- Staat
- -
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 10.09.2023
- Impfdatum
- 06.12.2021
- Beginn
- 07.08.2023
- Tage bis Beginn
- 609,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Agitation
Ammonia normal
Atelectasis
Blood gases normal
Blood glucose normal
Blood lactic acid
Blood thyroid stimulating hormone normal
Brain natriuretic peptide increased
COVID-19
Chest X-ray abnormal
Cough
Drug level
Dyspnoea
Encephalopathy
Glycosylated haemoglobin normal
Hyporesponsive to stimuli
Hypoxia
Symptomtext
Patient is a 50 y.o. male patient of Physician with history of DM2, Hyperlipidemia, Hypertension, Hypothyroidism and Schizoaffective disorder presented to Emergency Department with cough, congestion and generalized flu like symptoms. Patient transferred to hospital due to hypoxia and lactic acidosis. Sepsis due to Covid-19 Virus Infection Met sepsis criteria with T 101.1, HR 128, lactate 3.3 Date of onset of symptoms: 8/5/23 Symptoms present on admission: tachycardia, fevers, congestion, cough, shortness of breath, myalgias Date of covid positive test: 08/07/23 Vaccination status: vaccinated Imaging: CXR- low lung volumes with pulmonary vascular congestion and bibasilar atel Patient is a 50 y.o. male patient of Physician with history of DM2, Hyperlipidemia, Hypertension, Hypothyroidism and Schizoaffective disorder presented to Emergency Department with cough, congestion and generalized flu like symptoms. Patient transferred to hospital due to hypoxia and lactic acidosis. Sepsis due to Covid-19 Virus Infection Met sepsis criteria with T 101.1, HR 128, lactate 3.3 Date of onset of symptoms: 8/5/23 Symptoms present on admission: tachycardia, fevers, congestion, cough, shortness of breath, myalgias Date of covid positive test: 08/07/23 Vaccination status: vaccinated Imaging: CXR- low lung volumes with pulmonary vascular congestion and bibasilar atelectasis Oxygen requirements on admission: 2L Current oxygen requirements: RA Medical therapy: dexamethasone from 8/7, remdesivir from 8/8. Stopped after 8/9 due to resolved O2 requirement Consultants following: None Anticipated special isolation end date: 8/16 based on symptoms Acute metabolic encephalopathy, improved According to patients caregiver, patient is verbal and active at baseline Only responsive to sternal rub on arrival Vitals were stable with unremarkable ABG TSH WNL, ammonia WNL CTH unremarkable Awake alert and interactive 8/8; resumed haldol at reduced dose 8/8 and full dose 8/9; transient sedation after full dose haldol, adjusted per below Acute respiratory failure with hypoxia, resolved Due to COVID Not on oxygen at home but requiring 2L NC on admission CXR as above Flu and rapid strep screens negative BNP 294, no sign of peripheral volume overload COVID per above Weaned to RA 8/9, then needed 1L again after sedation with home haldol, back to RA since Lactic acidosis Lactate 3.3 down to 2.0 after 2.6L bolus in total DM2, non insulin dependent Blood glucose 169 on labs in the ER A1c was 4.3 10/2022, repeat pending Holding home Metformin Glucose rising with steroid use and resuming diet Monitor accu checks and start SSI Lantus QAM while on steroid Resume home regimen on discharge Hypothyroidism Continue home Synthroid Schizoaffective personality disorder MRDD Patient has 24 hour supervision with home health aids Unsure of legal guardianship Held home Thorazine and Haldol due to lethargy VPA level 65 Resumed haldol at 5mg BID 8/8, increased back to home dose of 20mg BID 8/9 as he was becoming more agitated. Quite lethargic after first dose of 20mg; decreased to 10mg BID to resume 8/10 and continue at that dose on discharge Advised to resume thorazine in one week Further per the discretion of his outpatient psychiatrist, follows up once monthly
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 26.05.2023
- Impfdatum
- 13.12.2021
- Beginn
- 19.09.2022
- Tage bis Beginn
- 280,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE NON ST ELEVATION MI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 13.12.2021
- Beginn
- 03.03.2023
- Tage bis Beginn
- 445,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Anticoagulant therapy
Asthenia
Atrial fibrillation
Blood creatinine normal
Blood glucose increased
Bradycardia
Bronchial wall thickening
C-reactive protein normal
Cough
Diarrhoea
Glomerular filtration rate decreased
Glucose tolerance impaired
Glycosylated haemoglobin increased
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Symptomtext
The patient is a 77 y.o. female patient of a MD with history of chronic back pain, GERD, HLD, paroxysmal afib on coumadin, HTN, and peripheral neuropathy presented to the Hospital with cough and weakness. Acute hypoxic respiratory failure d/t COVID-19 pneumonia P/w 1 week history of headache, dry cough, and weakness. Pt reporting diarrhea x 2 days, now resolved (took imodium at home). Mild wheezing on exam, improved Pt fully vaccinated plus one booster Afebrile. Pt initially hypoxic at 87%, now satting >94% on room air ambulating CRP nl CXR: Perihilar coarsened interstitial markings and bronchial wall thickening Decadron 6mg daily for 10 days Encourage IS use PT/OT/SW Acute kidney injury vs CKD Initial Cr 1.1 remain at same level x 3, probably pt's baseline. GFR 50. Likely prerenal given poor PO intake secondary to diarrhea and COVID UA and urine culture ordered P Atrial fibrillation HTN/ HLD HDS on admission, slightly bradycardic ~ 59 Continue coumadin, flecainide, and diltiazem Pharmacy consulted for warfarin dosing, therapeutic now 3.5 Pre- DM Hba1c 5.9 BS elevated in context of steroids therapy. Diet education before discharge Chronic back pain PRN tylenol
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 31.03.2023
- Impfdatum
- 13.12.2021
- Beginn
- 01.03.2023
- Tage bis Beginn
- 443,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Adrenal insufficiency
Ammonia normal
Anticoagulant therapy
Asthenia
Basal ganglia infarction
Blood cortisol
Blood creatinine increased
Blood folate increased
Blood glucose normal
Blood lactic acid normal
C-reactive protein increased
COVID-19
Cardiac failure
Cardiac failure chronic
Cerebral small vessel ischaemic disease
Chest X-ray abnormal
Symptomtext
Patient is a 80 y.o. male patient of MD with history of CHF, CKD, Depression, DM Type 2, CAD, Hypertension, Peripheral Neuropathy, nephrolithiasis, TIA, Chronic diarrhea, Hyperlipidemia presented to Hospital with shortness of breath weakness, Fever and Cough . Pt medically ready for discharge, but lives alone with wife who is also admitted. Possible discharge of both on 3/5 Acute hypoxic respiratory failure due to Sepsis due to COVID-19 Infection hypoglycemia, tachypnea, fever up to 102.7 on adm. Now resolved Symptoms since 2/27, weakness, Fever and Cough. Tested positive 3/1/2023. Vaccinated x 2 plus 1 booster. Chest x-ray prominence of the bronchovascular markings Lactic acid unremarkable, CRP; 48.6. Procal nl Initially required 4 L of supplemental oxygen, now weaned to baseline room air. Started on dexamethasone, changed to Prednisone due ot adrenal insufficiency Received a Rocephin azithromycin, no clear signs of bacterial infection and procal nl so discontinued Cont IS/PEP Dizziness Intermittent for weeks now improved Orthostatic VS normal Meclizine ordered. PT/ OT consulted. Ambulating with walker AKI On CKD Stage 3 Hypokalemia Admission CR 2.58, baseline 1.7-2.1. Cr 1.9 at discharge On Lasix, dose recently decreased by Nephrologist as outpt. Avoid Nephrotoxic agent Nephrology consulted, Lasix ordered IV x 2. Will cont PO lasix 40 mg daily and resume BID at discharge PO potasium Adrenal insufficiency In context of acute infection. Hypoglycemia and hypotension on adm. Cortisol 3.8 random Pt with hx of DM, hypoglycemic on adm, has remained off medication and with BS <180 despite steroids treatment. Started on prednisone 40 mg, will wean to 20 mg at discharge x 7 days, then 10 x 7 days then cont 5 mg until seen by PCP Thrombocytopenia Platelets 138k, probably due ot COVID and sepsis. No signs of bleeding Monitor. DM with neuropathy Pt presented with hypoglycemia, required multiple doses of dextro, will stop MIVF w/ D5 now. Etiology multifactorial, poor PO intake and noted adrenal insufficiency Hba1c 6 Pt with hx of DM, hypoglycemic on adm, has remained off medication and with BS <180 despite steroids treatment. On Amaryl and Tresiba at baseline, will hold at this time, will not cont at discharge as pt controlled on steroids. Cont SSI Acute metabolic encephalopathy- resolved History of TIAs, cerebral infarcts stroke Does have occasional intermittent baseline confusion. Now complicated by hypoxemia COVID, acute on chronic renal failure and hypoglycemia CT head without contrast mild chronic small vessel white matter changes. Remote bilateral basal ganglia lacunar infarcts. Remote right thalamic lacunar infarct. Ammonium nl. B12/ folic elevated Chronic HFpEF Hx of PAF on coumadin Bradycardia, sinus Shortness of breath cough likely triggered by COVID infection. No other signs of volume overload. Does not have acute exacerbation Echocardiogram 2/8/2023 with EF 65.0 %. ProBNP 4656. Cont coumadin, pharmacy to dose, INR therapeutic. Strict input and outputs, daily weights Fluid restriction. Contaminated Blood culture BC 1/2 + Coag neg Staph. Monitor
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 19.03.2023
- Impfdatum
- 08.12.2021
- Beginn
- 28.01.2023
- Tage bis Beginn
- 416,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Agitation
Alanine aminotransferase increased
Anticoagulant therapy
Aspartate aminotransferase increased
Atrial fibrillation
Bladder catheterisation
Blood creatinine increased
Blood culture negative
Blood lactic acid
Brain natriuretic peptide increased
COVID-19
Cardiac failure
Cardioversion
Catheter site haemorrhage
Chest X-ray abnormal
Communication disorder
Symptomtext
Patient is a 72 y.o. male of MD with history of rheumatoid arthritis, mitral valve regurgitation, hypertension, hyperlipidemia, CAD s/p CABG, atrial fibrillation, HFrEF with improved EF and recent COVID infection presented to the hospital with altered mental status and shortness of breath. He developed increasing oxygen requirements requiring high flow nasal cannula and eventually intubation on 2/1. Respiratory failure due to multifocal pneumonia, possible volume overload on background of lung disease from recent COVID infection. Completed 7-day course of Zosyn on 2/4. Briefly extubated on 2/5 however required reintubation. On 2/11 developed worsening hypotension, tachycardia and increase in inflammatory markers being started on broad-spectrum antibiotic for likely HAP. S/p trach/PEG 2/13. Acute respiratory failure with hypoxia Found to be hypoxic requiring 2 L nasal cannula at outside ED Thought multifactorial to a combination of edema, pneumonitis and recent COVID infection Increased oxygen requirements after admission requiring HHF and subsequently intubated on 2/1/23 Extubated and reintubated on 2/5 after developing increased work of breathing CT chest abdomen pelvis with contrast 2/11: Moderate marked bilateral pulmonary infiltrates Completed course of decadron Failed vent weaning due to mental status S/p Trach/PEG 2/13 Vent needs improving, tolerating PSV trials well, anticipate that he can be liberated from the vent over the next 1-2 weeks while at Select Toxic Metabolic Encephalopathy Reportedly had some AMS prior to presentation, but A&Ox 3 on presentation Course complicated by respiratory failure requiring intubation/sedation Has had agitation with sedation wean while intubated Now off of sedation, he is alert, trying to communicate via writing messages but nonsensical, suspect he has ongoing delirium Continue scheduled seroquel and oxycodone Sepsis Hypotension HAP BP as low as 81/56 at outlying ED, lactic acid 4.1 Hypotension thought secondary to sepsis although possibly due to medication Chest x-ray: Diffuse bilateral lung infiltrates, stable when compared to recent on 1/3/2023 Echo 11/2022: EF 58%, mild LVH, improved LV function when compared to prior Repeat Echo with EF 35%, severely enlarged LA in the setting of afib with RVR Completed 7d course of zosyn on 2/4 Hypotension and rising WBCs on 2/11; CT chest with persistent bilateral pulm infiltrates Blood cx from 2/11 with NGTD Sputum cx with growth of Serratia marcescens; pansensitive MRSA probe neg, stop Vanc Cefepime narrowed to ceftriaxone, continue through 2/18 Urinary Retention Failed TOV on 2/13 Attempted straight caths but had difficulty with some bleeding Foley replaced 2/14 Will need to re-attempt once able to mobilize Acute on Chronic HFpEF Echo 11/2022: EF 58%, mild LVH, improved LV function when compared to prior BNP 8860, increased from 2752 two weeks prior Chest x-ray: Diffuse bilateral lung infiltrates, stable when compared to recent on 1/3/2023 Repeat Echo with EF 35% in the setting of afib with RVR Cardio consulted, discussed adding beta-blocker if pressure tolerates Good response to lasix over 3L out 2/2 - 2/3 No need for further diuresis at this time Recent COVID infection Symptom onset 1/7/2023, tested positive on 1/12/2023 Vaccination status: Vaccinated Was outside of window for Paxlovid but treated briefly with Decadron Completed 20d isolation on 2/1 Completed a long course of IV decadron AKI Serum creatinine 1.42 on admission Baseline appears to be 0.7?0.9 Cr stable at baseline Transaminitis AST 156, ALT 163 on admission, Transaminases elevated in the setting of hypotension and shock liver LFTs now trending down, nearly normalized CAD Atrial fibrillation Hypertension s/p CABG S/p cardioversion in 6/2022 Was on amiodarone and carvedilol as an outpatient; amio stopped due to elevated LFTs, was not effective at rhythm control previously Transition off heparin gtt to eliquis HR intermittently elevated Increase metoprolol to 50mg BID (on coreg at home but due to soft Bps doubt he will tolerate) Holding home lisinopril and lasix due to low normal BPs Rheumatoid arthritis Home plaquenil and methotrexate held on admission Resumed home prednisone 10mg BID and plaquenil Continue hold methotrexate
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 20,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 16.12.2021
- Beginn
- 05.01.2023
- Tage bis Beginn
- 385,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Acute myocardial infarction
Anticoagulant therapy
Blood bicarbonate decreased
Blood culture
COVID-19
Cardiac stress test abnormal
Confusional state
Echocardiogram normal
Ejection fraction
Escherichia bacteraemia
Hyporesponsive to stimuli
Intensive care
Leukocytosis
Mental status changes
Metabolic acidosis
Myocardial ischaemia
Nephrectomy
Symptomtext
"Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: ""86 yo female, with PMH significant for OSA on CPAP, asthma, bipolar depression, HTN, who presented from nursing home to the ED today due to decreased responsiveness and fevers Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) treated in intensive care unit setting initially for urosepsis, E coli bacteremia, NSTEMI 1/7 Transferred to general floor 1/8 Underwent nuclear cardiac stress tests-ischemia of the lateral wall, mild 1/ 10 Seen by Cardiology, started on beta-blocker 1/11 Planned discharge to SNF on hold due to rising leukocytosis, leukocytosis improved down to 14 K the time of discharge Altered mental status, Improving gradually, most likely due to urosepsis Has significantly improved History of bipolar depression Continue with Tegretol and Cymbalta History of asthma Oxygen p.r.n., albuterol inhalers History of OSA On CPAP NSTEMI Appreciate cardiology consultation, echo showed normal LVEF of 55-60%, mild AS Giving IV heparin for 48 hours On aspirin, beta-blocker nuclear stress test,1/ 9 , as Cardiology, mild reversible defect, in the lateral wall consistent with mild ischemia, Cardiology recommended to treated medically , with beta-blocker, patient already on aspirin Urosepsis with E coli bacteremia Was on Levophed in intensive care unit setting Weaned of Levophed On ceftriaxone from 01/05, anticipate total course of antibiotic of 10 days at least Leukocytosis improving, has normalized 1/11 significant rise in leukocytosis to 19 K, planned discharge to SNF on hold No fever, patient does not look toxic, currently on IV Rocephin Has anion gap acidosis with bicarb of 15, check lactic acid, do sepsis workup, including blood culture History of hypertension PTA antihypertensives on hold Acute kidney injury, solitary right kidney, status post left nephrectomy Due to urosepsis, improving renal function Possible cognition impairment, move Moca scoring by speech, checked vitamin B12. Normal Condition at the time of discharge- Vss Constitutional: No distress, elderly, 2 liters/minute HENT: Normocephalic, Atraumatic, Pupils Reactive, Normal oropharynx, Nose normal. Cardiovascular: Normal heart rate, Normal rhythm, No murmurs, No rubs, No gallops. Respiratory: Normal breath sounds, No respiratory distress, No wheezing, No chest tenderness. GI: Bowel sounds normal, Soft, No tenderness, No masses, No pulsatile masses. Extremities: Intact distal pulses, No edema, No tenderness, No cyanosis, No clubbing. Neurologic: Alert & oriented x 2 , confused at times, No focal deficits noted. Skin: Warm and dry Issues Requiring Follow Up: (Who, what, when, and how communicated?) Losartan & Aldactone are on hold till f/u BMP & CBC , renal function improvement To follow-up on tolerance and efficacy of Augmentin"""
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 7,0
- Labordaten
- Covid PCR detected on 01/05/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular Essential hypertension, benign Acute on chronic diastolic congestive heart failure CAD (coronary artery disease) Mixed hyperlipidemia Chronic heart failure with preserved ejection fraction (HFpEF) Integumentary Dermatitis Psychological Bipolar depression Respiratory Asthma OSA (obstructive sleep apnea) Urinary Acute cystitis without hematuria Other Hiatal hernia Fibromyalgia Primary osteoarthritis of left hip Encounter for long-term (current) use of medications Sepsis secondary to UTI Hypokalemia Hypomagnesemia Elevated troponin Abnormal cardiovascular function study Bacteremia due to Escherichia coli
- Andere Medikamente
- acetaminophen (TYLENOL) 650 mg CR tablet Take 1 tablet by mouth every 8 (eight) hours as needed for Pain. albuterol (PROVENTIL HFA; VENTOLIN HFA; PROAIR) 90 mcg/actuation inhaler Inhale 2 puffs into the lungs every 4 (four) hours as needed
- Allergien
- Latuda [Lurasidone]Unknown Crestor [Rosuvastatin]Myalgia
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 12.01.2023
- Impfdatum
- 03.12.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 34,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Death
Dyspnoea
Endotracheal intubation
Laboratory test abnormal
Pulmonary embolism
Symptomtext
shortness of breath called 911 around noon admitted to ER around 1pm tests in ER determined Bilateral Pulmonary Embolism Pushed meds to help dissolve clots Intubated to help breath as meds were pushed Passed away before being transferred from ER to ICU around 11:30pm same day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 17.12.2022
- Impfdatum
- 06.03.2021
- Beginn
- 01.05.2022
- Tage bis Beginn
- 421,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cerebral disorder
Cerebrovascular accident
Dysarthria
Facial paralysis
Magnetic resonance imaging head abnormal
Symptomtext
Minor stroke. Drooping face, slurred speech. Symptoms subsided after 5 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- MRI showed a small spot on brain.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lisinopril Sertraline Multivitamins
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 22.09.2022
- Impfdatum
- 12.01.2022
- Beginn
- 08.08.2022
- Tage bis Beginn
- 208,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Acute respiratory failure
Adrenal mass
Anaemia
Angiogram pulmonary abnormal
Anticoagulant therapy
Anxiety
Atrial fibrillation
Blood creatinine increased
COVID-19 pneumonia
Cardiogenic shock
Cardiomegaly
Chronic kidney disease
Chronic obstructive pulmonary disease
Condition aggravated
Constipation
Coronary artery disease
Diastolic dysfunction
Symptomtext
A 58 y.o. female patient of CNP with history of HTN, HLD, COPD, chronic hypoxemic respiratory failure, chronic HFPEF who presented with respiratory distress. Symptoms worsened overnight with altered mental status, required intubation. Shock. Cardiogenic vs Septic; Aspiration Pneumonia; Pneumonia due to COVID-19; CT pulmonary arteries on 8/8/2022: cardiomegaly with sm-mod pericardial effusion; left lower lobe multi segmental mucoid; impaction; negative for PE; Status post intubation on 8/9; No longer requiring pressors; ID following; Repeat echo pending; Critical care signed off; Discontinue cefepime; Finished dexamethasone and remdesivir; Covid-19 Virus Infection; Date of onset of symptoms: 8/8/2022; Symptoms present on admission: shortness of breath, altered mental status, fever; Date of covid positive test: 8/8/2022; Vaccination status: vaccinated; Imaging: CTA pulmonary arteries; Oxygen requirements on admission: 8L; Current oxygen requirements: BiPAP; Medical therapy: steroids; pending hepatic panel - Remdesivir; Consultants following: Pulm CC, ID; Anticipated special isolation end; date: 8/17/2022; Completed treatment; Acute on chronic hypoxemic respiratory failure; COPD; Wears 3.5 liters chronically; AVAPs; Intubated initially; Currently on NC; Continue with nebs, antibiotics; extubated on 8/10; Critical care signed off; Acute Kidney Injury on CKD stage III, with ATN; CKD stage III with baseline creatinine 0.79-1. Likely due to shock; Creatinine peaked at 1.96; Renal neg for stones or hydronephrosis, 5.7 cm adrenal gland mass noted; Continue close monitoring, monitor urine output; Resolved; Acute metabolic encephalopathy -resolved; DM Type II; HgA1c on 6/11/2022: 5.9; Accucheck every 4 hours with ISS coverage; HFpEF; Pericardial Effusion TTE on 7/12/2022: LVEF 66%, grade II diastolic dysfunction, large pericardial effusion; echo densities attached to visceral pericardium. Repeat TTE. Hold diuretics, diurese as BP allows. Paroxysmal Atrial Fibrillation; Eliquis discontinued in mid July due to pericardial effusion; Hold Metoprolol while hypotensive.; Currently rate controlled. Maintain K>4, Mag >2. Adrenal gland mass; On right per renal ultrasound; Also noted on CT pulmonary angiogram, 5.7 cm; Will handle acute issues at this time and Patient follow-up as outpatient; HTN; Hold antihypertensive medications while on vasoactive medications. Restarted metoprolol. Consider adding lisinopril/hydrochlorothiazide and amlodipine as able. Dyslipidemia. Continue Atorvastatin, Chronic Anemia. Baseline hemoglobin 8-9. Currently 10.8. Continue Ferrous sulfate, Coronary Artery Disease; Continue aspirin, statin; Hold anti hypertensive medications. Severe malnutrition, POA; Consult dietitian; Constipation; Chronic history; Reports no BM since admission; On colace and miralax; Anxiety; Tremors; Patient is on Xanax and paroxetine at home as well as trazodone; Trazodone restarted on 8/13; Per patient request, will restart Xanax on 8/14; Continue paroxetine Patient stable for discharge today home with home health. However patient's home getting treatment for bugs, therefore discussed with social work case management and patient will be remaining in the hospital until this is completed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 12,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 15.12.2021
- Beginn
- 15.07.2022
- Tage bis Beginn
- 212,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angiogram cerebral abnormal
Arteriogram carotid abnormal
Atherectomy
Cardiac arrest
Cerebral artery occlusion
Cerebral mass effect
Computerised tomogram head abnormal
Craniectomy
Death
Electroencephalogram abnormal
Haemofiltration
Haemorrhage intracranial
Hydrocephalus
Intensive care
Intra-cerebral aneurysm operation
Intracranial aneurysm
Muscle twitching
Resuscitation
Symptomtext
Admission Date: 7/15/2022 PRESENTING PROBLEM: Subarachnoid hemorrhage Intracranial hemorrhage HOSPITAL COURSE: Patient is a 75 year old with a PMHx of ESRD on HD, Type 2 diabetes, CHF, HTN, HLD, GERD, SBO, diverticulitis, abdominal abscess s/p ex lap with colostomy and chronic pancreatitis that presented 7/15/2022 with an acute spontaneous subarachnoid hemorrhage. A head CT was completed that revealed a large left frontotemporal ICH, diffuse SAH, 8 mm MLS, and hydrocephalus. CTA head/neck demonstrated concern for Left MCA aneurysm. Patient was taken emergently to the OR for left MCA aneurysm clipping and left hemicraniectomy with ICH evacuation. Post operatively a DCA was completed that showed complete occlusion of left MCA aneurysm w/small neck remnant, head CT with stable postoperative findings, slight worsening of hydrocephalus, improvement in MLS to 6 mm. Patient also had an EVD placed for obstructive hydrocephalus. Patient was admitted to the Neuro ICH for subarachnoid hemorrhage management. She was started on CRRT given ESRD. Postoperatively, patient was weaned off sedation but remained a GCS <8. Right facial and upper extremity twitching was noted and EEG placed which demonstrated focal status epilepticus with left frontal origin. She was started on keppra and valproic acid with minimal improvement. Therefore, pt started on versed infusion. On 7/18, pt continued to be in focal status, therefore she was administered 4mg ativan, versed increased to 0.5mg/kg/hr and loaded with fosphenytoin with subsequent cardiac arrest. Resuscitation efforts attempted, family present at bedside and DPOA requested efforts cease. Please see critical event notes for further detail. Time of death 0928 on 7/19/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 diabetes mellitus, without long-term current use of insulin History of left breast cancer Gastroesophageal reflux disease without esophagitis ESRD on peritoneal dialysis Essential hypertension Hyperlipidemia Normocytic anemia Nausea & vomiting Abdominal pain SBO (small bowel obstruction) Gastrointestinal dysmotility Other chest pain CHF (congestive heart failure) Type 2 diabetes mellitus treated with insulin Acute diverticulitis Intra-abdominal abscess s/p ex lap, Hartmann's, end colostomy on 7/20/2020 with Dr. Septic shock Colostomy in place Other chronic pancreatitis ESRD on hemodialysis Type 2 diabetes mellitus with both eyes affected by proliferative retinopathy without macular edema, with long-term current use of insulin Retinal detachment, tractional, left eye Presbyopia of both eyes Primary insomnia Chest pain Numbness and tingling of left upper extremity SAH (subarachnoid hemorrhage) Acute respiratory failure with hypoxia Ventilator dependence
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 10 MG tablet atorvastatin (LIPITOR) 80 MG tablet B Complex-C-Folic Acid (RENA-VITE RX) 1 MG TABS calcium acetate, Phos Binder, (PHOSLO) 667 MG CAPS carvedilol (COREG) 6.25 MG t
- Allergien
- Nitroglycerin-Headache
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 06.07.2022
- Impfdatum
- 13.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Death
Epistaxis
Failure to thrive
Fatigue
Gastrointestinal haemorrhage
Gingival bleeding
Immune thrombocytopenia
Laboratory test
Melaena
Multimorbidity
Normocytic anaemia
Oesophagogastroduodenoscopy
Platelet transfusion
Thrombocytopenia
Transfusion
Ultrasound liver
Symptomtext
12/28/2021 to emergency room for nosebleeds, gum bleed, melena, GI bleed and fatigue. Severe thrombocytopenia and acute on chronic normocytic anemia. Required transfusion of blood and platelets. Treated for ITP. Stabilized and discharged on 01/04/2022. Multiple comorbid conditions. Failure to thrive. Patient died 01/14/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 8,0
- Labordaten
- EDG; liver ultrasound; multiple bloodwork labs
- Aktuelle Erkrankungen
- Moderate protein-calorie malnutrition; surgical wound infection; Osteomyelities of right ankel; Cellulitis
- Vorgeschichte
- Congestive heart failure; controlled type 2 diabetes; Bradycaria; liver chirrhosis
- Andere Medikamente
- Vancomycin; Lovenox; Linezolid; Marinol; aspirin; Acetaminophen; Cephalexin; Tamsulosin; Vitamin D3; Amodipine; Atorvastatin; Vitamin D3; iron; Januvia
- Allergien
- Sulfa; Cipro; Levaquin; Starlix; Amoxicillin-Pot Claval
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 06.12.2021
- Beginn
- 15.01.2022
- Tage bis Beginn
- 40,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Syncope
Symptomtext
Collapsed and died.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Medical Examiner/Coroner
- Aktuelle Erkrankungen
- High Blood Pressure
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- High Blood Pressure Pills
- Allergien
- N/A
- Vorherige Impfungen
- Bedridden one day following vaccine
- Staat
- ME
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 01.12.2021
- Beginn
- 03.03.2022
- Tage bis Beginn
- 92,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Angiogram cerebral abnormal
Apallic syndrome
Brain oedema
Cardiac telemetry normal
Cerebral artery occlusion
Cerebral infarction
Cerebral ischaemia
Cerebrovascular accident
Computerised tomogram abdomen normal
Computerised tomogram head abnormal
Computerised tomogram thorax normal
Decompressive craniectomy
Echocardiogram
Ejection fraction
Gastrostomy
Glycosylated haemoglobin increased
Hemiparesis
Low density lipoprotein normal
Symptomtext
Presented to the hospital with right sided weakness and small L MCA stroke 3/3/22, which evolved to a large hemispheric left MCA stroke 3/8/22 with malignant cerebral edema requiring decompressive hemicraniectomy 3/9/22. Examination remained poor with essentially vegetative state. She underwent tracheostomy and PEG tube placement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 18,0
- Labordaten
- CTA with perfusion 3/3: small area of ischemia L MCA, distal M3/4 occlusion on the left MRI brain 3/3: small area of distal infarct L MCA CT brain 3/7, 8: evolving large area of infarct L MCA distribution, significantly progressed from prior CT brain 3/9 post L hemicraniectomy TTE 3/3 normal EF 55%, no wall motion abnormality, grade 1 PFO US bilateral LE and UE 3/8 negative for DVT CT chest/abd/pelvis 3/14 negative for malignancy CTV pelvic floor 3/14 negative for pelvic DVT LDL 122 3/4 A1C 11.2 3/8 telemetry with no evidence of atrial fibrillation during admission
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertensnion Diabetes Hyperlipidemia
- Andere Medikamente
- amlodipine 10 atorvastatin 80 insulin detemir dulaglutide hctz 25mg lisinopril 40mg metformin 1000mg BID spironolactone 75mg
- Allergien
- milk
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 24.02.2022
- Impfdatum
- 27.12.2021
- Beginn
- 04.02.2022
- Tage bis Beginn
- 39,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute kidney injury
Asthenia
Azotaemia
COVID-19
Cystitis
Death
Delirium
Fatigue
Gastrointestinal stoma complication
Hyperkalaemia
Metabolic acidosis
Metabolic encephalopathy
SARS-CoV-2 test positive
Septic shock
Symptomtext
Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 1/14/2021, 1/31/2021 and 12/27/2021. Presented to ED 2/4/2022 c/o generalized weakness, fatigue, and high output from his ostomy. Admitted for septic shock, acute cycstitis, Covid19 requiring O2. Course c/b AKI w/azotemia, hperkalemia, metabolic acidosis and acute metabolic encephalopathy delirium. Tx'd w/decadron and Tylenol. Transitioned to comfort care instituted and expired 2/17/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 13,0
- Labordaten
- COVID-19 Positive on 2/4/2022 using the SARS assay platform
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Acne, BPH, Claudication, Colostomy, COPD, CKD, DM2, Hypertension, GERD, Hypercholesterolemia, Hyperlipidemia, Hypothyroidism, Macular degeneration, Malnutrition, Mild cognitive impairment, Multinodular goiter s/p thyroidectomy, PVD, Peritoneal Carcinomatosis, Recurrent UTI, Renal cyst, Vitamin D Deficiency.
- Andere Medikamente
- Acetaminophen, Albuterol, Amlodipine, Aspirin, Cetirizine, Cyanocobalamin, Diclofenac, Doxycycline, Duloxetine, Fenofibrate, Finasteride, Flonase, Folic Acid, Gabapentin, Levothyroxine, Lisinopril, Loperamide, Multivitamin, Omeprazole, Sim
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Acute respiratory failure
Alanine aminotransferase normal
Anion gap
Aspartate aminotransferase normal
Asthenia
Atelectasis
Basophil count decreased
Basophil percentage decreased
Blood albumin decreased
Blood alkaline phosphatase normal
Blood bicarbonate decreased
Blood bilirubin normal
Blood calcium decreased
Blood chloride increased
Blood creatinine increased
Blood glucose normal
Blood potassium normal
Symptomtext
Hospitalized (12.19.21 - 12.22.21); COVID-19 positive (12.10.21); Fully vaccinated PLUS Booster - moderna d/c summary: Discharge Summary MD (Physician) ? ? General Medicine Hospitalist D/C Summary BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider at Discharge: DO Admission Date: 12/19/2021 Discharge Date: 12/22/2021 Active Hospital Problems Diagnosis Date Noted POA ? Acute hypoxemic respiratory failure due to COVID-19 12/19/2021 Yes ? CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min 12/19/2021 Yes ? CLL (chronic lymphocytic leukemia) 12/19/2021 Yes ? Pneumonia due to COVID-19 virus 12/19/2021 Yes ? Junctional bradycardia 12/19/2021 Yes Resolved Hospital Problems Diagnosis Date Noted Date Resolved POA ? Acute on chronic diastolic congestive heart failure 12/19/2021 12/22/2021 Yes Pre-Existing Active Problems Diagnosis Date Noted POA ? Anemia 11/18/2020 Unknown ? Complete heart block 02/01/2020 Unknown ? Microscopic colitis 03/03/2010 Unknown DISCHARGE DISPOSITION: The patient was discharged to SNF No future appointments. Appointments Needing to be Scheduled Contact information for follow-up DO Specialty: Family Medicine Relationship: PCP - General Next Steps: Follow up Instructions: Please call to schedule a post-hospitalization follow-up appointment with your Primary Care provider in 7-10 days. At your appointment, talk to your provider about how you are feeling since being in the hospital. Instructions for after discharge Adult Diet Complete by: As directed Daily Weights Complete by: As directed Early and Progressive Mobility Complete by: As directed Occupational Therapy Evaluate and Treat at Receiving Facility Complete by: As directed Physical Therapy Evaluate and Treat at Receiving Facility Complete by: As directed DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute hypoxemic respiratory failure due to COVID-19 [U07.1, J96.01] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: The patient is a 94-year-old female with a history of CLL on venetoclax, CKD stage 4, chronic diastolic heart failure, stasis dermatitis of her lower extremities as well as junctional bradycardia, who presented with increasing shortness of breath, cough and hypoxia on 12/19. Patient is fully vaccinated with Moderna vaccination including recent booster. The patient had the onset COVID symptoms on 12/16 with a positive test on 12/19. Chest x-ray performed in the emergency department showed prominent interstitial opacities with a component of interstitial pulmonary edema. COVID testing was negative and the patient was admitted and started on dexamethasone and remdesivir. ProBNP was elevated on admission at 8461, and the patient received 1 dose of IV Lasix. Patient's creatinine subsequently increased to 1.81, and further doses of Lasix were held. Remdesivir was discontinued due to worsening renal function. With supportive care and further treatment with dexamethasone the patient had improvement in her respiratory status, appetite and oral intake. She was seen by PT/OT who recommended subacute rehab. As patient was clinically stable, with stable renal function, stable O2 saturations on 2 L/Min she was transition to oral dexamethasone and discharged to skilled nursing on 12/22/2021. CONSULTATIONS None INPATIENT PROCEDURES None PHYSICAL EXAM: BP 100/73 | Pulse (!) 41 | Temp 36.4 ?C (Axillary) | Resp 20 | Wt 66.7 kg | SpO2 97% | BMI 27.06 kg/m? Physical Exam Vitals and nursing note reviewed. Constitutional: General: She is not in acute distress. Appearance: Normal appearance. She is well-developed. HENT: Head: Normocephalic. Ears: Comments: Significant presbycusis present Mouth/Throat: Mouth: Mucous membranes are moist. Pharynx: No oropharyngeal exudate. Eyes: Conjunctiva/sclera: Conjunctivae normal. Cardiovascular: Rate and Rhythm: Regular rhythm. Bradycardia present. Heart sounds: No murmur heard. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: No wheezing. Comments: Diminished breath sound Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: General: Normal range of motion. Cervical back: Normal range of motion and neck supple. Right lower leg: No edema. Left lower leg: No edema. Skin: General: Skin is warm. Findings: No rash. Neurological: Mental Status: She is alert and oriented to person, place, and time. H&P: Attestation signed by MD at 12/20/2021 1:55 PM Patient did have some complaints of shortness of breath at the bedside and did have some mild coarse breath sounds heard bilaterally. Otherwise, patient overall seems to be doing fairly well. Agree with continued use of diuretics. Patient asymptomatic in regards to intermittent bradycardia. Will monitor clinically. Will need subacute rehab. Baseline renal function from early 2020 shows creatinine of approximately 1.6 - 1.7 on average. Expand All Collapse All Hide copied text Hover for details CHIEF COMPLAINT: Acute hypoxemic respiratory failure due to COVID-19 Assessment/Plan ASSESSMENT / PLAN: * Acute hypoxemic respiratory failure due to COVID-19 Assessment & Plan Likely multifactorial with COVID and CHF On 4L NC Continue lasix and dexamethasone Wean oxygen as tolerated Pneumonia due to COVID-19 virus Assessment & Plan Symptom onset: 12/16 Isolation: Severe Respiratory, if improved/afebrile antipyretics consider deescalation on 1/4 due to immune compromised status Vaccination Status: Vaccinated in Feb/March, has had booster although unsure of date Continue supplemental O2, Titrate/wean to maintain SpO2>92% Continue Dexamethasone 1/10 Continue Remdesivir 1/5, will have to continue to monitor renal function closely Encourage Self Prone, IS, deep breathing and ambulation as tolerated Symptomatic Treatment: Anti Tussives, Anti Emetics, Analgesics VTE PPx: Lovenox 40mg SQ q24 Daily CBC, CMP, CRP, D-Dimer Monitor I/O, daily weight, creatinine Maintain net neutral to negative fluid balance q24 Code Status: DNR Junctional bradycardia Assessment & Plan Seen by cardiology at Hospital last month, no intervention needed. Daughter states that they spoke with Dr. who said a pacemaker was not needed as her heart never stops and she does not have symptoms with her bradycardia EKG showing junctional rhythm with rate of 46 CLL (chronic lymphocytic leukemia) Assessment & Plan On venetoclax for CLL, hold with acute infection Follows with palliative care as an outpatient CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min Assessment & Plan Renal function appears better than baseline Continue to monitor with diuresis Acute on chronic diastolic congestive heart failure Assessment & Plan Patient had an echo in 11/2021 with EF 70% BNP elevated today 8461 CXR showing pulmonary edema vs infiltrates Given IV lasix 20 mg in ER, continue with BID IV lasix Monitor I/O, daily weights Subjective HISTORY OF PRESENT ILLNESS: Patient is a 94 y.o. female who presents today with shortness of breath, hypoxia and weakness. The patient has a complex medical history including CKD 4, CLL, bradycardia, CHF, previous DVT not on anticoagulation. She is very hard of hearing and so cannot provide a lot of history due to not understanding all of my questions. I did speak with her daughter on the phone to assist with the history. The patient was hospitalized at Hospital from 11/14-11/19 for a UTI, metabolic encephalopathy and CHF. She was discharged to rehab. Daughter reports that after 9 days she had improved and was told she did not need rehab but was unable to return home so went to another facility for respite. While there she has had increasing shortness of breath but her oxygen levels have been above 90 so she did not need oxygen. The facility reported that over the last 2-3 days she has had increasing weakness. Her daughter states she was there yesterday and she seemed to be at her baseline. Today the patient was found to be hypoxic and so EMS was called and she was brought to the ER for evaluation. The patient states that she occasionally has been having achy chest pain but does not have any today. She has some shortness of breath and an occasional cough. She states she has been tired and had some chills. In the ER the patient was found to be COVID positive. She had an elevated BNP at 8461. Her troponin was indeterminate with a delta of 3. She had no leukocytosis, a negative procal. Her EKG showed junctional rhythm with a rate of 46 and some ST and T wave abnormalities. She had a CXR showing prominent interstitial opacities bilaterally possible pulmonary fibrosis and or interstitial pulmonary edema and bibasilar atelectasis vs infiltrate. She was hypoxic requiring supplemental oxygen and was given lasix. The hospitalist team was contacted for admission and further management. Patient Active Problem List Diagnosis ? Microscopic colitis ? Complete heart block ? Anemia ? Acute hypoxemic respiratory failure due to COVID-19 ? Acute on chronic diastolic congestive heart failure ? CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min ? CLL (chronic lymphocytic leukemia) ? Pneumonia due to COVID-19 virus ? Junctional bradycardia Review of Systems Constitutional: Positive for activity change, chills and fatigue. Negative for fever. HENT: Negative for congestion and sore throat. Eyes: Negative for visual disturbance. Respiratory: Positive for shortness of breath. Negative for cough. Cardiovascular: Positive for chest pain (intermittent) and leg swelling. Gastrointestinal: Positive for abdominal pain. Negative for nausea, vomiting and diarrhea. Genitourinary: Negative for difficulty urinating and dysuria. Musculoskeletal: Negative for back pain and falls. Neurological: Positive for weakness. Negative for dizziness and light-headedness. Endo/Heme/Allergy: Positive for easy bleeding or bruising. Skin: Positive for wound. Negative for rash. Objective OBJECTIVE: BP 124/55 | Pulse (!) 47 | Temp 36.4 ?C (Axillary) | Resp 28 | Wt 66.7 kg | SpO2 99% | BMI 27.06 kg/m? Physical Exam Constitutional: General: She is not in acute distress. Appearance: Normal appearance. She is not diaphoretic. HENT: Head: Normocephalic and atraumatic. Ears: Comments: Very hard of hearing Mouth/Throat: Mouth: Mucous membranes are moist. Pharynx: Oropharynx is clear. Eyes: Extraocular Movements: Extraocular movements intact. Conjunctiva/sclera: Conjunctivae normal. Cardiovascular: Rate and Rhythm: Regular rhythm. Bradycardia present. Pulses: Normal pulses. Heart sounds: Normal heart sounds. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: No wheezing. Comments: Lung sounds diminished in bilateral bases, some scattered fine crackles bilaterally Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: Right lower leg: Edema present. Left lower leg: Edema present. Comments: LLE>RLE edema Skin: General: Skin is warm and dry. Comments: See photo below of wound on right shin Neurological: Mental Status: She is alert and oriented to person, place, and time. Psychiatric: Mood and Affect: Mood normal. Behavior: Behavior normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- Comprehensive Metabolic Panel (CMP) (Abnormal) Collected: 12/22/21 0549 Order Status: Completed Specimen: Blood, Venous Updated: 12/22/21 0750 Sodium Level 141 134 - 146 mmol/L Potassium Level 3.9 3.4 - 5.0 mmol/L Chloride 112 98 - 112 mmol/L HCO3 18 Low 21 - 29 mmol/L Anion Gap 11 9 - 18 mmol/L Glucose Level 87 70 - 99 mg/dL Blood Urea Nitrogen 37 High 8 - 20 mg/dL Creatinine 1.51 High 0.50 - 1.10 mg/dL MDRD eGFR 32 Low >=60 mL/min/1.73 m2 CG eCrCl -- Calcium Level Total 8.6 8.6 - 10.4 mg/dL Protein Total 4.9 Low 6.0 - 8.0 g/dL Albumin Level 2.8 Low 3.5 - 5.0 g/dL Bilirubin Total 0.3 0.2 - 1.0 mg/dL Alkaline Phosphatase 100 35 - 104 IU/L Alanine Aminotransferase 10 10 - 40 IU/L Aspartate Aminotransferase 14 10 - 40 IU/L C Reactive Protein (CRP), Blood Level (Abnormal) Collected: 12/22/21 0549 Order Status: Completed Specimen: Blood, Venous Updated: 12/22/21 0750 C-Reactive Protein 25.8 High <=5.0 mg/L D-Dimer (Abnormal) Collected: 12/22/21 0549 Order Status: Completed Specimen: Blood, Venous Updated: 12/22/21 0729 D-Dimer Quant 960 High 0 - 500 ng/mL FEU Complete Blood Count w/Differential (Abnormal) Collected: 12/22/21 0549 Order Status: Completed Specimen: Blood, Venous Updated: 12/22/21 0651 White Blood Cell 4.96 4.00 - 10.80 x10*3/uL Red Blood Cell 3.40 Low 4.20 - 5.40 x10*6/uL Hemoglobin 10.9 Low 12.0 - 16.0 g/dL Hematocrit 32.9 Low 37.0 - 47.0 % Mean Cell Volume 96.8 80.0 - 100.0 fL Mean Cell Hemoglobin 32.1 27.0 - 33.0 pg Mean Cell Hemoglobin Concentration 33.1 32.0 - 37.0 g/dL Red Cell Diameter Width 12.4 11.0 - 16.0 % NRBC Absolute Count 0.00 0.00 - 0.01 x10*3/uL NRBC Automated 0.0 0.0 - 0.1 %WBC Platelet 124 Low 140 - 400 x10*3/uL Mean Platelet Volume 11.5 High 7.4 - 11 fL Neutrophil Automated 77.2 35.0 - 80.0 % Immature Granulocyte Automated 0.4 0.0 - 0.6 % Lymphocyte Automated 8.3 Low 20.0 - 50.0 % Monocytes Automated 13.3 High 2.0 - 12.0 % Eosinophil Automated 0.4 0.0 - 6.0 % Basophil Automated 0.4 0.0 - 2.0 % Neutrophil Absolute Count 3.83 1.80 - 7.80 x10*3/uL Immature Granulocyte Absolute Count 0.02 0.00 - 0.05 x10*3/uL Lymphocyte Absolute Count 0.41 Low 1.00 - 4.00 x10*3/uL Monocyte Absolute Count 0.66 0.00 - 0.90 x10*3/uL Eosinophil Absolute Count 0.02 0.00 - 0.50 x10*3/uL Basophil Absolute Count 0.02 0.00 - 0.20 x10*3/uL DR CHEST 2 VIEWS FRONTAL AND LATERAL Resulted: 12/19/21 0350 Order Status: Completed Updated: 12/19/21 0352 Narrative: EXAMINATION: Frontal and Lateral View Chest EXAM DATE: 12/19/2021 3:26 AM TECHNIQUE: Frontal and lateral views INDICATION: Chest Pain or Dyspnea. COMPARISON: 2/1/2020 ENCOUNTER: Not applicable _________________________ Impression: Stable right chest port. The catheter tip is in the mid-lower superior vena cava. There are prominent interstitial opacities bilaterally suggesting underlying pulmonary fibrosis. A component of interstitial pulmonary edema is not excluded. There is also bibasilar atelectasis versus infiltrate. No pneumothorax. No other change.
- Aktuelle Erkrankungen
- hospitalized hospital 11/14-11/19 ? UTI, metabolic encephalopathy & CHF - Discharge Diagnosis Concern for urinary tract infection at admission ruled out by previous physician with suspicion that pyuria and urinary retention secondary to immobility -Patient was continued on ceftriaxone and with negative urine cultures discontinued by previous provider -Foley catheter is since been removed, patient passed a voiding trial -Renal ultrasound without evidence of hydronephrosis
- Vorgeschichte
- Past Medical History: Diagnosis Date ? Anemia ? Anxiety ? Bradycardia ? CHF (congestive heart failure) ? CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min ? CLL (chronic lymphocytic leukemia) ? Depression ? DVT (deep venous thrombosis) ? GERD (gastroesophageal reflux disease) ? Gout ? Heart block ? HLD (hyperlipidemia) ? Hypertension ? Hypothyroid ? Lymphedema ? Microscopic colitis ? Recurrent Clostridioides difficile infection ? Tumor lysis syndrome
- Andere Medikamente
- allopurinol 100 mg oral tablet = 1 tab(s), Oral, BID, Start Date: 11/14/21 Artificial Tears preserved ophthalmic solution 1 drop(s), OPTH, BID, PRN for dry eyes, # 10 mL, Start Date: 11/14/21 aspirin enteric coated 81 mg oral tablet = 1 t
- Allergien
- bactrim - diarrhea cipro XR - diarrhea penicillins - rash
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 02.05.2023
- Impfdatum
- 21.03.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 47,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pericarditis
Symptom recurrence
Symptomtext
ACUTE PERICARDITIS, UNSPECIFIED 7/16/2022 & 9/18/2022 -- RECURRENCE OF SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 10.12.2021
- Beginn
- 11.05.2022
- Tage bis Beginn
- 152,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back injury
COVID-19
Cough
Headache
Pain
Productive cough
Pulmonary oedema
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough infection with COVID19. I woke up on 5/11 with dry hacking cough. Later that day developed fever, headache, body aches. Was prescribed Paxlovid by PCP (via telehealth visit) and started taking it that afternoon. I had injured my back on 5/6 and was prescribed (via telehealth visit on 5/9) Methylprednisolone 4Mg Dose Pack , which I started taking that day. Per PCP instructions when receiving Paxlovid prescription I stopped taking the Methylpredisolone immediately, last does was 5/10 at bedtime (about 10 PM). COVID symptoms stayed for about 3 days. I did experience some "COVID rebound" symptoms 6-8 days after starting Paxlovid, primarily recurrence of cough - primarily in the morning, about 5-15 after getting out of bed, mildly productive, prompted by some fluid/mucus in lungs. Once lungs are clear minimal coughing during the day. This has been getting better but I am still experiencing this lingering morning cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary oedema
- Hospital-Tage
- -
- Labordaten
- Rapid Antigen test for COVID19
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity, high cholesterol, depression, anxiety
- Andere Medikamente
- Bupropion, Omeprazole, Famotidine, Atorvastatin, Acebutolol
- Allergien
- Feraheme
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 09.03.2021
- Beginn
- 04.02.2022
- Tage bis Beginn
- 332,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Atrial fibrillation
Blindness
Cerebellar stroke
Chronic obstructive pulmonary disease
Dyskinesia
Electroencephalogram normal
Endotracheal intubation
Lethargy
Nystagmus
Positive airway pressure therapy
Respiratory acidosis
Seizure like phenomena
Symptomtext
Patient is a 78 yo M with hx paroxysmal atrial fibrillation, dilated cardiomyopathy with systolic and diastolic CHF, arthrosclerotic heart disease, mixed hyperlipidemia, moderately differentiated invasive ductal carcinoma of the left breast in a male s/p bilateral mastectomy, history of alcoholism and peptic ulcer who presented with lethargy and seizure like activity. No reported focal neurological deficits. Patient did have some visual loss that was improving early in hospitalization. Patient found to have bilateral occipital lobe and right cerebellar stroke. Patient started on ASA, continued eliquis, lipitor. Patient with worsening lethargy and respiratory acidosis in PM on 2/6. Suspect multifactorial in setting of ativan from CIWA protocol, COPD. Patient intubated on 2/6 after patient did not improve with BiPAP. Patient started on steroids. Patient has been on precedex and fentanyl for sedation. After intubation patient was noted to have seizure like activity with vertical nystagmus and jerking of extremities. Patient loaded on keppra and started on 500 mg BID for maintenance. STAT EEG and did not show epileptic activity on 2/7 or 2/8 but patient having intermittent seizure like activity. Keppra increased to 1000 mg BID. Routine exam may have not captured event. We cannot do continuous EEG monitoring at or facility. No recurrent episodes since increasing keppra. Hospitalization also complicated by Afib w/ RVR. Tikosyn discontinued due to QTC prolongation and diltiazem gtt started 2/7. Pt transferred for higher level of care to hospital on 2/8.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebellar stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood pressure measurement
Blood test
Blood thyroid stimulating hormone
Body temperature
Cardiac flutter
Chest X-ray
Chest discomfort
Chest pain
Electrocardiogram
Full blood count
Heart rate
Hyperhidrosis
Inappropriate schedule of product administration
Laboratory test
Metabolic function test
Oxygen saturation
Syncope
Troponin
Symptomtext
heart was fluttering/flutter was really bad; woke up at 3 AM and fainted; like a pressure/ felt like there was a lot of pressure in her chest/ She felt like someone had their knee right in the center of her chest, between her breasts; had severe chest pain; sweating; Inappropriate schedule of vaccine administered; This spontaneous case was reported by a consumer and describes the occurrence of CARDIAC FLUTTER (heart was fluttering/flutter was really bad) and SYNCOPE (woke up at 3 AM and fainted) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Anaphylaxis, Hives and Hay fever. Previously administered products included for Product used for unknown indication: COVID-19 VACCINE NRVV AD26 (Time: 10:00 AM; Lot/Batch: 206A21A; Route and body site: Left arm) on 19-Jun-2021. Past adverse reactions to the above products included No adverse event with COVID-19 VACCINE NRVV AD26. Concurrent medical conditions included Fruit allergy (anaphylaxcic shock, swelling, difficulty breathing, hives) since 12-Apr-1998. On 03-Dec-2021 at 11:30 AM, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Dec-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). On 04-Dec-2021, the patient experienced CHEST PAIN (had severe chest pain). 04-Dec-2021, the patient experienced HYPERHIDROSIS (sweating). On 04-Dec-2021 at 3:00 AM, the patient experienced CARDIAC FLUTTER (heart was fluttering/flutter was really bad) (seriousness criterion medically significant), SYNCOPE (woke up at 3 AM and fainted) (seriousness criterion medically significant) and CHEST DISCOMFORT (like a pressure/ felt like there was a lot of pressure in her chest/ She felt like someone had their knee right in the center of her chest, between her breasts). On 03-Dec-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. On 04-Jan-2022 at 1:00 PM, CARDIAC FLUTTER (heart was fluttering/flutter was really bad), SYNCOPE (woke up at 3 AM and fainted) and CHEST DISCOMFORT (like a pressure/ felt like there was a lot of pressure in her chest/ She felt like someone had their knee right in the center of her chest, between her breasts) had resolved. At the time of the report, CHEST PAIN (had severe chest pain) and HYPERHIDROSIS (sweating) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood pressure measurement: 138/80 (High) 138/80. On an unknown date, Blood test: normal (normal) Normal. On an unknown date, Blood thyroid stimulating hormone: normal (normal) Normal. On an unknown date, Body temperature: 98 degrees f (normal) 98 degrees f. On an unknown date, Chest X-ray: normal (normal) Normal. On an unknown date, Electrocardiogram: normal (normal) Normal. On an unknown date, Full blood count: normal (normal) Normal. On an unknown date, Heart rate: abnormal (abnormal) heart is beating really hard/rapid heart beat and 76 (normal) 76. On an unknown date, Laboratory test: 19 (normal) 19 and normal (normal) Normal. On an unknown date, Metabolic function test: normal (normal) Normal. On an unknown date, Oxygen saturation: 97 % (normal) 97 %. On an unknown date, Troponin: normal (normal) Normal. Symptoms experienced by the patient reported as irregular heart rate/palpitations, heart rate greater than 100 beats per min, chest tightness, decreased level of consciousness, feeling hot. Event cause the patient to seek medical care. Patient was on emergency room/department from 18-Dec-2021 to 19-Dec-2021. No concomitant medication information was provided. No treatment medication was provided. Company Comment - This is a spontaneous case concerning a 61-year-old female patient with no relevant medical history provided, who experienced the serious and unexpected event of cardiac flutter and the expected event of syncope. On 03-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine). The events occurred 1 day after the second dose of mRNA-1273 vaccine, and had resolved on the same day. The rechallenge was unknown. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 04-Jan-2022: Follow-up information was received and had no new information. On 15-Jan-2022: Follow up received as medical history, lab data and event added.; Sender's Comments: This is a spontaneous case concerning a 61-year-old female patient with no relevant medical history provided, who experienced the serious and unexpected event of cardiac flutter and the expected event of syncope. On 03-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine). The events occurred 1 day after the second dose of mRNA-1273 vaccine, and had resolved on the same day. The rechallenge was unknown. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood pressure; Result Unstructured Data: 138/80; Test Name: Blood work; Result Unstructured Data: Normal; Test Name: TSH; Result Unstructured Data: Normal; Test Name: Body temperature; Result Unstructured Data: 98 degrees f; Test Name: Chest x-ray; Result Unstructured Data: Normal; Test Name: EKG; Result Unstructured Data: Normal; Test Name: Hemogram/PLTS; Result Unstructured Data: Normal; Test Name: heart rate; Result Unstructured Data: heart is beating really hard/rapid heart beat; Test Name: Pulse rate; Result Unstructured Data: 76; Test Name: Respiration; Result Unstructured Data: 19; Test Name: Sensitive; Result Unstructured Data: Normal; Test Name: BMP; Result Unstructured Data: Normal; Test Name: oxygen saturation; Result Unstructured Data: 97 %; Test Name: Troponin; Result Unstructured Data: Normal
- Aktuelle Erkrankungen
- Fruit allergy (anaphylaxcic shock, swelling, difficulty breathing, hives)
- Vorgeschichte
- Medical History/Concurrent Conditions: Anaphylaxis; Hay fever; Hives
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Blood thyroid stimulating hormone
Cardiac flutter
Chest X-ray
Chest discomfort
Chest pain
Electrocardiogram
Full blood count
Heart rate
Inappropriate schedule of product administration
Laboratory test
Metabolic function test
Syncope
Troponin
Symptomtext
heart was fluttering/flutter was really bad; woke up at 3 AM and fainted; had severe chest pain; like a pressure/ felt like there was a lot of pressure in her chest/ She felt like someone had their knee right in the center of her chest, between her breasts; Inappropriate schedule of vaccine administered; This spontaneous case was reported by a consumer and describes the occurrence of CARDIAC FLUTTER (heart was fluttering/flutter was really bad) and SYNCOPE (woke up at 3 AM and fainted) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for Product used for unknown indication: COVID-19 VACCINE NRVV AD26. Past adverse reactions to the above products included No adverse event with COVID-19 VACCINE NRVV AD26. On 03-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Dec-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). On 04-Dec-2021, the patient experienced CARDIAC FLUTTER (heart was fluttering/flutter was really bad) (seriousness criterion medically significant), SYNCOPE (woke up at 3 AM and fainted) (seriousness criterion medically significant), CHEST PAIN (had severe chest pain) and CHEST DISCOMFORT (like a pressure/ felt like there was a lot of pressure in her chest/ She felt like someone had their knee right in the center of her chest, between her breasts). On 03-Dec-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. In December 2021, CHEST DISCOMFORT (like a pressure/ felt like there was a lot of pressure in her chest/ She felt like someone had their knee right in the center of her chest, between her breasts) had resolved. At the time of the report, CARDIAC FLUTTER (heart was fluttering/flutter was really bad) had not resolved and SYNCOPE (woke up at 3 AM and fainted) and CHEST PAIN (had severe chest pain) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood test: normal (normal) Normal. On an unknown date, Blood thyroid stimulating hormone: normal (normal) Normal. On an unknown date, Chest X-ray: normal (normal) Normal. On an unknown date, Electrocardiogram: normal (normal) Normal. On an unknown date, Full blood count: normal (normal) Normal. On an unknown date, Heart rate: abnormal (abnormal) heart is beating really hard. On an unknown date, Laboratory test: normal (normal) Normal. On an unknown date, Metabolic function test: normal (normal) Normal. On an unknown date, Troponin: normal (normal) Normal. No concomitant medication information was provided. No treatment medication was provided. Company comment:This is a spontaneous case concerning a 61-year-old female patient with no relevant medical history provided, who experienced the serious and unexpected event of Cardiac flutter with the non-serious unexpected events of Inappropriate schedule of vaccine administered, Chest discomfort, and Chest pain. On 03-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine). The event of Inappropriate schedule of vaccine administered occurred on the same day, with all other events occurring on the following day. The rechallenge was unknown since there's no information about the first two doses. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report; Sender's Comments: This is a spontaneous case concerning a 61-year-old female patient with no relevant medical history provided, who experienced the serious and unexpected event of Cardiac flutter with the non-serious unexpected events of Inappropriate schedule of vaccine administered, Chest discomfort, and Chest pain.On 03-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine). The event of Inappropriate schedule of vaccine administered occurred on the same day, with all other events occurring on the following day. The rechallenge was unknown since there's no information about the first two doses. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood work; Result Unstructured Data: Normal; Test Name: TSH; Result Unstructured Data: Normal; Test Name: Chest x-ray; Result Unstructured Data: Normal; Test Name: EKG; Result Unstructured Data: Normal; Test Name: Hemogram/PLTS; Result Unstructured Data: Normal; Test Name: heart rate; Result Unstructured Data: heart is beating really hard; Test Name: Sensitive; Result Unstructured Data: Normal; Test Name: BMP; Result Unstructured Data: Normal; Test Name: Troponin; Result Unstructured Data: Normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 01.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Pyrexia
Syncope
Symptomtext
Patient states he began to experience chills, syncope, and fever reaching 102.8 at around 7pm on 12/23, and had to go to the ED on 12/24 where he had to remain overnight and was treated with IV fluids and acetaminophen. He was told his syncope was unrelated to the vaccine, and is not certain if he received any other medications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Unknown, patient was admitted to the ED.
- Aktuelle Erkrankungen
- Patient denies other illnesses
- Vorgeschichte
- CHF, GERD, COPD, ADHD, diabetes, HTN, bipolar disorder
- Andere Medikamente
- Zonisamide, ropinirole, pantoprazole, stiolto, metformin er, methylphenidate, Trulicity, tizanidine, albuterol inhaler, baclofen, Trintellix, mirtazapine, olanzapine, atorvastatin, gabapentin, oxybutynin er, furosemide, Tamsulosin, duloxeti
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anaphylactic reaction
Blood test
Urticaria
Symptomtext
Hives all over body. Anaphylaxis and taken to a local Hospital Emergency Room in December 24th 2021. Taken to an urgent care on December 17th 2021 to seek allergy testing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- Blood drawn at local Clinic on December 17th 2021. Results pending. Instructed to call for results on Wednesday December 29th 2021
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None since childhood until now.
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Additional Details: Patient passed out and came to quickly. Monitored him for about an hour.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- 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 pain
Syncope
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Fainting/Syncope-Mild, Additional Details: Patient fainted after receiving the vaccine. Ambulance arrived to take patient to the nearby hospital. Patient recovered alert and oriented x 3. BP 107/88; HR 86; Oxygen 97%; RR 18. Patient declined ER visit via ambulance. Stayed outside the clinic for 15 minutes and went shopping inside.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Severe, Additional Details: Pregnant (newly pregnant) patient fainted upon vaccination. She stated she has a history of fainting with injections from when she was younger, but did not inform the immunizer since it had not happened in a long time. She fainted and pharmacist and pharmacy intern lowered to safety, she was responsive within about 20 to 30 seconds. Made patient wait about 30 minutes before having family member drive her home, and informed her she should let her OB know this happened.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Systemic: Patient fainted while she was seated waiting for 15 minutes-Mild.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Head injury
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Additional Details: pt fell and hit his head, paramedicas came and found him to be responsive and let him go after 20 minutes of observation. Seemed to be focused afterward, could stand without any problems
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 14.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exposure during pregnancy
Human chorionic gonadotropin normal
Thrombosis
Ultrasound scan normal
Vaginal haemorrhage
Symptomtext
Pregnancy through IVF due date 8/12/21 Approximately an hour after receiving the vaccine, I started having severe vaginal bleeding (more than 1 pad per hour) with large blood clots consistent with a miscarriage. The heavy bleeding lasted for approximately 5 hours and then lightened to a medium period rate, by the next morning it was just spotting and as of today (12/13) I am still experiencing some spotting. An ultrasound and HCG test showed that there is still one healthy embryo. A second ultrasound will be taken on 12/15 to confirm. It is uncertain if there had original been multiples or what caused the bleeding. A tissue sample was not taken.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- Ultrasound and HCG (12/10)
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- Pre-natal vitamin, Progesterone in Oil, Estragon
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Cardiac monitoring abnormal
Dizziness
Fall
Head injury
Heart rate decreased
Hyperhidrosis
Hypotension
Interchange of vaccine products
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Hypotension-Severe, Systemic: Weakness-Medium, Additional Details: Fainted shortly after receiving Moderna booster. First 2 doses had been Pfizer. Patient reported almost fainting after Pfizer but not until after event. Hit forehead on hard floor, had a small cut, will probably bruise. Severe sweating. EMTs performed heart monitoring and decided to admit to hospital. Heart rate was measured as low as 38 BPM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Syncope
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: patient fainted-Medium, Additional Details: patient passed out about 20 seconds after recieving vaccine she regained conciousness after about 5-10 seconds she stuck around the pharmacy for 30 minutes instead of the 15 minutes and she was given water and snacks incase low blood sugar was also part of the issue. Patient seemed okay when she left.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.12.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Severe, Additional Details: THE PATIENT DESCRIBED FEELING LIGHTHEADED AFTER HIS VACCINATION. HE BECAME ALMOST UNRESPONSIVE WHILE SITTING IN THE VACCINE ADMINISTRATION AREA WHEREBY I WENT TO GET a staff member FOR ASSISTANCE. WE WERE ABLE TO GET THE PATIENT INTO A SUPINE POSITION AND staff member MEASURED HIS BLOOD PRESSURE, WHICH WAS APPROXIMATELY 70/50. Staff member WAS UNABLE TO GET A O2 READING ON THE PULSOXIMETER AT WHICH POINT WE CALLED 911. THE PATIENT LEFT ON HIS OWN AFTER EVALUATION BY THE EMTS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.05.2023
- Impfdatum
- 23.02.2022
- Beginn
- 20.05.2023
- Tage bis Beginn
- 451,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood lactic acid increased
COVID-19
Hypotension
Hypoxia
Leukocytosis
Pneumonia
Pneumonia aspiration
SARS-CoV-2 test positive
Sepsis
Speech disorder
Tachycardia
Vomiting
Symptomtext
Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: "Patient, 62 yo non-verbal female with history of CVA, dysphagia, aphasia, hemiparesis, PEG tube, schizophrenia and diabetes who presented to the ER from her residential facility for concern of emesis and hypoxemia. She was found to be COVID+ with bilateral aspiration pneumonia. On initial presentation she was found to be septic with hypotension, tachycardia, leukocytosis and elevated lactic acid. She was initially requiring oxygen and decadron for hypoxemia however was able to wean off of the oxygen with good saturation on room air. Initially started on zosyn for aspiration pneumonia and was able to be transitioned to Augmentin for a 5 day course. She was able to resume tube feeds, tolerated well and oxygenation remained good and she was discharged back to her residential facility with continue supportive care for COVID and augmentin for aspiration pneumonia."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- 4,0
- Labordaten
- COVID-19 detected PCR on 5/20/23.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN (hypertension) (Chronic) Schizophrenia (Chronic) Tobacco abuse (Chronic) Dyslipidemia (Chronic) Cognitive disorder Hemiplegia affecting left nondominant side Dysphagia as late effect of stroke Nonverbal Aphasia as late effect of stroke Hemiparesis affecting left side as late effect of cerebrovascular accident
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 17.04.2023
- Impfdatum
- 25.11.2022
- Beginn
- 11.04.2023
- Tage bis Beginn
- 137,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaemia
Atelectasis
Blood gases abnormal
COVID-19
Chest X-ray abnormal
Dyspnoea
Fatigue
Fibrin D dimer increased
General physical health deterioration
Lung infiltration
Pancytopenia
Platelet transfusion
Pneumonia bacterial
Red blood cell transfusion
Renal function test
Respiratory alkalosis
SARS-CoV-2 test positive
Thrombocytopenia
Symptomtext
Reason for Admission: dyspnea 2/2 COVID vs. Bacterial pneumonia Brief Summary of Hospital Stay: patient is a 66 YO male with h/o lung transplant for IPF, MDS, CKD IV, HTN, hypothyroidism, OSA, CHF presenting for evaluation of subjective dyspnea without the need of oxygen. Found to be COVID positive and pancytopenic. He is following with facility and Dr. Per facility transplant specialist ok to be treated here and may be transferred there any time the need would arise or if he would worsen. Got one unite of irradiated PRBCs, was treated with Remdesivir (discussed with Dr. - transplant specialist, that in spite of his CKD stage IV ok to give; 3 days per protocol if not needing oxygen, if needing oxygen, then total of 5 days, completed 5 days prior to discharge), Rocephin and doxycycline - as discussed with facility specialist; Still the patient continued to decline clinically and started requiring oxygen. Chest x-ray showed likely increased infiltrates vs atelectasis. Regimen was switched to Doxy, vanc and zosyn and decadron added. ABG showed mild respirator alkalosis. Changes were made in discussion with Dr. On day 3, due to worsening clinical status decision was made to transfer to transplant service and he was gracefully accepted there. A bed was available the same night, however patient decided to wait until the morning due to being extremely tired, however the bed was not available in the morning any more. On day 5 a bed became available again and patient was discharged. D-dimer elevated on arrival, but about his baseline and improved on day 3, troponins elevated but downtrending during the stay. Kidney function stable. Due to worsening thrombocytopenia and anemia he received irradiated platelet and PRBC transfusions prior to discharge in discussion with hem/onc on call Dr.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 4,0
- Labordaten
- COVID Positive PCR 4/10/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 14.04.2023
- Impfdatum
- 20.12.2021
- Beginn
- 25.02.2022
- Tage bis Beginn
- 67,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adult failure to thrive
Hypotension
Symptomtext
I95.9 HYPOTENSION 2/25/2022 HYPOTENSION I95.9 HYPOTENSION 2/25/2022 FAILURE TO THRIVE SYNDROME, ADULT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 10.01.2022
- Beginn
- 13.03.2023
- Tage bis Beginn
- 427,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chronic obstructive pulmonary disease
Computerised tomogram thorax abnormal
Condition aggravated
Dyspnoea
Exposure to SARS-CoV-2
Hypoxia
Laboratory test normal
Lung opacity
Pneumonia
SARS-CoV-2 test positive
Wheezing
Symptomtext
Patient Is a 54-year-old female with a past medical history of COPD on 2 L nasal cannula chronically, HFpEF, hypertension, hyperlipidemia, hypothyroidism, GERD, IBS who presents with shortness of breath and wheezing. Patient states that last week her mother was admitted to the hospital with COVID-19. She picked her mother up from the hospital upon discharge and had to spend some time with her to help care for her. She received a DuoNeb as well as Decadron in the ED, ultimately able to be weaned down to 2 L however she still had significant wheezing. She had a CT chest which is negative for PE though she does have right middle lobe attenuation of the bronchial tree consistent with a superimposed pneumonia. Lab work in ED is otherwise unremarkable. She did test positive for COVID-19. Patient states she is vaccinated and has received 2/3 boosters. Patient is admitted to surgical unit for acute on chronic hypoxia, COPD exacerbation and COVID-19 infection. Clinical Summary Patient was treated with decadron and remdesivir for COVID-19 as well as Azithro. Patient's breathing improved to where she no longer needed oxygen and wasn't wheezing. I discussed with the patient, she should receive 3 doses of Remdesivir to prevent progression of COVID since she is at high risk. Patient states though she has to get home to take care of her husband. Will DC with short decadron taper and 2 more days of Azythromycin. Patient has inhalers at home. Patient instructed to return if she wheezes and to isolate for 10 days. Discharge diagnosis COVID-19 Infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 04.01.2023
- Impfdatum
- 07.04.2021
- Beginn
- 14.11.2022
- Tage bis Beginn
- 586,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
11/14/22 presents to ED for "shortness of breath". PMHx of "hypertension, HFpEF LVEF 60, ESRD on HD (Monday, Wednesday, Friday), chronic anemia"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 11/14/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 19.12.2022
- Impfdatum
- 17.12.2021
- Beginn
- 25.07.2022
- Tage bis Beginn
- 220,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Dyspnoea
Fatigue
Feeling abnormal
Headache
Hypogeusia
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I woke up with a scratchy throat and throughout the day I started to feel fatigued. By that evening I had a fever about 99 or 100. Next morning I just felt a little icky, as the day went on I became more fatigued and the fever came back, definitely over 100. The day after that I went to an urgent care, thinking it was a sinus infection. They tested me for COVID-19, test came back positive. They weren't able to prescribe anything due to my current medications. I went home to isolate as best I could. Wore a mask whenever I left my room, and was able to mostly stay in my master suite but the rest of my household did end up coming down with it as well. I was still feverish off and on for a few days, definitely had a headache. Never lost my sense of taste and smell, but at some point my sense of taste was lessened. It was probably a good week that I isolated, after the symptoms had cleared up I started having issues breathing and had to use my inhaler more.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid test positive (07/28/22)
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Depression; Diabetes; Overweight
- Andere Medikamente
- Vitamin C; metformin; sertraline; lisinopril; ONE A DAY multivitamin; melatonin; ADVAIR DISKUS, JARDIANCE; PLAVIX; SINGULAIR; pravastatin; ZYRTEC; DUONEB; albuterol
- Allergien
- Allergic to the smell of rubbing alcohol; hand sanitizers; bleach; most cleaning products
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 10.12.2021
- Beginn
- 01.11.2022
- Tage bis Beginn
- 326,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dysphagia
Migraine
Nausea
Pain
Pharyngeal swelling
Rash
Respiratory tract congestion
SARS-CoV-2 test positive
Sinus headache
Sinusitis
Urticaria
Symptomtext
Developed rash within 12-24 hours of getting vaccine. About 8 months after getting my vaccine I contracted COVID. Began as a sinus headache and turned into a migraine that lasted 5 days. Mild fever 99 degrees, body aches, nausea, swollen throat and difficulty swallowing. Lot of coughing and congestion. Around day 3 I developed hives similar to what I had when I received vaccine. Around day 5 I reached out to allergist because I was beginning to show signs of a sinus infection. Most symptoms lasted one to two weeks with cough persisting for four weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- COVID-19 test x 6, 4 positive and 2 negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Hypothyroid
- Andere Medikamente
- SYNTHROID; QVAR; NASACORT; black cohosh, methylfolate; B12; omega; mg glycinate; ca with vitamin D3; probiotic; allergy shots
- Allergien
- NSAIDs; corn; shrimp
- Vorherige Impfungen
- Typically react strongly to all vaccines. Showing mild symptoms of whatever vaccine I have received.
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 15.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anti-cyclic citrullinated peptide antibody negative
Asthenia
Joint lock
Joint noise
Mobility decreased
Musculoskeletal stiffness
Pain in extremity
Red blood cell sedimentation rate normal
Symptomtext
12 days after receiving my first booster shot, I developed significant stiffness, pain and decreased strength and range of motion in my right hand. I woke up that evening and on making a fist, my pinky locked and clicked when it did bend. My right hand was very stiff and sore (4/10). These symptoms have continued and are still present. I have decreased strength and range of motion in the right hand daily and extreme stiffness with pain after inactivity (at night or after naps). I had no arthritic symptoms prior to this and symptoms are not getting better. I have slight stiffness in left hand.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- CCP negative Sed Rate 9
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 06.01.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 236,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Abdominal pain
Arthralgia
Chest pain
Symptomtext
chest pain, abdominal pain, arthralgias
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 18.12.2021
- Beginn
- 20.08.2022
- Tage bis Beginn
- 245,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chest pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 22.08.2022
- Impfdatum
- 10.03.2021
- Beginn
- 18.08.2022
- Tage bis Beginn
- 526,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Illness
Productive cough
Respiratory tract congestion
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID infection. Sympoms of shortness of breath, mild congestion, and productive cough. Unsure of onset of illness. Positive COVID test collected 08/18/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- Positive SARS-COV-2 (COVID-19) by NAA collected 08/18/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Obesity, COPD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 20.06.2022
- Impfdatum
- 04.01.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 156,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Asymptomatic COVID-19
Blood creatinine normal
Blood electrolytes normal
Cardiac failure
Cardiac monitoring normal
Orthostatic hypotension
SARS-CoV-2 test positive
Symptomtext
Discharge Physician: MD Primary Care Clinician at Discharge: Admission Date: 6/9/2022 Discharge Date: 6/11/2022 PRESENTING PROBLEM: Orthostatic hypotension Generalized weakness COVID-19 virus infection HOSPITAL COURSE: 69-year-old woman with chronic systolic heart failure (EF 23%), ischemic cardiomyopathy, coronary artery disease with ICD, mitral regurgitation (severe) and CKD stage 4 presented to the hospital with generalized weakness. She is found to be orthostatic we positive and was given judicious fluid boluses in the emergency department given her heart failure. She remained orthostatic and symptomatic and thus was admitted to the medical service. COVID-19 testing was positive though she was asymptomatic and without hypoxemia on ambient air. Review of medical records revealed that she was on hydrochlorothiazide/spironolactone/torsemide as well as lisinopril as prescribed by a Heart Clinic. These medications were held and the patient was provided very judicious IV fluid hydration overnight. Cardiac monitoring revealed no acute malignant arrhythmias. Electrolytes were within normal limits and creatinine was at baseline. Her symptoms did resolve. Measured orthostatic vital signs did reveal resolution of orthostatic hypotension. She was discharged on 06/11/2022. She was instructed to hold hydrochlorothiazide until her next visit with a Heart Clinic. She was discharged in good condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Orthostatic hypotension
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- Hospitalization Discharge Provider: MD Primary Care Provider: MD Admission Date: 12/2/2021 Discharge Date: 12/09/2021 Presenting Problem: Acute on chronic systolic congestive heart failure (HCC)
- Vorgeschichte
- Mitral regurgitation Type 2 diabetes mellitus with stage 3b chronic kidney disease, without long-term current use of insulin (HCC) Hypertension associated with diabetes (HCC) Eczema Coronary artery disease History of coronary angioplasty with insertion of stent Hyperlipidemia associated with type 2 diabetes mellitus (HCC) Severe major depression without psychotic features (HCC) NPDR (nonproliferative diabetic retinopathy) (HCC) Chronic systolic congestive heart failure (HCC) Ischemic cardiomyopathy ICD (implantable cardioverter-defibrillator), single, in situ Acute kidney injury superimposed on chronic kidney disease (HCC) Iron deficiency anemia Chronic kidney disease due to type 2 diabetes mellitus (HCC) Orthostatic hypotension
- Andere Medikamente
- aspirin 81 MG tablet clopidogrel (PLAVIX) 75 MG tablet dapagliflozin (FARXIGA) 10 MG TABS tablet dulaglutide (TRULICITY) 3 MG/0.5ML injection glipiZIDE (GLUCOTROL) 5 MG tablet lisinopril (PRINIVIL,ZESTRIL) 5 MG tablet mirtazapine (REM
- Allergien
- MetforminOther MorphineNausea and Vomiting
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 16.06.2022
- Impfdatum
- 01.04.2021
- Beginn
- 07.05.2022
- Tage bis Beginn
- 401,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Asymptomatic COVID-19
COVID-19
Condition aggravated
Joint range of motion decreased
Pain in extremity
SARS-CoV-2 test positive
Sickle cell anaemia with crisis
Symptomtext
Pt to ED 5/7 c/o sickle cell crisis, with pain to both arms and right leg. COVID+ 5/7, No other respiratory symptoms, not a candidate for antiviral therapy for COVID-19 infection. 5/8 Pt states he is having more pain in his arms. It is hard for him to lift them. 5/9 pt has remained AO x 4 throughout shift. No complaints of pain or weakness. No COVID-19 symptoms. Pt discharged 5/10.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 4,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Sickle cell pain crisis Sickle cell crisis Obesity (BMI 30-39.9) Chest pain, unspecified type History of pulmonary embolism
- Andere Medikamente
- apixaban (ELIQUIS)5 MG PO Tab, folic acid (FOLATE) 1 MG PO Tab
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 18.01.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 124,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest X-ray abnormal
Pneumonia aspiration
SARS-CoV-2 test positive
Symptomtext
aspiration pneumonia after testing positive for covid 5/22/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia aspiration
- Hospital-Tage
- -
- Labordaten
- covid positive CXR 5/22/22: Clinical history: Drug overdose; tachycardia; concern for aspiration Single frontal view of the chest was obtained and compared to exam from 11/15/2020. Heart is not enlarged. Scattered hazy opacities within the right lung could be artifactual; however, an infiltrative process would be difficult to exclude. The lungs and pleural spaces are otherwise clear. Pneumothorax is not seen. IMPRESSION: Questionable hazy opacities within the right lung could relate to an underlying infectious or inflammatory processes. Fluid overload is considered less likely.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- major depression/anxiety, ruptured ovarian cyst, hx multiple drug overdoses
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 10.02.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 87,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Arthralgia
Atelectasis
Atrial fibrillation
Back pain
Blood bicarbonate increased
Blood gases
Blood pH normal
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Chest pain
Chronic respiratory failure
Confusional state
Cough
Dyspnoea
Electrocardiogram abnormal
Exposure to SARS-CoV-2
Fatigue
Symptomtext
ED visit (5.6.22); Hospitalized w/ COVID (5.8.22); COVID-19 positive (5.1.22 / 5.8.22); Fully vaccinated PLUS two boosters. BRIEF OVERVIEW: Discharge Provider: Primary Care Provider: Admission Date: 5/8/2022; Discharge Date: May 13, 2022; DETAILS OF HOSPITAL STAY:PRESENTING PROBLEM: Hypoxia [R09.02]; Pneumonia due to COVID-19 virus [U07.1, J12.82]; COVID-19 [U07.1]; HOSPITAL COURSE: Pt is a 78 yr old F with PMHx of chronic hypoxic respiratory failure on 8L via NC at baseline, COPD, CAD, CHF, A-Fib, HTN, HLD, depression, OSA and obesity, presented to the ER on 5/8 with c/o worsening dyspnea. She is fully vaccinated, tested positive on 5/1 for COVID-19 and received molnupiravir (an antiviral) on 5/3 as outpatient. However, she continued to experience fatigue, hypoxia which prompted her ED visit. In the ER, she was borderline febrile, normotensive, tachycardic and tachypneic, maintaining appropriate oxygen saturations on 15 L/min NRB mask. Initial venous gas showed normal serum pH with likely chronically elevated pCO2 of 56 and bicarbonate of 30. Other initial labs show stable renal dysfunction, elevated proBNP, normal procalcitonin, normocytic anemia, and her COVID-19 screen is again positive. EKG showed A-Fib with RVR. CXR shows patchy bibasilar opacities suggestive of atelectasis vs infiltrate/pneumonia without significant interval change from imaging 2 days ago. Admitted for further management - started on Decadron x 10 days, Remdesivir x 5 days for COVID-19 PNA. There was concern for superimposed bacterial infection - Pulmonary consulted and empiric IV Cefepime/Doxycycline initiated. Sputum cultured attempted but unsuccessful. Clinically - her symptoms improved with return to baseline of her oxygen demands. On 5/11 - patient had left shoulder pain while attempting to move in bed. X ray concerning for left shoulder dislocation. Ortho consulted - felt it was chronic left rotator cuff tear with plans for outpatient follow up. PT/OT recommend Home with assist and home health. She was transitioned to oral Ceftin/Doxycyline for 3 more days to complete a total of 7 days of Antibiotics, as well as Decadron for total of 10 days. We reviewed stopping Amlodipine and reducing Lisinopril to 10 mg once daily as blood pressures well controlled in the hospital. Also discussed resuming Azithromycin daily once completion of current antibiotics - patient and son voiced understanding. She is discharged on 05/13/2022 in stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- 4.22.22 - PCP appointment for med check - chronic respiratory failure, chronic low back pain, intermittent confusion; 5.1.22 - patient called nurse triage for yellow phlegm and cough, sort throat, burning chest, HA - son COVID positive; COVID positive 5.1.22; Told to contact monoclonal antibody clinic. Will prescribe Paxlovid if not a MAB candidate. 5.6.22 - clinically worsened, presented to ED.
- Vorgeschichte
- Atrial fibrillation (HCC); OSA (obstructive sleep apnea); Tobacco abuse- quit smoking July 2013; COPD (chronic obstructive pulmonary disease) (HCC); Essential hypertension; Depression; Hypercholesterolemia; Environmental allergies; Chronic pain of left knee CAD (coronary artery disease); Stage 3 chronic kidney disease (HCC); Obesity, morbid (HCC) Platelets decreased (HCC); Community acquired pneumonia of right lower lobe of lung Chronic low back pain without sciatica, unspecified back pain laterality; Chronic respiratory failure with hypoxia (HCC); Leg edema, right; Frequent urination at night; Atrial fibrillation, unspecified type (HCC).
- Andere Medikamente
- Albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA); inhaler;apixaban (ELIQUIS); Aspirin chewable tablet; atorvastatin (LIPITOR) 40 MG tablet; azithromycin (ZITHROMAX) 250 MG tablet; benzonatate (TESSALON) 100 MG capsule; budesonide/f
- Allergien
- Hydrochlorothiazide-Hives
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 18.01.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 100,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test normal
Computerised tomogram head normal
Dizziness
Epistaxis
Exposure during pregnancy
Fall
Head injury
Hypertension
Pain
Sleep disorder
Speech disorder
Urine analysis normal
Symptomtext
Early Morning April 28.2022. I had woken up in the middle of the evening to use the restroom. Probably between 430 and 530am. At some point I believe I fell and hit my head on the counter. I had goose eggs on the right side of my head and there were things knocked off of the counter with pain on the right side of my body. My son came to wake me up because I hadn't woken him for school. He struggled to wake me and was finally able to call my mother who looked me over. When she arrived, I wasn't able to form full sentences and was struggling to get even one word out. She ended up taking me to the ER after calling my OB. Once we got to the ER they did a urine sample and blood work and a mental evaluation to rule out a stroke. They were concerned specifically about my inability to speak properly which lasted from about 9am-2pm that day. My speech ability gradually returned and improved from one word at a time to full sentences. They also did a CT scan for blood bleeds and monitored my blood pressure which was high. But they attributed that to nerves. They then sent me to labor and delivery for monitoring of the baby. The baby seemed fine and was moving as expected. The doctor came in and mentioned seizure activity and suggested that I see a neurologist. I had an appointment after that with a doctor and am waiting on an appointment with the neurologist. I haven't had any other episodes but have had moments of dizziness that pass after resting for a bit. I am also monitoring my blood pressure regularly. 20 weeks pregnant at time of adverse event. Estimated due date September 13, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Urine Test-no abnormalities-April 28th; Blood Work-no abnormalities- April 28th; CT Scan-no brain bleeds- April 28th
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Celiac Disease
- Andere Medikamente
- Prenatal Vitamin
- Allergien
- Gluten; codeine; trazodone; LAMICTAL
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 15.12.2021
- Beginn
- 12.04.2022
- Tage bis Beginn
- 118,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Cough
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
cough, shortness of breath
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 4/12/22 +Covid test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 13.12.2021
- Beginn
- 01.02.2022
- Tage bis Beginn
- 50,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
COVID-19
Chest X-ray
Cough
Dyspnoea
Electrocardiogram
Fatigue
Headache
Heart rate increased
Nausea
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
COVID breakthrough. The first 2 weeks of infection I had runny nose, headache, cough, tiredness. The following 3-4 weeks I developed long COVID symptoms which included, extreme fatigue, nausea, shortness of breath, and increased heartbeat. I am still experiencing some of the symptoms until this day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID test- positive; EKG; Bloodwork; Chest X-ray
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Amitriptyline
- Allergien
- Cipro
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 28.03.2021
- Beginn
- 29.03.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Aura
Condition aggravated
Head discomfort
Ill-defined disorder
Impaired work ability
Loss of personal independence in daily activities
Magnetic resonance imaging abnormal
Migraine
White matter lesion
Symptomtext
After the first injection, my migraines went from approximately 1-2 a month to 15--18 a month. Subsequently, I have been unable to hold down a job, participate in life, attend church or spend quality time with my family. I spend half of a month in a dark room, in bed, alone and away from my entire family. Sometimes I get an aura as a warning that my migraines are about to come on, sometimes I just get intense pressure immediately. My general practitioner and neurologist have tried to help me with multiple medications, but nothing seems to work. My chronic migraines typically last 1--2 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- I had an MRI without IV contrast on 12/10/2021. Findings include Mild ill-defined and punctate T2 hyperintense areas in the supratentorial white matter are compatible with chronic small vessel ischemic change. Mild/minimal chronic small vessel ischemic change within the pons.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- -Chronic migraine but not as often as I have now. -Arthritis in lower spine -Compressed disc in lower spine -Sciatic nerve down left leg -Bunion on left foot
- Andere Medikamente
- Doxycycline Hyclate 100mg cap, Topiramate 100mg tablet, Venlafaxine HCL 75mg tab, Gabapentin 300 mg tab, Clonazepam .5 mg tab, Fluticasone Prop 50 mcg spray, Oxycodone-Acetaminophen 10-325 tablet, Lisinopril 10 mg tablet, Ubrelvy 100 mg tab
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 12.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pneumonia
Pruritus
Urticaria
Symptomtext
Itching and hives all over body, pneumonia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Bees
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Dyspnoea
Erythema
Fatigue
Gait disturbance
Hypersomnia
Memory impairment
Nausea
Nodule
Skin warm
Swelling
Vertigo
Symptomtext
Day 1: Red, small hard knot, feverish to touch Day 2: Larger knot, sill feverish Day 3 - 6 Vertigo - unable to walk/care for self/nauseated--stayed in bed and with meds slept majority of time slept and unable to remember what was going on--could not move head without getting dizzy (vertigo) Day 7 - 10: Vertigo seemed better/improving, but still dizzy Day 11: Vertigo better/swelling gone All the while breathing difficulty and that continues through this date/tired when gets up to do anything//concerned about permanent damage as well as blood sugars
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Vertigo medication (meclizine)
- Aktuelle Erkrankungen
- Allergic reaction to diabetic meds/came off and was feeling much better.
- Vorgeschichte
- Diabetes II, obesity, back and arthritis issues, high blood pressure
- Andere Medikamente
- Do not tolerate many meds related to diabetes, I will provide a listing if deemed this is common of folks taking the booster.
- Allergien
- Morphine, Victoza, other diabetic meds, statins, Amoxycillin, cats, dogs
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 27.02.2022
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Immediate post-injection reaction
Incorrect route of product administration
Injection site pain
Injection site swelling
Limb injury
Paraesthesia
Symptomtext
Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Additional Details: Patient states sharp pain at injection site immediately after vaccination. He was told pain would go away in 2-3 days, but hasn't resolved. He didn't take any pain meds at the time, but dr has advised on ibuprofen and possible further testing. States administration of vaccine felt like stabbing motion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 08.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Paraesthesia
Sleep disorder
Symptomtext
I'm experiencing continued tingling/burning sensation on my arms (i believe referred to as paresthesia). It has been present for the past few months, which aligns with when I got my booster shot. Initially it was primarily at night, disrupting sleep, but now it often persists all day long. It is worse in my left arm, but present in both.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dyspnoea
Flushing
Nausea
Symptomtext
5 minutes after my 2nd dose vaccination, I experienced the following: shortness of breath, flushed face, chills, nausea. Overall I experienced these symptoms for 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Estradiol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 09.01.2022
- Tage bis Beginn
- 31,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood test normal
Dizziness
Dyspnoea
Urine analysis normal
Vertigo
X-ray normal
Symptomtext
1/9 Was walking thru a new house and started feeling weak and short of breath. And got quickly worse with shifting and later felt like I was on a boat(Vertigo) When I kept my head still it was fine but if I moved my head in the slightest it started again swaying. I asked to go to urgent care and I never ask to go see a doctor always saying it will pass. When I got there I got Xray, physical, blood and urine and when I was checked by moving my head I got REALLY DIZZY and the room itself seemed to be spinning fast. Was given meclizine for treatment and was advised ENT. I was taking the meclizine on and off since but it seems to be tapering off. Went to see my PCP but he was out of office and was seen by the PA. Only had a physical and agreed that I needed to see an ENT. This will happen on 1/26, and still dealing with vertigo.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 1/9 X-ray (normal) 1/9 Blood and Urine(normal)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Long CoVid, Osteoarthritis, Insulin Resistance from PCOS, GURD, Tendonitis, Asthma, HBP, Tachacardia,
- Andere Medikamente
- Norvasc, Zepeda, Zyrtec, Colcrys, Flonase, Hydrochlorothiazide, Metformin, Singular, Protonix, Klor-con, D3, C, Zinc, Iron
- Allergien
- Amoxicillin, Aspirin, Fruit(Fructose), Medical Adhesive
- Vorherige Impfungen
- All Covid shots gave puffy and painful lymph nodes for about 2weeks, Moderna 1st March 20,2021, 2ndApril 17,2021, 57yr old
- Staat
- NJ
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Chills
Dizziness
Dyspnoea
Fatigue
Headache
Injection site pain
Pain
Palpitations
Tachycardia
Symptomtext
Onset of heart palpitations with tachycardia, SOB, and left sided chest pain approximately 12 hours after vaccination. Additional symptoms: body aches, fatigue, dizziness, headache, chills, severe pain at injection site. I assessed my own vital signs using my fitness watch and resting heart rate remained between 105-110bpm, blood pressure < 120/80mmHg and my SpaO2 remained at or above 97%. After 12 hours of symptoms that were not subsiding I self treated with 400mg OTC ibuprofen and approximately 3 hours later all side effects resolved resting heart rate returned to my baseline of 55-60bpm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 01/10/2022 I was scheduled to receive a Hepatitis B booster for pre-employment physical. I consulted with the physician who auscultated my heart and lungs and found no abnormal sounds and normal vitals. Therefore I received Hepatitis B vaccine.
- Aktuelle Erkrankungen
- Anxiety
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 04.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Lymphadenopathy
Urticaria
Symptomtext
After my first dose (04/1/21), my right arm where I got the vaccine became red and itchy 9 days after my vaccine, it lasted for a day, then went away. I didn't have the same "Covid arm" reaction after my second dose, though I had swollen lymph nodes in my armpits and was very ill for a few days. I have had hives everyday since 8 days after my booster shot (12/04/21) as well as swollen lymph nodes in my armpits. A close friend has had the same issue, 10 days after receiving the Moderna vaccine - persistent hives and swollen lymph nodes that have lasted since then.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Influenza Flu
- Allergien
- none
- Vorherige Impfungen
- swollen arm from 1st Covid vaccine (8 days after administration).
- Staat
- OH
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac flutter
Cardiac stress test
Chest pain
Lymphadenopathy
Palpitations
X-ray
Symptomtext
Swollen glands behind the ear at the jaw line, severe chest pain and heart palpitations, fluttering accelerated pulse. Further testing required. X-rays reveal possibility of a swollen heart valve. Patient has no history of heart problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Stress test and x-ray 1/05/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Fibromyalgia
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 14.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood test
Computerised tomogram normal
Dyspnoea
Gastrooesophageal reflux disease
Hypersensitivity
Pruritus
Urticaria
Symptomtext
Dec 23 evening - experienced itchiness on head and arms Dec 24 morning - woke with allergic reaction symptoms -> severe itchiness/hives on torso, arms and head, acid reflux, shortness of breadth, low energy, took over the counter Benadryl every 4 hours throughout day, symptoms got better Dec 25 morning - woke with allergic reaction symptoms -> severe itchiness/hives on torso, arms and head, acid reflux, shortness of breadth, low energy, took over the counter Benadryl every 4 hours throughout day, symptoms got better Dec 26 morning - woke with allergic reaction symptoms at 1am -> severe itchiness/hives on torso, arms and head, acid reflux, shortness of breadth, low energy -> went to The local hospital ER, administered steroid, Zyrtec and Pepcid and released Dec 26 day -symptoms got better up until 2pm then declined again Dec 27 morning - woke with allergic reaction symptoms at 1am -> severe itchiness/hives on torso, arms and head, acid reflux, shortness of breadth, low energy -> administered Epi pen for tree nut allergy, went to The local hospital ER, administered steroid, Zyrtec and Pepcid and released Dec 27 day - prescription picked up for aforementioned medicines, started that during the day symptoms improved Dec 28 day - saw primary care -> no confirmed diagnosis, symptoms NOT for food allergy, suspect symptoms from Moderna booster shot administered on Dec 14, did blood work Dec 29 day - blood work indicated possible blood clot and infection Dec 30 evening - had CT scan of torso performed -> no blood clots Dec 31 - Jan 5 - symptoms are hives on skin on arms and head when irritated or scratched, shortness of breath at times, acid reflux at times, elevated resting heart rate ~80bpm (typically 60), lower energy level
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Dec 28 blood work Dec 30 CT scan of torso
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- trazadone and gabapentin to aid with sleep
- Allergien
- tree nut allergy
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abnormal behaviour
Amnesia
Blood creatine phosphokinase normal
Blood thyroid stimulating hormone normal
Chest X-ray normal
Chest pain
Chills
Confusional state
Dizziness
Dyspnoea
Electrocardiogram normal
Fibrin D dimer normal
Full blood count normal
Hallucination
Headache
Lethargy
Metabolic function test normal
Palpitations
Symptomtext
Within 24 hours of the 3rd dose, (Booster), I developed fever, chills, shortness of breath and headache. Between 24-48 hours after, I became very lethargic and confused. I do not remember Tuesday 12/13/21 at all. I was hallucinating and not acting normal according to my wife. Starting on Wednesday 12/14/21, I began to have substernal chest pain, fluctuating in pain throughout the day with increased headaches and tachycardia. The chest pain has been increasing everyday and the tachycardia happens multiple times a day now unprovoked. With the tachycardia i get short of breath and dizzy. On Wednesday 12/23/21, the pain in my chest with the tachycardia was to the point that I went to Emergency Room. I have had a follow up with my PCP on 12/29/21 and now have an Echocardiogram scheduled for 1/6/22. I continue to have tachycardia throughout the day with palpitations that are only increasing in pain and duration. I never had these issues prior to my Covid Booster. Nothing in my medical history has changed in the past year.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 12/23/21 Emergency Room - 12 lead (SVT), D Dimer, CPK, PTT, Protime, HS Troponin I, BMP, CBC, TSH 3rd Generation, Assay Free Thyroxine. All within normal ranges. Chest X-Ray Normal. Echocardiogram scheduled for 1/6/22 at Hospital.
- Aktuelle Erkrankungen
- None. I have never had any cardiac issues in my life.
- Vorgeschichte
- ADHD
- Andere Medikamente
- Adderall 20mg, Prozac 20mg, Prozason 4mg
- Allergien
- Sulfa allergy, I have had bad reactions to the first 2 vaccines. No food or other products
- Vorherige Impfungen
- All Moderna, age 32, 12/30/20, 1/29/21, 12/13/21, IM Injection, Moderna
- Staat
- MN
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 05.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest pain
Dyspnoea
Laboratory test normal
Peripheral swelling
Pruritus
Urticaria
Symptomtext
10 days after receiving my COVID-19 booster shot (Moderna), I developed urticaria (hives) on different areas of my body. It started with my head feeling itchy around 6:00 p.m. on 12/15/2021. 12 hours later I had hives on my torso, arms, legs, back, neck, etc. Over the next 5 days I continued to have horribly itchy hives that moved to different areas of my body. My hands and feet became extremely swollen for 2 days due to the hives and my itching. I went to urgent care on 12/16/2021, and they prescribed me Claritin, Benadryl, and Methylprednisone. These were not helping much. I went back to urgent care, and then they sent me to the ER, on 12/19/2021 because I started to feel worse (hives persisted, some chest pain and trouble breathing, and extremely swollen hands and feet). They prescribed me Pepcid and Claritin. They did some tests at the ER but did not determine a cause for any of my symptoms. I was at the ER for about 8 hours. On 12/20/2021, I went to a dermatologist, who prescribed me higher doses of Zyrtec, and Prednisone to take once I finished the Methylprednisone. Now since 12/21/2021, I have had less hive breakouts, and the last day I had any hives was 12/26/2021 around 4:00 a.m. I am still taking medications. Also to note, I have no known food allergies or allergies to substances (lotions, beauty products, etc) and had not eaten or started using anything new around the time my hives started. My only known allergy is amoxicillin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Polycystic ovary syndrome
- Andere Medikamente
- Sprintec (birth control) Spironolactone
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.12.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Migraine
Oropharyngeal pain
Pain
Pain in extremity
Tenderness
Symptomtext
Very sore left arm, hurts when I move it. Tender arm. Sore throat, migraine, chills, body aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Mobility decreased
Vomiting
Symptomtext
Severe vomiting for 2 days, unable to rise from bed for 4 days, chills, no fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Sore throat
- Vorgeschichte
- n/a
- Andere Medikamente
- Shingles vaccine
- Allergien
- Shrimp
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Mechanical urticaria
Scratch
Urticaria
Symptomtext
Received Moderna Booster on 12-7-21. Symptoms of hives began to appear on 12-14-21. The hives started on my scalp and neck. The past week the hives have worsened. I have developed dermatographia (skin writing) and will get hives for 10-40 minutes on any location that is scratched. Seams of clothing will also trigger hive development.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- Junel-fe
- Allergien
- sulfa drugs
- Vorherige Impfungen
- Moderna vaccination#2, 28yo received on 5-11-21, hives that lasted 3 days
- Staat
- GA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysgeusia
Dysphagia
Dyspnoea
Flushing
Hyperhidrosis
Throat tightness
Symptomtext
Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Medium, Systemic: Flushed / Sweating-Medium, Additional Details: Metallic taste in mouth
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 18.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Chills
Condition aggravated
Lymphadenopathy
Nausea
Oedema peripheral
Vomiting
Symptomtext
Nausea and chills began 9 hrs after dose, vomiting began 15 hours after dose and lasted for 3 hours. Chills and nausea abated after 24 hours, swollen and painful armpit began 36 hours after dose and continues currently at 48 hours post-dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Similar reaction to second COVID vaccine (but no swollen lymph nodes)
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Chromaturia
Decreased appetite
Dehydration
Nausea
Pain
Pruritus
Pyrexia
Vomiting
Symptomtext
PATIENT STATES HE HAD A SEVERE REACTION TO HIS BOOSTER SHOT. HE INITIALLY HAD JOINT PAIN THE EVENING OF THE VACCINE. HE THEN WORSENED OVER THE NEXT DAYS TO HAVE CHILLS, FEVER, ACHES, LOSS OF APETITE, NAUSEA, VOMITING, DEHYDRATION WITH DARK THICK URINE (LIKE HONEY). THOSE SYMPTOMS LASTED APPROXIMATELY 3 DAYS AND THEN HE BEGAN TO RECOVER. ON 12/13 HE REPORTED THAT HE BEGAN FEELING ITCHY ON HIS ENTIRE BODY. HE REPORTED TAKING TYLENOL AND IBUPROFEN AND DRINKING LOTS OF FLUIDS. I ADVISED PATIENT TO SEEK TREATMENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- DIABETES, HYPERTENSION
- Andere Medikamente
- GLIMEPERIDE, SILDENAFIL, ATORVASTATIN, LISINOPRIL, TESTOSTERONE INJECTION, PANTOPRAZOLE, CARVEDILOL, TOUJEO, ALBUTEROL, INSULIN LISPRO
- Allergien
- SULFA DRUGS
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Fatigue
Hypertension
Pain
Tachycardia
Symptomtext
Systemic: Body Aches Generalized-Medium, Systemic: Dizziness/Lightheadedness-Medium, Systemic: Exhaustion/Lethargy-Medium, Systemic: Hypertension-Severe, Systemic: Tachycardia-Medium.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest X-ray
Chest pain
Fatigue
Heart rate abnormal
Heart rate increased
Irregular breathing
Symptomtext
Chest pain, irregular breathing, heart rate skipping, fast heart rate and fatigue. The time course was from 8pm on 12/13/2021 until now at 3:41pm on 12/14/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Chest x-ray and blood work being done right now. Other tests requested also; possibly ECG or EKG. Possibly getting an MRI and seeing a cardiologist based on preliminary results. Patient is currently in the emergency room awaiting results.
- Aktuelle Erkrankungen
- Nothing
- Vorgeschichte
- Endometriosis
- Andere Medikamente
- Probiotics gummies, hair, skin and nails vitamins, iron supplement, and glucosamine
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Limb injury
Paraesthesia
Symptomtext
Site: Pain at Injection Site-Severe, 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
- MD
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Chest pain
Computerised tomogram
Dyspnoea
Pain
Pain in extremity
Painful respiration
Symptomtext
about 24 hrs after vaccine (12/8, evening) - chest pain (left upper chest), rather severe at times, difficulty expanding chest, some shortness of breath. Some pain into left arm. Subsided later that evening. Some achiness in chest Thursday 12/9 Friday 12/10 - chest pain seemed to return, more localized to just left of sternum. Pain with expansion of chest and some shortness of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Emergency department visit (12/10) to rule out serious problems (heart issues or blood clot). Blood work and CT Scan (due to history of clotting) showed nothing of concern.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Migraine, Blood clotting disorder (heterozygous factor v leiden) and history of PE
- Andere Medikamente
- none that day. Have prescription for zolmitriptan
- Allergien
- amoxicillin and related antibiotics
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 12.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Paraesthesia
Symptomtext
Systemic: Headache-Medium, Additional Details: Patient reported a headache tingling sharp pain in the back of her head. We asked her to wait for further observation. She said she was fine after 15 min and left
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse reaction
Balance disorder
Dizziness
Dyspnoea
Malaise
Paraesthesia oral
Swollen tongue
Tremor
Symptomtext
Patient received vaccine at 6:15 and reported not feeling well at 7:00--described tingling tongue, off balance , and light headed. At 7:05 she said her tongue felt fat and she was having trouble walking due to balance uncertainty. I gave her diphenhydramine 50mg intramuscularly at 7:10. She reported she was going to pass out and was very shaky . I called 911 and reported adverse reaction. Ems Arrived and checked vitals and gave her the option of going to hospital but said she was feeling better. i monitored her until 7:25 and her son picked her up but returned when they got to the front door because her tongue was swelling again. She reported she could not breathe and I injected epinephrine .3mg into outer thigh and had coworker call 911. was transported to Hospital. At 9pm she was still under observation but feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- history of vertigo
- Andere Medikamente
- n/a
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 10.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Hypertension
Interchange of vaccine products
Symptomtext
Systemic: Chest Tightness/Heaviness/Pain-Medium, Systemic: Hypertension-Medium, Additional Details: Patient got a booster of Moderna. His first 2 doses were Pfizer. After the booster was administered he experienced chest tightness, which he described as feeling like having anxiety but he was not anxious. His blood pressure was 146/97. He said his baseline is high but was not sure of the level. He experienced this for about 2.5 hours and is now completely back to normal everyday activities.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Palpitations
Symptomtext
Heart palpitations
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi vitamin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Hypoaesthesia oral
Paraesthesia
Symptomtext
Pt received her booster dose of Moderna on 12/1/21. She called Health Department on 12/3/21 to report a few hours after her booster shot she started experiencing some numbness and tingling around her left eye and left side of her mouth. Pt reports she did not notify her primary care doctor or seek emergency evaluation. Pt reports she still feels like she had lidocaine around the left side of her face. Public Health Nurse advised pt she needs to seek urgent evaluation right away. Pt verbalized understanding and agreed to the plan of care. Public Health Nurse tried to call pt back on 12/7 for follow up however while on the phone the pt said she had to go abruptly since she was at work. Pt did state was still experiencing some of the same symptoms but they seemed to be improving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- urgent eval was advised
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 07.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Chills
Confusional state
Dizziness
Fatigue
Headache
Injection site pain
Muscle spasms
Myalgia
Nausea
Palpitations
Symptomtext
48 hrs * Cold Chills * Stomach Spasms * Nausea * Dizziness * Loss of balance * Confusion * Fatigue * Muscle & headaches * Palpitations * Sore injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Moderna #1
- Staat
- MI
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Paraesthesia
Symptomtext
PATIENT COMPLAINED OF FACIAL TINGLING AFTER 15 MINUTES OF RECEIVING THE VACCINE. 25 MG OF DIPHENHYDRAMINE WAS GIVING ORALLY. PATIENT USED THE RESTROOM AND THEN LEFT AT 2:10PM STATING "SHE IS FINE"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ASPIRIN
- Allergien
- BACTRIM, FELDENE, RELAFEN
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Condition aggravated
Headache
Injection site pain
Myalgia
Nausea
Night sweats
Symptomtext
Moderate injection site pain, worst at 6-7hrs after injection, improving by 9am the next morning. Chills, night sweats, headache, myalgias, nausea started at 4am. All except headache resolved by 9am the next morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Had a mild pharyngitis 3 weeks prior
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- Moderate injection site pain, 25yo, 1/9/21 & 2/6/21, moderna covid vaccine
- Staat
- CT
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 13.11.2023
- Impfdatum
- 10.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Nerve conduction studies
Neuralgia
Pain in extremity
Symptomtext
Bilateral hand numbness and night pain--medial nerve sx saw orth and primary MD symptoms persist
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- 3/24 2022 nerve teasts--outcome--no treatment will help--learn to live with it--which I have using various items to get tasks done
- Aktuelle Erkrankungen
- Psoriati Arthritis
- Vorgeschichte
- previous bilateral knee replacements
- Andere Medikamente
- ASA 81 mgm Crestor 5 mgm Pantoprazole 40 mgm
- Allergien
- Sulfa Emycin Dilaudid Vicodin Renografin Synvisc Lobster Clams Scallops
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 27.04.2023
- Impfdatum
- 11.04.2023
- Beginn
- 25.04.2023
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pruritus
Urticaria
Vaccine positive rechallenge
Symptomtext
I have received 2 booster shots, both the Moderna brand. While I had no significant reaction to either of my initial doses, I think I may be allergic to the booster. My first booster was on 12/27/21 and starting 1/7/22, exactly 2 weeks after, I began having a reaction that consisted of painful and itchy hives all over my body that didn't respond to anything and lasted consistently for about a month following. My second dose of the booster was on 4/11/23 and starting 4/25/23, also exactly 2 weeks later, I developed painful and itchy hives that have not responded to anything. With still being in the presumable month if this follows the first time, I don't know how long it will last.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- I had a doctor's appointment about a week after the hives started in 2022, where I was told to put on lotion and hope for the best. That did not work.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Birth control (vienva) and Vitamin C gummies
- Allergien
- Treenuts
- Vorherige Impfungen
- Described under Item 18, I was 20 at the time of vaccination and 21 at the time of the initial adverse event.
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 06.02.2023
- Impfdatum
- 06.02.2023
- Beginn
- 03.02.2023
- Tage bis Beginn
- -
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Erythema
Joint swelling
Lymphadenopathy
Peripheral swelling
Pyrexia
Tenderness
Symptomtext
Fever over 103 for over 48h Joint redness, tenderness, swelling at 72h (hands and knees with difficulty walking stairs, and I am active) Balance distortion Severe redness with swelling of entire upper L arm, dark reddened area, extremely tender, has appeared adjacent to inj site Axillary lymphadenopathy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- I will have RF, ANA, and CRP drawn at my PCP this week.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HTN hypothyroidism menopause
- Andere Medikamente
- HCTZ 12.5 mg Losartan 100 mg levothyroxine 125mcg Armour thyroid 90mcg Amlodipine 10mg Bio-identical hormone pellets
- Allergien
- Morphine sulfate
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 14.12.2021
- Beginn
- 08.08.2022
- Tage bis Beginn
- 237,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Headache
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Tested positive 08/08/2022 - I had chills with a fever. A headache, sore throat and body aches. Tested positive again 11/07/2022 - I had a headache, a sore throat and mild body aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- at home rapid COVID-19 test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No- doesn't recall
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 13.12.2022
- Impfdatum
- 10.12.2021
- Beginn
- 04.10.2022
- Tage bis Beginn
- 298,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Exposure to SARS-CoV-2
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Started having a sore throat and stuffy nose and little cough. It didn't really get much worse than that. I waited a day I took an at home test and it was negative, but my wife had already been diagnosed with COVID-19. I then went to a clinic and after I got the positive reading a telehealth was scheduled. I was then prescribed PAXLOVID the symptoms didn't get any worse and by the time the medication was gone I had no more issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Amlodipine; meloxicam; vitamin D3; vitamin B12
- Allergien
- N/A
- Vorherige Impfungen
- Flu, chills and fever 2000 or 2001
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 13.12.2021
- Beginn
- 12.11.2022
- Tage bis Beginn
- 334,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Malaise
SARS-CoV-2 test positive
Symptomtext
positive covid test in fully vaccinated, boostered, symptomatic pt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 03.12.2021
- Beginn
- 13.10.2022
- Tage bis Beginn
- 314,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Influenza like illness
Malaise
Maternal exposure before pregnancy
Pregnancy
SARS-CoV-2 test positive
Symptomtext
I woke up not feeling well before going to work so I tested before going to work as I did I have flu like symptoms. I consulted with my doctor which changed the course of my prenatal care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 at home test was positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prenatal vitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 30.09.2022
- Impfdatum
- 07.01.2021
- Beginn
- 27.06.2021
- Tage bis Beginn
- 171,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Abdominal pain
Computerised tomogram abdomen
Full blood count
Lipase
Pancreatitis acute
Pancreatitis chronic
Ultrasound abdomen
Symptomtext
Acute pancreatitis Hospitalized for 2 days Abdominal pain - worsened upon eating Chronic Pancreatitis May 2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 1,0
- Labordaten
- Lipase CBC Abdominal CT scan Abdominal ultrasound
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Zofolt Vitamin D3
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 20.09.2022
- Impfdatum
- 09.12.2021
- Beginn
- 16.09.2022
- Tage bis Beginn
- 281,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chest discomfort
Cough
Fatigue
Headache
Myalgia
Symptomtext
fatigue, cough, myalgias, headaches, chest tightness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 15.12.2021
- Beginn
- 22.01.2022
- Tage bis Beginn
- 38,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Asymptomatic COVID-19
COVID-19
Colitis
Computerised tomogram abdomen abnormal
Constipation
Electrolyte imbalance
Faecal disimpaction
Faecaloma
Nausea
Rectal fissure
SARS-CoV-2 test positive
Surgery
Vomiting
Symptomtext
Moderna Dose 1 2/19/21 (023M20A) Moderna Dose 2 3/19/21 (026A21A) Moderna Dose 3 12/15/21 (029H21B) COVID Positive 2/5/22 2/5/22: 68-year-old male patient with a history of muscular dystrophy, hypertension, s/p pacemaker placement several years ago is wheelchair-bound at home. There is a caretaker who helps him. Patient has been constipated for more than 2 weeks. He has had very little flatus. His abdominal pain has been slowly getting worse. Patient has had some nausea and only 1 episode of vomiting. Since the pain was getting worse, patient came to the hospital for further evaluation. The pain is located in all the quadrants of the abdomen. Patient has not had any bloody stools. He denies any fever/chills associated with abdominal pain. A CT of the abdomen/pelvis shows evidence of significant amount of stool impaction. Surgeon was called from the emergency room for consultation. 2/9/22: 68-year-old male patient with a history of muscular dystrophy, hypertension, s/p pacemaker placement several years ago is wheelchair-bound at home. There is a caretaker who helps him. Patient has been constipated for more than 2 weeks. He had very little flatus. His abdominal pain was slowly getting worse. Patient has had some nausea and only 1 episode of vomiting. Since the pain was getting worse, patient came to the hospital for further evaluation. The pain was located in all the quadrants of the abdomen. Patient had no bloody stools. He denied any fever/chills associated with abdominal pain. A CT of the abdomen/pelvis shows evidence of significant amount of stool impaction. Surgeon was called from the emergency room for consultation. Patient had manual disimpaction of the stool on 02/05 per surgery in the OR. Patient was also noted to have rectal colitis and started on Levaquin and Flagyl. Patient subsequently was able to have bowel movements without difficulty. Patient also had perirectal fissure, wound nurse was consulted. Patient was also tested positive for SARS-CoV-2 infection but he was totally asymptomatic and was not placed on any oxygen. He did not require any treatment with remdesivir or dexamethasone as he did not complain of any shortness of breath. His electrolyte abnormalities were corrected. Patient was stable at the time of discharge. He was discharged home with VNA. He will complete the course of antibiotics as prescribed for treating rectal colitis. I did discuss with the patient's caregiver and all questions were answered. Patient will follow-up with primary care physician in 1 week. Patient was advised high-fiber diet and stool softeners advised to be continued to prevent is further episodes of severe constipation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- muscular dystrophy HTN pacemaker placement wheelchair bound
- Andere Medikamente
- APAP 1000 mg Po QD vitamin D 50 mcg PO QD cyanocobalamin 1000 mcg PO QD docusate 50 mg PO BID lisinopril 5 mg Po QD metoprolol 25 mg PO BID multivitamin 1 tab PO QD
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 28.06.2022
- Impfdatum
- 16.12.2021
- Beginn
- 19.06.2022
- Tage bis Beginn
- 185,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Ear pain
Exposure to SARS-CoV-2
Nasal congestion
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Streptococcus test
Vaccine breakthrough infection
Symptomtext
Breakthrough covid case. Presented to ER with c/o of bilateral ear pain, nasal congestion, sore throat, body aches, cough and exposure to covid. Hx of Moderna vaccine x 3. Prescribed Paxlovid. DC home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- 6/19/22: Cepheid covid test, strep A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- asthma DM2 depression GERD HTN Hyperlipidemia hypothyroidism
- Andere Medikamente
- Albuterol duloxetine mometasone pregabalin acyclovir aspirin artorvastatin citalopram diclofenac na ergocalciferol fluticasone glipizide levothyroxine losartan spironolactone cyanocobalamin ketotifen hydroxyzine loratidine
- Allergien
- amlodipine cipro flagyl hydromorphone medrol meloxicam metformin metronidazole motrin solumedrol
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 22.12.2021
- Beginn
- 30.05.2022
- Tage bis Beginn
- 159,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
COVID-19
Cardiac disorder
Illness
Pain
SARS-CoV-2 test positive
Urticaria
Symptomtext
I now I got a COVID from a party. My symptoms started 2 day after the party. I was weak with body ache. I tested at home and was negative. I tested two days later and was positive. During the sickness I took day quill and night quill. I developed hives and heart complications, post viral reaction. I take prednisone for the hives. And I take hydro steroids' for the hives.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- None
- Andere Medikamente
- Trintellix, bivanes
- Allergien
- None
- Vorherige Impfungen
- Dose 1 of Moderna 12/28/2020 ? Lot# 039K20A ? Left ? Hospital - Recovered I feel like 99 percent. The had gave the shot in my ve
- Staat
- VA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 16.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Oropharyngeal pain
Pyrexia
Quarantine
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I started getting a sore throat, congestion, cough and fever. I decided to test after my son also came down with symptoms and we had been on a two road trip. I used went to a pharmacy clinic and had a PCR COVID 19 test that came back positive. I was told to quarantine for fourteen days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- PCR COVID 19
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Ulcerative Colitis; Pituitary Adenoma; Sleep Apnea
- Andere Medikamente
- Cabergoline; trazadone; mesalamine
- Allergien
- Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 08.12.2021
- Beginn
- 04.06.2022
- Tage bis Beginn
- 178,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Fatigue
Feeling abnormal
Oropharyngeal pain
Pain
Pyrexia
Renal pain
Respiratory tract congestion
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID-19 case: When I woke up my throat was hurting and experienced congestion. Also felt feverish and had body aches. My kidneys felt sore and achy. I had cough, brain fog and fatigue. I took a rapid test and it came back negative. I felt a little better the next day but decided to test again and it still came back negative. I took some Ibuprofen and cough syrup on both days. On Monday 06/06/2022 I still wasn't feeling better so I went to Urgent Care and had a rapid test and a PCR test and I got my results back on 06/08/2022 and it showed I was positive for COVID-19. I was given Claritan D and cough syrup. I'm starting to feel better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 06/04/2022:Rapid test: Negative 06/05/2022: Rapid test: Negative 06/06/2022: Rapid and PCR: Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vyvanse
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 07.12.2021
- Beginn
- 18.05.2022
- Tage bis Beginn
- 162,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Fatigue
Headache
Malaise
Myalgia
Pain in extremity
SARS-CoV-2 test
Symptomtext
I had mild symptoms -- just tiredness and sore arm for a few hours following vaccination. I did not get COVID until 6 months after this dose.... I was very sick for 2 days -- cough, head ache, aching muscles, chills. Day 3 was very tired and cough remained for 7-10 days getting gradually better each day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID home test 5/18
- Aktuelle Erkrankungen
- No illnesses but I had received vaccinations for Yellow Fever and Typhoid about a week before getting sick for upcoming travel... so not sure if my immune system was taxed with those.
- Vorgeschichte
- Mild-Moderate Ulcerative Colitis
- Andere Medikamente
- I did not have an adverse reaction to the vaccination -- I just got COVID and was sick 6 months after my 3rd COVID shot -- or first booster. My current meds had no bearing on this. Someone called me from CDC and asked me to complete this.
- Allergien
- penicillin, peaches, red wine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 25.05.2022
- Impfdatum
- 10.12.2021
- Beginn
- 20.05.2022
- Tage bis Beginn
- 161,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Back pain
COVID-19
Fall
Fatigue
SARS-CoV-2 test positive
Symptomtext
5/17 s/p fall, weakness, fatigue, presented to Emerg. center on 5/20 w weakness, fatigue, and back pain. home test positive for covid on 5/19, tested at hospital PCR on 5/20. Was prescribed Paxlovid on 5/19-5/24 as op, Unclear if actually given. in hospital treated w decadron and remdesivir
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- covid home test on 5/19 and covid PCR on 5/20 positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension, diabetes, hx stroke, s/p hip replacement, COPD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 17.12.2021
- Beginn
- 19.05.2022
- Tage bis Beginn
- 153,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Malaise
SARS-CoV-2 test positive
Symptomtext
Up to date with vaccination admitted to hospital with symptomatic COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 3,0
- Labordaten
- COVID PCR pos 5/19/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 28.01.2021
- Beginn
- 09.05.2022
- Tage bis Beginn
- 466,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood pressure increased
COVID-19
Cough
Diarrhoea
SARS-CoV-2 test positive
Symptomtext
WEAKNESS, DIARRHEA, ELEVATED BLOOD PRESSURE, COUGH,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- POSITIVE COVID TEST
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Impaired fasting glucose 6/13/2005 Panhypopituitarism (HRC) 10/13/2010 Cognitive Disorder NOS 10/15/2010 HTN (hypertension) (ACG) 7/7/2012 Hyperlipidemia 6/7/2003 Cesarean Delivery 5/11/2004 Craniopharyngioma 10/18/2005 cranial radiation 2005 Hyperprolactinemia 5/18/2006 Pulmonary Nodule 6/20/2006 Bursitis Pes Anserine 3/30/2007 DJD Knee 3/30/2007 Obesity 3/30/2007 Vertigo 8/26/2010 Herpes Zoster NOS 1/7/2011 TIA (transient ischemic attack) Memory impairment (HRC) Stroke (HRC) 8/2015 L frontal lobe, R sided weakness Acute respiratory failure (HRC) 11/22/2010 Stroke (HRC) 2/9/2017 L MCA stroke, Infected prosthetic knee joint (HRC)
- Andere Medikamente
- B COMPLEX-C OR Multiple Vitamins-Minerals (THERA-M) ALBUterol sulfate HFA 108 (90 Base) MCG/ACT inhaler magnesium hydroxide (MILK OF MAGNESIA) 400 MG/5ML suspension calcium citrate-vitamin D (CITRACAL+D) 315-200 MG-UNIT ta
- Allergien
- Ibuprofen Statins-Hmg-Coa Reductase Inhibitors
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Peripheral swelling
Symptomtext
Worsened swelling in toes and fingers and hand pain, felt to be pesudogout.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, hypercholesterolemia, impaired fasting glucose, osteoarthritis, pseudogout
- Andere Medikamente
- -
- Allergien
- Ciprofloxacin, colchicine, keflex
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 07.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Pruritus
Sensation of foreign body
Urticaria
Symptomtext
I woke up on the 17th of December 2021, with an itching scalp. The next day, I started getting hive like bumps all over my body. It was getting worse as the day went on so I did a telehealth visit and they prescribed me Zyrtec, but it just kept getting worse. Later, it started to feel like I had a chunk of apple stuck in my throat and went to urgent care and they gave me liquid steroid and a Benadryl and that helped a lot! They prescribed more antihistamines and steroids, but I was just taking Zyrtec and eventually I was able to ween myself off of the Zyrtec after about a month and a half.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Blood Panel
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Magnesium Zinc, B Complex, Liquid B12 Complex, Liquid Vitamin D complex
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 09.12.2021
- Beginn
- 13.01.2022
- Tage bis Beginn
- 35,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blindness
Immunisation reaction
Infection
Ophthalmic herpes simplex
Pain
Symptomtext
Herpes Simplex virus that was in my right eye became very active casuing substantial pain, loss of vision and infection on the surface and below the surface. My cornea transplant surgeon and I determine the covid booster activated the virus. Months of treatment later and i still don't have the vision I had prior to the booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Opthamalogy appointments 3/24/22, 3/4/22, 2/24/22, 2/18/22, and 2/2/22
- Aktuelle Erkrankungen
- kerataconus, cornia transplant recovery
- Vorgeschichte
- kerataconus
- Andere Medikamente
- valacyclovir 500 mg, loteprednol eye drops, OTC tears
- Allergien
- sulpha
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 10.12.2021
- Beginn
- 06.04.2022
- Tage bis Beginn
- 117,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chills
Cough
Pyrexia
Symptomtext
chills, fever, cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 4/6/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 14.04.2022
- Impfdatum
- 01.12.2021
- Beginn
- 03.03.2022
- Tage bis Beginn
- 92,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Pyrexia
Respiratory tract congestion
Symptomtext
Patient presented to the hospital with fever and was found to have COVID. Had fever and congestion a week prior. Given 2L NC and steriods.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HF, diabetes, HLD, NSTEMI, ESRD, CAD
- Andere Medikamente
- asa, lantus, lidocaine-prilocaine,
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 20.04.2021
- Beginn
- 20.04.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Influenza like illness
Injection site pain
Pain
Pyrexia
Vaccine positive rechallenge
Symptomtext
I experienced injection site soreness, fever, chills, body aches, fatigue, and general flu like symptoms. These symptoms lasted for just over 48 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Narcolepsy
- Andere Medikamente
- Methylphenidate; Zyrtec; D Vitamin; Spironolactone; Vitamin D3
- Allergien
- Macrodantin; Vicodin
- Vorherige Impfungen
- Same reaction to Moderna Dose 1 although milder.
- Staat
- NJ
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 01.12.2021
- Beginn
- 23.03.2022
- Tage bis Beginn
- 112,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Diarrhoea
Fatigue
Injection site discolouration
Injection site induration
Injection site mass
Injection site pain
Injection site swelling
Joint swelling
Pyrexia
Urticaria
Vomiting
Symptomtext
Injection site swelling, burning and hard raised lump for 2 weeks that darkened on second week. Hives down left arm and left chest within 24 hours. Fever of 101.2?F for 72 hours post injection. Joint swelling and pain, especially on left-side of body. Vomiting and diarrhea for 72 hours post injection. Extreme fatigue for 1 week post injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Mushroom, yellow #6, Cephalexin, Codeine, Penicillin, Cipro antibiotics, pollen, animal dander/hair and mold
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 19.03.2022
- Impfdatum
- 05.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Erythema
Immune system disorder
Immunisation reaction
Impaired work ability
Pruritus
Swelling
Swelling face
Urticaria
Symptomtext
I couldn't go out and work with these side effects.; side effects my immune system is reacting worse to the Moderna covid booster shot; immune system affected; not sure why exactly I got this reddish swelling on my face,started on my neck, shoulders, hands, thighs, hands, and forearms; not sure why exactly I got this reddish swelling on my face,started on my neck, shoulders, hands, thighs, hands, and forearms; not sure why exactly I got this reddish swelling on my face,started on my neck, shoulders, hands, thighs, hands, and forearms; feels burning; itching; getting hives,I didn't recover from hives.,everyday hives,Everyday I am getting hives at different times, hives at least one time in a day.; This spontaneous case was reported by a consumer and describes the occurrence of SWELLING FACE (not sure why exactly I got this reddish swelling on my face,started on my neck, shoulders, hands, thighs, hands, and forearms), ERYTHEMA (not sure why exactly I got this reddish swelling on my face,started on my neck, shoulders, hands, thighs, hands, and forearms), SWELLING (not sure why exactly I got this reddish swelling on my face,started on my neck, shoulders, hands, thighs, hands, and forearms), BURNING SENSATION (feels burning) and PRURITUS (itching) in a 32-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 05-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Jan-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced SWELLING FACE (not sure why exactly I got this reddish swelling on my face,started on my neck, shoulders, hands, thighs, hands, and forearms), ERYTHEMA (not sure why exactly I got this reddish swelling on my face,started on my neck, shoulders, hands, thighs, hands, and forearms) and SWELLING (not sure why exactly I got this reddish swelling on my face,started on my neck, shoulders, hands, thighs, hands, and forearms). In January 2022, the patient experienced BURNING SENSATION (feels burning), PRURITUS (itching) and URTICARIA (getting hives,I didn't recover from hives.,everyday hives,Everyday I am getting hives at different times, hives at least one time in a day.). On an unknown date, the patient experienced IMPAIRED WORK ABILITY (I couldn't go out and work with these side effects.), VACCINATION COMPLICATION (side effects my immune system is reacting worse to the Moderna covid booster shot) and IMMUNE SYSTEM DISORDER (immune system affected). The patient was treated with HYDROXYZINE HCL at a dose of for 1 month; CETIRIZINE HYDROCHLORIDE (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) at an unspecified dose and frequency and TRIAMCINOLONE ACETONIDE (KENALOG [TRIAMCINOLONE ACETONIDE]) on 15-Feb-2022 for Hives, at a dose of took shot for hives. At the time of the report, SWELLING FACE (not sure why exactly I got this reddish swelling on my face,started on my neck, shoulders, hands, thighs, hands, and forearms), ERYTHEMA (not sure why exactly I got this reddish swelling on my face,started on my neck, shoulders, hands, thighs, hands, and forearms), SWELLING (not sure why exactly I got this reddish swelling on my face,started on my neck, shoulders, hands, thighs, hands, and forearms), BURNING SENSATION (feels burning), PRURITUS (itching), IMPAIRED WORK ABILITY (I couldn't go out and work with these side effects.) and VACCINATION COMPLICATION (side effects my immune system is reacting worse to the Moderna covid booster shot) had not resolved and IMMUNE SYSTEM DISORDER (immune system affected) and URTICARIA (getting hives,I didn't recover from hives.,everyday hives,Everyday I am getting hives at different times, hives at least one time in a day.) was resolving. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant products were not provided. It was reported that patient went to a dermatologist and on her first visit, the doctor said it is due to booster shot side effects. He explained about side effects her immune system was reacting worse to the Moderna covid booster shot. The doctor suggested to take steroid(Kenalog) shot. Everyday she was experiencing hives at different times. This case was linked to MOD-2022-512781 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 16-Mar-2022: Follow-up received contains significant information- event added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 11.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Neck mass
Pain
Swelling
Symptomtext
About two or three days after the vaccine I felt a lump under my chin almost to my neck. So I made a appointment to see my primary care doctor and he advised that it could be a reaction from the vaccine. The doctor said that we would keep a eye on it for now and come back in May for a follow up. If I come back and the bump is still there he will then send me out to have biopsy. I've notice that it will feel big at times like it has increased in size and other times it will feel like smaller in size. There are some days when I feel slight pain more of a discomfort feeling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Losartan 25mg, Hydrochlorothiazide 12.5mg, Singulair 10mg, Vitamin D 5,000mg, Turmeric, Fish Oil, Magnesium
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 15.03.2022
- Impfdatum
- 11.12.2021
- Beginn
- 09.02.2022
- Tage bis Beginn
- 60,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Diarrhoea
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I got Covid after Dose 3 started experiencing congestion and diarrhea. About a week later I was treated for a cough and my symptoms lasted for a week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Rapid (results positive)
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma; Fibromyalgia; Migraines
- Andere Medikamente
- Topamax, Effexor, Buspar
- Allergien
- WELLBUTRIN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 04.12.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Diarrhoea
Muscle spasms
Symptomtext
Bad cramps followed by diarrhea for 10 days, never had strange stomach pains like that.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Vertigo
- Vorgeschichte
- Allergies
- Andere Medikamente
- Zyrtec, Prilosec, Lo Loestrin FE, calcium supplements, multi vitamin, turmeric supplement
- Allergien
- Sulfa drugs, peanuts, eggs
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 06.12.2021
- Beginn
- 18.02.2022
- Tage bis Beginn
- 74,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Cough
Fatigue
Malaise
Oropharyngeal pain
SARS-CoV-2 test negative
Symptomtext
I was very fatigued. Then, I had a sore throat, and bad cough. Then, I took a home COVID-19 test, negative result. The next day, I still was not feeling well. I still had the bad cough, sore throat, and fatigue. Then later that day, I lost my taste. After 4 days, my taste came back. I took a total of 4 COVID-19 tests, all negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test.
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- Blisovi, Citalopram, Valacyclovir
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 07.03.2022
- Impfdatum
- 03.12.2021
- Beginn
- 12.01.2022
- Tage bis Beginn
- 40,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antinuclear antibody increased
Arthralgia
Autoimmune disorder
Blood test
COVID-19
Dizziness
Hypoaesthesia
Nasal congestion
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
COVID symptoms started 01/12/2022 with sore throat. On the 13th and 14th, the sore throat started to get worse, and on the 14th he had a low grade fever. On the 15th he received the positive COVID test and his fever was gone that day. 01/17/22 the symptoms were better. He also had a little bit of nose congestion. The 21st he had the antigen test, and it was negative. The COVID test was on the 15th. 1 month after being fully recovered he had finger numbness, joint pain, and dizziness. He seen his doctor and did some tests and said his ANA antibody was high which indicated an auto immune disorder. He is still experiencing those symptoms. He is seeing immunology today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- COVID (01/15/22), Antigen (01/21/22), Bloodwork (01/21/22)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 1 Diabetes
- Andere Medikamente
- Insulin, Fiber, Probiotic
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 20.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chronic spontaneous urticaria
Pruritus
Urticaria
Symptomtext
Chronic spontaneous urticaria (CSU) developed 11 or 12 days after getting the booster and it still has not gone away. I went to a clinic, where they thought it was scabies but it did not improve with treatment. I then went to my dermatologist, Dr who also couldn?t pin point what caused it. She prescribed me 20 mg Zyrtec daily to help with the constant itching. I finally realized what the cause was when I began talking with others online who had the same condition and their doctors were attributing it to the moderns booster. Symptoms are intense itchyness and hives constantly throughout the day and night. I?ve never had hives before, and have never had an allergic reaction to anything.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chronic spontaneous urticaria
- Hospital-Tage
- -
- Labordaten
- Scabies treatment on 1/5/22, did not help my condition. Dermatologist visit on 2/7/22, I was prescribed 20 mg Zyrtec daily which has helped improve my symptoms.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Celiac disease
- Andere Medikamente
- Celexa 10mg daily, birth control daily.
- Allergien
- I have celiac disease, gluten.
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 08.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Dizziness
Interchange of vaccine products
Joint swelling
Peripheral swelling
Pyrexia
Ultrasound scan
Symptomtext
The swelling occurred in both in her right and left elbows; Both arms also have swelling on the outer side of the divet of the elbow. The swelling was the diameter of a golf ball and stuck out about 1 centimeter from the arm; running a low grade fever ever since she received the booster dose; Interchange of vaccine products; patient was dizzy for 7 weeks after getting the booster dose; This spontaneous case was reported by a consumer and describes the occurrence of JOINT SWELLING (The swelling occurred in both in her right and left elbows) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) 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 vaccine and pfizer vaccine. Past adverse reactions to the above products included No adverse event with pfizer vaccine and pfizer vaccine. Concurrent medical conditions included Autoimmune disorder, Hashimoto's disease, Chronic fatigue syndrome and Lyme disease (Lyme disease neurological involvement). On 08-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Dec-2021, the patient experienced PYREXIA (running a low grade fever ever since she received the booster dose) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). In December 2021, the patient experienced DIZZINESS (patient was dizzy for 7 weeks after getting the booster dose). On 29-Dec-2021, the patient experienced JOINT SWELLING (The swelling occurred in both in her right and left elbows) (seriousness criterion medically significant) and PERIPHERAL SWELLING (Both arms also have swelling on the outer side of the divet of the elbow. The swelling was the diameter of a golf ball and stuck out about 1 centimeter from the arm). On 08-Dec-2021, INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) had resolved. In January 2022, DIZZINESS (patient was dizzy for 7 weeks after getting the booster dose) had resolved. At the time of the report, JOINT SWELLING (The swelling occurred in both in her right and left elbows) and PERIPHERAL SWELLING (Both arms also have swelling on the outer side of the divet of the elbow. The swelling was the diameter of a golf ball and stuck out about 1 centimeter from the arm) outcome was unknown and PYREXIA (running a low grade fever ever since she received the booster dose) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood test: normal (normal) normal. On an unknown date, Ultrasound scan: normal (normal) normal. The patient had a Moderna Booster dose on 08-Dec-2021 following her primary series of the Pfizer vaccine. On 29-DEC-2021 the patient first noticed a swelling on the inside of her right elbow. The swelling occurred on the body side of the divet of the elbow. A few hours later swelling started on the left elbow. The patient believed that the swelling was linked to the booster dose. The patients Orthopedics surgeon believed that the swelling was connected to the Moderna booster shot. No Concomitant medications were reported. No treatment medications were reported. Company comment. This spontaneous case concerns a 55 ? year ? old, female patient with relevant medical history of Lyme disease, who experienced the unexpected serious important medical event of joint swelling. Since the patient received the booster dose of mRNA-1273 vaccine, she experienced low graded fever. Three weeks later, she first noticed swelling on her right elbow, and a few hours later swelling started on the opposite side. Both arms also were swelling. The patient consulted an orthopedic surgeon, blood tests and ultrasound were performed with normal result. It is mentioned she had dizziness during 7 weeks after mRNA ? 1273 dose. No treatment is reported. The mentioned medical history could be a confounder. The patient previously had two doses of Pfizer COVID vaccine. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 55 ? year ? old, female patient with relevant medical history of Lyme disease, who experienced the unexpected serious important medical event of joint swelling. Since the patient received the booster dose of mRNA-1273 vaccine, she experienced low graded fever. Three weeks later, she first noticed swelling on her right elbow, and a few hours later swelling started on the opposite side. Both arms also were swelling. The patient consulted an orthopedic surgeon, blood tests and ultrasound were performed with normal result. It is mentioned she had dizziness during 7 weeks after mRNA ? 1273 dose. No treatment is reported. The mentioned medical history could be a confounder. The patient previously had two doses of Pfizer COVID vaccine. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Test Name: bloodwork; Result Unstructured Data: normal; Test Name: ultrasound; Result Unstructured Data: normal
- Aktuelle Erkrankungen
- Autoimmune disorder; Chronic fatigue syndrome; Hashimoto's disease; Lyme disease (Lyme disease neurological involvement)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site pain
Symptomtext
sore injection site left arm; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (sore injection site left arm) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 vaccination. Previously administered products included for Drug use for unknown indication: Pfizer vaccine (Patient received the Pfizer vaccine for primary vaccination series) and Pfizer vaccine. Past adverse reactions to the above products included No adverse drug reaction with Pfizer vaccine and Pfizer vaccine. On 08-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Dec-2021, the patient experienced VACCINATION SITE PAIN (sore injection site left arm). At the time of the report, VACCINATION SITE PAIN (sore injection site left arm) outcome was unknown. Concomitant medications and treatment information were not provided by reporter. The patient had a sore injection site left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Back pain
Pain
Renal pain
Urinary incontinence
Symptomtext
Severe mid back pain slightly to the left (kidney) combined with urinary incontinence developed on day six after vaccine and continues now into day 10.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- anemia
- Vorgeschichte
- ulcerative colitis
- Andere Medikamente
- none
- Allergien
- Night shades, shellfish
- Vorherige Impfungen
- Debilitating fatigue unable to perform ADLs or work, all over wondering inflammatory pain.
- Staat
- CT
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 10.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 20,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Mechanical urticaria
Peripheral swelling
Pruritus
Urticaria
Symptomtext
Dermatographia, burning and itching sensation in hands and feet, swollen forearms, hives. Taken a course of MethylPREDNISolone and Loratadine with no or little effect.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Non
- Vorgeschichte
- Non
- Andere Medikamente
- Non
- Allergien
- Non
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Symptomtext
Patient is reporting pain in elbow joint. Has had pain since 01/05/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Herpes zoster
Rash
Symptomtext
initially started as a burning sensation on the left side of his body; rashes starting to come out; shingles really bad; This spontaneous case was reported by a consumer and describes the occurrence of HERPES ZOSTER (shingles really bad), BURNING SENSATION (initially started as a burning sensation on the left side of his body) and RASH (rashes starting to come out) in a 45-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 vaccination. No Medical History information was reported. On 06-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Jan-2022, the patient experienced HERPES ZOSTER (shingles really bad) and RASH (rashes starting to come out). On an unknown date, the patient experienced BURNING SENSATION (initially started as a burning sensation on the left side of his body). At the time of the report, HERPES ZOSTER (shingles really bad), BURNING SENSATION (initially started as a burning sensation on the left side of his body) and RASH (rashes starting to come out) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant product use was not provided by the reporter. Patient was prescribed with an antiviral. Reportedly, Patient went to an immediate care clinic. Additionally, It was reported that patients second dose of vaccine was schedule on 03-Feb-2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 04.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Symptomtext
A week after the 3rd dose, I got full body hives. They are still happening. I am only taking ZYRTEC to subdue the itchiness. I did see Dr. on December 30, 2021, she recommended higher dose of ZYRTEC and recommended PEPCID and she did prescribe Prednisone. Prednisone did not help. She has recommended to continue the higher dose of ZYRTEC 3-4 OTC 10mg so 30 mgs daily and continue taking PEPCID. I will schedule a follow-Up soon. I still have the hives.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- The only thing I was taking was BP CHARLOTTE 24 FE I have been taking that last 5 years.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
Asthenia
Hypersomnia
Illness
Malaise
Nausea
Pyrexia
SARS-CoV-2 test
Vaccination site erythema
Vaccination site warmth
Symptomtext
was not feeling well/did not feel good; was sleeping 18-20 hours a day; was still very sick/is seriously ill, has serious illness; Had no taste; No smell; Had no energy; Fever/patient ran fever on/off/ran high fever; Nauseous; her arm turned hot that evening/it was hot to the touch; arm was red hot; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (her arm turned hot that evening/it was hot to the touch), MALAISE (was not feeling well/did not feel good), HYPERSOMNIA (was sleeping 18-20 hours a day), ILLNESS (was still very sick/is seriously ill, has serious illness) and AGEUSIA (Had no taste) in a 19-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 28-Dec-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Dec-2021, the patient experienced VACCINATION SITE WARMTH (her arm turned hot that evening/it was hot to the touch) and VACCINATION SITE ERYTHEMA (arm was red hot). On an unknown date, the patient experienced MALAISE (was not feeling well/did not feel good), HYPERSOMNIA (was sleeping 18-20 hours a day), ILLNESS (was still very sick/is seriously ill, has serious illness), AGEUSIA (Had no taste), ANOSMIA (No smell), ASTHENIA (Had no energy), PYREXIA (Fever/patient ran fever on/off/ran high fever) and NAUSEA (Nauseous). At the time of the report, VACCINATION SITE WARMTH (her arm turned hot that evening/it was hot to the touch), MALAISE (was not feeling well/did not feel good), HYPERSOMNIA (was sleeping 18-20 hours a day), AGEUSIA (Had no taste), ANOSMIA (No smell), ASTHENIA (Had no energy), VACCINATION SITE ERYTHEMA (arm was red hot) and NAUSEA (Nauseous) outcome was unknown and ILLNESS (was still very sick/is seriously ill, has serious illness) and PYREXIA (Fever/patient ran fever on/off/ran high fever) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In December 2021, SARS-CoV-2 test: negative (Negative) A negative test prior to the 1st dose of Moderna vaccine. On an unknown date, SARS-CoV-2 test: negative (Negative) Went it to get the covid-19 test again and it was negative and negative (Negative) Negative. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No Concomitant product use was reported. The reporter was calling on behalf of their daughter who was the patient and stated that after the patient received the 1st dose of the Moderna vaccine, their arm turned hot that evening, arm was red hot, it was hot to the touch, started with a fever and was not feeling well. The reporter stated that the patient had a negative test prior to the 1st dose of Moderna vaccine as the patient was exposed to someone on 22-Dec-2021. The reporter stated that the patient did not feel good, went it to get the covid-19 test again and it was negative. The daughter went to the urgent care as she was still very sick, and the urgent care told the patient to go to the hospital to get a swab test. The patient ran fever on/off, had no taste, no smell, nauseous, had no energy and was sleeping 18-20 hours a day which stated was not like patient. The patient went for a 4th test as the patient had all the symptoms of Covid-19 and the test was also negative on the 4th try. The reporter stated that the patient was seriously ill and was going back to work or else patient could lose their job. The reporter stated that this had lasted 9 days, and all the patient's symptoms coincide with the Covid virus, was seriously ill, had serious illness and ran high fever. No treatment information was provided. Company comment:This is a case concerning a 19-year-old female patient with no medical history provided, who experienced the unexpected AESI events of Hypersomnia, Ageusia, Anosmia and other nonserious events. These events occurred on unknown date after patient received the first dose of mRNA-1273. There is no medical assessment or treatment has been informed and outcome was reported as unknown. Reportedly, SARS-CoV-2 test was negative which was done on unknown date prior to vaccination and on unknown date after the vaccination. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Sender's Comments: This is a case concerning a 19-year-old female patient with no medical history provided, who experienced the unexpected AESI events of Hypersomnia, Ageusia, Anosmia and other nonserious events. These events occurred on unknown date after patient received the first dose of mRNA-1273. There is no medical assessment or treatment has been informed and outcome was reported as unknown. Reportedly, SARS-CoV-2 test was negative which was done on unknown date prior to vaccination and on unknown date after the vaccination. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 test; Test Result: Negative ; Result Unstructured Data: Went it to get the covid-19 test again and it was negative; Test Name: Covid-19 test; Test Result: Negative; Result Unstructured Data: Negative; Test Date: 202112; Test Name: Covid-19 test; Test Result: Negative; Result Unstructured Data: A negative test prior to the 1st dose of Moderna vaccine.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Maternal exposure during breast feeding
Pain in extremity
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Pain in the left arm with 1st shot) and MATERNAL EXPOSURE DURING BREAST FEEDING (Patient breastfeeding administered with first 2 shots) in a 29-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 vaccination. Concomitant products included MAGNESIUM and ZINC for Supplementation therapy. On 26-Dec-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Dec-2021, the patient experienced MATERNAL EXPOSURE DURING BREAST FEEDING (Patient breastfeeding administered with first 2 shots). On 27-Dec-2021, the patient experienced PAIN IN EXTREMITY (Pain in the left arm with 1st shot). On 26-Dec-2021, MATERNAL EXPOSURE DURING BREAST FEEDING (Patient breastfeeding administered with first 2 shots) had resolved. On 29-Dec-2021, PAIN IN EXTREMITY (Pain in the left arm with 1st shot) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment medication use was not provided by the reporter. Patient had accidentally got second dose on 10Jan2022, 2 weeks after first shot, earlier and out of the normal indications to get vaccinated, 1 month apart. She realized of that mistake and went to see 3 different physicians to ask them if there was anything wrong about it. All of the 3 HCPs told her there was no problem. Still, she was concern and mentioned currently breastfeeding when vaccinated and experienced just pain in left arm 1 day following vaccination, and it stopped 1 or 2 days after every shot. This case was linked to MOD-2022-449534 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- MAGNESIUM; ZINC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 11.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Pruritus
Symptomtext
Severe itching and Dermotographia beginning 14 days after vaccine. Severe itching for 7 days. Dermotographia is ongoing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Lymphadenopathy
Musculoskeletal pain
Pain
Spinal pain
Tenderness
Symptomtext
Chills, fatigue, severe body aches especially shoulder blade and up spine for 24 hours. Enlarged lymph node in neck on side where injection was. That lasted 3 days. Sore to touch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hashimotos Asthma
- Andere Medikamente
- Metformin Levothyroxine Daily vitamin
- Allergien
- Amoxicillin Orange juice Dye Yellow Lake 6 and Yellow 6
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Nausea
Pain
Pyrexia
Symptomtext
Fever, chills, body ache, bad headache, nausea. 36 hours in bed. No eating, no meds
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Successful A-fib with ablation 10 months ago
- Andere Medikamente
- Atorvastatin. Eliquis Calcium. Vitamin B. Flaxseed oil
- Allergien
- Hydralazine
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pain
Injection site pruritus
Injection site warmth
Symptomtext
Pain, redness, warm at injection site and Itching x 5 days. Tylenol helped to sleep at night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lisinopril Levothyroxine Estratest
- Allergien
- Tetanus toxoid Down/feathers Codeine
- Vorherige Impfungen
- Tetanus toxoid - anaphylaxis, 19 years old (1971)
- Staat
- VA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Inappropriate schedule of product administration
Myalgia
Pyrexia
Symptomtext
Inappropriate schedule of vaccine administered; Tiredness; Body aches; Fever; This spontaneous case was reported by a consumer and describes the occurrence of FATIGUE (Tiredness), MYALGIA (Body aches), PYREXIA (Fever) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) in a 35-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029h21b) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer (1st dose) on 03-May-2021 and Pfizer (2nd dose) on 24-May-2021. Past adverse reactions to the above products included No adverse event with Pfizer and Pfizer. Concomitant products included VITAMINS NOS for an unknown indication. On 23-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In December 2021, the patient experienced FATIGUE (Tiredness), MYALGIA (Body aches) and PYREXIA (Fever). On 23-Dec-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). On 23-Dec-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. At the time of the report, FATIGUE (Tiredness), MYALGIA (Body aches) and PYREXIA (Fever) had not resolved. No medical history was provided by the reporter. The patient reported following vaccination with the booster dose, the patient started to experience tiredness, body aches, fever and stated that the symptoms were ongoing. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- VITAMINS NOS.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 26.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Rash
Symptomtext
10 days after Moderna covid booster i developed a rash like condition when pressure or scratched on skin. It was diagnosed as dermatographia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- Scratched skin
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Delirium
Fatigue
Gait disturbance
Joint swelling
Myalgia
Pain in extremity
Peripheral swelling
Symptomtext
muscle and joint pain, delirious, exhausted for 3 days. Then swelling and pain in left hand, hip, and knee with difficulty walking. Now I have terrible swelling and pain in left ball of foot and can't walk.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- migraines
- Andere Medikamente
- Metropolol, Cymbalta, Pregabalin, Lithium
- Allergien
- Soy, mold
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Hyperhidrosis
Immediate post-injection reaction
Injection site reaction
Lymph node pain
Lymphadenopathy
Myalgia
Oropharyngeal pain
Pain
Pyrexia
Swelling
Tonsillar hypertrophy
Symptomtext
Muscle soreness at the administration site began almost immediately after vaccination and got worse as the day went on. It was still present, but milder the next day, and completely resolved on day 3 after vaccination. Approximately 100 degree fever, chills, and headache started around 6 hours after vaccination and lasted for at least 7 hours until bedtime. Woke up during the night with sweats. The fever, headache, chills and sweats were gone upon waking up the next morning. Around bedtime that same night on the day of vaccination, throat began mild aching. The mild aching progressed into a sore throat the next day with swollen tonsils and neck lymph nodes. The swelling and pain steadily got worse until the 5th day of symptoms, when the swollen lymph nodes also ached. On day 6 (today), the pain and swelling are marginally less than the previous day, but it is yet unclear if this indicates a trend to recovery. The pain and swelling fluctuate throughout the day and respond well to NSAIDs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- No testing done for AEs.
- Aktuelle Erkrankungen
- Mild food poisoning that resolved day of vaccination
- Vorgeschichte
- Nummular dermatitis, folliculitis
- Andere Medikamente
- Tri-luma cream
- Allergien
- -
- Vorherige Impfungen
- Pfizer COVID-19 vaccine, both doses, in April and May 2021. Aged 22. Strong headache that did not respond to NSAIDs lasting appr
- Staat
- NY
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Symptomtext
Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Pain in jaw
Parotitis
Swelling face
Symptomtext
-Left jaw pain/swelling -> acute parotitis -Left neck lymph node swelling -> acute cervical lymphadenopathy Onset of symptoms occurred within 24 hours of Moderna Booster Vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in jaw
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes Hypothyroidism, Hypertension, Lupus
- Andere Medikamente
- cyclobenzaprine HCl; diclofenac sodium; diltiazem HCl; duloxetine HCl; Ajovy Autoinjector; gabapentin; hydroxychloroquine sulfate; levothyroxine sodium; lovastatin; metformin HCl; naproxen; olanzapine; omeprazole; ondansetron; propranolol H
- Allergien
- Lisinopril
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Pain in jaw
Parotitis
Swelling face
Symptomtext
-Left jaw pain/swelling -> acute parotitis -Left neck lymph node swelling -> acute cervical lymphadenopathy Onset of symptoms occurred within 24 hours of Moderna Booster Vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in jaw
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes Hypothyroidism, Hypertension, Lupus
- Andere Medikamente
- cyclobenzaprine HCl; diclofenac sodium; diltiazem HCl; duloxetine HCl; Ajovy Autoinjector; gabapentin; hydroxychloroquine sulfate; levothyroxine sodium; lovastatin; metformin HCl; naproxen; olanzapine; omeprazole; ondansetron; propranolol H
- Allergien
- Lisinopril
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Oral pain
Vomiting
Symptomtext
He had a sore mouth. Vomit about 4 to 5 times and also had diarrhea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Benazepril, Nexium, HCTZ, aspirin
- Allergien
- mushrooms
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cheilitis
Feeding disorder
Pain
Stomatitis
Symptomtext
Her mouth on the right side broke out in sores. She could not wear her top teeth. The sore came out on her lips upper and lower. Very painful and also on the right side of her nose. She couldn't eat. She called her doctor and her prescribed her some antibiotics and after a few days it started to heal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Pregabalin, Levothyroxine, Amlodapine, HCTZ, Primaren, Nortriptyline, baby aspirin
- Allergien
- codeine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Hyperhidrosis
Induration
Injection site pain
Injection site swelling
Pain in extremity
Peripheral swelling
Pyrexia
Skin warm
Symptomtext
Pain, extreme swelling at injection site. Skin hard and hot to the touch. Fever, chills, sweating. Outcome is my arm is still extremely swollen, painful, hard, red, hot amd still feverish
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Atorvastatin 80mg Iron bid Aspirin 81 mg
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pustule
Injection site swelling
Soft tissue infection
Symptomtext
Patient's left deltoid injection site has a red raised bump and the redness traveled down to the elbow. There was also a small pustule at the injection site. Sent her to doctor who sent her to ER to rule out need for bloodwork. Was diagnosed with tissue infection from vaccine administration and prescribed cephalexin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- diabetes, hyperlipidemia, hypertension
- Andere Medikamente
- metformin, irbesartan, rosuvastatin, levothyroxine, hydrocortisone and clobetasol for flares prn
- Allergien
- sulfa
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Injection site discolouration
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Received vaccine booster on 12/13/21, last night when patient was getting ready for bed, she noticed redness, warmth, swelling, purple/blueish area (not at vaccine injection site) but to the side of it. The site is itchy. She is concerned she has cellulitis. This nurse advised her to contact her PCP for a visit or telehealth visit, etc. Advised to use ice on/off, hydrocortisone/benadryl cream, benadryl oral for itching. No difficulty breathing, shortness of breath, tongue swelling, hives, etc.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discolouration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 12.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Patient called on 12/15/2021 to report arm side effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Inappropriate schedule of product administration
Nausea
Vomiting
Symptomtext
started experiencing headaches, nausea, and vomiting; started experiencing headaches, nausea, and vomiting; started experiencing headaches, nausea, and vomiting; Husband reported his wife received the MODRNA booster dose on 09-Dec-2021/first PFIZER dose on 20-Jan-2021/ second PFIZER dose on 12-Feb-2021; This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (started experiencing headaches, nausea, and vomiting), NAUSEA (started experiencing headaches, nausea, and vomiting), VOMITING (started experiencing headaches, nausea, and vomiting) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Husband reported his wife received the MODRNA booster dose on 09-Dec-2021/first PFIZER dose on 20-Jan-2021/ second PFIZER dose on 12-Feb-2021) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer (The IM injection was given into the right arm with lot number EL9263.) on 20-Jan-2021 and Pfizer (The IM injection was given into the right arm with lot number EN2601.) on 12-Feb-2021. Past adverse reactions to the above products included No adverse event with Pfizer and Pfizer. On 09-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Dec-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Husband reported his wife received the MODRNA booster dose on 09-Dec-2021/first PFIZER dose on 20-Jan-2021/ second PFIZER dose on 12-Feb-2021). On 10-Dec-2021, the patient experienced HEADACHE (started experiencing headaches, nausea, and vomiting), NAUSEA (started experiencing headaches, nausea, and vomiting) and VOMITING (started experiencing headaches, nausea, and vomiting). On 09-Dec-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Husband reported his wife received the MODRNA booster dose on 09-Dec-2021/first PFIZER dose on 20-Jan-2021/ second PFIZER dose on 12-Feb-2021) had resolved. At the time of the report, HEADACHE (started experiencing headaches, nausea, and vomiting), NAUSEA (started experiencing headaches, nausea, and vomiting) and VOMITING (started experiencing headaches, nausea, and vomiting) outcome was unknown. Patient has no known food or drug allergies. Concomitant medications include Vitamins. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Axillary pain
Fatigue
Infection
Lymph node pain
Myalgia
Pruritus
Vaccination site erythema
Vaccination site mass
Vaccination site pain
Vaccination site warmth
Symptomtext
looked like an infection; itchy; warm and hot to the touch; bump/red bumpy circle; it hurt all the way to the armpit/the whole shoulder and armpit area hurt quite significantly; red patch/path started growing on vaccine site; pain spread to the lymph nodes in my armpit; whole shoulder hurt quite significantly; It was sore; fatigue; body aches; This spontaneous case was reported by a consumer and describes the occurrence of INFECTION (looked like an infection), PRURITUS (itchy), VACCINATION SITE WARMTH (warm and hot to the touch), VACCINATION SITE MASS (bump/red bumpy circle) and AXILLARY PAIN (it hurt all the way to the armpit/the whole shoulder and armpit area hurt quite significantly) in a 24-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) 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 vaccine (The patient got Pfizer first shot on 05-APR-2021, Lot no: ER8737.) on 05-Apr-2021, PFIZER VACCINE (The patient got Pfizer second shot on 07-MAY-2021 and Lot no: EW0173.) on 07-May-2021. Past adverse reactions to the above products included No adverse event with PFIZER VACCINE and Pfizer vaccine. Concomitant products included ESCITALOPRAM OXALATE (LEXAPRO) for Anxiety, LEVOTHYROXINE for an unknown indication. On 06-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Dec-2021, the patient experienced FATIGUE (fatigue) and MYALGIA (body aches). On 08-Dec-2021, the patient experienced INFECTION (looked like an infection), PRURITUS (itchy), VACCINATION SITE WARMTH (warm and hot to the touch), VACCINATION SITE MASS (bump/red bumpy circle), AXILLARY PAIN (it hurt all the way to the armpit/the whole shoulder and armpit area hurt quite significantly), VACCINATION SITE ERYTHEMA (red patch/path started growing on vaccine site), LYMPH NODE PAIN (pain spread to the lymph nodes in my armpit), ARTHRALGIA (whole shoulder hurt quite significantly) and VACCINATION SITE PAIN (It was sore). At the time of the report, INFECTION (looked like an infection), PRURITUS (itchy), VACCINATION SITE WARMTH (warm and hot to the touch), VACCINATION SITE MASS (bump/red bumpy circle), AXILLARY PAIN (it hurt all the way to the armpit/the whole shoulder and armpit area hurt quite significantly), FATIGUE (fatigue), MYALGIA (body aches), VACCINATION SITE ERYTHEMA (red patch/path started growing on vaccine site), LYMPH NODE PAIN (pain spread to the lymph nodes in my armpit), ARTHRALGIA (whole shoulder hurt quite significantly) and VACCINATION SITE PAIN (It was sore) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient was also taking birth control medications concomitantly. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LEVOTHYROXINE; LEXAPRO
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Rash
Rash erythematous
Rash papular
Rash pruritic
Symptomtext
This was a booster shot following two Pfizer vaccines in April 2021. painful itchy red raised rash on vaccine arm below the injection site. topical treatments, over counter pain reliever, warmth helped with pain, ice for the itching
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- low thyroid
- Andere Medikamente
- Atorvastatin, levothroxine
- Allergien
- latex, crab, gentamycin, Demerol, codeine
- Vorherige Impfungen
- Flu Nov 2020 pain severe swelling in shoulder age 58
- Staat
- MI
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Headache
Hot flush
Nausea
Pyrexia
Renal pain
Symptomtext
The 11th: headache, nausea The 12th: Fever 101F, Joint pain, Headache, sharp kidney pain, nausea. The 13th: hot flashes, fever 99F, kidney pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin gummies
- Allergien
- Some high level pain medication makes me feel sick and dizzy.
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Covid Arm - Red circle around injections, hot, swollen and itchy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Hyperpyrexia
Peripheral swelling
Pruritus
Rash
Symptomtext
Severe itching, arm was swollen for one week, rash, high fever for two days, and chills
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Humalog Levothroxycine
- Allergien
- Sulfa and Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 12.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Headache
Injection site erythema
Lymphadenopathy
Malaise
Pain
Toothache
Symptomtext
Woke up with swollen armpit and painful..like fluid buildup in my right arm. Still painful today the 4th day after shot. Red spot at injection site. Can't close arm all the way down without pain/discomfort. Headache Malaise Mild tooth pain upper and lower on right site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- HRT Del Estrogen IM Testosterone cream Vit D Armour thyroid Magnesium Multi vitamin Collagen Biotin
- Allergien
- NKA
- Vorherige Impfungen
- Age 54 Moderna 04/28/2021 Sore arm Fever Chills Headache Dizzy
- Staat
- PA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 11.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Urticaria
Symptomtext
started at least 4 hours later welt at injection site that got to the size of a half dollar.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 11.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Lymph node pain
Lymphadenopathy
Myalgia
Tenderness
Symptomtext
A day after vaccination, patient noticed lymph node had become swollen, and tender. Day 2 and 3 after vaccination was the worse swelling wise . On Day 4 patient noticed more pain on inner bicep and pain that has been travelling down to elbow and is painful to touch. If lift arm up can fell pain in arm pit area/ node area. Still swollen but not as much as day 2 and 3.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Lisinopril/HCTZ Daily Vitamin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Epistaxis
Fatigue
Headache
Injection site pain
Pyrexia
Symptomtext
Pt. states that after receiving the 2nd dose of Moderna 12/08/2021, started experiencing symptoms 12/10/2021 of headache, low-grade fever, pain at the injection site, fatigue, and nose bleed with clots (15mins). Symptoms have subsided, tenderness at the injection site continues. No noted Primary visit/communications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Cherries
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Deafness unilateral
Ear discomfort
Ear swelling
Fatigue
Vision blurred
Symptomtext
First couple of days felt tired but no other systems, woke up Saturday 12/4 and had no hearing in my left ear and my shoulder had a large knot. Had some blurred vision while at work that day and hearing was like a loud vibration. I thought it was ear wax but nothing relieved the pressure. Got appointment at nearest clinic since the store that gave the shot did not have one. Nurse told me I had severe swelling in my left year and some irritation in my right ear. My right ear hasn't lost earing but I do hear a lot of popping. My left ear is still without sound after 2 days of MethyIPREDNISolone Tablets, USP 4mg. Nurse told me to contact my family doctor after steroids are done if still can't hear. I am waiting for a call back from family doctor to get an appointment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Clinic did not do a covid test on me. Nurse looked in my ears and said she would give me steroids and told me to take Mucinex for possible congestion relief and told me to call my doctor if no improvement.
- Aktuelle Erkrankungen
- None was feeling great.
- Vorgeschichte
- Stage 4 Colon/liver/diaphram cancer in remission
- Andere Medikamente
- Tirosint 250 mcg
- Allergien
- medical Adhesive
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Urticaria
Symptomtext
welt 2 inches in diameter at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NKI
- Vorgeschichte
- N/A
- Andere Medikamente
- deprovera
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site rash
Injection site swelling
Injection site warmth
Pyrexia
Symptomtext
Large, swollen, red rash over and around the injection site. Hot and painful to the touch. 101 fever for 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism Anxiety
- Andere Medikamente
- Effexor XR 150 mgs Levothyroxine 75 mcgs
- Allergien
- Penicillin
- Vorherige Impfungen
- Moderna - 2nd Dose, 2/24/2021 - 102 fever, chills, aches
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Chills
Cold sweat
Fatigue
Headache
Malaise
Musculoskeletal stiffness
Nausea
Pain
Pyrexia
Rash
Symptomtext
12/6: Day of vaccine within a couple of hours I developed rash on both lower legs starting from below the knee to the ankles took a Benadryl because it kept getting worse, I also got a really bad headache and took 2 Tylenols (I have a picture of the rash) 12/7: Rash was still there not as bad, woke up with body aches, neck stiffness couldn't turn my neck to the left, fatigued, malaise, chills, nausea, GI issues, as the night approached I started feeling worse, came down with a fever & cold sweats was like this throughout the whole night, took 5 Tylenols throughout the day 12/8: still having cold sweats, fever was gone, chills, GI issues, body aches not as bad as day before, neck stiffness not as bad, took 1 Tylenol, rash still there not as bad 12/9: still having GI issues, rash still there not as bad but now it looks like tiny blood spots and it's only on the left leg (i have a picture)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hashimotos/hypothyroidism, pcos
- Andere Medikamente
- sertraline, np thyroid
- Allergien
- penicillin, tetracycline
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Heart rate increased
Pain
Pain in extremity
Pyrexia
Symptomtext
Woke with pain in arm and general body aches. Had mild fever (99.0) around 9:00am followed by chills. Around 2:45pm, my watch alerted me that my heart rate was high even though I was sitting down over a period of 10 minutes. Heart rate was between 120 and 125 during this time. I then took my blood pressure and received a reading of 122/84 with a pulse of 119. I took my pulse again at 3:00pm and it was still 117-120.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- mild hypertension, gout
- Andere Medikamente
- Losartan Potassium. Allopurinol, Glucosamine-Chondroitin, Vitamin D3.
- Allergien
- Ace Inhibitors
- Vorherige Impfungen
- similar reaction minus elevated heart rate with 2nd dose of Moderna vaccine. Vaccine date - 03/11/2021 Lot# 032M20A
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
Site: Pain at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aggression
Anger
Dizziness
Fatigue
Headache
Nausea
Pain
Symptomtext
Patient called on 12/6/21 to inform us of an adverse reaction she is experiencing after receiving a vaccine from us on 12/2/2021. Patient states she has been experiencing the following adverse effects: extreme headache, lightheadedness, nausea, fatigue and achy. Patient states headache is most bothersome. Symptoms started on Friday 12/3/2021 and have been progressively getting worse since then. I instructed the patient to call her primary care to discuss, due to her statement that symptoms have been getting worse. Patient was very angry and aggressive, stating she knew she shouldn't have received this vaccine. She also sounded as though she was not going to contact her primary care, stating she doesn't have time for all this, she needs to get back to work. I urged her to contact them anyways, informing her that we typically would not expect side effects to continue to worsen. Unsure if she will be taking my advice.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.12.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Dysphagia
Eye swelling
Mouth swelling
Pruritus
Swelling face
Swollen tongue
Throat tightness
Symptomtext
Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Severe, Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Severe, Systemic: Dizziness / Lightheadness-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Nodule
Pain
Symptomtext
On the evening of my booster shot, I started to have body aches, which is what I had after the first two shots. No big deal. One the morning after my booster, I currently have a small lump on the left side, base of my neck as well as a gigantic swollen lymph node on my left armpit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- one week prior: sinus infection.
- Vorgeschichte
- -
- Andere Medikamente
- Tri-Sprintec.
- Allergien
- -
- Vorherige Impfungen
- swollen left armpit lymph node after Dose 1 (Jan. 7, 2021) and Dose 2 (Feb. 4, 2021) of the Moderna vaccine, age 26-27.
- Staat
- NC
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Pain
Pyrexia
Symptomtext
fever, chills, body aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- vitamins
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 05.11.2023
- Impfdatum
- 15.10.2023
- Beginn
- 15.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Bacterial test
Chlamydia test
Differential white blood cell count
Full blood count
Herpes simplex test
Metabolic function test
Mononucleosis heterophile test
Neisseria test
Platelet count
Smear vagina
Treponema test
Viral test
Vulval disorder
Vulvovaginal ulceration
Symptomtext
Skin lesion on vulva supected lipschutz ulcer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bacterial test
- Hospital-Tage
- -
- Labordaten
- Syphilis Antibody Cascading Reflex Cbc (Includes Diff/plt) Comprehensive Metabolic Panel Bv/vaginitis Panel Dna Probe Chlamydia/n. Gonorrhoeae Rna, Tma, Urogenital Monospot Heterophile Ab Herpes Simplex Virus Culture
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Lexapro 20mg daily
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 02.08.2023
- Impfdatum
- 14.12.2021
- Beginn
- 10.01.2023
- Tage bis Beginn
- 392,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breakthrough COVID-19
Symptomtext
Breakthroguh Covid-19 Infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Anemia, CKD, Aortic aneurism, Cirrhosis of liver, COPD, ESRD
- Andere Medikamente
- Flonase, Gabapentin, Lactulose, Midodrine, Omeprazole, Propranolol, Renvela, Xifaxan, Zinc acetate
- Allergien
- No known Allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 05.07.2023
- Impfdatum
- 06.12.2021
- Beginn
- 21.01.2022
- Tage bis Beginn
- 46,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 2/18/21 lot# 023M20A; Moderna 3/18/21 lot# 002B21A; Moderna 12/6/21 lot# 029H21B;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 21.04.2023
- Impfdatum
- 17.12.2021
- Beginn
- 08.08.2022
- Tage bis Beginn
- 234,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 2/3/21 Lot# 007M20A; Moderna 3/3/21 Lot# 023M20A; Moderna 12/17/21 Lot# 029H21B
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 14.03.2023
- Impfdatum
- 04.12.2021
- Beginn
- 11.06.2022
- Tage bis Beginn
- 189,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 3/11/21 Lot# 044A21A; Moderna 4/8/21 Lot# 025B21A; Moderna 12/4/2021 Lot # 029H21B
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 13.03.2023
- Impfdatum
- 09.12.2021
- Beginn
- 09.03.2023
- Tage bis Beginn
- 455,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case. Moderna 1/7/21 011L20A, 2/4/21 012L20A and 12/9/21 029H21B
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID test 3/9/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 08.03.2023
- Impfdatum
- 14.12.2021
- Beginn
- 01.12.2022
- Tage bis Beginn
- 352,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 1/28/21 Lot# 007M20A; Moderna 4/8/21 Lot# 018B21A; Moderna 12/14/21 Lot# 029H21B
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 08.03.2023
- Impfdatum
- 14.12.2021
- Beginn
- 01.08.2022
- Tage bis Beginn
- 230,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 1/28/21 Lot# 007M20A; Moderna 4/8/21 Lot# 018B21A; Moderna 12/14/21 Lot# 029H21B
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 07.03.2023
- Impfdatum
- 04.12.2021
- Beginn
- 19.01.2022
- Tage bis Beginn
- 46,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 1/8/21 Lot# 012L20A; Moderna 2/5/21 Lot# 038K20A; Moderna 12/4/21 Lot# 029H21B
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 06.12.2021
- Beginn
- 11.10.2022
- Tage bis Beginn
- 309,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after three vaccines Moderna 2/27/21 Lot# 010A21A; Moderna 3/27/21 Lot# 017B21A; Moderna 12/6/21 Lot# 029H21B
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 09.12.2021
- Beginn
- 09.01.2023
- Tage bis Beginn
- 396,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough case dose 1 Moderna 1/7/21 011L20A dose 2 Moderna 2/4/21 012L20A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ 1/9/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 29.12.2022
- Impfdatum
- 04.12.2021
- Beginn
- 28.12.2022
- Tage bis Beginn
- 389,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 12/28/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 24.03.2021
- Beginn
- 04.10.2022
- Tage bis Beginn
- 559,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
This is 64 y.o. male who presented for the above procedure. Postoperative course was uncomplicated. Diet was advanced to regular diet and patient was taking sufficient PO intake to maintain hydration. Pain was controlled on PO medications. Patient was ambulating. The patient was deemed stable for discharge on 10/6/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 10/4 SARS-CoV-2 -COVID-19 by NAA, Micro -- detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 19.09.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 89,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Mental status changes
SARS-CoV-2 test positive
Unevaluable event
Symptomtext
HOSPITALIZATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 14.11.2022
- Impfdatum
- 15.12.2021
- Beginn
- 19.09.2022
- Tage bis Beginn
- 278,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chemotherapy
Chronic lymphocytic leukaemia
SARS-CoV-2 test positive
Symptomtext
09/19/22 admitted to Oncology for "CLL, inpatient chemo". PMHx of "A-fib, Arrhythmia, Arthritis, AS, bilateral lower extremity edema, bleeding tendency, chronic renal failure, CLL, Congestive heart failure"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 09/19/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 08.12.2021
- Beginn
- 03.10.2022
- Tage bis Beginn
- 299,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Respiratory tract congestion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory tract congestion
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 01.11.2022
- Impfdatum
- 17.02.2021
- Beginn
- 06.09.2022
- Tage bis Beginn
- 566,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vascular access malfunction
Symptomtext
09/06/22 presents to EC ED for "dialysis access malfunction". PMHx of "HTN, Type II DM, COPD, ESRD on HD, Anxiety/Depression, and PVD"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 09/06/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 03.12.2021
- Beginn
- 07.09.2022
- Tage bis Beginn
- 278,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 10.12.2021
- Beginn
- 06.08.2022
- Tage bis Beginn
- 239,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cough
Respiratory tract congestion
Symptomtext
cough, congestion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- 20,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 23.08.2022
- Impfdatum
- 08.12.2021
- Beginn
- 20.08.2022
- Tage bis Beginn
- 255,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough dose 1 Pfizer 1/31/21 EL9261 dose 2 Pfizer 2/21/21 EM9810
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ test on 8/21/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 18.08.2022
- Impfdatum
- 07.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 13,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Ibuprofen, magnesium glycinate, calcium, NAC, zinc, thyroid supplement (herbal), endocrine supplement (herbal)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 09.12.2021
- Beginn
- 25.01.2022
- Tage bis Beginn
- 47,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
Symptomtext
Can't smell or taste since a month after having vaccine. I had to get vaccine since I'm in healthcare field. Never had Covid prior or during my vaccine. Did not go back for any other vaccines. Left the healthcare field.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ageusia
- Hospital-Tage
- -
- Labordaten
- None because no one, including scientists and docs have any data or facts that can be proven. Everyone is blaming this on unknown previous medical condition, which is just an excuse to say, lets charge tons to money to see what's going on. Wow, this was a real sham! Docs are raking in the money and not able to do anything, but ask you to put your life savings in their pocket and never have an idea of what to do!
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- one a day vitamins
- Allergien
- sulfa, but no food or other allergies
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 11.08.2022
- Impfdatum
- 09.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 18Jan2021 as dose 1, single (Lot number: 042L20A), in left arm, on 17Feb2021 as dose 2, single (Lot number: 030M20A), in left arm and on 09Dec2021 as dose 3 (booster), single (Lot number: 029H21B) at the age of 53 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: ESOMEPRAZOLE, start date: 07Nov2012, stop date: 06Aug2022; ZYRTEC ALLERGY, start date: 04Jul2016, stop date: 06Aug2022. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: positive, notes: tested positive for COVID; Negative, notes: tested negative within 8 days of first positive test; positive, notes: tested positive again. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient had no known allergies. Patient started Paxlovid the evening she tested positive for COVID. She did very well and tested negative within 8 days of first positive test. She began having symptoms again, after 8 days of finishing full 5-day course of Paxlovid. She tested positive again on the 9th day after finishing full 5-day course of Paxlovid. Patient anti-viral medication included Paxlovid for COVID 19 Treatment. Treatment started on 22Jul2022 and stopped on 26Jul2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: covid-19 virus test; Result Unstructured Data: Test Result:positive; Comments: tested positive for COVID; Test Name: covid-19 virus test; Result Unstructured Data: Test Result:Negative; Comments: tested negative within 8 days of first positive test.; Test Name: covid-19 virus test; Result Unstructured Data: Test Result:positive; Comments: tested positive again
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- ESOMEPRAZOLE; ZYRTEC ALLERGY
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 29.07.2022
- Impfdatum
- 19.01.2022
- Beginn
- 18.07.2022
- Tage bis Beginn
- 180,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asymptomatic COVID-19
Hip fracture
Periprosthetic fracture
Symptomtext
Pt presented to the hospital with hip had a periprosthetic fracture non operatiable. pt asymptomatic for covid, transferred back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ETHO, Copd, CHF, Dementia, DM, BPH
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 29.07.2022
- Impfdatum
- 10.12.2021
- Beginn
- 28.07.2022
- Tage bis Beginn
- 230,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Symptomtext
Patient developed COVID after being vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 07.12.2021
- Beginn
- 06.05.2022
- Tage bis Beginn
- 150,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Respiratory tract congestion
Rhinorrhoea
Symptomtext
congestion, rhinorrhea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory tract congestion
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccines were administered beyond use date after thaw process; This spontaneous case was reported by a paramedic and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccines were administered beyond use date after thaw process) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 17-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 17-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccines were administered beyond use date after thaw process). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccines were administered beyond use date after thaw process) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient age was reported as 72 years and 6 months. No concomitant medications were reported. On 10-Jun-2022, the vaccination facility was notified of an audit that was done and it was informed that vaccines were administered beyond use date after the thaw process. There was no patient that had any adverse reactions and no reports of any reactions after the administration of these vaccines. The patient got Moderna with vaccine Ndc code 80777027399. It was unknown whether the patient was ever diagnosed/tested positive for COVID-19. It was unknown whether the patient had any acute illness at the time of vaccination and up to one month before it. It was unknown whether the patient had any chronic or long-standing health conditions. Prescriptions, over the counter medications, dietary supplements or herbal remedies being taken at the time of vaccination and/or at the time of adverse event was unknown. 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
- RI
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- 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
Symptomtext
Vaccine that was administered beyond use date after thaw process; This spontaneous case was reported by a paramedic and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that was administered beyond use date after thaw process) in a 28-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 18-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 18-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that was administered beyond use date after thaw process). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that was administered beyond use date after thaw process) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient age was reported as 28 years and 08 months. No concomitant medications were reported. On 10-Jun-2022, the vaccine facility staff was notified of an audit that was done and they were made aware of vaccines that were administered beyond use date after the thaw process. Patient had not reported any adverse reactions after the administration of the vaccine. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2022-542869 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-542869:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- 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
Symptomtext
Vaccine that administered beyond use date after the thaw process; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process) in a 66-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. It was unknown if patient ever had tested or diagnosed positive for COVID. It was unknown if patient had Acute or Chronic/ long-standing illnesses at the time of vaccination or up to 1 month prior to vaccination. Information about other vaccines given within 1 month prior to Moderna COVID-19 vaccine was unknown. On 18-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 18-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient age reported in the source document as 66 years 10 months. No concomitant medication information was provided. On 10-Jun-2022, medical was notified about an audit that was done and they were then made aware of vaccines that were administered beyond use date after the thaw process. Reporter stated that there was no patient that had any adverse reactions and there were no reports of any reactions after the administration of vaccines. Vaccine NDC code- 80777-0273-99 No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient ever had tested or diagnosed positive for COVID. It was unknown if patient had Acute or Chronic/ long-standing illnesses at the time of vaccination or up to 1 month prior to vaccination. Information about other vaccines given within 1 month prior to Moderna COVID-19 vaccine was unknown.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine that administered beyond use date after the thaw process/expired vaccine administered; This spontaneous case was reported by a paramedic and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) in a 26-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. It was unknown whether the patient was ever diagnosed/tested positive for COVID-19. It was unknown whether the patient had any acute illness at the time of vaccination and up to one month before it. It was unknown whether the patient had any chronic or long-standing health conditions. On 17-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 17-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient age was reported as 26 years and 4 months. Prescriptions, over the counter medications, dietary supplements or herbal remedies being taken at the time of vaccination was unknown The vaccines were administered beyond use date after the thaw process. The patient did not had any adverse reactions and no reports of any reactions after the administration of these vaccines. The patient got Moderna with vaccine Ndc code 80777027399. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown whether the patient was ever diagnosed/tested positive for COVID-19. It was unknown whether the patient had any acute illness at the time of vaccination and up to one month before it. It was unknown whether the patient had any chronic or long-standing health conditions.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- 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
Symptomtext
Vaccines that were administered beyond use date after thaw process; This spontaneous case was reported by an HCP and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccines that were administered beyond use date after thaw process) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 20-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 20-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccines that were administered beyond use date after thaw process). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccines that were administered beyond use date after thaw process) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications was reported. It was unknown if the patient was tested positive or diagnosed with COVID-19. It was unknown if acute illnesses at the time of vaccination and up to one month before. And it was unknown if chronic or long-standing health conditions. The vaccine was used beyond use date of some lot numbers for Moderna that were administered to patients. There was no adverse reaction noted or reported to the reporter ever regarding after administration of vaccine. No treatment drug details was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- 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
Symptomtext
Vaccines that were administered beyond use date after thaw process; This spontaneous case was reported by an HCP and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccines that were administered beyond use date after thaw process) in a 29-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 17-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 17-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccines that were administered beyond use date after thaw process). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccines that were administered beyond use date after thaw process) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient age was reported as 29 years and 09 months. No concomitant medications were reported. It was reported that the vaccines were administered beyond use date after the thaw process. Patient had not reported any adverse reactions after the administration of the vaccine. 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
- RI
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- 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
Symptomtext
Vaccines that were administered beyond use date after thaw process; This spontaneous case was reported by an HCP and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccines that were administered beyond use date after thaw process) in a 31-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. It was unknown if patient had ever diagnosed positive with Covid-19. It was unknown if patient had any acute illness at the time of vaccination or up to one month before. It was unknown if patient had any chronic or long-standing health conditions. On 19-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 19-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccines that were administered beyond use date after thaw process). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccines that were administered beyond use date after thaw process) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient age was reported as 31 years 10 months. No concomitant drug reported. It was reported vaccine administrated beyond use date after the thaw process. There was no patient that had any adverse reactions and no reports of any reactions after the administration of the vaccines. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient had ever diagnosed positive with Covid-19. It was unknown if patient had any acute illness at the time of vaccination or up to one month before. It was unknown if patient had any chronic or long-standing health conditions.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
vaccine administrated beyond use date after the thaw process; This spontaneous case was reported by an HCP and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine administrated beyond use date after the thaw process) in a 35-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 20-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 20-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine administrated beyond use date after the thaw process). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine administrated beyond use date after the thaw process) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient age was reported as 35 years 3 months. No concomitant drug reported. It was reported vaccine administrated beyond use date after the thaw process. There was no patient that had any adverse reactions and no reports of any reactions after the administration of the vaccines. 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
- RI
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine that administered beyond use date after the thaw process; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process) in a 27-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 21-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 21-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Age of the patient was reported as 27 year 8 months. No concomitant drug information was provided. The patient had received Moderna Covid-19 vaccine that were given beyond the 30 day use by date after the thaw process. No patient had any adverse reactions and no reports of any reactions after administration of the vaccine was noted. No treatment drug information was received. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- 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
Symptomtext
Vaccine that administered beyond use date after the thaw process; This spontaneous case was reported by an HCP and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process) in a 28-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. It was unknown if patient was diagnosed/tested positive for COVID-19, had acute illness at the time of vaccination and up to one month before, or had chronic or long-lasting illness. It was unknown if patient had taken any prescriptions, over the counter medication, dietary supplements or herbal remedies at the time of vaccination. On 21-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 21-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. The age of the patient was reported as 28 years 11 months. No concomitant medications were reported. The patient had no adverse reaction after the vaccine administration. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient was diagnosed/tested positive for COVID-19, had acute illness at the time of vaccination and up to one month before, or had chronic or long-lasting illness. It was unknown if patient had taken any prescriptions, over the counter medication, dietary supplements or herbal remedies at the time of vaccination.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- 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
Symptomtext
Vaccine that administered beyond use date after the thaw process/expired vaccine administered; This spontaneous case was reported by a paramedic and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 17-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 17-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications was reported. The reporter informed that, the vaccine was used beyond use date of some lot numbers for Moderna that were administered to patients. There was no adverse reaction noted or reported to the reporter ever regarding after administration of vaccine. It was unknown if the patient was tested positive or diagnosed with COVID-19. It was unknown if acute illnesses at the time of vaccination and up to one month before. And it was unknown if chronic or long-standing health conditions. No treatment drug details was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- 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
Symptomtext
Vaccine was administered beyond use date after the thaw process; This spontaneous case was reported by an HCP and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered beyond use date after the thaw process) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. It was unknown if the patient had ever been diagnosed or tested positive for COVID-19. It was reported, acute illness at the time of vaccination and up to one month before and chronic or long-standing health conditions were unknown. On 19-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 19-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered beyond use date after the thaw process). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered beyond use date after the thaw process) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient's age was reported as 59 years 7 months. No concomitant medications were provided by the reporter. No adverse reactions were reported by the patient after the administration of vaccine. Vaccine Ndc code was reported as 80777-0273-99. No treatment medications were provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if the patient had ever been diagnosed or tested positive for COVID-19. It was reported, acute illness at the time of vaccination and up to one month before and chronic or long-standing health conditions were unknown.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine that administered beyond use date after the thaw process/expired vaccine administered; This spontaneous case was reported by a paramedic and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) in a 28-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 18-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 18-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient age was reported as 28 years 10 months. No concomitant medication information was provided. On 10-Jun-2022, medical was notified about an audit that was done and they were then made aware of vaccines that were administered beyond use date after the thaw process. Patient got Moderna with vaccine Ndc code 80777-0273-99. Reporter stated that there was no patient that had any adverse reactions and there were no reports of any reactions after the administration of vaccines. No treatment medication were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- 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
Symptomtext
Vaccine that administered beyond use date after the thaw process/expired vaccine administered; This spontaneous case was reported by an emergency medical technician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) in a 24-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 18-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 18-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient's age was reported as 24 years and 8 months old. No concomitant medication information was provided. On 10-Jun-2022, medical was notified about an audit that was done and they were then made aware of vaccines that were administered beyond use date after the thaw process. Patient got Moderna with vaccine Ndc code. Reporter stated that there was no patient that had any adverse reactions and there were no reports of any reactions after the administration of vaccines. No treatment medication were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine that administered beyond use date after the thaw process/expired vaccine administered; This spontaneous case was reported by a paramedic and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 17-Jan-2022, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 17-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient age was reported as 59 year 8 months. No concomitant medications were reported No treatment medications were reported It was unknown if patient had acute illness at the time of vaccination and up to one month before. It was unknown if patient had been diagnosed with or tested positive for COVID-19. Patient reported no adverse reactions after the administration of vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- 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
Symptomtext
Vaccine that administered beyond use date after the thaw process/expired vaccine administered; This spontaneous case was reported by a paramedic and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) in a 41-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 22-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant drug information was provided. Patient age was reported as 41 years and 9 months. It was reported that vaccine was administered beyond use date to patients. There was no adverse reaction noted or reported regarding these administrations. No treatment drug information was provided. This case was linked to MOD-2022-542869 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- 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
Symptomtext
Vaccine that administered beyond use date after the thaw process/expired vaccine administered; This spontaneous case was reported by a paramedic and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) in a 46-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 18-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 18-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient age was reported as 46 years 7 months. No concomitant medication information was provided. On 10-Jun-2022, medical was notified about an audit that was done and they were then made aware of vaccines that were administered beyond use date after the thaw process. Patient got Moderna with vaccine Ndc code. Reporter stated that there was no patient that had any adverse reactions and there were no reports of any reactions after the administration of vaccines. No treatment medication were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 25.06.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine that administered beyond use date after the thaw process/expired vaccine administered; This spontaneous case was reported by a paramedic and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) in a 21-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 17-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 17-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant drug information was reported. Patient age was reported as 21 years and 6 months. It was reported that vaccine was administered beyond use date to patients. There was no adverse reaction noted or reported regarding these administrations. Vaccine number code was reported as 80777027399. No treatment drug information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 25.06.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- 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
Symptomtext
Vaccine that administered beyond use date after the thaw process/expired vaccine administered; This spontaneous case was reported by a paramedic and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) in a 22-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 17-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 17-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thaw process/expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant drug information was provided. Patient age was reported as 22 years and 8 months. It was reported that vaccine was administered beyond use date to patients. There was no adverse reaction noted or reported regarding these administrations. Vaccine number 1 code was reported as 80777027399. No treatment drug information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 25.06.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- 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
Symptomtext
Vaccine that administered beyond use date after the thawprocess; This spontaneous case was reported by a paramedic and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thawprocess) in a 20-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 prophylaxis. No Medical History information was reported. On 19-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 19-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thawprocess). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that administered beyond use date after the thawprocess) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. The patient's age was reported as 20 years and 6 months. No concomitant medication was provided. It was reported that vaccine was administered beyond use date to the patients. There was no adverse reaction noted or reported regarding these administrations. No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
COVID-19/Ear ache,Head pressure; Interchange of vaccine products; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (COVID-19/Ear ache,Head pressure) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029h21b) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer (Dose number: 1, Batch/Lot no: el3247, location of injection : Right Arm, Administration time: 1.00 PM, Route of administration: Intramuscular) on 02-Mar-2021, Pfizer (Dose number: 2, Batch/Lot no: er8732, location of injection : Right Arm, Administration time: 2.00 PM and Route of administration : Intramuscular) on 02-Apr-2021. Past adverse reactions to the above products included No adverse event with Pfizer and Pfizer. Concurrent medical conditions included Drug allergy (Allergy to unknown drug). Concomitant products included VITAMIN C [ASCORBIC ACID] for an unknown indication. On 23-Mar-2022 at 5:00 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Mar-2022, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). On 08-Jun-2022, the patient experienced COVID-19 (COVID-19/Ear ache,Head pressure). At the time of the report, COVID-19 (COVID-19/Ear ache,Head pressure) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 30-May-2022, SARS-CoV-2 test: negative (Negative) Negative. On 01-Jun-2022, SARS-CoV-2 test: negative (Negative) Negative. On 08-Jun-2022, SARS-CoV-2 test: positive (Positive) Positive. The patient did not received any other vaccine within 4 weeks prior to Covid vaccine. Hospitalization prolonged and treatment received was reported as No. Company Comment: This spontaneous case of Interchange of vaccine products concerns a 55-year-old female patient, with previous Pfizer vaccinations, who experienced the unexpected of COVID-19. The event occurred approximately 2 months 14 days after receiving the third dose of mRNA-1273 Vaccine. The patient had a positive SARS-CoV-2 test result. Treatment information was not provided. The outcome of the event was reported as unknown. The patient's medical history of previous Pfizer vaccinations remain as confounders for the occurrence of the event. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.; Sender's Comments: This spontaneous case of Interchange of vaccine products concerns a 55-year-old female patient, with previous Pfizer vaccinations, who experienced the unexpected of COVID-19. The event occurred approximately 2 months 14 days after receiving the third dose of mRNA-1273 Vaccine. The patient had a positive SARS-CoV-2 test result. Treatment information was not provided. The outcome of the event was reported as unknown. The patient's medical history of previous Pfizer vaccinations remain as confounders for the occurrence of the event. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220530; Test Name: Nasal swab test; Test Result: Negative; Result Unstructured Data: Negative; Test Date: 20220601; Test Name: Nasal swab test; Test Result: Negative; Result Unstructured Data: Negative; Test Date: 20220608; Test Name: Nasal swab test; Test Result: Positive; Result Unstructured Data: Positive.
- Aktuelle Erkrankungen
- Drug allergy (Allergy to unknown drug)
- Vorgeschichte
- -
- Andere Medikamente
- VITAMIN C [ASCORBIC ACID]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 96,0
- Geschlecht
- M
- Eingang
- 08.06.2022
- Impfdatum
- 08.12.2021
- Beginn
- 07.06.2022
- Tage bis Beginn
- 181,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 06.12.2021
- Beginn
- 25.05.2022
- Tage bis Beginn
- 170,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 07.12.2021
- Beginn
- 10.05.2022
- Tage bis Beginn
- 154,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
Interchange of vaccine products; Tested positive for covid on 5/10; had symptoms; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (Tested positive for covid on 5/10; had symptoms) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 vaccination. Previously administered products included for Drug use for unknown indication: Pfizer / BioNTech (Dose 1, Batch number EW0151, Location of injection: Left Arm.) on 12-Apr-2021, Pfizer / BioNTech (Dose 2, Batch number EW0173 and Location of injection Left arm) on 03-May-2021. Past adverse reactions to the above products included No adverse event with Pfizer / BioNTech and Pfizer / BioNTech. Concurrent medical conditions included Ehlers-Danlos syndrome, Mast cell activation syndrome, Postural orthostatic tachycardia syndrome, Chronic migraine, Autoimmune disorder NOS (l kely autoimmune condition), ADHD, Obsessive-compulsive disorder, Obstructive sleep apnea syndrome and Fruit allergy (Pineapple). Concomitant products included EPTINEZUMAB (VYEPTI [EPTINEZUMAB]) from 17-Dec-2020 to an unknown date, BOTULINUM TOXIN TYPE A (BOTOX) from 23-Aug-2021 to an unknown date and TOPIRAMATE (TROKENDI XR) for an unknown indication. On 07-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-May-2022, the patient experienced COVID-19 (Tested positive for covid on 5/10; had symptoms). On an unknown date, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 11-May-2022 to 15-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (Tested positive for covid on 5/10; had symptoms) had not resolved and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 10-May-2022, SARS-CoV-2 test: positive (Positive) Positive. On 16-May-2022, SARS-CoV-2 test: negative (Negative) Negative. On 21-May-2022, SARS-CoV-2 test: negative (Negative) Negative. On 23-May-2022, SARS-CoV-2 test: positive (Positive) Positive. It was reported that patient started experiencing symptoms on 09 May 2022, Patient tested positive again and symptoms worsened. Overall symptoms from COVID reported as chest pain, shortness of breath, cough, sneezing, congestion, chills, fever. Paxlovid eliminated chills and fever. Device Date was reported as 24 May 2022 Company comment: This spontaneous case concerns a 27-year-old female patient with no relevant medical history who experienced the unexpected non serious AESI of COVID 19 which occurred approximately 5 months after the administration of third dose of mRNA-1273 vaccine in COVID 19 vaccination series. Symptoms (chest pain, shortness of breath, cough, sneezing, congestion, chills and fever) started on 9-May and tested positive for COVID 19 on 10-May. Patient received NIRMATRELVIR, RITONAVIR (Paxlovid) as treatment for COVID 19 from 11-May to 15-May. Patient tested negative on 16-May. Symptoms recurred 5 days later which worsened after 2 days and again tested positive for COVID 19. Patient received 2 doses of Tozinameran vaccine about 7, and 8 months respectively prior from the last dose (interchange of vaccine products noted). The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 27-year-old female patient with no relevant medical history who experienced the unexpected non serious AESI of COVID 19 which occurred approximately 5 months after the administration of third dose of mRNA-1273 vaccine in COVID 19 vaccination series. Symptoms (chest pain, shortness of breath, cough, sneezing, congestion, chills and fever) started on 9-May and tested positive for COVID 19 on 10-May. Patient received NIRMATRELVIR, RITONAVIR (Paxlovid) as treatment for COVID 19 from 11-May to 15-May. Patient tested negative on 16-May. Symptoms recurred 5 days later which worsened after 2 days and again tested positive for COVID 19. Patient received 2 doses of Tozinameran vaccine about 7, and 8 months respectively prior from the last dose (interchange of vaccine products noted). 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: 20220510; Test Name: COVID-19 virus test; Test Result: Positive ; Result Unstructured Data: Positive; Test Date: 20220516; Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220521; Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220523; Test Name: COVID-19 virus test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- ADHD; Autoimmune disorder NOS (l kely autoimmune condition); Chronic migraine; Ehlers-Danlos syndrome; Fruit allergy (Pineapple); Mast cell activation syndrome; Obsessive-compulsive disorder; Obstructive sleep apnea syndrome; Postural orthostatic tachycardia syndrome
- Vorgeschichte
- -
- Andere Medikamente
- VYEPTI [EPTINEZUMAB]; BOTOX; TROKENDI XR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 09.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Computerised tomogram normal
Interchange of vaccine products
Vaginal haemorrhage
Symptomtext
On my third dose, January I had light unexplained vaginal bleeding. I was sent to a Gynecologist and they could not figure the source of this. I have had a hysterectomy. It was this unexplained light bleeding. It wasn't requiring a menstrual pad, but it was definitely bleeding. It happened once in October and December and recently three times in January 2022. I am fine now and I have not had any issues I've gotten my second booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Computerised tomogram normal
- Hospital-Tage
- -
- Labordaten
- Pelvic Exam 01/2021 normal. Pelvic Exam 01/2021 normal. CAT scan 01/2021 normal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Celiac Disease; Diabetes due to damaged pancreas
- Andere Medikamente
- Insulin base dose 40 units; metformin; glipizide 1.5mg; venlafaxine; pravastatin 40 mg; oxybutynin chloride; Ziac 2.5 mg; dexamethasone; Allegra 60 mg; fish oil omega 3; vitamin E; Tylenol arthritis; Advil; Osteo-Biflex; Centrum silver
- Allergien
- Celiac disease; dapsone; erythromycin; penicillin
- Vorherige Impfungen
- Pfizer 67 years old 04/09/2021, I had trouble swallowing food and eating and drinking. I had terrible upper back back. I had a l
- Staat
- MD
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 08.12.2021
- Beginn
- 17.05.2022
- Tage bis Beginn
- 160,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
Positive rapid antigen test rebound on Day +4 after finishing the 5-day course of Paxlovid; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (Positive rapid antigen test rebound on Day +4 after finishing the 5-day course of Paxlovid) in a 26-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 vaccination. No Medical History information was reported. On 08-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-May-2022, the patient experienced COVID-19 (Positive rapid antigen test rebound on Day +4 after finishing the 5-day course of Paxlovid). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 09-May-2022 to 13-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (Positive rapid antigen test rebound on Day +4 after finishing the 5-day course of Paxlovid) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: negative (Negative) Negative on day 5 of Paxlovid treatment and positive (Positive) Positive rapid antigen test rebound on Day 4 after finishing the 5 day course of Paxlovid treatment.. No concomitant medication information provided. No treatment medication information provided. On 08-Dec-2021, the patient received booster dose of Moderna COVID-19 Vaccine. Patient tested positive for COVID-19 on day 4th of Paxlovid treatment. After finishing the 5 days course symptoms were cough and congestion which was persisted steadily during that time. Rapid antigen test returned negative on the day 5 of paxlovid treatment. Company Comment: This spontaneous case concerns a 26-year-old female patient, with Co-suspect drug Paxlovid, who experienced the unexpected ADR of COVID-19. The event occurred approximately 5 months after receiving the third dose of mRNA-1273 Vaccine. The patient was treated with PAXLOVID for COVID-19, however the patient had persistent symptoms of cough and congestion and tested positive again after 4 days of treatment. The outcome of the event was reported as not resolved. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.; Sender's Comments: This spontaneous case concerns a 26-year-old female patient, with Co-suspect drug Paxlovid, who experienced the unexpected ADR of COVID-19. The event occurred approximately 5 months after receiving the third dose of mRNA-1273 Vaccine. The patient was treated with PAXLOVID for COVID-19, however the patient had persistent symptoms of cough and congestion and tested positive again after 4 days of treatment. The outcome of the event was reported as not resolved. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: Negative on day 5 of Paxlovid treatment; Test Name: COVID-19 virus test; Test Result: Positive ; Result Unstructured Data: Positive rapid antigen test rebound on Day 4 after finishing the 5 day course of Paxlovid treatment.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
I have had persistent ringing in my ears for six months
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- I have begun hearing a persistent ringing in my ears. It is more prevalent in my left ear than the right, but it exists in both ears. I did not consent to this side effect, I am not happy with this side effect, I need it to be solved because it has been over six months with no end in sight.
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 11.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 16.12.2021
- Beginn
- 17.01.2022
- Tage bis Beginn
- 32,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Hospitalization within 6 weeks of COVID vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 03.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 29,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear discomfort
Tinnitus
Symptomtext
Tinnitus and fullness in ears
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear discomfort
- Hospital-Tage
- -
- Labordaten
- 3/22/2022 Hearing test-Normal except for minor high pitched sound (age related) Physical examination by specialist- no infection or fluid in ears
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seasonal allergies
- Andere Medikamente
- Wellbutrin, Rosuvastatin, Prilosec, Claritin, Flonase, Vivelle Dot
- Allergien
- Sulfa, Methylprednisone Dos-Pak, Banana
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Pt received dose #2, was given outside the recommended timeframe of 28 days for Moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none, spoke with patient, no adverse effects per pt
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- long standing
- Andere Medikamente
- Risperdal 2mg po qhs; Symbicort 80-4.5 bid; Boost oral liquid po,; Methadone Hcl 30mg po Prozac 20mg po qam; Diphenhydramine 50mg qhs
- Allergien
- Adhesive tape
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 03.12.2021
- Beginn
- 26.01.2022
- Tage bis Beginn
- 54,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
covid-19 illness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
vaccine was administered greater than 12 hours post first vial puncture; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine was administered greater than 12 hours post first vial puncture) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 029H21B) for COVID-19 vaccination. No Medical History information was reported. On 09-Feb-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine was administered greater than 12 hours post first vial puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vaccine was administered greater than 12 hours post first vial puncture) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Date and time vial was first punctured: 08Feb2022 at 9:32am in vaccination room with an average room temp of 74 degrees F. No concomitant medication were reported. No treatment information were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 03.12.2021
- Beginn
- 11.02.2022
- Tage bis Beginn
- 70,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
The patient has not experience any adverse events, but the vaccine was inadvertently administered within 1 month of the patient receiving monoclonal antibody therapy (BAM infusion) for COVID-19. The facility that provided the patient's information did not indicate he had received the infusion, yet after vaccination they reported he had in fact received the BAM infusion on 1/4/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Endotracheal intubation
Feeling abnormal
Moaning
Pulse absent
Unresponsive to stimuli
Symptomtext
Approximately 15 hours post vaccine administration long term care facility resident was found in her room stating she "felt terrible". When nurse was repositioning patient the patient moaned and went unresponsive. SpO2 was 69%. When EMS arrived resident was responsive stating she "felt terrible". Report from ED stated that upon arrival to ED patient had no pulse and was intubated and admitted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Endotracheal intubation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prior to vaccination, patient had been treated for pneumonia.
- Vorgeschichte
- Congestive Heart Failure, lymphedema, hypertensive heart disease, hyperlipidemia, dependent on supplemental oxygen, GERD
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- Impfdatum
- 08.12.2021
- Beginn
- 03.02.2022
- Tage bis Beginn
- 57,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Inappropriate schedule of product administration
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after it had been punctured for greater than 12 hours) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) in a 19-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 042J21A and 029H21B) for COVID-19 vaccination. No Medical History information was reported. On 08-Dec-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Feb-2022 at 11:05 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 03-Feb-2022 at 11:05 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after it had been punctured for greater than 12 hours.) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). On 03-Feb-2022 at 11:05 AM, EXPIRED PRODUCT ADMINISTERED (Dose administered after it had been punctured for greater than 12 hours.) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient had not reported any symptoms and not received any additional doses, medications or treatments at that time. No concomitant medications were reported. 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
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 16.12.2021
- Beginn
- 28.01.2022
- Tage bis Beginn
- 43,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Positive COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 10.02.2022
- Impfdatum
- 16.12.2021
- Beginn
- 19.01.2022
- Tage bis Beginn
- 34,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Positive COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 16.12.2021
- Beginn
- 14.01.2022
- Tage bis Beginn
- 29,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Positive COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 09.12.2021
- Beginn
- 11.01.2022
- Tage bis Beginn
- 33,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Positive COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 21.12.2021
- Beginn
- 12.01.2022
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Positive COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Moderna booster vaccine given too early (in left deltoid). Second dose of Moderna was 11/10/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Booster given early. Second dose was given10/03/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Has heart stint
- Andere Medikamente
- Has a blood thinner from stnt procedure. Does not remember med or dose
- Allergien
- None voiced
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
vaccine given too early
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- 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
Upon entering in vaccination administration data in to the Immunization Information System website, it was noted that patient received COVID PFR booster on 1/21/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Dx: SBO,Diverticulitis (Augmentin thru 1/27), AKI, UTI (Cipro thru 1/28).
- Vorgeschichte
- _Parkinsons, HTN, HLD, Bradycardia, NSTEMI, Anxiety, Insomnia, obstipation.
- Andere Medikamente
- tylenol, aspirin, boost, carbidopa-levodopa, cipro, clonidine, ferrous sulfate, genteal tears, levothyroxine, losartan, mirtazapine, simvastatin, vitamin d3, vitamin e, voltaren
- Allergien
- no known drug allergies
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
Client in nursing home and had documentation and at nursing home as having 2 Moderna vaccines. A Moderna vaccine was given and upon entering into state Registry that afternoon a 3rd dose had been entered by a pharmacy that day from 11/24/2021. Family and Nursing home contacted. No adverse reaction as of 1/27/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Anemia.
- Vorgeschichte
- Anemia; Heart problems; Hypertension.
- Andere Medikamente
- Multi vitamin; B12; Eliquis; Amerilide; Potassium
- Allergien
- Sulfa.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 26.01.2022
- Tage bis Beginn
- 48,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 1/25/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nervousness
Symptomtext
Vaccine given In Left Deltoid. Patient anxious about getting vaccine. Discussed and gave words of support. Patient wanted vaccine. After vaccine patient felt shakey. Took vital signs BP 162/100 per electronic BP cuff, Temp 97.9 F, P:100 SP02 99%. Patient stated she took medication today but did not eat yet. Given water, gave words of support and performed manual BP 10 min later and BP was 142/82. Patient stated she felt better has history of HTN was going to eat lunch and would call emergency if she starts experiencing Chest pain SOB or any concerns or will call provider if starts to have questions or concerns. Encouraged to follow up with provider. Patient stated she felt better and wanted to Continue to work. Supervisor present and aware of situation .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nervousness
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN DM
- Andere Medikamente
- Amlodipine Losartan Januvia Glipizide
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 16,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Herpes zoster
Symptomtext
developed shingles and then additional spots all over body per client a week after the shingles started had J&J vaccine for her first dose 6-22-2021 lot # 204A21A, also right arm IM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- shingles by diagnosis 1-20-2022 on right side of neck/ shoulder and armpit area- started before the other "spots/ rash appeared) 1-1-2022
- Vorgeschichte
- none reported
- Andere Medikamente
- none reported
- Allergien
- allergic to: pollen
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Error: Booster Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 16.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Scheduled for Moderna follow-up (second dose 0.5ml) received half dose (0.25ml). Patient called to come back for other half (0.25ml) of dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Almond, tree nuts
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
On the CDC sheet, patient checked and listed that she is severely immunocompromised. She was given a booster of 0.25ml of Moderna vaccine instead of a 3rd shot (0.5ml).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Vaccine clinic administration of first dose Moderna to 15 year old young man.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 20,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Menstrual disorder
Symptomtext
Menstruation change. Amenorrhea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amenorrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypothyroidism, Hashimoto's Thyroiditis
- Andere Medikamente
- Synthroid, Vyvanse, Singular
- Allergien
- Tetanus shot allergy
- Vorherige Impfungen
- Tetanus shot in 1987 -very hot, red, swollen arm. Pfizer Covid vaccine - dose 1, 4/7/21 - hot, swollen arm at injection site.
- Staat
- NY
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
Patient was mistakenly given moderna vaccine dose (0.25ml) instead of pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Patient registered for pfizer booster but received moderna booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 15.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Error: Booster Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 13.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Inappropriate schedule of product administration
No adverse event
Wrong product administered
Symptomtext
inadvertently injected a second (duplicate) moderna covid booster (0.25mL) instead of a flu shot. Subsequently administered IM flu shot to offer flu protection as requested. No know adverse event associated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Burning sensation
Peripheral swelling
Swelling face
Symptomtext
My face swelled up substantially and was very tight and burned a bit. My arms and legs swelled a little. I took a Benadryl and the swelling went down within an hour.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Burning sensation
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- sudden hearing loss 3 weeks prior to vaccination
- Vorgeschichte
- Pelvic organ prolapse
- Andere Medikamente
- estradiol patch .0375 mg 1/week estradiol .1 mg 3 x week vaginally desvenlafaxine 50 mg 1 x day simvastatin 40 mg 1 x day trazodone 100 mg 1 x day triamterene-hydrochlorothiazide 37.5-25 mg tab 1 x day docusate sodium 500 mg 1 x day
- Allergien
- sulfa drugs, cilantro, mint
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 04.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Epistaxis
Symptomtext
About 3 hours after vaccine my nose began to profusely bleed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Epistaxis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Heartburn Headaches
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -