my 4th dose on 04/21/2022 and my COVID-19 symptoms started on 07/06/2022 extreme fatigue; headache; facial pain; Extremely tired. on 07/10/2022 i went to the Urgent care where they prescribed me PAXLOVIC but I didn't take because I was feeling better. Instead I took ibuprofens for my symptoms and drank a lot of liquids. I tested on 07/14/2022-07/16/2022 negative for positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Common immune Deficiency; Depression; Gerd; Asthma; Allergies, Glaucoma ; sleep Apnea;
- Andere Medikamente
- Albuterol; Latanoprost; Singular; Trazadone; Allegra ; Omeprazole; Gam Unix with Benadryl
- Allergien
- Compodine; iodine contrast
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 21.04.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 65,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aphonia
COVID-19
Headache
Nasal congestion
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
Starting 06/25/2022, I did an at home test which was negative. I had a really bad sore throat, headaches and congestion. On 06/26/2022, I went to the clinic to get the PCR test which came back positive. I called my doctor the next day on Monday 06/27/2022. They prescribed me PAXLOVID which my husband picked up for me. I took that as instructed and my last dose was on 07/02/2022. The headaches went away pretty fast. I had a very bad sore throat and sort of lost my voice. By Thursday 06/30/2022 I felt better and even better on 07/01/2022. I kept up my fluid intake and sucked on a lot of throat lozenges. Also, I took extra ZYRTEC daily to help with nasal/sinus congestion. By 07/04/2022, I felt basically back to my normal self. The sore throat was the worst part of this infection and by Friday 07/01/2022 I was feeling better and by that Monday 07/04/2022 I was feeling much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- At-home COVID-19 test (06/25/2022): negative; COVID-19 PCR test (06/26/2022): positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Cholesterol; Mild Anxiety
- Andere Medikamente
- Atorvastatin; PAXIL; multivitamin; ZYRTEC; vitamin D
- Allergien
- None
- Vorherige Impfungen
- After 1st and 2nd dose of COVID 19 vaccines, I had chills and body aches for 18 hours after the vaccine.
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Malaise
Pruritus
Scratch
Symptomtext
Around April 18th, 2022 I noticed I was scratching my neck and face. It kind of looked like a rash, but not raised or hot. Might have been from scratching but it was very itchy and extended from my cheek to my neck. I was subconsciously scratching so I started t pay attention to it and it would grow a little at a time. After 7 days, around April 27th, 2022 I started taking Allegra and it would help. If I stopped taking it, it would flare back up. It eventually started to subside sometime in May but I still take it because it comes back if I don't. I did not seek medical attention for this event. I self treated. I mentioned it to her recently when I was seen for COVID-19 symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroid; Hot Flashes-Menopause;
- Andere Medikamente
- Synthroid; Paroxetine- low dose; L-lysine; Fish oil- Omega 3; Probiotic- Bio Complete 3; Black Cohosh Root; Vitamin C
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 21.07.2022
- Impfdatum
- 20.04.2022
- Beginn
- 26.06.2022
- Tage bis Beginn
- 67,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Campylobacter test positive
Cough
Culture positive
Diarrhoea
Fatigue
Nasopharyngitis
SARS-CoV-2 test
Somnolence
Symptomtext
I developed cold symptoms on June 26th, I was on vacation with a number of relative. In hindsight, I think all 11 of us contracted COVID-19. It last about a week, I believe on the 1st of July I developed fatigue and kept napping and also developed diarrhea. The diarrhea went on for 6/7 days even after we returned from vacation. The tiredness was gone, the cold symptoms were gone but the diarrhea remained. I spoke with Doctor office and they took some culture that revealed Campylobacter, so unknown if it was related to COVID-19. Doctor prescribed an antibiotic, and that cleared it up. I also seem to have an upper respiratory cough that I cannot get rid of that seems to come and go.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- at home COVID-19 antigen test; GI cultures
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multivitamin; Tamsulosin; Finasteride
- Allergien
- Lactose Intolerant
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 21.07.2022
- Impfdatum
- 18.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 44,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Laboratory test
Pyrexia
Respiratory tract congestion
Throat irritation
Symptomtext
I had a scratchy throat, and a little congested. After I spoke with my doctor's office, I was prescribed PAXLOVID and took it for five days. I felt I had a very mild case. My wife never got it, as I isolated away from her. My fever got up to 100. My case only lasted about 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- At home test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Prostate cancer 2014; Bladder cancer
- Andere Medikamente
- Lovastatin; multivitamin; vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 18.04.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 64,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
COVID-19
Cough
Fatigue
Headache
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
In June I contracted Covid. I had nasal drip, congestion, headache and fatigue. I also had a low grade fever, and a bit of a stomach ache. I was out travelling. Two days later I began coughing and I came home and I tested and came back positive. The doctor prescribed me Paxlovid. My symptoms by this point was only fatigue, runny nose, and a cough. In 2 days all my symptoms went away. In total it lasted about 8 days before I tested negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- COVID test with positive result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Pacemaker; diabetes; cholesterol; high blood pressure
- Andere Medikamente
- Metformin HCL; Parica; Carvedilol; Rosuvastatin; Montelukast; Falcarinol; Omeprazole; Lantus; Calcium + D3; B12; Iron; Vitamin C; D3; Zinc
- Allergien
- Sulfa Drugs; Victoza
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 13.04.2022
- Beginn
- 18.07.2022
- Tage bis Beginn
- 96,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Foreign travel
Lacrimation increased
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Vaccine breakthrough infection
Symptomtext
Breakthrough Case of COVID-19; a scratchy throat, Slight Fever and watery eyes. I went and got tested and it came back positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19 Positive Test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Kidney Disease; Hypertension
- Andere Medikamente
- Benazetril; Nifedipine; Chlorthalidone; Spironolactone; Atenolol; Baby Aspirin.
- Allergien
- Cholesterol Medicine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 18.04.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 90,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Symptomtext
I started having headaches, chills, fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Glaucoma
- Andere Medikamente
- Lisinopril; montelukast; eye drops; brimonidine; brinzolamide; ROCKLATAN; pregabalin
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 13.04.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 88,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blepharitis
COVID-19
Pyrexia
SARS-CoV-2 test positive
Symptomtext
7/10 Very inflamed right upper eyelid, Slight fever 99.9. 7/10 Televisit with doctor who prescribed Paxlovid. Symptoms remained the same. Symptoms seemed to be about the same and things didn't noticeably change.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- 7/10 At home COVID 19 rapid test, positive.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Allergies
- Andere Medikamente
- Propranolol; Flonase; Calcium; Vitamin d3.
- Allergien
- Dogs; Cats; Mountain Cedar; Mold; Tobacco; Grasses; and Trees
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 31.03.2022
- Beginn
- 09.07.2022
- Tage bis Beginn
- 100,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Adrenal mass
Bile culture negative
Biopsy liver abnormal
COVID-19
Cholecystitis acute
Cholecystostomy
Computerised tomogram abdomen abnormal
Computerised tomogram thorax abnormal
Convalescent plasma transfusion
Cough
Hepatic mass
Hepatitis viral test negative
Hepatobiliary scan abnormal
Hepatocellular carcinoma
Imaging procedure abnormal
Inflammation
Jaundice
Symptomtext
Discharge Provider: MD Primary Care Provider: MD Admission Date: 7/6/2022 Discharge Date: Jul 15, 2022 PRESENTING PROBLEM: Liver mass [R16.0] HOSPITAL COURSE: Patient is a 73-year-old male with history of type 2 diabetes mellitus, hypertension and remote alcohol abuse who presented with abdominal pain and jaundice. Initially, he presented to Hospital, where imaging confirmed multifocal liver mass, and labs showed elevated LFTs. He was transferred to different Hospital for further workup. Upon admission, the patient was placed on IV fluids and gastroenterology was consulted. Hepatitis panel was done and returned negative. IR was consulted for liver biopsy, which was performed on 07/08. Results returned consistent with hepatocellular carcinoma. There was initially concern for adrenal nodule on initial imaging. He had follow-up MRCP as well as noncontrast abdominal CT, both of which confirmed benign etiology of adrenal nodule. Following admission, he developed cough, sputum production and intermittent fevers. Initial COVID testing in Hospital was negative, but repeat testing on 7/9 returned positive. As he was not hypoxemic, he was not felt to be a candidate for Decadron. Due to his elevated LFTs, he was not appropriate to be given remdesivir. He was provided treatment with convalescent plasma. For his newly diagnosed hepatocellular carcinoma, Oncology was consulted. They recommending outpatient follow-up in clinic to discuss potential treatment options. Initial imaging showed findings concerning for acute cholecystitis. Surgical Oncology was consulted for evaluation. They recommended HIDA scan for further evaluation. HIDA scan was done on 7/9, and was consistent with acute cholecystitis. Patient was started on IV Zosyn. Surgical Oncology did not feel that he was a surgical candidate, and recommended Interventional Radiology for cholecystostomy drain placement. IR was consulted, and cholecystostomy drain was placed on 7/11. Infectious disease was also consulted and they recommended to continue IV zosyn. Bile cultures have been negative. CT abdomen, pelvis and thorax with IV contrast was done on 7/13/22 and showed .arge liver mass smilar compared with 7/5/2022. Cholecystostomy drain with decompressed gallbladder and decreased pericholecystic inflammation. No findings suspicious for metastatic disease in the chest. Enlarged prostate with heterogeneous enhancement. This is nonspecific but carcinoma and have increased enhancement on CT. PSA was 4.06. Urology was consulted and they recommended outpatient follow-up with urology in 1-3 months with repeat PSA. CT did show left adrenal nodule and this was discussed with endocrinology. Endocrinology recommended outpatient aldo:renin screen for primary aldosteronism and 1 mg overnight dexamethasone suppression test. The patient was advised to follow-up with PCP for adrenal nodule and outpatient testing. On the day of discharge, the patient denied any nausea, vomiting or abdominal pain. He was tolerating diet. No fever or chills. He denied any chest pain or SOB. His vital signs have been stable. His LFTs have improved. The patient was discharged home in stable medical condition
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- OME (otitis media with effusion) ETD (eustachian tube dysfunction) Nasopharyngeal neoplasm, not found on scope Irregular heart beat Asthma Diabetes mellitus (HCC) Hyperlipidemia Hypertension Liver mass Adrenal adenoma, left
- Andere Medikamente
- amLODIPine (NORVASC) 5 MG tablet ciprofloxacin (CIPRO) 500 MG tablet Coenzyme Q10 (CO Q 10 PO) Cyanocobalamin (VITAMIN B-12 PO) Docusate Calcium (STOOL SOFTENER PO) FOLIC ACID PO Glucosamine HCl 500 MG TABS lisinopril (PRINIVIL,ZESTR
- Allergien
- DoxycyclineNausea and Vomiting, GI Upset Sulfa Drugs
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 90,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Oropharyngeal pain
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
04/11/2022 Vaccination 07/10/2022 I experienced coughing mid morning. I did a test at home that day COVID-19 NEGATIVE. Symptoms worsened to congestion, body aches, fatigue, sore throat. 07/11/2022 I did a PCR test and it was COVID-19+ Tessalon Perles prescribed by Doctor. Waiting to see if they are going to push for the anti viral medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19+
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Motrin, Odenton
- Allergien
- Cephalosporins; Erythromycin; Tree nuts
- Vorherige Impfungen
- Flu; near syncope
- Staat
- HI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 90,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Decreased appetite
Diarrhoea
Fatigue
Feeling cold
Headache
Hypersomnia
Influenza like illness
Muscle spasms
Nausea
Oxygen saturation decreased
Pain in extremity
SARS-CoV-2 test positive
Sinus headache
Throat irritation
Upper-airway cough syndrome
Symptomtext
On July 10th, after monitoring for several days, I had post nasal drip and a scratchy throat. I did a home COVID-19 test and it was positive. I contacted Dr., a friend of mine. Sine he knows my history of asthma, he suggested that I go to the hospital to get monoclonal antibodies. After I left the hospital, walking back to the car, I felt very cold and have shivers. After I drove home while feeling like I had a really bad flu. I isolated from my family in bed. I had no appetite. I took Nyquil every six hours for my throat. I had some chicken soup and within 15 minutes I had uncontrollable diarrhea. I began to have a very irritating, unproductive cough. I have been sleeping a lot because I am so fatigued. My oxygen level has been lower than normal for me. As of today I have my appetite back a bit and feel a little better. PO2 today is 93. When I had the diarrhea, I was also nauseous at the time. I also had a headache, kind of like a sinus headache. Today I have a mild sinus headache. My muscles cramped in my right leg and the left leg. My calves were sore on day one.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test, positive; PCR COVID-19 rapid test, positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; PVCs; Herpes; High Cholesterol; Macular Degeneration; Benign Prostate Hypotrophy; Nocturnal Leg Cramps from Spinal Injury; Acid Reflux
- Andere Medikamente
- Lutein; Metoprolol; Robaxin; Flomax; Lipitor; Prilosec; Colace; Valium; Valtrex; Multi Vitamin; Fluticasone Propionate; Spiriva; Albuterol
- Allergien
- Latex; Ambien
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 90,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Feeling abnormal
Headache
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
On last Thursday 7/11/22 I came inside from working out in yard. I thought I had just seasonal allergies flaring up. My wife suggested I take an at home test, which was immediately positive. I called my doctor immediately to see if I qualified for any sort of special treatment. I was connected to nurse helpline. My symptoms were significantly worse the next day. I was prescribed PAXLOVID. I started that Friday. I took 3 doses and stopped due to the steroid inhaler I am taking. I was told it could affect my heart. I then had the monoclonal antibody infusion. Symptoms were fatigue, congestion, extreme headache, cough. After first two doses of PAXLOVID I did start to feel significantly better. I am significantly better today and sleeping well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home test, PCR, Monoclonal Antibody Infusion.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- Steroid inhaler; clonazepam; AVODART
- Allergien
- Seasonal allergies; horse dandruff; cat dandruff; dog dandruff; brazil nuts; mold; dust; VICODIN; lactose intolerant
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 07.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Laboratory test abnormal
Memory impairment
Nodule
Oropharyngeal pain
Skin cancer
Wound
Symptomtext
Around 04/18 I had a sore throat and I let it go for a couple days. I talked to the doctor and asked him if it was possible that I had ingested glass. There were nodules in my throat and the doctor told my they were my tonsils and I explained they have been removed for some years now. I never tested myself until 04/27 and, I was positive. I isolated for about 5 days. I had a open sore on my face that I notices around the 05/01 and I called the doctor and they confirmed it was skin cancer 05/30. I will say I did have some issues with memory its still a little foggy but not as bad.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- High Blood Pressure; High A1C; High Cholesterol
- Andere Medikamente
- Atorvastatin; Flosemide; Metformin
- Allergien
- Erythromycin; Flagel
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 10.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 56,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
COVID-19
Chest X-ray abnormal
Decreased appetite
Fatigue
Lung opacity
Malaise
Painful respiration
SARS-CoV-2 test positive
Symptomtext
This 4th dose was actually the only time that I did not get at all sick from the vaccine. However, I contracted COVID (for the 3rd time) at the beginning of June 2022. I was sick for most of June, with it getting worse as time went on. My symptoms for this third case were very different than the first 2. In fact, I was sure it was just allergies for the first week, until it hurt to breathe. At that point, I went to the urgent care near my home and tested positive for COVID. Ten days later, I felt worse than ever. It still hurt when I breathed, I was exhausted with no energy, and I experienced loss of appetite (I pretty much could only eat one small meal a day). I went back to urgent care where they did a chest X-ray and prescribed prednisone and two antibiotics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID rapid test - positive June 9, 2022 Chest X-ray - June 19, 2022; Results - "Impression: Patchy bilateral lower lobe opacities could be due to peribronchial cuffing can be seen with a small airway disease or viral bronchitis or could be due to low lung volumes."
- Aktuelle Erkrankungen
- Long COVID (from spring 2020 )
- Vorgeschichte
- Rheumatoid arthritis, asthma
- Andere Medikamente
- Rx: Benicar, Spironolactone, Indapamide, Simvastatin, Methotrexate, Montelukast, BREO Ellipta, Cimzia infusion, Hydroxyzine (for long-COVID insomnia), Amitriptyline (for long-COVID headache), Metronidazole (for long-COVID facial rash) OTC:
- Allergien
- Penicillin, sulfa drugs, environmental (mold, pet hair, hay fever)
- Vorherige Impfungen
- COVID and Shingles - just the standard issues
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 88,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Discharge
General physical health deterioration
Influenza
Influenza virus test positive
Ocular discomfort
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Friday morning when i left i had a little sore throat and thought it was from sleeping on my back but on my way home it was getting worse and i got some drainage and my eys are bother me so i stopped to get some food and did a test before i went it. The test was weakly positive and i got worse and worse as i was going home. And i stopped at the er and got them to see me and they swapped for COVID-19 and flu i came back positive for both and they gave me Thermoful and Paxolvid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 -positive Flu- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Shif Culnery Arteries, Hypertensions, Low Obesity, Gout, Hyperthyroid, GURD, Diabetes, Typertolocis, Multiped Herna Disk
- Andere Medikamente
- Berlinta, Elpuranal, Losarton, Elferloxine, Vespa, Ecotrin, Everfatin, Mestermin, Quicsambi, Lingaglimtin, Etimberal, Amtopersal Sodium DR tabs
- Allergien
- Sulfur, Old Iodine Contrast, Eye Lubricant's
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 07.04.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 81,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
COVID-19
Fatigue
Headache
Pyrexia
Rhinorrhoea
SARS-CoV-2 test
Throat irritation
Symptomtext
Approximately 2 months after my 4th dose vaccination I contracted COVID-19 and experienced the following symptoms: Headache, Fever, Runny nose, Scratchy throat, Loss of smell and taste and Fatigue. I did not take anything for treatment and just decided to speak to my Doctor. He prescribed me with over the counter medications and basically to just let my symptoms run its course. As of today 07/08/2022 my symptoms have been better but I still have a low grade fever and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Multivitamins; Diltiazem
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 07.04.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 77,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Feeling abnormal
Malaise
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
COVID-19 case. I've had a cough for 2 weeks. I had fever, congestion. I didn't need to go to the hospital but I was pretty sick. I felt awful. I took Paxlovid for 5 days and was put on an inhaler.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- at home COVID-19 test - negative, second test - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- None
- Allergien
- Ampicillin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 73,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Nasal congestion
SARS-CoV-2 test positive
Symptomtext
COVID-19 case I thought I was having an allergy attack. My daughter's household all had COVID-19 and we were just with them. I tested and was positive. I called my Dr. and he advised don't take the antiviral medication . I never had a temperature and my pulse ox was fine. I had a little nasal congestion and fatigue but that's waning at this point. My experience was pretty minimal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- at home COVID-19 test - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Rheumatoid Arthritis
- Andere Medikamente
- Folic acid; Hydroxychloroquine; Simvastatin
- Allergien
- Codeine; Shellfish; Phenergan
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 57,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
Malaise
SARS-CoV-2 test positive
Symptomtext
On 06/02 my husband tested positive and I was still negative. I went in to get a PCR I was still negative Friday. And on Saturday I woke up with bad symptoms and my doctor called in PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 - positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Heart murmur
- Andere Medikamente
- ZYRTEC; multivitamin; collagen; coQ10; baby aspirin; glucosamine
- Allergien
- Iodine; azithromycin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 57,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Symptomtext
Sore scratchy throat, chills, slight body aches, slight fever 99.5. There was of 6 of us that all got COVID-19, my wife and i were the last 2 to show signs. We picked this up traveling, we were wearing our mask and test negative the Friday before we left. And after visiting, the oldest member test positive Tuesday the following week and then everyone else got sick. My symptoms game back June 11 and last 3 days and my fever went to 100.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid- positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multi Vitamins, Co-q-ten, Probiotics
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 05.04.2022
- Beginn
- 22.06.2022
- 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
Malaise
Nasal congestion
Pyrexia
SARS-CoV-2 test positive
Symptomtext
COVID-19. I received my 2nd booster shot on 06/24/2022 and my COVID-19 symptoms started on 06/23/2022 at around 04:00AM low grade fever; nose clogged up; nasal congestions; cough. I tested positive on the 06/24/2022. The same day I did tele visit with a nurse prescribed me PAXLOVID for 5 days. I tested positive again for COVID-19 on 07/05/2022. I went to the urgent care to get treated for COVID-19. Urgent care prescribed me albuterol; prednisone; MUCINEX DM over the counter medication; doxycycline. I am currently on the medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Diabetics
- Andere Medikamente
- Metformin; ADELINA; albuterol; ZYRTEC; nasal spray; montelukast; gabapentin; levothyroxine
- Allergien
- Environmental allergies; antibiotics
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.07.2022
- Tage bis Beginn
- 91,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Extra dose administered
Malaise
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Three months after 4th dose of Moderna, started feeling sick with fever and cough in the evening of 7/3/2022. Took a home test and it came back positive. Called Dr. and he prescribed PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Home Covid test.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- WELLBUTRIN; naltrexone; progesterone; estrogen; testosterone; omeprazole; FLONASE; MYRBETRIQ; multivitamin; calcium; bone supplement, D3 vitamin; GABA supplement; curcumin; pregnenolone; coQ10; 5 HTP; CLARITIN; magnesium; melatonin; focused
- Allergien
- Food sensitivities
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 01.04.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Decreased appetite
Fatigue
Nasal congestion
Nausea
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
My symptoms started on 06/19/2022, I woke up with a sore throat, coughing and nasal congestion. As the day went on, I had more coughing and chest congestion. I did a home test for COVID-19 and the result was positive. I called my doctor and left a message. He called back later, and I explained my symptoms and that I tested positive, he prescribed PAXLOVID. I began taking an over-the-counter cough medicine and TYLENOL. There was a mix up with the prescription, so I started it on Monday 06/20/2022. I felt worse on Monday, very tired, coughing, nasal and chest congestion, low or no fever, low appetite and my stomach felt queasy; my oxygen was good as I had monitored it. Once I started to take the PAXLOVID I gradually started feeling better. Fortunately, I slept well each night. I believe it was Wednesday, 06/23/2022 I had a video chat with my doctor who was checking in with me. I kept feeling better although tired. The cough medicine helped a lot. I believe I had another virtual visit on 06/25/2022. I told my doctor how much better I was feeling, and I continued to improve each day. I had one more virtual visit on 06/28/2022, I was told that some people have a rebound case of COVID-19 after finishing the PAXLOVID about the 10-14th day afterwards. I was feeling back to normal by the 10th day. I tested days 10-14 all came back negative, and my oxygen level has remained high.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 06/19/2022 home test for COVID-19 and the result was positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Environmental Allergies; Depression; High Blood pressure; High Cholesterol
- Andere Medikamente
- Bupropion; montelukast; rosuvastatin; ramipril; fluticasone nasal spray; estradiol; fexofenadine; vitamin D
- Allergien
- Environmental allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 73,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Cough
Fatigue
Headache
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 06/16/2022 with symptoms of fatigue, sore throat, congestion, cough, loss of smell and taste, headache, and fever of 101 at highest point. I was prescribed Paxlovid on 06/18/2022, but I was called back and instructed not to take it due to being on Estradiol. I was prescribed Guaiatussin and a cough pill as an alternative to Paxlovid. My symptoms began to improve after 5 days, but I am still experiencing lingering symptoms of cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal home test was positive on 06/18/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hashimotos Disease
- Andere Medikamente
- Levoxo; Estradiol; Magnesium; Probiotic; Vitamin D
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 02.04.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I had a fever of 101.8F, body aches and some sniffles. I took a home COVID-19 Test that came back positive. I called the COVID-19 chat, they asked all the questions that I answered and then asked if I wanted the Paxlovid and let them know that I did want it. I started taking it immediately.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 Test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Lisinopril, Metoprolol
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 01.04.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 90,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Headache
Malaise
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 06/30/2022 with symptoms of chest congestion, headache, fatigue, and elevated temperature. My doctor recommended I take Claritin, Robitussin, and Tylenol to treat the symptoms. I was ill for 5 days before my symptoms began to resolve. I am still currently experiencing chest congestion, fatigue, but my other symptoms are improving so far.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal home test was positive on 06/30/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthama; Allergies; Eczema; Migraines
- Andere Medikamente
- Symbicort; Multivitamin; Calcium; Vitamin D; Vitamin B12; Magnesium; Probiotics; Albuterol
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 01.04.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 67,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Malaise
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 06/07/2022 with symptoms runny nose, congestion, sore throat, and fatigue. I was prescribed PAXLOVID on 06/08/2022 via a telemedicine visit. I was ill for 2 days before my symptoms began to improve, and it was a very mild case. I am fully recovered with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal home test was positive on 06/08/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Sleep Apnea; Hypertension; High Cholesterol
- Andere Medikamente
- Calcium; multivitamin; simvastatin; lisinopril; melatonin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 31.03.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Rhinorrhoea
SARS-CoV-2 test positive
Secretion discharge
Sneezing
Symptomtext
On June the 17th I was sneezing and couching , lots of mucus, light headache, extreme fatigue and I also had a runny nose. I did not have a fever but had a 99.9 temperature for a few days. The day before I tested negative for COVID-19 rapid home test. On June the 20th I took a second test and it came back positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Diabetic ; Heart ; Blood Clot ; Severe Arthritis
- Andere Medikamente
- Warfarin; Levothyroxine; Metformin; Rosuvastatin; Probiotics; B complex strength ;Vitamin D3 ; Coq10 Enzyme ; PataDay
- Allergien
- Citric
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 01.07.2022
- Impfdatum
- 31.03.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 90,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Feeling abnormal
Headache
Productive cough
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID-19 on 6/29/2022. When I woke up I had a headache, phlegm in my throat, and congestion. I was prescribed PAXLOVID and I am still feeling kind of bad because it has only been 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 6/29/22 positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; BPH
- Andere Medikamente
- Lisinopril; amlodipine; tamsulosin; multivitamin; glucosamine; vitamin D; iron supplement
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 30.06.2022
- Impfdatum
- 30.03.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 47,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Headache
Heart rate increased
Lung disorder
Malaise
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
05/16/2022 I did not have really bad symptoms, but felt a little bit of funniness in my lungs. I also had bad headaches, a little bit of a cough and runny nose. On 5/18/2022I I test positive with a home COVID test. I had a runny nose and my heart started beating crazy, 155 beats per minute. I called my cardiologist and called my PCP on the following day, 5/19/2022. My PCP put me on Paxlovid. I started taking Paxlovid on that day. My heart rate was at 150 beats per minute for around 30 hours, then it went back to normal. I gradually started feeling better. The Paxlovid was hard on my stomach, and I had a chemical or metal taste. On 5/25/2022, I tested negative for COVID. On 5/31/2022, I noticed I had a cough again. I read that people on Paxlovid were having rebounds. I tested positive for COVID again that day. My symptoms were not as bad. I just had a cough and runny nose for about 3 days. I have now recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 3 COVID tests, 2 were positive , 1 was negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; AFIB
- Andere Medikamente
- Metropole; Singular; Allopurinol; Atorvastatin; Lisinopril; Baby aspirin; Vitamin D3; COQ10; Sal Palmetto; Turmeric; Multi Vitamin; Valacyclovir
- Allergien
- Pistachios
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 30.06.2022
- Impfdatum
- 30.03.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 73,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Fatigue
Feeling abnormal
Headache
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
My symptoms began progressively. I had a runny nose and a mild headache on about 06/11/2022 and 06/12/2022. Then I woke up with a raging headache on 06/13/2022 so I took a COVID-19 Test which came back positive. I was on a cruse ship at the time and contacted the medical department and they did a PCR which also came back positive. Other symptoms I experienced was that I lost my sense of taste and smell which still have not come completely back, I felt very fatigued and basically, I felt nasty.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 06/13/2022 took a home test, positive and a PCR test, positive.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High Blood Pressure; High Cholesterol
- Andere Medikamente
- Pantoprazole sod DR; ramipril; spironolactone; low dose aspirin; atorvastatin; finasteride; tamsulosin HCL; calcium; vitamin D; multivitamin; AREDS 2
- Allergien
- No allergies.
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 05.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Joint range of motion decreased
Pain in extremity
X-ray limb
Symptomtext
Injection site reaction in left arm. 3 days later started having similar pain in right arm deltoid muscle. Pain in right arm got worse with pain limiting range of motion. Even using left arm, could cause severe pain in right arm. This has continued for 2 months. Saw an orthopedic PA on May 12, 2022 for the pain. He said it could be bursitis or rotator cuff tendonitis. He gave me a steroid shot in my right shoulder. It didn't help. I took a 5 day regimen of prednisone. That did not help either. He recommended that I get a MRI and see a shoulder specialist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- Had an x-ray of my right shoulder and arm.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 3 auto immune related conditions
- Andere Medikamente
- Premarin, vitamin A
- Allergien
- -
- Vorherige Impfungen
- Just soreness and redness at injection site
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 16.04.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 38,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Headache
Impaired work ability
Pain
SARS-CoV-2 test
SARS-CoV-2 test positive
Somnolence
Symptomtext
I didn't have any reaction to the vaccine, but i did catch covid in May 2022. I had a bad headaches and body aches. All I have been doing is sleeping. I taste everything and I have been eating fine. I just sleep all day. I have been out of work for about 2 weeks. I was prescribed Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- PCR Covid Test- Positive (5/24/2022) Rapid Test- Negative (5/24/2022) Covid Antigen- awaiting results (6/1/2022)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Psoriatic Arthritis
- Andere Medikamente
- Amlodipine Losartan Humira
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 22.04.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 33,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Feeling abnormal
Oropharyngeal pain
Pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Started with daughter who tested positive on 5/23 or possibly after visiting patients throughout the week. Wednesday night 5/25, started with a sore throat. Thursday 5/26, I felt okay, later that evening I felt worse again. Friday, Saturday, Sunday had initially bad cough, sore throat, not much of a runny nose. Everything went away, then body aches, runny nose, congestion. No fever. Feeling very tired, body aches. Cough, runny nose, and sore throat have gone away. In process of recovery.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 05/26/2022 at-home COVID test negative. 05/27/2022 at-home COVID test negative. 05/27/2022 PCR COVID test positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoporosis
- Andere Medikamente
- Forteo injection; mirtazapine; vitamin D; calcium; niacinamide; Tylenol as needed
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 19.04.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Nasal congestion
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Covid positive on 5/11/22. Stuffy, runny nose, constant cough, fever On 5/12/22 began Paxlovid for 5 days Symptoms were gone by 5/14/22 Tested negative on 5/17/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Antigen test positive on 5/11/22 Antigen test positive on 5/15/22 Antigen test negative on 5/17/22 and again on 5/21/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 25.05.2022
- Impfdatum
- 12.04.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 37,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
COVID-19
Chills
Fatigue
Headache
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Starting experiencing throat soreness on 5/19. I tested positive for Covid on 5/20. I started experiencing extreme fatigue which persisted throughout the weekend accompanied by chills and high temperature. Experienced headaches and coughing. Tele doctor on 5/23. Sore throat started to fade on 5/23 and feeling better on 5/24.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 18,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Fatigue
Immunisation reaction
Pain
Pyrexia
Symptomtext
10/27 received my first booster, had fever and achiness for 3 days after. Then I was fine. On 11/15/21 began running a low grade fever (99.5-100) with tiredness which lasted till 11/23. Called my PCP and was advised fever was probably a virus and to let it run it's course. Second booster on 4/8 with fever and achiness for 3 days. Then fine till 4/26/22, began running low grade fever with tiredness again which lasted till 5/16/22. We had moved so saw new PCP 5/9/22 who felt it was a reaction to vaccine. She administered Prevnar 20 that day. This may account for the additional days of low grade fever. She felt it was my body's reaction due to Fibromyalgia and did not administer a COVID test. I am feeling fine at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Fibromyalgia
- Andere Medikamente
- Triamterene, Potassium, Rosuvastatin, Toprol XL Vitamin C,D,B12, Magnesium Citrate, Multi-Vitamin, Mucinex, 81mg Aspirin
- Allergien
- None
- Vorherige Impfungen
- See notes in item 18
- Staat
- VA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 30.04.2022
- Tage bis Beginn
- 23,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Cough
Nasopharyngitis
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test negative
Sinus disorder
Symptomtext
Have had a severe cold, congestion, sinuses, etc. fever chills controlled by tylenol / advil. Took 3 covid home tests all negative... saw PA after cold was getting better... Never had a cold this long or this bad and wondered if impacted by vaccine effects on immune system. Am still recovering but still have a lot in my head (sounds like a bad cold still)... coughing is much less both day and night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- None
- Andere Medikamente
- Allopurinol, Levothyroxine, Lipitor
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oedema
Pruritus
Symptomtext
On 05/08/22 developed intense pruritus at fingertips and DIP joints, progressing to palmar aspect of hands at joints; then periorbital, perioral itching, minimal edema; progressed then to forehead and upper arms/deltoids (B) pruritus. Patient has self-administered oral diphenhydramine 25mg TID and topical hydrocortisone 0.1% for some relief. Seen in clinic 05/19/22 and continued pruritus treated with methylprednisolone 4mg tablet taper (12mg x4days, 8mg x4days, 4mg x4days).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No acute illness at vaccination or reaction time
- Vorgeschichte
- COPD, stage IV; Oxygen dependence; GERD w/o bleeding; Depression; Hyperlipidemia; Tobacco Dependence; Vitamin D deficiency; BPH
- Andere Medikamente
- Albuterol MDI 90mcg 2inh q4-6hrs; atrovastatin 20mg QD; Hydrocodone-apap 10-325mg QID prn; ipratropium/albuterol 0.5/3mg per 3mL vial via nebulizer QID;
- Allergien
- NDKA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear pain
Facial pain
Headache
Lymph node pain
Neck pain
Pain in jaw
Pharyngeal swelling
Symptomtext
severe ear jaw and neck pain left side of face and headache--thought i had an inter ear infection was prescribed a z pac--used heat and ice on and off nothing helped--after a week it finally eased up now i still have some pain but my lympth node on the left side of throat is swollen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- estradiol, lisinopril
- Allergien
- dairy,
- Vorherige Impfungen
- moderna covid 19 1st booster 9/14/2021, headache and leg pain,
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 09.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vaccination site pain
Symptomtext
Pain at injection Site Right Arm after first shot; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (Pain at injection Site Right Arm after first shot) in a female patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 vaccination. The patient's past medical history included Cat bite (on the left hand) on 28-Feb-2022 and Surgery (left hand) on 14-Mar-2022. Previously administered products included for Cat bite: Rabies shot (right arm). Past adverse reactions to the above products included No adverse event with Rabies shot. Concurrent medical conditions included Asthma. On 09-Apr-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 09-Apr-2022, the patient experienced VACCINATION SITE PAIN (Pain at injection Site Right Arm after first shot). In April 2022, VACCINATION SITE PAIN (Pain at injection Site Right Arm after first shot) had resolved. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. Concomitant medications included asthma medications. At the beginning of Mar-2022, prior to vaccination, the patient was at hospital for cat bite. The patient had pain at injection site and the pain lingered for about 2 weeks. No treatment medication was provided. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma
- Vorgeschichte
- Medical History/Concurrent Conditions: Cat bite (on the left hand); Surgery (left hand)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 12.04.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Headache
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test positive
Sinusitis
Symptomtext
I thought I was experiencing a sinus infection because I had a sore throat. I was coughing, having a headache, and my nasal passage was congested. I had started taking ADVIL sinus medication and it helped a little bit but it started progressing. I called my PCP first and they said they don't do the throat swab, so I needed to go the urgent care or ER. So, I went to the urgent care not far from my house. They asked me about my symptoms, and I told them and they asked if I wanted to get a COVID test while I was there. They tested me and it came back positive. They did another COVID test and sent it to the lab and it would take 3 days to make sure. (PCR) They wanted to verify that it was positive again. They gave me digital COVID-19 results. That also came back positive the next day. He gave me a prescription for PAXLOVID. I asked about a prescription for the cough since I was still coughing. He prescribed Benzonatate and I've been taking those. Benzonatate 3 times a day and PAXLOVID twice daily one in the morning and in the evening. Planning to go get retested this coming Friday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 05/13/2022 - Rapid COVID Test - Positive; 05/13/2022 - PCR COVID Test - Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HIV Positive; High blood pressure; Acid Reflux
- Andere Medikamente
- Amlodipine; BIKTARVY; Vitamin D; NEXIUM as needed
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 31,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Malaise
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough Covid infection on 5/16/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Symptoms began 5/16/2022 At-home Covid test on 5/17/2022--positive PCR test at Clinic on 5/18/2022--positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 17.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 37,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Myalgia
Oropharyngeal pain
Pulmonary congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I started getting symptoms of sore throat, chest congestion, runny nose, and muscle aches. This lasted about 5 days. I did an at home COVID-19 test which was positive. I contacted my doctor and was told no use to get the antiviral drug.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- COVID-19 test
- Aktuelle Erkrankungen
- Light cold; sore throat
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Exposure to SARS-CoV-2
Malaise
SARS-CoV-2 test positive
Symptomtext
Experienced pretty severe symptoms the two days following vaccine. Exposed to Covid on May 7 and tested positive on May 12. Was prescribed Paxlovid for symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Covid-19 test
- Aktuelle Erkrankungen
- Cold Sore
- Vorgeschichte
- CHF; Non compaction cardiomyopathy; Status post cardiac arrest in 2011
- Andere Medikamente
- Ramipril; carvedilol; mg oxide; vitamin D; simvastatin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 11.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site bruising
Injection site reaction
Symptomtext
Site: Bruising at Injection Site-Mild, Systemic: Bruising and "Pooling" of vaccine below injection site-Mild, Additional Details: Patients states there was a bruise that formed a line all the way around her arm above her elbow, and just above that she thinks it was the vaccine "pooling". Resolve within 2 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Allergic respiratory symptom
COVID-19
Cough
Fatigue
Headache
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I tested positive after using an at-home COVID-19 kit on 05/03/2022. I've had symptoms similar to my seasonal allergy symptoms but a bit more severe. I've suffered from runny nose, cough, fatigue, body aches, fever, and a headache. I went to a pharmacy to complete an antigen test on 05/04/2022, and the results came back positive again for COVID-19. My physician prescribed Paxlovid for a five-day treatment course. The first two days, my symptoms were persistent but mild as the Paxlovid was working. I finished the prescription on 05/09/2022 and currently feeling pretty much better. I still feel more fatigue than normal, but all of my other symptoms have pretty much subsided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 tests - 05/03/2022 and 05/04/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Arthritis Asthma Seasonal Allergies Psoriasis
- Andere Medikamente
- Montelukast Meloxicam Magnesium Citrate Melatonin Vitamin B6 supplement Vitamin D3 supplement
- Allergien
- Seasonal Allergies Iodine Gladium
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 23.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Illness
Malaise
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID-19 breakthrough: Symptoms for this round of illness was much worse than first round.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Benazepril Atorvastatin
- Allergien
- Atorvastatin
- Vorherige Impfungen
- Shingles: date unknown
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 02.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Diarrhoea
Flatulence
Pain
Symptomtext
It all started with bloating and gas like feeling in my stomach that I could not release. That led me to pain then lead me to the GI doctor. He did a brief exam in the office and gave me medication - Dicyclomine 20mg 1 tablet 3x daily before meals as needed. GI doctor also has me taking a probiotic Align He scheduled me for some testing as well. Also experiencing diarrhea, hasn't gone away yet. I've never experienced GI problems in the past. This was a pretty drastic change. This coming Saturday, I will be going for a stomach scan.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 05/14/2022 - Upcoming stomach scan. If GI doctor sees anything of concern, will schedule future appointments. 07/14/2022 - Future coloscopy & endoscopy
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lupus Type 2 Diabetes Blood Pressure HX of Nerve Damage
- Andere Medikamente
- Levothyroxine 88mcg Losartan Fenofibrate 145mg Atorvastatin 20mg Amlodipine Besylate 10mg Metformin 1000mg PM Metformin/SYNJARDY 25/1000mg AM Trulicity: one injection weekly in abdomen Vitamin C
- Allergien
- Penicillin Sulfa
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 04.04.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Feeling abnormal
Malaise
Respiratory tract congestion
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I contracted COVID-19 on 5/3/2022 with symptoms of congestion, scratchy throat, slight cough, slight brain fog, slight fatigue, and I was ill for about 7 days. I was prescribed Cefuroxime Axetil 500mg 2xdaily for 7 days, and Methylprednisolone 4mg dose pack 6 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swabs were positive 5/5/2022.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension High Cholesterol Cataract Surgery
- Andere Medikamente
- Lisinopril 40mg Atorvastatin 20mg Amlodipine 10mg Hydroxyzine 25mg twice daily Carvedilol 3.125mg twice daily Multivitamin Aspirin 81mg Vitamin C 500mg Vitamin E 180 Vitamin D3 25mg 1000iu Apple Cider Vinegar Gummies Ashwagandha
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 29.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Antinuclear antibody positive
Arthralgia
Back pain
Blood test abnormal
Joint stiffness
Neck pain
Pain in extremity
Ultrasound Doppler normal
Symptomtext
First: hip pain, right neck soreness. First days: Back and hip pain, Upper leg pain and aches, Tightness around my knees. Bilateral. Subsequent days and weeks: All of the above, but not always all at once. Sometimes with increased intensity. Sometimes with less intensity. Sometimes accompanied by fleeting pain in different areas of my back, legs, and knees. Some neck pain. Dr. discontinued Simvastin on April 18th. Prescribed Cyclobenzaprine to take at bedtime to facilitate ability to sleep.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Blood tests - Positive speckled ANA. Ultrasound of my legs?no vein problem responsible for the trouble.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypertension, Diabetes, Osteoarthritis,.
- Andere Medikamente
- Ramipril, Elliquis, Januvia, Glimepiride, Farxiga, Omeprazole, Methenamine Hipp, Montelulcast, Mometasone Curate, simvastatin, Estrace Cream, Lorazepam. Vitamin C, Fish Oil, Vitamin D.
- Allergien
- Macrodantin, Pyridium?actual allergies. Codeine, Vicodin, Erethromycin?intolerances. Almonds?allergy.
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 09.04.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 24,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Headache
Nasopharyngitis
SARS-CoV-2 test positive
Symptomtext
Tested positive for COVID 19 four weeks after 4th dose of the vaccine. Symptoms were severe headache, bad cold, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home Rapid COVID 19 test kit.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypothyroid, High Cholesterol, Osteoporosis, Migraines, IBS
- Andere Medikamente
- Synthroid, Zocor, Pepcid, Forteo, Calcium, Magnesium, Vitamin D
- Allergien
- Penicillin, Clindamycin, Bactrim, Tramadol, Nickel
- Vorherige Impfungen
- Typhoid vaccine - fever, nausea - within 90 minutes of vaccine. Age 35, 1/1990
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 32,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Headache
Respiratory tract congestion
SARS-CoV-2 test positive
Upper-airway cough syndrome
Symptomtext
I contracted COVID-19 on 05/03/2022 with symptoms of post nasal drip cough, congestion, very mild headache if I exerted myself, and fatigue. I was prescribed Paxlovid on 05/07/2022 and my symptoms have fully resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab 05/06/2022 was positive.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Type II diabetes Prostate cancer Type 3 kidney disease Heart stint Morbid obesity
- Andere Medikamente
- Atorvastatin 80mg nightly Amlodipine besylate 5mg daily Metformin 500mg twice daily Pioglitazone 3mg daily Allopurinol 300mg daily Atenolol 50mg daily Jardine's 25mg daily Lisinopril 20mg daily Trulicity injectable Insulin u500 Latanoprost
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 02.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Nerve compression
Pain
Pain in extremity
Sleep disorder
Symptomtext
04/08/2022 My Right arm began hurting. The pain radiates from the vertebrae and numbness in the right arm. It got to where I could not sleep and had numbness in my right index finger. I went to the hospital. The doctor told me it is because the nerve from the vertebrae is being pinched. He prescribed Diclofenac Na 1 % and a muscle relaxer which I have not received yet. I am still having issues. I use ice and it helps with symptoms some.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Degenerative Arthritis
- Andere Medikamente
- Atorvastatin Glucosamine Chondroitin Iron COQ10 B Complex Vitamin Fish Oil Simethicone Vitamin D3
- Allergien
- Zocor
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 08.05.2022
- Impfdatum
- 18.03.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bladder pain
Discomfort
Hypertonic bladder
Interchange of vaccine products
Micturition urgency
Nausea
Ultrasound scan
Urethral pain
Urine analysis
Symptomtext
Shortly after my first covid vaccine, I developed serious symptoms of overactive bladder, including constant urgency, pressure and pain in the bladder and urethra. I had the two vaccines a month apart and had severe bladder symptoms from a few days after the first vaccine through the fall, in August or September. The symptoms gradually declined to almost normal by November. When i had a flareup of the bladder symptoms again after my first booster (3rd vaccine) in early December 2021, I wondered if it may be related. In this case, the symptoms only However, I am a strong supporter of vaccination and assumed it was a coincidence. As i am over 60 and was going to travel to visit my ailing parents, i obtained a 2nd booster the first of May 2022. The next day, my bladder symptoms returned. Again, not nearly as significant as the first occurrence, but still moderately significant (pressure, pain, urgency, nausea) for several days, gradually declining, although still not returned to normal as of the date of this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bladder pain
- Hospital-Tage
- -
- Labordaten
- I have had several urinalysis, ultrasound. Diagnosis was overactive bladder. I had never before had any bladder issues and, rather, have long had a very strong bladder (no trips to the bathroom at night).
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- None
- Andere Medikamente
- none
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 07.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Peripheral swelling
Rash
Symptomtext
developed unknown rash, swelling of the hands, dermatographia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- Went to urgent care 4/28/2022, treated for hives, received methylprednisolone injection in buttocks and prescription for methylprednisolone to take over 5 day period.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 06.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain
Swelling
Symptomtext
Patient called in on 5/6/22. Patient having redness as big as a "softball," with pain and swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes, hypertensive kidney disease.
- Andere Medikamente
- -
- Allergien
- strawberry, bees
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 11.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 17,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
COVID-19
Cough
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough Case of COVID-19 I had no side effects for the vaccine except for a mild shoulder pain for about 24 hours, then I was fine, I had a mild cough around the 18th of April, which I did not take any medicine for, Pryor to my return from Ireland , on 04/28/2022, I tested positive for COVID-19 but I had not other symptoms but the mild cough, the only reason that I took a test was because it was required for me to do so before I could get on the plane.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test
- Aktuelle Erkrankungen
- Melanoma Skin Cancer of Right Shoulder, taken off on March 17, 2022
- Vorgeschichte
- Hypertension Thyroid Disorder
- Andere Medikamente
- Losartan 100mg 1xdaily Estradiol Patch 0375mg 2x per week Levothyroxine 50mcg 1xdaily Bactrim, 2xdaily Calcium 1200mg Multivitamin
- Allergien
- Codeine Macrobid
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site extravasation
Symptomtext
Error: Leaking from Injection Site-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site extravasation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 23.04.2022
- Tage bis Beginn
- 16,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal X-ray
Abdominal discomfort
Abdominal pain
Abdominal tenderness
Blood test
Computerised tomogram abdomen abnormal
Constipation
Discomfort
Lipase normal
Medical diet
Sleep disorder
Symptomtext
I was awakened about an hour after going to bed with excruciating pain in my abdomen and couldn't get comfortable. When I stood up and walked around it was still there. It was so bad I considered calling the ambulance to go to the hospital. When I woke up it was still hurting but not the excruciating pain from earlier. I went to Urgent Care and by then the pain was still there, my whole abdomen was very tender and uncomfortable. They told me to go to the ER. They did tests and sent me home with referral to GI specialist. I was placed on a clear liquid diet for 3 days - by Tuesday it was better but still painful in the upper abdomen. As the week wore on the pain dissipated. Tomorrow I will see the GI specialist. As the week progressed I progressed to a pancreatic diet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Urgent Care xray of the abdomen - looked like my bowel was full ER blood draw - lipase was 11.98 CAT SCAN of Abdomen - possible pancreatitis
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- asthma
- Andere Medikamente
- Multivitamin, Vit D3, Macuhealth (for eyes), Acetyl L-Carnipine, Flovent, Rostasis, Fosamax,
- Allergien
- Shrimp, Beer
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 01.05.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Diarrhoea
Exposure to SARS-CoV-2
Headache
Influenza like illness
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
On 04/28/2022, I had a PCR test done since my wife was not feeling well. Her PCR test came back positive on 04/30/2022 and mine came back negative. I got the 2nd booster on 05/01/2022 and the following day I ended up testing positive (05/02/2022). The first two days, I had some flu-like symptoms (congestion, headache, fever, body aches and diarrhea) and my doctor has me on Paxlovid which has helped. I have some congestion currently but nothing like before Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID PCR test (04/30/2022): Negative, COVID at home test (05/02/2022): Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension and High Cholesterol
- Andere Medikamente
- Atorvastatin, Olmesartan and Amlodipine
- Allergien
- None
- Vorherige Impfungen
- 2nd Moderna shot: Body aches and lethargy. Flu shot sometimes makes me tired
- Staat
- MS
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure fluctuation
Dizziness
Immunisation reaction
Symptomtext
Starting the next day after receiving the vaccine, when I woke up, I began to experience dizziness. When I rotated from a prone position to a sitting position, I would become very dizzy. Also, during different parts of the day I would experience dizziness. I would stay dizzy for about 5-10 seconds then it would resolve. I will be going in to see the doctor soon. After speaking over the phone, they believe its a change in blood pressure from going from sitting to standing or laying down to sitting or standing. My endocrinologist said its a known side effect of the booster that normally resolves in a day or two, but mine has not. My neurologist also believe its likely a result of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- History of Migraines, High blood pressure, Type II Diabetes, High Cholesterol and History of one Seizure
- Andere Medikamente
- Crestor 40mg; Actose 30mg; Kepra XR 500mg; Farxiga 10mg; Janumet 50/1000mg; Losartan Potassium 50mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- 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: nein
Injection site erythema
Symptomtext
redness of upper arm 7x7
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- high blood pressure, high cholesterol
- Andere Medikamente
- amlodepine, omega 3, testosterone cream
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 20,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Exposure to SARS-CoV-2
Nasopharyngitis
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test negative
Symptomtext
Was exposed (in close contact for more than 15 minutes) with two people on 4/23 and 4/24 who tested positive for COVID on 4/25 and 4/26. On 4/25 had a sore throat and runny nose. On 4/26 was very congested and had a slight fever and body aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- On 4/26 went to Hospital COVID test site and had a PCR test. The test came back negative on 4/27. Rapid antigen tests on 4/25, 4/26 and 4/27 were all negative. Conclusion is that I have a bad cold.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, seasonal allergies
- Andere Medikamente
- fluticasone propionate (Flonase), loratadine (Claritin)
- Allergien
- -
- Vorherige Impfungen
- Pneumococcal 23-Val Ps Vaccine
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site mass
Injection site pain
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Left arm: Pain, Swelling, Lump around injection site, Itching, warm, red
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cvs Phamracy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site rash
Rash pruritic
Symptomtext
The next day after the vaccine, I had a rash on the injection site that lasted 24 hours. This has happened on the first dose that was reported as well but was much worse. I put cortisone cream on the site which did help the itching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Moderna 1st dose - large raised rash on injection site lasted 1 week
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 14.04.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
Neck pain
Nerve compression
Neuralgia
Pain
Pain in extremity
Symptomtext
I already had some cervical pain before the vaccine. But maybe a day or 2 after the vaccine, I had left sided pain, left back pain, left shoulder all down my left arm into middle left finger-down the nerve line, like a pinch nerve, very aggravating. I am still experiencing the symptoms but its not as intense. I've been experiencing extreme nerve pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None after receiving the vaccine.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Breast Cancer Survivor
- Andere Medikamente
- Diltiazem ER; Famotidine; Flonase; Alprazolam
- Allergien
- Most Fruits; Antibiotics; Latex
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site swelling
Lymphadenopathy
Pyrexia
Tinnitus
Symptomtext
Site: Swelling at Injection Site-Medium, Systemic: Fever-Medium, Systemic: Lymph Node Swelling-Severe, Systemic: Tinnitus-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Back pain
Discomfort
Head discomfort
Headache
Injection site pain
Muscular weakness
Oropharyngeal pain
Pain
Pain in extremity
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Body Aches Generalized-Mild, Systemic: pressure/pain by left ear that migrated to left side of back, down left arm, and on left side of throat.-Mild, Systemic: Weakness-Mild, Additional Details: left arm weakness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Peripheral swelling
Symptomtext
Swollen arm; Arm hurts really bad; This spontaneous case was reported by a consumer and describes the occurrence of PERIPHERAL SWELLING (Swollen arm) and PAIN IN EXTREMITY (Arm hurts really bad) in an 18-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 vaccination. Patient had no allergies, had not tested positive for Covid 19 and did not take any concomitant medication. On 21-Apr-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 21-Apr-2022, the patient experienced PERIPHERAL SWELLING (Swollen arm) and PAIN IN EXTREMITY (Arm hurts really bad). The patient was treated with IBUPROFEN for Adverse event, at an unspecified dose and frequency. At the time of the report, PERIPHERAL SWELLING (Swollen arm) and PAIN IN EXTREMITY (Arm hurts really bad) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. The patient stated that patient actively experienced above symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient had no allergies, had not tested positive for Covid 19 and did not take any concomitant medication.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Feeling abnormal
Loss of personal independence in daily activities
Malaise
Myalgia
Nausea
Symptomtext
she has not been the same since; still feels sick; Has not been able return to normal activities; Lack of energy; Intermitted muscle ache all over body; Nauseated; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (she has not been the same since), MALAISE (still feels sick), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (Has not been able return to normal activities), ASTHENIA (Lack of energy) and MYALGIA (Intermitted muscle ache all over body) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 11-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In April 2022, the patient experienced FEELING ABNORMAL (she has not been the same since), MALAISE (still feels sick), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (Has not been able return to normal activities), ASTHENIA (Lack of energy), MYALGIA (Intermitted muscle ache all over body) and NAUSEA (Nauseated). At the time of the report, FEELING ABNORMAL (she has not been the same since), MALAISE (still feels sick), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (Has not been able return to normal activities), ASTHENIA (Lack of energy), MYALGIA (Intermitted muscle ache all over body) and NAUSEA (Nauseated) had not resolved. No concomitant medications were reported. No treatment information was provided. This case was linked to MOD-2022-547047.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 14.04.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test normal
Fatigue
Immunisation reaction
Pyrexia
SARS-CoV-2 test negative
Symptomtext
I had a low grade fever that went up and down for about 6 days. I ended up in my doctor's office on 4/19. They did not test for Covid since I had already tested negative multiple times at home. They advised that it may be a reaction to the vaccine and that I should continue to monitor my symptoms. Within two days after that, my fever had gone away and I've been alright since then with the exception of some abnormal levels of fatigue that has remained since the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home Covid Tests-negative; Blood Tests-4/19-nothing found.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Synphroid Nutra fill Magnesium
- Allergien
- Sulfa; cephalosporins
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 29.03.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 11,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Blood electrolytes normal
Chills
Fatigue
Full blood count normal
Headache
Immediate post-injection reaction
Liver function test normal
Lymphocyte count
Myalgia
Protein total decreased
Symptomtext
immediate sx were: chills, fatigue, myalgias/arthragias, headache; after ~5 d, return of fatigue, headaches, same quality as all prior fatigue, headaches s/p Moderna shots (I never thought to check BP with those headaches, as expected with vax). Note my first booster, 8/18/21, was full dose given prior to EUA, and the booster antecedent to these sx was EUA half dose. continued into week 11th April so i checked my BP and had SBP 155-165 and DBP 85-95. prior to that i had rare intermittent labile BP not sustained and not with headaches. Saw my oncologist 18Apr for routine check up and shared this and BPs and on 19APR started amlodipine 5 mg qhs with regulation of BP by d3 (today). I am a practicing oncologist; follicular lymphoma x 17 yr, active disease returned Aug21 on watch and wait, no immediate concern by my doctor that these sx related to the lymphoma
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- today 22Apr normal CBC, electrolytes, hepatic mineral panel with exception of lymphocyte count 0.9/dL and total protein 6.1g/dl, stable values for me. normal exam except palpable sq small lymphoma lesions
- Aktuelle Erkrankungen
- ongoing hypogammaglobulinemia secondary to rituximab follicular lymphoma active, watch and wait mild occasional lability in blood pressure
- Vorgeschichte
- ongoing hypogammaglobulinemia secondary to rituximab follicular lymphoma active, watch and wait
- Andere Medikamente
- IVIg q4w premarin, vitD3, cymbalta senna restasis ocular rabeprazole
- Allergien
- some adhesives
- Vorherige Impfungen
- after Shingrix, fever, myalgias, arthralgias, fatigue, chills, fatigue
- Staat
- PA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast pain
Fatigue
Mastitis
Symptomtext
The day after the vaccine I experienced fatigue. The Saturday following the vaccine I developed a sore breast. I saw the Dr the following Tuesday and was dx'd w/ Mastitis. I was put on Keflex and antibiotics and warm compresses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism, Osteo-arthritis
- Andere Medikamente
- Atorvastatin, Thyroxine, D3, Selenium, B12, Melatonin, Magnesium, Turmeric, Biotin
- Allergien
- Bactrim, Flagyl, Erythromycin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 18.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Asthenia
Influenza like illness
Loss of personal independence in daily activities
Malaise
Pain
Symptomtext
Woke 12 hours after receiving vaccine with extreme joint/body aches, weakness. Felt as if I had major case of Flu. After 12 hours started to improve but was unable to really function all day. Following morning I was back to normal. This happened with my second shot lasting only 12 hours; 3rd shot (booster but was full dose) was sick for 36 hours then fine. I asked for Pfizer for 4th booster but was advised to stay with Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None. Did not contact physician
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Celecoxib. 100 MG 1Xday; Myrbetriq ER 50 MG 1Xday; Escitalopram 10 MG. 1 x day.
- Allergien
- Codine and penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Confusional state
Fall
Nausea
Pain
Pyrexia
Symptomtext
Developed severe chills an hour after she received vaccine. Reports fever for 2 days (did not check temperature). Continued to have mild weakness, nausea, mild body aches for almost 10 days. Daughter reported she fell out of bed and was confused.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None, patient declined.
- Aktuelle Erkrankungen
- Acute exacerbation of chronic back pain
- Vorgeschichte
- Rheumatoid arthritis, chronic mild anemia, CKD stage III, hyperlipidemia, hypertension, chronic hyponatremia, monoclonal gammopathy, nicotine dependence
- Andere Medikamente
- Atenolol, cetirizine, chlorthalidone, ezetimibe, Flovent, folic acid, gabapentin, ibuprofen, methotrexate, rosuvastatin
- Allergien
- Pravastatin, lovastatin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 20.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria chronic
Symptomtext
AFTER 11 DAYS DEVELOPED CHRONIC URTICARIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria chronic
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test abnormal
Fatigue
Infectious mononucleosis
Mononucleosis heterophile test positive
Somnolence
Symptomtext
EXTREME FATIGUE DURING THE DAY CAUSING ME TO FALL ASLEEP FOR SEVERAL HOURS EVEN AFTER HAVING A FULL NIGHT OF SLEEP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- BLOOD TEST SHOWED ACTIVE MONONUCLEOSIS INFECTION
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- GLUTEN INTOLERANCE
- Andere Medikamente
- VITAMINS D3, k, c, Bs. ZINC, COLLAGEN, FISH OIL, BIO-IDENTICAL HORMONES
- Allergien
- GLUTEN AND GRAINS
- Vorherige Impfungen
- SEVERAL DAY OF MENSTRUAL BLEEDING AFTER MODERNA COVID-19 VACCINE #1 IN FEB. 2021
- Staat
- PA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Injection site pruritus
Symptomtext
Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 12,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Lip swelling
Pharyngeal swelling
Pruritus
Rash erythematous
Tongue erythema
Urticaria
Symptomtext
4/13/22: Intense itching (multiple body parts: arms, torso front/back, groin, ankles, palms of hands, bottom of feet, inner ears, and scalp). Red Rash, Welts, Swollen lip (only half left side) + raised welt on Tongue, Slightly swollen throat 4/14/22 Went to ER: Given Benadryl shot (which offered no relief.) ER performed no tests. 4/17/22 Post care: Healthcare provider offered no other testing. Treatment plan consisted only of treating the symptoms with Prednisone (high dose). I deferred due to contraindication with my history of heart arrhythmia. Requested tests, bloodwork, so I could assess, then make decision for this Rx, they offered NO blood tests. They did not refer me Allergy/Immunology.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hashimoto?s (hypothyroidism), PLDTS, WPW, Pre-Sacral mass (benign)
- Andere Medikamente
- Vitamins: C, D, E, B-12 Magnesium, Calcium, Selenium
- Allergien
- penicillin, loradatine, erythromycin
- Vorherige Impfungen
- 2/27/21 MODERNA COVID-19 Vacc. DOSE 2 Lot# 023M20A Two weeks after this Covid Vacc, experienced very swollen lymph glands (unde
- Staat
- MA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Fatigue
Headache
Myalgia
Nausea
Symptomtext
The following day, severe muscle and joint pain, nausea, fatigue, headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Gluten sensitive
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 15.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pain
Pain in extremity
Product administered at inappropriate site
Symptomtext
Patient complains of "dead arm"/pain in shoulder radiating down arm. Vaccine may have been given too high in the arm (joint space)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 14.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 14,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Hypoaesthesia
Pain in extremity
Periarthritis
Symptomtext
pt states that he experienced frozen shoulder, including arm pain and finger numbness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Symptomtext
Systemic: Allergic: Itch Generalized-Medium, Additional Details: Pt developed a full body rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Body temperature increased
Chills
Feeling abnormal
Immunisation reaction
SARS-CoV-2 test negative
Symptomtext
I had the vaccine, and I was fine for the first 27 hours. Then on 4/5 at 3:30pm I started to feel not so great, and I took my temp in the evening and it was 100.2 degrees and when I went to bed it was 100.4 degrees. I also had chills and achy joints. Then on 4/6 my temp was 99.1 degrees then it rose to 100.7 degrees. It got up as high as 101.6 degrees that day. I took an at home COVID test and it came back negative. On the 4/7 my temp was 101.4 degrees at 2:15 in the morning. I took two Tylenol and when I woke up later it went down. Then it rose again throughout the day reaching 101.4 degrees. That night I decided to contact my doctor and explained my symptoms. Then the next morning I noticed my temp was going down. The doctor called me back and informed me that she thought it was a reaction to the vaccine. Then on 4/8 my temp went from 98.9 to 101.4 degrees. From 4/9-4/10 I noticed that my temp started to revert back to normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes Type 2
- Andere Medikamente
- Metformin; Simvastatin; Vitamin B
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Impaired work ability
Limb discomfort
Nausea
Pain
Pyrexia
Sick leave
Symptomtext
Fever, body ache, leg discomfort, headache nausea All started about 12 hours after the shot, and have been treated with Tylenol Once Tylenol wears off, the headache and fever come back I had to call in sick, as I wasn?t able to work today
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- One a day vitamin , Mirena IUD
- Allergien
- Grapefruit
- Vorherige Impfungen
- Similar ADRs with the second shot of Pfizer (but to a lesser degree), and with the first booster of Moderna Both occasions requi
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Eye pain
Headache
Pyrexia
Vomiting
Symptomtext
Patient has a headache; eyes hurt, weak, vomiting and fever since 4/6/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Erythema
Pruritus
Scratch
Skin discolouration
Symptomtext
Moderna second booster shot was administered on April 6, 2022 to patient. She never had any problem with the other Moderna vaccines. She said her arm began to itch the day after (4/7/22) by Saturday (4/9/22) her arm was very red and pink from her scratching where the itching was located. She is fine otherwise no other symptoms or adverse effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hyperthyroidism, hypertension
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- 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: nein
Extra dose administered
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Symptomtext
Site: Itching at Injection Site-Medium, 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
- -
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Back pain
Headache
Pain in extremity
Symptomtext
leg pains, back pains, headache starting the day after the vaccine was administered and since. Very bad reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- seasonal allergy medicine. vitamins
- Allergien
- Prednizone
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 25.03.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Pruritus
Swelling
Symptomtext
Extreme skin itching about 1 week post Moderna booster resulting in Urticaria Dermatographia. Itching skin results in raised hives upon scratching skin surface.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 10.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Induration
Inflammation
Pain
Pruritus
Urticaria
Symptomtext
After receiving Moderna booster, patient developed a large, hard, itchy, welt that was inflamed and sore. Patient had not experienced any similar reaction to previous doses and is concerned that the administration of the vaccine was improperly performed. Patient was seen by her physician and given a course of an antibiotic to treat possible cellulitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 09.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Body temperature
Feeling abnormal
Inappropriate schedule of product administration
Lymph node rupture
Lymphadenopathy
Pyrexia
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of LYMPH NODE RUPTURE (Thinks lymph node is ruptured) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Iron deficiency anemia (Iron deficiency anemia during menopause (its gone now)). Previously administered products included for Drug use for unknown indication: PFIZER vaccine (primary series and first booster dose). Past adverse reactions to the above products included No adverse event with PFIZER vaccine. Concurrent medical conditions included Fibroids. On 04-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Apr-2022, the patient experienced LYMPH NODE RUPTURE (Thinks lymph node is ruptured) (seriousness criterion medically significant), FEELING ABNORMAL (Felt like a truck hit her /was miserable throughout the night), LYMPHADENOPATHY (Swelling of the lymph node / lymph nodes were large grape-life / firm under the armpit/swollen/lymph node is bulging/swelling like a outward down), AXILLARY PAIN (Her entire armpit was like a bee stung / states it is painful), PYREXIA (Had a 102 F. temp.) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient had primary series and first booster dose as PFIZER and 2nd booster shot as Moderna). At the time of the report, LYMPH NODE RUPTURE (Thinks lymph node is ruptured), FEELING ABNORMAL (Felt like a truck hit her /was miserable throughout the night), LYMPHADENOPATHY (Swelling of the lymph node / lymph nodes were large grape-life, / firm under the armpit/swollen/lymph node is bulging/swelling like a outward down), AXILLARY PAIN (Her entire armpit was like a bee stung / states it is painful), PYREXIA (Had a 102 F.) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient had primary series and first booster dose as PFIZER and 2nd booster shot as Moderna) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 04-Apr-2022, Body temperature: 102 (High) 102 F. The weight of patient was reported as 125 (unit was not reported). Patient had primary series and first booster dose of PFIZER and second booster shot of Moderna. It was reported that patient had swelling of the lymph nodes, lymph nodes were large grape-life and firm under the armpit. She stated it was painful and swollen. She used to put hot water under the arm and it was no longer firm but her entire armpit was like a bee stung. She stated that, the lymph node was not firm anymore and had bulged and swelling like outward down. She was thinking could that possibly be a lymph node rupture. No concomitant and treatment medication information was reported. Company comment: This spontaneous case concerns a 58-year-old female patient with history of interchange of vaccine products, who experienced the unexpected serious (medically significant) event Lymph node rupture, on same day after a dose of mRNA-1273. The patient experienced fever, axillary pain, and enlarged firm lymph nodes in the armpit which subsequently softened after hot fomentation, and she felt that the nodes had ruptured. At the time of reporting, the event outcome was unknown. Previously the patient had taken 3 doses of Pfizer vaccine (inappropriate schedule of vaccine administration). The benefit-risk relationship of mRNA-1273 is not affected by this report. Sender's Comments: This spontaneous case concerns a 58-year-old female patient with history of interchange of vaccine products, who experienced the unexpected serious (medically significant) event lymph node rupture, on same day after a dose of mRNA-1273. The patient experienced fever, axillary pain, and enlarged firm lymph nodes in the armpit which subsequently softened after hot fomentation, and she felt that the nodes had ruptured. At the time of reporting, the event outcome was unknown. Previously the patient had taken 3 doses of Pfizer vaccine (inappropriate schedule of vaccine administration). The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210404; Test Name: Body temperature; Result Unstructured Data: 102 F.
- Aktuelle Erkrankungen
- Fibroids
- Vorgeschichte
- Medical History/Concurrent Conditions: Iron deficiency anemia (Iron deficiency anemia during menopause (its gone now)).
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nausea
Retching
Vaccine positive rechallenge
Symptomtext
dry heaves, naseau
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ms
- Andere Medikamente
- dimethyl fumorate, baclofem, desmotressin acetate, citalopram hydrobromide, vitamin d, calcium, multi vitamin, fluticasone,
- Allergien
- latex, mold
- Vorherige Impfungen
- Moderna 004f21a 70 dry heaves, naseau
- Staat
- IL
- Alter
- 94,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenopia
Fatigue
Symptomtext
pt became very tired and had a hard time keeping his eyes open, paramedics were called, pt was able to keep eyes open when paramedics arrived
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Feeling hot
Urticaria
Symptomtext
over heated, hives on back
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- zolpidem
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pruritus
Symptomtext
Patient reports itchiness at injection site 24 hours post injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 31.03.2022
- 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 pruritus
Injection site swelling
Symptomtext
Site: Itching at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Feeling cold
Headache
Pain
Symptomtext
Night of getting the vaccine she was freezing cold and her joints started to hurt. The next morning she had a terrible headache and felt achy all over.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- seizure disorder, high blood pressure COPD, neuropathy
- Andere Medikamente
- dilantin, neurontin, amlodipine, lyrica, centurium silver, folic acid, flonase inhaler, azelastine, trelegy
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 02.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 31.03.2022
- 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 rash
Injection site swelling
Injection site urticaria
Skin discolouration
Symptomtext
Pt got shot on 3/30/2022. Noted more rash like hives on injection site left upper deltoid on 3/31/2022 in AM. Noted more redness and swelling. Site location felt sore. Tried ice compresses which made it worse he felt. No meds taken. Sought treatment at Health Center on 4/2/2022. Saw Dr. , D.O. He was given allergy pack (Loratadine 10mg one tab po daily x 7 days, and Benadryl as needed. Short ice compresses with towel buffer advised 5 minutes 3 times a day. Ok to shower with soap and water. Pat dry. Rash marked with purple been to see if rash spreads. Pt will follow up with appointment on 4/4/2022 to check on rash status. In the mean time, if any worsening pain/rash/change in symptoms, advise for ER evaluation here locally.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Seasonal allergies
- Andere Medikamente
- None
- Allergien
- NKDA. Seasonal allergies + dust
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 20.03.2022
- Impfdatum
- 19.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Symptomtext
Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Headache
Injection site erythema
Injection site induration
Injection site pruritus
Injection site swelling
Oedema peripheral
Pain in extremity
Pyrexia
Tinnitus
Symptomtext
Left arm sore and feels hard at injection site - began approximately 11 hours after injection - still painful, though less, and feels hard, on 03/18/22 at 11:30am Swelling , redness, and itching at injection site - began approximately 11 hours after injection - symptoms lessened but still obvious on 03/18/22 at 11:30 am Headache and buzzing in head - began approximately 11 hours after injection - alleviated by acetaminophen first taken when fever started - slight headache and buzzing in head on 03/18/22 at 11.30am Fever of 99.7 - began approximately 12 hours after injection - alleviated by acetaminophen - continued through mid day on 03/17/22 - no fever on 03/18/22 Pain and swelling under left arm - soft, bulbous area below armpit - pain began on 03/16/22 - swelling noted approximately 10:00pm on 03/17/22 - swelling remains
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- glucosamine chondroitin, brain booster, acetaminophen
- Allergien
- sulfa drugs, penicillin products, latex
- Vorherige Impfungen
- 2nd dose Moderna Covid vaccine - fever, sore/stiff arm, buzzing headaches - 61 yo, Moderna 017C21A
- Staat
- LA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Heart rate increased
Muscle swelling
Myalgia
Pain
Respiratory rate increased
Vaccine positive rechallenge
Symptomtext
tiredness and achiness began at 6:30pm 3/15/22, along with swollen pectoral muscle. All over achniness and tiredness worsened, along with swollen pectoral muscle, rapid heart rate and breathing, and chills began late that evening around midnight and lasted through 7am on 3/17/22. Achiness, chills, rapid heart rate and breathing subsided at that time. As of 11:15am on 3/17/22, pectoral muscle is still very swollen and painful and tiredness persists.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- spontaneous bilateral internal carotid artery dissections, causing multiple TIAs, requiring stenting in both left and right arteries
- Andere Medikamente
- aspirin 81 mg oral tablet 1/nightly, spironolactone 25 mg oral tablet 1/nightly, fluticasone 50 mcg/inh nasal spray 1 in each nostril nightly, levocetirizine 5 mg oral tablet 1/nightly, fluorometholone 0.1% ophthalmic suspension 1 drop in r
- Allergien
- hives with aleve
- Vorherige Impfungen
- Very similiar symptoms with 2nd Moderna Covid vaccine on 5/15/21, age 39
- Staat
- GA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 12.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 12.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pruritus
Symptomtext
Patient started experiencing pain and slight itching in the shoulder area the day after his 2nd dose of Moderna. I recommended diphenhydramine for treatment. I recommended that he seek medical treatment if his symptoms get worse and to call 911 or go to emergency room if he starts experiencing any difficulty breathing . He will follow up on any changes to his condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Gabapentin 300mg by mouth twice daily
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 12.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE; VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE; No adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE), PRODUCT STORAGE ERROR (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (No adverse event) in a female patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular use) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE), PRODUCT STORAGE ERROR (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE), PRODUCT STORAGE ERROR (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (No adverse event) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Intramuscular use) was unknown. For mRNA-1273 (Spikevax) (Intramuscular use), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and PRODUCT STORAGE ERROR (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE). No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 12.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case was reported for patient 10th out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:Master Case, Patient 10
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 12.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case is reported for patient 11 out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:Master case
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
- 12.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case is reported for patient 14 out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:Master case
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
- 12.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case was reported for patient 13th out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:Master Case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 12.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. This case contains information for patient 5 out of 16. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 11.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product temperature excursion issue
Symptomtext
vaccine given after expiration date due to temperature change in storage; vaccine given after expiration date due to temperature change in storage; no adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine given after expiration date due to temperature change in storage), PRODUCT TEMPERATURE EXCURSION ISSUE (vaccine given after expiration date due to temperature change in storage) and NO ADVERSE EVENT (no adverse event) in a female patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular use) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine given after expiration date due to temperature change in storage), PRODUCT TEMPERATURE EXCURSION ISSUE (vaccine given after expiration date due to temperature change in storage) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine given after expiration date due to temperature change in storage), PRODUCT TEMPERATURE EXCURSION ISSUE (vaccine given after expiration date due to temperature change in storage) and NO ADVERSE EVENT (no adverse event) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Intramuscular use) was unknown. For mRNA-1273 (Spikevax) (Intramuscular use), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (vaccine given after expiration date due to temperature change in storage) and PRODUCT TEMPERATURE EXCURSION ISSUE (vaccine given after expiration date due to temperature change in storage). Concomitant medication was not provided. It was unknown if the patient experienced any additional symptoms/events. Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.09.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No Adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No Adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 12-Apr-2022, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No Adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No Adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case is reported for patient 1st out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739843, US-MODERNATX, INC.-MOD-2023-739848, US-MODERNATX, INC.-MOD-2023-739857, US-MODERNATX, INC.-MOD-2023-739859, US-MODERNATX, INC.-MOD-2023-739861, US-MODERNATX, INC.-MOD-2023-739862, US-MODERNATX, INC.-MOD-2023-739864, US-MODERNATX, INC.-MOD-2023-739863, US-MODERNATX, INC.-MOD-2023-739867, US-MODERNATX, INC.-MOD-2023-739868, US-MODERNATX, INC.-MOD-2023-739839, US-MODERNATX, INC.-MOD-2023-739851 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739843:Patient 5 US-MODERNATX, INC.-MOD-2023-739848:Patient 7 US-MODERNATX, INC.-MOD-2023-739857:Patient 12 US-MODERNATX, INC.-MOD-2023-739867:Patient 10 US-MODERNATX, INC.-MOD-2023-739868:Patient 11 US-MODERNATX, INC.-MOD-2023-739861:Patient 14 US-MODERNATX, INC.-MOD-2023-739864:Patient 9 US-MODERNATX, INC.-MOD-2023-739863:Patient 16 US-MODERNATX, INC.-MOD-2023-739862:Patient 15 US-MODERNATX, INC.-MOD-2023-739859:Patient 13 US-MODERNATX, INC.-MOD-2023-739839:Patient 4 US-MODERNATX, INC.-MOD-2023-739851:Patient 8
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
- 11.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case is reported for patient 9 out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case is reported for patient 15th out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:Master case
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
- 11.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case is reported for patient 12 out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case is reported for patient 8th out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:Master case
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
- 11.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case was reported for patient 7th out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:Master Case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case is reported for patient 6 out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case is reported for patient 4th out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:Master case
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
- 11.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; HCP states that they administered shot to patient after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered shot to patient after their expiration date) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered shot to patient after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered shot to patient after their expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered shot to patient after their expiration date). No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. This case is reported for patient 3 out of 16 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No Adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No Adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No Adverse event) outcome was unknown. Not Provided For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No Adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. This case contains information for patient 2 out of 16. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 08.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product temperature excursion issue
Symptomtext
no adverse event; GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE; GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE), PRODUCT TEMPERATURE EXCURSION ISSUE (GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (no adverse event) in a 14-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular use) 1 dosage form. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and PRODUCT TEMPERATURE EXCURSION ISSUE (GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE), PRODUCT TEMPERATURE EXCURSION ISSUE (GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular use), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and PRODUCT TEMPERATURE EXCURSION ISSUE (GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE). Concomitant medication was not provided. 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
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 07.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product temperature excursion issue
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE; No adverse event; VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE), PRODUCT TEMPERATURE EXCURSION ISSUE (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (No adverse event) in a 60-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE), PRODUCT TEMPERATURE EXCURSION ISSUE (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and PRODUCT TEMPERATURE EXCURSION ISSUE (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE). Concomitant medication was not reported. It was unknown if the patient experienced any additional symptoms/events. Treatment medication was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 07.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product temperature excursion issue
Symptomtext
Vaccine given after expiration date due to temperature change in storage; Vaccine given after expiration date due to temperature change in storage; no adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine given after expiration date due to temperature change in storage), PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine given after expiration date due to temperature change in storage) and NO ADVERSE EVENT (no adverse event) in a male patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular use) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine given after expiration date due to temperature change in storage), PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine given after expiration date due to temperature change in storage) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine given after expiration date due to temperature change in storage), PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine given after expiration date due to temperature change in storage) and NO ADVERSE EVENT (no adverse event) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Intramuscular use) was unknown. For mRNA-1273 (Spikevax) (Intramuscular use), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Vaccine given after expiration date due to temperature change in storage) and PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine given after expiration date due to temperature change in storage). No concomitant medications were reported. It was unknown if the patient experienced any additional symptoms/events. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 06-Sep-2023: Follow up added with no new information received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 07.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product temperature excursion issue
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE; no adverse event; VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE), PRODUCT TEMPERATURE EXCURSION ISSUE (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (no adverse event) in a 31-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular use) 1 dosage form. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE), PRODUCT TEMPERATURE EXCURSION ISSUE (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular use), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and PRODUCT TEMPERATURE EXCURSION ISSUE (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE). Concomitant medications were not reported. It was unknown if the patient experienced any additional symptoms/events. Treatment medications were not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 99,0
- Geschlecht
- F
- Eingang
- 06.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 06.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 06.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 06.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 06.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 06.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 06.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 96,0
- Geschlecht
- F
- Eingang
- 06.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 06.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 06.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 06.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 06.09.2023
- Impfdatum
- 01.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 06.09.2023
- Impfdatum
- 01.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 06.09.2023
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 02.08.2023
- Impfdatum
- 05.04.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 190,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines moderna 2/12/21 lot# 015M20A; Moderna 3/2/21 lOt# 002B21A; Moderna 11/8/21 lot# 034F21A; Moderna 4/5/22 lot# 048L21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 24.07.2023
- Impfdatum
- 21.03.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 137,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test
Symptomtext
He had covid for a whole week, felt tired, sneezing; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (He had covid for a whole week, felt tired, sneezing) in a 71-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 21-Mar-2022, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Aug-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced COVID-19 (He had covid for a whole week, felt tired, sneezing). On 16-Jul-2023, COVID-19 (He had covid for a whole week, felt tired, sneezing) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In August 2022, SARS-CoV-2 test: Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication not reported. Treatment medication not reported. This case was linked to US-MODERNATX, INC.-MOD-2023-734135 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-734135:Wife case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202208; Test Name: Covid-19 test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 97,0
- Geschlecht
- F
- Eingang
- 21.06.2023
- Impfdatum
- 23.05.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 24,0
- 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 Pfizer 3/29/21 Lot# ER8730; Pfizer 4/23/21 lot# Ew0172; Pfizer 3/6/22 lot# FK9895
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID+
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 21.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Audiogram abnormal
Ear discomfort
Tinnitus
Symptomtext
I developed a Pulsatile Tinnitus on my left ear. I had like a hard bit on my ear, I spoke to the doctor in a radiology department, they did a Pure-tone audiometry.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Audiogram abnormal
- Hospital-Tage
- -
- Labordaten
- 13JULY2022- Pure-Tone Audiometry- Hearing block
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Losartan; Oxybutynin; Multi Vitamins; Vitamin D; Calcium; Magnesium; Zinc; Fish Oil; Potassium; Probiotic; Aleve
- Allergien
- Clindamycin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 22.04.2023
- Impfdatum
- 01.08.2022
- Beginn
- 14.02.2023
- Tage bis Beginn
- 197,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal mass
Computerised tomogram abdomen abnormal
Magnetic resonance imaging abnormal
Symptomtext
Abdominal mass
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal mass
- Hospital-Tage
- -
- Labordaten
- CAT scan, MRI
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- psoriasis, psoriatic arthritis, hypothyroidism
- Andere Medikamente
- Tirosint, methotrexate
- Allergien
- penicillin, codine
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 12.04.2023
- Impfdatum
- 06.04.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 86,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Computerised tomogram normal
Diplopia
Fall
Laboratory test abnormal
Magnetic resonance imaging normal
Myasthenia gravis
Parkinson's disease
Symptomtext
I went to the ER because of a fall, and a double vision, they did a lot of tests, I stayed overnight, and I was referred to a Neurologist. The doctor said I have Parkinson's disease and Myasthenia gravis, this affected my eye only.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Computerised tomogram normal
- Hospital-Tage
- 1,0
- Labordaten
- 2022 Lab work, Myasthenia Gravis; 2022 CT scan, not stroke; 2022 MRI, normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetic
- Andere Medikamente
- Vitamin D; FLONASE
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 10.04.2023
- Impfdatum
- 01.04.2022
- Beginn
- 31.07.2022
- Tage bis Beginn
- 121,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphonia
Laboratory test normal
SARS-CoV-2 test negative
Symptomtext
Started to lose voice when talking, this comes and goes. Sought care form an ENT 8/29/2022, COVID-19 test, negative, scope negative. No further testing performed as no results found. ENT Proscribed prednisone to no effect. Condition continues at time of reporting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aphonia
- Hospital-Tage
- -
- Labordaten
- 29AUG2022, COVID-19 test, negative, scope negative
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Magnesium; Preservision
- Allergien
- Morphine; Sporionox
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 04.04.2023
- Impfdatum
- 01.04.2022
- Beginn
- 26.03.2023
- Tage bis Beginn
- 359,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Moderna 1/28/21 Lot# 028L20A; Moderna 2/25/21 Lot# 004M20A; Moderna 11/10/21 Lot# 033F21A; Moderna 4/21/22 Lot# 048L21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 16.04.2022
- Beginn
- 17.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
tinnitus, buzzing in ear, not constant, but frequent After the next booster on 9/12/22, same location, Moderna lot AS71443, intramuscular, left arm. the tinnitus became constant and at times is louder than others, and difficult to ignore
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- sertraline Meloxicam dutasteride
- Allergien
- penicillin neosporin tramadol
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 30.03.2023
- Impfdatum
- 29.04.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 213,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Moderna 1/6/21 Lot# 012L20A; Moderna 3/3/21 Lot# 012L20A; Moderna 12/22/21 Lot# 060H21A; Moderna 4/29/22 Lot#048L21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 97,0
- Geschlecht
- M
- Eingang
- 28.03.2023
- Impfdatum
- 21.04.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 131,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 1/14/21 Lot# 012L20A; Moderna 2/11/21 Lot# 010M20A; Moderna 4/21/22 Lot# 048L21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 22.11.2022
- Impfdatum
- 28.03.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 65,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Computerised tomogram
Haemorrhage
Metastatic neoplasm
Positron emission tomogram
SARS-CoV-2 test
Symptomtext
patient got COVID-19; previous cancer spread; periodic bleeding; This spontaneous case was reported by a patient and describes the occurrence of METASTATIC NEOPLASM (previous cancer spread) and HAEMORRHAGE (periodic bleeding) in an 87-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Bladder cancer (bladder cancer, malignant tumor with abdomen metastasis removed on 2019) in 2010, Appendicitis, Surgery in 2019 and Nephrectomy in 2017. Concurrent medical conditions included Allergy to antibiotic, Pain, Fever and Sleep disorder NOS. Concomitant products included PARACETAMOL (TYLENOL) for Pain and Fever, ALPRAZOLAM (XANAX) for Sleep disorder NOS. On 28-Mar-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In June 2022, the patient experienced HAEMORRHAGE (periodic bleeding) (seriousness criterion medically significant). In July 2022, the patient experienced METASTATIC NEOPLASM (previous cancer spread) (seriousness criterion medically significant). On 07-Sep-2022, the patient experienced COVID-19 (patient got COVID-19). On 20-Sep-2022, COVID-19 (patient got COVID-19) had resolved. At the time of the report, METASTATIC NEOPLASM (previous cancer spread) and HAEMORRHAGE (periodic bleeding) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2022, Computerised tomogram: previous cancer spread again. In 2022, Positron emission tomogram: previous cancer spread again. On 20-Sep-2022, SARS-CoV-2 test: (Negative) 13 days later. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Flu shot on 01-Oct-2022. The patient took multivitamin supplements. No treatment medications were reported. Company Comment: This is a spontaneous case, reported by a patient, concerning an 87-year-old female patient with relevant medical history of Bladder cancer with abdominal metastasis, who experienced the unexpected serious (medically significant) events of Metastatic neoplasm and Haemorrhage, which occurred approximately 4 months after receiving the fourth dose of mRNA-1273 vaccine as the first booster dose of COVID-19 vaccine. Patient also received 3 doses of Moderna COVID-19 vaccine prior and 1 dose of Bivalent Moderna COVID-19 vaccine after. It was reported that the patient's previous cancer had spread and also had periodic bleeding. Patient also had COVID-19 infection approximately 5 months and 1 week post mRNA-1273 vaccination, and was resolved after 13 days confirmed by a negative SARS-CoV-2 test. Patient also underwent CT scan and PET scan which revealed spread of the previous cancer. No further details about the clinical course and treatments were provided. Outcome of the events Metastatic neoplasm and Haemorrhage were unknown. The medical history of Bladder cancer with abdominal metastasis remain as confounders for the events. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to US-MODERNATX, INC.-MOD-2022-673532, US-MODERNATX, INC.-MOD-2021-291235, US-MODERNATX, INC.-MOD-2021-674168, US-MODERNATX, INC.-MOD-2021-674162 (Linked Report).; Sender's Comments: This is a spontaneous case, reported by a patient, concerning an 87-year-old female patient with relevant medical history of Bladder cancer with abdominal metastasis, who experienced the unexpected serious (medically significant) events of Metastatic neoplasm and Haemorrhage, which occurred approximately 4 months after receiving the fourth dose of mRNA-1273 vaccine as the first booster dose of COVID-19 vaccine. Patient also received 3 doses of Moderna COVID-19 vaccine prior and 1 dose of Bivalent Moderna COVID-19 vaccine after. It was reported that the patient's previous cancer had spread and also had periodic bleeding. Patient also had COVID-19 infection approximately 5 months and 1 week post mRNA-1273 vaccination, and was resolved after 13 days confirmed by a negative SARS-CoV-2 test. Patient also underwent CT scan and PET scan which revealed spread of the previous cancer. No further details about the clinical course and treatments were provided. Outcome of the events Metastatic neoplasm and Haemorrhage were unknown. The medical history of Bladder cancer with abdominal metastasis remain as confounders for the events. The benefit-risk relationship of mRNA-1273 is not affected by this report. US-MODERNATX, INC.-MOD-2022-673532:Bivalent booster US-MODERNATX, INC.-MOD-2021-291235:Dose 3 US-MODERNATX, INC.-MOD-2021-674168:Dose 2 US-MODERNATX, INC.-MOD-2021-674162:Dose 1
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 2022; Test Name: CT scan; Result Unstructured Data: previous cancer spread again; Test Date: 2022; Test Name: PET scan; Result Unstructured Data: previous cancer spread again; Test Date: 20220920; Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: 13 days later
- Aktuelle Erkrankungen
- Allergy to antibiotic; Fever; Pain; Sleep disorder NOS
- Vorgeschichte
- Medical History/Concurrent Conditions: Appendicitis; Bladder cancer (bladder cancer, malignant tumor with abdomen metastasis removed on 2019); Nephrectomy; Surgery
- Andere Medikamente
- XANAX; TYLENOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 07.04.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 208,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Admitted to hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 21.10.2022
- Impfdatum
- 12.04.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 191,0
- 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 3/12/21 Moderna 044A21A dose 2 4/9/21 Moderna 018B21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ test on 10/20/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 20.10.2022
- Impfdatum
- 29.04.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 159,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back disorder
Musculoskeletal discomfort
Tendon disorder
X-ray limb abnormal
Symptomtext
After my vaccination I started to come down with symptoms that I have had physical therapy for both mid back lower back and neck. 09/27/2022 Cortisone shot in shoulder greatly improved my right shoulder and will being physical therapy for it, however neck is worse. X-ray done before cortisone shot. Physical therapy has greatly improved my symptoms for my hip and back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back disorder
- Hospital-Tage
- -
- Labordaten
- X-Ray: Right Shoulder: Diagnosed with Tendon related issues. 09/27/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; Microvalve Prolapse
- Andere Medikamente
- Atenolol; Benazepril; Chlorthalidone; Levothyroxine; Multi-Vitamin; CoQ10
- Allergien
- Penicillin; Sulfa; Emicin; Macro Danton
- Vorherige Impfungen
- January for 2021 when I started to come down with symptoms. Right hip was replaced in 2013 and then after the 1st COVID-19 Vacci
- Staat
- KY
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 31.03.2022
- Beginn
- 20.09.2022
- Tage bis Beginn
- 173,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Unevaluable event
Symptomtext
Admitted to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 03.05.2022
- Beginn
- 11.09.2022
- Tage bis Beginn
- 131,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Admitted to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 03.04.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 160,0
- Dosis
- 4
- 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 dose 1 3/11/21 Moderna 001B21A dose 2 4/8/21 Moderna 045A21A dose 3 11/7/21 Moderna 058F21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ 9/10/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 29.08.2022
- Impfdatum
- 24.03.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 151,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after three vaccines Moderna 8/5/21 Lot# 041C21A ; Moderna 9/2/21 Lot# 041C21A; Moderna 3/24/22 Lot# 048L21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 04.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acoustic stimulation tests abnormal
Deafness neurosensory
Sudden hearing loss
Symptomtext
Sudden sensorineural hearing loss
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests abnormal
- Hospital-Tage
- -
- Labordaten
- Hearing Test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Essential Hypertension, Hypothyroidism, Hyperlipidemia, DM II diet controlled
- Andere Medikamente
- Gabapentin, Diltiazem, Levothyroxine, Metoprolol Succinate, Simvistatin, Triamterene Hydrochlorothiazide, Low Dose Aspirin, Omega 3
- Allergien
- Accupril
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 20.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 01.08.2022
- 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
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 20.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 01.08.2022
- 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
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 20.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 20.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 07.04.2022
- Beginn
- 06.08.2022
- Tage bis Beginn
- 121,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Pt tested positive for COVID on 08/06/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 10.08.2022
- Impfdatum
- 04.04.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 128,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Extra dose administered
Symptomtext
Patient has had 4 COVID vaccinations and developed COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- -
- Geschlecht
- U
- Eingang
- 09.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine experienced multiple warm excursions and was administered past it's expiry date), PRODUCT STORAGE ERROR (Vaccine was above 5F for a total of 20 reported hours and reached a max temperature of 19.4F (is true max, 75.2F was most likely battery change)) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 01-Aug-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 01-Aug-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine experienced multiple warm excursions and was administered past it's expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was above 5F for a total of 20 reported hours and reached a max temperature of 19.4F (is true max, 75.2F was most likely battery change)) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine experienced multiple warm excursions and was administered past it's expiry date), PRODUCT STORAGE ERROR (Vaccine was above 5F for a total of 20 reported hours and reached a max temperature of 19.4F (is true max, 75.2F was most likely battery change)) 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 (Vaccine experienced multiple warm excursions and was administered past it's expiry date) and PRODUCT STORAGE ERROR (Vaccine was above 5F for a total of 20 reported hours and reached a max temperature of 19.4F (is true max, 75.2F was most likely battery change)). Concomitant product use was not provided by the reporter. Moderna product was stored in the freezer (prior to moving to the fridge). Vaccine experienced multiple warm excursions and was administered past its expiry date. The vaccine was damaged out at the time of report. Lot 048L21A was delivered on 17-Mar-2022. Vaccine was moved to the fridge on 31-Jul-2022 and administered on 01-Aug-2022 and vial removed from fridge and punctured at 1:00pm. The vaccine was above 5F for a total of 20 reported hours and reached a max temperature of 19.4F (was true max, 75.2F was most likely battery change). The reporting interval changes on 07-Apr-2022 at 9:13am from a 5-minute reporting interval to a 15-minute reporting interval. There was missing freezer temperature data from 09-Jun-2022 to 18-Jul-2022. The sharp spike was most likely when the team changed the battery and placed the TempAlert device back in the freezer. When the data came back there were two warm excursions. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 05.08.2022
- Impfdatum
- 28.04.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 97,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines ; Moderna 1/27/21 Lot# 032H20A; Moderna 1028/21 Lot# 076C21A; Moderna 4/28/22 Lot# 048L21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- external COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 27.07.2022
- Impfdatum
- 21.04.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 80,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Rhinorrhoea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
On 7-8-2022, I started noticing an occasional cough and runny nose. I took a home Covid19 test and it showed negative results. On 7-9-2022, I tested positive for Covid19 using a home test. I went to the clinic on 7-10 and was tested for Covid19 again with positive results. The pharmacist gave me a prescription for Paxlovid. I am doing very well now and recovered. I am reporting my breakthru case of Covid19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 7-8-2022 home Covid19 test with negative results 7-9-2022 home Covid19 test with positive results 7-10-2022 Covid19 test at clinic
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN, Gout, Glaucoma
- Andere Medikamente
- Allopurinol; Lisinopril; Amlodipine Besylate; Atorvastatin; Baby Aspirin; Zinc; Lycopene; VitD; VitC
- Allergien
- Sulfa Drugs
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Patient was given an expired vaccine, patient did not report any side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Patient was given an expired vaccine, patient did not report any side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient was given an expired vaccine, patient did not report any side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Yes
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
None/Vaccine Expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None At This Time
- Aktuelle Erkrankungen
- Unknown/None Listed
- Vorgeschichte
- Unknown/None listed
- Andere Medikamente
- Unknown/None Listed
- Allergien
- None listed
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient was given an expired vaccine, patient did not report any side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient was given an expired vaccine, patient did not report any side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient was given an expired vaccine, patient did not report any side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
None Reported/Vaccine Expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None At This Time
- Aktuelle Erkrankungen
- Unknown/None Listed
- Vorgeschichte
- Unknown/None Listed
- Andere Medikamente
- Unknown/None Listed
- Allergien
- Unknown/None Listed
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was given an expired vaccine, patient did not report any side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Yes
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
None at this time/Vaccine Expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None at this time
- Aktuelle Erkrankungen
- Unknown/None Listed
- Vorgeschichte
- Unknown/None Listed
- Andere Medikamente
- Unknown/None Listed
- Allergien
- Unknown/None Listed
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient was given an expired vaccine, patient did not report any side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
None Reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- None reported
- Aktuelle Erkrankungen
- Unknown/None listed
- Vorgeschichte
- Unknown/None Listed
- Andere Medikamente
- Unknown/None listed
- Allergien
- Unknown/None listed
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- -
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 02.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Suspected COVID-19
Symptomtext
This spontaneous report received from a patient via other manufacturer Pfizer concerned a 58 year old male. Initial information was processed with the additional information received on 15-JUL-2022 and 18-JUL-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: hyperthyroidism, and penicillin allergy. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 042A21A, expiry: unknown) dose was not reported, 1 total, administered on an unspecified date at 12:00 to left arm for covid-19 prophylaxis. Concomitant medications included bupropion hydrochloride (Wellbutrin), levothyroxine sodium (Synthroid) and sertraline hydrochloride (Zoloft) for drug used for unknown indication. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26.cov2.s (Dose number in series 1). The patient additionally received non-company Moderna vaccine (elasomeran) (dose number in series 2) (form of admin, route of admin not reported, batch number: 048L21A, expiry: unknown) dose was not reported, administered on 02-APR-2022 at 12:00 to left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with second dose of Moderna vaccine (elasomeran) (Dose number in series 2). The patient received another non-company Pfizer biontech Covid-19 vaccine (Tozinameran) (Dose number in series 3) (form of admin, route of admin not reported, batch number: unknown, expiry: unknown) dose was not reported, administered on 02-JUN-2022 at 12:00 to left arm for covid-19 prophylaxis. On an unspecified date in 2022, patient had covid-19 (Dose number in series 3). The patient received non company suspect Paxlovid (form of admin, route of admin and batch number were not reported and expiry: unknown) dose was not reported, administered on 21-JUN-2022 for covid-19 treatment. Patient received last dose of Paxlovid on 25-JUN-2022. On 04-JUL-2022 at 08:00, the patient experienced covid rebound after paxlovid five day treatment. (Dose number in series 3). The action taken with covid-19 vaccine ad26.cov2.s, elasomeran and tozinameran was not applicable and action taken with Paxlovid was treatment discontinued. The patient had not recovered from covid rebound after paxlovid five day treatment. This report was non-serious. This report was associated with product quality complaint number: 90000242596. The suspected product quality complaint has been confirmed to be the reported allegation was not confirmed and the root cause was determined to be not manufacturing related. Batch and lot tested and found within specifications based on the PQC evaluation/investigation performed. Sender's Comments: V0- Medical assessment comment is not required as per standard procedure as case was assessed as non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Suspected COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hyperthyroidism; Penicillin allergy
- Vorgeschichte
- -
- Andere Medikamente
- WELLBUTRIN; ZOLOFT; SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 18.04.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 51,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
I was going in for a CT scan and I just had my car dropped off. I was sent to get a routine COVID-19 test and it came back positive and I was sent home. I was totally unaware and was just told to report any symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 11.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Dose administered after manufacturer date of expiry; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. The patient was administered with first Booster dose. The vial was thawed for the first time on 11Jul2022. On 11Jul2022, the vial was initially stored in the refrigerator. The vial did not undergo any temperature excursions. No treatment medication information was provided. This case was linked to MOD-2022-608562, MOD-2022-608557 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 95,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 11.07.2022
- Beginn
- 11.07.2022
- 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 (dose administered after manufacturer date of expiry) in a 95-year-old female patient who received mRNA-1273 (Moderna COVID-19 vaccine/lot# batch/lot# 048L21A) for COVID-19 immunization. No medical history reported. On Jul 11, 2022, patient received a dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On Jul 11, 2022, patient administered expired product (dose administered after manufacturer date of expiry). At the time of the report, administered expired product (dose administered after manufacturer date of expiry) outcome unknown. The reporter did not provide any causality assessments, concomitant medication or treatment information. Patient administered the second booster dose. Vial thawed for the first time on Jul 11, 2022. The number of doses per vial: 3. On Jul 11, 2022, vial initially stored in the refrigerator. Vial did not undergo any temperature excursions. This case linked to MOD-2022-608564 (patient link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 11.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Dose administered after manufacturer date of expiry; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that the patient received first booster dose of Moderna vaccine on 11-Jul-2022 from a vial containing 3 doses. It was reported that the vial was initially stored in the refrigerator on 11-Jul-2022. The vial was thawed for the first time on 11-Jul-2022. The vial did not undergo any temperature excursions. The reporter asked what action needs to be taken further in regards to the expired vaccine administration. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2022-608564, US-MODERNATX, INC.-MOD-2022-608562 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-608564:3rd Patient (same reporter) US-MODERNATX, INC.-MOD-2022-608562:2nd Patient (same reporter)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 85,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test
Symptomtext
Got Covid 7/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid test
- Aktuelle Erkrankungen
- Nonhodgkins lymphoma in remission since 11/18 Rheumatoid arthritis
- Vorgeschichte
- -
- Andere Medikamente
- Sulindac 200 mg Levothyroxine .025 mg Omeprazole 20 mg Fexofenodrene 180 mg Pseudoephedrine 30 mg Multivitamin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 07.04.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 69,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Laboratory test normal
Magnetic resonance imaging normal
Speech disorder
Symptomtext
First was an episode of disconnect between a word I had in my mind and trying to speak that word. I could talk but I couldn't get the word I wanted to use even if I knew what it was. It went away. I did see a doctor and had an MRI. I was told if this happened again to go to the ER. The second episode on 07/22 at 8:30AM my husband called the ambulance and they went through the entire stroke protocol. I was told to start taking a regular aspirin everyday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Laboratory test normal
- Hospital-Tage
- -
- Labordaten
- MRI - it was normal. Stroke protocol tests - nothing abnormal.
- Aktuelle Erkrankungen
- Temporary dizziness
- Vorgeschichte
- Osteoporosis; Glaucoma; Fusion
- Andere Medikamente
- Loratadine; spironolactone; coQ10
- Allergien
- Strawberries; statin drugs; gabapentin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Patient presents to medical facility for 2nd booster dose of Moderna Covid vaccine. When documenting in log, lot number states Modera lot 048L21A expiration date of 7/8/2022. Vaccination administered 7/13/2022. No adverse reaction noted during observation window, Follow up scheduled.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ND00233 Overweight Personal history of nicotine dependence Age 55 and older Essential (primary) hypertension Hyperlipidemia, unspecified Gout, unspecified Rash and other nonspecific skin eruption
- Andere Medikamente
- Metoprolol Succinate ER 25 MG Tablet Extended Release 24 Hour, Sig: 1 tablet Orally QHS Start Date: 07/07/2022 KOP: Yes DrugSource: In House Pharmacy Stop Date: 12/04/2022, Atorvastatin Calcium 20 MG Tablet, Sig: 1 tablet Orally QHS Start D
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Medical unit: Patient presents for 1st booster dose of Moderna Covid vaccination. Previous vaccination Jannsen 5/14/2021 When documenting vaccine administration in eCW, the lot # noted expiration date of 07/08/2022. Vaccine administer to patient on 7/13/2022. No adverse reactions noted during required post vaccination observation period. Scheduled for follow-up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- iBUPROFEN 600 MG
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 11.07.2022
- Impfdatum
- 09.04.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 44,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Infection
Polymerase chain reaction positive
Symptomtext
Breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Infection
- Hospital-Tage
- -
- Labordaten
- PCR test positive 05/25/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- BPH, Right bundle block
- Andere Medikamente
- Atorvastatin, levothyroxine, Vitamin D, Fish oil
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Costochondritis
Symptomtext
Two days after vaccination I had extreme costochondritis I called my doctor and he recommended I take Aleve and use heat I took one Tylenol and one Aleve.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Costochondritis
- Hospital-Tage
- -
- Labordaten
- No.
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- Hypertension, Glaucoma, Acid reflux
- Andere Medikamente
- Labetalol, Pepcid, Zioptan, Vitamin D, Vitamin B12, Baby aspirin
- Allergien
- Codeine, Sulpha, Penicillin
- Vorherige Impfungen
- Pneumonia vaccine
- Staat
- NJ
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 29.04.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 27,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Exposure to SARS-CoV-2
Head discomfort
Nasal congestion
Nasopharyngitis
Respiratory tract congestion
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Upper-airway cough syndrome
Symptomtext
The week prior to my symptoms beginning, my wife and two children had contracted Covid. On 05/26, I began to experience head cold like symptoms, congestion, coughing, stuffiness. I do suffer from seasonal allergies, but I went ahead and took an at home Covid test which came up negative. I was experiencing head stuffiness, cough, persistent nasal drip that lasted from Thursday, 5/26 to the following Monday morning. I went for a PCR test on 05/27 which came back positive. I had a telemedicine visit after receiving my results and the doctor prescribed Flonase, Sinex nasal spray and a Wixela inhaler. I was also taking Tamiflu cough and cold to help treat the symptoms. They did send a prescription for a Medrol pack which I never ended up using. I was still testing positive for Covid until this morning 06/09, 14 days after testing positive originally.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- Rapid Covid Test-negtive-05/27; PCR Covid Test - positive- 05/27
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Sleep Apnea; I.T.B; Elevated Cholesterol
- Andere Medikamente
- Zyrtec Rosuvastatin Multivitamin Vitamin D Zinc Vitamin K Curcumin Supplement
- Allergien
- Lactose; gluten
- Vorherige Impfungen
- 2nd dose of Moderna. Relapse of ITP. Connection to vaccine not established. Age 56.
- Staat
- NE
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 08.06.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Moderna shot and inadvertently had the Moderna in the freezer and the freezer was not approved for over 30 days of storage; They used two vials from the freezer after 30 days to administer them to 4 patients; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They used two vials from the freezer after 30 days to administer them to 4 patients) and PRODUCT STORAGE ERROR (Moderna shot and inadvertently had the Moderna in the freezer and the freezer was not approved for over 30 days of storage) in an 81-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. No Medical History information was reported. On 18-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They used two vials from the freezer after 30 days to administer them to 4 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Moderna shot and inadvertently had the Moderna in the freezer and the freezer was not approved for over 30 days of storage). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They used two vials from the freezer after 30 days to administer them to 4 patients) and PRODUCT STORAGE ERROR (Moderna shot and inadvertently had the Moderna in the freezer and the freezer was not approved for over 30 days of storage) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. Reporter stated that it was notified to them that their upright freezer (two separate doors for freezer and fridge) was not good to use after 30 days. They normally pull the vials out before the 30 days to thaw. Reporter further stated that they wanted to have a stand alone freezer because of an automatic defrost cycle on some two door freezer/fridge combinations. The vial was initially stored in the refrigerator on 17-May-2022 (1 vial) and 19-May-2022 (1 vial). The temperature had not gone out of range at all, and the vial did not undergo any temperature excursions Reporter further stated that the patients had not contacted them about any problems. No treatment medication were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Inadvertently had the Moderna in the freezer and the freezer was not approved for over 30 days of storage; Used two vials from the freezer after 30 days to administer them; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT STORAGE ERROR (Inadvertently had the Moderna in the freezer and the freezer was not approved for over 30 days of storage) and EXPIRED PRODUCT ADMINISTERED (Used two vials from the freezer after 30 days to administer them) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. No Medical History information was reported. On 18-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Used two vials from the freezer after 30 days to administer them). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Inadvertently had the Moderna in the freezer and the freezer was not approved for over 30 days of storage). At the time of the report, PRODUCT STORAGE ERROR (Inadvertently had the Moderna in the freezer and the freezer was not approved for over 30 days of storage) and EXPIRED PRODUCT ADMINISTERED (Used two vials from the freezer after 30 days to administer them) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. Reporter stated that it was notified to them that their upright freezer (two separate doors for freezer and fridge) was not good to use after 30 days. They normally pull the vials out before the 30 days to thaw. Reporter further stated that they wanted to have a standalone freezer because of an automatic defrost cycle on some two door freezer/fridge combinations. The vial was initially stored in the refrigerator on 17-May-2022 (1 vial) and 19-May-2022 (1 vial). The temperature had not gone out of range at all, no temperature excursion happened. The patient received booster dose. Reporter further stated that the patients had not contacted them about any problems. 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
- NE
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 18.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
used two vials from the freezer after 30 days to administer them; used two vials from the freezer after 30 days to administer them; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (used two vials from the freezer after 30 days to administer them) and PRODUCT STORAGE ERROR (used two vials from the freezer after 30 days to administer them) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. No Medical History information was reported. On 18-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (used two vials from the freezer after 30 days to administer them) and PRODUCT STORAGE ERROR (used two vials from the freezer after 30 days to administer them). At the time of the report, EXPIRED PRODUCT ADMINISTERED (used two vials from the freezer after 30 days to administer them) and PRODUCT STORAGE ERROR (used two vials from the freezer after 30 days to administer them) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant mediations were not reported On 17-MAY-2022 the vial was initially stored in the refrigerator. 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
- WI
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 04.06.2022
- Impfdatum
- 12.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
Very similar to the initial Covid-19 symptoms; Interchange of vaccine products; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (Very similar to the initial Covid-19 symptoms) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) in a 72-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. Previously administered products included for Drug use for unknown indication: Pfizer / BioNTech (Dose Number: 3 Batch/Lot No: N/A Location of injection: Arm Left) on 04-Oct-2021. Past adverse reactions to the above products included No adverse event with Pfizer / BioNTech. Concurrent medical conditions included Drug allergy. On 12-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced COVID-19 (Very similar to the initial Covid-19 symptoms) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). On 22-May-2022, COVID-19 (Very similar to the initial Covid-19 symptoms) had resolved. At the time of the report, INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 16-May-2022, SARS-CoV-2 test: positive (Positive) Positive. The patient previously received a COVID-19 Vaccine. The patient had past drug history (unknown drug) due to which patient experienced reaction Allergy. Patient developed recurrence of nasal congestion, rhinorrhea, cough, and headache on 16-May-2022. Very similar to the initial Covid- 19 symptoms. The patient did not experienced fever. Rapid Covid-19 antigen test was positive. Symptoms resolved after about one week on 22-May-2022. The patient received unknown drug of Pfizer from 07-May-2022 to 11-May-2022 for Treatment of COVID-19. The device date was reported as 27-May-2022. Company comment-This spontaneous case concerns a 72-year-old male patient with no relevant medical history reported, who experienced the unexpected non serious AESI of Covid 19 infection on an unknown date after receiving the 4th dose of mRNA-1273 vaccine in the covid 19 vaccination series. It was reported that the patient was treated with Pfizer drug starting on 7-May-2022 for covid 19 treatment for 5 days. Details of the onset date, lab results and symptoms of this initial Covid 19 infection and its outcome was not reported. Patient had recurrence of nasal congestion, cough, rhinorrhea and headache similar to initial Covid 19 infection five days after completion of Pfizer drug. Rapid Covid-19 antigen test was positive and symptoms resolved after 1 week. Patient has received a dose of TOZINAMERAN 190 days prior to mRNA-1273 vaccine (interchange of vaccine products). The current pandemic situation of COVID 19 may remain as confounder and elderly age remains a risk factor to the event Covid-19. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Event seriousness assessed per medical judgement.; Sender's Comments: This spontaneous case concerns a 72-year-old male patient with no relevant medical history reported, who experienced the unexpected non serious AESI of Covid 19 infection on an unknown date after receiving the 4th dose of mRNA-1273 vaccine in the covid 19 vaccination series. It was reported that the patient was treated with Pfizer drug starting on 7-May-2022 for covid 19 treatment for 5 days. Details of the onset date, lab results and symptoms of this initial Covid 19 infection and its outcome was not reported. Patient had recurrence of nasal congestion, cough, rhinorrhea and headache similar to initial Covid 19 infection five days after completion of Pfizer drug. Rapid Covid-19 antigen test was positive and symptoms resolved after 1 week. Patient has received a dose of TOZINAMERAN 190 days prior to mRNA-1273 vaccine (interchange of vaccine products). The current pandemic situation of COVID 19 may remain as confounder and elderly age remains a risk factor to the event Covid-19. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Event seriousness assessed per medical judgement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220516; Test Name: Rapid Covid-19 antigen test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Drug allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Inadvertently had the Moderna in the freezer and the freezer was not approved for over 30 days of storage; They used two vials from the freezer after 30 days to administer them to 4 patients; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They used two vials from the freezer after 30 days to administer them to 4 patients) and PRODUCT STORAGE ERROR (Inadvertently had the Moderna in the freezer and the freezer was not approved for over 30 days of storage) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. No Medical History information was reported. On 20-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They used two vials from the freezer after 30 days to administer them to 4 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Inadvertently had the Moderna in the freezer and the freezer was not approved for over 30 days of storage). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They used two vials from the freezer after 30 days to administer them to 4 patients) and PRODUCT STORAGE ERROR (Inadvertently had the Moderna in the freezer and the freezer was not approved for over 30 days of storage) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant drug was reported. No treatment drug was reported. Reporter stated that it was notified to them that their upright freezer (two separate doors for freezer and fridge) was not good to use after 30 days. They normally pull the vials out before the 30 days to thaw. Reporter further stated that they wanted to have a stand alone freezer because of an automatic defrost cycle on some two door freezer/fridge combinations. The vial was initially stored in the refrigerator on 17-May-2022 (1 vial) and 19-May-2022 (1 vial). The temperature had not gone out of range at all, no temperature excursion happened. The patient received booster dose. Reporter further stated that the patients had not contacted them about any problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 12.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 antibody test
Symptomtext
This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (Covid-19 prior to Pfizer (Z-PAK) treatment) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. Concurrent medical conditions included Sjogren's disease and Allergy. On 12-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced COVID-19 (Covid-19 prior to Pfizer (Z-PAK) treatment). The patient was treated with AZITHROMYCIN (Z-PAK) at an unspecified dose and frequency. At the time of the report, COVID-19 (Covid-19 prior to Pfizer (Z-PAK) treatment) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 18-May-2022, SARS-CoV-2 antibody test: positive (Positive) Positive. No concomitant medication was reported. Co-suspect product included Pfizer started from 7-May-2022 to 12-May-2022 for COVID-19 treatment. Patient had not taken any medications within 2 weeks of starting COVID-19 treatment. Treatment product included steroid inhaler. Device date was reported as 27-May-2022. Company Comment: This spontaneous case concerns a 67-year-old female with no relevant medical history reported, who experienced the unexpected non-serious AESI event of COVID-19 unspecified days after receiving the fourth dose of mRNA-1273 vaccine. It was reported that patient was treated with Pfizer (Z-PAK) from 7th May to 12th May 2022 and with steroid inhaler for Covid-19. 6 days after stopping treatment she had a resurgence of COVID symptoms and tested positive with rapid test. The current pandemic situation of COVID-19 may remain as confounder to the event Covid-19. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Sender's Comments: This spontaneous case concerns a 67-year-old female with no relevant medical history reported, who experienced the unexpected non-serious AESI event of COVID-19 unspecified days after receiving the fourth dose of mRNA-1273 vaccine. It was reported that patient was treated with Pfizer (Z-PAK) from 7th May to 12th May 2022 and with steroid inhaler for Covid-19. 6 days after stopping treatment she had a resurgence of COVID symptoms and tested positive with rapid test. The current pandemic situation of COVID-19 may remain as confounder to the event Covid-19. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220518; Test Name: COVID-19 Rapid test; Test Result: Positive; Result Unstructured Data: Positive.
- Aktuelle Erkrankungen
- Allergy; Sjogren's disease
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 11.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 20,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
Symptoms were gone on 5/25. Tested negative with an at home test on 5/26. Symptoms returned on 5/27 -diarrhea, sneezing, congestions. The symptoms are milder this time, no cough; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (Symptoms were gone on 5/25. Tested negative with an at home test on 5/26. Symptoms returned on 5/27 -diarrhea, sneezing, congestions. The symptoms are milder this time, no cough) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. Co-suspect product included non-company product NIRMATRELVIR, RITONAVIR (PAXLOVID) for COVID-19 treatment. Concurrent medical conditions included Asthma and Drug allergy. On 11-Apr-2022 at 12:00 PM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-May-2022, the patient started NIRMATRELVIR, RITONAVIR (PAXLOVID) (unknown route) at an unspecified dose. In May 2022, the patient experienced COVID-19 (Symptoms were gone on 5/25. Tested negative with an at home test on 5/26. Symptoms returned on 5/27 -diarrhea, sneezing, congestions. The symptoms are milder this time, no cough). At the time of the report, COVID-19 (Symptoms were gone on 5/25. Tested negative with an at home test on 5/26. Symptoms returned on 5/27 -diarrhea, sneezing, congestions. The symptoms are milder this time, no cough) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 26-May-2022, SARS-CoV-2 test: negative (Negative) Negative. No concomitant medication information was provided. It was reported as on 27-May-2022 the symptoms returned as diarrhea, sneezing and congestions. The symptoms were milder and no cough. It was also reported that no need to use inhaler. Patient was not taking any medications/products within 2 weeks of starting COVID-19 treatment Patient did not received any treatment. Company comment: This spontaneous case concerns a 64-year-old female patient, with no relevant medical history, who experienced the unexpected, non-serious AESI of COVID-19, approximately a month after the fourth dose of mRNA-1273 vaccine. No details of previous doses were provided. As per source document, symptoms were gone while she was under Paxlovid treatment and had a negative home test, but a day after she experienced milder symptoms of diarrhea, sneezing and congestion. Concomitant PAXLOVID remains as a confounder for the event. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 64-year-old female patient, with no relevant medical history, who experienced the unexpected, non-serious AESI of COVID-19, approximately a month after the fourth dose of mRNA-1273 vaccine. No details of previous doses were provided. As per source document, symptoms were gone while she was under Paxlovid treatment and had a negative home test, but a day after she experienced milder symptoms of diarrhea, sneezing and congestion. Concomitant PAXLOVID remains as a confounder for the event. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220526; Test Name: Tested negative with an at home test; Test Result: Negative ; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- Asthma; Drug allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 31.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
vial left in fridge and was not thrown out after 30 day beyond use date; Dose administered after 30-day use by date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day use by date) and PRODUCT STORAGE ERROR (vial left in fridge and was not thrown out after 30 day beyond use date) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 vaccination. No Medical History information was reported. On 03-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 03-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vial left in fridge and was not thrown out after 30 day beyond use date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day use by date) and PRODUCT STORAGE ERROR (vial left in fridge and was not thrown out after 30 day beyond use date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant drugs were not reported. Treatment medications were not provided. It was reported that the vial was initially stored in refrigerator on 22-Mar-2022. The vial did not undergo any temperature excursion. It was also reported that the vials were un-opened but administered to 7 patients 11 days after the beyond use date on different dates of 3 doses administered on 28-Apr-2022, 1 dose administered on 03-May-2022 and 3 doses were administered on 05-May-2022. This case was linked to MOD-2022-577179, MOD-2022-577174 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 27.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 20,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Confirmed Breakthrough 1st - 02/06/2021 Moderna 007M20A 2nd - 03/09/2021 Moderna 023M20A 3rd - 10/26/2021 Moderna 049C21A 4th -- 05/04/2022 Moderna 048L21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive Covid Test - 5/24/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 27.05.2022
- Impfdatum
- 30.03.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 32,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
COVID-19
SARS-CoV-2 test
Symptomtext
COVID-19; COVID-19 recurrent; This spontaneous case was reported by a physician and describes the occurrence of COVID-19 (COVID-19 recurrent) and COVID-19 (COVID-19) in a 63-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. Co-suspect product included non-company product NIRMATRELVIR, RITONAVIR (PAXLOVID) for COVID-19 treatment. Concurrent medical conditions included Overweight. Concomitant products included PRAVASTATIN for an unknown indication. On 30-Mar-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-May-2022, the patient started NIRMATRELVIR, RITONAVIR (PAXLOVID) (unknown route) at an unspecified dose. On 09-May-2022, the patient experienced COVID-19 (COVID-19). In May 2022, the patient experienced COVID-19 (COVID-19 recurrent). On 13-May-2022, COVID-19 (COVID-19) had resolved. At the time of the report, COVID-19 (COVID-19 recurrent) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 09-May-2022, SARS-CoV-2 test: positive (Positive) Very positive test. On 13-May-2022, SARS-CoV-2 test: negative (Negative) Negative. In May 2022, Body temperature: 101 (High) 101 F. On 21-May-2022, SARS-CoV-2 test: positive (Positive) Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient reported have started getting COVID symptoms Sun (08-May-2022), On 09-May-2022 patient tested very positive and started Paxlovid. Symptoms were fever to 101F, cough, body aches, sinus symptoms and sneezing. Patient stated that started feeling much better within 24-48 hours and was minimally symptomatic with negative rapid test on last day of Paxlovid, Friday,13-May-2022. Within 2-3 days after Paxlovid finished started to get symptoms of reinfection: no fever, but plus body aches, cough, severe sinus and cold symptoms. It felt like a new infection as it started with nasal and sinus burning like an early cold. Symptoms were significantly present with markedly positive rapid test on Sat, 21-May-2022, at the time of report. Company comment: This is a spontaneous case concerning a 63-years-old male patient with no relevant medical history, who experienced the unexpected non-serious adverse events of special interest, COVID-19 (COVID-19) and COVID-19(Covid-19 recurrent) which occurred 1 month 9 days after receiving the fourth dose of mRNA-1273 vaccine. The patient developed COVID symptoms on 09-May-2022 and tested very positive and started with Paxlovid treatment. Symptoms were fever to 101F, cough, body aches, sinus symptoms and sneezing, were better within 24-48 hours and was minimally symptomatic with negative rapid test on last day of Paxlovid, 13-May-2022. Within 2-3 days after completed Paxlovid started to get symptoms of body aches, cough, severe sinus cold symptoms without fever. Symptoms were significantly present with markedly positive rapid test on 21-May-2022, at the time of report. SARS-CoV-2 test was positive as on 09-May-2022 and 21-May-2022. Ongoing Covid 19 pandemia could be considered as confounder to the event. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Event seriousness assessed as per medical judgement.; Sender's Comments: This is a spontaneous case concerning a 63-years-old male patient with no relevant medical history, who experienced the unexpected non-serious adverse events of special interest, COVID-19 (COVID-19) and COVID-19(Covid-19 recurrent) which occurred 1 month 9 days after receiving the fourth dose of mRNA-1273 vaccine. The patient developed COVID symptoms on 09-May-2022 and tested very positive and started with Paxlovid treatment. Symptoms were fever to 101F, cough, body aches, sinus symptoms and sneezing, were better within 24-48 hours and was minimally symptomatic with negative rapid test on last day of Paxlovid, 13-May-2022. Within 2-3 days after completed Paxlovid started to get symptoms of body aches, cough, severe sinus cold symptoms without fever. Symptoms were significantly present with markedly positive rapid test on 21-May-2022, at the time of report. SARS-CoV-2 test was positive as on 09-May-2022 and 21-May-2022. Ongoing Covid 19 pandemia could be considered as confounder to the event. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Event seriousness assessed as per medical judgement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body temperature
- Hospital-Tage
- -
- Labordaten
- Test Date: 202205; Test Name: Body temperature; Result Unstructured Data: 101 F; Test Date: 20220509; Test Name: COVID-19 virus test; Test Result: Positive ; Result Unstructured Data: Very positive test; Test Date: 20220513; Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220521; Test Name: COVID-19 virus test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Overweight
- Vorgeschichte
- -
- Andere Medikamente
- PRAVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 14,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Interchange of vaccine products
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Confirmed Breakthrough - 4/15/2022 1st Dose - J&J - 6/15/2021 2nd Dose - Moderna - 4/1/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 4/15/2022 Positive COVID test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acoustic stimulation tests
Tinnitus
Symptomtext
Ringing in both ears. Its started after my 1st vaccination in April 2021, its grew louder after my 2nd vaccination in March 2021. I was referred to an audiologist by my Doctor. I was basically told that it might disappear as suddenly a it appeared and to keep updating my Doctor. I was able to ignore it for the most part although it became bothersome in the evening. There was no noticeable change after my 3rd vaccination in October 2021, however it got "louder" after the 4th in April 2022. I have advised my Doctor of this and we are discussing the possibility of a 2bd referral.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- On 4/23/2021 my hearing was tested
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Sleep Apnoea, Type 2 Diabetes, High Blood Pressure
- Andere Medikamente
- Victoza, Humulim 70/30, Enalapril, Amlodipine, Furosemide, Spironolactone, Diltiazem,Metformin, Protonix,Atorvastatin, Gabapentin, Melatonin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was initially stored in the refrigerator on 22March2022 and administration of vaccine on 10May2022; patient got a dose after the use by date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient got a dose after the use by date) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 22March2022 and administration of vaccine on 10May2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 048L21A) for COVID-19 vaccination. No Medical History information was reported. On 10-May-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 10-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient got a dose after the use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 22March2022 and administration of vaccine on 10May2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient got a dose after the use by date) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 22March2022 and administration of vaccine on 10May2022) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. Concomitant and Treatment medications was not provided by the reporter. The hcp wanted to know if the dose was considered as viable or do they need to re-dose. One doses vials administered after 30-day use By date. On 22-Mar-2022, the vial was initially stored in the refrigerator. On 10-May-2022, the vaccine was administered. The vial does not undergone any temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Vaccine was administered patient on 05/10/2022. As per manufacturer expiry date of vaccine was 07/08/2022 but beyond use date was 04/21/22. Contacted the patient and patient has no adverse reaction due to vaccine. There was no temperature excursion during storage of vaccine since vaccine was received at pharmacy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 15.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyskinesia
Symptomtext
Right hand index finger started involuntary jerking
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyskinesia
- Hospital-Tage
- -
- Labordaten
- None. It went away within the day
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High BP under control
- Andere Medikamente
- Amlodopine, nystatin, lisoprine
- Allergien
- Comparing, sulfa
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 30.03.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 39,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Increased bronchial secretion
Paranasal sinus hypersecretion
SARS-CoV-2 test positive
Symptomtext
On May 08, 2022, I tested positive for COVID, this has been very mild. The symptoms have been mucus in my sinus cavities and lungs. I have been using Afrin at night, over the counter mucus relief, and prescription cough medication as needed. No fever, my oxygen has stayed within normal range.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High Blood Pressure, High Cholesterol, Incontinence
- Andere Medikamente
- High blood pressure medication, Cholesterol medication, Flomax
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 19.04.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
I contracted covid on 5/4.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Allegra
- Allergien
- erythromycin, peanuts, nightshades
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 30.04.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nodule
Swelling
Symptomtext
Lump/swelling on right and left side of areas right above collar bone
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nodule
- Hospital-Tage
- -
- Labordaten
- None. Advised by physician to wait 4 weeks to see if swelling subsides. Sent physician email, no office visit.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Slow FE iron pills and allergy pills(Claritin 24 hr reditabs)
- Allergien
- Pollen & dust only
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Computerised tomogram
Echocardiogram
Immunisation reaction
Laboratory test
Memory impairment
Symptomtext
around 9:45 p.m., sudden onset of forgetfulness, could not remember getting COVID booster earlier in the day. called 911 tranported to Hospital, given many test to include: CT stroke alert panel, echo cardiogram, PHVC cardiology consult, lab Events occurred in peri-vaccination period for second mrna covid booster administration. Conclusion : a reactions to the 2nd moderna booster shot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Computerised tomogram
- Hospital-Tage
- 3,0
- Labordaten
- stated above
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- Eliquis 5MG 2x per day, Lisinopril 2.5 1x per day
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 19.02.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 65,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Fall
SARS-CoV-2 test positive
Symptomtext
04/25/22 presents to EC ED for "fall". PMHx of "schizophrenia"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 04/25/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 01.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Systemic: Lymph Node Swelling-Mild, Additional Details: pt husband reports that patient developed lump in neck and md told her most likely due to COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Clonus
Serotonin syndrome
Therapy change
Symptomtext
Serotonin syndrome, withdrawal of SSRI, addition of lower dose different SSRI, slow recovery
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Clonus
- Hospital-Tage
- -
- Labordaten
- Clonus evaluation
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- MDD, GAD, Environmental allergies
- Andere Medikamente
- Prozac, Buspirone, Ativan, Trazadone, Align Probiotic, Vitamins B, C, D, Fish Oil, Quercetin
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
Patient presented for their second dose of COVID vaccine. Patient did not have his card present at time of visit but stated that he was due for his second dose of Moderna vaccine. At time of vaccination, MA and provider did not check patient's vaccine history. Following vaccination it was identified that the patient had actually received Pfizer for their first vaccine dose 20 days prior. Patient received incorrect vaccine at the incorrect interval (1 day early)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Psoriasis
Skin exfoliation
Symptomtext
I had a breakout of psoriasis. So a big scaly of patches of skin. First time it was on the ankle then it spread to the upper legs, then upper arms, my chest, my sides and belly, all over my upper and lower back, and back of leg. My husband had a prescription for it since he and my daughter have it so I used some of his medicine, until I saw my own doctor and got my own prescription of probetisol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Psoriasis
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoarthritis; Prediabetes; Sensitive Skin
- Andere Medikamente
- Synthroid; Nadolol; Doxycycline; Amlodipine; Lisinopril; Cyclobenzaprine Omeprazole; Metformin; Naproxen; Fish Oil; Glucosamine; Biotin
- Allergien
- Sensitivity to a Crestor
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Laryngitis
Symptomtext
Laryngitis; coughing like there is something is in his thorat; This spontaneous case was reported by a consumer and describes the occurrence of LARYNGITIS (Laryngitis) and COUGH (coughing like there is something is in his thorat) in an 80-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Flu vaccine (Yearly intramuscular Flu vaccine) in 2021. Past adverse reactions to the above products included No adverse event with Flu vaccine. Concurrent medical conditions included Blood pressure high (No Recent change in status such as improvement or worsening.), Penicillin allergy and Drug allergy. On 04-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 05-Apr-2022, the patient experienced LARYNGITIS (Laryngitis) and COUGH (coughing like there is something is in his thorat). At the time of the report, LARYNGITIS (Laryngitis) and COUGH (coughing like there is something is in his thorat) had not resolved. Relevant concomitant medications reported high Blood pressure medication of unknown brand. Patient did not had COVID positive test or diagnosis. No treatment information was provided. This case was linked to MOD-2022-547050, MOD-2022-547043, MOD-2022-547048 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood pressure high (No Recent change in status such as improvement or worsening.); Drug allergy; Penicillin allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 25.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 10.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Atrial fibrillation
Body temperature increased
Symptomtext
ATRIAL FIB, INCREASED TEMP LASTED 4 TO 6 DAYS THEN WENT AWAY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- NOT KNOWN PT IS A MEDICAL DR.
- Aktuelle Erkrankungen
- NOT KNOWN
- Vorgeschichte
- NOT KNOWN
- Andere Medikamente
- NOT KNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 22.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
patient received second booster too early. first booster on 1/14/22 so second booster should have been on or after 5/14/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
Resident received her first booster vaccine of COVID-19 Moderna on 2-3-2022. She was administered a second booster vaccine of COVID-19 Moderna on 4-19-2022. This second booster dose was administered less than 4 months after the first booster dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None. Monitoring in place. No adverse effects noted.
- Aktuelle Erkrankungen
- Resident is on palliative and supportive care. No illnesses noted one month prior.
- Vorgeschichte
- POLYNEUROPATHY, UNSPECIFIED Acute Neurologic UNSPECIFIED DEMENTIA WITHOUT BEHAVIORAL DISTURBANCE COVID-19 Pulmonary MAJOR DEPRESSIVE DISORDER, RECURRENT, MODERATE INSOMNIA OSTEOPOROSIS WITHOUT CURRENT PATHOLOGICAL FRACTURE ABNORMAL WEIGHT LOSS ENCEPHALOPATHY, UNSPECIFIED Acute Neurologic RETENTION OF URINE, UNSPECIFIED UNSPECIFIED HEARING LOSS, UNSPECIFIED EAR HYPERLIPIDEMIA, UNSPECIFIED OBSTRUCTIVE SLEEP APNEA ESSENTIAL (PRIMARY) HYPERTENSION CALCULUS OF GALLBLADDER AND BILE DUCT WITH ACUTE CHOLECYSTITIS WITHOUT OBSTRUCTION UMBILICAL HERNIA WITHOUT OBSTRUCTION OR GANGRENE NGASTRO-ESOPHAGEAL REFLUX DISEASE WITHOUT ESOPHAGITIS MAJOR DEPRESSIVE DISORDER, RECURRENT, UNSPECIFIED VITAMIN D DEFICIENCY, UNSPECIFIED CONTRACTURE, OTHER SPECIFIED JOINT Non-Surgical Orthopedic/Musculoskeletal ENCOUNTER FOR PALLIATIVE CARE FUNCTIONAL QUADRIPLEGIA VENOUS INSUFFICIENCY (CHRONIC) (PERIPHERAL) PERIPHERAL VASCULAR DISEASE, UNSPECIFIED Cardiovascular and Coagulations
- Andere Medikamente
- Melatonin Tablet 1 MG Give 1 tablet by mouth at bedtime for Insomnia Gabapentin Capsule 100 MG Give 1 capsule by mouth three times a day for Pain Losartan Potassium Tablet 25 MG Give 1 tablet by mouth one time a day for HTN Memantine HCl Ta
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 28.03.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 17,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
The patient should have been given 0.5 mL of the vaccine solution for a "full dose" but instead was only given 0.25 mL or a "half dose". She contacted our office on 4/14/22 when she became aware of the dose mix-up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraine headaches
- Andere Medikamente
- Sumatriptan 50mg tablet
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Menstruation irregular
Symptomtext
This was my first booster. My original vaccine was administered 3/10/21 and was a Jannsen vaccine. My side effect from the booster was a fully cycle of my period after just finishing a complete cycle 15 days before this. I started to spot on 4/9 and on 4/10 I had a full period 13 days early,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstruation irregular
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Lupus Myelitis, Asthma, Acid Reflux, Depression
- Andere Medikamente
- Hydroxychloroquine, Montelukast, Citalopram
- Allergien
- Tree nuts
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
no adverse effect.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 15.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
no adverse effect.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 15.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
A few days after receiving the Second Moderna booster on 4/1/22 I have experienced nonstop ringing in my ears. 24/7 high pitched ringing, continuous.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
Patient received Moderna full dose instead of Moderna booster dose. Patient was immediately notified of the dosing error. Patient reported no reaction immediately following the vaccine administration. No adverse reactions observed or reported, patient waited 15-20 minutes after injection before leaving clinic site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Extra dose administered
Occipital neuralgia
Symptomtext
1. 4 days after this Moderna dose, onset of L occipital neuralgia, which continues. 2. An approximate 15 min episode of atrial fibrillation, identified with Kardia mobile app
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Rheumatoid Arthritis Normal tension glaucoma
- Andere Medikamente
- Methotrexate 15 mg/ week Metoprolol succionate ER 50 mg BID Plaquenil 200 mg daily Folic Acid 1 mg daily Simvastatin 19 mg daily One A Day Wonens 50+ multivitamin Citar Citracal + D3 one caplet daily Alphagan P Ophthalmic bid Dorzolamide O
- Allergien
- Nadolol Pentazocine-Acetaminophen Clindamycin Latanoprost Aspirin Naproxen
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Phlebitis
Symptomtext
Patient has confirmed phlebitis from moderna vaccine. Followed up with MD but otherwise ok. no hospitalization.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Phlebitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation reaction
Symptomtext
pt got covid arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunisation reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Given 0.5mL of Moderna as booster dose after receiving Johnson & Johnson initial dose in 2021. Should have received 0.25mL of Moderna. Attempted to notify patient via phone and mail.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Abnormal Pap, Adnexal pain
- Vorgeschichte
- Asthma, GERD, Anxiety, Depression, Back Pain
- Andere Medikamente
- ProAir HFA Zoloft Ibuprofen
- Allergien
- Morphine, Darvocet, Codeine, Aspirin, Vicodin, Keflex, Iodine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
received a full "3rd" dose which is the second that been administered to patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- History of Breast Cancer, with radiation treatment
- Vorgeschichte
- Cancer
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 09.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Speech disorder
Symptomtext
Patient received 2nd Booster of Moderna. After several minutes, pt's wife and himself approach pharmacy counter and states that the pt is unable to speak. FAST technique was done on pt. Pt was completed all tasks other than speech (which resolved completely after several minutes). Informed pt's wife to call MD ASAP and inform of the possible TIA and to inform us of outcome. MD diagnosis confirmed possible TIA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Speech disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 09.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injury associated with device
Symptomtext
Error: Patient Accidentally Stuck by Needle-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injury associated with device
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 09.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
administration error. Patient was given 0.25 ml rather than 0.5 ml as a first dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 78,0
- 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: ja
Interchange of vaccine products
Symptomtext
Patient had gotten pfizer for all 3 shots so far and accidently got moderna for their 4th booster. Got 0.25mL of Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was refrigerated more than 12 hours after 1st puntured/ kept less than 10 minutes in room temperature while drawing; Expired moderna vaccine dose administered to patient/Dose administered greater than 12 hours post puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine dose administered to patient/Dose administered greater than 12 hours post puncture) and PRODUCT STORAGE ERROR (The vial was refrigerated more than 12 hours after 1st puntured/ kept less than 10 minutes in room temperature while drawing) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Apr-2022 at 9:00 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Apr-2022 at 9:00 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine dose administered to patient/Dose administered greater than 12 hours post puncture). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was refrigerated more than 12 hours after 1st puntured/ kept less than 10 minutes in room temperature while drawing). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine dose administered to patient/Dose administered greater than 12 hours post puncture) and PRODUCT STORAGE ERROR (The vial was refrigerated more than 12 hours after 1st puntured/ kept less than 10 minutes in room temperature while drawing) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. The vial was initially stored in the refrigerator on 22-Mar-2022 Date and time the vial was first punctured on 04-Apr-2022 at 09.00 am PST There was no temperature excursion. No treatment medication were provided. This case was linked to MOD-2022-533520 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Dose administered greater than 12 hours post puncture; Dose administered greater than 12 hours post puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered greater than 12 hours post puncture) and PRODUCT STORAGE ERROR (Dose administered greater than 12 hours post puncture) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Apr-2022 at 9:00 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Apr-2022 at 9:00 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered greater than 12 hours post puncture). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Dose administered greater than 12 hours post puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered greater than 12 hours post puncture) and PRODUCT STORAGE ERROR (Dose administered greater than 12 hours post puncture) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Patient took the second booster dose. The vial was initially stored in the refrigerator on 22 Mar 2022. The vial was first punctured on 04 Apr 2022 at 9 am. The vial was stored in fridge post puncture. The vial did not undergo any temperature excursions. Total amount of time the vial was exposed to room temperature range was less than 10 total minutes while drawing but otherwise the vial was in the fridge. The vial exposed to room temperature for greater than 24 hours. No treatment medications were reported. This case was linked to MOD-2022-533442 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
CLIENT IS IMMUNOCOMPROMISED AND WAS RECEIVING A 1ST BOOSTER DOSE OF MODERNA (4TH VACCINATION). CLIENT WAS GIVEN A FULL MODERNA DOSE (0.5ML) INSTEAD OF A BOOSTER DOSE (0.25ML).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
pt given vaccine that had expired 12 hours prior, vaccine was refrigerated, no temperature excursions, manufacturer contacted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
pt was given a vaccine from a vial that had expired 12 hours prior. Vial had been refrigerated the entire time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 04.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
patient was inadvertently administered 0.5ml instead of 0.25ml dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Flushing
Hyperhidrosis
Symptomtext
Systemic: Flushed / Sweating-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Flushing
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 03.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
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
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Patient was given 0.5ml dose of Moderna for booster instead of 0.25ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
A 16-year-old patient should not have received Moderna vaccine per the EUA. Patient advised to receive an age-appropriate Pfizer dose in 28 days to complete her primary series per COVID-19 administration errors and deviations guidelines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
How was the vial stored post puncture? RT/fridge? RT the whole time.; Booster dose administered 27 hours and 8 minutes post puncture; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Booster dose administered 27 hours and 8 minutes post puncture) and PRODUCT STORAGE ERROR (How was the vial stored post puncture? RT/fridge? RT the whole time.) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Mar-2022 at 2:16 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Mar-2022 at 2:16 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Booster dose administered 27 hours and 8 minutes post puncture). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (How was the vial stored post puncture? RT/fridge? RT the whole time.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Booster dose administered 27 hours and 8 minutes post puncture) and PRODUCT STORAGE ERROR (How was the vial stored post puncture? RT/fridge? RT the whole time.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. Number of doses/vials: 1 booster dose. On 28-Mar-2022 at 11:24 AM, the vial was initially stored in the refrigerator The vial was first punctured minutes after taking it out of the refrigerator. The vial was stored at room temperature (RT) (8? to 25?C= 46? to 77?F) the whole time post puncture. Dose was administered >12hours post puncture. The vial did not undergo any temperature excursions. No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 30.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysgeusia
Symptomtext
A day or 2 after the first dose EVERYTHING I started eating/drinking had a metallic taste to it. I can taste things still but the metallic taste overtakes most flavors/scents. It has lasted over a month and I assumed maybe I had bad batches of the food in my house. I have since replaced the food in my house and the metallic taste is there no matter what I eat or drink and has not dulled yet which is concerning to me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysgeusia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 24.03.2022
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
Patient received second booster dose of Moderna COVID19 vaccine. Patient did not present with any symptoms or adverse events post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Type 2 diabetes, hypertension, sleep apnea
- Vorgeschichte
- Type 2 diabetes, hypertension, sleep apnea
- Andere Medikamente
- Metformin ER 500mg, Wegovy 0.25mg/ml, Esomeprazole 40mg, Losartan 50mg tabs, topiramate 25mg, finasteride 1mg
- Allergien
- No known allergy
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 19.03.2022
- Impfdatum
- 19.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
MODERNA COVID SHOT GIVEN TO 17 YEAR OLD PATIENT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 12.03.2022
- Beginn
- 12.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient given a dose of Moderna from yesterday's vial that had been at room temp for 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 12.03.2022
- Beginn
- 12.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
shot was given with moderna that had been at room temp for 24 hours. pt had similar side effects as those receiving a shot not over exp. time
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 13.03.2022
- Beginn
- 13.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine was administered more than 12 hours post puncture
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NONE
- Andere Medikamente
- NA
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 13.03.2022
- Beginn
- 13.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Vaccine was administered more than 12 hours post puncture. THERE WAS NO ADVERSE EVENT
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
- CA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 13.03.2022
- Beginn
- 13.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
Vaccine administered more than 12 hours post puncture. NO ADVERSE EVENTS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 13.03.2022
- Beginn
- 13.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
dose given >12 hour post-puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (dose given >12 hour post-puncture) in a 21-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 13-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (dose given >12 hour post-puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (dose given >12 hour post-puncture) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Date and time vial was first punctured: 12Mar2022 at 10:18 AM The vial was stored post puncture at room temperature. No concomitant and treatment medication were reported. The vial did not undergo any temperature excursions. The vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) for 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired dose administered (booster); This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered (booster)) in a 47-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048L21A) for COVID-19 vaccination. Previously administered products included for COVID-19 vaccination: J&J (First dose) on 12-Mar-2021. Past adverse reactions to the above products included No adverse event with J&J. On 08-Mar-2022 at 9:45 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 08-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered (booster)). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered (booster)) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided by the reporter. No treatment details were provided. Patient height was reported as 5'6". It was reported that the dose was administered more than 12(US) hours post puncture. The vial was initially stored in the refrigerator on 07-Mar-2022 and vial was first punctured 07-Mar-2022 at 2:30 PM. Vaccine did not undergo any temperature excursions the vial was exposed to room temperature range (8 degree Celsius to 25 degree Celsius equal to 46 degree to 77 degree Fahrenheit) under 5 minutes per HCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -