- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 02.10.2023
- Impfdatum
- 06.05.2022
- Beginn
- 09.09.2023
- Tage bis Beginn
- 491,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Blood gases abnormal
Blood iron decreased
Blood pH abnormal
Blood pH decreased
COVID-19
Chest X-ray normal
Chronic obstructive pulmonary disease
Condition aggravated
Dementia
Disorientation
Dyspnoea
Fall
Glycosylated haemoglobin normal
Hypercapnia
Hypoxia
Lethargy
Liver function test normal
Symptomtext
Patient is a 66 y.o. female who presented from ECF on 9/9/2023 with increased dyspnea and lethargy - found to have marked hypercapnia requiring persistent BiPap in the ED. History significant for COVID-19 Dx ~4 days PTA. Acute on Chronic Hypercapnic and Hypoxic Respiratory Failure Respiratory Acidosis Acute Exacerbation of COPD - With significant COPD history, likely exacerbated by sedating medications and COVID-19 infection. - Presentation VBG pH 7.20, pCO2 undetectably high (~120). - Initially required Bipap for hypercapnia - Currently weaned down to 4L NC (3L NC at baseline) - pt was started in BIPAP on admission - respiratory status improving, ABG's improved; pH normalized and pt taken off bipap - Continuing triple inhaler therapy. Unable to give Duo-nebs due to hospital policy with COVID - cont azithromycin. - Continuing steroid therapy for COPD and COVID as below. COVID-19 - Presented with: hypoxia, hypercapnia - Symptom onset: on 9/5 (approximately 5 days PTA) - Positive COVID-19: 9/6 at ECF and positive here on admission 9/10. - Vaccination status: Unknown - CXR showed no evidence of airspace consolidation. - Oxygen status: on BiPap on admission; now down to 3-4 L NC - Decadron: Yes. Expected end date 9/19 - Remdesivir: yes, end date 9/12 - DVT prophylaxis:Lovenox - Serial COVID labs ordered: No Acute Metabolic Encephalopathy Dementia - acute component due to hypercapnia above. Also some contribution possible from benzo/opiate use and acute infectious process. - pt with underlying dementia; per pt's brother pt with some baseline confusion though seems she is currently not at her baseline - awake and alert though disoriented on exam; follows commands; right sided upper ext weakness noted and chronic - given recent falls at ECF, will obtain CT head to ensure no acute bleed - pt's home scheduled ativan, gabapentin and prn morphine held on admission due to mentation - today pt now awake and alert though disoriented; follows commands - called ECF and confirmed pt on 1 mg ativan scheduled tid - will resume ativan at low dose 0.5 mg tid here and restart gabapentin lower dose at 100 mg tid - will hold prn morphine still Hx of Opiate Use Disorder with Chronic Opiate Dependence Suspected Benzodiazepine Dependence - Complex history, previously on Methadone on last discharge from OH (7/2022). ECF med list with Suboxone TID, Morphine PRN, and Lorazepam tid scheduled - Continue suboxone; adding back half home dose ativan tid - holding prn morphine Major Depressive Disorder - Continue home Buspar 20mg TID and Prozac 30mg daily. Dementia - Per history. - Continue home Aricept. Thrombocytopenia - Acute, suspected in the setting of acute viral infection as above. - PLT 106 on admission and down to 90 today - B12 normal; iron studies low with normal ferritin - monitor Hx of Hypertension Hx of DM2 - Previously on Amlodipine and Metformin, but since discontinued. Suspect in the setting of possible Hospice admission. - hgbA1c 5.1% - Continue to monitor BPs Hx of CVA - With noted RUE weakness chronically. - Continue home ASA 81mg. Hx of Hepatitis C - Unclear treatment history. LFTs within normal limits on admission. - Continue OP follow-up
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 26.04.2022
- Beginn
- 24.12.2022
- Tage bis Beginn
- 242,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Angiogram pulmonary abnormal
Anticoagulant therapy
Blood culture negative
Blood lactic acid decreased
Bronchial secretion retention
COVID-19
Computerised tomogram thorax abnormal
Cough
Dyspnoea
Emphysema
Haemoptysis
Hiatus hernia
International normalised ratio increased
Lung opacity
Malaise
Overgrowth fungal
Pneumonia
Pneumonia viral
Symptomtext
Patient is a 81 y.o. female patient of local MD with history of COPD, osteoporosis, squamous cell carcinoma of the tongue, arctic aneurysm, recent diagnosis of PE on Coumadin for anticoagulation is presenting with chief complaint of shortness of breath, cough with green sputum for about a week. Covid-19 Virus Infection Date of onset of symptoms: A week ago was around 12/18. Symptoms present on admission: Yes Date of covid positive test: 12/24 Vaccination status: vaccinated Imaging: CTPA?no acute PE with mild bilateral lower lung GGO which could reflect underlying mild pneumonitis. Borderline prominent heart size with suspected mild pulmonary hypertension. Extensive bilateral centrilobular and bullous emphysema with large hiatal hernia Oxygen requirements on admission: 3L patient is on 3 L oxygen chronically. Current oxygen requirements: 2-3 lit Medical therapy: Decadron started 12/27 given into no above home O2 demands. Remdesivir started 12/27 per HCP Consultants following: HCP Anticipated special isolation end date: 1/4/23 Breathing improving Pneumonia- viral CT pulmonary angiogram shows mild bilateral lower lung groundglass opacities at the right middle, bilateral lower lobes and left lingula. Findings reflect underlying mild pneumonitis. Afebrile. Vital stable. Oxygen saturation 96% on 3 L oxygen. Lactic acid 2.7, WBC 3.8. She was initiated on Rocephin CAP. Procalcitonin <0.06. Stop Rocephin, Check urine antigen- negative BC negative at 48 hours Sputum culture normal flora after 24 hrs with heavy growth yeast. Discussed with HCP- likely a commensal mucinex Incentive spirometry/PEP Episode of hemoptysis 1/01- now resolved- likely due to recent pulmonary infection in the setting of AC use Pulmonary consulted. 1/02 CT chest demonstrated developing segmenta and subsegmental bronchial airway endobronchial density likely due to mucus plugging. Mild multifocal bilateral lower lung ground-glass opacities/pneumonitis have intervally decreased when compared to CT 12/24/2022. Recent history of pulmonary embolism in November 2022 Hemoptysis. She is compliant with Coumadin, INR 2.7-- > 2.5 Patient reports specks of blood in the sputum for last 2 days prior to admission. Now ressolved CT chest as above. Continue Coumadin- dosing per pharmacy. Given return, consult pulm for evaluation Increase mucinex to 1200mg BID COPD Chronic respiratory failure She is on 3 L oxygen at baseline. Doxycycline- complete course Resume home inhalers.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 13.01.2023
- Impfdatum
- 22.04.2022
- Beginn
- 22.12.2022
- Tage bis Beginn
- 244,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Blood bicarbonate decreased
Blood creatinine increased
Blood culture negative
Blood urea increased
COVID-19
Chest X-ray abnormal
Cough
Dyspnoea
Electrocardiogram normal
Glycosylated haemoglobin increased
Hypotension
Lung infiltration
Malaise
Metabolic acidosis
SARS-CoV-2 test positive
Troponin increased
Symptomtext
Patient is a 61 y.o. male who is a patient of DO with significant medical history of HTN, bipolar disorder, cardiomyopathy, GERD, HFrEF, HLD, OSA presented to Hospital with dyspnea and hypotension. Acute respiratory failure with hypoxia Covid-19 Virus Infection Possible community acquired bacterial pneumonia Date of onset of symptoms: 12/17/22 Symptoms present on admission: malaise, dyspnea, cough Date of covid positive test: 12/17/22 Vaccination status: vaccinated Imaging: CXR with bibasilar infiltrates concerning for bacterial overlay, Though generally uncommon with covid - will check micro data and include antibiotics Cultures: Blood cultures no growth to date. Sputum culture, pneumonia urine antigens ordered Oxygen requirements on admission: 4L Current oxygen requirements: None Medical therapy: Decadron, Rocephin, Azithromycin Discharge Rx: Decadron to complete 10 days, Omnicef to complete 7 days, azithromycin to complete 5 days AKI on CKD Metabolic acidosis BUN 66 / Cr 2.72, Bicarb 16 Baseline Cr ~ 1.5 with some baseline variation With both AKI and acidosis, as well as contraindication to repeated bolus with resp failure Bicarb drip started on admission Nephrology consulted Creatinine improved to 1.65 on 12/25 Bicarbonate improved to 23 on 12/25 Follow-up with patient's primary nephrologist as outpatient Hypotension, resolved HTN Chronic HTN but reportedly hypotensive at home Told to hold antihypertensives and presents normotensive to mildly hypertensive Coreg, hydralazine, nifedipine resumed Valsartan to be held until follow-up with nephrology PAF Coreg for rate control Eliquis for stroke prophylaxis S/p pacer Chronic pancreatitis Continue Welchol and Creon Elevated troponin Troponin 73, chronically elevated, delta flat In absence of chest pain EKG paced without any convincing evidence of ischemia No further inpatient work-up DM2 with longterm insulin use A1c 7.1 Lantus and SSI Mood disorder Continue Depakote, Abilify, Buspar Decrease Nocturnal Ativan with respiratory failure OSA Nonadherent to CPAP Monitor on continuous pulse ox Chronic HFrEF With recovered EF at 55% Sept '21 Continue Coreg Hold Lasix initially with AKI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 12.04.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 230,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Angiogram pulmonary abnormal
Blood pressure increased
COVID-19
Chronic obstructive pulmonary disease
Condition aggravated
Cough
Dyspnoea
Hypoxia
Malaise
Pneumonia
Pulmonary mass
SARS-CoV-2 test positive
Tachypnoea
White blood cell count increased
Symptomtext
Patient is a 74 y.o. male patient of DO pmh copd, htn, schizophrenia who presents to ED with increasing shortness of breath and cough. Acute respiratory failure with hypoxia Pneumonia of right lower lobe due to infectious organism Acute exacerbation of COPD On presentation?hypoxic to 80%, tachypneic with respiratory rate to 26 WBC 13.79 CT PA with mild tree-in-bud nodules in the right middle and right lower lobes which may be infectious or inflammatory. Continue with dexamethasone, scheduled inhaler, omnicef and zithromax On 1 L of oxygen. To wean to RA Wean oxygen as tolerated, encourage incentive spirometry WBC up to 16 < 10, today, down to 13 Patient feels better, SOB improved so will DC home once fully weaned off oxygen. Patient advised to follow-up with his PCP. Covid-19 Date of onset of symptoms: 11/16/22 Symptoms present on admission: shortness of breath, cough Date of covid positive test: 11/18/2 Vaccination status: fully vaccinated per patient and received 4 total vaccinations Imaging: ct as above Oxygen requirements on admission: 3 to 4LNC Current oxygen requirements: 1 L Medical therapy: dexamethasone started 11/28/2022. S/p Paxlovid therapy for 5 days Consultants following: None Special isolation DC'd Essential hypertension BP elevated 140's to 170's Continue lisinopril 40 mg p.o. daily Hydrochlorothiazide 12.5 mg p.o daily increased to 25 mg daily BP better controlled Schizophrenia On invega q28 days, continue depakote and loxapine Family Contact Information Code Status: Full Code Quality Measures ? DVT Prophylaxis: Lovenox ? Foley Catheter: Absent Disposition ? Discharge Location: Home ? Estimated Discharge Date: 12/2/2022 ? Outpatient Testing: None
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 16.03.2021
- Beginn
- 01.07.2022
- Tage bis Beginn
- 472,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Death
Endotracheal intubation
Mental status changes
SARS-CoV-2 test positive
Septic shock
Symptomtext
pt brought to ED via ambulance for AMC and worsening respiratory status; required intubation; positive for COVID; septic shock; pt passed away that same day in the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 22.04.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 193,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal distension
Acute respiratory failure
Bacteraemia
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Chronic obstructive pulmonary disease
Condition aggravated
Death
Dyspnoea
General physical health deterioration
Malnutrition
Pneumonia
Positive airway pressure therapy
SARS-CoV-2 test positive
Staphylococcus test positive
Therapy cessation
Thrombocytopenia
Symptomtext
Patient is a 75 y.o. female of MD with history of COPD that presented to Hospital with shortness of breath for 1 week. Patient was positive for COVID-19 and CXR concerning for multifocal pneumonia. Patient required BiPAP since admission and was DNR DNI. She gradually continued to decline and became unresponsive to physical stimulation and painful stimulation. Additionally, patient's abdomen is distended due to air from BiPAP. Discussed at length with family members we decided patient should be DNRCC and be taken off the BiPAP. Comfort orders were placed, BiPAP was removed. Patient expired at 1245 on 11/7/2022. Acute hypoxic respiratory failure secondary to multifocal pneumonia from Covid-19 Virus Infection Acute COPD exacerbation secondary to pneumonia Concern for Viral Sepsis due to COVID pneumonia, POA Date of onset of symptoms: 1 week Symptoms present on admission: Shortness of breath Date of covid positive test: 11/1/2022 Vaccination status: vaccinated Imaging: Chest x-ray shows multifocal pneumonia Oxygen requirements on admission: BiPAP Current oxygen requirements: BiPAP with supplemental oxygen FiO2 40% Medical therapy: Completed course of remdesivir. Was being given steroids. Bacteremia Blood culture turned positive with staph species. This is likely contaminant. Discontinued vancomycin. Thrombocytopenia Possibly related to viral infection Nutrition Patient unable to take adequate nutrition being BiPAP dependent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 14.11.2022
- Impfdatum
- 11.03.2021
- Beginn
- 26.10.2022
- Tage bis Beginn
- 594,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood glucose increased
COVID-19
Death
Hypotension
Lethargy
SARS-CoV-2 test positive
Speech disorder
Unresponsive to stimuli
Symptomtext
Pt to ED 10/26 for high blood sugar. PT COVID+ 10/26. Patient is non verbal, monitor shows ST, BP is low. 10/27 Pt is lethargic, unable to follow commands, no signs of pain/discomfort. Pt expired 10/28.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 3,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acute respiratory failure with hypoxia and hypercapnia ...
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG PO Tab; amLODIPine (NORVASC) 10 MG PO Tab; aspirin 81 MG PO Chew Tab; atorvastatin (LIPITOR) 40 MG PO Tab; Cholecalciferol (vitamin D) 25 MCG (1000 UT) PO Tab; Dextrose, Diabetic Use, (glucose) 4 GM PO Chew Ta
- Allergien
- Sulfa antibiotics
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 91,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 11.04.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 156,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal distension
Acinetobacter bacteraemia
Acute respiratory failure
Aspartate aminotransferase increased
Blood bilirubin increased
Blood creatinine increased
Blood lactic acid
C-reactive protein increased
COVID-19
Cardio-respiratory arrest
Chest X-ray abnormal
Computerised tomogram head normal
Computerised tomogram spine
Contusion
Death
Edentulous
Endotracheal intubation
General physical health deterioration
Symptomtext
Moderna COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. Rec'd Moderna vaccine on 1/11/2021, 2/8/2021, 9/18/21 and 4/11/22. Admitted for acute hypoxemic resp failure 2/2 PNA in severe resp distress, Tachypnea 40s, O2 sat 70s, pink frothy sputum, BL Ronchi, distended abd, bruises, edentulous. In ED, placed on Airvo 60L/60% with O2 sat 84-89%, rapidly declined requiring emergent intubation. Pertinent labs include COVID-19 positive, Lactic acid 2.2-- >1.9, Procal 3.90, CRP 1.9, Troponin 40-- >38, NT-proBNP 20679, Scr 1.41, bilirubin 1.2, AST 55, and PLTs 118. CXR c/w RLL infiltrate. Influenza A/B. Head & Cervical spine CT w/o acute injury. Admitted to ICU s/p intubation for HLOC. Febrile at 103, v-paced rhythm 80-90s, and SBP 102-140s. Dx'd w/Acute hypoxemic resp failure 2/2 COVID, Acinetobacter, and Moraxella pneumonia and also developed Acinetobacter Bacteremia. Ex'd 9/14/22 after code blue for PEA arrest. After 20 minutes of CPR, family withdrew care. Tx'd with remdesivir, cefepime, vancomycin, unasyn, methylprednisolone, and metronidazole
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 10,0
- Labordaten
- covid + 9/04/22 - This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HFreF-CAD, Afib/Vfib on eliquis s/p ACID, TIA, Aortic dissection, HTN, HLD, CAD, COPD, CKD-II, BPH, GIB/GERD, anemia of chronic disease
- Andere Medikamente
- albuterol, atorvastatin, carvedilol, furosemide, multivitamin, xarelto, silver sulfadiazine, tiotropium, trazodone, vitamin a/c/e/zinc/copper
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 14.03.2022
- Beginn
- 17.09.2022
- Tage bis Beginn
- 187,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
COVID-19
COVID-19 pneumonia
Condition aggravated
Death
Delirium
Dyspnoea
Fatigue
Insomnia
Interstitial lung disease
SARS-CoV-2 test positive
Symptomtext
Moderna COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. Rec'd Moderna vaccine on 1/13/2021, 2/10/2021, 10/15/2021 and 3/14/22. Presented to ED 09/12/22 w/increasing SOB and O2 needs. In ER, patient in afib RVR, HFNC 60L/60%, given IV MP 100, vanc/cefe, lasix, diltiazem gtt. Admitted for afib, Covid PNA and interstitial lung dx. Episodes of delirium w/decreased sleep, improved with nightly prn precedex. Cont'd increasing O2 demands, eventually max'd on Airvo. Became increasingly tired, requested to change status to DNR. Expired on 9/17/22. Tx'd w/remdesivir, methylprednisolone, bactrim, doxycycline, vancomycin, cefepime, and acyclovir.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 6,0
- Labordaten
- covid 19 + 9/13/22 - This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ILD/UIP,Squamous cell lung cancer s/p SBRT, afib on eliquis, chronic steroids for ILD flare
- Andere Medikamente
- amlodipine, apixaban, ascorbic acid, atorvastatin, biotin, carboplatin, vitamin d3, dexamethasone, gemcitabine, omega 3, loratidine, losartan, magnesium, multivitamin with minerals, naproxen, nitedanib, ondansetron, PEG 3350, prednisone, pr
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 19.09.2022
- Impfdatum
- 25.03.2021
- Beginn
- 01.07.2022
- Tage bis Beginn
- 463,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Death
General physical health deterioration
Hypophagia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
pt in Health and Rehab; on hospice; pt had a positive COVID test on 7/8/22; pt gradually declined with increase in congestion; poor oral intake; pt passed away in the facility
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- VASCULAR DEMENTIA, ALZHEIMER'S DISEASE, HYPOTHYROIDISM, HLD, GERD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 23.03.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 24,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adult failure to thrive
Condition aggravated
Death
Symptomtext
Patient tolerate vaccine well day of administration. Reported patient in hospice care, cause of death was adult failure to thrive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Adult Failure to Thrive
- Vorgeschichte
- Adult Failure to Thrive Weakened immune system History of leukemia
- Andere Medikamente
- Unknown
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 02.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Resident passed away 5 days after getting the booster dose. Received Primary Moderna vaccine on 8/20/2021 and 9/17/2021. Booster dose on 3/2/2022. Resident died on 3/7/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- S/P cardiac cath, complex CAD
- Vorgeschichte
- Hypertension, Diabetes, Hyperlipidemia, Pyelonephritis, mild mitral regurgitation, renal stones diverticulosis, cardiomyopathy, anemia, systolic- diastolic cardiac dysfunction, history of cerebral artery occlusion with cerebral infarction.
- Andere Medikamente
- Protonix, Lisinopril, Carvedilol, Vit D3, Crestor, Gabapentin, Aspirin, Insulin, Jardiance, Plavix
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 03.03.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Agitation
Condition aggravated
Headache
Hypersensitivity
Pain in extremity
Productive cough
Respiratory arrest
Resuscitation
Seizure
Speech disorder
Symptomtext
Patient presented to the pharmacy for her second Moderna COVID-19 vaccine. Patient was unable to fill the form out herself, so I had to assist the patient with the questions. Patient stated she had no problems with her first Moderna vaccine 4 weeks ago. I asked the patient how she felt post injection and she stated she did not feel the injection. Patient rolled down her arm sleeve and when I felt her shoulder to make sure the bandage was not removed, the patient stated her arm felt sore. I advised the patient to wait at least 15 to 30 minutes to make sure she felt okay. Patient walked to observation area and sat with her mother. Approximately 10 minutes later, mom told a technician at the register she thought the patient was having an "allergic reaction". The technician alerted me (the pharmacist) and I immediately went to the patient to determine the situation. Mom stated patient was "having trouble talking", which is what happens when patient is having an allergic reaction. My staff called a code white to have management come to the pharmacy for assistance and also called EMS/911. I advised mom and patient I could give liquid Benadryl & mom agreed (patient shook her head yes). I then attempted to administer 5 mL of Diphenhydramine (12.5mg/5mL) to the patient using an oral syringe; I was only able to give the patient about 2mL before patient shook her head that she did not want anymore medication and made a face as if the medication tasted bad. About a minute later patient started holding her head between her hands stating her head hurt. Patient was becoming pretty agitated and I asked if mom and patient about moving the patient to the floor. Mom stated no, that placing her on the floor would make the head pain worse. Within a few minutes, patient appeared to be having a seizure. We then moved the patient from the chair to the floor and placed patient on her side in case she vomited. Patient did not vomit but had a little bit of spit up. It then appeared the patient had stopped breathing. At this point, patient was placed on her back and three chest compressions were given. Patient immediately started breathing. EMS arrived at this point and gave Versed IM because the patient was starting to have yet another seizure. Patient was then transported by EMS to the hospital. Patient left the pharmacy awake and more coherent of her surroundings after receiving the Versed and the seizure had stopped.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory arrest
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Patient did not state any recent illnesses within the past month.
- Vorgeschichte
- Patient stated seizure history on consent form (takes medications for seizures but unable to provide accurate medication list).
- Andere Medikamente
- Patient stated she takes medications for a seizure history. However, she was unable to provide medication names on consent form. This pharmacy does not fill medications for this patient either.
- Allergien
- Patient stated allergic to cinnamon and other foods but not able to provide further details. Patient stated no allergies to medications. (Topiramate and aspirin allergy per our file). Patient received first dose of Moderna on 02/03/2022 without problems.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 12.01.2023
- Impfdatum
- 16.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Cough
Gait inability
Influenza virus test negative
Pain
Paralysis
Pyrexia
SARS-CoV-2 test negative
Skin laceration
Symptomtext
Narrative: 3/172022 ED visit: Pt presented to agency ED with c/o general weakness since yesterday. Pt said he got COVID vaccine yesterday. Denies SOB. Has some cough, body aches at home. He states he woke up with 104 temp today. 3/24/22 - Pt states he is doing okay but says last Wednesday (3/16) he had his COVID booster and the next day he woke up and "felt paralyzed" as he says he could not move. He went to a community ED but after being sent home, he decided to come to the facility. He says a few hours later he felt better and was allowed to be discharged. He says he was having fever and could not walk so he tried crawling but skinned his legs in the process. He is much better today and has no complaints.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- -
- Labordaten
- COVID19 and FLU tests are NEGATIVE today Vital Signs * Temperature 102.5 F (39.2 C) Pulse 98 Respirations 18 Blood Pressure 145/76 Pain scale recorded: 0 Pulse Oximetry 94 Room Air
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 16.12.2022
- Impfdatum
- 27.04.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 223,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram cerebral abnormal
Anticoagulant therapy
Asymptomatic COVID-19
Cerebral venous thrombosis
Electroencephalogram normal
Hypoaesthesia
Idiopathic intracranial hypertension
Magnetic resonance imaging head normal
Neurological symptom
Paraesthesia
SARS-CoV-2 test positive
Symptomtext
"Patient with 3 COVID vaccines who admitted to hospital after COVID detected test for left sided numbness. Provider d/c note: ""Hospital Course: No notes on file These were her acute medical issues addressed: 1. Transient L sided paresthesias. No acute CVA on imaging(brain MRI); could have been a TIA? EEG - unremarkable. No seizure activity. -- consulted Neurology. Neurologic symptoms of transient nature. Unclear source. 2. ? L cortical venous thrombosis by Cerebral angiogram 11/28/22. -- continue with Eliquis BID. -- diagnosed by conventional angiography on 11/28/2022. 3. Migraines. -- continued Topamax/ Neurontin/ Nortriptyline 4. ?Psudotumor cerebri 5. HTN -- cont Amlodipine 6. Obesity -- BMI 48.8 7. OSA 8. Polypharmacy. DC'd redundant medications from her medication list. 9. COVID-19 positive: Asymptomatic. NOT hypoxic at all Vaccinated x 2 and boosted x 1. DC home with paresthesia symptoms completely resolved. Will follow up with Neurology as previously scheduled."""
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebral venous thrombosis
- Hospital-Tage
- 3,0
- Labordaten
- COVID Detected PCR on 12/6/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular Migraine Primary hypertension Cerebral venous thrombosis of cortical vein without infarction Respiratory Obstructive sleep apnea Asthma Other Morbid obesity (HCC) Folate deficiency B12 deficiency Iron deficiency anemia secondary to inadequate dietary iron intake Dysarthria Cervical disc disease with myelopathy Transient neurologic deficit Seizure-like activity (HCC)
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 25.09.2022
- Impfdatum
- 29.04.2022
- Beginn
- 30.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electric shock sensation
Insomnia
Nausea
Pain in extremity
Paraesthesia
Suicidal ideation
Vibratory sense increased
Symptomtext
I am a 67 yr old extremely healthy vegan woman, runner. I haven't been to the doctor for an illness in over 12 yrs. After the 4th Moderna booster I got extreme soreness in my 3rd and 4th rt toes. I thought it was from running with new shoes. A week later pins and needles started in both feet, primarily my left, and some pins and needles in my hands. The pins and needles have never subsided. I've had insomnia and feelings like a buzzing and electric current going through my body for hours at a time. I have been suicidal, several times, which I have never been before in my life. It has been 5 months now and this is continuing. I found a vaccine forum online where thousands of others are reporting similar symptoms. Sometimes I'm okay with it and other times I'm just holding on. I am pro-vaccine and feel it has saved 100s of thousands of lives, but this has affected me terribly. I hope that the FDA and CDC can help us.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Little nausea after 4/29/2022 which was my 2nd Moderna booster
- Vorgeschichte
- None
- Andere Medikamente
- B12
- Allergien
- None that I know of
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 15.08.2022
- Impfdatum
- 13.05.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 19,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test abnormal
Catheterisation cardiac
Coronary arterial stent insertion
Dizziness
Electrocardiogram
Fatigue
Haemorrhage
Head injury
Impaired driving ability
Laboratory test abnormal
Nausea
Syncope
Symptomtext
On 06/01/2022 I woke up with extreme exhaustion. While in the shower I felt nauseated and lightheaded. I fainted and hit my head on the door handle of the shower. I was bleeding and was taken to the ER. While I was there they did a number lab work some did come out as abnormal also had a borderline ECG. They kept my 1 day and diagnosed my with syncope. I did have the same feeling throughout the next few days. I did see my primary doctor and ended up having a heart cath and placed two stents. I still am dealing with fatigue and sometimes light headed to the point I do not feel comfortable driving. I have had some of these symptoms previously but now it seems like it is more frequent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 1,0
- Labordaten
- Multiple blood draws 06/01/2022 some abnormal. ECG 06/01/2022 borderline.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure; High Cholesterol; Coronary Artery Disease
- Andere Medikamente
- CRESTOR; ramipril; PEPCID; aspirin; coQ10; vitamin D; multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 02.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Chest X-ray
Dyspnoea
Dyspnoea exertional
Electrocardiogram
Fatigue
Hypersomnia
Night sweats
Pulmonary oedema
Symptomtext
I was really tired for 3 or 4 days, sleeping 12 hours at night and 6 hours during the day. Then that went away but the thing that bothered me the most was shortness of breath. It is not unusual for someone my age but unusual for me. I would go up my steps, which is 14 steps, and I was out of breath. I would also have night sweats. I ended up going to the ER and they did a bunch of tests on me. They took blood twice, they were checking to see if I had a heart attack. I was there for 5 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary oedema
- Hospital-Tage
- -
- Labordaten
- Blood work; chest x ray; EKG twice. They said I had fluid in my lungs but could not hear anything in scope.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Afib
- Andere Medikamente
- Rosuvastatin Gelation Warfarin Centrum Multivitamin
- Allergien
- Amoxicillin
- Vorherige Impfungen
- Moderna, 2nd dose
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 23,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Amnesia
Angiogram cerebral abnormal
Anticoagulant therapy
Arteriogram carotid abnormal
Arteriosclerosis
Blood test normal
Cerebral arteriosclerosis
Computerised tomogram head normal
Confusional state
Dyspepsia
Electrocardiogram normal
Memory impairment
NIH stroke scale
Neurological examination normal
Repetitive speech
SARS-CoV-2 test negative
Transient global amnesia
Troponin normal
Symptomtext
Symptoms of confusion, memory loss began around 8:00 AM on April 22, 2022. The previous night, patient had heartburn but was otherwise okay. Patient's partner drove her to the Emergency Room at a Hospital where she was evaluated by an ER physician for possible stroke or heart attack. Vital signs were taken, blood work was done, a brain CT scan was done, and patient was admitted. Patient was administered Plavix and 81 mg. aspirin. Later testing took place as detailed below. Patient's memory returned after about three hours, but the three hours were never recalled. Diagnosis was Transient Global Amnesia. WE DO NOT KNOW THAT THIS WAS RELATED TO THE VACCINE!! ER doctor's note at admission: Patient is a 70-year-old female with history of GERD, valvular heart disease, migraine headaches, woke up feeling well except for some heartburn. Her partner noticed her confusion and loss of memory that began around 8 AM on April 22. Specifically he states that she was forgetting what season it was and was forgetting conversations they were having and was having repetitive questioning and seemed confused. Her speech was never slurred and she never had a headache or diplopia or dysarthria or dysphagia or focal weakness or numbness. She never had vertigo or ataxia. Currently her symptoms are resolving and her mental status seems to be at baseline but still has loss of memory for some of the events of this morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- NIH stroke scale
- Hospital-Tage
- 1,0
- Labordaten
- CT head read as negative. CT angio head and neck shows minimal atherosclerotic disease only. Blood work including troponin are negative. Rapid COVID-negative. EKG is normal with a heart rate of 73. Code stroke called on arrival by the nurse. Signs and symptoms most consistent with transient global amnesia. NIH stroke scale is now 0 and tPA not indicated. Neurologic exam remains normal. ER physician discussed the case with Dr. (neurologist) who wanted the patient started on a baby aspirin daily and 75 mg of Plavix daily. Discussed case with second Dr. who agrees to admit.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mitral and tricuspid valve repair; arthritis; high BP, anxiety
- Andere Medikamente
- Bupropion SR 150 mg; Rosuvastatin 10 mg; Omeprazol 40 mg; Verapamil ER 180 mg; Paroxetine 20 mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 29.03.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 13,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
C-reactive protein normal
Diplopia
Full blood count abnormal
Glycosylated haemoglobin normal
Lipids normal
Magnetic resonance imaging head normal
Magnetic resonance imaging normal
Metabolic function test normal
Red blood cell sedimentation rate normal
Thyroid function test normal
VIth nerve paralysis
White blood cell count decreased
Symptomtext
Developed left Abducens Nerve palsy, double vision
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- VIth nerve paralysis
- Hospital-Tage
- -
- Labordaten
- MRI of Brain and Orbit negative . CBC showed WBC low at 2.9, rest normal Comprehensive panel , thyroid panel , lipid panel ,sed rate and C rp , Hemoglobin A1C we?re all normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- BPH, arthritis, hypothyroidism
- Andere Medikamente
- Tamsulosin, finasteride, levthyroxine, meloxicam, B complex
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 09.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blood test
Dizziness
Fatigue
Fear
Influenza like illness
Loss of consciousness
Muscular weakness
Pain
Pyrexia
Symptomtext
I had flu like symptoms with dizziness, fever, body aches. On the second day I was very dizzy and then I passed out. I woke up on the bathroom floor. I have no idea how long I was passed out for and I was alone. This was very scary for me. I felt exhaustion and muscle weakness. I did report this to my doctor. My Endocrinologists and he suggested that I not have another COVID-19 vaccine. My muscle pain and nerve issues remained the same after the 1st and 2nd dose of Moderna which was reported also.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Blood work
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Brain tumor non-cancerous; fibromyalgia; unilateral vestibular hypofunction; hypothyroidism; brain injury
- Andere Medikamente
- Cabergoline; Synthroid; Liothyronine; Multivitamin; Vitamin D; Magnesium
- Allergien
- Morphine; Sulfa
- Vorherige Impfungen
- Moderna - 1st dose and 2nd dose E- report 834152, 834159
- Staat
- TX
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 12.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Computerised tomogram normal
Electrocardiogram normal
Immunisation reaction
Loss of consciousness
Magnetic resonance imaging normal
Symptomtext
Patient stated that the day after she received the vaccine - she "blacked out" on two different occasions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- She saw her dr and said dr had several tests performed: EKG, MRI, CT scan and all came out normal. The doctor then asked if by chance she had received any recent vaccines and she said she had gotten the Covid shot the day before this happened. Patient says that after telling office about the vaccine that they looked into it further and decided that she had experienced her reaction as a result of the COVID vaccine.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anaphylactic reaction
Blood pressure abnormal
Confusional state
Dizziness
Eye swelling
Hypoaesthesia
Hypotension
Loss of consciousness
Mouth swelling
Paraesthesia
Paraesthesia oral
Pulse abnormal
Swelling face
Swollen tongue
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Allergic: Anaphylaxis-Severe, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Severe, Systemic: Confusion-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Hypotension-Severe, Systemic: Numbness (specify: facial area, extremities)-Severe, Systemic: Tingling (specify: facial area, extemities)-Severe, Additional Details: <10 mins post moderna booster pt reported "feeling faint and tingling lips." pt received previous vaccine doses 5/12/21+6/9/21 without issue. h/o anaphylaxis to lactose. symptoms began to worsen: pulse faint, bp undetectable, loss conciousness (<1min). came to upon arrousal, still weak pulse/tingling mouth. administered epi x 1, ems arrived and took over care. transported to er.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 21.09.2023
- Impfdatum
- 05.11.2022
- Beginn
- 18.08.2023
- Tage bis Beginn
- 286,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pneumonia
Pneumonia bacterial
Superinfection
Symptomtext
8/18/2023 - 8/20/2023 (2 days) Date of Admission: 8/18/2023 Discharge Date: 08/20/23 Discharge Disposition: Home or Self Care past medical history of hypertension, hyperlipidemia, pre diabetes, peripheral neuropathy, peripheral arterial disease, osteoarthritis, chronic disease stage I, obesity. no indication for Decadron due to no hypoxia or requirement of oxygen. On remdesivir currently day 3. On empiric Rocephin and Zithromax in hospital to cover for probable superimposed community-acquired bacterial pneumonia as the symptoms going on for more than 10 days. 012M20A 1/28/2021 Moderna 002A21A 3/1/2021 037F21A 11/9/2021 033K212A 4/18/2022 014H22A 11/5/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 14.03.2023
- Impfdatum
- 12.03.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 137,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arrhythmia
Blood pressure increased
COVID-19
Cardiac disorder
Electrocardiogram ambulatory
SARS-CoV-2 test positive
Symptomtext
I had my vaccination on 03/10/2022. On 07/27/2022 I went to the pharmacy and tested COVID-19 positive. I received the results on 07/30/2022. I was provided monoclonal antibodies as a course of treatment. On 08/17/2022 I was still COVID-19 positive. I was prescribed PAXLOVID. I started to have some cardiac events with increase in blood pressure with arrhythmia after testing COVID-19 positive. I did wear a heart monitor for 30 days. I am scheduled for an Echocardiogram on 04/04/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- 07/27/2022 COVID-19 positive 08/17/2022 COVID-19 positive 12/14/2022 to 01/11/2023 I wore a heart monitor for 30 days.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; Osteoarthritis; Immune Compromised
- Andere Medikamente
- Lisinopril; LASIX; propranolol; acyclovir; amlodipine; potassium; calcium; vitamin D; iron; probiotic; EVUSHELD
- Allergien
- Codeine; sulfa; CIPRO; NSAIDS
- Vorherige Impfungen
- Flu vaccination; achy with sore arm and low-grade fevers; COVID-19 vaccinations fever achiness
- Staat
- MI
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 03.03.2023
- Impfdatum
- 08.03.2022
- Beginn
- 24.02.2023
- Tage bis Beginn
- 353,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blood lactic acid normal
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Cough
Exposure to SARS-CoV-2
Hyperkalaemia
Hypotension
Hypoxia
Liver function test increased
Pneumonia
Procalcitonin increased
Respiratory failure
SARS-CoV-2 test positive
White blood cell count normal
Symptomtext
Discharge Physician: MD Primary Care Physician: MD Date of Admission: 2/24/2023 Discharge Date: 2/28/2023 Room Number: PRESENTING PROBLEM: Pneumonia of right lower lobe due to infectious organism Pneumonia due to COVID-19 virus COVID-19 Patient is a 61 y.o. male past medical history down syndrome, achalasia and dysphagia with feeding tube in place, anemia, elevated LFTs and GERD who presents with cough and weakness. Hospitalized from 1/31-2/2 with abdominal wall cellulitis and pneumonia and completed 5 days of Azithromycin and rocephin. In the Emergency Department, he was noted to have hypoxia down into the 80s at times and required 2L NC. He tested positive for COVID in the ER. Per report other residents at his AFC and care givers also positive. His procal was elevated at 0.62 and CXR showed concern for worsening of right lung with multifocal pneumonia. He had normal lactic acid and WBC and did not meet sepsis criteria. He did have some softer blood pressures in the ER but improved with IVF. He was noted to have hyperkalemia and elevated LFTs but LFTs were similar to recent admit. He was given IVF and started on azithromycin and rocephin in the ER but switched to cefepime on admit. He was admitted to the hospitalist team for COVID, respiratory failure and pneumonia. Patient was able to wean oxygen. He was continued on antibiotics (and discharged to complete 5 day coarse of antibiotics) and decadron during admit. His labs improved, vitals and lung sounds improved. Patient was able to ambulate out of bed the day of discharge. Patient is clinically improved and hemodynamically stable for discharge. Discussed plan of care for discharge with AFC and guardian including outpatient follow-up with PCP within 7 days. They voiced understanding and were agreeable with plan of care for discharge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- 3/8/2022 Medical group Cellulitis of abdominal wall
- Vorgeschichte
- MR (mental retardation), severe Down syndrome Allergic rhinitis GERD (gastroesophageal reflux disease) Anxiety Other dysphagia Esophageal achalasia with dysphagia NPH (normal pressure hydrocephalus) Gastrostomy tube in place Elevated BP without diagnosis of hypertension DNR (do not resuscitate) Feeding tube dysfunction, initial encounter Abdominal wall cellulitis Normocytic anemia COVID-19 Thrombocytopenia
- Andere Medikamente
- acetaminophen (TYLENOL) 32 MG/ML suspension ALPRAZolam (XANAX) 1 MG tablet betamethasone dipropionate 0.05 % cream carbamide peroxide (DEBROX) 6.5 % otic solution clotrimazole-betamethasone (LOTRISONE) cream fluticasone (FLONASE) 50 MCG/ACT
- Allergien
- Chloral Hydrate LactoseDiarrhea
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 05.05.2022
- Beginn
- 23.10.2022
- Tage bis Beginn
- 171,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Influenza virus test positive
Pneumonia
Respiratory syncytial virus test positive
SARS-CoV-2 test positive
Symptomtext
Date of Admission: 10/23/2022 Date of Discharge: 10/25/2022 Admission Diagnosis: Community acquired pneumonia of right upper lobe of lung Hospital Principal Problem (Discharge Diagnoses): Shortness of breath
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 10/23 Covid-19, Flu, RSV by NAA, Detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 55,0
- Geschlecht
- U
- Eingang
- 20.12.2022
- Impfdatum
- 13.04.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 250,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dyspnoea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 21.10.2022
- Impfdatum
- 16.04.2021
- Beginn
- 31.08.2022
- Tage bis Beginn
- 502,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest pain
Dizziness
SARS-CoV-2 test positive
Symptomtext
08/31/22 presents to ED for "chest pain" "lightheadedness". PMHx of "heavy alcohol use, DVT, subdural hematoma, delirium tremens, Warnicke encephalopathy"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 08/31/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 18.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Diverticulum
Symptomtext
I had my vaccination on 04/18/2022. About a week later my Diverticulosis flare-up and was continuous for every 3-4 weeks. I could take the Ibuprofen to get it under control but the flare-ups were persistent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diverticulosis; Allergies; Gout; Kidney Stones
- Andere Medikamente
- Allegra; Allopurinol; Potassium Citrate
- Allergien
- Penicillin, Vancomycin
- Vorherige Impfungen
- Covid-19 03/29/2021 Diverticulosis Flare-up
- Staat
- OH
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 08.04.2022
- Beginn
- 05.09.2022
- Tage bis Beginn
- 150,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Confusional state
Dyspnoea
Mental status changes
SARS-CoV-2 RNA
SARS-CoV-2 test
COVID-19
SARS-CoV-2 test positive
Symptomtext
Symptoms include shortness of breath and confusion in mental status.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- SARS-CoV-2 Antigen specimen collection 9/5/22 2019 Novel Coronavirus RNA specimen collection 9/9/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular disease, Hypertension, Chronic Renal Disease, and Cancer
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 08.04.2022
- Beginn
- 05.09.2022
- Tage bis Beginn
- 150,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Confusional state
Dyspnoea
Mental status changes
SARS-CoV-2 RNA
SARS-CoV-2 test
COVID-19
SARS-CoV-2 test positive
Symptomtext
Symptoms include shortness of breath and confusion in mental status.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- SARS-CoV-2 Antigen specimen collection 9/5/22 2019 Novel Coronavirus RNA specimen collection 9/9/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular disease, Hypertension, Chronic Renal Disease, and Cancer
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 04.04.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 171,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Feeling abnormal
Hyperaesthesia
Lymphadenopathy
Mobility decreased
Nasal congestion
Rhinorrhoea
SARS-CoV-2 test positive
Tenderness
Symptomtext
9/22/2022, I thought it was allergies from working out in the yard. I had a runny nose, cough, head congestion. On Friday, 9/23/22, the same symptoms were increased, fatigue, brain fog, so I tested at home and it was negative. All weekend it was the same symptoms, coughing more, very fatigue. I did not feel like getting off the couch. My head was foggy and spinning. On Sunday I felt a little bit better and on Monday I felt worse again and I had a swollen lymph node on my neck. On Tuesday it was worse and more swollen. Sore to touch and that area was so tender. I tested on Tuesday, 9/27/2022 and it was positive. I did a telehealth over the phone with my provider. She started me on the PAXLOVID. I take vitamin D 2000 mg for my osteoporosis and the doctor increased that to 4000 mg. 10/7/2022, it has been 2 weeks, and I still feel like I have a little brain fog and I still have been coughing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- 9/23/2022 COVID-19 home test negative, 9/27/2022 COVID-19 home test positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; osteoporosis
- Andere Medikamente
- Lisinopril; omeprazole; CELEBREX; vitamin D; folate; SINGULAIR
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 11.09.2022
- Impfdatum
- 14.03.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Joint injury
Limb injury
Pain in extremity
Paraesthesia
Symptomtext
Site: Pain at Injection Site-Medium, Systemic: Joint Pain-Medium, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Additional Details: Patient is experiencing prolonged pain in his left arm and shoulder. He saw his primary care MD with no resolution. He does not want to pay out of pocket for additional testing or therapy. Escalating to Risk to coordinate treatment options that will not require the patient to pay out of pocket.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 97,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 15.04.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 126,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Blood potassium increased
Blood urine present
COVID-19
Dyspnoea
Glomerular filtration rate decreased
Hyperkalaemia
Laboratory test
Prohormone brain natriuretic peptide
SARS-CoV-2 test positive
Urine analysis abnormal
Urine leukocyte esterase positive
White blood cell count increased
White blood cells urine positive
Symptomtext
Discharge Provider: DO Primary Care Provider: NP Admission Date: 8/19/2022 Discharge Date: 8/22/2022 PRESENTING PROBLEM: COVID-19 Acute kidney injury (HCC) AKI (acute kidney injury) (HCC) COVID HOSPITAL COURSE: Patient is a 97 y.o. male who presents today with a history of hypertension, hyperlipidemia, chronic obstructive pulmonary disease, coronary artery disease, a flutter. Patient presented to a local emergency department from a residential facility after staff noted patient was somewhat short of breath. Patient was given a nebulized breathing treatment with no improvement. When EMS was called they noted patient was not wheezing and found him to have no respiratory distress. They then proceeded to bring patient to emergency department for further evaluation. Upon arrival to the emergency department patient was not showing any signs of respiratory distress. Initial workup showed patient tested positive for COVID-19. Lab work showed acute kidney injury with decreased GFR of 34 with previous readings normal. ProBNP was 26 44. WBC 12.8, potassium 5.7. UA showed large leukocytes, large blood, urine WBC >180. Patient was then started on IV Rocephin. Patient was given 20 mg IV Lasix for the elevated BNP and elevated potassium level. Emergency department provider did talk to patient's daughter and she confirmed patient as a do not resuscitate. Hospital Services was contacted and accepted patient for admission for acute kidney injury and hyperkalemia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Unspecified dementia without behavioral disturbance (HCC) Fall from ground level Multiple rib fractures Pulmonary hypertension (HCC) Atrial flutter (HCC) Encephalopathy Bradycardia Malnutrition due to starvation (HCC) COVID-19 Acute cystitis
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin 81 MG enteric coated tablet benzonatate (TESSALON) 100 MG capsule dexamethasone (DECADRON) 6 MG tablet (Expi
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Apathy
COVID-19
Dyspnoea
Dysstasia
Fatigue
Fear
Feeling abnormal
Headache
Impaired work ability
Laziness
Loss of personal independence in daily activities
Malaise
Nasal congestion
Nasal discomfort
Oropharyngeal pain
Rash
Respiratory tract irritation
SARS-CoV-2 test positive
Symptomtext
My partner had symptoms several days before i did, Then i came down with them 3 days later. It started with sinus and fatigue. I couldn't breathe and very clogged nose and it was burning. I had a very light sore throat. I think the thing in my throat was the first symptom. And then i woke up and my head was stuffy. I really didn't wanna do anything. I tried to work but couldn't. On day 8 i got slammed with a major headache and brain fog. It was scary. I was on Paxlovid. It really scared me, i called the doctor and everyone, day 9/10 i had heavy brain fog. on day 10 i tested negative. I just felt crappy and fatigue and lazy over the next week but it was getting better. I had skin legions. i was breaking out everywhere. And all that went away as the brain fog went away. One of the trail symptoms is it feels like i have something that i needed to cough up. cough drops were helpful. Its only this week i would say over the weekend i started feeling better. Monday was the first day i could go to work. A week ago Wednesday i was feeling kinda good and then i was like great im gonna go run a errand and i went out and stop by some markets and gas and i couldn't stand up. I got 2 more days of rest and got better. And yesterday by back of throat symptoms started again and i gave up and took and nap, im just tired.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19- positive PCR- positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hyperthyroidism, Over Weight
- Andere Medikamente
- Levophyroxine; Acyclovir; Naproxin; Baclofin; Oxycodone;
- Allergien
- Eggs; Vicodin; Garlic
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 22.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Heart rate irregular
Hypoaesthesia
Migraine
Paraesthesia
Thirst
Vertigo
Vision blurred
Symptomtext
I waited an hour after receiving the injection due to my health hx of allergic reactions.I left the Health Dept approx at 3:50 pm. I felt fine during this time and had no sx. As I was driving home I suddenly felt extreme fatigue and blurred vision. I drove the 15 minutes to my house and immediately went to lie on my bed. I fell asleep and awoke at 11:43 pm. I didn?t feel any better at that time but vision had cleared some. I was very thirsty and tired. I went back to sleep and did not wake up until 11:42 the next morning. As I stood up my head was spinning,I had a severe headache and still so tired. The more I moved the worse it got. This continued continually for a week, then I started having tingling and numbness in my hands and fingers and my heart felt it was beating irregular. These sx continued for 2 days. I almost went to the ER but decided not to because I have no insurance.Mine days after sx started they just disappeared. Since then I?ve had occasional headaches but over the past day I?ve had a severe migraine like headache and numbness in my hands. Nothing with my meds or daily routine have changed. I did not go back and get the second vaccine and I never reported this to the health department but I am tomorrow
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None as of yet
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Alpha-Gal Allergy Linear Morphea Scleroderma Rheumatoid Arthritis Vitamin B 12 deficiency
- Andere Medikamente
- Smarty Pants Womens Multivitamin Vitamin B12 injection 1ml IM q monthly
- Allergien
- Beef Pork Dairy Per blood testing
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 09.04.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 41,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Blood pressure increased
COVID-19
Cough
Dyspnoea
Fatigue
Feeling abnormal
Heart rate increased
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 05/20/2022 with symptoms of cough, brain fog, loss of taste, fatigue, congestion, shortness of breath, blood pressure is elevated, and heart rate is elevated. I was prescribed Paxlovid but was instructed to take it if my symptoms worsened, but they have not. I fly every week have traveled outside the country frequently for work; I've been on over 300 trips. I was also prescribed benzonatate for cough which has worked really good for my cough. My symptoms have remained very mild, and I am on day 3 of my illness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab was positive on 05/20/2022.
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- Meniere disease; Hypertension
- Andere Medikamente
- Multivitamin Vitamin D Flavonoid Betahistine Losartan 100 mg Triamterene Flomax
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- 06.04.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 26,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Exercise tolerance decreased
Fatigue
Headache
Pain
Pulmonary pain
SARS-CoV-2 test
Symptomtext
On May 2, 2022, I noticed my lungs started burning when I was at the gym working out, doing my normal routine of rowing machine, kettle bell swings and box step ups. I could not finish my normal routine. On Wednesday I felt better so I mowed the grass, it took me four hours. I was tired and had a headache and went to bed at 06:30PM ET. On Thursday I woke up with my body achy and a headache would come and go. I took TYLENOL to help ease the pains of both. I tried to go to the gym on Friday but I could not do any part of my routine. I went to the doctor today May 19, 2022, after seven days of taking TYLENOL since I am still achy and the headache still comes and goes. I will get the results of my COVID-19 test later tonight. My doctor has prescribed me Amoxicillin 500mg 2 (1000mg) capsules by mouth three times daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Thyroid Disease; High Cholesterol; Prostate; Cancer (multi); Acid Reflux; GERD
- Andere Medikamente
- SYNTHROID; Pravastatin; FLOMAX; Finasteride; Prednisone; Carvedilol; Losartan; FLONASE; CLARITIN; Diclofenac
- Allergien
- Urva
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 16.03.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 26,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Anxiety
Blood iron normal
Blood thyroid stimulating hormone normal
Condition aggravated
Depression
Full blood count normal
Iron binding capacity total normal
Laboratory test normal
Panic attack
Serum ferritin normal
Suicidal ideation
Thyroxine normal
Weight increased
Symptomtext
extreme hair loss, weight gain, increase in anxiety/panic attacks, worsening depression & suicidal thoughts
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- labs completed 04/2022 & CBC/Ferr/Iron+TIBC/T4/TSH-- normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- anxiety, depression, ADHD, migraines
- Andere Medikamente
- prozac 60mg, vyvanse 50mg, propranolo ER 60mg, Junel Fe, Lunesta 2mg, MVI, B12
- Allergien
- NKDA, NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 11.05.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Heart rate irregular
Immediate post-injection reaction
Pallor
Palpitations
Symptomtext
Immediately after vaccination, discussed her history of emphysema and discussed the fitting of the N95 mask to her face for good protection. A few minutes later, while under observation the client reported feeling dizzy and having palpitations. Her pulse was irregular with some very strong beats and some weaker; she was pale. We assisted her to recline on a cot and recommended removal of the mask for increased fresh air, considering her symptoms. She recovered well with the observation of other RN, who also found there were some concerns about her morning medication and hydration. She was given water to drink. She was held until she felt really well for 15 additional minutes, and then she headed off to Bible Study, (saying she felt well enough to go shopping) confirming that she had a cell phone with her and would stop driving immediately if she had any symptoms. Called her at home at 3:30 pm and she reported having a very good day. ( in review note that her vaccine appointment information requested reasonable accommodation "required a place to sit if standing for long periods is required", and she reported a prior history of a severe allergic reaction). RN 5/11/22 3:45 pm. Pt reported that on the morning of 5/11/22, due to early morning dose of thyroid medication that she had nothing to eat or drink prior to vaccintion. Pt also reports hisotry of insomnia averaging about 4 hours of sleep a night. PHN 5/13/22 08:30
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- emphysema
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 11.04.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
COVID-19
Condition aggravated
Malaise
Nausea
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Tinnitus
Symptomtext
Congestion, runny nose, loss of sense of smell, some nausea (but that may be from the Paxlovid), and generally not feeling well. Also, not sure if it?s the Covid, but have been having random loud tinnitus (ringing) in my right ear, which I hope only remains random since I already have permanent tinnitus in my left ear which may be due to having Covid in April/May 2020. Did Covid rapid test on 05/11/2022 and had a positive result. Called doctor and was prescribed Paxlovid. Am currently taking Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Took Rapid Covid test on 05/11/2022 and had Positive result.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Amlodipine Besylate (Norvasc) 2.5mg ? 1x Tamsolosin (Flomax) 0.4mg ? 1x, AM & PM Finasteride 5mg ? 1x Acyclovir 400mg ? 1x Latanoprost Opthalmic Solution ? 0.005% - 1 drop each eye, PM Dorzolamide HCL Ophthalmic Solution ? 2% - 1 drop each
- Allergien
- Scallops Bee stings Pollen
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Body temperature increased
Dyspnoea
Symptomtext
7:30 pm c/o shortness of breath with temp of 100.5, at 7:45 continued to c/o shortness of breathe with temp of 102.5, at 8:30pm Antacid 2 tabs and Tylenol 650mg was given, at 8:36pm Provider orderes received to send out to Hospital emergency. at 9:10pm EMS arrived to unit, and at 9:23 patietn had left the unit. At 12:30 am patietn returned to facility Temp 99.2, denies complaints with no new orders received from the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Pateitn was sent to ER. No free world records noted in chart.
- Aktuelle Erkrankungen
- HTN, Hyperlipidemia, Presence of artificial Hip Joint
- Vorgeschichte
- HTN, Hyperlipidemia, Presence of artificial Hip Joint
- Andere Medikamente
- Atenolol, Atrovastin, Fluphenazine, Lisinopril
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Muscle spasms
Pain
Product administered at inappropriate site
X-ray
Symptomtext
The shot nurse gave me my shot and I said it felt like the needle hit the bone and when I got in my car my back shoulder blade was in a spasm, in a few days I could not move the shoulder or lift my arm with throbbing pain. Pain still exists in the area at time of this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- X-ray
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Amlodipine; Philips colon health; turmeric; One A Day 50 plus
- Allergien
- Penicillin; cat dander
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Dyspnoea
Pyrexia
Symptomtext
Chest pain, shortness of breath, fever 101
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Sent to ER.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- iddm, htn,
- Andere Medikamente
- Novolin insulin, norvasc, prozac, metformin, aspirin
- Allergien
- lithium
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 11.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Myalgia
Skin discolouration
Skin exfoliation
Tremor
Symptomtext
shaking Chills severe muscle and joint pain 36hrs after the shot the skin on my palms turned white and peeled off.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Asthma HTN
- Andere Medikamente
- valsartan 320mg QD, Metoprolol tartrate100mg BID, HCTZ 25mg QD, Levothyroxine 75mg QD, Metformin 500mg BID, Ducosate sodium 100mg QD, Cetirizine 10mg QD, Montelukast 10mg QHS, and Ezetimibe 10mg QHS
- Allergien
- Floroquinalones red man syndrome, Hymenoptera stings hyper sensitive to the venom
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Condition aggravated
Extra dose administered
Herpes zoster
Inflammation
Joint swelling
Symptomtext
Developed shingles two days after booster. This is the third time I've developed shingles since I started the COVID-19 vaccinations; two of the three times were within a few days of an injection. Generally speaking, I have a significant inflammatory response to the vaccine: joint pain and swelling that last several days. I have assumed this is because I have EDS. I often get joint swelling when I'm ill.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Ehlers Danlos, Chiari, kidney disease
- Andere Medikamente
- Diamox, Nortriptyline, Prilosec, Vitamin D, Calcium, Magnesium, Alpha Lipoic acid
- Allergien
- Vicodin, Tramadol HCL, Sulfadiazine, Fentanyl, Erythromycin base, Soma, Latex
- Vorherige Impfungen
- Moderna COVID-19 vaccines: previously reported a cutaneous hypersensitivity reaction that lasted several weeks. Joint pain and s
- Staat
- NJ
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Axillary pain
Chest pain
Nausea
Symptomtext
Chest pains under arm, nausea an hour after administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Rosuvastatin 10 mg
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 17.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Condition aggravated
Fatigue
Headache
Muscle twitching
Skin reaction
Urine analysis
Urticaria
Symptomtext
The day after, fatigue, headache and some chills. Then 2 days later, just the fatigue. Starting last Tuesday, I've broken out in hives. I've never had any skin reactions before. Also experienced some muscle twitching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Urine analysis.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin
- Allergien
- None
- Vorherige Impfungen
- moderna vaccine- chills
- Staat
- PA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 04.04.2022
- Impfdatum
- 21.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 8,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Fibrin D dimer increased
Joint swelling
Oedema peripheral
Peripheral swelling
Prealbumin
Symptomtext
Individual met with medical provider in clinic on 3/29/22 morning 9am and relayed concern for swelling in ankles, feet. Medical provider documented this as "slight +1 edema BLE at ankles, very mild". Follow-up monitoring by provider team warranted D-dimer labs, and 3/30/22 provider documentation to reflect bilat +2 pretibial/ankle and foot pitting edema, pretibial area with diffuse PAD appears red casting, +dp, cap rf<3, musk: ilat ankle/foot/toes with full AROM w/o limitation. Encouraged ankle pumps, BLE elevation and increasing daily physical activity, knee ted hose given, reviewed d-dimer 0.88, will trial short course lasix and create f/u appt for eval, discussed low socium diet and reviewed s/s worsening and when to contact medical.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- D-dimer 0.88 (0-0.5) prealbumin 17.9 (17-42)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 03.04.2022
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Tachycardia
Vomiting
Symptomtext
Dizziness, Nausea Vomiting & Tachycardia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 22.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Balance disorder
Blindness
Blood pressure increased
Chills
Coordination abnormal
Decreased appetite
Dizziness
Dysarthria
Eyelid disorder
Fatigue
Feeding disorder
Feeling abnormal
Feeling of body temperature change
Gait inability
General physical health deterioration
Grip strength decreased
Haematemesis
Headache
Symptomtext
She got her vaccine, hours after the vaccine she got a fever. Her fever was 102.2, it went up that evening after 8:00 PM to 103.7 and it stayed that way until the next day to around 11:00 AM, and subsided. She then had a runny nose, was very tired, lethargic and she had a very bad headache. The next day she was even more tired, loss her appetite and could not eat without nausea, and head hurting very bad until her vision was not correct. The day after that 3/24/22 she really felt bad to the point that she felt uncoordinated, was shaking, still unable to eat, low grade temperature, chills and headache. She threw up that night for the first time. Then on 3/25/22 she woke up and had trouble balancing very badly, vision was blurred, her eyes were crossing, unable to eat still, no appetite. After 3 hours she had uncontrollable sneezing, and rolled over to the right and could not control her balance. She feels her head is airy and light, things are spinning and then started to have projectile vomiting every 15 minutes. Her husband called 911, she was sweating profusely and unable to move, could not open her eyes, could barely speak. The EMT's came quickly and was unresponsive and her temperature apparently was over 106, her BP was 170/94. They took her to the local Medical Center, where she was still throwing up, heart rate still low and unresponsive. When she became aware she was throwing up the lining of her stomach, bile and blood. She was still unable to sit up, still was unable to talk, was slurring her speech. They put in an IV, her heart was low in the 50s, and her BP was still high, she could not see the monitor herself, but could hear the alarms going off alerting it was too high. They kept asking her questions about her health, and could not give then any answers as to what would have caused this. They sent her home without being able to walk, her equilibrium is still off, her head is light and feels like something is making her topple over and her body is giving way to it throwing her down. She is gradually able to sip and eat light foods which just started yesterday, 3/28/22, and cannot grab things or walk. She is just uncoordinated right now. She has a diaper on due to incontinence and has think mucous and is sneezing, and the drainage in thick in the back of her throat. Her sputum is think as well. She still cannot see straight, but has not run a fever. She has been monitoring her BP and her last reading was 157/87 2 hours ago, heart rate 62. She is getting cold/hot flashes and is shaking at times. They kept her in the hospital until Saturday and could not find anything wrong with her, and discharged her not able to walk. She informed them that she had the vaccine, and had been having symptoms ever since, and did not give her many instructions. She had a knee replacement on 12/23/21 and she was given instructions on what to do prior to getting the vaccine and took 7 weeks of aspirin, and then was OK to get the vaccine. Had no reaction to the first vaccine at al.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- In the ER, blood work.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Asthma, cervical cancer 3 years, spinal stenosis, degenerative disc disease, degenerative joint disease, osteoarthritis.
- Andere Medikamente
- Flexeril, BC powder.
- Allergien
- Latex, pork, Ibuprofen, Tylenol, Gabapentin, Topamax, Meloxicam, Hydrocodone.
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 28.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chest pain
Chills
Fatigue
Feeling hot
Heart rate increased
Lymphadenopathy
Nausea
Pain
Pyrexia
Rash
Rash erythematous
Tenderness
Vomiting
Symptomtext
Fever of 102, severe chills, severe body aches, chest pain, rapid heart rate, joint pain, nauseau and vomitting, fatigue, red painful rash on left arm which was hot and painful to touch, swollen lymph nodes in arm pit and above collar bone on left side, most symptoms lasted about 6 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Crohns
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Lisinopril, simvistatin
- Allergien
- Nonw
- Vorherige Impfungen
- Covid, moderna
- Staat
- OR
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 27.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 26.03.2022
- Tage bis Beginn
- 5,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood creatine phosphokinase normal
C-reactive protein
Chest X-ray normal
Chest pain
Electrocardiogram abnormal
Fibrin D dimer normal
Full blood count normal
Metabolic function test normal
Red blood cell sedimentation rate normal
Tachycardia
Troponin normal
Symptomtext
Chest pain and tachycardia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- ecg, cxr, troponin, CRP, CPK, CMP, ESR, D-dimer, CBC - some changes on ecg, otherwise no abnormal findings, waiting on CRP
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- asthma
- Andere Medikamente
- -
- Allergien
- meclocycline
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 24.03.2022
- Impfdatum
- 23.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Eye haemorrhage
Palpitations
Symptomtext
PALPITATIONS, BLOOD DRIPPING FROM EYE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HEART
- Andere Medikamente
- BRILINTA 90MG, PRAVASTATIN 40MG, PANTOPRAZOLE 40MG, METOPROLOL ER 50MG.
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 14.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
C-reactive protein abnormal
C-reactive protein increased
Chest discomfort
Chest pain
Computerised tomogram coronary artery normal
Dyspnoea
Electrocardiogram abnormal
Muscle spasms
Sinus bradycardia
Troponin normal
Symptomtext
Vaccine on the 14th and intermittent chest pain in the epigastric/mid sternum region without radiation started on the 15th -- no SOB, palpitations, edema or radiation of pain . CP is at rest and with activity, feels like a spasm and lasts for couple of seconds. VS at office 11/60 and HR 68. Pt is active, wt 157, BMI 27, works out daily and eats clean. No hx of GERD or acid reflux. EKG in office on 3/17 sinus bradycardia -- not ready by cardiologist. Troponin negative at less than 6 on 3/17 and CRP 20 and CRP high sensitivity 24.5. Pt sent to cardiologist whom completed other labs and EKG -- results not obtained yet but normal per pt and bradycardia. CT coronary/angiography on 3/22/22 is negative, no plaque or stenosis, calcium score is zero. CP increased and SOB on 3/18. By 3/23 CP has decreased to very seldom and SOB has decreased.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG, CRP, Troponin, CTA -- all detailed above
- Aktuelle Erkrankungen
- bradycardia
- Vorgeschichte
- bradycardia, cervicalgia
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 17.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Symptomtext
Paresthesia (pins and needles) of the hands bilaterally
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes Asthma
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 14.03.2022
- Impfdatum
- 14.03.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Dizziness
Dysphagia
Dyspnoea
Eye movement disorder
Throat tightness
Symptomtext
Patient received Moderna vaccine dose 2 at 0826. At 0842 patient c/o chest tightness, then he reported difficulty breathing, and then throat tightness. He further complained that he was having problems swallowing, felt like he was going to pass out. Eyes rolled. Did not lose consciousness. I called 9-1-1...at 0846, RN administered 0.3 mL epinephrine IM left thigh. BP at 0850 was 162/96, respirations = 18. HR at 0853 was 106, EMS arrived and transported patient to Local Hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, COPD, obesity, GERD, sleep apnea, neuropathy
- Andere Medikamente
- amlodipine, docusate, indomethacin, Januvia, losartan, MiraLAX, pramipexole, rosuvastatin, tizanidine, topiramate
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Chills
Cyanosis
Decreased appetite
Dehydration
Fatigue
Hyperhidrosis
Hypoaesthesia
Nausea
Pain
Pruritus
Rash
Urine odour abnormal
Symptomtext
4 days - COViD fingers and toes (blue discoloring skin) 4 days - Numbness in fingers and toes 1 day-Rash 1-day - Bumps 1 day - Itching 2 days - Back Pain 1 day - Nausea 1 day - Chills 2 days - Fatigue 1 day - Sweating 2 days - Foul Smelling Urine 4 days - Body Aches 4 days - Joint Pain 2 days - Loss of Appetite Treatment - increased water intake, ibuprofen, Benadryl and Tylenol
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 02.03.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Exposure during pregnancy
Symptomtext
PATIENT IS A 27 YEAR OLD, 35 WEEKS PREGNANT, FEMALE. PATIENT RECEIVED A MODERNA 0.5 ML VACCINE TO HER RIGHT DELTOID @ 11:55 A.M. WITHIN 5 MINUTES OF RECEIVING THIS INJECTION, PATIENT COMPLAINED OF NEW ONSET CHEST PAIN. PATIENT STATED SHE HAD NOT EATEN ANYTHING PRIOR TO RECEIVING THE VACCINE. PATIENT'S VITAL SIGNS WERE ALL NORMAL BP 130/72, PULSE 83, RR 16. PATIENT DENIED SOB. EMS WAS CALLED AND TRANSPORTED PATIENT TO ER. AT DISCHARGE, PATIENT WAS A&oX4, WALKING, TALKING, NO ISSUES.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Dizziness
Symptomtext
Patient began feeling dizzy and lightheaded starting about 5 minutes after IM injection. Patient was offered some water and crackers and a place where she could lay down if she felt like she was going to pass out. Patient continued to sit out front of the pharmacy for a period of 30 minutes until she was feeling better. We contacted an emergency contact for the patient to come pick her up at the pharmacy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- asthma
- Vorgeschichte
- asthma, smoker
- Andere Medikamente
- n/a
- Allergien
- nkda
- Vorherige Impfungen
- Patient indicated that they had a similar reaction following yearly flu shot
- Staat
- NC
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Chest pain
Dizziness
Pain in extremity
Symptomtext
approximately 10 mins after shot patient noted burning in arm that extended to chest and "a little lightheaded". VS reassuring, exam unremarkable. No signs of anaphylaxis. Symptoms improved upon discharge, VS remained stable. Last follow up was at 1500 2/24/22 (2 hours after shot), reported feeling better. Arm sore.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, hypothyroidism, sinus tachycardia, GI issues with certain foods
- Andere Medikamente
- Synthroid 25mg Dextroamphetamine-amphetamine 15mg Propranolol 10mg
- Allergien
- Red dye in face paint and red lipstick (facial swelling) Bees: unknown reaction Dairy & Olive Oil: GI upset
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 13.02.2022
- Impfdatum
- 12.02.2022
- Beginn
- 13.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Chills
Condition aggravated
Dyspnoea
Heart rate increased
Insomnia
Nausea
Oedema peripheral
Pain
Pyrexia
Restlessness
Vomiting
Symptomtext
Full body aches, swollen right armpit, naseau, vomiting, restlessness, inability to sleep, chills, presumed fever, increased resting heart rate (up by 40+ bpm compared to normal), shortness of breath, anxiety
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Intracranial Hypertension, Asthma
- Andere Medikamente
- Acetazolamide (500mg Daily), CBD+CBG Oil (.75-1.5 ml daily)
- Allergien
- -
- Vorherige Impfungen
- Reaction to flu vaccine, approx. 11 years old (2004), intense dehydration, vomiting, rash, and body aches over the course of a w
- Staat
- MN
- Alter
- -
- Geschlecht
- F
- Eingang
- 12.10.2023
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Pain
Pain in extremity
Symptomtext
sore left arm; body aches; headache; fatigue; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (sore left arm), PAIN (body aches), HEADACHE (headache) and FATIGUE (fatigue) in a female patient of an unknown age who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch nos. AS7148B and 033K21-2A) for COVID-19 prophylaxis. The patient's past medical history included Autoimmune disorder in 2005, Arthropod bite in 2005 and Lyme disease (with MS Symptoms). On 05-Apr-2022, the patient received fourth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 13-Sep-2022, received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced PAIN IN EXTREMITY (sore left arm), PAIN (body aches), HEADACHE (headache) and FATIGUE (fatigue). At the time of the report, PAIN IN EXTREMITY (sore left arm), PAIN (body aches), HEADACHE (headache) and FATIGUE (fatigue) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter did not provide any causality assessments. Concomitant medication not reported. Treatment medication not reported. The patient was on blood pressure medication. The patient received her fourth vaccine on 05-Apr-2022 vaccine listed as Spikevax moderna on the card lot number 033K21-2A expiration date 20-May-2022. Patient received the vaccine in her left arm. Patient had a sore left arm, body aches, headache, and fatigue. The patient received her fifth vaccine on 13-Sep-2022 vaccine listed as Moderna Bivalent Spikevax lot number AS7148B expiration date is not known. Patient received the vaccine in her left arm. Patient had a sore left arm, body aches, headache, and fatigue. This case was linked to US-MODERNATX, INC.-MOD-2023-744170 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-744170:case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Autoimmune disorder; Disequilibrium syndrome; Lyme disease (with MS Symptoms)
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthropod bite; Blood pressure abnormal (The patient was blood pressure medication.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 13.09.2022
- Beginn
- 24.03.2023
- Tage bis Beginn
- 192,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dizziness
Fatigue
Headache
Pyrexia
SARS-CoV-2 test positive
Sacroiliac joint dysfunction
Symptomtext
Tested positive for Covid - 19 on March 24, 2023. Cough, Sore throat, head ache, fever, tiredness Tested negative with BinaxNow Test on 3/31/2023 Still have coughing , headache and or light-headedness, and sore throat occassionaly during each day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- OnGo Home test tested positive 3/24/2023 Tested negative with BinaxNow Test on 3/31/2023
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- GERDS
- Andere Medikamente
- Pantoprozole Sodium 40 mg twice a day, Calcium 600 mg D3 20 mcg
- Allergien
- Demerol
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 11.04.2023
- Impfdatum
- 07.04.2022
- Beginn
- 22.03.2023
- Tage bis Beginn
- 349,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Had cough and fever and sore throat starting night of March 19. Tested negative for Covid Mach 20 when fever and other symptoms appeared but tested positive March 22.. Began Paxlovid March 23,2023 following Virtual appointment March 22, 2023 with primary physician, DO. Did not take Atorvastin, per Dr. for 10 days after initiating Paxlovid for 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- At home Covid Test test showing positive to Covid 19 on March 22, 2023
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure; High Cholesterol
- Andere Medikamente
- Atorvasatin Calcium 5mg 1 x day; Losartan Potasium 100 mg 1 x day; Vitamin D 25 mcg; Omeprazole 20 mg; Naicin 500mg L-Arginine 500 mg
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 05.04.2023
- Impfdatum
- 30.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Vaccination site pain
Symptomtext
This spontaneous case was reported by a patient family member or friend and describes the occurrence of VACCINATION SITE PAIN (pains on their left shoulders (injection site).) and ARTHRALGIA (having pain in other joints - right shoulder and the knees. For his wife - she complains about the pain too) in an adult female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: JANSSEN COVID-19 VACCINE. Past adverse reactions to the above products included No adverse event with JANSSEN COVID-19 VACCINE. Concurrent medical conditions included Pollen allergy. On 30-Mar-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VACCINATION SITE PAIN (pains on their left shoulders (injection site).) and ARTHRALGIA (having pain in other joints - right shoulder and the knees. For his wife - she complains about the pain too). At the time of the report, VACCINATION SITE PAIN (pains on their left shoulders (injection site).) and ARTHRALGIA (having pain in other joints - right shoulder and the knees. For his wife - she complains about the pain too) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. Patient received 1st booster dose on 25-Oct-2021, lot number 014F21A. The patient and husband got the 2nd booster dose of the Moderna Covid- 19 vaccine, they have been experiencing pains on their left shoulders (injection site). Patient complains about the pain too. Patient husband stated that they never got sick before they got the shot. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Pollen allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 04.10.2022
- Impfdatum
- 02.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
Blood test
Chest X-ray
Echocardiogram
Electrocardiogram
Exercise electrocardiogram
Headache
Heart rate increased
Laboratory test
Symptomtext
I had a headache with this vacine that I did not have with others. It lasted 2 days and it was strong. Then a few weeks later I noticed my apple watch and noticed my heart rate just went up for no reason while reason. I talked to my doctor and they ran some tests, and I was diagnosed now with afib and being treated for it, which I did not have prior to the vaccine. I don't have a history of it in my family, I dont smoke nor drink, not overweight. It came out of no where.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- EKG, bloodwork, heart xray. All were inconclusive and no results. I was not having afib attack at the moment. Did a tredmill test and noticed something wrong and another ultrasound and noticed the pumping in my heart and was diagnosed with afib after I was with the artery. I am currently awaiting to see if I had heart disease.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Levothyroxine, Lipotor generic, vitamin D3, vitamin B12, folic acid, eye vitamins, omega 3, calcium.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 12.01.2021
- Beginn
- 29.08.2022
- Tage bis Beginn
- 594,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
COVID-19
Nausea
SARS-CoV-2 test positive
Vomiting
Symptomtext
08/29/22 presents to ED for "nausea and vomiting as well as abdominal pain". PMHx of "Crohn's disease, CKD stage III, aortic sclerosis, mitral valve regurgitation, and diastolic dysfunction"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- 08/29/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 04.09.2022
- Impfdatum
- 31.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Diarrhoea
Rash
Rosacea
Vertigo
Symptomtext
This was my second booster and I got a terrible rash from chest to my neck and throat which laster 6 weeks and I developed rosacea on my cheeks, chin and nose and eyes. which I still have 9/2022 and will have always although I am seeing a doctor for light treatment. I also had diarrhea and still have to a lesser extent. I wish I never got it. After my second Moderna shot I got vertigo for 4 weeks and still am not as steady as I was but the vertigo is gone thank goodness. The rash I was told by Dr. that I had enough in me already and the 2nd booster make my whole immune system get messed up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- I saw several doctors for rash and they said take benedryn for 6 weeks!
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- losartan every day , water pill twice a week
- Allergien
- a few antibiotics
- Vorherige Impfungen
- 2nd moderna vaccine vertigo for a few weeks
- Staat
- IL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 26.08.2022
- Impfdatum
- 21.01.2021
- Beginn
- 03.06.2022
- Tage bis Beginn
- 498,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Covid 19 documented by positive PCR. Symptoms: sore throat, headache, cough, fatigue (physical and mental) Paxlovid Recovered @ 19 days with some lingering fatigue and nighttime cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Positive PCR, normal pulse-ox
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Idiopathic urticaria
- Andere Medikamente
- Prempro .3/1.5, Fexofenadine, probiotic, calcium, vitamin C, vitamin D, vitamin B complex
- Allergien
- Penicillin, sulfa, other unknown
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 27.04.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 77,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Nasal congestion
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I received the vaccine on 04/27/2022. On 07/13/2022 I woke up with stuffy nose, congestion, cough and tired. On the 07/15/2022 I took a home test for Covid-19 and was positive. After I went to my local clinic and was prescribed cough medicine and NOHIST DM liq. Was told to take 5mil. 3x a day as needed. Symptoms lasted 3-4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Levothyroxine; fish oil; calcium; aspirin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 19.04.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 87,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Respiratory tract congestion
Throat irritation
Symptomtext
Covid-19 I tested positive on July 15th i experienced congestion, coughing, scratchy throat, and fatigue that was the first day and the second day i was prescribed paxlovid around 11am and while taking paxlovid i started to feel better and symptoms started to subside.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; Hyperlipidemia; Asthma
- Andere Medikamente
- Chloridone; Atorzastin; Calcium; Vitamin D; Maccuhealph; Fish oil;
- Allergien
- Percodan
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 20.04.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 19,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Erythema
Fatigue
Headache
Herpes zoster
Lymphadenopathy
Muscle strain
Myalgia
Neuralgia
Oral pain
Pain
Rash
SARS-CoV-2 test positive
Symptomtext
My friends tested positive and I started noticing that the roof of my mouth was very sore. I had more of that pain and I was very tired. Those were the only symptoms during my COVID-19 diagnosis. I didn't test negative until the 5/23. I noticed the fatigue the most. The shingles I noticed on Sunday, 7/17, morning I noticed I had swollen gland under my arm. That night I had a lot of pain and it felt like a pulled/sore muscle. By Monday afternoon the pain was worse and I had three tiny red dots in a row on my shoulder and that clued me in to it being shingles. That afternoon I called the doctor and they gave me an antiviral prescription. I had a small rash on my back near bra and front upper chest area. Its not spearing but the patches are conjoining into a bigger piece. I also ad a raging headache on Tuesday. Gabapentin is helping with the nerve pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- ARMOUR thyroid; B complex; latanoprost; ginkgo; vitamin C; multivitamin; magnesium; calcium citrate; vitamin D; fish oil
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 20.07.2022
- Impfdatum
- 15.04.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 89,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Malaise
SARS-CoV-2 test positive
Sneezing
Symptomtext
I received my vaccine on 04/05/2022. On July 13/2022 I started feeling ill during the day. Persistent cough and sneezing. on 07/17/2022 I went to the doctor after testing positive for Covid-19. I was prescribed Paxlovid. Started feeling better same day after taking medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Blood Pressure; Gout;
- Andere Medikamente
- vitamin b6; Allopurinol; fish oil; Co que-10; Super B Complex; Jardiance; Levo Thyroxine; Vitamin C; Glucosamine; , Calcium; ; allergy relief ; iron; adult vitamin; vitamin d3; losartan; terazosin; pravastatin. ashwagandha
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 18.04.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 81,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Productive cough
SARS-CoV-2 test positive
Sinus disorder
Symptomtext
04/18/2022 vaccination. 07/08/2022 I had sinus discomfort from sinus and asthma but felt I was coughing a lot more. I was a lot more fatigue. Productive cough, uncontrollable. 07/09/2022 antigen COVID-19 positive. Physician put me on PAXLOVID. I am still have a small amount of fatigue and I am still coughing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Hypertension; Obese
- Andere Medikamente
- Atorvastatin; amlodipine; montelukast; chlorthalidone; calcium; PEPCID; budesonide; BREO inhaler
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 24.02.2021
- Beginn
- 11.07.2022
- Tage bis Beginn
- 502,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Insomnia
Nasal congestion
Pain
Productive cough
SARS-CoV-2 test positive
Symptomtext
Ache all over, stuffy head, cough with heavy phlegm, trouble sleeping at onset day zero; gradually felt better until day 5 when felt tired all over; started paxlovid on day 5; positive at home tests on day 2 and day five; negative test on day 8 and feeling fine (day 8 equals day 4 of paxlovid which I will finish on its 5 day course).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home antigen tests on days 2(+), 5(+), and 8(-)..
- Aktuelle Erkrankungen
- Nine
- Vorgeschichte
- High BP
- Andere Medikamente
- Lisinopril 20 mg Vitamin D 6000 iue
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 12.02.2021
- Beginn
- 24.06.2022
- Tage bis Beginn
- 497,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Candida infection
Oropharyngeal pain
Pain
Productive cough
Pyrexia
Streptococcus test negative
Symptomtext
Developed a severe sore throat and productive cough began on 6/24/2022, Initially treated with amoxicillin for 10 days, but three days into this the throat swab for suspected strep infection came back negative. I was not comfortable quitting the antibiotics mid-coursse, so I finished the 10 days. PCP believed I was suffering from Thrush and treated me with NYSTATIN, which I did until the bottle was empty on 7/18/2022; on which day I woke up with general body aches, productive cough, and a very mild fever 99,3 (normal for me is 97.7).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Test for strep
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Atorvastatin 40mg daiy, tadalAfil 5mg daily, clonazepam .5mg daily, testosterone cypionate .5mls weekly, omeprazole 20mg daily, melatonin 12mg daily,
- Allergien
- roxicet/percocet (minor hives)
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 03.04.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 83,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Fatigue
Headache
Influenza virus test positive
Muscular weakness
Pain
Pain in extremity
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
On 6-21-2022, I started having fatigue, leg weakness and aching, headache, body aches and chills. The next day, I had a temp of 100.3 so I took tylenol. I called the doctors office and went in that afternoon to test for Covid19. They tested me for the flu and Covid19. The rapid testwas negative and they sent the test off for a PCR. There were no medications prescribed and they told me to alternate tylenol and aleve. My fever broke on 6-23 and I started to feel a little better. I was feeling alot better by 6-24. The PCR came back positive on 6-25-2022. The doctors office called me back on 6-27 to tell me the PCR was positive. I am recovered now and I am reporting my breakthrough case of Covid19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 6-22-2022 Flu and Covid 19 test at doctors office, flu negative, rapid antigen negative, PCR came back a few days later as positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Irregular heartbeat, Diabetes type 2, Borderline heart disease/high blood pressure
- Andere Medikamente
- Escitalopram, Metformin, Atorvastatin, Vit D2, OTC pain relief as needed
- Allergien
- Horseradish
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 89,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Nausea
Vertigo positional
Symptomtext
Starting 07/06/2022, I woke up dizzy and nauseous. It went away in the middle of the day. I didn't think to much about it. I woke up the next day on 07/07/2022, I woke up dizzy and didn't think I could drive to my mammogram. So, after the appointment, my husband took me to the urgent care right next door. They said I likely had benign paroxysmal positional vertigo and I was prescribed meclizine. I was told to take them 3 times daily and rest. If I was not better by 7/11/2022 it was recommended I follow up with an ENT. As of today, 07/11/2022, I am fine and having no symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; High Blood Pressure
- Andere Medikamente
- Felodipine; Losartan; Albuterol inhaler; Claritin; Mucinex ER; Advair HFA; Montelukast; Glucosamine; Calcium, Magnesium and Zinc; Vitamin D3; Vitamin B12; Vitamin C
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 22.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 10,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Periarthritis
Symptomtext
Seen in clinic 7/7/2022 with 2-3 month hx of left shoulder pain, new diagnosis made of left adhesive capsulitis. Pt didn't specifically link it to the vaccine, but the timing raises the possibility of a causal link. He is having similar but much milder symptoms in the right (non-vaccinated) arm, however, so may be unrelated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- physical exam
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- voltaren gel
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 05.07.2022
- Impfdatum
- 01.04.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 76,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
COVID-19
Fatigue
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
In the evening of June 16th around 9pm I noticed I was more tired than I usually am at that time. I attributed it to the hike I did that day. The following day after a full night sleep, I woke up and realized I was still tired, a low level sore throat. I also took my temperature and it was 101.4 degrees. After a couple of hours I did a home COVID-19 test and it showed that I was positive. I quarantined myself. I had a telehealth appointment and was able to get a PAXLOVID prescription. I noticed my symptoms decreasing over the course of June 18th and 19th. By June 20th I had no more symptoms. I went to the hospital on the 22nd to get a PCR test and it showed positive so I continued quarantining. I went again on the 27th and that showed I was negative. I returned to work on the 30th and haven't had any symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test- Positive; PCR COVID test- positive; At home COVID-19 test- negative; PCR COVID-19 test- negative.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Idiopathic Pulmonary Fibrosis; Anticoagulated due to history of blood clots; Low Cholesterol
- Andere Medikamente
- Fenofibrate; warfarin; famotidine; niacin; vitamin D; krill oil; multivitamin; vitamin C; biotin; doxylamine succinate
- Allergien
- Hay fever
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 01.07.2022
- Impfdatum
- 31.03.2022
- Beginn
- 26.06.2022
- Tage bis Beginn
- 87,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dysphonia
Fatigue
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
It started with nasal congestion, sore throat and then followed with dry cough. I also had fatigue. It started Sunday and I did the at home test on Tuesday and tested positive for COVID-19. I called my PCP and we had a virtual appointment. I reported that my blood oxygen level was normal. I was advised by the doctor and prescribed PAXLOVID. As of today, my nasal congestion and sore throat have gone away. Cough has gone away. My voice is lower than normal and I still have fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test, positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Calcium; vitamin D3; magnesium; coQ10; amlodipine; LIPITOR; latanoprost
- Allergien
- Cat dander
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 25.02.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 124,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site swelling
Symptomtext
Patient reported swelling/bump at the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 20.04.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 28,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Rash
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Urticaria
Symptomtext
After we took the rapid test, it came back negative, we still contacted the doctor to let her know. She said because of my underlying conditions, she wanted me to get a PCR test because it would be more accurate to be safe. My husband and I both went on 5/20/2022 to the local hospital area and had the PCR test. The results came back that night positive. That was during the weekend so I couldn't get into the doctor's office. We knew what we needed to do. We did contact my doctor's office that Monday on the 23rd. We had a video visit and talked about symptoms which were mild. Just a cough, no fever or anything. My doctor noted that I could get the monoclonal antibody infusion. We went in on May 24 for the infusion. Bebtelovimab. At the time we had to wait for an hour and there was no reaction at the time. On the 28th, I started getting hives and a rash on neck shoulder and chest area. I called the urgent number and they said to take Benadryl. By the next day I contacted my doctor and she said to take Benadryl as well. She recommended I report this as well. The company contacted me about my symptoms as well. Delayed reaction 24 hours after. We talked about the life of the medicine, etc. learning as we have all this happening. Doctor noted to continue the Benadryl and to use anti itch cream and if they get worse to come back. They're fading and with the Benadryl hopefully this part will be over.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- 05/18/2022 at-home COVID Rapid test negative. 05/20/2022 PCR COVID test positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis; High blood pressure; CPPD (Pseudogout); Hx of thyroidectomy; Hx of parathyroidectomy
- Andere Medikamente
- Hydrochlorothiazide; Synthroid; atenolol; captopril; Norvasc; vitamin D; Tylenol or Advil as needed
- Allergien
- Penicillin; binders of medication; Calan binder anaphylactic reaction; fillers of medication; kiwi; seafood; other foods
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 01.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 12,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Headache
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
On 5/25 I developed a dry cough, congestion, runny nose, and a headache. I took an at home Covid test and that was positive, so I went to my local hospital and verified my results. I had a telehealth appointment with my doctor who advised that I not take my pravastatin and prescribed Paxlovid, vitamin C, and zinc lozenges. I'm done with the medication now and feeling about 95% better. I really began feeling better around 3 days after I started the medication. The only thing I have now is a little bit of a cough and that is improved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Covid test 5/25 positive.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Heart Condition.
- Andere Medikamente
- Probiotic; Prevacid; Entresol; magnesium; vitamin D; multivitamin; Pravastatin
- Allergien
- None.
- Vorherige Impfungen
- Shingrix, chills 24 hours after injection.
- Staat
- OK
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.05.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Pruritus
SARS-CoV-2 test
Symptomtext
extreme itching without hives or rash; Paxlovod "rebound" with negative post-treatment test converting to positive (day four post-treatment) with recurrence of symptoms three days following completion of medication course; This spontaneous case was reported by a physician and describes the occurrence of PRURITUS (extreme itching without hives or rash) and COVID-19 (Paxlovod "rebound" with negative post-treatment test converting to positive (day four post-treatment) with recurrence of symptoms three days following completion of medication course) in a 62-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. Co-suspect product included non-company product NIRMATRELVIR, RITONAVIR (PAXLOVID) for COVID-19 treatment. Patient had no known allergy. Concurrent medical conditions included Asthma and Hypertension. Concomitant products included FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE (ADVAIR) and CETIRIZINE for an unknown indication. On 15-Mar-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-May-2022, the patient started NIRMATRELVIR, RITONAVIR (PAXLOVID) (unknown route) at an unspecified dose. On 15-May-2022, the patient experienced PRURITUS (extreme itching without hives or rash) and COVID-19 (Paxlovod "rebound" with negative post-treatment test converting to positive (day four post-treatment) with recurrence of symptoms three days following completion of medication course). At the time of the report, PRURITUS (extreme itching without hives or rash) and COVID-19 (Paxlovod "rebound" with negative post-treatment test converting to positive (day four post-treatment) with recurrence of symptoms three days following completion of medication course) was resolving. Not Provided DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: negative (Negative) negative and positive (Positive) positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Comedication also included Monteleukast. Device Date : 24May2022 Company Comment: This is a spontaneous case concerning a 62-year-old, male patient with concurrent medical conditions of Asthma and Hypertension, who experienced the unexpected non-serious events of Pruritus, Covid-19. The events occurred 61 days after the fourth dose of mRNA-1273 COVID 19 Vaccine. Patient was tested for SARS-CoV-2 test, initial results was negative then tested positive. Patient was treated with nirmatrelvir, ritonavir tablets at an unspecified dose. The events were reported as resolving. The concurrent medical conditions of Asthma and Hypertension remains a confounder. The benefit-risk relationship of mRNA-1273 COVID 19 Vaccine, is not affected by this report.; Sender's Comments: Company Comment: This is a spontaneous case concerning a 62-year-old, male patient with concurrent medical conditions of Asthma and Hypertension, who experienced the unexpected non-serious events of Pruritus, Covid-19. The events occurred 61 days after the fourth dose of mRNA-1273 COVID 19 Vaccine. Patient was tested for SARS-CoV-2 test, initial results was negative then tested positive. Patient was treated with nirmatrelvir, ritonavir tablets at an unspecified dose. The events were reported as resolving. The concurrent medical conditions of Asthma and Hypertension remains a confounder. The benefit-risk relationship of mRNA-1273 COVID 19 Vaccine, is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Test; Test Result: Negative ; Result Unstructured Data: negative; Test Name: COVID-19 Test; Test Result: Positive ; Result Unstructured Data: positive
- Aktuelle Erkrankungen
- Asthma; Hypertension
- Vorgeschichte
- Comments: Patient had no known allergy.
- Andere Medikamente
- ADVAIR; CETIRIZINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 01.04.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Headache
Oropharyngeal pain
Tinnitus
Vaccine breakthrough infection
Symptomtext
***********COVID BREAK THROGH CASE ************* May 18 I started having a sore throat and some cough but no fever. That lasted for two days I tested on Wednesday (negative) and Friday (positive). The symptoms continued I still have a sore throat and coughing. I started getting headaches on Sunday and that lasted until Thursday along with sore throat and ring in my ears.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Multi Vitamin Calcium
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Immediate post-injection reaction
Menstruation irregular
Muscle spasms
Nausea
Vaginal haemorrhage
Symptomtext
Immediately after my first dose I started spotting. By day 3 it was very heavy vaginal bleeding. Alongside the bleeding I have been getting lightheaded, nauseous and experiencing heavy cramping. This is very unusual for me to have heavy bleeding longer than 4 days in a row. I am positive this came from the vaccine because not only did the problem arrive the same day but it was too early for my normal period. The type of cramps are also more severe than what I'm normally use to. I reported this to my job and took time off but the problem still persist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 15.05.2022
- Impfdatum
- 11.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Cellulitis
Haematoma
Lymphadenopathy
Pyrexia
Subcutaneous abscess
Symptomtext
Left axililla cellulitis abscess,, fever, soft >4cm hematoma in area of left axillia lymph node presenting 24 hours post vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Biktarvey Zoloft
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 13.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Lymphadenopathy
Menstruation irregular
Pain in extremity
Symptomtext
Sore arm, swollen lymph nodes to neck, arm, underarm and lower back, missed menstrual but still have all the symptoms of having it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Almost a month has passed, been going to PT to relieve lower back pain that never went away.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Xyzal
- Allergien
- Egg Yolk, Peanuts, Shrimp.
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 18.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspepsia
Mechanical urticaria
Pruritus
Sensation of foreign body
Skin reaction
Urticaria
Symptomtext
I got the Modern booster shot on February 18, 2022. On the morning of February 28, 2022, I woke up with severe itching under my bra line. In the following days, I experienced uncontrollable itching and dermatographia - what I characterized at the time as hives or welts. Every time I would scratch my skin, and sometimes even when I didn't, big red welts would appear. They would go away soon after they appeared and tended to migrate all over my body, including stomach, back, neck, chest, legs, arms, face, forehead, and ears. The same morning I noticed the itching, I also had really, really severe heartburn - like I'd swallowed a pill that was stuck in my throat and acid was coming up to meet it. It's now May, and even though my symptoms have abated somewhat, I'm still dealing with this. I take Claritin and Pepcid daily and have received two steroid shots.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- None specific to this condition.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Feeling hot
Headache
Induration
Pain in extremity
Product administered to patient of inappropriate age
SARS-CoV-2 test
Tuberculin test
Symptomtext
Red arm; Hard; Hot to the touch; Sore arm; Headache; 17 year old patient received first dose of Moderna COVID-19 vaccine; This spontaneous case was reported by a nurse and describes the occurrence of ERYTHEMA (Red arm), INDURATION (Hard), FEELING HOT (Hot to the touch), PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (17 year old patient received first dose of Moderna COVID-19 vaccine) and PAIN IN EXTREMITY (Sore arm) in a 17-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient had no ear infection or allergy flare-ups. The patient's past medical history included Sexually transmitted infection (risk of sexually transmitted infection), Fracture of ankle, Ear infection (no recent ear infection.), Laryngitis, Vomiting, Urinary tract disorder (urinary symptoms) and COVID-19 (Tested positive to COVID a year ago (before the vaccine)) in 2021. Concurrent medical conditions included Anxiety, Asthma, Eczema, Family stress (family tension, lots of tension in the family), GERD, Generalized anxiety disorder (GAD), Insomnia (Recent change in status improvement sleeping okay), Migraine (migraines 3-4 a month), Photophobia, Posture abnormal (poor posture) and Tick bite. Concomitant products included ETHINYLESTRADIOL;NORETHINDRONE and ETHINYLESTRADIOL, NORETHISTERONE ACETATE (JUNEL) for Birth control, ALBUTEROL [SALBUTAMOL], FEXOFENADINE, FLUTICASONE PROPIONATE (FLONASE [FLUTICASONE PROPIONATE]) and IBUPROFEN for an unknown indication. On 04-Apr-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) .5 milliliter. On 04-Apr-2022, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (17 year old patient received first dose of Moderna COVID-19 vaccine). On an unknown date, the patient experienced ERYTHEMA (Red arm), INDURATION (Hard), FEELING HOT (Hot to the touch), PAIN IN EXTREMITY (Sore arm) and HEADACHE (Headache). At the time of the report, ERYTHEMA (Red arm), INDURATION (Hard), FEELING HOT (Hot to the touch), PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (17 year old patient received first dose of Moderna COVID-19 vaccine), PAIN IN EXTREMITY (Sore arm) and HEADACHE (Headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, SARS-CoV-2 test: positive (Positive) Positive. On an unknown date, Tuberculin test: result not provided Result not provided. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. No other vaccines were administered within 1 month prior to Moderna COVID-19 vaccine Reporter states that her 17 year old daughter received the Moderna vaccine as the 1st shot, they were going to receive the 2nd dose from Pfizer at the time of report. No Treatment information was reported. Most recent FOLLOW-UP information incorporated above includes: On 05-May-2022: New Reporter added, Patient Initials updated. Medical History added. Lab data added. Concomitant medication (Junel) added. New events added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: COVID-19 test; Test Result: Positive ; Result Unstructured Data: Positive; Test Name: PPD test; Result Unstructured Data: Result not provided
- Aktuelle Erkrankungen
- Anxiety; Asthma; Eczema; Family stress (family tension, lots of tension in the family); Generalized anxiety disorder (GAD); GERD; Insomnia (Recent change in status improvement sleeping okay); Migraine (migraines 3-4 a month); Photophobia; Posture abnormal (poor posture); Tick bite
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (Tested positive to COVID a year ago (before the vaccine)); Ear infection (no recent ear infection.); Fracture of ankle; Laryngitis; Sexually transmitted infection (risk of sexually transmitted infection); Urinary tract disorder (urinary symptoms); Vomiting; Comments: The patient had no ear infection or allergy flare-ups.
- Andere Medikamente
- ALBUTEROL [SALBUTAMOL]; ETHINYLESTRADIOL;NORETHINDRONE; FEXOFENADINE; FLONASE [FLUTICASONE PROPIONATE]; IBUPROFEN; JUNEL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.05.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Skin discolouration
Tenderness
Symptomtext
Patient reported tiredness, chills, tenderness, and no bump. She also complained of a green dot the size of a small freckle. She said it occurred after her first Covid-19 vaccine and has not resolved. It looks like a green dot tattoo. She said she is not having any side effects currently, minus the green dot which has not resolved yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- N/A
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 09.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 23,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
Chills
Lymphadenopathy
Pain
Pain in extremity
Pyrexia
Symptomtext
I recieved vaccine at work. Normal side effects: sore arm, fever, chills, body aches, swollen lymph node in arm pit on the side I got the shot. Over time I noticed I could not smell things like I used too. I didn't notice it at first. I stopped smelling my coffee brew but I could smell my coffee when I got within a foot of the pot. I have 2 kiddos in diapers and always said their poop didn't smell and my husband would laugh at me. Around April 17th I realized I had moderate loss of my smell and it had been gone for several weeks after my first COVID vaccine. I had vaccine number 2 on May 4th and my smell is further diminished.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Escitalipram, multivitamin, zyrtec, flonase
- Allergien
- Clindamycin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 06.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysphagia
Dysphonia
Pruritus
Urticaria
Symptomtext
I woke covered in hives and it was intensely itchy. I took an Allegra and it gave 80% relief. I woke Saturday and I was worse, my scalp, neck and back was covered with hives. I went to urgent care and was diagnosed with Urticaria. It also became hard for me to swallow and I became hoarse. I went to ER and was given an Epi-Pen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypothyroidism Hyperlipidemia Depression
- Andere Medikamente
- Synthroid 112mcg Rosuvastatin 20mg Sertraline 150mg Magnesium 500mg CoQ10 100mg Turmeric
- Allergien
- Lanolin
- Vorherige Impfungen
- TDAP, swollen arm.
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 18.03.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 28,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Angioedema
Erythema
Pain
Skin exfoliation
Swelling
Symptomtext
In April traveled by car to family ranch, where I experienced angio-edema reaction to my face and eyes. This is a family ranch to which I travel 2 to 6 times a year, but this past year this was the third time I experienced this facial reaction. The first time was in July, the second time was in November, and this was my third reaction. All three times I required steroids and was required to stay out of the sun. I experienced peeling of my skin, swelling, pain, and reddening of my skin. The only reason I wonder if there is a connection to the vaccines is that I have continually visited this ranch at various seasons without previously having had more than hayfever(these occurred in the summer, fall, and early spring)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None that I know of., other than going to clinic and ER for observation.
- Aktuelle Erkrankungen
- allergies
- Vorgeschichte
- Allergies, Menagioma Brain Tumor (removed surgery 2/20/2019); lymphodema, arthritis
- Andere Medikamente
- Valsartan, Kepra, D-3, B-12, L-Lysine, Preservavision, Krill
- Allergien
- Penicillin, Ampicillin, Keflex, adhesive tape, Lipator
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 30.04.2022
- Beginn
- 30.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain
Product administered to patient of inappropriate age
Symptomtext
As stated by the employee, MA, who gave the vaccine - "The patient came in with her grandparents for their COVID vaccines. Upon arrival to the office I advised that they would be receiving the Moderna vaccine as we are out of the Pfizer at this time. Patient and grandparents agreed. After administering the vaccines, I noticed the patient was under the age of 18. Once I realized what I had done, I went directly to another employee, MA, and then together we reported the incident to (Family Medicine provider) who advised that there wasn't anything life threatening connected with administering the vaccine. The information was then given to (Pediatrician) who stated he would contact the patient's parents." No treatment course indicated by Dr. To date, the patient/parents have not reported any serious side effects or symptoms. As indicated in the patients, Dr. spoke to the parents on 5/2/22 documented as "spoke with mom - she had no fever but was achy yesterday. She felt better today and went to school. I apologized for patient getting the Moderna vs. the Pfizer and we did address the issue with the MA who gave it and will proceed to have our clinical manager review the process to make sure it does not happen again. Mom voices understanding and will call me with any questions."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None indicated by Dr.
- Aktuelle Erkrankungen
- - None
- Vorgeschichte
- - ADHD, GERD with esophagitis, and mild intermittent asthma
- Andere Medikamente
- Based on patient currently taking Azelastine twice daily, Arnuity Ellipta once daily, and Dexmethylphenidate ER once daily
- Allergien
- - NKDA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 14.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Dizziness
Electrocardiogram normal
Fall
Fatigue
Feeling abnormal
Night sweats
Symptomtext
After vaccine I had a normal reaction of feeling fatigued, and there was a point within days of the vaccine that I felt like I was in a fog or daze, and has lasted up until a couple days ago. A week after my booster vaccine, when I would get up and get dizzy and I fell back twice. That is when I gave a call to 911, I went to the ER by ambulance, blood work, EKG. I was released the same day after about 8 hours. Since then I have felt in a daze and I can't really think straight or focus on anything in general. The daze is starting to go away. I have set up an appointment with a neurologist. I also had night sweats the first two nights post vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Blood work: normal ranges, EKG: clear and normal.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- CML; Heart issues; Bicuspid Aorta
- Andere Medikamente
- Flecainide acetate 15mg; Levothyroxine; Baby aspirin 81mg; TKI Sprycel
- Allergien
- Erythromycin; Bananas
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 8,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
Atrial flutter
Blood test normal
Chest X-ray
Echocardiogram
Electrocardiogram abnormal
Headache
Injection site erythema
Injection site pruritus
Injection site reaction
Pyrexia
SARS-CoV-2 test negative
Symptomtext
I had a reaction at the injection site it was red and itchy and I developed a low grade fever of 99.8 with a headache. They lasted for 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Chest X ray Unknown, Blood work Normal, COVID-19 Text negative, EKG abnormal Afib with Flutter, TEE normal
- Aktuelle Erkrankungen
- Sinus Issues/ Infection
- Vorgeschichte
- Diabetes type 2, Venous Insufficiency, Hypertension, Hyperlipidemia, Coronary Artery Disease , Chronic Back pain, Abnormal Pulmonary Function, Asthma
- Andere Medikamente
- Metoprolol 50 mg, Atorvastatin 10mg, Plavix 75 mg, Hydrolyzing 25 mg, HTZ 25mg, Furosemide 40 mg, Aspirin 81mg, Metformin 1000 mg, Multivitamin Gold with Vitamin K, Vitamin C 500 mg , Omega Fish Oil 1200 mg, Calcium Supplement 500mg, Col Q
- Allergien
- Latex, Penicillin, Benadryl
- Vorherige Impfungen
- -
- Staat
- GU
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Headache
Nausea
Symptomtext
Patient started to experience dizziness, nausea and frontal headaches about 45 minutes after vaccine was administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diverticulitis, Hypertension, Impaired Fasting Glucose, Gout, Hypercholesterolemia, Hypertriglyceridemia, History of positive PPD reactor
- Andere Medikamente
- Fenofibrate 160mg; Losartan 25mg; Allopurinol 300mg
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 19.03.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 33,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Bone pain
Diarrhoea
Headache
Nausea
Pain
Pain in extremity
Symptomtext
bone pain; pain when lifting arm, pain when moving arm, painful to move arm up and down; pain from arm to elbow to shoulder; joint pain, shoulder pain; slight headache; felt nauseated; had loose stools; This spontaneous case was reported by a consumer and describes the occurrence of BONE PAIN (bone pain), PAIN (pain when lifting arm, pain when moving arm, painful to move arm up and down), DIARRHOEA (had loose stools), PAIN IN EXTREMITY (pain from arm to elbow to shoulder) and ARTHRALGIA (joint pain, shoulder pain) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 19-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 21-Apr-2022, the patient experienced DIARRHOEA (had loose stools) and NAUSEA (felt nauseated). On an unknown date, the patient experienced BONE PAIN (bone pain), PAIN (pain when lifting arm, pain when moving arm, painful to move arm up and down), PAIN IN EXTREMITY (pain from arm to elbow to shoulder), ARTHRALGIA (joint pain, shoulder pain) and HEADACHE (slight headache). At the time of the report, BONE PAIN (bone pain), PAIN (pain when lifting arm, pain when moving arm, painful to move arm up and down), DIARRHOEA (had loose stools), PAIN IN EXTREMITY (pain from arm to elbow to shoulder), ARTHRALGIA (joint pain, shoulder pain), NAUSEA (felt nauseated) and HEADACHE (slight headache) outcome was unknown. No concomitant medications were reported. Patient stated that she usually does not get headaches. No treatment medications were reported. This case was linked to MOD-2022-547032, MOD-2022-547037 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Hypoaesthesia
Neurological examination normal
Symptomtext
Since receiving the vaccine I had extreme fatigue that I only had once in my life before. I also had numbness on the left side of my face. That's the same symptom I felt when I had the Guillain-Barre syndrome 17 years ago. The numbness on the left side of my face only happened that one time since getting the vaccine. I also don't think that I have been experiencing anymore fatigue either.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Neurological exam- normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Pravastatin 20mg 1xday Ibandronate 150mg tablet 1xmonth
- Allergien
- Bee; Clindamycin; some Codeines; blood that's not washed (IGA)
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Contusion
Injection site bruising
Injection site erythema
Pain in extremity
Sensory disturbance
Skin warm
Symptomtext
pt states her left arm had fever and was red around the injection site. It became bruised and it spread from the injection site to the left breast nipple. It was painful underneath her arm and felt wet even though she has not perspired. She saw her PA and was to apply ice to the affected areas. These symptoms lasted about 2 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Gutta Psoriasis, HBP, Diabetes, Chlorestoral,
- Andere Medikamente
- metoprolol 100mg atorvastatin 80mg, losartan 25mg, sumatriptan 100mg, tramadol 50mg methotrexates on Fridays 10mg folic acid 1mg hydroxyzine 25 mg vitamin D3
- Allergien
- sulfa morphine
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 20.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Limb injury
Symptomtext
Site: Pain at Injection Site-Medium, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 18.04.2022
- Impfdatum
- 25.03.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Erythema
Inflammation
Lymphoedema
Pruritus
Urticaria
Symptomtext
Member developed lymphedema in left axillary approximately 24-48 hours from initial booster dose. Symptoms self resolved within 72 hours. Approximately 12-14 days after booster, patient developed total body urticaria. Patient developed raise, eurythmic, itchy, purpura clustered in any area that presented with pressure. Examples would be back, arms, and buttocks when sitting. Hands if driving. Any point in contact when laying on a bed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Member was seen in local ED within 48 hours of initial Urticaria outbreak. Patient was given diphenhydramine 25mg and methylprednisolone dose pack for inflammatory response. Patient seems to have reacted positively to medication with symptoms lessening but still present. Patient has an appointment with Immunology, date TBD.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Patient is prescribed Motrin 800mg and Methocarbamol 750mg prior to COVID-19 booster.
- Allergien
- No known allergies at this time.
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Oral mucosal eruption
Rash
Urticaria
Symptomtext
Pt reported on 3/25/22 in visit signs of hives and rash on left arm and mouth since Monday (3/21/2022), Patient concerns possible body reaction from the moderna vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Patient took antihistamines (Benadryl) and reaction went away in two days. Patient is doing well now.
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- Hyperlipidemia, Depression, Low back pain, COPD, Tobacco user.
- Andere Medikamente
- Unknown.
- Allergien
- Gabapentin: hives, itching, pruritus, rash, shortness of breath Ketorolac: Rash, shortness of breath, Penicillin: rash, hives, itching, pruritus, anaphylaxis, swelling Tramadol: Shortness of Breath Vancomycin:: itching, Pruritus, rash Vicodin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Eye irritation
Eye pruritus
Eye swelling
Hyperhidrosis
Nausea
Ocular hyperaemia
Swelling
Vertigo
Vomiting
Symptomtext
4/1/2022 at 2:00 eyes began itching and where becoming red and swollen. (left was worse than right). Swelling and redness where worse on 4/2. On 4/3 began experiencing extreme dizziness and vertigo. I was experiencing excessive sweats. Took OTC meds for vertigo. Drank cold water trying to cool off and ease vertigo. Became very nauseous and began vomiting. Laid down and took 3 hour nap. Vertigo was slightly better and no vomiting. Was able to get into see doctor and was advised to take Benadryl. Benadryl altered my sleep so I had to stop taking it. On 04/13/2022 vertigo and nausea have subsided. Eye irritation has improved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension; Hyperlipidemia
- Andere Medikamente
- Levothyroxine Meloxicam Amlodipine Simvastatin Losartan Baclofen Ca Vitamin D3 Multi-vitamin Biotin
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Incorrect dose administered
Myalgia
Symptomtext
Patient was given full dose instead of booster dose (half of dose) of Moderna vaccine. Patient experienced muscle soreness and headache symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Skin cancer, depression, anxiety
- Andere Medikamente
- Aspirin, escitalopram, famotidine, hydroxyzine, dexamethasone, metoprolol succinate, naratriptan, ondansetron
- Allergien
- No known allergies documented.
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 10.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 10.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Covid arm rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Valsartan 160 mg Ezetimibe 10mg. Omeprazole Allopurinol Vitamin D
- Allergien
- Flu vaccine, sulfa drugs, codeine, keflex, statins
- Vorherige Impfungen
- Guillain barre-flu shot
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 09.04.2022
- Impfdatum
- 28.02.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pruritus
Urticaria
Symptomtext
Itchiness started on scalp, then down to neck, back of neck and ears covered in hives, then down to back of body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Confusional state
Erythema
Feeling abnormal
Injection site erythema
Injection site pain
Peripheral swelling
Swelling face
Symptomtext
sore at sight of injection. red swelling continues to extend past injection site down the arm over night, face feels like swelling. after injection about 30 minutes felt confused a little foggy. overall felt odd so took two acetaminophen, 100 mg and went to bed, next day felt better but redness at site had spread down my arm, took two Benadryl and felt better Had only one Benadryl so took it. pharmacy will deliver more tpday and will continue and call doctor today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COPD, Hiatal Hernia, SLE not diagnosed by doctor, Asthma, Diabetes Type 2
- Vorgeschichte
- COPD, Asthma
- Andere Medikamente
- Atenolol, atorvastatin, levothyroxine, amlodipine, vitamin D, Advair, Spiriva,
- Allergien
- dust, grasses, chocolate, corn
- Vorherige Impfungen
- fatigue, redness at site of injectiom
- Staat
- PA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Oxygen saturation
Pain
Vaccination site erythema
Vaccination site movement impairment
Vaccination site pain
Vaccination site rash
Symptomtext
Achiness; Could not barely lift arms for 3 days; Pain in the injection site; Tiredness; Redness in the injection site,; rash an inch in diameter in the injection site for 6 days; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (Achiness), VACCINATION SITE MOVEMENT IMPAIRMENT (Could not barely lift arms for 3 days), VACCINATION SITE PAIN (Pain in the injection site), FATIGUE (Tiredness) and VACCINATION SITE ERYTHEMA (Redness in the injection site,) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K212A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for COVID-19 immunisation: Pfizer COVID 19 vaccine (First dose , LOT : EWO177) on 01-Jul-2021 and Pfizer COVID 19 vaccine (Second dose) on 22-Jul-2021. Past adverse reactions to the above products included No adverse event with Pfizer COVID 19 vaccine and Pfizer COVID 19 vaccine. Concurrent medical conditions included Penicillin allergy. On 28-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Mar-2022, the patient experienced PAIN (Achiness), VACCINATION SITE MOVEMENT IMPAIRMENT (Could not barely lift arms for 3 days), VACCINATION SITE PAIN (Pain in the injection site), FATIGUE (Tiredness), VACCINATION SITE ERYTHEMA (Redness in the injection site,) and VACCINATION SITE RASH (rash an inch in diameter in the injection site for 6 days). The patient was treated with HYDROGEN PEROXIDE for Adverse event, at an unspecified dose and frequency. On 30-Mar-2022, VACCINATION SITE MOVEMENT IMPAIRMENT (Could not barely lift arms for 3 days) had resolved. On 02-Apr-2022, VACCINATION SITE RASH (rash an inch in diameter in the injection site for 6 days) had resolved. At the time of the report, PAIN (Achiness) and VACCINATION SITE PAIN (Pain in the injection site) had not resolved and FATIGUE (Tiredness) and VACCINATION SITE ERYTHEMA (Redness in the injection site,) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Oxygen saturation: 97-98% (normal) 97-98%. No concomitant medications were reported. Treatment given was washing with water, hot compress and applying hydrogen peroxide on the injection site area. Patient reports that she was still experiencing pain and could not barely lift arms for 3 days, and rash an inch in diameter in the injection site for 6 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Name: Oxygen level; Result Unstructured Data: 97-98%
- Aktuelle Erkrankungen
- Penicillin allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.04.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Feeling cold
Pain
Symptomtext
Began to feel very cold on Friday 3/3/22, 12 hrs after vaccine booster. Friday evening I went to bed and woke up shivering and teeth chattering. My husband covered me with 4 blankets and I continued to shiver and teeth chattering for another 30 minutes. The next morning I was achy all over and spent the day in bed. The next day (Sunday) I felt better, just very sore from shivering.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dermatitis
Rash
Rash erythematous
Rash papular
Rash pruritic
Skin lesion
Symptomtext
48 hours after my booster I started to develop a rash. In a few hours it covered my torso, arms and legs. Itchy, bumpy, lesions that then resolved into what looks like a sunburn.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Dermatologist examined my and conclude it was a generalized dermatitis reaction to the booster shot. Treated with a steroid shot and cortisone cream.
- Aktuelle Erkrankungen
- Head cold that started about 6 days before my booster. I was mostly recovered by April 1st but had been taking Tylenol PM, Naproxen and Meloxicam the previous 6 days to manage fever & body aches (not all at once but scattered over the 6 days). I was seen by a physician for my cold symptoms. Tested for Covid (1 rapid PCR, 3 home tests), strep and flu - all tests were negative. Physician diagnosed a cold.
- Vorgeschichte
- None
- Andere Medikamente
- thyroxine, progesterone, estradiol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 27.03.2022
- Impfdatum
- 10.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Musculoskeletal stiffness
Pyrexia
Swelling
Urticaria
Symptomtext
Presented with normal fever symptoms the day following the shot. However, experienced severe hives, swelling, stiffness, and joint pain around 2 weeks following the shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Effexor, Wellbutrin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 26.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain lower
Appendicectomy
Appendicitis
Computerised tomogram abdomen abnormal
Symptomtext
Booster dose given afternoon Monday March 21. Pt woke on Tuesday March 22 at 8 a.m. with RLQ abdominal pain; ER found appendicitis requiring surgical extraction. Pt reported no pain or GI problems prior to Tuesday morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain lower
- Hospital-Tage
- 2,0
- Labordaten
- Abd CT and bw at Emergency Room Tuesday, March 22. Discharged after surgery.
- Aktuelle Erkrankungen
- Anal Fistula, Allergic Rhinitis
- Vorgeschichte
- Anal fistula/fissure; fistulotomy 9/16; seton insertion procedure 3/12/21
- Andere Medikamente
- -
- Allergien
- Penicillin V
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 22.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Pain in extremity
Pregnancy
Symptomtext
I was giving booster doses of moderna vaccine at a group, I also offered any staff a booster if they wanted it. Patient is an employee there and she said she needed her booster, she said she had an appointment on 03/15/22 for her booster but had to cancel due to car trouble, I asked her for her immunization card and she didn't have it but she said she was over due for her booster, so I gave her the shot. When we went to imput the info on the computer we discovered she wasn't due for another month. I called patient 03/24/22, she said she felt fine other than a little soreness in her arm and she did discover she was pregnant today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- denies
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 03.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Hot flush
Nausea
Pain
Symptomtext
I got my booster shot on 3/3/22. Since my booster shot I've had body aches, fatigue, chills, slight headache, occasional periods of hot flashes, and occo. waves of nausea almost every evening starting around 4-5p for the last 2.5 weeks and lasting most of the night. Every morning I get up I feel better, but then it starts all over again the next evening. I previously was vaccinated on 8/12/21 and 9/8/21 with only 2 days of symptoms post each initial shots. I left the medical professional section blank because I have not seek any medical care regarding my symptoms yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- none *this vaccine that I got was just a booster shot I got on 3/3/22. I was previously vaccinated on 8/12/21 and 9/9/21 with the Moderna vaccine .
- Vorgeschichte
- None.
- Andere Medikamente
- Wellbutrin; Probiotic; Multi Vit; Vit D2; Omeprazole; Valtrex; Citrucel.
- Allergien
- Dilaudid and Amoxicillin.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 22.03.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Dizziness
Haematemesis
Pyrexia
Rhinorrhoea
Vomiting
Symptomtext
PATIENT RECEIVED 3 VACCINES ON 3/10/22: MODERNA, SHINGRIX, AND PREVNAR 20. PATIENT REPORT STARTING TO HAVE SYMPTOMS AT NIGHT ON 3/10/22l FEVER, THROWING UP AND WITH BLOOD LIGHT RED COLOR, DIZZINESS, COUGH, RUNNY NOSE. THIS LAST FOR 3 DAYS BUT STILL HAVE MINOR SYMPTOMS FOR ABOUT 1-2 WEEKS. PT TOOK TYLENOL AND ROBITUSSIN OVER THE COUNTER TO HELP WITH SYMPTOMS. PATIENT IS OKAY NOW.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD-USING INHALER
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 21.03.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Disorientation
Dizziness
Fatigue
Feeling abnormal
Gait disturbance
Malaise
Symptomtext
During the night after the vaccine, the patient woke up in the middle of the night not feeling well. He says he remembers walking to the bathroom, didn't know where he was or what he was doing, and kind of "blacked out". He said he fell into the door but caught himself so he didn't fall to the ground. He says now he feels like he has "long covid" complaining of fatigue and brain fog
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Had covid month prior to vaccine
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Asthenia
Burning sensation
Nausea
Rash
Urticaria
Symptomtext
Ardor of joints and pelvis. Nausea, weakness. At day #10 after the shot, I woke up with a rash. Went to emergency room on day #11 and was diagnosed with an urticaria. Prescription for 6 days: Methylprednisolone and Hydroxyzine. As of today, still with the problem.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- In process
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Panadol; Multivitamin
- Allergien
- Prior to vaccine, No
- Vorherige Impfungen
- COVID Moderna 2021-04-21 2021-05-19
- Staat
- -
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Flushing
Head discomfort
Hyperhidrosis
Symptomtext
Pt reported flushing/sweating, dizziness, head pressure. Vitals: 152/106, 83, 18, 99% RA -- > 147/102 Pt AxOx3. Per pt, BP is at his BL. Instructed pt to f/u w/ PCP regarding BP. Pt states that he feels ok to drive home. Pt ambulated w/ steady gait. Not changes notes. Per clinic lead pt ok to drive home w/ instructions to call EMS if symptoms worsen. Pt given juice and crackers. Pt states that he feels better prior to departure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: adjustment disorder w/ mixed disturbance, Alcohol use disorder. Inguinal hernia s/p repair
- Andere Medikamente
- N/A
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 16.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Rash
Symptomtext
Patient is a staff member at the clinic. Patient is immunocompromised and came to mobile clinic yesterday to receive her booster shot. Her 3rd dose was 10/04/2022. She reported that her 2nd and 3rd doses had quickly affected her and that she had felt increased heart rate and sweating afterwards. Patient would still like to continue with booster shot for complete protection. She was given 0.25mL of Moderna (lot #033K21-2A) IM in her left deltoid at 1511. About 15 minutes after injection, she reported increased tiredness and fatigue. RN goes over to assess patient and palpates heart rate. Heart rate is within normal limits and there is not increased sweating observed. RN sees a mild rash on patient's chest. Patient denies any increased difficulty breathing, swelling/tightness in throat, or any increased itchiness. RN observes patient is speaking in full sentences, normal rhythm, and normal breathing positioning. RN suggests that provider come out to see patient due to rash. Provider FNP comes outside 20 minutes after injection. Suggests patient come lay down on exam table and have 1 Benadryl. Patient given 25 mg of Diphenhydramine about 25 min after injection. RN continue to observe patient and confirm not increased difficulty breathing or worsening symptoms. Patient does report increased fatigue. She says it is similar to how she felt after 2nd and 3rd dose. Patient heads home at 1641 after reviewing ER precautions with RN and home care for the next few days. Patient also, has epi-pen at home and know how to use it should anything change.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Gait disturbance
Insomnia
Limb discomfort
Pain in extremity
Peripheral swelling
Skin discolouration
Symptomtext
Patient was vaccinated with booster Moderna on 3/4/22. Patient states no discomfort over the weekend but noticed discomfort on Monday 3/7/22 when walking to class. Patient reports having swollen, discolored, painful toes. Pain and discomfort from toes keeping patient up at night and making it difficult to walk. Patient states discomfort increased around 3/14/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Amphetamine/Dextroamphetamine 15 mg
- Allergien
- NKA/NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 14.03.2022
- Impfdatum
- 18.02.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 19,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Mechanical urticaria
Pruritus
Symptomtext
After about 14 days, patient developed Dermatographias, with pruritus.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Malaise
Symptomtext
I suffered a small stroke before the vaccine and started feeling sick with headache at 9pm which lasted about 6 days took doctor prescribed Nurtec, Ubrelvy and Sumatriptan 50mg. Headaches have subsided with OTC Benadryl.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 02.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Injection site pain
Peripheral swelling
Symptomtext
Localized erythema, arm swelling, and pain at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Breast cancer, stage 1, estrogen receptor negative, right C50.911, Z17.1 Health care maintenance Z00.00 Acquired hypothyroidism E03.9 Need for COVID-19 vaccine Z23 History of hepatitis C Z86.19 Essential hypertension, benign I10 Depression with anxiety F41.8 Night sweats R61
- Vorgeschichte
- Resolved Updated Circulatory Migraine Create Overview Change Dx Resolve -2 yr MD HYPERTENSION, BENIGN ESSENTIAL Create Overview Change Dx Resolve -6 days MD Digestive Reflux esophagitis Create Overview Change Dx Resolve -2 yr MD History of hepatitis C Edit Overview Change Dx Resolve -6 days MD Overview Genotype 1B. Endocrine OBESITY Create Overview Change Dx Resolve -10 yr MD HYPOTHYROIDISM, ACQUIRED Create Overview Change Dx Resolve -1 yr MD Hyperlipidemia, mixed Create Overview Change Dx Resolve -3 yr MD Nervous HEARING LOSS Create Overview Change Dx Resolve -3 yr MD CARPAL TUNNEL - SAW DR. Create Overview Change Dx Resolve -8 yr MD Reproductive Edit Overview Change Dx Resolve -6 yr PT Overview replaced due to ICD-10 go-live Breast cancer, stage 1, estrogen receptor negative, right Edit Overview Change Dx Resolve -6 days MD Oncology Treatment Summary Overview 6/2018 Adenomyosis Create Overview Change Dx Resolve -6 yr MD Respiratory Snoring Create Overview Change Dx Resolve -10 yr MD Sinusitis, chronic Create Overview Change Dx Resolve -2 yr MD Mild intermittent asthma without complication Create Overview Change Dx Resolve -3 yr MD Allergic conjunctivitis and rhinitis, bilateral Create Overview Change Dx Resolve -7 yr MD Immune Sjogren's syndrome Create Overview Change Dx Resolve -4 yr MD Integumentary Lichen planus Create Overview Change Dx Resolve -7 yr MD Dry skin dermatitis Create Overview Change Dx Resolve -4 yr MD Musculoskeletal Spinal stenosis of lumbar region with neurogenic claudication Edit Overview Change Dx Resolve -1 yr MD Overview Dr.: surgery April 2018 Primary osteoarthritis of right knee Create Overview Change Dx Resolve -3 yr MD Polyarthritis Create Overview Change Dx Resolve -1 yr MD Patellofemoral arthralgia of right knee Create Overview Change Dx Resolve -2 yr MD Fibromyalgia Create Overview Change Dx Resolve -6 yr PT Urinary Neurogenic bladder Edit Overview Change Dx Resolve -2 yr MD Overview Post-op Psychiatric POST TRAUMATIC STRESS SYNDROME Create Overview Change Dx Resolve -10 yr MD DEPRESSION and ANXIETY Create Overview Change Dx Resolve -6 days MD Chronic pain syndrome Create Overview Change Dx Resolve -4 yr MD Other sweats Create Overview Change Dx Resolve -6 days MD Sleep disorder, falling asleep during the day and falling Create Overview Change Dx Resolve -4 yr MD IG A DEFICIENCY Create Overview Change Dx Resolve -2 yr MD HYPERGLYCEMIA Edit Overview Change Dx Resolve -6 yr PT Overview Problem list replacer utility Health care maintenance Create Overview Change Dx Resolve -6 days MD Fall at home Create Overview Change Dx Resolve -6 yr MD Epigastric pain Create Overview Change Dx Resolve -3 yr MD
- Andere Medikamente
- (RANITIDINE HCL) 150 MG CAPS RANITIDINE HCL 150 MG ORAL CAPSULE 3 years ago ascorbic acid (VITAMIN C) 500 mg chewable tablet Take 4 tablets by mouth Daily. 6 days ago Cholecalciferol (VITAMIN D3) 2000 UNITS CAPS 1 by mouth twice a day
- Allergien
- Allergies Latex Latex Not Specified 10/2/2015 Past Updates SEVERE Sulfa Antibiotics Sulfa Antibiotics Hives Not Specified 6/16/2004 Past Updates
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 07.03.2022
- Impfdatum
- 02.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Loss of personal independence in daily activities
Pain
Pain in extremity
Sleep disorder
Symptomtext
Arm was killing me; It hurts/ Sore; Couldn't even play golf; Discomfort; Been up all morning; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Arm was killing me), PAIN (It hurts/ Sore), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (Couldn't even play golf), DISCOMFORT (Discomfort) and SLEEP DISORDER (Been up all morning) in a 72-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. The patient's past medical history included COVID-19 in September 2021. On 02-Mar-2022 at 10:30 AM, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 03-Mar-2022, the patient experienced PAIN IN EXTREMITY (Arm was killing me). 03-Mar-2022, the patient experienced PAIN (It hurts/ Sore), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (Couldn't even play golf), DISCOMFORT (Discomfort) and SLEEP DISORDER (Been up all morning). At the time of the report, PAIN IN EXTREMITY (Arm was killing me), PAIN (It hurts/ Sore), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (Couldn't even play golf), DISCOMFORT (Discomfort) and SLEEP DISORDER (Been up all morning) had not resolved. The action taken with mRNA-1273 (Spikevax) (Intramuscular) was unknown. No Concomitant medication reported. The patient stated that as a treatment put a hot towel on his arm and his shoulder. Patient had no swelling, no redness. Patient went through some yuck and that kind of stuff, what people go through, Almost passed after about 9-11 days then paitent felt better. There was some discomfort; it was not severe pain. No Treatment medication reported. This case was linked to MOD-2022-501358 (Patient Link). Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 05.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 05.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Myalgia
Pyrexia
Symptomtext
Chills, muscle aches, high fever of 102.6
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Epileptic
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Neck pain
Pain in extremity
Vision blurred
Symptomtext
Patient received booster today. Denies any problems with last two covid vaccines. Has pain in left arm and neck and slight blurred vision in left eye that started 15 min after vaccine. BP 198/110 SP02 97% 90:P Temp 36.9. Reported to pharmacist advised to give 1 Benadryl 25 mg. Patient in agreement took 25 mg Benadryl. Rechecked BP 160/98 P 80. Patient denies being seen or calling 911. Is award to call 911 with SOB or CP or gets worse . Also states will follow up with provider on BP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- History of HTN 2 years ago
- Vorgeschichte
- None.
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Injection site erythema
Injection site warmth
Myalgia
Nausea
Vomiting
Symptomtext
Large red, warm to touch at injection site, nausea, vomiting, headache, fatigue, muscle ache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Arthritis, Asthma, Chronic Bronchitis, Heart Failure
- Andere Medikamente
- Lipitor, Spiriva, Symbicort, Buspar, Prozac, Flonase, Prilosec, Oxybutynin, Pro Air
- Allergien
- Iodine,
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 03.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Malaise
Postpartum haemorrhage
Vaginal haemorrhage
Symptomtext
-Onset of postpartum bleeding (lochia alba on 03/02/2022) after it had already ceased, accompanied with my typical PMS symptoms (headache, general malaise/fatigue). Small streaks of blood appeared when wiping in otherwise clear discharge prior to onset of lochia alba. Reminder that lochia alba stage had already been completed and spontaneously restarted after vaccination with significant amounts of lochia alba. Also currently experiencing chest pains 2 days later. It is important to mention that just 7 hours after my 1st vaccination on 01/31/2022, I experienced Premature Rupture of Membranes and significant bleeding/passing of clots at only 19 weeks pregnant (I have submitted a separated VAERS report for this incident). I went into preterm labor at 20 weeks and my baby passed away due to not being viable. No pregnancy concerns nor complications prior to vaccination; What happened to me and my baby still remains unexplained. I TRULY hope all will consider that this vaccine may be causing hormonal/reproductive disturbances, especially in women of color.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Migraine GERD Scoliosis/Chronic Pain Asthma (not complicated)
- Andere Medikamente
- Omeprazole Prenatal Vitamin D3
- Allergien
- N/A
- Vorherige Impfungen
- Preterm Premature Rupture of Membranes accompanied with severe vaginal bleeding/passing of clots at 19 weeks pregnant; Preterm l
- Staat
- KY
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Erythema
Influenza like illness
Peripheral swelling
Pyrexia
Symptomtext
Patient complained of fever, cough, flu-like symptoms, and softball size redness and swelling of arm which lasted 48-52 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Cholesterol Blood pressure Obese
- Andere Medikamente
- Lisinopril Meloxicam Finasteride Lovastatin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Pain in extremity
Pruritus
Rash
Skin warm
Swelling
Vaccination site reaction
Symptomtext
developed covid arm immediately after injection. Raised, very itchy, hot to touch, very painful, rash is circular and big.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Multi Vitamin, Calcium Citrate, Biotin
- Allergien
- Strawberries, TamiFlu, Latex sensitivity, mineral oil
- Vorherige Impfungen
- 08/12/2021
- Staat
- AR
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 18.12.2023
- Impfdatum
- 22.04.2022
- Beginn
- 29.11.2023
- Tage bis Beginn
- 586,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
Hospitalized with COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Cancer (bladder), Coronary Artery Disease, Congestive Heart Failure, Hyperlipidemia, Hypertension, Reflux and Other (AFib)
- Andere Medikamente
- unknown
- Allergien
- ACE Inhibitors Allergy (Unknown, Verified 11/29/23 08:11) Allergic Reactions codeine [Codeine] Allergy (Verified 11/29/23 08:11) Syncope Penicillins Allergy (Verified 11/29/23 08:11) Rash pregabalin [From Lyrica] Allergy (Verified 11/29/23 08:11) "Drunk funny feeling" propoxyphene HCl [From Darvon] Allergy (Verified 11/29/23 08:11) N/V tramadol Allergy (Verified 11/29/23 08:11) Itching
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 06.12.2023
- Impfdatum
- 14.04.2022
- Beginn
- 02.12.2023
- Tage bis Beginn
- 597,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 2 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- positive covid pcr 12/2/23
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- COPD, B/l PE, HTN, HLD, HFpEF, GERD
- Andere Medikamente
- unknown
- Allergien
- sulfa
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 05.11.2023
- Tage bis Beginn
- 570,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
hospitalized with covid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- DMII, HTN, HLD, Osteoporosis, Afib, Aphasia 2/2 CVA, Chronic B/L Cellulitis, Depression, and Anxiety
- Andere Medikamente
- unknown
- Allergien
- cefdinir, dabigatran etexilate
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 16.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 06.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 22.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 22.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 91,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 22.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product administration duration
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product administration duration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product administration duration
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product administration duration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product administration duration
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product administration duration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product administration duration
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product administration duration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product administration duration
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product administration duration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product administration duration
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product administration duration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
VACCINE WAS STORED IN AN UNAPPROVED STORAGE UNIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 16.08.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
PATIENT RECEIVED VACCINE AFTER BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- LOPID
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 16.08.2023
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
PATIENT RECEIVED VACCINE AFTER BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 19.07.2023
- Impfdatum
- 22.02.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 287,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
Positive for Covid-19; This spontaneous case was reported by a pharmacist and describes the occurrence of COVID-19 (Positive for Covid-19) in a 75-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 033K212A) for COVID-19 prophylaxis. Concurrent medical conditions included Penicillin allergy. On 22-Feb-2022 at 3:34 PM, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) .5 milliliter. On 06-Dec-2022, the patient experienced COVID-19 (Positive for Covid-19). At the time of the report, COVID-19 (Positive for Covid-19) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 06-Dec-2022, SARS-CoV-2 test: Positive. The action taken with mRNA-1273 (Spikevax) (Intramuscular) was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2023-731472 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-731472:Bivalent case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221206; Test Name: Covid-19 virus test; Test Result: Positive
- Aktuelle Erkrankungen
- Penicillin allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 14.06.2023
- Impfdatum
- 08.03.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 274,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Angina unstable
Symptom recurrence
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE UNSTABLE ANGINA ANGINA, UNSPECIFIED 12/8/2022 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Angina unstable
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 08.06.2023
- Impfdatum
- 24.03.2022
- Beginn
- 03.06.2023
- Tage bis Beginn
- 436,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines ; Moderna 8/2/21 lot# 005C21A; Moderna 8/31/21 lot# 033C21A; Moderna 3/24/22 Lot# 033K212A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 14.03.2023
- Impfdatum
- 19.04.2022
- Beginn
- 05.11.2022
- Tage bis Beginn
- 200,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Moderna 2/25/21 Lot# 031L20A; Moderna 3/25/21 Lot# 045A21A; Moderna 11/6/21 Lot# 939906; Moderna 4/19/22 Lot# 033K21-2A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 14.02.2023
- Impfdatum
- 11.05.2022
- Beginn
- 13.02.2023
- Tage bis Beginn
- 278,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
hospitalized with covid; fully vaccinated with 1 booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Cancer (Bladder Cancer ), Hyperlipidemia, Hypertension and Other (AFIB)
- Andere Medikamente
- unknown
- Allergien
- Statins, codeine, dilaudid, codeine sulfate, hydrocodone compound, morphine sulfate, narcotics
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 20.01.2023
- Impfdatum
- 16.01.2023
- Beginn
- 16.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Expired vaccine administered to a patient; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered to a patient) and NO ADVERSE EVENT (no adverse event) in an adult patient of an unknown gender who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 16-Jan-2023, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 16-Jan-2023, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered to a patient). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered to a patient) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered to a patient). No concomitant medications were reported. No treatment details were reported. Most recent FOLLOW-UP information incorporated above includes: On 17-Jan-2023: Follow-up information included reporter added, patient's age group added and product details updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 23.12.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adverse reaction
Symptomtext
My Parkinsons medicine quit working for about 4 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Adverse reaction
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Parkinsons, rheumatoid arthritis, occupational asthma
- Vorgeschichte
- Same as above - my parkinsons medicine quit working for 4 weeks after the booster shot.
- Andere Medikamente
- Mirapex er, singlet 50/200, 25/100, Singulair, plaquenil, amantadine, celebrex, Adderall, orthotricycline, methotrexate , folic acid
- Allergien
- Yellow dye no 5
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 30.08.2021
- Beginn
- 18.11.2022
- Tage bis Beginn
- 445,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
patient hospitalized
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 19,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 14.04.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 242,0
- 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 6/3/21 005C21A dose 2 Moderna 7/1/21 043B21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ 12/12/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 09.12.2022
- Impfdatum
- 22.02.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 282,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 62-year-old female patient received BNT162b2 (BNT162B2), on 22Feb2022 as dose number unknown, single (Lot number: 033K21-2A) at the age of 61 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "HIV", start date: 1995 (ongoing), notes: HIV since 1995. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Dec2022, outcome "unknown" and all described as "Treatment of COVID-19".Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical information:No Other medication in 2 weeks. Paxlovid was taken as COVID 19 Treatment.Treatment start date was 02Dec2022.Treatment stop date was 05Dec2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- HIV infection (HIV since 1995)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.12.2022
- Impfdatum
- 29.05.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Unevaluable event
Symptomtext
No adverse event; 4 adult patients received Monovalent vaccine 9 day after MFG expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 29-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date). No concomitant medications were reported. 8 adult patients received monovalent vaccine Beyond manufacture Expiration Date. It was reported that expiry date of vaccine had not been extended.It was unbroken cartons. Vial size was reported as 5.5 mL. Vial was initially stored in the refrigerator 20-MAY-2022 and 28-MAY-2022. 4 adult patients on 21-MAY-2022 and 4 more adult patients on 29-MAY-2022. Vial did not undergo any temperature excursions. No treatment information was provided. This case contains information for the 7th of 8 adult patients described by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-679408, US-MODERNATX, INC.-MOD-2022-679413, US-MODERNATX, INC.-MOD-2022-679412 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-679408:same reporter US-MODERNATX, INC.-MOD-2022-679412:same reporter US-MODERNATX, INC.-MOD-2022-679413:same reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.12.2022
- Impfdatum
- 29.05.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Unevaluable event
Symptomtext
No adverse event; 4 adult patients received Monovalent vaccine 9 day after MFG expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 29-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date). No concomitant medications were reported. 8 adult patients received monovalent vaccine Beyond manufacture Expiration Date. It was reported that expiry date of vaccine had not been extended.It was unbroken cartons. Vial size was reported as 5.5 mL. Vial was initially stored in the refrigerator 20-MAY-2022 and 28-MAY-2022. 4 adult patients on 21-MAY-2022 and 4 more adult patients on 29-MAY-2022. Vial did not undergo any temperature excursions. No treatment information was provided. This case contains information for the 7th of 8 adult patients described by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-679408, US-MODERNATX, INC.-MOD-2022-679413, US-MODERNATX, INC.-MOD-2022-679412 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-679408:same reporter US-MODERNATX, INC.-MOD-2022-679412:same reporter US-MODERNATX, INC.-MOD-2022-679413:same reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.12.2022
- Impfdatum
- 29.05.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Unevaluable event
Symptomtext
Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022; no adverse event; 4 adult patients received Monovalent vaccine 9 day after MFG expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date), PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022) and NO ADVERSE EVENT (no adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 29-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date), PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022). No concomitant medications were reported. 8 adult patients received monovalent vaccine Beyond manufacture Expiration Date. It was reported that expiry date of vaccine had not been extended. It was unbroken cartons. Vial size was reported as 5.5 mL. Vial was initially stored in the refrigerator 20-MAY-2022 and 28-MAY-2022. 4 adult patients on 21-MAY-2022 and 4 more adult patients on 29-MAY-2022. Vial did not undergo any temperature excursions. No treatment information was provided. This case contains information for the 6th of 8 adult patients described by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-679408, US-MODERNATX, INC.-MOD-2022-679142, US-MODERNATX, INC.-MOD-2022-679409, US-MODERNATX, INC.-MOD-2022-679410, US-MODERNATX, INC.-MOD-2022-679412, US-MODERNATX, INC.-MOD-2022-679414, US-MODERNATX, INC.-MOD-2022-679415 .; Sender's Comments: US-MODERNATX, INC.-MOD-2022-679408:same reporter US-MODERNATX, INC.-MOD-2022-679142:same reporter US-MODERNATX, INC.-MOD-2022-679409:same reporter US-MODERNATX, INC.-MOD-2022-679410:same reporter US-MODERNATX, INC.-MOD-2022-679412:same reporter US-MODERNATX, INC.-MOD-2022-679414:same reporter US-MODERNATX, INC.-MOD-2022-679415:same reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.12.2022
- Impfdatum
- 29.05.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Unevaluable event
Symptomtext
Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022; no adverse event; 4 adult patients received Monovalent vaccine 9 day after MFG expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date), PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022) and NO ADVERSE EVENT (no adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 29-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date), PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022). No concomitant medications were reported. 8 adult patients received monovalent vaccine Beyond manufacture Expiration Date. It was reported that expiry date of vaccine had not been extended. It was unbroken cartons. Vial size was reported as 5.5 mL. Vial was initially stored in the refrigerator 20-MAY-2022 and 28-MAY-2022. 4 adult patients on 21-MAY-2022 and 4 more adult patients on 29-MAY-2022. Vial did not undergo any temperature excursions. No treatment information was provided. This case contains information for the 6th of 8 adult patients described by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-679408, US-MODERNATX, INC.-MOD-2022-679142, US-MODERNATX, INC.-MOD-2022-679409, US-MODERNATX, INC.-MOD-2022-679410, US-MODERNATX, INC.-MOD-2022-679412, US-MODERNATX, INC.-MOD-2022-679414, US-MODERNATX, INC.-MOD-2022-679415 .; Sender's Comments: US-MODERNATX, INC.-MOD-2022-679408:same reporter US-MODERNATX, INC.-MOD-2022-679142:same reporter US-MODERNATX, INC.-MOD-2022-679409:same reporter US-MODERNATX, INC.-MOD-2022-679410:same reporter US-MODERNATX, INC.-MOD-2022-679412:same reporter US-MODERNATX, INC.-MOD-2022-679414:same reporter US-MODERNATX, INC.-MOD-2022-679415:same reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.12.2022
- Impfdatum
- 29.05.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Unevaluable event
Symptomtext
Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022 beyond MFG expiry date.; no adverse event; 4 adult patients received Monovalent vaccine 9 day after MFG expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date), PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022 beyond MFG expiry date.) and NO ADVERSE EVENT (no adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 29-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022 beyond MFG expiry date.) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date), PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022 beyond MFG expiry date.) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022 beyond MFG expiry date.). No concomitant medications were reported. 8 adult patients received monovalent vaccine Beyond manufacture Expiration Date. It was reported that expiry date of vaccine had not been extended. It was unbroken cartons. Vial size was reported as 5.5 mL. Vial was initially stored in the refrigerator 20-MAY-2022 and 28-MAY-2022. 4 adult patients received vaccine on 21-MAY-2022 and 4 more adult patients on 29-MAY-2022. Vial did not undergo any temperature excursions. No treatment information was provided. This case contains information for the 5 out of 8 adult patients described by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-679408, US-MODERNATX, INC.-MOD-2022-679413, US-MODERNATX, INC.-MOD-2022-679142, US-MODERNATX, INC.-MOD-2022-679409, US-MODERNATX, INC.-MOD-2022-679410, US-MODERNATX, INC.-MOD-2022-679414, US-MODERNATX, INC.-MOD-2022-679415 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-679413:same reporter US-MODERNATX, INC.-MOD-2022-679408:same reporter US-MODERNATX, INC.-MOD-2022-679142:same reporter US-MODERNATX, INC.-MOD-2022-679409:same reporter US-MODERNATX, INC.-MOD-2022-679410:same reporter US-MODERNATX, INC.-MOD-2022-679414:same reporter US-MODERNATX, INC.-MOD-2022-679415:same reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.12.2022
- Impfdatum
- 29.05.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Unevaluable event
Symptomtext
Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022 beyond MFG expiry date.; no adverse event; 4 adult patients received Monovalent vaccine 9 day after MFG expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date), PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022 beyond MFG expiry date.) and NO ADVERSE EVENT (no adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 29-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022 beyond MFG expiry date.) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date), PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022 beyond MFG expiry date.) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 28-MAY-2022 and dose was administered in 29-MAY-2022 beyond MFG expiry date.). No concomitant medications were reported. 8 adult patients received monovalent vaccine Beyond manufacture Expiration Date. It was reported that expiry date of vaccine had not been extended. It was unbroken cartons. Vial size was reported as 5.5 mL. Vial was initially stored in the refrigerator 20-MAY-2022 and 28-MAY-2022. 4 adult patients received vaccine on 21-MAY-2022 and 4 more adult patients on 29-MAY-2022. Vial did not undergo any temperature excursions. No treatment information was provided. This case contains information for the 5 out of 8 adult patients described by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-679408, US-MODERNATX, INC.-MOD-2022-679413, US-MODERNATX, INC.-MOD-2022-679142, US-MODERNATX, INC.-MOD-2022-679409, US-MODERNATX, INC.-MOD-2022-679410, US-MODERNATX, INC.-MOD-2022-679414, US-MODERNATX, INC.-MOD-2022-679415 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-679413:same reporter US-MODERNATX, INC.-MOD-2022-679408:same reporter US-MODERNATX, INC.-MOD-2022-679142:same reporter US-MODERNATX, INC.-MOD-2022-679409:same reporter US-MODERNATX, INC.-MOD-2022-679410:same reporter US-MODERNATX, INC.-MOD-2022-679414:same reporter US-MODERNATX, INC.-MOD-2022-679415:same reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.12.2022
- Impfdatum
- 21.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Unevaluable event
Symptomtext
Adult patient received Monovalent vaccine 1 day after MFG expiration date; No adverse event; Patient received Monovalent vaccine after MFG expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received Monovalent vaccine after MFG expiration date), PRODUCT STORAGE ERROR (Adult patient received Monovalent vaccine 1 day after MFG expiration date) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 21-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 21-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received Monovalent vaccine after MFG expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Adult patient received Monovalent vaccine 1 day after MFG expiration date) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received Monovalent vaccine after MFG expiration date), PRODUCT STORAGE ERROR (Adult patient received Monovalent vaccine 1 day after MFG expiration date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Patient received Monovalent vaccine after MFG expiration date) and PRODUCT STORAGE ERROR (Adult patient received Monovalent vaccine 1 day after MFG expiration date). Pharmacist was calling to report that 8 adult patients received Moderna COVID-19 vaccine beyond manufacture expiration date. No concomitant medications were reported. MFG Expiration date was 20May2022 (agent checked, it had not been extended). It was unbroken cartons. Vial size was reported as 5.5 ml. The vial was initially stored in the refrigerator on 20-MAY-2022 and 28-MAY-2022 The vaccine was administered to 4 adult patients on 21-MAY-2022 and 4 more adult patients on 29-MAY-2022 The vial did not underwent any temperature excursions. No treatment medications were reported. This case contains information for the 3rd of 8 adult patients described by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-679408, US-MODERNATX, INC.-MOD-2022-679413, US-MODERNATX, INC.-MOD-2022-679412 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-679408:same reporter US-MODERNATX, INC.-MOD-2022-679412:same reporter US-MODERNATX, INC.-MOD-2022-679413:same reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 01.12.2022
- Impfdatum
- 21.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Vial was initially stored in the refrigerator on 20-MAY-2022 and dose was administered in 21-MAY-2022 beyond MFG expiry date.; No adverse event; Patient received Monovalent vaccine 1 day after MFG expiration date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received Monovalent vaccine 1 day after MFG expiration date.), PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 20-MAY-2022 and dose was administered in 21-MAY-2022 beyond MFG expiry date.) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 21-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 21-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received Monovalent vaccine 1 day after MFG expiration date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 20-MAY-2022 and dose was administered in 21-MAY-2022 beyond MFG expiry date.) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received Monovalent vaccine 1 day after MFG expiration date.), PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 20-MAY-2022 and dose was administered in 21-MAY-2022 beyond MFG expiry date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Patient received Monovalent vaccine 1 day after MFG expiration date.) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 20-MAY-2022 and dose was administered in 21-MAY-2022 beyond MFG expiry date.). No concomitant medications were reported. 8 adult patients received monovalent vaccine Beyond manufacture Expiration Date. It was reported that expiry date of vaccine had not been extended.It was unbroken cartons Vial size was reported as 5.5 mL. Vial was initially stored in the refrigerator 20-MAY-2022 and 28-MAY-2022. 4 adult patients on 21-MAY-2022 and 4 more adult patients on 29-MAY-2022. Vial did not undergo any temperature excursions. No treatment information was provided. This case contains information for the 2nd of 8 adult patients described by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-679142, US-MODERNATX, INC.-MOD-2022-679409, US-MODERNATX, INC.-MOD-2022-679410, US-MODERNATX, INC.-MOD-2022-679412, US-MODERNATX, INC.-MOD-2022-679413, US-MODERNATX, INC.-MOD-2022-679414, US-MODERNATX, INC.-MOD-2022-679415 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-679142:Adult patient 1, same reporter US-MODERNATX, INC.-MOD-2022-679409:same reporter US-MODERNATX, INC.-MOD-2022-679410:same reporter US-MODERNATX, INC.-MOD-2022-679412:same reporter US-MODERNATX, INC.-MOD-2022-679413:same reporter US-MODERNATX, INC.-MOD-2022-679414:same reporter US-MODERNATX, INC.-MOD-2022-679415:same reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 01.12.2022
- Impfdatum
- 29.05.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
4 adult patients received Monovalent vaccine 9 day after MFG expiration date; no adverse event; 4 adult patients received Monovalent vaccine 9 day after MFG expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date), PRODUCT STORAGE ERROR (4 adult patients received Monovalent vaccine 9 day after MFG expiration date) and NO ADVERSE EVENT (no adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 29-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (4 adult patients received Monovalent vaccine 9 day after MFG expiration date) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date), PRODUCT STORAGE ERROR (4 adult patients received Monovalent vaccine 9 day after MFG expiration date) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 9 day after MFG expiration date) and PRODUCT STORAGE ERROR (4 adult patients received Monovalent vaccine 9 day after MFG expiration date). No concomitant medications were reported. Pharmacist was calling to report that 8 adult patients received Moderna COVID-19 vaccine Beyond manufacture Expiration Date. MFG Expiration date was 20 May 2022 (MI agent checked, it has not been extended). It was unbroken cartons. Vial size was reported as 5.5 ml. The vial was initially stored in the refrigerator on 20-MAY-2022 and 28-MAY-2022 4 adult patients on 21-MAY-2022 and 4 more adult patients on 29-MAY-2022 The vial did not undergo any temperature excursions. This case contains information for the 8th of 8 adult patients described by the reporter. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 01.12.2022
- Impfdatum
- 21.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
4 adult patients received Monovalent vaccine 1 day after MFG expiration date; no adverse event; 4 adult patients received Monovalent vaccine 1 day after MFG expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 1 day after MFG expiration date), PRODUCT STORAGE ERROR (4 adult patients received Monovalent vaccine 1 day after MFG expiration date) and NO ADVERSE EVENT (no adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 21-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 21-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 1 day after MFG expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (4 adult patients received Monovalent vaccine 1 day after MFG expiration date) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 1 day after MFG expiration date), PRODUCT STORAGE ERROR (4 adult patients received Monovalent vaccine 1 day after MFG expiration date) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (4 adult patients received Monovalent vaccine 1 day after MFG expiration date) and PRODUCT STORAGE ERROR (4 adult patients received Monovalent vaccine 1 day after MFG expiration date). Pharmacist is calling to report that 8 adult patients received Moderna COVID-19 vaccine Beyond manufacture Expiration Date. No concomitant medications were reported. MFG Expiration date was 20May2022 (agent checked, it has not been extended). It was unbroken cartons. Vial size was reported as 5.5 ml. The vial was initially stored in the refrigerator on 20MAY2022 and 28MMAY2022 4 adult patients on 21MAY2022 and 4 more adult patients on 29MAY2022 The vial did not undergo any temperature excursions. No concomitant medications were reported. This case contains information for the 1st of 8 adult patients described by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 30.11.2022
- Impfdatum
- 29.05.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 30.11.2022
- Impfdatum
- 21.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 21.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 29.11.2022
- Impfdatum
- 09.03.2022
- Beginn
- 25.11.2022
- Tage bis Beginn
- 261,0
- 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 4/23/21 Lot# 048B21A; Moderna 5/21/21 Lot# 033C21A; Moderna 3/9/22 Lot# 033K21-2A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 10.11.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Pt admitted to the hospital 11/1 with Covid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 9,0
- Labordaten
- Covid test positive 11/9
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Acute on chronic systolic heart failure, A-fib, chronic kidney disease, Diabetes, End stage renal disease, implantable cardioverter defribrillator, ischemic cardiomyopathy, proteinuria, secondary hyperparathyroidism of renal origin, and warfarin anticoagulation
- Andere Medikamente
- Unknown
- Allergien
- Eggs, fish, seafood
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 15.04.2022
- Beginn
- 16.10.2022
- Tage bis Beginn
- 184,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case after 4 vaccines Moderna 1/28/21 Lot# 037K20A; Moderna 2/27/21 Lot# 027L20A; Moderna 10/25/21 Lot# 939903; Moderna 4/15/22 Lot# 033K21-2A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 20.10.2022
- Impfdatum
- 01.04.2021
- Beginn
- 18.10.2022
- Tage bis Beginn
- 565,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Fall
SARS-CoV-2 test positive
Subdural haematoma
Symptomtext
Pt has a history of COPD, schizophrenia, and polysubstance abuse, and currently lives in a facility. He suffered a ground level fall and was noted to have a subdural hematoma. He was awaiting transfer to hospital care at the facility when his COVID test came back positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 17.03.2022
- Beginn
- 15.10.2022
- Tage bis Beginn
- 212,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 26.09.2022
- Impfdatum
- 04.04.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 171,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 2 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 9/22/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- CLL in remission Chronic Thrombocytopenia Hx of Kidney stones Hx of BPH
- Andere Medikamente
- unknown
- Allergien
- penicillins
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 88,0
- Geschlecht
- U
- Eingang
- 10.09.2022
- Impfdatum
- 08.06.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Vaccine expired on 20May2022 ,stored in refrigerator on 7Jun2022 and administered on 8Jun2022; No adverse event; patient received Moderna Covid-19 vaccine that was expired and past the Manufacturers; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received Moderna Covid-19 vaccine that was expired and past the Manufacturers), PRODUCT STORAGE ERROR (Vaccine expired on 20May2022 ,stored in refrigerator on 7Jun2022 and administered on 8Jun2022) and NO ADVERSE EVENT (No adverse event) in an 88-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 08-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received Moderna Covid-19 vaccine that was expired and past the Manufacturers). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 20May2022 ,stored in refrigerator on 7Jun2022 and administered on 8Jun2022) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received Moderna Covid-19 vaccine that was expired and past the Manufacturers), PRODUCT STORAGE ERROR (Vaccine expired on 20May2022 ,stored in refrigerator on 7Jun2022 and administered on 8Jun2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (patient received Moderna Covid-19 vaccine that was expired and past the Manufacturers) and PRODUCT STORAGE ERROR (Vaccine expired on 20May2022 ,stored in refrigerator on 7Jun2022 and administered on 8Jun2022). No concomitant drug information was provided. Vial was initially stored in refrigerator on 7Jun2022. Vial had not undergone any temperature excursion issue. It was unknown if the patient had allergies to any food, medication, or other products. It was also unknown if the patient had received any other vaccine 1 month prior to Moderna vaccine and had any COVID-19 positive test or diagnosis previously. It was also unknown if the adverse event caused the patient to seek medical care (office visit, Urgent care, ER, hospitalized). No adverse event was reported. No treatment drug information was provided. Most recent FOLLOW-UP information incorporated above includes: On 01-Sep-2022: Follow-up received, updated suspect drug information and I narrative. On 02-Sep-2022: Follow-up received contains no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 86,0
- Geschlecht
- U
- Eingang
- 10.09.2022
- Impfdatum
- 08.06.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
The vial had expired on 20-May-2022 and was initially stored in the refrigerator on 07-Jun-2022 that was administered on 08-Jun-2022; No adverse event; The patient received Moderna COVID-19 vaccine 19 days after the expiration date and also past the manufacturers expiration date; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The patient received Moderna COVID-19 vaccine 19 days after the expiration date and also past the manufacturers expiration date), PRODUCT STORAGE ERROR (The vial had expired on 20-May-2022 and was initially stored in the refrigerator on 07-Jun-2022 that was administered on 08-Jun-2022) and NO ADVERSE EVENT (No adverse event) in an 86-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. It was unknown if the patient had ever been diagnosed or tested positive for COVID-19. Chronic and acute illness at the time of vaccination and one month prior was unknown. Allergies to medication, food and other products were not applicable. Other vaccines given within 1 month prior to Moderna COVID-19 vaccine was unknown. It was unknown if the patient had chronic or long-standing health conditions. On 08-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The patient received Moderna COVID-19 vaccine 19 days after the expiration date and also past the manufacturers expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial had expired on 20-May-2022 and was initially stored in the refrigerator on 07-Jun-2022 that was administered on 08-Jun-2022) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The patient received Moderna COVID-19 vaccine 19 days after the expiration date and also past the manufacturers expiration date), PRODUCT STORAGE ERROR (The vial had expired on 20-May-2022 and was initially stored in the refrigerator on 07-Jun-2022 that was administered on 08-Jun-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (The patient received Moderna COVID-19 vaccine 19 days after the expiration date and also past the manufacturers expiration date) and PRODUCT STORAGE ERROR (The vial had expired on 20-May-2022 and was initially stored in the refrigerator on 07-Jun-2022 that was administered on 08-Jun-2022). It was unknown if the patient had prescriptions, over the counter medications, dietary supplements or herbal remedies being taken at the time of vaccination or at the time of adverse event. No concomitant medication was reported. Moderna booster doses were given to 27 patients 19 days after expiration date of 20-May-2022. On 07-Jun-2022, the vial was initially stored in the refrigerator. The vial had not undergone any temperature excursions. It was unknown if an adverse event had caused the patient to seek medical care office visit, Urgent care, emergency room, hospitalized and unknown if the symptoms were improved or worsened. The patient had not experienced any adverse events. No treatment medication was reported. This case was linked to US-MODERNATX, INC.-MOD-2022-630785. Most recent FOLLOW-UP information incorporated above includes: On 01-Sep-2022: Follow up received contains significant information: Suspect vaccine details were added, correct expiration date, and narrative updated. On 02-Sep-2022: Follow up received contains non-significant information: Narrative was updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2022-630785:Same 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. Chronic and acute illness at the time of vaccination and one month prior was unknown. Allergies to medication, food and other products were not applicable. Other vaccines given within 1 month prior to Moderna COVID-19 vaccine was unknown. It was unknown if the patient had chronic or long-standing health conditions.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- U
- Eingang
- 10.09.2022
- Impfdatum
- 08.06.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Vaccine expired on 20-May-2022 and stored in refrigerator on 07-Jun-2022 and administered on 08-Jun-2022; No adverse event; Patient administerd booster dose of expired Moderna Covid-19 vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient administerd booster dose of expired Moderna Covid-19 vaccine), PRODUCT STORAGE ERROR (Vaccine expired on 20-May-2022 and stored in refrigerator on 07-Jun-2022 and administered on 08-Jun-2022) and NO ADVERSE EVENT (No adverse event) in a 79-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient administerd booster dose of expired Moderna Covid-19 vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 20-May-2022 and stored in refrigerator on 07-Jun-2022 and administered on 08-Jun-2022) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient administerd booster dose of expired Moderna Covid-19 vaccine), PRODUCT STORAGE ERROR (Vaccine expired on 20-May-2022 and stored in refrigerator on 07-Jun-2022 and administered on 08-Jun-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Patient administerd booster dose of expired Moderna Covid-19 vaccine) and PRODUCT STORAGE ERROR (Vaccine expired on 20-May-2022 and stored in refrigerator on 07-Jun-2022 and administered on 08-Jun-2022). No concomitant medications were reported. The patient received booster dose. It was reported that the medical assistant saw that the expiration date was 20-Jun-2022 when looked that up before however medical assistant had nothing in writing or printed to confirm the expiration date of 20-Jun-2022. Patient received Moderna Covid-19 vaccine that was expired and past the Manufacturers expiration date. It was reported that the vial was initially stored in the refrigerator on 07-Jun-2022. The vial did not undergo any temperature excursions. The patient did not experienced any adverse events. No treatment information was reported. Most recent FOLLOW-UP information incorporated above includes: On 01-Sep-2022: Live follow up received contains product dose details added. Expiry date updated. On 02-Sep-2022: Live follow up received contains non significant information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 03.09.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Expired vaccine was kept in refrigerator a week before administration; No adverse event; Vaccine expired on 20-May-2022 and was administered on 16-Jun-2022; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022 and was administered on 16-Jun-2022), PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator a week before administration) and NO ADVERSE EVENT (No adverse event) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 16-Jun-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 16-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022 and was administered on 16-Jun-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator a week before administration) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022 and was administered on 16-Jun-2022), PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator a week before administration) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022 and was administered on 16-Jun-2022) and PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator a week before administration). Concomitant drugs were not reported. The patient received second booster dose. The patient had not reported any adverse reactions. Number of doses/vials were 7 doses/1 vial. It was reported that the reporter did not know when the vial was initially stored but states that vaccines were usually put in refrigerator a week before administration. The vial did not undergo any temperature excursion. Treatment medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 03.09.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Expired vaccine was kept in refrigerator/HCP did not know but states that vaccines are usually put in refrigerator a week before administration; No adverse event; Expired vaccine administered to patients; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered to patients), PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator/HCP did not know but states that vaccines are usually put in refrigerator a week before administration) and NO ADVERSE EVENT (No adverse event) in a 47-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 16-Jun-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 16-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered to patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator/HCP did not know but states that vaccines are usually put in refrigerator a week before administration) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered to patients), PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator/HCP did not know but states that vaccines are usually put in refrigerator a week before administration) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered to patients) and PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator/HCP did not know but states that vaccines are usually put in refrigerator a week before administration). No concomitant drug was reported. It was reported that patient was administered to 7 patients past the expiration date, from Moderna lot number 033K21-2A with an expiration date of 20MAY2022. The patients not reported any adverse reactions. HCP did not know but stated that vaccines were usually put in refrigerator a week before administration. Vial did not undergoes temperature excursion. No Treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
The vial was initially stored in the refrigerator, vaccines are usually put in refrigerator a week before administration.; No adverse event; Expired vaccine administered to patients; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered to patients), PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator, vaccines are usually put in refrigerator a week before administration.) and NO ADVERSE EVENT (No adverse event) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 16-Jun-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 16-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered to patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator, vaccines are usually put in refrigerator a week before administration.) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered to patients), PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator, vaccines are usually put in refrigerator a week before administration.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered to patients) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator, vaccines are usually put in refrigerator a week before administration.). Total 7 doses were given 1 vial. The reporter did not knowhow vial was stored but stated that vaccines are usually put in refrigerator a week before administration. The vial did not undergo any temperature excursions. Patient was given 1st booster dose. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 02.09.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Expired vaccine was kept in refrigerator a week before administration; No adverse event; Vaccine expired on 20-May-2022 was administered on 16-Jun-2022; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022 was administered on 16-Jun-2022), PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator a week before administration) and NO ADVERSE EVENT (No adverse event) in a 61-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 16-Jun-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 16-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022 was administered on 16-Jun-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator a week before administration) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022 was administered on 16-Jun-2022), PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator a week before administration) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022 was administered on 16-Jun-2022) and PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator a week before administration). Concomitant drugs were not reported. The patient received first booster dose. The patients had not reported any adverse reactions. Number of doses/vials were 7 doses/1 vial. It was reported that the reporter did not know when the vial was initially stored but states that vaccines were usually put in refrigerator a week before administration. The vial did not undergo any temperature excursion. Treatment medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 02.09.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Expired vaccine was kept in refrigerator; No adverse event; Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022), PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator) and NO ADVERSE EVENT (No adverse event) in a 55-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 16-Jun-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 16-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022), PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022) and PRODUCT STORAGE ERROR (Expired vaccine was kept in refrigerator). No concomitant medications were reported. The patient had received second booster dose. Number of doses/vials were 7 doses/1 vial. The vial did not undergo any temperature excursions. The Healthcare Professional (HCP) did not know the date the vial was initially stored in the refrigerator but stated that vaccines were usually put in refrigerator a week before administration. Patient had not reported any adverse reactions. No treatment details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
expired vaccine kept in refrigerator; No adverse event; Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022), PRODUCT STORAGE ERROR (expired vaccine kept in refrigerator) and NO ADVERSE EVENT (No adverse event) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 16-Jun-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 16-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (expired vaccine kept in refrigerator) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022), PRODUCT STORAGE ERROR (expired vaccine kept in refrigerator) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022) and PRODUCT STORAGE ERROR (expired vaccine kept in refrigerator). No concomitant medications were reported. Number of doses/vials were 7 doses/1 vial. The Healthcare Professional (HCP) did not know the date the vial was initially stored in the refrigerator but stated that vaccines were usually put in refrigerator a week before administration. The reporter wanted to know about the stability of this lot number and recommendation for next steps for the patients impacted due to this. The patients had not reported any adverse reactions. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
The vial was initially stored in the refrigerator, vaccines are usually put in refrigerator a week before administration.; The patients did not report any adverse reactions; Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022), PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator, vaccines are usually put in refrigerator a week before administration.) and NO ADVERSE EVENT (The patients did not report any adverse reactions) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 16-Jun-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 16-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator, vaccines are usually put in refrigerator a week before administration.) and NO ADVERSE EVENT (The patients did not report any adverse reactions). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022), PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator, vaccines are usually put in refrigerator a week before administration.) and NO ADVERSE EVENT (The patients did not report any adverse reactions) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (The patients did not report any adverse reactions) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 20-May-2022/Patient received vaccine on 16-Jun-2022) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator, vaccines are usually put in refrigerator a week before administration.). No concomitant medications were reported. Dose administered after 30-day Use By Date or after manufacturer date of expiry. Number of doses/vials were 7 doses/1 vial. The Healthcare Professional was not knowing the date the vial was initially stored in the refrigerator but stated that vaccines were usually put in refrigerator a week before administration. The vial had not undergone any temperature excursions. The reporter wanted to know about the stability of this lot number and recommendation for next steps for the patients impacted due to this. The patients had not reported any adverse reactions. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 103,0
- Geschlecht
- M
- Eingang
- 30.08.2022
- Impfdatum
- 14.04.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 133,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalization with covid; fully vaccinated with booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 8/25/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Congestive Heart Failure, Hypertension and Other (BPH/Periphral neuropathy)
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 30.08.2022
- Impfdatum
- 29.04.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 118,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Hospitalization with COVID-19 despite full vaccination with 2 boosters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID-19 PCR 8/24/2022.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Coronary artery disease, CVA, hyperlipidemia, hypertension, peripheral vascular disease (with vascular stent) and valve replacement-bleed in right eye
- Andere Medikamente
- Unknown
- Allergien
- Dermagran, Sulfa, Tetracycline, Zinc acetate
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 103,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 14.04.2022
- Beginn
- 23.08.2022
- Tage bis Beginn
- 131,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Hospitalized with COVID-19; fully vaccinated with 2 boosters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID-19 PCR 8/23/2022.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Asthma, coronary artery disease, COPD, hypertension, reflux and other (histoplasmosis)
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 14.04.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 130,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Hospitalized with COVID-19; fully vaccinated with 3 boosters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID-19 PCR 8/22/2022.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Coronary artery disease and hypertension
- Andere Medikamente
- Unknown
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 13.08.2022
- Impfdatum
- 12.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysgeusia
Symptomtext
Narrative: Patient received 2nd booster dose of Moderna vaccine on 4/12/22. On 4/13/22, patient reported to nurse that he had a metallic taste in his mouth.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysgeusia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 13.08.2022
- Impfdatum
- 17.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Optic ischaemic neuropathy
Optical coherence tomography
Visual field tests
Visual impairment
Symptomtext
Non-arteritic anterior Ischemic optic neuropathy. Partial vision loss OD, no treatment available. Vision loss remains stable and is not debilitating. Disc at risk was present for several years w/o vision loss before incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Optic ischaemic neuropathy
- Hospital-Tage
- -
- Labordaten
- Visual fields, Ophthalmic exam, OCT.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Low back pain , nasal obstruction , aortic sclerosis, hyperlipidemia
- Andere Medikamente
- Bisoprolol-hydrochlorothiazide 1.25-3.12 MG tablets qd Famoditine 20 mg hs Aspirin 81 mg qd (Vazalore) Losartan 25 mg tablet qd Latanoprost 0.005% 1gtt ou qd Tylenol 1000 mg 3-4/day prn Lipitor 40 mg qd Apomorphine/Oxytocin 4mg/100iu prn
- Allergien
- Allergies: Bactrim->rash morphine->histamine release severe itching. Paper tape Zyrtec->trigeminy Skelaxin->bigeminy NSAIDS->dyspepsia
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
The facility did not have a prior history of COVID vaccinations on this patient and they were trying to complete a primary series what they thought was needed, a 2nd dose. Based on the state database, this was the patient's 4th dose, but a full dose of Moderna was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 05.04.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 114,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Covid vaccine breakthrough case: Dose 1 Pfizer 3/8/21 EN6202 Dose 2 Pfizer 3/29/21 ER2613
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid+ on 7/28/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.07.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Circumstance or information capable of leading to medication error
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (scanned the vaccine box to pull up the expiration date it states 20-May-2022 but portal has the expiration date listed as 31-Dec-2069) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (scanned the vaccine box to pull up the expiration date it states 20-May-2022 but portal has the expiration date listed as 31-Dec-2069). At the time of the report, CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (scanned the vaccine box to pull up the expiration date it states 20-May-2022 but portal has the expiration date listed as 31-Dec-2069) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was provided by the reporter. No treatment medications was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 28.07.2022
- Impfdatum
- 08.03.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 139,0
- 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 4/22/21 Lot# 030A21A; Moderna 05/20/21 Lot# 005C21A; Moderna 3/8/22 Lot# 033K21-2A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 24.07.2022
- Impfdatum
- 14.02.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 136,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Inappropriate schedule of product administration
SARS-CoV-2 test
Symptomtext
second dose was more than a months after his first dose, and it had expired on the 20May2022.; he received and expired vaccine for his second dose; This spontaneous case was reported by a patient and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (second dose was more than a months after his first dose, and it had expired on the 20May2022.) and EXPIRED PRODUCT ADMINISTERED (he received and expired vaccine for his second dose) in a 30-year-old male patient who received mRNA-1273 (Spikevax) (batch nos. 033K21-2A and 033K21-2A) for COVID-19 vaccination. Concurrent medical conditions included Hay fever. On 14-Feb-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 30-Jun-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 30-Jun-2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (second dose was more than a months after his first dose, and it had expired on the 20May2022.) and EXPIRED PRODUCT ADMINISTERED (he received and expired vaccine for his second dose). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (second dose was more than a months after his first dose, and it had expired on the 20May2022.) and EXPIRED PRODUCT ADMINISTERED (he received and expired vaccine for his second dose) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: (Positive) Positive. No concomitant medication was provided. No treatment medication were provided. No other vaccines were received by the patient within 1 month prior to Moderna COVID-19 vaccine. It was reported that patient had never experienced a similar event in the past. The AE did not cause patient to seek medical care (office visit, Urgent care, ER, hospitalized). The patient had COVID + test or diagnosis in Jan2022 or Dec2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Hay fever
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 106,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
hospitalization with covid; fully vaccinated with 3 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- COPD on 2 L home oxygen at night, bilateral carotid artery stenosis S/P B/L CEA, bilateral PAD S/P revascularization, and recent stent in common iliac artery, hypertension, and hyperlipidemia
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 99,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 96,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 2 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 3,0
- Labordaten
- positive covid PCR 7/16/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Asthma, Hyperlipidemia, Hypertension, Thyroid and Other (Arthritis)
- Andere Medikamente
- unknown
- Allergien
- unknown abx
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 23.04.2021
- Beginn
- 09.07.2022
- Tage bis Beginn
- 442,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Leukemia CLL
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 31.03.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 99,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID infection.,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 06.07.2022
- Impfdatum
- 01.04.2022
- Beginn
- 12.06.2022
- Tage bis Beginn
- 72,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Impaired work ability
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
The day I noted that I had sinus congestion and coughing. The next day I was still coughing and congested and I took a COVID-19 home test and it turned positive very quickly. Then I went to my doctor for a confirmatory test and it was positive. I was given a 5 day treatment of PAXLOVID. Within 24 hours my symptoms were slowly going away. By the time I finished my 5 day treatment I felt perfectly normal. I was able to continue working again when I was taking treatment but I was working remotely.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test, COVID-19 test.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; High Cholesterol; BPH
- Andere Medikamente
- Lisinopril; finasteride; rosuvastatin; aspirin; multivitamin; vitamin D; coQ10; calcium
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 15.04.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 74,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with 2 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- positive covid pcr 6/28/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Congestive Heart Failure, Hyperlipidemia, Hypertension, Peripheral Vascular Dz (carotid artery stenosis), Thyroid (hypo) and Other (dementia; chronic back pain; osteoarthritis; valvular heart disease; pAfib )
- Andere Medikamente
- unknown
- Allergien
- Sulfa, aripiprazole, clarithromycin, rivastigmine, rivastigmine tartrate, ciprofloxacin, ciprofloxacin, HCL
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 29.03.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 41,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Influenza like illness
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
03/2022 vaccination. 05/09/2022 sniffles, runny nose. I had thought that it was allergies. 05/10/2022 felt flu like symptoms. I tested COVID-19 at home; positive. With my cancer history they put me on PAXLOVID. Felt better within 4 days tested negative within 4 days. Testing negative presently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Lung Cancer right upper lobe removed January 2019; Carotid Cancer head and neck radiation November 2019
- Andere Medikamente
- NORVASC; lisinopril; hydrochlorothiazide; metformin; levothyroxine; multivitamin; aspirin
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 29.06.2022
- Impfdatum
- 14.03.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 101,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Electroencephalogram
Metabolic encephalopathy
Urinary tract infection
Symptomtext
pt presented with with covid, uti and metabolic encephalopathy. treated with antibiotics, eeg done. Discharged to HCF
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Alzheimer's, CKD, Hypothyroidism
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vaccine was given. Vaccine had been expired for four days. Moderna has been notified and we are waiting for a response from them as to what the next steps are. Update: Moderna informed today; "The vaccine administered on May 24, 2022 from lot number 033K21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vaccine was given. Vaccine had been expired for four days. Moderna has been notified and we are waiting for a response from them as to what the next steps are. Update: Moderna informed clinic today; "The vaccine administered on May 24, 2022 from lot number 033K21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 25.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Patient was inadvertently administed with the 11 days of expired vaccine that was initially stored in the refrigerator on 27 May 2022; Patient was inadvertently administed with the vaccine 11 days after expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was inadvertently administed with the vaccine 11 days after expiration date.) and PRODUCT STORAGE ERROR (Patient was inadvertently administed with the 11 days of expired vaccine that was initially stored in the refrigerator on 27 May 2022) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer (primary series.) on 22-Feb-2021 and Pfizer (primary series.). Past adverse reactions to the above products included No adverse reaction with Pfizer and Pfizer. On 31-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 31-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was inadvertently administed with the vaccine 11 days after expiration date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Patient was inadvertently administed with the 11 days of expired vaccine that was initially stored in the refrigerator on 27 May 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient was inadvertently administed with the vaccine 11 days after expiration date.) and PRODUCT STORAGE ERROR (Patient was inadvertently administed with the 11 days of expired vaccine that was initially stored in the refrigerator on 27 May 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. The patient had no known allergies.It was unknown whether the patient had been diagnosed with/ tested positive for COVID 19. Acute and Chronic illness at the time of vaccination and up to one month before was reported as none. Number of doses/vials administered were reported as one vial and the vial had not undergone any temperature excursions. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vaccine was given. Vaccine had been expired for four days. Moderna has been notified and we are waiting for a response from them as to what the next steps are. Update: Moderna informed Facility today; "The vaccine administered on May 24, 2022 from lot number 033K21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vaccine was given. Vaccine had been expired for four days. Moderna has been notified and we are waiting for a response from them as to what the next steps are.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vaccine was given. Vaccine had been expired for four days. Moderna has been notified and we are waiting for a response from them as to what the next steps are.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vaccine was given. Vaccine had been expired for four days. Moderna has been notified and we are waiting for a response from them as to what the next steps are.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 24.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vaccine was given. Vaccine had been expired for four days. Moderna has been notified and we are waiting for a response from them as to what the next steps are.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
vaccine was expired (4 days), manufacture was notified, Moderna is evaluation the effectiveness of the expired vaccine and we are waiting for a response.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine was expired (4 days), manufacture was notified, Moderna is evaluating the effectiveness of the expired vaccine and we are waiting for a response.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine was expired (4 days), manufacture was notified, Moderna is evaluating the effectiveness of the expired vaccine and we are waiting for a response. Note: her first two vaccines were
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine was expired (4 days), manufacture was notified, Moderna is evaluating the effectiveness of the expired vaccine and we are waiting for a response.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine was expired (4 days), manufacture was notified, Moderna is evaluating the effectiveness of the expired vaccine and we are waiting for a response.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine was expired (4 days), manufacture was notified, Moderna is evaluating the effectiveness of the expired vaccine and we are waiting for a response.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine was expired (4 days), manufacture was notified, Moderna is evaluating the effectiveness of the expired vaccine and we are waiting for a response.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 07.03.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 72,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoxia
Sepsis
Urinary tract infection
Symptomtext
Sepsis, hypoxi and UTI, treated with iv antibiotics and fluids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoxia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypothyroidism, unhealing ulcer, chf, MS, pulmonary hypertension
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was taken out from freezer and stored initially in refrigerator on 20-Apr-2022, expired on 20-May-2022 and administered on 24-May-2022; Patient was given expired (4 days expired) Moderna vaccine on 24-May-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was given expired (4 days expired) Moderna vaccine on 24-May-2022) and PRODUCT STORAGE ERROR (Vaccine was taken out from freezer and stored initially in refrigerator on 20-Apr-2022, expired on 20-May-2022 and administered on 24-May-2022) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K212A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer (Dose number-1, dose and unit-0.3 milliliter, Batch number (EN6207), Route of administration- Intramuscular, Anatomical location-Right deltoid) on 22-Mar-2021, Pfizer (Dose number-2, dose and unit-0.3 milliliter, Batch number (EW0151), Route of administration- Intramuscular, Anatomical location-Left deltoid) on 12-Apr-2021, Pfizer (Dose number-3, dose and unit-0.3 milliliter, Batch number (FF2593), Route of administration- Intramuscular and Anatomical location-Left deltoid) on 30-Nov-2021. Past adverse reactions to the above products included No adverse event with Pfizer, Pfizer and Pfizer. On 24-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 24-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was given expired (4 days expired) Moderna vaccine on 24-May-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was taken out from freezer and stored initially in refrigerator on 20-Apr-2022, expired on 20-May-2022 and administered on 24-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient was given expired (4 days expired) Moderna vaccine on 24-May-2022) and PRODUCT STORAGE ERROR (Vaccine was taken out from freezer and stored initially in refrigerator on 20-Apr-2022, expired on 20-May-2022 and administered on 24-May-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications information was reported. On 24-May-2022, the patient was given expired (4 days expired) Moderna vaccine lot 033K21-2A (manufacturer expiration date 20-May-2022) Intramuscular 0.25mL as a fourth dose. Vial was taken out of freezer and was initially stored in the refrigerator on 20-Apr-2022. Out of freezer expiration date was 20-May-2022. The vial did not undergo any temperature excursion. No treatment medications were provided. This case was linked to MOD-2022-575471 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 20.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Moderna vaccine manufacturer expiration date 20-May-2022 was taken out of the freezer on 20-Apr-2022 and administered on 24-May-2022; Patient was given expired (4 days expired) Moderna vaccine; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was given expired (4 days expired) Moderna vaccine) and PRODUCT STORAGE ERROR (Moderna vaccine manufacturer expiration date 20-May-2022 was taken out of the freezer on 20-Apr-2022 and administered on 24-May-2022) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: PFIZER (Dose: 1, Lot/Batch number: EL3302, Dose/volume: 0.3 ml, Route and Body site: Intramuscular, left deltoid.) on 25-Jan-2021, PFIZER (Dose: 2, Lot/Batch number: EL9264, Dose/volume: 0.3 ml, Route and Body site: Intramuscular, left deltoid.) on 18-Feb-2021, PFIZER (Dose: 3, Lot/Batch number: FF8841, Dose/volume: 0.3 ml and Route: Intramuscular.) on 14-Oct-2021. Past adverse reactions to the above products included No adverse event with PFIZER, PFIZER and PFIZER. On 24-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 24-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was given expired (4 days expired) Moderna vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Moderna vaccine manufacturer expiration date 20-May-2022 was taken out of the freezer on 20-Apr-2022 and administered on 24-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient was given expired (4 days expired) Moderna vaccine) and PRODUCT STORAGE ERROR (Moderna vaccine manufacturer expiration date 20-May-2022 was taken out of the freezer on 20-Apr-2022 and administered on 24-May-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. Moderna vaccine lot 033K21-2A manufacturer expiration date 20-May-2022 was taken out of freezer on 20-Apr-2022. Out of freezer expiration date was 20-May-2022. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 59,0
- Geschlecht
- U
- Eingang
- 18.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vaccine expired on 20-May-2022 and initially stored in refrigerator and administered on 27-May-2022; Expired vaccine doses administered 3 patients/ 3 booster doses administered after manufacturer date of expiry; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine doses administered 3 patients/ 3 booster doses administered after manufacturer date of expiry) and PRODUCT STORAGE ERROR (The vaccine expired on 20-May-2022 and initially stored in refrigerator and administered on 27-May-2022) in a 59-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 27-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 27-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine doses administered 3 patients/ 3 booster doses administered after manufacturer date of expiry). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vaccine expired on 20-May-2022 and initially stored in refrigerator and administered on 27-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine doses administered 3 patients/ 3 booster doses administered after manufacturer date of expiry) and PRODUCT STORAGE ERROR (The vaccine expired on 20-May-2022 and initially stored in refrigerator and administered on 27-May-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that, the reporter noticed the box did not have a expiration date so she scanned the code and noticed the expiration date was 20-May-2022. The vial was initially stored in the refrigerator on 27-May-2022. The vial did not undergo any temperature excursion. No treatment medications were provided. This case was linked to MOD-2022-587906, MOD-2022-587910 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 55,0
- Geschlecht
- U
- Eingang
- 18.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
On 27May2022, 1 vial was placed in the refrigerator from which 2 doses (0.25mL booster doses) were administered.; Expired vaccine doses administered 3 patients/3 booster doses administered after manufacturer date of expiry; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine doses administered 3 patients/3 booster doses administered after manufacturer date of expiry) and PRODUCT STORAGE ERROR (On 27May2022, 1 vial was placed in the refrigerator from which 2 doses (0.25mL booster doses) were administered.) in a 55-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 27-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 27-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine doses administered 3 patients/3 booster doses administered after manufacturer date of expiry). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (On 27May2022, 1 vial was placed in the refrigerator from which 2 doses (0.25mL booster doses) were administered.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine doses administered 3 patients/3 booster doses administered after manufacturer date of expiry) and PRODUCT STORAGE ERROR (On 27May2022, 1 vial was placed in the refrigerator from which 2 doses (0.25mL booster doses) were administered.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that the vial did not undergo any temperature excursions. No concomitant medications were reported. No treatment medications were reported. This case was linked to MOD-2022-589616 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 15-Jun-2022: Significant follow-up received: Patient details (age) added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Patient received a 1st dose of Moderna. Moderna is not approved for patients under 18.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 25,0
- Geschlecht
- U
- Eingang
- 17.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine doses administered 3 patients/3 booster doses administered after manufacturer date of expiry; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine doses administered 3 patients/3 booster doses administered after manufacturer date of expiry) in a 25-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K212A) for COVID-19 prophylaxis. No Medical History information was reported. On 24-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 24-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine doses administered 3 patients/3 booster doses administered after manufacturer date of expiry). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine doses administered 3 patients/3 booster doses administered after manufacturer date of expiry) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information were given. Reporter stated that on 24-May-2022, 1 vial was placed in the refrigerator from which 1 dose (0.25 mL booster dose) was given. No temperature excursions were reported. No treatment information were given. This case was linked to MOD-2022-589616 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 15-Jun-2022: Follow up contains significant information: Patient demographics (age) added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
administered with expired vaccine; This spontaneous case was reported by a patient and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. Concurrent medical conditions included Immunocompromised. On 26-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine) outcome was unknown. No concomitant drug was reported. It was reported that patient took second booster dose on 26-May-2022 (Expiry date: 20-May-2022) No Treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Immunocompromised
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
administered with expired vaccine; This spontaneous case was reported by a patient and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. Concurrent medical conditions included Immunocompromised. On 26-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered with expired vaccine) outcome was unknown. No concomitant drug was reported. It was reported that patient took second booster dose on 26-May-2022 (Expiry date: 20-May-2022) No Treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Immunocompromised
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine doses administered 3 patients/3 booster doses administered after manufacturer date of expiry; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine doses administered 3 patients/3 booster doses administered after manufacturer date of expiry) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 24-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 24-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine doses administered 3 patients/3 booster doses administered after manufacturer date of expiry). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine doses administered 3 patients/3 booster doses administered after manufacturer date of expiry) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Reporter stated that on 24May2022, 1 vial was placed in the refrigerator from which 1 dose (0.25mL booster dose) was given. No temperature excursions were reported. No concomitant medication information were given. No treatment information were given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The patient received dose from the expired vaccine (20-May-22), which was administered on 03-Jun-22, after 30-day Use By Date or after manufacturer date of expiry; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The patient received dose from the expired vaccine (20-May-22), which was administered on 03-Jun-22, after 30-day Use By Date or after manufacturer date of expiry) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033k21-2a) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer (First booster dose) on 26-Oct-2021. Past adverse reactions to the above products included No adverse event with Pfizer. Concurrent medical conditions included Drug allergy (Amiodarone), Drug allergy (Dabigatran) and Sulfonamide allergy (Sulfa drugs, Sulfonamides). On 03-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The patient received dose from the expired vaccine (20-May-22), which was administered on 03-Jun-22, after 30-day Use By Date or after manufacturer date of expiry). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The patient received dose from the expired vaccine (20-May-22), which was administered on 03-Jun-22, after 30-day Use By Date or after manufacturer date of expiry) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was unknown if the patient ever had COVID-19 positive test or diagnosis. Patients medical history was not relating to mentioned adverse event and both acute and chronic illness at the time of vaccination. The patient does not received any vaccine within 1 month prior to Moderna COVID-19 vaccine. Concomitant product use was not provided by the reporter. It was unknown if the patient had experienced similar adverse event in the past. The event does not caused the patient to seek medical care. Number of doses or vials and date the vial was initially stored in the refrigerator were unknown. The vial did not undergone any temperature excursions. Treatment information was not provided. This case was linked to MOD-2022-583804.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy (Dabigatran); Drug allergy (Amiodarone); Sulfonamide allergy (Sulfa drugs, Sulfonamides)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 10.06.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired dose administered; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 10-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication details was reported. Number of doses or vials includes 1 dose from 1 vial. The vial was initially taken out from the freezer, thawed, and used on 10Jun2022. Never put in the refrigerator for storage. The vial did not undergo any temperature excursions. This was the patient's 2nd booster dose administered in their left arm. Patient was not experiencing any symptoms. No treatment was given. No treatment medication details was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Discovered 6/13/22, that patient above had received a vaccination that expired 5/20/2022. The date of vaccination was 5/27/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Discovered 6/13/22, that patient above had received a vaccination that expired 5/20/2022. The date of vaccination was 5/27/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 20,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Discovered 6/13/22, that patient above had received a vaccination that expired 5/20/2022. The date of vaccination was 5/24/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
pt received an exp dose of moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
pt received an exp moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
pt received an exp dose of moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
pt received an exp dose of covid vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
pt received an exp dose of moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
pt received an exp dose of moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
pt received an exp dose of moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
pt received an exp dose of moderna covid vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (possible that doses were given after expiration date) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (possible that doses were given after expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (possible that doses were given after expiration date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided by the reporter. It was reported they have 20 vials of Moderna vaccine, Caller not know if they had a shelf life extension. They have quite a bit of it in the freezer. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
The patient's first dose of Moderna was administered on 2/3/2022. The second dose of Moderna was administered too early, on 2/15/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired dose administered to a patient; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered to a patient) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 27-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered to a patient). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered to a patient) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Patient received 1st booster dose. Reporter stated no adverse events were reported by the patient after getting the vaccine. Date the vial was initially stored in the refrigerator was reported as 27 Apr 2022. The vial not underwent any temperature excursions. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
PATIENT GIVEN EXPIRED VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
PATIENT GIVEN EXPIRED VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
PATIENT GIVEN EXPIRED VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
PATIENT GIVEN EXPIRED VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
PATIENT GIVEN EXPIRED VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
PATIENT GIVEN EXPIRED VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
PATIENT GIVEN EXPIRED VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
COVID -19; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (COVID -19) in a 52-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. Concurrent medical conditions included Hypertension. Concomitant products included ACETYLSALICYLIC ACID (BABY ASPIRIN), ATORVASTATIN CALCIUM (LIPITOR), ESCITALOPRAM OXALATE (LEXAPRO), MELATONIN and TELMISARTAN for an unknown indication. On 07-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced COVID-19 (COVID -19). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 12-May-2022 to 16-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (COVID -19) had not resolved. Patient didn't had any allergies. The patient taking any other medications/products within 2 weeks of starting COVID-19 treatment. The patient previously receive a COVID-19 Vaccine. On 22-May-2022 relapse of COVID symptoms occurred 5-6 days after taking Paxlovid. Relapse of COVID symptoms 5-6 days after taking Paxlovid. Device Date : 23May2022. Company Comment: This spontaneous case concerns a 52-year-old male patient with no relevant medical history reported, who experienced the unexpected non-serious AESI event of COVID-19 unspecified days after receiving fourth dose of mRNA-1273 vaccine. It was reported that patient was treated with Paxlovid from 12-May-2022 to 16-May-2022 and had a relapse of COVID symptoms 5-6 days after taking Paxlovid. The current pandemic situation of COVID-19 may remain as confounder to the event Covid-19. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.; Sender's Comments: This spontaneous case concerns a 52-year-old male patient with no relevant medical history reported, who experienced the unexpected non-serious AESI event of COVID-19 unspecified days after receiving fourth dose of mRNA-1273 vaccine. It was reported that patient was treated with Paxlovid from 12-May-2022 to 16-May-2022 and had a relapse of COVID symptoms 5-6 days after taking Paxlovid. The current pandemic situation of COVID-19 may remain as confounder to the event Covid-19. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hypertension
- Vorgeschichte
- -
- Andere Medikamente
- BABY ASPIRIN; LIPITOR; LEXAPRO; MELATONIN; TELMISARTAN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine administered on 20-may-2022 and freezed on 25-may-2022; patient received an expired Moderna booster dose; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received an expired Moderna booster dose) and PRODUCT STORAGE ERROR (Vaccine administered on 20-may-2022 and freezed on 25-may-2022) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 25-May-2022 at 10:17 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 25-May-2022 at 10:17 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received an expired Moderna booster dose). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine administered on 20-may-2022 and freezed on 25-may-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received an expired Moderna booster dose) and PRODUCT STORAGE ERROR (Vaccine administered on 20-may-2022 and freezed on 25-may-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant drugs were not reported. Treatment medications were not provided. It was reported that the vial was stored in refrigerator on 25-May-2022 and was pulled straight out of freezer and thawed out. The vial did not undergo any temperature excursion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 16.04.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
PATIENT RECEIVED A MODENA VACCINE AT AGE 12. SHOULD HAVE RECEIVED PFIZER. PER CDC, DOSE DOESN'T HAVE TO BE REPEATED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 25.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 47,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
Tested negative with home antigen test 3 days after completion of Paxlovid and tested positive again 8 days later; This spontaneous case was reported by a physician and describes the occurrence of COVID-19 (Tested negative with home antigen test 3 days after completion of Paxlovid and tested positive again 8 days later) in a 62-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033k21-2a) for COVID-19 vaccination. The patient's past medical history included Low back pain. Concurrent medical conditions included Reflux gastritis, Prostatic hypertrophy, Asthma and Drug allergy. On 01-Apr-2022 at 9:00 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-May-2022 at 5:00 PM, the patient experienced COVID-19 (Tested negative with home antigen test 3 days after completion of Paxlovid and tested positive again 8 days later). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 04-May-2022 to 09-May-2022 for COVID-19 prophylaxis, at an unspecified dose and frequency. At the time of the report, COVID-19 (Tested negative with home antigen test 3 days after completion of Paxlovid and tested positive again 8 days later) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 12-May-2022, SARS-CoV-2 test: negative (Negative) Negative. On 18-May-2022, SARS-CoV-2 test: positive (Positive) Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications details were not reported by the reporter. Patient tested negative with home antigen test 3 days after completion of Paxlovid five day course. Felt better afterwards and then tested positive again 8 days later, experienced symptoms of congestion, cough, headache and mild fever and so far, not as severe as symptoms before starting Paxlovid. Device Date was reported as 18-May-2022. Company Comment: This is a Spontaneous case concerning a 62-year-old male patient, with no relevant medical history, who experienced the unexpected, non-serious AESI of COVID-19, approximately 1 month and a half after the fourth dose of mRNA-1273 vaccine. No information about previous doses was disclosed. Patient reported he tested negative with home antigen test 3 days after completion of Nirmatrelvir, Ritonavir (Paxlovid) 5 day course. Felt better afterwards and then tested positive again 8 days later. He experienced symptoms of congestion, cough, headache and mild fever, not as severe as symptoms before starting Paxlovid. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This is a Spontaneous case concerning a 62-year-old male patient, with no relevant medical history, who experienced the unexpected, non-serious AESI of COVID-19, approximately 1 month and a half after the fourth dose of mRNA-1273 vaccine. No information about previous doses was disclosed. Patient reported he tested negative with home antigen test 3 days after completion of Nirmatrelvir, Ritonavir (Paxlovid) 5 day course. Felt better afterwards and then tested positive again 8 days later. He experienced symptoms of congestion, cough, headache and mild fever, not as severe as symptoms before starting Paxlovid. 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: 20220512; Test Name: COVID-19 antigen test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220518; Test Name: COVID-19 antigen test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Asthma; Drug allergy; Prostatic hypertrophy; Reflux gastritis
- Vorgeschichte
- Medical History/Concurrent Conditions: Low back pain
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Product administered to patient of inappropriate age
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 14.04.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 36,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Moderna 12/30/20 Lot#025J20A Moderna 1/27/21 Lot# 25J20A; Moderna 11/3/21 Lot# 076C21A Moderna 4/14/22 Lot# 033K21-2A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 5/20/22 COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
1st Modern Booster given too soon - given 2 months after second dose instead of 5 months
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Patient received 0.25ml of Moderna COVID-19 vaccine on 5/18/2022. Patient has no history of receiving a COVID-19 vaccine and eleigible to receive a first dose in a COVID-19 vaccine series. An additional 0.25ml of Moderna was administered immediately after. The patient received a total of 0.5ml of Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- back pain, COPD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asymptomatic COVID-19
SARS-CoV-2 test
Vaccine breakthrough infection
Symptomtext
Asymptomatic Breakthrough COVID infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive Nucleic Acid Amplification (NAA)/Polymerase Chain Reaction (RT-PCR) on 5/18/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Osteomyelitis, end stage renal disease, hypertension, obesity, systolic heart failure, irritable bowel disease
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 30.03.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 30,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested Covid positive 4/29/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home rapid antigen 4/29/22: Positive PCR 4/30/22 POSITIVE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Allergic asthma ( mild), apnea (mild), lower back issues (multi factorial)
- Andere Medikamente
- Montelukast, gabapentin, albuterol, fluticasone, calcium citrate, bariatric multivitamin
- Allergien
- -
- Vorherige Impfungen
- Shingrix, 2 shots a few months apart 2021Age 67
- Staat
- CO
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
No adverse events reported, patient was given a vaccine that was not recommended for her age group.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- Larin Fe 1/20 (28) 1 mg-20 mcg (21)/75 mg (7) tablet TAKE ONE TABLET BY MOUTH ONE TIME DAILY
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Symptomtext
Patient received the 1st dose J&J on 4/28/21, 1st dose booster Moderna 3/25/22, and 2nd booster Moderna 5/6/22. No adverse reactions reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- GERD, vitamin D deficiency
- Andere Medikamente
- N/A
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 08.05.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient received a third booster of Moderna by mistake 2 months after the second booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, Hyperlipidemia
- Andere Medikamente
- Norvasc, Gemfibrozil, Sertraline, Remeron, Prozac
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
The patient received 2 doses of 0.25 mL Moderna COVID 19 Vaccine - the equivalent of (0.5mL) this is the correct amount of vaccine for the 2nd dose of Moderna mRNA vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
The patient received 2 doses of 0.25 mL Moderna COVID 19 Vaccine - the equivalent of (0.5mL) this is the correct amount of vaccine for the 2nd dose of Moderna mRNA vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
On April 18, 2022, A Licensed Immunized 10 patients with an expired dose of Moderna, which I immediately realized when I filed the documents and stopped the vaccination process. The Covid-19 Vaccine delivery document stated that deadline date and time to use these vaccines was day 6 of month 4 and year 2022 at 7:10am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
On April 18, 2022, A Licensed Immunized 10 patients with an expired dose of Moderna, which I immediately realized when I filed the documents and stopped the vaccination process. The Covid-19 Vaccine delivery document stated that deadline date and time to use these vaccines was day 6 of month 4 and year 2022 at 7:10am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
On April 18, 2022, A Licensed Immunized 10 patients with an expired dose of Moderna, which I immediately realized when I filed the documents and stopped the vaccination process. The Covid-19 Vaccine delivery document stated that deadline date and time to use these vaccines was day 6 of month 4 and year 2022 at 7:10am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
On April 18, 2022, A Licensed Immunized 10 patients with an expired dose of Moderna, which I immediately realized when I filed the documents and stopped the vaccination process. The Covid-19 Vaccine delivery document stated that deadline date and time to use these vaccines was day 6 of month 4 and year 2022 at 7:10am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
On April 18, 2022, I Licensed Immunized 10 patients with an expired dose of Moderna, which I immediately realized when I filed the documents and stopped the vaccination process. The Covid-19 Vaccine delivery document stated that deadline date and time to use these vaccines was day 6 of month 4 and year 2022 at 7:10am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
On April 8, 2022, A Licensed Immunized 10 patients with an expired dose of Moderna, which I immediately realized when I filed the documents and stopped the vaccination process. The Covid-19 Vaccine delivery document stated that deadline date and time to use these vaccines was day 6 of month 4 and year 2022 at 7:10am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
On April 8, 2022, I Licensed Immunized 10 patients with an expired dose of Moderna, which I immediately realized when I filed the documents and stopped the vaccination process. The Covid-19 Vaccine delivery document stated that deadline date and time to use these vaccines was day 6 of month 4 and year 2022 at 7:10am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
On April 8, 2022, I Licensed Immunized 10 patients with an expired dose of Moderna, which I immediately realized when I filed the documents and stopped the vaccination process. The Covid-19 Vaccine delivery document stated that deadline date and time to use these vaccines was day 6 of month 4 and year 2022 at 7:10am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
On April 8, 2022, I Licensed Immunized 10 patients with an expired dose of Moderna, which I immediately realized when I filed the documents and stopped the vaccination process. The Covid-19 Vaccine delivery document stated that deadline date and time to use these vaccines was day 6 of month 4 and year 2022 at 7:10am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
On April 8, 2022, A Licensed Immunized 10 patients with an expired dose of Moderna, which I immediately realized when I filed the documents and stopped the vaccination process. The Covid-19 Vaccine delivery document stated that deadline date and time to use these vaccines was day 6 of month 4 and year 2022 at 7:10am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 73,0
- Geschlecht
- U
- Eingang
- 05.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
2 of my patients received expired Moderna Covid-19 vaccine. Both were booster doses (0.25mL).; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (2 of my patients received expired Moderna Covid-19 vaccine. Both were booster doses (0.25mL).) in a 73-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (2 of my patients received expired Moderna Covid-19 vaccine. Both were booster doses (0.25mL).). At the time of the report, EXPIRED PRODUCT ADMINISTERED (2 of my patients received expired Moderna Covid-19 vaccine. Both were booster doses (0.25mL).) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient received 2nd booster dose. No concomitant medications was provided by the reporter. It was unknown if patient had any Allergies to medications, food and other products or patient was diagnosed or tested positive for COVID-19. It was unknown if the patient had chronic or long-standing health condition and if patient received other vaccines within one month prior to any dose of Moderna COVID-19 Vaccine. The Vial was initially stored in refrigerator 30-MAr-2022 and Dose administered after 30-day Use By Date or after manufacturer date of expiry Vial did not undergo any temperature excursions. Expired Vaccine was administered on 23-Apr-2022. No treatment medications was provided by the reporter. This case was linked to MOD-2022-555023 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 74,0
- Geschlecht
- U
- Eingang
- 05.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received expired Moderna Covid-19 vaccine(0.25 mL); This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received expired Moderna Covid-19 vaccine(0.25 mL)) in a 74-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. It was unknown regarding allergies (medications, food, and other products). Reported unknown if patient ever had COVID positive test or diagnosis and stated unknown history related to mentioned adverse event and both acute and chronic illnesses at the time of vaccination. Unknown if patient received other vaccines given within 1 month prior to Moderna COVID-19. . On 29-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received expired Moderna Covid-19 vaccine(0.25 mL)). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received expired Moderna Covid-19 vaccine(0.25 mL)) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was provided by the reporter. The vial was initially stored in the refrigerator on 30Mar2022. Patient received 2nd booster dose on 29Apr2022. It was reported unknown that the adverse event cause patient to seek medical care (office visit, Urgent care, ER, hospitalized): Unknown the patient has experienced a similar event in the past. The vial did not undergo any temperature excursion. No treatment medications was provided by the reporter. This case was linked to MOD-2022-555070 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown regarding allergies (medications, food, and other products). Reported unknown if patient ever had COVID positive test or diagnosis and stated unknown history related to mentioned adverse event and both acute and chronic illnesses at the time of vaccination. Unknown if patient received other vaccines given within 1 month prior to Moderna COVID-19.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Accidentally gave a 5th dose of moderna vaccine to patient and another dose of flu vaccine. I forgot to run a Immunization report before evaluating patient's immunization history. Afterwards, when I was entering the info in the Immunization database, I saw patient already got flu vaccine (8/14/21 and Moderna (2 doses at Health Clinic (3/1/21, 3/29/21) AND pharmacy (11/03/21, 1/24/02)). I notified the pharmacists at pharmacy and store, and spoke to the health office. Patient denied every getting any aforementioned shots above. She told myself and tech that this was her first shot at the drop-off station. After a 15 minute observation period, patient didn't report any adverse outcomes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Moderna that has BUD of 3/30/22 administered; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna that has BUD of 3/30/22 administered) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 28-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 28-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna that has BUD of 3/30/22 administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna that has BUD of 3/30/22 administered) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications reported. No treatment reported It was reported that the vial administered has an expiration of 5/20/22, and a BUD of 3/30/22 to one person this was done today which is 4/28/2022. The reported wanted to know if it was recommended for the individual to be revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient given a vaccine that had expired 04/23/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- None
- Allergien
- Sulfa, Penicillin, Metoprolol
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient given vaccine that expired 04/23/22 @15:30 pm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoarthritis, Hyperlipidemia, Allergic Rhinitis, Chronic Pain syndrome,
- Andere Medikamente
- None
- Allergien
- Cortisone, Doxycycline, Gabapentin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Screened pt for COVID booster. Pt had lost card; looked up pts information in agency entry system which showed that pt had initial doses of Moderna series, but no booster shot. Re-wrote new COVID card and administered booster. Later in day upon doing data entry, it is recognized that pt is already in our documenting system but under another date of birth, at the same location, indicating that we may have previously given pt his 1st booster dose 1/10/22 and pt would not be due for 2nd booster until around 5/10/22. If this data is correct, pt was given 2nd booster shot less than 2 weeks early.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Not known
- Vorgeschichte
- Not known
- Andere Medikamente
- Not known
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 24.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- N/A
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Exposure to SARS-CoV-2
SARS-CoV-2 test positive
Symptomtext
patient tested positive for covid after exposure to daughter who had tested positive 4 days earlier
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- SARS-CoV-2 (COVID-19) Detected Abnormal Final Methodology Final Nucleic Acid Amplification (NAA)/Polymerase Chain Reaction (RT-PCR). Detected on 4/24/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- diabetes hypertension arythmia, heart disease, CHF gastric cancer
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 25.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient given Moderna in 21 days instead of 28 days or more. He has not had any symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.04.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Thaw on 18-Mar-2022 and took vaccine on 21-Apr-2022; Received a booster dose from an expired Moderna vial; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received a booster dose from an expired Moderna vial) and PRODUCT STORAGE ERROR (Thaw on 18-Mar-2022 and took vaccine on 21-Apr-2022) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 21-Apr-2022 at 10:20 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Apr-2022 at 10:20 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received a booster dose from an expired Moderna vial). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Thaw on 18-Mar-2022 and took vaccine on 21-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received a booster dose from an expired Moderna vial) and PRODUCT STORAGE ERROR (Thaw on 18-Mar-2022 and took vaccine on 21-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. concomitant product was not reported. patient received a booster dose from an expired Moderna vial. Thaw date reported on 18-Mar-2022. Treatment product was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 23.04.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Administered \some vaccine that were expired a week ago. It was kept in the fridge.; Patients were administered an "expired" vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients were administered an "expired" vaccine) and PRODUCT STORAGE ERROR (Administered \some vaccine that were expired a week ago. It was kept in the fridge.) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients were administered an "expired" vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Administered \some vaccine that were expired a week ago. It was kept in the fridge.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients were administered an "expired" vaccine) and PRODUCT STORAGE ERROR (Administered \some vaccine that were expired a week ago. It was kept in the fridge.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant information was provided. It was reported that the vaccines expired a week ago. The vial did not undergo any temperature excursions. Vials were stored in the refrigerator on 28-Feb-2022. Patient was administered with second booster dose. No treatment information was provided. This case was linked to MOD-2022-543481 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Pt given booster dose on 4/21/22 from a vial that expired on 4/18/22. Moderna was contacted and their report shows that the dose maintained the necessary protection so no repeat dose was recommended to the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 22.04.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Administered some vaccine that were expired a week ago. It was kept in the fridge; Patients were administered an expired vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients were administered an expired vaccine) and PRODUCT STORAGE ERROR (Administered some vaccine that were expired a week ago. It was kept in the fridge) in a 76-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients were administered an expired vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Administered some vaccine that were expired a week ago. It was kept in the fridge). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients were administered an expired vaccine) and PRODUCT STORAGE ERROR (Administered some vaccine that were expired a week ago. It was kept in the fridge) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Date the vial was initially stored in the refrigerator on 28-Feb-2022. No concomitant medication was reported. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 22.04.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
administered some vaccine that were expired a week ago. It was kept in the fridge.; patients were administered an "expired" vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patients were administered an "expired" vaccine) and PRODUCT STORAGE ERROR (administered some vaccine that were expired a week ago. It was kept in the fridge.) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patients were administered an "expired" vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (administered some vaccine that were expired a week ago. It was kept in the fridge.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patients were administered an "expired" vaccine) and PRODUCT STORAGE ERROR (administered some vaccine that were expired a week ago. It was kept in the fridge.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications information was reported. It was reported that the vaccines expired a week ago. The vial did not undergo any temperature excursions. Vials were stored in the refrigerator on 28-Feb-2022 This case was linked to MOD-2022-543471 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
patients were administered an "expired" vaccine; Vials were stored in the refrigerator on 28Feb2022 and were all administered on 18April2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patients were administered an "expired" vaccine) and PRODUCT STORAGE ERROR (Vials were stored in the refrigerator on 28Feb2022 and were all administered on 18April2022) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patients were administered an "expired" vaccine) and PRODUCT STORAGE ERROR (Vials were stored in the refrigerator on 28Feb2022 and were all administered on 18April2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patients were administered an "expired" vaccine) and PRODUCT STORAGE ERROR (Vials were stored in the refrigerator on 28Feb2022 and were all administered on 18April2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications information was reported. It was reported that the vaccines expired a week ago. The vial did not undergo any temperature excursions. Vials were stored in the refrigerator on 28-Feb-2022. Treatment medications were not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- M
- Eingang
- 22.04.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
administered some vaccine that were expired a week ago. It was kept in the fridge.; patients were administered an "expired" vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patients were administered an "expired" vaccine) and PRODUCT STORAGE ERROR (administered some vaccine that were expired a week ago. It was kept in the fridge.) in a 69-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A.) for COVID-19 vaccination. No Medical History information was reported. On 18-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patients were administered an "expired" vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (administered some vaccine that were expired a week ago. It was kept in the fridge.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patients were administered an "expired" vaccine) and PRODUCT STORAGE ERROR (administered some vaccine that were expired a week ago. It was kept in the fridge.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant drug was reported. It was reported that seven patients were administered an expired vaccine. Vials were stored in the refrigerator on 28-Feb-2022 and were all administered on 18-Apr-2022. The vial did not undergo any temperature excursions. No treatment medications were reported. This case was linked to MOD-2022-543471-KC, MOD-2022-543474-CH, MOD-2022-543476-LH, MOD-2022-543479-DF, MOD-2022-543481-RK, (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial was stored in refrigerator on 28-Feb-2022 and administered on 18-Apr-2022; Patients were administered an expired vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients were administered an expired vaccine) and PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 28-Feb-2022 and administered on 18-Apr-2022) in a 93-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients were administered an expired vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 28-Feb-2022 and administered on 18-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients were administered an expired vaccine) and PRODUCT STORAGE ERROR (Vial was stored in refrigerator on 28-Feb-2022 and administered on 18-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The vials did not go with any temperature excursions. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 22.04.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Administered some vaccine that were expired a week ago. It was kept in the fridge.; Patients were administered an "expired" vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients were administered an "expired" vaccine) and PRODUCT STORAGE ERROR (Administered some vaccine that were expired a week ago. It was kept in the fridge.) in a 90-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients were administered an "expired" vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Administered some vaccine that were expired a week ago. It was kept in the fridge.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients were administered an "expired" vaccine) and PRODUCT STORAGE ERROR (Administered some vaccine that were expired a week ago. It was kept in the fridge.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant were reported. The vaccines expired a week before administering it. The vial did not undergo any temperature excursions. The vials were stored in the refrigerator on 28-Feb-2022. The was administered with second booster dose. No treatment were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Inappropriate schedule of product administration
No adverse event
Symptomtext
Administered vaccine 2 weeks and 1 day to soon. No adverse outcome.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Inappropriate schedule of product administration
No adverse event
Symptomtext
Vaccination administered 2 weeks and 1 day to soon. No adverse outcome for client.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Vaccination administered 2 weeks and 1 day to soon. No adverse outcome for client.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- No
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received vaccine with expired BUD) and PRODUCT STORAGE ERROR (Administered after the 30 day use by date) in a 62-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. Patient had no known drug allergy and also the patient did not have any acute illness at the time of vaccination and up to one month before. Patient had never been diagnosed with/tested positive for COVID-19. Concurrent medical conditions included Paroxysmal atrial fibrillation (No recent change), Depression (No recent change) and Monoclonal B-cell lymphocytosis (No recent change). Concomitant products included FLECAINIDE ACETATE, PAROXETINE, LISINOPRIL, METOPROLOL SUCCINATE and ASPIRIN [ACETYLSALICYLIC ACID] for an unknown indication. On 08-Apr-2022 at 8:30 AM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 08-Apr-2022 at 8:30 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine with expired BUD). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Administered after the 30 day use by date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received vaccine with expired BUD) and PRODUCT STORAGE ERROR (Administered after the 30 day use by date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered EXPIRED PRODUCT ADMINISTERED (Received vaccine with expired BUD) to be not related. No further causality assessment was provided for PRODUCT STORAGE ERROR (Administered after the 30 day use by date). The by use date of vaccine was labelled as 18-Mar-2022. On 18-Feb-2022, the vial was initially stored in refrigerator. The vaccine was stored in refrigerator between 2-8 degree Celsius and there was no temperature excursion. No symptoms or side effects were reported by the patient. The event did not cause patient to seek medical care. The reporter did not report any other potential causes. It was unknown if patient experience similar events in the past. No additional doses treatments or medications have been administered in response. This case was linked to MOD-2022-536509 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Depression (No recent change); Monoclonal B-cell lymphocytosis (No recent change); Paroxysmal atrial fibrillation (No recent change)
- Vorgeschichte
- Comments: Patient had no known drug allergy and also the patient did not have any acute illness at the time of vaccination and up to one month before. Patient had never been diagnosed with/tested positive for COVID-19.
- Andere Medikamente
- FLECAINIDE ACETATE; PAROXETINE; LISINOPRIL; METOPROLOL SUCCINATE; ASPIRIN [ACETYLSALICYLIC ACID]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Product storage error; Received vaccine with expired BUD; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received vaccine with expired BUD) and PRODUCT STORAGE ERROR (Product storage error) in a 45-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. Co-suspect product included non-company product TETANUS VACCINE for an unknown indication. It was reported that patient had not been diagnosed with/tested positive for COVID-19. It was reported that patient had no acute illnesses at the time of vaccination and upto one month before. Concurrent medical conditions included Drug allergy (Cefdinir), Drug allergy (Codeine), Drug allergy (Doxycycline Hyclate), Drug allergy (Erythromycin), Drug allergy (Lamictal), Drug allergy (Lisinopril), Drug allergy (Lithium Carbonate), Drug allergy (Peniillin drugs), Drug allergy (Tramadol), Drug allergy (Wellbutrin), Drug allergy (Amitriptyline), Type 2 diabetes mellitus (No recent change), Bipolar disorder (No recent change), Major depression (No recent change), Hyperlipidemia (No recent change) and Asthma (No recent change.). Concomitant products included ATORVASTATIN, CELECOXIB (CELEBREX), GABAPENTIN and CLONAZEPAM (KLONOPIN) for an unknown indication. On 05-Apr-2022, the patient received dose of TETANUS VACCINE (Intramuscular) 1 dosage form. On 05-Apr-2022 at 10:45 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 05-Apr-2022 at 10:45 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Received vaccine with expired BUD). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Product storage error). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received vaccine with expired BUD) and PRODUCT STORAGE ERROR (Product storage error) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered EXPIRED PRODUCT ADMINISTERED (Received vaccine with expired BUD) to be not related. No further causality assessment was provided for PRODUCT STORAGE ERROR (Product storage error). Concomitant medication included Ability 30 mg/daily by oral route of administration. It was reported that vial was initially stored in refrigerator between 2-8 degree Celsius on 18-Feb-2022. It was reported that vial did not undergo any temperature excursions. It was reported that patients did not have any symptoms or side effects. It was reported that this was patient's first moderna booster dose. No treatment medications were reported. This case was linked to MOD-2022-536509.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma (No recent change.); Bipolar disorder (No recent change); Drug allergy (Wellbutrin); Drug allergy (Tramadol); Drug allergy (Peniillin drugs); Drug allergy (Lithium Carbonate); Drug allergy (Lisinopril); Drug allergy (Lamictal); Drug allergy (Erythromycin); Drug allergy (Doxycycline Hyclate); Drug allergy (Codeine); Drug allergy (Cefdinir); Drug allergy (Amitriptyline); Hyperlipidemia (No recent change); Major depression (No recent change); Type 2 diabetes mellitus (No recent change)
- Vorgeschichte
- Comments: It was reported that patient had not been diagnosed with/tested positive for COVID-19. It was reported that patient had no acute illnesses at the time of vaccination and upto one month before.
- Andere Medikamente
- ATORVASTATIN; CELEBREX; GABAPENTIN; KLONOPIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 24.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oral herpes
Symptomtext
I got some cold sores following my vaccine. This lasted for about three and a half weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oral herpes
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Wellbutrin; Lipitor; Pantoprazole; Famotidine; Alprazolam; Arimidex
- Allergien
- Fentanyl; NSAIDs
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 19.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood thyroid stimulating hormone
Full blood count
Laboratory test normal
Tinnitus
Symptomtext
Tinnitus developed that night after the vaccine. Right ear greater than the left. Have had mild tinnitus for 10 plus years easily managed with white noise. This new onset is several times louder. No treatment yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood thyroid stimulating hormone
- Hospital-Tage
- -
- Labordaten
- Normal chemistries, TSH, CBC
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, coronary artery disease, hypothyroidism
- Andere Medikamente
- Atenolol, Protonix, Synthroid, Crestor, aspirin 81 mg, famotidine, Vascepa
- Allergien
- Sulfa, cephalosporins
- Vorherige Impfungen
- Pfizer Covid vaccine on 1-21-2021. Mild flushing. No subsequent trouble with Pfizer on 2-23-21 and 10-19-21.
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 19.04.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
A patient was administered a dose from a vial that had been open for 22 h; A patient was administered a dose from a vial that had been open for 22 h; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (A patient was administered a dose from a vial that had been open for 22 h) and PRODUCT STORAGE ERROR (A patient was administered a dose from a vial that had been open for 22 h) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 14-Apr-2022 at 3:30 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 14-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (A patient was administered a dose from a vial that had been open for 22 h). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (A patient was administered a dose from a vial that had been open for 22 h). At the time of the report, EXPIRED PRODUCT ADMINISTERED (A patient was administered a dose from a vial that had been open for 22 h) and PRODUCT STORAGE ERROR (A patient was administered a dose from a vial that had been open for 22 h) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant drugs were not reported. Treatment medications were not provided. It was reported that patient received booster dose. It was reported that the vial went from the freezer to thawing process at room temperature on13-Apr-2022 at 05:00 pm, (thawing process 2 h) and was first punctured at 13-Apr-2022 at 07:00 pm. No temperature excursion occurred and vials were stored in room temperature for 22 hours. The expiry date of the vial was reported as 20-May-2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Administered vaccine from a vial that was punctured more than 12 hours; Administered an expired dose of the Moderna COVID-19 vaccine from a vial that was punctured more than 12 hours; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered an expired dose of the Moderna COVID-19 vaccine from a vial that was punctured more than 12 hours) and PRODUCT STORAGE ERROR (Administered vaccine from a vial that was punctured more than 12 hours) in a 91-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 12-Apr-2022 at 12:30 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 12-Apr-2022, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered an expired dose of the Moderna COVID-19 vaccine from a vial that was punctured more than 12 hours). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Administered vaccine from a vial that was punctured more than 12 hours). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered an expired dose of the Moderna COVID-19 vaccine from a vial that was punctured more than 12 hours) and PRODUCT STORAGE ERROR (Administered vaccine from a vial that was punctured more than 12 hours) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vial was initially stored in the refrigerator on 24-Mar-2022. The vaccine was punctured on 11-Apr-2022 at 12:54 pm. Post puncture the vail was stored in refrigerator. The vial did not undergo any temperature excursions. No Treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 18.04.2022
- Impfdatum
- 17.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient presented for second dose of Moderna on 3/17/2022. He received a 0.5ml dose of Moderna in right deltoid. Afterward it was discovered he had received his first dose of Moderna on 3/4/2022, making the interval between doses too close. Patient received a repeat second dose of Moderna on 4/14/2022 per CDC guidelines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received a dose of the Moderna COVID-19 vaccine from a vial that was punctured more than 12 hours previously; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received a dose of the Moderna COVID-19 vaccine from a vial that was punctured more than 12 hours previously) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Janssen COVID-19 vaccine in March 2021 and Pfizer COVID-19 vaccine in October 2021. Past adverse reactions to the above products included No adverse event with Janssen COVID-19 vaccine and Pfizer COVID-19 vaccine. On 07-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received a dose of the Moderna COVID-19 vaccine from a vial that was punctured more than 12 hours previously). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received a dose of the Moderna COVID-19 vaccine from a vial that was punctured more than 12 hours previously) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Medical history was not provided by the reporter. Patient was not on any concomitant medications. Reporter stated that, a patient received the first booster dose of the Moderna COVID-19 vaccine from a vial that was punctured more than 12 hours previously on 06-Apr-2022. The patient had not reported any adverse reactions at this time. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 15.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Psychotic disorder
Symptomtext
Psychosis: began on post-vaccination day 3.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Psychotic disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Dyshidrotic Eczema flare
- Vorgeschichte
- Anxiety, depression, sleep apnea
- Andere Medikamente
- Zoloft, atorvastatin, Wellbutrin
- Allergien
- Prozac
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 14.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
No reaction to vaccine, incorrect vaccination given for 3rd booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Pt was given an expired dose of vaccine. Vial was placed in frig on 3/24/22 and punctured on 4/11/22 at 1254 pm and expired on 12/12/22 at 0054. Dose was drawn up on 12/12/22 at 1230pm. Provider was notified and Moderna company was contacted for support and I am awaiting their call back on plan of care. No adverse reaction occurred.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 24.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 23.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Incorrect dose administered
Symptomtext
Patient received full dose of Moderna vaccine instead of the intended booster (half dose). Patient experienced similar side effects with first vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Breast cancer, allergic rhinitis, osteoporosis, hypothyroidism
- Andere Medikamente
- Albuterol, cholecalciferol, levothyroxine, triamterene/hydrochlorothiazide
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was administered a full dose of the Moderna vaccine in error instead of the intended booster (half dose). Patient is not experiencing any side effects as a result of this over administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Multiple myeloma, cardiac amyloidosis, pulmonary hypertension, chronic kidney disease, gastroespohageal reflux disease
- Andere Medikamente
- Acyclovir, allopurinol, apixaban, bumetanide, cholecalciferol, fluroruracil, niacinamide, omeprazole, potassium chloride, senna/docusate, sildenafil
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 09.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
patient that came in 14 years old with Pfizer 1st and second dose and was given the Moderna booster; This spontaneous case was reported by a physician and describes the occurrence of PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (patient that came in 14 years old with Pfizer 1st and second dose and was given the Moderna booster) in a 14-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer (Pfizer 1st dose lot#EW0183) on 08-Jun-2021 and Pfizer (Pfizer 2nd dose lot#EW0180) on 29-Jun-2021. Past adverse reactions to the above products included No adverse event with Pfizer and Pfizer. On 01-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Apr-2022, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (patient that came in 14 years old with Pfizer 1st and second dose and was given the Moderna booster). At the time of the report, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (patient that came in 14 years old with Pfizer 1st and second dose and was given the Moderna booster) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Reported stated that the patient had not reported any side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received a dose from a vial past the 30 day use by date) and PRODUCT STORAGE ERROR (Date of refrigeration 24Feb2022 and Date of administration 04April2022) in a 53-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 04-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received a dose from a vial past the 30 day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date of refrigeration 24Feb2022 and Date of administration 04April2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received a dose from a vial past the 30 day use by date) and PRODUCT STORAGE ERROR (Date of refrigeration 24Feb2022 and Date of administration 04April2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication details were reported. Reporter stated that the date of refrigeration was 24-Feb-2022 and the vial did not undergo any temperature excursions. And the dose was Patient's booster dose. No treatment medication details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
The patient did not have an adverse reaction, the patient was asymptomatic. The appropriate dose was given 7 days early. The patient was notified of the early dose and advised to return for the appropriate time for the vaccine to be effective. the patient was rescheduled for the correct time for his second dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- no
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Underdose
Symptomtext
1150H - vaccinator was handed a moderna .25ml vaccine instead of a pfizer .30ml 1205H - vaccinator reported incident to the nurse in charge 1211H - nurse in charge contacted supervisor after advising patient, NIC was advised to educate patient on the need to receive the same dosage of moderna today to be considered fully vaccinated 1215H - patient agreed then refused by the time of the second administration 1225H - called supervisor and was advised to educate patient that he needs to get the pfizer dose .30ml in 5 mos to be considered fully vaccinated 1230H - patient was educated. Patient did not have any adverse reaction to the shot during the observation period of 30 minutes and agreed that he understood the education 1235H - patient left the clinic
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
Covid vaccine error - wrong vaccine given to complete primary series, minimal waiting period not followed; no adverse event reported per the pt, office staff will check on patient daily x1 wk
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- No illness at the time of vaccine, Left acute otitis media - 3 wks ago
- Vorgeschichte
- HTN, GERD, Tachycardia, Migraine headaches, Depression
- Andere Medikamente
- Lisinopril, Amlodipine, Protonix, Metoprolol, Celexa, Gabapentin
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Differential white blood cell count
Expired product administered
Full blood count
Lipids
Metabolic function test
No adverse event
Urine analysis
Symptomtext
Expired Moderna dose administered to patient on 04/04/22 vaccine Exp Date: 04/03/22 with no adverse effects noted after 15 minutes observation Charge Nurse notified Vaccine Manager LPN made aware Patient made aware f/u appt with provider today for evaluation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Differential white blood cell count
- Hospital-Tage
- -
- Labordaten
- Test done today, that were ordered on the visit of March-15-2022: Urinalysis; CBC with differential; Lipid Panel; Comprehensive Metabolic Panel.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Penicillin.
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient given booster dose of 0.25mL, when she was due for Moderna #2. A second dose of 0.25mL was given to equal 0.5mL for dose #2
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- NA
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
14 year old child was given moderna vaccine instead of pfizer. No known problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none known
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- menorrhagia, eczema and allergic rhinitis
- Andere Medikamente
- cetirizine 1mg/ml take 5ml by mouth daily
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 04.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
This 19-year-old male received his first dose of the Covid-19 vaccine mRNA Moderna on March 11, 2022. On April 1st, 2022, the patient was administered his second dose of the Covid-19 vaccine moderna which is 21 days earlier than his scheduled dose. Patient experienced no adverse effects from this vaccine. On April 4th, 2022, I spoke with prescriber who states that patient is doing okay and experienced no adverse effects from the early vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
The patient received their 1st booster 12/15/2021. This means they were eligible to receive their 2nd booster on or after 4/15/2022 (4 months after their 1st booster). The 2nd booster was administered/given to them 4/3/2022. This is 12 days early. They were given their 2nd booster 12 days early.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No illness the date of vaccination. Unknown for one month prior.
- Vorgeschichte
- Unknown at time of vaccination.
- Andere Medikamente
- Unknown
- Allergien
- No allergies reported.
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 04.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine vial was left out for longer than 24 hours on the counter, Medical Assistant did not notice that date on the vial and administered expired vaccine to the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Anxiety [F41.9] Atrial fibrillation (CMS/HCC) [I48.91 Barrett's esophagus [K22.70] Benign prostatic hyperplasia with nocturia Chronic post-thoracotomy pain [G89.22] Coronary artery disease [I25.10] Degenerative joint disease [M19.90] Diverticulosis [K57.30] Diverticulosis [K57.90] Dumping syndrome [K91.1] Encounter for antineoplastic chemotherapy [Z51.11] Esophageal cancer (CMS/HCC) [C15.9] Barrett esopahgus in situ carcinoma ETOH abuse [F10.10] Fracture [T14.8XXA] ? clavicle and left shoulder GERD (esophageal reflux) [K21.9] Hiatal Hernia [K44.9] Hyperlipidemia [E78.5] Hypertension [I10] Left shoulder pain [M25.512] post fall at work, surgery, chronic persistent discomfort Osteoarthritis gen'l [M15.9] Pain, chronic [G89.29] 2018 Neck and lower back Palpitations [R00.2] PMR (polymyalgia rheumatica) (CMS/HCC) [M35.3] Polymyalgia rheumatica syndrome (CMS/HCC) [M35.3] 3/29/2011 -7/10 diagnosed by Dr. and treated with prednisone Reflux esophagitis [K21.00] Trigger finger of right hand [M65.30] 2018 Right index, middle, and ring finger Vitamin D deficiency [E55.9]
- Andere Medikamente
- amLODIPine (NORVASC) 10 MG tablet Take 1 tablet by mouth daily. Needs office visit for further refills HYDROcodone-acetaminophen (NORCO) 5-325 MG per tablet Take 1 tablet by mouth daily as needed for Pain. Do not start before March 30, 2022
- Allergien
- Lipitor
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 02.04.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Vaccination site swelling
Symptomtext
swelling on the injection site on the left side; 4th shot on 28Mar2022; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE SWELLING (swelling on the injection site on the left side) and EXTRA DOSE ADMINISTERED (4th shot on 28Mar2022) in a 61-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. Concurrent medical conditions included Rheumatoid arthritis (started 20 years ago, Patient had it entire life, still the same). On 28-Mar-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form and first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 28-Mar-2022, the patient experienced EXTRA DOSE ADMINISTERED (4th shot on 28Mar2022). On 30-Mar-2022, the patient experienced VACCINATION SITE SWELLING (swelling on the injection site on the left side). At the time of the report, VACCINATION SITE SWELLING (swelling on the injection site on the left side) and EXTRA DOSE ADMINISTERED (4th shot on 28Mar2022) outcome was unknown. No concomitant medication was reported. Patient had never been diagnosed with or tested positive for COVID-19. No other vaccines given within 1 month prior to Moderna COVID-19 vaccine. Patient stated they have received 3 shots of Moderna COVID-19 vaccine and had no problems with it. Treatment medication was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Rheumatoid arthritis (started 20 years ago, Patient had it entire life, still the same)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 01.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Date: 4/1/2022 staff member came in, 0940 for a booster shot their third vaccine. They completed the pre-vaccination worksheet. I verbally went over the pre-vaccination paperwork with them. They reported no adverse reactions to previous injections of Moderna. I administered Moderna vaccine at 0945, a booster dose, of 0.25 ml in left deltoid. Vial lot # 033K21-2A and expiration date 04/09/2022. The employee did not have their vaccine card. I completed a new card, using their previous vaccination information from the program for them. At 0945 I administered 0.25 ML of Moderna booster dose and monitored them for 15 minutes. The employee showed no signs or symptoms of adverse reactions to this vaccination. The employee was alert and verbally responsive. Registered Nurse, on duty, assessed employee post injection and found no signs or symptoms of anaphylaxis or negative side effects. At 1000 the employee walked out of clinic without showing any signs of difficulty. After checking the employee's vaccination dates against the memo providing instructions for vaccinations I saw that I administered the vaccine 2 months too soon. The correct date of the third dose of Moderna should have been given on 6/28/2022. I alerted the Registered Nurse on duty to what happened and was directed to alert the Nurse Consultant III.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 42,0
- Geschlecht
- U
- Eingang
- 01.04.2022
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental overdose
Symptomtext
gave 4th dose of the Moderna Covid-19 vaccine of 0.5mL instead of 0.25mL dose.; This spontaneous case was reported by an other health care professional and describes the occurrence of ACCIDENTAL OVERDOSE (gave 4th dose of the Moderna Covid-19 vaccine of 0.5mL instead of 0.25mL dose.) in a 42-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033K21-2A) for COVID-19 vaccination. No Medical History information was reported. On 23-Mar-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 23-Mar-2022, the patient experienced ACCIDENTAL OVERDOSE (gave 4th dose of the Moderna Covid-19 vaccine of 0.5mL instead of 0.25mL dose.). At the time of the report, ACCIDENTAL OVERDOSE (gave 4th dose of the Moderna Covid-19 vaccine of 0.5mL instead of 0.25mL dose.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental overdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
Gave 5th dose of moderna 1 month after receiving 4th dose. No symptoms noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Cancer
- Vorgeschichte
- Depression, cancer
- Andere Medikamente
- Buspirone, Gabapentin, Glucosamine, Letrozole, Pantoprazole, Revlimid, Sertraline, Trazodone.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 30.03.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Second dose of vaccine was given 21 days after first dose rather than 28 days after first dose. First dose given 3/4/22, and second dose was given 03/25/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -