- Staat
- MN
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 05.06.2023
- Impfdatum
- 19.05.2022
- Beginn
- 12.03.2023
- Tage bis Beginn
- 297,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
Dyspnoea
Exposure to SARS-CoV-2
Oxygen saturation increased
Positive airway pressure therapy
Productive cough
Respiratory failure
SARS-CoV-2 test positive
Symptomtext
Patient with history of ESRD on nightly peritoneal dialysis and diabetes. He was brought to the ED by EMS on 3/12/23 with shortness of breath and productive cough that has been present for the past three days. Notably, he lives with someone who was recently ill with COVID. When EMS arrived, the patient's O2 saturations were 30% on room air and increased to 80% after being placed on a non-rebreather mask. A COVID PCR test done in the ED also resulted positive. Ultimately, the patient was admitted 3/12/23 - 3/16/23 with discharge diagnoses including acute respiratory with hypoxia and COVID-19. Notably, the patient was on Decadron in the hospital. During admission, eh required BiPAP, but was weaned off oxygen by discharge. Of note, the patient has received the primary COVID vaccine series and one booster dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 22.03.2023
- Impfdatum
- 11.11.2022
- Beginn
- 19.03.2023
- Tage bis Beginn
- 128,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Patient expired 3/19/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Amniotic band syndrome with right lung and arm agenesis, restrictive lung disease, chronic hypoxic respiratory failure, scoliosis, Jarcho Levine syndrome, neurogenic bladder, neurogenic bowel
- Andere Medikamente
- Unknown
- Allergien
- Erythromycin, sulfa antibiotics, gentamicin, nitrofurantoin trimethoprim, vancomycin, latex, morphine, fosfomycin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 10.02.2023
- Impfdatum
- 03.05.2022
- Beginn
- 06.02.2023
- Tage bis Beginn
- 279,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
SARS-CoV-2 test positive
Symptomtext
Death on 02/06/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Positive COVID-19 test on 01/02/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COVID-19, HTN, HLD, Mass of pancreas
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 07.02.2023
- Impfdatum
- 17.10.2022
- Beginn
- 27.11.2022
- Tage bis Beginn
- 41,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Asthenia
COVID-19
Cough
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Patient history of dementia. Patient seen in the ED on 11/27/22 with weakness. Patient tested positive for COVID-19 on 11/25 at his living facility after developing a cough and chest congestion. The morning of 11/27, patient's wife found the patient on the floor and was concerned about his weakness. Repeat COVID PCR test in the ED on 11/27 also positive. Ultimately, patient admitted 11/27/22 for acute hypoxic respiratory failure due to COVID-19 infection. He did require supplemental O2 during his admission, however, was able to be weaned off and tolerating room air by discharge. Patient discharged 12/3/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 11.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Aphasia
Balance disorder
Cerebrovascular accident
Dizziness
Magnetic resonance imaging head abnormal
Nausea
Neurological symptom
Vertigo
Symptomtext
Woke in AM feeling very dizzy, with serious balance issues; motion in peripheral vision; slight nausea. Cautioned by primary care physician in June to get immediate care if experiencing stroke symptoms (acute stroke diagnosed on June 17, 2022 MRI - recent within 2 - 3 weeks prior to MRI - however, experienced no common symptoms of stroke) (Moderna Booster vaccine on 4/15/22). Went to Urgent Care, Dr. examined and determined symptoms to be consistent with vertigo. No additional MRI was ordered, however, later visit w/neurologist has ordered an MRI to rule out 2nd stroke. Still waiting for appointment for MRI. Symptoms of vertigo slowly disappeared within approximately 2 weeks. June 17, 2022 MRI discovered evidence of Acute Stroke, Left. Small acute/subacute left cortical infarct parietal gray matter. MRI was ordered on June 9, 2022 by primary care physician at annual physical due to complaints of some problem with word retrieval. No other symptoms were experienced. Was advised the stroke was recent, within 2 - 3 weeks prior to MRI. (Moderna booster administered prior to stroke on 4/15/22)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- Waiting for appointment for MRI
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension - managed w/medication
- Andere Medikamente
- Metoprolol 25 mg;Amlodipine-Valsarstan 5-160;Atorvastatin 10mg; Clopidogrel 75 mg; fluticasone 50 mcg; Dietary Supplements: Calcium +D 650 MG; tart cherry (Clopidogrel and Atorvastatin prescribed when MRI determined stroke in June 2022)
- Allergien
- Penicillin; Toletin; Advised to avoid NSAIDs
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 97,0
- Geschlecht
- F
- Eingang
- 09.01.2023
- Impfdatum
- 03.05.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 237,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
SARS-CoV-2 test positive
Symptomtext
Death on 12/26/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Positive Covid-19 results on 12/28/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Suspected MI; OSC: COVID-19; CKD Stage 3; DM2; HTN; HLD; obesity
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 08.12.2022
- Impfdatum
- 09.05.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 210,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Acute myocardial infarction
Alanine aminotransferase normal
Albumin globulin ratio decreased
Anion gap
Anticoagulant therapy
Antiplatelet therapy
Aspartate aminotransferase normal
Atrial fibrillation
Blood albumin decreased
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium normal
Blood chloride normal
Blood creatinine normal
Blood glucose normal
Blood potassium normal
Blood sodium normal
Blood urea increased
Symptomtext
COVID+ 12/5/2022. Vaccination status - moderna x3 BRIEF OVERVIEW: Discharge Provider: Primary Care Provider: Admission Date: 12/5/2022 Discharge Date: 12/7/2022 Active Hospital Problems Diagnosis Date Noted POA ? COVID-19 virus infection 12/05/2022 Yes ? Acute on chronic diastolic congestive heart failure (HCC) 12/16/2020 Yes ? CAD (coronary artery disease) 10/13/2022 Yes ? Paroxysmal atrial fibrillation (HCC) 05/13/2022 Yes ? Type 2 diabetes mellitus with diabetic polyneuropathy, without long-term current use of insulin (HCC) 11/15/2019 Yes ? COPD (chronic obstructive pulmonary disease) (HCC) 04/06/2015 Yes ? B12 deficiency 12/05/2022 Yes ? Hypothyroidism 12/16/2020 Yes ? Acute on chronic diastolic heart failure (HCC) DETAILS OF HOSPITAL STAY: Clinical Narrative: The patient was admitted with COVID-19 lower respiratory tract infection/pneumonia. As result she also suffered from a heart failure exacerbation which required diuresis. She was also wheezing given her tobacco history was felt to have an exacerbation of chronic obstructive pulmonary disease. She was treated for chronic obstructive pulmonary disease exacerbation and COVID-19 pneumonia with corticosteroids, per protocol. She received remdesivir given her hypoxia on presentation. She received gentle continue diuresis at suspect to her heart failure. She did respond serially with these interventions. She will be discharged home today and is in a stable & improved condition. Please see the following problem-list oriented Hospital Course below: COVID-19 virus infection Assessment & Plan Unclear contribution to current respiratory issue. However, will check inflammatory markers, give vitamins, start Remdesivir, give Solumedrol 40mg TID. Treat for CAP as well with Rocephin/azithromycin. Low threshhold to de-escalate antiviral/antimicrobial tx if makes continued improvement on diuresis. 12/5 - chest x-ray appearance consistent with alveolar infiltrates from viral pneumonia. Remains on remdesivir. Also being treated for a kidney acquired pneumonia. She does, however, report improvement with the diuretic and repeat chest x-ray will be obtained in the a.m. Likely beneficial to stay somewhat on the dry side. 12/6 - improving. Chronic obstructive pulmonary disease exacerbation improving as well. Possibly home as early as tomorrow afternoon. 12/7 - treated for COVID-19 pneumonia given the degree of hypoxia on admission. Pulmonary infiltrates. Three days of remdesivir. Improvement. IV Decadron daily. The patient does not want to complete a full 5 days of therapy and the literature supports stopping it after Day 3 for people that improve sufficiently/considerably. This will be respected. The patient will be discharged home today with continued corticosteroid dosing and concurrent therapy for possible bacterial superinfection. * Acute on chronic diastolic congestive heart failure (HCC) Assessment & Plan Echo in Oct 2022 with EF 52%. Pulmonary congestion on CXR. Diurese with Lasix 40mg BID x3 doses; monitor response. Continue Toprol, Spironolactone, lisinopril. 12.5 - Lasix dosing decreased. Replace potassium. Recheck chest x-ray in a.m. 12/7 - doing well. Responded to the Lasix dosing. Acute on chronic diastolic congestive heart failure. Exacerbation of. Exacerbated by COVID-19 lower respiratory tract infection/pneumonia. Improved. CAD (coronary artery disease) Assessment & Plan NSTEMI in Oct 2022 with LHC showing severe 2V disease, unable to stent. Already infarcted. Continue Plavix. EF at that time 54%. 12/7 - continue with antiplatelet therapy, statin, and secondary prevention. Paroxysmal atrial fibrillation (HCC) Assessment & Plan Controlled. Continued Eliquis, Toprol Type 2 diabetes mellitus with diabetic polyneuropathy, without long-term current use of insulin (HCC) Assessment & Plan Recent A1c was 6.9, not on any hypoglycemics. Monitored. Stable. COPD (chronic obstructive pulmonary disease) (HCC) Assessment & Plan This is in hx, but not on chronic inhalers. Give sch duonebs, Symbicort, mucinex. 12/5 - continue nebs and present treatment. 12/7 - chronic obstructive pulmonary disease exacerbation secondary to COVID-19 will restrict tract infection/pneumonia. Improved nebulized therapies and concurrent corticosteroids. Tobacco cessation discussed. B12 deficiency Assessment & Plan Replete. Continue at home. Follow CBC outpatient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 2,0
- Labordaten
- Lab Results Component Value Date WBC 10.41 12/06/2022 RBC 4.43 12/06/2022 HGB 11.9 (L) 12/06/2022 HCT 37.3 12/06/2022 MCV 84.2 12/06/2022 PLATELET 218 12/06/2022 NEUTABSOLU 8.94 (H) 12/06/2022 Lab Results Component Value Date GLUCOSE 179 (H) 12/06/2022 SODIUM 140 12/06/2022 POTASSIUM 3.9 12/06/2022 CHLORIDE 102 12/06/2022 ANIONGAP 12 12/06/2022 BUN 26 (H) 12/06/2022 CREATININE 0.71 12/06/2022 CALCIUM 9.2 12/06/2022 TOTALPROTE 7.3 12/06/2022 ALBUMIN 3.3 (L) 12/06/2022 GLOBULIN 3.7 07/15/2014 AGRATIO 1.0 07/15/2014 ALKALINEPH 86 12/06/2022 AST 17 12/11/2020 ASTP5P 17 12/06/2022 ALT 14 12/11/2020 ALTP5P 13 12/06/2022 BILIRUBINT 0.9 12/06/2022 EGFR 89 12/06/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diagnosis Date ? Allergic ? Asthma ? Backache ? Bladder tumor 10/2019 ? Brain aneurysm 11/8/2006 ? Cancer (HCC) Bladder Ca - resection 11/2019 ? Cataract ? Cellulitis of leg, left 10/10/2017 resolved with Keflex therapy ? CHF (congestive heart failure) (HCC) ? COPD (chronic obstructive pulmonary disease) ? Delayed emergence from general anesthesia ? Diabetes mellitus (HCC) ? Disorder of eye, unspecified 4/1/15 MRSA conjunctivitis ? Fall 07/23/2019 ? Glaucoma ? Heart trouble ? History of chicken pox ? Hyperlipidemia ? Hypertension ? Kidney failure ? Neuropathy of lower extremity, unspecified laterality ? Obesity ? Osteoarthritis pain located knees ? Osteoporosis ? Rheumatoid arthritis(714.0) joints involved hips & knees ? Shingles on her back for 3 months ? SOBOE (shortness of breath on exertion) ? Stroke (HCC) 2006 - had stroke at time of brain surgery - lasted about 16 hours - no residual
- Andere Medikamente
- Albuterol Sulfate 108 (90 Base) MCG/ACT 2 puffs Inhalation 4 times daily PRN Amitriptyline HCl 25 MG TAKE 1 TABLET BY MOUTH EVERY NIGHT Atorvastatin Calcium 20 mg Oral Daily, for cholesterol Citalopram Hydrobromide 20 mg Oral Daily Cyanocob
- Allergien
- Cozaar [Angiotensin Receptor Blockers]Hives, Shortness of Breath Macrobid [Nitrofurantoin]Anaphylaxis PenicillinsHives, Shortness of Breath, Swelling Shellfish AllergyAnaphylaxis TetracyclineHives, Shortness of Breath Cardura [Doxazosin]Hives, Rash Flu Virus VaccineHives Sular [Calcium Channel Blockers]Hives, Swelling Sulfa DrugsHives, Swelling Shellfish
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 18.11.2022
- Impfdatum
- 17.05.2022
- Beginn
- 30.10.2022
- Tage bis Beginn
- 166,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute kidney injury
Acute left ventricular failure
Acute respiratory failure
Aortic arteriosclerosis
Asthenia
Chronic obstructive pulmonary disease
Computerised tomogram thorax abnormal
Condition aggravated
Death
Dyspnoea at rest
COVID-19 pneumonia
Cardiac failure congestive
Cardiac valve disease
Cardiomegaly
Chest X-ray abnormal
Dyspnoea exertional
Emphysema
Essential hypertension
Symptomtext
Admitted 10/30/2022 with chief complaint SOB. Onset of symptoms was gradual starting several days ago with been gradually worsening course since that time. Reports SOB at rest and exertion, associated productive cough, weakness. Active Problems: Essential hypertension, benign Centrilobular emphysema (CMS/HCC) Diastolic CHF (CMS/HCC) COPD, moderate (CMS/HCC) Adenocarcinoma of left lung (CMS/HCC) Other hyperlipidemia Acute hypoxic respiratory failure, Acute on chronic diastolic heart failure, COVID-19 infection pneumonia, Acute systolic heart failure, Hypoxia is multifactorial, DDX, radiation pneumonitis, HF, COVID or a combination of these. Pulmonology consulted. Patient clearly expressed that he does not want to be intubated. Inpatient hospice. Continue Lasix 40 mg IV b.i.d. and spironolactone. Continue atorvastatin, Coreg. Continue PPI Dexamethasone 6 mg iv daily 11/6/2022: Cause of death: Acute hypoxemic respiratory failure due to COVID-19 infection and acute combined congestive heart failure. Confounding factors include left lung adenocarcinoma, valvular heart disease and acute kidney injury.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 7,0
- Labordaten
- 10/30/2022: RAPID SARS-COV-2 BY PCR Detected CXR 10/30/2022 Stable right MediPort. Median sternotomy changes. The heart is borderline enlarged and stable in size. Tortuous thoracic aorta with diffuse atheromatous calcifications. Pulmonary vessels are normally distributed. Moderate size right pleural effusion with superimposed hazy airspace opacities. Dense consolidation in the left upper lung, which was also present on prior CT chest of the chest and may reflect posttreatment changes. No pneumothorax
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Past Medical History: ? Acquired phimosis 5/5/2016 ? Acute, but ill-defined, cerebrovascular disease ? Anemia ? erosive gastritis on egd ? Aortic valve disorders 2006aortic stenosis-mild ? Benign neoplasm of colon Colon Polyp ? Benign neoplasm of rectum and anal canal ? Carotid artery disease ? Cerebral infarction (CMS/HCC) 2006No residual weakness ? DM (diabetes mellitus) ? Duodenitis 5/23/16 ? Embolism and thrombosis of arteries of lower extremity 12/15/2016 ? Essential hypertension, benign 1983 ? Gastritis 5/23/16 ? Gastroesophageal reflux disease ? Malignant neoplasm of prostate (CMS/HCC) 12/12/03PSA of 5.31 on 6/11/06 ? Monoclonal paraproteinemia released by dr--follow lab ? Osteoarthritis ? hyperlipidemia ? Personal history of colonic polyps 3/21/12 ? Polyneuropathy in other diseases classified elsewhere ? Postoperative urethral stricture 3/11/04 ? PVD (peripheral vascular disease) (CMS/HCC) 12/2016 ? S/P tricuspid valve replacement ? Scrotal edema ? Sinusitis, chronic ? Spinal stenosis, lumbar region, without neurogenic claudication lumbar ? Tricuspid valve stenosis
- Andere Medikamente
- unknown
- Allergien
- ?Amoxicillin -Throat swelling- either from prophylactic amox or from numbing solution the dentist used ?Penicillins ANAPHYLAXIS Throat swelled shut ?Quinolones PRURITUS itching palms ?Sulfamethoxazole-Trimetho prim GI UPSET, DIZZINESS, CONSTIPATION, Anorexia and Other
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 01.06.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 82,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Pt died in hospital on 8/22/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Coronary artery disease-severe, multivessel, post CABG on 3/15 Resp failure - trach 3/25 - vent Pseudomonas pneumonia with septic shock - VV ECMO stopped on 3/29 Pre-op acute hypoxic respiratory failure secondary to COPD exacerbation from chronic bronchitis - Required intubation 3/3, Extubated 3/7 (before heart surgery) Acute renal failure - prior CVVHD, now on intermittent dialysis Probable OSA Newly diagnosed systolic CHF, EF 40-45% Type 2 diabetes Hyperlipidemia BPH VRE bacteremia 3/27 Ischemic extremities -post left aka, left below the elbow amputation, right transmetatarsal and right transmetacarpal amputations COVID exposure (wife), unvaccinated status. He tested negative on 04/22 and 4/29. Afib / flutter 4/29 Hypothermia, lethargy 5/5-possible new sepsis -Recent sputum culture grew carbapenem resistant Pseudomonas, sensitive to Levaquin and gentamicin -sternal wound infection became apparent on 05/06 , growing sensitive Pseudomonas
- Vorgeschichte
- COPD Type 2 diabetes Hypertension Hyperlipidemia BPH Alcoholism
- Andere Medikamente
- Xanax Aspirin Pulmicort Citrate Cardizem Lexapro Lasix NPH insulin Proamatine Protonix Deltasone Renvela NACHL
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 19.05.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 85,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
I discussed options with her and her husband 8/12. RTAC for CRRT offered, not likely to change outcome, she and her husband were very clear that they desire transition to comfort care. This occurred and she died shortly thereafter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Delirium. Anxiety. Depression Acute hypoxemic resp failure, multifactorial, s/p trach 2/17 - COVID pneumonia, in recovery phase - recent aspiration pneumonia, ABX completed 2/25 - Volume overload - Chronic R pleural effusion, s/p R thoracentesis 2/11 - PFO - Weakness HTN hx Afib, SSS, PM in situ AKI/CKD4-5, requiring HD Hypophosphatemia PBC/AIH, s/p OLT 2011 Recent Veillonella parvula bacteremia, ABX completed 2/25 C.diff colitis Hypothyroidism Pancytopenia (HIT neg) Anemia of chronic disease and critical illness Severe protein calorie malnutrition Severely debilitated state after prolonged critical illness
- Vorgeschichte
- cirrhosis due to PBC/AIH, s/p OLT 2011, PFO, chronic R pleural effusion, HTN, Afib (on flecainide and apixaban), PM for SSS, CKD4-5, secondary hyperparathyroidism, hypothyroidism, anemia of chronic disease, depression, COVID vaccinated/boosted.
- Andere Medikamente
- midodrine potassium and sodium phos Amiodarone Citrate dextrose Cardizem Lomotil Lasix Gabapentin Guaifensin Atrax Synthroid Cytomel Mag oxide Remeron Protonix Rapamune Sodium Bicard sodium Chloride Tacrolimus Ursodiol
- Allergien
- Azathioprine, doxycycline, Mycophenolate, Oxycodone, Pramipexole, Prednisone, Rifampin, Sertraline, Sulfa
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 09.06.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 26,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Agonal respiration
Apnoea
Bradycardia
Cardio-respiratory arrest
Death
Endotracheal intubation
Life support
Pulse absent
Unresponsive to stimuli
Symptomtext
We discussed her inability to have a tracheostomy and overall goals of care/code status. She currently meets criteria for extubation this morning. She is agreeable to removing her breathing tube at this time. When asked if she'd like to have the breathing tube re-placed if she needed it, she clearly indicated that she does not want the tube or breathing machine. She has requested to be a DNI. At this time, she wishes to remain full code without intubation. A Code Blue was paged where Patient was found unresponsive, with agonal respirations and significant bradycardia upon arrival. She became pulseless. ACLS protocol was initiated per the patients wishes. She was bagged via mask but not intubated. After approx. 2 minutes of compressions we had ROSC. Her daughter at the bedside requested that when her heart stops again, we allow her to pass peacefully. Morphine 4 mg IVP was ordered for comfort. Shortly after, she became apenic and pulseless. She was pronounced deceased at 1230 pm on 7/5/22. Family was present at the bedside.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardio-respiratory arrest
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Salivary gland cancer Pharyngeal-cutaneous fistula remote h/o salivary gland tumor s/p resection/radiation Malnutrition Scleroderma Restrictive lung disease Aspiration pneumonia Acute hypercapnic respiratory failure Hyponatremia Recurrent aspiration pneumonitis Pleural effusion
- Vorgeschichte
- Hypertension GERD Degenerative disc disease Peripheral neuropathy Hypothyroid
- Andere Medikamente
- Xanax Lovenox Pepcid Robitussin Synthroid Prednisone Sodium Chloride Tab
- Allergien
- Bactrim Latex Sulfa antibiotics Tylenol
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 28.01.2021
- Beginn
- 09.06.2022
- Tage bis Beginn
- 497,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Cerebrovascular accident
Magnetic resonance imaging head abnormal
Paraesthesia
Symptomtext
mild stroke 40 days after second Moderna booster; He has tingling in his right hand and right foot.; This spontaneous case was reported by a patient and describes the occurrence of CEREBROVASCULAR ACCIDENT (mild stroke 40 days after second Moderna booster) in a 66-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Patient had never tested positive for COVID. Concurrent medical conditions included Seasonal allergy and Asthma. On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 28-Oct-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 20-Apr-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 09-Jun-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced CEREBROVASCULAR ACCIDENT (mild stroke 40 days after second Moderna booster) (seriousness criteria hospitalization and medically significant). In 2022, the patient experienced PARAESTHESIA (He has tingling in his right hand and right foot.). The patient was treated with ACETYLSALICYLIC ACID (ASPIRIN 81) for Stroke, at a dose of 81 milligram; CLOPIDOGREL BESYLATE (CLOPIDOGREL [CLOPIDOGREL BESYLATE]) for Stroke, at a dose of 75 milligram and ATORVASTATIN CALCIUM TRIHYDRATE (ATORVASTATIN [ATORVASTATIN CALCIUM TRIHYDRATE]) for Stroke, at a dose of 80 milligram. At the time of the report, CEREBROVASCULAR ACCIDENT (mild stroke 40 days after second Moderna booster) and PARAESTHESIA (He has tingling in his right hand and right foot.) was resolving. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Patient went to emergency room on 10-Jun-2022. Patient had not experienced a similar event in the past. Company comment: This spontaneous case concerns a 66 year old male patient, with no relevant medical history reported, who experienced the serious (hospitalization, medically significant), unexpected adverse event of special interest Cerebrovascular accident (mild stroke 40 days after second Moderna booster), which occurred 1 month, 20 days after the fourth dose of mRNA-1273 vaccine administration, which prompted the patient to go to the emergency room 1 day after. The outcome of the event was reported as resolving. The benefit -risk relationship of mRNA -1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 66 year old male patient, with no relevant medical history reported, who experienced the serious (hospitalization, medically significant), unexpected adverse event of special interest Cerebrovascular accident (mild stroke 40 days after second Moderna booster), which occurred 1 month, 20 days after the fourth dose of mRNA-1273 vaccine administration, which prompted the patient to go to the emergency room 1 day after. The outcome of the event was reported as resolving. The benefit -risk relationship of mRNA -1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma; Seasonal allergy
- Vorgeschichte
- Comments: Patient had never tested positive for COVID.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 19.05.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Aortic dissection
Death
Symptomtext
Daughter called to report that her mother passed away on 5/26/2022 and wanted to provide some information because she has gotten her Moderna booster 6 days prior to her passing. She is not use the death was related to the vaccine administration but wanted to report it anyway. She stated her mother received her first Moderna booster on 11/21/21 and on 11/24/21 she has a varicose vein rupture and she was seen in the ER and released. This vaccine is not listed in the system. Her daughter then reported she got her 2nd Moderna booster at the local County Health Department on 5/19/2022 and on 5/22/2022 had severe abdominal pain and was sent to the hospital and diagnosed with an aortic dissection and place on comfort care and she passed on 5/26/2022. Her daughter was reporting in case it could have been due to the Moderna vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 4,0
- Labordaten
- no information provided. Pt was admitted to local hospital on 5/22/22 and stayed there until she passed on 5/26/22.
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- Atrial fibrillation
- Andere Medikamente
- Daughter only reported Elloquis
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 22.11.2022
- Impfdatum
- 28.04.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 189,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anticoagulant therapy
COVID-19
Cardiac failure
Chest discomfort
Chest pain
Chills
Cough
Diabetes mellitus
Dizziness
Dyspnoea
Hypertension
Nausea
Pyrexia
Supraventricular tachycardia
Thrombosis
Symptomtext
Patient is a 61 y.o. female patient of MD with a history of chest pain and dizziness. Patient states that she has been diagnosed with blood clots in her legs recently and was started on Eliquis yesterday. States that she has been having inferior substernal chest pains a mix of sharpness and pressure, over the last 3 days. Does note that she feels short of breath. States that she has been having fevers and chills. Does note that she has been dizzy. States that her husband is here in the hospital for chest pain and she has been with him upstairs. States that the symptoms were such that she felt that she needed to be evaluated as she became deeply concerned. Has had a dry cough. States that she thought that she was "just getting a cold". Has also felt nauseated over the last 4 days, worse over the last 3 days. Denies additional clinical concerns at this time. No hypoxia, pt stabilized dced home , eliquis resumed from outpt dvt Discharge Diagnoses: Covid Dm Htn Dvt HFpEF SVT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 10.05.2022
- Beginn
- 15.08.2022
- Tage bis Beginn
- 97,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal distension
Abdominal pain lower
Aortic valve disease
Aortic valve replacement
Aortic valve stenosis
Arteriosclerosis coronary artery
Aspiration pleural cavity
Atrial fibrillation
Blood culture
COVID-19 pneumonia
Catheter site haemorrhage
Central venous catheterisation
Chest tube insertion
Coronary artery bypass
Culture
Culture urine
Echocardiogram
Ejection fraction decreased
Symptomtext
Discharge Provider: Primary Care Provider: MD Admission Date: 8/15/2022 Discharge Date: 9/16/2022 PRESENTING PROBLEM: Coronary arteriosclerosis in native artery [I25.10] Aortic valve disease [I35.9] Arteriosclerotic coronary artery disease [I25.10] Aortic valve stenosis, critical [I35.0] Coronary artery arteriosclerosis [I25.10] Aortic stenosis, severe [I35.0] HOSPITAL COURSE: The patient was seen in the office and was found to be a candidate for Coronary artery bypass grafting x1 using endoscopically harvested left saphenous vein, aortic valve replacement, intra op TEE, TEE INTRAOPERATIVE. The procedure was performed on 8/15/2022. The procedure went well and the patient was transferred to the CVRU per routine. 8/19: Patient needs to be pushed as far as pulmonary rehab and activity. Renal panel Q 6 hrs. CI 2.4-3.6 The patient developed covid pneumonia as well as aifb with rvr and hypotension. She required critical care for several days. 8/21: ECHO 8/18 with reduced EF of 20%. May need AHFconsult. Now improved will tfer to 7hc. 8/22: ECHO 8/18 with reduced EF of 20%. AHF consult. WBC trending up- UA positive- culture ordered. Afib RVR this am, Amio bolus/gtt. Continue Midodrine for hypotension. 8/23: cefepime started per ID for urine culture 8/24: holding tube feeds for abdominal distention, encourage oral intake, continue bilateral pleural drains. 8/25: continue lasix per AHF recommendations, keep bilateral pleural drains, out of bed to chair today 8/26: out of covid isolation, started ambulating in room. Bilateral pleural tubes remain. Corpak remains with tube feeds on hold. Eating more - continue calorie count. 8/27: Remove chest tube after walk today, if output remains low, continue calorie count, increase activities. 8/28: Continue nocturnal tube feeding. Anticipate discharge to rehab in 1-2 days. 8/29: C/o lower abdominal pain. UA positive- per discussion with Dr. will wait for culture results prior to treating with ABX, since WBC is going down and patient is not febrile. KUB showed nonobstructive supine bowel gas pattern. Transfuse 1 unit of PRBC today. Weight trending up. Cardiology managing heart failure, started Milrinone today. IR central PICC ordered. Continue nocturnal tube feeding. Poor oral calorie intake. 8/30: Bleeding from chest tube and PICC line site. Hold Heparin. WBC trending up, obtain blood cultures. Heart failure managed by cardiology. 8/31: Patient now NSR, WBCs continue to trend up. CXR ordered. Monitor blood and urine cultures Discuss leukocytosis with ID and attending. 9/1: Intermittent a-fib, Patient continues to not tolerate tube feeds, Starting with TPN and lipids today, d/c corpak. Vascular consulted. IR consulted for thoracentesis and draining fluid collection of the left psoas muscle. 9/2: Nutrition recommending jejunal corpak instead of TPN and lipids. Jejunal corpak placed today. Hgb 7 this morning - 2PRBCs given plus extra dose of lasix Bed side right thoracentesis performed by CTS PA - 800ml off, asked RN to send culture of the fluid. Discussed psych consult for depression medication - not interested at this time. Discuss having the patient go outside if she can tolerate sitting up - Patient was interested in this but was not able to due to procedures. IR planning on aspiration of left psoas fluid collection. 9/4: psychiatry consulted at the request of a daughter from out of town - remeron started. Tube feeds running at 20ml/hr around the clock due to not tolerating 40ml/hr. 9/5: ancef started for left knee endo site warmth and erythema 9/6: Amiodarone and milrinone drips per AHF. Replace K+, phos and Mag. Warmth/erythema of left knee EVH site improving. Heart failure managing diuretics and antihypertensives. ECHO completed, EF- 45%, no pericardial effusion. 9/7: Continue Ancef for warmth/erythema of left knee EVH site, order written for patient to o outside with RN 9/9: Left knee looking much improved. Restart calorie count due to patient telling IR she did not want PGJ. Disccused the importance of getting her to rehab and the need for PGJ. Patient agreed to get PGJ if she is not able to take in enough calories during the calorie count. 9/10: Continue Calorie count. PJG pending for Monday. Needs PT/OT 9/11: continues to have poor oral intake. TF via corpak. Anticipate PGJ Monday 9/12: PGJ placed 9/13:Continue calorie count. continues to have poor oral intake. TF via corpak. Patient c/o pain after PGJ placement. Plan for d/c to rehab on Thursday 9/14: IR to remove tunneled PICC today, continue tube feeding. Anticipate discharge to rehab tomorrow. 9/15: Patient is ready for SAR discharge, when bed available. 9/16: Patient is in stable condition. Patient was c/o pain at the PGJ site, CT completed by IR, no concerns noted. She denies shortness of breath or chest pain. Sternal incision clean dry and Intact. Having bowel movements. Discharge to rehab today. Discharge instructions given. CXR from today reviewed with Dr., right pleural effusion, No intervention required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 32,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Coronary artery spasm Severe aortic stenosis, s/p AVR 8/15/22 MR (mitral regurgitation) Subclavian steal syndrome Carotid stenosis CVA (cerebral infarction) DDD (degenerative disc disease), lumbar BCC (basal cell carcinoma of skin) HTN (hypertension) IFG (impaired fasting glucose) Posterior vitreous detachment of left eye Dermatochalasis of both upper eyelids Osteoporosis Occlusion of left subclavian artery Glaucoma suspect of both eyes Mitral valve annular calcification Coronary artery disease involving native coronary artery of native heart without angina pectoris Arteriosclerotic coronary artery disease, s/p CABG 8/15/22 Postoperative anemia due to acute blood loss Acute on chronic combined systolic and diastolic heart failure COVID-19 Atrial fibrillation RVR AKI (acute kidney injury) Chronic kidney disease Dysphagia UTI (urinary tract infection) Leukocytosis New cardiomyopathy, unknown etiology EF 20%, improved to 45% Physical deconditioning Psoas hematoma, left, secondary to anticoagulant therapy Bilateral pleural effusion Failure to thrive in adult Celiac artery stenosis & stenosis Protein calorie malnutrition
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet amiodarone (PACERONE) 200 MG tablet amLODIPine (NORVASC) 5 MG tablet Ascorbic Acid (VITAMIN C PO) aspirin 81 MG chewable tablet Cholecalciferol (VITAMIN D) 1000 UNITS CAPS hydrALAZINE (APRESOLINE) 10 MG
- Allergien
- Iodine LatexFatigue Persantine [Dipyridamole] Simvastatin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 03.05.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 65,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Anaemia
Atelectasis
Blood culture positive
Bradycardia
Bronchiectasis
COVID-19
Chest X-ray normal
Computerised tomogram abdomen abnormal
Condition aggravated
Culture urine positive
Electrocardiogram ambulatory abnormal
Escherichia test positive
Fatigue
Gram stain positive
Haemoglobin decreased
Hypotension
Intensive care
Symptomtext
Admission Date: 7/7/2022 Discharge Date: Jul 12, 2022 PRESENTING PROBLEM: Sepsis (HCC) [A41.9] HOSPITAL COURSE: per ICU transfer summary: 85 year old female with hx of dementia on Aricept, RA on Arava and prednisone 5 mg.daily, HTN, chronic anemia who presented to ED with fatigue. Found to have urinary tract infection and AKI as well as acute on chronic anemia with Hemoccult-positive stool, HGB 5.9. Additionally was COVID positive with a normal chest x-ray but 2 L oxygen requirement. CT scan of the abdomen and pelvis showed a punctate nonobstructing right renal stone but no ureteral calculi or hydronephrosis. Also showed bronchiectasis and chronic airspace disease RML and mild atelectasis. She was given IV fluids (1250 ml) however remained hypotensive therefore was started on nor epinephrine for ongoing hypotension. Ultimately transferred to Blodgett intensive care unit for further care. Received 1 unit packed red blood cells en route to ICU. On arrival to ICU received second unit of blood. Did not require pressors in ICU. One of two blood cultures positive for GNR. Rocephin changed to 2 grams Q24, new cultures sent. Awaiting urine culture. Bradycardia noted, patient with history of the same. Holter completed 6/21 no evidence of high grade av block or symptoms with bradycardia. Patient improved this Am 7/8. Off nasal canula eating a diet and actually hypertensive. AKI contiues to improve. Will hold home triamterene with HCTZ additional day and hopefully kidney function returns to baseline 7/9. Plan to transfer to GMB today. Hospitalist Summary: Patient was continued on IV Rocephin. Repeat Blood Cx were negative at 4 days. Urine Cx grew E. Coli - resistant to Ampicillin, and intermediate to Cipro. GI did not feel patient had a bleed so they signed off (Admission hgb was 5.9 and went up above 12 after two units (and stayed there) suggesting first value was lab error. Other workup included Chest X ray which showed small bilateral pleural effusions. Patient continued to improve - transitioned to Ceftin (per discussion with ID pharmacy) to complete a total of 10 days of antibiotic therapy. Her home Dyazide was discontinued and she was started on Norvasc 5 mg daily. Her renal function had normalized prior to discharge. COVID Precautions information provided. I discussed with patient, husband and daughter at bedside the following on 7/11: - Close BP monitoring - Lasix as needed for leg swelling - Outpatient PCP followup for labs within 1 week (CBC and CMP) - Outpatient Colonoscopy/EGD consideration with GI. Patient was otherwise back to baseline and discharged home in stable condition on 07/12/2022. Epic message sent to PCP For follow up labs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic venous insufficiency Osteoporosis Vitamin D deficiency Macular degeneration Varicose veins of leg with complications, bilateral Bronchiectasis (HCC) PSVT (paroxysmal supraventricular tachycardia) (HCC) HTN (hypertension), benign Scoliosis, unspecified scoliosis type, unspecified spinal region Rheumatoid arthritis involving multiple sites with positive rheumatoid factor (HCC) Iron deficiency anemia Septic shock (HCC) UTI (urinary tract infection) AKI (acute kidney injury) (HCC) Acute on chronic blood loss anemia Acute respiratory failure with hypoxia (HCC) COVID-19 virus infection
- Andere Medikamente
- alendronate (FOSAMAX) 70 MG tablet ALFALFA PO amLODIPine (NORVASC) 5 MG tablet Ascorbic Acid (VITAMIN C PO) Calcium Phosphate-Cholecalciferol (CVS CALCIUM-VITAMIN D) 250-400 MG-UNIT chewable tablet cefuroxime (CEFTIN) 500 MG tablet ch
- Allergien
- Dyazide [Triamterene]
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 33,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anticoagulant therapy
Bladder catheterisation
Blood loss assessment
Bradycardia foetal
COVID-19
Caesarean section
Complication of pregnancy
Delivery
Ecchymosis
Electrocauterisation
Exposure during pregnancy
Fatigue
Foetal heart rate deceleration abnormality
Foetal heart rate indeterminate
Foetal hypokinesia
Foetal monitoring abnormal
Foetal non-stress test abnormal
Haemorrhage subcutaneous
Symptomtext
Patient is a 32 y.o. G5P0040 female at 31w0d with Estimated Date of Delivery: 8/17/22 who presents today with preterm contractions and decreased fetal movement. She was diagnosed with COVID-19 on 6/9 and since then had been having cramping/contractions which increased in severity and frequency on 6/15 which promped her to come into triage. She reports the contractions were every 10 minutes or so. She denies LOF and vaginal bleeding. She now reports improved fetal movement but is concerned due to her history of prior losses. She reports her COVID-19 symptoms are improving but she continues to feel fatigued and is having a headache. She denies vision changes and a RUQ pain. The patient is a 32 y.o. G5P0040 at 31w1d who was admitted to labor and delivery for observation due to preterm contractions, decreased fetal movement and variable decelerations noted on NST in traige. Her pregnancy is complicated by COVID-19 in pregnancy, chronic hypertension, history of recurrent miscarriage (for which she is on Lovenox 40 mg BID, Prograf 4 mg and Synthroid). She was also on Prednisone earlier in pregnancy and is on insulin for steroid induced hyperglycemia. On admission, she received betamethasone and was started on IV magnesium for neuroprotection. She was noted to have persistent fetal bradycardia (105-107) that did not improve with fetal resuscitation methods. Her c-EFM was reviewed with the MFM team and the decision was made to proceed with a cesarean section due to category II fetal heart tones remote from delivery. Due to her recent Lovenox dose, she required general anesthesia. Patient is a 32 y.o. G5P0141 who is POD#1 from a pLTCS for Category II FHT remote from delivery who developed significant bleeding from her c-section incision refractory to pressure and was taken to the OR for exploration of her wound. REMARKABLE FINDINGS: - Pfannenstiel incision, oozing, with ecchymosis and with approximately 8x5 cm area of induration - Subcutaneous tissue with infiltrating clot, tracking toward the right flank - area of active bleeding from the inferior skin a SURGICAL COMPLICATIONS: None TECHNIQUE: The patient was taken to the operating room, where general anesthesia was obtained without difficulty. She was placed in a dorsal, supine position and prepped and draped in the usual manner. The existing Pfannenstiel incision was opened using his scalpel. 3-0 Vicryl was removed from the subcutaneous tissue using pickups and suture scissors. An area of active bleeding was noted along the anterior portion of the skin incision 3 inches in from the right corner, which was cauterized with the Bovie. The wound was explored and the fascia was noted to be intact. Approximately 20 mL of clot and loose blood was removed from the wound. Bovie cautery was used to obtain hemostasis. An area of persistent bleeding was noted deep in the subcutaneous tissue just inferior to the right corner of the skin incision. 3-0 Vicryl was used in figure-of-eight fashion and hemostasis was obtained. The wound was irrigated and suctioned. No active bleeding was noted. The subcutaneous tissue was irrigated and excess fluid removed with suction. The subcutaneous tissue was reapproximated using 3-0 Vicryl in a runnig fashion. The transverse skin incision was repaired with 3-0 Stattafix. Swift-set skin glue was applied. A pressure dressing The patient tolerated the procedure well. EBL 20 mL. Sponge, lap and needle counts correct x2. No antibiotics were indicated. The patient was transferred to the recovery room in good condition. Dr was present and scrubbed for the entire procedure. Intake Transfuse RBC 300.00 mL Plasma-Lyte-A infusion 700.00 mL sodium chloride 0.9% (NS) infusion 900.00 mL Total Intake 1900 mL Output Est. Blood Loss 20 mL Anesthesia Foley Output 600 mL Total Output 620 mL Net Net Volume 1280 mL Estimated Date of Delivery: 08/17/22 31w 1 D preterm male born 1.52 kg
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- 5,0
- Labordaten
- Group B Streptococcus (GBS), PCR [392185784] (Abnormal) Collected: 06/16/22 0125 Order Status: Completed Specimen: Swabbed Collection from Vaginal/Rectal Updated: 06/17/22 1014 Group B Strep PCR Streptococcus agalactiae (Group B) Abnormal Comment: Detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Circulatory Pre-existing essential hypertension affecting pregnancy, antepartum Infectious/Inflammatory COVID-19 affecting pregnancy in third trimester Nervous Seizure disorder during pregnancy, antepartum Genitourinary Preterm contractions Endocrine/Metabolic Mixed hyperlipidemia MTHFR gene mutation Steroid-induced hyperglycemia Other MFM PLAN OF CARE History of recurrent miscarriages Delivery by classical cesarean section
- Andere Medikamente
- ibuprofen (MOTRIN) 600 MG tablet CALCIUM PO cholecalciferol (VITAMIN D) 50 MCG (2000 UT) capsule Insulin Pen Needle (BD ULTRA-FINE MINI PEN NEEDLE 5 MM X 31G) levothyroxine (SYNTHROID) 25 MCG tablet metFORMIN (GLUCOPHAGE) 500 MG tablet Pren
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- 07.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 18,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Blood test
COVID-19
Chest X-ray abnormal
Feeling abnormal
Malaise
SARS-CoV-2 test positive
Scan brain
Thrombosis
Ultrasound Doppler abnormal
Ultrasound scan
Symptomtext
I did not have an adverse reaction to the vaccine but I tested positive on 05/25/2022. I started to feel bad on 05/25 and I went to the ER and they tested me for Covid 19 and it was positive. I did not take anything to relieve my symptoms from Covid. I was re-test on 5/28 and it was still positive. I was admitted to the hospital on 5/28 because I felt really bad. I was in the hospital for seven days. I had blood clots in my legs and chest and they blood thinners.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- 7,0
- Labordaten
- Covid 19 - via nose swabs times two and they both positive. Blood test, several ultra sounds, chest x-ray, ultra sound over my legs and chest several times. Also scanned my head to check for blood clots.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Centrum vitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 11.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fatigue
Headache
Interchange of vaccine products
Mobility decreased
Nausea
Pain in extremity
Presyncope
Pyrexia
Vaccination site rash
Vision blurred
Symptomtext
within 4 hours i had a headache, nausea, fatigue, and then next day I was lightheaded and almost passed out 3x in a couple hours (this was 24 hours after the shot). Felt feverish and unable to get off the couch but worst part was feeling like my vision was clouding over, nauseated, and i was about to pass out. Every time i tried to get up or walk, i felt like i was going to faint. This lasted about 2-3 hours and then i was just fatigued. Arm was very sore day 2 and i had a rash about 3 inches below vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- IBS and arythmia
- Andere Medikamente
- Synthroid, Norvasc, multivit, L-lysine, Vit D
- Allergien
- Sulpha drugs, tetracycline, Cipro, tetanus, betadine
- Vorherige Impfungen
- similar symptoms when i took a sulpha drug. Also had fatigue and headache with Pfizer vaccination but nothing as severe as this
- Staat
- WI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Anal incontinence
Asthenia
Basilar artery occlusion
Computerised tomogram head abnormal
Culture urine positive
Echocardiogram abnormal
Ejection fraction
Escherichia test positive
Facial paralysis
Headache
Hemiparesis
Influenza A virus test negative
Influenza B virus test
Left atrial dilatation
Moaning
Nausea
Respiratory syncytial virus test negative
SARS-CoV-2 test negative
Symptomtext
Patient received vaccination above through Health Department on 5/3/22. She developed a headache shortly after. On 5/7/22, she presented to our emergency department with nausea, vomiting, and weakness. CT scan of head showed no acute abnormalities, but showed an old stroke. Patient was given fluids and Zofran. Patient was discharged home and instructed to follow-up with her primary care provider. On the evening of 5/7/22, she presented to our ED again unresponsive and moaning. Repeat head CT scan showed no acute abnormalities, but showed an old stroke. UA is positive for UTI. Admitted for UTI and weakness. Upon arrival to med/surg, patient was found to have bit her own tongue, incontinences of bowel and bladder, and demonstrated facial droop and right-sided weakness. Repeat CT done and resulted with acute left vertebral artery occlusion in the left basilar artery. Not a candidate for thrombectomy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- First 2 CT of head results were negative for acute abnormalities. Third CT of head was positive for acute left vertebral artery occlusion in the left basilar artery. Urine culture is positive for Escherichia coli. Negative for COVID-19, Flu A, Flu B, and RSV. ECHO results: left atrium is mildly dilated. Ejection fraction of 55-60%.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Acute gouty arthritis, GERD, Hypertension, Hypothyroidism, CT scan shows old previous stroke
- Andere Medikamente
- Levothyroxine 137mcg daily, Potassium chloride 10mEq daily, Losartan 100mg daily, Simvastatin 40mg daily, Bupropion 300mg XL daily, Indapamide 2.5mg daily, Amlodipine 15mg daily, Metoprolol 25mg ER daily, Tylenol 325mg every 4 hours as ne
- Allergien
- ACE inhibitors, aspirin, penicillin
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 02.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Blood test
Electrocardiogram abnormal
Eye movement disorder
Eye pain
Facial paralysis
Lacrimation increased
Loss of personal independence in daily activities
Neurological symptom
Symptomtext
Patient stated that she could not drink out of a bottle on 05/04/2022. that same night, patient stated her eyes were watering and painful. The following morning, the patient stated she attempted to drink out of a straw and was unable to. Patient stated she did not take any over the counter medications for her symptoms. on 05/06/2022, Patient stated that she was unable to close her left eye and the left side of her face began to droop. Patient reported to the Emergency room at Medical Center that same Friday, and stated she was given Valtrex 1g to take 2 tabs per day as prescribed by a Bio-neurosurgeon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- Patient stated that Medical Center ran a blood panel. They also performed an EKG on the bases that her symptomology was in line with stroke symptoms. Patient stated after being seen, the doctor diagnosed it as bells palsy and will follow up with her PCM Dr. on 05/09/2022. After her follow up, Dr. prescribed Prednisone 20mg 2xd and to follow up in September unless any additional symptoms occur. Patient stated she also has an eye Dr. appointment on June 2nd @ 0910 with Dr.
- Aktuelle Erkrankungen
- Patient stated nothing to report.
- Vorgeschichte
- Diabetes type 2, Gasopresus, high blood pressure,
- Andere Medikamente
- Pantoprazole 40mg 1xd, Extended Metformin 500mg 2xd, Lantus Insulin 10cc 1xd, Glimipride 4mg 2xd, Jardiance 25mg 1xd, Simvastatin 5mg 1xd, Lisinopril 20mg 1xd, Amlodipine 5mg 1xd, Nova log PRN, Celebrex 1xd, Cholestyramine 1 scoop daily, Vi
- Allergien
- Neosporin, Gabapentin, Erythromycin, other mycins, Prednisone, Pramipexole Dihydro
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 20.10.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Hypokinesia
Tachycardia
Symptomtext
Chest pain; tachycardia; could not move; This spontaneous case was reported by a consumer and describes the occurrence of CHEST PAIN (Chest pain), TACHYCARDIA (tachycardia) and HYPOKINESIA (could not move) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 immunisation. Previously administered products included for COVID-19 immunisation: Pfizer BioNTech COVID-19 vaccine (dose 1; chest pains for 9 months) on 13-Mar-2021, Pfizer BioNTech COVID-19 vaccine (dose 1) on 13-Mar-2021, Pfizer BioNTech COVID-19 vaccine (dose 1) on 13-Mar-2021, Pfizer BioNTech COVID-19 vaccine (dose 2) on 16-Aug-2021 and Pfizer BioNTech COVID-19 vaccine (dose 2) on 16-Aug-2021. Past adverse reactions to the above products included Chest pain with Pfizer BioNTech COVID-19 vaccine; Chills with Pfizer BioNTech COVID-19 vaccine; Costochondritis with Pfizer BioNTech COVID-19 vaccine; Myocarditis with Pfizer BioNTech COVID-19 vaccine; and Tachycardia with Pfizer BioNTech COVID-19 vaccine. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced CHEST PAIN (Chest pain) (seriousness criterion hospitalization), TACHYCARDIA (tachycardia) (seriousness criterion hospitalization) and HYPOKINESIA (could not move) (seriousness criterion hospitalization). The patient was hospitalized on 03-Jun-2022 due to CHEST PAIN, HYPOKINESIA and TACHYCARDIA. At the time of the report, CHEST PAIN (Chest pain), TACHYCARDIA (tachycardia) and HYPOKINESIA (could not move) outcome was unknown. No concomitant drug was reported. On 03-Jun-2022, the patient was hospitalized overnight. No treatment drug was reported. Company Comment: This is a Spontaneous case concerning a 64-year-old female patient with medical history of interchange of vaccine administration, COVID-19 vaccine, Pfizer BioNTech COVID-19 vaccine 1st and 2nd dose with adverse events of chest pains for 9 months, tachycardia, and myocarditis. The patient received 3rd dose with mRNA-1273 and on an unknown date and latency experienced the serious (per hospitalization) unexpected events of Chest pain, Tachycardia and Hypokinesia. The mentioned medical history of adverse reactions after first and second dose with Pfizer BioNTech remains a confounder. No further clinical information or diagnostic tests results were disclosed for analysis. No concomitant medication or treatment information was reported. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 06.07.2023
- Impfdatum
- 02.02.2021
- Beginn
- 06.11.2022
- Tage bis Beginn
- 642,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Confusional state
Encephalopathy
Tachycardia
Symptomtext
Reported Symptoms: 10010300:CONFUSION; 10014625:ENCEPHALOPATHY; 10043071:TACHYCARDIA; 10084268:COVID-19; Narrative: Patient received three doses of Pfizer and one dose of Moderna COVID 19 vaccine. The patient presented to the ED on 6 November 2022 with confusion and tachycardia. The patient was admitted with COVID 19. The patient was treated with diltiazem. The patient was discharged on 16 November 2022 in stable condition. Reported per EUA. Other Relevant HX: Other: covid encephalopathy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 06.07.2023
- Impfdatum
- 02.02.2021
- Beginn
- 06.11.2022
- Tage bis Beginn
- 642,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Confusional state
Encephalopathy
Tachycardia
Symptomtext
Reported Symptoms: Confusion; Encephalopathy; Tachycardia; Narrative: Patient received three doses of Pfizer and one dose of Moderna COVID 19 vaccine. The patient presented to the ED on 6 November 2022 with confusion and tachycardia. The patient was admitted with COVID 19. The patient was treated with diltiazem. The patient was discharged on 16 November 2022 in stable condition. Reported per EUA. Other Relevant Hx: Other: covid encephalopathy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 11.05.2023
- Impfdatum
- 10.05.2022
- Beginn
- 01.04.2023
- Tage bis Beginn
- 326,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
04/01/23 presents to ED for "breathing problem". PMHx of "hypertension, hyperlipidemia, CHF, BPH"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 04/01/23 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 04.05.2023
- Impfdatum
- 05.05.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 215,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Blood test
COVID-19
Cough
Decreased appetite
Dysstasia
Eye pain
Fatigue
Hyperhidrosis
Malaise
Mobility decreased
Oropharyngeal pain
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sleep disorder
Symptomtext
On 12/6/2022, I began to have a sore throat at around 8 or 9 AM. I knew that wasn't feeling well, but I went about my normal activities. Over the next three to four hours, the sore throat continued to get worse. At about 1-2 PM, I arrived at my physical therapy appointment, and I was wearing a mask. I didn't feel very well, but I did my therapy. Over the two hours I was there, I could tell that I was getting sicker, as I had fatigue and soreness. I felt like I was starting to get a fever. I finished my appointment, and my condition continued to get worse and worse by the minute. I came home and had a little bit of soup. I knew I was sick at this point, but I wasn't sure exactly what it was. I went to bed and woke up around midnight with coughing, fever, sweats, body aches, malaise, runny nose, fatigue, and eye pain. I couldn't even get out of bed. I remained in bed and tried drinking some water and getting some sleep, but it didn't help. My symptoms all got worse. I didn't have an appetite. At about 10 AM on 12/7/2022, I was able to take a home antigen test, and I got a positive result. I called my cardiologist for advice, and I was told that if my condition worsened, I was to either see my PCP or go to the ER. I went to the ER on 12/8/2022. I had tried to combat my symptoms with OTC medicines, but nothing worked. At this point, I was too weak to stand, so a neighbor (who also had COVID-19 and was less ill) took me to the ER. At the ER, I underwent blood work and was put on a breathing machine. I was given various intravenous fluids and medications. After about nine hours, I felt a little better. The hospital was overcrowded, and no hospital beds were available, so I was released with prescriptions for PAXLOVID and an albuterol inhaler. They told me to come back to the ER if I had any more issues. I took the medicines and spent two and a half weeks in bed. I tested negative on day 14 and day 16. It was a slow recovery, but I did eventually recover.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- 07DEC2022 home antigen test, positive result; 21DEC2022 home antigen test, negative result; 23DEC2022 home antigen test, negative result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Inflammatory Bowel Disease; Arrhythmogenic Right Ventricular Cardiomyopathy Dysplasia; Atrial Fibrillation; Long QT Syndrome; Genetic Bicuspid Aortic Valve Disease; PAI-1 Mutation 4G/5G Genotype; Vascular Occlusion; Hypothyroidism; Crohn's Disease; Exocrine Pancreatic Insufficiency; Subcutaneous Implantable Cardioverter Defibrillator; Subclavian Premounted Stent System
- Andere Medikamente
- Sotalol; ELIQUIS; atorvastatin; spironolactone; levothyroxine; CYMBALTA; gabapentin; metoprolol; nitroglycerin; AMBIEN; folic acid; baby aspirin; vitamin B12; iron; vitamin D; dicyclomine; ZENPEP; potassium
- Allergien
- LOVENOX; standard bandage and surgical adhesives; opioids
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 24.04.2023
- Impfdatum
- 23.04.2022
- Beginn
- 21.04.2023
- Tage bis Beginn
- 363,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Dyspnoea
Malaise
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I realized i was very sick 21APR2023 and was so congested I had trouble breathing, I took antihistamines and called my wife who stated with my conditions I needed to go to the hospital. I wen tto the hospital and was hospitalized. i am in the hospital while i am giving this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 3,0
- Labordaten
- 22APR2023 COVID-19 Test-Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Amlodipine; Predezone; Potassium Citrate; Nexium; Cenokot; Vitamin B12; Vitamin D3; Aspirin; Zyrtec; Q10; Crestor; Acetaminophen ; Tylenol; Fish Oil
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 23.04.2023
- Impfdatum
- 29.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 33,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests abnormal
Condition aggravated
Tinnitus
Symptomtext
Tinnitus in right ear. Diagnosed my ENT. No treatment available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Hearing test and exam
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Tinnitus started after Moderna.
- Andere Medikamente
- Estradiol tablets
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 20.04.2023
- Impfdatum
- 19.04.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Cardiac monitoring
Cardiac stress test
Computerised tomogram
Decreased appetite
Dizziness
Fatigue
Mobility decreased
Palpitations
Symptomtext
On 06/19/2022, at 03:00PM, I had severe fatigue, heart palpitations, loss of stamina. Treatment was lots of bed rest. Eventually I was issued prescriptions. I also had severe dizziness and appetite loss. There were many CT Scans and stress tests and heart monitoring sessions, I do not know dates and details.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Loss of stamina
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Lisinopril; simvastatin; multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 17.04.2023
- Impfdatum
- 23.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Blood chromium
Blood test
Bursitis
Condition aggravated
Discomfort
Gait disturbance
Headache
Joint swelling
Muscle spasms
Nerve compression
Pain
Pain in extremity
Peripheral coldness
Pyrexia
Skin tightness
Spinal X-ray abnormal
X-ray normal
Symptomtext
After I got my first Moderna booster, I had intermittent pre-existing pain that worsened. The pain extended from the back of my thigh toward my knee. The pain was in both legs, but it was worse in the left leg. It felt sort of like sitting on a tennis ball on the left side., and it sometimes caused me trouble walking. My doctor took X-rays, but he found no anomalies, so he guessed it was bursitis. He recommended physical therapy, which I received for about eight weeks. After the therapy sessions ended, I still did the exercises that I had learned. The discomfort was no better or worse than before, but the exercises helped decrease the intensity of the pain. Between May and September 2022, I was fine. I still had some intermittent discomfort, but it didn't interfere with my ability to go about my normal activities. On 9/18/2022, I received my second Moderna booster (AS7143C). The pain returned about three weeks afterwards. The pain was in the same part of the legs that it had been prior to my getting physical therapy, and I also had trouble walking again. I went to an orthopedic surgeon, because I felt like something was wrong. I underwent X-rays, and no structural anomalies were present. The surgeon then told me that it was likely ischial bursitis that had been activated. He then recommended that I get physical therapy, which I didn't start until 4/4/2023. In the meantime, I did the exercises that I had learned in my previous physical therapy sessions. They helped lessen the intensity of the pain, but the skin around my left thigh started to feel tight. I continue to experience the feeling of tightness at the time of this writing. I got my third Moderna booster (067H22A) on 3/29/2023. The third booster was a different experience. When I received the third booster, a cold sensation ran down my arm, and I had never experienced that before. I then immediately felt a momentary pain or swelling in my left hip. I then had a low-grade fever that lasted for about two days and a headache that lasted for about five days. I don't normally get headaches, so this was unusual. The bursitis(?) flared up again in both legs, and I had trouble walking. When I went to see the physical therapist on 4/4/2023, I felt fine and nothing hurt, both before and after the therapy. I had no trouble walking, and everything was perfect. When the therapist touched my left hip, she said that she could feel a tightness on the back of the left thigh, a lump. To her, it felt like a muscle spasm. The pain returned a few days later, though. On 4/11/2023, I saw my doctor again. The doctor did more X-rays and looked higher up in my spinal column to see if there was a pinched nerve. He couldn't find anything structurally wrong, so he sent me back to physical therapy. He also decided that I should undergo bloodwork to check my chromium and cobalt levels, because he wanted to rule out any possibility of toxicity caused by my shoulder and hip replacements. I am currently awaiting the test results.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- History of Two Shoulder and Two Hip Replacements
- Andere Medikamente
- Cod Liver Oil
- Allergien
- Bee Stings; Hydrocodone; Oxycodone; Meloxicam; Zyrtec; Keflex; Tramadol; Shrimp
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 12.09.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 49,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
Blood test
COVID-19
Cardiac monitoring
Cardiac stress test
Cough
Electrocardiogram normal
Feeling jittery
Palpitations
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Thyroid function test
Symptomtext
10/31/22 I thought I had allergies with a runny nose and sneezing, and maybe a bit of a cough. This lasted for about four days. On 11/4/22 I lost my sense of taste and smell. I took a home COVID test which was positive. I took another COVID test on 11/6 and 11/8 which were positive. And on 11/10/22, my COVID test was negative. I had stopped sneezing and my nose was not running. I have recovered from those symptoms. On 11/14/22 I felt jittery. On 11/16/22 I was having heart palpitations and still have them. I had an EKG that was normal. I wore a heart monitor for a week starting on 11/28/22 and do not have the results. I go for a stress test tomorrow, 12/14/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Home COVID test: 3 positive and 1 negative; EKG was normal; Wore a heart monitor and do not have the results yet; Blood work done for Thyroid, no results back.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 Diabetes
- Andere Medikamente
- Levothyroxine; fenofibrate; atorvastatin; metformin ER; baby aspirin; vitamin D2; CLARITIN; vitamin B12; calcium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 19.05.2022
- Beginn
- 05.08.2022
- 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
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
On Friday I tested because I felt like I was getting a cold, I wanted to make sure it was not COVID-19. The home COVID-19 came back negative, so we went our excursion. I was scheduled for a sleep study on the Monday after that weekend and the test I took a test at the lab before I went in for the sleep study and this COVID-19 test came back positive. My symptoms were mild, I got over them in five days. The shortness of breath lasted for almost three weeks. I do feel like I have completely recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test negative; rapid COIVD-19 test positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetic; High Blood Pressure, High Cholesterol; Familia Benign Tremors
- Andere Medikamente
- No
- Allergien
- Bupropion; lidocaine; betadine; MUCINEX
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 09.06.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 144,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Dyspnoea
Emphysema
Lung opacity
Oxygen saturation decreased
COVID-19
Cardiac stress test normal
Cardiac telemetry normal
Chest X-ray abnormal
Chronic obstructive pulmonary disease
SARS-CoV-2 test positive
Troponin normal
Symptomtext
Discharge Attending of Record: MD Primary Care Provider: MD Documenting Provider: PA-C Admission Date and Time: 10/31/2022 8:29 PM Discharge Date and Time: 11/03/2022 1:09 PM Positive Covid Date: 11/1/2022 Admission Diagnosis: 1. Dyspnea Discharge Diagnosis: 1. Dyspnea with history of severe pulmonary emphysema and hypoxia 2. COVID-19 infection with no evidence for COVID pneumonia The patient is an 83-year-old male with history of severe emphysema, moderate chronic obstructive pulmonary disease with exacerbations who presented to the emergency department with increasing dyspnea. He did have a workup in the emergency department of a chest x-ray that did show chronic changes of pulmonary emphysema along with persistent opacity along the lateral aspect to the left upper lung which could represent scar less likely pneumonia. Emergency department did place the patient into the observation unit for further workup of the cause of his dyspnea. His it did see that the patient was having a chronic obstructive pulmonary disease exacerbation he was given steroids along with duo nebulized treatments. We also did order a Lexiscan Myoview cardiac stress test to ensure that his dyspnea was not a cardiac equivalent. Patient had stable troponins with no life-threatening arrhythmias on telemetry. Lexiscan Myoview did not show any signs of ischemia. Secondary to patient's history of severe emphysema pulmonology was consulted who did recommend a film array. His COVID-19 was negative initially been on film array it was positive. Pulmonology did feel that steroids and DuoNebs were appropriate. Patient was overall feeling improved. He was desatting his oxygen on ambulation so pulmonary rehab was consulted and they did set him up for home oxygen. Repeat chest x-ray does not show any evidence of infiltrate. At this time pulmonology feels comfortable discharging home with a long week of steroids which was written. He does have his inhalers at home and will have home oxygen. He will follow-up with his pulmonologist in the next couple of weeks as he does have an appointment. No antibiotics are recommended by pulmonology at this time. He feels improved upon discharge. He will come back with any progressive symptoms or concerns but is sent home feeling overall improved. He did see physical therapy and occupational therapy while here who did not recommend any additional modalities.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pulmonary emphysema (HCC), severe. History of Cryptogenic organizing pneumonia (HCC), dx'd 2005 with flares., with LUL nodule noted 11/2020 Right Pneumothorax, 11/05. Spontaneous. Rhinitis, allergic Hemoptysis Postinflammatory pulmonary fibrosis (HCC) COPD with acute exacerbation (HCC) Nodule of lower lobe of left lung Dyspnea Shortness of breath Carotid stenosis, left Supraventricular arrhythmia HTN (hypertension) Aortic stenosis MGUS (monoclonal gammopathy of unknown significance) Tobacco Abuse, in Remission. 42 pack years. Quit '98 IFG (impaired fasting glucose) Dyslipidemia Rosacea Osteopenia Skin lesion, with granulomatous features. Noted 11/2020. T12 compression fracture (HCC) Low testosterone in male Elevated alkaline phosphatase level Other closed displaced fracture of proximal end of left humerus with routine healing, subsequent encounter Generalized anxiety disorder
- Andere Medikamente
- albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin EC 81 MG enteric coated tablet fluticasone (FLONASE) 50 MCG/ACT nasal spray fluticasone-umeclidin-vilant (TRELEGY ELLIPTA) 100-62.5-25 MCG/INH i
- Allergien
- Mucinex Hydrochlorothiazide W-triamterene Lipitor [Atorvastatin] Pravastatin Simvastatin Doxycycline Ciprofloxacin Lovastatin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 06.05.2022
- Beginn
- 27.08.2022
- Tage bis Beginn
- 113,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Cough
Decreased appetite
Depersonalisation/derealisation disorder
Exposure to SARS-CoV-2
Fatigue
Headache
Influenza like illness
Mobility decreased
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Sensory loss
Sneezing
Symptomtext
08/27/22 I started to feel achy and tired, and I was out of sorts. I started to sneeze, cough, slight aches and a headache. I was just not feeling like myself. I had been exposed to COVID. On 8/28/22 I tested negative with a home test. I stayed in bed for about a week. I was very tired. My fatigue lasted 3 weeks. I had low grade fever, coughing, very congested, flu like symptoms, lost my sense of taste and smell and had no appetite. It took three weeks to get my strength back. On 9/1/22, I had a tele visit with my physician. He told me to rest, but did not feel I should take PAXLOVID because my symptoms were not bad enough to warrant. He recommended I take vitamin D, vitamin C, zinc for two weeks and drink plenty of fluids and rest. I was to take cough medicine and decongestant if I needed it. My sense of smell and taste took about a month to return. After that, I felt better. My physician recommended I do not take my last booster for 3 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- COVID tests, negative and positive.
- Aktuelle Erkrankungen
- TIGAN; sulfa drugs; erythromycin
- Vorgeschichte
- Digestive tract issues; reflux; lower back pain
- Andere Medikamente
- Pantoprazole; famotidine; SYNTHROID; raloxifene; sucralfate; estradiol; PHILLIPS COLON HEALTH; PHILLIPS FIBER GOOD GUMMIES; MIRALAX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 19.01.2021
- Beginn
- 06.09.2022
- Tage bis Beginn
- 595,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Atrial fibrillation
COVID-19
Condition aggravated
SARS-CoV-2 test positive
Symptomtext
09/06/22 presents to ED for "A. fib". PMHx of "A. fib."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 09/06/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 05.06.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Condition aggravated
Cough
Dizziness
Fatigue
Headache
Hypoaesthesia
Paraesthesia oral
Throat tightness
Head discomfort
Hypoaesthesia oral
Impaired work ability
Incomplete course of vaccination
Malaise
Migraine
Nausea
Oral pruritus
Pharyngeal paraesthesia
Symptomtext
She got her vaccine, she felt ok and they told her to walk around. She went up one aisle and wrapped around, felt dizzy, came around the other aisle to go back to have a sit in the waiting area instead of waiting around. The dizziness got worse and she began to get pressure/headache. One of the techs saw her sitting down and she asked if she was OK, and she informed her that she was not and not feeling well, that she was dizzy and had a headache. She told her to have a seat for the 15 minutes and that maybe she needed to sit down a while. A minute or 2 later her throat started tingling, similar to her reaction to pineapples. She started coughing, and at that point another tech was walking back from somewhere and asked her if she was ok and she informed her that her throat was feeling like it was about to close. She asked if she had just received the vaccine, and told her that she was not feeling well. At the same time with the tingling of her throat her mouth began to itch, felt like an allergic reaction to something. She told her she would get her some water and some Benadryl. They had her take the Benadryl which she took and they had her sit there and the 15 minutes had passed. All of a sudden her mouth started, in the corners of her mouth first started going numb. She was thinking what was happening, and the longer she sat there the numbness went from the corners of her mouth to the tip of her nose like she had anesthesia from a dentist. The numbness went down to her chin area across her whole entire mouth. The tech said and asked if she was getting numbness on her mouth and she told her yes, and she said the same thing happened to her and that she should be fine. She told her that she felt like her whole face was going numb. The other tech that gave her the Benadryl told her that she needed to get home before the Benadryl kicked in before she wasn't able to drive home. She went home, laid down, and her throat was feeling better. The next day her headache was gone, the dizziness was gone, but the numbness had not gone and she still could not feel her mouth. That portion of her face in her cheek and the area from the tip of her nose to her chin. She then called on 6/8/22 the pharmacy and informed them that the symptoms had not gone away, and that is when the pharmacist made the report that we already have on file (2313040). He spoke to the techs that were there at the time of her vaccine, and apologized for what had taken place and that she should have never been sent home, and that the reactions were not good after receiving the vaccine. He then informed her that he would not give her another vaccine due to her reaction. He did ask her in detail what the techs had told her. They told her that they would see her in a couple of weeks for her next vaccine, and he said that NO they will not see her and to consider herself exempt and that she should not receive another dose of the vaccine. She did not see a doctor as she does not have one and had no insurance and could not afford for her to go to the UC. Once she went home and Benadryl took effect she no longer felt that her life was in danger. About 2 days after she spoke with the pharmacist the numbness had gone away, 6/10/22-6/11/22. She has not had any other symptoms since she got the numbness back. She felt very tired, sluggish, just very exhausted feeling like she could not do a lot for several weeks up to a month after the vaccine. She actually started feeling better sometime in July. She could barely do her normal routine, and no energy to do anything else and would come home and rest. She has a history of migraines when she was in her 20's, and has noticed that she has been having migraines more often since the vaccine. She has had 3 major migraines situations since the vaccine, sensitive to the light, nausea, tension headache which has happened twice. The first time she had that feeling she was able to lie down and had been off of work and just had the pressure behind her eyes and able to catch them early and take medicine to relieve her symptoms. The other two she was not able to catch and lost 2 days of work from these symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure prn, anxiety and panic disorder.
- Andere Medikamente
- Gabapentin, Klonopin, Hydrochlorothiazide.
- Allergien
- Latex, betadine/iodine, pineapples.
- Vorherige Impfungen
- Flu vaccine many years ago. She gets really sick and nauseous every time she has had the flu vaccine and makes her feel like she
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 16.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal loss of weight
Alopecia
Anaemia
Blood creatinine increased
Blood iron decreased
Blood test abnormal
Blood thyroid stimulating hormone decreased
Condition aggravated
Extra dose administered
Haemoglobin decreased
Vitamin D decreased
Symptomtext
After receiving my fourth dose of Moderna, my hair started falling out in large amounts. I had seen some hair loss in the previous few months, but it was noticeably worse after that fourth dose. I have very fine hair, but it started falling out to the point where you could see bald patches. My hair line also began to recede about an inch back. I was also losing weight very quickly without trying. I lost 22 pounds. My hair loss got so bad, that I felt the need to purchase a wig. On 06/20/2022, my doctor sent me to have some extensive blood tests. I'm still waiting on some of the results, but the results that have come in have shown low thyroid levels, low iron to the point of anemia, Creatinine levels were high, vitamin D was low, hemoglobin was low, along with other abnormalities. The second round of blood tests they did showed similar results. I am going to see a rheumatologist and an endocrinologist in a few weeks for further investigation. There is a concern that some medications I am on may be causing some of these test results.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Blood test 06/20/2022 abnormal findings; Additional Blood testing 08/19/2022 abnormal findings.
- Aktuelle Erkrankungen
- COVID-19 like symptoms lasting a week but multiple negative COVID-19 tests
- Vorgeschichte
- Lupus; Rheumatoid Arthritis; Hypothyroid; Sleep Apnea
- Andere Medikamente
- Vitamin B; vitamin D; hydroxychloroquine; olmesartan-HCTZ; spironolactone; pantoprazole; levothyroxine; bupropion-HCL; dextroamphetamine ER; alprazolam; meloxicam
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 23.08.2022
- Impfdatum
- 20.05.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 51,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Back pain
Blood cholesterol normal
Dyspepsia
Fatigue
Full blood count normal
Grip strength decreased
Haematocrit normal
Haemoglobin normal
Influenza virus test negative
Laboratory test normal
Lipids normal
Migraine
Muscle tightness
Musculoskeletal stiffness
Platelet count normal
Red blood cell count normal
SARS-CoV-2 test negative
Symptomtext
On or about July 10th I began having severe exhaustion. It lead to heartburn even when I didn't eat. I had severe migraine and weakness. These symptoms lasted from July 26 through the 28th of July. My back began to hurt on the July 24 through the 27th. The pain was in my lower back, stiff and tight. The weakness I had felt like I could not get a grip on anything to hold and I was shaky. No matter what position I was in my back hurt for several days. I contacted my doctor and was advised to take ibuprofen and drink fluids. The weakness and the migraine concerned the doctor and I was scheduled for tests on August 1st. No diagnosis was offered as the tests were all normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- COVID-19, negative; CBC, normal; Non Fasting Lipid, normal; Thyroid, normal; Influenza, negative; White Blood Cell, in range; THC, in range; Cholesterol, in range; Red Blood Cell, in range; Platelet, in range; Hemoglobin, in range; Hematocrit, in range;
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Prozac
- Allergien
- Kiwi
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 12.05.2022
- Beginn
- 11.08.2022
- Tage bis Beginn
- 91,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Blood test
Chest X-ray
Computerised tomogram
Condition aggravated
Electrocardiogram
Hypertension
Pain in extremity
Symptomtext
Very high blood pressure, perhaps related to medication changes, worsening leg and back pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 8/11/2022 CAT scan of head, Lung X-ray, ECG, Blood tests.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Depression, Sleep Apnea, Acid Reflux, High Blood Pressure, High Cholesterol, Back and Leg Pain. Obesity.
- Andere Medikamente
- Baby Aspirin, HCTZ, Losartan. Meloxicam, Gabapentin, Pantoprazole, Finasteride, Tamsulosin, Parnate, Pravastatin, Quetiapine, Melatonin, Vitamin D3, Vitamin B12, Metamucil, Medrol Pack.
- Allergien
- Codeine
- Vorherige Impfungen
- 3/31/2021 Moderna Covid Vaccune - I had an ocular migraine 4 days after my second shot
- Staat
- MN
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 07.05.2022
- Beginn
- 15.08.2022
- Tage bis Beginn
- 100,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Asthenia
COVID-19
Cough
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Weakness, cough, SOB
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- positive COVID
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 11.08.2022
- Impfdatum
- 28.04.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 63,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Condition aggravated
Cough
Influenza like illness
Malaise
Nasal congestion
Pain
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Reporting breakthrough Covid 19 case Started to feel sick on June 30th and tested positive on July 3rd via home test. Body aches like similar to the flu - high fever about 5-6 degrees above normal - cough and stuffy head. Pain in old injuries that are 40 years old and have not been an issue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Covid positive test 7/3/22 Covid negative test 7/12/22
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Migraines
- Andere Medikamente
- Botox (200 units every 3 months) Paroxetine 10mg - daily Verapamil 240mg - daily Claritin 10mg - daily Famotidine 20 mg - daily Meloxicam 15mg - daily Krill Oil 500mg - daily Alpha Lipoic Acid 300mg - daily Vitamin D3 125mg - daily
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 16.05.2022
- Beginn
- 12.06.2022
- Tage bis Beginn
- 27,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19 pneumonia
Cystitis
Malaise
Pneumonia
SARS-CoV-2 test negative
Urine analysis abnormal
White blood cells urine positive
Symptomtext
On June 12, 2022, I got really sick and had a bladder infection. Two days later, I went to the ER because I thought I was having a heart attack and they diagnosed me with pneumonia. They said that they thought it looked like COVID pneumonia and I've never had pneumonia before. They tested me for COVID-19, and I was negative. My blood oxygen level was also at 90 and they advised that if it got any lower to come back. The bottom of my left lung is missing due to a surgery that I had many years ago, so I believe that I may have been affected more harshly than others may have been. I've been monitored closely by my doctor since these events. As of 08/10/2022, I am still on an antibiotic. I have been prescribed multiple antibiotics over this span of time since none have been able to get rid of the white blood cells that were discovered on a uranalysis that cannot be explained.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- -
- Labordaten
- Urinalysis white blood cells found 08/02/2022; PCR COVID-19 test negative 06/14/2022; at home COVID-19 test negative 06/2022.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Ascending Aortic Aneurism; A-fib; Ablation.
- Andere Medikamente
- Multivitamin; losartan HCTZ; ELIQUIS; propafenone; metoprolol; cranberry.
- Allergien
- Incense.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 05.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 12,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal discomfort
Abdominal pain
Abdominal pain upper
Chest X-ray
Computerised tomogram abdomen
Diarrhoea
Dizziness
Endoscopy upper gastrointestinal tract abnormal
Faeces discoloured
Feeling hot
Flushing
Full blood count
Gastrointestinal ulcer
Gastrointestinal ulcer haemorrhage
Haemoglobin decreased
Headache
Tachycardia
Symptomtext
Headache, upset stomach, abdominal pain/stomach ache daily post vaccine. Some days more than others. 5/17/22 11:00 AM Flushing, feeling hot, tachycardia. 1215 had bowel movement dark purple/ black in color, liquid. Light headed, pulse 125-135. Taken to ER via ambulance at 1:30. Had 4 more liquid bm. Admitted to hospital 5/17 11pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- 2,0
- Labordaten
- Chest xray, CT abdomen, upper endoscopy, cbc. Hg from 14.6 down to 10.4 in 4hrs. Upper endoscopy showed ulcer, no longer bleeding.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, HTN, athritis
- Andere Medikamente
- Losartin 50mg, Aleve qd, Zyrtec qd, Melatonin 5g qhs, Agilease bid, Calcium Bid
- Allergien
- Erythromycin,bees
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 01.08.2022
- Impfdatum
- 06.05.2022
- Beginn
- 31.07.2022
- Tage bis Beginn
- 86,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Cough
Dyspnoea
Dyspnoea at rest
Mental status changes
Symptomtext
7-31-2022 patient presented to our ER with c/o SOB while resting. Pt was already aware that he had covid. Pt also c/o weakness, AMS and coughing. Pt was admitted for further evaluation and treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CVA, Diabetes, hyperlipidemia, hypertension, Heart disease with CABG
- Andere Medikamente
- Aspirin 81 mg po daily mirtazapine 15 mg po HS ramipril 10 mg po daily glipizide 5 mg po bid clopidogrel 75 mg po daily folic acid 1 mg po daily lexapro 5 mg po daily metoprolol succinate 50 mg po daily atorvastatin 40 mg po hs januvia 100
- Allergien
- penicillin sulfa
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 26.04.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 93,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest discomfort
Cough
Dizziness
Dyspnoea
Epistaxis
Eye irritation
Fatigue
Headache
Ocular discomfort
Parosmia
Respiratory tract congestion
SARS-CoV-2 test positive
Taste disorder
Symptomtext
I contracted COVID-19 on 07/28/2022 with symptoms of dizziness, chest tightness, cough, difficulty breathing, headache, congestion, pressure and burning in eyes, senses of smell and taste diminished, bloody nose, and fatigue. I was not prescribed any medications. I was ill for 5 days before my symptoms began to improve. I have not recovered as of yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid antigen test was positive on 07/29/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Metformin; Tegratol; Adderall; Trazadone; Multivitamin
- Allergien
- Clindamycin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 29.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 20,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Immediate post-injection reaction
Injected limb mobility decreased
Injection site pain
Laboratory test normal
Pain in extremity
Sleep disorder
Symptomtext
The symptoms started immediately after the shot was given I had pain in my arm. It moved into the shoulder and down my arms. Within 2 weeks it crossed over to my right shoulder. The pain is not as heavy but it wakes me up at night. I can still feel the pain where the injection was given. The pain started down my arm and then traveled up into shoulder. Then the crossed over into my right shoulder. I have lost mobility in my left arm along with strength. The doctor completed several test and was not able to find anything, I have seen 4 specialist and been seen in the emergency room. No abnormalities were determined. I am scheduled to see other doctors after this as I am still in pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- No additional testing done after 4th dose
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes; Prostate Cancer; Foot Neuropathy
- Andere Medikamente
- Humalog; Eli Gard; Quinapril; Carvedilol; Rosuvastatin; Zinc Sulfate; Vascepa; Lyrica; Pantoprazole; Tamsulosin; Align Probiotic
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 27.07.2022
- Impfdatum
- 26.04.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 71,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Borrelia test negative
Diarrhoea
Dyspnoea
Fatigue
Influenza A virus test negative
Influenza B virus test
Malaise
Nausea
Pain
Post-acute COVID-19 syndrome
Pyrexia
Respiratory syncytial virus test negative
SARS-CoV-2 test negative
Symptomtext
I was fatigued, a little tired. In May I tested negative but I was not sick, it was just a requirement to travel. In July I got sick I went to the doctor, I had fever, fatigue, nausea, diarrhea, difficulty breathing, body ache, I had the test again and it was negative but the doctor said it was Long COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- May 2022 COVID-19 negative; July 12th, 2022 FLU A & B test negative; July2022 RSV test negative; July 2022COVID-19 negative; July 2022 Lyme test negative; July 2022 blood test normal.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Hydroxychloroquine; benazepril; pazopanib; omeprazole
- Allergien
- N/A
- Vorherige Impfungen
- Flu shot, 67 years.
- Staat
- GA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 20.04.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 82,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Fatigue
Headache
Nasal obstruction
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Symptomtext
On the evening of the 11th of July I started to get a headache and it was difficult to keep my glasses on and a scratchy throat. On Tuesday the 12th I went on about my regular day and came back and after lunch fell asleep and woke up with the same headache as Monday but worse. I took some TYLENOL and it only dulled the pain some. No other symptoms. I woke up between 2/3 am on the 13th and I wasn't breathing well. I used the pulse oximeter and my oxygen saturation was 92. My nostril were clogged so I used FLONASE. I took a COVID-19 at home test and it was positive. I called my Dr. and they sent me PAXLOVID and started it on the evening of the 12th. I had a fever that went to 102. On the 14th I had a tele visit. By Friday I was feeling 70% better and still with a low 99.3 fever. By Mon 18th I did not have any symptoms and completed the PAXLOVID. I still had a bit of fatigue. Now I don't even have fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 at home test - positive.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Acid reflux
- Andere Medikamente
- PROTONIX; eye drop; ZYRTEC; calcium; vitamin D3
- Allergien
- Penicillin; sulfur
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 02.06.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 48,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Cough
Dyspnoea
Dyspnoea exertional
Fatigue
Headache
Myalgia
Oropharyngeal pain
Respiratory tract congestion
Symptomtext
Symptoms thus far have included headache, increased fatigue, increased weakness, increased shortness of breath especially dyspnea on exertion, myalgias, sore throat, coughing congestion. Mentions that the reason she presented to the clinic was the notable increased shortness of breath which has been worsening over the past few days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 02.05.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 9,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac flutter
Cardiac monitoring abnormal
Electrocardiogram abnormal
Palpitations
Tachycardia
Troponin
Symptomtext
Heart palpitations, heart flutterings. Wore a heart monitor for 15 days and these also showed up on the monitor. They happen at night or if I am taking a nap.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- tachycardia, troponin - performed twice. EKG (hospital)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- history of pneumonia, but have not had pneumonia for at least 10 years. Prior to this episode I haven't used my inhaler for 3 years. The prescription container was expired
- Andere Medikamente
- Ondansetron (as needed, occasionally); famotidine; Floragen 3; Vitamin D3-2,000 units; ocuvite-lutein tabs - 2 daily; zinc 50 units; albuterol inhaler - as needed
- Allergien
- -
- Vorherige Impfungen
- lame knees
- Staat
- GA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 36,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dyspnoea
Influenza like illness
SARS-CoV-2 test positive
Symptomtext
I developed a racking cough and difficulty breathing including an onset of what felt like a very terrible flu.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Covid home test result was positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Amlodipine; irbesartan; hydrochlorothiazide; doxazosin mesylate
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 28.06.2022
- Impfdatum
- 08.06.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Electrocardiogram abnormal
Tachycardia
Symptomtext
About 28 hours after the injection, I began having episodes of Atrial Fibrillation and tachycardia. These only lasted for 5-20 minutes. The episodes were fairly frequent for about 48 hours then decreased frequency. ( I have a device that records a 30 second ECG. so I have documentation of these episodes. I have never had an episode of atrial fibrillation but my sister has and that is why we have a device in the house Highest heart rate recorded was 185 beats per minute while sitting. ) I called my physician whose nurse suggested I consider going to the ER if the episodes continued. Because of the brevity of the episodes I did not feel like going to the ER would be helpful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- I have an appointment with a primary care provider this week to discuss this issue. I continue to have brief episodes once a day or less, I have requested a cardiology consultation before I have any additional vaccinations.
- Aktuelle Erkrankungen
- Fluid in right ear
- Vorgeschichte
- Chronic Fatigue Syndrome, Restless leg syndrome, mild depression, occasional migraines, seasonal allergies, GERD
- Andere Medikamente
- zoloft, Chlortrimeton, Musinex, Mirapex, Pepcid, multivitamin, Vitamin C, Chromium picolinate, calcium/magnesium. Just finished a short course of Prednisone for fluid in the ear.
- Allergien
- sulfa drugs, macro bid, saccharine,
- Vorherige Impfungen
- typical reactions of low fever and pain with previous Moderna vaccinations and previous booster
- Staat
- MI
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 09.04.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 72,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Abdominal pain upper
Alcohol use
Asthenia
Asthma
Asymptomatic COVID-19
Back pain
Blood alcohol increased
COVID-19
Cerebral atrophy
Cerebral small vessel ischaemic disease
Chest X-ray abnormal
Chronic obstructive pulmonary disease
Computerised tomogram head abnormal
Condition aggravated
Confusional state
Contusion
Cough
Symptomtext
Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 6/20/2022 Discharge Date: 6/21/2022 Condition on discharge: Stable Patient is a 76 y.o. female with PMH of asthma, COPD, GERD, depression, hyperlipidemia, urge urinary incontinence, Etoh use/abuse, who presented to Hospital Emergency Department on 6/21/22 with weakness. She notes that she had a bad fall the other day, was seen in ER and was sent home. She states "since being home I am not doing well. Im in a lot of pain in my head and back." She notes that her back pain is the mid/lower back and she rates the pain at 8/10. She notes "I have always had a bad back but not in this spot, always lower." She has bruising to the right side of her head. She notes that when she called her doctors office yesterday morning they recommended that she call an ambulance and come into the hospital. She has been able to get up and move around at home using a walker. She notes that she gets dizzy and lightheaded. She states "I can't walk on my own right now and I keep losing my train of thought. I cant stay focused." She notes that she has had trouble focusing since her fall. She notes that the right side of her head where she has the bruising is painful and rates the pain at 7/10. She has been taking Tylenol at home for the pain. She is uncertain as to how she fell but states "every part of my body got hit." She is uncertain if she passed out when she fell. She also notes that her upper abdomen feels tight and sore. She has been having some SOB that she first noticed yesterday and states "I woke up out of my sleep because I couldn't breath." She notes that she coughs all the time but that is not different than normal and she denies wheezing. She denies chest pain or palpitations. She is struggling to remember what day it is. She is feeling tired all the time. She denies fever or chills. She notes "I eat if I think about it but if I dont think about it then I dont." She notes that she lives alone and is unaware of any sick contacts She is vaccinated and boosted against COVID. She has never had COVID before. She notes that she drinks alcohol daily and drinks two bourbon and water. She notes that her last drink was Monday night. CT head completed in the ER showing no acute intracranial abnormality identified. Stable chronic microvascular ischemic changes and volume loss of the brain. CXR showing nonspecific mild hazy and streaky bilateral lower lung opacities which could represent atelectasis or pneumonia in the proper clinical setting. Redemonstrated background findings of COPD. She was COVID positive and did require 2L NC when oxygen dropped to 88%. Her labs were essentially normal. Vitals were stable. She was admitted for weakness, confusion and COVID 19. She was admitted for observation. Mild asymptomatic COVID-19 infection, she is status post for Moderna COVID vaccines. At this point she was on room air and doing well so no need for Decadron or home oxygen. She should stay in respiratory isolation for 9 more days. For her asthma/chronic obstructive pulmonary disease she will continue her home medication Symbicort, Spiriva, albuterol, and Singulair. Her chest x-ray show no acute changes. Regarding low back pain and recent falls, she will continue take Tylenol 500-1000 mg q.6 hours p.r.n.. She had x-ray of lumbosacral spine which show no acute fracture, she has diffuse osteopenia, mild dextroconvex curvature of the lumbar spine, and severe degenerative changes at L5-S1. She was seen by PT, OT and they recommend home health care with home OT and PT. she should follow-up with the primary care physician in 1 or 2 weeks. Patient alcohol level was 183. She claims that she drinks II alcoholic drinks at night. She was seen by medical social worker, she was offer resources for alcohol treatment but she declined. She does not believe that she has any alcohol problem. Generalized weakness most likely due to alcohol use, chronic low back pain, and COVID infection. Per PT and OT she was recommended home OT and PT. She was evaluated by SLP for cognitive evaluation she did very well. She was also negative for concussion syndrome. She was discharged home on June 21, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma Urgency incontinence Restless legs syndrome (RLS) Hyperlipidemia Tricuspid regurgitation Mitral regurgitation Environmental allergies COPD (chronic obstructive pulmonary disease) Esophageal reflux Alcohol abuse Recurrent major depressive disorder, in partial remission H/O tobacco use, presenting hazards to health Tremor of both hands Confusion and disorientation COVID-19 virus infection Generalized Weakness and recent fall
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler atorvastatin (LIPITOR) 10 MG tablet benzonatate (TESSALON) 100 MG capsule Blood Pressure Monitoring (BLOOD PRESS
- Allergien
- Zpak [Macrolides]Hives Environmental PrednisoneHives
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 06.05.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dyspnoea
Exposure to SARS-CoV-2
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Symptoms developed were primarily congestion, coughing, difficulty breathing (mild), low grade fevered that persisted on first day only. Please note the onset of these symptoms came after 3 days of exposure from my son living in household who had much worse symptoms including severe coughing and fever. My son?s symptoms developed about 48 hours after returning from a business trip where we were both exposed to other team members who later tested positive for COVID19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID19 Rapid Diagnostic test performed by Pharmacy on Friday 6/10/2022 at 10:30 AM; Results were positive (RX 2895885-07878).
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Acutane
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 04.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac monitoring
Electrocardiogram
Palpitations
Symptomtext
16 hours after receiving booster heart racing to 180 and uncontrollable palpitations
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- 4 separate EKG in emergency , monitored and given meds Metoprolol tartrate and 14 day zito heart monitor
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High blood pressure under control with meds and exercise
- Andere Medikamente
- Fluoxetine ,Amlodipine Lisinopril
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 20.04.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 43,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood erythropoietin
Blood lactate dehydrogenase
Blood test
Dizziness
Dyspnoea
Feeling cold
Haemoglobin decreased
Haptoglobin
Laboratory test
Reticulocyte count
Symptomtext
With my regular check up with primary care, they did lab work. The blood work showed a drop in hemoglobin down to 9. I still have more tests, but I don't have all the results yet. The hematologist also noted some tear-drop shaped blood cells. They ran the tests for them but haven't gotten the results back yet for that either. The hematologist requested additional tests. The additional tests were for erythropoietin level, reticulocyte count, LDH, and haptoglobin, waiting for results. Tests were done two days ago. The hematologist also said depending on the results, we may also need to do a bone marrow test. My PCP is thinking that some of the symptoms I've been complaining about is the result of the hemoglobin level. Symptoms have been feeling cold a lot lately, out of breath at times without doing anything, and getting dizzy a lot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Blood work, hemoglobin dropped to 9. Additional tests: erythropoietin level, reticulocyte count, LDH, and haptoglobin, waiting for results.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure; Type 2 Diabetes; ADD
- Andere Medikamente
- Cyclobenzaprine 10mg; empagliflozin 10mg; ADDERALL 30mg total daily; semaglutide 0.5mg injection; amlodipine 10mg; omeprazole 40mg; bupropion 300mg; cetirizine 10mg; gabapentin 300mg; magnesium 250mg every other day; diltiazem 240mg; metfor
- Allergien
- Penicillin; phenobarbital; clindamycin; lisinopril
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 02.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Back pain
Chest pain
Dyspnoea
Sleep disorder
Symptomtext
Sharp stabbing chest pains began for the first week on left side and progressively worsened to all areas of upper chest and back. Shortness of breath and anxiety. I?m also having trouble sleeping
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No know drug or food allergy
- Vorherige Impfungen
- Hpv vaccine (other info unknown)
- Staat
- MN
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Dyspnoea
Dyspnoea exertional
Interchange of vaccine products
Paraesthesia
Symptomtext
This was 2nd covid booster. Doctor recommend Moderna for 2nd covid booster. The first three vaccinations were Pfizer. There was no reaction for 15 minutes, but when leaving clinic and walking to the car I had extreme shortness breath with chest pressure, and minimal pain in upper left chest area. This extreme reaction continued for several hours, but took about three days to diminish. Currently, I have shortess of breath when climbing stairs and walking short distances. Most of the time I am unable to take a deep breath, and feel as if I cannot breath when in a confined area. At times the tingling pain is still in the upper left chest area, but goes away in a couple of hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure, Thyroid, Osteoporosis, Glaucoma,Vascular Disease, Migraines
- Andere Medikamente
- Levothyroxin Gabepentin Atorvastatin Lisinopril Lantanoprost, Timolol, Osteo Vegan, Osteo VSC, Vitamin K, Probiotic, Excedrin Migraine,
- Allergien
- Gluten intolerant
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 30.04.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Chills
Headache
Hypertension
Joint swelling
Laboratory test
Lymphadenopathy
Malaise
Mastication disorder
Pain in extremity
Pain in jaw
Ultrasound Doppler abnormal
Symptomtext
So when I got the vaccine I had a sore arm and chills. The following Saturday I had a terrible pain on my right side of my jaw. I took some meds. The next morning I took some Aleve and it helped the pain. I went to bed the net night and I got up my right leg was in pain. An then when I woke up on Monday morning it was the right leg that was in some terrible pain. An then I was able to get a doctor appt and my doctor didn't know why I was having that pain in both of my legs, because I am a healthy person. So she took my blood pressure and it was high. She asked if I wanted a steroids shot and I said no. I wanted to see if it would just go away. She said that she don't like taking shots or medicine if she don't have to. The pain just went away the second week of May 2022. I still can't chew on that side of my jaw. Then my hand started aching and when I wake up in the morning my right leg is still aching. I am still having bad headaches as well. So I went to the doctor on yesterday and I had a mark on my right leg and my doctor did and ultra sound and found my lump nodes to be swollen and my ankles are swollen. She said that I have the symptoms of COVID but I didn't have COVID and my doctor said that I may have theses symptoms for at least another 3 months. Test was ran. My tests haven't come back as of yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Blood Panel, Ultra sound test haven't come back yet.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Mirtazapine 30mg, Bell Bladder Tea, and Montmorency Cherry Juice,
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Body temperature increased
Chest pain
Chills
Dyspnoea
Fatigue
Mobility decreased
Pain
Pyrexia
Symptomtext
The evening after getting the vaccine developed severe chills and high fever (104), body aches, shortness of breath and couldn't get out of bed. High temp and fatigue lasted for following week. Still experiencing occasional low-grade fever, chest pain and shortness of breath. Went to the dr week of 5/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Bloodwork
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Aspirin
- Allergien
- Penicillin, Lidocaine
- Vorherige Impfungen
- Fainted after 1st flu shot
- Staat
- MD
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Diarrhoea
Extra dose administered
Tremor
Symptomtext
About 3 hours after vaccine she developed chills, could not get warm and started shaking violently. This lasted lasted 12 hours. She developed diarhea after this and still has it today but it is getting some better. She contacted her oncologist for medical advice. She had the Covid Virus after getting the 2nd covid vaccine dose that lasted 7 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cancer X 3 (2 non Hodgkin's lymphoma and 1 breast cancer) Anxiety
- Andere Medikamente
- Synthroid, omeprazole, pravastatin, 81mg aspirin, Vitamin D, Xanax, Ziprasidone, Anastrozole, B12
- Allergien
- sulfa codeine erythromycin Biaxin Tamiflu
- Vorherige Impfungen
- pt says she was told she had a reaction after her one of the Covid doses but she cannot not remember. She states she has had so
- Staat
- NE
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 12.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 11,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase normal
Albumin globulin ratio
Anion gap
Aspartate aminotransferase normal
Asthenia
Atrioventricular block second degree
Basophil percentage decreased
Blood albumin decreased
Blood alkaline phosphatase increased
Blood bilirubin increased
Blood calcium decreased
Blood chloride normal
Blood creatinine normal
Blood glucose normal
Blood potassium normal
Blood sodium normal
Blood urea nitrogen/creatinine ratio
Blood urea normal
Symptomtext
Pneumonia, Sepsis Chief Complaint Arrived via Rescue. Reports patient had low SpO2 and fever. Squad arrived to find pt lethargic, 98.8 temp and 92% on room air. History of Present Illness 81-year-old male presents to emergency department via ambulance for evaluation of lethargy, weakness, low SPO2 and a fever this morning. The patient resides at assisted living facility and staff reported that the patient was not wanting to get up this morning and was lethargic, they checked a temperature and reported that he had a fever as well as a oxygen level of 86% on room air. They notified family of patient's symptoms. The patient does complain of a sore throat. Has an occasional cough. He denies any chest pain or shortness of breath. He has been fully vaccinated against COVID-19. Staff did report that the patient had a fall on Saturday, reported that the patient slipped out of his chair. Fall was witnessed. He does have a history of falls. Family was notified. Family reports that the patient was at his baseline yesterday. The patient is anticoagulated on Eliquis due to atrial fibrillation. He denies a headache or dizziness. He denies any neck or back pain. He denies any chest pain or shortness of breath. He denies abdominal pain, nausea, vomiting or diarrhea. He denies any other sites of pain. Review of Systems Constitutional: Positive for fever, no chills, positive for weakness and fatigue Eye: No recent visual problems ENT: No ear pain, nasal congestion, positive sore throat Respiratory: No shortness of breath, ocass cough, no wheezing Cardiovascular: No Chest pain, Gastrointestinal: No abdominal pain, nausea, vomiting, diarrhea, Genitourinary: No dysuria, no frequency Musculoskeletal: No back pain, neck pain Integumentary: No rash Neurologic: Alert & oriented X 4, no headache, no dizziness, no numbness or tingling All systems otherwise negative/review of systems reviewed as documented in chart Physical Exam Vitals & Measurements T: 37.1 ?C (Oral) HR: 88(Peripheral) HR: 87(Monitored) RR: 16 BP: 127/66 SpO2: 98% HT: 186.000 cm WT: 108.000 kg BMI: 31.220 O2 Therapy: Room air General: Alert and oriented, well nourished, no acute distress. Eye: PERRL, EOMI, normal conjunctiva. HENT: Normocephalic, clear tympanic membranes, normal hearing, moist oral mucosa. Neck: Supple, non-tender, no lymphadenopathy. Lungs: Faint crackles bilateral lower lobes, diminished right lower lobe, clear to auscultation bilateral upper lung fields, non-labored respiration. Heart: Normal rate, regular rhythm, no murmur,trace-1+ pedal edema. Abdomen: Soft, non-tender, non-distended, normal bowel sounds, no masses. Musculoskeletal: No deformity, no tenderness or swelling. Skin: Skin is warm, dry and pink. Neurologic: Awake, alert and oriented x 3, no focal neuro deficits, globally weak. Psychiatric: Cooperative, appropriate mood and affect. Assessment/Plan 1. Pneumonia J18.9 Afebrile, non-toxic appearing. Presented to ED for lethargy, eval of hypoxia and reported fever from facility. Sp02 92% on room air. The patient has known dementia, family reports the patient is lethargic today and is not his normal. The patient does respond appropriately to questions. The patient does complain of generalized weakness. ECG shows sinus tachycardia with second-degree AV block, no ST segment elevation. He does have crackles bilateral lower lobes, diminished right lung base. 1 view chest x-ray shows right lower lobe infiltrate. The patient does have an elevated white blood cell count 18,000, procalcitonin normal at 0.27, CRP elevated at 4.3. Curb 65 score is 2 points placing the patient in a moderate risk group. Ordered levofloxacin IV for the patient. We will closely monitor SPO2. Current SPO2 94%. COVID swab was negative. Plan to admit the patient for observation due to increased risk for worsening symptoms. Orders: SARS-CoV-2 (COVID-19) PCR (GeneXpert), Nares/Nasal Swab, Stat collect, 05/23/22 8:30:00, Stop date 05/23/22 8:30:00, Nurse collect, No, Yes, 05/23/22, Unknown, No, Yes, Not Pregnant Urinalysis with Microscopic Standard, Urine, Stat collect, 05/23/22 7:43:00, Stop date 05/23/22 7:43:00, Nurse collect XR Chest 1 View Portable, 05/23/22 7:43:00, Routine, 05/23/22 7:43:00, Lethargic, No, Transport Mode: Stretcher, , No, , No, Rad Type Notified Dr of admission. Risk Statement (what is the risk to this patient if they are NOT hospitalized): Risk for worsening mental decline due to infection, risk for falls leading to injury due to weakness related to infection, risk for sepsis, risk for hypoxia leading to respiratory arrest and/or death. ADMISSION LEVEL: Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Lab Results Test Name Test Result Date/Time Sodium Level 138 mEq/L 05/23/2022 08:03 Potassium Level 4.0 mEq/L 05/23/2022 08:03 Chloride Level 103 mEq/L 05/23/2022 08:03 CO2 26 mmol/L 05/23/2022 08:03 Anion Gap 12 mmol/L 05/23/2022 08:03 Glucose Level 96 mg/dL 05/23/2022 08:03 BUN 17 mg/dL 05/23/2022 08:03 Creatinine Level 1.1 mg/dL 05/23/2022 08:03 BUN/Creat Ratio 15 05/23/2022 08:03 GFR AA 81 05/23/2022 08:03 GFR Non AA 67 05/23/2022 08:03 Calcium Level 8.2 mg/dL 05/23/2022 08:03 Bili Total 1.1 mg/dL 05/23/2022 08:03 Alk Phos 126 unit/L (High) 05/23/2022 08:03 AST/SGOT 29 unit/L 05/23/2022 08:03 ALT/SGPT 33 unit/L 05/23/2022 08:03 Protein Total 6.5 g/dL (%) 05/23/2022 08:03 Albumin Level 3.0 g/dL (%) (Low) 05/23/2022 08:03 Globulin 3.5 gm/dL (High) 05/23/2022 08:03 A/G Ratio 1 05/23/2022 08:03 CRP 4.3 mg/dL (High) 05/23/2022 08:03 Procalcitonin PMC 0.27 ng/mL 05/23/2022 08:03 WBC 18.8 x10^3/mcL (High) 05/23/2022 08:03 RBC 4.25 x10^6/mcL (Low) 05/23/2022 08:03 Hgb 12.9 g/dL (%) (Low) 05/23/2022 08:03 Hct 40 % (Low) 05/23/2022 08:03 MCV 93 fL 05/23/2022 08:03 MCH 30 pg 05/23/2022 08:03 MCHC 32 g/dL (%) 05/23/2022 08:03 RDW 19.3 % (High) 05/23/2022 08:03 Platelet 233 x10^3/mcL 05/23/2022 08:03 Auto Lymph % 2 % 05/23/2022 08:03 Auto Neut % 80 % (High) 05/23/2022 08:03 Auto Mono % 14 % (High) 05/23/2022 08:03 Auto Eos % 0 % 05/23/2022 08:03 Auto Baso % 0 % 05/23/2022 08:03 Neut Abs# 15.0 x10^3/mcL 05/23/2022 08:03 Blood Glucose, Capillary. POC 94 mg/dL 05/23/2022 07:35 Diagnostic Results Chest x-ray ED provider interpretation, focal infiltrate noted right lower lobe ECG ECG shows sinus rhythm with second-degree AV block. No ST segment elevation.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- atrial fibrillation, BPH, hypertension, hyperlipidemia, peripheral vascular disease, hypothyroidism
- Andere Medikamente
- amiodarone apixaban atorvastatin enalapril finasteride levothyroxine lorazepam
- Allergien
- red dye, cephalosporins, sulfa drugs
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 19.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Body temperature increased
Fatigue
Migraine
Muscle spasms
Paraesthesia
Restlessness
Sleep disorder
Symptomtext
PATIENT EXPERIENCE RESTLESSNESS BEGINNING SHORTLY AFTER MIDNIGHT-ON & OFF AWAKENING THROUGHOUT THE EARLY MORNING HOURS. THIS MORNING WOKE UP WITH A MIGRAINE, TINGLING HANDS, LEG SPASMS, BACK PAIN, AND EXTREME FATIGUE IN SPITE OF TYLENOL DOSES.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- TEMPERATURE TAKEN 5-20-22 AT 8:30AM & IN SPITE OF RECENT TYLENOL DOSE, SHE HAD 100.4 TEMPERATURE.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- MIGRAINES
- Andere Medikamente
- UNKNOWN
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Heart rate increased
Hypertension
Ventricular extrasystoles
Symptomtext
I received my 2nd booster shot on 04/22/2022 and on the same day I experienced that my heart beat was really fast, my blood pressure was very high, that I almost called 911 and PVC wasn't normal. My blood pressure stayed for 22 weeks. My heart rate was high for 3 weeks and my heart rate is 55-57 which is normal and it was 70-80. On May 13/2022, it finally settled down. I called my doctor I told her that I was taking extra on my blood pressure med and she said it was ok to do that and it stated coming down. At night, my PVC was high so I was taking vallum to lowered it down. I did EKG before I got my booster shot and it was ok but after the vaccine everything went out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- thyroids, hypertension, PVC
- Andere Medikamente
- regular meds- levothyroxine, amlodipine besylate, atorvastatin, losartan -hctz, vitamin multi, glucosamine, omega3 therapy, calcium, once a week alendronate sodium
- Allergien
- codeine, artificial fragrances, seasonal allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 09.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 11,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Pruritus
Symptomtext
Had the feeling in both hands that pins were being poked in all areas and became very itchy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- No tests visited my dermatologist
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- 27.04.2022
- Beginn
- 15.05.2022
- Tage bis Beginn
- 18,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Dyspnoea
Fatigue
Headache
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
After dose 4 vaccine, I started having shortness of breath, headache and fatigue. I did a home Covid test on 5-8 and it was positive. The next day, I called my doctor on 5-9 and he had me go to an urgent care for a follow up test. I had a follow up Covid test on 5-9. It also came back positive and I was given a prescription for Paxlovid to take over 5 days. I had problems getting the Paxlovid and I am just on day 2 but I am feeling much better today. Headaches and shortness of breath have decreased. I am reporting my breakthrough case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Home test Covid on 5-8-2022 then Office Covid test on 5-9-2022, both positive results.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Arthritis; PTSD
- Andere Medikamente
- Amlodipine 10mg daily, Chondroitin (osteobioflex) 1 daily, Atorvastatin 20mg 3 times weekly, Hydrochlorothiazide 25mg daily, Lisinopril 40mg daily, OTC Magnesium lactate 84mg daily, Metoprolol 100mg daily, Vit B complex OTC daily, OTC Mens
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 16.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Erythema
Paraesthesia
Urticaria
Symptomtext
Severe, severe hives all over and severe redness of face, as well as burning and prickly feeling on face. I began taking Benadryl when the symptoms first occurred. I ended up going to Hospital Urgent Care to seek treatment because, as time went on, I was not getting any relief. I was then prescribed p\Prednisone, which I am taking, and also told to increase dose and continue to take Benadryl.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type II Diabetes, High Cholesterol, Hashimoto?s Thyroiditis
- Andere Medikamente
- Ozempic, Simvastatin, Lisinopril, levothyroxine, Glucosamine/Chondroitin, Cranberry tablets, Turmeric, Magnesium, Vitamin D
- Allergien
- Penicillin, latex
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 30.04.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Laboratory test
Pneumonia
Symptomtext
I couldn't breath so I went to the hospital, they ran a lot of test. I was diagnosed with pneumonia and admitted into the hospital for a week. I was prescribed levofloxacin 750mg and prednisone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 6,0
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- COPD; IBS; Emphysema; Heart Disease.
- Andere Medikamente
- Clopidogrel 75mg; losartan 50mg; escitalopram 20mg; metoprolol 100mg; atorvastatin 40mg; ranolazine 2000mg; diltiazem 180mg; Trelegy; Centrum silver; vitamin B.
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Pain in extremity
Peripheral swelling
Symptomtext
Arm swollen days later. Painful. Unable to lift with arm. Plan to go to doctor today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 14.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Chills
Diarrhoea
Dizziness
Erythema
Fatigue
Feeding disorder
Flushing
Migraine
Nausea
Pain in extremity
Sleep disorder
Swelling
Swelling face
Throat tightness
Vomiting
Symptomtext
1. my throat started to close within 10 minutes, plateaued at 15 minutes, went away at 40 minutes 2. face and neck and upper chest swelled and flushed red for 4 days 3. severe nausea--I'm still mildly nauseous 4. vomiting --1 day 5. diahhreah--I still have mild diahhreah 6. migraine headaches that didn't respond to Tylenol or Aspirin initially and woke me out of sound sleep at 2 am; lasted for 4 days 7. dizziness- 8 days 8. extreme fatigue--I'm still moderately fatigued 9. sever sore arm--arm is slightly sore now 10. chest pain in the middle of my chest, went away upon lying down, upon getting up came back, lasted 3 days, I still feel it occasionally 11. inability to eat solid foods for 4 days due to vomiting and nausea 12. severe chills at night and in the day--I still get chills at night occasionally
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Celiac disease, post lyme hypersensitivity, supra gastric belching, rapid transit, failed peristalsis low LES pressure
- Andere Medikamente
- Magnesium, vitamin D, Vitamin C, calcium citrate, fish oil, lutein, Refresh eye drops, Biotin,
- Allergien
- gluten, Reglan, Baclofen, sulfa drugs, sulfites, sulfates, doxycycline, flatly, copra, cortisone, betamethasone, lanolin, wool, aloe, ducal temporary dental cement
- Vorherige Impfungen
- Zostra 2010, got a mild case of shingles extraquadvalient flu vaccine 10/21--chills, body aches, headaches, exhaustion for 2 wee
- Staat
- PA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 11.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Condition aggravated
Dizziness
Dyspnoea
Feeling abnormal
Gait disturbance
Hyperhidrosis
Hypophagia
Mobility decreased
Muscular weakness
Night sweats
Pain
Pain in extremity
Tachycardia
Symptomtext
Patient COMPLAINED OF WEAKNESS AND NOT FEELING RIGHT, WAS TACHYCARDIC
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Patient WAS TAKEN TO THE HOSPITAL DUE TO INCREASE INCREASE WEAKNESS AND TACHYCARDIC
- Aktuelle Erkrankungen
- HISTORY OF LEG PAIN/FOOT PAIN, HAS BEEN COMPLAIN OF INCREASE PAIN TO RIGHT FOOT AND LEG, DOES HAVE HISTORY OF FRACTURE TO RIGHT LEG AND FOOT WITH PINS AND SCREWS. THIS MORNING COMPLAINS WERE INCREASE WEAKNESS TO LEGS: Patient was seen as a medical emergency this morning. He called the emergency at 0630 due to weakness and not feeling right. He stated that he had his COVID Moderna Booster 5/11/22 and initially felt great and was able to go outside. Later last night he stated that his body just started to ache and overall he felt terrible. Throughout the night he stated that the body aches increased along with sweating through his clothing, mild shortness of breath, dizziness, and weakness. He was able to eat dinner yesterday, but today has not ate so far. He stated that he has been drinking increased fluids including water and coffee to try and stay hydrated. He stated that he was so weak he could barely get out of his bed and needed assistance to walk up the stairs. He does admit that he has never told this provider that prior to this he was seeing cardiology for a medical history of heart failure. He does not remember what medications he was on for this, but remember the doctors name and which hospital he worked through.
- Vorgeschichte
- PSORIASIS PAIN IN LIMBS DEPRESSIVE DISORDER
- Andere Medikamente
- TYLENOL 500MG BID REMERON 15 MG DAILY ARISTOCORTA CREAM BID
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Dyspnoea
Electrocardiogram
Joint swelling
Lip swelling
Peripheral swelling
Pyrexia
Rash
Respiratory tract congestion
Symptomtext
Arm and shoulder swelling, rash down back congestion, fever lips swollen and struggling to breathe, possible viral illness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Blood, EKG
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- COPD
- Andere Medikamente
- Claritin D, albuterol sulfate, budesonide, singular
- Allergien
- peanuts, sulfa products
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Dizziness
Fatigue
Mobility decreased
Nausea
Pyrexia
Retching
Sleep disorder
Vomiting
Symptomtext
About 9 pm, 11 hours after booster, high fever of 101 which lasted all night., upset stomach. About 14 hours after booster, severe nausea, dry heaving, some throwing up, light headed, didn't want to move because of nausea. Lasted several hours. No sleep. Next morning, nausea almost gone, very tired. Fever abated by mid morning. Fatigue the two days after booster. I had no symptoms with first three shots except for sore arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Had UTI confirmed on 4/11. Took cefpodoxime Proxetil 100 MG antibiotic for 5 days, last day was April 17th. Also took probiotic for approximately from April 14 to approximately April 20.
- Vorgeschichte
- Diagnosed with Afib in 2012 but heart monitor test in 2021 did not show it.
- Andere Medikamente
- Vitamin B2,100mg daily; D3,1000IU daily
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest pain
Chills
Computerised tomogram
Dyspnoea
Dyspnoea exertional
Fatigue
Fibrin D dimer increased
Muscle contracture
Pain
Pain in extremity
Pain in jaw
Pyrexia
Scan with contrast
Symptomtext
I started having chest pain periodically. It felt like a muscle contraction. It was for a few days. I had pain in my upper left arm that was there for several days before. On the 21st I experienced shortness of breath. I got short of breath carrying groceries to the car. I also had pain in my jaw. I also had fever, chills, and achiness the day following vaccination. My D-dimer test came back abnormal. I was given a CAT scan for blood clots. This afternoon I have a stress test and they want to do a Holter monitor. I continue to have fatigue and shortness of breath episodes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Blood Test CAT Scan Chest with Contrast CAT Scan
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- GERD Elevated Tryptase Levels Arthritis
- Andere Medikamente
- Synthroid Evoxac Nexium Baclofen Fish Oil Baby Aspirin Calcium Vitamin B12 Vitamin D3 Magnesium Probiotic Cholestoff
- Allergien
- Penicillin Erythromycin Hyoscyamine Tape Adhesive Tobacco Smoke Celery Avocado Grapes Strawberries Lettuce
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 08.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Joint injury
Limb injury
Pain
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
- NC
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypotension
Nausea
Urinary incontinence
Visual impairment
Symptomtext
Developed hypotension, complete loss of bladder control (which I did not know until felt wet), nausea, and dim vision.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Osteoarthritis
- Andere Medikamente
- Naproxen, Famotidine, Omeprazole, Percocet, PreserVision 2, Omega 3, Vitamin C and D, Calcium, CBD gummies
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 25.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Arrhythmia
Atrioventricular block
Blood test
Cardiac pacemaker insertion
Chest X-ray
Computerised tomogram
Echocardiogram
Electrocardiogram
Headache
Immune-mediated adverse reaction
Myocardial necrosis marker
Tachycardia
Symptomtext
On 04/25/2022 ,I went to sleep with a headache, I woke up with heart arrhythmia. I went to the ER on the 04/26/2022, as I was in tachycardia, I developed a heart block. My medications have been changed from Aspirin 81mg once a day to Eliquis 5mg twice a day. I have had to get a pace maker put in. The doctors feel the immune response to the fourth dose of the vaccine caused the arrhythmia. The doctors say my medications may change as they monitor my heart through the pace maker.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- Chest x-ray, Cardiac ultra sound, CAT scan, Bloodwork for heart enzymes, EKG, Echocardiogram
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Sotolal 80mg 1 po bid, Vitamin D 1 po qd, Levothyroxine 125mcg 1 po qd, Linzess 1 po qd, Multivitamin 1 po qd, Omeprazole 20mg 1 po qod, Vesicare 5mg 1 po qod, Estridial Cream topically biw, Aspirin 81mg 1 po qd
- Allergien
- NKDA, KKFA
- Vorherige Impfungen
- COVID-19
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 27.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Fatigue
Palpitations
Symptomtext
Approximately a few days after my 2nd booster shot (Dose 4), I experienced the following symptoms: Fatigue, Raising heart palpitations, Tightness in the chest. I took my daily medication of baby aspirin to help ease my condition. I called my doctor and was advised that it's not unusual for them to hear for senior people to get the same symptoms after getting vaccinated. After a day, I was feeling back to normal again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin B12, Vitamin D3, Zinc, L-lysine, Aspirin, Flonase
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Heart rate
Insomnia
Symptomtext
difficulty breathing; difficulty sleeping; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (difficulty breathing) and INSOMNIA (difficulty sleeping) in a 73-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Apr-2022, the patient experienced DYSPNOEA (difficulty breathing) and INSOMNIA (difficulty sleeping). At the time of the report, DYSPNOEA (difficulty breathing) and INSOMNIA (difficulty sleeping) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 20-Apr-2022, Heart rate: elevated (abnormal) elevated. Concomitant medications was not provided by the reporter. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220420; Test Name: elevated heart rate; Result Unstructured Data: elevated
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 23.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Contusion
Mobility decreased
Pain in extremity
Peripheral swelling
Symptomtext
Severe pain began on top of my left foot in the evening( about 32 hours after receiving my Moderna second booster). I had only had Pfizer brand vaccines for my 3 previous vaccines. The pain felt like a piece of heavy machinery had been dropped on top of my foot. I was unable to bend the foot to flex it up or down within the hour and it began to rapidly swell. I had not injured my foot or bumped it since getting the vaccine (rested for 24 hours after getting the second booster). My husband who happens to be a physician examined it and said it was terrible swollen and bruised above the swelling. The pain was about a 9.5 on a scale of 1-10. I took Acetaminophen and iced it for an hour. The swelling was totally gone in the morning when I woke up and I had no pain whatsoever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Vestibular neuritis
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- -
- Allergien
- Bee stings; Latex sensitivity
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Abdominal distension
Abdominal pain lower
Adverse reaction
Condition aggravated
Diverticulitis
Inflammation
Pain
Pyrexia
Vaccine positive rechallenge
Symptomtext
On Booster 3 I experienced a severe 9 day Diverticulitis event, thought to be random and surgery was considered, but being in middle of a covid surge, it was avoided. I got a CT abdomen and antibiotics, fever to 104, negative covid test x 3. Then I got Covid shot 4 last week. Within a day I started to experience again symptoms of Diverticulitis, same symptoms, pain, inflamation, abdominal bloating, LLQ pain, fever: I started the Levoquin and gram negative antibiotics within 6 hours of definitive symptoms. They still lasted four solid days, but not to the extent as the first major event after Moderna 3. Moderna 4 had the same time of onset of symptoms, and when the connection was made to the proximity of both events, I felt it important to report this adverse reaction. Going forward what do I do wrt vaccination, a different type or do I pre treat with Levoquin before the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- September 14th, Dr. : CBC (Right shift), CMP, PSA (lower quadrant pain as well with abdominal distention), CT abdomen with contrast: GI urgent consult, then EGD/Colonoscopy with confirmed diverticulitis on CT. Covid shot 4: no test, I just took the antibiotics and persisted
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Irritable Bowel Syndrome, GERD, Diverticulosis
- Andere Medikamente
- Prolosec 20mg; Phentermine 37.5mg; ASA 87mg
- Allergien
- Keflex
- Vorherige Impfungen
- Just to the Covid Shot #3, then followed by #4 with same symptoms
- Staat
- OH
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 22.11.2023
- Impfdatum
- 16.11.2023
- Beginn
- 16.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Headache
Nausea
Pain
SARS-CoV-2 test negative
Vomiting
Symptomtext
Patient started to exhibit hours after vaccine nausea, vomiting , diarrhea, headache and body aches. She reports she was up all night vomiting. She thought she may have had COVID and took 3 COVID test at home which came back negative. Her nausea and vomiting last through the night but then went away. She is now still feeling headache and body ahces. She presented to clinic today 11/22 with symptoms and wanted to get another COVID test and evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 11/22/23- COVID test negative.
- Aktuelle Erkrankungen
- patient states she had a little congestion but related that to allergies. She recently visited another city.
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 27.10.2023
- Impfdatum
- 06.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Myalgia
Pyrexia
Symptomtext
head and body/aches; body/aches; fever; fatigue; This spontaneous case was reported by a patient and describes the occurrence of HEADACHE (head and body/aches), MYALGIA (body/aches), PYREXIA (fever) and FATIGUE (fatigue) in a 63-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 056M21A) for COVID-19 prophylaxis. The patient was not diagnosed with/ tested positive for COVID-19. Previously administered products included for Anxiety: Clonazepam since 21-Apr-2020; for Product used for unknown indication: Pfizer on 19-Feb-2021, Pfizer on 09-Mar-2021, Pfizer on 09-Oct-2021 and Flu vaccine on 01-Oct-2023. Past adverse reactions to the above products included No adverse event with Clonazepam, Flu vaccine, Pfizer, Pfizer and Pfizer. Concurrent medical conditions included Osteoporosis (just). On 06-May-2022, the patient received fourth dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced HEADACHE (head and body/aches), MYALGIA (body/aches), PYREXIA (fever) and FATIGUE (fatigue). At the time of the report, HEADACHE (head and body/aches), MYALGIA (body/aches), PYREXIA (fever) and FATIGUE (fatigue) had resolved. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. After each of her 6 COVID vaccinations, Patient have experienced head and body/aches, fever, and fatigue for approximately 36 hours. Patient would like to know was it unusual to have fevers, a few aches and fatigue after having the Moderna Spikevax vaccine. She reported it packed more of a punch this time. This one hit her pretty hard. She was feeling well last night and then started feeling achy and had a fever but not high. She was really sick on Sunday night after she got the vaccine and typically has a fever. She was just concerned since it was 36 hours after the vaccine that she was still experiencing these reactions. No treatment information was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-743743 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 10-Oct-2023: Live follow up received contains reference number added. On 23-Oct-2023: Live Follow up received: Date of administration of suspect vaccine, historical vaccine, events has been added, and batch number updated, narrative was updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-743743:Monovalent case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Osteoporosis (just)
- Vorgeschichte
- Comments: The patient was not diagnosed with/ tested positive for COVID-19.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- F
- Eingang
- 11.10.2023
- Impfdatum
- 02.05.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Symptomtext
she has experienced a soreness whenever she lays down on her left arm/shoulder; This spontaneous case was reported by a consumer and describes the occurrence of ARTHRALGIA (she has experienced a soreness whenever she lays down on her left arm/shoulder) in an 87-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 056M21A) for COVID-19 prophylaxis. No Medical History information was reported. On 02-May-2022, the patient received fourth dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 02-May-2022, after starting mRNA-1273 (Spikevax), the patient experienced ARTHRALGIA (she has experienced a soreness whenever she lays down on her left arm/shoulder). At the time of the report, ARTHRALGIA (she has experienced a soreness whenever she lays down on her left arm/shoulder) had not resolved. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. She had received 5 doses of the Moderna COVID-19 vaccines on: 3-MAR-2021 with lot number 038K20A, On 31-MAR-2021, lot number 023M20A, On 26-NOV-2021, lot number 058H21A, On 2-MAY-2022, lot number 056M21A. On 20-SEP-2022, lot number AS7148B After receiving the injection of the Moderna vaccine on 2MAY2022 she had experienced a soreness whenever she lays down on her left arm/shoulder. Other times if she' sleeping it hurts so bad that it wakes her up. No vaccines 4 weeks prior to COVID-19 vaccines. No medications or treatments provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 05.10.2023
- Impfdatum
- 02.05.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pain
Pain in extremity
Symptomtext
Patient says she experienced a sore arm and pain in shoulder that never went away. She believes it was from vaccine. She has pain in shoulder in middle of the night and states throbbing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 09.06.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 114,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
Loss of personal independence in daily activities
Oropharyngeal pain
Productive cough
Respiratory syncytial virus test positive
Rhinorrhoea
SARS-CoV-2 test positive
Streptococcus test negative
Throat irritation
Symptomtext
On 9/28/2022, I was exposed to COVID-19. On 10/1/2022, I went to a party at noon. While I was there, I noticed my nose was running a little, and I had a slight tickle in the back of the throat. After about an hour, I left and went home. I took a nap and ended up sleeping until the morning of 10/2/2022. When I woke up, I had a painful, burning sensation in the back of the throat, plus phlegm. This continued for about five days and then began to subside. I was not able to function for another week. On 10/2/2022, I took a home antigen test and got a positive result. I had a telehealth visit with a local urgent care clinic on 10/3/2022, and I was prescribed Paxlovid, which I began taking 10/6/2022. I had no perceived improvement after beginning the medicine, but my symptoms also did not worsen. I took OTC Mucinex and Ricola lozenges to help treat the symptoms, but they weren't very effective. After about a week, I began to feel a little better. I felt much better after two weeks, but it took a month before I felt like I was back to normal. On 11/30/2022, I was again exposed to COVID-19. On 12/3/2022, I began to develop a sore throat, but it was less intense than it had been in October. I thought I had strep throat. I had sore throat and runny nose that continued for several days, but I powered through them and continued with my normal activities. Since I had recently had COVID-19, I didn't think I could possibly get it again so soon. On 12/9/2022, I went to a local urgent care clinic to undergo a strep test. A throat swab was performed, and I was given a brief physical exam before I was sent home. I learned within minutes after being tested that I was negative for streptococcus, but on 12/10/2022, I found out that I had tested positive for COVID-19 and RSV. I was offered Paxlovid, but I decided not to take it, because my symptoms this time around were less severe than they had been the first time around. I just treated my symptoms with OTC Mucinex and Ricola lozenges, but they didn't seem to help much. Because the symptoms were less severe this time, I was able to function well enough to work from home. I just took lots of naps and slept a lot. The symptoms lasted for about two weeks. It took a full month before I returned to my pre-COVID-19 functioning level.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 02OCT2022 - Home Antigen Test - Positive Result; 09DEC2022 - Throat Swab -- Negative for Streptococcus, Positive for COVID-19 and RSV
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Overweight
- Andere Medikamente
- Mountain Peak Nutritionals HTN Support; Baby Aspirin; Vitamin C; Zinc; Vitamin D; Vitamin K; Vitamin E; Vitamin A
- Allergien
- Sulfa Drugs
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 30.05.2023
- Impfdatum
- 26.04.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 12,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
I have been experiencing chronic head-to-toe hives for the past year. Hives started two weeks after my second Moderna booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- No tests, just visual confirmation of condition as conducted by my allergist/immunologist.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- sulfa (as a child)
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 16.05.2023
- Impfdatum
- 14.05.2022
- Beginn
- 04.02.2023
- Tage bis Beginn
- 266,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Computerised tomogram abnormal
Dacryostenosis acquired
Fatigue
Increased viscosity of upper respiratory secretion
Lacrimation increased
Malaise
Nasal congestion
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I started feeling sick with nasal congestion, stuffiness in my head and had a sore throat. I took a COVID-19 Home Test which was expired, and it was negative. The next day it was the same symptoms but i was tired. I was a little better the next day but was completely better. Two days later I took another test and that was positive. I did reach out to my health care provider, and they did offer me Methyletrednisolone and I did take that. I now have lingering issues. I have developed watery eyes and I have seen my eye doctors about this. I have been told that I have blocked tear ducts but they water. I also have major congestion. I have had a CT Scan and they see that I have some mucus built up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Famotine; Florajen; Multivitamin; Low Dose Aspirin; Vitamin D3; Clopidogrel; Lisinopril; Omega Three Fish Oil; Osteobiflex; Crestor; Metoprolol
- Allergien
- Sulfa; Penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 15.05.2023
- Impfdatum
- 15.05.2022
- Beginn
- 28.02.2023
- Tage bis Beginn
- 289,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Cardiovascular symptom
Electrocardiogram
Herpes zoster
Malaise
Pain in extremity
Symptomtext
I had my vaccination on 05/15/2022. I started to feel unwell on 02/28/2023. I went to my primary doctor on 03/03/2023 with feelings of heart attack symptoms with left arm pain. I could not be upright without pain in my arm. I had an EKG on this date. I went to the emergency room on 03/05/2023 as my symptoms were much worse. I was determined to have Shingles by default. I had a repeat EKG. I presently feel better on 05/15/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- 03/03/2023 and 03/05/2023 EKG 03/05/2023 Blood Panel
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism; History of Migraines
- Andere Medikamente
- Synthroid; Olive Leaf Extract
- Allergien
- N/A
- Vorherige Impfungen
- Shingles vaccinations; flu like symptoms 12/2021 and 03/2022
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 15.05.2023
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2023
- Tage bis Beginn
- 365,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain
Back pain
Computerised tomogram normal
Dyspepsia
Electrocardiogram normal
Full blood count normal
X-ray normal
Symptomtext
I had lower back and abdominal pain. I went to Urgent Care, where they sent me to the emergency room. They ran a lot of tests on me, EKG, two CAT scans, CBC bloodwork, X-rays. All tests came back as normal, showing nothing that should be causing the pain that I am experiencing. I was given medication to help reduce acid before I eat and something for pain. I am starting to feel better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- 12MAY2023 EKG - normal; 12MAY2023 CAT scan - normal; 12MAY2023; CBC bloodwork - normal; 12MAY2023 - X-rays - normal
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Gout
- Andere Medikamente
- Enalapril; Metoprolol Tartrate; Meloxicam; Montelukast; Allopurinol; Cranberry Capsule; Allergy Nasal Spray
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 15.05.2023
- Impfdatum
- 13.05.2022
- Beginn
- 20.03.2023
- Tage bis Beginn
- 311,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test abnormal
COVID-19
Chills
Headache
Oxygen saturation decreased
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I was positive for COVID-19 pn 19MAR2023, I had fever and chills headache and a respiratory congestion. My blood levels were low, I went to the emergency room and they gave me paxlovid that was regulated for me because of my liver issues. They were concerned because my oxygen has been abnormal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 19MAR2023 COVID-19- Test- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroid; Hyperlipidemia; Depression
- Andere Medikamente
- Lavasa Thyroid; Venlafaxine; Rosuvastatin; Albuterol; Turmeric
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 12.05.2023
- Impfdatum
- 09.05.2022
- Beginn
- 11.05.2023
- Tage bis Beginn
- 367,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Decreased appetite
Fatigue
Inflammation
Lethargy
Symptomtext
I started feeling exhausted struggled to eat and was Lethargic couldn't eat Sunday the 15th went to urgent care I was diagnosed with an inflammatory reaction I was prescribed 800 mg ibuprofen after taking first dose started to recover from event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid test
- Aktuelle Erkrankungen
- Penicillin: Amoxicillin
- Vorgeschichte
- Asthma, Chronic Sinusitis
- Andere Medikamente
- Multivitamin: Vitamin D3: Cinnamon: Elderberry: Probiotic: Biotin: Fish Oil: Echinacea: Kariva: Xyzal: Zolpidem: Rivatriptan
- Allergien
- Scopolamine
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 03.05.2023
- Impfdatum
- 29.04.2022
- Beginn
- 19.03.2023
- Tage bis Beginn
- 324,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Discomfort
Exposure to SARS-CoV-2
Feeling of body temperature change
Headache
Malaise
Pain
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse reaction to the vaccine. After being exposed to COVID-19, I started feeling ill on 03/16/2023. I had body aches and uncomfortable. I had extreme hot and cold symptoms with a headache when I went to the urgent care center. I tested positive for COVID-19 on 03/19/2023. I took an assortment of vitamins per my mothers-in-law direction, and it helped me recover faster. As of today, I am feeling better with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 19MAR2023 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Dairy
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 28.04.2023
- Impfdatum
- 24.04.2022
- Beginn
- 19.04.2023
- Tage bis Beginn
- 360,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Fatigue
Pain
SARS-CoV-2 test positive
Symptomtext
On 19APR2023 in the evening I had chills and fever that never reached over 99.4 but very bad chills and aches. Fatigue hit me hard that night. I slept well and the next morning I felt better and went to a funeral as an Usher which I was committed to do I stayed away from people and hugged nobody. I slept eleven hours total that Thursday fatigue was gone by Friday but coughing started and remained terrible through 24APR2023 but has been getting better since then. I am still testing positive as of this date 28APR2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 22APR2023 COVID-19 test, positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- COREG; amlodipine; XANAX; MIRAPEX; multivitamin; D3; biotin
- Allergien
- Sulfa; gabapentin
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 25.04.2023
- Impfdatum
- 24.04.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 144,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Dizziness
Fear
Heart rate increased
Illness
Loss of personal independence in daily activities
Malaise
Myalgia
SARS-CoV-2 test positive
Visual impairment
Wheezing
Symptomtext
I began to have muscle aches on the night of 9/15/2022 while I was in bed. I immediately knew that I was sick. I got up and took a home antigen test and got a negative result. On 9/16/2022, the muscle aches worsened. On 9/17/2022, I tested positive on a home antigen test. On 9/18/2022, I called the doctor's office and notified them of my situation. I was advised to stay home and rest and take vitamin C and Flonase. They also told me to use my albuterol inhaler if I ever had any trouble breathing; in the first week of my illness, I was wheezing during my illness, so I did end up using the inhaler. After about seven days, I felt like I could do more, so I attempted to do some light gardening. When I bent over three times in succession, though, I became very lightheaded. This scared me, because I had never fainted before. I thought that I might faint, though, so I immediately sat down. My heartrate was very fast at this point, and my vision went dim. I just sat quietly and waited until the feeling passed. That was when I realized that I had not yet recovered from the COVID-19 and that I should stay indoors and recuperate. At about two and a half weeks after the symptom onset, I finally had energy again. It was then that I resumed normal activities.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- 15SEPT2022 - Home Antigen Test - Negative Result; 17SEPT2022 -Home Antigen Test - Positive Result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes, Type II; Atrial Fibrillation; Acid Reflux; Hypertension
- Andere Medikamente
- Eliquis; Invokana; Metoprolol Tartrate; Prevacid Rx; Potassium Chloride; Losartan; Hydrochlorothiazide; Amlodipine Besylate; Albuterol Inhaler; Women's Probiotic; Daily Fiber; Glucosamine Potassium Sulfate Chloride; Calcium Citrate Plus D3
- Allergien
- Penicillin; Metoprolol Sulfate; Statins
- Vorherige Impfungen
- In 1974, I received a cholera vaccination. I had a fever above 102 and was bedridden afterwards for the rest of the evening.
- Staat
- CT
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 20.04.2023
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Cough
Fatigue
Musculoskeletal stiffness
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I tested positive for Covid-19 on January 15, 2023. I experienced chills, flexibility was off, fatigue, fever of 101. 00, bad cough. I was taking Tylenol for my symptoms and also Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Hypertension
- Andere Medikamente
- Matzim; Atorvastatin; Aspirin; Valsartan;
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 13.04.2023
- Impfdatum
- 20.05.2022
- Beginn
- 16.02.2023
- Tage bis Beginn
- 272,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Fatigue
Pain
Respiratory tract congestion
SARS-CoV-2 test negative
Wheezing
Symptomtext
2/16/2023 I was feeling fatigued, body aches, bad cough and congestion. I tested with an at home COVID Test and it was negative. I tested again for COVID on 2/20/23 and it was negative. I had an appointment with the doctor on 2/20/23 and was prescribed steroids. I called back on 2/22/23 and was prescribed an antibiotic. I was wheezing very badly. This lasted for four weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 18FEB23-At Home COVID Test- Negative; 20FEB23- At Home COVID Test- Negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Camahort Inhaler, Omeprazole, Crestor, Albuterol Inhaler, Lasix, Trazadone, Turmeric, Flonase, Agilease, Omega 3, Calcium with Vitamin D
- Allergien
- Hydrocodone, Oxycodone
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 17.03.2023
- Impfdatum
- 07.12.2022
- Beginn
- 23.01.2023
- Tage bis Beginn
- 47,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Feeling hot
Malaise
Pain
Paranasal sinus discomfort
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Assuming "adverse event" means when I had covid beginning on 1/23/23, my initial symptoms that first day were tiredness. On Day 2-5, I had a fever that ranged from 101-102 F. On Day 2, I took ibuprofen. After Day 5, the fever subsided. After that, I felt tired for about 3 weeks. Also, I felt like something in my sinuses right behind my nose--I wasn't congested but my sinuses felt clogged or some sort of odd pressure. That lasted for about 3 weeks. Occasionally, during the four week period of recovery, I would feel feverish and achy but I never had a fever except for the first few days. I sporadically took Mucinex during the period I wasn't feeling well but I don't think it made a difference. I did contact my doctor's office on 1/24/23 via their portal and they prescribed rest, fever reducers, cough medicine and mucinex, as needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Took a home rapid test on 1/24/23 which was positive. Took a home rapid test on 1/30/23 which was positive. Took a home rapid test on 2/3/23 which was negative.
- Aktuelle Erkrankungen
- None. Was seeing some temporary elevated blood pressure which is normal now.
- Vorgeschichte
- High cholesterol
- Andere Medikamente
- Rosuvastatin, Estrace, metamucil, multi vitamin
- Allergien
- Ancef, Lipotor
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 07.03.2023
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Symptomtext
Patient called reporter on 3/7/23, and stated that she had a red blotchy area surrounding injection site and then spread around her arm but remained localized, denied raised areas or itching and resolved in about 1 week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- Patient stated none
- Aktuelle Erkrankungen
- Multiple Sclerosis
- Vorgeschichte
- Multiple Sclerosis
- Andere Medikamente
- unknown
- Allergien
- patient states multiple allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 06.05.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 96,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cold type haemolytic anaemia
Cough
Diarrhoea
Fatigue
Haemoglobin decreased
Lymphocytosis
Monoclonal B-cell lymphocytosis
Oropharyngeal pain
Rash
SARS-CoV-2 test positive
Sinus disorder
Yellow skin
Symptomtext
On 05/06/2022 I received my Covid-19 vaccine. On 08/10/2022 I started having diarrhea, sore throat, cough, extreme fatigue, sinus issues; face started getting yellow; and breakouts on face. I tested positive on 08/11/2022 for Covid-19. Symptoms lasted about two weeks. Since Covid-19 I was diagnosed with Cold Agglutinin Disease , Monoclonal B -Cell and Lymphocytosis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Covid-19 - Positive; Hemoglobin- Decreased
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Armour Thyroid; Pristiq; Multivitamin; Vitamin D3; Vitamin C; Calcium; Vitamin B12; Vitamin B6; Biotin; Omega 3; Ginko;
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 06.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 21,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Attention deficit hyperactivity disorder
Bronchitis
COVID-19
Fatigue
Heart rate increased
Narcolepsy
SARS-CoV-2 test positive
Throat irritation
Wheezing
Symptomtext
On 06/06/2022 I received my Covid-19 vaccine. On 06/27/2022 I woke up feeling a little scratchy throat. I tested positive for Covid-19 two days after. I started getting bronchitis. After reaching out to my doctor I was prescribed PAXLOVID for 5 days. Symptoms started to lift after 3 days and by the 5th day tested negative for Covid-19. Post Covid effects are ADHD, Chronic Fatigue/narcolepsy, wheezing, elevated heart race, are the results of having Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- PCR (06/29/2022) positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Bronchitis; Sleep Apnea; GERD; Lactose intolerance; Fodmap Intolerance; Rosacea; BPH; Erythromelalgia; Brachioradial Pruritus; MCI; Dry eye disease; vitamin D deficiency; vitamin B12 deficiency; IBS; Fibromyalgia; Chronic fatigue Syndrome
- Andere Medikamente
- Lactase; SINGULAIR; MUCINEX; FLONASE; FLOVENT; coQ10; vitamin D2; vitamin B12
- Allergien
- Latex; sulfa drugs; iodine base Ct scan contrast dye; codeine
- Vorherige Impfungen
- Monkey pox 09/02/2022; 54; Site reaction that led to a big lesion on arm size of quarter dollar.
- Staat
- WV
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Contusion
Hyperaesthesia
Nodule
Pain
Pain in extremity
SARS-CoV-2 test negative
Symptomtext
My adverse event started after receiving the 4th dose. It happened within 20 minutes. My left arm was sore, and painful to touch. It lasted for 10 days. I also noticed a knot on my elbow. It was very painful to do anything or to lift. Between my thumb and index finger it was all black and bruised. I used a heating pad on my elbow for the knot. I thought it was normal but it concerned me when it took long time to heal. There wasn't much to do about it. I didn't seek care from my doctor. It resolved by itself.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- 25JAN2023 COVID-19 test negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D; elderberry; aspirin; probiotics; cranberry
- Allergien
- None
- Vorherige Impfungen
- Middle school, I had a second MMR and I passed out.
- Staat
- AL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 12.01.2023
- Impfdatum
- 13.07.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 138,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
COVID-19
Chills
Headache
Nasal congestion
Nasal discomfort
Pyrexia
SARS-CoV-2 test positive
Symptomtext
It was a real bad burning in my nose and nasal congestion. I thought it was a sinus infection because I get those frequently. I also had chills and a fever, and a headache. My blood pressure was also up. I took an at home COVID-19 test and it came back positive. I went to the doctor the next day and took another COVID-19 test which also came back positive. I was given PAXLOVID. It was also noted after the COVID-19 infection that I had some hypertension. I was told to take zinc and vitamin C, and I was put on low dose amlodipine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 28NOV2022 at home COVID-19 test positive; 29NOV2022 rapid COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Reflex Sympathetic Dystrophy; Palpitations
- Andere Medikamente
- Metoprolol; low dose naltrexone; levocetirizine; memantine; zinc; vitamin C; fish oil; vitamin D; MUCINEX; FLONASE
- Allergien
- BIAXIN; AZO GANTRISIN
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 01.01.2023
- Impfdatum
- 18.02.2021
- Beginn
- 01.01.2023
- Tage bis Beginn
- 682,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Decreased appetite
Nasopharyngitis
Pyrexia
Rhinorrhoea
SARS-CoV-2 test
Symptomtext
Cold like symptoms, fever 101.3 runny nose loss of appetite non productive cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- covid rapid tested
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Dementia, Alzheimer's, hyperlipidemia, cervicalgia, left bundle block vit d deficiency
- Andere Medikamente
- Colace, tab-a-vite Trazodone, vit b-1 vit d
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 30.12.2022
- Impfdatum
- 15.01.2021
- Beginn
- 09.12.2022
- Tage bis Beginn
- 693,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Chemotherapy
Computerised tomogram thorax normal
Malaise
Nasal congestion
Oxygen saturation decreased
Symptomtext
Patient was seen and examined. She was getting chemotherapy today with taxol and incidentally noted to have O2 desat to lowest of 89% for a brief second then comes back up to ~93. Her Heme/Onc physician was concerned for PE and asked that she be evaluated in ER. She was never symptomatic. In ER CTPE was negative and no other acute cardiopulmonary issues were identified. She had COVID19 about 3 weeks ago with mild symptoms and remains with nasal congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 29.12.2022
- Impfdatum
- 27.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antinuclear antibody positive
C-reactive protein increased
Fatigue
Joint stiffness
Musculoskeletal stiffness
Polyarthritis
Rheumatoid factor positive
Tenderness
Symptomtext
New onset polyarthritis, morning joint stiffness and fatigue persistent since the injection and still currently present. Tenderness and stiffness MCPs both hands and shoulders.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- +ANA screen on 08/25/2022. On 11/10/2022 elevated CRP 2.26 (N<1), +rheumatoid factor IgM 4.9 (N<3.5), ANA panel negative
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Diabetes type II, hypertension, hyperlipidemia
- Andere Medikamente
- ASA 81mg/d, atorvastatin 40mg/d, glimepiride 2mg 1/2 daily, losartan 25mg/d, metformin 500mg/d, omeprazole 20mg/d, calcium carbonate 500mg/d, magnesium oxide 500mg/d
- Allergien
- lisinopril (lips swelling)
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 28.11.2022
- Impfdatum
- 21.09.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 68,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Congestion, runny nose, sore throat
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Positive COVID-19 results via binaxnow rapid test on 11/28/2022
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- pneumonitis d/t inhalation of food and vomit, other pulmonary embolism without acute cor pulmonate, heart failure, dysphagia, a-fib, rhabdomyolysis, retention of urine, sepsis, history of falling, hypertension, major depressive disorder, hypothermia, unspecified injury of head, GERD, other chronic pain, cystitis, acute kidney failure, acute respiratory failure with hypoxia, constipation, urinary tract infection
- Andere Medikamente
- Align, antacid, celexa, cranberry-VitC-lactobacillus, docusate, dorzolamide, eliquis, fluticasone, furosemide, albuterol INH, lumigan, nitrostat, nystatin, pantoprazole, polyethylene glycol, prednisone, preserVision, senna tolterodine, tyle
- Allergien
- Amlodipine, gabapentin, tetanus toxoids
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 25.11.2022
- Impfdatum
- 25.05.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Capillaritis
Capillary leak syndrome
Inflammation
Livedo reticularis
Purpura
Rash
Rash erythematous
Scratch
Skin discolouration
Skin haemorrhage
Symptomtext
I experienced purpura, bleeding under the skin, and was diagnosed with Capillaritis. My capillaries are inflamed and leaking. I experienced red dots all over my legs, arms, and they began to merge with one another. I also had what looked like scratches, but were dots in lines, from this on my legs, stomach, and thighs. This occurred around 2 weeks after my dose. I had no itching, pain, rash, or raised blotches. I experienced 2 days of the spreading, darkening, and this gradually got lighter, but I have scattered remnants that has remained. My legs have a mottled appearance due to this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Blood work at local urgent care
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Arthritis; Hodgkin's Lymphoma history
- Andere Medikamente
- SYNTHROID; atorvastatin; vitamin C; CENTRUM seniors; CALTRATE D for women; vitamin E; turmeric; glucosamine chondroitin; lysine; flaxseed oil
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 16.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Nasal congestion
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I had very mild nasal congestion, a cough for a day, and slight fever no higher than 101. I tested positive for COVID-19 at home. I started to feel better after 3 days but, I was still tested positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19 test, 05/25/2022, positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; Hypothyroidism; High Cholesterol
- Andere Medikamente
- Atorvastatin; levothyroxine; losartan
- Allergien
- Contrast dye
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 09.11.2022
- Impfdatum
- 06.05.2022
- Beginn
- 15.10.2022
- Tage bis Beginn
- 162,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Ear infection
Nasopharyngitis
Oropharyngeal pain
SARS-CoV-2 test positive
Sinus disorder
Symptomtext
Sore throat on 14 Oct 2022, again on 15 Oct 2022. Tested at home, positive for Covid 19. Went to Little Clinic for confirmation test the same day. No treatment administered because I had been on three courses of progressively stronger antibiotics from The Little Clinic for ear infection, and since I had been having cold and sinus like symptoms for a month (tested negative for covid a few weeks prior), and any possible exposure data wasn't known, we couldn't pinpoint a date for Covid symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Covid 19 nasal swab test at Little Clinic.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 Diabetes Coronary Artery Disease Arthritis
- Andere Medikamente
- Fish oil Low dose aspirin Atorvastatin Metformin Omeprazole Atenolol Hydrochlorothiazide Trulicity weekly injection Pregabalin Meloxicam Benadryl, as needed Lactase, as needed Gas relief chewables, as needed
- Allergien
- Codeine Fenofibrate Adhesive sensitivity
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 10.05.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 114,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Oropharyngeal pain
Rhinorrhoea
Symptomtext
I experienced a sore throat, headache, heavy fatigue and nasal drip.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Amlodipine; Hydrochlorothiazide
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 26.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Malaise
Myalgia
Nausea
Pyrexia
Symptomtext
Headache, Myalgia, Fever, nausea, malaise, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- yes, Moderna Vaccine 1st Dose
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 08.11.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Insomnia
Myalgia
Nausea
Symptomtext
Headache, Myalgia, difficulty sleeping, nausea Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- yes, moderna covid vaccine previous dose
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 08.11.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Insomnia
Myalgia
Nausea
Symptomtext
Headache, Myalgia, difficulty sleeping, nausea Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- yes, moderna covid vaccine previous dose
- Staat
- AZ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 02.05.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 158,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest discomfort
Chills
Cough
Ear pain
Feeling abnormal
Headache
Oropharyngeal pain
Pain
Respiratory syncytial virus infection
Respiratory tract congestion
SARS-CoV-2 test positive
Throat irritation
Symptomtext
It started with a sore throat that didn't go away, then went to my head then my right ear. I was achy and kept a headache the whole time. I had chills, cough and little congestion. I felt rundown like I wanted to lay around and do nothing. The symptoms fluctuated in severity some days they were 7 and others a nagging 5. I was told to take OTC on the 7th and I was told it was RSV. When it didn't go away I tested for COVID-19 and it was positive. I was given a Z-PAK. I'm not testing positive now but still feel rundown and sometimes still feel it in my chest and throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Severe Crohn's disease; Bipolar; Inflammatory arthritis; Alfa 1 antitrypsin deficiency
- Andere Medikamente
- Magnesium; ibuprofen; MUCINEX; BENADRYL; dicyclomine; FLONASE; progesterone; KLONOPIN; testosterone cream; estradiol; protonic; pregnenolone; NURTEC
- Allergien
- A lot of them
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 29.04.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 134,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenopia
COVID-19
Cough
Decreased appetite
Diarrhoea
Fatigue
Headache
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
My eyes were really heavy and tired. I developed a runny nose and a cough. I also had extreme fatigue and a headache for 1 or 2. I developed a fever of around 100 degrees. I also had 1 day of diarrhea and loss of appetite. I tested myself on September 10, using a home COVID-19 test kit and it was positive. I contacted my doctor the next day who recommended isolation and prescribed PAXLOVID. My symptoms did not improve much from the medication. It took about 2 weeks for the symptoms to go away. I had a lingering cough for about 2 days after the 2 weeks. I have currently completely recovered from all my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 test positive September 10, 2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- TYLENOL; metoprolol; simvastatin; triamterene hydrochlorothiazide
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 01.11.2022
- Impfdatum
- 30.04.2022
- Beginn
- 17.09.2022
- Tage bis Beginn
- 140,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Chills
Dizziness
Feeling abnormal
Memory impairment
Nausea
Pain
Parosmia
SARS-CoV-2 test positive
Sleep disorder
Taste disorder
Symptomtext
I woke up on October 17 and was a little dizzy, extremely nauseated, achy and I had a funny taste in my mouth. I took my morning medicine. I smelled something in the restaurant I went to and immediately became nauseated to the point I had to lay down in the back of my car. I started to have some chills and was achy and decided to take a test. I contacted my doctor she prescribed PAXLOVID. I took the first dose and made myself eat so I could take meds. The next day I was still achy but no longer had the chills. By Monday, I felt like a different person. I was not back to normal, but I felt better. I tested on Thursday and was no linger positive. I am still having some brain fog now but not as often. I am having to write things down. I still don't have my full energy back and I am not sleeping as I was previously.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID 19 home test October 17, 2022 positive
- Aktuelle Erkrankungen
- Mild allergies
- Vorgeschichte
- Diabetic; Coughing Asthma
- Andere Medikamente
- WELLBUTRIN XR; MUCINEX; metformin HCLER; atorvastatin; dicyclomine; meloxicam; metoprolol; JARDIANCE; losartan HTZ; famotidine; ZYRTEC; BENADRYL; benzonatate; VASCEPA; cyclobenzaprine; hydrocodone; furosemide; OZEMPIC; TUSSIONEX cough; mult
- Allergien
- DOLOBID; morphine; barley; malt; beer; seasonal allergies
- Vorherige Impfungen
- COVID-19 2nd dose Moderna vaccine flu like symptoms
- Staat
- IL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 31.10.2022
- Impfdatum
- 29.04.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 178,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
COVID-19
Headache
Insomnia
Pain
Productive cough
Pyrexia
SARS-CoV-2 test positive
Sneezing
Symptomtext
On October 24th I noticed increased sneezing and unusual coughing. Later that night, I noticed joint aches and pain. I could not sleep thought the night from the symptoms. I scheduled a COVID-19 test. I tested for COVID-19 on the morning of October 25th. It was positive. I called my primary care provider as the provided that tested me did not treat for my symptoms at that time. The symptoms are mild, but they have been long lasting. My cough is productive. I haven't had any GI symptoms. I have developed a headache which is unusual for me. I continue to have the same symptoms as day one, and I am on day 7 now. I will seek an appointment with my doctor before returning to work to make sure I'm medically clear. I've been treating symptoms with over-the-counter medication. I added a supplement called ULTIMATE IMMUNITY. I take two tablets twice a day. I've only had a low-grade fever ranging from 99.1-degrees to 100.3-degrees.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- 10/25/2022 at home COVID-19 positive; 10/25/2022 rapid COVID-19 positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hiatal Hernia
- Andere Medikamente
- AZURETTE birth control pill; omeprazole; melatonin; ZYRTEC; red yeast rice; ubiquinol; turmeric; vitamin C; B complex; omega 3; vitamin D3; calcium; magnesium; probiotics; multivitamin
- Allergien
- Seasonal; sulfa drugs; nickel
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 17.06.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 87,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Head discomfort
Headache
Nasal congestion
SARS-CoV-2 test positive
Sinusitis
Upper-airway cough syndrome
Symptomtext
I had a severe sinus infection with nasal drip. I also had facial fullness with a headache and stuffiness. By the end of that week, I tested myself to see if I had COVID-19. I believe I contracted the virus around the 10th of September. I spoke to my doctor who called in a Z-PAK and told me to take vitamin C and zinc. Within a few days, I got better. At this point I have completely recovered from all my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test September 13,2022 positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes, Hypertension; Arthritis; Depression; Fibromyalgia
- Andere Medikamente
- Metformin; vitamin B complex; vitamin D3; GEMTESA; LYRICA; CYMBALTA; glipizide; prazosin; trazodone; metoprolol; ABILIFY; MAXZIDE; losartan; buspirone; ADDERALL; meloxicam
- Allergien
- BACTRIM; TYLOX; amoxicillin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 22.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Laboratory test
Nail discolouration
Nail disorder
Rash pruritic
Symptomtext
Horrible itching rash on my chin to my breast and chest and my toes, nail beds of my toes turning bruised and loosing toe nails. The dermatogoit gave me predizone, Dr. (dermatology)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash pruritic
- Hospital-Tage
- -
- Labordaten
- dermatologist tested me for lupus and auto immune diseases
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- Just get parts replaced
- Andere Medikamente
- Celebrex, Topamax, lamotrigine, venzendi , multi vitamin, Vit,. C, Vit. D3, B12, Glucosamine Chondroid Sulfate
- Allergien
- Mineral Oil, Flu vaccine
- Vorherige Impfungen
- Flu vaccine approx. 15 years I got GBS
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 14.10.2022
- Impfdatum
- 14.04.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 169,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Diarrhoea
Malaise
SARS-CoV-2 test positive
Symptomtext
I had a fever of 99.9 degrees. I still have sense of taste and smell but I did have diarrhea. I pretty much had all the symptoms with COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Controlled High Blood Pressure
- Andere Medikamente
- Clonidine; labetalol
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 29.06.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Hypoaesthesia
Injection site nodule
Injection site pain
Insomnia
Neck pain
Pain
Pain in extremity
Symptomtext
She got her vaccine, had sore arm and pain and it never went away and getting worse. She cannot fell her index finger, cannot feel her thumb, and at the elbow area she is growing a knot in that area, ? whether it's a blood clot or not. She went to the pharmacy and told them about her arm, and they tell her that the symptoms should go away. She then told her to report it to us. She went to her doctor and saw them, told her about it a few times, and prescribed some pain medicine which she did not take unless it's really bad, but is not a pill person for pain. They did not run any tests, and is going to go to a new doctor on Tuesday as her previous provider left the practice. The pain goes from the injection site itself, and then extends up the back of her neck on the left side like a sharp shocking pain that shoots up to the back of her neck. It goes up the shoulder to the neck. She cannot sleep on that side as when she does it feels tired, and feels like it weighs about 100#. It just hurts all of the time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site nodule
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure.
- Andere Medikamente
- Amlodipine 10 mg, Lisinopril/HCTZ 20/25 mg.
- Allergien
- Penicillin, Tetracycline, Amoxicillin.
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Gait disturbance
Musculoskeletal stiffness
Pain in extremity
Symptomtext
Generalized stiffness pain, leg leg pain especially the knees with an unstable gait. Her gait improved but it took 4 months for her symptoms to be much better. Knee is still can be more stiff than she had prior to the Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- No studies have been done
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypercholesteremia
- Andere Medikamente
- Atorvastatin, Fish Oil, Calcium and vitamin D3, Naproxen
- Allergien
- blood pressure pill?
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 27.04.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 84,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Feeling abnormal
Nasopharyngitis
Oropharyngeal pain
Pain
Symptomtext
On 7/19 I was experiencing fatigue and tested positive on 7/20. I was prescribed paxlovid the same date and eventually began to feel better. On 7/30 I began to feel a lot worse with cold symptoms including sore throat and body aches. Doctor would not re-prescribe paxlovid. After about five days I began to feel a little bit better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Crestor; baby aspirin; Calcium
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 15.02.2021
- Beginn
- 26.08.2022
- Tage bis Beginn
- 557,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Fatigue
Laboratory test abnormal
SARS-CoV-2 test positive
Symptomtext
08/26/22 presents to ED for "Fatigue, abnormal labs". PMHx of " hypertension, hyperlipidemia, sick sinus syndrome status post pacemaker, bladder cancer and CKD 3"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 08/26/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 01.09.2022
- Impfdatum
- 23.05.2022
- Beginn
- 28.08.2022
- Tage bis Beginn
- 97,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Decreased appetite
Oropharyngeal pain
Symptomtext
Activity change, appetite change and sore throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 27.08.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Erythema
Pain of skin
Skin warm
Swelling
Symptomtext
Narrative: Patient received COVID 19 Vaccine (Moderna) on 4/13/22. The patient complained of redness, swelling, and warmth and tenderness to the touch on 16 April 2022. The patient was treated with a warm compress. Reported per EUA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain of skin
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 17.05.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 63,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Oropharyngeal pain
SARS-CoV-2 test
Vaccine breakthrough infection
Symptomtext
I experienced sore throat, fatigue and a breakthrough case of COVID-19 that lasted for 8 days then I tested negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Blood pressure, High cholesterol
- Andere Medikamente
- Lovastatin, Losartan
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 18.08.2022
- Impfdatum
- 17.05.2022
- Beginn
- 09.07.2022
- Tage bis Beginn
- 53,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood donation
COVID-19
Cough
Extra dose administered
Fatigue
Pyrexia
Symptomtext
I got Covid seven weeks after the fourth booster. I had 100.1 degree fever for about three days, cough, and fatigue. I had a virtual appointment with a PA. She suggested Robitussin DM, Tylenol if needed, rest and lots of fluids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none. The only difference was that I gave blood on 07/07/2022
- Vorgeschichte
- none
- Andere Medikamente
- Vitamins: Calcium, Vitamin D, Vitamin C, Iron
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 17.08.2022
- Impfdatum
- 09.05.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Biopsy uterus normal
Ultrasound uterus normal
Uterine dilation and curettage
Uterine polyp
Vaginal haemorrhage
Symptomtext
On May 10, I started to have some pretty intense back pain which I never had before. This lasted for a couple of weeks. On May 23, I had vaginal bleeding. I went to my urogynecologist who sent me to an oncologist because they could not get a tissue sample. The oncologist did a DNC on July 06th and it showed that there was benign polyps blocking the neck of the uterus. The removed it and biopsied which confirmed they were normal with no sign of cancer there or in the uterine wall. I have had no further issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Biopsy-July 06th, 2022-Polyps located-Benign Sonogram-May 23, 2022-No findings
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Amlodipine; Calcium; Vitamin D; Famotidine; Lovastatin; Propranolol; Fosamax; Glucosamine Chondrodite; Vitamin C; Vitamin B12; Melatonin; Metamucil
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 12.05.2022
- Beginn
- 23.07.2022
- Tage bis Beginn
- 72,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Nasopharyngitis
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
7/23/2022 I had mild cold symptoms with a sore throat. It started getting worse with a fever. I had to take Tylenol. I tested positive for COVID-19. I was given Paxlovid and completed the full 5 day prescription. I started feeling better by the 6th day. I started having cold symptoms again and tested positive for COVID-19. At this moment I feel a lot better and no longer tested positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multi vitamin; Vitamin D; Vitamin B 12; Turmeric
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 10.08.2022
- Impfdatum
- 09.05.2022
- Beginn
- 04.07.2022
- Tage bis Beginn
- 56,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
COVID-19
Chills
Cough
Decreased appetite
Myalgia
Pain
Pyrexia
Symptomtext
Pt. stated 4th of July weekend he contracted Covid while at the mall, he was asymptomatic and did not know. Pt had chills, fever, cough. he had loss of taste. Severe body and muscle ache, no appetite. Pt. stated he has rare cancer. High fever for 5 days. Was put on PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- No labs or x-rays
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Anxiety; Epilepsy; ADHD
- Andere Medikamente
- Sleep medications; anxiety
- Allergien
- Sulphur
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 08.05.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 61,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Headache
SARS-CoV-2 test positive
Symptomtext
I received cough; headache and fatigue about 7 days, but, cough is still there. My doctor prescribed PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- I tested positive COVID 19 on 07/08/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- I was taking mycophenolate.
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 08.08.2022
- Impfdatum
- 05.05.2022
- Beginn
- 24.07.2022
- Tage bis Beginn
- 80,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Feeling abnormal
Impaired work ability
Nasal congestion
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I was probably exposed on Tuesday, 07/19/2022 at work. I just started feeling sort of bad and woke up with a fever on 07/24/2022. I took an at home COVID-19 test which was positive. I ran a fever for around 2 days. I got my fever down, but I just felt really wiped out for 2 more days after that. Altogether, I missed 5 days of work. I stayed really well hydrated, I did not lose appetite or sense of taste or smell. I had a real sore throat for at least the whole 5 days. I also had a really stuffy head and nose for closer to 10 days. I emailed my doctor's office after testing positive for COVID-19 who advised that I just use over the counter medication to mitigate my symptoms until they improved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test-07/24/2022-positive
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- One a Day Multivitamin; Lutein.
- Allergien
- Penicillin; C-chlor.
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 06.05.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 65,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
SARS-CoV-2 test positive
Symptomtext
On July 10, 2022, I tested positive for COVID-19. That Friday I tested myself because I was having COVID-19 like symptoms and it was negative but when I re-tested on July 10th, I tested positive. I contacted my doctor and she stated that I did not need Paxlovid because of my age and I wasn't high risk.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Tested posted on COVID-19 on July 10th, 2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Rosuvastatin
- Allergien
- Sulfur
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 05.08.2022
- Impfdatum
- 05.05.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 71,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Malaise
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
I contracted COVID-19 on 07/15/2022 with symptoms of cough, sneezing, runny nose, congestion, and fatigue. I was not prescribed any medication. I was ill for 4 days before my symptoms began to resolve. I am fully recovered with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab home test was positive on 07/15/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Zinc; vitamin D3; vitamin C; red yeast rice; CENTRUM silver multivitamin; ZYRTEC
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 05.08.2022
- Impfdatum
- 03.05.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 50,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Headache
Oropharyngeal pain
Pain
Pyrexia
Symptomtext
I had a sore throat, headache, mild fever, body ache, and cough. I was giving 2 different antibiotics. I was given Paxlovid to take for 5 days. I started feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Baclofen; Calcium Citrate; Vitamin C; Vitamin D; B12; Magnesium Citrate; Finasteride; Multi Vitamin; Zinc
- Allergien
- Sulfur; Milk; Corn; Soy; Nut
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 04.08.2022
- Impfdatum
- 29.04.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dysphonia
Malaise
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 07/16/2022 with symptoms of cough, congestion, hoarseness, chest congestion, runny nose, and fever of 101. I was prescribed PAXLOVID on 07/19/2022. I was ill for 8 days before my symptom began to resolve. My symptoms returned and worsened on 07/28/2022. I began to improve on 08/03/2022 but my symptoms have not fully resolved yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab home test was positive on 07/18/2022; COVID-19 PCR was positive on 07/21/2022; COVID-19 rapid nasal swab home test was negative on 07/24/2022; COVID-19 PCR was positive on 07/28/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism; High Cholesterol; Pre-diabetic
- Andere Medikamente
- SYNTHROID; gabapentin; vitamin B12; REPATHA; aspirin; magnesium; coQ10; probiotic; metformin
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 04.08.2022
- Impfdatum
- 04.05.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 56,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asymptomatic COVID-19
Herpes zoster
Musculoskeletal pain
Pain
Pruritus
Rash vesicular
SARS-CoV-2 test positive
Symptomtext
29Jul2022-Started experiencing pain in right shoulder blade. Had experienced some itching in that area also a few days before but had attributed that to a slight sunburn I got in middle of June. Pain worsened over next several days and on 03July2022, I broke out in a small rash of blisters about the size of a 50 cent piece. Sent picture to my son, who is a physician and was told it looked like shingles. He referred me to ships doctor who diagnosed me with Shingles and gave me acyclovir 800mg to take qid until pack of 35 tablets was gone. Upon returning home on 09July2022, I still was in pain and was seen by my primary physician on 11Jul2022. I was given gabapentin 100mg to take until pain was better. Pain is currently resolving, but I still have some episodes of significant pain. I travelled again during week 15July2022 and 22Jul2022. Several people on my tour appeared sick at the end of the trip so I tested myself and my husband, by PCR test and were negative. However Sunday, 24Jul2022, I woke up feeling like I had a sinus infection. I did a rapid test and was positive (very faint line) so I repeated to make sure. My husband did not have symptoms then but felt worse as day went on so he tested positive that afternoon. He also received 4th dose of Moderna on the same day I did at the same pharmacy and with same lot number. We both tested negative by PCR on 29Jul2022 and 30Jul2022. However he tested positive and I tested negative on a rapid test on30Jul2022. We have just tested negative on rapid test on 03Aug2022 and neither of us have symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal pain
- Hospital-Tage
- -
- Labordaten
- See AE info for PCR and rapid Covid test results and dates
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes, Seasonal Allergies, High Blood Pressure (controlled)
- Andere Medikamente
- Toprol, Enalapril, Allegra, Vitamin D3, AREDS II, Metformin
- Allergien
- Cephalosporins, Pepcid
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.08.2022
- Impfdatum
- 03.05.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 42,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
Fatigue
Feeling abnormal
Hypersomnia
Impaired work ability
Nasopharyngitis
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Coworker that came to work with a cold, the next day my coworker then called me and stated that she was positive for COVID-19. On Wednesday I started to feel like I was coming down with a cold. By Thursday morning I went into the doctor's office for a visit. COVID-19 test was done and I was positive. I was given a prescription for an anti-viral but it was not Paxlovid. I started taking it right away and felt bad for about 2 days. 5 days I stayed home and then afterwards I went back to work. My main symptoms were feeling fatigued and I slept a lot, low grade fever for a few days. As of today I feel back to normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test: Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Anxiety; Acid Reflux;
- Andere Medikamente
- Vitamin D3; Turmeric; Multivitamin; Calcium; Zinc; Magnesium; Flonase; Allegra; Collagen; Inhaler; Celexa; Amlodipine; Lovastatin; Metoprolol;
- Allergien
- Sulfa; Nickel; Dust Mites; Medical Adhesive Tape;
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 03.08.2022
- Impfdatum
- 04.05.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 83,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Nasopharyngitis
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I had scratchy throat; cough; cold-like symptoms; and fever for about 5 days and I took Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- I tested positive COVID-19; 07/26/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- I had high blood.
- Andere Medikamente
- I was Amlodipine; Rosuvastatin; Levothyroxine; Calcium and fish oil.
- Allergien
- I am allergic to Penicillin.
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 30.04.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 82,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chills
Cough
Fatigue
Nasal congestion
Oropharyngeal pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
We were on a cruise and I had taken some test kits on the cruise. I tested myself since my husband had already tested positive. I developed chills, fever and nasal congestion. I also had a sore throat along with fatigue. I contacted the medical unit on the cruise ship who did another test on us. We had 2 days remaining on the cruise so we had to wait until the cruise was over and immediately went to the urgent care. We started the treatment. I started to anti viral at that time. My fever and chills had subsided by then. I am still testing positive and still have a cough and a runny nose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 Rapid test July 21, 2022 positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- FOSAMAX; vitamin D
- Allergien
- KEFLEX; CIPRO
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 30.04.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 55,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chills
Cough
Nasal congestion
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Sinus headache
Symptomtext
Tested positive for COVID-19 6/24/2022. Started Paxlovid same day. Symptom-free by 2 days after completion of Paxlovid. Then developed rebound. Symptoms included sore throat, nasal congestion, fever, chills, cough and rebound sinus headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Positive RAT.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- BPH, GERD, spinal stenosis, history of pulmonary carcinoid, history of renal cell carcinoma
- Andere Medikamente
- Tamsulosin, Pantoprazole, Cetirizine, Vitamin D3
- Allergien
- Diethylcarbamazine - GERD
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 21.05.2022
- Beginn
- 31.07.2022
- Tage bis Beginn
- 71,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Fatigue
Myalgia
Symptomtext
fatigue, myalgias
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 30.04.2022
- Beginn
- 04.07.2022
- Tage bis Beginn
- 65,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aphonia
Body temperature increased
COVID-19
Chest discomfort
Dysphagia
Dysphonia
Exposure to SARS-CoV-2
Fatigue
Loss of personal independence in daily activities
Oropharyngeal pain
Productive cough
Pyrexia
SARS-CoV-2 test positive
Sleep disorder
Somnolence
Symptomtext
On 07/04/2022 someone who I had recently traveled with informed me that they were positive for COVID-19. I then tested for COVID-19 with an at home test and was positive. I had difficulty swallowing, a sore throat, and a strange feeling in my chest but was not coughing much but a few days later I began to develop a cough that was producing phlegm. After testing positive I called my doctor who prescribed PAXLOVID. My symptoms were progressively worse each day. I was very fatigued and had to nap a lot and my voice was extremely horse to the point that I would lose my voice after speaking for as little as 20 minutes. I had to order food in for at least a week because I could not cook. I had a temperature of 103. My doctor advised that I use TYLENOL to treat my fever, but I couldn't swallow the pills. I couldn't sleep through the night due to the inability to swallow. After taking the PAXLOVID I began to feel better but it took at least 2 weeks before I was able to cook again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test 07/04/2022 positive.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Thrombosis
- Andere Medikamente
- Baby aspirin; CRESTOR; ELIQUIS; bio-curcumin; CARTILAGE HX; CATALASE HX; coQ10; INFLAMMUNE; krill; women's multivitamin; lutein; resveratrol; probiotic; vitamin C; zinc; quercetin; COLLAGEN HX; bone powder with vitamin D and calcium; COCOA
- Allergien
- Orange; milk chocolate; peanut; shrimp.
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 28.07.2022
- Impfdatum
- 27.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
COVID-19
Chest discomfort
Cough
Fatigue
Feeling abnormal
Headache
Nasal congestion
Oropharyngeal pain
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
I woke up with intense headache several times. I also had upset stomach, mental fogginess, and fatigue. The very next day I started having nasal congestion and sneezing. So, I took an at home test which came back positive. I started isolating for 5 days and got plenty of rest. I had a virtual doctor's appointment. My doctor told me to take EXCEDRIN after giving her all my symptoms and drink plenty of fluid. I ask were there any downside to taking PAXLOVID and she said that most people have returning symptoms, so I just took over the counter. By the 3rd day I started coughing bad and had chest tightening. The next day I started having a sore throat which I took HALLS for and all the other symptoms (headache, upset stomach, and body aches) had started to resolve. By Friday I only had congestion, fatigue, and some couching at night until maybe Tuesday. On July 7th was the day I tested negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Estradiol
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 27.07.2022
- Impfdatum
- 26.04.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 65,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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 congestion, headache, fever, and fatigue. I was prescribed PAXLOVID on 07/01/2022. I was ill for 7 days before my symptoms began to resolve. I have lingering fatigue, but all of my other symptoms are fully resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab home test was positive on 06/30/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Osteopenia
- Andere Medikamente
- Pravastatin; amlodipine; vitamin C; calcium; vitamin B complex; vitamin D3
- Allergien
- N/A
- Vorherige Impfungen
- Dose 2 Moderna COVID-19 my eyelids swelled for 12 hours at age 72 on 02/23/2021.
- Staat
- TX
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 25.04.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 55,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Chills
Cough
Oropharyngeal pain
SARS-CoV-2 test positive
Sneezing
Symptomtext
I had been traveling and because I was sneezing and had a sore throat, I tested and, it was positive. I had no fever. It was mainly sneezing and coughing and a sore throat. And I put it into my my-charts system, and my doctor recommended that I visited a doctor that was in chain. I had chills and sneezing, and I thought I had hay fever. I was out of town and drove back to my house and I was positive again. I then I went to a local urgent care, and they tasted me again. Urgent care recommended me to another hospital to get me the mono antibodies done.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 2 at home COVID-19 tests positive. COVID-19 test positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- A Fib; High Blood Pressure; High Cholesterol; PVC; Obese; Arthritis
- Andere Medikamente
- Amiodarone; ELIQUIS; losartan; metoprolol; rosuvastatin; coQ-10; vitamin D3
- Allergien
- Hay fever; Contact Dermatitis; diclofenac
- Vorherige Impfungen
- Sore arm for all vaccines
- Staat
- WA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 25.04.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 72,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Feeling abnormal
Headache
Impaired work ability
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Somnolence
Tension headache
Symptomtext
I was tired and feeling run down. I thought maybe I just wasn't sleeping well. The night of July 6th, I started to feel achy, like if I was coming down with something. I went to get a PCR test and it was negative. 2 days later I was feeling fine, and then the day after, it all hit. I took a home COVID test and it was positive. I was congested and incredibly fatigued. I was trying to work but I had to sleep after every other. To this day I can only work very few hours before I have to lay down and nap. I work a desk job so I am not doing labor. The top part of my head feels like its to tight. I currently am experiencing still heavy fatigue and a headache even though I just recently tested negative again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- PCR COVID test with positive result.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- CLARITIN
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 25.04.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 64,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Chest discomfort
Chills
Decreased appetite
Ear pain
Fatigue
Headache
Hypersomnia
Nasal congestion
Oropharyngeal pain
Pain in jaw
Pyrexia
SARS-CoV-2 test positive
Weight decreased
Symptomtext
Starting 06/28/2022, I had a headache, nasal congestion, sore throat, fatigue, chills, my jaw hurt and my ears hurt, and I felt like I had a sinus infection. I called my doctor on 06/29/2022 and they told me to take a COVID-19 test before coming in. I took the At-Home COVID-19 test which was positive. I called her back and asked if I could get Paxlovid. After having a telehealth visit, she called in a prescription for the Paxlovid. I was not able to get the Paxlovid until 06/30/2022 due to the local pharmacy not being able to dispense it. Before starting it, I slept a lot and experienced all the symptoms that were noted above plus occasional chills, fever and my chest felt heavy. I did lose my sense of taste and smell, and I lost weight due to not being hungry. After starting the Paxlovid, within 2 days, I started feeling so much better. By that Sunday, 07/03/2022, I felt almost 100% better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- At-Home COVID-19 test (06/29/2022): Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure; High Cholesterol
- Andere Medikamente
- Lisinopril; Simvastatin; OTC allergy pills; Extra Strength Tylenol as needed
- Allergien
- None
- Vorherige Impfungen
- Measles vaccine caused me to break out in a rash and I got the flu after receiving the vaccine for it in 2014
- Staat
- MO
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 22.04.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 79,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Oropharyngeal pain
Respiratory tract congestion
Symptomtext
Sore throat, cough, congestion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Vertigo, Graves? disease
- Andere Medikamente
- Meclizine, calcium, levothyroxine, flonase, glucosamine, olmesartin,, atovastatin, fenofibrate, Probiotic
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 22.04.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 63,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
Nasopharyngitis
SARS-CoV-2 test positive
Symptomtext
Started feeling cold like symptoms on 06/23/2022 and tested positive for COVID with a home test. Had telahealth appt was was prescribed Paxlovid. Had lingering symptoms for 1 month. Have fully recovered now 7/25/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin B-12; Vitamin D3; Daily Multivitamin; Glucosamine; Luton Zia Xanthan; Calcium; Fish Oil
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 23.04.2022
- Beginn
- 22.07.2022
- 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
Chest discomfort
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
Developed chest tightness, runny nose and sneezing and fever on 7/22. Tested positive that day. Spoke to doctor on 7/23 and received Paxlovid which I am currently taking.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Pantoprazole; Vitamin D;
- Allergien
- Penicilin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 23.04.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 87,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Oropharyngeal pain
Productive cough
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
On July 19, 2022, I had a little bit of sore throat. The next day I had a slight fever and runny nose. I took a home test and it was positive. I spoke with Dr. and he prescribed PAXLOVID and started that day. After that my symptoms decreased. As of today, July 25, 2022 I feel pretty good other than a dry cough and occasional it is productive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test, positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Lisinopril; LIPITOR; vitamin D3
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 21.04.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 47,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Influenza like illness
Nasal congestion
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Sneezing
Throat irritation
Symptomtext
I started to have a scratchy throat. Within 24 hours I developed a fever of 101, cough, sore throat, nasal congestion, and sneezing. I felt like I had the flu. The next day I took a COVID-19 test at home that came back positive. I had a virtual meeting with a doctor to get PAXLOVID. My flu like symptoms lasted for about 2 weeks. For about 5 weeks I had a cough, and felt really fatigued.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Irritable Bowel Syndrome
- Andere Medikamente
- Vitamin C
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 24.07.2022
- Impfdatum
- 23.07.2022
- Beginn
- 24.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Injection site pain
Pain
Pyrexia
Symptomtext
He had soreness at the injection site area almost immediately. He woke up with aches, chills, and a slight to medium headache around 4:00 a.m., and was definitely feverish (hot to the touch) by 8 a.m. He's unusually tired. He has mild chills and a mild headache (it's 12:11 p.m. on the 24th, so about 20 hours after the vaccination.) This is his 2nd Covid booster and his first Moderna dose. He previously had Pfizer for his 2-series vaccination and first booster. His first Covid booster was in late December. (I selected dose number in the series as 4--two primary and two boosters.)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- similar symptoms after previous Covid vaccinations
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 21.04.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 62,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Malaise
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 06/22/2022 with symptoms of cough, runny nose, congestion, and fatigue. I was prescribed molnupiravir, doxycycline, and guaifenesin with codeine on 06/24/2022. I was ill for 3 to 4 days before my symptoms began to resolve. I am fully recovered, but I have a lingering runny nose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid home test was positive on 06/22/2022; COVID-19 PCR was positive on 06/24/2022; COVID-19 rapid home test was negative on 06/29/2022.
- Aktuelle Erkrankungen
- Stye in lower right eyelid
- Vorgeschichte
- Lungs are "dirty" after 35 years of Smoking Cannabis discontinued use in 2014 but lungs are noticeably occluded
- Andere Medikamente
- Atorvastatin; coQ10; finasteride; alfuzosin; diltiazem; cephalexin; erythromycin ophthalmological ointment
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 15.04.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 88,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Ear pain
Head discomfort
Headache
Injection site erythema
Injection site warmth
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Vertigo
Symptomtext
On 4-15-2022, I got my vaccine and the next morning, I had a red/warm know at the injection site that lasted a couple of days. On 7-12-2022, I woke up with head congestion, cough and low grade fever of 99.7. I took a home Covid19 test with positive results. On the next day, 7-13, my temp elevated to 100.4, I had a headache, sore throat, body aches, vertigo, bilateral ear pain along with symptoms that started on 7-12. I had a telehealth visit with my PCP and he prescribed paxlovid. I started taking it on 7-14 for 5 days and my temp got up to 100.9. On 7-18, I took another home Covid 19 test with negative results. On 7-19, I took another home Covid19 test and it was positive again with most of my symptoms returning. I am reporting a breakthru case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- Covid19 home tests on 7-12 positive result - 7-18 with negative result - 7-19 with positive result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seasonal Allergies, Hypertension, Hyperlipidemia, Hx CVA with resulting hx of Seizures, Meibomium Gland Dysfunction, Restless Leg Syndrome, Sleep Apnea (Central and Obstructive), Asthma
- Andere Medikamente
- Aspirin; Flonase; Hydroeye softgels; Levetiracetam ER; Singulair; Mirapex; Crestor; Lisinopril/HCTZ; Xiidra; Zyrtec; ProAir inhaler; Symbicort inhler
- Allergien
- Bactrim; Augmentin, Cefzil; Plaquenil; Fluoroquinolone
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 21.04.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 81,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Exercise tolerance decreased
Fatigue
Headache
Malaise
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
Starting 07/11/2022, I got a bad sore throat and head congestion. At first, I thought it was allergies but I knew it was the wrong time of the year. The next morning I felt relatively good but by mid-day I was having more symptoms and by that evening I took an at-home COVID-19 test which was positive. The next morning, I had severe body aches, fever, cough, head congestion and sore threat. I contacted my doctor's office right away. They got back to me and recommended the monoclonal antibody (bebtelovimab) treatment. So, I got that on 07/13/2022 and by the next day I felt substantially better. On 07/15/2022, I was feeling even better. By 07/16/2022, I was feeling much better but still fatigued. The next day I felt almost completely back to normal but by the end of the day I still had some mild fatigue. Yesterday, 07/21/2022, I thought I was feeling back to my normal self so I went for a bike ride for about 2 miles, but by the end of it I was having symptoms again (body aches, headache and malaise) and was concerned. I am hoping that with more rest, I will get back to normal. I contacted my doctor this morning who said to rest and I took an at-home test which was positive. They told me to ignore it and that I could test positive for another 45 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At-home COVID-19 test (07/12/2022): positive; At-home COVID-19 test (07/21/2022): negative; At-home COVID-19 test (07/22/2022): positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type II Diabetes
- Andere Medikamente
- Dutasteride; metformin; atorvastatin; aspirin; CENTRUM for men; melatonin; JARDIANCE
- Allergien
- Hay fever
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 13.04.2022
- Beginn
- 02.07.2022
- Tage bis Beginn
- 80,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Fatigue
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Throat irritation
Symptomtext
After my tour bus trip returned on June 26, 2022, I tested negative for COVID 19 for the next several days. I began to feel tired with raspy throat and congestion on July 2, 2022. I tested again on July 3, 2022 and was positive. I also had a slight fever. I lost my taste and smell during this infection, but didn't actually realize it until a couple of weeks later. My fever went away after 3 days. My other symptoms improved by the 28th. I didn't regain my taste and smell until July 16th.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test, negative; Home COVID-19 test, positive.
- Aktuelle Erkrankungen
- Congestion
- Vorgeschichte
- Aortic Valve
- Andere Medikamente
- Alopurinol; COLCRYS; LIPITOR; fosinopril; hydrochlorothiazide; warfarin; TOPROl; vitamin E; baby aspirin; multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 14.04.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 69,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Headache
Hypersomnia
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19. I had a sore throat for possibly four days. I also had a headache for maybe 3 days. I was very tired and fatigued. I slept and spent all day in bed on 06/23/2022. I received treatment of Paxlovid on the morning of 06/23/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 Test - Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- 2nd dose of Pfizer - sore arm and flu-like symptoms
- Staat
- HI
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 14.04.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 52,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Cough
Diarrhoea
Ear infection
Exposure to SARS-CoV-2
Hyperhidrosis
Nausea
Oropharyngeal discomfort
Oropharyngeal pain
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sinus disorder
Symptomtext
I received my second COVID-19 booster, which was from Moderna, on 4/14/2022. On about 6/3/2022, I was informed that one of my colleagues had tested positive for COVID-19. I did a home that day, and I got a positive result. On about 6/4/2022, I contacted a telehealth, and I was sent to a place to get a PCR, which ultimately also yielded a positive result. I was prescribed a 5-day course of Paxlovid. On the evening of 6/5/2022, I started to get a sore throat, fever, sweating, chills, body aches, nausea, and diarrhea. The symptoms continued and then they improved on 6/9/2022 or 6/10/2022. At one point, I thought I had gotten over it, but then I had a rebound around 7/4/2022. During my rebound, my symptoms were more focused in the sinuses. I also developed an ear infection, for which I took amoxicillin. At the time of this writing, I'm mostly over it, though I have sniffles, a lingering cough and a ticklish sensation in the throat. It's possible that they're residual symptoms of COVID-19, but they could also possibly be due to allergies. In fact, I am due to see an allergist sometime soon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Multiple Myeloma; Perforated Foramen Ovale of the Heart (Caused an Infarct in the Left Occipital); Right-Sided Blindness in Both Eyes.
- Andere Medikamente
- Propranolol; Amlodipine; Famotidine; Vitamin B1; Levocetirizine; Vyvanse; Baclofen; Ibuprofen; Wellness Formula Multivitamin; Vitamin D.
- Allergien
- Dairy; Bee and Wasp Stings.
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 07.07.2022
- Beginn
- 09.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Burning sensation
Erythema
Fatigue
Injection site pain
Limb discomfort
Pain in extremity
Peripheral swelling
Pruritus
Symptomtext
I did develop a sore arm that lasted for 48 hours. It was painful when he did the injection. Then, it was the sore arm, tiredness and fatigue the next day. The 24 hours after, I felt fatigued more than usual. Saturday morning on July 9, I noted that my legs were feeling itchy, and they were both below the calf area. The next day when I could actually look, I noticed that it started to look red and developed especially on the left leg. It was beet red color. It started itching more and I noticed that there was blistering forming on the back of my left leg on the lower portion. On the right side, on the inner part of my leg, I noticed more redness, itching, and burning. I still have it, but it?s not as intense now. As of yesterday, it seemed to start subsiding. I did see a NP on Monday, July 11 and he didn?t have any answers. He didn?t think it was related to the vaccine, but he wasn?t sure. I still think it could be related because that?s the only thing I did that was different. I didn?t eat anything different or take any new medications. The vaccine was the only thing that happened. He told me to use Kenalog ointment to use for the itching. I?ve been using some CeraVe over the counter anti-itching lotion and that seemed to help. I just get these intense urges to scratch and I refrain from that because they do blister. But they are super uncomfortable. The redness looks to be subsiding, but the itchiness hasn?t. If I touch it, it does begin to itch. However, it?s not as intense as it was. The legs also did feel tight, like swelling or irritation in the legs. The symptoms are improving, but not fully recovered at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Blood work 07/11/2022 - indicated low hemoglobin at 10.2, not a new event
- Aktuelle Erkrankungen
- Recently diagnosed with anemia within the last month
- Vorgeschichte
- Colon Cancer; Possible Liver Cancer; Atrial fibrillation; Hypertension
- Andere Medikamente
- Metoprolol Succinate ER; HCTZ; Ascorbic Acid; Vitamin C; Vitamin D3; COQ10; Iron; Parasol; Chromium Picolinate; Xarelto; Magnesium; Potassium; Fiber Gummy
- Allergien
- Sulfa; Lisinopril; Ibuprofen; Aleve
- Vorherige Impfungen
- 2nd Dose COVID-19 Moderna vaccine, 05/04/2021, age 74 - Similar symptoms of legs becoming red, swollen, and itchy, but more wide
- Staat
- KY
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 11.07.2022
- Impfdatum
- 23.05.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 11,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Back pain
COVID-19
Computerised tomogram normal
Cough
SARS-CoV-2 test positive
Throat irritation
Vertigo
Symptomtext
When I caught COVID-19 I had a scratchy throat and a cough that lasted for 5 days. I had no fever and nothing else. I took some Delsym cough syrup. Since then I have had stomach cramping and an increase in vertigo. I also have been having back pain now. I went to the ER for my stomach cramps and back pain. I was prescribed dicyclomine. That medication didn't help anything. I saw my doctor today and he doesn't know what is causing this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- 6/4/2022- At Home COVID-19 Test- Positive; 7/3/2022- CAT Scan- Normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Psoriatic Arthritis; Hypertension; Atrial Fibrillation; Meniere?s Disease, Sleep Apnea, Scoliosis
- Andere Medikamente
- Simponi Aria; Xarelto; Tamsulosin; Metoprolol; Amlodipine; Rosuvastatin; Montelukast; Hydrochlorothiazide; Ramipril
- Allergien
- Flagyl; Neomycin; Sulfa Drugs
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 15.01.2021
- Beginn
- 09.06.2022
- Tage bis Beginn
- 510,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Diarrhoea
SARS-CoV-2 test positive
Symptomtext
diarrhea, cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- 8,0
- Labordaten
- positive covid test 6/9
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension Lower GI bleed Osteoarthritis Chronic lumbar radiculopathy Major depressive disorder Anxiety
- Andere Medikamente
- ALPRAZolam (XANAX) 0.5 mg oral tablet amLODIPine-benazepril (LOTREL) 10-20 mg oral capsule atenolol (TENORMIN) 50 mg oral tablet celecoxib (CELEBREX) 200 mg oral capsule cholecalciferol, vitamin D3, 1000 unit (25 mcg) oral tablet colchicine
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 05.07.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site cellulitis
Symptomtext
07/07/2022: Patient reported developing cellulitis from the Moderna vaccine that she was given on 07/05/22 on her left arm. Patient was seen by physician and she was diagnosed with cellulitis, she is currently on antibiotic therapy and is using ice to reduce the swelling. DPM was notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Aspirin, NSAIDS
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 27.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Pyrexia
Swelling
Urticaria
Symptomtext
Fever, weakness, hives beginning on left nipple to groin anterior side only, denies drainage or blistering. Reports some small "little bumps." (patient described feeling like she was getting shingles again.)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- lupus
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 25.05.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Headache
Oedema peripheral
Swelling
Symptomtext
Having pitted Edema in lower extremities: severe swelling: headaches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Blood work
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Season allergies: Arthritis
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 21.06.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Nausea
Vomiting
Symptomtext
Patient experiences 24 hours of intermittent nausea and weakness with two episodes of vomiting. Patient experienced no fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Dementia
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 38,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest discomfort
Cough
Diarrhoea
Fatigue
Headache
Malaise
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
I contracted COVID-19 on 06/20/2022 with symptoms of headache, sneezing, sore throat, cough, congestion, chest tightness, fatigue, and diarrhea. I tested positive after returning home from a trip. I received Monoclonal Antibodies on 06/22/2022. I was ill for 5 days before my symptoms began to improve, but I am not fully recovered as of yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab home test was positive on 06/21/2022
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- 2 rounds of Breast Cancer, High Cholesterol
- Andere Medikamente
- Remedex, Crestor, Zyrtec, Doxylamine Succinate, Tylenol, Calcium
- Allergien
- Demerol
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 21.06.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Chills
Cough
Diarrhoea
Headache
Myalgia
Pyrexia
Vomiting
Symptomtext
A few hours after I got vaccinated I notice that my temperature slowly started going up. The next day I had chills and my fever was up to 103 . I throw up once and also had diarrhea. I had a headache for two days and up to today I still have soar muscles . Until today I have a occasional cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- Ph Positive CML
- Vorgeschichte
- High Cholesterol Hypertension
- Andere Medikamente
- Sprycel Atorvastatin Lisinopril
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 19.05.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 33,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
COVID-19
Cough
Decreased appetite
Fatigue
Headache
Myalgia
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I had muscle aches, very tired and fatigue, a terrible sore throat and a heavy cough. I felt extremely weak, bad congestion, and loss of appetite. When I felt my headache progressing worse, I took an at-home COVID-19 on 06/21/2022 and it came back positive. So I went to the emergency room when my symptoms got worse, and they tested me again as I began experiencing a terrible fever. Their test as well came back positive. During my overnight stay, EUA-Bebtelovimab monoclonal antibody treatment. As of today (06/24/2022), I'm starting to feel better but not completely 100% yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- 1,0
- Labordaten
- COVID-19 Tests: 06/21/2022 & 06/22/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Absolute Anemia, High Blood Pressure, Arthritis, Hypothyroidism, Obesity
- Andere Medikamente
- Levothyroxine, Atenolol, Lisinopril, Atorvastatin, Vitamin B-12, Centrum Silver
- Allergien
- Sulfur Drugs
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Injection site pain
Symptomtext
Vaccine administering error: At our COVID vaccination clinic, patient was accidentally given Moderna COVID vaccine (18 and up) 0.3 ml instead of 0.25ml as the 2nd COVID vaccine booster. Patient was contacted the same day and notified this vaccine administering error. Then patient was contacted again the next day to follow up. Patient did not have any other signs or symptoms except pain in the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hypertension Vitamin D deficiency Quantiferon-TB test reaction without active tuberculosis Ankylosing spondylitis of lumbosacral region Osteomalacia
- Andere Medikamente
- Amlodipine 5 mg Rifampin 300 mg Omeprazole 20 mg Ibuprofen 400 mg Cosentyx Pen 150 mg/ml
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Injection site pain
Product administration error
Symptomtext
Vaccine administering error: At our COVID vaccination clinic, patient was accidentally given Moderna COVID vaccine (18 and up) 0.3 ml instead of 0.25ml as the 2nd COVID vaccine booster. Patient was contacted the same day and notified this vaccine administering error. Then patient was contacted again the next day to follow up. Patient did not have any other signs or symptoms except pain in the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hypothyroidism Hyperlipidemia Elevated fasting blood sugar
- Andere Medikamente
- Lipitor 10 mg Ibuprofen 600 mg Tylenol 500 mg Fosamax 70 mg Calcium 500 mg + Vit D 10 mcg Vitamin D3 25 mcg
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Injection site pain
Symptomtext
Vaccine administering error: At our COVID vaccination clinic, patient was accidentally given Moderna COVID vaccine (18 and up) 0.3 ml instead of 0.25ml as the 2nd COVID vaccine booster. Patient was contacted the same day and notified this vaccine administering error. Then patient was contacted again the next day to follow up. Patient did not have any other signs or symptoms except pain in the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hypertension Hyperlipidemia Type 2 diabetes Mellitus controlled by diet LTBI
- Andere Medikamente
- Losartan 100 mg Allopurinol 100 mg Aspirin 81 mg Metformin 500 mg Pravastatin 20 mg Vitamin D3 50 mcg
- Allergien
- Atorvastatin -- Hepatotoxicity
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Injection site pain
Vaccination error
Symptomtext
Vaccine administering error: At our COVID vaccination clinic, patient was accidentally given Moderna COVID vaccine (18 and up) 0.3 ml instead of 0.25ml as the 2nd COVID vaccine booster. Patient was contacted the same day and notified this vaccine administering error. Then patient was contacted again the next day to follow up. Patient did not have any other signs or symptoms except pain in the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hyperlipidemia Low Back Pain Osteoporosis Prediabetes Minimal cognitive impairment
- Andere Medikamente
- Meclizine 12.5 mg Mirtazapine 15 mg Flonase 50 mcg
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Injection site pain
Vaccination error
Symptomtext
Vaccine administering error: At our COVID vaccination clinic, patient was accidentally given Moderna COVID vaccine (18 and up) 0.3 ml instead of 0.25ml as the 2nd COVID vaccine booster. Patient was contacted the same day and notified this vaccine administering error. Then patient was contacted again the next day to follow up. Patient did not have any other signs or symptoms except pain in the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Coronary artery disease Acute gastric ulcer Bilateral inguinal hernia Type 2 diabetes mellitus Hypertension Hyperlipidemia
- Andere Medikamente
- Aspirin EC 81 mg Metoprolol 100 mg Lipitor 80 mg Amlodipine 5 mg Protonix 40 mg Ventolin HFA 90 mcg Famotidine 40 mg
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Injection site pain
Product administered to patient of inappropriate age
Symptomtext
Vaccine administering error: At our COVID vaccination clinic, patient was accidentally given Moderna COVID vaccine (18 and up) 0.3 ml instead of 0.25ml as the 2nd COVID vaccine booster. Patient was contacted the same day and notified this vaccine administering error. Then patient was contacted again the next day to follow up. Patient did not have any other signs or symptoms except pain in the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Unknown.
- Vorgeschichte
- Type 2 diabetes mellitus; Hyperlipidemia; Vitamin D deficiency; Anemia.
- Andere Medikamente
- Multiple Vitamins for Women.
- Allergien
- No Known Allergies.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Injection site pain
Vaccination error
Symptomtext
Vaccine administering error: At our COVID vaccination clinic, patient was accidentally given Moderna COVID vaccine (18 and up) 0.3 ml instead of 0.25ml as the 2nd COVID vaccine booster. Patient was contacted the same day and notified this vaccine administering error. Then patient was contacted again the next day to follow up. Patient did not have any other signs or symptoms except pain in the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hyperlipidemia Goiter Osteoporosis Allergic rhinitis
- Andere Medikamente
- Loratadine 10 mg Hydroxyzine 25 mg Calcium 500-Vit D3 400 unit Fosamax 70 mg Vitamin D3 25 mcg
- Allergien
- Ibuprofen--eye redness, mild
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Injection site pain
Product administration error
Symptomtext
Vaccine administering error: At our COVID vaccination clinic, patient was accidentally given Moderna COVID vaccine (18 and up) 0.3 ml instead of 0.25ml as the 2nd COVID vaccine booster. Patient was contacted the same day and notified this vaccine administering error. Then patient was contacted again the next day to follow up. Patient did not have any other signs or symptoms except pain in the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Allergic rhinitis Benign prostatic hyperplasia Hyperlipidemia Hypertension COPD Type 2 diabetes mellitus with stage 3 chronic kidney disease
- Andere Medikamente
- Hyzaar 100 mg - 25 mg Flonase 50 mcg Aspirin EC 81 mg Flomax 0.4 mg Lipitor 20 mg Pepcid 40 mg Amlodipine 5 mg Omeprazole 20 mg Combivent 20 mcg-100 mcg
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Injection site pain
Symptomtext
Vaccine administering error: At our COVID vaccination clinic, patient was accidentally given Moderna COVID vaccine (18 and up) 0.3 ml instead of 0.25ml as the 2nd COVID vaccine booster. Patient was contacted the same day and notified this vaccine administering error. Then patient was contacted again the next day to follow up. Patient did not have any other signs or symptoms except pain in the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Unknown.
- Vorgeschichte
- Hyperlipidemia; Allergic rhinitis; DM type 2; Hepatitis B carrier; Anemia.
- Andere Medikamente
- Glipizide; Lipitor; Metformin; Flonase .
- Allergien
- No Known Allergies.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Injection site pain
Symptomtext
Vaccine administering error: At our COVID vaccination clinic, patient was accidentally given Moderna COVID vaccine (18 and up) 0.3 ml instead of 0.25ml as the 2nd COVID vaccine booster. Patient was contacted the same day and notified this vaccine administering error. Then patient was contacted again the next day to follow up. Patient did not have any other signs or symptoms except pain in the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- DM Type II Hypertension Hyperlipidemia
- Andere Medikamente
- Atenolol 50 mg Losartan 50 mg Hydrocil oral power Gemfibrozil 600 mg Pravastatin 20 mg Oys 500/Vit D 400 Aspirin EC 81 mg Glipizide 5 mg-Metformin 500 mg Jardiance 10 mg Basaglar Kwikpen U Insulin
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
COVID-19
Chills
Computerised tomogram
Headache
Extra dose administered
Injection site reaction
Muscle spasms
Nausea
Immediate post-injection reaction
Impaired work ability
Inflammation
Loss of personal independence in daily activities
Neck pain
Neurological symptom
Pyrexia
X-ray
Rash pruritic
Symptomtext
Immediately after the 2nd Moderna booster I had severe muscle spasms starting in my R shouder rotator cull area; the spasms continued across my upper back, shoulders , neck and into my head/scalp. I almost fell down in the pharmacy area, but was able to get to a chair near the shot area, then to proceed a few steps toward the coffee area, ger a decaf coffee and rest at a table for about 10 min. I was on my lunch break from university where I was currently teaching and needed to get back to students in the painting studio - but never made it back. I was helped to my car and was able to drive about a 1/2 mile to our hospital where I was checked into Emergency. I was there having multiple tests until after 9 pm. The hospital was concerned about stroke symptoms, the continuing muscle spasms through my upper body Right side. I was discharged with medicine for the spasms, but then had to return several days later with fever, chills, nausea, headache and full-blown COVID. I had to stay at home for two weeks, needing to have the university hire a substitute faculty member to finish the course I teach. I also needed to hire a helper for my basic home tasks and some personal care. I am still needing weekly check-ups and physical therapy for the muscle spasms and rampant inflammation on my right side above my legs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Emergency Room on May 24, 2022 : full check up of vital signs; CT scan of upper body to groin area; 2nd hospitalization repeated checks with addition of x-rays; doctor's referral this past week (June15) more follow up with local surgeon's office regarding R shoulder and neck pain.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- in remission from Multiple Myeloma
- Andere Medikamente
- levothyroxine; senior multivitamin, vitamins C, B, e, MG, CA, lutein, alpha lipoic acid, focus factor
- Allergien
- penicillin and some mycin antibiotics
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Injection site pain
Wrong product administered
Symptomtext
Vaccine administering error: At our COVID vaccination clinic, patient was accidentally given Moderna COVID vaccine (18 and up) 0.3 ml instead of 0.25ml as the 2nd COVID vaccine booster. Patient was contacted the same day and notified this vaccine administering error. Then patient was contacted again the next day to follow up. Patient did not have any other signs or symptoms except pain in the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Benign essential hypertension Hyperlipidemia History of cerebrovascular accident with residual deficit CKD stage G3a/A2, GFR 45-59 and albumin creatinine ratio 30-299 mg/g Left-sided weakness Type 2 diabetes mellitus without complication Vitamin D deficiency Depression, unspecified depression type Adjustment disorder with depressed mood Benign prostatic hyperplasia Hemiparesis Minimal cognitive impairment
- Andere Medikamente
- 04/05/2022 ASPIRIN EC 81 mg 90 TAKE 1 TABLET BY MOUTH ONCE DAILY. 04/05/2022 HYDROCHLOROTHIAZIDE 12.5 mg 90 TAKE 1 CAPSULE BY MOUTH ONCE DAILY. 04/05/2022 GLIPIZIDE ER 5 mg 90 Take 1 tablet by mouth every day with breakfast 01/11/2022 NATUR
- Allergien
- No Known Allergies.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 31,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Nasal congestion
Oral pain
Oropharyngeal pain
Pain
Paranasal sinus discomfort
Rash
SARS-CoV-2 test positive
Throat irritation
Symptomtext
Tested positive on 6/17. Spoke to dr and started paxlovid. Developed scratchy throat and sinus pressure that got progressively worse. Next day, had sore throat and nasal congestion and mouth pain w/ body aches. No fever. Intermittent chills. Developed rash following day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High BP
- Andere Medikamente
- Toporal, adamine, vit d3, lutein, zeaxathnine, mulberry,
- Allergien
- augmentin, sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Feeling hot
Headache
Injection site pain
Irritability
Neuralgia
Symptomtext
Pain at injection site, extreme headache, Temperature 101 degrees, joint pain, nerve pain/irritated feels hot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Metoprolol, Rosuvastin, Acyclovir, baby aspirin Multiple vitamin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 19.01.2021
- Beginn
- 13.06.2022
- Tage bis Beginn
- 510,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Injection site rash
Injection site reaction
Pain
Rash erythematous
Rash pruritic
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
1st shot 01/19/21 large red itchy rash encircling the shot site. 2nd shot 2/16/21 moderate, red itchy rash encircling the shot site, body aches, low energy, runny nose. 1st booster 12/17/21 same symptoms as 2nd shot. 2nd booster 05/20/22 no rash, no symptoms. 6/13/22 positive test result for Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- Covid test performed 6/13/2022 - Positive result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Thyroid and recently diagnosed type 2 Diabetes
- Andere Medikamente
- Vitamin C, D, Lipoflavonoid, Metformin, Triam/HCTZ, Levothyrox
- Allergien
- Scallops
- Vorherige Impfungen
- 2nd vaccine for whooping cough .... body aches and runny nose
- Staat
- NE
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 27,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Headache
Injection site pain
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I received my vaccine on 05/23/2022. There was no immediate reaction. The following day my arm where I received the vaccine was sore. Each day after I had gotten better. On the morning of 06/19/2022 I woke up around 7 AM with a scratchy throat, minor headache and cough. I went to work did two rapid test which was negative. I then did a PCR and was diagnosed with Covid. I was prescribed PAXLOVID and since taking the medication symptoms have subsided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Covid PCR
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Lisinopril; lovastatin; TYLENOL PM
- Allergien
- Peanuts; walnut; intolerance to NORCO
- Vorherige Impfungen
- Minor injection site soreness after any shot.
- Staat
- NC
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 27.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 35,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Nasopharyngitis
Oropharyngeal pain
Respiratory tract congestion
Streptococcus test negative
Symptomtext
sore throat and congestion, cold
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- strep throat negative
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Celexa
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 07.06.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Joint range of motion decreased
Pain
Symptomtext
pain, limited range of motion right shoulder
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- pantoprazole 40mg, rsouvastatin 5mg, creon 12,000-36,000 units, metoprolol tartrate 50mg, levothyroxine 75mcg
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 04.05.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Extra dose administered
Fatigue
Headache
Influenza like illness
Oropharyngeal pain
SARS-CoV-2 test
Secretion discharge
Vaccine breakthrough infection
Symptomtext
For the Second and Forth shot of the vaccine, I did have mild flu like symptoms for a day or so but they went away. Breakthrough Case of COVID- I had a sore throat, a cough, Mucus, very bad headache, and fatigued.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID Test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis, Sleep Apnea, Cancer Survivor.
- Andere Medikamente
- Synthroid, Iliothyronine, Zolpidem, Ashawaganda, Vitamin, 12, Vitamin, C, Vitamin, D, Magnesium.
- Allergien
- All Antibiotics, Latex, Penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 14.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Injection site erythema
Injection site pain
Injection site rash
Injection site warmth
Myalgia
Nausea
Pyrexia
Vomiting
Symptomtext
Started with pain is the area of the shot and the fatigue, muscle pain, chills, nausea then fever, vomiting and now a big read rash on the injection site that is very hot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- I am on Oxygen due to Covid-19
- Vorgeschichte
- N?A
- Andere Medikamente
- Yes
- Allergien
- Valume
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 16.06.2022
- Impfdatum
- 18.05.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 26,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Balance disorder
COVID-19
Chills
Cough
Dizziness
Dry throat
Fatigue
Feeling abnormal
Pain
Pyrexia
SARS-CoV-2 test positive
Somnolence
Symptomtext
Starting 06/13/2022, I started having coughing, chills and fever. On 06/14/2022, I tested Positive for COVID, and went to urgent care where I was prescribed Paxlovid. I started the Paxlovid on 06/15/2022. My entire body has been aching, my throat was dry and I felt horrid. . 06/15/2022 I started getting dizzy and had to steady myself. So far to this day I have had a day and a half of the Paxlovid, and I am starting to feel slightly better but I am very fatigued and feel the need to nap throughout the day (which I do not like to do).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lisinopril, Simvastatin, Centrum Silver and Vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 03.05.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 37,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Bronchospasm
COVID-19
Cough
Headache
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Sleep disorder
Symptomtext
On 6/8/2022, I had a cough, headache, and sore throat. I took a home test for COVID, and the result was negative. On 6/9/2022, I took another home test, which yielded a positive result. The cough and headache were worse on 6/9/2022. I also had a runny nose and aching joints. My cough was so bad that my sleep was disrupted by bronchial spasms, and I had to use my albuterol inhaler. On 6/10/2022 or 6/11/2022, I began taking NyQuil for nighttime relief, and I was able to sleep well. During the day, I took Mucinex, Tylenol, and dextromethorphan, all of which eased the symptoms and provided temporary relief. On 6/10/2022, I called my doctor's office, and I was prescribed Paxlovid. Two or three days after beginning the Paxlovid, I started to feel a little better and was able to do some household chores. I was also able to take my dog for a walk for the first time since having COVID on the evening of 6/14/2022. I did another home test on 6/14/2022, and I got another positive result, though the pink line was just barely discernible. At the time of this writing, I still have an intermittently runny nose (which may be due at least in part to my asthma) and intermittent cough. I feel better than I did at the beginning of my illness, as I have been sleeping better. Since the beginning of the pandemic, I have taken various precautionary measures, including masking. However, about five days before I developed symptoms, I went to my granddaughter's high graduation party, which was held outdoors, and I didn't wear a mask. None of the 50 or so guests wore masks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Intermittent asthma, iliotibial band syndrome, back pain and sciatica resulting from bulging disk in lumbar area.
- Andere Medikamente
- Gabapentin, multivitamins, fish oil, calcium, vitamin D3, vitamin C, magnesium, Prevagen, vitamin K2, Advil, Tylenol, flax seed oil, Pepcid, albuterol inhaler, Alvesco inhaler, Ricola cough drops, Magna Life Leg and Back Pain Relief, Flonas
- Allergien
- Demerol, PABA.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 14.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Oral pruritus
Throat irritation
Symptomtext
itching throat and palate
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oral pruritus
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- CKD stage 3 Endometriosis History of radical nephrectomy Hyperlipidemia Proctocolitis
- Andere Medikamente
- unknown
- Allergien
- adhesive tape
- Vorherige Impfungen
- Covid vaccine, Moderna
- Staat
- IL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 14.05.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Cough
Gingival blister
Laryngitis
Pain
SARS-CoV-2 test negative
Throat irritation
Tooth abscess
Wheezing
Symptomtext
On the 16th of May, I got an itchy throat. I thought it was allergies. The next day, on the 17th, I started with a cough. The cough went on until the 31st. During that time, on the 20th, I had a temp of 99 and, on the 22nd, it went up to 101. I had an asthma prepared pack because, as of April, my doctor diagnosed me with asthma. She prescribed a pack that included MEDROL. I started the MEDROL and my laryngitis started on the 19th. I had a video visit with my doctor on the 24th. She told me to switch off the MEDROL to prednisone. I took prednisone from the 24th to the 30th. She also told me to start a Z-PAK on the 24th and that was 5 days. It ended on the 28th. She also had me start a medication that included guaifenesin and codeine. I wheezed worse. During this time, I was also talking albuterol in a nebulizer. I ran out of albuterol so the next batch of albuterol solution was DUONEB - ipratropium bromide and albuterol sulfate inhalation solution. During this time, I couldn't blow more than 220 or 230 so we were doing more of the inhalation therapy. I wasn't getting better so she prescribed another Z-PAK. I took that from June 1st to the 5th. On June 6th, I thought I had a sinus infection. It was intense. Within a day, I ended up with a huge blister on my gum over one of my teeth. It ended up being a dental abscess. That was 3 days of pain. It deflated on the 8th. I had to see an oral surgeon and will be having it removed on Tuesday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- At home Covid test - negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Afib; Arthritis
- Andere Medikamente
- Olmesartan medoxomil; levothyroxine; ELIQUIS; amlodipine; pravastatin; B complex vitamin; vitamin D3; TYLENOL
- Allergien
- Iodine; cinnamon; red dye; cilantro; season allergies especially to mold and pollen; bandage adhesive; tracer dye for bone scans; CELEBREX; MUCINEX; NYQUIL; guaifenesin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 05.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Bone disorder
Bone fragmentation
Muscular weakness
Pain
Scoliosis
Spinal X-ray abnormal
Urinary tract infection
Symptomtext
On the 7th I was leaving the grocery store and my legs stopped working. I almost collapsed in the parking lot. What saved me was my shopping cart. The next week I had an appointment with my doctor already anyways. I talked to him about it, and he gave me a prescription for x-rays and I did that a week and a half later. The next week after that, I had another appointment with my doctor, and he said that there was a lot of bone debris in the middle of my spine and the bones in my neck were straight. And some scoliosis. I have been trying to get an appointment with an orthopedic doctor. Haven?t had luck with that yet. I was also prescribed methocarbamol to try and help with the pain, but it hasn?t been working too well. Also, The beginning of June, I was also having really bad lower back pain. The doctor noted it could have just been a UTI, but no scans were done to confirm anything. Antibiotics did make pain less, but still having back pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- X-Ray: a lot of bone debris in the middle of my spine and the bones in my neck were straight. Some scoliosis
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 Diabetes, Rheumatoid Arthritis, Fibromyalgia, PCOS, High cholesterol, Gastroesophageal Reflux Disease, Carpal Tunnel
- Andere Medikamente
- Methotrexate, Sulfasalazine, Metformin, Buspirone, Bupropion, Prescription Folic Acid, Prescription Vitamin D, Nexium, Simvastatin, Fiber, Glucosamine, Iron, Turmeric, Magnesium, Vitamin C, Multivitamin and Super B Complex, Biotin
- Allergien
- Penicillin, Mangoes, Several skin allergies (ex: juices of shellfish can cause hives if it gets in contact with skin), Soaps
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 03.05.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 13,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Rash approximately 2 weeks after my second covid moderna booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- No tests done
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High cholesterol , glaucoma
- Andere Medikamente
- Lipitor , birth control, travprost eye drops, sumatriptan when needed. One a day vitamin
- Allergien
- Codine, Naproxen
- Vorherige Impfungen
- Moderna- Covid Vaccine shot #2 covid arm
- Staat
- MN
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 07.06.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Vaccination site erythema
Vaccination site mass
Vaccination site pruritus
Vaccination site warmth
Symptomtext
Patient called Public Health on 6/10/2022 at approximately 1522 hours. Patient noted that she had redness, itching, warmth, and a lump within three inches of the vaccination site. Patient noted that she called her primary care provider and they advised OTC topical anti-itch cream and benadryl medication as needed. They also directed the patient to seek additional care if the condition persists or worsens. Public health staff shared with patient the CDC What to Expect After Getting a COVID-19 Vaccination including common reactions and care such as a cool compress at the injection site. Patient encouraged to follow provider recommendations and contact public health if additional resources are needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Patient reports have skin rash reactions when bandages are used. A bandage was not provide to the patron per their request.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Burning sensation
Contusion
Injection site pain
Pain
Sleep disorder
Tenderness
Symptomtext
Patient reports she did not have any pain the day of vaccination but the next day her shoulder and collar bone were very sore. She thought this was strange because it's usually my arm that is sore (second booster dose). Her injection pain has been getting worse to the point that it wakes her up in the middle of the night. It is extremely sensitive to the touch (feels like she have a gigantic bruise) and has a burning sensation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- n/a to be done
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 04.06.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Injection site erythema
Injection site warmth
Pain
Symptomtext
Patient experienced some pain the day of the injection in the afternoon, but she was more concerned about the 2 inch square very warm, red area that appeared below the injection site 2 days later on Monday and Tuesday (vaccine administered on Saturday). I spoke with her on Wednesday and she said she did not require any medication or treatment for the reaction and that it had started to fade a little bit on Wednesday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 18.05.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 16,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Exposure to SARS-CoV-2
Fatigue
Headache
Nasopharyngitis
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Sinus disorder
Symptomtext
I woke up on 06/03 and felt really tired and had sinus issues and sore throat. I attributed that to my recent travel. But I took a home Covid test which was negative. Later that day I went ahead and went to a local clinic to take a PCR test. I received positive results the next morning on 06/04. Before I received my results, I was informed that some of the family I was traveling had turned up positive for Covid. I was experiencing head cold like symptoms like congestion and headache which lasted through till Monday. I was treating symptoms with over the counter medications until Monday morning when I called my doctor, who prescribed Paxlovid which I began on Monday evening, and by Tuesday, my symptoms had greatly improved and have continued to improve each day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home Covid test-negative-06/03, PCR Covid test-positive-06/03
- Aktuelle Erkrankungen
- Two Colds
- Vorgeschichte
- None
- Andere Medikamente
- Fish Oil, Vitamin D, Calcium
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Burning sensation
Discomfort
Hypoaesthesia
Neuralgia
Pain
Symptomtext
About 14 hours after patient received booster dose (0.25ml) of Moderna Covid vaccine, he developed severe pain in all joints of his body. He also reports his nerves were "on fire" and that there was noticeably increased numbness in extremities. The pt went to his primary physician who prescribed a high dose prednisone taper. This course of treatment did little to relieve nerve symptoms. Pt also states that he is in as much pain as he was in before his recent back surgery even though, prior to the booster dose, he was experiencing positive healing and improvement. He has additional follow-up appts to further address the pain and discomfort.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Major back surgery in January 2022. Was healing well from surgery
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 07.06.2022
- Impfdatum
- 22.04.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 39,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
COVID-19
Cough
Exposure to SARS-CoV-2
Fatigue
Headache
Nasal congestion
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I had been notified the day before that I had been exposed by a family member to COVID. I woke up the next morning and had a scratchy throat. I thought I better get tested to make sure. I got tested at about 11:30AM and as the day progressed, I started to get really tired. My nose was stuffy. I was notified at 07:00PM that night of the 31st that I tested positive on the rapid test. I also had PCR test as well that same day. On the next day, I received those results at 04:30PM and they came back positive. I ran a temperature of 102.5. Stuffy nose and dull headache across my forehead. I had a cough, but it was every once in a while. I felt more like my allergies were bad instead of COVID, except the temperature. I drank a lot of fluids and stayed in bed until Thursday. Thursday, I had no temperature and Friday as well. Still had the runny nose. I'm fine now. I get tired but I feel fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 05/31/2022 Rapid COVID test positive. 05/31/2022 PCR COVID test positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Tetracycline; erythromycin; mushrooms
- Vorherige Impfungen
- A previous flu vaccine, fever of 101, ill for 5 days after.
- Staat
- IL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 08.05.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 25,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Decreased appetite
Fatigue
Oropharyngeal pain
Pyrexia
Sleep disorder
Streptococcus test negative
Vaccine breakthrough infection
Symptomtext
Breakthrough case of Covid, sx onset 06/02/2022. Sx began on 06/02/2022, I woke up with a sore throat, low grade fever, fatigued and I had not slept well the night before. The sore throat was not getting better. I went to urgent care to get a rapid strep test, which was negative. The rapid Covid test was negative that I took at home. Urgent care recommended a PCR test. Results came back Saturday 06/04/2022. I was extremely fatigued, throat was very sore, fever was 100.5. I have a pulse oximeter and my O2 level was at about 94%. I slept all day Saturday, most of Sunday. I did take some MUCINEX last night before bed and when I got up, I was still a little fatigued and I have not had much of an appetite. I have been drinking plenty of fluids. No other sx currently, my appetite is coming back slowly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 06/03/2022 Rapid test Friday morning at home negative. 06/03/2022 Friday afternoon a local hospital PCR was positive Rapid strep test was negative
- Aktuelle Erkrankungen
- Mild cold nothing severe just some sneezing and coughing
- Vorgeschichte
- No I don't
- Andere Medikamente
- Fluoxetine; LAMICTAL; rosuvastatin
- Allergien
- Z-PAK; strawberries
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 05.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Rash
Urticaria
Symptomtext
DEVELOPED RASH/HIVES ON LEFT SIDE OF NECK/UPPER SHOULDER. TOOK BENADRYL AND RASH WENT AWAY. RASH HAS NOT RETURNED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 04.06.2022
- Impfdatum
- 02.06.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Hives all over upper thighs starting the morning I woke up two days after receiving the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- PCN
- Vorherige Impfungen
- Smaller reaction to my second dose of Moderna as well on May 7, 2021. Didn?t think anything of it at the time. Had hives appear
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 21.04.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 35,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Fatigue
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
5-26-2022, I started noticing a sore throat, fatigue and head congestion and I took a home Covid test that was negative. I retook another home test on 5-27 and it was negative as well. On 5-30, 2022, I took another home test and it was positive. I called the doctor on 5-30 and went to the urgent care. They prescribed a cough medicine with codeine and told me to come back if it got worse. I am much better today. I am reporting my breakthrough case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 3 home Covid home tests, 2 negative and 1 positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Rabeprazole 20mg daily; montelukast 10mg daily; Advair inhaler 250/50 1 inh bid; albuterol inh 90mcg as needed; calcium 600mg with vit d daily; magnesium 500mg daily; multivitamin daily
- Allergien
- Aleve; mustard
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 03.06.2022
- Impfdatum
- 01.03.2021
- Beginn
- 24.05.2022
- Tage bis Beginn
- 449,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Head discomfort
Influenza virus test
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Vaccinated on Mar 1 & 29, 2021; Boosted on Oct 29, 2021 & Apr 26, 2022; On May 24, 2022 I had a cough, head congestion and a slight fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Visited Walk In. Administered a flu test and a covid test. I tested positive for covid.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Atorvastatin.
- Allergien
- Penicillin.
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 21.04.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 42,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Headache
Oropharyngeal pain
Pain
Paranasal sinus hypersecretion
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I started getting symptoms of sore and scratchy throat. I had a slight headache with sinus drainage, body aches, and fever. I did an at home COVID-19 test on 6/2/2022 that was positive. I did a telehealth visit with my doctor and was not prescribed anything. Today my symptoms have got worse and stronger.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anemia; Diverticulitis; Sleep Apnea
- Andere Medikamente
- Thyroid Medications
- Allergien
- Penicillin; sulfa; morphine
- Vorherige Impfungen
- Moderna Dose 1, 2, 3 - Rash.
- Staat
- HI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 24.03.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 25,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test abnormal
Dry eye
Eyelid ptosis
Fatigue
Myasthenia gravis
Symptomtext
In April 2022, I was flying out of the area. When I reached my destination, my eyes felt dry. Also, the right eyelid had drooped. It may have started a day or two prior, but I didn't notice it, as I thought I was just tired. However, it was definitely noticeable when I reached my destination. We stayed where we were for 5 days. When we returned home, I made an appointment with my doctor. I saw a physician's assistant and underwent a blood test that was ordered by the doctor. It was found that my blood had very high levels of acetylcholine, and it is suspected that I have myasthenia gravis. I am scheduled to see the physician's assistant again on 6/4/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Pinched nerve in the neck.
- Vorgeschichte
- One lobe of thyroid gland previously surgically removed; bone spur on right foot; suspected myasthenia gravis.
- Andere Medikamente
- Synthroid; ibuprofen.
- Allergien
- Pine nuts.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 19.04.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dermatitis contact
Exposure to toxic agent
Pruritus
Symptomtext
I was exposed to poison ivy on 5/20/2022 but was not aware of it at the time. A day or two later I began noticing skin reactions to the exposure. The adverse event is the extremeness of the reaction, much greater than experienced in prior exposures. I contacted my personal physician and he prescribed Triamcinolone Acetonide Cream USP 1mg/g. After application for three days the extreme reaction was not subsiding so my personal physician prescribed Methylprednisolone Tablets, USP 4 mg, 21 tablet course for 6 days. Basic comfort was restored, but some itching remained, though greatly reduced. The initial major rashes are recovering but other patches, some seem to be new areas, are flaring up (itchiness without the pimpling) periodically.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lexapro
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 02.05.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 20,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Influenza like illness
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Tested positive for COVID-19 on 5/24/2022 after experiencing flu like systems with fever previous two day.. Personal physician prescribed Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Two independent home tests results were positive for Covid-19.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HBP
- Andere Medikamente
- High Blood Pressure medications.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- 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
Arthralgia
Immediate post-injection reaction
Pain
Symptomtext
Deep pain in left shoulder joint immediately upon administration. Pain continued to intensify over the next 30 - 45 minutes. Dull pain in left shoulder, worse during the night. Persists and is increased when raising arm, especially above head, rotating arm out to left side or attempting to lift objects with left hand/arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Evaluated 06/01/2022 by patient's PCP
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HBP (controlled)
- Andere Medikamente
- metoprolol xl 25mg, losartan 25mg, atorvastatin 20mg, vitamin D 2000 units, multivitamin, aspirin 81mg E.C.
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 01.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac flutter
Dizziness
Symptomtext
Client reports has felt like heart fluttering and like he is going to pass out several times since he received the vaccine yesterday morning, client advised to see Primacy Care Physician for further evaluation/treatment promptly, client verbalized understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Unknown at this time
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 13.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Chills
Cough
Decreased appetite
Fatigue
Headache
Nausea
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test negative
Somnolence
Streptococcus test negative
Symptomtext
On May 23 started feeling sore throat and fatigue,tested negative on an at home antigen test but by May 25 the sore throat was severe, had 101.1 degree fever, chills, nausea, headache, overall body aches and tested positive on at home antigen test so I went to Mather Hospital where they gave me an infusion of monoclonal antibodies. I slept almost the entire day and the next day I felt a little better. Fever broke, chills subsided, still sore throat, little appetite and coughing and congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- A strep test was administered and that came back negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- high blood pressure GERD high cholesterol
- Andere Medikamente
- Enalapril, Metoprolol, atorvastatin, zetia, prilosec, Vitamin D, CoQ 10, glucosamin chondroitin, Super C + zinc, calcium, multivitamin
- Allergien
- codeine, hydrocodone, flagyl, clindamycin, gabapentin
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 29.05.2022
- Impfdatum
- 26.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Conjunctivitis
Eye irritation
Fatigue
Malaise
Nasopharyngitis
Rhinorrhoea
Swelling of eyelid
Upper-airway cough syndrome
Symptomtext
Dose administered on April 26 by Pharmacy at clinic. First symptoms of Covid appeared on April 29. I thought it was a cold with runny nose, post-nasal drip, fatigue, no fever. Runny nose lingered for several weeks. Not sure when conjunctivitis symptoms first appeared because complicated by fact that I'd had eyelid surgery on April 6. Eye lids were swollen and eyes irritated from drops and ointments having to apply several times daily. Conjunctivitis diagnosed at Immediate Care - and antibiotic eye drops began on May 20. Infection resolved by May 23 when I saw my eyelid surgeon for 6-week post-op visit. She took me off antibiotics and now on 3x daily eye drops, Refresh PM eye ointment in pm and Lumify in am. Irritation subsiding, but not yet fully resolved (see #20 below).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Had eyelid surgery (bilateral ptosis repair, ectropion repair) on April 6; eyelids were still swollen when Covid symptoms first appeared. Since eyes, themselves, were also irritated, I cannot be certain when conjunctivitis began.
- Vorgeschichte
- Arthritis
- Andere Medikamente
- latanoprost, dorzolamide-timolol, Soothe-XP eye drops, doxycycline, multi-vitamin, biotin, vitamin D3, estradiol (patch and vaginal cream)
- Allergien
- sulfa, penicillin (allergist says I have outgrown), cipro (rxn. to caffeine, not a true allergy)
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 28.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Fatigue
Headache
Interchange of vaccine products
Pain
SARS-CoV-2 test negative
Symptomtext
"Screaming" headache (started @ 8pm, increased til midnight, continued til 10am next day), extreme fatigue, body aches, diarrhea (2 days). Took Tylenol which lessened headache and body aches somewhat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- At-home Covid-19 test 5/25/21, 1pm, negative result.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Aortic heart valve replacement (11/2015).
- Andere Medikamente
- Atorvastatin and Warfarin.
- Allergien
- Penicillin.
- Vorherige Impfungen
- Similar adverse reaction as noted above, ill for 4 days, 57, 4/6/21, Janssen C-19, Lot 201A21A. Unreported.
- Staat
- VA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 25,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest discomfort
Diarrhoea
Fatigue
Productive cough
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 05/23/2022 with symptoms of runny nose, congestion, fatigue. On 05/26/2022 my symptoms worsened and I woke up with chest tightness, and a productive cough. I was not prescribed any medication when I went to the urgent care on 05/26/2022. I have also experienced diarrhea sporadically. My cough is not as productive today, but I still have a runny nose as well. My symptoms are worse in the mornings. I am beginning to feel better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab was positive on 05/26/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Zoloft; Altase; Zocor; women's multivitamin; elderberry; coQ10
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 27.05.2022
- Impfdatum
- 26.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fall
Mental status changes
Pyrexia
Symptomtext
Pt developed a fever approx 12hours after vaccine administration. He had mental status changes and fell in his home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Prior COVID-19 Dx (2/2021), quadraplegic, coronary artery disease, aortic stenosis, chronic indwelling catheter (2ndary to being paralyzed). Had a previous rxn to C-19 reaction
- Andere Medikamente
- -
- Allergien
- Levofloxacin, latex
- Vorherige Impfungen
- The patient received Moderna COVID-19 Vaccine 0.25 ml IM. Series: Series 3 on 11/5/21,. Admitted to the hospital 24hours l
- Staat
- CO
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 27.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 20,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Oropharyngeal pain
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID-19 Case: It started as a sore throat and cough, I called my doctor and he prescribed Paxlovid. The symptoms subsided after 72-hours. After a few days I started to feel better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 05/25/2022- PCR COVID-19 Test=Positive
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- Mild Hypertension; Gastroesophageal Reflux Disease (GERD)
- Andere Medikamente
- Multivitamins Fish Oil
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site erythema
Injection site infection
Injection site pain
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Patient experienced swollen, red, itchy, hot, sore arm around injection site 2 days after injection. Another pharmacist suggested going to Emergency Room and site was confirmed as infected
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 11.05.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 11,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Malaise
Nasal congestion
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough Covid Symptoms first developed on 05/22/2022 Symptoms: cough, sore throat, runny/stuffy nose, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Binax nasal swab positive on 05/24/2022 (home test)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure sleep apnea osteoporosis
- Andere Medikamente
- Celexa Pepsid Losartan Potassium Restasis Omega 3 Calcium
- Allergien
- Lisinopril Sulfa Codeine
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash erythematous
Rash papular
Symptomtext
Red raised bumps on back. Slightly itchy. Unilateral and somewhat symmetrical.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cold sore Migraines
- Vorgeschichte
- Chronic migraines
- Andere Medikamente
- Acyclovir Sumitriptan
- Allergien
- Tetracycline
- Vorherige Impfungen
- Covid 19 moderna
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 19.04.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Headache
Nasopharyngitis
Oropharyngeal pain
Pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
A little over 1 month after vaccination, 5-21-2022, I started feeling cold symptoms such as runny nose, cough, severe headache, congestion, sore throat and body aches. I took a home Covid test on 5-21 and 5-22 and both were negative. I also took a home test on 5-23 and it was positive. I had a telehealth visit with the doctor on 5-23 and they prescribed Paxlovid. I have started taking it and I am feeling much better. I am reporting a breakthrough case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 3 home Covid tests, 2 were negative and 1 positive result.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Metamucil 1 cap daily, Calcium Citrate 1 daily, Vit D3 2000units daily, Estradiol .5mg twice weekly
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Chills
Computerised tomogram head
Full blood count
Laboratory test
Lipids
Magnetic resonance imaging head
Metabolic function test
Pyrexia
Transient ischaemic attack
Ultrasound Doppler
Urine analysis
Symptomtext
The same day as booster felt chills, fevers for 5 days. Went to the ER and was admitted to hospital. While there had a TIA. Cardiologist has recommended Holter Monitor. Hospital stay was 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- 3,0
- Labordaten
- CBC, BMP, CMP, Lipid panel, Cardiac markers, CT Head, Chest Xray, MRI Brain, Urinalysis, Bi lateral carotid US
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Thyroid, Depression, Herpies
- Andere Medikamente
- Liothyronine, Acyclovir, Tretamine,
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 16.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site discolouration
Injection site dryness
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Skin exfoliation
Symptomtext
Two days after the vaccine shot the area where it was injected was very swollen and red and very hot to the touch. I used ice and Benadryl cream per my physician since it had a bit of an itch to it. It improved over the next week, however, my skin became brown in color and seemed dry. By the 8th day, the brown area started to peel. It is like I have a bad sunburn in that one area. The skin under the skin that peeled off is very pink and delicate and I am scared of infection or a sunbrun.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discolouration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Xiidra eye drops, Buspur, Klonopin, vitamin D-3, tumeric, probiotic, and milk thistle
- Allergien
- Aspirin (Phenyl Salicylate) Hyoscyamine (Phenyl Salicylate) Phenergan (Ethylenediamine Dihydrochloride) Zyrtec and Xyzal (Ethylenediamine Dihydrochloride) Propolis (Cera Alba/beeswax/honey) Dodecyl gallate (Try to avoid Benzoic Acid) Ethylenediamine Dihydrochloride Gluten Soy
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 26.04.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 12,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dysphonia
Fatigue
Headache
Hyperhidrosis
Nasal congestion
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Vaccine breakthrough infection
Symptomtext
Breakthrough case of COVID 05/08/2022. Fever stayed with me, sweats, headache, no cough, a little hoarseness and scratchy throat and exhaustion, went through the course of PAXLOVID then started with a stuffy nose, nothing fierce, could be allergies form the pollen. It lasted about 4 days, before the 5th day I was feeling better. I am really glad I got that booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 05/10/2022 Home test positive.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetes Type I; Hypertension; high cholesterol; bilateral radiculopathy; chronic pain; glaucoma; allergies; asthma; GERD; Barret's Esophagus; obesity
- Andere Medikamente
- Valsartan; metoprolol; metformin; atorvastatin; gabapentin; Lantus; lansoprazole; metoclopramide; albuterol; Symbicort; iron; multivitamin; magnesium; Metamucil; Florastor; Zaditor (eye drop); latanoprost; Voltaren gel; Xyzal; Flonase (rx);
- Allergien
- Lyrica; Topamax; ibuprofen; naproxen; seasonal allergies; dust; cats
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 25.04.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 23,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
COVID-19
Chills
Cough
Fatigue
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Tested positive for COVID, May 18th Chills, fever, runny nose, dry cough, tremendous fatigue, stomach ache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Tested positive for COVID, May 18th
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes, High Blood Pressure, Cardio Vascular
- Andere Medikamente
- Jardiance, Inspra, Indapamide, Benazapril, Dilitiazem,Metformin, Multi-vitamin, Fish Oil, VitaminsB12, C. D, Echinacea, Magnesium, Turmeric, Saw Palmetto and CO Q10
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Symptomtext
The day after the shot, I had severe pain in my right hip joint. I've had bursitis in my hip except it's been many years since a flare up. I did have it last October after my 3rd vaccine but didn't think much of it. I didn't have any problems prior then when I got the shot, it was grief in my hip. I didn't think about it back with the 3rd vaccine and didn't mention it. I talked to Dr. and I'm taking diclofenac sodium and did that for 2 weeks and some physical therapy (exercises to do). He finally gave me a cortisone injection. I'm going in on Wednesday to probably get another injection and follow up. After the injection, everything was okay, and the pain went away. The pain diminished slowly within a day or so.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Allergies
- Andere Medikamente
- Osphena 60mg 1x day; ibandronate sodium 150mg 1x monthly (last day of month); azelastine nasal spray; Allegra Allergy OTC; Viactiv 2x day; multivitamin 1x day; eye vitamin; lutein; zeaxanthin 1x day; biotin 1x day
- Allergien
- Penicillin; tetracycline; peppers; chilis; environmental allergies
- Vorherige Impfungen
- 3rd COVID Moderna: 10/28/2021, Bursitis flare up in the right hip as well.
- Staat
- GA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 21.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal X-ray
Bacterial test positive
Blood test abnormal
Chills
Constipation
Gastrointestinal disorder
Pain
Prostatitis
Pyrexia
Urinary tract disorder
Symptomtext
12 hours after booster had body aches and fever which lasts about 24 hours then felt fine Approx 8 days after booster vaccine had severe chills and overall body aches - fever spiked to 102 on third day - led to acute prostatitis and GI problems - urinary issues seem to be resolved with antibiotic and now FloMax - still in treatment for GI issues
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Blood panel showed mild bacterial load but not in subsequent tests (approx May 4) More recent abdominal x-ray shows mild to moderate constipation (May 19) Mostly recovered from urinary issue - still in treatment for GI issues
- Aktuelle Erkrankungen
- Lower back pain - L4/L5 damage Gastro-Intestinal bloating
- Vorgeschichte
- Heart attack about 10 years ago
- Andere Medikamente
- Atorvastatin, aspirin, Vitamin D, Clonazepam, Ezetimibe, Lisinipril, Meloxicam, Nebivolol, Fish Oil
- Allergien
- None known
- Vorherige Impfungen
- short term reaction to COVID 2nd and 3rd shots - resolved within 2 days
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 8,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Ear discomfort
Feeling abnormal
Headache
Laboratory test normal
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Sputum discoloured
Symptomtext
5/13 Sore throat and coughing started. 5/14 Sore throat and very bad cough. Fever 100.6, ears and head felt fuzzy, took Tylenol and Tussin DM to treat symptoms. Fever lasted all day. 5/15 No fever, but symptoms continued otherwise. 5/16, No fever, but cough improved, though sounded wet. All other symptoms same. 5/17 No change in symptoms. Took at home Covid test, which was positive. 5/18 Headache all day, metallic taste in mouth. 5/19 No change. 5/20 produced dark yellow sputum.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Pneumonia test also negative, Rapid test at Urgent care positive. prescribed Paxlovid on 2/17.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Glaucoma
- Andere Medikamente
- Zyrtec D, Latanoprost, B complex with C, K2, fish oil, turmeric, vitamin d, b12, calcium Caltrate, probiotic, lutein vision complex
- Allergien
- Sulfa drugs, epinephrine, maximite's, adhesive tape
- Vorherige Impfungen
- Shingrix, 10/13/2019. Arm swelled up, very sore to touch. Dose 1 of shingrix. 3/11/2021, Arm swelled up greatly 3/11-3/15, Co
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 06.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 11,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
COVID-19
General physical condition abnormal
Glassy eyes
Insomnia
Nasal congestion
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
On Tuesday night I was not able to sleep well and had nasal congestion and my back was sore. I had been out weeding and thought maybe it was allergies from being in the garden. I had been at a wedding over the weekend but was very cautious. I went to work and my co-workers thought my eyes looked glassy and I just didn't look right. I took a test and it was positive. I called my Dr who had me test again two hours later and he got me Paxlovid. I really only had the body aches, I had a fever Wednesday night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Covid Test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Cholesterol
- Andere Medikamente
- Calcium, Vitamin D3, Magnesium, Turmeric, Multivitamin, Simvastatin
- Allergien
- Sulfa; peaches; plums; nectarines
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 13.05.2022
- Beginn
- 14.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Fatigue
Myalgia
Oropharyngeal pain
Respiratory disorder
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
The following symptoms iccured the day after I had the booster shot. Sore throat Persistent cough Muscle aches Fatigue Then, on and off for about a week I had upper respiratory tightness and cough. No fever at all.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Negative PCR test 3 days after booster Positive at home test 6 days after booster
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Biotin Levothyroxine Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 26.04.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 13,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
Nasopharyngitis
Productive cough
SARS-CoV-2 test positive
Symptomtext
Travelled to and back home at beginning of May. On 5/7 I began feeling cold-like symptoms w/ a productive cough. I tested positive on 5/9 and contacted my Dr and got Paxlovid and took it for 5 days. I was sick up until 5/14. I re-tested on 5/18 and was negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Hydrochlorothiazide, Synthroid, Zyrtec, Vitamin D
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 20.05.2022
- Impfdatum
- 16.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Malaise
Nausea
Vaccination site pain
Symptomtext
Malaise; Lightheadedness; Pain at the injection site / sore arm; Chills; Nausea; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (Malaise), DIZZINESS (Lightheadedness), VACCINATION SITE PAIN (Pain at the injection site / sore arm), CHILLS (Chills) and NAUSEA (Nausea) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. No Medical History information was reported. On 16-May-2022 at 3:30 PM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-May-2022 at 5:00 AM, the patient experienced MALAISE (Malaise), DIZZINESS (Lightheadedness), VACCINATION SITE PAIN (Pain at the injection site / sore arm), CHILLS (Chills) and NAUSEA (Nausea). On 17-May-2022 at 8:00 AM, MALAISE (Malaise), DIZZINESS (Lightheadedness), CHILLS (Chills) and NAUSEA (Nausea) had resolved. At the time of the report, VACCINATION SITE PAIN (Pain at the injection site / sore arm) had not resolved. Concomitant product use was not provided by the reporter. The patient received second booster on 16-May-2022 at 3:30 PM afternoon and experienced several AEs on 17-May-2022 between 5:00 AM to 8:00 AM morning. They were the most significant of all 4 shots. The patient experienced pain at the injection site, chills, malaise, nausea and lightheadedness. Events had subsided, except for a sore arm. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 13.05.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chest discomfort
Fatigue
Myalgia
Pain
Pruritus
Pyrexia
Rash
Urticaria
Symptomtext
Myalgia, Arthralgia, Fever, SkinRash, Rash, UrticariaPruritus, "Generalized vaccine symptoms such as body aches, tiredness, etc starting aroun 1400 that day. Slight chest tightness and low grade fever-100.3 that evening 2000. Rash/hives on hands/chest/arms 5/13/2022 1100 - came to Occupational health office: Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac stress test abnormal
Catheterisation cardiac normal
Chest X-ray
Dizziness
Echocardiogram
Headache
Heart rate irregular
Peripheral swelling
Scan with contrast normal
Symptomtext
One day in March 2022 I got hot and lightheaded. I went to see the cardiologist and they did a stress test. I failed it. The doctor said my heartbeat was irregular. They checked me in the hospital on May 3, 2022. On May 4, 2022, they did a heart catheterization and inserted dye through my heart to watch the circulation. They didn't find any blockages. I am going to see a specialist tomorrow to see what's going on with the electrical part of my heart because it's beating out of sync. When I was at the hospital hey changed my medications. They changed my losartan potassium to 50mg. They told me to stop taking triamterene. They put me on Lipitor, but I had reactions from it so I took myself off of it. I started just taking the Rosuvastatin. I was given atorvastatin 20mg 2x night. I took it at home until May 10th because I was having headaches, and my hands and feet swelled up. I stopped taking it and then everything went back to normal. They also added metoprolol 25mg and a baby aspirin 81mg 1x night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- 2,0
- Labordaten
- Imaging; Stress test- failed, showed irregular heartbeat; Chest X-ray; Heart Echocardiogram
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Neuropathy; Type 2 Diabetic; High Blood Pressure (controlled); High Cholesterol (controlled); Breast Cancer Removal Surgery (4/4/2019); Sleep Apnea
- Andere Medikamente
- Letrozole 2.5mg tablet morning; Levothyroxine 75mcg tablet morning; Losartan Potassium 100mg tablet 1x morning; Triamterene-HCTZ 37.5-25mg tablet 1x morning; Rosuvastatin 10mg tablet 1x night; Vitamin D3 50mcg capsule 1x morning; Omega 3 2,
- Allergien
- Hydrocodone
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 09.05.2022
- Beginn
- 14.05.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Nasal congestion
SARS-CoV-2 test positive
Symptomtext
I registered with VSAFE and reported that I had tested positive for Covid I had a virtual doctor visit I was prescribed Paxlovid which I was to take for 5 days and I am still stuffy in the head and fatigued.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- I registered with VSAFE and reported that I had tested positive for Covid after taking a Covid test.
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- High blood pressure; premature atrial contractions; High Cholesterol
- Andere Medikamente
- Evista; Ziac; vitamin D3; calcium; pro and prebiotic; losartan
- Allergien
- Bactrim; Ceftin; hydrocodone; gluten; wheat
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 01.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Pain
Pain of skin
Symptomtext
Rash on upper arm-same as injection arm. Stinging and soreness. Treated with analgesic cream.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- None. Consulted by phone with primary doctor with pictures
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Levoraxan
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 30.04.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash erythematous
Rash pruritic
Symptomtext
Approximately 2 two weeks after receiving the vaccine I developed a rash. It started on the back of my neck, it was red and itchy. Rash kind of moves around. It has been on my scalp, stomach, back, arms, legs, feet. It stays in 1 place for about 20 mins and then moves somewhere else. Zyrtec, betamethasone, and antihistamine helps a little.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Thyroid
- Andere Medikamente
- Advil; Synthroid
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Feeling of body temperature change
Pain
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
*******************COVID BREAKTHROUGH CASE********************************* Severe body aches; Chills; I think I had a temperature but never took it. Dr prescribed Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- May 1st home test -positive; May 2nd PCR the next day at the pharmacy -Positive as well.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertention
- Andere Medikamente
- Vyvanse Unithroid Cymbalta Tramadol Valsartan
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 14.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Neuralgia
Rash
Symptomtext
PATIENT DEVELOPED SHINGLES DAY AFTER RECEIVING 2ND BOOSTER SHOT OF MODERNA. DIAGNOSIS WAS CONFIRMED DURING TELEMEDICINE APPOINTMENT WITH DR. PATIENT HAD PAINFUL RASH ON BACK AROUND BRA STRAP AREA. GIVEN 7-DAY COURSE OF VALACYCLOVIR 1 GRAM TID. AND GABAPENTIN 300MG TO TAKE AS NEEDED FOR NERVE PAIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- DM TYPE 2, HYPERTENSION, HYPOTHYROIDISM, ATHEROSCLEROTIC DISEASE
- Andere Medikamente
- ASPIRIN 81MG , CLOPIDOGREL 75MG, LEVEMIR, LISINOPRIL 20MG, METFORMIN ER 500MG, NIFEDIPINE ER 90MG,
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 16.04.2022
- Beginn
- 17.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Pain
Symptomtext
Left upper arm/shoulder pain when lifting arm to dress etc that hasn't improved, have not yet sought treatment but plan to.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain
Symptomtext
I woke up and was very achy so I took Tylenol every 6 hrs to keep the pain away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Propranolol Triamterene Potassium Levothyroxine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 09.05.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Eye pruritus
Oral mucosal blistering
Pruritus
Symptomtext
Patient experienced mouth blisters, itchy eyes/ears. Transferred to Emergency Department. Received diphenhydramine, famotidine, and albuterol. She recovered and was discharged home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hyperlipidemia, hypertension
- Andere Medikamente
- Albuterol, budesonide, epinephrine, fluticasone, ondansetron
- Allergien
- Amlodipine (hives), azithromycin (anaphylaxis), losartan (anaphylaxis), fruit (anaphylaxis), peanuts (anaphylaxis), lorazepam (rash), hydrocodone (rash), meloxicam (hives), mupirocin (rash), nystatin (rash), sulfa drugs (rash)
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Malaise
SARS-CoV-2 test
Vaccine breakthrough infection
Symptomtext
Breakthrough case of COVID on 11th and began Paxlovid on that evening. Symptoms were mild but began resolving on the 12th.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Antigen X2; PCR X1; Was tested for Omicron about 1 month ago due to being in a study and results returned negative.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Vit-D Losartan Turmeric Mult-vit mag Flaxseed Emergen-C
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Incorrect dose administered
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
WE GAVE A MODERNA BOOSTER DOSE TO PT AND HE IS UNDER 18. HE SHOULD HAVE RECEIVED A PFIZER BOOSTER DUE TO PATIENT AGE (15). THE MOTHER CAME IN WITH HER CHILDREN AND REQUESTED MODERNA BOOSTER FOR HERSELF AND KIDS AND WE DID NOT VERIFY THE PATIENT AGE APPROPRIATELY BEFORE PHARMACIST ADMINISTERED THE INCORRECT VACCINE BOOSTER. PHARMACIST REALIZED THE ERROR ALMOST IMMEDIATELY AFTER THE INCORRECT DOSE. MOTHER WAS THERE AS WELL AS PATIENTS TWIN BROTHER AND OLDER SIBLING. PATIENT HAD NO ADVERSE EVENT FROM THE INCORRECT DOSE , HE STAYED FOR ABOUT 30 MINUTES TO BE OBSERVED. PHARAMCIST FOLLOWED UP WITH MOHTER FOLLOWING DAY AND SEVERAL DAYS LATER AND PATIENT HAD NO ADVERSE EVENTS AS A RESULT OF THE MODERNA VACCINE DOSE BEING GIVEN INCORRECTLY, SHE STATED PATIENT FELT A LITTLE FATIGUED THE NEXT DAY BUT WAS OTHERWISE NORMAL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 09.05.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Petechiae
Rash
Symptomtext
A diffuse petechial rash covering legs, spreading to back, head, and ears.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- Losartan, Amlodipine
- Allergien
- dust mites and mold; no other allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angioedema
Pyrexia
Symptomtext
Fever & Angioedema Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Myalgia
Symptomtext
Myalgia & Arthralgia Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site warmth
Symptomtext
Approximately one inch below the injection site the skin became red, hot and inch. It was irregular shaped but basically round and about 2 inches in diameter. It lessened in redness today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, high cholesterol
- Andere Medikamente
- Creator 40 mg Efexir 150mg
- Allergien
- -
- Vorherige Impfungen
- After Covid vaccines- aches, fatigue, chills, and headache
- Staat
- MA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 23.04.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 13,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Oropharyngeal pain
Rhinorrhoea
Viral test
Symptomtext
Sore throat, chills, runny nose, headache, and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Home test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Alendronate Atenolol Pravastatin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood sodium decreased
Blood test
Computerised tomogram head normal
Confusional state
Fatigue
Mental status changes
Symptomtext
Moderna #4 given 5/6/22 9:30 am, in the afternoon patient was at his daughters house feeling tired. He went home to rest and later on that evening reported by daughter she was acting strange, Yelling at family "get the f** out", not responding to them to open the door. EMS came over took patient to hospital. noted by reports was admited with AMS/confusion. Hospital course vitals stable, blood work stable except for Na 126 that improved to 130 next day and normal CT of head. Patient was discharged next day AMA as he did not want to stay any longer. Family took him home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- poorly controlled diabetic
- Vorgeschichte
- poorly controlled diabetic
- Andere Medikamente
- Active Outpatient Medications Status ========================================================================= 1) ACCU-CHEK GUIDE (GLUCOSE) TEST STRIP USE TEST STRIP ACTIVE AS DIRECTED TO TEST BLOOD GLUC
- Allergien
- SIMVASTATIN - Signs/symptoms: HEADACHE
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 26.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site swelling
Pyrexia
Symptomtext
Fever. Injection site red and swollen for several days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes HTN Breast Cancer Hyperlipidemia Cardiomyopathy Asthma
- Andere Medikamente
- Enalapril Maleate 20 mg metFORMIN 1000 mg Rosuvastatin Calcium 20 mg Aspirin 81 mg Iron Supplement 325 (65 Fe) MG Vitamin B-12 1000 MCG T Vitamin B1 100 mg
- Allergien
- Omeprazole- headache
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 08.05.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Symptomtext
Hives on forearms, took Benadryl to relieve itching
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, High Cholesterol, Hypogonadism, Lipodystrophy HIV - 1988, AIDS (PCP), 1990 Hyperthyroidism, Gallbladder disease, Graves? disease, and Type 1 Diabetes, 1999
- Andere Medikamente
- Levothyroxine Esomeprazole (Nexium) Dapsone Lisinopril Genvoya Fluxetine (Prozac) Atenolol Azelastine HCI OR Nasalcort Finasteride Duloxetine HCL Hydroxyzine Pam Montelukast Acyclovir Rosuvastatin Calcium Silodosin (Rapaflo) XYZAL Cypiona
- Allergien
- Sulfa drugs (turn purple), Tramadol (aggressive), Klonopin (depression), Primidone (lethargy), Epinephrine (low BG)
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Decreased appetite
Headache
Lethargy
Symptomtext
I have had mild reactions to the other COVID-19 vaccines. I woke up that morning with a headache, chills, and lethargic. I also did not have an appetite. By 5/2/2022 I felt better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoporosis Glaucoma in both eyes Afib Bradycardia Valvular Heart Disease
- Andere Medikamente
- Latanoprost Dorzolamide Timolol Eventy injections on 4/19/2022 given once monthly
- Allergien
- Bananas Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Blood test
Computerised tomogram
Lipase increased
Magnetic resonance imaging
Muscle spasms
Pancreatitis
Symptomtext
The previous 3 vaccines were Pfizer. Starting 04/28/2022, I ended up having an extreme epigastric pain that was across the upper abdomen at the diaphragm level. It came out of the blue right after I ate breakfast with a friend. I went to the ER and they did lab work and my lipase was way higher than normal (1,731 u/L) standard range 13-60 u/L). So, they admitted me to the hospital for precaution because the treatment for pancreatitis is nothing by mouth so all I had for 3 days was IV fluids. I was discharged home and I was to continue my meds. I was told to see my PCP and I saw him yesterday. I am still having cramps to this day but to be expected when your epigastric system gets off track.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- 5,0
- Labordaten
- Bloodwork CT Scan MRI done in the hospital
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Intermittent Allergic Sinusitis Diabetes Type II Hypertension
- Andere Medikamente
- Amlodipine Besylate Lisinopril Metformin Lantus Insulin
- Allergien
- Sensitive to anti-cholesterol drugs
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Injection site rash
Product administered at inappropriate site
Symptomtext
Minor rash around injection site approximately 3-5 cm, rash appearing lower in the arm suggesting incorrect administration (subcutaneous) lower than the deltoid muscle. Patient stated vaccine was administered lower than the deltoid. Patient treating rash with OTC cream and will follow-up if any changes. Pharmacist scheduled follow-up for next day. Today 05/05 patient returned to pharmacy to show rash and question revaccination. Providing administration errors revaccination guidance documentations for recommendations in case of subcutaneous administration to patient for guidance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Tramadol
- Allergien
- Iodides
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Lethargy
Symptomtext
Systemic: Chills-Medium, Systemic: Exhaustion/Lethargy-Severe, Systemic: Headache-Medium.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Throat irritation
Symptomtext
The patient complained of diffuse itching on the skin of her upper body and arms and itching on the back of her throat approximately 8 minutes after the vaccine administration. The patient had brought her own cetirizine 10mg from home and took it, I provided a glass of water to the patient. The patient stated she was feeling better 11 minutes later and went home. The patient called from home to report she was feeling even better with no more issues 1 hour later, approximately 12:30p.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 01.05.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tension headache
Tinnitus
Symptomtext
TINNITUS. I actually began experiencing a pronounced ringing in my ears in August 2021, nearly 4 months after receiving my second dose of the initial Moderna vaccine series. The ringing in my ears continued for the next several months. I received a first booster (3rd shot) on 11/27/21 and continued to notice tinnitus thereafter, sometimes louder, sometimes softer. I decided to have my hearing tested in February 2022 -- and had an aural test on 2/21/22. The results were that my hearing is nearly perfect, even at my age. Still, the tinnitus persisted off and on. Perhaps it got a little better as time went on? Hard to say. I thought it was due to hypertension, which I have recently begun managing with drugs. YESTERDAY, I got my 2nd booster (4th total shot). Today, my tinnitus is very, very strong. And my head feels tight, like someone is squeezing it with their hands. I understand this is merely anecdotal evidence and that it's difficult to establish causality here, but I wanted my story to count toward the statistics -- as I see that there are multiple accounts worldwide of tinnitus occurring perhaps as a result of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tension headache
- Hospital-Tage
- -
- Labordaten
- Aural exam 02/21/2022 resulted in diagnosis of tinnitus in both ears, but hearing considered excellent.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension (managed with drugs)
- Andere Medikamente
- Fish oil Finasteride Atorvastatin Losartan
- Allergien
- N/A
- Vorherige Impfungen
- Tinnitus, commencing late-August 2021, four months after receiving 2nd does of Moderna Covide vaccine on 5/1/21, age at time 52
- Staat
- TN
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 01.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injection site rash
Rash
Symptomtext
Rash beginning with injection site and moving over entire torso.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- right knee replacement 1 week prior to vacination
- Vorgeschichte
- copd
- Andere Medikamente
- Fosinaphril, Amlodapine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 27.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Fatigue
Feeling abnormal
Headache
Neck pain
Pain
Somnolence
Swelling
Symptomtext
Felt horrible starting in the middle of the night after receiving vaccination: Headache and aching all over (but especially in neck) Following onset of symptoms, took 1000mg acetominephen at 6 am, 12:30 pm, and 8:30 pm. Spent most of day in bed and much of it sleeping. Second morning after vaccination: Left armpit swollen and very sore. Neck still a little sore. Still a little tired. Other symptoms have abated. May go back to bed for a few hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Mild hemophilia A - Factor VIII baseline 25-30% Osteopenia Depression Borderline high cholesterol
- Andere Medikamente
- Bupropion 300 mg Anastrozole 1 mg Centrum Silver for women Citalopram 20 mg Calcium 600 mg with D3 10 mcg D3 12.5 mcg
- Allergien
- -
- Vorherige Impfungen
- Fatigue. 50yo. 4/6/2021. COVID. Janssen.
- Staat
- NC
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Contusion
Fatigue
Headache
Limb discomfort
Musculoskeletal discomfort
Pain in extremity
Peripheral swelling
Symptomtext
Patient could not bend joint between leg and foot/ could not put weight on foot; It was swollen and bruised where the swelling was; It was swollen and bruised where the swelling was; Patient could not bend the joint between where the leg and foot meet/the joint did not work at all, it was excruciating/ it came on pretty suddenly; Joint pain/the joint did not work at all, it was excruciating; Fatigue; Headache; bone crushing joint pain on her left foot, pretty excruciating; This spontaneous case was reported by an other health care professional and describes the occurrence of LIMB DISCOMFORT (Patient could not bend joint between leg and foot/ could not put weight on foot), CONTUSION (It was swollen and bruised where the swelling was), PERIPHERAL SWELLING (It was swollen and bruised where the swelling was), MUSCULOSKELETAL DISCOMFORT (Patient could not bend the joint between where the leg and foot meet/the joint did not work at all, it was excruciating/ it came on pretty suddenly) and ARTHRALGIA (Joint pain/the joint did not work at all, it was excruciating) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for Product used for unknown indication: Pfizer COVID-19 (Patient's previous doses were all pfizer). Past adverse reactions to the above products included No adverse event with Pfizer COVID-19. On 22-Apr-2022 at 12:40 PM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In April 2022, the patient experienced LIMB DISCOMFORT (Patient could not bend joint between leg and foot/ could not put weight on foot), CONTUSION (It was swollen and bruised where the swelling was), PERIPHERAL SWELLING (It was swollen and bruised where the swelling was), MUSCULOSKELETAL DISCOMFORT (Patient could not bend the joint between where the leg and foot meet/the joint did not work at all, it was excruciating/ it came on pretty suddenly), ARTHRALGIA (Joint pain/the joint did not work at all, it was excruciating), FATIGUE (Fatigue), HEADACHE (Headache) and PAIN IN EXTREMITY (bone crushing joint pain on her left foot, pretty excruciating). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) at an unspecified dose and frequency. At the time of the report, LIMB DISCOMFORT (Patient could not bend joint between leg and foot/ could not put weight on foot), CONTUSION (It was swollen and bruised where the swelling was), PERIPHERAL SWELLING (It was swollen and bruised where the swelling was), MUSCULOSKELETAL DISCOMFORT (Patient could not bend the joint between where the leg and foot meet/the joint did not work at all, it was excruciating/ it came on pretty suddenly), ARTHRALGIA (Joint pain/the joint did not work at all, it was excruciating) and PAIN IN EXTREMITY (bone crushing joint pain on her left foot, pretty excruciating) had resolved and FATIGUE (Fatigue) and HEADACHE (Headache) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information provided. It was reported that about 32 hours later after the vaccine, she suddenly felt like a huge piece of machinery stomped on the top of her left foot. She elevated her foot, and about a half hour later she went upstairs, she realized she could not put any weight on her foot and she reports it was swollen and bruised. She put ice on it, fell asleep, and when she woke up the swelling was totally gone, and no pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Asthenia
Back pain
Decreased appetite
Headache
Immediate post-injection reaction
Injection site pain
Insomnia
Symptomtext
Around 9:00 pm on the day of the shot I began having lower back, shoulder, an d knee aches, followed by a headache. Arm was sore from shot almost immediately and worsened over the day. Took ibuprofen for aches, but didn?t help. Problems sleeping that night and woke up the next morning with a severe head headache and lower back pain. Overall loss of energy. Injection site continued to be sore. Loss of appetite. Purchased Theraflu Nighttime and began taking that around 1:00 pm the day following the injection. Theraflu helped me sleep but didn?t take away the symptoms of sore lower back and headache. Continued taking Theraflu into that night and early the next day. Began feeling better two days following injection with a mild headache persisting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High cholesterol, high tryglecerides
- Andere Medikamente
- Lisinopril, pioglitazone, Jardiance, repatha sureclick 140 mg, zetia, Vascepa, Metformin, baby aspirin, daily vitamin supplement, vitamin d3 supplement, loratadine.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiomegaly
Erythema
Pain in extremity
Vomiting
Symptomtext
Patient experienced a swollen heart, red and sore arm and multiple sessions of vomiting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diaphragm surgery and COPD
- Andere Medikamente
- Aspirin, Nexium, Clonazepam, Buproprion, Losartan, Fenofibrate, Atorvastatin, Gabapentin, Sertaline, Clobetasol, Loratadine, Dicyclomine
- Allergien
- Season allergies (hay,grass)
- Vorherige Impfungen
- Flu Shot
- Staat
- NJ
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Injection site erythema
Injection site induration
Injection site swelling
Pain
Productive cough
Respiratory tract congestion
Sluggishness
Sputum discoloured
Symptomtext
1. upper left arm has significant swelling, turned reddish and was very firm to touch 2. chills, body soreness, sluggish, congestion with heavy yellowish flam and cough 3. still experiencing mild symptoms a full week later and date of this report 4. my primary care doctor prescribe a 5 day dose of Cefuroxime Axetil 250 MG - one every 12 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- virtual visit with primary care doctor on April 21, 2022.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure high cholesterol Gout
- Andere Medikamente
- Atorvastatin 10 MG - once daily TELMISARTAN - 80 MG - once daily Allopurinol; 300 mg - once daily
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Symptomtext
Patient expereinced itching with 1st booster of Moderna. Same expereince with two other doses. Patient had taken Zyrtec 10 mg PO prior to arrival per MD recommendation. Started having itching in observation after approx 5 mins, no other symptoms. Dr. notified and 25mg of Benadryl given PO. Patient expressed some improvement and no other symptoms. Advised per Dr. for patient to take Benadryl 25mg Q6H if needed. Also informed of need to call emergency if any symptoms of breathing problems or throat swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- anemia, anxiety, asthma, atherosclerosis, diverticulitis, fatty liver, bariatric surgery, GERD, migraine, obesity, allergic rhinitis, MI
- Andere Medikamente
- Evolcumab, tramadol, cyclosporine, zithromax, biacodyl, simethicone, singulair, zyrtec.
- Allergien
- cipro, adhesive tape, amoxicillin, atrovastatin, cephalexin, erythomycin, pantoprazole, penicillin, pravastatin, simvastin
- Vorherige Impfungen
- Moderna
- Staat
- IN
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Hot flush
Lethargy
Myalgia
Nausea
Pain in extremity
Symptomtext
Nausea, extreme chills, headache, lethargy, muscle aches, sore arm, hot flashes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/a
- Andere Medikamente
- Diva Vegan Multivitamin Tri Femynor 28-day
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Symptomtext
APPROXIMATELY 10 MINUTES AFTER VACCINATION PATIENT REPORTED DIZZINESS, POSSIBLE DIFFICULTY BREATHING. 0.3MG EPINEPHRINE WAS ADMINISTERED, PATIENT WAS MONITORED, AND PATIENT WENT TO THE HOSPITAL WITH E.M.T.S. BLOOD PRESSURE WAS NORMAL, AND PATIENT REMAINDED CONSCIOUS. SHE COULD SPEAK.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOW
- Vorgeschichte
- NO
- Andere Medikamente
- UNKNOWN
- Allergien
- LATEX (RASH) SENSITIVITY TO BENADRY (MAKES HER HYPER)
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- 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: ja
Arthralgia
Back pain
Neck pain
Pain in extremity
Symptomtext
Joint pain, hands, back, neck
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Neck pain
Pain in extremity
Symptomtext
severe neck pain, arms, headache, legs, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Lantus, Metformin, Gabapentin, Atorvaststin, Venlafaxine, Meloxicam, Losartan, Glipizide, Levothyroxine
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 31.08.2023
- Impfdatum
- 03.05.2022
- Beginn
- 27.09.2022
- Tage bis Beginn
- 147,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood loss anaemia
Obstructive sleep apnoea syndrome
Symptomtext
G47.33 ADULT OBSTRUCTIVE SLEEP APNEA 11/15/2022 ANEMIA DUE TO BLOOD LOSS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood loss anaemia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 21.06.2023
- Impfdatum
- 17.05.2022
- Beginn
- 16.06.2023
- Tage bis Beginn
- 395,0
- 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 2/25/21 lot# 031M20A; Moderna 3/25/21 lot# 045A21A; Moderna 12/7/21 lot# 045J21A; Moderna 5/17/22 lot# 056M21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 95,0
- Geschlecht
- F
- Eingang
- 21.06.2023
- Impfdatum
- 11.05.2022
- Beginn
- 16.06.2023
- Tage bis Beginn
- 401,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 08.06.2023
- Impfdatum
- 25.04.2022
- Beginn
- 20.08.2022
- Tage bis Beginn
- 117,0
- 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 1/27/21 lot# 007M20A; Moderna 2/24/21 lot# 010A21A; Moderna 10/27/21 lot# 939905; MOderna 4/25/22 lot# 056M21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 31.05.2023
- Impfdatum
- 02.06.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 162,0
- 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 Moderan 2/5/21 lot# 038K20A; Moderna 3/5/21 lot# 030A21A; Moderna 12/4/21 lot# 939909; Moderna 6/2/22 Lot# 056M21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 24.05.2023
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Symptomtext
lip swelling without respiratory problem, open air, vital signs normal, given loratadine 10 mg Stat, then daily PRN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip swelling
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 18.05.2023
- Impfdatum
- 06.05.2022
- Beginn
- 07.05.2023
- Tage bis Beginn
- 366,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fluid retention
Nasal congestion
SARS-CoV-2 test positive
Upper respiratory tract congestion
Symptomtext
5/7/23 I was really congested, upper respiratory and nasal. I started coughing a few days later, which really hurt because of a fall I had several days before. On 5/11/23, I went to a walk-in clinic and had a COVID test, results pending. I was prescribed a Z-Pack and a steroid thinking it was a virus. After being prescribed these medications, my COVID results came back positive. I called my PCP and was prescribed Molnupiravir and a nebulizer. I took the Molnupiravir for five days. I am now dealing with significant fluid retention and have a call into my doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 11MAY23-COVID Test-Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- COPD, Coronary Artery Disease
- Andere Medikamente
- Losartan, Metoprolol, Atorvastatin, Baby Aspirin, Hydrochlorothiazide, Vitamin D, Vitamin B, Magnesium, Anoro Inhaler, Albuterol Inhaler
- Allergien
- Amoxicillin, Rosemary,Gabapentin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 17.05.2023
- Impfdatum
- 13.10.2022
- Beginn
- 26.11.2022
- Tage bis Beginn
- 44,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Prostate cancer
- Vorgeschichte
- Prostate cancer
- Andere Medikamente
- Lisinopril/HCTZ; Multivitamin; Vitamin D; Probiotic
- Allergien
- Aspirin; Ciproflaxin; Shrimp/Lobster; Dairy
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 09.05.2023
- Impfdatum
- 29.04.2022
- Beginn
- 23.03.2023
- Tage bis Beginn
- 328,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Mental status changes
SARS-CoV-2 test positive
Symptomtext
03/23/23 presents to ED for "altered mental status". PMHx of "anemia, DM 2, HTN, hypothryroidism"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 03/23/23 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 27.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 35,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Janus kinase 2 mutation
Platelet count increased
Symptomtext
I have had my platelets counted on several occasions. When I had my platelets counted in August 2019, they were 360,000, which is considered within normal range. However, the first time the platelet count was outside of normal range was in November 2019, and then it was 451,000. In January 2020, it was again within normal range at 417,000. In February 2021, it was at 425,000, which is also considered to be within normal range, However, in June 2022, my platelet count was at 494,000 which is well outside of normal range. In December 2022, it was 599,000. In January 2023, it was 571,000. Most recently, on 3/22/2023, it was at 565,000. I don't know if there is any correlation between my the COVID-19 vaccines and boosters, but prior to getting my elevated reading in June 2022, I received a booster on 4/27/2022. I have no discernable symptoms, but I am consulting a hematologist, who has informed that a genetic mutation, JAK 2V617F, was detected. I am due to see my hematologist again on 6/14/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Janus kinase 2 mutation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Severe Degenerative Disk Disease; Osteoporosis; Herniations in Neck and Back; Neuropathy in Hands and Feet; Left Posterior Tibialis Tendon Problem; Full Tear of Right Rotator Cuff Supraspinatus Tendon; Premature Ventricular Contractions
- Andere Medikamente
- Levothyroxine; lisinopril; rosuvastatin; oxycodone; estradiol cream; gabapentin; trazodone; ibuprofen; multivitamin; fish oil; beetroot; coQ10; vitamin D3; super B complex; possibly quercetin
- Allergien
- Cat dander; bermuda grass
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 25.04.2022
- Beginn
- 05.04.2023
- Tage bis Beginn
- 345,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Herpes zoster
Symptomtext
Acute Zoster L5S1 not sure if related, prob stress from THR, but question was any need to visit a doctor since last covid-19 vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none other than THR 3 mths prior
- Vorgeschichte
- HTN, GERD, SPIN AL STENOSIS- s/p fusion ch LBP, neurcardiogenic syncope, allergic rhinitis, restless legs, iron def , s/p ORIF left hip fx with ch hip pain(labral tear at THR 12/22)
- Andere Medikamente
- B-12,500mcg/ centrum silver/pepcid 20mg q am/ ferrous sulfate 325mg wmf/protonix 40mg q day/losartan 50mg q d/ mirapex 1mg q hs/ Neurontin 600mg q hs/zoloft 50mg q hs/ pro Tylenol 1 gm q 8hr/ prn ultram 50mg at hs--ch hip pain
- Allergien
- feline--urticaria bactrim--nausea iodine soap--rash
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 05.04.2023
- Impfdatum
- 30.09.2022
- Beginn
- 15.02.2023
- Tage bis Beginn
- 138,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test
Symptomtext
Got Covid- mild. Had Paxlovid and took it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- home test
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- mild controlled asthma
- Andere Medikamente
- rosuvostatin 40, montelukast 10
- Allergien
- sulfur, ampicillin
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 29.03.2023
- Impfdatum
- 15.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abnormal menstrual clots
Anaemia
Blood test abnormal
Heavy menstrual bleeding
Menstrual disorder
Oligomenorrhoea
Ultrasound scan
Symptomtext
I received the Moderna booster on 7/15/22 and on 7/26/2022 started having what I thought was a normal period however it never stopped bleeding. I had continuous bleeding some days lighter and some days much heavier (could have gone to the ER, but I am an ER nurse so monitored myself at home). This bleeding was unlike any I had ever had prior. There were chunks of what looked like cotton candy endometrium floating in the toilet bowl (grey pink tissue). I had very frequent clots I could often feel passing and the consistency of the bleeding was unlike a normal period for me. These symptoms lasted until 11/28/2022 culminating in the worst bleeding I have had so far and then stopped. Normal periods resumed after this in December and have been normal since. To note, thought I am a postpartum person I had had several normal periods prior to this event, even after having COVID I had no abnormality to my periods whatsoever. There were no other rapid changes in my lifestyle or the care of my child (nursing etc.) nor any pregnancies, so I believe I have a baseline to compare.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abnormal menstrual clots
- Hospital-Tage
- -
- Labordaten
- I saw a midwife NP in September where I had blood work performed, pelvic exam, and ultrasound. All were fairly normal with perhaps some anemia. On November 17, I had a follow up with my PCP and recommended to see a traditional OBGYN but was not able to see them before the bleeding subsided.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypermobile joints
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 29.03.2023
- Impfdatum
- 17.05.2022
- Beginn
- 23.03.2023
- Tage bis Beginn
- 310,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 3/23/23
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Leukocytosis SHOCK, Septic Primary Metabolic Alkalosis, Secondary Respiratory Acidosis Hyponatremia Hyperkalemia Acute Kidney Injury, Prerenal vs ATN, Non-oliguric Elevated Glucose Hyperphosphatemia Rhabdomyolysis Asymptomatic Bacteruria CAD s/p stenting Hypertension Hyperlipidemia Anxiety COPD, not in exacerbation GERD Diabetes, uncontrolled, type 2 Chronic Pain Paroxysmal A Fib
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 13.03.2023
- Impfdatum
- 07.06.2022
- Beginn
- 04.03.2023
- Tage bis Beginn
- 270,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 2 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- positive covid pcr 3/1/23
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- CAD, HFrEF, Chronic Anemia, HTN, HLD, Hypothyroidism, DMII
- Andere Medikamente
- unknown
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 07.03.2023
- Impfdatum
- 07.06.2022
- Beginn
- 05.03.2023
- Tage bis Beginn
- 271,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 2 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 3/4/23
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Hyperlipidemia, Renal Disease (Urinary incontinence) and Other (arthritis, Bronchitis, B/l PE, Chronic back and leg pain)
- Andere Medikamente
- unknown
- Allergien
- codeine, morphine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 27.05.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 55,0
- 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 4/3/21 Lot# 026B21A; Moderna 5/1/21 Lot# 017C21A; Moderna 11/18/21 Lot# 077C21B; Moderna 5/27/22 Lot# 056M21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 22.02.2023
- Impfdatum
- 01.03.2021
- Beginn
- 01.10.2022
- Tage bis Beginn
- 579,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tinnitus, constant ringing in both ears, stronger in left. no treatment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- none to date
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 14.02.2023
- Impfdatum
- 11.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 12,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 2 vaccines Moderna 11/17/21 Lot# 939909; Moderna 5/11/22 Lot# 056M21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 94,0
- Geschlecht
- M
- Eingang
- 02.02.2023
- Impfdatum
- 24.05.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 170,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Moderna 3/4/21 Lot# 029A21a; Moderna 4/1/21 Lot# 028A21A; Moderna 11/17/21 Lot# 939909; Moderna 5/24/22 Lot# 056M21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) in a 75-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 13-May-2022, the patient received fourth dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). No concomitant medication was provided. The BUD of the vaccine was provided was 12May2022. Treatment medication was not provided by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Follow up received contains non significant information.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date) and NO ADVERSE EVENT (No adverse event) in a 70-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 13-May-2022, the patient received fourth dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date). No concomitant medication was provided. The BUD of the vaccine was provided was 12May2022. Treatment medication was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (No adverse event) in a 54-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 13-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). No concomitant medication information provided. Pharmacist reported that they have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30 day beyond use date. Before use date reported was 12-May-2022. No treatment information provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live Significant follow up received: Patient information and vaccination details updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (No adverse event) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 13-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). No concomitant medication information provided. Pharmacist reported that they have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30 day beyond use date. Before use date reported was 12-May-2022. No treatment information provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live Significant follow up received: Patient information and vaccination details updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (No adverse event) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 13-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). No concomitant medication information provided. Pharmacist reported that they have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30 day beyond use date. Before use date reported was 12-May-2022. No treatment information provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live Significant follow up received: Patient information and vaccination details updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Patient had been administered with the Moderna vaccine which were beyond the 30day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (no ad) in a 69-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 17-May-2022, the patient received fourth dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 17-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On an unknown date, the patient experienced NO ADVERSE EVENT (no ad). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (no ad) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no ad) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). No concomitant medication was reported. No treatment medication was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Non significant Live Follow up; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; vaccine used which were beyond the 30-Day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine used which were beyond the 30-Day beyond use date) and NO ADVERSE EVENT (no adverse event) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 17-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine used which were beyond the 30-Day beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine used which were beyond the 30-Day beyond use date) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (vaccine used which were beyond the 30-Day beyond use date). Concomitant products were not reported. It was reported that patient received monovalent dose that was administered beyond 30 day beyond use date. The use by date of lot 056m21a was reported as 12-May-2022. Treatment medications were not reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Non significant Live Follow up received.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; vaccine used which were beyond the 30-Day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine used which were beyond the 30-Day beyond use date) and NO ADVERSE EVENT (no adverse event) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 17-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine used which were beyond the 30-Day beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine used which were beyond the 30-Day beyond use date) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (vaccine used which were beyond the 30-Day beyond use date). Concomitant products were not reported. It was reported that patient received monovalent dose that was administered beyond 30 day beyond use date. The use by date of lot 056m21a was reported as 12-May-2022. Treatment medications were not reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Non significant Live Follow up received.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; vaccine used which were beyond the 30-Day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine used which were beyond the 30-Day beyond use date) and NO ADVERSE EVENT (no adverse event) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 17-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine used which were beyond the 30-Day beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine used which were beyond the 30-Day beyond use date) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (vaccine used which were beyond the 30-Day beyond use date). Concomitant products were not reported. It was reported that the 30 day beyond use date of lot 056m21a was 12-May-2022. Treatment medications were not reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Non significant Live Follow up received.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; BUD was reported as 17-May-2022 and vaccine was administered on 12-May-2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (BUD was reported as 17-May-2022 and vaccine was administered on 12-May-2022) and NO ADVERSE EVENT (No adverse event) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 17-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (BUD was reported as 17-May-2022 and vaccine was administered on 12-May-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (BUD was reported as 17-May-2022 and vaccine was administered on 12-May-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (BUD was reported as 17-May-2022 and vaccine was administered on 12-May-2022). Concomitant product use was not provided by the reporter. Treatment information was not provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Follow-up received contains additional no new information was received.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 16.05.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; BUD was reported as 12-May-2021 and vaccine was administered on 16-May-2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (BUD was reported as 12-May-2021 and vaccine was administered on 16-May-2022) and NO ADVERSE EVENT (No adverse event) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 16-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (BUD was reported as 12-May-2021 and vaccine was administered on 16-May-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (BUD was reported as 12-May-2021 and vaccine was administered on 16-May-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (BUD was reported as 12-May-2021 and vaccine was administered on 16-May-2022). Concomitant product use was not provided by the reporter. Treatment information was not provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Follow-up received contains additional no new information was received.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 16.05.2022
- Beginn
- 16.05.2022
- 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
No adverse event
Symptomtext
No adverse event; BUD was reported as 12May2022 and vaccine was administered on 16-May-2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (BUD was reported as 12May2022 and vaccine was administered on 16-May-2022) and NO ADVERSE EVENT (No adverse event) in a 68-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 16-May-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 16-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (BUD was reported as 12May2022 and vaccine was administered on 16-May-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (BUD was reported as 12May2022 and vaccine was administered on 16-May-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (BUD was reported as 12May2022 and vaccine was administered on 16-May-2022). Concomitant product use was not provided by the reporter. Treatment information was not provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Follow-up received contains additional no new information was received.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 16.05.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date) and NO ADVERSE EVENT (No adverse event) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 16-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date). No concomitant medication was reported. Pharmacist reported that they have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 monovalent and 20 bivalent) which were beyond the 30 days beyond use date. No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live Significant Follow-up received; Patient information and vaccinations details updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date) and NO ADVERSE EVENT (No adverse event) in a 63-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 13-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date). No concomitant medication was reported. Pharmacist reported that they have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 monovalent and 20 bivalent) which were beyond the 30 days beyond use date. No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live Significant Follow-up received; Patient information and vaccinations details updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) in a 68-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056m21a) for COVID-19 prophylaxis. No Medical History information was reported. On 13-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). The beyond use date (BUD) of the vaccine was reported as on 12-May-2022. The patient received the vaccine at a pharmacy. No concomitant medication reported. No treatment medication reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Follow-up document received on 24-Jan-2023 with no new information.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
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
- 20.01.2023
- Impfdatum
- 01.06.2022
- Beginn
- 20.01.2023
- Tage bis Beginn
- 233,0
- 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
COVID vaccine breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 1/20/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 16.01.2023
- Impfdatum
- 16.02.2021
- Beginn
- 08.01.2023
- Tage bis Beginn
- 691,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Hospitalization following a positive COVID-19 test
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- AFIB, hypertension, hypercholesteremia, osteoarthritis, an appendectomy, and a hysterectom
- Andere Medikamente
- Ferrous Sulfate, Methotrexate, folic acid
- Allergien
- Celecoxib
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 09.01.2023
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient accidentally received an expired Moderna vaccine) and NO ADVERSE EVENT (No adverse event) in a 63-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 056M21A) for COVID-19 prophylaxis. On 15-Dec-2022, the patient received first dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) .5 milliliter. On 15-Dec-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient accidentally received an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient accidentally received an expired Moderna vaccine) and NO ADVERSE EVENT (No adverse event) outcome was unknown. Concomitant Medication use information was not provided by reporter. It was unknown that the patient ever been diagnosed with/ tested positive for COVID-19. Patient had no acute illnesses at the time of vaccination and up to one month before. It was unknown that the patient had any chronic or long-standing health conditions. It was reported that no prescriptions, over the counter medications, dietary supplements, or herbal remedies being taken at time of vaccination and/or at the time of the adverse event. Most recent FOLLOW-UP information incorporated above includes: On 06-Jan-2023: Follow up received that contains significant information includes updated patient details, updated reporter details, added medical history, updated suspect product details, event details and update narrative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient had no allergy.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 05.01.2023
- Impfdatum
- 29.01.2021
- Beginn
- 16.11.2022
- Tage bis Beginn
- 656,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Gastrointestinal haemorrhage
SARS-CoV-2 test positive
Symptomtext
11/16/22 presents to ED for "GI Bleeding". PMHx of "A. Fib , prostate cancer s/p radiation, COPD on 2 L, hypothyroid, CHF"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 11/15/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 29.12.2022
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine was expired on Oct, 12, 2022. Have been unable to contact patient, and patient will be notified that he needs to been re-vaccinated 6 weeks from 12/15/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Elevated Blood Pressure Irregular Cardiac Rhythm
- Andere Medikamente
- None
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 22.12.2022
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- 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; patient accidentally received an expired Moderna vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient accidentally received an expired Moderna vaccine) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 056M21A) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Dec-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) Unknown. On 15-Dec-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient accidentally received an expired Moderna vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient accidentally received an expired Moderna vaccine) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown Route), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (patient accidentally received an expired Moderna vaccine). No concomitant and treatment medication information was not reported. Most recent FOLLOW-UP information incorporated above includes: On 19-Dec-2022: Live Follow up- Significant information include suspect product change from MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5) to Spikevax and narrative updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 17.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Suicidal ideation
Symptomtext
Hospitalization: 12/1/2022 - 12/4/2022 (3 days) Presentation to the ED: suicidal ideation COVID + date: 12/1/2022 Treatment: NONE -Asymptomatic. Discharge to: HOME. MODERNA LOT # 031H21A 11/16/2021 MODERNA LOT # 056M21A 4/30/2022 MODERNA BIVALENT LOT # 042H22A 12/17/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- BILATERAL MASECTOMY D/T BREAST CANCER ON ORAL CHEMO, DEPRESSION, CVA, TREMORS, SEIZURES, HLD, HTN, T2D.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 07.11.2022
- Beginn
- 04.12.2022
- Tage bis Beginn
- 27,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Encephalopathy
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 12/4/2022 - 12/7/2022 (3 days) Presentation to the ED: acute encephalopathy. COVID + date: 12/4/2022 Treatment: IV dexamethasone and Remdesivir Discharge to: Home. 1. Moderna Lot # 030L20A 1/26/2021 2. Moderna Lot # 013M20A 2/23/2021 3. Moderna Lot # 066F21A 11/15/2021 4. Moderna Lot # 056M21A 4/24/2022 5. Moderna BiValent booster Lot # GH9702 11/7/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- dementia, hypertension, afib, pacemaker, malignant neoplasm of the large intestine.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 12.07.2022
- Beginn
- 18.12.2022
- Tage bis Beginn
- 159,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Moderna 3/20/21 Lot# 030A21A; Moderna 4/17/21 Lot# 007B21A; Janssen 11/24/21 Lot#1855191; Moderna 7/12/22 Lot# 056M21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 11.03.2021
- Beginn
- 06.11.2022
- Tage bis Beginn
- 605,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
11/06/22 presents to EC ED for "cough, chest congestion". PMHx of "SLE, seizures, CAD with CABG, htn, CHF (EF 35%), ESRD on dialysis"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 11/06/22 SARS-CoV-2 (COVID-19) detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 17.05.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 216,0
- 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
COVID vaccine breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 12/20/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 15.12.2022
- Impfdatum
- 18.05.2021
- Beginn
- 31.08.2022
- Tage bis Beginn
- 470,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested positive for COVID via at-home test on 8/31/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- At-home test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- lisinopril 10mg
- Allergien
- morphine oysters
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 13.05.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 207,0
- 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 case Pfizer 2/2/21 EL3248, 2/23/21 EN6200 and boosted 10/12/21 FF8847 and 5/13/22 Moderna 056M21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID test on 12/6/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
requested pfizer, but got moderna booster in error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 10.11.2022
- Impfdatum
- 01.09.2021
- Beginn
- 12.09.2022
- Tage bis Beginn
- 376,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Mental status changes
SARS-CoV-2 test positive
Symptomtext
09/12/22 presents to ED for "altered mental status". PMHx of "schizophrenia, thrombocytopenia, prior ESBL UTI, HAP"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 09/12/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 25.07.2022
- Beginn
- 30.10.2022
- Tage bis Beginn
- 97,0
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 3 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 10/30/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- frequent UTIs (ESBL neg Ecoli), fecal/urinary incontinence, seasonal allergies, CVA/lacunar infarct HTN, HLD, hypothyroidism, & Chronic HFpEF
- Andere Medikamente
- unknown
- Allergien
- Augmentin, gabapentin, latex, adhesive tape, cipro, achromycin, effexor, anti-inflammatories, mycins
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 21.04.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 154,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rhinorrhoea
SARS-CoV-2 test
Sneezing
Throat irritation
Symptomtext
I had sneezing, a running nose and a scratchy throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rhinorrhoea
- Hospital-Tage
- -
- Labordaten
- At home rapid COVID-19 test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma; High blood pressure; High cholesterol
- Andere Medikamente
- FLONASE; FOSAMAX; SINGULAIR; PRAVACHOL; HYDRODIURIL; CELEBREX; SYMBICORT (inhaler); PRILOSEC; magnesium; calcium w/ vitamin D; fish oil
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 25.10.2022
- Impfdatum
- 11.05.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 161,0
- 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 Pfizer 3/15/21 Lot# EN6207; Pfizer 4/6/21 Lot# Er8733; Pfizer 10/18/21 Lot# 30145BA; Moderna 5/11/22 Lot# 056M21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- External COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 24.03.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 214,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
COVID-19 immunisation
SARS-CoV-2 test
Vaccination failure
Symptomtext
CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from other company (Pfizer) via a patient concerned a 55-year-old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: asthma, and sulfa 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: 026D21 A expiry: UNKNOWN) dose was not reported, administered 1 in total on 24-MAR-2021 for covid-19 prophylaxis. Age at time of vaccination 54 years old. On 23-SEP-2022, the patient experienced confirmed clinical vaccination failure following vaccination with covid-19 vaccine ad26.cov2.s (Dose number in series 1). Patient received non-company suspect vaccine included: elasomeran (Moderna vaccine) (Dose number in series 2) (batch number: 056M21A expiry: UNKNOWN, form of admin, route of admin, and were not reported) dose was not reported, administered on 24-OCT-2021 for covid-19 prophylaxis. On 24-OCT-2021, the patient experienced revaccination with different covid-19 vaccine following vaccination with elasomeran (Dose number in series 2). Patient received non-company suspect vaccine included: elasomeran (Moderna vaccine) (Dose number in series 3) (batch number: 056MZ1 A expiry: UNKNOWN, form of admin, route of admin, and were not reported) dose was not reported, administered on 13-MAY-2022 for covid-19 prophylaxis. No concomitant medications were reported. On 23-SEP-2022, the patient experienced confirmed covid-19 infection. Laboratory data included: COVID-19 virus test Positive following vaccination with elasomeran (Dose number in series 3). Patient received non-company drug included: paxlovid (batch number: Unknown expiry: Unknown, form of admin, route of admin, and were not reported) dose was not reported, administered from 23-SEP-2022 to 27-SEP-2022 for covid-19 treatment. On 28-SEP-2022, Laboratory data included: COVID-19 virus test Positive. On 01-OCT-2022, Laboratory data included: COVID-19 virus test Negative, patient started feeling better and then again started feeling sick. On 04-OCT-2022, Laboratory data included: COVID-19 virus test Positive. The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, and elasomeran was not applicable. The patient was recovering from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure and revaccination with different covid-19 vaccine was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint, and reference number requested. Sender's Comments: V0:20221027458-covid-19 vaccine ad26.cov2.s- Confirmed Clinical Vaccination failure. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220923; Test Name: COVID-19 VIRUS TEST; Test Result: Positive; Test Date: 20220928; Test Name: COVID-19 VIRUS TEST; Test Result: Positive; Test Date: 20221001; Test Name: COVID-19 VIRUS TEST; Test Result: Negative; Test Date: 20221004; Test Name: COVID-19 VIRUS TEST; Test Result: Positive.
- Aktuelle Erkrankungen
- Allergic reaction to antibiotics; Asthma
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 31.05.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 134,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 2 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 10/12/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Acute Covid infection Poor PO intake Protein calorie malnutrition (BMI 18.6) generalized weakness 3rd degree AV block HTN Glaucoma
- Andere Medikamente
- unknown
- Allergien
- Penicillins
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 29.09.2022
- Impfdatum
- 27.06.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 44,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram normal
Nasopharyngitis
Parosmia
Post-acute COVID-19 syndrome
SARS-CoV-2 test negative
Sinusitis
X-ray dental normal
Symptomtext
I did not have a reaction to the vaccine. On 08/10/2022 I began feeling symptoms that was unique and I tested for COVID-19 with a home test which was negative. My primary symptom was I sensed smells that where not there (exhaust fumes) and continues to this day. I've been to the dentist to see if I had any dental issues that would cause this symptom a everything was within normal range. I had CT scan and was within normal range. My doctor determined that I have long COVID-19 but I have never tested positive for COVID-19. My doctor has tried me on a different prescription to see if that will help with my symptoms. For a few days we tried albuterol inhaler, we tried ipratropium nasal spray, one week course of antibiotic doxycycline (deep sinus infection), nasal rinse with a steroid budesonide. I have had cold symptoms the last five days and have not tested positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Computerised tomogram normal
- Hospital-Tage
- -
- Labordaten
- CT scan showed no abnormalities. Full x-rays of my mouth.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 28.09.2022
- Impfdatum
- 27.09.2022
- Beginn
- 27.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Patient given 0.5ml instead of 0.25 ml for his #2 booster and the patient is not complaining of any symptoms at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 14.09.2022
- Impfdatum
- 27.05.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 110,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Fully vaccinated and boosted twice
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 22.04.2022
- Beginn
- 28.08.2022
- Tage bis Beginn
- 128,0
- 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 2/25/21 Lot# 010A21A; Moderna 3/25/21 Lot# 018B21A; Moderna 12/30/21 Lot# 060H21A; Moderna 4/22/22 Lot# 056M21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 07.09.2022
- Impfdatum
- 13.05.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 104,0
- 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 2/4/21 Lot# 013M20A; Moderna 3/4/21 Lot# 030A21A; Moderna 11/9/21 Lot# 939905; Moderna 5/13/22 Lot# 056M21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 27.08.2022
- Impfdatum
- 23.04.2022
- Beginn
- 24.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Psoriasis
Symptomtext
My whole body broke out with Psoriasis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Psoriasis
- Hospital-Tage
- -
- Labordaten
- Dermatology did the tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Pantoprazole 20% Rosuvastatin 5mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 25.08.2022
- Impfdatum
- 04.05.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 113,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, Vitamin B12, hypertension, diverticulitis, glaucoma, urinary incontinence, polyp of colon, chronic frontal sinusitis, autoimmune thyroiditis, hypothyroidism, dementia
- Andere Medikamente
- Acetaminophen 325mg, Buspirone 5mg, Donepezil 5mg, Fluocinolone acetonide, Hydrochlorothiazide 25mg, Klor-Con 10MEQ, Latanoprost 0.005%, Levothyroxine 50mcg, Melatonin 3mg, Olanzapine 2.5mg, Trazodone 50mg, Vitamin B-12 1000mcg
- Allergien
- Bactrim, Keflex
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 25.08.2022
- Impfdatum
- 04.05.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 110,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hyperlipidemia Mild Congntive Impairment Hypthyroidsim Chronic Obstructive Pulmonary Disease ALzheimer's Disease Type 2 Diabetes Mellitus Without Complications Age-Related Osetoporosis Major Depressive Disorder Low Back PainPaxysmal Atrial Fibrillation
- Andere Medikamente
- Acetaminophen 500 mg tabs PRN, three times a day Citalopram Hydrobromide 20 mcg Digoxin 125 mcg Docu Soft 100 mg caps Fluticasone-Sameteri 250-50mg Levtryoxine Sodium 25mcg Lidocaine 5% Patch daily Memenatine 5 mg Tabs Muxienc 600 mg Olanz
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 16.05.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 62,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
COVID-19
Feeling abnormal
SARS-CoV-2 test positive
Symptomtext
05/16/2022 I had vaccination. On 07/16/2022 I was traveling that evening. I drove home from feeling a little out of sorts. On 07/17/2022 my temperature was 102. 07/18/2022 I took a COVID-19 at home test and it was positive. On 07/19/2022 I sought medical attention and was prescribed Plaxovid. I started the medication that evening and for the 5 day period. I am feeling reasonably good presently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body temperature increased
- Hospital-Tage
- -
- Labordaten
- COVID-19 Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Myasthenia Gravis; Irregularity in heart valve; Hernia; Enlarged Prostate
- Andere Medikamente
- Pyridostigmine; Finasteride; Terazosin; Amlodipine; Toprol; Lisinopril; Chlorthalidone
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 15.08.2022
- Impfdatum
- 15.05.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 56,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthma
COVID-19
Cellulitis
Symptomtext
Covid-19 kicked up my asthma and went on a nebulizer with albuterol and steroid for a few days. I called my doctor and they wanted me to get the infusion or PAXLOVID but by the time I got to the Dr. the window had closed. They put me on a steroid and my symptoms didn't improve. I was evaluated at an urgent care facility the following weekend and they added an antibiotic and by that time there was a case of cellulitis in my left leg. The following week I was recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthma
- Hospital-Tage
- -
- Labordaten
- COVID-19- positive on the 10th.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Cardiomyopathy; Lymphedema
- Andere Medikamente
- Diltiazem; vitamin D; low dose aspirin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 15.08.2022
- Impfdatum
- 07.06.2021
- Beginn
- 01.07.2022
- Tage bis Beginn
- 389,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Vitiligo
Symptomtext
new onset Vitiligo on legs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vitiligo
- Hospital-Tage
- -
- Labordaten
- upon physical exam on 8/15/22 dr confirmed vitiligo
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- Errin, Bisopropyl
- Allergien
- sulfa medications
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 12.05.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 70,0
- 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
Tested positive for COVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- At-home COVID Antigen Test - Positive - 7/24/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Lovastatin, Metamucil, Glucosamine/Chondroitin, Vitamin D
- Allergien
- Do not tolerate codeine well; allergic to Iodine
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 06.07.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 30,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
This spontaneous case was reported by a nurse and describes the occurrence of INCORRECT DOSE ADMINISTERED (Patient inadvertently given dose from different age group.) and NO ADVERSE EVENT (No adverse event) in an 18-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. AR4504B and 056M21A) for COVID-19 vaccination. Patient had no known allergies. It was unknown if patient ever had COVID positive test or diagnosis. On 06-Jul-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) .5 milliliter. On 05-Aug-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to .5 milliliter. On 05-Aug-2022, after starting mRNA-1273 (Spikevax), the patient experienced INCORRECT DOSE ADMINISTERED (Patient inadvertently given dose from different age group.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, INCORRECT DOSE ADMINISTERED (Patient inadvertently given dose from different age group.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for INCORRECT DOSE ADMINISTERED (Patient inadvertently given dose from different age group.). No concomitant medications were reported. It was unknown if other vaccines given within 1 month prior to Moderna vaccine. It was reported that 18yr old patient was inadvertently given 0.5mL dose from a purple vial Lot number AR4504B, which was slated for 6-11 year old age group and 18 plus booster dose. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient had no known allergies. It was unknown if patient ever had COVID positive test or diagnosis.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 05.05.2022
- Beginn
- 03.08.2022
- 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
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Break through Covid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- PCR test positive 08/05/2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 04.08.2022
- Impfdatum
- 03.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
No known adverse side effects occurred. Patient given a 0.5mL dose for their booster shot, but should have received a 0.25mL dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 04.08.2022
- Impfdatum
- 26.02.2021
- Beginn
- 26.05.2022
- Tage bis Beginn
- 454,0
- Dosis
- 4
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
SARS-CoV-2 test positive
Symptomtext
On May 26, I tested positive for COVID. My great niece and nephew, who I care for tested positive on 5/21/22. My niece who was fully vaccinated and boosted with one shot tested positive on 5/24/22. My other great niece tested positive on the 24th also. My sister also tested positive on 5/26. The twin girls who are 3 were to young to be vaccinated. Their daycare center stopped requiring masks in March and stopped notifying parents in May when someone tested positive at the center. My 6 year old nephew was also vaccinated We always wore masks in public.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Low platelet count but does not require treatment Seasonal allergies Mike asthma which does not require treatment
- Andere Medikamente
- Levothyroxine Fluticasone propionate nasal spray Zyrtec Centrum silver Citracal Womens propbiotic B-6
- Allergien
- None but I often have several side effects to medications so My doctors monitor what they give me.
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 04.08.2022
- Impfdatum
- 04.05.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 89,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I started getting symptoms of a runny nose, cough and congestion. I took a COVID-19 test that was positive. I contacted my doctor. I was prescribed Paxlovid and an inhaler. My symptoms are getting better today. I had to stop taking my blood pressure medication due to taking Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID-19 test.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- History of a stoke
- Andere Medikamente
- Lisinopril; Atorvastatin; Plavix; Allopurinol; Multivitamin; Flax seed oil; Cetirizine
- Allergien
- Grass
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 29.04.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 90,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Nasal congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
It started with runny nose. I thought it was my allergies. I was sneezing a lot and then I started coughing. I tested positive at home. I saw the doctor on Saturday. I did not get PAXLOVID because my symptoms were not too bad. I am feeling fine as of today. My nose is just a little stuffy. Last night I still tested positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test, positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; High Cholesterol; Hypothyroidism
- Andere Medikamente
- ATACAND; NORVASC; SYNTHROID; CRESTOR; baby aspirin
- Allergien
- Environmental
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID case confirmed by PCR. Initial positive antigen test at home on 7/25/22. Negative test on 7/30/22 after treatment with Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- At home antigen test 7/25 PCR (Saliva test) taken 7/26, positive result received 7/27
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure, gout, HSV-1
- Andere Medikamente
- Hydrochlorothiaziade, allopurinol
- Allergien
- gentamicin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 80,0
- Geschlecht
- U
- Eingang
- 24.07.2022
- Impfdatum
- 21.07.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
A dose of Moderna Covid-19 vaccine was administered to a patient at 10a today (21Jul2022) from a vial that was punctured at 11:45a on 20Jul2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (A dose of Moderna Covid-19 vaccine was administered to a patient at 10a today (21Jul2022) from a vial that was punctured at 11:45a on 20Jul2022) in an 80-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 prophylaxis. No Medical History information was reported. On 21-Jul-2022 at 10:00 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 21-Jul-2022 at 10:00 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (A dose of Moderna Covid-19 vaccine was administered to a patient at 10a today (21Jul2022) from a vial that was punctured at 11:45a on 20Jul2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (A dose of Moderna Covid-19 vaccine was administered to a patient at 10a today (21Jul2022) from a vial that was punctured at 11:45a on 20Jul2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment details were reported. Number of doses/vial was Single dose The vial was initially stored in the refrigerator on 14-Jul-2022 Vial was first punctured on 20-Jul-2022 at 11:45 am Vial was stored in the refrigeration post puncture Vial did not undergo any temperature excursions
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 20.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 42,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac monitoring
Cough
Electrocardiogram
Extrasystoles
Nervousness
Symptomtext
At the very beginning of June I noticed my heart would skip a beat and I would feel it in my chest and I am familiar with that because sometimes medications trigger that and I couldn't figure out what I was doing differently, so I was a little perplexed why. For awhile I was nervous, so 3 weeks ago I seen my cardiologist and he did a heart monitor to capture the image of it to see what it is. He put in a stent about 3-4 years ago and I wanted to make sure I didn't have a blockage again but he didn't think it was and that it was a rhythm issue but wanted to make sure. It's very random and does it more in the evening than daytime, or I feel it anyways more in the evening. It causes me to to cough a lot when it happens and other than that I am waiting on results from EKG once he gets the report back and we will see what is going on.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac monitoring
- Hospital-Tage
- -
- Labordaten
- EKG July 2022 (unknown results).
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Cholesterol; High blood pressure
- Andere Medikamente
- Allopurinol; BYSTOLIC; losartan; aspirin; fenofibrate, NEXLETOL; ZETIA; ONE A DAY vitamin; coQ10; vitamin D.
- Allergien
- Codeine; epinephrine
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 28.06.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
hospitalized with covid; fully vaccinated with 2 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- afib, OSA (only using nasal strip, no CPAP)
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 20.07.2022
- Impfdatum
- 04.03.2021
- Beginn
- 01.06.2021
- Tage bis Beginn
- 89,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tinnitus both ears
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 91,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalization with dx other than COVID-19, COVID-19 incidental finding
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 07/19/2022 COVID positive test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Lung cancer, diabetes, hypertension, hx of CVA
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 18.04.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 48,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Discharge
Hypersensitivity
SARS-CoV-2 test positive
Symptomtext
04/18/2022 Vaccination Traveled to the other country 06/05/2022 Started to experience what you thought was extreme allergies. 06/07/2022 COVID-19 POSITIVE home test 06/08/2022 COVID-19 POSITIVE test at Doctor office. Prescribed Plaxovid. I still have a little bit of drainage and cough but I think it may be a little bit of allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 POSITIVE
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Wellbutrin; Lipitor; Toperal XL; Claritin; Hydrochlorothiazide; Irvesartam; Krill Oil; Vitamin D3; Vitamin E; Vitamin B Complex
- Allergien
- Biaxin
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 16.04.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 74,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test
Vaccine breakthrough infection
Symptomtext
I had a breakthrough case of COVID-19 confirmed by a home test on July 4, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home antigen test July 4, 2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Autoimmune disease (Susac's syndrome)
- Andere Medikamente
- Gabapentin, Lexapro, Propranolol, Probiotics, EpiCor
- Allergien
- PCN and Zithromax
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- 08.03.2021
- Beginn
- 06.07.2022
- Tage bis Beginn
- 485,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Nasal congestion
Sneezing
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; Sneezing; stuffy nose; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 08Mar2021 at 13:00 as dose number 2, single (Lot number: ENG206) at the age of 69 years, in left arm and on 04Oct2021 at 13:00 as dose number 3, (booster), single (Lot number: FD84218), in left arm for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), from 25Apr2022 at 13:00 (Lot number: 056M21A) to 25Apr2022 at 13:00 at single (dose number 4, (booster), single) for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), (Batch/Lot number: unknown) at single (dose number unknown, single) for covid-19 immunisation. There were no concomitant medications. The following information was reported: SNEEZING (non-serious) with onset 06Jul2022 at 03:00, outcome "recovering"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 06Jul2022 at 03:00, outcome "unknown" and all described as "Treatment of COVID-19"; NASAL CONGESTION (non-serious) with onset 06Jul2022 at 03:00, outcome "recovering", described as "stuffy nose". The patient underwent the following laboratory tests and procedures: Blood pressure measurement: high. Therapeutic measures were taken as a result of drug ineffective, covid-19. Therapeutic measures were not taken as a result of sneezing, nasal congestion. Clinical course: Patient had no known allergies. Patient received Paxlovid for COVID 19 Treatment from 27Jun2022 to 02Jul2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 03.06.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 2 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 7/14/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Hypertension, Obstructive Sleep Apnea and Renal Disease
- Andere Medikamente
- unknown
- Allergien
- celecoxib, glycopyrrolate, hydrocodone, lansoprazole, latex
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 20.05.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 55,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
Hospitalization with COVID-19. Fully vaccinated with 2 boosters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Type II NIDDM, hyperlipidemia, hypertension, reflux, DJD; myasthenia gravis and colon polyps
- Andere Medikamente
- Unknown
- Allergien
- Adhesive, Propoxyphene HCl
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 16.04.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 87,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated with 2 boosters. COVID breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 96,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 25.05.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 43,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated with one booster. COVID breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- 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: ja
Product storage error
Symptomtext
Vaccine was given outside of 12 hour interval
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 07.05.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 55,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Patient hospitalized while vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 68,0
- Geschlecht
- U
- Eingang
- 07.07.2022
- Impfdatum
- 16.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Illness
Symptomtext
I have two booster; I got sick; This spontaneous case was reported by a patient and describes the occurrence of ILLNESS (I have two booster; I got sick) in a 68-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 prophylaxis. Concurrent medical conditions included Asthma. Concomitant products included FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE (ADVAIR) for Asthma, LAMOTRIGINE for an unknown indication. On 16-May-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. On an unknown date, the patient experienced ILLNESS (I have two booster; I got sick). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) on 30-May-2022 for COVID-19 treatment, at a dose of 3 tablets for 5 days. At the time of the report, ILLNESS (I have two booster; I got sick) outcome was unknown. Patient took two booster Moderna Covid-19 vaccine, and got sick, they put patient on Paxlovid. Patient seems to work fine about five days after finishing Paxlovid. Patient started getting like cold symptoms and that was about two days ago cold symptoms, yellow sputum which is now turning more clear and patient took a covid test and it was positive so, patient think he had rebound covid. Symptoms reported by patient as very very tired. Patient further stated that patient was not experiencing side effect because of the vaccination it was due to Paxlovid. Patient was taking cold medications, herbal cold medications because he thought he had cold when one's he finished Paxlovid and symptoms came back like cold but today he tested positive for covid." When probed if adverse events are worsening, improved and persisting. Patient stated, "No well he don't if it is a covid rebound is a side effect of Paxlovid. Most recent FOLLOW-UP information incorporated above includes: On 08-Jun-2022: Upon internal review on 05-July-2022, significant correction was performed. Moderna vaccine was removed from historical vaccine and added in product tab. Removed the classification of Tracking only.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Illness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma
- Vorgeschichte
- -
- Andere Medikamente
- ADVAIR; LAMOTRIGINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 99,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 03.05.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Patient brought to the emergency department by EMS for weakness on 6/6. COVID-19 PCR testing was positive on that day (6/6), however patient had a previous positive test on 5/20. The patient was admitted from 6/6-6/8. This meets criteria for vaccine breakthrough case review.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 29.06.2022
- Impfdatum
- 20.06.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysmenorrhoea
Postmenopausal haemorrhage
Symptomtext
post menopausal menstrual bleeding. light. some cramping. Same occurred following 1st booster Moderna lot 939909 in November of 2021 but did not immediately connect event to vaccination. No menstrual bleeding following Pfizer 1st dose 03-02-2021 EN6198 or dose 2 Pfizer 03-23-2021 ER2613
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysmenorrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- sulfa
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 28.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Electrocardiogram abnormal
Heart rate increased
Symptomtext
Rapid Heart Beat (155)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram abnormal
- Hospital-Tage
- -
- Labordaten
- ECG confirmed rapid heart beat
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- pAFIB, Hypertension
- Andere Medikamente
- Hydralazine, Losartan, ASA 81mg, Eliquis, Metoprolol, Atorvastatin,
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Vaccine administering error: At our COVID vaccination clinic, patient was accidentally given Moderna COVID vaccine (18 and up) 0.3 ml instead of 0.25ml as the 2nd COVID vaccine booster. Patient was contacted the same day and notified this vaccine administering error. Then patient was contacted again the next day to follow up. Patient did not have any other signs or symptoms except pain in the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- CKD stage 2 Type II DM Hypertension Hyperlipidemia Chronic non alcoholic liver disease
- Andere Medikamente
- Colace 100 mg Victoza injection 0.3 mg/0.1 ml Basaglar Insulin 100 unit/ml Vitamin D3 25 mcg Os-Cal 500- Vit D3 5 mcg Metformin 1000 mg Lisinopril 5 mg Lipitor 10 mg Ecotrin 81 mg Metoprolol 50 mg
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 14.05.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 32,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bronchitis viral
COVID-19
Cough
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Mainly, I have had a runny nose that went into my chest that has made me cough a lot. I called in to virtual doctor and she issued me prednisone and cough pearls since it sounded dry at the time. It kept getting worse and 4 days later I did another virtual visit with my doctor who said it sounded like I had a viral bronchitis. My COVID-19 test finally came back positive. I received an Albuterol inhaler with cough syrup as well as Doxycycline.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bronchitis viral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- sinus infection
- Vorgeschichte
- Thyroid, hypertension, skin cancer
- Andere Medikamente
- Sinthroid, Iodine, Claritin.
- Allergien
- Sulfa, coconut, magnesium sulfate, penicillin.
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 16,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Positive test for COVID-19 on June 19, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure, high cholesterol, treated (late 2016) latent tuberculosis, borderline obesity (~30 BMI)
- Andere Medikamente
- Lisinopril 20mg Simvastatin 20mg Aspirin 81mg Hydrochlorothiazide 12.5mg B3 Supplement 2000iu Melatonin 1mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial initially stored in refrigerator on 10-May-2022 should have been discarded by 10-Jun-2022 and was administered on 13-Jun-2022; Dose administered after 30-day Use By Date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date) and PRODUCT STORAGE ERROR (Vial initially stored in refrigerator on 10-May-2022 should have been discarded by 10-Jun-2022 and was administered on 13-Jun-2022) in a 64-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 056M21A) for COVID-19 prophylaxis. No Medical History information was reported. On 13-Jun-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 13-Jun-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 initially stored in refrigerator on 10-May-2022 should have been discarded by 10-Jun-2022 and was administered on 13-Jun-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date) and PRODUCT STORAGE ERROR (Vial initially stored in refrigerator on 10-May-2022 should have been discarded by 10-Jun-2022 and was administered on 13-Jun-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The reporter stated they had a vaccine they moved from freezer to fridge on 10-May-2022. And according to information sheet they were good for 30 days, but it looked like there had been a couple of doses given this week. The vaccine should had been discarded on 10-Jun-2022 but the patient was given a second dose of the series on 13-Jun-2022. The dose was administered after 30-day Use by Date. It was also reported that the vial had not undergone any temperature excursions and the patient had not called to report any side effects. No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 14.05.2022
- Beginn
- 12.06.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
Came down with COVID 4 weeks after getting a 4th dose of Moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Levothyroxine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 15.06.2022
- Beginn
- 15.06.2022
- 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 initially stored in refrigerator on 10-May-2022 should have been discarded by 10-Jun-2022 and was administered on 15-Jun-2022; It looks like there has been a couple of doses given this week. It should have been discarded on 10June2022 and a second booster dose was given 15June2022.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (It looks like there has been a couple of doses given this week. It should have been discarded on 10June2022 and a second booster dose was given 15June2022.) and PRODUCT STORAGE ERROR (Vial initially stored in refrigerator on 10-May-2022 should have been discarded by 10-Jun-2022 and was administered on 15-Jun-2022) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Jun-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (It looks like there has been a couple of doses given this week. It should have been discarded on 10June2022 and a second booster dose was given 15June2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial initially stored in refrigerator on 10-May-2022 should have been discarded by 10-Jun-2022 and was administered on 15-Jun-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (It looks like there has been a couple of doses given this week. It should have been discarded on 10June2022 and a second booster dose was given 15June2022.) and PRODUCT STORAGE ERROR (Vial initially stored in refrigerator on 10-May-2022 should have been discarded by 10-Jun-2022 and was administered on 15-Jun-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that patient received a second booster dose. Concomitant drugs were not reported. It was reported that the vial was moved from freezer to fridge on 10-May-2022 and should have been discarded on 10-Jun-2022 and was administered 2 doses to patient on 13-Jun-2022 and 15-Jun-2022. The vial did not undergo any temperature excursion. It was also reported that patients have not called to report any side effects. This case was linked to MOD-2022-590656 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 18.06.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental underdose
Inappropriate schedule of product administration
Symptomtext
Received 2nd dose more than 35 days after the first dose; Patient received half dose booster instead of the 2nd primary full dose; This spontaneous case was reported by a nurse and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Received 2nd dose more than 35 days after the first dose) and ACCIDENTAL UNDERDOSE (Patient received half dose booster instead of the 2nd primary full dose) in a 20-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 056M21A) for COVID-19 prophylaxis. No Medical History information was reported. On 16-Jun-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 16-Jun-2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Received 2nd dose more than 35 days after the first dose) and ACCIDENTAL UNDERDOSE (Patient received half dose booster instead of the 2nd primary full dose). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Received 2nd dose more than 35 days after the first dose) and ACCIDENTAL UNDERDOSE (Patient received half dose booster instead of the 2nd primary full dose) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. Nurse stated 2nd primary dose was given as a half dose by mistake. Nurse stated that, the patient received half dose booster by mistake, instead of the 2nd primary full dose. The 2nd dose was administered more than 35 days after the first Moderna COVID-19 primary full dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 17.06.2022
- Impfdatum
- 15.06.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Pt scheduled for a Moderna booster shot. Pt had previously had 2 full doses of Moderna vaccine on 3/9/21 & 2/9/21. Pt had a booster dose on 11/5/21. Pt's father self reported pt was immunocompromised. Once immunocompromise status was entered into the pt's chart the dose recommendation changed from no dose recommended to FULL dose due. However, booster dose was administered. Education provide to father & pt that full dose should have been given based on report of immunocompromise. Father declined for pt to receive any additional dosing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 16.06.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Patient administered 0.25ml booster dose for 2nd dose in primary series. Moderna called and recommended that (per CDC) patient be given 2nd half of dose same day. Patient notified and states she will return to clinic before end of business.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 10.06.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental overdose
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL OVERDOSE (Pharmacist administered a first Moderna booster dose to a patient with a volume of 0.5ml instead of 0.25ml. This came from a Primary Series and a booster dose vial so the patient received too high) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer vaccine (The patient received Pfizer vaccine for her Primary series of Covid-19 vaccine). Past adverse reactions to the above products included No adverse event with Pfizer vaccine. On 10-Jun-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 10-Jun-2022, the patient experienced ACCIDENTAL OVERDOSE (Pharmacist administered a first Moderna booster dose to a patient with a volume of 0.5ml instead of 0.25ml. This came from a Primary Series and a booster dose vial so the patient received too high). At the time of the report, ACCIDENTAL OVERDOSE (Pharmacist administered a first Moderna booster dose to a patient with a volume of 0.5ml instead of 0.25ml. This came from a Primary Series and a booster dose vial so the patient received too high) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Patient does not report any other adverse reactions or side effects. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental overdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna case ID CEA-2628: lot number 056m21a maintained the activity neccessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna case ID CEA-2628: lot number 056m21a maintained the activity neccessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case. lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna lot number 056m21a maintained the activity neccessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna case ID CEA-2628: lot number 056m21a maintained the activity neccessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- silodosin, finasteride, amlodipine-olmesartan
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna lot number 056m21a maintained the activity neccessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- atorvastatin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 01.06.2022
- 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
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- penicillins
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 01.06.2022
- 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
Vaccine stored under refrigeration beyond 30 days. Moderna case ID CEA-2628: lot number 056m21a maintained the activity neccessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna: lot number 056m21a maintained the activity neccessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- dicyclomine, temazepam, tramadol, lisinopril-hctz, olavix
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- anucort
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- risperidone, levoxyl,
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- egg
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- eliquis, prevident, flomax,
- Allergien
- sulfa
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- xanax, ambien, lipitor, adderall, venlafaxine, geodon, trazodone, impramine
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- lisinopril.HCT, phentermine, augmentin, norco,
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- hydromorphone, amoxicillin, trazodonefluconazole, trazodone, crestor, losartan, docusate, allopurinol zofran,
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- adderall, buproprion,
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- gabapentin, zolpidem, clenpiq, potassium cl, olmesartan, furosemide
- Allergien
- ceftin, penicillamine
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- finasteride, lasix, ropinirole, metformin, warfarin, potassium cl, dicloxacillin, coreg, lipitor, irbesartan
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Moderna Case ID CEA-2628: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- shingrix, crestor, finasteride, losartan
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine stored under refrigeration beyond 30 days. Modera Case ID CEA-2628 result: lot number 056M21A maintained the activity necessary to protect against the SARSCoV-2 (COVID-19) virus at time of administration. Did not contact patient per no action required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- shingrix,
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 11.06.2022
- Impfdatum
- 11.06.2022
- Beginn
- 11.06.2022
- 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
Vaccine was administered 2 days after the Beyond-Use-Date of 6/9/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 31,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I was congested with a small cough. I took a cold pill the night before; I woke up at 5 in the morning and was even more congested. I was visiting family, and tested the day before and it was negative. The next morning, I woke up and took an at-home COVID-19 test, and it came back positive. So I got up and went to a mobile clinic up some blocks. I took an antigen and PCR COVID-19 test, and both tests came back positive. I called my doctor back home when I got to a hotel to isolate; the doctor prescribed me Paxlovid and began my treatment. Now I'm feeling better and took at-home test yesterday that came back negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 Tests: 06/04/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Osteopenia, Hay Fever
- Andere Medikamente
- Boniva Supplement, Allergy Eye Drops
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 15.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Hemiparesis
Interchange of vaccine products
Pupillary reflex impaired
Scan
Sensory disturbance
Symptomtext
Two days later, patient reported "buzzing " sensation to her face. Primarily right side of face and down to chin. Had increased weakness to her right side and right pupil sluggish. She was sent to the ED and then returned to our facility the same day when no acute issues were found. Per patient, similar symptoms to one of her previous strokes. Per husband, patient had a heart attack after her initial Covid vaccination series (pfizer) and did not want her to get the booster but patient wanted it so chose to go with the Moderna for the booster since it was a smaller dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- There were multiple blood tests and scans done at the hospital. I do not have access to those.
- Aktuelle Erkrankungen
- Cerebral Infarction
- Vorgeschichte
- COPD, HTN, CHF, CKD 3, DM2, athersclerotic heart disease, non rheumatic mitral valve insufficiency, thrombocytopenia, A. Fib
- Andere Medikamente
- Esetimibe, Fluoxetine, Aspirin EC, Furosemide, Lantus, Victoza, Xarelto, Atorvastatin, Omeprazole, Levothyroxine, Metoprolol, Pregabalin, Trazodone
- Allergien
- Metformin, Metocloparamide, Plavix, adhesive tape, atorvastatin (cough), gabapentin, Latex
- Vorherige Impfungen
- Per husband, this patient had a heart attack after her initial Covid series with Pfizer.
- Staat
- CT
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 25.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 37,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Covid 19 positive. Mild case- only needed to speak with MD on the phone. No live office visit required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- PCR and multiple antigen tests starting 6/4/22
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- mild controlled asthma
- Andere Medikamente
- cholesterol, asthma
- Allergien
- sulfa, ampicillin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 03.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Mycobacterium tuberculosis complex test
Symptomtext
Patient scheduled for Nurse visit that included Tb test and Covid booster. The vaccine was a prerequisite for a class.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mycobacterium tuberculosis complex test
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.06.2022
- 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 temperature excursion issue
Symptomtext
Product was administered after having been exposed to 45 hours of out-of-range temps reaching a Max 0f 13.4 C/Freezer was exposed to excursions; Administration after 45 hours excursion; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Product was administered after having been exposed to 45 hours of out-of-range temps reaching a Max 0f 13.4 C/Freezer was exposed to excursions) and EXPIRED PRODUCT ADMINISTERED (Administration after 45 hours excursion) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 056M21A) 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 (Administration after 45 hours excursion). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Product was administered after having been exposed to 45 hours of out-of-range temps reaching a Max 0f 13.4 C/Freezer was exposed to excursions). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Product was administered after having been exposed to 45 hours of out-of-range temps reaching a Max 0f 13.4 C/Freezer was exposed to excursions) and EXPIRED PRODUCT ADMINISTERED (Administration after 45 hours excursion) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. It was reported that the product was administered after having been exposed to 45 hours of out-of-range temps reaching a max of 13.4 C. The date the vial was initially stored in the refrigerator was reported as unknown. It was reported that provider removed vials from freezer as needed, stored in the refrigerator and did not mark BUD date or keep vaccine tracking records. It was reported that freezer was exposed to excursions but the provider contacted and indicated the vaccine was considered viable. Treatment information was not provided. This case was linked to MOD-2022-583131 (E2B Linked Report).; Sender's Comments: MOD-2022-583131:MOD-2022-583493 (same reporter 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
- 08.06.2022
- Impfdatum
- 02.05.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product temperature excursion issue
Symptomtext
product was administered after having been exposed to 45 hours of out-of-range temps reaching a Max 0f 13.4 C/Freezer was exposed to excursions; administration after 45 hours excursion; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (product was administered after having been exposed to 45 hours of out-of-range temps reaching a Max 0f 13.4 C/Freezer was exposed to excursions) and EXPIRED PRODUCT ADMINISTERED (administration after 45 hours excursion) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 056M21A) for COVID-19 vaccination. No Medical History information was reported. On 02-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 02-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administration after 45 hours excursion). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (product was administered after having been exposed to 45 hours of out-of-range temps reaching a Max 0f 13.4 C/Freezer was exposed to excursions). On 02-May-2022, EXPIRED PRODUCT ADMINISTERED (administration after 45 hours excursion) had resolved. At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (product was administered after having been exposed to 45 hours of out-of-range temps reaching a Max 0f 13.4 C/Freezer was exposed to excursions) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. It was reported that the product was administered after having been exposed to 45 hours of out-of-range temps reaching a max of 13.4 C. The date the vial was initially stored in the refrigerator was reported as unknown. It was reported that provider removed vials from freezer as needed, stored in the refrigerator and did not mark BUD date or keep vaccine tracking records. It was reported that freezer was exposed to excursions but the provider contacted and indicated the vaccine was considered viable. No treatment medication was provided. This case was linked to US-MODERNATX, INC.-MOD-2022-583493 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 06-Jun-2022: Follow-up received updated start date of Moderna Vaccine, event verbatim and event start date.; Sender's Comments: US-MODERNATX, INC.-MOD-2022-583493:MOD-2022-583493 (same reporter case)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 29.04.2022
- 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 test
Symptomtext
COVID-19 prior to Paxlovid treatment; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (COVID-19 prior to Paxlovid treatment) in a 54-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. Concurrent medical conditions included Type 1 diabetes mellitus, Hypothyroidism and Drug allergy (unknown drug allergy). Concomitant products included INSULIN ASPART (NOVOLOG) from 18-May-2022 to 01-Jun-2022 for an unknown indication. On 29-Apr-2022 at 12:30 PM, 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 Paxlovid treatment). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 18-May-2022 to 23-May-2022 for COVID-19 treatment, at a dose of 1 dosage form. At the time of the report, COVID-19 (COVID-19 prior to Paxlovid treatment) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 26-May-2022, SARS-CoV-2 test: negative (Negative) Negative covid test result 3 days after finishing paxlovid. On 01-Jun-2022, SARS-CoV-2 test: positive (Positive) positive test result 9 days after finishing Paxlovid. The patient received unspecified medications/products within 2 weeks of starting COVID-19 treatment. After 5 days of all doses of Paxlovid treatment, patient felt extreme fatigue, runny nose, slight cough, allergy-like symptoms. Patient tested COVID-19 negative 3 days after finishing Paxlovid and tested positive 9 days after finishing Paxlovid. The device date was reported as 01-Jun-2022. Company comment: This spontaneous case of concerns a 54-year-old female patient, with no relevant medical history, who experienced the unexpected, non-serious AESI of COVID-19. The event was reported with no onset date; hence, latency to the fourth dose of mRNA-1273 vaccine cannot be assessed. No details of previous doses were provided. As per source document, she received Paxlovid as COVID-19 treatment 19 days after the fourth dose of mRNA-1273 vaccine, and after 5 days of treatment she experienced extreme fatigue, runny nose, slight cough, allergy-like symptoms. Three days after finishing Paxlovid she had a negative test and was tested positive 9 days after finishing Paxlovid. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case of concerns a 54-year-old female patient, with no relevant medical history, who experienced the unexpected, non-serious AESI of COVID-19. The event was reported with no onset date; hence, latency to the fourth dose of mRNA-1273 vaccine cannot be assessed. No details of previous doses were provided. As per source document, she received Paxlovid as COVID-19 treatment 19 days after the fourth dose of mRNA-1273 vaccine, and after 5 days of treatment she experienced extreme fatigue, runny nose, slight cough, allergy-like symptoms. Three days after finishing Paxlovid she had a negative test and was tested positive 9 days after finishing Paxlovid. 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: COVID - 19 Test; Test Result: Negative ; Result Unstructured Data: Negative covid test result 3 days after finishing paxlovid; Test Date: 20220601; Test Name: COVID - 19 Test; Test Result: Positive ; Result Unstructured Data: positive test result 9 days after finishing Paxlovid.
- Aktuelle Erkrankungen
- Drug allergy (unknown drug allergy); Hypothyroidism; Type 1 diabetes mellitus
- Vorgeschichte
- -
- Andere Medikamente
- NOVOLOG
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 07.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
No adverse event
Symptomtext
2nd booster dose of Moderna given today at the clinic. A nurse gave .5ml Moderna instead of 0.25ml dose. Client is feeling well with no adverse reaction as of 11:45am today. Client has been notified of this error and is calm and understanding. She is happy to be notified and not concerned of receiving a higher dose than what is recommended at this time. Client does not notice any adverse side effects at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 07.06.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Patient received 2nd booster dose of Moderna vaccine that he was not eligible for. Patient received Moderna vaccine doses on 2/10/21, 3/10/21, 11/27/21. Patient is a 47 year old and is not immunocompromised.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Extra dose administered
Vaccine breakthrough infection
Symptomtext
Fully vaccinated and boosted twice. COVID infection breakthrough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 06.06.2022
- Impfdatum
- 25.05.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 11,0
- 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
COVID vaccine breakthrough case.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 5/30/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 05.06.2022
- Impfdatum
- 22.04.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure high cholesterol Both under control with the above medications
- Andere Medikamente
- Chlorthalidone 25mg Atorvastatin 5mg Aspirin 81mg Advil 200mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- U
- Eingang
- 04.06.2022
- Impfdatum
- 28.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
vial was initially stored in the refrigerator from the freezer on 27-Apr-2022 and the doses were administered on 28-May-2022; Administered with vaccine that is past beyond the 30 day use; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered with vaccine that is past beyond the 30 day use) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator from the freezer on 27-Apr-2022 and the doses were administered on 28-May-2022) in a 62-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. Previously administered products included for Drug use for unknown indication: Janssen on 29-Mar-2021 and Pfizer on 18-Dec-2021. Past adverse reactions to the above products included No adverse event with Janssen and Pfizer. On 28-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered with vaccine that is past beyond the 30 day use). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator from the freezer on 27-Apr-2022 and the doses were administered on 28-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered with vaccine that is past beyond the 30 day use) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator from the freezer on 27-Apr-2022 and the doses were administered on 28-May-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vial was initially stored in the refrigerator from the freezer on 27-Apr-2022 and the doses were administered on 28-May-2022. No adverse events had been reported by patient at the time of the call. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- U
- Eingang
- 04.06.2022
- Impfdatum
- 28.05.2022
- Beginn
- 28.05.2022
- 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
The vial was initially stored in the refrigerator from the freezer on 27-Apr-2022 and the doses were administered on 28-May-2022.; administered with vaccine that is past beyond the 30 day use; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator from the freezer on 27-Apr-2022 and the doses were administered on 28-May-2022.) and EXPIRED PRODUCT ADMINISTERED (administered with vaccine that is past beyond the 30 day use) in a 61-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Janssen on 24-Mar-2021 and Pfizer on 18-Dec-2021. Past adverse reactions to the above products included No adverse event with Janssen and Pfizer. On 28-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with vaccine that is past beyond the 30 day use). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator from the freezer on 27-Apr-2022 and the doses were administered on 28-May-2022.). At the time of the report, PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator from the freezer on 27-Apr-2022 and the doses were administered on 28-May-2022.) and EXPIRED PRODUCT ADMINISTERED (administered with vaccine that is past beyond the 30 day use) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vial was initially stored in the refrigerator from the freezer on 27-Apr-2022 and the doses were administered on 28-May-2022. No treatment medications were reported. This case was linked to MOD-2022-581520 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 01-Jun-2022: Follow up received on 01/Jun/2022: Upon follow up the case was upgraded to valid from invalid. added patient initials, date of birth, added historical vaccine, updated suspect coding and added event of product storage error which was missed in previous version.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 03.06.2022
- Impfdatum
- 28.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product use issue
Symptomtext
Vaccine was given beyond BUD of vaccine. Vaccine refrigerated 4/27 1020 and vaccine given 5/28 0820. One day over BUD. No reported adverse effect after vaccine given which affected 7 patients.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Interchange of vaccine products
Symptomtext
Patient received Moderna first dose on 2/10/2021 and second dose on 3/10/2021. Patient is not considered immunocompromised. Patient received Moderna first booster on 11/10/2021 and Pfizer second booster on 4/20/2022. Patient was administered a third Moderna booster on 5/31/2022. Third booster given outside of current FDA booster recommendations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknow
- Vorgeschichte
- CAD, Fuch's, Glaucoma, High Blood Pressure, Hypthyrodism, Hypertension, Stenosis, Hearking Loss, Type 2 Diabetes, GERD, Osteoporosis, and Dementia.
- Andere Medikamente
- Acetaminophen, Amlodipine, Aspirin, Chlohexidine, Cholecalciferol, docusate senna, flonase, flm forte liquifilm, imdur xr, lasix, levothyroid, loperamide, metoprol tartrate, nitrogylcerin, ocular lubricant, omeprazole, pravachol, proventil,
- Allergien
- Lovastation, Simvastatin, and Codeine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient was not eligible for the vaccine booster (48 years old). No adverse reactions to vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Abnormal cervical pap
- Andere Medikamente
- Amlodipine, prenatal s, obago (hydroquinone/vitamin c)
- Allergien
- Augmentin
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 02.06.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Wrong product administered
Symptomtext
Patient requested covid vaccine in error but he wanted the shingrix vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient received first dose on 3/11/2021 and second dose on 3/16/2022. First booster provided on 5/31/2022 which was too early based upon current FDA recommendations for time separation between initial series and booster dose for Moderna. Patient is not considered immunocompromised.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Type 2 Diabetes Dementia/Alzheimer's Anemia
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient not considered immuncompromised and under age 50 but was given a 2nd booster doses of Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 11.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fungal infection
Immediate post-injection reaction
Therapy non-responder
Vaccine positive rechallenge
Vertigo
Symptomtext
As I sat at the pharmacy during the 15 minute wait after my vaccination, I immediately felt some vertigo. I didn't report it to a pharmacist as I didn't feel like there was anything to be done about it. A week later, I started treating a yeast infection. I have so far taken 4 Fluconazole tablets. The infection will not go away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fungal infection
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Had been getting over vertigo which may have been attributed to the Covid booster I had in October of 2021. Had recovered from that long (4 month) episode which has just started up again since my May 11th booster.
- Vorgeschichte
- irritable bowel and acid reflux, pudendal neuralgia
- Andere Medikamente
- Chlordiazepoxide/Clidinium 5/2.5 mg , omeprazole 20mg, probiotic pearls, Magnesium Citrate, 125mg
- Allergien
- Sulfa - hives Penicillin products, stomach issues
- Vorherige Impfungen
- Same issues. Yeast infection and vertigo. Age 62, vaccination date 10-22-21, Covid-19 Moderna booster , lot number unreadable
- Staat
- WI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Patient received 4th booster ~1 week early. 3rd booster was received 1/11/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient was given booster by local Care Center staff too early. 2nd dose was administered 3/11/22 and booster given 5/27/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- gabapentin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- -
- Geschlecht
- M
- Eingang
- 30.05.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The unpunctured vaccine vial was stored in the refrigerator for 38 days and administered to this patient 8 days after the 30-day Use By Date; Received expired 1st booster dose 8 days after 30-day Use By Date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired 1st booster dose 8 days after 30-day Use By Date) and PRODUCT STORAGE ERROR (The unpunctured vaccine vial was stored in the refrigerator for 38 days and administered to this patient 8 days after the 30-day Use By Date) in an adult male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. No Medical History information was reported. On 25-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired 1st booster dose 8 days after 30-day Use By Date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The unpunctured vaccine vial was stored in the refrigerator for 38 days and administered to this patient 8 days after the 30-day Use By Date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received expired 1st booster dose 8 days after 30-day Use By Date) and PRODUCT STORAGE ERROR (The unpunctured vaccine vial was stored in the refrigerator for 38 days and administered to this patient 8 days after the 30-day Use By Date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Reporter thinks that the patient is in his 60's but not 100 percent sure. No concomitant medications was reported. Patient received the expired first booster dose of Moderna COVID-19 vaccine. 30-days use by date was reached on 17 May 2022. Vial did not undergo any temperature excursions. No treatment was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 26.05.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.05.2022
- 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
No adverse event
Product storage error
Symptomtext
Vaccine was administered past the 30 day refrigerator expiration date by MA. Moderna and state health department were notified on day of administration. Patient notified today. No known adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Unknown
- Andere Medikamente
- Torvastatin, Irbesartan.
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.05.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- 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
1 dose was given past 30 day use by date; 1 dose was given past 30 day use by date; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (1 dose was given past 30 day use by date) and PRODUCT STORAGE ERROR (1 dose was given past 30 day use by date) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 056M21A) for COVID-19 vaccination. No Medical History information was reported. On 23-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 23-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (1 dose was given past 30 day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (1 dose was given past 30 day use by date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (1 dose was given past 30 day use by date) and PRODUCT STORAGE ERROR (1 dose was given past 30 day use by date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. On 19Apr2022, the vial was initially stored in the refrigerator. The vial did not undergo any temperature excursions. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
PATIENT WAS TO RECEIVE 0.25ML BOOSTER DOSE BUT INSTEAD RECEIVED FULL 0.5ML DOSE. NO ADVERSE AFFECTS REPORTED BY PATIENT WHEN NOTIFIED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
PATIENT WAS TO RECEIVE 0.25ML BOOSTER DOSE BUT INSTEAD RECEIVED FULL 0.5ML DOSE. NO ADVERSE AFFECTS REPORTED BY PATIENT WHEN NOTIFIED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LIPITOR 10MG
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
PATIENT WAS TO RECEIVE 0.25ML BOOSTER DOSE BUT INSTEAD RECEIVED FULL 0.5ML DOSE. NO ADVERSE AFFECTS REPORTED BY PATIENT WHEN NOTIFIED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
PATIENT WAS TO RECEIVE 0.25ML BOOSTER DOSE BUT INSTEAD RECEIVED FULL 0.5ML DOSE. NO ADVERSE AFFECTS REPORTED BY PATIENT WHEN NOTIFIED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
PATIENT GIVEN FULL DOSE INSTEAD OF BOOSTER DOSE. PATIENT TOLERATED WELL. NO KNOWN SIDE AFFECTS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HYPERTENSION,TYPE II DM, HYPERLIPIDEMIA
- Andere Medikamente
- ROSUVASTATIN 10MG, METFORMIN 500MG, OMEPRAZOLE 20MG, ALLOPURINOL 400MG, LISINOPRIL 20MG
- Allergien
- CODEINE
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 14.05.2022
- Beginn
- 14.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Anticoagulant therapy
Blood test
Cardiac ventricular disorder
Catheterisation cardiac abnormal
Chest discomfort
Echocardiogram abnormal
Electrocardiogram
Myocardial necrosis marker increased
Stress cardiomyopathy
Symptomtext
A few hours after receiving the vaccine, I went to the hospital because I was having pressure in my chest. When I went to the ER they took my vitals and ran some test. I had elevated heart enzymes. They put me in an observation unit and kept me overnight. The next day, I had a echocardiogram which showed abnormalities in my left ventricle. They scheduled me for a heart catherization. They said I had a heart attack. On May 16, 2022, they gave me the heart catherization which ruled out a heart attack but shown that I had broken heart syndrome. I was prescribed baby Aspirin, Lipitor, Lisinopril, and Metoprolol Succinate. The doctors said it should resolve in about 1 or 2 months. I was released on May 17th. I would still get another vaccine if recommended.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anticoagulant therapy
- Hospital-Tage
- 4,0
- Labordaten
- EKG, Blood work, Echocardiogram- showed abnormalities in my left ventricle
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Calcium, Vitamin D, Duloxetine, Melatonin, Trazadone, Amlodipine Besylate
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired medication given to patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
No adverse event
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
Patient came in for a booster shot of covid vaccine. He was given Moderna by mistake as he is not 18 years of age yet. He was previously given the Pfizer, but mistakenly got moderna this time. No adverse reaction and provider and parents were notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- None needed. No reaction
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 19.05.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
Staff were unaware that patient had already received his first Moderna Booster dose at the previous facility on 2/18/22. Patient inadvertently administered the second Moderna Booster dose only 3 months after receiving their first booster dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A.
- Vorgeschichte
- Allergic rhinitis, osteoarthritis, hypertension, and Vitamin D deficiency.
- Andere Medikamente
- -Loratadine 10 mg as needed -Metamucil 1 tsp powder Oral Q8H PRN for Constipation -Preparation H ointment prn to rectal area for Dx -Lactulose 10g/15ml give 15 ml syrup every 24 hours prn NTE 1x/24 hours -Colace 100mg PO qday x30days DX:
- Allergien
- NKA.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 18,0
- Dosis
- 3
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysuria
Micturition urgency
Urinary tract infection
Symptomtext
UTI - burning, urgency, etc. phone visit on 5/20: Prescribed antibiotic and pyridine. 5/23: symptoms resolving
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysuria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Amnesia
Hypersomnia
Interchange of vaccine products
Somnolence
Unresponsive to stimuli
Symptomtext
She got her 4th booster at home (homebound). She got the vaccine on Tuesday late afternoon. To her knowledge and recollection she had no reaction to that. On Wednesday a CNA came as they always do, she slept OK that evening. She know that the nurse came and changed some dressings on her stomach. She does not remember her coming, but knows it happened, and apparently she just went to sleep after eating breakfast and then does not remember that or what she ate. She apparently fell asleep after the nurse left. She then woke up and it was dark and remembers it was 1:00 AM Thursday and had lost the entire previous day. Her roommates thought she was dying and told her that as she did not respond and would not wake up. She has been OK since waking up on Thursday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amnesia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Diabetes, Cardiomyopathy, arthritis all over her body, bedbound due to lower spine stenosis, neuropathy, GERD.
- Andere Medikamente
- Primidone, Methanamine, Vitamin D, Gabapentin, Vitamin C.
- Allergien
- Penicillin and it's derivatives.
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 16.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Swelling face
Symptomtext
30 hours later swelling of lip and cheek
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
Pt. received dose of Moderna from a vial that was outside the discard timeframe. Vial was still stored at proper storage temp. Moderna manuf. notified. Due to, proper storage & no other negative factors, per Moderna vaccine dose "Maintained activity against COVID-19". Dose valid Per Moderna. Doses increased risk for microbial infection the father outside the discard window as it is for MDV. No known injury to patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Dementia, Anxiety, Depressive disorder, Alzheimer's disease, Neuropathy, Supraventricular tachycardia, Orthostatic Hypotension, Benign prostatic hyperplasia, Skin lesion, Ataxic gait, History of malignant neoplasm of colon, History of sick sinus syndrome, history of colonoscopy, cataract surgery, arthroscopy knee surgery, tonsillectomy, Prostate Surgery - Urolift, Cancer Surgery - Colostomy, Pacemaker
- Andere Medikamente
- donepezil, fludrocortisone, HOLLIHESIVE SKIN BARRIER 4" x 4" WAFER, HOLLISTER Eaches, Ipratropium bromide, memantine, New Image Flexwear Barrier 2 3/4", Ostomy Supplies, QUEtiapine, Sertraline, Tamsulosin, Topiramate, Vitamin D3,
- Allergien
- Citalopram, Penicillin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- 27.04.2022
- Beginn
- 14.05.2022
- Tage bis Beginn
- 17,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Amaurosis fugax
Anticoagulant therapy
Blindness unilateral
Blood test normal
Electrocardiogram ambulatory
Magnetic resonance imaging normal
Symptomtext
I had a partial loss of vision in the upper half of my right eye. It lasted for 10 seconds before it started to dissipate on it's own. It gradually started to clear up. On May 15th, I went to my eye Doctor. He explained I should go to the emergency room to be checked for possibility of stroke. I went to ER at 5:00PM that same day and sent me home with a heart monitor. I haven't had any reoccurrence since. Omaurosis Fugax is what I was diagnosed with. I was put on 325 mg of Aspirin per day since the event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amaurosis fugax
- Hospital-Tage
- -
- Labordaten
- Bloodwork- Normal; MRI- Normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Migraines; Arthritis
- Andere Medikamente
- Diphenoxylate Hydrochloride 2.5 mg, I take 2 tabs 3 times a day Tamsulosin Hydrochloride 1 capsule once a day Alprazolam .25 mg, I take .5 tablet once a day Amoxicillin 500 mg, I take one a day Ipratropium Nasal Spray, .6% , I take one shot
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 09.05.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac discomfort
Chest X-ray normal
Chest discomfort
Electrocardiogram normal
Extrasystoles
Inflammation
Symptomtext
That night I laid down and went to bed but as I was falling asleep my heart felt strange but it didn't last long so I went to sleep. The next morning, I listened to my heart with a stethoscope and noticed 2 or 3 distinct skipped beats per minute. I emailed my doctor who reached out to confirm that there were no other concerning symptoms associated. By 5/11, I was feeling a lot of strange sensation in my chest. Since I've never had an issue like this in the past, I called my doctor again and made an appointment on 5/12 to see a doctor at my PCPs office. He did a chest xray and an ekg. He stated that I was probably experiencing some mild inflammation due to the vaccine. I felt better for a few days but on Monday, 5/16 the sensation in my chest returned and I was hearing at least 4 skipped beats per minute. I called my doctor again and I'm scheduled to do a holter monitor starting on 5/26 for further diagnosis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac discomfort
- Hospital-Tage
- -
- Labordaten
- Xray 5/12-normal EKG 5/12-normal
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypertension Thyroid issue
- Andere Medikamente
- Lisinopril 5mg once daily Levothyroxine 100micrograms daily Metronidazole 0.75% gel applied to nose twice daily Multivitamin Citrocal 400mg Tylenol 500mg daily Benefiber 2 teaspoons Refresh Plus Lubricant Eye drops
- Allergien
- Augmentin Bactrim
- Vorherige Impfungen
- Swine Flu Vaccine-Age-20's-I fainted.
- Staat
- MO
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 02.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Swollen lymph nodes in left groin area
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- Multi-vitamin, fish oil, glucosamine, vit d, Lexapro, Singulair, Zyrtec
- Allergien
- Sulfa, wheat
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
No adverse event
Symptomtext
NO ADVERSE REACTION. ADMINISTRATION ERROR REPORT, INADVERTENTLY GIVEN A MIXED PRIMARY SERIES. PATIENT'S FIRST VACCINE WAS PFIZER, FOR THE 2ND VACCINE ON 5/10/22 PT WAS GIVEN MODERNA 0.25ML.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hyperlipidemia, Hypertension, Urinary Incontinence
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 09.05.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Patient received larger dose of Moderna vaccine than needed (full dose). She had already received full dose of Moderna three times in the primary series and needed booster dosing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CNS lymphoma, paraplegia, hyperlipidemia, hypertension, allergic rhinitis
- Andere Medikamente
- Atorvastatin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 91,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Oxygen saturation abnormal
Symptomtext
Narrative: Pt was monitored closely. Oxygen saturation and activity level returned to baseline after 2 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oxygen saturation abnormal
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 08.03.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 58,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
PATIENT WAS ADMINISTERED THE SECOND BOOSTER 0.25 ML TOO SOON. NO NOTED REACTIONS AT THIS TIME.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HYPERTENSION, TYPE 2 DIABETES
- Andere Medikamente
- NOVOLIN 70/30, MAGNESIUM OXIDE, ROPINIROLE, PRALUENT PEN 75 MG, AMITRIPTYLINE, ASPIRIN 80 MG, CELEBREX, CLOPIDIDOGREL, FUROSEMIDE, GABAPENTIN, GLIMEPIRIDE, RELION/NOVOLIN R, ISOSORBIDE MONONITRATE, LISINOPRIL, METOPROLOL SUCCINATE ER, OMEGA
- Allergien
- NONE LISTED
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
A moderna booster dose was given to a patient under age 18. No known adverse reaction occurred. The patient had received pfizer for their primary series, but requested moderna for their booster. The administering pharmacist did not notice the patient was only 17 until after the vaccine had been administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- NONE KNOWN
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 08.05.2022
- Impfdatum
- 25.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Liver disorder
Liver function test increased
Symptomtext
Vaccination resulted in hospitalization in subsequent days after vaccination. Per hospital report, pt LFTs rose significantly after the vaccination resulting in hospitalization.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Liver disorder
- Hospital-Tage
- 10,0
- Labordaten
- LFT elevation secondary to vaccination reported by hospital. Effects on liver resulted in hospitalization of patient.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 07.05.2022
- Impfdatum
- 30.04.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Symptomtext
Patient experienced blisters on her toes and feet, she explained to me she thought it was from her boot because she has tendonitis, but then a day later discovered the blisters on her foot without the boot. She saw the podiatrist and he said to monitor the blisters and do not pop them. I advised her the same advise. She will follow up with her doctor on Monday this week. I saw the blisters and they look exactly like subepidermal blistering eruptions, possibly due to mRNA vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blister
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- tendonitis
- Vorgeschichte
- -
- Andere Medikamente
- steroids for tendonitis
- Allergien
- codeine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 07.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Poor quality product administered
Product temperature excursion issue
SARS-CoV-2 test
Symptomtext
vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) for 3 hours; vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) for 3 hours/dose administered >12/24 hours post puncture; Patient received a second booster and are not immunocompromised or over 50 years of age; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) for 3 hours), POOR QUALITY PRODUCT ADMINISTERED (vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) for 3 hours/dose administered >12/24 hours post puncture) and EXTRA DOSE ADMINISTERED (Patient received a second booster and are not immunocompromised or over 50 years of age) in a 48-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. Patient did not had acute and chronic illnesses at the time of vaccination. Other vaccines given within 1 month prior to Moderna COVID-19 vaccine (type, brand, lot, route, dose #) no. The patient's past medical history included COVID-19 on 11-Sep-2020. Previously administered products included for Drug use for unknown indication: JANSSEN COVID-19 VACCINE (Booster dose) and JANSSEN COVID-19 VACCINE (Primary series). Past adverse reactions to the above products included No adverse event with JANSSEN COVID-19 VACCINE and JANSSEN COVID-19 VACCINE. Concurrent medical conditions included Drug allergy (Accutane allergy). On 03-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-May-2022, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) for 3 hours/dose administered >12/24 hours post puncture) and EXTRA DOSE ADMINISTERED (Patient received a second booster and are not immunocompromised or over 50 years of age). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) for 3 hours). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) for 3 hours), POOR QUALITY PRODUCT ADMINISTERED (vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) for 3 hours/dose administered >12/24 hours post puncture) and EXTRA DOSE ADMINISTERED (Patient received a second booster and are not immunocompromised or over 50 years of age) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 11-Sep-2020, SARS-CoV-2 test: positive (Positive) Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. Date the vial was initially stored in the refrigerator: 29-Apr-2022. On 29-Apr-2022 at 8:00 AM vial was first punctured. The vial was stored in fridge post puncture. Vial was moved from freezer to refrigerator. Total amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F):3 hours. Maximum or minimum temperatures reached, as applicable (specify temp is in C or F) were not known and duration was 3 hours. Storage condition at the time of the excursion was refrigerated storage. Visual inspection noting any vaccine state change: (e.g. were frozen vials thawed, were thawed vials re-frozen, were they visualized at all) no. Any previous excursions with the impacted vial was reported as no. It was stated that, event did not cause patient to seek medical care. There were no other potential causes and patient did not experience similar event in the past. Treatment medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- Test Date: 20200911; Test Name: COVID-19; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Drug allergy (Accutane allergy)
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19; Comments: Patient did not had acute and chronic illnesses at the time of vaccination. Other vaccines given within 1 month prior to Moderna COVID-19 vaccine (type, brand, lot, route, dose #) no.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 06.05.2022
- Impfdatum
- 14.04.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 21,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Nasal congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
I had nasal congestion, sneezing, coughing and this is all minor. The worst thing was seeing the positive result. I ended up doing a video health meeting and received a prescription of Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID-19 Test 05/05/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Levothyroxine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 06.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Extra dose administered
Product temperature excursion issue
Symptomtext
Vial did under went a temperature excursion; Patient received a Dose administered greater than 12 hours post puncture; Patient received a second booster and are not immunocompromised or over 50 years of age; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received a Dose administered greater than 12 hours post puncture), EXTRA DOSE ADMINISTERED (Patient received a second booster and are not immunocompromised or over 50 years of age) and PRODUCT TEMPERATURE EXCURSION ISSUE (Vial did under went a temperature excursion) in a 40-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. The patient had no allergies. The patient never had COVID-19 positive test or diagnosis. The patient had no acute or chronic illnesses at the time of vaccination. Previously administered products included for Product used for unknown indication: janssen for primary series and booster (primary series and booster). Past adverse reactions to the above products included No adverse event with janssen for primary series and booster. On 03-May-2022 at 11:15 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-May-2022 at 11:15 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received a Dose administered greater than 12 hours post puncture). 03-May-2022 at 11:15 AM, the patient experienced EXTRA DOSE ADMINISTERED (Patient received a second booster and are not immunocompromised or over 50 years of age). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vial did under went a temperature excursion). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received a Dose administered greater than 12 hours post puncture), EXTRA DOSE ADMINISTERED (Patient received a second booster and are not immunocompromised or over 50 years of age) and PRODUCT TEMPERATURE EXCURSION ISSUE (Vial did under went a temperature excursion) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The patient was not immunocompromised. Other vaccines given within 1 month prior to Moderna vaccine reported as no. The adverse event did not cause patient to go for office visit, urgent care, ER and hospital. The vial was initially stored in the refrigerator on 29 Apr 2022 and was first punctured on 29 Apr 2022 at 8AM. The vial was stored in fridge post puncture and did undergo temperature excursion. The vial was exposed to room temperature range (8 to 25 degree Celsius or 46 to 77 degree F) for 3 hours. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no allergies. The patient never had COVID-19 positive test or diagnosis. The patient had no acute or chronic illnesses at the time of vaccination.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Extra dose administered
Product temperature excursion issue
Symptomtext
3 patients received a Dose administered >1224 hours post puncture; 3 patients received a second booster and are not immunocompromised or over 50 years of age; They state also that this vial did under went a temperature excursion; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (3 patients received a Dose administered >12/24 hours post puncture), EXTRA DOSE ADMINISTERED (3 patients received a second booster and are not immunocompromised or over 50 years of age) and PRODUCT TEMPERATURE EXCURSION ISSUE (They state also that this vial did under went a temperature excursion) in a 36-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: janssen (Patient received Janssen as primary series and booster dose.). Past adverse reactions to the above products included No adverse event with janssen. On 03-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (3 patients received a Dose administered >12/24 hours post puncture), EXTRA DOSE ADMINISTERED (3 patients received a second booster and are not immunocompromised or over 50 years of age) and PRODUCT TEMPERATURE EXCURSION ISSUE (They state also that this vial did under went a temperature excursion). At the time of the report, EXPIRED PRODUCT ADMINISTERED (3 patients received a Dose administered >12/24 hours post puncture), EXTRA DOSE ADMINISTERED (3 patients received a second booster and are not immunocompromised or over 50 years of age) and PRODUCT TEMPERATURE EXCURSION ISSUE (They state also that this vial did under went a temperature excursion) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient had no Allergies No concomitant medication information provided. No treatment medication information provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- -
- Geschlecht
- U
- Eingang
- 05.05.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Patient Administered vaccine on 27-APR at 10:57am, post 24Hr duration of 26-Apr at 10:46am.; Patient Administered vaccine on 27-APR at 10:57am, post 24Hr duration of 26-Apr at 10:46am.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient Administered vaccine on 27-APR at 10:57am, post 24Hr duration of 26-Apr at 10:46am.) and PRODUCT STORAGE ERROR (Patient Administered vaccine on 27-APR at 10:57am, post 24Hr duration of 26-Apr at 10:46am.) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 056m21a) for COVID-19 vaccination. No Medical History information was reported. On 27-Apr-2022 at 10:57 AM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 27-Apr-2022 at 10:57 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient Administered vaccine on 27-APR at 10:57am, post 24Hr duration of 26-Apr at 10:46am.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Patient Administered vaccine on 27-APR at 10:57am, post 24Hr duration of 26-Apr at 10:46am.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient Administered vaccine on 27-APR at 10:57am, post 24Hr duration of 26-Apr at 10:46am.) and PRODUCT STORAGE ERROR (Patient Administered vaccine on 27-APR at 10:57am, post 24Hr duration of 26-Apr at 10:46am.) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant drug reported. Moderna vaccine was administered past the allowed 24 hours of room temperature allowance and past the allowed 12 hours after puncture. The vial was moved from the freezer to the fridge and believes on 15-April. Vial was moved to room temperature for initial use at 10:46 am on 26-April and punctured at that time. The last dose was administered on 27-April at 10:57 am. No treatment information was provided by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 02-May-2022: Significant Live FU received, Lot no. updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong technique in product usage process
Symptomtext
Patient was administered vaccine that was greater than 12 hours post first vial puncture. Patient did not exhibit any adverse reaction post administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- atorvastatin, escitalopram, ketotifen ophthalmic solution
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Patient was administered vaccine that was greater than 12 hours post first vial puncture. Patient did not exhibit any adverse reaction post administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- dyslipidemia, pre-diabetes
- Andere Medikamente
- atorvastatin, Suboxone, buspirone, docusate, duloxetine, metformin
- Allergien
- No Known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong technique in product usage process
Symptomtext
Patient was administered vaccine that was greater than 12 hours post first vial puncture. Patient did not exhibit any adverse reaction post administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Accutane
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient received 0.5 ml vs 0.25 ml dose for their first booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- COPD, Diverticulosis, HTN, Gout
- Andere Medikamente
- Allopurinol, Diltiazem, Eliquis, Finasteride
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient received 0.5mL dose vs 0.25mL dose for the booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, hearing loss, history of stroke, hyperaldosteronism, insomnia
- Andere Medikamente
- Albuterol, Carvedilol, Diltiazem, Eliquis
- Allergien
- NTG transdermal
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 27.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lip discolouration
Tongue discolouration
Symptomtext
Employee complained of blackening of lips and tongue 1 day after receiving the vaccines. It has since resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip discolouration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 02.05.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
2ND DOSE WAS BOOSTER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- HAS NOT RECEIVED ANY ADDITONAL HEALTH CARE SERVICES.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- DM 2 hypertenion
- Andere Medikamente
- tylenol and Ibuprofen PRN
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
The patient was supposed to receive a Shingrix shot but received a Moderna vaccine. After getting in touch with the patient, she has stated she was feeling fine and there was no adverse reaction to the vaccine at this time. Patient was understanding and will be coming in for the correct vaccine on a different day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HYPERTENSION
- Andere Medikamente
- N/A
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient administered 2nd Moderna booster dose but did not qualify for the dose. Patient does not meet the age requirement and does not have an immunocompromising condition. No current adverse events noted at this time from the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- N/A.
- Vorgeschichte
- Asthma.
- Andere Medikamente
- Claritin 10 mg PPO q24hrs PRN. Xopenex 2 puffs q6hrs PRN NTE 4x/day.
- Allergien
- NKA.
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Pharmacy administered a Moderna Vaccination after the vial was punctured and at room temperature for longer than 12 hours. The vial was punctured on 4/21/2022 @ 08:37 AM, which means the vial expired on 04/21/2022 @ 08:37 PM. The vial was left out overnight and was used for patients' vaccination on 04/22/2022 @ 10:22 AM. Patient has been called multiple times but has yet to be reached by the pharmacy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- NO known health conditions
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The Pharmacy administered a Moderna Vaccination after the vial was punctured and at room temperature for longer than 12 hours. The vial was punctured on 4/21/2022 @ 08:37 AM, which means the vial expired on 04/21/2022 @ 08:37 PM. The vial was left out overnight and was used for patients' vaccination on 04/22/2022 @ 10:31 AM. Patient has been called multiple times but has yet to be reached by the pharmacy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- No known health conditions
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Pharmacy administered Moderna Vaccination after the vial was punctured and at room temperature for longer than 12 hours. The vial was punctured on 4/21/2022 @ 08:37 AM, which means the vial expired on 04/21/2022 @ 08:37 PM. The vial was left out overnight and was used for patients' vaccination on 04/22/2022 @ 11:12 AM. Patient has been notified and has had no adverse events related to vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None reported
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- 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: ja
Expired product administered
No adverse event
Symptomtext
Pharmacy administered Moderna Vaccination after the vial was punctured and at room temperature for longer than 12 hours. The vial was punctured on 4/21/2022 @ 08:37 AM, which means the vial expired on 04/21/2022 @ 08:37 PM. The vial was left out overnight and was used for patients' vaccination on 04/22/2022 @ 11:44 AM. Patient has been notified and has had no adverse events related to vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- 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: ja
Expired product administered
Symptomtext
Pharmacy administered the Moderna vaccination 14 hours after the vial's expiration time. The vial was punctured on 4/21/2022 @ 8:37 AM, which means the vial was due to expire at 8:37 PM (12 hours after first puncture). The vial was left out overnight on 04/21/2022 and the expired vial was administered to patient at 11:59 AM on 04/22/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 16.04.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Herpes zoster
Symptomtext
Shingles on left front side of abdomen.Previously, I had received 3 doses of the Pfizer covid vaccine. The 4th vaccine was the first time I had received the Moderna vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- Confirm by Nurse Practitioner, on April 20 2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Rheumatoid arthritis
- Andere Medikamente
- Methotrexate; Prolia, injection; Simponi Aria; Zoloft;Montelukast, 10 mg, 1xDay Folic Acid; Vit C;Vit D3; Flonase; Losartan; Lovastatin; Levocetirizine; Esomeprozole; Fish oil; Hair&Nail supp; Azelastine; Trazodone.
- Allergien
- Options (itching).
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired Booster doses administered >12 hours post puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered >12 hours post puncture) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered >12 hours post puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered >12 hours post puncture) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. On 20APR2022 vial was initially stored in the refrigerator. On 21APR2022 at 8:45AM Date and time vial was first punctured. Concomitant medications were not reported. 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
- KY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired Booster doses administered >12 hours post puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered >12 hours post puncture) in a 68-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered >12 hours post puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered >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 medication was reported. No treatment medication was reported. Patient received expired booster dose (more than 12 hours after first puncture). Date the vial was initially stored in the refrigerator 20-Apr-2022. Vial did not undergo any temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired Booster doses administered greater than 12 hours post puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered greater than 12 hours post puncture) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Apr-2022 at 8:00 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered greater than 12 hours post puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Booster doses 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. Concomitant medications was not provided by the reporter. On 20 Apr 2022, the vial was initially stored in refrigerator. On 21 Apr 2022 at 8:45 AM, the vial was first punctured. On 22 Apr 2022 from 10:30 AM to 12:00 PM, vaccine was administered. The vial does not undergone any temperature excursions. Total amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F): 27 and half hours. The vial exposed to room temperature for >24 hours. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
the vial exposed to room temperature for more than 24 hours and then administered; Expired Booster doses administered >12 hours post puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered >12 hours post puncture) and PRODUCT STORAGE ERROR (the vial exposed to room temperature for more than 24 hours and then administered) in a 68-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered >12 hours post puncture). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (the vial exposed to room temperature for more than 24 hours and then administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered >12 hours post puncture) and PRODUCT STORAGE ERROR (the vial exposed to room temperature for more than 24 hours and then administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. The vial was initially stored in the refrigerator on 20-APR-2022. The vial was first punctured on 21-APR-2022 at 8:45AM. The vaccine on 22-APR-2022 from 10:30AM to 12:00PM. The vial did not undergo any temperature excursions. Total amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) was 27 and half hours. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered greater than 12 (US) hours post puncture) in a 64-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 056M21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered greater than 12 (US) hours post puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Booster doses administered greater than 12 (US) 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 provided. Moderna COVID-19 Vaccine was administrated on 22 APR 2022 from 10:30 AM to 12:00 PM. It was reported that vial was initially stored in the refrigerator on 20 APR 2022 and was first punctured on 21 APR 2022 at 8: 45 AM. Vial was stored at room Temperature post puncture and did not undergo temperature excursions. Vial was exposed to room temperature for more than 24 hours within the range 8 degree to 25 degree C which was equal to 46 degree to 77 degree F for 27 and half hours. No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 25.04.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient received a booster dose just 1 month after completing primary series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 25.04.2022
- Impfdatum
- 18.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspepsia
Symptomtext
I had very severe heartburn. I rarely get heartburn. I am taking OTC medication for it. I also noticed on my 2nd dose which was Pfizer that I had got heartburn as well. I went to my doctor and suggested taking an OTC heartburn medication. It is still continuing to this day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspepsia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Pre-diabetic
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Pfizer 2nd dose - heartburn
- Staat
- IL
- Alter
- 69,0
- Geschlecht
- M
- 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: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Atrial fibrillation
Blood glucose increased
Blood test abnormal
Electrocardiogram normal
Glucose urine present
Myocardial necrosis marker normal
Urine analysis abnormal
Urine ketone body present
Symptomtext
Prolonged Atrial Fibrillation (4 and 1/2 Hrs) Chemically converted by Calcium channel blocker to sinus rhythm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- EKG, Full blood workup with normal results excepting elevated blood glucose, uranalysis with elevated glucose and ketones. Normal heart enzymes during episode and after conversion. All 4/16/2022 at the ER
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 Diabetes, Hypertension, Gout
- Andere Medikamente
- Allopurinol 200mg QD, Lipitor 10mg QD, Janumet XR 100-1000 BID, Jardiance 10mg QD, Multivitamin, Vitamin B-12 500mg QD, Vitamin D 5000IU QD, Aspirin 80mg QD
- Allergien
- Naproxen withdrawl allergy
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 22.04.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysstasia
Lethargy
Mental status changes
Swollen tongue
Throat irritation
Symptomtext
1110 Moderna booster administered. 1135 patient c/o scratchy throat. Patient states that throat felt scratchy, and tongue started to swell. Patient was instructed to sit in chair and had a decreased mental status about one minute later. Patient was lethargic so staff assisted him to the floor and elevated his legs. Patient stated that he ate chips prior to symptoms starting. 911 was called at 1140. Tongue swelling worsened. EPI administered at 1142 into right thigh through jeans. Patient denies history of allergies, no known drug, food, or environmental allergies. History of anxiety and depression. Patients takes medications for anxiety/depression. No other meds taken. Patient denies SOB. No stridor, wheezing, or hives noted. EMS arrived at 1148. Patient was able to stand with EMS assistance. Patient was transported to the ED by EMS. Tongue still slightly swollen when patient left with EMS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysstasia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Anxiety/Depression
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 14.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Aggression
Disorientation
Symptomtext
disorientation, aggression
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aggression
- Hospital-Tage
- -
- Labordaten
- Hospital concurrent
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- psoriatic arthritis, schizoaffective bi polar 2 adhd
- Andere Medikamente
- Lithium, propanolol, adderall, ziprasidone
- Allergien
- none
- Vorherige Impfungen
- -