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Reporte zur Charge 029H21B

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

252Reporte angezeigt
8Todesfaelle
54Hospitalisiert
2Lebensbedrohlich
5Bleibende Schaeden
MI 44 RI 22 OH 14 CA 12 IL 11 TX 11 NC 11 GA 9 MA 9 CT 9 NY 8 MN 7

VAERS 2680708

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2637255

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2607589

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2607451

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2599121

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2586274

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2559209

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2536046

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2454642

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2391009

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2359704

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2238089

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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

VAERS 2190406

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2136986

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 1974954

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

kritisch
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
-

VAERS 2624679

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

schwer
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
-

VAERS 2317638

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

schwer
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
-

VAERS 2098546

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

schwer
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
-

VAERS 2050106

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

schwer
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
-

VAERS 2013370

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

schwer
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
-

VAERS 1997304

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

schwer
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
-

VAERS 1984779

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

schwer
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
-

VAERS 1970960

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

schwer
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
-

VAERS 1962122

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

schwer
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
-

VAERS 1962114

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

schwer
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
-

VAERS 1959214

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

schwer
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
-

VAERS 1959086

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

schwer
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
-

VAERS 1954498

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

schwer
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
-

VAERS 1947319

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

schwer
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
-

VAERS 1943534

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

schwer
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
-

VAERS 1931919

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

schwer
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
-

VAERS 1931907

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

schwer
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
-

VAERS 1924273

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

schwer
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
-

VAERS 2636026

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2616037

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2615340

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2613391

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2550370

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2536660

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2530105

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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.

VAERS 2477308

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2429694

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2421011

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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

Symptomtext

chest pain

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2417215

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2324237

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2322004

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2292734

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2280667

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2278160

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2245769

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2220344

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2209289

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2201432

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2157823

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2147496

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2109370

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

moderat
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
-

VAERS 2087665

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2063817

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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

VAERS 2024777

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2021535

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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).

VAERS 2019586

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 2006024

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 1992419

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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

VAERS 1985939

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 1981807

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

moderat
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
-

VAERS 1963724

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

moderat
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
-

VAERS 1963252

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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

VAERS 1962943

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

moderat
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
-

VAERS 1961824

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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)

VAERS 1955090

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 1954508

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 1948208

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 1947314

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

moderat
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
-

VAERS 1943901

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 1942506

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21B

moderat
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
-

VAERS 1940718

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

moderat
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
-

VAERS 1939026

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 1932144

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 1928678

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 1928362

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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

VAERS 1925146

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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
-

VAERS 1916430

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

moderat
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

VAERS 2713239

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2621935

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

mild
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.

VAERS 2576585

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge 029H21B

mild
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
-

VAERS 2533302

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2530133

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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

VAERS 2528938

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

mild
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
-

VAERS 2523020

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2465414

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2452120

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2366176

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2338893

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2335860

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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

VAERS 2325989

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2317349

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2313188

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2294370

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2286940

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2280928

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2266373

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2260427

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
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VAERS 2258463

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

mild
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
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VAERS 2236055

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2233725

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21b

mild
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
-

VAERS 2220425

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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.

VAERS 2209371

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2188850

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2182354

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2180002

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2178470

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2173310

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2162766

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2138014

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2101114

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2087401

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2068488

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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.

VAERS 2059243

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2058519

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2053790

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2043659

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2042002

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2037559

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2033257

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2029559

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 2019947

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1998035

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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)

VAERS 1984051

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

mild
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
-

VAERS 1981125

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1975287

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

mild
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
-

VAERS 1975094

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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

VAERS 1974476

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1955010

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1955010

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1963345

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1963327

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1959952

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1958897

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

mild
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
-

VAERS 1955072

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1954482

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

mild
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
-

VAERS 1946915

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1946895

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1946719

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

mild
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

VAERS 1944457

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1944227

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

mild
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
-

VAERS 1943504

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1942631

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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

VAERS 1942463

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1942191

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1940235

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1939542

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1939346

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1936337

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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

VAERS 1936121

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1932781

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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

VAERS 1929063

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1924700

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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
-

VAERS 1924276

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21B

mild
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
-

VAERS 1921279

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

mild
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.

VAERS 1920569

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

mild
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
-

VAERS 2709921

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

gering
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
-

VAERS 2664953

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2652745

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2619060

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2596208

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2595626

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2593234

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2593230

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2592454

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2567691

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2555851

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2545844

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2539092

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 1656085

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2507282

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2496694

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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

Symptomtext

congestion

Weitere VAERSDATA-Felder
Praegender Schweregrund
Respiratory tract congestion
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2494975

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2440796

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2429638

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2418190

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2414680

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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

Symptomtext

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
-

VAERS 2412685

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2408139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 029H21B

gering
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
-

VAERS 2396435

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

gering
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
-

VAERS 2396354

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2379403

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2355887

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2355886

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2355884

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2355883

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335757

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335756

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335755

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335754

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335740

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335737

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335735

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335732

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335560

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335517

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335514

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335512

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335509

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335137

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335135

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2335126

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2318407

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

gering
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
-

VAERS 2313056

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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

Symptomtext

covid

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2306960

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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

Symptomtext

covid

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2306107

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2293118

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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

VAERS 2292337

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2285772

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2226011

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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

Symptomtext

None

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
-

VAERS 2226004

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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

Symptomtext

No symptoms

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
-

VAERS 2211262

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2206459

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2162511

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2134622

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2115679

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2110085

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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

Symptomtext

None stated.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Unevaluable event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2109978

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2109949

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2107114

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2102061

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2101684

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2101625

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2098810

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2098807

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2080341

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2079883

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2079654

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 029H21B

gering
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
-

VAERS 2071969

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

gering
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
-

VAERS 2068618

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2068478

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2065559

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2050847

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2045792

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2038202

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21B

gering
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
-

VAERS 2031537

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2025282

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 2006233

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

gering
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.

VAERS 1985449

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 1971111

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 1959379

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

gering
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
-

VAERS 1951824

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

gering
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
-

VAERS 1943126

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 1940069

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 1936524

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

gering
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
-

VAERS 1935397

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-

VAERS 1929068

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029h21b

gering
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
-

VAERS 1923549

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 029H21B

gering
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
-