- Staat
- -
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 28.06.2023
- Impfdatum
- 07.01.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 164,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pulmonary embolism
Pulmonary infarction
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE PULMONARY EMBOLISM W INFARCTION, UNSPECIFIED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 07.02.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Thrombosis
Symptomtext
Per pt spouse, pt suffered blood clot and died.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None reported
- Andere Medikamente
- -
- Allergien
- KNDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 09.01.2023
- Impfdatum
- 07.01.2022
- Beginn
- 29.11.2022
- Tage bis Beginn
- 326,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Chest pain
Dyspnoea
Fatigue
Influenza virus test
Malaise
Pulmonary embolism
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I was feeling really tired and congested. On November 30th I ended going to the hospital with chest pain and I had a pulmonary embolism. I was in the hospital until December for that through December 2nd but they never tested me for COVID-19. I ended up having shortness of breath, fever, congestion, and was not feeling well. I ended up going to an urgent care and tested positive for COVID-19. I have some lingering shortness of breath today but over all I have recovered from COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- COVID-19 antigen test; Influenza test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Polycystic Ovary Disease
- Andere Medikamente
- Sertraline; buspirone; loratadine
- Allergien
- Peanuts; sulfa drugs
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 30.12.2021
- Beginn
- 23.12.2022
- Tage bis Beginn
- 358,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute left ventricular failure
Acute respiratory failure
Ammonia increased
Asthma
Blood creatinine increased
Blood thyroid stimulating hormone normal
Brain natriuretic peptide increased
COVID-19
Chest X-ray abnormal
Chronic left ventricular failure
Computerised tomogram head abnormal
Cough
Diabetic diet
Dyspnoea
Ejection fraction normal
Fatigue
Hepatic encephalopathy
Symptomtext
Assessment and Plan Patient is a 70 y.o. female patient of CNP with history of atrial fibrillation, diabetes mellitus, chronic diastolic heart failure, HOCM, nonsustained V. tach, status post ICD device, OSA on CPAP, who presented to the emergency room with altered mental status, congestion, shortness of breath, cough, phlegm production. Acute hepatic encephalopathy-resolved CT head-non acute (prior ischemic dx) On BiPAP with improvement Hold home gabapentin TSH-4.66 (mild elevation) Ammonia level 99>68 Patient admits she is not taking her lactulose regularly DC home today, patient informed to take lactulose to prevent recurrence Acute on chronic hypoxemic hypercarbic respiratory failure-resolved Asthma with exacerbation-resolved OSA Start the patient albuterol MDI, Symbicort, dexamethasone BiPAP as above if needed She is on 3L of nasal cannula at baseline in addition to CPAP nightly Acute on chronic diastolic heart failure Moderate pulmonary hypertension Hypertrophic cardiomyopathy Ejection fraction 60 to 65% BNP of 2700 Patient on Bumex 4 mg twice daily at home Continue metolazone and spironolactone Stop Bumex per nephrology and monitor for now Covid-19 Virus Infection Date of onset of symptoms: 12/22/22 Symptoms present on admission: Shortness of breath, cough cold, congestion Date of covid positive test: 12/23/22 Vaccination status: vaccinated Imaging: Chest x-ray personally reviewed, bilateral pulmonary venous congestion, mild left pleural effusion Oxygen requirements on admission: 3L Current oxygen requirements: 3L Medical therapy: steroids Consultants following: ID Anticipated special isolation end date: 1/2/22 AKI on CKD III Creatinine baseline around 2 Presenting creatinine 2.41 Bumex as above Increased to 3.1 on 12/25 Nephrology consulted- recs appreciated Lower extremity wounds Mainly on left, right appears improved Consult wound care Atrial fibrillation Nonsustained V. tach s/p ICD Coumadin, dosed by pharmacy Elevated troponin demand ischemia, trend troponin every 3 hours Troponin of 86 and then 88 Diabetes mellitus Diabetic diet Edo consulted- recs appreciated Increase as needed while on steroids Hyperthyroidism Continue home Levothyroxine TSH 4.66 Lower extremity Ulcer Follows with Podiatry outpatient Continue dressings left leg Xeroform, 4x4, kerlix, ace wrap and right leg kerlix with ace wrap Morbid obesity due to excess calories BMI 44 Encouraged on lifestyle modification GERD Continue daily PPI Chronic fatigue PT/OT eval and treat
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.07.2022
- Tage bis Beginn
- 182,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anticoagulant therapy
COVID-19
Death
Diarrhoea
Gastrointestinal haemorrhage
Symptomtext
pt had a recent hospitalization (unsure on date and length of time) with a dx of COVID and GI bleed; general surgery consult said pt did not have a significant bleed and was able to be put back on anticoagulant; was dc'd to home with diarrhea; had been home 4 days before family was unable to reach pt, called for a welfare check; EMS found pt with no signs of life; brought to ED for evaluation; pt pronounced deceased at Hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CAD, DM, HTN, HLD, STROKE
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 26.10.2022
- Impfdatum
- 28.12.2021
- Beginn
- 05.09.2022
- Tage bis Beginn
- 251,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Death
Symptomtext
Narrative: on hospice
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 19.09.2022
- Impfdatum
- 28.12.2021
- Beginn
- 02.08.2022
- Tage bis Beginn
- 217,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anticoagulant therapy
COVID-19
Cardiac telemetry
Dyspnoea
Echocardiogram normal
Ejection fraction normal
Electrocardiogram abnormal
Fatigue
Hypokalaemia
Left atrial enlargement
Malaise
Pulmonary embolism
SARS-CoV-2 test positive
Tachycardia
Ultrasound Doppler normal
Symptomtext
OBSERVATION DISCHARGE NOTE Assessment and Plan Patient is a 70 y.o. female patient of DO with history of COVID 19, HTN, depression MS, HLD presented with tachycardia and sob. Bilateral PE COVID 19 Did not feel well the week of July 18th. Positive home COVID test July 25th. Symptoms of fatigue and sob. Husband also tested positive Vaccinated status: vaccinated and boostered O2 sats >90% on RA EKG - SR LA enlargement Telemetry - SR VR 70s Echocardiogram - no right heart strain. EF 60-65% Venous doppler LE: No evidence of deep or superficial vein thrombosis in the right or left lower extremities Lovenox on admission Consult pharmacy regarding NOAC - cost and education please She is requesting discharge home this morning. Pending results of echocardiogram, venous doppler and cost of NOAC will plan on discharge hoe later today. Hypokalemia Replace and recheck HTN SBP 130s MS Very well controlled per patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 29.08.2022
- Impfdatum
- 29.12.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Angiogram pulmonary abnormal
Atelectasis
Bronchial wall thickening
COVID-19
Chest tube insertion
Death
Dyspnoea
Emphysema
Encephalopathy
Endotracheal intubation
Fibrin D dimer increased
Haemoglobin decreased
Lung consolidation
Lung infiltration
Mechanical ventilation
Pleural effusion
Pneumonia
Positive airway pressure therapy
Symptomtext
The patient was transferred to the Hospital on 03/05/2022 for a higher level of care from the Medical Center. He had a recent COVID infection, became SOB, and was diagnosed with bilateral PNA and sepsis. CTA of chest was obtained d/t elevated D dimer which was negative for pulmonary embolus or aortic dissection. Had significant interval worsening in the appearance of the lungs with increased infiltrates superimposed on chronic emphysema with areas of nodular consolidation, bronchial wall thickening, and trace bilateral pleural effusions and atelectasis. The patient's hgb was low and received 2 units of PRBC. On the floor, the patient was treated with Rocephin in addition to DuoNeb breathing treatments. The patient had a complicated course requiring oral intubation and mechanical vent when he failed Bipap. He could not be weaned from vent, and underwent chest tube placement for left-side pneumo. The patient was taken off sedation but remained unresponsive. The patient had profound encephalopathy. The patient expired on 04/01/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 21.04.2021
- Beginn
- 28.01.2022
- Tage bis Beginn
- 282,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Death
Symptomtext
Narrative: Patient passed away due to COVID-19. He had received the COVID-19 vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 93,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 25.01.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 74,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest X-ray abnormal
Cough
Death
Dyspnoea
Hypoxia
Lung infiltration
Urinary tract infection
Symptomtext
Presented to ED, Hospital, with c/o cough and hypoxia. Patient was diagnosed with Covid-19 on 04/10/2022. Since then he has had SOB and nonproductive cough. Chest Xray revealed some bilateral pulmnary infiltrates. Patient was also found to have a UTI and started on Macrobid for 7 days. Patient was discharged home with home health. Patient expired on 05/13/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 22.03.2021
- Beginn
- 06.03.2022
- Tage bis Beginn
- 349,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Anticoagulant therapy
Blood test
Computerised tomogram
Dyspnoea
Heart rate increased
Pulmonary embolism
Thrombectomy
Ultrasound scan
X-ray
Symptomtext
Booster shot was administered 27 December 2021. Developed shortness of breath and increased heart rate starting about 15 February 2022. Hospitalized on 6 March 2022 and diagnosed with unprovoked multiple pulmonary embolisms without DVT . Was treated with heparin and with a thrombectomy to remove embolisms from lungs. Received oxygen therapy while in hospital and while recovering at home. Continuing to recover and taking Eliquis regularly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 4,0
- Labordaten
- X-Ray 3/6/22 Cat Scan 3/6/22 Ultrasounds 3/6/22 Blood tests ongoing
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure High Cholesterol Obesity Seasonal Allergies
- Andere Medikamente
- Verapamil Lisinopril Metoprolol Hydrochlorothiazide Simvastatin Xyrtec Daily Multivitamin Daily Fish Oil Vitamin D3
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 07.01.2022
- Beginn
- 21.08.2022
- Tage bis Beginn
- 226,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bronchoscopy
COVID-19
COVID-19 pneumonia
Candida test positive
Culture positive
Decreased appetite
Diarrhoea
Dyspnoea
Endotracheal intubation
Herpes zoster
Intensive care
Klebsiella test positive
Productive cough
Pyrexia
SARS-CoV-2 test positive
Weight decreased
Symptomtext
74 yo M PMH CKD 2/2 chronic glomerulonephritis s/p renal transplant in 2008, COVID-19 pneumonia 7/27, HTN, OSA, paroxysmal afib, possible COPD vs asthma and extensive occupational exposure in cement production plant who presented 8/21 as a transfer for evaluation of persistent fevers. Patient tested positive for COVID pneumonia on 7/27 and afterwards he had shingles on his left arm that was treated with acyclovir for 1 week. After treatment, his fever persisted along with diarrhea and loss of appetite with a 23 pound weight loss. He also has worsening acute on chronic dyspnea with mildly productive cough. Patient was taken for bronchoscopy with BAL and transferred to MICU 8/25 for postprocedure management s/p intubation for bronchoscopy. Treated empirically with Cefepime, doxy, azithromycin, Rocephin and IV steroids decadron 10mg BID for suspected persistent COVID-19 PNA. Respiratory culture +Klebsiella and rare Candida. He was extubated 8/27 to nasal cannula and tolerating well since that time. Spoke with patient's wife re: home care services. States she is not sure they will be needing at this time. States they will be staying in nearby condo for a few days and then travel back home. Verbalizes unsure if they will go to outpatient therapy vs home care. States she will look into it once home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 12,0
- Labordaten
- 8/21 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 23.12.2021
- Beginn
- 15.01.2022
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain lower
Alanine aminotransferase normal
Albumin globulin ratio
Alpha-1 anti-trypsin
Anion gap
Antimitochondrial antibody
Antinuclear antibody negative
Aspartate aminotransferase normal
Basophil count
Basophil percentage
Blood albumin normal
Blood alkaline phosphatase normal
Blood bilirubin increased
Blood calcium normal
Blood chloride normal
Blood creatinine normal
Blood glucose normal
Blood immunoglobulin A
Symptomtext
Pink rash on genital area and nausea from early to mid January, 2022, saw primary care physician 1/31/2021. Rash was consistent with previous rash from 8/2020, which was also instance of a positive COVID-19 test. Diagnosed as dermatitis and prescribed a topical cream to treat the rash which resolved after a few weeks of use. Omeprazole was offered, but refused. Nausea issues persisted with loose and frequent stools and lower abdominal pain. Saw a new provider 3/2/2022 for second opinion. Omeprazole was ordered along with blood and fecal labs. Based on results, Cipro and Flagyl were ordered for a week due to possible GI infection and inflammation. Probiotic was also started during course of antibiotics. Symptoms improved somewhat after course of antibiotics. Referred to gastroenterologist for consult. On 3/28/2022 additional labs ordered, abdominal ultrasound, and scheduled for upper and lower endoscopy. Endoscopy completed 4/11/2022, noted gastritis, esophogitis, and ulcerated terminal ilium. Concern for possible Crohn's disease was noted and Mesalamine and famotodine were ordered. Episode of syncope occurred 4/22/2022, medication was stopped and lab work ordered. Mesalamine was stopped and switched to Sulfasalazine. GI issues are still being monitored.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- 3/3/2022: IMMUNOGLOBULIN A , 156mg/DL; DEAMIDATED GLIADIN IGA 0.3 U/mL; TTG IGA <0.5 U/mL; Complete Blood Count w/o diff: WBC 7.81 10(3)/mcL, RBC 5.94 10(6)/mcL, HGB 17.3 g/dL, HCT 49.8%, MCV 83.8fL, MCH 29.1pg, MCHC 34.7 g/dL, Platelet Count 221 10(3)/mcL, RDW 11.6%, MPV 11.1fL. 3/4/2022: OCCULT BLOOD - IFOB negative; Ova and parasite - none seen; C DIFF PCR Toxin B negative; STOOL WBC LACTOFERIN positive; Stool culture no salmonella, shigella, or e coli, negative for campylobacter antigen, shiga toxin 1 and 2 not detected 4/23/2022 CBC with auto diff: WBC 7.80 10(3)/mcL, RBC 5.99 10(6)/mcL, HGB 17.5g/dL, HCT 48.9%, MCV 81.6fL, MCH 29.2pg, MCHC 35.8g/dL, Platelet Count 206 10(3)/mcL, RDW 12.4%, MPV 10.7fL, Neutrophils 63%, Lymphocytes 27.1%, Monocytes 6.8%, Eosinophils 2.6%, basophils 0.5%, absolute neutrophils 4.9 10(3)/mcL, absolute lymphocytes 2.11 10(3)/mcL, absolute monocytes 0.53 10(3)/mcL, absolute eosinphil 0.20 10(3)/mcL, absolute basophils 0.04 10(3)/mcL Assay Lipase 20 U/L Comprehensive Metabolic Panel: SODIUM 138 mmol/L POTASSIUM 3.9 mmol/L CHLORIDE 100 mmol/L CO2, VENOUS 27 mmol/L ANION GAP 11.0 mmol/L GLUCOSE 94 mg/dL BUN 11 mg/dL CREATININE, BLOOD 0.95 mg/dL BUN/CREATININE RATIO 12 ratio TOTAL PROTEIN 7.8 g/dL ALBUMIN 4.8 g/dL A/G RATIO 1.6 CALCIUM 9.7 mg/dL T BILI 1.6 mg/dL SGOT (AST) 20 U/L SGPT (ALT) 28 U/L ALKALINE PHOSPHATASE 59 U/L GFR, EST. NONAFRICAN >60 GFR, EST. AFRICAN >60 5/13/22: Abdominal ultrasound: Liver appears normal in echogenicity without intrahepatic biliary dilatation or focal hepatic mass lesions. Antegrade portal vein flow. Normal flow visualized hepatic veins. No abnormality on chroma images. No hepatic surface nodularity. The gallbladder is normal in size. There is a 4 mm echogenic oval lesion along the nondependent wall of the mid gallbladder body. No internal blood flow. Consideration would include tumefactive adherent sludge or polyp. Definitive shadowing gallstones are not seen. No gallbladder wall thickening or pericholecystic fluid. Reported sonographically negative Murphy's sign per scanning technologist. The common duct is normal in diameter at 0.4 cm. There are portions of the pancreatic head and tail which are obscured by overlying bowel gas. The visualized pancreas is sonographically unremarkable. Right kidney measures 10.5 cm in length. No shadowing calculus, hydronephrosis, or renal mass lesion. Alpha-1 Antitrypsin total 126 mg/dL IRON 139 mcg/dL TRANSFERRIN 239 mg/dL TIBC, CALCULATED 299 mcg/dL % SATURATION * 46 % Assay Ferritin 202ng/mL ANTINUCLEAR ANTIBODIES ANA Screen negative titer, Antinuclear autoantibodies not detected by IFA at a 1:80 screening dilution of HEp-2 cells. Assay Ceruloplasmin 25 mg/dL ANTI-SMOOTH MUSCLE ANTIBODY <1:10 titer Anti-Mitochondrial Antibody <1:10 titer Hepatitis non detected CALPROTECTIN, F <50.0 mcg/g
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- asthma
- Andere Medikamente
- Loratadine, multivitamin, albuterol
- Allergien
- flovent, cats
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 16.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Cardiac failure congestive
Cardiac imaging procedure abnormal
Cardiac ventricular thrombosis
Cardiomegaly
Cardiomyopathy
Dyspnoea
Echocardiogram abnormal
Ejection fraction decreased
Implantable defibrillator insertion
Multiple gated acquisition scan abnormal
Symptomtext
Shortness of breath, enlarged heart, thrombus in my left ventricle, low ejection fracture, congestion heart failure, cardiomyopathy. Wore life vest for four month and finally had to get a internal cardiac defibrillator on June 3, 2022. I have been on a heart failure protocol of medication since the end of January 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac ventricular thrombosis
- Hospital-Tage
- 4,0
- Labordaten
- Echocardiogram showed EF of 25%, cardiac MRI showed EF 18%, and MUGA scan showed EF 23%.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension and gout
- Andere Medikamente
- Benazpril 40mg, norvaz 5 mg, allupournol 200 mg.
- Allergien
- Iodine and shellfish
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 13.01.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 102,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Bell's palsy
Blood test normal
Influenza like illness
Nasopharyngitis
Symptomtext
Developed Bell's Pausly after third (booster) Maderna shot. Patient has never tested positive for moderna nor had the virus, but completed all three Moderna shots. 1. Moderna 01/09/21. 2. 02/06/2021 3. 01.13/2022. Experienced flu/cold ;like symptoms (worse reaction of the three) with booster Moderna shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- Normal blood tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Adult Onset Diabetes
- Andere Medikamente
- developed Bell's Paulsy. Diagnosed on April 26, 2022 at Center Emergency Department
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 18.04.2022
- Impfdatum
- 20.01.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 40,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vocal cord paralysis
Symptomtext
The patient annotated "Parlayed left Vocal chord" Patient was seen at another clinic and is getting care. Patient did no give any specification on treatment nor where he was seen as a result of the reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vocal cord paralysis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Patient Listed Rotator Cuff and Left Shoulder with no other specification.
- Vorgeschichte
- None Listed
- Andere Medikamente
- None Listed
- Allergien
- None Listed
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 06.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dyspnoea
Electrocardiogram ambulatory
Heart rate abnormal
Insomnia
Myocarditis
Palpitations
Symptomtext
After receiving my booster, a week later I was short of breath, a tight feeling in my chest, and my heart felt like it was pounding uncontrollably. It got to the point where I couldn't sleep because the beating of my heart was so loud. I contacted my cardiologist and he stated I had all the symptoms of myocarditis. To get rid of it I was taking 400 mg of ibuprofen 4 times a day for 5 days. My heart rate has been off and have been prescribed metoprolol PRN when symptoms show. I have been struggling and having many of these similar issues as before. I was given a heart monitor for a week and will be seeing my cardiologist this following week to discuss findings.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Heart monitor: Results pending.
- Aktuelle Erkrankungen
- From my first vaccine I started to have heart palpitations and it continued to get worse. It started to have issues with the electric system with my heart. I did have an ablation done in December 2021. Everything was fine after the surgery and I was feeling great until the booster.
- Vorgeschichte
- Hashimoto's Thyroid Disease.
- Andere Medikamente
- Armor Thyroid 90mg daily; Simvastatin 10mg daily.
- Allergien
- Penicillin.
- Vorherige Impfungen
- Janssen 1st Vaccine Date: 03/29/2021 Lot: 1808978 : From my first vaccine I started to have heart palpitations and it continued
- Staat
- OH
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 20.11.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 41,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Echocardiogram
Electrocardiogram abnormal
Pericarditis
Symptomtext
ON 31 DECEMBER, I EXPERIENCED ACUTE SYMPTOMS OF WHAT WAS EVENTUALLY DIAGNOSED AS PERICARDITIS. I SPENT THE EVENING OF 31 DECEMBER IN THE HOSPITAL EMERGENCY ROOM, WHERE IT WAS NOT DIAGNOSED. ON 2 JANUARY, I SPENT THE AFTERNOON IN THE HOSPITAL, WITH ACUTE SYMPTOMS. BEFORE GOING TO HOSPITAL ON 2 JANUARY, I WENT TO URGENT CARE, WHO SENT ME TO HOSPITAL BECAUSE AN EKG WAS ABNORMAL. DR. CONFIRMED THE DIAGNOSIS OF PERICARDITIS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- I RECEIVED EKG TESTS AT HOSPITAL. DR. ORDERED ANOTHER EKG AND AN ECHOCARDIOGRAM. HE FORMALLY DIAGNOSED ME WITH PERICARDITIS AND HAS HAD ME ON A DRUG REGIMEN OF ADVIL AND COLCHICINE. I AM STILL ON IT, AS I CONTINUE TO EXPERIENCE CHEST PAIN SYMPTOMS.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- TETRACYCLIN
- Vorherige Impfungen
- I DEVELOPED TINNITUS AFTER RECEIVING MY FIRST MODERNA SHOT IN MARCH 2021.
- Staat
- NC
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 35,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: ja
C-reactive protein increased
Echocardiogram abnormal
Pericardial effusion
Pericarditis
Red blood cell sedimentation rate increased
Symptomtext
Pericarditis, Admitted to the Hospital, NSAID and Colchicine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- 2,0
- Labordaten
- Elevated ESR and CRP, Pericardial effussion on Echo
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HTN
- Andere Medikamente
- Cymbalta, Losartan
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deep vein thrombosis
Dysstasia
Pain in extremity
Ultrasound scan
Symptomtext
Began experiencing pain in my right leg on 1/10/2022. Symptoms increased over the next few days. On 1/21/2022 experienced severe pain and was unable to stand on right leg. Office visit on 1/24/2022 led to diagnosis of DVT in right leg. Began taking Xarelto 1/24/2022. Started wearing compression stocking. Status: Continuing discomfort in leg but became fully ambulatory after 10 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Ultrasound 1/24/2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LOW DOSE ASPIRIN 1X DAILY
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anaphylactic reaction
Dyspnoea
Pharyngeal swelling
Symptomtext
Anaphylactic reaction after first vaccine and post Amoxicillin/allergic reaction; Swelling in throat after first vaccine and post Amoxicillin; Could not breath after first vaccine & post Amoxicillin; This spontaneous case was reported by a pharmacist and describes the occurrence of ANAPHYLACTIC REACTION (Anaphylactic reaction after first vaccine and post Amoxicillin/allergic reaction), PHARYNGEAL SWELLING (Swelling in throat after first vaccine and post Amoxicillin) and DYSPNOEA (Could not breath after first vaccine & post Amoxicillin) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 vaccination. Co-suspect product included non-company product AMOXICILLIN for Tooth infection. Previously administered products included for Tooth infection: Amoxicillin from 23-Dec-2021 to 31-Dec-2021. Past adverse reactions to the above products included No adverse event with Amoxicillin. Concurrent medical conditions included Tooth infection. On 06-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Jan-2022, the patient started AMOXICILLIN (unknown route) 1 dosage form. On 18-Jan-2022, the patient experienced ANAPHYLACTIC REACTION (Anaphylactic reaction after first vaccine and post Amoxicillin/allergic reaction) (seriousness criterion medically significant), PHARYNGEAL SWELLING (Swelling in throat after first vaccine and post Amoxicillin) (seriousness criterion medically significant) and DYSPNOEA (Could not breath after first vaccine & post Amoxicillin) (seriousness criterion medically significant). At the time of the report, ANAPHYLACTIC REACTION (Anaphylactic reaction after first vaccine and post Amoxicillin/allergic reaction), PHARYNGEAL SWELLING (Swelling in throat after first vaccine and post Amoxicillin) and DYSPNOEA (Could not breath after first vaccine & post Amoxicillin) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant Medication use information was not provided by reporter. On 18J AN 2022 restarted Amoxicillin for tooth infection again and ended up in the hospital with an allergic reaction. Patient thought that she had developed allergy to Amoxicillin and having anaphylactic reaction to amoxicillin. Treatment Medication use information was not provided by reporter. Company comment: This is a spontaneous case concerning a 57-year-old, female patient with concomitant medication of Amoxicillin, who experienced the unexpected serious events of pharyngeal swelling and dyspnea and expected serious event of anaphylactic reaction. The events anaphylactic reaction, pharyngeal swelling and dyspnea occurred 12 days after the first dose of mRNA-1273 vaccine administration. The events were described as, the patient received Amoxicillin treatment for approximately one week for tooth infection with the last dose of 6 days prior to the first dose of mRNA-1273 vaccine administration. 12 days after the first dose of mRNA-1273 vaccine administration, patient restarted with Amoxicillin for the same indication and the within the same day patient experienced throat swelling and could not breath and ended up in the hospital. No reported treatment information. The outcome of the events anaphylactic reaction, pharyngeal swelling and dyspnea were unknown. The concomitant medication of Amoxicillin remain confounder. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 31-Jan-2022: Seriousness criteria updated for event Anaphylactic reaction.; Sender's Comments: This is a spontaneous case concerning a 57-year-old, female patient with concomitant medication of Amoxicillin, who experienced the unexpected serious events of pharyngeal swelling and dyspnea and expected serious event of anaphylactic reaction. The events anaphylactic reaction, pharyngeal swelling and dyspnea occurred 12 days after the first dose of mRNA-1273 vaccine administration. The events were described as, the patient received Amoxicillin treatment for approximately one week for tooth infection with the last dose of 6 days prior to the first dose of mRNA-1273 vaccine administration. 12 days after the first dose of mRNA-1273 vaccine administration, patient restarted with Amoxicillin for the same indication and the within the same day patient experienced throat swelling and could not breath and ended up in the hospital. No reported treatment information. The outcome of the events anaphylactic reaction, pharyngeal swelling and dyspnea were unknown. The concomitant medication of Amoxicillin remain confounder. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Tooth infection
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Electrocardiogram normal
Fall
Fatigue
Gait inability
Loss of consciousness
Lymphadenopathy
Malaise
Symptomtext
A few days after my #3 dose for Moderna, I began to feel sick and fatigued, where one of the nodes in my armpit swelled. After coming home from work, I came home took a nap and then went to the bathroom and all of a sudden a huge sense of dizziness came over me and I hit my doorway and fell on the floor and went unconscious. I was unable to walk for a bit and crawled to my bed. I have continued to have multiple dizziness spells that are progressively getting worse that are lasting about 15-20 minutes each and have gotten worse in intensity and more frequent. My doctor is referring me to a cardiologist to make sure everything is okay. Planning to use a long-term monitor for heart during dizziness spells. At the moment my doctor does not want to give me anything as of yet since they are unsure of what is going on. I am still fatigued as well. It is now at the point where I cannot go through an entire day without taking a nap.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- EKG was unremarkable. Blood work is planned within the next few weeks.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- Prenatal Vitamin, and Zyrtec
- Allergien
- Spearmint and Eucalyptus and Aloe
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Dizziness
Loss of consciousness
Symptomtext
Light headed, Weak, Loss of consciousness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Chills
Dizziness
Loss of consciousness
Pain
Palpitations
Peripheral coldness
Sleep disorder
Symptomtext
I recieved my vaccine yesterday afternoon and have been having severe chills for hours. my body feels like it?s on fire and my toes & fingers are so cold. i?m starting to not sure if this is normal my whole body hurts and i?ve passed out twice. my heart rate is feels like it keeps racing and it wakes me up. I?m still not feeling good but i think my fever has went down some. I just got really dizzy and passed out after getting up to go to the bathroom and my heart rate laying in bed was consistently in the 140s or so for a few hours. I have a cardiology appointment today so I figured i?ll just see what they say
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Pt to follow up with cardiology today
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- -
- Andere Medikamente
- Northera
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anaphylactic reaction
Drug hypersensitivity
Symptomtext
She has always been able to take amoxicillin, but after her Moderna shot she had an anaphylactic allergic reaction to Amoxicillin. She believes it could be related to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- 1/18/21 not sure. She went to the emergency room and was discharged.
- Aktuelle Erkrankungen
- 12/23/21 AMOXIL FOR 10 DAYS infected tooth 1/6/22 Moderna shot 1st one 1/18/22 AMOXIL. infected tooth
- Vorgeschichte
- thyroid disorder
- Andere Medikamente
- armour thyroid
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypotension
Syncope
Symptomtext
patient fainted shortly after receiving vaccinations . Calle 911 and kept patient calm and applied cool compress to forehead. Ems arrived and took patient to hospital for precaution due to low blood pressure. Patient was released later in day after receiving IV fluids to help raise blood pressure. Patient is feeling fine after treatment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- metoprolol tartrate 25mg and fluoxetine 40mg
- Allergien
- oxycodone and morphine related products
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Headache
Myocarditis
Symptomtext
Mom said patient started having bad headache and chest hurting....took patient to ER and ER said patients heart was inflammed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 2,0
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Injection site pain
Loss of consciousness
Nausea
Vomiting
Symptomtext
Vomiting/nausea, 1 hour Passing out, 15 minutes Fatigue, over 12 hours Pain at injection site, no redness/itchiness, over 12 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Vasovagal syncope, hypotension, supraventricular tachycardia
- Andere Medikamente
- Prozac, turmeric supplements, birth control pills, mesalamine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Loss of consciousness
Nausea
Pyrexia
Symptomtext
Pt stated that 12 hrs after she received her first dose of Moderna vaccine, she experienced some side effects i.e., fever ,chills, nausea, dizzy. Seh said she passed out cold. The side effects lasted about 24-48hrs. She is feeling much better today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none noted
- Vorgeschichte
- none noted
- Andere Medikamente
- none noted
- Allergien
- none noted
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Generalised tonic-clonic seizure
Seizure
Symptomtext
Tonic-clinic non-epileptic seizure during sleep. Taken to ER via ambulance. No treatment given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Generalised tonic-clonic seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Amphetamine salts 10mg Zinc 50mg Levocetirizine dihydrochloride 5mg 24hr
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysarthria
Seizure
Swollen tongue
Vomiting
Symptomtext
As the patient was sitting out in the lobby, within 11 minutes of receiving her booster (#3 dose) she began having a seizure that lasted around 2 to 3 minutes. After the seizure stopped, we noticed the patients' tongue became swollen and she wasn't talking clearly. She wanted water, after she took a drink she began to throw-up. We called 991 to have EMS take her to the ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- unknown.
- Aktuelle Erkrankungen
- no other known illnesses
- Vorgeschichte
- unknown she doesn't usually fill with local pharmacy
- Andere Medikamente
- unknown medication list, this patient doesn't fill her prescriptions with local pharmacy
- Allergien
- no known allergies, per VAR patient didn't list any allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Presyncope
Vomiting
Symptomtext
Patient stated she was feeling light-headed and like she might pass out after receiving vaccines. She remained sitting and was given water. She did vomit, but after a few minutes, she stated she was feeling better. She did not complain of any difficulty breathing and there were no signs of a rash or hives.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Syncope
Symptomtext
AFTER ADMINISTERING MODERNA 1ST DOSE @ 1747, ABOUT 5 MINUTES LATER PT'S FELT DIZZY, SWEATING, HAD SOME WATER, PT'S WAS WITH MOTHER, PT'S SAID HE FAINT , OR FEEL THIS WAY EVERY TIME HE GETS VACCINE BECAUSE PT'S IS AFRAID OF NEEDLE. PT'S JUST WANTED SOME WATER AND SAID HE IS GETTING BETTER. @ 1810 PT'S TOOK TYLENOL 500MG (2 TABLETS). PT'S FELT ALRIGHT TO LEAVE ~@1815; MOTHER SAID SHE WILL DROP OFF HER SON AND BE WITH HIM. PT;S FEELING FINE TO LEAVE PHARMACY WITH MOTHER. DP 01/03/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 26.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Immediate post-injection reaction
Nausea
Paraesthesia
Syncope
Symptomtext
Pt fainted immediately post flu vaccine administration, was only unconscious for a few seconds- approx 30 sec. , - immunizing certified technician immediately braced pt's slump forward in chair. Pt did not report any other adverse reactions. Pt was instructed to sit in immunization room for at least 5 minutes. - reported ok - her mother was with her & they were instructed to wait in waiting area for a few more mins. Later in afternoon, Mom called & reported that patient was again feeling very dizzy, nauseous, and her hands were tingly. Mom was instructed to monitor & if there was any increased adverse reactions including difficulty breathing to call 911. Checked on patient the next day & she reported no residual issues... feeling just fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Pt (post-event) reported fainting has occurred previously.
- Staat
- WV
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 03.03.2023
- Impfdatum
- 23.09.2022
- Beginn
- 16.10.2022
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase normal
Anion gap
Aspartate aminotransferase normal
Basal ganglia infarction
Basophil count decreased
Basophil percentage
Blood albumin normal
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium normal
Blood chloride normal
Blood creatinine
Blood creatinine increased
Blood glucose normal
Blood potassium normal
Blood sodium normal
Blood urea nitrogen/creatinine ratio
Blood urea normal
Symptomtext
ED note by Dr. 10/16/22: "Chief Complaint Patient presents with ? Numbness HISTORY OF PRESENT ILLNESS Patient, is a 82 y.o.male who presents to the Emergency Department with numbness tingling his left arm hand. He also has weakness in his left grip. He states this started occurring around 6:00 p.m. yesterday. He says he was watching football on could hold onto the remote causing him to have concern why he may be weak. He had no difficulty with speech trouble walking. He had no trauma associated with this change in sensation and grip strength. He says entire left arm feels weak as well as somewhat on his left leg but is able to ambulate without difficulty. Does not take any blood thinners, had a history of stroke, have any chest pain or shortness of breath. REVIEW OF SYSTEMS The pertinent positive and negative symptoms are as per HPI. All other systems reviewed and are negative." "CLINICAL IMPRESSION 1. Atraumatic subdural hematoma 2. Left arm weakness DISPOSITION/PLAN Admitted" H&P by Dr. on 10/16/22: "PCP: MD Chief Complaint: Left hand weakness and numbness HPI: Patient is a 82 y.o., male with a history of essential hypertension, CKD who presents with left hand weakness and numbness that began yesterday around 6:00 p.m.; this morning when he woke up his symptoms continued. He denies hitting his head or falling down, denies any difficulty with walking, talking. No headaches, blurry vision, nausea/vomiting, chest pain, shortness of breath, diarrhea, dysuria. In the ED, CT brain suggestive of mixed density subdural hematoma over right frontal and parietal convexity without midline shift. ED physician discussed these findings with Neurosurgery, who recommended admission for observation and repeat imaging in the morning. COVID-19 vaccination status: Received vaccine x2 and booster x2. COVID-19 test: Negative today." "Assessment/Plan: Patient is a 82 y.o., male who presents with the following: 1. Subdural hematoma, nontraumatic -CT findings as above; neurosurgery consulted by ED, recommend MRI tomorrow to rule out underlying CVA as well. -hold off aspirin, neuro checks q.4 hours. -fall precautions. 2. Essential hypertension -resume lisinopril, metoprolol with holding parameters. 3. Hyperlipidemia -resume statin. 4. COPD without exacerbation -resume home inhaler regimen. 5. Chronic GERD -resume PPI. 6. CKD stage IIIA -serum creatinine currently around baseline, will continue to monitor and avoid nephrotoxic agents. 7. Normocytic anemia -hemoglobin currently stable, will order iron panel, vitamin B12 and folate levels. "
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 3,0
- Labordaten
- EXAM: Temperature: 37.2 ?C (98.9 ?F) Heart Rate: 68 BP (Non-Invasive): (!) 141/54 Respiratory Rate: 18 SpO2: 98 % Labs: I have reviewed all lab results. Lab Results for Last 24 Hours: Results for orders placed or performed during the hospital encounter of 10/16/22 (from the past 24 hour(s)) POC FINGERSTICK GLUCOSE - BMC/JMC (RESULTS) Result Value Ref Range GLUCOSE, POC 161 (H) 60 - 100 mg/dl COMPREHENSIVE METABOLIC PANEL, NON-FASTING Result Value Ref Range SODIUM 140 136 - 145 mmol/L POTASSIUM 4.7 3.5 - 5.1 mmol/L CHLORIDE 105 96 - 111 mmol/L CO2 TOTAL 27 23 - 31 mmol/L ANION GAP 8 4 - 13 mmol/L BUN 17 8 - 25 mg/dL CREATININE 1.37 (H) 0.75 - 1.35 mg/dL BUN/CREA RATIO 12 6 - 22 ESTIMATED GFR 52 (L) >=60 mL/min/BSA ALBUMIN 3.7 3.4 - 4.8 g/dL CALCIUM 9.2 8.8 - 10.2 mg/dL GLUCOSE 94 65 - 125 mg/dL ALKALINE PHOSPHATASE 101 45 - 115 U/L ALT (SGPT) 13 10 - 55 U/L AST (SGOT) 18 8 - 45 U/L BILIRUBIN TOTAL 0.7 0.3 - 1.3 mg/dL PROTEIN TOTAL 6.5 6.0 - 8.0 g/dL TROPONIN-I Result Value Ref Range TROPONIN I 11 7 - 30 ng/L CBC WITH DIFF Result Value Ref Range WBC 8.5 3.7 - 11.0 x10?3/uL RBC 4.06 (L) 4.50 - 6.10 x10?6/uL HGB 12.8 (L) 13.4 - 17.5 g/dL HCT 39.2 38.9 - 52.0 % MCV 96.6 78.0 - 100.0 fL MCH 31.5 26.0 - 32.0 pg MCHC 32.7 31.0 - 35.5 g/dL RDW-CV 14.2 11.5 - 15.5 % PLATELETS 178 150 - 400 x10?3/uL MPV 9.2 8.7 - 12.5 fL NEUTROPHIL % 73 % LYMPHOCYTE % 14 % MONOCYTE % 9 % EOSINOPHIL % 3 % BASOPHIL % 1 % NEUTROPHIL # 6.20 1.50 - 7.70 x10?3/uL LYMPHOCYTE # 1.18 1.00 - 4.80 x10?3/uL MONOCYTE # 0.80 0.20 - 1.10 x10?3/uL EOSINOPHIL # 0.25 <=0.50 x10?3/uL BASOPHIL # <0.10 <=0.20 x10?3/uL IMMATURE GRANULOCYTE % 0 0 - 1 % IMMATURE GRANULOCYTE # <0.10 <0.10 x10?3/uL PT/INR Result Value Ref Range PROTHROMBIN TIME 11.1 9.4 - 12.5 seconds INR 1.00 Imaging Studies: XR CHEST PA AND LATERAL Result Date: 10/16/2022 PROCEDURE DESCRIPTION: XR CHEST PA AND LATERAL CLINICAL INDICATION: Chest pain TECHNIQUE: PA and lateral views of the chest. COMPARISON: Chest x-ray 12/11/2019. FINDINGS: Heart: Normal. Mediastinum: No mass or widening. Hila: Normal, no mass. Pulmonary vascularity: Normal Lungs: No mass or airspace opacity. Pleura: No pleural effusion. No pneumothorax. Bones: No osseous lesion. Sternotomy wires again visualized. No acute cardiopulmonary process. Radiologist location ID: CT BRAIN WO IV CONTRAST Result Date: 10/16/2022 Patient Male, 82 years old. CT BRAIN WO IV CONTRAST performed on 10/16/2022 4:39 PM. REASON FOR EXAM: left arm numbness RADIATION DOSE: 1431.10 mGy.cm TECHNIQUE: Multiplanar nonenhanced images of the brain COMPARISON: None FINDINGS: A mixed density subdural hematoma overlying the right frontal and parietal convexity with maximum thickness 7 mm on coronal plane without midline shift. Small area of tissue loss within the right parietal lobe. No hydrocephalus. Patchy white matter lucencies are nonspecific but could relate to chronic microvascular ischemic changes. Chronic lacunar infarct in the right basal ganglia. No evidence of an acute major vascular territory infarct. A mixed density subdural hematoma overlying the right frontal and parietal convexity without midline shift. Findings were discussed with Dr. at 6: 05:00 PM on October 16, 2022. Radiologist location ID ECG: per my read - No results found for this visit on 10/16/22 (from the past 720 hour(s)).
- Aktuelle Erkrankungen
- Patient Active Problem List Diagnosis Date Noted ? Subdural hematoma 10/16/2022 ? CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min 10/16/2022 ? Normocytic anemia 10/16/2022 ? Organic impotence 04/04/2019 ? Prostate cancer screening 04/04/2019 ? Poor historian ? Essential hypertension ? GERD (gastroesophageal reflux disease) 11/06/2017 ? Screening for colon cancer 11/06/2017 ? Benign prostatic hypertrophy (BPH) with incomplete bladder emptying 07/20/2017 ? Hiatal hernia 01/25/2014 ? Hypertension 01/24/2014 ? Hyperlipidemia 01/24/2014 ? CAD (coronary artery disease) 01/24/2014
- Vorgeschichte
- Past Medical History: Diagnosis Date ? Arthritis hands ? Colon polyp ? Congestive heart failure (CHF) S/P Right CEA; Carotid Doppler-small amout of plaque in left carotid bulba and ICA ? Coronary artery disease S/P 3-Vessel CABG 1990 ? Dysphagia ? Essential hypertension ? Extensive tattoos ? H/O cardiovascular stress test 1/25/14 Normal myocardial perfusion study, EF 52%; No focal dyskinesia ? Hearing loss ? Heartburn no recent symptoms ? Hiatal hernia ? History of PFTs 09/21/2017 Severe Obstructive airways disease ? Hyperlipidemia ? Pneumonia 10/23/2015 ? Poor historian ? Poor historian ? Problems with swallowing ? Shortness of breath with walking hills ? Snores Pt. has never been tested for sleep apnea ? Wears glasses Past Surgical History: Procedure Laterality Date ? HX ADENOIDECTOMY childhood ? HX APPENDECTOMY childhood ? HX CAROTID ENDARTERECTOMY Right 2011 ? HX CHOLECYSTECTOMY 6/10/98 ? HX COLONOSCOPY Past ? HX CORONARY ARTERY BYPASS GRAFT 1990 3 vessel ? HX HEART CATHETERIZATION 1990's ? HX LAP CHOLECYSTECTOMY ? HX TONSILLECTOMY childhood ? HX UPPER ENDOSCOPY 11/06/2014
- Andere Medikamente
- Medications Prior to Admission Prescriptions albuterol sulfate (PROVENTIL OR VENTOLIN) 90 mcg/actuation Inhalation HFA Aerosol Inhaler Take 2 Puffs by inhalation Every 6 hours as needed for Other ANORO ELLIPTA 62.5-25 mcg/actuation
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 30.12.2021
- Beginn
- 08.01.2023
- Tage bis Beginn
- 374,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blood creatinine increased
Blood electrolytes abnormal
Blood glucose increased
Blood sodium decreased
Blood thyroid stimulating hormone decreased
COVID-19
Computerised tomogram head normal
Confusional state
Diarrhoea
Hyponatraemia
Hypophagia
Impaired self-care
Leukocytosis
Mental status changes
SARS-CoV-2 test positive
Thyroxine free increased
Tremor
Symptomtext
"Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: ""86 YO female with past medical history significant for CAD s/p CABGx2, aortic stenosis s/p AVR, arthritis, DM2 with neuropathy, HLD, hypertension, PVD, and renal artery stenosis, hx of UTIs, with baseline dementia, who presented to ED with progressive weakness and AMS that began 3-4 days ago. She reports that she was sick on the 12/22 from a respiratory infection likely bacteria because she was on antibiotics (unsure which one prescribed in the clinic), but did not require oxygen at home or hospitalization. Since this infection she has not been the same. She has been more week, shaky, and confused. Daughter reports patient has been having loose stools. Denies any falls, recent travels, or sick contacts. She has not been eating and drinking since about Christmas time. She has not had anything to eat or drink today. Denies fever, chills, chest pain, shortness of breath or any other complaints. Initial vitals were stable. Leukocytosis 15.4, elevated glucose, slight increase in Cr from baseline 0.8-1.0, and hyponatremia 130 were noted on labs. TSH significantly decrease <0.01, and free T4 elevated to 2.2. UA negative for infection, but has some hyaline casts. CT head with no acute findings. Per duaghter the patient cannot care for herself at home. She will be admitted to secure placement or establish home care as well as to be worked up and treated for thyroid and electrolyte abnormal labs. Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) Patient was admitted to the medical service. She was given IV hydration. She was treated with insulin for her DM - metformin was held. She was treatedly with methimazole, but this was discontinued. She was considered for an ECF, but covid was positive. Her activity level improved. She was d/c home."""
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- 8,0
- Labordaten
- Covid PCR detected on 01/10/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular CAD (Coronary Artery Disease) s/p CABG Aortic Valve Stenosis s/p AVR PVD (peripheral vascular disease) HTN (hypertension) Hyperlipemia Renal artery stenosis TIA (transient ischemic attack) Endocrine Diabetes mellitus Diabetic peripheral neuropathy Subacute thyroiditis Integumentary Intertrigo Other Sinus tachycardia by electrocardiogram Abnormal head CT Debility COVID-19 virus infection Encephalopathy due to COVID-19 virus
- Andere Medikamente
- acetaminophen (TYLENOL EXTRA STRENGTH) 500 mg tablet Take 1,000 mg by mouth every 8 (eight) hours as needed for Pain. Indications: pain carvediloL (COREG) 12.5 mg tablet Take 1 tablet by mouth 2 (two) times daily with meals. citalopram (
- Allergien
- DyesNausea And Vomiting
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 13.01.2023
- Impfdatum
- 22.12.2022
- Beginn
- 03.01.2023
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain upper
Arthralgia
COVID-19
Chest pain
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 1/3/2023 - 1/5/2023 (2 days) Presentation to the ED: epigastric/left-sided chest and left shoulder pain. COVID + date: 1/3/2023. Treatment: no current indication for remdesivir or steroids. Discharge to: Home. 044A21A 3/9/2021 031B21A 4/5/2021 059H21A 1/6/2022 moderna bivalent AS7166B 12/22/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- MALT-lymphoma, GERD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 18.04.2021
- Beginn
- 10.10.2021
- Tage bis Beginn
- 175,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cardiac failure acute
Cardiac failure chronic
Cardiac failure congestive
Dyspnoea
Respiratory viral panel
SARS-CoV-2 test positive
Symptomtext
Date of Admission: 10/10/2022 Date of Discharge: 10/24/2022 Admission Diagnosis: CHF (congestive heart failure), HA class I, acute on chronic, combined (CMS/HCC) Shortness of breath Hospital Principal Problem (Discharge Diagnoses): COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 14,0
- Labordaten
- 10/11 Respiratory Virus Panel By PCR, SARS-CoV-2 -COVID-19 Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 22.11.2022
- Impfdatum
- 27.12.2021
- Beginn
- 07.11.2022
- Tage bis Beginn
- 315,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Aspiration pleural cavity
Blood culture positive
Blood gases normal
COVID-19
Chest X-ray abnormal
Cough
Culture negative
Device leakage
Device occlusion
Dyspnoea
Gastroenterostomy
Hypoxia
Laboratory test abnormal
Legionella test
Lethargy
Leukocytosis
Lung opacity
Pleural effusion
Symptomtext
COVID + - reported as approximately 10/29/22. Vaccination status - pfizer x2 + moderna x1 BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: MD Admission Date: 11/7/2022 Discharge Date: Nov 9, 2022 Active Hospital Problems Diagnosis Date Noted POA ? Community acquired bacterial pneumonia 11/07/2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Community acquired bacterial pneumonia HOSPITAL COURSE: 46-year-old female with a past medical history significant for cerebral palsy as well as epilepsy presents due to cough and lethargy. Of note, patient had been tested in the outpatient setting and was found positive for COVID-19 approximately 10 days prior to admission and had received paxlovid. She was previously vaccinated. In the ER the patient was hypoxic on room air 87% but did require as much as 7 L at 1 point. Chest x-ray showed a possible left lower lobe infiltrate. Labs were remarkable for leukocytosis. Patient started on ceftriaxone, azithromycin, and thought to warrant admission to the hospital. Patient was able to wean down to 2 L of oxygen during her hospital stay and was continued on this early on. She remained afebrile. Urine Legionella and urine Streptococcus pneumoniae antigens came back negative but she was continued on antibiotics. Although 1 blood culture did come back positive, this was found to be coagulase-negative Staph and was thought to be likely a contaminant. Patient had clinical improvement according to her mother who was at her side throughout her hospitalization. Eventually, the patient was able to wean down to room air oxygen. As the patient had returned almost her baseline state and was on room air and afebrile, she was thought to be appropriate for discharge home on 11/09/2022. She was discharged in stable condition and transition to liquid suspension of antibiotics to complete a 5 day course of antibiotic therapy for possible community-acquired pneumonia. BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: MD Admission Date: 11/13/2022 Discharge Date: Nov 18, 2022 Active Hospital Problems Diagnosis Date Noted POA ? Cerebral palsy 11/13/2022 Yes ? Pneumonia 11/07/2022 Yes ? Focal epilepsy DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Pleural effusion Pleural effusion, left HOSPITAL COURSE: 46 y.o. female with PMHx of severe developmental delay, cerebral palsy, epilepsy who presented with increased work of breathing, gurgling/coughing, and fever of 101.4. Patient lives at home with parents who are her caretakers. She was recently hospitalized 11/07/2022-11/09/2022 with community acquired pneumonia. She was treated with rocephin and azithromycin and discharged on Augmentin which she completed last night. Per mother, the patient was doing well since day of discharge. In the emergency room, the patient was tachycardiac and tachypnic. Labs showed a leukocytosis. Chest xray revealed a left sided complete opacification and large left pleural effusion. VBG was stable. O2 saturations remained in mid 90s on 2L NC. She was admitted to hospitalist. IR and ID consulted. IR performed L thoracentesis. Fluid studies neg for empyema, cultures did not isolate a bacteria. ID was consulted to comment on two separate occasions of blood cultures with staph epidermidis. They state it was likely from difficult venipuncture and contamination with no need to treat. They recommended completing course of antibiotics for PNA with Augmentin, through 11/19. During hospital stay patient also had PGJ tube replaced as it had been leaking. On 11/15 the tube became clogged and IR consulted again for replacement which was done on 11/17. She was evaluated for repeat thoracentesis on left, but no fluid collection and after deep suctioning she returned to her baseline breathing and appeared comfortable to family. Given the working PGJ tube and respiratory stability, she was discharged in stable condition home on 11/18. She will complete Augmentin through 11/19. CONSULTS / RECOMMENDATION: Infectious disease Interventional radiology
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Abnormal EEG Seizure-like activity Nonepileptic episode Focal epilepsy Cerebral palsy
- Andere Medikamente
- Acetaminophen 650 mg Per G Tube Every 6 hours PRN Collagenase 250 UNIT/GM No dose, route, or frequency recorded. Estradiol 0.1 MG/24HR Pttw, 1 patch Transdermal TWICE PER WEEK 0.025 MG/24HR Pttw, No dose, route, or frequency recorded. levOC
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 24.03.2021
- Beginn
- 11.07.2022
- Tage bis Beginn
- 474,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19 pneumonia
Symptomtext
Pt with lung cancer, on chemotherapy, admitted to hospital for covid pneumonia, requiring 2L oxygen, started on remdesivir and steroids
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 12.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Magnetic resonance imaging head normal
Migraine
Tinnitus
Symptomtext
Tinnitus started two days after receiving booster, is constant and has not resolved. Increased migraines, 30+ migraines from date of injection through March. Started nortriptyline which resolved migraines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- MRI Brain 4/22/22 - normal study
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Migraines Iron Deficiency Anemia Vitamin D Deficiency
- Andere Medikamente
- Vitamin D 50,000 IU Elderberry gummy Magnesium
- Allergien
- Latex Aspirin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 01.07.2021
- Beginn
- 01.05.2022
- Tage bis Beginn
- 304,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
Oropharyngeal pain
Paracentesis
SARS-CoV-2 test positive
Symptomtext
was found to be COVID positive with mild sore throat and some shortness of breath persisting after paracentesis but much improved and remains on room air, afebrile, no cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Eczema
Fatigue
Myalgia
Nausea
Oropharyngeal pain
Symptomtext
Severe muscle aches as I had when having Mono, sore throat, extreme fatigue and nausea. Eczema flare up on neck, ears and lower extremities with Prednisone 10mg tabs taken
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma, Eczema, Dormant TB carrier with 6 month of INH preventative drug therapy
- Vorgeschichte
- Eczema, Asthma, Dormant TB, Mono at age 35, history of pneumonia and bronchitis
- Andere Medikamente
- 25MG HYDROYZINE TABS, FLUTICASONE PROPIONATE 0.05% PRN, WOMENS MULTI VITAMIN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 21.12.1921
- Beginn
- 23.12.2021
- Tage bis Beginn
- 36.527,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Insomnia
Mobility decreased
Pain in extremity
Symptomtext
Pain in left arm. intermittent for months after 1st shot (Moderna 036B21A ), 2nd shot (Moderna 023C21A) and booster (Moderna 059H21A). Last pain event so sever, unable to move arm . Took non-aspirin pain reliever just to get sleep. Next morning the pain had decreased, but was still present
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multiple Vitamins, Calcium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Condition aggravated
Diarrhoea
Dizziness
Eye haemorrhage
Eye infection viral
Eye pain
Feeling cold
Headache
Nausea
Oral herpes
Pain
Symptomtext
Headache and dizzy within 2 hours of injection, 8 hours later body aches, teeth chattering chills, headache, dizzy, nausea and diarrhea and left eye pain. Was in bed fully clothed from head to foot covered completely with covers to stay warm all day and night Thursday the 24th, Friday the 25th all the same as Thursday eye pain increasing and fever blisters (cold sores) starting in left nostril and on bottom lip, took Tylenol and Ibuprofen, didn't work. Saturday the 26th, eye pain worse, went back to clinic, was told she saw bleeding in my left eye. Sunday 27th eye pain even worse and travelling to right eye, and headache is only getting worse, called eye doctor, scheduled appointment with him for Monday 28th at 8:10 a.m., says no bleeding in eye(s), but there appears to be a virus most likely from the COVID vaccine that has caused not only the virus in the eyes but flare up of fever blisters (cold sores) prescribed antibiotic and steroid drops for eyes, and extra Acyclovir for fever blisters (cold sores).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- COVID and Flu test done at a facility on Saturday 03/26/22
- Aktuelle Erkrankungen
- Sinus Infection and upper respiratory infection, long haulers from COVID - cognitive, and neurological.
- Vorgeschichte
- Osteoporosis, neck and lower back disk degeneration, blood clot in lung, mild asthma, herpes simplex virus 2 on and around lips, in and around nose.
- Andere Medikamente
- Acyclovir 400 mg.; Low dose aspirin 81 mg.; CoQ10; Omega 3 Fish Oil; Zinc; Vitamin C; B 12; Super B Complex; Turmeric; Biotin; Ginko Biloba; Loratidine 10 mg.
- Allergien
- Cipro, Codiene, Indocin, Lyrica, Sulfa. Seasonal allergies, hayfever.
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphonia
Bronchial irritation
Cough
Dyspnoea
Symptomtext
Patient experienced a dry cough and bronchial irritation the morning following the Moderna booster. Patient lost her voice on day 2. She is having difficulty speaking and pushing out air. Her oxygen saturations remain good.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Adverse reaction to pertussis vaccine
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Joint range of motion decreased
Mobility decreased
Myalgia
Rash
Swelling
Symptomtext
Swelling, rash, & red arm Mobility issues with moving my arm Muscle pain Range of motion has changed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Ibuprofen
- Allergien
- Phenobarbital
- Vorherige Impfungen
- 1st & 2nd dose of Moderna
- Staat
- VA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Decreased appetite
Dyspnoea
Fatigue
Headache
Nausea
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I started with a fever that progressed to fatigue, loss of appetite, diarrhea and a severe headache. So I decided to take an at-home COVID-19 test on 02/17/2022 to see if I had COVID, and it came back positive. So I contacted my doctor and informed them about my positive diagnosis, so I have a virtual appointment on 02/22/2022 at 11:45AM ET to receive further information for treatment and possible medication to help me recover. As of now, I'm still having shortness of breath, a bad headache, nausea, and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 test: 02/17/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Crohn's disease
- Andere Medikamente
- N/A
- Allergien
- Iodine
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 10.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Brain natriuretic peptide increased
Catheterisation cardiac abnormal
Coronary artery occlusion
Coronary artery stenosis
Cough
Dyspnoea
Echocardiogram abnormal
Ejection fraction decreased
Electrocardiogram ST segment depression
Troponin increased
Ventricular assist device insertion
Symptomtext
Patient arrived to emergency department complaining of 3 day history of shortness of breath and coughing. He was found to have significantly elevated BNP and elevated troponins with significant ST depression on EKG. Echo findings included an ejection fraction of 15-20%. Left heart catheterization was performed and found 90% stenosis in left main artery, total occlusion in left circumflex, 99% stenosis in proximal left anterior descending artery, 80% stenosis in mid left anterior descending artery, 50-60% stenosis in proximal right coronary artery, and total occlusion in distal right coronary artery. Impella device was placed and patient was transferred emergently to outside facility for evaluation for CABG.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- psoriatic arthritis rheumatoid arthritis hyperlipidemia tobacco abuse cervical disc disease
- Andere Medikamente
- Albuterol 90 mcg/actuation inhaler PRN atorvastatin 20 mg daily diclofenac 100 mg daily folic acid 1 mg daily HCTZ 12.5 mg daily methotrexate 15 mg once weekly oxycodone 10 mg BID sulfasalazine 1 g BID turmeric root extract 1000 mg BID
- Allergien
- Prednisone
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Dyspnoea
Full blood count
Wheezing
Symptomtext
Vaccine Monday. Thursday felt SOB. Ran during fitness assessment Friday and was seen in the clinic for O2 sat 89%, wheezing. Improved with steroids and beta agonist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Normal CXR and CBC.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Allergic urticaria
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Chest pain
Electrocardiogram normal
Neck pain
Pain
X-ray normal
Symptomtext
Pain developed on the left side of my chest on 2/4/22. The pain is when ever I?m breathing or moving around. It?s especially sharp when laughing, burping, coughing, sneezing. Sitting upright is the most comfortable state to be in. The pain did reach into my shoulder and neck, but has since subsided and now remains in the chest. Treated it with Tylenol and a heating pad to no effect. Went to urgent care on 2/5/22. Vitals were taken, x ray, ecg, and examination were performed. Nothing was reported as abnormal. I was referred to a cardiologist and prescribed naproxen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- X ray and ecg done on 2/5/22.
- Aktuelle Erkrankungen
- Covid 19 at the beginning of January 2022.
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 11.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Pain in jaw
Symptomtext
JAW PAIN AND CHEST PAIN WHICH LASTED COUPLE OF DAYS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Dizziness
Emotional distress
Feeling hot
Malaise
Tremor
Symptomtext
Gave vaccine at about 5:40pm. Patient soon after felt faint, hot and overall not well. Upon observation, she was also shaking and appeared distressed. She was not sure what was happening and probably thought it was anxiety. She didn't have any reactions prior. I talked to her to get her to calm down a little, offered her a lollipop (to increase her sugar intake) and had her sit. She felt better after 15 minutes and she left after verbally confirming she was feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 17.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Condition aggravated
Dizziness
Fatigue
Immunodeficiency
Multiple sclerosis
Muscle spasticity
Symptomtext
Had what acted like an MS flare after most recent full dose #3 (full dose because immunocompromised with B cell depleting agent Ocrevus for MS) with worse dizziness, worse balance, worse spasticity and profound fatigue beginning 1-2 days after vaccination and lasting 3-4 weeks. This happened after dose #2 as well beginning on 4/24/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None. Reported to MS neurologist and PCP.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Multiple sclerosis, migraine, POTS, GERD
- Andere Medikamente
- Ocrevus, Vyepti, pregabalin, protonix, Migrelief, butterbur, ubiquinol, fish oil, flaxseed oil, calcium citrate, magnesium,, multivitamin.
- Allergien
- Cefaclor (hives), tizanidine (hypotension), boswellia (itching).
- Vorherige Impfungen
- after Moderna dose #2 on 4/24/21. Similar to this reaction but lasted longer, about 5 weeks.
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Heart rate increased
Injection site urticaria
Symptomtext
On the 22nd, I experienced shortness of breathe and elevated heartrate, it became worse on the 23rd. That evening, I noticed a large hand size hive at the injection site. I went to the doctor on the 24th and was evaluated by the doctor and was told to come back on the morning on the 25th. My shortness of breathe went away on the 24th, on the 25th the hive receded in size and the doctor state I was clear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Allegra D, Calcium, Magnesium, Zinc, Evening Primrose Oil capsule, Biotin, Vitamin D
- Allergien
- Biaxin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Chills
Dysmenorrhoea
Feeling abnormal
Headache
Heart rate irregular
Menstruation irregular
Pain
Palpitations
Pyrexia
Tachycardia
Vertigo
Symptomtext
12 hours after 2nd dose, 103 fever, body aches, chills, headache for 48 hours. 24 hours-2 weeks after 2nd dose: Tachycardia/irregular heart beat/heart palpitations and extreme vertigo/brain fog. I work at an OBGYN and spoke with one of the NP's who gave me xanax for anxiety. States am having true heart palpitations but marked it off as anxiety. ~1 month post vaccine: Still having issues with my heart beat. Headache and brain fog has not gone away since the vaccine. Now having a menstrual period 2 weeks early with extremely heavy cramping. Am currently saving money to try to see cardiologist. Have a referral for a neurologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- None yet.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Oral birth control
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Food aversion
Headache
Migraine
Myalgia
Night sweats
Pain
Pruritus
Pyrexia
Urticaria
Symptomtext
Around 10 pm aches and muscle soreness were noted. Throughout the night following the booster shot I also experienced chills, fever, very strong headache, and aversion to food. I also got a migraine the next day. These were treated with rest and Tylenol and were resolved. On 1/24/22 I noticed strong itching sensation when I got up at 6 am. It was especially strong on my scalp. Throughout the day I had travelling hives on my body especially my back, neck, chest, and arms. I treated it with 1% hydrocortisone cream which gave temporary mild relief. On 1/25/22 I had more severe hives that appeared and disappeared on various parts of my body, especially my ears, neck, arms, and trunk. I took Benadryl and used the 1% hydrocortisone cream but was still very itch most of the day. The issue has not been resolved at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None at this time.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Migraines, acne.
- Andere Medikamente
- Fish oil supplement and women's multivitamin
- Allergien
- None. Suspected infant allergies to sulfa and suprax but managed sulfa medication fine as an adult. Fall seasonal allergies as a child but grown out of as an adult.
- Vorherige Impfungen
- No reaction other than a sore arm after Moderna shot #1 on 4/5/21. After Moderna shot #2 on 5/3/21 (patient age: 34), I experien
- Staat
- IL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Dyspnoea
Eye swelling
Fluid retention
Inflammation
Musculoskeletal pain
Nerve compression
Pain in extremity
Peripheral swelling
Pruritus
Swelling
Swelling face
Urticaria
Symptomtext
Significant pain & swelling in left arm shoulder to hand lasting 3 days, inflammation & pain spread to shoulder blade & back, pinching nerves, retaining fluid, swollen face & eyes 2 days. On day 12 hives, mostly on left arm, Dr visit. Took Benadryl and daily dose of Xyzal. Prescribed Prednisone 20 mg for 5 days. Day 13 hives spread throughout top 1/2 of body, head to hips. Day 14 hives continued to spread and become more raised, intense itching, shortness of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Na
- Vorgeschichte
- Allergies
- Andere Medikamente
- Zoloft, multivitamin, Xyzal
- Allergien
- Penicillin, pets, environmental
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse event
Dizziness
Injection site infection
Injection site rash
Lymph node pain
Nausea
Nervousness
Pain
Paraesthesia
Symptomtext
Adverse event: Woke up 2 days later feeling dizzy and shaky. She noticed potential infection and rash localized to shot administration. Pain radiating to lymph nodes, tingly fingers and nausea. Treatment: Benadryl for rash; went to urgent care Sunday morning. She was prescribed cephalexin and Zofran. She is considering a doppler if not feeling better by Tuesday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Fibromyalgia
- Vorgeschichte
- Fibromyalgia
- Andere Medikamente
- Claritin
- Allergien
- NSAIDs, Sulfa, Pineapples
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chest X-ray normal
Electrocardiogram normal
Fatigue
Flushing
Headache
Hypertension
Laboratory test normal
Psychomotor hyperactivity
Symptomtext
I went into the Rheumatologist for my routine appt 01/14/2022 and my BP was 193/107. I felt hyper and face was flushed. I had a recheck on the opposite arm (left arm) and it was diastolic 106 to a reading of 131-even while rested it was going up. They sent me to the ER same day around noon a couple of blocks away. They checked my BP again and it was Initially 214/125 and pulse 77 respirations 18 O2 sat 99%. I was prescribed Clonidine 0.01mg 1 time dose. I was kept in the ER and rested about and checked again 149/102. I had a slight headache the whole time but that continued and felt very fatigued. I was discharged and told to f/u with PCP. I did f/u with my PCP and have checked my BP and most are normal, headache went away on the 16th, and just some BP readings high. My PCP is continuing to monitor my BP for the next few weeks. Before this happened my BP was actually running a little low so they did not want to increase my BP medication. I also have been taking Benadryl 50mg at night because my BP runs higher at night and to help me sleep.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- EKG 01/14/2022 Labs 01/14/2022 Chest X-ray 01/14/2022 All results were normal
- Aktuelle Erkrankungen
- Stomach issues some heartburn and IBS symptoms two weeks before.
- Vorgeschichte
- Lupus Dermatomyositis Overlap Syndrome, Chronic back condition
- Andere Medikamente
- Hydroxychloroquine Plaquenil 200MG, Lisinopril 10MG 1x daily, Celebrex 200MG daily, Vitamin D3 2000IU, Juice Plus capsules 2 daily
- Allergien
- Penicillin, Diflucan, Flonase, Seasonal Allergies, Cat Allergies, Not sure if I am allergic to Flu vaccine, I had a huge welt. But I haven't a reaction from the last two.
- Vorherige Impfungen
- I did get a welt one time on my left arm due to my flu vaccine but I have been fine for the last two flu shots.
- Staat
- AL
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest X-ray
Chest discomfort
Chest pain
Computerised tomogram
Costochondritis
Decreased appetite
Dry mouth
Dyspnoea
Electrocardiogram
Fatigue
Gastrooesophageal reflux disease
Muscular weakness
Oesophagogastroduodenoscopy
Pain in extremity
Ultrasound biliary tract
Symptomtext
Two days after receiving vaccine, I had arrived at work and felt the need to take a deep breath. After that, my chest became tight followed by shortness of breath. That evening began having severe reflux with pain at the lower sternum. In the following days chest tightness continued along with shortness of breath and calves became extremely sore. Reported to ED 4 days after symptoms began, cardiology workup and blood work was normal. Lost appetite with dry mouth two days after ER visit and experiencing weakness in arms and legs. Scheduled appointment with PCP. Diagnosed with reflux brought on by the shot. Sent home with meds. That evening extreme chest pain and shortness of breath with fatigue. Went to ED by Ambulance. Blood work, cardiology workup and CT scan were all normal. Sent home with additional medicine. All symptoms persisted until the following week. Saw PCP again to be evaluated for Guillain Barre syndrome; was negative. Sent back home and told to "ride it out". Three weeks post vaccine, still pain in calves, weakness in limbs, random heart burn, tightness in chest and sometimes shortness of breath. Had EGD which was negative and waiting to do a gallbladder ultrasound. Currently also on multiple supplements and OTC meds. Now suspected that I may also have Costochondritis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Chest x-ray, EKG, blood work in ED - 1/2/22 Chest x-ray, EKG, blood work, CT Scan w/ contrast in ED - 1/5/22 EGD - 1/14/22 Gallbladder U/S - 1/19/22
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High cholesterol.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 01.01.2022
- Beginn
- 02.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Gait disturbance
Pain
Paraesthesia
Symptomtext
Extreme weakness, joints and muscles not wanting to function or hold me up. I often need a cane. I am not able to walk far without holding onto something. Pain levels are higher. This started within 24 hours and progressed to its worst within 2 weeks. It's been 18 days and the "buzzing" is at an all time high in my nerves. I haven't contacted a doctor because of the long-term small fiber neuropathy and moving. I do not have a GP set until Feb 4th. I am avoiding people due to the spread of Omicron and COVID-19. Going to call for an earlier appointment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Small fiber neuropathy, clinical depression, PTSD, IBS, chronic sinus infections, severe allergies
- Vorgeschichte
- Small fiber neuropathy, clinical depression, PTSD, IBS, chronic sinus infections, severe allergies
- Andere Medikamente
- Gralise, Celebrex, Ubrelvy, B2, B12, D3, Alpha Lipoic Acid, Acidophilus, CoQ10, Allegra, Guaifenesin, Benadryl, Nasacort
- Allergien
- Lyrica, Nortriptyline, Lexapro, Flonase, Dymista, Cymbalta, Savella, Sprix, severe reactions to allergy shots
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Migraine
Symptomtext
Migraine-like headache; This spontaneous case was reported by a consumer and describes the occurrence of MIGRAINE (Migraine-like headache) in a 34-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Johnson and Johnson COVID-19 vaccine (2nd dose) and Johnson and Johnson COVID-19 vaccine (1st dose). Past adverse reactions to the above products included No adverse event with Johnson and Johnson COVID-19 vaccine and Johnson and Johnson COVID-19 vaccine. On 10-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Jan-2022, the patient experienced MIGRAINE (Migraine-like headache). On 10-Jan-2022, MIGRAINE (Migraine-like headache) had resolved. Concomitant and treatment medication was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chest discomfort
Dyspnoea
Fatigue
Headache
Injection site pain
Rash
Urticaria
Symptomtext
Left shoulder/injection site pain. Pressure around the heart, slight difficulty breathing with exertion, fatigue, headache, joint pain and mild rash/hives.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Borderline hypertension.
- Andere Medikamente
- Amlodipine, Fish oil, Turmeric Curcumin, Red Yeast Rice, CoQ10
- Allergien
- None
- Vorherige Impfungen
- Age 63. Moderna COVID19 2nd dose. 3/4/2021: Lethargy, dizziness, headache, joint pain, liver pain eye pain, cold extremities and
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 16.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Mouth swelling
Pharyngeal swelling
Rash
Swollen tongue
Symptomtext
Severe rash spread all over body. Controle by clinic visit and steroid shots. Rash and swelling made it to mouth, tongue and throat which ended up putting me in hospital due to breathing problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 4,0
- Labordaten
- Unknown at this time.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Amlodipine/Olmesartan 5/40 Fish oil Multi vitamin 50+ age BioTE ADK-5 Testosterone Gel 1.62% 4 pumps a day
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Diarrhoea
Feeling abnormal
Interchange of vaccine products
Retching
Renal impairment
Urine analysis
Vomiting
Tremor
Symptomtext
Violently threw up for several hours. Had to go to the ER. Kidneys shut down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Blook & urine work at Diagnostic labs.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- stress
- Andere Medikamente
- Valacyclovir 500 mg 1 daily (prevention) Amlodipine 10 mg Lithium 150 mg Duloxetine 30 mg 2 daily (am/pm)
- Allergien
- sulfa, bacatracin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Neck pain
Pain
Rash
Vaccination site pain
Symptomtext
The pain is worse with movement and when lifting heavy objects; a little rash like little white dots over this area; chest pain; chest pain is localized to the breast bone, and in his neck area.; Sore left arm; This spontaneous case was reported by a consumer and describes the occurrence of CHEST PAIN (chest pain), NECK PAIN (chest pain is localized to the breast bone, and in his neck area.), PAIN (The pain is worse with movement and when lifting heavy objects), RASH (a little rash like little white dots over this area) and VACCINATION SITE PAIN (Sore left arm) in a 61-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 vaccination. The patient's past medical history included COVID-19 (He stayed overnight in a hospital with that diagnosis, but does not recall receiving any treatments) on 10-Dec-2020, Cough (since before taking the vaccine) and Cold (since before taking the vaccine). On 31-Dec-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Jan-2022, the patient experienced VACCINATION SITE PAIN (Sore left arm). On 02-Jan-2022, the patient experienced CHEST PAIN (chest pain), NECK PAIN (chest pain is localized to the breast bone, and in his neck area.) and RASH (a little rash like little white dots over this area). On an unknown date, the patient experienced PAIN (The pain is worse with movement and when lifting heavy objects). The patient was treated with GUAIFENESIN (MUCINEX) at an unspecified dose and frequency; IBUPROFEN at an unspecified dose and frequency and ALCOHOL at an unspecified dose and frequency. At the time of the report, CHEST PAIN (chest pain) and NECK PAIN (chest pain is localized to the breast bone, and in his neck area.) had not resolved, PAIN (The pain is worse with movement and when lifting heavy objects) and RASH (a little rash like little white dots over this area) outcome was unknown and VACCINATION SITE PAIN (Sore left arm) had resolved. No prior history of myocarditis or pericarditis. No Concomitant medication was reported. Patient had chest pain on 2 JAN 2022 which had continued up until that day. This chest pain was localized to the breast bone, and in his neck area. These was also a little rash like little white dots over this area. The pain was worse with movement and when lifting heavy objects. This case was linked to MOD-2022-448106 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Cold (since before taking the vaccine); Cough (since before taking the vaccine); COVID-19 (He stayed overnight in a hospital with that diagnosis, but does not recall receiving any treatments)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Immediate post-injection reaction
Pain
Paraesthesia
Pyrexia
Symptomtext
Immediately had tingling in your hand and still having the tingling a couple weeks later pain in the area for a couple days had the fever for 2 days body aches and headaches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Patient said that the technician gave her the shot very aggressively and she immediately felt the tingling and still feels it.
- Aktuelle Erkrankungen
- some stomach issues
- Vorgeschichte
- no
- Andere Medikamente
- Vitamin b12 Vitamin k2 calcium multivitamin magnesium vitamin d3 phosphatidylerine
- Allergien
- monistat some contact solutions
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Chills
Erythema
Heart rate increased
Nodule
Pain
Swelling
Symptomtext
Local soreness, redness, knot, swelling Body aches, chills, chest pain, elevated heart rate
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Interchange of vaccine products
Paraesthesia
Symptomtext
Client received the 1st COVID vaccine Janssen 11/30/21. Client reports that approximately 1 hour after receiving his 1st dose he started having left sided numbness and tingly from the shoulder to his waist. Client reports that the symptoms lasted roughly 1-2 days. Client did not follow-up with primary care physician. Client denies any medical underlying conditions, no known allergies, and not currently taking any medications. Client requesting Moderna as a booster dose. At 1346, Co-lead elevated medical consult to Vaccine Operation Team for review. At 1350, Co-lead received response from Dr. approving Moderna Booster Dose. Client notified of the approval and at 1356 Client was administered Moderna Booster Vaccine (Lot #059H21A, Exp 3/27/22). Client was observed and no adverse reactions nor symptoms were noted. Client education on adverse reactions and when to seek care. Client completed observation without complaint and left vaccination center with steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cyanosis
Feeling cold
Pallor
Skin discolouration
Tremor
Vomiting
Symptomtext
Patient turned pale, blue lips and circles around eyes. He started to shake heavily and felt cold. After about 5 minutes he vomited and shook heavily for about 30 minutes. We were able to warm him up with a blanket. He felt better after about 45 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Pain
Paraesthesia
Symptomtext
Developed tingling, numbness, pain and strange pulsating in outer extremities (including calf, foot, forearm, midarm and hand) on same side of body as where the dose of Moderna booster was administered (right). These symptoms developed on 01/06/2022 (2 days after the dose was administered).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Metoprolol, Suboxone, Pantoprazole, Lantus, Humalog
- Allergien
- Ativan, Zoloft
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Diarrhoea
Fall
Mobility decreased
Muscular weakness
Symptomtext
Patient received his booster around 1pm on Monday, January 3rd. His wife said he was still in bed at noon on Tuesday and had severe muscle weakness. He could not get out of bed at all. He then started with severe, uncontrolled diarrhea. He was so weak that he could not get to the bathroom or out of the bed. Wednesday morning the diarrhea had continued and the patient fell. His wife came to the pharmacy around lunch time to report his reaction. She had called his PCP and was told to get Imodium and feed him a bland diet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Wife reports that he was healthy the morning of vaccination.
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye swelling
Fatigue
Hypoaesthesia oral
Lip swelling
Myalgia
Paraesthesia oral
Periorbital swelling
Symptomtext
A patient got her second dose of the Moderna vaccine on 1/4/22 around 4 pm at the pharmacy. The patient called the pharmacy in the morning and said that she woke up with the typical side effects of the booster (muscle aches and tiredness), but also had swelling in her lips and eyes. She said that it started early in the morning and she does not feel any pain but her lips feel a little numb/tingly. She said there is puffiness but no redness. She patient reported no other abnormal side effects and stated that it is just the puffiness/swelling of the eyes and lips that concerned her. She said she isn't having any trouble breathing, rash, dizziness, fast heartbeat, or swelling in the throat. The patient reported no other foods or triggers in the past 24 hours that may have caused the effect. The patient was advised that she should contact her doctor directly for further guidance and monitoring. She was advised that if her symptoms get any worse resembling those of an allergic reaction, she should seek medical help immediately. The patient's doctor was contacted by the pharmacy as well to report the patient's symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None per patient
- Vorgeschichte
- None per patient
- Andere Medikamente
- Unknown
- Allergien
- None per patient
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest X-ray
Chest pain
Electrocardiogram
Pleurisy
Chest discomfort
Dyspnoea
Symptomtext
After getting the booster shot I started having pain in my chest couple hours after shot. Gradually getting worse each day. Ending up in the ER at local hospital. Diagnosis was pleurisy. I've not been sick or do I take any medications. I do not smoke and in very good shape.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Chest X-ray, EKG, and blood work. Jan 1 2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Levaquin
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 24.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Illness
Impaired work ability
Palpitations
Vomiting
Symptomtext
Threw up all the way home. Heart racing uncontrollably. Severely sick for 10 days still recovering - by far worse than any flu. The event has resulted in a working disability hopefully temporarily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- insomnia
- Andere Medikamente
- Seroquel
- Allergien
- lactose intolerant
- Vorherige Impfungen
- Pfiser 2nd dose temp. adverse reaction lasted 3 days
- Staat
- AZ
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 24.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure systolic increased
Chest pain
Heart rate increased
Interchange of vaccine products
Sick relative
Symptomtext
1st two doses were Pfiser had NO side effects. Did not have tooth abscess during either This Moderna booster caused my Systolic Blood Pressure to exceed 200 for 3 days in a row with fast heart rate above 100 putting me in the ER and lucky to survive. My significant other became EXTREMELY sick for 10 days and got her booster the same time I did. We are still trying to recover from 2 weeks ago. What a nightmare! There must be something wrong with that Moderna Lot # and please let us know asap.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 1,0
- Labordaten
- ER for severe chest pain high BP & potential heart attack on 12-28.
- Aktuelle Erkrankungen
- Tooth abscess - active infection at time of booster
- Vorgeschichte
- hypertension
- Andere Medikamente
- Brilinta, Metoprolol. lisinopril
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 28.12.2020
- Beginn
- 28.12.2021
- Tage bis Beginn
- 365,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Breast pain
Breast swelling
Decreased appetite
Dysmenorrhoea
Fatigue
Feeling abnormal
Fluid retention
Illness
Lymphadenopathy
Menstruation irregular
Mobility decreased
Muscle spasms
Myalgia
Pain
Pain in extremity
Somnolence
Swelling
Symptomtext
Within 24 hours of receiving the Moderna booster I became very ill with extreme body aches - joints and muscular. This lasted for 48 hours until I began taking 800 mg of Ibuprofen. I also experienced extreme fatigue, sleeping 10-12 hours a day. I didn't feel well with the first vaccination, was fine with the 2nd vaccination, but this was the worst I had experienced. By the 4th day, the pain was manageable with 800mg of Ibuprofen every 12 hours, but fatigue continues. Starting 24 hours after the shot, my left arm/shoulder had swollen glands all around to the point I couldn't use my arm and felt like I needed a sling to find relief standing because it was painful to hang at my side. The most concerning issue is that despite my menstrual cycle being regular and just ending six days prior, by the 4th day after the shot, my breasts became extremely sore, swollen, and I began cramping. On the 5th day, it's as if I'm having another menstrual cycle with bleeding and cramps. I've also gained six pounds despite not having much of an appetite that seems related to fluid retention. I'm now on the 8th day since my shot, menstruating, swollen, joints aching, and extreme fatigue and brain fogginess.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- I have an appointment with my hematologist scheduled in general to monitor my iron levels, but am calling to make an appointment with my general practitioner.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Low Iron Spinal Stenosis/Degenerative Disc
- Andere Medikamente
- Pristiq 50mg/daily
- Allergien
- Reglan
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Dry mouth
Dyspnoea
Hypersensitivity
Illness
Influenza virus test
Insomnia
Lymphadenopathy
Nausea
Pruritus
Pyrexia
SARS-CoV-2 test
Symptomtext
Neck really itching; Gland on neck; Nausea; Allergic reaction; Fever; Hard time breathing; Dry cough non stop; Dry mouth; Been really really sick; Not sleeping well at all; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (Hard time breathing), COUGH (Dry cough non stop), DRY MOUTH (Dry mouth), INSOMNIA (Not sleeping well at all) and ILLNESS (Been really really sick) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 (had IV for treatment) in August 2021. On 28-Dec-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Dec-2021, the patient experienced INSOMNIA (Not sleeping well at all). On 29-Dec-2021, the patient experienced DYSPNOEA (Hard time breathing), COUGH (Dry cough non stop), DRY MOUTH (Dry mouth), ILLNESS (Been really really sick), HYPERSENSITIVITY (Allergic reaction), PYREXIA (Fever) and NAUSEA (Nausea). On 01-Jan-2022, the patient experienced PRURITUS (Neck really itching) and LYMPHADENOPATHY (Gland on neck). At the time of the report, DYSPNOEA (Hard time breathing), COUGH (Dry cough non stop), DRY MOUTH (Dry mouth), INSOMNIA (Not sleeping well at all), ILLNESS (Been really really sick), PRURITUS (Neck really itching), HYPERSENSITIVITY (Allergic reaction), PYREXIA (Fever), LYMPHADENOPATHY (Gland on neck) and NAUSEA (Nausea) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In August 2021, SARS-CoV-2 test: positive (Positive) Positive. On an unknown date, Influenza virus test: negative (Negative) Negative. On an unknown date, SARS-CoV-2 test: negative (Negative) Negative. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient was on two blood thinners. No treatment information was reported. It was reported that the patient was fine before the shot and went to the doctor on an unspecified date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Name: Flu test; Test Result: Negative; Result Unstructured Data: Negative; Test Name: COVID-19 Test; Test Result: Negative; Result Unstructured Data: Negative; Test Date: 202108; Test Name: COVID-19 Test; Test Result: Positive; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (had IV for treatment).
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dehydration
Flushing
Speech disorder
Symptomtext
Patient left the facility and went to eat at a neighboring restaurant where she lost ability to communicate, became flush, and EMS was called. When we followed up with the patient that same evening, patient states she was treated for dehydration and released from the hospital after receiving IV fluids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- bladder infection
- Vorgeschichte
- COPD, GERD, Depression, neuropathy
- Andere Medikamente
- Tizanidine, gabapentin, rosuvastatin, sertraline, trazadone, folic acid. divalproex ER, advair, d3
- Allergien
- NSAIDS, Penicillins
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse event
Chest pain
Chills
Injection site pain
Pain
Symptomtext
Experienced chest pain, especially on exertion, for 2 days after receiving COVID booster vaccination. Received vaccine on 12/30/21, adverse event began on 12/31/21, continued on 1/1/22. Less in severity on 1/1/22. Accompanied by body aches, injection site soreness and slight chills on 12/31/21. Vaccinated with Pfizer for initial series in December 2020 and January 2021 and received Moderna as booster in December 2021. 23 weeks pregnant at time of booster vaccination, estimated date of delivery April 2022. First pregnancy. Of note I am a pharmacist for a health system.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Ferrous sulfate supplement
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 27.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arrhythmia
Electrocardiogram abnormal
Enzyme activity normal
Full blood count
Heart rate increased
Palpitations
Sinus arrhythmia
White blood cell count normal
Symptomtext
Within 24 hours of receiving my booster, I had a sudden onset of heart palpitations and a racing heart. My pulse was around 100 BPM and would not go down. I could tell I was experiencing arrhythmia. It was diagnosed yesterday from the Hospital to be Sinus Arrhythmia. I had an EKG, complete blood comprehensive panel and checked my blood enzymes. The enzymes were excellent. There was no indication of myocarditis or pericarditis. Based on my blood work, my white blood cell count was normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- I had an EKG, complete blood comprehensive panel and checked my blood enzymes. The enzymes were excellent. There was no indication of myocarditis or pericarditis. Based on my blood work, my white blood cell count was normal. The EKG indicated sinus arrhythmia.
- Aktuelle Erkrankungen
- I was not experiencing any illness
- Vorgeschichte
- I have high blood pressure (controlled); high cholesterol (controlled); arthritis in my knee; my right knee replaced; left hip replaced
- Andere Medikamente
- Metoprolol; Lisinopril; HCTZ; Atorvastatin; Acyclovir; Vitamin D; Zinc
- Allergien
- I do not have any allergies
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Incorrect route of product administration
Injection site pain
Mobility decreased
Pain
Symptomtext
Patient said shot was painful at time of administration. He said, in about 4 hours, he could not move his arm and was in extreme pain so he went to the emergency room. The doctor there told him that it looked as if the shot was given too high on the arm. He was prescribed an anti-inflammatory but is still complaining of pain today(monday 12/20)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- not known
- Vorgeschichte
- not known
- Andere Medikamente
- not known
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 02.08.2023
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Aphasia
Musculoskeletal stiffness
Pyrexia
Symptomtext
stiffness of my neck and shoulder; Not able to speak; Alopecia; fever; This spontaneous case was reported by a patient and describes the occurrence of ALOPECIA (Alopecia), MUSCULOSKELETAL STIFFNESS (stiffness of my neck and shoulder), APHASIA (Not able to speak) and PYREXIA (fever) in a 37-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 prophylaxis. The patient had no medical history, concomitant disease or risk factor. On 13-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 14-Jan-2022, the patient experienced PYREXIA (fever). On 27-Jan-2022, the patient experienced ALOPECIA (Alopecia). In July 2022, the patient experienced MUSCULOSKELETAL STIFFNESS (stiffness of my neck and shoulder) and APHASIA (Not able to speak). At the time of the report, ALOPECIA (Alopecia) had not resolved and MUSCULOSKELETAL STIFFNESS (stiffness of my neck and shoulder), APHASIA (Not able to speak) and PYREXIA (fever) outcome was unknown. Concomitant medication was not reported. Patient had fever next day after booster shot. 2 weeks later, had alopecia on beard and 2.5 month later, had alopecia on hair. It was still continuing as of 28-Jul-2023. In Jul-2022, patient was not able to speak and had sever stiffness of neck and shoulder. Treatment medication was not reported. It was unknown if the patient experienced any additional symptoms/events. There were no lab data/results available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no medical history, concomitant disease or risk factor.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 02.06.2023
- Impfdatum
- 07.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Rash
Urticaria
Symptomtext
recurrent daily urticaric rash controlled with antihistamine BID dosing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 21.01.2022
- Beginn
- 27.08.2022
- Tage bis Beginn
- 218,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Anti-cyclic citrullinated peptide antibody
Arthralgia
Arthroscopy
Bacterial test
Borrelia test
Full blood count
Joint swelling
Laboratory test
X-ray
Symptomtext
Severe chronic joint pain in right knee, left ankle, and left hip. Also, severe chronic swelling in right knee and left ankle. Has lasted for over five months. Still no official diagnosis or cause. Have had breast implants (silicon) for three years. Just had them removed a couple of weeks ago. Believe it's from the implants, not the vaccine, but am unsure at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- CBC, CCP antibody, Lyme disease test, bacterial infection test (multiple times), RA, knee scope, and x-ray.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- NP Thyroid 90mg, Zinc, B vitamin, magnesium
- Allergien
- Wheat, eggs, tomato, some nuts
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 22.12.2021
- Beginn
- 28.08.2022
- Tage bis Beginn
- 249,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test abnormal
Dysphagia
Heart rate increased
Hyperthyroidism
Insomnia
Neck pain
SARS-CoV-2 test negative
Thyroid function test abnormal
Thyroxine increased
Tri-iodothyronine increased
Ultrasound scan
Symptomtext
I received my 3rd dose on 12/22/2021. After 1 year my adverse event started on 08/28/2022 in the morning around 8:00AM I felt pain in my neck. I couldn't swallow. I didn't think much about it. I went to a doctor who did a blood test. My thyroid level was high. My T3 and T4 was high. I had fast heartbeat. I had difficulty sleeping. I was experiencing Hyperthyroidism. I had 4 blood test and 1 ultrasound. My doctor prescribed me atenolol for about 1 week. By the 3rd blood test all of my symptoms resolved. This is the first time it happened to me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- 22DEC2022 COVID-19 test negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 21.11.2022
- Impfdatum
- 21.11.2021
- Beginn
- 21.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Incorrect route of product administration
Pain
Symptomtext
Patient called the pharmacy on 11/21/2022 and stated that he has been in pain since he got the shot last year. He stated that the pharmacist may have gave him the shot between the shoulder and joint. He complains of numbness and serious pain which he has seen a doctor for. He claimed an EMT was done and that his PCP recommended rehab.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- acid reflux hyperlipidemia hypothyroidism BPH
- Andere Medikamente
- Tylenol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 23.09.2022
- Impfdatum
- 26.01.2022
- Beginn
- 03.09.2022
- Tage bis Beginn
- 220,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
SARS-CoV-2 test positive
Symptomtext
Tested COVID positive, symptoms include cough and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- 3,0
- Labordaten
- Nasopharyngeal test and nasal swab collected 9/03/2022 detected 2019 Coronavirus RNA on 9/03/2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular disease.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 10.01.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 168,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Headache
Nasopharyngitis
Pain in jaw
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
On June 27, 2022 I tested positive for COVID-19. Four days before I had a really bad cold. I had headaches, my jaw was hurting, runny nose, and a bunch of coughing. I ran a low-grade fever the following days. I contacted my doctor and they sent me a z pack and that did not help so I started taking my asthma medicine to help with my breathing. I kept testing positive for a week and a half.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- June 27, 2022 tested positive for COVID-19 Prescribe a Z Pack
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma Diabetes
- Andere Medikamente
- Zertec Samotidine Benadryl Steels oftener Fiber supplements Adviarhfa Inhaler as needed Singular Spirivarestimat
- Allergien
- Codeine Sulfa Naproxen
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 18.03.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 298,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Frustration tolerance decreased
SARS-CoV-2 test
Tinnitus
Headache
SARS-CoV-2 test positive
Symptomtext
This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (a week after getting the booster, I tested positive for COVID/mild COVID/a week after that I got a really bad headache for one day), TINNITUS (tinnitus started on that day and hasn't gone away/it's there 24/7/worse at night when I try to lie down/it's very pronounced for the first 1.5 hours in the morning/still dealing with it/signals in her brain are pulling this sound) and FRUSTRATION TOLERANCE DECREASED (it was extremely depressing when I found out that ENT couldn't help me) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 059H21A, 044B21A and 045A21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 15-Apr-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to .5 milliliter. On 03-Jan-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 10-Jan-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced COVID-19 (a week after getting the booster, I tested positive for COVID/mild COVID/a week after that I got a really bad headache for one day). On 17-Jan-2022, the patient experienced TINNITUS (tinnitus started on that day and hasn't gone away/it's there 24/7/worse at night when I try to lie down/it's very pronounced for the first 1.5 hours in the morning/still dealing with it/signals in her brain are pulling this sound) and FRUSTRATION TOLERANCE DECREASED (it was extremely depressing when I found out that ENT couldn't help me). At the time of the report, COVID-19 (a week after getting the booster, I tested positive for COVID/mild COVID/a week after that I got a really bad headache for one day), TINNITUS (tinnitus started on that day and hasn't gone away/it's there 24/7/worse at night when I try to lie down/it's very pronounced for the first 1.5 hours in the morning/still dealing with it/signals in her brain are pulling this sound) and FRUSTRATION TOLERANCE DECREASED (it was extremely depressing when I found out that ENT couldn't help me) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 10-Jan-2022, SARS-CoV-2 test: (Positive) Positive.- No concomitant medications was reported. The patient had gone to the ENT but has not had any luck diagnosing or treating her symptoms. Her ENT had dismissed this stating that the signals in her brain are pulling this sound up based on a childhood memory. Patient said that the pitch of the tinnitus was like crickets chirping at night time. Event headache was the reported symptom of COVID-19. No treatment medications was reported. Company Comment: This is a spontaneous case concerning a 51-year-old, female patient with no reported medical history, who experienced the unexpected non-serious events of (AESI) Covid-19, Tinnitus and Frustration. The event Covid-19, occurred 7 days after the third dose of mRNA-1273 Vaccine. While the events Tinnitus and Frustration occurred 14days after the third dose of mRNA-1273 Vaccine. Patient tested positive for SARS COV-2. No further details on clinical course and treatment received were reported. The events were reported as not resolved. The benefit-risk relationship of mRNA-1273 Vaccine, is not affected by this report. Sender's Comments: This is a spontaneous case concerning a 51-year-old, female patient with no reported medical history, who experienced the unexpected non-serious events of (AESI) Covid-19, Tinnitus and Frustration. The event Covid-19, occurred 7 days after the third dose of mRNA-1273 Vaccine. While the events Tinnitus and Frustration occurred 14days after the third dose of mRNA-1273 Vaccine. Patient tested positive for SARS COV-2. No further details on clinical course and treatment received were reported. The events were reported as not resolved. The benefit-risk relationship of mRNA-1273 Vaccine, is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220110; Test Name: Covid-19 virus test; Test Result: Positive; Result Unstructured Data: Positive.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.08.2022
- Impfdatum
- 31.12.2021
- Beginn
- 22.04.2022
- Tage bis Beginn
- 112,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test
Biopsy skin abnormal
Blood test
Guttate psoriasis
Hypersensitivity
Injection related reaction
Lip swelling
Rash
Skin test positive
Symptomtext
severe face, neck rash, extreme swollen lips, no preg
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- series of steriods, antibiotics, cortisone cream, dupexent, patch test, allergy blood work-up, over 3 months beginning April 21 through August 27, 2022. Food allegies normal high for cows mild ( I don.t drink milk);, patch test pos for neosporum; severe allergic reaction 3 days after the dupenent 3rd injection, rash arms, legs, neck, face. Biopsy of the right upper extremity Aug 27, 2022, pos for gut psorisis (way different rash than the original face/neck rash, had a severe reaction to the 3rd Dupexent shot
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- in good heath
- Andere Medikamente
- none
- Allergien
- severe hives, rashes on face and neck, severe swelling lips, mostly lower lip
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 04.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Injection site erythema
Injection site induration
Injection site pain
Injection site rash
Injection site warmth
Pyrexia
Symptomtext
Fever, chills, headache, fatigue - began about 12 hours after injection and lasted until approximately 36 hours after injection. Red, sore, painful, hard, hot rash at injection site - began about 12 hours after injection and has not subsided even after 56 hours after injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- allergic to penicillin
- Vorherige Impfungen
- fatigue, fever, chills after 2nd dose of Pfizer vaccine, subsided within 36 hours.
- Staat
- -
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 22.12.2021
- Beginn
- 30.07.2022
- Tage bis Beginn
- 220,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Cough
Fatigue
Pyrexia
Symptomtext
fatigue, fever, cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 31.07.2022
- Impfdatum
- 22.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Pruritus
Symptom recurrence
Urticaria
Symptomtext
Skin itchiness and light hives along with dermatographia began appearing all over my body a couple days after receiving the Moderna booster shot. I was prescribed once daily Fexofenadine 180mg after reporting symptoms to my doctor, neither me or my doctor had suspected the vaccine as the cause of this, but some other possible allergen was never determined. The allergy medicine gets rid of the symptoms, but without taking it they return just as bad as when they started.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Sertraline - 150mg Trazodone - 50mg
- Allergien
- G6PD Deficiency
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 24.02.2021
- Beginn
- 10.07.2022
- Tage bis Beginn
- 501,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
COVID-19
Cough
Pain
SARS-CoV-2 test positive
Symptomtext
Pt admitted for right hip pain, but no acute fracture or dislocation. Pt is COVID positive with a mild cough that is nonproductive and some generalized body aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 11.01.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 100,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cough
Disturbance in attention
Fatigue
Influenza A virus test negative
Influenza B virus test
Night sweats
Productive cough
Pyrexia
SARS-CoV-2 test negative
Sneezing
Streptococcus test negative
Symptomtext
Possible breakthrough case of COVID-19. Symptoms began April 21, dry occasionally productive cough, sneezing, fatigue, trouble concentrating, fever over 104F, extreme night sweats. Fever controlled with Advil, Tylenol had little effect. Fever subsided evening of April 26, after 24 hours unmedicated fever free ended quarantine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid at-home tests on April 20, two on 21,22 - all negative. COVID-19 PCR test, strep, influenza A and B on April 23 at urgent care - all negative. Covid at-home tests on April 27 and 28 - both negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 31.12.2021
- Beginn
- 25.06.2022
- Tage bis Beginn
- 176,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Myalgia
Oropharyngeal pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
I just had a sore throat, muscle aches, runny nose, sneezing. My fever got to 101.2. This lasted for about 2 days. It definitely was not severe. I feel much better today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- PCR test positive. At home test positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D3; biotin
- Allergien
- Iodine IV; penicillin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Joint range of motion decreased
Symptomtext
Per PCP report, client reports pain in left deltoid region with decreased shoulder range of motion since he received his Moderna vaccine on 3/25/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- bilateral foot deformity, obesity, hypertension
- Andere Medikamente
- hydrochlorothiazide 25 mg 1 tablet by mouth daily
- Allergien
- cat dander mold
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Humerus fracture
Injection site pain
Loss of personal independence in daily activities
Pain
Symptomtext
Soreness in left arm from injection site (patient claims to be high) and any range of motion. This includes reaching up, scratching neck, reaching back, putting on clothes, turning/mopping, and general daily activities. Left arm is compound fracture of humorous. Patient has titanium plate roughly 8 inches long. No issues in the past with any other immunizations. First time receiving a vaccine in left arm. This has been going for for roughly 5 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- NO DRUGS WERE BEING TAKEN AT THE TIME OF VACCINATION
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 18.05.2022
- Impfdatum
- 03.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Rash papular
Scratch
Urticaria
Symptomtext
Since 14 February he has complained of recurrent episodes of generalized itching and rashes described as raised, red, itchy welts which can occur anywhere on his body, especially at sites of pressure or where his skin is scraped or scratched. Lesions last less than 24 hours, affected his palms and soles, and resolve without post-inflammatory changes. He denies laryngeal, pulmonary, GI, neurologic, and cardiovascular symptoms with these episodes. Episodes not associated with heat, exercise, sweating, cold, foods, medications, NSAIDs, IV contrast, latex exposure, known infections, or insect bites/stings. He received his Moderna COVID-19 vaccine booster dose on 3 February, 11 days prior to onset of symptoms. He has used oral antihistamines with benefit. He denies constitutional symptoms. UCT score today is 20 (2, 2, 3, 3, 1, 4, 2, 3). No history of adverse reactions to prior vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- 1) Myopia 2) PFB
- Andere Medikamente
- None
- Allergien
- Sulfa antibiotic (by report, does not recall reaction). No known food, latex, or venom allergies.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 27.01.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 42,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Lymphadenopathy
Nausea
Ultrasound lymph nodes
Symptomtext
Okay, I was like really nauseous about 10 hours after, I had that for a couple of days, I vomited a couple times and I had the chills as well. It was not that different from my other two doses. Until I got the enlarged lymph nodes around 03/11/2022. I noticed it when I was taking a shower. The only other time I had an enlarged lymph node that lasted a few days within my 1st vaccine and it was very painful at the time. I could not even lift my arm really. The node after the 3rd dose took like 3-4 weeks to go down slowly. The doctor posterior cervically lymph adenopathy, he feels a reactive lymph node and feels it is not cancer. Repeat ultrasound is scheduled in about 2 weeks. I do not feel anything currently, I think it went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Ultrasound, posterior cervically lymph adenopathy.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 28.12.2021
- Beginn
- 11.05.2022
- Tage bis Beginn
- 134,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vomiting
Symptomtext
vomiting, positive COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 15.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Diarrhoea
Fatigue
Nausea
Retching
Vomiting
Symptomtext
The next day after vaccine, I felt tired. I started getting chills, very nauseous. I then started vomiting. I could not even keep down water. I tried treating at home with Pedialyte and I still kept throwing up. I threw up about 4 more times. I did not have anything to vomit and had dry hives. I ate breakfast the next morning and kept vomiting more. I did a telehealth visit and they said it could be the vaccine. The day after that, I had more vomiting and diarrhea on until the night. This stopped on 1/20/2022 but the weakness continued until 1/22/2022. I also did a follow up with my doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Autoimmune disease
- Andere Medikamente
- Metformin
- Allergien
- Penicillin; Levaquin; peanuts
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 17.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Blood glucose increased
Decreased appetite
Dizziness
Extra dose administered
Nausea
Vertigo
Symptomtext
Two days following injection I was light headed, loosing balance and room circling. vertigo. Symptoms went away next day, but today the symptoms are back and worse... this is day 4. I am also nauseated and lack of appetite. I am afraid to walk without holding onto a wall for furniture. I had three previous injections with no problems, this was my second booster shot. Is this unusual and how long may it last?
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Blood pressure was fine. Suger a little high this morning but had a late dinner yesterday. My diabetes had been under control with my medication.
- Aktuelle Erkrankungen
- Diabetes
- Vorgeschichte
- History of bladder cancer with surgery Nov. 2019, Gallbladder removed Sept. 2021 Several back operations, screw in C2-3 after auto accident. Bilateral knee replacements.
- Andere Medikamente
- Losartin 25 mg. one daily, Metformin 1000 twice a day, Glimepride 2mg once daily, Low dose aspirin daily, Rosuvastatin 20 mg 1 daily, Vitamins: Folic acid 400 mg 1 daily, B12 1000 mg 1 daily, D3 25 mcg. 1daily, Fish Oil 1200 1 daily.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 15.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Fatigue
Feeding disorder
Haemoglobin decreased
Hypersomnia
Muscular weakness
Night sweats
Splenomegaly
Symptomtext
I on march 22nd, 2022 my temperature went up to 102 and remained for 4 days. I was unable to eat, had night sweats, fatigue and muscle weakness. I was taking multiple 2 hour naps. With lymphoma I have my blood drawn each month. My hemoglobin was on 13 grams usually. On Monday 04/11/2022 my hemoglobin was just under 9 grams. I am feeling good today and normal. My spleens enlarged in March by 2 centimeters. It still is technically within normal limits.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Splenic Marginal Zone Lymphoma; Congenital hemolytic anemia (had it since I was 11 years old)
- Andere Medikamente
- 3200 micrograms of Folic acid, Ocuvite, Vitamin D3 125% of RDA.
- Allergien
- Mild allergy to Eggs; Amoxicillin; Tetracycline; Tetanus booster
- Vorherige Impfungen
- Tetanus Booster, 1980
- Staat
- SC
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 11.02.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 57,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Heavy menstrual bleeding
Symptomtext
As a user of the hormonal birth control, Mirena IUD, I do not have monthly menstruation which has been consistent over the length of 9 years of use of IUD. On 03/09/2022 experienced sudden and heavy vaginal bleeding after 9 years of monthly menstruating not occurring while being prescribed and using Mirena IUD birth control. Heavy and unusual bleeding accompanied by intense abdominal cramps has not subsided for a period of 5 days. Bleeding amount and duration is also inconsistent with prior menstrual history without birth control, in which pervious periods where light- 3 to 4 days of bleeding with minimal to no cramps.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- To be updated once doctor appointment concludes
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None
- Andere Medikamente
- Mirena IUD
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 24.03.2022
- Impfdatum
- 28.12.2021
- Beginn
- 14.01.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation reaction
Pruritus
Urticaria
Symptomtext
My first 2 Moderna vaccines did not give me any adverse reactions. It was upon my 3rd (booster) dose that I noticed some strange symptoms right about 2 weeks following the shot. The first symptom was an itchy scalp, legs, and palms. This went on for about a day before I noticed that I was developing hives in my groin area, scalp, hands, legs, and some patchy spots on my abdomen. I did not initially link it to possibly being a vaccine reaction, and took Benedryl to lessen the symptoms. After about a week of on and off taking Benedryl, which helped greatly but made me constantly drowsy, I switched to a non-drowsy Zyrtec. It is important to note that I had no change in diet, activity, clothing, food, no new medications or supplements, no changes in soaps or detergents (I am a creature of habit and routine). I did not immediately inform a medical professional as the symptoms, while persistent, have been lessening (though at a painstakingly slow rate). Just recently I visited Dr. and informed him of the situation, to which he referred me to this site to report my symptoms. At this time, it has been roughly 3 months of symptoms. Half a dose of Zyrtec once a day allows for the symptoms to almost completely disappear. Though, if I scratch or irritate my skin even mildly (even just scrubbing lightly in the shower) , hives will appear for a few minutes before dissipating again. I am going tomorrow for blood work as well. I am currently off Zyrtec per my doctor as to not skew the bloodwork. I've noticed some hives come and go but not as intense at it was 3 months ago. It seems this reaction is extremely slow to work out of my system. I've never experienced any reaction like this before in my life and the only change that I can think of was the booster shot. I hope that you can find this information helpful in the event others may be experiencing similar symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 19.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Peripheral swelling
Rash
Symptomtext
Patient had redness by the injection site. Patient also stated her bicep is twice the size. Lastly patient has rashes on her body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Phentermine 30mg Junel 1/20
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Limb discomfort
Pain in extremity
Peripheral swelling
Symptomtext
swelling in their arm/ sometime swells up; wants to know what's its making arm felling wrong. tiered of hurting/ arm hurts so bad; This spontaneous case was reported by a consumer and describes the occurrence of PERIPHERAL SWELLING (swelling in their arm/ sometime swells up), LIMB DISCOMFORT (wants to know what's its making arm felling wrong.) and PAIN IN EXTREMITY (tiered of hurting/ arm hurts so bad) in an 81-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059h21a) for COVID-19 vaccination. Concurrent medical conditions included Cholesterol. On 31-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In January 2022, the patient experienced PERIPHERAL SWELLING (swelling in their arm/ sometime swells up), LIMB DISCOMFORT (wants to know what's its making arm felling wrong.) and PAIN IN EXTREMITY (tiered of hurting/ arm hurts so bad). At the time of the report, PERIPHERAL SWELLING (swelling in their arm/ sometime swells up), LIMB DISCOMFORT (wants to know what's its making arm felling wrong.) and PAIN IN EXTREMITY (tiered of hurting/ arm hurts so bad) had not resolved. Concomitant drugs included cholesterol medicine. It was reported that patient was planning to take X-rays for the arm and visited orthopedic doctor. It was reported that the events worsened. Treatment medications were not provided. This case was linked to MOD-2022-510135, MOD-2022-510205, MOD-2022-510214 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cholesterol.
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 28.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test negative
Rash
Urticaria
Symptomtext
patient has had reoccurring rash/hives
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- patient states she was referred to allergist who performed allergy testing and everything came back negative
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- mixed hyperlipidemia, vitamin d deficiency, hypertension, coronary atherosclerosis, supraventricular tachycardia, heart valve replacement, OSA,
- Andere Medikamente
- aspirin, calcium, Cardizem, loratadine, multivitamin, nitroglycerin, rosuvastatin, vitamin d
- Allergien
- codeine, penicillins, sulfa antibiotics, tree nuts
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 05.03.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amblyopia
Headache
Injection site induration
Injection site pain
Injection site swelling
Muscle spasms
Vomiting
Symptomtext
1. Pain, swollen, and hard at the injection site. 2.vomitting 3. Headaches, 4. Lazy Right eye, and spasms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/a
- Andere Medikamente
- Tylenol
- Allergien
- N/a
- Vorherige Impfungen
- Dizziness, headaches, nausea, and vomiting. Age: 33 yrs old Moderna vaccine 1 and 2 Date: 1st dose: 08/14/21 2nd dose: 09/
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 24.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Urticaria
Symptomtext
Starting approximately one week after my Moderna booster, I started to experience daily rash / hive flare ups at various areas of my body. The flare ups and hive patch outbreaks continue to this day and are ongoing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitex (chaste) berry supplement
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 07.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Lethargy
Menstruation delayed
Menstruation irregular
Pain
Pyrexia
Symptomtext
Delayed Menstrual cycle. Menstrual cycle began in between doses of the COVID19 vaccine (1st dose: 12/07/2021). Cycle start date was 12/21/2021 and lasted 47 days, 19 days longer than typical. The second menstrual cycle post vaccination has also been irregular, with cycle start date 02/06/2022 and is currently delayed longer than typical, by two days and counting. Other non-menstrual adverse effects: headache, fever, body ache, lethargy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 03.03.2022
- Impfdatum
- 17.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Computerised tomogram abnormal
Pancreatitis
Symptomtext
Stomach pain 3 days after I got the booster. Got diagnosed with pancreatitis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Got a cat scan done that's how they determined I had pancreatitis
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes, back pain
- Andere Medikamente
- None
- Allergien
- Keflex , walnuts , pecans
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 11.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adverse reaction
Erythema
Rash pruritic
Skin warm
Swelling
Type IV hypersensitivity reaction
Symptomtext
Patient received her first dose of Moderna shot intramuscularly in her left arm on 01/11/2022. She reported today 02/28/22 that she experienced delayed adverse reactions one week after getting the shot. The adverse reactions experienced were an itchy rash on the left arm, right arm and torso; hotness, redness and swelling the size of a tennis ball on the left arm. She reported a telehealth visit with her doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash pruritic
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Lamictal, Sulfa Drugs, Doxycycline, Monistat, Bacitracin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal discomfort
Asthenia
COVID-19
Decreased appetite
Diarrhoea
SARS-CoV-2 test positive
Sluggishness
Somnolence
Symptomtext
Next day after the shot, I had upset stomach and diarrhea. That following Thursdays I became sluggish and drain. I went to the hospital tested positive for COVID. I didn't have a appetite and only wanted to sleep.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Sertraline
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Pruritus
Urticaria
Symptomtext
Ten days post Moderna booster, scalp and ears began itching / tingling (mid morning). Within 30 minutes, hives on scalp and ears began, lymph nodes on back of neck were swollen and sore. Palms of hands became intensely itchy, hives began showing up on inner arms and wrists, thighs, stomach, and back. Hive patches seemed to move and became much worse when itched. I started by taking Benadryl. It helped a bit, but not much. Went to general physician one day after onset of symptoms, was told to take antihistamines, no known cause. Daily after the doctor visit, I take 180mg fexofenadine (am), 10mg famotidine (once am, once pm), and 10mg cetirizine (pm). I still have very itchy skin, but no hives. Dermatographia is everywhere, but worse on limbs and stomach. Flares happen in the evening. No other allergies, no difference in product use or foods. Will see allergist / immunologist shortly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- None yet. Bloodwork to be completed in April.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none apart from infrequent migraines
- Andere Medikamente
- Women's once a day supplement, vitamin C, vitamin D, magnesium, spironolactone, Ubrelvy as needed (once per month, usually)
- Allergien
- Possibly sulfa antibiotics, nothing else.
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 08.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Urticaria
Vaccination complication
Symptomtext
Ten days after booster began with hives all over my head,neck,stomach,arms, Palma of hands and feet. I was seen four times by provider we tried prednisone with some relief but returned after done. Zertec twice a day with acid reducer as well. Sent to dermatologist where they confirmed it was from booster. Was instructed to take up to four zertec a day. Periodically I have been taking Benadryl as well. I continue to have hives and dermagrapgia to this day but still taking zertec
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Ulcerative colitis, anxiety, kidney stone
- Andere Medikamente
- Sulfasalzine, sertraline, folic acid, Simvastatin, vitamin d3
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 19.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 15,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Symptomtext
Dermatographia that started 15 days after the third covid vaccine (the booster). Has been ongoing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- None - self diagnosed
- Aktuelle Erkrankungen
- Common cold
- Vorgeschichte
- None
- Andere Medikamente
- Multi-vitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site discomfort
Injection site pain
Symptomtext
patient reported today via phone that she is still having a throbbing and burning sensation at the injection site but it is not a visible reaction, and its been past the 7 to 10 days that usually these types of symptoms resolve so i advised her on that and to contact her pcp to see if they want to see her or have any suggestions for her.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discomfort
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 31.12.2020
- Beginn
- 22.01.2022
- Tage bis Beginn
- 387,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Nasal congestion
Pain
Sneezing
Throat irritation
Symptomtext
Scratchy throat, bronchial pain, sneezing, coughing, stuffy post nasal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure, high cholesterol
- Andere Medikamente
- Zetia, Lisinopril, multivitamin, vitamin D, red yeast rice, COQ10, probiotic, ashwaghanda, Zyrtec, fish oil, colace, Ristela
- Allergien
- Reglan
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Muscular weakness
Pain in extremity
Phlebitis
Pruritus
Rash
Symptomtext
Patient reports sx beginning hours after vaccination. Sx include: rash on R arm and bilateral legs, GI upset, intermittent Itching all over her body, swollen, bulging veins all over, L arm weakness and pain. She did not seek medical attention even though she was advised. She said there was too much traffic. She was also advised to take Benadryl and she states she didn't know what that was and didn't have any. Most of the symptoms have subsided and has an appointment to see her doctor tomorrow 02/15/2022 at 8am. I advised her to call me after her appointment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism Hypertension
- Andere Medikamente
- levothyroxine 100mcg 1 QD losartan 100mg 1 QD Vitamin C 1000mg Calcium Citrate 500mg + Magnesium 80mg + Zinc 10mg Vitamin E 180mg Magnesium 400mg Vitamin D3 200mg Calcium 1200mg Vitamin B-12 1000mcg Super B Complex Co Q 10 300mg
- Allergien
- IVP dye - anaphylaxis Alendronate 70mg - dizziness and GI complaints
- Vorherige Impfungen
- 60 years ago Yellow Fever swollen arm and fever
- Staat
- WI
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 13.02.2022
- Impfdatum
- 21.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 11,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Blister
Erythema
Erythema multiforme
Eye pruritus
Fatigue
Gait disturbance
Pain in extremity
Peripheral swelling
Pharyngeal swelling
Pruritus
Rash
Rash erythematous
Skin lesion
Urticaria
Symptomtext
Severe skin itching started 1/26/2022. Symetrical full body rash started 2/1/22, red target lesions. Swollen hands, feet and thighs, redness started 2/3/22. Seen at walkin 2/4/22, diagnosed with urticaria started on prednisone. Throat thickness. Difficulty walking from severe foot pain. Severe hand pain and knee pain. Extreme fatigue. Itchy eyes. Blister lesions right wrist. Seen again by PCP on 2/10/22 diagnosed with erythema multiforme.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma, seasonal allergies, depression, anxiety
- Andere Medikamente
- montelukast 10 mg daily, sertraline 50 mg daily, vitamin c 500mg daily, fiber capsule daily, fexofenadine 180 mg daily, melatonin 10mg night, midnight sleep aid
- Allergien
- pseudoephedrine
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Rash
Urticaria
Symptomtext
On 1/22/2022 I woke up and I had little bumps all over my body. I thought it may of been bug bites or something since it was so long after the vaccine. The bumps turned into hives, I tried to use cortisone cream but it didn't help. I started taking Zyrtec, I was having to take it twice a day to keep the hives away, they lasted for about 1 week. I am still having to take the Zyrtec 1xday to keep the hives away, if I don't take it they come back. I went to the health clinic at my college and I was advised that I had dermatographia. I was just advised to keep taking the Zyrtec.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Birth Control ( Xulane ) / Change out birth control patch 1x a week.
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Lip swelling
Swollen tongue
Urticaria
Symptomtext
patient called the day after getting her moderna booster shot and said she had hives and swelling of lips and tongue.she said she took an otc allergy med she thought was benadryl(generic). she was told to go to the er. after checking on the patient the next day the patient said she got bloodwork and vitals taken at the er but left as there was a lot of people there and she took more benadryl. the patient said the hives seemed to be getting better and she was feeling better than before
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- bloodwork/vitals at er
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- hydroxyzine effexor tramadol seroquel lopressor ventolin lipitor
- Allergien
- no known allergys
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Burning sensation
Erythema
Loss of personal independence in daily activities
Mechanical urticaria
Pruritus
Rash
Sleep disorder
Symptomtext
Intense burning, itching, redness all over body starting approx 10 days after injection. Could not be controlled with oral antihistamines, was interfering with daily life and sleep. Received steroid injection and oral steroid course, which then allowed itching to be controlled by oral antihistamines. It has now been over 1 month and still have dermatographia symptoms (rash appears after any friction on skin). Taking Zyrtec daily to control itching, nothing is controlling friction rash.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- 1/18 - went to urgent care received 125mg Solu-Medorl injection 1/21 - started 6 days of MethyLPREDNISolone Tablets 4mg
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- rosacea acne
- Andere Medikamente
- 10mg CBD sublingual supplement
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 10.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 28,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash papular
Skin irritation
Urticaria
Symptomtext
Irritated and itchy skin all over body resulting in very pronounced raised hives and rash. First noticed in scalp but present on entire body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Amphetamine salt combo 30mg xr
- Allergien
- None. Seasonal grass seed/grass pollen.
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 10.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Facial pain
Gastrointestinal disorder
Pain in extremity
Peripheral swelling
Pruritus
Urticaria
Symptomtext
reports of itchy skin and digestive issues for the last week post MODERNA covid booster. Reported broke out in hives over much of body (back, neck, and torso). subsided with benadryl, - started having pain along face about 1 week after the vaccine. Also reports of pain and swelling in hands. - no similar reaction to first two doses of moderna. Rx for prednisone, antihistamine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Benign essential hypertension
- Andere Medikamente
- hydroCHLOROthiazide levocetirizine (XYZAL)
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Erythema
Inflammation
Pruritus
Symptomtext
On day 10 (Sun, Feb 6th) in the evening, I started getting very itchy on my stomach. Overnight it continued and moved around my trunk and head/scalp. Has continued ever since and worsened slightly. No raised hives, but red inflamed, burning areas as it moves around and itches. After 48 hours of constant itching, I took Zyrtec, which alleviated the redness and itchiness. Today is day 13 from the date of my booster shot that I believe triggered this undesired immune response.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None known
- Andere Medikamente
- Daily Multivitamin and glucosamine 1500mg with MSM 1500mg
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- 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
Myalgia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Grip strength decreased
Influenza like illness
Pain
Pain in extremity
Pyrexia
Symptomtext
Later that evening I began to have a fever and flu-like body aches, mainly pulsating through my hands and feet. After the aches went away 48 hrs later, I have still experienced piercing pain in my hand, mainly through my index finger. It feels like it should look very swollen, but it doesn?t. I can?t grip things like dishes or the steering wheel without pain or sometimes at all. I?ve never had arthritis but I would guess this is what severe arthritis feels like.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Trocanteric bursitis which is unrelated
- Andere Medikamente
- Generic Birth control pills
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 11.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lethargy
Oropharyngeal pain
Pain
Pruritus
Pyrexia
Respiratory tract congestion
Urticaria
Symptomtext
Sore body, fever, and lethargy night of 1/11/22. Ended symptoms on 1/12/22. Then on the night of 1/21/22, developed itchy hives that appear randomly on entire body, even palms and soles of feet. Sore throat and congestion that lasted for a week. Hives come and go on random areas of the body still up to today's date, 2/6/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Pain
Pyrexia
Swelling
Symptomtext
Fever 102.1, chills, headache, body aches x48 hours, swollen axilla today is day3.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN, hypothyroid
- Andere Medikamente
- Losarten, HCTZ, Amlodapine, synthroid
- Allergien
- None
- Vorherige Impfungen
- 2 Covid vaccines 1/14/21, 2/11/21 fever/body aches/headache
- Staat
- KY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Bone pain
Symptomtext
States severe pain started in L shoulder, elbow , wrist and collar bone 12 hours afterModerna injection. Was seen by her pmd. spoke with Pt today states she still has pain in these areas but it has decreased some.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- htn
- Andere Medikamente
- HCTZ, Tenormin
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pruritus
Injection site swelling
Symptomtext
Itching at the injection site from 07JAN22 - 13JAN22. Redness and swelling at the injection site for 1 week following vaccination. Patient did not take any treatments or seek medical care for this event. Symptoms eventually subsided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- Not seen by provider
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- CHRONIC SINUSITIS
- Andere Medikamente
- FLONASE, ALLEGRA
- Allergien
- NONE
- Vorherige Impfungen
- TUBERSOL SKIN TEST,
- Staat
- NJ
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Pruritus
Rash
Urticaria
Symptomtext
4 to 6 hours after I received the vaccine I started with a hive like rash. It wasn't very itchy until the next day. The hives started on the back of my right arm. I did a virtual visit with my doctor and he told me to take OTC antihistamine and use hydrocortisone cream. The itching and rash still spread so I went to the ER. They gave me a steroid injection on my left side. I was prescribed Methylprednisolone 4mg and Hydroxyzine HCL 25mg. The rash is now controlled, but the itching is still continuous. The hives are going away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- I had tested positive for Covid-19 the next morning after receiving the vaccine.
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D, Vitamin C, Multivitamin
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Injection site warmth
Pain
Symptomtext
Got Moderna vaccine on Tuesday (02/01/21) morning at about 10 45 am or so. Today (02/03/21) noticed the area was a little swollen, very red and hot to the touch and a softball sized area around where the shot was given is sore to the touch. Took ibuprofen yesterday since she was achy and felt fine today when she woke up. However, she noticed the area when taking a shower about 10 minutes ago. Advised to go to urgent care to get it checked out to make sure not infected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- DIABETES, HTN, CHOLESTEROL
- Andere Medikamente
- -
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pain
X-ray normal
Symptomtext
PATIENT STATES MORNING AFTER VACCINATION, HER RIGHT SIDE AND SHOULDER BEGAN HURTING AND CONTINUES. HER WHOLE BODY ACHES AS WELL. NO RELIEF FROM MEDICATION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- PATIENT WENT TO DR. HAD AN XRAY AND NOTHING WAS DISCOVERED
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- DIABETES, HIGH BLOOD PRESSURE, HIGH CHOLESTEROL, ARTHRITIS, GERD
- Andere Medikamente
- ATORVASTATIN 40MG, PANTOPRAZOLE 40MG, HCTZ 25MG, AMLODIPINE 5MG, GLIPIZIDE 5MG, MELOXICAM 15MG, LISINOPRIL 40MG, METFORMIN 1000MG
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Urticaria
Symptomtext
Hives occurring all over the body throughout the day Dermatographia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hashimotos Thyroidosis
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site nodule
Injection site pain
Injection site warmth
Symptomtext
Patient developed knot at injection site that is hot and painful, but not red.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site nodule
- Hospital-Tage
- -
- Labordaten
- None at this time.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Codeine, Morphine, Macrolides
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eosinophil count increased
Erythema
Laboratory test normal
Mechanical urticaria
Pruritus
Symptomtext
Full body itchiness and dermatographia starting 12 days after the booster. No changes to diet, new soaps, lotions, detergents, etc. Given 40mg of prednisone for 5 days and xyzal. This drastically reduced symptoms. After course of prednisone itchiness and redness is back
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- Normal blood lab work done on 1/19/2022. Eosinophils relative was high. Other results normal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Poultry (chicken, turkey, etc) Bactrim (sulfa drugs) Ceclor
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (very sore arm) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 vaccination. The patient's past medical history included Abdominal pain, Diarrhea and Constipation. Previously administered products included for Abdominal pain: Tylenol (Patient has IBS and sometimes she would have abdominal pain and diarrhea or constipation which would be relieved by Tylenol). Past adverse reactions to the above products included No adverse event with Tylenol. Concurrent medical conditions included Irritable bowel syndrome (Patient has IBS which was diagnosed long before to getting the 1st dose of the vaccine). On 29-Dec-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Dec-2021, the patient experienced PAIN IN EXTREMITY (very sore arm). On 31-Dec-2021, PAIN IN EXTREMITY (very sore arm) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. Treatment medication was not provided by the reporter. Patient is scheduled to have her 2nd dose on 26-JAN-2022. This case was linked to MOD-2022-461324 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Irritable bowel syndrome (Patient has IBS which was diagnosed long before to getting the 1st dose of the vaccine).
- Vorgeschichte
- Medical History/Concurrent Conditions: Abdominal pain; Constipation; Diarrhea
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Full body hives
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- vitamin c, vitamin B, turmeric, glucoasime and chondroitin. Mirena IUD
- Allergien
- NKA no food or drug allergies otherwise noted
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash erythematous
Symptomtext
A red rash has appeared all over my body about a week after I got the Moderna ? dose booster shot. I previously had the two Moderna vaccines but did not experience a rash like this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Lymphadenopathy
Pain
Pain in extremity
Symptomtext
Note: my first 2 series in my COVID-19 vaccine was Pfizer. I decided to cross boost. Approximately 36 hours after receiving a Moderna COVID-19 booster, along with the typical side effects (sore arm, swollen lymph nodes, chills) I had a burning pain that would come and go about every 10 minutes way down in my lower right pelvis region (felt like ovary/fallopian tube area). This pain and burning went on all day. 12 hours. The next day it was completely gone. I knew it was related to my booster. I never felt this burning pain before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None. Occurred on a Sunday. If the pain persisted beyond, my plan was to seek medical help but it only lasted one day.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- I always take a multi vitamin, biotin, magnesium, zinc and a probiotic daily.
- Allergien
- Oral allergy to raw apples, peaches, kiwi, plum.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site induration
Injection site pain
Injection site pruritus
Injection site swelling
Nasal congestion
Rhinorrhoea
Sneezing
Symptomtext
Patient came today at 10:42am today for a consultation and asking to report to VAEARS for her adverse reaction. She got Moderna Booster on Friday of 1/21/22. On the night of 1/21/22, she starting to experience nasal congestion, sneezing, running nose, her injection site was red, very itchy, raised harden bump on the injection site pain, and the border of the red swollen area diameter keep getting bigger everyday. She have been taking benadryl everyday (still taking it up until today) and apply ice on the injection site area, and it did help alleviated most of the symptoms. Patient is very concern and insisted on marking on her profile of having allergic reaction to Moderna due to the severe itchiness on her injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- No per patient.
- Vorgeschichte
- hypercholesteronemia, hypertension, WPW sundrome, fibromyalgia
- Andere Medikamente
- Taking multivitamin Vitafusion for women.
- Allergien
- Sulfa-hives head to toe, throat and tongue swelling up, Latex-rash
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Blood test
C-reactive protein increased
Hypoaesthesia
Neck pain
Pain
Pain in extremity
Pruritus
Urticaria
Symptomtext
On 1/10/2022, I started getting hives that would appear on random parts of my body, which would last about 30 minutes, then disappear and reappear elsewhere on my body. These hives are extremely painful and itchy. On 1/11/2022, I started having severe left arm pain that radiated from my neck down to my fingers. It gave my hand a numb feeling. On 1/12/2022, this left arm pain started radiating into my right arm and down my back. To this date, I continue to deal with these hives and body pain. I reported to the ER on 1/12 due to the severe arm pain resulting in no relief. I reported to an Urgent Care on 1/14 with continued hives and body pain and was prescribed a hydrocortisone cream and told to take Zyrtec allergy medicine to help with the hives.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Blood tests completed in the ER on 1/13/2022. Results shows heightened C-Reactive Protein levels.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Birth control (norethindrone 0.35 mg tablet)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 02.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Cough
Gait disturbance
Nausea
Oropharyngeal pain
Pain
Pyrexia
Rash
Symptomtext
Sore throat, rash, fever over 100, body aches, nausea. All listed symptoms lasted for 3 days. Aches continued then side pain with back ache. Difficult to walk. Continuous cough to this day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- PENICILLIN AND OTHER SULFEUR DRUGS
- Vorherige Impfungen
- 2nd vaccine headaches and body aches for 24 hours. Occasional headaches for 4 months
- Staat
- ME
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Swelling
Urticaria
Symptomtext
January 7th: Sudden onset of hives, intense itchiness with redness, swelling went to urgent care next day perscribed otc antihistamines 2xqd, benadryl to assist at night.. currently on 1 claritin in am a 2 benadryl at night. has improved significantly but still persists
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- depression
- Andere Medikamente
- birth control: lo Loestrin fe , zoloft 50mg
- Allergien
- metronidazole
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 23.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Disturbance in attention
Fatigue
Hypersomnia
Pain
SARS-CoV-2 antibody test negative
SARS-CoV-2 test negative
Symptomtext
Severe fatigue, aches, chills, very poor mental clarity. I could not function at all. Went to bed and slept 13 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Prior to the vax, I took both an antibody and antigen test, both were negative. Previous 2nd dose administered 11 months prior, Feb 2021.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthritis
Limb discomfort
Movement disorder
Musculoskeletal discomfort
Pain
SARS-CoV-2 test
Symptomtext
Making arthritis horrible in left hand and right knee; Bare the pain to go to the bathroom, a lot of pain, hurts like hell; Hard to move; Feels like bubbles of air in between areas in her back so she had to hold her left arm up to move a little bit; Experienced the same feeling in neck and back; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 16-Jan-2022 and was forwarded to Moderna on 16-Jan-2022. This spontaneous case was reported by a consumer and describes the occurrence of ARTHRITIS (Making arthritis horrible in left hand and right knee), MUSCULOSKELETAL DISCOMFORT (Experienced the same feeling in neck and back), PAIN (Bare the pain to go to the bathroom, a lot of pain, hurts like hell), MOVEMENT DISORDER (Hard to move) and LIMB DISCOMFORT (Feels like bubbles of air in between areas in her back so she had to hold her left arm up to move a little bit) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 vaccination. Co-suspect product included non-company product INFLUENZA VACCINE (FLU) for an unknown indication. Concurrent medical conditions included Arthritis. Concomitant products included FAMOTIDINE (PEPCID [FAMOTIDINE]), GABAPENTIN, METOPROLOL, LEVOTHYROXINE, TOPIRAMATE, ALENDRONATE SODIUM (ALENDRONATE), METFORMIN, NORTRIPTYLINE, ROSUVASTATIN, ROPINIROLE, TIZANIDINE, VITAMIN B COMPLEX (SUPER B COMPLEX [VITAMIN B COMPLEX]), ZOLPIDEM TARTRATE (AMBIEN) and HYDROCODONE for an unknown indication. On 09-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form and dose of INFLUENZA VACCINE (FLU) (unknown route) 1 dosage form. On 12-Jan-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced MUSCULOSKELETAL DISCOMFORT (Experienced the same feeling in neck and back). On 15-Jan-2022, the patient experienced ARTHRITIS (Making arthritis horrible in left hand and right knee), PAIN (Bare the pain to go to the bathroom, a lot of pain, hurts like hell), MOVEMENT DISORDER (Hard to move) and LIMB DISCOMFORT (Feels like bubbles of air in between areas in her back so she had to hold her left arm up to move a little bit). The patient was treated with HYDROCODONE for Adverse event, at an unspecified dose and frequency. At the time of the report, ARTHRITIS (Making arthritis horrible in left hand and right knee), MUSCULOSKELETAL DISCOMFORT (Experienced the same feeling in neck and back), PAIN (Bare the pain to go to the bathroom, a lot of pain, hurts like hell), MOVEMENT DISORDER (Hard to move) and LIMB DISCOMFORT (Feels like bubbles of air in between areas in her back so she had to hold her left arm up to move a little bit) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 15-Jan-2022, SARS-CoV-2 test: negative (Negative) Negative. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient reported that last wednesday she started experiencing a nick on the left side of her neck, like she slept wrong on the pillow, then thursday it moved to the right side of neck and the left was better, then friday experienced the same feeling in neck and back, on saturday it got a lot worse, horribly bad, hard to move, feels like bubbles of air in between areas in her back so she had to hold her left arm up to move a little bit, bare the pain to go to the bathroom, a lot of pain, hurts like hell, making arthritis horrible in left hand and right knee. Patient doesnot want to go to the hospital Patient has taken some of the hydrocodone but it has not really helped. Company comment This case concerns a 65-year-old female patient, with medical history of Arthritis and having received INFLUENZA VACCINE on the same day of the administration of mRNA-1273 vaccine, who experienced the unexpected non-serious events of ARTHRITIS (AESI), MUSCULOSKELETAL DISCOMFORT, PAIN, MOVEMENT DISORDER and LIMB DISCOMFORT. The events started 3 days after the administration of the first dose of mRNA-1273 vaccine and continued appearing during the following 3 days. Patient?s medical history of Arthritis remains as a confounder, and having received INFLUENZA VACCINE makes this drug a co-suspect drug. Patient does not want to go to the hospital. Patient has taken some of the hydrocodone but it has not really helped. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This case concerns a 65-year-old female patient, with medical history of Arthritis and having received INFLUENZA VACCINE on the same day of the administration of mRNA-1273 vaccine, who experienced the unexpected non-serious events of ARTHRITIS (AESI), MUSCULOSKELETAL DISCOMFORT, PAIN, MOVEMENT DISORDER and LIMB DISCOMFORT. The events started 3 days after the administration of the first dose of mRNA-1273 vaccine and continued appearing during the following 3 days. Patient?s medical history of Arthritis remains as a confounder, and having received INFLUENZA VACCINE makes this drug a co-suspect drug. Patient does not want to go to the hospital. Patient has taken some of the hydrocodone but it has not really helped. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220115; Test Name: Covid test; Test Result: Negative ; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- Arthritis
- Vorgeschichte
- -
- Andere Medikamente
- PEPCID [FAMOTIDINE]; GABAPENTIN; METOPROLOL; LEVOTHYROXINE; TOPIRAMATE; ALENDRONATE; METFORMIN; NORTRIPTYLINE; ROSUVASTATIN; ROPINIROLE; TIZANIDINE; SUPER B COMPLEX [VITAMIN B COMPLEX]; AMBIEN; HYDROCODONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site bruising
Injection site erythema
Injection site induration
Injection site pain
Injection site pruritus
Injection site rash
Injection site warmth
Symptomtext
Two days after receiving my Moderna covid vaccine booster I developed a hot, red a few inches distal to the injection site. It felt and looked 3 or 4 small bites/pinpricks, each about an inch in diameter with a hard, red center, painful and itchy, over appx a 3x3in area, 3-6in distal from where I was injected. The rash doubled in size, growing to 8 or 9 little red pinpricks over a 6x8ish area, got hotter, harder, and more painful over the next day. It stared to subside on the 4th day post-injection, and was gone by six days post-injection. I also developed a large bruise at the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no medical conditions
- Vorgeschichte
- nonsmoker, no drinking
- Andere Medikamente
- 50ug synthroid
- Allergien
- slight seasonal environmental allergies; no other allergies to foods or drugs
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Nausea
Pyrexia
Vomiting
Symptomtext
Fever, chills, fatigue, nausea, vomiting. Severe vomiting lasting 2 days post vaccine. Recorded temperature at 101 then later at 95.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/a
- Andere Medikamente
- N/a
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Laryngitis
Lymphadenopathy
Nasopharyngitis
Oropharyngeal pain
Paranasal sinus discomfort
SARS-CoV-2 test negative
Sinus congestion
Streptococcus test negative
Throat irritation
Symptomtext
December 31st had swollen lymph nodes, one went away quickly but still have one receding under left arm. 01/05 In the evening had sore throat and the start of laryngitis, when the morning came it was full blown laryngitis, scratchy and sore throat, sinus pressure and congestion. Called Dr. and set up an appt. 01/06 and it was done at 10am. Advised to get covid and strep throat tests. 01/07 My rapid test results was negative and Strep test was negative. Called Doctor and stated head cold with laryngitis and was advised to take liquids and bed rest. 01/08 On the evening I was recovering and had a few symptoms left and by the 11th was fully recovered. Only thing left is the receding lymph node under left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 01/06 CoVid and Strep test( both negative)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoarthritis, Pinched nerve(numbing sensation)
- Andere Medikamente
- Equate Multivitamin, Ibuprofen, Spring Valley Potassium, Leg Cramp Supplement
- Allergien
- Banana, Peanut
- Vorherige Impfungen
- Covid, Pfizer 2nd dose, 01/18/2021, age 34, under left arm swollen lymph for 3 weeks
- Staat
- IA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Scratch
Skin warm
Urticaria
Symptomtext
Developed hives and scratch like rash all over the body. It would come and go and move. Hot to the touch and itchy. Went to the doctor and began Zyrtec. As of now have had hives for 15 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Have not done labs yet. Was waiting to see if it would resolve on its own per doctor. Told to wait a couple weeks.
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- Low thyroid function
- Andere Medikamente
- Birth control Levothyroxine
- Allergien
- Allergic to penicillin/amoxicillin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Pain in extremity
Peripheral swelling
Symptomtext
Patient had arm soreness and swelling . Also experiencing low back pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Hypersensitivity
Limb discomfort
Urticaria
Symptomtext
PATIENT CALLED IN TODAY TO REPORT AN ADVERSE REACTION TO THE MODERNA VACCINE. SHE IS HAVING REDNESS/IRRITATION IN THE ARM SHE GOT HER VACCINE. THIS SEEMS TO BE A VERY DELAYED REACTION. SHE GOT HER VACCINE OVER TWO WEEKS AGO, ON JANUARY 4, 2022. SHE SAID SHE STARTED NOTICING THE REDNESS ABOUT A WEEK AGO. IT ISN'T CAUSING HER PAIN. SHE SAID IT LOOKS JUST RED AND IRRITATED BUT DOESN'T APPEAR TO BE INFECTED IT LOOKS MORE LIKE SOME WELTS/APPEARS TO BE MORE ALLERGIC REACTION. SHE WAS WONDERING ABOUT TRYING BENADRYL. I TOLD HER THAT WOULD BE A GREAT PLAN TO START WITH SOME BENADRYL AND THAT SHE COULD ALSO TAKE IBUPROFEN IF NEEDED. DISCUSSED SIGNS OF CELLULITIS TO WATCH FOR REDNESS THAT STAYS AROUND OR SPREADS/HEAT/PAINFUL. ADVISED TO CONTACT DOCTOR IF HER SYMPTOMS SEEM TO WORSEN OR DO NOT IMPROVE AT ALL. ALSO TOUCHED BASE WITH HER DR OFFICE AND SPOKE TO EMPLOYEE WHO SAID SHE WOULD REACH OUT TO THE PATIENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE SHARED
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- SERTRALINE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Bone pain
Motion sickness
Pollakiuria
Symptomtext
Cannot hold anything on her stomach. Uncontrollable peeing and motion sickness. Bones are painful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bone pain
- Hospital-Tage
- -
- Labordaten
- No.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Lexapro
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Headache
Induration
Nodule
Pain in extremity
Peripheral swelling
Symptomtext
Left arm redness, soreness, swollen, hard knot, frequent headaches. All symptoms still after 10 days and going.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Upcoming doctor appt on Wednesday, 01/26/2022
- Aktuelle Erkrankungen
- Migraines
- Vorgeschichte
- Meralgia Paresthetica, Lumbar Disc Degeneration, Lumbar Radiculopathy, Myalgia, Migraines,
- Andere Medikamente
- Gabapentin 300 mg at bedtime, Ibuprofen 800mg at bedtime, Nortriptyline 20mg at bedtime, Aimovig injector shot (1 shot per month) given 01/05/2022
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Symptomtext
itchiness on her body; rash; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (itchiness on her body) and RASH (rash) in a 42-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059h21a) for COVID-19 vaccination. Concomitant products included GABAPENTIN for an unknown indication. On 06-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Jan-2022, the patient experienced PRURITUS (itchiness on her body) and RASH (rash). The patient was treated with CALAMINE for Adverse event, at an unspecified dose and frequency; LORATADINE (CLARITIN [LORATADINE]) for Adverse event, at an unspecified dose and frequency and DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for Adverse event, at an unspecified dose and frequency. At the time of the report, PRURITUS (itchiness on her body) and RASH (rash) was resolving. It was reported that after 3 days Calamine, Claritin, Benadryl which didn't helped. This case was linked to MOD-2022-454578 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- GABAPENTIN.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 14.05.2021
- Beginn
- 15.01.2022
- Tage bis Beginn
- 246,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Malaise
Symptomtext
positive test and symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Lymphadenopathy
Symptomtext
Lymphadenopathy, left clavicle for 9 days. Joint pain right shoulder and left side of body for 7 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi vitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Myalgia
Urticaria
Symptomtext
On Tuesday, 01/11, I had muscle pain from my shoulders down. I started developing hives on my face at around 16:00 on Wednesday, 01/12. Next morning, 01/13 it spread to forearms and chest. This is when I called my nurse. I had these symptoms (albeit more severe) after my second dose in May again 2 days after the vaccination and was on a holding pattern to go to an ER with anaphylaxis. The problem solved within 2 days with Zyrtec and Benadryl this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hyperlipidemia Hormone disorder Cervical agenesis
- Andere Medikamente
- Estradiol Valerate 3.5 mg/ml injected weekly (injected on 01/06/2022 at 08:28 PM) Vitamin C Vitamin B Complex Culturelle Women's Healthy Balance
- Allergien
- No known allergies.
- Vorherige Impfungen
- Hives 2 days after, Age 46 y.o., Vaccinated on 05/25/2021 with Moderna COVID-19 Vaccine (Intra Muscular).
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling abnormal
Muscle tightness
Symptomtext
Patient DOB 04/17/1961 received the Moderna booster lot #059H21A expires 01/27/2022 at 07:44am. The client completed her observation period without incident but returned to the vaccine table at 08:50 am with complaints of dizziness, feeling like she was "floating", and "tightness" in her left leg. The client said she was "folding laundry" when she started feeling "dizzy". She said she looked up from the laundry and the dizziness got better. The client said she did not feel like she was going to pass out but still felt like she was "floating". She said the leg "tightness" started when she was doing laundry. The client reported a history of "feeling dizzy" after vaccination. The client denied any pertinent medical history and does not take any medications. The client was alert and oriented x 4, her breathing was regular and unlabored, and her skin color was appropriate for ethnicity. At 08:56am, RN checked the client's vital signs. BP 120/82, HR 76, RR 20, SpO2 97%, no complaints of pain. RN, gave the client a juice to drink. At 09:00 vitals were retaken. BP 120/78, HR 72, RR 16, SpO2 97%, and no complaints of pain. The client said the "floating feeling? was going away. She reported that her left leg still felt tight. Vitals were taken again at 09:05 am, BP 118/75, HR 73, RR 20, SpO2 97%, and no complaints of pain. The client said the "dizziness" went away. RN educated the client to report history of dizziness next time she got a shot and to return if symptom came back. RN also talked to the client about following up with her primary care provider if the leg tightness did not resolve. The client felt she may have injured herself while doing laundry. The client stood up and her BP was rechecked. BP 120/84 in standing position. The client walked away with a steady gait and returned to the vaccination table at 10:30am and said she was still feeling fine, then departed again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- The client denied having any health problems.
- Vorgeschichte
- The client denied having any health problems.
- Andere Medikamente
- The patient denied taking any medications. She said she takes supplements but did not name the supplements.
- Allergien
- The client denied having allergies.
- Vorherige Impfungen
- Dizziness.
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Symptomtext
rash around injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- sinus problems
- Vorgeschichte
- tracheal bronchomalasia, asthma, osteoarthritis, chronic sinusitis, myopic degeneration, diabetes
- Andere Medikamente
- methadone, dexilant, ropinirole, clonazepam, propranolol, montelukast, q-var, budesonide nasal spray,, vitamin c, multivit, zinc,
- Allergien
- iodine, CT dye, tegaderm tape, augmentin, erythromycin , clarithromycin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Rash; This spontaneous case was reported by a consumer and describes the occurrence of RASH (Rash) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 vaccination. Concurrent medical conditions included Type 2 diabetes mellitus. Concomitant products included METFORMIN for Type 2 diabetes mellitus, PRAVASTATIN and HYDROCHLOROTHIAZIDE, LISINOPRIL (LISINOPRIL/HYDROCHLOROTHIAZIDE) for an unknown indication. On 11-Jan-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 an unknown date, the patient experienced RASH (Rash). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for Rash, at an unspecified dose and frequency. At the time of the report, RASH (Rash) had not resolved. Patient stated they have stopped taking their daily medicine due to the rash.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Type 2 diabetes mellitus
- Vorgeschichte
- -
- Andere Medikamente
- METFORMIN; PRAVASTATIN; LISINOPRIL/HYDROCHLOROTHIAZIDE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 15,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pruritus
Urticaria
Symptomtext
About 2 weeks after getting the Moderna booster vaccine I began getting daily hives. The hives start at generally 6 or 7pm each day and last for about 2 or 3 hours. Occasionally I will get them again later in the night while I am in bed. I have seen a doctor at my regular physician's office on January 12th who prescribed me a topical steroid cream to use on the hives (triamcinolone acetonide). He also recommended using Benadryl. I have used both the steroid cream and Benadryl with minimal relief. I have also used a cool washcloth compress which helps a little. The hives are extremely itchy and appear mostly on my shoulders, back, torso, and arms. I occasionally experience them on my hands, legs, feet, and scalp. The hives are round and oval but also longer/irregular shapes especially if I scratch them. The hives don't seem to have any trigger that I can determine. There have been no changes to anything in my routine, no new foods added to my diet and I am usually not doing anything when they come on. The only thing that has happened was the Moderna booster shot 2 weeks prior to the onset of the hives. I have been experiencing the daily hives for almost 2 weeks now at this point. I will be seeing a dermatologist in the middle of February.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None yet. The doctor just looked at the photo of the hives I have on my phone and looked at my skin during my appointment on January 12th.
- Aktuelle Erkrankungen
- I was getting over a regular cold at the time I got the Moderna booster vaccine
- Vorgeschichte
- None
- Andere Medikamente
- Prenatal vitamin
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site reaction
Rash erythematous
Skin infection
Symptomtext
Pt has experienced bruising and several dark red rashy spots around the injection site. She did not report having a fever but has taken Ibuprofen around the clock since time of vaccine. She states her dr told her it was a skin infection from the vaccine. She did not tell whether or not her dr saw her in person
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 16.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Hypoaesthesia
Lymph node pain
Lymphadenopathy
Pain in extremity
SARS-CoV-2 test positive
Throat irritation
Symptomtext
After receving my booster shot, the next day was the normal sore arm. I then started to feel it migrate and become sore in my lymph node in my armpit (left arm, same as shot). Friday, 1/14, it was the size of a softball. I took an anti-inflammatory and the swelling started to shrink. Saturday, 1/15 at night, my throat started to itch and I was having numbness in the vaccinated arm. Today, Sunday, 1/16, visited the urgent care to rule out sepsis. No sign of sepsis but tested positive for Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- Positive test result from Urgent Care. Also ruled out sepsis in the lymph node.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Cholesteral
- Andere Medikamente
- High Cholesteral Medicine, Vitamin D, Mulitvitamin complex
- Allergien
- None, only environmental allergies (bees, wasps, red ants)
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Lip swelling
Lymph node pain
Pain
Swelling face
Symptomtext
I did a booster shot with Moderna on 1/12/22 and got a side reaction: swollen area around lips, including lower lip, chin and partially lower cheeks. At the evening on 1/14 the symptoms started developing, I massaged the area a bit, drank some water and went to bed. At night I woke up as the aforementioned area got worse (pain, more swollen). I took a pill of Benadryl, applied some Hydrocortisone ointment and went to bed. I could sleep till morning as symptoms pertained. In the morning I scheduled a call with my medical provider (1:50 pm PST) and took one more antihistamine pill (Claritin). I still have one part of my face (left one) bigger than other. Some mild side effects I got on a second day after booster: pain in left under armpit (lymph knot), weakness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 01.01.2022
- Beginn
- 02.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Peroneal nerve palsy
Sciatica
Symptomtext
Patient had moderna booster on 1/1/22. She reported severe pain in left leg the evening of 1/2/22. She was diagnosed with drop foot (new diagnosis) and sciatica (which she has had before)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Musculoskeletal stiffness
Pruritus
Vaccination site swelling
Symptomtext
Swelling at the vaccine site, tightness, itching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hashimotos Thyroiditis, PCOS
- Andere Medikamente
- Vitamin C 1000MG
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Sensitive skin
Symptomtext
3 hrs after taking the vaccine he started getting skin sensitivity on his face. He look in the mirror and started see little red bumps on his face. He took Benadryl a it got better a little. When he woke up the next day the bumps spreaded from his face to down his neck.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- synopsis, herniated disc, asthma, synaptic issues on right side
- Andere Medikamente
- no
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Patient stated he has a rash on his torso. And a rash on his face. Patient was instructed to make an appointment with a doctor for further inspection. Patient has a high likely of having shingles.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Injection site erythema
Injection site pain
Injection site swelling
Injection site warmth
Symptomtext
warm red area at site of injection with soreness and swelling that has lasted multiple days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- reviewed by clinician at facility that stated to her that the injection was given below the deltoid
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Pruritus
Throat irritation
Urticaria
Symptomtext
Allergic reaction-hives, itching, scratchy throat
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cough
Fatigue
Influenza virus test negative
Nausea
Pain
Pyrexia
Respiratory syncytial virus test negative
Urticaria
Symptomtext
several days later, started with high fever (104) with body aches and the development of hives on her arms, legs and upper chest as well as fatigue, cough and nausea. Went to the ED on 01/01/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Negative flu and RSV on 01/01/2022.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Lisinopril 5 mg HS
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Pain
Pain in extremity
Symptomtext
Booster immunizaton was administered at 0.5ml vs 0.25ml. Patient c/o sore arm and minimal body aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Fatigue
Impaired work ability
Incorrect dose administered
Pain
Symptomtext
Booster immunization administered at 0.5ml instead of 0.25ml. Patient c/o body aches, tired, chills and missed work 1/13/22 and 1/14/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest discomfort
Chills
Fatigue
Impaired work ability
Incorrect dose administered
Pain
Symptomtext
Booster immunization given at 0.5 instead of 0.25. Patient is tired, has chills/body aches, heavy chest and missed work 1/13/22 and 1/14/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Fatigue
Impaired work ability
Incorrect dose administered
Pain
Pain in extremity
Symptomtext
Booster COVID immunization given at 0.5 instead of 0.25ml. Patient's arm very sore and tired with body aches. Missed day of work on 1/13/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Nausea
Pain in extremity
Symptomtext
Patient was given 0.5ml for a booster. Sore arm and nausea for 24 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Symptomtext
Patient was treated previously with antibodies around 30 days prior. Patient experienced diarrhea the morning after receiving her booster shot. Patient symptoms resolved on their own, discussed with the pharmacy about a week later and reporting followed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Had COVID and was treated with antibodies 30 days prior
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 09.01.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Pruritus
Rash erythematous
Skin swelling
Symptomtext
12/27/21 Moderna booster injection. 01/8/22 burning, red rashes all over with itching symptoms. Thereafter raised skin. Took Zyrtec and topical cream/lotion or hydrocortisone application. Relief strategy helps stop burning, itching and raised skin. But, red rash continue. If relief strategy is paused, then within a day, all adverse events reappear
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
9 days after receiving the Moderna booster I developed hives all over my body. I have never been allergic to anything nor did I have a reaction to the first and second dose of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zinc / vitamin C
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Pruritus
Urticaria
Symptomtext
Hives and intense itching all over my torso, back, down my arms and the top of my thighs between my leg. I took diphenhydramine 3 doses every 4 hrs. This did not help at all so then I took ceitrizine hydrochloride and continues with the hiphenhydramine every 4 hrs. This gave a tiny bit of relief from the itching. The hives resolved almost completely in 30 hrs and by 54 hrs everything was gone. This was from the moderna booster. 9 months previously i received a one dose of the johnson and johnson. I hate to think what would have happened if I had a full dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- osteoarthritis
- Andere Medikamente
- none
- Allergien
- No allergies or sensitivities show in multiple tests from multiple doctors but I get asthma in the spring and shellfish causes my glands in my neck to swell even though the tests show nothing.
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Malaise
Symptomtext
BOOSTER; 1 hour after getting vaccine, patient got covid like symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Feeling abnormal
Feeling hot
Pruritus
Somnolence
Symptomtext
At 10:38 a.m , patient stated " I'm hot, why am I so hot?" Then removed her jacket. Vitals were taken at 10:40 a.m. as :B/P 132/108, p 87, O2 99, resp 18. Patient was kept seated in observation area for furter evaluation. Patient stated " I feel like I'm floating out of my chair" at 10:50a.m.; vitals were taken : B/P 126/101 p 89 O2 99, resps 19. Patient appeared drowsy. Patient was repeatedly asked orientation questions. Pt. stated " What, I'm confused." Patient was able to answer question and was shown to be A/O x4. Patient stated she was very sleepy. At 10:56 a.m. Emergency Services were called and notified of situation, while on phone with EMs patient complained of itching to both arms. EMS stated not to give her anything PO or IM including the Benadryl that we carry. At 10:56 patient was made aware EMS would be arriving to transport her to hospital for further evaluations. Patient stated "No, I don't do hospitals, My brother died in that hospital." Vitals taken at 11:06 : B/P 139/107, P 89, Resps 17, O2 99. EMS arrived at 11:12 to examine patient further. Patient initially refused examination, then agreed. Patient was examined by EMS and stated " Whatever this is it'll pass, God got me". EMS VItal machine read BP 137/87, P 87, O2 99% at 11:20 a.m. and at 11:21 a.m. vitals read 133/93 BP, P 87 and O2 100%. Patient refused hospital transport by EMs. Patient states she has a doctor's appointment at 1:20p.m. and if she's not feeling better by then she'll go to hospital. EMS departed at 11:30a.m. Pt. was kept in observation area for further evaluation. Patient ate lunch and walked out of observation area at 12p.m.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- DIABETES
- Vorgeschichte
- DIABETES
- Andere Medikamente
- DIABETIC MEDICATION PER PATIENT
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Fatigue
Headache
Injection site swelling
Lymph node pain
Lymphadenopathy
Pain
Pyrexia
Swelling
Symptomtext
Swelling of the left arm at injection site the size of an orange less than 12 hours after Booster. Low grade fever of 100.5 chills, body aches, tiredness and headache. The symptoms lasted all day. took Benadryl and Tylenol to relive symptoms. Had to repeat every 4 hours with Tylenol. By the next day the swelling was the size of a grapefruit. The lymph nodes in armpit are sore and swollen. On Monday at 7am went to primary care office to be seen. I still had a low fever they marked the redness with surgery marker and was told to monitor the swelling. Take pictures and send in via patient portal. Tuesday sent pictures of the swelling spreading was given a script of cephalexin to take for 7 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No other illnesses
- Vorgeschichte
- None
- Andere Medikamente
- Lexapro 10 milligrams, Zinc, Vitamin D
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site swelling
Tissue injury
Symptomtext
Swelling at injection site and tissue damage (possibly cellulitis)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- She was advised to go see a dr. In the meantime, she was advised to take Motrin or Tylenol, use an ice pack, and take some Benadryl
- Aktuelle Erkrankungen
- Na
- Vorgeschichte
- Na
- Andere Medikamente
- Na
- Allergien
- Na
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Dizziness postural
Erythema
Headache
Hyperhidrosis
Peripheral coldness
Skin discolouration
Symptomtext
The client reported dizziness to EMT and requested for her blood pressure to be obtained. RN responded. The client reported dizziness and sweating in her hands. Vitals obtained at 12:20PM were as follows BP 156/92, HR 69, O2 99%. The client reported a history of hypertension and stated that she has a medication prescribed. The client reported to RN that she did not take the prescribed medication this morning. The client subsequently stated to RN that she takes the medication as needed or when she experiences symptoms of high blood pressure. The client stated her current symptoms are normal for her when she experiences an episode of high blood pressure. The client reported feeling something on her cheek and removed her mask. RN noted an area of increased pink color that was approximately one inch in diameter. The client's family member reported the client has a history of rosacea and flushing when she is stressed. The client denied any other s/s of anaphylaxis. Client reported a history of anaphylaxis after taking penicillin and sulfa medications as a child. The client is not prescribed an Epi-Pen currently. The client stated her dizziness had resolved. Vitals obtained at 12:26 PM were as follows BP 165/96, HR 67, O2 99%. The client denied any current dizziness. The client stated when she experiences an episode of high blood pressure that drinking water and taking her medication help improve her symptoms. The client was provided water and began drinking it. RN noted mild diffuse redness across the client's chest. The client's family member stated this was normal for the client. The client denied any other signs or symptoms of anaphylaxis. The client denied any symptoms following her first or second doses of Moderna COVID vaccine. Vitals obtained at 12:32 PM were as follows BP 148/92, HR 69, O2 99%. The client denied any current dizziness or sweating of her palms. The client reported a slight headache and rated the pain at a 2 out of 10 on a 10 point scale. The client stated she commonly experiences headaches with stress and high blood pressure. The client stated her hands felt cold. The client stated she did eat a small sandwich and drank coffee today. The client stated she had not consumed any water today. The diffuse redness was still present on the client's chest and the spot on her right cheek. Repeat vitals obtained at 12:42PM were as follows: BP 156/92, HR 67, O2 99%. The client reported new onset of dry mouth, sweating and coldness of her hands, and headache still present. The client stated the pain of the headache was a 2 on a 10 point scale. RN provided education to the client on possible adverse reactions and when to seek medical care. RN recommended the client follow up with a medical provider regarding her blood pressure. The client voiced understanding of this education. The client stood up unassisted from the anti-gravity chair. The client reported slight dizziness upon standing but stated that she felt "okay to leave." RN offered continued observation. The client declined and stated that she would like to leave the vaccination site. The client's family member confirmed he was driving the client home. The client ambulated unassisted with a steady gait out of the observation area at 12:48 PM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hypertension
- Andere Medikamente
- HTN medication as needed
- Allergien
- Anaphylaxis to penicillin and sulfa medications
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Symptomtext
PATIENT HAS SWOLLEN LYMPH NODES UNDER THE ARMS AND IN THE COLLARBONE AREA. IT STARTED THE DAY FOLLOWING THE SHOT AND HAS BECOME PROGRESSIVELY MORE SWOLLEN AND PAINFUL. PATIENT WILL CONTACT THEIR PRIMARY CARE DR FOR AN OFFICE VISIT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- HAD THE FLU A FEW WEEKS BEFORE. TOOK TAMIFLU FOR IT
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
patient reported today that she had a full body rash that was unresolved with benadryl and topical antihistamine/steroid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- pt has history of asthma, pulmonary disease
- Vorgeschichte
- asthma, pulmonary disease
- Andere Medikamente
- none reported
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Throat irritation
Symptomtext
Patient began feeling lightheaded, dizzy, chills, and scratchy throat after given vaccine. Patient was monitored for 45 minutes - given water and snacks - until feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None STated
- Vorgeschichte
- Unknown
- Andere Medikamente
- None stated
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Rash
Symptomtext
Patient came to the pharmacy 1/9/22 reporting what she believed was an allergic reaction to the vaccine she received 1/6/22. She reported a rash covering her upper left arm down to her wrist & a rash on her legs behind her knees. Patient was advised to take benadryl for the the rash & seek medical attention if it got worse or any difficulty breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site inflammation
Injection site nodule
Injection site pruritus
Symptomtext
within a week my upper left arm formed a softball size knot, red, inflammed and itching under the skin. continued to spread down my left arm to elbow, contacted my PCP and she prescribed me steriods and antibiotics, still have symptoms, not as bad, swelling will go away and come back, itching has began to calm down, site still red and forming a pattern in circular motion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- blood pressure, diabetes, depression, chorlesterol
- Allergien
- codiene, biaxin, bactrum, sulfur
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site warmth
Symptomtext
INJECTION SITE REDNESS AND WARM TO TOUCH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- HYDROCORTISONE CREAM AND TYLENOL
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Symptomtext
The patient developed itching in the arm near the injection site about 20 to 30 minutes after receiving the vaccine. She took a loratadine since that is what she normally takes after getting a vaccine due to the itching. We also gave her an ice pack to place on the arm. We had her to stay in the pharmacy waiting area for about 45 min to an hour to monitor her reaction. She began to feel better after taking the loratadine and applying the ice pack.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- ASTHMA
- Vorgeschichte
- ASHTMA, HYPERTENSION
- Andere Medikamente
- BLOOD PRESSURE AND , MED FOR ASTHMA (UNKNOWN)
- Allergien
- AMLODIPINE??
- Vorherige Impfungen
- She informed me after the vaccination that she has developed itching in the past after receiving a vaccine.
- Staat
- AL
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Blood blister
Bone pain
Dizziness
Headache
Injection site erythema
Injection site pain
Injection site swelling
Lip swelling
Nasopharyngitis
Pelvic pain
Peripheral swelling
Pyrexia
Symptomtext
Red swollen painful feverish injection site. Febrile 100.0, dizziness, headache, severe bone pain worse in the lower back and pelvic region. Cold like symptoms and swollen lips with blood blisters. Also right arm is swollen from shoulder to elbow
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Bisoprolol, zyrtec d, zinc, vitamin c, vitamin d3, lexapro,
- Allergien
- Cipro, hydrocodone, feldene, latex, pineapple, banana
- Vorherige Impfungen
- Swollen lymph nodes, red swollen painful injection site, headache, dizziness, heart palpitations, severely swollen arm, febrile
- Staat
- CO
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abnormal behaviour
Blood glucose decreased
Dizziness
Glassy eyes
Hyperhidrosis
Slow response to stimuli
Symptomtext
The patient had been asked to stay for observation and the pharmacist located him seated. He was slow to respond when pharmacist was trying to give him written information on the vaccine and stated he was dizzy. His mother took note of the conversation and recognized he was not acting normal and called EMS. During this time he was given a glass of water to drink, his eyes initially looked glazed over but patient remained conscious although very slow to respond. He also broke out in a sweat. He stated that his throat was not closing and there were no signs of swelling around his lips or mouth observable. He remained seated and revived after the drink of water stating he felt better. Emergency personnel arrived and took him to the ambulance to check his vitals. Family members reported low blood glucose levels. The patient was not transported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none stated and patient filled out none on sheet
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Fatigue
Headache
Injection site pain
Injection site rash
Lethargy
Lymph node pain
Nausea
Pain
Pyrexia
Symptomtext
Fever 99.6 Extreme body aches Nausea Headache Fatigue Diarrhea Rash at injection site Sore at injection site Pain in the glands on arm of injection site Lethargy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity
- Andere Medikamente
- Prozac, lamictol,
- Allergien
- Percocet, Aderol
- Vorherige Impfungen
- March 30, 2021, Pfizer COVID vaccine dose 2, age 49, Fever, rash at injection site, fatigue, pain at injection site, body ache
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Urticaria
Symptomtext
I?ve developed prettt extensive hives and a rash that won?t seem to go away just over a week after my 3rd dose of Moderna. Antihistamines and Prednisone have been prescribed, but aren?t fully helping. Nothing else has changed in my life- no new foods, personal care products, etc. the Vaccine has been the only change, and now the hives are pretty intense. Will be following up with an allergist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Wellbutrin xl 300mg
- Allergien
- Sulfa-antibiotics
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Injection site erythema
Injection site warmth
Malaise
Pain in extremity
Symptomtext
Patient called pharmacy today at about noon to report "redness/hot-to-touch" on her injection site (3.5"x3.5" size of baseball). The problem started Wednesday evening (vaccination was done Monday night about 6 pm). She had the usual headache, fatigue/malaise and sore arm until Wednesday. The redness localized on the injection site. It does not radiate down the arm. Patient didn't seem to able to use ice pack at work. I suggested she place ice pack on area tonight/weekend and take APAP. She can't take other NSAIDs as she is currently on diclofenac. I also suggested her to contact her doctor as well. I will follow-up with her when I work tomorrow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hip pain; high blood pressure; migraine; GERD
- Andere Medikamente
- N/A
- Allergien
- Quinolones
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vomiting
Symptomtext
Patient has anxiety with vaccines and shots. Patient was fine after receiving the vaccine but vomited while they were waiting for any potential side-effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pyrexia
Symptomtext
slight fever but feels fine today
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- mitral valve prolapse
- Vorgeschichte
- mitral valve prolapse
- Andere Medikamente
- tacrolimus, amlodipine
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 17.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Chills
Fatigue
Hyperpyrexia
Lymphadenopathy
Malaise
Myalgia
Nausea
Pain in extremity
Pyrexia
Symptomtext
I received 2 doses of the Pfizer Vaccine initially in Jan/Feb 2021, then did the heterologous boost with Moderna in December 2021. I started having chills, fever, muscle aches around 12-14 hrs post shot. At 16 hours post shot I developed a 106.6 (hyperpyrexia) degree fever. The fever was managed with ibuprofen at home and brought down to about 101-102 that lasted until about 30 hours post. Felt very ill, nauseous, muscle aches, sore arm. tiredness for about 24 hours. I had very swollen lymph nodes (lymphadenopathy) for 6 days post shot, and generally feelings of tiredness. My menstrual cycle was missed. I have not have a period for 37 days now (as of 1/7/21), typical menstrual cycle length is 27 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Mild suspected food poisoning. Just stomach pain.
- Vorgeschichte
- None.
- Andere Medikamente
- Spironolactone
- Allergien
- Suspected penicillin.
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Headache
Nausea
Pain
Pain in extremity
Pyrexia
Symptomtext
Headache, fever, nausea, body aches, sore arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Ibuprofen
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Muscular weakness
Pain in extremity
Symptomtext
arm pain, dizziness, generalized muscle weakness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- none
- Andere Medikamente
- Xulane
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site warmth
Symptomtext
redness, burning, warm to touch at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- latex
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cold sweat
Dizziness
Feeling cold
Feeling hot
Nausea
Vertigo
Symptomtext
Patient received booster dose of Moderna. At the end of the 15 minute observation period patient stated he felt dizzy. Staff had patient sit back down for awhile to see if he felt better. Patient complained of the "room spinning," he felt warm and his hands felt clammy. We started a fan to help cool him off. After a few minutes he said he felt cold and a little nauseous. Patient was coherent and could speak. He said he ate earlier in the day. He denied any previous reactions after a vaccine. After another 20 minutes or so, he still reported he felt dizzy and it wasn't going away. He was not accompanied by anyone. He requested paramedics be called. They came to the pharmacy, checked him out and chose to transport him to a hospital. I did not receive any information or vitals from the paramedics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Unknown.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Ibuprofen
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 04.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Rash erythematous
Symptomtext
Patient received a rash red rash on the upper arm . recieved the moderna on 12-27-2021 and the afluria on 12-21-2021. both on on left arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Was healing from a hospitalization and sickness
- Vorgeschichte
- Hypertension and Asthma
- Andere Medikamente
- many
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Lethargy
Sinus pain
Toothache
Symptomtext
Booster shot 8 months after 2nd COVID shot. All 3 have been moderna. Extreme fatigue, moderate headache that comes and goes, extreme lethargy, sinus/tooth pain. No fever. No cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- age 44. 03/29/21 Moderna 038A21A. 04/26/21 Moderna 038A21A
- Staat
- MD
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Axillary pain
Peripheral swelling
Rash
Swelling
Symptomtext
Arm swollen again rash, arm pit & side swollen, pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- fish oil, lactose, calcium, fiber
- Allergien
- Pertussis
- Vorherige Impfungen
- Moderna 2nd shot & Pertussis
- Staat
- TX
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 02.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Injection site pain
Lethargy
Symptomtext
Chills (resolved within 12 hours), pain in arm at injection site (ongoing), lethargy (lasted ~24 hours)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- T1DM, hypothyroidism, HLD, uterine fibroids
- Andere Medikamente
- Levothyroxine, lisinopril, rosuvastatin, vitex
- Allergien
- Latex allergy, pork intolerance
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Injection site reaction
Urticaria
Symptomtext
Pt. states that after receiving the 2nd dose of Moderna 12/31/2021, started experiencing symptoms 01/01/2022 of headaches and welp running across the Left arm at the injection site. No noted Primary visit/communications. Self-Treating with Tylenol and Benadryl. Covid + 09/13/2021 received Covid Antibodies 09/14/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HBP, Asthma, Diabetes
- Andere Medikamente
- Zyrtec, Propanil, Monaclasp, Ometprosal, Metaphorim, Trazadone, Vitamin D3, Genial, Oxycodone, Amitriptyline
- Allergien
- Lasinapril, Lyrica
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anal incontinence
Angina pectoris
Hypoglycaemia
Malaise
Nausea
Vomiting
Symptomtext
Severe nausea/vomiting, hypoglycemia, angina, loss of bowels, malaise.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- BP checked x 2: 20 min apart (both WNL) Pupils evaluated (PERRLA)
- Aktuelle Erkrankungen
- anxiety
- Vorgeschichte
- anxiety
- Andere Medikamente
- cymbalta, zoloft
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Dizziness
Fatigue
Oropharyngeal pain
Pain in extremity
Vomiting
Symptomtext
Diarrhea vomiting dizzy fatigue arm pain sore throat....last for 5 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- -
- Andere Medikamente
- Paroxetine
- Allergien
- Sulfur
- Vorherige Impfungen
- Flu shot 17 yrs ago
- Staat
- FL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Headache
Pain
Symptomtext
Headache- within 24 hours lasted for 3 days body ache- within 18 hours lasted for 3 days chills- within 18 hours, off and on for 3 days Fatigue- within 18 hours, lasted for 3 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes type 2, asthma, prothrombin 2 mutation, hemochromatosis
- Andere Medikamente
- Simvastatin, xyzal, xarelto, levemir, novolog, aspirin, actos
- Allergien
- Coconut, Benadryl, iodine
- Vorherige Impfungen
- Moderna Covid-19 2nd dose, same reaction as the booster
- Staat
- -
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site pain
Injection site swelling
Symptomtext
PATIENT REPORTS SWELLING AND PAIN IN ARM FROM THE INJECTION SITE TO BELOW THE ELBOW STARTING THE DAY AFTER VACCINATIONS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HX OF STROKE/CVD
- Andere Medikamente
- GABAPENTIN, METOPROLOL TARTRATE, FIORICET, BACLOFEN, ATORVASTATIN, KEPPRA, CLOPIDOGREL, SERTRALINE
- Allergien
- CODEINE
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- 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
Musculoskeletal stiffness
Symptomtext
Swollen lymph node under arm beginning approx 12 hours after injection. Stiff neck beginning approx 20 hours after injection. Tailbone pain on left side beginning approx 31 hours after injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Phentermine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Neck pain
Pain in extremity
X-ray
Symptomtext
extreme pain in left arm, shoulder, back of shoulder and left side of neck, was giving muscle relaxers. appt to see an otho dr Monday Jan 3
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- xray showed nothing
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- synthroid, protonix
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 02.01.2022
- Impfdatum
- 01.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Vision blurred
Vomiting
Symptomtext
Patient did not experience any adverse effects after first two doses of Moderna vaccine. 5 minutes after receiving booster (0.25mL) dose of Moderna, patient started experiencing blurry vision, dizziness and nausea. Gave ice pack to patient. Patient felt better after vomiting. Patient stated he did not eat anything all morning. He felt much better in about 10 minutes. Patient drank a bottle of water. I observed him for 30 minutes. He felt fine to leave.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Myalgia
Pain in extremity
Peripheral swelling
Pyrexia
Symptomtext
Severe pain in entire arm where vaccine was received about 12 hours after vaccine. Swelling in upper left arm also 12 hours after. Fever, chills, muscles aches less that 48 hours after vaccine. Severity of arm pain has not changed after 48 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 01.01.2022
- Impfdatum
- 19.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Decreased appetite
Dizziness
Eye discharge
Headache
Hypersomnia
Loss of personal independence in daily activities
Myalgia
Oral herpes
Pain in jaw
Pyrexia
Rash
Stomatitis
Symptomtext
Approx 12 hrs after dose, experienced fever, chills, jaw ache, muscle aches, eye discharge, headache, & dizziness. The fever and chills abated after a few hours; the headache persisted resulting in a lack of energy, appetite, or ability to do anything other than sleep for the next 24-30 hours. After that I noticed a rash covering my trunk with a few spots on back, arms, and legs. I also experienced mouth sores / fever blisters. Benedryl (oral & topical applications) have helped with rash although it has not disappeared. This was the booster dose. I had no reaction to 1st dose other than sore arm (injection site). 2nd dose caused fever, chills, headache & exhaustion but no rash & recovery much quicker than booster. I weigh between 100-105 lbs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Cephalosporins
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 31.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Dizziness
Fall
Symptomtext
Patient felt well sitting in vaccination room for a couple minutes. While walking to chair a few steps aware she suffered dizziness and loss of balance that led to a fall. She never lost consciousness and felt better almost immediately.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- EMS arrived and tested her 5 minutes later. She was alert and aware of surroundings. She declined further care.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypothyroidism
- Andere Medikamente
- levothyroxine
- Allergien
- no known allergies
- Vorherige Impfungen
- She claimed she had dizziness after a vaccine "years ago."
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Fatigue
Headache
Lymphadenopathy
Myalgia
Pyrexia
Symptomtext
Headache 12 hours after shot: Tylenol. Muscle and joint pain: Tylenol. Fever for 12 hours. Chills for 12 hours. Swollen arm glands. Since shot, still swollen: Tylenol, ibuprofen and heating pad. Felt tired since shot (including today).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Epilepsy
- Andere Medikamente
- Carbatrol; Zyrtec; Aspirin; Estradiol vaginal inserts; Ocuvite; Calcium; Multivitamin; Fiber capsules; Stool softener
- Allergien
- Penicillin; Etodolac; Flagyl
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Injection site erythema
Injection site pain
Lymphadenopathy
Sinus disorder
Symptomtext
Patient states that she began to feel tired 12/27/21 evening. She noticed redness and pain at the site a few hours after immunization as well. Swelling in her armpit started 12/28/21 and had not gotten better as of 12/29/21. She was also having sinus drainage.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- septra, penicillins
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Fatigue
Pyrexia
Symptomtext
Pt. states that after receiving the 3rd dose of Moderna 12/28/2021, started experiencing symptoms within 30mins of dizziness with continuing into the evening of fatigue, fever, and chills. No noted Primary visit/communications. Pt. still experiencing symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- Shingrix 12/2020 (flu-like symptoms lasting 3 days)
- Staat
- IN
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Nasal congestion
Nasopharyngitis
Pyrexia
Symptomtext
Low grade fever. Stuffy nose and cough like a head cold
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High cholesterol and blood pressure
- Andere Medikamente
- Lisinopril. Amlodipine. Rosuvastatin. Ubiquinol. Allergy relief medicine
- Allergien
- No
- Vorherige Impfungen
- Body ache and chills
- Staat
- KY
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Dysphonia
Electrocardiogram normal
Erythema
Heart rate increased
Interchange of vaccine products
Pharyngeal swelling
Speech disorder
Urticaria
Symptomtext
I previously received the Johnson and Johnson vaccine 3/3/31 and went to a Pharmacy to get a Moderna booster shot. Two days after injection on 12/25/21 I developed a few hives on the outside my both of my forearms. 50mg of Benadryl seemed to calm the reaction but give never completely faded. Later that night on the 25th some additional hives developed on my waist and backs of my knees. I took 50mg of Benadryl before bed. The next morning I woke with hives on all parts of both arms, beneath both arms around my crotch and waistline, back, shoulders, chest, neck and some redness on my face. Began prescription of 60mg of Prednisone and took first dose at approximately 12 noon. Benadryl was last taken at about 8pm. The next morning at 7am I woke with hives covering a significant amount of my body. Took daily dose of prednisone and took 50mg of Benadryl. At appx. 11am I took more Benadryl but reaction was only slightly impacted. Went out to eat lunch from 2-3 and people I was with noted my face and neck increasing in redness over the course of an hour. Took 50mg of Benadryl around 3-3:15. At 3:30 the decision was made to go to a local emergency department. While waiting to be seen by doctor I experienced chest tightness and my throat began to swell, speaking became difficult and my voice was lowered to a very low register. Quick evaluation when checking in to ED showed a 143 bpm heart rate. Upon seeing the doctor they administered epinephrine and Benadryl via IV and that calmed the reaction for some time but within 10-15 minutes hives retuned around my shoulders, chest, crotch. back, and down my arms. More Benadryl was given after about 30 minutes from original dose via IV. This calmed reaction again but it did not completely subside. Shortly after, I was released. I've continued taking 50mg of Benadryl every 4 hours and have seen a great reduction in symptoms but the hives continue to pop back up in smaller numbers especially with any lapses in taking Benadryl every 4 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- EKG, was negative - 12/27/21.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Fish oil pills, acidophilus, vitamin C
- Allergien
- No. Allergic to wasp stings
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Injection site rash
Symptomtext
Patient called pharmacy on 12/27/21 stating that she had side effects from her booster dose. She reported very high blood pressure that started occurring on 12/23/21 (vaccine given 12/22/21). Patient reported the following readings: 182/86, 170/94, 181/92, 188/93. Patient also reported developing a rash on her arm around the injection site. Patient said she was going to her doctor 12/27/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 26.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Discomfort
Incorrect route of product administration
Injection site erythema
Injection site pain
Injection site swelling
Injection site warmth
Myalgia
Skin swelling
Symptomtext
The Moderna booster dose (3rd shot) was injected into my left upper arm. It did not penetrate the deltoid muscle. The injection was subcutaneous only - not intramuscular. Beginning the evening following the shot there was a lot of swelling of the skin at the injection site, redness, warmth and pain. Into the next day 12/23/2021 these symptoms continued. I did not develop soreness in the muscles of the shoulder as I had with the two previous doses of Moderna vaccine. The swelling and discomfort of my skin was much greater.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Ear/bone infection
- Vorgeschichte
- Ear infection
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Pneumonia vaccine 2015.
- Staat
- FL
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cough
Dry throat
Interchange of vaccine products
Pruritus
Throat tightness
Symptomtext
pt had pfizer doses 1 & 2 previously -- 2nd pfizer dose given 4/9/2021 -- patient at clinic today to receive Moderna booster (half dose) -- dose given at 10:56, around 11:02 am she started experiencing itching on her chest, dry throat/cough -- 25mg po benadryl given -- medical response team called for assistance -- Dr. listened to her lungs which were clear at the time - BP 158/80 P:79 --- within 2 mins, her throat was becoming tight -- 0.30 epinephrine auto-injector administered --911 called for transport to ER for observation -- immediately symptoms (itching/throat tightness) resolved -- BP: 134/80 P:109 -- EMS arrived and transported to local ER --
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- anaphylaxis to IVP dye and flu vaccine -- ?? hives to bactrim and augmentin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Axillary pain
Fatigue
Hyperhidrosis
Lymphadenopathy
Oedema peripheral
Pain
Pyrexia
Sleep disorder
Symptomtext
A few hours after receiving the booster shot pain and swelling started to appear in the armpit of the arm where it was administered. I'm experiencing fatigue, pain, physical weakness, fever and extreme sweating during sleep. I also can't sleep well. The swelling of the lymph knots continues. The Lymph knot right in the armpit is noticeably swollen and hard and condition doesn't seem to improve, even two days after. First two doses of the vaccine were not as intense.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Possibly colonitis
- Andere Medikamente
- Ibuprophen Codemagnyl (Codeine tablet from DK, EU) Tylenol CBD oil
- Allergien
- possibly Tea Tree Oil
- Vorherige Impfungen
- First two doses of Moderna but not as intense.
- Staat
- PA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Disorientation
Hallucination
Headache
Heart rate irregular
Mood swings
Pain
Pyrexia
Sleep disorder
Symptomtext
Day after experienced body aches, head aches, and fever. Symptoms continued into second day but more mild. Night of second day began to feel disoriented, trouble recalling performed tasks, and mood swings. Early morning of third day awakened by fever and odd heart beat. Third day milder symptoms of disorientation, mild hallucinations with lights, shadows, or objects moving. Along with a discomfort in upper abdomen. Continued mood swings.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Advil
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 46,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- M
- Eingang
- 02.11.2023
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- F
- Eingang
- 02.11.2023
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 54,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 43,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 38,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- F
- Eingang
- 02.11.2023
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 54,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 20,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 02.11.2023
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 02.11.2023
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 67,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 68,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 36,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 02.11.2023
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 59,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 56,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 42,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 54,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 48,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 48,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 02.11.2023
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 64,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- F
- Eingang
- 02.11.2023
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 69,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 56,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 64,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- MN
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 01.11.2023
- Impfdatum
- 06.01.2022
- Beginn
- 30.10.2023
- Tage bis Beginn
- 662,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 01.11.2023
- Impfdatum
- 06.01.2022
- Beginn
- 30.10.2023
- Tage bis Beginn
- 662,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Unevaluable event
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- F
- Eingang
- 31.10.2023
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- F
- Eingang
- 31.10.2023
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 46,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 31.10.2023
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 31.10.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- 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
- 46,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- M
- Eingang
- 31.10.2023
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 31.10.2023
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 31.10.2023
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- F
- Eingang
- 31.10.2023
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 63,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 31.10.2023
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 59,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 39,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 29.12.2022
- Beginn
- 29.12.2022
- 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
- 23,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 37,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- F
- Eingang
- 31.10.2023
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- 65,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- 64,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 54,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 63,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 29.12.2022
- Beginn
- 29.12.2022
- 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
- 31.10.2023
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- F
- Eingang
- 31.10.2023
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 46,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 21,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 63,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 56,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 31,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- F
- Eingang
- 31.10.2023
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 51,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- 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
- 38,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 38,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 50,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- 31.10.2023
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 31.10.2023
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 19,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 31.10.2023
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 63,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 52,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- M
- Eingang
- 31.10.2023
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 71,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 30.12.2022
- Beginn
- 30.12.2022
- 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
- 48,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 31.10.2023
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 36,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 26.01.2021
- Beginn
- 26.01.2021
- 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
- M
- Eingang
- 31.10.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 31.10.2023
- Impfdatum
- 28.01.2021
- Beginn
- 28.01.2021
- 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
- 40,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 39,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 72,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 48,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 48,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- 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
- AR
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 26.01.2022
- Beginn
- 21.10.2023
- Tage bis Beginn
- 633,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
hospitalized for covid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- HTN CAD s/p 2 stents HLD H/O melanoma
- Andere Medikamente
- unknown
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 61,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 24,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product 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
- 32,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 29.12.2022
- Beginn
- 29.12.2022
- 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
- F
- Eingang
- 31.10.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 31.10.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 88,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- 88,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- 31.10.2023
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- 31.10.2023
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- 31.10.2023
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- 31.10.2023
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- 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
- 47,0
- Geschlecht
- M
- Eingang
- 31.10.2023
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Incorrect dose administered
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
- 30.10.2023
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 70,0
- Geschlecht
- F
- Eingang
- 30.10.2023
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 30.10.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 56,0
- Geschlecht
- M
- Eingang
- 30.10.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 23,0
- Geschlecht
- F
- Eingang
- 30.10.2023
- Impfdatum
- 29.12.2022
- Beginn
- 29.12.2022
- 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
- 65,0
- Geschlecht
- F
- Eingang
- 30.10.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 52,0
- Geschlecht
- F
- Eingang
- 30.10.2023
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 32,0
- Geschlecht
- F
- Eingang
- 30.10.2023
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 56,0
- Geschlecht
- M
- Eingang
- 30.10.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- M
- Eingang
- 30.10.2023
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- F
- Eingang
- 30.10.2023
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 32,0
- Geschlecht
- F
- Eingang
- 30.10.2023
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product 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
- 39,0
- Geschlecht
- F
- Eingang
- 30.10.2023
- Impfdatum
- 06.01.2021
- Beginn
- 06.01.2021
- 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
- 23,0
- Geschlecht
- M
- Eingang
- 30.10.2023
- Impfdatum
- 26.01.2021
- Beginn
- 26.01.2021
- 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
- FL
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 25.09.2023
- Impfdatum
- 02.01.2022
- Beginn
- 20.09.2023
- Tage bis Beginn
- 626,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adult failure to thrive
COVID-19
Cardiac failure congestive
Diabetes mellitus
Gait disturbance
Generalised oedema
Loss of personal independence in daily activities
Urinary tract infection
Symptomtext
Hospitalization for ambulatory dysfunction, COVID-19 (high risk of complication), decreased activities of daily living, failure to thrive, anasarca, CHF, diabetes, UTI on dates 9/20/2023- 9/23/2023. Treated with vitamin D 25 mcg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Adult failure to thrive
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- metformin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- 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
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
- CA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 02.08.2023
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- CA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 02.08.2023
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- 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
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
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.07.2023
- Impfdatum
- 18.06.2022
- Beginn
- 18.06.2022
- 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
Symptomtext
No adverse event; Patient received Moderna Covid-19 monovalent vaccine on 18-JUN-2022 which was expired in 27-MAR-2022; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 18-JUN-2022 which was expired in 27-MAR-2022) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 18-Jun-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 18-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 18-JUN-2022 which was expired in 27-MAR-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 18-JUN-2022 which was expired in 27-MAR-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 assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 18-JUN-2022 which was expired in 27-MAR-2022). No concomitant medication was reported. It was reported that 4 doses of the Moderna Covid-19 vaccine were administered on 18-JUN-2022. 3 doses of Moderna Covid-19 vaccine were administered on 22-June-2023. No treatment information was reported. This case contains information for patient 1 out of 7. This case was linked to US-MODERNATX, INC.-MOD-2023-731896, US-MODERNATX, INC.-MOD-2023-731899, US-MODERNATX, INC.-MOD-2023-731901, US-MODERNATX, INC.-MOD-2023-731900, US-MODERNATX, INC.-MOD-2023-731898, US-MODERNATX, INC.-MOD-2023-731897 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-731896:Patient 2 (18-JUN-2022) US-MODERNATX, INC.-MOD-2023-731899:Patient 5 (22-JUN-2023) US-MODERNATX, INC.-MOD-2023-731901:Patient 7(22-JUN-2023) US-MODERNATX, INC.-MOD-2023-731900:Patient 6 (22-JUN-2023) US-MODERNATX, INC.-MOD-2023-731898:Patient 4 (18-JUN-2022) US-MODERNATX, INC.-MOD-2023-731897:Patient 3 (18-JUN-2022)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.07.2023
- Impfdatum
- 22.06.2022
- Beginn
- 22.06.2022
- 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
Symptomtext
No adverse event; Patient received Moderna Covid-19 monovalent vaccine in June of 2022. The vaccine expired in March 27, 2022; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine in June of 2022. The vaccine expired in March 27, 2022) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Jun-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 22-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine in June of 2022. The vaccine expired in March 27, 2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine in June of 2022. The vaccine expired in March 27, 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 assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine in June of 2022. The vaccine expired in March 27, 2022). No concomitant information was reported. Suspect product dosage text was reported as unknown. No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2023-731892 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-731892:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.07.2023
- Impfdatum
- 22.06.2022
- Beginn
- 22.06.2022
- 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
Symptomtext
No adverse event; Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2022 which was expired in 27-MAR-2022; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2022 which was expired in 27-MAR-2022) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Jun-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 22-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2022 which was expired in 27-MAR-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2022 which was expired in 27-MAR-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 assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2022 which was expired in 27-MAR-2022). No concomitant medication was reported. Dosage text was reported as unknown. No treatment information was reported. This case contains information for patient 6 out of 7. This case was linked to US-MODERNATX, INC.-MOD-2023-731892 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-731892:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.07.2023
- Impfdatum
- 22.06.2023
- Beginn
- 22.06.2023
- 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; Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2022 which was expired by 27-MAR-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2022 which was expired by 27-MAR-2022) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Jun-2023, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 22-Jun-2023, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2022 which was expired by 27-MAR-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2022 which was expired by 27-MAR-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 assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2022 which was expired by 27-MAR-2022). No concomitant medication was reported. It was reported that 4 doses of the Moderna Covid-19 vaccine were administered on 18-JUN-2022. 3 doses of Moderna Covid-19 vaccine were administered on 22-June-2023. No treatment information was reported. This case contains information for patient 5th out of 7. This case was linked to US-MODERNATX, INC.-MOD-2023-731892 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-731892:Master case patient 1
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.07.2023
- Impfdatum
- 22.06.2023
- Beginn
- 22.06.2023
- 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; Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2023 which was expired in 27-MAR-2022; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2023 which was expired in 27-MAR-2022) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Jun-2023, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 22-Jun-2023, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2023 which was expired in 27-MAR-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2023 which was expired in 27-MAR-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 assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2023 which was expired in 27-MAR-2022). No concomitant medication was reported. It was reported that 4 doses of the Moderna Covid-19 vaccine were administered on 18-JUN-2022. 3 doses of Moderna Covid-19 vaccine were administered on 22-June-2023. No treatment information was reported. This case contains information for patient 6th out of 7. This case was linked to US-MODERNATX, INC.-MOD-2023-731892 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-731892:Master case patient (1)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.07.2023
- Impfdatum
- 18.06.2022
- Beginn
- 18.06.2022
- 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
Symptomtext
No adverse event; 7 patients received Moderna Covid-19 monovalent vaccine in June of 2022. The vaccine expired in March 27, 2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (7 patients received Moderna Covid-19 monovalent vaccine in June of 2022. The vaccine expired in March 27, 2022) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 18-Jun-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 18-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (7 patients received Moderna Covid-19 monovalent vaccine in June of 2022. The vaccine expired in March 27, 2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (7 patients received Moderna Covid-19 monovalent vaccine in June of 2022. The vaccine expired in March 27, 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 assessment was provided for EXPIRED PRODUCT ADMINISTERED (7 patients received Moderna Covid-19 monovalent vaccine in June of 2022. The vaccine expired in March 27, 2022). No concomitant medication was reported. The dosage text was reported as unknown. It was reported that 4 doses of the Moderna Covid-19 vaccine were administered on 18-Jun-2022 and 3 doses of Moderna Covid-19 vaccine were administered on 22-Jun-2022. The expiry date was reported as 27-Mar-2022. No treatment information was reported. This case contains information for patient 3rd out of 7 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-731892 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-731892:MASTER CASE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.07.2023
- Impfdatum
- 22.06.2023
- Beginn
- 22.06.2023
- 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; Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2023 which was expired in 27-MAR-2022; This spontaneous case was reported by a medical assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2023 which was expired in 27-MAR-2022) and NO ADVERSE EVENT (No adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Jun-2023, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 22-Jun-2023, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2023 which was expired in 27-MAR-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2023 which was expired in 27-MAR-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 assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient received Moderna Covid-19 monovalent vaccine on 22-JUN-2023 which was expired in 27-MAR-2022). No concomitant medication was reported. It was reported that 4 doses of the Moderna Covid-19 vaccine were administered on 18-JUN-2022. 3 doses of Moderna Covid-19 vaccine were administered on 22-June-2023. Expiry date was reported as 27-Mar-2022. No treatment information was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-731892 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-731892:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 14.05.2023
- Impfdatum
- 10.01.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 26,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Amenorrhoea
Immediate post-injection reaction
Symptomtext
I was 52 and still had regular menstruation. My period stopped after the COVID-19 booster. It stopped immediately. While I think I was approaching menopause, it is not typically a sudden full stop.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amenorrhoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- multi-vitimin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 06.04.2023
- Impfdatum
- 08.02.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 82,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
COVID-19; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (COVID-19) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 prophylaxis. Concurrent medical conditions included Chronic lymphocytic leukemia (Indolent) and Pollen allergy. On 08-Feb-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In May 2022, the patient experienced COVID-19 (COVID-19). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) for COVID-19, at an unspecified dose and frequency. At the time of the report, COVID-19 (COVID-19) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. Patient felt like she had a cold by the end of the week patient was fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Chronic lymphocytic leukemia (Indolent); Pollen allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 04.04.2023
- Impfdatum
- 29.12.2021
- Beginn
- 03.04.2023
- Tage bis Beginn
- 460,0
- 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 4/6/21 Lot# 016B21A; Moderna 5/4/21 Lot# 009C21A; Moderna 12/29/21 Lot# 059H21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 14.03.2023
- Impfdatum
- 04.01.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 321,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 3/7/21 Lot# 030A21A; Moderna 4/6/21 Lot# 018B21A; Moderna 1/4/22 Lot# 059H21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 03.03.2023
- Impfdatum
- 17.07.2022
- Beginn
- 18.12.2022
- Tage bis Beginn
- 154,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bronchitis
COVID-19
Chest X-ray abnormal
SARS-CoV-2 test positive
Symptomtext
Admitted for bronchitis with COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bronchitis
- Hospital-Tage
- 73,0
- Labordaten
- PCR testing, CXR
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, HTN, CKD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 14.01.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 55,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal uterine bleeding
Abortion spontaneous
Amenorrhoea
Endometrial atrophy
Infertility female
Maternal exposure before pregnancy
Pregnancy
Pregnancy test positive
Pregnancy with contraceptive device
Smear cervix
Ultrasound uterus abnormal
Uterine dilation and curettage
Symptomtext
Pregnancy (30 days after second Moderna vaccine) with in date, correctly placed, and fully functional IUD. Subsequent miscarriage in which a surgical D & C had to be performed for a missed miscarriage. Amenorrhea and infertility sustained for 7 months in combination with uterine endometrial lining noted to be fairly thin at 5.5 mm during ultrasound with no plausible explanation or cause.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abnormal uterine bleeding
- Hospital-Tage
- -
- Labordaten
- Ultrasound for Amenorrhea- 10/19/2022 Pap smear- 09/21/2022 Suction Dilatation & Curettage- 05/27/2022 Abnormal uterine bleeding and Positive pregnancy test with IUD- 04/18/2022
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Melatonin, Unisom, hormonal, IUD Mirena
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 20.02.2023
- Impfdatum
- 20.12.2021
- Beginn
- 19.07.2022
- Tage bis Beginn
- 211,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Underdose
Wrong product administered
Symptomtext
Patient received first dose 0.25 ml on 20-Dec-2021 and second dose 0.25 ml on 19-Jul-2022; No adverse event; 11 patients instead of 20 patients who were inadvertently administered with the monovalent vaccine instead of the bivalent booster dose; Patient received first dose 0.25 ml on 20-Dec-2021 and second dose 0.25 ml on 19-Jul-2022; This spontaneous case was reported by a pharmacist and describes the occurrence of WRONG PRODUCT ADMINISTERED (11 patients instead of 20 patients who were inadvertently administered with the monovalent vaccine instead of the bivalent booster dose), UNDERDOSE (Patient received first dose 0.25 ml on 20-Dec-2021 and second dose 0.25 ml on 19-Jul-2022), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received first dose 0.25 ml on 20-Dec-2021 and second dose 0.25 ml on 19-Jul-2022) and NO ADVERSE EVENT (No adverse event) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. AR6965B, 05N322A and 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 20-Dec-2021 at 10:21 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 19-Jul-2022 at 9:43 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .25 milliliter. On 20-Jan-2023 at 10:09 AM, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .5 milliliter. On 19-Jul-2022 at 9:43 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received first dose 0.25 ml on 20-Dec-2021 and second dose 0.25 ml on 19-Jul-2022). On 20-Jan-2023 at 10:09 AM, the patient experienced WRONG PRODUCT ADMINISTERED (11 patients instead of 20 patients who were inadvertently administered with the monovalent vaccine instead of the bivalent booster dose). On an unknown date, the patient experienced UNDERDOSE (Patient received first dose 0.25 ml on 20-Dec-2021 and second dose 0.25 ml on 19-Jul-2022) and NO ADVERSE EVENT (No adverse event). At the time of the report, WRONG PRODUCT ADMINISTERED (11 patients instead of 20 patients who were inadvertently administered with the monovalent vaccine instead of the bivalent booster dose), UNDERDOSE (Patient received first dose 0.25 ml on 20-Dec-2021 and second dose 0.25 ml on 19-Jul-2022), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received first dose 0.25 ml on 20-Dec-2021 and second dose 0.25 ml on 19-Jul-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered WRONG PRODUCT ADMINISTERED (11 patients instead of 20 patients who were inadvertently administered with the monovalent vaccine instead of the bivalent booster dose) and NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for UNDERDOSE (Patient received first dose 0.25 ml on 20-Dec-2021 and second dose 0.25 ml on 19-Jul-2022) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received first dose 0.25 ml on 20-Dec-2021 and second dose 0.25 ml on 19-Jul-2022). Concomitant medications were not reported. The patient received all doses in left side of body. It was reported that Moderna monovalent vaccine was administered to approximately 20 patients from 11-Jan-2023 to 21-Jan-2023, instead of the Moderna bivalent booster. HCP wanted to know if these patients can receive the Moderna bivalent booster shot after that incorrect dose, and how long should they wait to receive it. The patient did not experience similar event in the past. The event did not cause patient to seek medical care. No other potential causes for the event. Upon follow up they stated that there were only 11 patients instead of 20 patients who were inadvertently administered with the monovalent vaccine instead of the bivalent booster dose. Treatment information was not provided. This case pertains to 13th of the total 20 patients. This case was linked to US-MODERNATX, INC.-MOD-2023-704234 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Follow up received wherein the patient demographics, product and narrative updated. On 25-Jan-2023: Live follow-up document received contains no new information. On 06-Feb-2023: Significant follow up received contains route of administration added, event verbatim and narrative updated. On 06-Feb-2023: Follow-up document received contain no new information. On 07-Feb-2023: Follow-up document received contain no new information. On 15-Feb-2023: Significant follow-up received contains reporter details added, patient details added, suspect details added, event details and causality updated, narrative updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704234.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 18.02.2023
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Underdose
Wrong product administered
Symptomtext
No adverse event; There were only 11 patients instead of 20 patients who were inadvertently administered with the monovalent vaccine instead of the bivalent booster dose/ Patient was to get Bivalent but received monovalent; 0.25 ml received for Dose 1 instead of 0.5 ml; This spontaneous case was reported by a pharmacist and describes the occurrence of WRONG PRODUCT ADMINISTERED (There were only 11 patients instead of 20 patients who were inadvertently administered with the monovalent vaccine instead of the bivalent booster dose/ Patient was to get Bivalent but received monovalent), UNDERDOSE (0.25 ml received for Dose 1 instead of 0.5 ml) and NO ADVERSE EVENT (No adverse event) in a 69-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. AR6965B, 7H593 and 059H21A) for COVID-19 prophylaxis. It was unknown if patient was ever been diagnosed with/ tested positive for COVID-19. Patient had no acute illnesses at the time of vaccination and up to one month before. Patient had no chronic or long-standing health conditions. Patient did not had any prescriptions, over-the-counter medications, dietary supplements, or herbal remedies taken at time of vaccination and/or at the time of the adverse event. Patient had no known drug allergies. On 20-Dec-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 19-Jan-2022, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .5 milliliter. On 20-Jan-2023, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .5 milliliter. On 20-Dec-2021 at 10:21 AM, the patient experienced UNDERDOSE (0.25 ml received for Dose 1 instead of 0.5 ml). On 20-Jan-2023 at 10:49 AM, the patient experienced WRONG PRODUCT ADMINISTERED (There were only 11 patients instead of 20 patients who were inadvertently administered with the monovalent vaccine instead of the bivalent booster dose/ Patient was to get Bivalent but received monovalent). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, WRONG PRODUCT ADMINISTERED (There were only 11 patients instead of 20 patients who were inadvertently administered with the monovalent vaccine instead of the bivalent booster dose/ Patient was to get Bivalent but received monovalent), UNDERDOSE (0.25 ml received for Dose 1 instead of 0.5 ml) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered WRONG PRODUCT ADMINISTERED (There were only 11 patients instead of 20 patients who were inadvertently administered with the monovalent vaccine instead of the bivalent booster dose/ Patient was to get Bivalent but received monovalent) and NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for UNDERDOSE (0.25 ml received for Dose 1 instead of 0.5 ml). Concomitant medication was not provided. HCP stated that they had a situation at the pharmacy where Moderna monovalent vaccine was administered to approximately 20 patients from 11-Jan-2023 to 21-Jan-2023, instead of the Moderna bivalent booster. Later upon follow up reporter called back on 06-Feb-2023 at 3:35pm and stated that there were only 11 patients instead of 20 patients who were inadvertently administered with the monovalent vaccine instead of the bivalent booster dose. Patient administered the Dose 1 at 10:21 am on 20-Dec-2021, Dose 2 at 10:07 am on 19-Jan-2022 and Dose 3 at 10:49 am on 20-Jan-2023. Treatment information was not reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704234 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Follow-up received on 24-Jan-2023 with patient details and vaccination date added. On 25-Jan-2023: Follow-up document received on 25-Jan-2023 with no new information. On 06-Feb-2023: Follow-up document received on 06-Feb-2023 with no new information received. On 06-Feb-2023: Follow-up information received on 06-Feb-2023 includes vaccine route of administration, event verbatim and I-narrative supplement were updated. On 07-Feb-2023: Follow-up document received on 07-Feb-2023 contains no new information. On 15-Feb-2023: Upon receipt of the follow-up for the case MOD-2022-704882 on 15-Feb-2023, it was identified that the case MOD-2022-704882 was created with year 2022 however Initial IRD of the report was 23-Jan-2023. Hence, the case MOD-2022-704882 was nullified from the database and a newcase MOD-2023-710801 was created. Follow-up document received on 15-Feb-2023 for the case MOD-2022-704882 with Vaccination details and Event added.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704234:Master
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient was ever been diagnosed with/ tested positive for COVID-19. Patient had no acute illnesses at the time of vaccination and up to one month before. Patient had no chronic or long-standing health conditions. Patient did not had any prescriptions, over-the-counter medications, dietary supplements, or herbal remedies taken at time of vaccination and/or at the time of the adverse event. Patient had no known drug allergies.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 06.01.2022
- Beginn
- 16.02.2023
- Tage bis Beginn
- 406,0
- 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
- TX
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 13.01.2023
- Impfdatum
- 12.01.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 264,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Atrial fibrillation
Chest discomfort
Electrocardiogram abnormal
Heart rate increased
Laboratory test abnormal
Symptomtext
I woke up early on the 3rd of October. I knew something was not correct. My chest didn't feel normal. I checked my pulse and saw I had a very fast heartbeat. I laid in bed for a while waiting for a change it didn't. My smart watch EKG said I was in AFIB. I called my local Cardiologist, left a message. I got my wife up and taken to the ER where I was admitted. I was diagnosed very quickly that I was in AFIB. I don't know what all they did to me. I was admitted and put on IV's and at least two different medications. CARDIZEM was the medication given that I noticed when they. MULTAQ was another medication. When they discharged me the put me on MULTAQ 400mg twice a day. And I was taking ELIQUIS at that time I have Leiden Factor 5 G mutation. It is genic and I take ELIQUIS for the rest of my life. They increased that dosage as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- 1,0
- Labordaten
- 03Oct2022 Multiple test, all abnormal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Low Density Lipoproteins
- Andere Medikamente
- Vitamin D3; super K; multivitamin; fish oil; SLO-NIACIN; rosuvastatin; ELIQUIS
- Allergien
- N/A
- Vorherige Impfungen
- 10/31/1969 Flu vaccination chills and body aches 6 hours later.
- Staat
- KY
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 31.01.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 332,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54-year-old male patient received BNT162b2 (BNT162B2), on 25Dec2020 at 11:00 as dose 1, single (Lot number: EL0140), in left arm, on 19Jan2021 at 16:00 as dose 2, single (Lot number: FJ1686), in left arm and on 31Jan2022 at 16:00 as dose 3 (booster), single (Lot number: 059H21A) at the age of 53 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: penicillin" (unspecified if ongoing). Concomitant medication(s) included: OMEPRAZOLE, start date: 01Aug2020. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 29Dec2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (03Jan2023) negative, notes: Tested negative; (07Jan2023) positive, notes: Tested positive immediately with 2 covid tests; (07Jan2023) positive, notes: Tested positive immediately with 2 covid tests; (29Dec2022) positive, notes: Tested positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Other medication in 2 weeks: Yes. The patient received Antiviral drug Paxlovid from 29Dec2022 to 02Jan2023 for the treatment of COVID-19. Other medical history: Pacemaker implanted 03Jun2022. Not on medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230103; Test Name: covid; Test Result: Negative ; Comments: Tested negative; Test Date: 20230107; Test Name: covid; Test Result: Positive ; Comments: Tested positive immediately with 2 covid tests; Test Date: 20230107; Test Name: covid; Test Result: Positive ; Comments: Tested positive immediately with 2 covid tests; Test Date: 20221229; Test Name: pcr; Test Result: Positive ; Comments: Tested positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy
- Andere Medikamente
- OMEPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 09.01.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 204,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Female sex hormone level abnormal
Heavy menstrual bleeding
Vaginal haemorrhage
Symptomtext
I was passing palm sized blood clots. I wouldn't stop bleeding after my period. I ended up having to go to the emergency room. I was prescribed iron and constipation medication. I was also prescribed a month of birth control to regulate the hormones and control the bleeding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Female sex hormone level abnormal
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Avocado; latex
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Neurological symptom
Symptomtext
stroke like symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neurological symptom
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- lexipro
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 29.12.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 29.12.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 29.12.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Given past 30 day fridge use by date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Given past 30 day fridge use by date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Given past 30 day fridge use by date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Given past 30 day fridge use by date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Given past 30 day fridge use by date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Given past 30 day fridge use by date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Given past 30 day fridge use by date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Given past 30 day fridge use by date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Given past 30 day fridge use by date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Given past 30 day fridge use by date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Given past 30 day fridge use by date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 24.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent dose administered after the BUD to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) in a 26-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 24-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient). It was reported that it was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Patient ID was reported as Unknown. Concomitant product use was not provided by the reporter. It was reported that 77 Monovalent doses administered after the BUD to patients 12 and up. Breakdown of doses were as follows- 37 doses from Lot 059H21, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 24.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Monovalent doses administered after the BUD to patients; no adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 61-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medication information was reported. 77 Monovalent doses administered after the BUD to patients 12 and up. Breakdown of doses is as follows- 37 doses from Lot 059H21, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A No treatment medication information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 24.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent dose administered after the BUD to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient) and NO ADVERSE EVENT (No adverse event) in a 33-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 24-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient). It was reported that it was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Patient ID was reported. Concomitant product use was not provided by the reporter. It was reported that 77 Monovalent doses administered after the BUD to patients 12 and up. Breakdown of doses were as follows- 37 doses from Lot 059H21, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- -
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 22.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Monovalent doses administered after the BUD to patient; no adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) in an adolescent male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient). No concomitant medication information was provided. No treatment medications were provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 18.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Monovalent doses administered after the BUD to patients; no adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 47-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 18-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medication information was reported. 77 Monovalent doses administered after the BUD to patients 12 and up. Breakdown of doses is as follows- 37 doses from Lot 059H21, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A No treatment medication information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- 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
No adverse event
Symptomtext
no adverse event; Monovalent dose administered after the BUD to patients.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patients.) and NO ADVERSE EVENT (no adverse event) in a 50-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 26-May-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 26-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patients.). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patients.) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patients.). No concomitant medications were reported. It was unknown whether patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 24.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent dose administered after the BUD to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) in a 57-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 059H21A and 058A22-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 28-Jul-2022, received dose of mRNA-1273 (Spikevax) (Intramuscular) dosage was changed to 1 dosage form. On 24-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient). It was reported that it was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Concomitant product use was not provided by the reporter. It was reported that 77 Monovalent doses administered after the BUD to patients 12 and up. Breakdown of doses were as follows- 37 doses from Lot 059H21, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 20-Dec-2022: Live follow-up received: other dose details were updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 41-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 18-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 18-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). Patient ID was reported. It was unknown if the patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. No concomitant drug was reported. Reportedly, the patient was eligible for COVID-19 vaccine. No treatment drug was reported. This case was linked to MOD-2022-690879 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 43-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 18-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 18-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). Concomitant medication was not reported. Patient ID was reported as 5696088. It was unknown if the patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Reportedly, in this report the patient was eligible for COVID-19 vaccine. Breakdown of doses were reported as 37 doses from Lot 059H21, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A. Treatment medication was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 55-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 18-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 18-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). Patient ID was mentioned as 4961178. No concomitant medications was reported. It was reported that it was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was reported that 77 Monovalent doses administered after the BUD to patients 12 and up. Breakdown of doses is as follows- 37 doses from Lot 059H21, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A. Treatment information was not provided. This case was linked to MOD-2022-690803 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 27-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 04-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). Concomitant medication was not provided. It was reported that it was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was reported that 77 Monovalent doses administered after the BUD to patients 12 and up. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 30-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 04-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medications were reported. It was reported that 113 Bivalent doses were administered after the BUD to patients 12 and up. 51 doses were administered from Lot AS7140C, and 60 doses from Lot AS7148B. No treatment medications were reported. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 48-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 04-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) 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 (Monovalent doses administered after the BUD to patients). No concomitant medication information was provided. Total 77 Monovalent doses were administered after the BUD to patients 12 and up.37 doses from Lot 059H21, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A. It was unknown patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 30-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 04-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). It was unknown if the patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. No concomitant drug was reported. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 02.11.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 58-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 02-Nov-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 02-Nov-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant drug was reported. Patient ID was reported as Unknown It was unknown if the patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Reportedly, the patient was eligible for COVID-19 vaccine. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 43-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 04-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). It was unknown if the patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. No concomitant drug was reported. Reportedly, the patient was eligible for COVID-19 vaccine. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 29-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 04-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) 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 (Monovalent doses administered after the BUD to patients). It was reported as COVID19 Eligible. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. No concomitant medication were reported. 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
- CO
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 57-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 11-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 11-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant drug was reported. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 26-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 28-Jan-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 28-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medications were reported. Total 77 Monovalent doses were administered after the BUD to patients 12 and up.37 doses from Lot 059H21, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. 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
- CO
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 27-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 28-Jan-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 28-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). Concomitant product use was not provided by the reporter. It was reported that it was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was reported that 77 Monovalent doses administered after the BUD to patients 12 and up. Breakdown of doses is as follows- 37 doses from Lot 059H21, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 23-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 28-Jan-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 28-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). Patient ID was reported as Unknown. It was unknown if the patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. No concomitant drug was reported. Reportedly, the patient was eligible for COVID-19 vaccine. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) in a 30-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 04-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient). Patient ID was reported. Concomitant medication was not reported. Reportedly, in this report the patient was eligible for COVID-19 vaccine. Treatment medication was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 27-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 28-Jan-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 28-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medications were reported. No treatment details were reported. It was reported that it was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was reported that total 77 Monovalent doses were administered after the BUD to patients 12 and up. 37 doses from lot 059H21, 26 Doses from lot 065K21A and 12 doses from lot 058A22-2A.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient) and NO ADVERSE EVENT (No adverse event) in a 26-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 28-Jan-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 28-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient). Patient ID was reported. It was unknown if the patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. No concomitant drug was reported. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) in a 46-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 28-Jan-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 28-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient). Patient ID was reported. Concomitant medications details were not reported by the reporter. It was unknown if the patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Reportedly, the patient was eligible for COVID-19 vaccine. Treatment details were not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 48-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 28-Jan-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 28-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No relevant concomitant medications were reported. 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
- CO
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 34-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 28-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medications were reported. It was reported that it was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. 77 Monovalent doses administered after the BUD to patients 12 and up. It was reported that 37 doses from Lot 059H21A, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A were administered. 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
- CO
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 21.07.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 47-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 21-Jul-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 21-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medications were reported. It was reported that it was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. 77 Monovalent doses administered after the BUD to patients 12 and up. It was reported that 37 doses from Lot 059H21A, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A were administered. 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
- CO
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 19-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Jul-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 15-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medications were reported. It was reported that it was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. 77 Monovalent doses administered after the BUD to patients 12 and up. It was reported that 37 doses from Lot 059H21A, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A were administered. 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
- CO
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 48-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Jul-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 15-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medications were reported. It was reported that it was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. 77 Monovalent doses administered after the BUD to patients 12 and up. It was reported that 37 doses from Lot 059H21A, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A were administered. 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
- CO
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to Patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to Patients) and NO ADVERSE EVENT (No adverse event ) in a 50-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 11-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 11-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to Patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event ). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to Patients) 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 (Monovalent doses administered after the BUD to Patients). ID was reported as 7552537. Concomitant medications details were not reported by the reporter. It was unknown if the patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Total 77 Monovalent doses were administered after the BUD to patients 12 and up. Breakdown of doses was, 37 doses from Lot 059H21, 26 doses from Lot 065K21A and 12 doses from Lot 058A22-2A. Treatment details were not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 24.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 24.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 24.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 24.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
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
- 27.12.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
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
- 27.12.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- 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
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- 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
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- 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
No adverse event
Symptomtext
Inadvertent administration past the 30-day Use by Date of the Moderna vaccine. No Symptoms to report as no adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- -
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 04.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Monovalent doses administered after the BUD to patient; no adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) in an adolescent female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Intramuscular) was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patient). No concomitant medication information was provided. No treatment medications were provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 40-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 11-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 11-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). It was unknown if the patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. No concomitant drug was reported. Reportedly, the patient was eligible for COVID-19 vaccine. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- 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
No adverse event
Symptomtext
No adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 35-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 02-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 02-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medication details was reported. 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
- CO
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 42-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 28-Jan-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 28-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medications was provided. No treatment medications was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent dose administered after the BUD to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) in a 48-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 04-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient). No concomitant medications were reported. It was unknown whether patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Treatment information was not provided. This case was linked (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent dose administered after the BUD to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) in a 55-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 18-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 18-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent dose administered after the BUD to patient). No concomitant medications were reported. It was unknown whether patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 04.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Monovalent doses administered after the BUD to patients; No adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in a 62-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medication information was reported. 77 Monovalent doses administered after the BUD to patients 12 and up. Breakdown of doses is as follows- 37 doses from Lot 059H21, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A No treatment medication information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; Monovalent doses administered after the BUD to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) in a 48-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Feb-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 04-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No relevant concomitant medications were reported. 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
- CO
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.12.2022
- 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
No adverse event
Symptomtext
Monovalent doses administered after the BUD to patients; No adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) in an adolescent patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Monovalent doses administered after the BUD to patients). No concomitant medication information was reported. Monovalent doses administered after the BUD to patients 12 and up. Breakdown of doses is as follows- 37 doses from Lot 059H21, 26 doses from Lot 065K21A, and 12 doses from Lot 058A22-2A. No treatment medication information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 06.12.2022
- Impfdatum
- 07.01.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 332,0
- 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. Pfizer 4/13/21 EW0158, 5/4/21 EW0169 and boosted Moderna 1/7/22 059H21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID test on 12/5/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 29.11.2022
- Impfdatum
- 30.12.2021
- Beginn
- 19.11.2022
- Tage bis Beginn
- 324,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Chest X-ray normal
Cough
Laboratory test normal
Symptomtext
COVID+ 11/19/2022 Vaccination status - Pfizer x2, moderna x1 BRIEF OVERVIEW: Discharge Provider: PRIVATE DO Primary Care Provider: PRIVATE MD Admission Date: 11/19/2022 Discharge Date: Nov 23, 2022 Active Hospital Problems Diagnosis Date Noted POA ? COVID-19 11/20/2022 Yes ? Foster care (status DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: COVID-19 [U07.1] HOSPITAL COURSE: 25-year-old male with cerebral palsy and developmental delay resides at PRIVATE. Pt. presented to the ED with concerns of a cough. He was found to have COVID and admitted to the hospital. Chest x-ray and labs were unremarkable. No treatment was initiated as patient's O2 sats were WNL on room air throughout his admission. Pt. will follow up with his PCP outpatient. He will return to his PRIVATE in improved and stable condition. Attestation signed by PRIVATE, DO at 11/23/2022 5:09 PM I have personally interviewed and examined the patient on 11/23/2022. Management was discussed. I agree with the documented findings and plan of care in his/her note. Brief exam: Gen: Awake, NAD CV: RRR Lungs: CTAB Abd: Soft, ND/NT Ext: Contractures of LE bilaterally Brief history and medical decision making: Patient is a 25-year-old male with history as outlined below who presented to the emergency department with concerns of cough. He was found to have COVID with chest x-ray and blood work unremarkable. Patient did not require treatment for COVID during his stay due to no hypoxia and minimal symptoms. Discharge was delayed due to ability to return to his PRIVATE, however patient was discharged back to home in stable condition on 11/23/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pre-Existing Active Problems Diagnosis Date Noted POA ? Diplegic cerebral palsy (HCC) 12/14/2017 Unknown ? Agitation 04/21/2016 Unknown ? Behavior concern 04/21/2016 Unknown ? Anxiety 04/21/2016 Unknown ? Complex partial epilepsy (HCC) 02/10/2014 Unknown ? Hx of Neurological Testing (DO NOT EDIT) 08/26/2013 Unknown ? Static encephalopathy Unknown ? Spastic diplegia (HCC
- Andere Medikamente
- Albuterol Sulfate 2.5 mg Nebulization Every 4 hours PRN Baclofen 10 mg Oral 3 times daily Cetirizine HCl 10 mg Daily Cholecalciferol 25 MCG (1000 UT) Oral cloNIDine HCl 0.2 MG/24HR 1 patch Transdermal Weekly cloNIDine HCl,cloNIDine HCl,CloN
- Allergien
- Amoxicillin Rash Latex
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 07.11.2022
- Impfdatum
- 31.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
moderna covid vaccine administered to patient who was under 18. No adverse reaction to vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- moderna covid vaccine administered to patient who was under 18. No adverse reaction to vaccine administration.
- Aktuelle Erkrankungen
- moderna covid vaccine administered to patient who was under 18. No adverse reaction to vaccine administration.
- Vorgeschichte
- moderna covid vaccine administered to patient who was under 18. No adverse reaction to vaccine administration.
- Andere Medikamente
- moderna covid vaccine administered to patient who was under 18. No adverse reaction to vaccine administration.
- Allergien
- moderna covid vaccine administered to patient who was under 18. No adverse reaction to vaccine administration.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 29.12.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Exposure during pregnancy
Symptomtext
3rd pregnancy with a history of high blood pressure with two previous pregnancies. Expected due date 06/03/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure during pregnancy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- The patient is pregnant with a history of high blood pressure.
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 06.01.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 284,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 11.10.2022
- Impfdatum
- 29.12.2021
- Beginn
- 10.10.2022
- Tage bis Beginn
- 285,0
- 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 3/11/21 Lot# 023M20A; Moderna 4/11/21 Lot# 018B21A; Moderna 12/29/21 Lot# 059H21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 06.10.2022
- Impfdatum
- 28.12.2021
- Beginn
- 06.10.2022
- Tage bis Beginn
- 282,0
- Dosis
- 3
- Route/Site
- IM / RA
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
- MN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 28.12.2021
- Beginn
- 06.10.2022
- Tage bis Beginn
- 282,0
- Dosis
- 3
- Route/Site
- IM / RA
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
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 15.01.2022
- Beginn
- 20.08.2022
- Tage bis Beginn
- 217,0
- 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
Breakthrough Case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid + on 08/20/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 03.10.2022
- Impfdatum
- 13.01.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 261,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 28.09.2022
- Impfdatum
- 06.01.2022
- Beginn
- 27.09.2022
- Tage bis Beginn
- 264,0
- Dosis
- 3
- Route/Site
- IM / RA
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 COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 27.09.2022
- Impfdatum
- 28.12.2021
- Beginn
- 25.09.2022
- Tage bis Beginn
- 271,0
- 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 COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
The patient received the vaccine before the authorized age
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 20.09.2022
- Impfdatum
- 16.05.2021
- Beginn
- 20.09.2022
- Tage bis Beginn
- 492,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Animal scratch
COVID-19
Cellulitis
Cough
SARS-CoV-2 test positive
Symptomtext
Pt admitted for cellulitis of the right forearm post cat scratch. Pt stated that he tested positive on home test for COVID and was positive here. Pt had no fever, but just a cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Animal scratch
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 19.09.2022
- Impfdatum
- 06.01.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 251,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
covid + test in fully vaccinated pt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 28.12.2021
- Beginn
- 12.09.2022
- Tage bis Beginn
- 258,0
- 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
- MN
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 28.10.2021
- Beginn
- 07.09.2022
- Tage bis Beginn
- 314,0
- Dosis
- 2
- Route/Site
- IM / RA
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
- NY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 26.12.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Dermatitis
Eczema
Staphylococcus test
Symptomtext
Severe eczema, dermatitis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dermatitis
- Hospital-Tage
- 6,0
- Labordaten
- Staph infection
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Multi vitamin, advil
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 02.09.2022
- Impfdatum
- 12.07.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asymptomatic COVID-19
Computerised tomogram abnormal
Duodenal ulcer
Duodenitis
Faeces discoloured
Gastrointestinal wall thickening
Haemoglobin
Peptic ulcer
SARS-CoV-2 test positive
Symptomtext
Patient up to date on COVID vaccines who admitted with an incidental COVID test. Asymtpomatic for COVID. Provider d/c note: "90 year old male with a history of CKD stage III, anemia, BPH, hypertension, and osteoarthritis admitted with COVID and black stools. CT two weeks ago revealed proximal duodenal wall thickening, surrounding fat stranding, and a couple areas of suspected ulcer is in the duodenal bulb suspicious for peptic ulcer disease with neoplastic or other duodenitis. He was incidentally found to have COVID. Hospital Course: Pt was seen by GI who offered endoscopy. The pt declined endoscopy in favor of medical treatment. A full and detailed discussion of the risks and benefits of this course of action was held. Spouse and other family member (daughter or grandaughter) made aware of this decision as well and they agree. They understand it could be from cancer. His hemoglobin has stabilized with PPI therapy, which will continue. He remained asymptomatic in regards to COVID, in fact today he states, ""I feel great."" He has been instructed on quarantine measures. "
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- COVID detected PCR on 08/05/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Arthritis BPH CKD Glaucoma Hypertension Osteoarthritis
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 09.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 58-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Jan2022 as dose 3 (booster), single (Lot number: 059H21A) at the age of 58 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Htn" (unspecified if ongoing); "Hyperlipidemia" (unspecified if ongoing); "obesity" (unspecified if ongoing); "fmd" (unspecified if ongoing); "ACE inhibitors allergies" (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL SUCCINATE; ROSUVASTATIN; VIT D3; VIT B6. Past drug history included: Amlodipine, reaction(s): "Known allergies: Amlodipine"; Keflex, reaction(s): "Known allergies: keflex". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Aug2022) Positive; (unspecified date) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 included Paxlovid.; Sender's Comments: Based on the information currently available, a causal association between the reported event and BNT162b2 cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202208; Test Name: covid home test; Test Result: Positive ; Test Name: COVID-19 test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Drug allergy; Foot and mouth disease; Hyperlipidemia; Hypertension; Obesity
- Andere Medikamente
- METOPROLOL SUCCINATE; ROSUVASTATIN; VIT D3; VIT B6
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.08.2022
- Tage bis Beginn
- 212,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Asymptomatic COVID-19
Coagulopathy
Lethargy
SARS-CoV-2 test positive
Symptomtext
Patient received moderna vaccine on 3/18/21, 4/15/21, and 1/6/22. Presented to ER on 7/13/22. COVID positive on 8/6/22. Admitted on 7/13 for lethargy and patient lying on floor. The patient was ready to be discharged but then he had a positive COVID test without any COVID symptoms. He was kept in hospital for 3 more days and observed. He has not developed any fever, chills, diaphoresis. Discharged on 8/8/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- 26,0
- Labordaten
- 8/6/22 COVID19 positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Abnormal EKG 6/22/2016 ? Acquired coagulation factor inhibitor disorder 7/7/2022 ? Acquired coagulation factor inhibitor disorder 7/7/2022 ? Arthritis ? AV block, Mobitz 1 6/7/2019 ? Benign prostatic hyperplasia without lower urinary tract symptoms 2/1/2018 ? CKD (chronic kidney disease), stage III ? Former smoker ? GERD (gastroesophageal reflux disease) ? Gout ? Hypertension ? Hypertensive nephrosclerosis ? Ischemic cardiomyopathy ? Isolated proteinuria with morphologic lesion 6/4/2018 ? Non-ischemic cardiomyopathy ? Obesity, Class III, BMI 40-49.9 (morbid obesity) ? Osteoarthritis ? Pacemaker ? Parathyroid adenoma ? Sleep apnea with use of continuous positive airway pressure (CPAP) 4 cm h20
- Andere Medikamente
- Acetaminophen 650 mg Oral EVERY 4 HOURS PRN Albuterol Sulfate 108 (90 Base) MCG/ACT 2 Puffs Inhalation EVERY 6 HOURS PRN Calcitriol 0.25 mcg Oral DAILY Dexamethasone 2 mg Oral DAILY WITH BREAKFAST Enoxaparin Sodium 30 mg Subcutaneous DA
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 02.04.2021
- Beginn
- 31.07.2022
- Tage bis Beginn
- 485,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
Patient hospitalized with COVID after receiving vaccinations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 22.12.2021
- Beginn
- 01.08.2022
- Tage bis Beginn
- 222,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
hospitalization with covid; fully vaccinated with booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- HFpEF, Asthma, Neuropathy
- Andere Medikamente
- unknown
- Allergien
- amoxicillin, ibuprofen, penicillins, morphine
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 56,0
- Geschlecht
- U
- Eingang
- 29.07.2022
- Impfdatum
- 23.07.2022
- Beginn
- 23.07.2022
- 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
Expired vaccine stored and then administered; We gave 2 doses of expired Moderna Covid-19 vaccine to patients last month on 23Jul2022.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We gave 2 doses of expired Moderna Covid-19 vaccine to patients last month on 23Jul2022.) and PRODUCT STORAGE ERROR (Expired vaccine stored and then administered) in a 56-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 23-Jul-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 23-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (We gave 2 doses of expired Moderna Covid-19 vaccine to patients last month on 23Jul2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Expired vaccine stored and then administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (We gave 2 doses of expired Moderna Covid-19 vaccine to patients last month on 23Jul2022.) and PRODUCT STORAGE ERROR (Expired vaccine stored and then administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. Confirmed expiration date was reported as 27-Mar-2022. The vial was initially stored in the refrigerator on 23-Jul-2022. The vial did not undergo any temperature excursions. 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
- TX
- Alter
- 62,0
- Geschlecht
- U
- Eingang
- 29.07.2022
- Impfdatum
- 23.07.2022
- Beginn
- 23.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
the vial was initially stored in the refrigerator 23Jul2022; We gave 2 doses of expired Moderna Covid-19 vaccine to patients last month on 23Jul2022.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We gave 2 doses of expired Moderna Covid-19 vaccine to patients last month on 23Jul2022.) and PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator 23Jul2022) in a 62-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 23-Jul-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 23-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (We gave 2 doses of expired Moderna Covid-19 vaccine to patients last month on 23Jul2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator 23Jul2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (We gave 2 doses of expired Moderna Covid-19 vaccine to patients last month on 23Jul2022.) and PRODUCT STORAGE ERROR (the vial was initially stored in the refrigerator 23Jul2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. The vial was initially stored in the refrigerator on 23-Jul-2022. The vial did not undergo any temperature excursions. 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
- CA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 23.07.2022
- Impfdatum
- 16.07.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Moderna COVID-19 vaccine was administered after the published expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna COVID-19 vaccine was administered after the published expiration date) in a 19-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 16-Jul-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 16-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna COVID-19 vaccine was administered after the published expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna COVID-19 vaccine was administered after the published expiration date) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication information was provided. Moderna vaccine was given to 2 patients from the same lot number that was expired. Number of doses/vials-2 doses Date the vial was initially stored in the refrigerator administered on 10-Jul-2022 The vial was did not undergo any temperature excursions Patient had not reported any symptoms after receiving Moderna dose. No additional medications or treatments have been administered in response to this error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 17.07.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
administered the Moderna COVID-19 vaccine after the published expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered the Moderna COVID-19 vaccine after the published expiration date) in a 28-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 059H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Jul-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 17-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered the Moderna COVID-19 vaccine after the published expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered the Moderna COVID-19 vaccine after the published expiration date) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. The patient did not report any symptoms after receiving this dose of the vaccine. Treatment information was not provided. This case was linked to US-MODERNATX, INC.-MOD-2022-609499 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-609499:Patient 1 (Same reporter)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 28.12.2021
- Beginn
- 20.07.2022
- Tage bis Beginn
- 204,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 16.01.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 135,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Amniotic fluid volume decreased
Arrested labour
Bed rest
COVID-19
Caesarean section
Chest discomfort
Delivery
Maternal exposure before pregnancy
Premature labour
Respiratory tract congestion
SARS-CoV-2 test positive
Uterine contractions during pregnancy
Symptomtext
My due date was 07/16/2022, and I had a really smooth pregnancy with no complications until I contracted COVID-19. I contracted COVID-19 05/30/2022 with symptoms of scratchy chest, congestion, and on 06/01/2022 I began having contractions. I was admitted to the hospital on 06/01/2022 for my early labor contractions, and they were able to stop the labor. I was released after 2 nights in the hospital on bedrest. Due to low amniotic fluid which resulted due to my illness and my son being breach I had to have a C-Section. I was hospitalized for 3 days. My son was born weighing 4lbs 10 oz and he was in the hospital for 8 days before being release. We are both healthy and doing well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amniotic fluid volume decreased
- Hospital-Tage
- 2,0
- Labordaten
- COVID-19 rapid nasal home test was positive on 06/01/2022; COVID-19 PCR was positive on 06/01/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Prenatal Vitamin; Omega 3; Magnesium; Aspirin
- Allergien
- Benadryl
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 04.01.2022
- Beginn
- 09.07.2022
- Tage bis Beginn
- 186,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
Patient hospitalized for COVID while vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 06.01.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 170,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 15.01.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 172,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 26.03.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Suspected COVID-19
Vaccination failure
Symptomtext
SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a 51 year old female . Initial information was processed along with the additional information received on 08-JUL-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: pre diabetes, asthma, hypertension, hypothyroidism, penicillin allergy, and drug allergy (Advil, Leviquin, Zithromax, Metformin), and other pre-existing medical conditions included: Patient was not pregnant at the time of vaccination. The patient received first dose of covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805022 expiry: UNKNOWN) dose was not reported, administered 1 in total to the left arm on 26-MAR-2021 for prophylactic vaccination. Age at time of vaccination 50 years old. The patient received second dose of non-company suspect vaccine elasomeran (Moderna vaccine) (Dose number in series 2) (form of admin, route of admin were not reported, batch number: 059H21A expiry: UNKNOWN) dose was not reported, administered to the left arm on 07-JAN-2022 for prophylactic vaccination. Concomitant medications included hydrochlorothiazide, and levothyroxine sodium. On an unspecified date, the patient experienced suspected covid-19 infection (Dose number in series 2) which led to suspected clinical vaccination failure (Dose number in series 1). The patient was treated with non company suspect drug Paxlovid (form of admin, route of admin, batch number and expiry were not reported) dose was not reported, administered on 09-JUN-2022 to 16-JUN-2022 for the treatment of covid-19. On 24-JUN-2022, 08:00, the patient experienced rebound covid (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s, and elasomeran was not applicable. The outcome of the suspected covid-19 infection and suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000241596; Sender's Comments: V0. 20220715390-covid-19 vaccine ad26.cov2.s -suspected clinical vaccination failure . The event(s) has an unknown/unclear temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related..
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Suspected COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma; Drug allergy (Advil, leviquin, zithromax, metformin); Hypertension; Hypothyroidism; Penicillin allergy; Pre-diabetic
- Vorgeschichte
- Comments: Patient was not pregnant at the time of vaccination
- Andere Medikamente
- SYNTHROID; HYDROCHLOROTHIAZIDE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 31.12.2021
- Beginn
- 21.06.2022
- Tage bis Beginn
- 172,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccine breakthrough infection
Symptomtext
Breakthrough case of COVID-19 7 months post Vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Nobe
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- PCOS; Androgenetic Alopecia
- Andere Medikamente
- Amlodipine
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 28.06.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immunosuppression
Underdose
Symptomtext
The patient presented to receive his third dose of COVID vaccine. He received a booster (0.25 ml) dose. However, he is immunosupressed and should've received a full 0.5 ml, third primary series dose. The patient was not harmed, though he was undervaccinated. There is no record of the patient contracting COVID up to this date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunosuppression
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- low back pain
- Vorgeschichte
- h/o renal transplant, hypertension, diabetes, immunosupression, right foot drop
- Andere Medikamente
- Prograf, prednisone, Omeprazole, CellCept, minoxidil, Lasix, magnesium, Labetalol, glipizide, gabapentin, voltaren gel, aspirin, Norvasc
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 23.12.2021
- Beginn
- 13.06.2022
- Tage bis Beginn
- 172,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asymptomatic COVID-19
Bone operation
Medical device removal
SARS-CoV-2 test positive
Symptomtext
left distal femur replacement and radical resection of femur and femur hardware removal. Patient tested positive for COVID 19 but remained asymptomatic
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- 3,0
- Labordaten
- Positive COVID PCR test 6/13/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HYPERLIPIDEMIA, MIXED (272.2) Unknown Psychosexual dysfunction Unknown Essential tremor Unknown HYPERTENSION, BENIGN ESSENTIAL (401.1) Unknown ACNE ROSACEA (695.3) Unknown Psoriasis Unknown SOLAR LENTIGO (709.09) Unknown LUMBAGO (724.2) Unknown Fatigue 780.79 Unknown Benign prostatic hyperplasia without lower urinary tract symptoms 9/28/2012 Microalbuminuria 2/3/2014 Rectus diastasis, upper abdominal wall 9/9/2014 Actinic keratosis of left temple 11/7/2014 Actinic keratoses 4/20/2015 Onychomycosis 11/9/2015 Chronic left shoulder pain 5/9/2016 Tear of medial meniscus of right knee, current 5/8/2017 Severe obesity (BMI 35.0-39.9) with comorbidity 5/12/2017 Recurrent cold sores 5/18/2018 Squamous cell carcinoma, lip 12/5/2018 Controlled type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin 12/5/2018 Internal derangement of left knee (Chronic) 7/17/2019 Displaced supracondylar fracture with intracondylar extension of lower end of left femur, initial encounter for closed fracture (Chronic) 4/15/2020 OSA (obstructive sleep apnea) (Chronic) 7/30/2020 Atrial fibrillation, permanent 3/7/2020 Chronic anticoagulation 10/21/2020 Type 2 diabetes mellitus, without long-term current use of insulin 10/21/2020 Closed displaced supracondylar fracture of distal end of left femur with intracondylar extension with nonunion 10/21/2020 Postoperative anemia 3/7/2020 Alkaline phosphatase elevation 12/7/2020 Restless legs syndrome (RLS) 12/7/2020 Renal cyst, right (Chronic) 3/18/2021 Lymphadenopathy (Chronic) 6/15/2021 History of COVID-19 (Chronic) 9/20/2021 Lab test positive for detection of COVID-19 virus 9/21/2021 Stage 3a chronic kidney disease (Chronic) 10/25/2021 Wears dentures (Chronic) 10/25/2021 Iron deficiency anemia due to chronic blood loss 4/13/2022 Iron malabsorption 4/13/2022 Pain in bone fixation device, initial encounter 6/6/2022 Post-traumatic osteoarthritis of left knee 6/6/2022
- Andere Medikamente
- acetaminophen 500 mg Oral EVERY 6 HOURS PRN acetaminophen/diphenhydramine 25-500 mg 1 tablet Oral NIGHTLY PRN apixaban 5 mg Oral 2 times daily atenolol 100 mg Oral Daily atorvastatin calcium 40 mg Oral Daily calcium carb/vit D3/mineral
- Allergien
- Iodinated contrast Media - Throat swelling
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
patient received Moderna booster dose approved for 18 years and older.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- 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: unbekannt
Expired product administered
Symptomtext
Expired vaccine given, no reactions. Vaccine expired 3/27.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- 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: unbekannt
Expired product administered
Symptomtext
Expired vaccine given, no reactions. Vaccine expired 3/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- 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: unbekannt
Expired product administered
Symptomtext
Expired vaccine given, no reactions. Vaccine expired 3/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- 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: unbekannt
Expired product administered
Symptomtext
Expired vaccine given, no reactions. Vaccine expired 3/27
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
- 31.05.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
No symptoms, expired vaccine given. Vaccine expired 3/27/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
No symptoms, expired vaccine given. Vaccine expired 3/27/2022
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
- 31.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
No symptoms, expired vaccine given. Vaccine expired 3/27/2022
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
- 31.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
No symptoms, expired vaccine given. Vaccine expired 3/27/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
No symptoms, expired vaccine given. Vaccine expired 3/27/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
No symptoms, expired vaccine given. Vaccine expired 3/27/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
No symptoms, expired vaccine given. Vaccine expired 3/27/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
No symptoms, expired vaccine given. Vaccine expired 3/27/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -