VAERS Reports AS7164B

VAERS 2699399

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

kritisch

Staat: WA
Alter: 72,0
Geschlecht: M
Eingang: 20.10.2023
Impfdatum: 25.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Pain in extremity Pulmonary embolism

Symptomtext

Pulmonary embolism/ Pain behind his leg; PAIN BEHIND HIS LEG; This spontaneous case was reported by a patient family member or friend and describes the occurrence of PULMONARY EMBOLISM (Pulmonary embolism/ Pain behind his leg) and PAIN IN EXTREMITY (PAIN BEHIND HIS LEG) in a 72-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. Previously administered products included for COVID-19 prophylaxis: Moderna covid-19 vaccine (patient received dose 1 of monovalent Moderna COVID-19 vaccine, lot: 002A21A) on 26-Feb-2021, Moderna covid-19 vaccine (patient received dose 2 of monovalent Moderna COVID-19 vaccine, lot: 045A21A.) on 01-Apr-2021, Moderna covid-19 vaccine (patient received dose 3 of monovalent Moderna COVID-19 vaccine, lot: 939905..) on 27-Oct-2021, Moderna covid-19 vaccine (patient received dose 4 of monovalent Moderna COVID-19 vaccine and lot: 066K21A.) on 02-Apr-2022. Past adverse reactions to the above products included No adverse event with Moderna covid-19 vaccine, Moderna covid-19 vaccine, Moderna covid-19 vaccine and Moderna covid-19 vaccine. On 25-Oct-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On an unknown date, the patient experienced PULMONARY EMBOLISM (Pulmonary embolism/ Pain behind his leg) (seriousness criteria hospitalization and medically significant) and PAIN IN EXTREMITY (PAIN BEHIND HIS LEG) (seriousness criterion hospitalization). At the time of the report, PULMONARY EMBOLISM (Pulmonary embolism/ Pain behind his leg) and PAIN IN EXTREMITY (PAIN BEHIND HIS LEG) outcome was unknown. No concomitant drug was reported. No treatment drug was reported. Company comment- This is a regulatory authority case concerning a 72-year-old male patient with no medical history reported who experienced the unexpected and serious (hospitalization and medically significant) AESI pulmonary embolism along with the unexpected and serious (hospitalization) event pain in extremity. It was reported that after a dose of mRNA-1273.222 (Original/Omicron BA.4/5) vaccine, given as a 5th dose of COVID vaccine schedule the patient had pain behind his leg, was hospitalized, and had a pulmonary embolism. No further details were provided for medical review. The benefit-risk relationship of the mRNA-1273.222 (Original/Omicron BA.4/5) vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2689003

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

kritisch

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 30.09.2023
Impfdatum: 01.10.2022
Beginn: 02.09.2023
Tage bis Beginn: 336,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Angiogram pulmonary abnormal Atelectasis Blood culture positive Blood lactic acid COVID-19 COVID-19 pneumonia Chills Condition aggravated Cough Diuretic therapy Dyspnoea Electrocardiogram QT prolonged Electrocardiogram abnormal Glycosylated haemoglobin normal Hyperglycaemia Lung consolidation Lung disorder

Symptomtext

62 y.o. adult anesthesiologist patient of DO with history of rheumatoid arthritis on Humira, gout, osteoporosis, GERD, avascular necrosis, NIDDM2, HTN who presented to Hospital with fever, chills, cough, found to have COVID. Acute hypoxemic respiratory failure COVID-19 viral pneumonia Date of onset of symptoms: 8/28 Symptoms present on admission: cough, fevers, chills, dyspnea Date of COVID positive test: 9/2 Vaccination status: vaccinated (last booster in October 2022) Imaging: CTPA on admission with extensive ground-glass opacification throughout the lungs bilaterally, highly suggestive of COVID-19 pulmonary disease given the clinical history with more focal areas of airspace disease are present within the lung bases, suggesting atelectasis or consolidation, as well as small bilateral pleural effusions Oxygen requirements on admission: HHFNC max Current oxygen requirements: non-heated high flow at 5L Medical therapy: steroids for 10 days, diuresis for dry lung strategy, completed remdesivir; given dose of tocilizumab on 9/4 as well Urine antigens negative Consultants following: pulm, ID Anticipated special isolation end date: TBD pending clinical course, likely 20 day from symptom onset Much improved, likely home with home oxygen in next 24-48 hrs if stable on 3-4L Severe sepsis, resolved In setting of COVID-19 Lactic up to 2.9 on admission, since resolved Blood cultures 9/2 at FSED with 1/2 positive for staph hominis and 1/2 positive for staph epidermidis, therefore are contaminants Repeat blood cultures without growth Treatment of COVID as above Prolonged QTc, resolved EKG - sinus tachycardia with QTc 533 on admission Initially on levofloxacin, stopped QTc normalized Rheumatoid arthritis Immunosuppression due to drug therapy Patient on Humira weekly and methotrexate as needed as well as prednisone as needed (recently on 10 mg daily) Holding Humira, on dexamethasone as above, steroid taper then resuming home prednisone dosing following dexamethasone course NIDDM2 with hyperglycemia On metformin at home; Hgb A1c of 6.9% Hyperglycemia in setting of steroids and COVID at times Continue SSI, adjust as needed Essential hypertension On metoprolol at home, continue here with hold parameters at lower dose Resume home dose on discharge Hyperlipidemia Continue pravastatin

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2670161

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

kritisch

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 11.08.2023
Impfdatum: 13.10.2022
Beginn: 27.03.2023
Tage bis Beginn: 165,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Pulmonary embolism

Symptomtext

I26.99 ACUTE PULMONARY EMBOLISM 3/27/2023 ACUTE PULMONARY EMBOLISM

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2659927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge AS7164B

kritisch

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 24.07.2023
Impfdatum: 23.09.2022
Beginn: 14.03.2023
Tage bis Beginn: 172,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Deep vein thrombosis

Symptomtext

ACUTE DVT OF LEFT LEG, UNSPECIFIED VEIN ACUTE RESPIRATORY FAILURE

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2659362

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

kritisch

Staat: -
Alter: 90,0
Geschlecht: F
Eingang: 21.07.2023
Impfdatum: 27.09.2022
Beginn: 16.12.2022
Tage bis Beginn: 80,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Chronic respiratory failure Hypoxia Respiratory failure Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE RESPIRATORY FAILURE ACUTE HYPERCAPNIC RESPIRATORY FAILURE CHRONIC RESPIRATORY FAILURE CHRONIC HYPERCAPNIC RESPIRATORY FAILURE ACUTE ON CHRONIC HYPERCAPNIC RESPIRATORY FAILURE HYPOXEMIA 11/22/2022, 2/9/2023, 3/12/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2658882

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

kritisch

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 20.07.2023
Impfdatum: 30.09.2022
Beginn: 02.03.2023
Tage bis Beginn: 153,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute myocardial infarction

Symptomtext

ACUTE NON ST ELEVATION MI

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Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2636131

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

kritisch

Staat: -
Alter: 96,0
Geschlecht: F
Eingang: 24.05.2023
Impfdatum: 06.10.2022
Beginn: 03.01.2023
Tage bis Beginn: 89,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Cerebral artery occlusion Cerebrovascular accident Hypothyroidism

Symptomtext

I63.512 ACUTE STROKE DUE TO OCCLUSION OF LEFT MIDDLE CEREBRAL ARTERY 1/3/2023 HYPOTHYROIDISM

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2606051

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

kritisch

Staat: WA
Alter: 52,0
Geschlecht: F
Eingang: 29.03.2023
Impfdatum: 27.09.2022
Beginn: 16.03.2023
Tage bis Beginn: 170,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Cough Respiratory arrest

Symptomtext

I had what I thought was a cold. I was unable to breath and stop coughing. I went to the emergency room on March 19, 2023. After looking at my ears and throat. They prescribed Tessalon Pearls, Doxycycline, and a steroid. My symptoms improved after a couple of days. I am still taking the medication and am still suffering from the cough. I have not yet recovered from all my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory arrest
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Sjogren's Syndrome
Andere Medikamente: Leflunomide; Ambien; Zyrtec
Allergien: All Cillins; Sulfa Drugs; Keflex; Biaxin
Vorherige Impfungen: -

VAERS 2601855

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

kritisch

Staat: MN
Alter: 27,0
Geschlecht: M
Eingang: 22.03.2023
Impfdatum: 11.11.2022
Beginn: 19.03.2023
Tage bis Beginn: 128,0
Dosis: 5
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Patient expired 3/19/2023.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Amniotic band syndrome with right lung and arm agenesis, restrictive lung disease, chronic hypoxic respiratory failure, scoliosis, Jarcho Levine syndrome, neurogenic bladder, neurogenic bowel
Andere Medikamente: Unknown
Allergien: Erythromycin, sulfa antibiotics, gentamicin, nitrofurantoin trimethoprim, vancomycin, latex, morphine, fosfomycin
Vorherige Impfungen: -

VAERS 2575072

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

kritisch

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 03.02.2023
Impfdatum: 01.10.2022
Beginn: 13.01.2023
Tage bis Beginn: 104,0
Dosis: 5
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute kidney injury Acute respiratory failure Autopsy Bacterial test negative Blood gases abnormal Brain natriuretic peptide increased Bronchoscopy abnormal COVID-19 Cardiac failure congestive Catheterisation cardiac Chest X-ray abnormal Computerised tomogram head abnormal Computerised tomogram thorax abnormal Cough Death Dyspnoea Echocardiogram abnormal Ejection fraction decreased

Symptomtext

Discharge Provider: Primary Care Physician at Discharge: MD Admission Date: 1/13/2023 PRESENTING PROBLEM: Lung abnormality [J98.4] Acute on chronic respiratory failure [J96.20] HOSPITAL COURSE: Patient was a 73 y.o. male who is s/p bilateral lung transplant 7/25/18 for IPF, complicated by MDS with pancytopenia, systolic and diastolic heart failure (currently compensated), CAD s/p CABG, then stent (7/2022), atrial flutter. He had COVID-19 infection 12/2022 which was not treated. He presented on 1/13/2023 with worsening respiratory symptoms (dyspnea, cough, wheezing, increased work of breathing, mild desaturation and 1 L drop in home spirometry), CT showing bilateral nodular pulmonary infiltrates. He underwent bronchoscopy 1/13/22 and was admitted to the lung transplant service for IV antibiotics and ID consultation. During bronchoscopy he had bloody secretions on initial bronch, hemoptysis and worsening infiltrates post bronchoscopy. Bronchoscopy with negative bacterial cutlures, empiric abx stopped 1/17. CXR worsening, ECHO obtained and EF down to 30%, previously 60%, with basal to mid anterolateral and apical segments severely hypokinetic, moderate MR. BNP over 37,000. Heart failure team were consulted. 1/18 RHC with Swan placement demonstrated biventricular failure- lasix and Milrinone gtt started per AHF team. 1/21 CT thorax with worsening perihilar infiltrates. Course further complicated by worsening AKI for which nephrology was consulted. Underwent RHC 1/30 on milrinone 0.1, with low filling pressures and normal CO. Milrinone was weaned off. He had worsening respiratory failure 2/1 and didn't tolerate attempts at BiPAP even with Precedex gtt. He had worsening mental status with ABG showing only hypoxemia. CT head without new acute abnormality. Ct thorax showed extensive bilateral ground-glass opacities, worse from prior study. GOC discussion with wife, daughter, and son at bedside with concern for need for intubation. They decided to transition to comfort care. At 1745, he passed away Per Lung Transplant team request, a limited chest autopsy was requested. Family consented. Date of Death: 2/2/23 Time of Death: 5:45 PM Preliminary Cause of Death: Acute respiratory failure

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 20,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: IPF (idiopathic pulmonary fibrosis) OSA (obstructive sleep apnea) History of nicotine use History of psychiatric disorder Pulmonary fibrosis, s/p transplant 7/25/2018 Atial flutter CAD (coronary artery disease) Restless leg syndrome History of pulmonary embolism Other complications of lung transplant Steroid-induced diabetes Pseudoaneurysm History of atrial tachycardia Tachycardia Postoperative atrial fibrillation Hx of CABG Dyslipidemia Central Sleep Apnea on ASV Myocardial infarction Osteoporosis, unspecified osteoporosis type, unspecified pathological fracture presence Paroxysmal nocturnal dyspnea GERD with esophagitis Hiatal hernia BiPAP (biphasic positive airway pressure) ASV dependence Human metapneumovirus (hMPV) pneumonia Other specified anemias Primary insomnia Myelodysplastic syndrome Nonrheumatic aortic valve insufficiency Atypical atrial flutter Cardiomyopathy Pulmonary edema cardiac cause Acute respiratory failure Acute systolic congestive heart failure Ischemic cardiomyopathy Hyponatremia Moderate protein-calorie malnutrition Primary squamous cell carcinoma of left ear Anticoagulant long-term use Long term current use of anticoagulant therapy Actinic keratosis Arthritis Congenital pes planus, unspecified foot Elevated PSA History of cholecystectomy Status post lung transplantation Major depressive disorder, recurrent, moderate Polyp of colon Chronic alcoholism in remission Recurrent major depression in remission Sensorineural hearing loss, bilateral Spinal stenosis, lumbar region without neurogenic claudication Tobacco dependence in remission Unspecified cataract Unspecified disorder of refraction MDS (myelodysplastic syndrome) Lung abnormality Hemoptysis setting of abnormal CT scan demonstrating nodular opacities AKI on CKD 4 History of skin cancer Immunosuppressed status Multifocal lung consolidation Stress hyperglycemia Acute hypoxemic respiratory failure History of CVA (cerebrovascular accident)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet acyclovir (ZOVIRAX) 400 MG tablet apixaban (ELIQUIS) 5 MG tablet atorvastatin (LIPITOR) 40 MG tablet BMX compounded suspension buPROPion (WELLBUTRIN SR) 150 MG 12 hr tablet busPIRone (BUSPAR) 10 MG tabl
Allergien: Nsaids MoldOther PollenOther
Vorherige Impfungen: -

VAERS 2551323

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

kritisch

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 03.10.2022
Beginn: 28.12.2022
Tage bis Beginn: 86,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Acute respiratory failure COVID-19 Cardiac failure acute Cardiac failure congestive Condition aggravated Diuretic therapy Dyspnoea Hypoxia Malaise Nausea Pulmonary congestion SARS-CoV-2 test positive

Symptomtext

COVID+ 12/28/22. Vaccination Status- J&J x1, Pfizer x1 + Moderna BIVALENT x1 Discharge Summary MD (Physician) ? ? General Medicine BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: MD Admission Date: 12/28/2022 Discharge Date: Dec 29, 2022 Active Hospital Problems Diagnosis Date Noted POA ? Anemia 08/25/2022 Yes ? Chronic diastolic congestive heart failure 11/21/2016 Yes ? Depression 11/20/2013 Yes ? RA (rheumatoid arthritis) Yes ? Fibromyalgia Yes ? Hypertension Yes ? OSA (obstructive sleep apnea) 03/14/2013 Yes ? DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypoxia [R09.02] Acute on chronic congestive heart failure, unspecified heart failure type [I50.9] Acute hypoxemic respiratory failure due to COVID-19 [U07.1, J96.01] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 63 y.o. female with a history of OSA, rheumatoid arthritis, chronic diastolic heart failure, and hypertension who presents with shortness of breath and general malaise, found to be COVID-19+. There was radiographic evidence of mild pulmonary vascular congestion, the patient had not taken her lasix as she was very nauseated. She was admitted as she was very short of breath. In the ER she was given lasix IV and admitted to the hospital. She diuresed well and felt much better. She got one dose of remdesivir as well due to some hypoxia in the ER. Patient felt much better the day after admission. Patient was able to walk without shortness of breath or desaturation below 88%. Patient declined staying for 3 doses of remdesivir. She was fully vaccinated for COVID-19 and was feeling better. She was tolerating a general diet. She was instructed on signs and symptoms of when to return to the ER. She was instructed to continue taking her lasix, she was then discharged home in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: Office visit with Hosptial for Chief Complaint: Presents in follow up from recent CT scan and pelvic ultrasound that show right ovarian cyst. Will await OVA-1 result. If low risk would recommend serial monitoring with repeat pelvic ultrasound. If worsening pain and surgery necessary would refer to complex gyn
Vorgeschichte: OSA (obstructive sleep apnea) Nonischemic cardiomyopathy Hypertension RA (rheumatoid arthritis) Fibromyalgia Bilateral venous insufficiency Depression Morbid obesity with BMI of 45.0-49.9, adult IBS (irritable bowel syndrome) Current chronic use of systemic steroids Hx of bariatric surgery Chronic diastolic congestive heart failure NSTEMI (non-ST elevated myocardial infarction) Open bicondylar fracture of distal femur, left, sequela Vitamin D deficiency Malignant melanoma of torso excluding breast Pulmonary embolism Nausea AKI (acute kidney injury) Migraine headache Morbid obesity Ventricular premature beats Depression Fibrositis Chronic venous insufficiency Essential hypertension Irritable bowel syndrome Cardiomyopathy Rheumatoid arthritis Chest pain Closed fracture of tibial plateau, right, initial encounter Elbow fracture, right, sequela Acute on chronic diastolic heart failure Anemia
Andere Medikamente: Aspirin 81 mg Oral Daily Baclofen 10 mg Oral 3 times daily PRN buPROPion HCl 150 mg Oral Every other day Calcium Carb-Cholecalciferol 500-200 MG-UNIT 1 tablet Oral Daily Citalopram Hydrobromide 40 MG TAKE 1 TABLET DAILY dilTIAZem HCl Coated
Allergien: Oxycontin [Oxycodone]Anaphylaxis ErythromycinNausea/Vomiting/Diarrhea HydroxychloroquineNausea Only IbuprofenGI Upset LatexRash Motrin IbOther Neurontin [Gabapentin]Dizziness Phentermine Prozac [Fluoxetine]Anxiety Tape
Vorherige Impfungen: -

VAERS 2548059

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

kritisch

Staat: MN
Alter: 72,0
Geschlecht: M
Eingang: 02.01.2023
Impfdatum: 12.10.2022
Beginn: 31.12.2022
Tage bis Beginn: 80,0
Dosis: 5
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19

Symptomtext

Patient presented with acute hypoxic respiratory failure secondary to COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2543616

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

kritisch

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 21.09.2022
Beginn: 20.10.2022
Tage bis Beginn: 29,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Arteriogram coronary abnormal Atrioventricular block Blood cholesterol increased Blood test abnormal Diabetes mellitus Feeling abnormal Muscular weakness Myocardial infarction

Symptomtext

I want to start by saying I am a vegan. I never had a problem with cholesterol. I eat no meat, no cheese, no oil, etc. I had a heart problem 7 years ago. For the last 4 years I been on top of it, especially being a vegan. After the vaccine, my left arm felt tired. Which was weird because it had been 4-6 weeks since I had the shot. After feeling this and just run down through the day, I knew I was having a heart attack. It was the week before the November holiday when it hit me, around 11/14/2022. I was admitted into the hospital for 5-6 days. They did an angiogram and noticed I was blocked.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 5,0
Labordaten: Blood work panel to come back saying I am now a diabetic, and my cholesterol was high.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; arterial sorosis
Andere Medikamente: Metoprolol; vitamin D; magnesium; biotin
Allergien: NEOSPORIN
Vorherige Impfungen: -

VAERS 2528027

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

kritisch

Staat: WA
Alter: 50,0
Geschlecht: M
Eingang: 09.12.2022
Impfdatum: 11.10.2022
Beginn: 05.12.2022
Tage bis Beginn: 55,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Asthma COVID-19 COVID-19 pneumonia Condition aggravated

Symptomtext

Patient received Moderna COVID vaccine on 4/19/21, 5/17/21, and Moderna bivalent COVID vaccine on 10/11/22. On 11/28/22, patient was diagnosed with COVID infection in the community. On 12/5/22, patient admitted to our inpatient facility (med/surg unit) with acute respiratory failure with hypoxia (requiring 5-6L NC O2), COVID-19 pneumonia, and intermittent asthma with acute exacerbation due to COVID-19 infection and pneumonia. As of today (12/9/22), patient is still admitted in the med/surg unit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: history of intermittent asthma, obesity, ADD and anxiety
Andere Medikamente: albuterol inh, collagen, concerta er, fluticasone/salmeterol inh, guanfacine, claritin-d, methylphenidate, mvi
Allergien: amoxicillin/clavulanate
Vorherige Impfungen: -

VAERS 2491425

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

kritisch

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 28.09.2022
Beginn: 24.10.2022
Tage bis Beginn: 26,0
Dosis: 4
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Acute respiratory failure COVID-19 Cerebral ischaemia Cerebrovascular accident Cough Dysarthria Hypoaesthesia Imaging procedure abnormal Magnetic resonance imaging head abnormal Malformation venous Oxygen saturation decreased Paraesthesia Respiratory symptom SARS-CoV-2 test positive

Symptomtext

COVID + 10/25/22 - Vaccination Status - Moderna x4, including bivalent BRIEF OVERVIEW: Discharge Provider: Primary Care Provider: DO Admission Date: 10/24/2022 Discharge Date: Oct 26, 2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute CVA (cerebrovascular accident) [I63.9] Cerebrovascular accident (CVA), unspecified mechanism [I63.9] COVID-19 virus infection [U07.1] HOSPITAL COURSE: 68 y.o. old female with hx of COPD, tobacco abuse, HLD, and anxiety/depression who was admitted for 4 day history of LUE numbness/tingling and episode of dysarthria with imaging showing early/subacute ischemic CVA in the right central sulcus. Neurology was consulted. An MRI of the brain was done. There was findings of congenital venous malformations. Neurosurgery was consulted. They did not feel there was anything to be done in patient emergently. They recommended follow-up with their team in 2-4 weeks. This information was placed in her discharge paperwork. Pt also with ongoing cough and recent viral URI symptoms with most recent symptom onset about 10 days prior to admission with patient found to be COVID-19 positive. Pt initially maintaining her saturations on room air, but developed acute hypoxic respiratory insufficiency with O2 sats down to 85% on room air. Pt started on supplemental O2 via NC with quick improvement with initiation of dexamethasone and remdesivir. PT OT evaluated the patient and patient felt she was at baseline and did not require Sar placement. Patient required a small amount of O2 with ambulation and this was arranged prior to discharge. Patient felt ready to go home and was medically stable for discharge.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD (chronic obstructive pulmonary disease) Tobacco use disorder Hyperlipidemia
Andere Medikamente: Albuterol Sulfate 108 (90 Base) MCG/ACT 2 puffs Inhalation Every 6 hours PRN Alendronate Sodium 70 mg Oral Every Sunday ALPRAZolam 0.5 mg Oral Nightly PRN Atorvastatin Calcium 20 mg Oral Daily, for cholesterol Cyanocobalamin 15,000 Units O
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2482097

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164B

kritisch

Staat: IL
Alter: 37,0
Geschlecht: M
Eingang: 25.10.2022
Impfdatum: 05.10.2022
Beginn: 08.10.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: unbekannt Erholt: ja

Adenovirus test Blood HIV RNA Borrelia test positive C-reactive protein increased Chest X-ray abnormal Angiogram pulmonary abnormal Blood HIV RNA below assay limit Blood culture negative Blood immunoglobulin G normal Blood immunoglobulin M Borrelia test negative Cardiac dysfunction Cardiac imaging procedure abnormal Chest pain Chills Computerised tomogram thorax Cytomegalovirus test negative Dyspnoea

Symptomtext

Vaccinated for flu and covid on 10/5. Had symptoms of fever and fatigue on 10/6 and 10/7 which are typical for patient after covid vaccines (this was his 5th dose). He is high risk because of obesity. On saturday, 10/8 he started having a rash and shortness of breath and he sought care at an urgent care who transferred him to an ED. HE was found to have orthopnea, LE edema, and DOE with elevated troponin (200s). Cardiac MRI was recommended but couldn't be done in a timely manner so he was transferred to our ED and admitted for myocarditis. Troponins were already decreasing and CRP was >100. Rash was present and thought to be more typical of viral exanthem but all viral studies were negative (see below). He remained febrile until 10/13 and defervesce and rash began to fade. He was also digressed and treated for hypertension. trops and crp were decreasing and patient was less symptomatic. he was d/ced home.

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Praegender Schweregrund: Gynaecomastia
Hospital-Tage: 5,0
Labordaten: TTE with moderately decreased LV function trop reported as >200, 36 on admit here, <5 in clinic 10/24 crp 225 on admit, 92 at discharge, and 6 in clinic 10/25 ASO negative, lyme antibodies positive confirmatory western blot negative, mycoplasma IgG pos IgM neg, parvo dna neg, parvo IgG pos IgM neg, rubella IgG equivocal IgM neg, spotted fever group IgG neg IgM neg, measles IgG pos IgM neg, HIV viral load and western blot neg, cmv per serum neg, legionella urine neg, cxr volume increased no pneumonia, ebv per serum neg, full rvp neg, adenovirus dna serum neg, echovirus serum pcr neg, enterovirus pcr serum neg, hav serum pcr neg
Aktuelle Erkrankungen: awaiting the arrival of a sleep apnea machine.
Vorgeschichte: OSA
Andere Medikamente: tylenol occasionally but not on day of vaccination.
Allergien: None
Vorherige Impfungen: -

VAERS 2485620

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

kritisch

Staat: NC
Alter: 52,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 30.09.2022
Beginn: 10.10.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Catheterisation cardiac normal Echocardiogram normal Electrocardiogram normal Myocardial infarction Troponin increased

Symptomtext

I had a heart attack, I had a n indicated heart attack due to the rise in troponin levels,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: ECG, Heart sonogram and a Heart Catherization all results normal. No blockage detected or noted.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Estradiol
Allergien: Sulfa; Fennel
Vorherige Impfungen: 03/24/2021 COVID-19 Moderna

VAERS 2628408

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

schwer

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 08.05.2023
Impfdatum: 21.10.2022
Beginn: 30.04.2023
Tage bis Beginn: 191,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain COVID-19 Change in seizure presentation Chest X-ray abnormal Condition aggravated Electrocardiogram QT prolonged Electroencephalogram normal Endotracheal intubation Intensive care Intentional medical device removal by patient Malaise Pneumonia Secretion discharge Seizure Status epilepticus Stridor Swallow study

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 4/30/2023 Discharge Date: May 3, 2023 PRESENTING PROBLEM: Status epilepticus (HCC) Seizures (HCC) HOSPITAL COURSE: Patient is a 57yoF who was admitted with breakthrough seizures in the setting of CAP. She has a known seizure disorder for which she has taken Dilantin for many years. She was diagnosed with COVID about 5 weeks ago, and was improving, then for the past 3 weeks has noticed increasing mucous production and not feeling well. She also has had increasing frequency of her baseline seizures. She had multiple seizures and presented to a local ED. She was given 5mg Versed and 3G Keppra, and as she was not returning to baseline, was intubated and sedated. She was transferred to an ICU for further care. On admission, she was placed on EEG and after determining she was not actively seizing, her sedation was weaned. Her CXR was consistent with a RLL pneumonia and she was started on a 5d course of Unasyn for CAP. Later in the day, she self extubated and had noted stridor that was treated successfully with steroids and racemic epinephrine. She has continued to improve clinically and passed a bedside swallow evaluation. She transferred out of the ICU to the general floor. She worked with PT/OT and did not require subacute rehab. She remained seizure free. She was transitioned from Unasyn to augmentin for her pneumonia for 5 days. She complained of significant abdominal pain, was evaluated by GI who recommended increasing PPI to BID. She will continue to hold seroquel due to prolonged QTc. Follow up with her PCP and neurology outpatient. PT/OT recommended home with assist. Patient is discharging in improved and stable condition

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Praegender Schweregrund: Change in seizure presentation
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: History of substance use Anxiety and depression
Andere Medikamente: buprenorphine-naloxone (SUBOXONE) 8-2 MG buPROPion (WELLBUTRIN XL) 150 mg 24 hr tablet dicyclomine (BENTYL) 10 mg capsule diphenoxylate-atropine (LOMOTIL) 2.5-0.025 MG per tablet dorzolamide-timolol (COSOPT) 22.3-6.8 MG/ML ophthalmic soluti
Allergien: None
Vorherige Impfungen: -

VAERS 2612475

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

schwer

Staat: PA
Alter: 58,0
Geschlecht: F
Eingang: 10.04.2023
Impfdatum: 08.10.2022
Beginn: 20.01.2023
Tage bis Beginn: 104,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arteriosclerosis Computerised tomogram normal Echocardiogram normal Electrocardiogram ambulatory normal Electrocardiogram normal Full blood count normal Loss of consciousness Ultrasound Doppler

Symptomtext

I passed out, I was taken to the emergency room. I was kept overnight for observation. Once I got into the emergency room they started running tests, CAT scan, EKG, echocardiogram, CBC bloodwork. All tests came back negative, I was kept in the hospital overnight for observation. I was released the next day with advice to see my PCP. I was then ordered to wear a Holter monitor for a month and a carotid ultrasound. The Holter monitor did not show anything, the ultrasound showed age related plaque.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: 20JAN2023 CAT scan - negative; 20JAN2023 Echocardiogram - negative;20JAN2023 EKG - negative; 20JAN2023 CBC Bloodwork - negative; 27JAN2023 Holter Monitor - negative; 21FEB2023 Carotid Ultrasound - some plaque
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Alpha Lipoic Acid
Vorherige Impfungen: -

VAERS 2604937

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

schwer

Staat: MD
Alter: 82,0
Geschlecht: F
Eingang: 28.03.2023
Impfdatum: 25.09.2022
Beginn: 12.11.2022
Tage bis Beginn: 48,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Chest X-ray abnormal Chest discomfort Computerised tomogram thorax abnormal Dyspnoea Echocardiogram abnormal Pericardial effusion Pulmonary oedema

Symptomtext

I got very short of breath, I felt like someone hit me in my chest, I could not breath. My doctor told me to go to the emergency room and I was admitted to the hospital on November 14, 2022. They found fluid around my heart and in my lungs. They said this is what was causing my shortness of breath. My doctors have changed my medications and added some to my daily regime. It took me two months, but I feel that I back to being myself.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: -
Labordaten: 14NOV2022 CAT scan, fluid around the heart and in the lungs; 14NOV2022 Echocardiogram, fluid around the heart and in the lungs; 14NOV2022 Chest x-ray, fluid around the heart and in the lungs
Aktuelle Erkrankungen: No
Vorgeschichte: Atrial Fibrillation
Andere Medikamente: ELIQUIS; SYNTHROID; vitamin D with calcium; LIPITOR; PROLIA injection every 6 months; EPIPEN
Allergien: Sulfa; niacin; fentanyl; white face hornet
Vorherige Impfungen: -

VAERS 2569817

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

schwer

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 28.01.2023
Impfdatum: 29.09.2022
Beginn: 07.10.2022
Tage bis Beginn: 8,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Aura COVID-19 immunisation Dizziness Interchange of vaccine products Ischaemic stroke Laboratory test Ophthalmological examination Photophobia Visual impairment

Symptomtext

Interchange of vaccine products; Revaccination with different COVID 19 vaccine; visual issues; visual auras; was very sensitive to light; lightheadedness; ischemic strokes; This spontaneous case was reported by a consumer and describes the occurrence of ISCHAEMIC STROKE (ischemic strokes) in a 71-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Previously administered products included for COVID-19 prophylaxis: PFIZER BIONTECH COVID-19 VACCINE on 25-Jan-2021, PFIZER BIONTECH COVID-19 VACCINE on 25-Feb-2021, PFIZER BIONTECH COVID-19 VACCINE (1st booster on 28 Sep 2021) on 28-Sep-2021 and PFIZER BIONTECH COVID-19 VACCINE (2nd booster on 27 May 2022) on 27-May-2022. Past adverse reactions to the above products included No adverse event with PFIZER BIONTECH COVID-19 VACCINE, PFIZER BIONTECH COVID-19 VACCINE, PFIZER BIONTECH COVID-19 VACCINE and PFIZER BIONTECH COVID-19 VACCINE. On 29-Sep-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) 1 dosage form. In 2022, the patient experienced ISCHAEMIC STROKE (ischemic strokes) (seriousness criterion medically significant). On 07-Oct-2022, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced VISUAL IMPAIRMENT (visual issues), AURA (visual auras), PHOTOPHOBIA (was very sensitive to light) and DIZZINESS (lightheadedness). On an unknown date, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) and COVID-19 IMMUNISATION (Revaccination with different COVID 19 vaccine). At the time of the report, ISCHAEMIC STROKE (ischemic strokes) and DIZZINESS (lightheadedness) had resolved with sequelae and VISUAL IMPAIRMENT (visual issues), AURA (visual auras), PHOTOPHOBIA (was very sensitive to light), INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) and COVID-19 IMMUNISATION (Revaccination with different COVID 19 vaccine) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Laboratory test: had tests from top to bottom, and they haven't found any real red flags.. On an unknown date, Ophthalmological examination: didn't find any issues with eyes.. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter did not provide any causality assessments. No concomitant and treatment medications were reported. The patient did not receive any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was reported that the patient's doctor ordered an MRI on 3-Dec-2022. It was reported that she had 3 ischemic strokes. Estimated at the time that they had occurred 3-6 weeks prior to 3-Dec-2022, which would put it in the time frame when she was having the symptoms. The reporter stated that now she still gets some symptoms, but not as intense as the first time. Company comment: This spontaneous case concerns a 71-year-old, female patient with no medical history information reported, previously vaccinated with 4 doses of Pfizer Biontech COVID 19 vaccine, who experienced the unexpected serious (medically significant) event of ischemic stroke. Interchange of vaccine product and revaccination with different COVID 19 vaccine were also noted. The event was diagnosed approximately 2 months after a dose of mRNA-1273 bivalent BA.1(administered as the fifth dose) with symptoms starting approx. 8 days after 5th dose. As reported, patient had visual issues and visual auras and was very sensitive to light and had lightheadedness. Patient went to get an ophthalmology exam, but no issues with her eyes were found. These symptoms continued for a while, so MRI was done and doctors reported that patient had 3 ischemic strokes with estimation they had occurred 3-6 weeks prior to MRI (which was done 2 months after 5th dose). Reportedly, patient had tests from top to bottom, and they haven't found any real red flags. No further information about the events was provided. The benefit-risk relationship of mRNA-1273 bivalent BA.1 is not affected by this report.

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Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: -
Labordaten: Test Name: tests from top to bottom; Result Unstructured Data: had tests from top to bottom, and they haven't found any real red flags.; Test Name: an ophthalmology exam; Result Unstructured Data: didn't find any issues with eyes.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2545895

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

schwer

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 29.12.2022
Impfdatum: 05.10.2022
Beginn: 11.12.2022
Tage bis Beginn: 67,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute kidney injury Anticoagulant therapy Asthenia Bladder catheter replacement Bladder catheterisation Blood creatinine increased Blood culture negative COVID-19 Chest X-ray normal Condition aggravated Confusional state Culture urine positive Deep vein thrombosis Delirium Diabetes mellitus management Fall General physical health deterioration Haematemesis

Symptomtext

Patient is a 72 y.o. male admitted to the hospital on 12/11/2022 with reports of worsening confusion, and reported episode of emesis that appeared coffee ground in nature. He had recently been diagnosed with COVID, and was also found to have mild AKI and a possible UTI. Discharge Diagnosis and Associated Hospital Course Acute Metabolic/Toxic Encephalopathy Delirium Multifactorial, in the setting of AKI, COVID, and possible UTI. Intermittent confusion also noted over the past hospitalizations. May have some underlying cognitive impairment. Vitals stable, patient pleasantly confused (oriented to person/place) at discharge. Treating underlying infectious/metabolic processes. Stable to return on 12/13/22. Abnormal urinalysis With abnormal UA and encephalopathy. Unclear if indicative of active infection vs colonization, in setting of chronic Foley. Had been on Keflex and Methenamine for suppressive therapy for infections. Recent catheter exchange 12/7 with Urology. Urine culture growing >100 K proteus. Blood cultures negative. Patient received cefepime during admission. Culture reviewed, plan to discharge on Omnicef to complete 7 day total course. Resume prophylactic antibiotics once Omnicef completed. COVID-19 - Presented with: encephalopathy - Symptom onset: 12/10 - Positive COVID-19: 12/10 (reportedly positive 12/9 at facility) - Vaccination status: Vaccinated - CXR on admission showed no acute cardiopulmonary process - Oxygen status: Room Air - On Paxlovid per ID. Complete course as prescribed. - DVT prophylaxis: Resume Eliquis at dose of 2.5 mg BID at discharge. Coffee Ground Emesis Reported prior to admission. Patient unable to provide confirmatory history. Hemoglobin stable since arrival, no witnessed emesis or melena since arrival. Plan for 6 week course of PPI total. No GI consult pursued. Ok to resume anticoagulation at discharge. History of pulmonary embolism and proximal right lower extremity DVT Admitted to GMC 6/1 - 6/3/22 with submassive PE s/p successful catheter-directed thrombectomy on 6/2/22. Also found to have an acute proximal DVT of the right lower extremity at that time. Suspected to be provoked by recent long-distance car trip at that time. Repeat right lower extremity venous doppler on 10/17/22 with chronic DVT in the right popliteal and gastrocnemius veins, demonstrating partial resolution of previous thrombus. Cardiologist in October (Dr.) had recommended 2 additional months of anticoagulation at that time. At this time, patient has completed 6 months of therapeutic anticoagulation. In setting of COVID illness and current debility, recommend transition to Eliquis 2.5 mg BID as prophylactic dose until functional status improves. Follow-up with Dr. as directed. AKI on CKD III Likely in the setting of decreased PO intake, GI losses, and concomitant ACE-I therapy. Creatinine baseline 1.1-1.2, up to 1.46 on admission. Has improved with IV fluids to 1.03 at discharge. OK to resume ACE-I at discharge. Normocytic Anemia Noted on previous admission in the setting of hematuria. Hgb on discharge was 9.2. Hemoglobin currently stable at 10.1 at time of discharge, no witnessed evidence of GI bleeding. Follow-up lab work as outpatient at the discretion of outpatient providers. Insulin Dependent Diabetes Mellitus Type 2 Per history. Home regimen includes basal/bolus insulin (50 units Lantus and SSI) as well as Glimepiride. Current glycemic control adequate, had been on liquid diet during hospital stay. In setting of acute illness, will decrease Lantus from 50 to 40 units daily at discharge, sliding scale insulin coverage alone with meals. Avoid further use of sulfonylurea. Monitor glucose at facility and adjust regimen accordingly. Essential Hypertension Blood pressures currently controlled. Lisinopril held during admission, Ok to resume at discharge. Hx of Penile Cancer s/p partial penectomy Urethral stricture Vesicocutaneous fistula Urinary Retention S/p urethral dilation, bilateral hydrocelectomy in 9/2017. Has had a SPT in the past. Has a vesicocutaneous fistula at site of prior suprapubic tract. Follows with urology, Dr. Underwent urethral dilation on 10/21/22. Recent Urology visit on 12/7 with Foley catheter exchange at that time. Plan was for cystoscopy in 2 weeks time. He has had recent hematuria. Continue foley catheter. Continue Proscar. Had worsening memory issues on oxybutynin. Myrbetriq resumed on discharge. Follow-up with urology as outpatient as planned. Generalized Weakness Multiple Falls In the setting of progressive functional decline with multiple co-morbidities and hospitalizations. Recently discharged to. Plan to return at discharge for continued rehabilitation. Chronic LE Lymphedema L > R, noted on previous admission as well. Continue with OP evaluation at Lymphedema Clinic. Coccyx wounds Evaluated by wound care on 12/12, moisture associated wound to coccyx. Recommend ointment, and ongoing skin checks at facility. Obesity Continue to encourage lifestyle and dietary modification as able.

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2544820

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

schwer

Staat: NY
Alter: 87,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 19.10.2022
Beginn: 01.12.2022
Tage bis Beginn: 43,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Anticoagulant therapy Blood test COVID-19 Computerised tomogram thorax abnormal Dyspnoea Pneumonia Pulmonary thrombosis Thrombosis Ultrasound Doppler abnormal

Symptomtext

I got short of breath and it got worse. Prior to COVID I got pneumonia, so I had an oximeter and read that it was 79. I did not go to the ER and went to the local hospital because that is where my doctor. He told me I had blood clots in my lung and legs. They treated me with blood thinners and oxygen. I was there for 4 days.

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Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 4,0
Labordaten: Blood work; CT scan; ultrasound of both my legs
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure; allergic sinusitis; GERD
Andere Medikamente: Omeprazole; famotidine; nasal spray; hydrochloride; multivitamin; arthritis over the counter medication
Allergien: Penicillin; artificial sweetener
Vorherige Impfungen: -

VAERS 2480380

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

schwer

Staat: VT
Alter: 21,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Eye movement disorder Loss of consciousness Malaise Pallor Posture abnormal Vomiting

Symptomtext

Patient received Moderna COVID19 Bivalent Updated Booster 12+ 0.5ml in the right deltoid and Fluarix quad 0.5ml in the left deltoid. The patient then asked for some water and for a receptacle to vomit into. The patient lost color, stated she was feeling unwell and shortly thereafter she her head fell back, her eyes rolled back in her head and she lost consciousness. She came to quickly, but again lost consciousness a second time. She did come to again and asked for the pharmacist and technician to contact her mother who was out waiting in the car. 911 was called immediately after she lost consciousness the first time. EMS arrived and evaluated the patient. The patient and her mother decided to not seek further treatment at the hospital. The patient does have a history of passing out after blood draws, but has never passed out after vaccinations. This information was not disclosed to the pharmacy prior to administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Ehlers Danlos Type 3, Hypothyroidism, Hiatal Hernia, Chronic Depression, Chronic Nausea, Chronic Fatigue
Andere Medikamente: Unknown
Allergien: Peppermint, nickel and gluten
Vorherige Impfungen: -

VAERS 2465752

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

schwer

Staat: MN
Alter: 19,0
Geschlecht: F
Eingang: 30.09.2022
Impfdatum: 30.09.2022
Beginn: 30.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Balance disorder Fall Syncope

Symptomtext

About 5 minutes after receiving both shots, she lost balance and fainted, or nearly fainted. She fell into a chair, then slid down onto the floor. She was given some food and water and began to feel better over about 20 to 30 minutes.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None listed
Vorgeschichte: none listed
Andere Medikamente: Unknown
Allergien: None listed on profile
Vorherige Impfungen: -

VAERS 2459799

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

schwer

Staat: IL
Alter: 26,0
Geschlecht: M
Eingang: 24.09.2022
Impfdatum: 23.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Loss of consciousness Seizure

Symptomtext

Patient received the Covid vaccine in Left arm. Asked for a minute, then passed out and started seizing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: hospitalization 09/24/2022
Aktuelle Erkrankungen: No
Vorgeschichte: Depression
Andere Medikamente: Escitalopram 20mg, Nortripltyline 10mg
Allergien: NKA
Vorherige Impfungen: -

VAERS 2679972

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: WA
Alter: 61,0
Geschlecht: F
Eingang: 07.09.2023
Impfdatum: 18.11.2022
Beginn: 11.02.2023
Tage bis Beginn: 85,0
Dosis: 4
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia COVID-19 Fatigue Migraine SARS-CoV-2 test

Symptomtext

She has also had a chronic migraine which she feels is leveling out now; sore shoulder; fatigue; Covid 19; This spontaneous case was reported by a nurse and describes the occurrence of COVID-19 (Covid 19), MIGRAINE (She has also had a chronic migraine which she feels is leveling out now), ARTHRALGIA (sore shoulder) and FATIGUE (fatigue) in a 61-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Influenza vaccine. Past adverse reactions to the above products included No adverse event with Influenza vaccine. Concurrent medical conditions included Asthma, Irritable bowel syndrome (IBS), Allergy to NSAIDs (Gastric sensitivity) and Gluten intolerance. Concomitant products included FLUTICASONE PROPIONATE (FLOVENT) for Asthma, BACLOFEN, RIZATRIPTAN, PSEUDOEPHEDRINE, OXYMETAZOLINE HYDROCHLORIDE (DECONGESTANT [OXYMETAZOLINE HYDROCHLORIDE]) and FLUTICASONE PROPIONATE (FLONASE [FLUTICASONE PROPIONATE]) for an unknown indication. On 18-Nov-2022, the patient received fourth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 11-Feb-2023, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced COVID-19 (Covid 19). On an unknown date, the patient experienced MIGRAINE (She has also had a chronic migraine which she feels is leveling out now), ARTHRALGIA (sore shoulder) and FATIGUE (fatigue). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 30-Jan-2023 to 05-Feb-2023 at a dose of 1 dosage form. At the time of the report, COVID-19 (Covid 19), MIGRAINE (She has also had a chronic migraine which she feels is leveling out now), ARTHRALGIA (sore shoulder) and FATIGUE (fatigue) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 08-Feb-2023, SARS-CoV-2 test: Negative. On 13-Feb-2023, SARS-CoV-2 test: Negative. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter did not provide any causality assessments. On 24-NOV-2021, patient took third dose of Moderna vaccine with batch/Lot No: 939909 and location of injection was arm right. She had received all Moderna vaccines but was not sure of the number. Her last COVID-19 vaccine was a Moderna Bivalent BA.4/BA.5 vaccine administered in NOV2022. With the most recent dose she experienced a sore shoulder. With previous doses she had experienced a sore shoulder and was tired. After receiving the most recent dose she had COVID-19 with some continuing symptoms. This started in FEB2022 when she had bladder pain that was worse than her usual bladder pain. She also had a chronic migraine which she felt was leveling out now. She also had fatigue. She believed she has an undiagnosed history of interstitial cystitis and thought her increased bladder pain was due to a UTI. She had not taken any medications or treatments for her symptoms. She had rebound Covid after finishing course of treatment for Covid. This case was linked to US-MODERNATX, INC.-MOD-2023-739543 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 01-Sep-2023: Significant Follow-up received. Historical Vaccine added, Events updated, Suspect product updated, Paxlovid was updated as treatment medication; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739543:Monovalent dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 20230208; Test Name: Rapid tests; Test Result: Negative ; Test Date: 20230213; Test Name: Rapid tests; Test Result: Negative
Aktuelle Erkrankungen: Allergy to NSAIDs (Gastric sensitivity); Asthma; Gluten intolerance; Irritable bowel syndrome (IBS)
Vorgeschichte: -
Andere Medikamente: BACLOFEN; RIZATRIPTAN; PSEUDOEPHEDRINE; DECONGESTANT [OXYMETAZOLINE HYDROCHLORIDE]; FLONASE [FLUTICASONE PROPIONATE]; FLOVENT
Allergien: -
Vorherige Impfungen: -

VAERS 2623179

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: NY
Alter: 70,0
Geschlecht: F
Eingang: 28.04.2023
Impfdatum: 27.10.2022
Beginn: 02.04.2023
Tage bis Beginn: 157,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest discomfort Chills Fatigue Nasopharyngitis Pneumonia

Symptomtext

I was really tired and had chills for about day after receiving the vaccines. On 03/25/2023 I had a tightness in my chest. I went to my pharmacy, I took Mucinex, and it got progressively worse. I went to an urgent care 03/31/2023 and I got two antibiotics and prednisone. On 04/02/2023 I was diagnosed with pneumonia. As of today, I feel better, but I sound and feel like I have cold.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: AFIB
Andere Medikamente: Xarelto; Multivitamin; Vitamin D; Magnesium; Vitamin B12
Allergien: N/A
Vorherige Impfungen: -

VAERS 2622174

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: NY
Alter: 86,0
Geschlecht: M
Eingang: 27.04.2023
Impfdatum: 23.09.2022
Beginn: 29.09.2022
Tage bis Beginn: 6,0
Dosis: 5
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Angina pectoris Cardiac discomfort Cardiac disorder Cardiac stress test abnormal Catheterisation cardiac abnormal Chest discomfort Chest pain Colonoscopy normal Coronary arterial stent insertion Coronary artery occlusion Electrocardiogram abnormal Endoscopy normal Gastrointestinal disorder

Symptomtext

On September 29, 2022, six days after vaccination, I experienced chest pain while walking uphill. As I have been very lucky and had no major medical problems, I told myself that this can't be anything serious and turned around and went home. The next day I tried again and the chest pain returned. I, however, remained in denial and said to myself that this couldn't be anything, I don't have medical problems. On the third day, I tried again and the pain came sooner, so I went home and called my primary care physician's office at a local healthcare facility. They told me to go to the ER. I did. The ER team told me that there was some anomaly on my EKG and that I should see my primary physician promptly. The next day, the doctor I saw told me to get a stress test immediately and that if the HCF were unable to schedule it promptly I should go to another Cardiology facility. That is what I ended up doing. Dr. performed a stress test and told me I had a blockage and needed a prompt catheterization. That was done at another Hospital where the Cardiology facility placed one stent. The next day I was back in the ER with chest pain, was sent to the hospital, this time to the Medical Center where I was again in the cath lab where the Cardiology facility placed a second stent. This was followed by several weeks of angina pain/pressure and a second trip to a Medical Center in an ambulance and another cath lab exploration that found nothing. I did not want to have to be transported to another hospital for acute heart problems, so I switched my cardiology care to another healthcare facility so that it would be closer at hand and also integrated with my primary care practice. They did yet another catheterization, concluded as well that I had no further blockages, and that my continuing chest pain/pressure was a problem for the digestive diseases department. They performed a colonoscopy and endoscopy on me and found nothing so I was prescribed a regime of pantoprazol, simethicone, and Benifiber to relieve symptoms. That works imperfectly but it helps a lot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: See above
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure under control with 5mg lisinopril
Andere Medikamente: Lisinopril, Atorvastatin, Vitamin C, Vitamin D3, Riboflavin, Magnesium, CoQ-10, Chromium picolinate, Benfotiamine
Allergien: None
Vorherige Impfungen: -

VAERS 2616755

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 18.04.2023
Impfdatum: 11.11.2022
Beginn: 01.12.2022
Tage bis Beginn: 20,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Joint range of motion decreased Mobility decreased Pain Pain in extremity X-ray normal

Symptomtext

I experienced a loss of range of motion in my left arm. Upward, outward extension is painful. It became so bad, that I couldn't reach for the salt at the dinner table or pick up a glass of water easily. Any kind of reaching was extremely painful. I went to the doctor finally, on 12/12/2022. She gave me some very basic physical therapy exercises to relieve immediate pain. I was also treating with over-the-counter pain medication. I started physical therapy on 01/31/2023. I've been going twice a week. I do 25 minutes of exercises and 15 minutes of physical therapy manipulation. I've seen vast improvement. It's not all better. I don't have full range of motion or full confidence that movement won't be painful, but I can reach for my coffee without worrying.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 12DEC2022 - X-Ray - Nothing Abnormal Found
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Omeprazole; Singulair; Vitamin D3; Multivitamin; Turmeric; Calcium; Allergy Shot
Allergien: Insulin
Vorherige Impfungen: -

VAERS 2616320

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: VA
Alter: 54,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 14.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 18,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injected limb mobility decreased Injection site pain Injection site reaction Musculoskeletal discomfort Pain Periarthritis

Symptomtext

The health event presented with the beginnings of a frozen shoulder in my left sub deltoid. I have a limited range of motion. Specifically we're talking about anterior deltoid. Range of motion is limited when I start with my left arm extended and I try to reach back, I can really feel it in that deltoid. The pain is acute and sharp, then immediately goes away when I stop making that motion. There's still about 10-15% residual pain. With my hand extended or elbow bent, if I try to reach back, it hurts. The pain lingers for a second then goes away within a minute. I take ADVIL for my back, and that doesn't help with the shoulder much. When I subluxed my right shoulder, my left shoulder was okay. My doctor put me on a prescription called diclofenac 75mg twice daily for a week then I was on that for once a day for a week after that, then as needed. I didn't start taking that until my right shoulder was really bothering me. Stretching seems to help the right shoulder. When I came off the diclofenac, my left shoulder started bothering me. After my right shoulder was okay, my left shoulder was hurting more in January/February and it's been trending in discomfort up until now. I did finally get massage therapy which was on my left shoulder. That was 3 days ago. It definitely took the edge off. This is a standard Swedish massage. It seemed to have loosened up a little bit. The pain is not as sharp. I have scheduled for another massage therapy in about 2 to 3 weeks. If it really starts to come back, then I may have another appointment with an orthopedist. I could also continue to do the stretches for my subluxed shoulder on my left shoulder. It's so painful that I recently made the decision to get a Shingles vaccine in my right shoulder because of the left shoulder pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Subluxation of Right Shoulder from Bicycle Accident
Vorgeschichte: Ulnar Nerve Damage Bilaterally; Cervical Spine Issues Between C-5, C-6, C-7, C-8; Carpal Tunnel in Both Arms; Slight herniation between L5 and S1; Subluxation of Right Shoulder from Bicycle Accident; Benign Prostatic Hyperplasia; Spina bifida occulta; Meniere's Disease; Raynaud Phenomenon; 4cm Gyroid on Left Thyroid
Andere Medikamente: LEXAPRO; folate; vitamin B12
Allergien: KLONOPIN; nickel; environmental allergies
Vorherige Impfungen: 1st Moderna COVID-19 vaccine 04/17/2021, within an hour, I developed a 1.5 cm blister on my left shoulder about the size of a ma

VAERS 2616287

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: CO
Alter: 66,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 04.10.2022
Beginn: 09.11.2022
Tage bis Beginn: 36,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Nasal congestion Pharyngeal paraesthesia SARS-CoV-2 test positive

Symptomtext

I had a stuffy nose, a tingle in my throat and extremely tired.

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Praegender Schweregrund: Pharyngeal paraesthesia
Hospital-Tage: -
Labordaten: At home rapid COVID-19 test- positive 11/9/2022; COVID-19 test- positive 11/10/2022
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2614743

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 13.04.2023
Impfdatum: 10.10.2022
Beginn: 01.03.2023
Tage bis Beginn: 142,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood creatine phosphokinase normal Differential white blood cell count normal Echocardiogram abnormal Electrocardiogram ambulatory abnormal Electrocardiogram normal Full blood count normal Heart rate increased Metabolic function test normal Palpitations Tachycardia Thyroid function test normal X-ray normal

Symptomtext

In early March I started being awoken by a raising heartbeat at night. It was for no reason whatsoever. I happened to be going to my annua l checkup and told him about and he put me on a Holter monitor. He also ran an EKG and thyroid test and those came back normal. On the 24th I felt like my heart was racing all day. Before the results came back. The next morning, I went to the emergency room. My temperature was normal. My blood pressure was 127/81, mu oxygen was 100. While I was there, I was told by the doctors that my heart was going from 60 to 100 beats per minute and there was no indication as to why. They gave me Propranolol 40mg twice a day. The Holter monitor results showed slight abnormalities. I went to the cardiologist on the 29th and he ordered an echocardiogram which was not remarkable. I followed with my general practitioner just yesterday. My emergency room reason for visit was tachycardia and heart palpitations. I am now on beta blockers; I have not recovered from it.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: 20-21MAR2023 Holter monitor - slight abnormalities; 20MAR2023 EKG, Thyroid test- normal 25MAR2023 CBC auto differential-normal; 25MAR2023 CK imaging - normal; 25MAR2023 metabolic panel- normal; 25MAR2023 x-ray - normal; 25MAR2023 12 lead EKG- normal; 04APR2023 Echocardiogram - Not remarkable
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Benadryl
Allergien: Gluten intolerance
Vorherige Impfungen: -

VAERS 2613239

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: TX
Alter: 70,0
Geschlecht: M
Eingang: 11.04.2023
Impfdatum: 07.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 5,0
Dosis: 5
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Blood test Magnetic resonance imaging abnormal Medical device implantation Mobility decreased Musculoskeletal pain Myalgia Pain in extremity Rotator cuff syndrome

Symptomtext

I had my vaccination on 10/07/2022. On 10/12/2022 I started having muscle pains. These pains were manifesting on both shoulders and at the top of my legs and buttocks. It was difficult for me to move and I would have to gradually get my legs moving. I had a lot of pain in my shoulders. I could move my arms to the front of my body and near. I could not reach behind me or up above me. I contacted my physician in 10/2022. I stopped taking the alopurinol and testosterone. I was sent for blood panel. I was then referred to specialist for Neurology. I had an MRI of my right shoulder as it was the most painful. I was also referred to other specialty care and they put electrodes on my legs and put pins in my knees. I am still being followed up with specialty care. I was recommended by Neurology to have steroid injections. This made a substantial difference and the pain went away. I was then seen for my left shoulder. There was no tear but they treated with the same treatment. I was instructed to start Physical Therapy which I was doing daily. My legs improved dramatically with the physical therapy. I have had 2 months of pain free but the pain has started to come back the last 6 weeks and getting worse. I conversed with my doctor in 04/2023 and I have started back up with daily appointments the physical therapy.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 10/2022 MRI of Right shoulder, I had a partial tear on the rotator cuff
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Type II Diabetes; Gout; Low Testosterone
Andere Medikamente: Carvedilol; eplerenone; metformin; atorvastatin; magnesium; injections for testosterone
Allergien: N/A
Vorherige Impfungen: -

VAERS 2611465

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 07.04.2023
Impfdatum: 06.10.2022
Beginn: 11.02.2023
Tage bis Beginn: 128,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood test normal Dizziness Dyspnoea Electrocardiogram normal Fatigue Headache Malaise X-ray normal

Symptomtext

I had shortness of breath, fatigue, headache, dizziness. I didn't feel sick, I just felt lousy. I went to the hospital; they check me for my heart. They did an EKG, two sets of blood work, and an x-ray. Everything came back normal. They sent we home with no treatment. They told me to follow up with my primary care doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 14FEB2023 EKG - Normal; 14FEB2023 Blood work - Normal; 14FEB2023 Blood work- Normal; 14FEB2023 X-ray - Normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chronic Pain; Fibromyalgia
Andere Medikamente: Levothyroxine; Duloxetine; Atorvastatin; Ropinirole; Gabapentin; Baclofen; Meclizine; Albuterol; Fluticasone; Zyrtec; Magnesium; Vitamin D2; Aimovig
Allergien: Shellfish; Ibuprofen; Dilaudid; Amitriptyline; Nortriptyline; Morphine pill sensitivity
Vorherige Impfungen: -

VAERS 2607389

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: NJ
Alter: 73,0
Geschlecht: F
Eingang: 31.03.2023
Impfdatum: 29.09.2022
Beginn: 24.01.2023
Tage bis Beginn: 117,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anxiety Electrocardiogram normal Heart rate increased Tremor

Symptomtext

My heart started beating extremely fast, it felt as though my heart was going to jump right out of my chest. I had to anxiety attacks back-to-back at work. It left me feeling very shaky after the episode. I went to the closet urgent care. They took my blood pressure, ran an EKG, took my pulse-oxy, they also listened to my heart. All tests came back normal, but they could hear with the stethoscope extra heart beats. They diagnosed me anxiety. I was advised to follow up with my primary care physician who prescribed an anxiety medication and referred me to a psychiatrist. My psychiatrist and I discussed if the anxiety could possibly be long haul COVID-19 side effect as I had tested positive for COVID-19 in December 2022.

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: 24JAN2023 Blood pressure, normal; 24JAN2023 EKG negative; 24JAM2023 Pulse ox normal
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: SYNTHROID; liothyronine; CRESTOR; coQ10; vitamin D3; biotin; estradiol vaginal cream; XANAX
Allergien: CIPRO; latex; amoxicillin
Vorherige Impfungen: -

VAERS 2604945

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: AR
Alter: 62,0
Geschlecht: F
Eingang: 28.03.2023
Impfdatum: 26.09.2022
Beginn: 01.01.2023
Tage bis Beginn: 97,0
Dosis: 5
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Bronchitis Cardiomegaly Chest X-ray Dyspnoea Influenza virus test Loss of personal independence in daily activities Polymerase chain reaction SARS-CoV-2 test

Symptomtext

I had my vaccination on 09/26/2022. I started to experience shortness of breath in 01/2023. I went to urgent care on 03/16/2023 and was diagnosed with probable cardiomegaly and bronchitis. I was prescribed an antibiotic and inhaler. I currently feel much better on 03/28/2023. I am supposed to stay indoors with limited exercise for 3 weeks total. After 3 weeks I am supposed to call my doctor with a follow up to my condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 03/16/2023 Chest Xray COVID-19 Flu Pneumonia
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type II Diabetes 2018; Elevated Cholesterol; Hypertension
Andere Medikamente: Gensibrozil; Metformin; Vitamin C; Vitamin B12; Multivitamin; Fluvoxamine; Respirall; Vitamin D3; Fish Oil; Allergy medications; Diabetes supplies
Allergien: N/A
Vorherige Impfungen: -

VAERS 2604863

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: MA
Alter: 69,0
Geschlecht: M
Eingang: 28.03.2023
Impfdatum: 25.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 6,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthritis Muscular weakness Tremor

Symptomtext

I did not have an adverse reaction to the vaccine. In 10/2022, in both thighs on the inside I have noticed my muscles are very weak and they shake. I contacted my doctor, and it was determined that I have arthritis. I take TYLENOL or ADVIL to take care of the pain. I am not taking physical therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2577200

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: MI
Alter: 53,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 12.10.2022
Beginn: 31.01.2023
Tage bis Beginn: 111,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Angiogram pulmonary abnormal Bronchitis COVID-19 Cough Dyspnoea Pulmonary septal thickening Respiratory tract congestion SARS-CoV-2 test positive Splenic artery aneurysm

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 1/31/2023 Discharge Date: Feb 1, 2023 PRESENTING PROBLEM: COVID [U07.1] COVID-19 virus infection [U07.1] HOSPITAL COURSE: Patient is a 53 y.o. female without significant past medical history. She presented to the emergency department with complaint of shortness of breath. Recently tested positive for COVID and had worsening dyspnea at home and therefore presented to the ER for further evaluation. She had a CTA which showed no PE, bronchitis, interlobular septal thickening possibly related to pulmonary edema, and splenic artery aneurysm. She was started on steroids for her bronchitis and had great improvement in her symptoms. Also on mucinex and tessalon for cough and congestion. She will need to follow-up with her PCP regarding splenic artery aneurysm. Given marked improvement in her symptoms, she was discharged in stable condition on 2/1/23. She was enrolled in the Transition to Home monitoring program.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: 9/16/2022 Office Visit with my MD Non-recurrent acute suppurative otitis media of left ear with spontaneous rupture of tympanic membrane
Vorgeschichte: Idiopathic hypersomnia without long sleep time Encounter for screening colonoscopy Multiple acquired skin tags Ganglion cyst of dorsum of left wrist Memory disturbance COVID-19 virus infection
Andere Medikamente: Ascorbic Acid (VITAMIN C) 500 MG CAPS benzonatate (TESSALON) 100 MG capsule CALCIUM PO cholecalciferol (D3) 50 MCG (2000 UT) tablet Cyanocobalamin (VITAMIN B-12 CR PO) Ferrous Sulfate (IRON) 325 (65 FE) MG TABS guaiFENesin (MUCINEX) 600 MG
Allergien: Sulfa DrugsHives BactrimHives Erythromycin PenicillinsSwelling
Vorherige Impfungen: -

VAERS 2566808

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 23.09.2022
Beginn: 17.01.2023
Tage bis Beginn: 116,0
Dosis: 5
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Asthenia Blood creatinine normal COVID-19 Condition aggravated Cough Diabetic foot Diarrhoea Dizziness Glomerular filtration rate Hyperglycaemia Hypoglycaemia Insulin therapy Metabolic acidosis Metabolic function test abnormal Nausea Oxygen saturation decreased Renal impairment SARS-CoV-2 test positive

Symptomtext

COVID+ 1/17/2023. Vaccination status - Moderna x4 + Moderna BIVALENT booster Discharge Summary MD (Physician) ? ? General Medicine BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: MD Admission Date: 1/17/2023 Discharge Date: 01/19/2023 Active Hospital Problems Diagnosis Date Noted POA ? Diabetic ulcer of right midfoot associated with type 2 diabetes mellitus, with fat layer exposed 01/18/2023 Yes ? COVID 01/17/2023 Yes ? Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin Active Issues Requiring Follow-up: T2DM Diabetes Discharge Planning: ? The patient's wife is receiving OmniPod some time this week and will transition from V-Go which should make controlling his blood sugars easier. Should follow with outpatient provider to have this set up and pt/wife be trained in its use ? Transition back to V-GO not advised, as the patient's wife informed provider that pt has multiple episodes of hypoglycemia at home if he does not eat before bed + early in morning. Discharge Plan: ? Safe for discharge to home with ordered medication doses. Do not resume Vgo. Pt to start Omnipod when able/trained. ? Metformin use questionable in this pt due to age and declining renal function. However his dosage is within the perimeters of his reduced GFR (500mg twice daily), will need close monitoring by PCP. ? SGLT2 would be indicated due to CKD. This can cause fluctuations in glucose levels and would likely need insulin regimen adjustments Chronic Wounds ? DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: COVID HOSPITAL COURSE: Patient is a 85 y.o. male who presented with weakness, nausea, vomiting, diarrhea, lightheadedness x 2 days duration. He developed a cough so wife administered a COVID-19 test which was positive. He reported ongoing symptoms on adm. They are concerned about him going home with these symptoms, as his primary caregiver / spouse is also sick with COVID-19 and feeling unwell. Hemodynamically stable in the ED, desaturation on room air. Mild metabolic acidosis on CMP with creatinine at baseline. No leukocytosis. One hypoglycemic reading with three other normal readings. +covid-19 pcr. No cxr. Given 500cc NS once and dextrose in ED. He was weaned off supplemental o2 and evaluated by pulm rehab/pt/ot who stated patient would need home with pt but no oxygen on discharge. His course was complicated by hypoglycemic episodes after patient refused to remove his insulin pump on admission. Once pump removed from patient, consulted for labile glucose levels. He had adjustments made in his diabetes medications and had improvement in glu levels. He was discharged home in stable conditions with plans for close follow up and teaching of upcoming diabetes medication changes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: Inpt 8/26/22-8/31/22: Admission Date: 8/26/2022 Discharge Date: 08/31/2022 Admitting Physician: MD Attending Physician: MD Discharge Clinician: MD Primary Care Provider at Discharge: MD Active Hospital Problems Diagnosis Date Noted POA ? Diabetic ulcer of left foot associated with type 2 diabetes mellitus, unspecified part of foot, unspecified ulcer stage Patient was started on IV vancomycin and Zosyn after blood cultures collected. Podiatry consulted and =ultimately performed partial left hallux amputation with likely surgical cure. Dr of Podiatry will follow cultures and follow-up with patient. Discharged home on keflex for 7 days. Patient was continued on his insulin pump during this hospital stay.
Vorgeschichte: Personal history of prostate cancer CAD (coronary artery disease) Hypertension associated with diabetes Diabetic infection of right foot Mixed hyperlipidemia Persistent atrial fibrillation Stage 3 chronic kidney disease Ischemic cardiomyopathy OSA (obstructive sleep apnea) Atherosclerosis of artery of both lower extremities Carotid artery stenosis Ischemic cerebrovascular accident (CVA) Obesity (BMI 30-39.9) ICD (implantable cardioverter-defibrillator) in place Atherosclerosis of native artery of right lower extremity with ulceration of midfoot RLS (restless legs syndrome) Syncope, unspecified syncope type Presence of Watchman left atrial appendage closure device Aortic stenosis Chronic systolic heart failure Polyneuropathy associated with underlying disease Abnormal CBC Platelets decreased Other constipation Difficulty with CPAP full face mask use Diabetic foot infection Atherosclerosis of native arteries of left leg with ulceration of other part of foot Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin
Andere Medikamente: Aspirin 81 mg Oral Daily B Complex Vitamins 1 tablet Oral Daily Bacillus Coagulans-Inulin 1-250 BILLION-MG 1 Caplet Oral Daily Cinnamon 2,000 mg Oral Daily Coenzyme Q10 100 mg Oral Daily Empagliflozin 25 mg Oral Daily Furosemide 20 mg Oral
Allergien: Adhesive TapeRash
Vorherige Impfungen: -

VAERS 2566752

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: IL
Alter: 70,0
Geschlecht: F
Eingang: 24.01.2023
Impfdatum: 28.09.2022
Beginn: 25.12.2022
Tage bis Beginn: 88,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Dyspnoea Ear pain Fatigue Headache Malaise Productive cough Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

12/25/2022 Woke up around 6 am not feeling well. Had headache, earache, productive cough, congestion, and fatigue. Took at home COVID-19 test and it was negative. Woke up 12/26/2022 at 3AM, tested again, and it was negative. Symptoms continued to worsen. Called PCP on 12/27/2022 and was prescribed Paxlovid. Began Paxlovid and symptoms began to improve. All my symptoms have improved but still having breathing issues. Went back into PCP and was put on prednisone and it has helped resolve breathing issues

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: At home COVID-19 test x3 - 1 Negative 2 Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; COPD; narrowing in nerve endings; Atrial tachycardia;
Andere Medikamente: Dilopazim; Inopresol; Montelukast; Atorvastatin; lisinopril; hydrochlorothiazide; Advair; Albuterol PRN; Nebulizer duel Nebs PRN; Multivitamin; Ca; Vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 2544929

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: MI
Alter: 94,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 26.09.2022
Beginn: 29.09.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / RA

Tod: ja Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein

Asthenia Atrial fibrillation Blood test abnormal Breast disorder female Chest X-ray abnormal Choking Computerised tomogram abnormal Computerised tomogram breast abnormal Computerised tomogram liver abnormal Cough Decreased appetite Disorientation Dysphagia Feeling abnormal Gait disturbance Hepatic lesion Hypophagia Infection

Symptomtext

About three days after getting her shot, my mother woke up disoriented and unlike herself. She was lethargic and did not want to eat. She drank some tea and soup, and that's a quarter of what she usually eats. This was on Thursday evening, by that Friday she was not getting any better. I did a COVID-19 test on her. She was negative. It was hard for her to walk or move, I had to carry her to the bathroom. She was unable to get dressed. That Saturday she was worse and had to be physically lifted out of bed to go to the bathroom and she was completely weak and had extreme Flu like symptoms. She was coughing and when she tried to eat, she was having a very hard time swallowing and would choke on it. I called 911 to have the medics transfer to the hospital on that Saturday night around 9:30PM. They found at the ER she had lesions on liver, thyroid and right breast, Her X-Ray show her left lung was a third to a half clouded and the right lung a quarter to a third cloudy, and they diagnosed her with pneumonia. She was given medication at the hospital and an antibiotic regime for 5 to 6 days and it was not making any improvement. They changed the antibiotic and that was seemed to be making slight improvement, but then she developed sepsis. Then they made the choice to have a cardiologist change her meds due to her AFIB. The cardiologist changed the meds at 5 PM in the afternoon and didn't get more AFIB medication until 9AM the next morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 18,0
Labordaten: 01Oct2022 Blood work, infection; 01Oct2022 CT scan, lesions on liver, thyroid and right breast; 01Oct2022 Chest X-Ray, Left lung was a third to a half clouded and the right lung a quarter to a third cloudy, pneumonia
Aktuelle Erkrankungen: N/A
Vorgeschichte: Stroke in 2015
Andere Medikamente: Blood pressure medication; LIPITOR; atorvastatin; calcium; fish oil; vitamin E; ELIQUIS; diltiazem; memantine; pantoprazole; digoxin; centerline; potassium; TYLENOL; multivitamin; vitamin D3; glucosamine chondroitin.
Allergien: N/A
Vorherige Impfungen: -

VAERS 2543810

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: PA
Alter: 65,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 23.09.2022
Beginn: 01.12.2022
Tage bis Beginn: 69,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Back pain Blood test abnormal Chest X-ray abnormal Chest pain Electrocardiogram abnormal Eosinophil count Lung disorder Lymphocyte percentage decreased Musculoskeletal chest pain

Symptomtext

I had chest pains off and on for three days. It was an aching pain that had went through painfully from my chest, ribs and back. The pain was so bad I went to the ER. They performed testing I had to wait until my cardiologist came, and said things weren't any different from his last visit with me. He did not feel it was heart related. I feel better now it did take a couple of days. They do not know what caused this.

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Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: 20Dec2022 3 EKG irregularities; 20Dec2022 X-Ray, spots on lungs; 20Dec2022 3 blood work panels, irregular EOS too high 3 count, low lymph auto
Aktuelle Erkrankungen: N/A
Vorgeschichte: Celiac Disease; Osteoporosis; Osteoarthritis; Right Bundle Branch Heart Disease
Andere Medikamente: Albuterol; VALTREX; AMBIEN; ALLEGRA; FLONASE; AREDS; omega 3; glucosamine; calcium and D; RECLAST infusion
Allergien: Celiac disease; clarithromycin; bacterium
Vorherige Impfungen: -

VAERS 2509709

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

moderat

Staat: CA
Alter: 27,0
Geschlecht: M
Eingang: 16.11.2022
Impfdatum: 10.10.2022
Beginn: 09.11.2022
Tage bis Beginn: 30,0
Dosis: 4
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Electrocardiogram normal

Symptomtext

Chest Pain (left side, just under peck) 11/09 , went to see Dr 11/14 , got an EKG and all looked good. Planning on getting an Echo on 11/28 and Blood Work on 11/18 to see why chest pain is occuring.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG 11/14 - Looked Good.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Advil and Ibuprofen
Vorherige Impfungen: -

VAERS 2492708

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: MD
Alter: 73,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 26.09.2022
Beginn: 07.10.2022
Tage bis Beginn: 11,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test abnormal Chest pain Fatigue Goitre Headache Heart rate increased Heart rate irregular Hunger Neck pain Thyroiditis Ultrasound thyroid abnormal Weight decreased

Symptomtext

Began with intermittent painful spot on right side of neck. On 10/07/2022 pain spread to area from top on head to chest on the right side and swelling of thyroid. Fatigue, pulse sometimes over 100, irregular heartbeat, need to eat at least 4 times /day, small weight loss. Was mailed order for thyroid ultrascan which was performed 10/18/2022, blood test on 10/19/2022 at which point thyroiditis was diagnosed and I was told to stop taking Synthroid. From online publications I have read that this is "self-limiting" but I am beginning to wonder whose limits will be reached first. Thankfully the pain has subsided but not gone away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Thyroid ultrascan Radiology 10/18/2022, blood test Endocrine 10/19/2022
Aktuelle Erkrankungen: -
Vorgeschichte: wet macular degeneration
Andere Medikamente: 25mcg Synthroid 4xweek received monthly injection of Lucentis in right eye on 10/06/2022 Bluebonnet Eye Care 2xday Mega Food Women Over 55 One Daily Mykind plant iron & organic herbs 2 or 3 x week
Allergien: -
Vorherige Impfungen: original shingles shot, VAERS report filed

VAERS 2487323

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

moderat

Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 28.09.2022
Beginn: 29.09.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Incorrect route of product administration Mobility decreased

Symptomtext

On 10/24/22 the patient returned to the pharmacy for another immunization and wanted to let us know that her shoulder was still in pain from the updated Covid booster she had a month ago. She has difficulty raising her arm above her head. She will be having an appointment with her doctor and will bring this to his attention. She also noted that the vaccine was given higher than other vaccines she has received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2487292

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: CO
Alter: 70,0
Geschlecht: M
Eingang: 24.10.2022
Impfdatum: 05.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Asthenia Back pain COVID-19 Cough Dyspnoea Electrocardiogram normal Fatigue Feeling abnormal Feeling jittery Headache Heart rate irregular Malaise Nasal disorder Nausea Pain Poor quality sleep Pyrexia

Symptomtext

He got his vaccine, he didn't have any reactions when he first got the vaccine. Later that evening his shoulders were sore from the shots. The next day he had two sore shoulders as he had gotten 2 vaccines, one flu in one arm and the COVID in the other. He did feel a little weak, but felt like he was under the weather. The next day 10/7/22 he had an irregular heart beat, he felt tired and weak, had shortness of breath and felt sick, nausea. He started having body aches, hips, shoulders and lower back. On 10/8/22 he had the same symptoms with headache when he woke up and restless/jittery at night. He still had the other symptoms continuing from the 7th as well. On 10/9/22 he had the same symptoms including the previous ones continuing. He was sleeping poorly. Then on 10/10/22 he still felt bad. On 10/11/22 when he woke up that morning he did not have the irregular heart beat which was intermittent and then started having it in the afternoon and then started coughing a lot. He went to his doctor and said that he was having a reaction to the vaccine. He asked for an EKG and this was done and normal earlier and had no irregular heart beat when he saw the doctor. His condition got worse that afternoon. irregular heart beat started again and as the day went on in the evening with the coughing, still coughing and feeling sicker, but feeling a little better. He called back the doctor, and saw the medical assistant and they did a COVID test which was positive, and he did have a fever on 10/12/22 of 101.7. They prescribed Paxlovid tablets which he took for 5 days, and also told him to take Tylenol and Coricidin HBP for cough. He is feeling better than he did, but still not feeling great, feels still short of breath, coughing, nose issues. Cough medicine is helping. He has no history of irregular heart beat in the past.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG
Aktuelle Erkrankungen: None.
Vorgeschichte: High blood pressure, hypothyroidism.
Andere Medikamente: Losartan, Levothyroxine.
Allergien: Codeine (anaphylactic reaction of throat closing).
Vorherige Impfungen: Flu vaccine and Shingrix vaccine had sick feeling, soreness in the arms similar to what he has now in 2019.

VAERS 2481799

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: NC
Alter: 68,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 29.09.2022
Beginn: 05.10.2022
Tage bis Beginn: 6,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Condition aggravated Cough Eyelid margin crusting Nasal congestion Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19. I developed a sore throat on 10/05/2022 that progressively became worse. My other symptoms included nasal congestion, headaches, coughing, and crusting over my left eye whenever I woke up. The congestion, coughing, and crusting over my eye still persists. I was prescribed to take over the counter MUCINEX, FLONASE, and ROBITUSSIN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 7Oct2022 home COVID19 test positive; 12Oct2022 PCR test positive.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2471890

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: NJ
Alter: 63,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 01.10.2022
Beginn: 02.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site erythema Injection site pain Injection site pruritus Injection site reaction Paraesthesia Urticaria

Symptomtext

Large welt at injection site, which I still have. It's been very itchy and has not responded to hydrocortisone cream. The edges are still very red and itchy, as if I can feel it spreading. At times it feels like pin pricks or burning. It's 4 inches wide and about 3 inches high.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: HBP Osteoarthritis
Andere Medikamente: Lisinopril Metoprolol Omeprazole Claritin Skin, Hair and Nails dietary supplement
Allergien: Aspirin Sulfa Cipro
Vorherige Impfungen: -

VAERS 2471325

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

moderat

Staat: NY
Alter: 42,0
Geschlecht: M
Eingang: 07.10.2022
Impfdatum: 03.10.2022
Beginn: 03.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dehydration Fatigue Headache Nausea Pain Paraesthesia Sleep disorder Vomiting

Symptomtext

nausea; vomited; headache; achiness; tingling like pins and needles in his thumb; felt dehydrated; Took Ambien to go to sleep; fatigued; This spontaneous case was reported by a patient and describes the occurrence of PAIN (achiness), PARAESTHESIA (tingling like pins and needles in his thumb), DEHYDRATION (felt dehydrated), SLEEP DISORDER (Took Ambien to go to sleep) and FATIGUE (fatigued) in a 42-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Previously administered products included for Product used for unknown indication: Johnson COVID-19 vaccine, Pfizer COVID-19 vaccine and Pfizer COVID-19 vaccine (2 doses of Pfizer vaccine). Past adverse reactions to the above products included No adverse event with Johnson COVID-19 vaccine, Pfizer COVID-19 vaccine and Pfizer COVID-19 vaccine. On 03-Oct-2022, the patient received fourth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) 1 dosage form. On 03-Oct-2022, the patient experienced PAIN (achiness), PARAESTHESIA (tingling like pins and needles in his thumb), DEHYDRATION (felt dehydrated), SLEEP DISORDER (Took Ambien to go to sleep) and FATIGUE (fatigued). On 04-Oct-2022, the patient experienced NAUSEA (nausea), VOMITING (vomited) and HEADACHE (headache). The patient was treated with ZOLPIDEM TARTRATE (AMBIEN) at an unspecified dose and frequency. At the time of the report, PAIN (achiness) had not resolved and PARAESTHESIA (tingling like pins and needles in his thumb), DEHYDRATION (felt dehydrated), SLEEP DISORDER (Took Ambien to go to sleep), FATIGUE (fatigued), NAUSEA (nausea), VOMITING (vomited) and HEADACHE (headache) outcome was unknown. No concomitant medications was reported. After receiving the bivalent vaccine patient came home at 2:00 and felt fine. Patient ate a late lunch or an early dinner, laid down, and went to bed. Slight achiness when he woke up with light fatigue, and Felt a little tingling like pins and needles in his thumb. Woke up at 10:00 PM. Patient took Ambien to go to sleep. Patient felt dehydrated. Drank dehydrated soda. Around 1-2 AM he went to the bathroom with nausea, and vomited. Went back to sleep. Got up next day morning. Had a small protein cookie for breakfast. The more patient moved around felt achy. Had a headache. Laid down from 11-12:00 to 3:00. Woke up with continued achiness. No sore throat. No additional medications or treatments.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468477

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: MD
Alter: 30,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 04.10.2022
Beginn: 04.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Feeling hot Paraesthesia

Symptomtext

After patient received their Bivalent moderna vaccine they walked over to the waiting area and almost immediately reported feeling dizzy. They were instructed to sit down immediately and were being monitored by the Pharmacist on Duty. Patient did not improve and began to feel hot. They were then guided to the floor to lay on their back and feet elevated while another person called 911. This all occurred within 5-10 minutes of getting their vaccine. Patient remained alert and responsive to questions and reported feeling better and less dizzy but also tingling in their arms. Emergency services arrived and incident review will Responders. They took over and monitored patients vitals. Heart rate and blood pressure began to show signs of normal and they were then escorted to their vehicle by emergency responders.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: None
Andere Medikamente: none
Allergien: Mild allergic reaction to Penicillin
Vorherige Impfungen: -

VAERS 2465795

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 30.09.2022
Impfdatum: 24.09.2022
Beginn: 24.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Hyperhidrosis Mobility decreased Muscular weakness Musculoskeletal stiffness Pain Posture abnormal

Symptomtext

PT. STATED THAT AFTER RECEIVING THE VACCINE SHE EXPERIENCED NO STRENGTH IN ARMS AND LEGS, HAD THE CHILLS AND SWEATS, HER BODY WAS STIFF AND SHE SLITHERED OUT OF BED AND WAS ON THE FLOOR UNABLE TO MOVE FOR CONSIDERABLE AMOUNT OF TIME UNTIL SON FOUND HER. SHE TOOK TYLENOL FOR PAIN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: HAS DR. APPT. 9/26/22
Aktuelle Erkrankungen: N/A
Vorgeschichte: ADRENAL GLAND DISEASE AND MENOPAUSE
Andere Medikamente: N/a
Allergien: HEPERIN, MORHINE
Vorherige Impfungen: -

VAERS 2463199

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

moderat

Staat: WI
Alter: 70,0
Geschlecht: M
Eingang: 28.09.2022
Impfdatum: 26.09.2022
Beginn: 28.09.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Paraesthesia

Symptomtext

Numbness and tingling in fingers in left hand

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Lisinopril Pravastatin Hydochlorothiazide
Allergien: -
Vorherige Impfungen: -

VAERS 2716819

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: OH
Alter: 69,0
Geschlecht: F
Eingang: 22.11.2023
Impfdatum: 16.11.2023
Beginn: 16.11.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Diarrhoea Headache Nausea Pain SARS-CoV-2 test negative Vomiting

Symptomtext

Patient started to exhibit hours after vaccine nausea, vomiting , diarrhea, headache and body aches. She reports she was up all night vomiting. She thought she may have had COVID and took 3 COVID test at home which came back negative. Her nausea and vomiting last through the night but then went away. She is now still feeling headache and body ahces. She presented to clinic today 11/22 with symptoms and wanted to get another COVID test and evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 11/22/23- COVID test negative.
Aktuelle Erkrankungen: patient states she had a little congestion but related that to allergies. She recently visited another city.
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2639732

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

mild

Staat: WA
Alter: 68,0
Geschlecht: F
Eingang: 01.06.2023
Impfdatum: 23.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Gastrointestinal disorder Inflammatory bowel disease Irritable bowel syndrome Medical procedure Pain in extremity

Symptomtext

I had a sore arm for about a day after receiving the Moderna Dose 4 vaccine. Since receiving the first COVID-19 within two weeks, I have had both upper and lower gastrointestinal issues. I have had multiply procedure to diagnose and treat to my health issues. I have a history of gastrointestinal issues. As of yesterday, my doctor says I have irritable bowel syndrome and inflammatory disease.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Gastrointestinal
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2636086

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: CA
Alter: 60,0
Geschlecht: M
Eingang: 24.05.2023
Impfdatum: 28.09.2022
Beginn: 09.05.2023
Tage bis Beginn: 223,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Myalgia Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had congestion, slight fever, muscle aches, mild symptoms, I used a home COVID-19 test that came back positive. I called my doctor to have a telehealth visit to let her know that I had tested positive for COVID-19 and discuss my symptoms. She did prescribe the antiviral Paxlovid, that I was able to start taking that day. I started feeling better in two days and tested negative, six days later I tested positive again on Sunday, I am currently waiting my time in quarantine for five days to see if I do have two negative tests in a row.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: 12MAY2023 Home COVID-19 test - positive; 14MAY2023 Home COVID-19 test - negative; 21MAY2023 Home COVID-19 test - positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Omeprasole
Allergien: No
Vorherige Impfungen: -

VAERS 2635409

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: SC
Alter: 68,0
Geschlecht: F
Eingang: 23.05.2023
Impfdatum: 18.11.2022
Beginn: 18.04.2023
Tage bis Beginn: 151,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Feeling cold Headache Influenza B virus test positive Malaise Pain Respiratory tract congestion SARS-CoV-2 test negative Sneezing

Symptomtext

I went outside 18APR2023 and felt the effects of pollen immediately in my throat. That day and the days that followed I had congestion, headache, sneezing, I never had fever but chills and body aches so I stayed in the house due to not feeling well, I took my temperature but no fever. My symptoms began to worsen then and they lasted about three weeks, I took three COVID-19 tests all negative. 25APR2023 I thought I had a sinus infection and so I saw my doctor and was administered a tripple test which resulted in a positive Flu B. I was freezing with a chills after that and was prescribed TAMIFLU by my doctor, a seven day course. I was feeling better in a few days and back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 25APR2023 Influenza B test, positive.
Aktuelle Erkrankungen: None
Vorgeschichte: RA; Hypoglycemia; Hypothyroidism; Osteoporosis
Andere Medikamente: Levothyroxine; methylprednisolone; methotrexate; ORENCIA; FOSAMAX; oxybutynin ER
Allergien: None
Vorherige Impfungen: -

VAERS 2634620

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: KS
Alter: 62,0
Geschlecht: F
Eingang: 21.05.2023
Impfdatum: 19.05.2023
Beginn: 19.05.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Pain in extremity Peripheral swelling Skin discolouration Skin warm

Symptomtext

All 3 vaccines were give less than 1 inch apart per patient and were all able to be covered by 1 band aid. Patient's arm was hot to touch, painful, red/purple, and swollen to the size of a baseball. Patient was advised to apply ice, take Tylenol, and wait a couple of days to allow initial symptoms to resolve on their own. If it gets worse see PCP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Hyderlipidemia, Hydertension, Hypokalemia, migraine, muscle spasm, nervous system disease, pain or migraine, vaginitis
Andere Medikamente: Acetazolamide 250mg tab, Losartan/HCTZ 50/12.5mg tab, Metformin 500mg tab, and Simvastatin 40mg tab
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 2628425

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IL
Alter: 70,0
Geschlecht: M
Eingang: 08.05.2023
Impfdatum: 29.09.2022
Beginn: 27.02.2023
Tage bis Beginn: 151,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Exposure to SARS-CoV-2 Fatigue Malaise Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I was congested, had a cough, achy, very tired, I took a home COVID-19 test, that came back positive. My wife and I both were positive, so we called and had a telehealth visit with our Physician Assistant to let her know about our positive test and symptoms. She prescribed Paxlovid that I was able to start that evening. In forty-eight hours, I started feeling better, it did take a couple of weeks before I was really feeling like myself.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 28FEB2023 Home COVID-19 test - positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Lovastatin; Lotemax Eye Drop
Allergien: No
Vorherige Impfungen: -

VAERS 2627031

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge as7164b

mild

Staat: CA
Alter: 66,0
Geschlecht: M
Eingang: 05.05.2023
Impfdatum: 27.04.2023
Beginn: 27.04.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Infection Pain in extremity Skin warm Swelling

Symptomtext

Patient called on 5/4/23 to let us know he had experienced an adverse reaction to the prevnar vaccine. He states he went home after he was vaccinated and felt soreness and saw redness on his arm. He was not too worried about it. Second day he still had soreness, swelling, and red and warm, continued to third day. After third day he went to doctor who told him it was an infection and prescribed him an antibiotic (amoxicillin). It has been 8 days patient is still experiencing symptoms although he states it has lessened today (8th day).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: no per vaccine administration record
Vorherige Impfungen: -

VAERS 2627009

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IL
Alter: 59,0
Geschlecht: F
Eingang: 04.05.2023
Impfdatum: 01.05.2023
Beginn: 03.05.2023
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site erythema Injection site infection Injection site pain Injection site warmth Pain in extremity

Symptomtext

Patient experienced arm pain the day after her vaccination. Two days later she had redness on her arm around the injection site. She said it was warm to the touch and hurt. Patient said the next day the redness got bigger and was still warm to the touch. It was around 5 inches in length. Patient went to doctor and they stated it was an infection and patient was prescribed antibiotics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2624964

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 02.05.2023
Impfdatum: 23.09.2022
Beginn: 28.02.2023
Tage bis Beginn: 158,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chills Fatigue Lethargy Paranasal sinus hypersecretion SARS-CoV-2 test positive

Symptomtext

I felt very tired, I had chills, sinus drainage, I knew I had something I just wasn't sure what it was, I took a home COVID-19 test that came back positive. I called my doctor to discuss my positive test and symptoms, we decided I would take the antiviral Paxlovid. I was able to start the medication the next day. It took me took weeks to completely get over being lethargic. Even after having finished the five-day regimen, I felt tired, I did not want to do anything.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 01MAR2023 Home COVID-19 test - positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Flomax; Finasteride; Cetirizine; Multivitamin; Vitamin B Complex; Glucosamine
Allergien: No
Vorherige Impfungen: In 1972 I had a very strong reaction to a smallpox vaccine.

VAERS 2622477

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: TX
Alter: 49,0
Geschlecht: F
Eingang: 27.04.2023
Impfdatum: 22.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Arthritis Bursitis Joint range of motion decreased Ligament rupture Magnetic resonance imaging abnormal X-ray abnormal

Symptomtext

I got my fourth dose of Moderna COVID-19 vaccine in October 2022. Sometime in November 2022, I started having pain and reduced range of motion in the left shoulder. I saw my PCP in January 2023, and he referred me to a physical therapist. On about 1/24/2023, I began seeing a physical therapist. At the time of this writing, I still see the physical therapist usually twice weekly. Since I have been seeing the physical therapist, I now have less pain and slightly more range of motion. At this point, there is no set time limit for me to receive the therapy, so the length of time is at my discretion. I have taken Tylenol from time to time to treat the pain when it's bad enough, but I usually don't find it necessary. I also saw an orthopedist on 3/30/2023. He took X-rays, and I was diagnosed with arthritis. He gave me a steroid shot. After the steroid shot, I had slightly more range of motion, but it didn't last long. On 3/17/2023, I underwent an MRI of the left shoulder. Bursitis and a partial tear of a ligament were detected. No recommendations have been made with regard to the treatment of those conditions, though I have called them and am awaiting a reply.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 30MAR2023 - X-Rays - Arthritis Diagnosed; 17MAR2023 - MRI - Bursitis and Ligament Tear in Left Shoulder Detected
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Atomoxetine; Fluoxetine; Levothyroxine; Biotin; Calcium
Allergien: Sulfa Drugs; Seafood
Vorherige Impfungen: -

VAERS 2619973

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IN
Alter: 62,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 27.09.2022
Beginn: 24.03.2023
Tage bis Beginn: 178,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain upper COVID-19 Constipation Diarrhoea Headache Lethargy Nasopharyngitis Oropharyngeal pain Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 twice just eight weeks apart. The first time I contracted it in January, I had cold-like symptoms including head congestions, aches, chest congestion, sore throat, and general lethargy. However, this second time around in March, I had all of the same symptoms including headache, diarrhea and stomach pain/constipation. I took an at-home COVID-19 test on 01/28/2023 which came back positive; in March, I started having symptoms on 03/23/2023 and took a test on 03/26/2023. In January, I let it run its own course for self-recovery. In March, I contacted my doctor because the diarrhea wasn't stopping. He prescribed Imodium even though I didn't take since it ended on its own the next day. I started feeling better days following with no treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: 28JAN2023, 26MAR2023 -- COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Omeprazole; Meloxicam; Levothyroxine; Centrum Multivitamin; Melatonin; Iron; Magnesium; Aspirin
Allergien: Penicillin; Sulfa Drugs
Vorherige Impfungen: -

VAERS 2619860

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

mild

Staat: NY
Alter: 66,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 06.10.2022
Beginn: 01.12.2022
Tage bis Beginn: 56,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Dizziness Tinnitus

Symptomtext

Tinnitus. I'm not sure if the tinnitus began after COVID vaccine # 4 or beforehand. The Tinnitus worsened after dose # 4 causing me to seek follow-up medial care, which is still in progress.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: ER visit for ringing in the ear and dizziness.
Aktuelle Erkrankungen: diabetes hypertension GERDS
Vorgeschichte: Diabetes. Atypical chest pains, GERDS
Andere Medikamente: Imdur atorvastatin Meformin Renexa Metoprolol Dexilant NTG - PRN Vitamins - Magnesium, Vitamin B Complex, Probiotic, Calcium, Biotin, CoQ10, Krill Oil
Allergien: NKA
Vorherige Impfungen: -

VAERS 2618431

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MD
Alter: 81,0
Geschlecht: F
Eingang: 20.04.2023
Impfdatum: 17.10.2022
Beginn: 13.04.2023
Tage bis Beginn: 178,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Malaise Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

For three days I had mild symptoms, that I thought was just a cold or allergies. I then developed a bad cough, high fever, I used a home COVID-19 test that came back positive. I called my doctor; we discussed my symptoms. He prescribed the Lagevrio that I will be taking the last pills today. I only have a runny nose now but I feel fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 16APR2023 Home COVID-19 - positive
Aktuelle Erkrankungen: No
Vorgeschichte: Half a lung removed from cancer
Andere Medikamente: Vitamin D; Vitamin B; High Blood Pressure medication; High Cholesterol medication
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2616161

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IL
Alter: 74,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 10.10.2022
Beginn: 15.01.2023
Tage bis Beginn: 97,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Malaise SARS-CoV-2 test positive

Symptomtext

1/15/2023 I had a cough and it persisted for three days. I tested positive for COVID with an at home COVID test on 1/15/23. On 1/16/23 I called my primary care physician who prescribed Paxlovid. I took the Paxlovid for the five days. The symptoms disappeared and I felt better, and all is well. I continued to test positive for COVID for two or three weeks. I never tested negative for COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 15JAN2023-At Home COVID Test- Positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine, Simvastatin, Lalanoerost, Timodol, Multi Vitamin, Fish Oil
Allergien: None
Vorherige Impfungen: -

VAERS 2615388

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

mild

Staat: NM
Alter: 70,0
Geschlecht: F
Eingang: 14.04.2023
Impfdatum: 12.10.2022
Beginn: 13.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Feeling hot Muscular weakness

Symptomtext

I had very mild fever 100.0 and I had chills. I have muscle weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes type 2
Andere Medikamente: Metformin; Estrogen; Testosterone; Polyethylene; Aspirin; Vitamin D3; magnesium; calcium
Allergien: None
Vorherige Impfungen: -

VAERS 2615365

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 14.04.2023
Impfdatum: 17.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Blood pressure increased

Symptomtext

I went in to see my doctor for my knee, she noticed that my blood pressure was elevated. We thought this may be due to the pain of my hurting my knee, so we decided to watch my blood pressure, this was on October 20, 2022. On October 27 I went to my local fire department asked if they could check my blood pressure. My left arm was 215/100, my right was 185/85, they instructed me to contact my doctor immediately, which I did. I had a telehealth appointment on November 4, 2022, we discussed the blood pressure that the fire department had taken. She prescribed lisinopril for the blood pressure, currently it has been helping to keep my blood pressure normal, 101/60.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Levothyroxine; ZOLOFT; ibuprofen
Allergien: No
Vorherige Impfungen: -

VAERS 2614764

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 13.04.2023
Impfdatum: 12.10.2022
Beginn: 20.02.2023
Tage bis Beginn: 131,0
Dosis: 5
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Amnesia Brain fog COVID-19 Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had my vaccination on 10/12/2022. I started to have a sore throat on 02/20/2023. I tested COVID-19 negative from 02/20/2023 to 02/23/2023. The morning of 02/24/2023 I tested COVID-19 negative. I started to run a fever and have a very runny nose on that same day. I tested COVID-19 positive on the evening of 02/24/2023. I contacted my physician on 02/24/2023 and I requested PAXLOVID. I presently feel ok but I do still feel like I have brain fog and memory loss.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 02/20/2023 02/24/2023 test COVID-19 negative. 02/24/2023 test COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Situational Asthma
Andere Medikamente: Anastrozole; calcium; vitamin D; flax oil
Allergien: Codeine; penicillin; onions; bananas; nuts
Vorherige Impfungen: 1979 Tetanus shot; arm red and hot to touch

VAERS 2613990

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NM
Alter: 82,0
Geschlecht: M
Eingang: 12.04.2023
Impfdatum: 09.10.2022
Beginn: 06.04.2023
Tage bis Beginn: 179,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Cough Electrocardiogram abnormal Fatigue Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I noticed that I felt tired one day. I have the ability to take an EKG on my phone, so I did, and it was abnormal. this went on for several hours and then normalized. I went out in the yard to do some yard work and it happened again and then it normalized again. I went to the doctor, and they did an EKG there and it showed up again there. Then, on 4/8/23, I tested positive for COVID-19. I had a cough, congestion, and chills. I contacted my doctor and was prescribed Paxlovid. I am still dealing with these symptoms at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 01APR2023 EKG - Abnormal; 08APR2023 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Zyrtec; Vitamin B12; Vitamin D
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2613214

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: OH
Alter: 66,0
Geschlecht: F
Eingang: 11.04.2023
Impfdatum: 06.09.2022
Beginn: 28.03.2023
Tage bis Beginn: 203,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Dysgeusia Fatigue Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

3/28/2023 03:00 fatigue, chest congestion, runny nose. Tested with at home COVID-19 test, positive. Televisit with doctor who prescribed PAXLOVID and to treat symptomatically. That afternoon the PAXLOVID caused blood pressure to drop, and there was a very bitter taste in the mouth. After the 5-day course of PAXLOVID, I felt much better. There is a little chest congestion lingering at time of reporting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 28Mar2023 at home COVID-19 test, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 2 Diabetes
Andere Medikamente: Verapamil; RABELAIS; metformin; SYNTHROID; VESICARE; lisinopril; liothyronine; atorvastatin; low dose aspirin; probiotic; cranberry pill; iron supplement; multivitamin
Allergien: Mineral oil; BACTRIM; NEOSPORIN; ZOSTAVAX (shingles vaccine); TRULICITY
Vorherige Impfungen: Shingles vaccine, ZOSTAVAX. Injection site reaction, a large and red reaction at the site. 55 2012; All 5 COVID-19 vaccines left

VAERS 2613177

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IN
Alter: 68,0
Geschlecht: F
Eingang: 11.04.2023
Impfdatum: 07.10.2022
Beginn: 13.02.2023
Tage bis Beginn: 129,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal discomfort Ageusia Asthenia COVID-19 Fatigue Feeding disorder Feeling abnormal Hypersomnia Nausea Pyrexia SARS-CoV-2 test positive

Symptomtext

I was extremely tired, I had a low-grade fever, felt nauseous. I took a home COVID-19 test, it came back negative. I woke up feeling horrible, I called my doctor and explained to him that my stomach wasn't feeling good, I felt like something was brewing. He sent me to the lab to get test, my doctor wrote me a prescription for the Paxlovid. When I got home the dam burst wide open. I slept on and off twenty-four hours straight, only waking up to go to the bathroom or get something to drink. I did lose my sense of taste, I had nausea, it took four days before I could eat anything. My strength still has not returned to me one hundred percent, my energy is not back either.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 13FEB2023 Home COVID-19 test - negative; 14FEB2023 PCR COVID-19 test - positive
Aktuelle Erkrankungen: No
Vorgeschichte: Fibromyalgia; Hypertension; Hyperlipidemia
Andere Medikamente: Ambien; Lipitor; Vitamin C; Vitamin D; Olive Leaf Extract; Mullein Leaf Extract: Estrace Cream
Allergien: No
Vorherige Impfungen: -

VAERS 2613100

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IL
Alter: 65,0
Geschlecht: F
Eingang: 11.04.2023
Impfdatum: 06.10.2022
Beginn: 05.04.2023
Tage bis Beginn: 181,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cough Nasal congestion Oropharyngeal pain Pyrexia

Symptomtext

I had a fever for about 3-4 days, coughing, and nasal congestion. I also had a really sore throat which is how it started out and it lasted for about 3-4 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: PROLIA shot; calcium supplement; vitamin B; vitamin D; ALLEGRA; allergy shot
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2611401

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: PA
Alter: 69,0
Geschlecht: M
Eingang: 07.04.2023
Impfdatum: 06.10.2022
Beginn: 15.03.2023
Tage bis Beginn: 160,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Congestion, runny nose, body aches Started Tuesday evening late, tested positive Wednesday. Symptoms very mild- gone by Friday

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: At home testing- positive Wednesday at home test Tuesday- Negative
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure
Andere Medikamente: solifenacin 5 mg mirabegron 50 mg tamsulosin .4 mg multivitamin aspirin 81mg
Allergien: none
Vorherige Impfungen: -

VAERS 2610861

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MD
Alter: 79,0
Geschlecht: F
Eingang: 06.04.2023
Impfdatum: 05.10.2022
Beginn: 31.01.2023
Tage bis Beginn: 118,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Headache

Symptomtext

1/31/2023 I woke up and I had a headache in the back of my head, it felt like a sharp pain. I took Tylenol and it went away. It came back for a few days. I called my doctor, and he prescribed Neurontin. My headaches went away after a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: COPD
Andere Medikamente: Rosuvastatin, Trelegy Ellipta Inhaler, Albuterol , Protonics, Lisinopril, Vitamin D, Multi Vitamin, Zyrtec
Allergien: Prolia
Vorherige Impfungen: -

VAERS 2610340

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 27.09.2022
Beginn: 14.11.2022
Tage bis Beginn: 48,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Brain fog COVID-19 Chest X-ray normal Cough Fatigue Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

COVID-19 positive 11/15/2022.I had a sore throat, drippy nose, fatigue, coughing and brain fog. I reached out to my PCP and was prescribed a course of Paxlovid. After completing Paxlovid I had a rebound of all my COVID-19 symptoms. I reached out again to my PCP to get medication but he did not prescribe another dose of the medication. Om 12/07 I had a follow up with my Pulmonologist she ordered an Xray to rule out Pneumonia and it was clear. I was prescribed a 3?4-day supply of prednisone to take as needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 15Nov2022 COVID-19 test - positive 07Dec2022 Chest Xray - clear
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Albuterol inhaler; Baby aspirin; Brio Ellipta Inhaler; Zyrtec; Clonazepam; Flonase; Losartan; Singular; Nifedipine; pantoprazole; potassium; Rosuvastatin; Terbinafine; Triamterene
Allergien: Latex; Codeine
Vorherige Impfungen: -

VAERS 2610021

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 26.09.2022
Beginn: 23.03.2023
Tage bis Beginn: 178,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Ear pain Oropharyngeal pain SARS-CoV-2 test negative Streptococcus test negative

Symptomtext

I had a sore throat and pain in my ear. I was tested for COVID-19 and Strep and tested negative for both. I contacted my doctor and was prescribed Amoxicillin. I am feeling much better now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: 30MAR2023 COVID-19 Test - Negative; 30MAR2023 Strep Test - Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; High Blood Pressure; High Cholesterol; Hypothyroidism
Andere Medikamente: Synthroid; Hydrochlorothiazide; Atorvastatin; Zafirlukast; Xolair; Calcium; Vitamin D3; Probiotic; Multivitamin; Diclofenac Sodium
Allergien: Naproxen; Singulair; Bactrim
Vorherige Impfungen: -

VAERS 2609953

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

mild

Staat: OH
Alter: 67,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 03.10.2022
Beginn: 15.02.2023
Tage bis Beginn: 135,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anosmia COVID-19 Decreased appetite Diarrhoea Fatigue Musculoskeletal discomfort Ocular discomfort Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I tested positive n Feb 15 but on the 12 I started having a sore throat and having discomfort in my neck area. On the 14th I was hit with extreme exhaustion, and I had to cut my day short and go rest. I had a doctors appoint on the 15, I took a test before my appoint and was positive. I had a fever and some discomfort in my eye area. Then on Thursday I had decreased apatite and loss of most of the sense of smell. On Feb 17 and 20th, I had some diarrhea. Between these dates I stopped taking medication and I drank a large amount of water. I started taking the Paxlovid on the 17. I was sleeping for about 12 hours throughout the night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetic High Cholesterol; High Bood Pressure; Depression; Sleep Apnea
Andere Medikamente: Metformin; Atorvastatin; Fluoxetine; Amlodipine; Vitamin B12; Vitamin C; Vitamin D; Fish Oil; Multivitamin Hair skin and nails; Magnesium Oxid; Zinc
Allergien: Lisinopril; Clindamycin; Sulfa
Vorherige Impfungen: -

VAERS 2609905

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: DE
Alter: 71,0
Geschlecht: M
Eingang: 05.04.2023
Impfdatum: 03.10.2022
Beginn: 30.03.2023
Tage bis Beginn: 178,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Ageusia Anosmia Arthralgia COVID-19 Feeling abnormal Malaise Nasal congestion Pain Respiratory tract congestion SARS-CoV-2 test positive Sinus congestion

Symptomtext

Thursday afternoon started to feel a little off and through the evening. Friday 31MAR2023 when woke I felt ill and every joint hurt aches and and pains I never had a fever this prompted me to do a COVID-19 Test-Positive and it continued throughout the day. I called my Doctor and the nurse called me back .It was recommended to take Advil and Tylenol. I started to develop sinus and chest congestion. I took cough medicine Delsym 32MAR2023 Saturday I continued the regiment every twelve hours on Saturday I just felt horrible no fever but literally did nothing on Sunday started to fell a little better and never developed heavy chest congestion a lessening of the symptom but lost taste and smell and this now has continue to improve as of Tuesday the lasting symptoms are nasal congestion and aching in my hip joints but Advil takes care of that and today I feel pretty damn good. I felt well enough yesterday and today but still lack of smell and taste but was able to cut the lawn.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 31MAR2023 COVID-19 Test-Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; High Cholesterol
Andere Medikamente: Metformin; Multivitamin; Turmeric; Sau Palmetto; Red yeast rice; Vitamin K; Vitamin D; Areds; Glucosamine
Allergien: Chlorine
Vorherige Impfungen: -

VAERS 2609892

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: DE
Alter: 65,0
Geschlecht: U
Eingang: 05.04.2023
Impfdatum: 14.10.2022
Beginn: 26.12.2022
Tage bis Beginn: 73,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia COVID-19 Cough Diarrhoea Gastric disorder Malaise Nasopharyngitis Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I had some stomach issues and head cold like symptoms. I had diarrhea and the next day I began to have a sore throat and was feeling unwell. I started having a fever of around 101 on that Wednesday. After about 3 days it started coming down. I also had started coughing. The doctor did not prescribe any medications, just over the counter TYLENOL was taken. I started to feel better around January 2nd, 2023. Most of my symptoms were gone by the 3rd or 4th of January. I took about a month to feel my energy was back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 test positive December 29, 2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Seasonal Allergies; Osteoporosis; Osteopenia
Andere Medikamente: Baby aspirin; vitamin E; calcium with vitamin D; glucosamine; collagen; vitamin C; alendronate sodium tablets
Allergien: Sulfa
Vorherige Impfungen: Moderna dose 2 April 24, 2021 I developed Moderna arm after this vaccine. It was itchy red and hot for a day or so. I was 64 yea

VAERS 2609336

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NJ
Alter: 77,0
Geschlecht: F
Eingang: 04.04.2023
Impfdatum: 28.09.2022
Beginn: 02.12.2022
Tage bis Beginn: 65,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Brain fog COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

I tested positive for Covid-19 on December 2, 2022 I experienced fatigue; brain fog; I was also prescribed Paxlovid for my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes; Hypertension; High Cholesterol
Andere Medikamente: Amlodipine; Metformin; Lipitor; Tricor
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2609182

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IL
Alter: 68,0
Geschlecht: F
Eingang: 04.04.2023
Impfdatum: 30.09.2022
Beginn: 23.03.2023
Tage bis Beginn: 174,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Headache Oropharyngeal pain Pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had a runny nose, coughing, sore throat, headache, body aches very tires. I had been out of the country, so I used a home COVID-19 test that did come back positive. I called and had a telehealth visit with my doctor. I was prescribed the PAXLOVID on March 25, 2023, the headaches and body aches went away, the fatigue took another week. I have tested negative but I am still suffering from a cough and runny.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 24MAR2023 home COVID-19 test, positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Lisinopril; atorvastatin; latanoprost; glucosamine/chondroitin; CITRACAL
Allergien: Ampicillin
Vorherige Impfungen: -

VAERS 2607378

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: OH
Alter: 75,0
Geschlecht: F
Eingang: 31.03.2023
Impfdatum: 22.09.2022
Beginn: 15.03.2023
Tage bis Beginn: 174,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Blood test Computerised tomogram abnormal Dizziness Electrocardiogram abnormal Muscular weakness Vertigo positional

Symptomtext

I became dizzy, my legs were weak I called the ambulance, they checked vital signs and felt that I needed to the emergency room for further testing. Upon arriving at the emergency room, they EKG, CAT, scan, bloodwork, they felt I needed to stay overnight, for observation. It was determined I have benign paroxysmal positional vertigo; I was prescribed ANTIVERT to held with being dizzy that I took for ten days. I now have it to take as needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: 1,0
Labordaten: 15MAR2023 CAT scan positive for benign paroxysmal positional vertigo; 15MAR2023 EKG positive for benign paroxysmal positional vertigo; 15MAR2023 EKG positive for benign paroxysmal positional vertigo
Aktuelle Erkrankungen: No
Vorgeschichte: Rheumatoid Arthritis; High Blood Pressure; Atrial Fibrillation; Diabetes
Andere Medikamente: CULTURELLE; iron supplement; magnesium; lisinopril; metoprolol; omeprazole; ORENCIA infusion; XARELTO; spironolactone; levothyroxine: potassium: gabapentin
Allergien: SUDAFED; AUGMENTIN; glyburide; metformin; nickel; latex
Vorherige Impfungen: -

VAERS 2606628

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 30.03.2023
Impfdatum: 28.09.2022
Beginn: 01.03.2023
Tage bis Beginn: 154,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Clostridium test positive Diarrhoea Flatulence Norovirus test positive Stool analysis abnormal

Symptomtext

I was having eight to ten loose stools a day accompanied with a lot of gas pain. I called the doctor who prescribed some medication and asked for a stool sample. Once the results of the sample came back it showed positive for C-diff and Norovirus. I was given a prescription of vancomycin for 10 days. I will be giving another stool sample on April 5, 2023, to ensure that the medication has cleared up the C-diff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 13MAR2023 Stool sample, positive for C-diff and Norovirus
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension
Andere Medikamente: Spironolactone; lovastatin; amlodipine; vitamin D
Allergien: No
Vorherige Impfungen: 1950's Influenza vaccine, I was hospitalized.

VAERS 2606027

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MD
Alter: 68,0
Geschlecht: M
Eingang: 29.03.2023
Impfdatum: 27.09.2022
Beginn: 11.02.2023
Tage bis Beginn: 137,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

It felt more like a cold, I had a sore throat, cough, no fever. I used my home COVID-19 test, that came back positive. I called my doctor to discuss my symptoms and let him know I was positive for COVID19. I was prescribed the PAXLOVID that I started taking that evening. I started feeling better within a few days of taking the PAXLOVID antiviral. I was fatigued a few days after feeling better but it did not last long.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 11FEB2023 home COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure; High Cholesterol
Andere Medikamente: Amlodipine; metoprolol; vitamin B-12; vitamin D; potassium citrate; CRESTOR
Allergien: Lisinopril; benazepril
Vorherige Impfungen: -

VAERS 2605919

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

mild

Staat: WA
Alter: 70,0
Geschlecht: M
Eingang: 29.03.2023
Impfdatum: 27.09.2022
Beginn: 17.03.2023
Tage bis Beginn: 171,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Myalgia Respiratory tract congestion

Symptomtext

I had muscle aches and a lot of congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Omeprazole; Tamsulosin; Rosuvastatin; Amlodipine; Iron Pill
Allergien: Does not remember name of medication allergic too.
Vorherige Impfungen: -

VAERS 2605027

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: VA
Alter: 50,0
Geschlecht: F
Eingang: 28.03.2023
Impfdatum: 24.09.2022
Beginn: 01.12.2022
Tage bis Beginn: 68,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain lower Dyspepsia SARS-CoV-2 test negative

Symptomtext

My adverse event started on 12/2022. I had digestive issue along with lower abdominal pain. They referred me to a Rheumatologist which I am waiting on blood work result at the moment. I will be going for the results on 04/12/2023. They also referred me to a Gastroenterologist which I will be going to on 04/25/2023. As of now the doctors are trying to rule out the cause of the pain I am having which is why they haven't prescribed me any medication yet. It is an ongoing issue I am having.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain lower
Hospital-Tage: -
Labordaten: 28MAR2023 COVID-19 test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Undifferentiated Connective Tissue Disease
Andere Medikamente: PLAQUENIL; aspirin; multivitamin; ZYRTEC
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 2604831

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MD
Alter: 50,0
Geschlecht: F
Eingang: 28.03.2023
Impfdatum: 23.09.2022
Beginn: 04.02.2023
Tage bis Beginn: 134,0
Dosis: 5
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chills Cough Fatigue Impaired work ability Malaise Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

On February 4th I had the worst sore throat I could ever recall and started to develop fatigue. The day before my entire household had taken COVID19 tests at home and they were negative. On the 5th we were still sick and took another test and we were all glaringly positive. The next day I contacted my doctor because I was having chills, cough, still sore throat and tired. They prescribed Paxlovid. The cough started to clear pretty quickly but the fatigue lasted through the end of the week. The sore throat started getting better the day after Paxlovid. I contacted my employment and was told I could probably go back on February 15th but I worked telehealth because I was still fatigued and dragging. I went back to campus on February 22nd and was completely symptom free at that point.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 2022Feb3- COVID19 at home rapid test- (Negative); 2022Feb5th- COVID19 at home test- (posititve)
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypercholesterolemia
Andere Medikamente: Rosuvastatin; Multivitamin
Allergien: Pollen; Cats
Vorherige Impfungen: -

VAERS 2604792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge AS7164B

mild

Staat: MA
Alter: 41,0
Geschlecht: F
Eingang: 28.03.2023
Impfdatum: 23.09.2022
Beginn: 26.12.2022
Tage bis Beginn: 94,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Eye swelling Fatigue Hypersomnia Hypomenorrhoea Malaise Menstrual disorder Nasopharyngitis SARS-CoV-2 test positive

Symptomtext

I was at the onset of symptoms I had a general feeling of being tired or having a cold tired unwell I took a quick view tests and had a faint line followed up with a Flowflex test and had an immediate bright red result, I called my Doctors office and they gave a ne the Covid line I called the number that day or the next and was prescribed Paxlovid and I had a temperature of one hundred and two point five. I masked after my positive test and stayed masked including my family staying out of the house, I slept for days. On day nine I got COVID-19 rebound. I called the Doctors office and they said the rebound rate was five percent my Doctor said fifteen to twenty percent. I asked for information n the virus as to impact on the mensuration cycle none was available but my period is off cycle and has not returned frequency is the same the volume is low. I was really fatigued for a month afterwards including my eyes feeling like they were swollen as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 27DECCOVID-19 Test-Positive 04JAN2023 COVID-19 Test-Positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2604156

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NJ
Alter: 70,0
Geschlecht: F
Eingang: 27.03.2023
Impfdatum: 23.09.2022
Beginn: 03.02.2023
Tage bis Beginn: 133,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Headache Respiratory tract congestion SARS-CoV-2 test positive Upper-airway cough syndrome

Symptomtext

I had very mild symptoms except for fatigue. I did not have any fever. The first night I had a mild headache then congestion and postnasal drip. I tested positive on February 05, 2023, and was prescribed PAXLOVID on February 06, 2023. She said it was up to me to take the medication. I started to take the PAXLOVID, and it did not help. I gave me a horrible metallic taste in my mouth, but I had less fatigue. I tested positive for quite some time. I was down for the count for a month as I continued to test positive for a month. I was very isolated as people that knew me did not want to be around. At this time, I have completely recovered. The fatigue was a long-lasting symptom. It varies the way the doctors treat symptoms. I did not like that my doctor left it up to me to take the medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 home test February 03, 2023 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Simvastatin; vitamin D; calcium
Allergien: Ampicillin; amoxicillin; penicillin
Vorherige Impfungen: -

VAERS 2603348

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MD
Alter: 60,0
Geschlecht: M
Eingang: 24.03.2023
Impfdatum: 22.09.2022
Beginn: 03.01.2023
Tage bis Beginn: 103,0
Dosis: 5
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Headache Nasopharyngitis Pyrexia SARS-CoV-2 test positive

Symptomtext

On 01/03/203 I started to get a fever, cold like symptoms and headache. I tested Positive for Covid and contacted my doctor. I was prescribed Paxlovid for days and started to feel better. After testing negative for a few days I retested Positive for Covid-19 and symptoms returned.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Covid-19 test- positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multi vitamin
Allergien: Augmentin; Ceftin
Vorherige Impfungen: -

VAERS 2597113

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IN
Alter: 79,0
Geschlecht: M
Eingang: 15.03.2023
Impfdatum: 23.09.2022
Beginn: 19.02.2023
Tage bis Beginn: 149,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Feeling hot Nasopharyngitis Rhinorrhoea SARS-CoV-2 test positive Sneezing Throat irritation

Symptomtext

02/19/2023 I had a ticklish throat and no other symptoms. 02/20/2023 I had the symptoms of a heavy cold, extreme fatigue, coughing,sneezing, heavy nasal output I also felt feverish but my temp was normal. I took a home COVID-19 and tested positive. I had fatigue for about 2-3 weeks after onset.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 02/20/2023 - COVID-19 positive
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Xarelto; Furosemide; Metoprolol Tartrate; Atorvastatin; Colchicine; Amlodipine Besylate; Lisinopril HCTZ; Vitamin D; Fish Oil
Allergien: Allopurinol
Vorherige Impfungen: -

VAERS 2592372

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IL
Alter: 70,0
Geschlecht: F
Eingang: 07.03.2023
Impfdatum: 04.09.2022
Beginn: 29.12.2022
Tage bis Beginn: 116,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Bronchitis COVID-19 Cough Oropharyngeal pain SARS-CoV-2 test positive Wheezing

Symptomtext

I started have a sore throat and developed crazy coughing. I made an appointment with my doctor and had a telehealth appointment we discussed my symptoms by then I was wheezing. I was given a prescription for antibiotics. It took me about 8 to 10 days to get over the bronchitis. Once I got COVID-19 in February, I emailed the doctor and was prescribed, molnupiravir. I started taking it immediately I was still coughing five days later so I had a telehealth appointment and the doctor called in antibiotics to help me to finish get rid of the cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Home COVID-19 test positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Vitamins; AMITIZA; simvastatin; ZETIA; duloxetine; meloxicam; FLONASE spray; fish oil; vitamin C
Allergien: Latex
Vorherige Impfungen: -

VAERS 2575876

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 04.02.2023
Impfdatum: 26.09.2022
Beginn: 30.09.2022
Tage bis Beginn: 4,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Laboratory test normal Myalgia X-ray normal

Symptomtext

Developed significant widespread myalgias within several days of vaccine - and ongoing myalgias in both hips and right thigh

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: Labs and xrays normal
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism,osteopenia,past breast cancer (in remission), neuropathy from past chemotherapy
Andere Medikamente: Synthroid,Gabapentin,Turmeric, Vitamin D, Vitamin B12, Calcium
Allergien: Penicillin, sulfa
Vorherige Impfungen: -

VAERS 2575136

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

mild

Staat: MA
Alter: 58,0
Geschlecht: M
Eingang: 03.02.2023
Impfdatum: 22.09.2022
Beginn: 01.02.2023
Tage bis Beginn: 132,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain in extremity

Symptomtext

patient got the moderna covid bivalent booster dose on 9/22/22, he came to the pharmacy on 2/1/23 and said his left arm is still sore. Pharmacy contacts the office of PRIVATE to inform doctor regading this issue on 2/2/23.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2572116

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: WA
Alter: 71,0
Geschlecht: F
Eingang: 31.01.2023
Impfdatum: 31.10.2022
Beginn: 25.12.2022
Tage bis Beginn: 55,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Arthralgia Axillary mass Blood potassium decreased Limb discomfort Mammogram normal Mean platelet volume increased Ultrasound breast normal

Symptomtext

I noticed I had a lump in opposite armpit than injection site. I went to urgent care and received a mammogram and ultrasound. No explanation of lump. Doctor visit scheduled for next month. Mild discomfort in under arm. Severe pain in left shoulder after vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Mammogram 01/13/2023, Ultrasound 01/13/2023, Blood test, potassium low; MVP-elevated (01/03/2023)
Aktuelle Erkrankungen: No
Vorgeschichte: High Cholesterol; high blood pressure; Glaucoma; arthritis; asthma as a child
Andere Medikamente: Atorvastatin; AVOVIDA; bupropion; buspirone; estradiol; hydrochlorothiazide; latanoprost; levothyroxine; liothyronine; low dose aspirin; multivitamin; olmesartan; PROMETRIUM; rabeprazole; vitamin D3; B12; magnesium; PYCNOGENOL.
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2570040

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: CT
Alter: 66,0
Geschlecht: M
Eingang: 29.01.2023
Impfdatum: 05.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Loss of personal independence in daily activities Neuropathy peripheral Pain

Symptomtext

2 Weeks after the injection the patient began have extreme sensitivity to cold in fingers and feet. Such that he uses cotton gloves to fetch items from the refrigerator. Once he gets a chill in either extremity a chill runs through his body and the pain and discomfort is 10/10. It has limited his activity and exercise regime and impacts his life on daily basis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Trazadone 2 - 50mg at night (sleep) approx 1/6 of 1.25 meg Ambien tablet at night Tamsulosin - .4 mg at bedtime to improve emptying bladder and improve urine flow Venlafaxine - 50 mg with breakfast for depression.
Allergien: -
Vorherige Impfungen: -

VAERS 2563344

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: TX
Alter: 72,0
Geschlecht: F
Eingang: 19.01.2023
Impfdatum: 17.10.2022
Beginn: 10.01.2023
Tage bis Beginn: 85,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal distension Flatulence Oropharyngeal pain Rhinorrhoea

Symptomtext

Sore throat, runny nose, gas and bloating

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: hypo thyroid Sjogren.s syndrome Psoriatic Arthritis Osteoarthritis Depression
Andere Medikamente: Synthroid, Lumigan, Nexium, Hydroxychloroquine, Zoloft, Crestor, Buspirone, vitamin D, turmeric, COQ, Hydro Eye
Allergien: Tetracycline, NSAIDs, Percocet, zithromycin,Cipro, Vicodin
Vorherige Impfungen: -

VAERS 2561690

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: WA
Alter: 67,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 09.10.2022
Beginn: 10.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Decreased appetite Fatigue Pyrexia Throat irritation

Symptomtext

Started with scratchy throat; excessive coughing; low grade fever and fatigue with no appetite. Saw doctor 10/23/2022 prescribed doxycycline.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: Bronchiectasis
Vorgeschichte: Diabetes
Andere Medikamente: TYLENOL GR
Allergien: Grass
Vorherige Impfungen: -

VAERS 2560751

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MN
Alter: 67,0
Geschlecht: M
Eingang: 16.01.2023
Impfdatum: 14.10.2022
Beginn: 27.12.2022
Tage bis Beginn: 74,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood test abnormal COVID-19 Chills Cough Infection Nasopharyngitis Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

12/27 I had a very bad sore throat. By 12/30 I had chills and a slight fever (99). Went to urgent care where I tested positive on a PCR COVID-19 test. The 7 consecutive, prior days, I was negative on an at home COVID-19 test. Symptoms felt very cold like. Doctor determined there was an infection using a blood test. Prescribed azithromycin, and a mouthwash consisting of a mix of lidocaine, MAALOX, and BENADRYL. I was able to get a prescription as well for PAXLOVID that evening when the PCR results came in. Jan 5 I felt like improving. Symptoms tapered off after that with a cough that lingers to time of reporting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Dec30,2022 COVID-19 PCR positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Penicillin; tetracycline
Vorherige Impfungen: -

VAERS 2559699

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: CA
Alter: 70,0
Geschlecht: M
Eingang: 13.01.2023
Impfdatum: 01.10.2022
Beginn: 11.11.2022
Tage bis Beginn: 41,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal discomfort Blood test abnormal Diarrhoea Dysphagia Eating disorder Gastrointestinal pain Haematocrit decreased Haemoglobin decreased International normalised ratio normal Neutrophil count decreased Platelet count decreased Prothrombin level increased Red blood cell count decreased Retching Vomiting White blood cell count decreased

Symptomtext

gastrointestinal pain, explosive diarrhea, stomach upset, stopped eating 4 days , couldn't swallow or ingest anything, I was gagging and couldn't keep anything down. low white blood cells.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 29NOV2022 - Blood Test - abnormal and inconclusive ; 21DEC2022 - Blood Test - abnormal and inconclusive ; 27DEC2022 - Blood Test - abnormal and inconclusive ; 09JAN2023 - Blood Test - abnormal and inconclusive; 13JAN2023 - Blood Test - abnormal and inconclusive; 13JAN2023 Clotting Test - Prothrombin 13.2, INR 1.0, white blood count 3.8, red blood count 3.63, hemoglobin 12.8, hematocrit 38.9, platelets 143, absolute neutrophil .30
Aktuelle Erkrankungen: N/A
Vorgeschichte: Heart Failure; Pacemaker present
Andere Medikamente: Metoprolol; Succinate; Vitamin D3; Omega 3 Acid Capsule; Vitamin B12; Centrum Multivitamin for Men; Metformin; Vitia
Allergien: Penicillin; Lipitor; Vitia; Metformin; Metoprolol; Gabapentin;
Vorherige Impfungen: Penicillin

VAERS 2559485

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: PA
Alter: 67,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 13.10.2022
Beginn: 27.12.2022
Tage bis Beginn: 75,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Headache Nasopharyngitis Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I started having fever, headache, cough, runny nose cold like symptoms. I took naproxen for the headache and that did help. After finding out my grandson was positive for COVID-19, I then tested that night and was positive as well. Everything was closed because of Christmas so I called the doctor on Tuesday and was told to treat the symptoms. Then my children kept saying get medication so on the 29 of December I called the doctor and a prescription of PAXLOVID was sent to the pharmacy. The PAXLOVID did help all cold like symptoms went away all but the cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Metoprolol succinate; risedronate sodium
Allergien: N/A
Vorherige Impfungen: -

VAERS 2558776

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: VA
Alter: 57,0
Geschlecht: M
Eingang: 12.01.2023
Impfdatum: 07.10.2022
Beginn: 13.12.2022
Tage bis Beginn: 67,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Oropharyngeal pain Pyrexia Rhinitis SARS-CoV-2 test positive

Symptomtext

I had a low-grade fever and a minor sore throat. I also had rhinitis and that was it. I completed a COVID-19 PCR Test on December 13th, 2022, and the test was positive. I was prescribed Paxlovid. I did not treat the sore throat or rhinitis. My symptoms began to re solve and by day 5 of the Paxlovid, I tested negative on December 19 and 20, 2022. I tested positive again on a home test on December 21st, 2022. I also completed another PCR test and was positive again. I received my first negative home test on December 29, 2022, by that time all of the symptoms have gone away. I have remained negative since December 29, 2022, and I have been testing negative daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID-19 PCR Test on December 13th, 2022-Positive COVID-19 Home Test-December 22th, 2022-Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: HIV; Depression; Hypertension
Andere Medikamente: Dovato; Lipitor; Ibuprofen; Wellbutrin; Losartan HCTZ; Trazadone; Omeprazole; Daily Multi-vitamin
Allergien: Sulfa; Bees
Vorherige Impfungen: -

VAERS 2558760

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 12.01.2023
Impfdatum: 12.10.2022
Beginn: 02.01.2023
Tage bis Beginn: 82,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Headache Malaise Pyrexia Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

I noticed a scratchy throat and runny nose on the 2nd. I developed a general feeling of unwell. I had a cough and a fever of 101.0 along with a headache. I completed a home COVID-19 test and it was positive. I called my doctor's office and listed all the symptoms that I had. They called in a prescription for PAXLOVID. By Thursday the fever went away and by the next day I no longer had the cough. I do feel that I have completely recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 home test January 3rd, 2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: GERD; Chronic Lower Back Issue; Cholesterol; Mitral valve and Tricuspid Valve Insufficiency
Andere Medikamente: N/A
Allergien: BACTRIM; erythromycin; penicillin; PERCOCET
Vorherige Impfungen: -

VAERS 2556158

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IL
Alter: 66,0
Geschlecht: M
Eingang: 10.01.2023
Impfdatum: 23.09.2022
Beginn: 21.11.2022
Tage bis Beginn: 59,0
Dosis: 1
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia COVID-19 Cough Fatigue Foreign travel Headache Malaise Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Starting 11/21/2022, while traveling, I started feeling kind of uncomfortable with a little bit of a cough. I felt kind of crummy. When I got home that night, I was having a fever of 101.4 and a bad headache. I was having body aches from head to toe. I tested myself with an at-home COVID-19 test which was positive. I waited to call my doctor for a few hours to see if it's okay if I took the PAXLOVID that my wife had left over from when she had COVID-19 previously (she did not take it so it was a full course of it). The on-call doctor said it was okay to take it. I started it that night. I woke up the next day and had no body aches or headache. I had a mild cough but no fever. I still tested positive but I was feeling much better symptom wise. I only had a mild side effect from PAXLOVID which was the poor taste but by that Saturday I was done with isolation and I was fine until 12/4/2022, when I got back home and I started developing a cough again. No fever, just fatigue, cough and malaise, and I tested positive again for COVID-19 (rebound infection). After 5 days, I was negative again and it took me about another week to get rid of the cough and my energy to return to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At-home COVID-19 test (11/21/2022): positive; At home COVID-19 test (12/4/2022): positive; At-home COVID-19 test (12/08/2022): negative; At-home COVID-19 test (12/10/2022): negative
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure; High Cholesterol; Lower Back Pain; Coronary Artery Disease
Andere Medikamente: Olmesartan; rosuvastatin; gabapentin; baby aspirin; vitamin C; vitamin D; melatonin; acetaminophen
Allergien: REGLAN
Vorherige Impfungen: -

VAERS 2552492

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IA
Alter: 71,0
Geschlecht: F
Eingang: 06.01.2023
Impfdatum: 05.10.2022
Beginn: 30.11.2022
Tage bis Beginn: 56,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Cough Ear discomfort Influenza like illness Middle ear effusion Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test negative Sinusitis Tinnitus Upper-airway cough syndrome

Symptomtext

I received my 5th dose of Moderna Bivalent on 10/05/2022. My flu like symptoms started on 11/30/2022 in the morning around 8:00AM. I had a postnasal drip and sore throat. My head was clogged up. On the same day I had a Diabetes check so my doctor did a COVID-19 which was negative. I went to the urgent care on 12/30/2022. The symptoms moved up in my chest. I had a severe cough. I was diagnosed with a Sinusitis. Before visiting the urgent care I took over the counter cold medications such as DAYQUIL, NYQUIL, and albuterol inhaler. In the urgent care they prescribe me with amoxicillin and prednisone. I am still taking the antibiotics. Before the vaccines came out I came down with COVID-19 infection on October 2020. I still have some congestions in my head and some pressure in my ears. The urgent doctor told me that I had fluids in my ear which was why my ears were ringing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 06JAN2023 COVID-19 test negative
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes; Pace Maker 09/21/2021; Asthma
Andere Medikamente: Metformin; fluoxetine; XARELTO; metoprolol; vitamin C; vitamin D3; coQ10
Allergien: Silicone; NIASPAN
Vorherige Impfungen: -

VAERS 2552454

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IN
Alter: 67,0
Geschlecht: M
Eingang: 06.01.2023
Impfdatum: 06.10.2022
Beginn: 04.01.2023
Tage bis Beginn: 90,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Sinus congestion Sneezing

Symptomtext

I've been coughing, sneezing, with sinus congestion; I also have a runny nose and minor sore throat as of yesterday. I decided to take an at-home COVID-19 test in the evening of 01/05/2023, and it came back positive. I called my doctor this morning to tell him about my positive test, and he prescribed me PAXLOVID for treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID-19 test: 01/05/2023
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: ALEVE; CENTRUM'S men's vitamin; tamsulosin; atorvastatin; amlodipine; ramipril
Allergien: N/A
Vorherige Impfungen: -

VAERS 2551355

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 05.10.2022
Beginn: 19.12.2022
Tage bis Beginn: 75,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Fatigue Oropharyngeal pain Pain

Symptomtext

Sore throat fatigue body aches and a cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Coronary artery disease; Sjogren disease; Hypothyroidism
Andere Medikamente: Not applicable
Allergien: Cats; horses; seasonal allergies insect bites; bee stings
Vorherige Impfungen: -

VAERS 2550228

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: TX
Alter: 56,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 04.10.2022
Beginn: 28.12.2022
Tage bis Beginn: 85,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Fatigue Nasal congestion Oropharyngeal pain Pain Pain in extremity Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

After the vaccine, I woke up with a little soreness on my arm. My symptoms started on 12/28 I had running nose, fever, sore throat, and then that night chills, body ache, next day extreme fatigue. I had a COVID-19 test on Dec 30th the in the evening and it was positive. I called my doctor on 12/31 and prescribed PAXLOVID. My symptoms lasted for three days, but fatigue still continues, and also nose congestion. I started taking PAXLOVID on December 31st, today is my last day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 28DEC COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Myocarditis
Andere Medikamente: Lisinopril; VYVANSE; multivitamins; calcium; fish oil; coQ10
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2546903

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 25.09.2022
Beginn: 10.12.2022
Tage bis Beginn: 76,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Headache Paranasal sinus discomfort Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I woke up and I was congested with sinus pressure and headache, a low grade fever was also present. I decided to take a test for COVID-19 and it was positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVOID-19 test result of which was positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Breast cancer; Gird
Andere Medikamente: Anastrozole; Pepcid; Vitamin D
Allergien: Thiamazole
Vorherige Impfungen: -

VAERS 2545767

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: OH
Alter: 76,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 27.09.2022
Beginn: 19.12.2022
Tage bis Beginn: 83,0
Dosis: 5
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Exposure to SARS-CoV-2 Nasal congestion Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I had a stuffy nose and a sore throat. My husband was diagnosed with COVID-19 5 days prior. I did a COVID-19 at home test and I tested positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 19DEC2022 COVID-19 at home test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; High Cholesterol
Andere Medikamente: Metformin; letrozole; famotidine; FOSAMAX; ELIQUIS; metoprolol; atorvastatin; aspirin; calcium; AREDS 2 vitamins for eyes
Allergien: Triamterene; MAXIDE; terbinafine
Vorherige Impfungen: -

VAERS 2544986

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: AZ
Alter: 66,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 27.09.2022
Beginn: 15.11.2022
Tage bis Beginn: 49,0
Dosis: 6
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Aphonia Bedridden Bronchitis Chest X-ray normal Cough Diarrhoea Dizziness Fatigue Influenza virus test negative Nausea Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test negative Sinusitis

Symptomtext

Two months after COVID-19 vaccine I lost my voice with a sore throat and felt dizzy, lightheaded, congested, nauseous, with diarrhea and extreme fatigue; Had just started taking a new medication called BREZTRI and one of the possible side effects was having cold symptoms, so I thought I was just having a severe side effect; After being bedridden for 6 days I went to an urgent care, where I was tested for the Flu, COVID-19 and given a Chest X-ray, all results were negative; However I don't think the technician performed the COVID-19 test correctly, she barely stuck the swab in the testing fluid; I was told that I had Sinus infection and Bronchitis; I was prescribed the dual drug of amoxicillin with AUGMENTIN; Even though this was a month ago, I still have a dry cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Chest X-ray negative; Flu and COVID-19 negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Emphysema; High Cholesterol.
Andere Medikamente: Atorvastatin; estradiol; progesterone; IMODIUM; new medication BREZTRI
Allergien: Codeine; succinylcholine.
Vorherige Impfungen: -

VAERS 2544962

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MA
Alter: 59,0
Geschlecht: M
Eingang: 28.12.2022
Impfdatum: 26.09.2022
Beginn: 20.12.2022
Tage bis Beginn: 85,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Exposure to SARS-CoV-2 Headache Myalgia Pyrexia Rhinorrhoea SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

12/20/2022 I had been around people who were testing positive. I was having a runny nose. I tested negative with a COVID-19 home test. On Wednesday, 12/21/2022, the runny nose turned into a headache by the end of the day I went to an outdoor event, and I was shivering, and I was having muscle aches. I came home and tested positive with a COVID-19 home test. On Thursday morning, on 12/22/2022 I did a telehealth. They went through a checklist and told me I was eligible to receive PAXLOVID. They prescribed it on 12/22/2022 and I started taking it on that day. I started feeling better the next day, but probably the 24th of December I started feeling better. In time I stated not noticing the symptoms as much. My nose was not running, and headache and muscle aches went away pretty quickly, and I did not have a fever anymore after Wednesday night, 12/21/2022. 12/28/2022, I am feeling better, but I am still testing positive as of this morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 12/20/2022 COVID-19 home test negative; 12/21/2022 COVID-19 home test positive; 12/28/2022 COVID-19 home test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2544632

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: OH
Alter: 29,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 24.09.2022
Beginn: 12.12.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Headache Malaise Nasal congestion Oropharyngeal pain Pain in extremity SARS-CoV-2 test positive

Symptomtext

After receiving the vaccine, I felt tired, and my arm was sore for a day or two. On 12/12/2022, I began not feeling well with a headache and sore throat. On 12/13/2022, I tested positive for COVID-19 with a home test. I had a telehealth visit with my doctor and because I am young and in good health it was not recommended for me to take PAXLOVID. I took ibuprofen and acetaminophen for my symptoms. As of today, I continue to have a stuffy nose and cough. Stuffy nose and cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 13DEC2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: NUVARING; CLARITIN; FLONASE; multivitamin; fiber supplement
Allergien: N/A
Vorherige Impfungen: -

VAERS 2543847

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: OH
Alter: 66,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 23.09.2022
Beginn: 24.11.2022
Tage bis Beginn: 62,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Nasal congestion Oropharyngeal pain Pain Pruritus Pyrexia Rhinorrhoea SARS-CoV-2 test positive Sneezing Throat irritation

Symptomtext

11/24/2022 in the middle of the night I started to have a scratchy throat, itching, and sneezing. I decided to take a home COVID-19 test that did come out positive. I developed a severe sore throat, body aches, sneezing and a low grade fever. Nasal congestion, low grade fever and dripping nose for a few days. Sore throat was lasting for about 4 days that was extremely painful. I tried to take lozenges and TYLENOL however it did not improve. It started to improve by the 5th day. I began taking the PAXLOVID from Nov 24th night until completion. I am now doing fine and feeling completely normal. I did have a rebound of symptoms after 2 days post my last PAXLOVID dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 24NOV2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes Insipidus; History of Breast Cancer; High Blood Pressure; Spinal Stenosis; High Cholesterol
Andere Medikamente: Desmopressin; losartan; exemestane; vitamin D; calcium
Allergien: Penicillin; BACTRIM
Vorherige Impfungen: Moderna arm, from the original 2 vaccines. They both came about a week afterwards. Moderna 01/08/2021 & Moderna 02/05/2021

VAERS 2528955

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

mild

Staat: WA
Alter: 68,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 11.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Immunisation reaction Pruritus Rash Scratch Skin reaction Skin warm Urticaria

Symptomtext

10/12/22: Covid Arm Rash (which I get after each vaccine/booster). 3" diameter. Red/itchy/warm. 10/24/22: Scalp to feet full body rash began. Areas included scalp, face, eyelids, lips, ears (inside and outside) neck, back, chest, arms, waist, pubic area, groin, in between butt-cheeks, thighs, knees, shins, feet (tops/bottoms), hands (tops/bottoms, fingers). Everywhere. Symptoms: red spots, pencil-like scratches, hive-like patches. These were inches long and wide. Itchy-ness level 7. Affected areas come and go within say 1 hour then re-appear in a different area. Can't wear earrings, bra, compression socks. Did not work: benedryl, loratadine, hydrocortizone, triamcinolone. As of 12/12/22, symptoms are decreasing, As of 12/12/22, symptoms are decreasing, but still present. Important to note that these symptoms appear in one area for about an hour, disappear, then re-appear in another area. Some of the affected areas ranged from 3"x3" to 4"x8" for patch of say 6 pencil like scratches on back or 4"x4" raised/bumpy area on butt. Hives seem to be more common in warm folds (inside elbows, groin, stomach, waist). I have photos if you need them.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: n/a
Vorgeschichte: -
Andere Medikamente: Linzess, Multi-vitamin, Vitamin D
Allergien: Tape
Vorherige Impfungen: -

VAERS 2525643

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NY
Alter: 66,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 15.11.2022
Beginn: 27.11.2022
Tage bis Beginn: 12,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Rash Urticaria

Symptomtext

hives and skin rashes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2517460

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

mild

Staat: DC
Alter: 28,0
Geschlecht: F
Eingang: 27.11.2022
Impfdatum: 15.11.2022
Beginn: 25.11.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Mechanical urticaria Pruritus Rash erythematous Urticaria

Symptomtext

About ten (10) days after the second Moderna booster, I developed itching and dermatographia that lead to raised welts and red marks on my skin. The worst areas are around my neck and on my scalp. This happened for my first booster as well, but I did not connect it to the booster at the time and therefore did not report it. However, this is starting off the same as the first time. Zyrtec helps reduce the symptoms. The first time this happened, after the first Moderna booster, the issue eventually resolved after a month or two. I am planning to take Zyrtec again this time and document the length and severity of the symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Same adverse reaction after the first Moderna booster in 12/2021.

VAERS 2517033

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 25.11.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Asthenia Body temperature increased Dizziness Drooling Dysphagia Hypoaesthesia Hypoaesthesia oral Myalgia Pain Pharyngeal hypoaesthesia

Symptomtext

Within 30 minutes dizzy, faint and weak. Within 45 minutes numb nose to numb cheeks to numb face to numb lips to numb mouth to numb throat. Difficulty swallowing and drooling noted. Halted with 25 mg Benadryl liquid oral dose. 24 hours after vaccine noted body aches, muscle and joint soreness. Low grade fever 99.8 p.o. 36 hours after temp climbing- peaked at 102 p.o. 48 hours later. All s/s resolves in 72 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: EZETIMIBE/SIMVASTATIN 10-20mg,, MONTRLUKAST SODIUM 10mg., MVI, Vitamin D-3 5,000 IU, Magnesium 250 mg.
Allergien: Estrogen, statins, Measles vaccine, influenza vaccine, Pneumovax, Tuberculin derivative, shellfish/ (iodine products), dairy, plants (seeds, pollen, fruits, nuts, berries, vegetables, grasses, trees etc), eggs (albumin), latex, allergy (de-sensitizing) injections, small animal dander (cats, mice, rabbits etc), dust/dust mites, Formaldehyde/ flame retardant sprays or chemicals.
Vorherige Impfungen: Influenza vaccine @ age 21. Loss of consciousness. Measles @ age 2 body rash. Tuberculin testing- 10 cm hive @ injection site.

VAERS 2512355

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge AS7164B

mild

Staat: NY
Alter: 84,0
Geschlecht: F
Eingang: 19.11.2022
Impfdatum: 14.10.2022
Beginn: 07.11.2022
Tage bis Beginn: 24,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Rash Rash pruritic Urticaria

Symptomtext

generalized skin rash, like hives, very itchy on buttocks, thighs, legs, back, upper arms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, arthritis,
Andere Medikamente: Zyrtec 10 mg, qd; pravastatin 20mg qd; irbesartan 300mg qd; fluticasone prop. 50mcg/actuation nasal spray, 1 spray each nostril bid; 81mg asa qd; Linzess 72mcg capsule qd. Multiple vitamin, coQ 10, Ca, Mg, D,
Allergien: many
Vorherige Impfungen: previous Moderna Covid vaccine----rash

VAERS 2510865

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NJ
Alter: 45,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 01.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Pruritus Rash Rash erythematous Rash papular Rash pruritic Urticaria

Symptomtext

I started dealing with rashes breaking out all over my body. They were very red and very itchy. Sometimes raised and welty-looking, sometimes only red and itchy skin. The doctor has put me on a 6 day course of prednisone, and that seems to be controlling it for the most part right now. The only new thing introduced to my body was the booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Common cold about one to two weeks prior to vaccination
Vorgeschichte: High blood pressure being controlled by medication.
Andere Medikamente: Hydrochlorothiazide; Daily multivitamin; and daily Vitamin D.
Allergien: Sensitivity to nuts/seeds (not allergic, just stomach issues), sensitivity to latex/adhesive.
Vorherige Impfungen: Covid arm, 43, 3/6/21, Moderna Covid vaccine (1st shot)

VAERS 2509453

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 27.09.2022
Beginn: 12.10.2022
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Bronchitis COVID-19 Cough Fatigue Poor quality sleep Respiratory tract congestion SARS-CoV-2 test positive Sleep disorder

Symptomtext

My sister who had been traveling, came to stay with me. She had a bit of a cough, but we didn't think much of it until it had lasted around 3 days. At that point, on 10/12/2022, we each tested ourselves for COVID-19 and were positive. I contacted my doctor and had a phone consultation. He called in a prescription for PAXLOVID. I began taking that the day after I tested positive. I was feeling really tired but couldn't nap. I had a lot of head congestion and an unproductive cough. However, after the five days of the PAXLOVID, I was feeling fine. I continued to mask for the following five days. I did still have some congestion but was feeling good. After the additional five days of isolating, I felt much better and was able to go to the grocery store. After the recommended isolation time, I tested myself again and was negative. Three days after testing negative, I wanted to go see my elderly mother, so I tested myself again and I was actually positive. I went to my doctor's office to do a drive thru COVID-19 test and it was also positive. Two days before I tested positive again, I had spoken with my doctor who told me that it sounded like I was developing bronchitis. He called in a Z PAK and prednisone which I took to completion. When I tested positive again, my doctor told me that I could not take the PAXLOVID again, so he suggested a cold and flu medication and MUCINEX. 12 days after testing positive again, I was feeling better and tested negative again. I am still feeling a bit of fatigue in the evenings, but I am very active. Also, through all of this illness, I have not been able to sleep well. I have been tired, but unable to sleep through the night. I will sleep for a few hours and wake up and have trouble going back to sleep. Last night was the first night in some time that I was able to sleep for 5-6 hours straight.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 12OCT2022 at home COVID-19 test positive; 18OCT2022 at home COVID-19 test negative; 22OCT2022 at home COVID-19 test negative; 28OCT2022 PCR COVID-19 test positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Year-round Seasonal Allergies; Fibromyalgia; Arthritis
Andere Medikamente: Lisinopril; hydrochlorothiazide; naproxen; vitamin D3; calcium; magnesium; vitamin C; montelukast; diazepam
Allergien: Penicillin; sulfa
Vorherige Impfungen: Age 18 1965, Smallpox vaccine, swelling at injection site and fever for two weeks.

VAERS 2508728

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NY
Alter: 38,0
Geschlecht: M
Eingang: 15.11.2022
Impfdatum: 31.10.2022
Beginn: 14.11.2022
Tage bis Beginn: 14,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dyspepsia Impaired work ability Mechanical urticaria Pruritus Rash erythematous Urticaria

Symptomtext

Dermatographic urticaria and heartburn. I began to get terribly itchy the night of November 14, 2022, and awoke this morning to find that I had red welts all over my right neck. Eating breakfast, I developed terrible heartburn. I found more welts on the left side of my neck at work and had to come home early.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: I was diagnosed with dermatographic urticaria after my second COVID shot (also Moderna, on 4/15/2021), but it was largely managed until last night.
Aktuelle Erkrankungen: M/A
Vorgeschichte: Migraine
Andere Medikamente: Allegra; Amitriptyline.
Allergien: N/A
Vorherige Impfungen: Dermatographic urticaria, age 37, vaccination on 4/15/2021, Moderna COVID vaccine.

VAERS 2503222

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

mild

Staat: SC
Alter: 56,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 28.09.2022
Beginn: 23.10.2022
Tage bis Beginn: 25,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Fatigue Headache Insomnia Pain in extremity SARS-CoV-2 test negative

Symptomtext

I woke feeling like I had a cold or sinus infection a real bad cough came next I also had a real bad headache and could no sleep at night. My two COVID-19 tests were negative my Doctor prescribed medicine, I also was tacking Nyquil and Dayquil. I still have a cough and I am really tired and fatigued A weird thing is I have a real sore finger or knuckle.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Two COVID-19 tests negative.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Jinteli; Iron; Vitamin D3; Simvastatin; Cetirizine
Allergien: Sulfa; Ceclor; Septra; Augmentin
Vorherige Impfungen: -

VAERS 2501958

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: VA
Alter: 74,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 25.09.2022
Beginn: 06.11.2022
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Diarrhoea Malaise Nausea SARS-CoV-2 test positive

Symptomtext

I started to experience nausea, diarrhea and just the feeling of being unwell. I shared that information with the physician in the ER, she automatically stated that I had COVID-19. I received the anti-body infusion the same day as my visit. I was very surprised that I tested positive after being fully vaccinated plus I received all three booster shots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19
Aktuelle Erkrankungen: -
Vorgeschichte: Type II Diabetic; High BP; Arthritis; Asthma; Gout; Previous Blood Clot; Reflux
Andere Medikamente: Hydroxychloroquine; metformin; ELIQUIS; VICTOZA; HCTZ; furosemide; BREO; gabapentin; folic acid; alpha lipoic; coQ10; acetaminophen; multivitamin
Allergien: PERCODAN; PERCOCET; DILAUDID; DEMEROL; adhesive; SEFTIN; DICLOFINAC; TRIGENTA; INVOKANA; BACTRIM; CESALOR; BENEDRYL; codeine
Vorherige Impfungen: I had COVID arm after receiving each Moderna vaccine.

VAERS 2501834

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: OH
Alter: 66,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 01.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chills Fatigue Headache Malaise Nasal congestion Productive cough SARS-CoV-2 test positive

Symptomtext

Symptoms; productive cough; headache; nasal congestion; chills; fatigue and malaise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Home COVID 19 test positive on 10/31/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Type C Diabetes; High Cholesterol
Andere Medikamente: ADVAIR; propranolol; FLONASE; metformin; SINGULAIR; atorvastatin; omeprazole
Allergien: Ibuprofen; sulfa; bandage adhesive
Vorherige Impfungen: -

VAERS 2501811

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NY
Alter: 72,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 05.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Injection site mass Injection site rash Pyrexia

Symptomtext

After 24 hours patient developed a rash (subcutaneous lumps around injection site) which radiated to the other arm. Lumps fully disappeared after 2 weeks. Worst of it was within the first 5 days. Patient also experienced very high fever for 3 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site mass
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: anaphylaxis to PCN
Vorherige Impfungen: -

VAERS 2493899

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NY
Alter: 28,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 17.10.2022
Beginn: 23.10.2022
Tage bis Beginn: 6,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Fatigue Feeling abnormal Pyrexia Visual impairment

Symptomtext

day after shot (Oct 18) had low grade fever and fatigue, which resolved within 2 days on Oct 20. On Oct 23, I woke up with intense fatigue, brain fog and lightheadedness. It has now been 9 days and I still am having this affects along with disoriented vision.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Vyvanse 50mg, Yaz
Allergien: No
Vorherige Impfungen: -

VAERS 2493025

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

mild

Staat: NJ
Alter: 63,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 01.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain in extremity

Symptomtext

sore arm which she has gotten with all her vaccinations.; This spontaneous case was reported by a pharmacist and describes the occurrence of PAIN IN EXTREMITY (sore arm which she has gotten with all her vaccinations.) in a 63-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 vaccination. The patient had no allergies. No other vaccines were taken within 1 month prior to Moderna COVID-19 vaccine. There were no history relating to mentioned AE and both Acute and Chronic illnesses at the time of vaccination. No Medical History information was reported. Concomitant products included MONTELUKAST SODIUM (SINGULAIR), LEVOCETIRIZINE DIHYDROCHLORIDE (ALLEGRA [LEVOCETIRIZINE DIHYDROCHLORIDE]) and ALENDRONATE SODIUM (FOSAMAX) for an unknown indication. On 01-Oct-2022, the patient received fourth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) .5 milliliter. On an unknown date, the patient experienced PAIN IN EXTREMITY (sore arm which she has gotten with all her vaccinations.). At the time of the report, PAIN IN EXTREMITY (sore arm which she has gotten with all her vaccinations.) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter did not provide any causality assessments. Patient had dose 1 on 17 Mar 2021 with Lot number as 047A21A via unknown route and dose 2 on 14 Apr 2021 with lot number as 040B21A via unknown route. No treatment medication reported. This case was linked to MOD-2022-656967, MOD-2022-656961 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no allergies. No other vaccines were taken within 1 month prior to Moderna COVID-19 vaccine. There were no history relating to mentioned AE and both Acute and Chronic illnesses at the time of vaccination. No Medical History information was reported.
Andere Medikamente: SINGULAIR; ALLEGRA [LEVOCETIRIZINE DIHYDROCHLORIDE]; FOSAMAX
Allergien: -
Vorherige Impfungen: -

VAERS 2492630

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: OH
Alter: 24,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 09.10.2022
Beginn: 16.10.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Aphonia Chills Cough Dysphonia Headache Oropharyngeal pain Paranasal sinus discomfort Productive cough Pyrexia Respiratory symptom Rhinorrhoea Secretion discharge Sinus disorder Sneezing Throat irritation

Symptomtext

Sore throat started 10/16, became progressively worse and then severe for next couple days. Chills and feverish next day 10/17, then subsided. Then URI/sinus symptoms began (severe runny nose and sneezing, sinus pressure, headache, hoarseness, scratchy throat and losing voice). After OTC meds and prednisone symptoms began to improve. Towards end, developed an intermittent cough. Now I still have some runny nose and green mucus, coughing up phlegm occasionally. Voice is almost recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Fish oil, Adderall 10mg XR, Singulair 10mg, Zyrtec, Nasonex, Atorvastatin 10mg , multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2490122

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: VA
Alter: 43,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 13.10.2022
Beginn: 13.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Fatigue Laboratory test normal Nervousness Pain Urine analysis normal

Symptomtext

Later, that night around 6 I had the typical reaction very fatigue and joint pain and a low-grade fever of 100. Then I started having pain in the growing area and with the past shots it would normally be in the shoulders making difficult to even turn my neck. Here we are two weeks later, and I am still in so much pain that it is making me nervous. I called my Primary last week, and they did a UTI test and they also tried to test for blood cancer, but I declined that test. I go back for a follow up in a few weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: UTI neg, twisted ovary neg
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2486557

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NJ
Alter: 70,0
Geschlecht: F
Eingang: 23.10.2022
Impfdatum: 01.10.2022
Beginn: 02.10.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue

Symptomtext

Severe fatigue 10/02/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, hypothyroidism,depression
Andere Medikamente: Wellbutrin, synthroid, cytomel
Allergien: Cherries, peaches
Vorherige Impfungen: -

VAERS 2482852

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: RI
Alter: 31,0
Geschlecht: M
Eingang: 19.10.2022
Impfdatum: 22.09.2022
Beginn: 24.09.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test normal Dizziness Feeling abnormal Heart rate increased

Symptomtext

09/24/2022 I noticed I had a fast heart rate and for a little period of time and it stopped, I went to the doctor on 09/26/2022 and was experiencing light headiness and brain fog with the fast heartbeat. All blood work done that day came back negative, but I am still currently experiencing the brain fog, accompanied by being lightheaded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Blood panel 10/26/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: High blood pressure
Andere Medikamente: Lisinopril,
Allergien: Augmentin, seasonal allergeries
Vorherige Impfungen: -

VAERS 2480315

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: OH
Alter: 71,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 24.09.2022
Beginn: 28.09.2022
Tage bis Beginn: 4,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dry skin Pruritus Rash pruritic

Symptomtext

I first noticed some dry skin around 4 days after receiving my vaccine. I attributed it to dryness from frequent swimming. However, after I moisturized, my skin was no longer dry, but I was still itching. I had little bumps appearing on my legs, back, arms, chest, and now a little bit on my face that really itch. I spoke with my dermatologist who gave me some high potency hydrocortisone cream which helped quite a bit. He also advised that I double my ZYRTEC dosage which also helped. I continued using over the counter moisturizer as well. Things are getting progressively better but have not cleared up completely and I intend to call my doctor today for an additional prescription of hydrocortisone cream.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism; Grave's Disease; Chronic Urinary Tract Infections; Chronic Bronchitis; Rheumatoid Arthritis
Andere Medikamente: SYNTHROID; SINGULAIR; MACROBID; omeprazole; ZYRTEC; calcium; vitamin D; estradiol vaginal cream
Allergien: Latex; seasonal allergies; dust mites; mold; penicillin; COMPAZINE; TIGAN; BIAXIN; COX 2 Inhibitors
Vorherige Impfungen: -

VAERS 2478872

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 24.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Impaired work ability Movement disorder Pain in extremity Product administered at inappropriate site

Symptomtext

PATIENT STATED THAT AFTER GETTING THE VACCINE HER ARM WAS VERY SORE AND THAT SHE WAS IN SO MUCH PAIN THAT SHE COULD NOT MOVE HER ARM AT ALL. THIS CAUSED HER TO MISS 2 DAYS OF WORK AND SHE MADE A DOCTOR APPOINTMENT. THIS WAS ADVERSE REACTION IN WHICH SHE STATED PER HER MD THAT THE SHOT WAS GIVEN TO AGRESSIVE AND TO CLOSE TO OTHER VACCINE GIVEN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: UNNKOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2477242

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

mild

Staat: MI
Alter: 89,0
Geschlecht: F
Eingang: 13.10.2022
Impfdatum: 06.10.2022
Beginn: 08.10.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test normal Ear pain Facial pain Headache Neck pain

Symptomtext

2 days after the administration of vaccine you experienced sharp pain in the back of the head and neck and into the face and ear on the right side, comes and goes, pain lasts a few minutes. Back of head hurts, feels best sitting in the chair with a heating pad. Went to doctor on Monday who prescribed a muscle relaxer which did not help much. The sharper bursts of pain have improved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: Doctor did do bloodwork. No abnormal results
Aktuelle Erkrankungen: none
Vorgeschichte: bad knee, heart condition aortic stenosis with left bundle block
Andere Medikamente: b12 shot once monthly; trellegy ; fish oil, eye vitamin, baby aspirin
Allergien: sulfa allergy
Vorherige Impfungen: -

VAERS 2476306

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

mild

Staat: TX
Alter: 61,0
Geschlecht: F
Eingang: 12.10.2022
Impfdatum: 06.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site bruising

Symptomtext

Patient noticed bruise after she left the pharmacy when she took the bandaid off. still has the bruise. no pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Multivitamin
Allergien: none
Vorherige Impfungen: -

VAERS 2475529

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: TX
Alter: 68,0
Geschlecht: M
Eingang: 11.10.2022
Impfdatum: 01.10.2022
Beginn: 04.10.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal discomfort Arthralgia Body temperature increased COVID-19 Diarrhoea Headache Nausea Oropharyngeal pain Paranasal sinus discomfort Rhinorrhoea SARS-CoV-2 test positive Sinus disorder Sinus operation

Symptomtext

This was the second time I had COVID-19. Runny nose, sore throat, headache, sinus pressure, temp increase to 101, joint pain. The symptoms still continue but are better. I still have sinus involvement and drainage. I was given PAXLOVID 5 day course. I was also taking ADVIL and both reacted badly. I would say that NSAIDs and PAXLOVID do not mix at all. As a result of both I got nausea, acidic diarrhea and upset stomach. I'm still tested positive today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: COVID-19 test positive
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension; Asthma
Andere Medikamente: Olmesartan; metoprolol; fluticasone
Allergien: Azithromycin; KEFLEX; CELEBREX; gentamycin; codeine
Vorherige Impfungen: -

VAERS 2472771

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

mild

Staat: MN
Alter: 60,0
Geschlecht: F
Eingang: 09.10.2022
Impfdatum: 01.10.2022
Beginn: 02.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Injection site erythema Injection site pain Injection site swelling

Symptomtext

Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Headache-Medium, Additional Details: Swelling, redness, pain, and headache have improved significantly, but have not resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2472705

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NJ
Alter: 50,0
Geschlecht: F
Eingang: 08.10.2022
Impfdatum: 05.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Pyrexia

Symptomtext

High fever= 103.6 Slept Fever resolved several hours later

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2472493

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

mild

Staat: NH
Alter: 68,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Pruritus Rash

Symptomtext

The patient told me that she had a rash/itch after her first ever dose of moderna covid vaccine so her doctor told her to take a benadryl before each future dose. She forgot to take one this morning so she took a tablet right before her shot. vaccine administration was around 12:25pm and as she was waiting afterwards she said she was feeling itchy /rash on her chest and feeling a little itchy on her face at 12:51pm .I administered 25mg of liquid diphenhydramine at 12:56pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Blood pressure 131/78 pulse 80 at 1:00pm blood pressure 125/82 pulse 82 at 1:12pm
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: unknown
Allergien: penicillin, sulfur
Vorherige Impfungen: moderna covid vaccine 3/3/21 age 66 rash

VAERS 2464463

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

mild

Staat: MD
Alter: 75,0
Geschlecht: F
Eingang: 06.10.2022
Impfdatum: 26.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Injection site pain Injection site swelling Injection site warmth Pain in extremity Peripheral swelling Skin discolouration Skin warm

Symptomtext

9/26/2022 I had the appointment and I went there and there was a short wait. And then it was my turn they gave me the shot sitting down. The person giving me the shot sat to my left and there was nothing odd about that. It didn't hurt or anything. It seemed fine. The next day I woke up it was sore and swollen and when I touched it, it was warm and pinkish purple so there was clearly something wrong. I thought that it would go away but when it didn't I went to urgent care 9/29/2022. I called the pharmacy and she asked me some questions and said she would put it in the reporting system and told me to go to urgent care. I tried to see my PCP but they said they could not fit me in so I just went to an urgent care. They asked question and looked at it and suggested I put ice on it and take some ADVIL. I did not take the ADVIL but it did go away in a couple of days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Cracked tooth
Vorgeschichte: High Blood Pressure
Andere Medikamente: Blood pressure meds; multivitamin; vitamin D3; vitamin E; cranberry pill; vitamin C; zinc; turmeric; magnesium; low dose baby aspirin; elderberry
Allergien: N/A
Vorherige Impfungen: -

VAERS 2470278

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

mild

Staat: MN
Alter: 69,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 26.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Abdominal pain Computerised tomogram abdomen normal Fatigue Flank pain Laboratory test normal Pain in extremity Urine analysis normal

Symptomtext

I experienced right flank pain and right sided abdominal pain after my vaccine. This really went off for 5 days. I went to ER on day 4 and clinical follow-up on day 5 and I have gradually better since day 5. I still have right side flank pain, minimally bothersome at this point. I also felt fatigues and had a sore left arm. At the ER they did complete lab work, urine test and CT scan of the abdomen which tests were normal. I can say I am about 90% better today, not back to normal, well on the way to getting better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: Complete Lab work- normal; CT scan of the abdomen- normal; Urine test- normal
Aktuelle Erkrankungen: None
Vorgeschichte: History Of Migraine Headaches, Hypothyroidism; Border Line Elevated Cholesterol
Andere Medikamente: Ibuprofen; Synthroid; Atorvastatin; Metoprolol; Baby Aspirin
Allergien: Flora quinolone; Antibiotics, Terbinafine
Vorherige Impfungen: COVID-19 vaccines, experience a sore arm

VAERS 2467746

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: PA
Alter: 48,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 30.09.2022
Beginn: 30.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Asthenia Dizziness

Symptomtext

Patient became lightheaded and weak after vaccine. Has had previous episodes over the last few months, regardless of vaccainations. Patient taken from store by ambulance to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: No known
Vorgeschichte: No known
Andere Medikamente: No known
Allergien: No known
Vorherige Impfungen: -

VAERS 2467222

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

mild

Staat: OH
Alter: 70,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 23.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Arthralgia Joint range of motion decreased Loss of personal independence in daily activities

Symptomtext

Patient was vaccinated with Covid booster, and upon getting back home her shoulder was hurting. She called the pharmacy back to speak with RPH. After coming back into the pharmacy RPH advised patient to go to doctor to get evaluated. Patient complained of shoulder pain and limited range of motion. Patient reported to the emergency room and was released. Patient followed up with primary care prescriber the following week. Patient still reporting shoulder pain the following week including that it was hard to complete tasks around her farm and it was still hard to get dressed. Patient is doing physical therapy and strength exercises.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: hypertension
Andere Medikamente: Solifenacin 10mg Tablets, Alendronate 70mg, Losartan 50mg
Allergien: ace inhibitors
Vorherige Impfungen: -

VAERS 2467074

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

mild

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 26.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Injection site erythema Injection site rash Injection site swelling

Symptomtext

red with swelling and rash at site of reaction starting day after vaccine given and has lasted about a week so far

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2466868

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

mild

Staat: PA
Alter: 78,0
Geschlecht: F
Eingang: 02.10.2022
Impfdatum: 02.10.2022
Beginn: 02.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Pain Pruritus

Symptomtext

red, itchy, and sore, also itchy on side of body

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: simvastatin and ventolin
Allergien: iodides, penicillin, soy, fish derived
Vorherige Impfungen: -

VAERS 2465743

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

mild

Staat: IL
Alter: 75,0
Geschlecht: M
Eingang: 30.09.2022
Impfdatum: 22.09.2022
Beginn: 24.09.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Gait disturbance Hyperhidrosis Laboratory test normal Vertigo Vomiting

Symptomtext

Patient stated approximately 2 days after vaccines experienced vertigo, excessive sweating, vomiting, loss of stability. So much so he went to the hospital, and he was there from Sat to Tues. He said from the tests ran etc certain things were ruled out and it seemed that he was experiencing these symptoms due to the vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vomiting
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: mesalamine 1.2gm also received the high dose flu shot at the same time of covid moderna booster
Allergien: milk products,nsaid,corticosteroids
Vorherige Impfungen: -

VAERS 2463270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge AS7164B

mild

Staat: IA
Alter: 64,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 25.09.2022
Beginn: 26.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Cough Headache SARS-CoV-2 test positive

Symptomtext

I had my vaccination on 09/25/2022. I woke up on 09/26/2022 with a temperature cough and headache. I took an home test that was COVID-19 Negative. I went to Urgent Care on 09/27/2022 and tested COVID-19 Positive. I was told I could possibly take Plaxovid but was recommended by a friend to not take just yet due to recent vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 09/26/2022 COVID-19 Negative 09/27/2022 COVID-19 Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; High Cholesterol; Hypothyroidism
Andere Medikamente: Losartan; Levothyroxine; Atorvastatin; Amlodipine
Allergien: Penicillin
Vorherige Impfungen: Unwell with most vaccinations

VAERS 2463186

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: KY
Alter: 52,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 24.09.2022
Beginn: 25.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Herpes zoster Immediate post-injection reaction Injection site pain Pyrexia Rash

Symptomtext

Immediately after receiving my vaccine, I didn't notice much more than a sore arm at injection site. I did have a fever that night. The highest it got was around 102. I was taking Tylenol to treat that. When I woke up Sunday morning, I had a rash on my forehead more on the left than right side. The rash got progressively worse and spread to other places. I called my doctor Monday morning who was booked up, so I texted pictures of the rash on my face. From the photos, she was able to diagnose Shingles. She prescribed Valtrex. My face is still covered in a rash but I have not been running a fever anymore.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fluoxetine; Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2463181

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: MD
Alter: 71,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 27.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Extra dose administered Fatigue Pain Pyrexia

Symptomtext

Pt accidently received and extra dose of Moderna bivalent booster vaccine, within 2 weeks of receiving a Pfizer booster vaccine. Pt only developed fever at night of the vaccine and experienced fatigue and achiness the following morning. all symptoms were controllable by Tylenol extra strength according to pt.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2461127

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NY
Alter: 12,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 17.09.2022
Beginn: 17.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Pyrexia

Symptomtext

Patient received unauthorize dose of Moderna Bivalent. Mother reported fever and fatigue for 24 hours following however within 48 hours symptoms resolved. Mother denied any further complaints.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2460902

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NY
Alter: 12,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 17.09.2022
Beginn: 17.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Incorrect product formulation administered Pyrexia

Symptomtext

Patient received Moderna Bivalent as a booster when not yet authorized. Spoke to mother who reports 24 hours of fever and fatigue, however resolved within 48 hours post vaccine. Denied any complaints at time of phone call.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2459584

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

mild

Staat: NY
Alter: 68,0
Geschlecht: F
Eingang: 24.09.2022
Impfdatum: 21.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Diarrhoea Pain

Symptomtext

Diarrhea after first Bivalent booster shot; Achiness after first Bivalent booster shot; This spontaneous case was reported by a patient and describes the occurrence of DIARRHOEA (Diarrhea after first Bivalent booster shot) and PAIN (Achiness after first Bivalent booster shot) in a 68-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 vaccination. Concurrent medical conditions included Irritable bowel syndrome (Diagnosed many years ago. Patient normally tooks Imodium or Lomotil for IBS.). Concomitant products included LOPERAMIDE HYDROCHLORIDE (IMODIUM) and LOPERAMIDE HYDROCHLORIDE (LOMOTIL [LOPERAMIDE HYDROCHLORIDE]) for Irritable bowel syndrome. On 21-Sep-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 21-Sep-2022, the patient experienced DIARRHOEA (Diarrhea after first Bivalent booster shot) and PAIN (Achiness after first Bivalent booster shot). At the time of the report, DIARRHOEA (Diarrhea after first Bivalent booster shot) and PAIN (Achiness after first Bivalent booster shot) outcome was unknown. Patient received the first dose on 07-Feb-2021 (Lot: 030M20A), second dose on 07MAR2021 (Lot: 032M20A), First Monovalent Booster dose on 01NOV2021 (Lot: 032F21A) and 2nd Monovalent Booster dose on 27APR2022 (Lot: 057M21A). Patient states that got her 5th shot yesterday and she always had the same reaction after all Moderna COVID-19 shots. No treatment medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Irritable bowel syndrome (Diagnosed many years ago. Patient normally tooks Imodium or Lomotil for IBS.)
Vorgeschichte: -
Andere Medikamente: IMODIUM; LOMOTIL [LOPERAMIDE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2705204

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 28.10.2023
Impfdatum: 27.09.2022
Beginn: 14.08.2023
Tage bis Beginn: 321,0
Dosis: 5
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 SARS-CoV-2 test

Symptomtext

Tested COVID Positive; This spontaneous case was reported by a non-health professional and describes the occurrence of COVID-19 (Tested COVID Positive) in a patient of an unknown age and gender who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. Previously administered products included for Drug use for unknown indication: PFIZER BIONTECH COVID-19 VACCINE (LOT number EP7534) on 01-Apr-2021, PFIZER BIONTECH COVID-19 VACCINE (LOT number ER8737) on 22-Apr-2021, PFIZER BIONTECH COVID-19 VACCINE (LOT number PE3592 (Booster)) on 30-Aug-2021 and PFIZER BIONTECH COVID-19 VACCINE (LOT number FJ4991 (Second Booster)) on 11-May-2022. Past adverse reactions to the above products included No adverse event with PFIZER BIONTECH COVID-19 VACCINE, PFIZER BIONTECH COVID-19 VACCINE, PFIZER BIONTECH COVID-19 VACCINE and PFIZER BIONTECH COVID-19 VACCINE. Concomitant products included ATORVASTATIN and OMEPRAZOLE for an unknown indication. On 27-Sep-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 14-Aug-2023, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced COVID-19 (Tested COVID Positive). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) on 14-Aug-2023 for COVID-19, at a dose of UNK, bid, 3 pills. On 19-Aug-2023, COVID-19 (Tested COVID Positive) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 14-Aug-2023, SARS-CoV-2 test: Positive. On 19-Aug-2023, SARS-CoV-2 test: (Negative) No symptoms. On 26-Aug-2023, SARS-CoV-2 test: (Positive) Rebound covid. On 08-Sep-2023, SARS-CoV-2 test: Negative. On 14-Aug-2023 Patient tested positive and on 19-Aug-2023 after 5 days, tested negative and on 26-Aug-2023 patient again tested positive (rebound COVID) and on 08-Sep-2023, tested negative after 13 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230814; Test Name: COVID-19 VIRUS TEST; Test Result: Positive ; Test Date: 20230819; Test Name: COVID-19 VIRUS TEST; Test Result: Negative ; Test Date: 20230826; Test Name: COVID-19 VIRUS TEST; Test Result: Positive ; Test Date: 20230908; Test Name: COVID-19 VIRUS TEST; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ATORVASTATIN; OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2699058

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

gering

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 20.10.2023
Impfdatum: 28.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Blood pressure increased Flushing Heart rate increased

Symptomtext

After she received her COVID booster she had a sensation of being flushed with elevation of her blood pressure and pulse; she started taking some Benicar at request of physician with some improvement of her symptoms and blood pressure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood pressure increased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2677928

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: AR
Alter: 85,0
Geschlecht: F
Eingang: 30.08.2023
Impfdatum: 21.10.2022
Beginn: 26.08.2023
Tage bis Beginn: 309,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test positive

Symptomtext

hospitalized with covid; fully vaccinated with 2 boosters

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: positive covid pcr 8/26/23
Aktuelle Erkrankungen: unknown
Vorgeschichte: Diabetes (prediabetes), Hyperlipidemia, Hypertension and Other (essential tremor)
Andere Medikamente: unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2656010

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

gering

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 13.07.2023
Impfdatum: 28.09.2022
Beginn: 21.03.2023
Tage bis Beginn: 174,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Obstructive sleep apnoea syndrome Osteoarthritis

Symptomtext

OBSTRUCTIVE SLEEP APNEA 10/31/2022 OSTEOARTHRITIS OF LEFT HIP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Obstructive sleep apnoea syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648153

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: -
Alter: 95,0
Geschlecht: M
Eingang: 22.06.2023
Impfdatum: 19.06.2023
Beginn: 19.06.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Immunisation reaction Wrong product administered

Symptomtext

unknowm side effects due to the vaccine being administered today; Patient received bivalent vaccine as first dose; This spontaneous case was reported by a pharmacist and describes the occurrence of IMMUNISATION REACTION (unknowm side effects due to the vaccine being administered today) and WRONG PRODUCT ADMINISTERED (Patient received bivalent vaccine as first dose) in a 95-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. It was unknown if patient had any medical history, allergy, concomitant diseases and risk factor. Patient did not received any other vaccines in the 4 weeks prior to COVID-19 vaccine. On 19-Jun-2023, the patient received first dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 19-Jun-2023, the patient experienced IMMUNISATION REACTION (unknowm side effects due to the vaccine being administered today) and WRONG PRODUCT ADMINISTERED (Patient received bivalent vaccine as first dose). At the time of the report, IMMUNISATION REACTION (unknowm side effects due to the vaccine being administered today) and WRONG PRODUCT ADMINISTERED (Patient received bivalent vaccine as first dose) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter did not provide any causality assessments. No concomitant information was reported. No treatment information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Immunisation reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: It was unknown if patient had any medical history, allergy, concomitant diseases and risk factor. Patient did not received any other vaccines in the 4 weeks prior to COVID-19 vaccine.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2647550

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: OH
Alter: 69,0
Geschlecht: F
Eingang: 21.06.2023
Impfdatum: 19.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Therapeutic response unexpected

Symptomtext

The last 2 doses were Moderna and she claims that she was symptom free for at least 6 weeks after getting the doses; This spontaneous case was reported by a patient and describes the occurrence of THERAPEUTIC RESPONSE UNEXPECTED (The last 2 doses were Moderna and she claims that she was symptom free for at least 6 weeks after getting the doses) in a 69-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. The patient's past medical history included COVID-19 in March 2020. Previously administered products included for Product used for unknown indication: PFIZER BIONTECH COVID-19 VACCINE (First Dose, EN6203) on 05-Mar-2021, PFIZER BIONTECH COVID-19 VACCINE (Second Dose, ER2613) on 26-Mar-2021, PFIZER BIONTECH COVID-19 VACCINE (Third Dose, FF8814, First Booster) on 15-Oct-2021 and Senior flu vaccine (Aug/Sep2022). Past adverse reactions to the above products included No adverse effect with PFIZER BIONTECH COVID-19 VACCINE, PFIZER BIONTECH COVID-19 VACCINE, PFIZER BIONTECH COVID-19 VACCINE and Senior flu vaccine. Concurrent medical conditions included Asthma (She is on Symbicort which keeps her lungs under good condition), Allergy (Allergies), Arthritis, Hypertension (Her BP is fairly under control) and Depression (Treated for depression which is working very well). Concomitant products included BUDESONIDE, FORMOTEROL FUMARATE (SYMBICORT) for Asthma. On 19-Oct-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On an unknown date, the patient experienced THERAPEUTIC RESPONSE UNEXPECTED (The last 2 doses were Moderna and she claims that she was symptom free for at least 6 weeks after getting the doses). At the time of the report, THERAPEUTIC RESPONSE UNEXPECTED (The last 2 doses were Moderna and she claims that she was symptom free for at least 6 weeks after getting the doses) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter did not provide any causality assessments. Patient received fourth dose of Moderna on 22-APR-2022, with batch no being reported as 001M21A. Patient stated that she contracted Covid-19 in Mar2020 before she received the 1st dose of the Covid-19 vaccine which led to her having long Covid. The symptoms she mentions were fever and fatigue. She had been pretty much sick for 13 months and stated that she will be pretty lucky if she was 4 days symptom free but symptoms mentioned come back. The symptoms appeared when she was under a lot of stress like at the time of the call where she had now been taking Dayquil for 3-4 days. She was losing a lot of time at work. The 1st 3 doses were Pfizer and she claimed that she did not get relief of her long Covid symptoms after the shots. The last 2 doses were Moderna and she claims that she was symptom free for at least 6 weeks after getting the doses. Treatment information was not reported. Most recent FOLLOW-UP information incorporated above includes: On 14-Jun-2023: Live follow-up received and had no new information. On 14-Jun-2023: Follow-up received and added new event of unexpected therapeutic benefit and updated narrative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Therapeutic response unexpected
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy (Allergies); Arthritis; Asthma (She is on Symbicort which keeps her lungs under good condition); Depression (Treated for depression which is working very well); Hypertension (Her BP is fairly under control)
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: SYMBICORT
Allergien: -
Vorherige Impfungen: -

VAERS 2640436

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: WI
Alter: 65,0
Geschlecht: M
Eingang: 02.06.2023
Impfdatum: 21.10.2022
Beginn: 25.05.2023
Tage bis Beginn: 216,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Extra dose administered No adverse event

Symptomtext

Extra dose administered; No adverse event; Pharmacist states that they had 6 patients dosed with the bivalent vaccine which were administered one and two days beyond the BUD.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Pharmacist states that they had 6 patients dosed with the bivalent vaccine which were administered one and two days beyond the BUD.), EXTRA DOSE ADMINISTERED (Extra dose administered) and NO ADVERSE EVENT (No adverse event) in a 65-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch nos. AS7173B and AS7164B) for COVID-19 prophylaxis. No Medical History information was reported. On 21-Oct-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) .5 milliliter. On 25-May-2023, received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) dosage was changed to 1 dosage form. On 25-May-2023, the patient experienced EXPIRED PRODUCT ADMINISTERED (Pharmacist states that they had 6 patients dosed with the bivalent vaccine which were administered one and two days beyond the BUD.). On an unknown date, the patient experienced EXTRA DOSE ADMINISTERED (Extra dose administered) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Pharmacist states that they had 6 patients dosed with the bivalent vaccine which were administered one and two days beyond the BUD.), EXTRA DOSE ADMINISTERED (Extra dose administered) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Pharmacist states that they had 6 patients dosed with the bivalent vaccine which were administered one and two days beyond the BUD.) and EXTRA DOSE ADMINISTERED (Extra dose administered). No concomitant medication details was reported. The patient received the Moderna monovalent vaccine dose 1 on 05-Mar-2021, dose as unknown, route of administration as unknown, lot number 036A21A. The patient received the Moderna monovalent vaccine dose 2 on 02-Apr-2021, dose as unknown, route of administration as unknown, lot number 028A21A. The patient received the Moderna booster vaccine on 07-Dec-2021, dose as 0.25 ml, route of administration as unknown, lot number 031H21A. No treatment medication details was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-726797 (Linked Report). This case was linked to MOD-2023-726988 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 30-May-2023: Live Non-significant follow up information received. On 30-May-2023: Live Significant follow up information was received_Patient demography (initial, date of birth and age), Suspect product vaccine details (additional booster) and Narrative was updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-726797:Patient 1

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2636056

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: MD
Alter: 67,0
Geschlecht: F
Eingang: 24.05.2023
Impfdatum: 29.09.2022
Beginn: 21.03.2023
Tage bis Beginn: 173,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Exposure to SARS-CoV-2 Nasopharyngitis No adverse event SARS-CoV-2 test positive

Symptomtext

I did not have an adverse reaction to the vaccine. I was exposed to COVID-19 while on vacation. I tested positive for COVID-19 on 03/21/2023. I felt like it was a lingering cold. I contacted my doctor and got a prescription for Paxlovid. I tolerated the medication without any complications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 21MAR2023 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxine
Allergien: Diary; Penicillin
Vorherige Impfungen: -

VAERS 2617812

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 19.04.2023
Impfdatum: 19.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Intermenstrual bleeding

Symptomtext

Menstrual spotting randomly between cycles, between 2-7 days the past few months up to February.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intermenstrual bleeding
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Tylenol
Allergien: -
Vorherige Impfungen: -

VAERS 2613692

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: NJ
Alter: 69,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 25.09.2022
Beginn: 11.02.2023
Tage bis Beginn: 139,0
Dosis: 5
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cough Laboratory test abnormal Sinus congestion Sinusitis

Symptomtext

02/11/2023 I had a bad cough and sinus congestions. After testing positive for a sinus infection I was prescribed Amoxicillin and Prednisone. Symptoms lasted 3 weeks with lingering cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cough
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 2 Diabetes , High blood pressure; Coronary artery disease
Andere Medikamente: Atorvastatin; Lisinopril; Glimepiride
Allergien: N/A
Vorherige Impfungen: -

VAERS 2613683

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: MA
Alter: 57,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 07.10.2022
Beginn: 21.03.2023
Tage bis Beginn: 165,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Hypoaesthesia SARS-CoV-2 test positive

Symptomtext

3/21 had case of COVID-19 but reporting numbness that occurred after COVID-19. 4/2 began having numbness in my fingertips. Left side I went into my forearm, calves, and upper thigh. Right side starting at my collar bone and going all the way down. I experience the numbness on both sides but it is more pronounced on right side. Called PCP and they stated there was nothing that could be done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID-19 test positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Simvastatin
Allergien: Naproxen sodium
Vorherige Impfungen: -

VAERS 2610905

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: CO
Alter: 72,0
Geschlecht: F
Eingang: 06.04.2023
Impfdatum: 03.10.2022
Beginn: 12.12.2022
Tage bis Beginn: 70,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood urine present Cardiac monitoring normal Cystitis Electrocardiogram normal Full blood count normal Hemiparesis Magnetic resonance imaging normal Muscular weakness Transient ischaemic attack

Symptomtext

12/12/2023 I was on the phone and all of a sudden, I dropped the phone and had complete weakness in my left arm. I went to the ER, and I was diagnosed with a mini stroke (TIA), They gave me an EKG, MRI and a CBC, I was given a heart monitor to wear overnight for one month. The results were normal. I also want to report that I have had a bladder infection for the past 2 weeks and they have found blood in my urine. I am currently on antibiotics. I have a follow up appt with the Urologist on May 2nd.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood urine present
Hospital-Tage: -
Labordaten: 12Dec2022 EKG normal, 12Dec2022 MRI normal, 12Dec2022 CBC normal
Aktuelle Erkrankungen: None
Vorgeschichte: COPD
Andere Medikamente: Probiotic; multivitamin; OCUVITE; levothyroxine; atorvastatin; torsemide; RESTASIS; albuterol inhale; TRELEGY inhaler
Allergien: None
Vorherige Impfungen: -

VAERS 2610060

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 03.09.2022
Beginn: 03.12.2022
Tage bis Beginn: 91,0
Dosis: 5
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 5 vaccines Moderna 3/1/21 Lot# 010A21A; Moderna 3/29/21 Lot# 018B21A; Moderna 10/25/21 Lot# 02D621A; Moderna 3/31/22 Lot# 002M21A; Moderna 9/3/22 Lot# AS7164B

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2609389

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: WA
Alter: 74,0
Geschlecht: F
Eingang: 04.04.2023
Impfdatum: 03.10.2022
Beginn: 17.01.2023
Tage bis Beginn: 106,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chemotherapy Computerised tomogram pelvis Endometrial cancer Hysterectomy Scan Smear vagina Ultrasound scan Vaginal discharge

Symptomtext

It started with heavy vaginal discharge. I decided to go to the clinic to see what that was about; they did an endometriosis ultrasound, swabbing scan and a CT scan. They completed a hysterectomy procedure and additional swabbing for testing when they determined I had endometrial cancer (ferrous carcinoma), or practically uterine cancer. I'm currently undergoing chemotherapy for treatment in hopes of recovery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chemotherapy
Hospital-Tage: -
Labordaten: 17JAN2023 -- Ultrasound, CT Scan, & Endometriosis Scan
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Fosamax; Atorvastatin; Citracal; Vitamin D3; Vitamin C; Fish Oil; Loratadine; Melatonin
Allergien: Sulfa Drugs; Levaquin; Augmentin; Macrobid; Niaspan; Pepcid; Lopid; Ultram; Simvastatin; Cannabis-salve
Vorherige Impfungen: -

VAERS 2607993

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: FL
Alter: 70,0
Geschlecht: F
Eingang: 02.04.2023
Impfdatum: 28.09.2022
Beginn: 31.12.2022
Tage bis Beginn: 94,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Cough SARS-CoV-2 test positive

Symptomtext

Dry tickly cough and tiredness began 12/31/2022. Positive home test for Covid 19 on 1/1/2023.Went to Urgent Care on 1/2/2023, where positive test was confirmed. Started paxlovid and benzonate on 1/2/2023. Symptoms lessened by 1/5/2023 and resolved by 1/10/23. Negative home test on 1/8/2023. Overall symptoms were mild.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Home Covid 19 tests 1/1/2023 and 1/8/2023. Rapid test at Urgent care on 1/2/2023. (Vaccine given on 8/28/2022 was third booster.)
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: multivitamin, calcium
Allergien: no
Vorherige Impfungen: -

VAERS 2607554

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: NC
Alter: 69,0
Geschlecht: M
Eingang: 31.03.2023
Impfdatum: 26.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 5,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Atrial fibrillation Cardiac failure Cardiac operation

Symptomtext

I went for a year checkout, in October, the doctor sent me to the ER, in an ambulance; they kept me there for that evening. The Cardiologist gave instructions to transported me to another place. I was hospitalized for 4 days. I was diagnosed with atrial fibrillation; they gave me medicine. They gave me shot, that was in January. They schedule me to have in February a heart procedure,. My heart is functioning normally now, but I still being treated for a heart failure. I am taking a lot drugs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atrial fibrillation
Hospital-Tage: 4,0
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: COPD
Andere Medikamente: lisinopril;; atorvastatin; Omeprazole; Vitamin D; Multi Vitamins; Coq-10; Breztri
Allergien: Penicillin; Shellfish; Beat Stems
Vorherige Impfungen: -

VAERS 2607514

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 31.03.2023
Impfdatum: 29.09.2022
Beginn: 31.01.2023
Tage bis Beginn: 124,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Nasopharyngitis SARS-CoV-2 test positive

Symptomtext

1/31/2023 tested in the morning on an at home COVID-19 test, positive. Very mild cold symptoms. Televisit with doctor, who proscribed PAXLOVID. Symptoms lasted maybe 3 days with very mild cold symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 31Jan2023 at home COVID-19 test, positive.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Metoprolol succinate; lisinopril; tamsulosin; finasteride; hydrochlorothiazide; atorvastatin; gabapentin; calcium; multivitamin; vitamin D3; fish oil; coQ10; CLARITIN
Allergien: Bees; wasp stings
Vorherige Impfungen: -

VAERS 2606048

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: NC
Alter: 68,0
Geschlecht: M
Eingang: 29.03.2023
Impfdatum: 27.09.2022
Beginn: 28.12.2022
Tage bis Beginn: 92,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Brain injury Computerised tomogram head Hypoaesthesia Magnetic resonance imaging head abnormal Muscular weakness

Symptomtext

I woke up and the left side of my face felt numb. I had a small amount of weakness in my left arm. I got to the emergency room at 8AM. After about three hours, I had an MRI and had already had a CT scan.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Brain injury
Hospital-Tage: 1,0
Labordaten: 28DEC2023 MRI, one centimeter of damage to right side of thalamus; 28DEC2023 CT scan, doesn't remember results
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: SKELAXIN; SINGULAIR; ZETIA; XANAX; omeprazole
Allergien: N/A
Vorherige Impfungen: Pfizer 11/5/2021, I had a deep vein thrombosis 2 days later and has since been resolved

VAERS 2606007

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: MA
Alter: 55,0
Geschlecht: F
Eingang: 29.03.2023
Impfdatum: 27.09.2022
Beginn: 06.03.2023
Tage bis Beginn: 160,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Basal cell carcinoma Biopsy skin abnormal

Symptomtext

3/6/23 I was at my yearly dermatology appointment. I had a spot on my face which was biopsied and diagnosed with basal cell carcinoma from sun damage. I am supposed to have Mohs Surgery on May 1, 2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Basal cell carcinoma
Hospital-Tage: -
Labordaten: 8MAR23 Biopsy of spot on face, Basal Cell Carcinoma
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes; Genital Herpes
Andere Medikamente: VALTREX; multivitamin; vitamin D; vitamin B complex; calcium magnesium zinc; vitamin K; vitamin C; zinc.
Allergien: CIPRO; sulfa drugs; adhesives; shellfish; raw onions; eggplant; amoxicillin
Vorherige Impfungen: -

VAERS 2605038

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: PA
Alter: 43,0
Geschlecht: M
Eingang: 28.03.2023
Impfdatum: 22.09.2022
Beginn: 15.01.2023
Tage bis Beginn: 115,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Audiogram abnormal Deafness unilateral Magnetic resonance imaging normal Tinnitus

Symptomtext

In Jan 2023 I started experiencing a constant humming sound in my left ear. I visited an ENT and had a audiometry exam. It was confirmed that I have a significant amount of hearing loss in my left ear specifically high pitches. I was diagnosed with Tinnitus and have a follow up scheduled with an Audiology specialist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Audiogram abnormal
Hospital-Tage: -
Labordaten: 15Jan2023 MRI normal, 15Jan2023 Audiometry exam, hearing loss left ear.
Aktuelle Erkrankungen: None
Vorgeschichte: Lumbago (lower back pain)
Andere Medikamente: Atorvastatin; rabeprazole
Allergien: Sulfa drugs; cyclin drugs; cefprozil; ibuprofen; ADVIL; aspirin
Vorherige Impfungen: -

VAERS 2603983

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: MD
Alter: 42,0
Geschlecht: F
Eingang: 27.03.2023
Impfdatum: 23.09.2022
Beginn: 09.12.2022
Tage bis Beginn: 77,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Cough Epistaxis Influenza virus test negative Nasopharyngitis Respiratory syncytial virus test negative Respiratory tract congestion SARS-CoV-2 test negative Sinusitis

Symptomtext

Around December 9, I began having cold symptoms. Symptoms did not improve and I began having nose bleeds when I would cough. I went to urgent care and was diagnosed with a sinus infection. I was prescribed amoxicillin and told to switch to Claritin from Zyrtec. Completed course of Amoxicillin and symptoms improved during treatment but returned much worse when antibiotic was completed. Returned to a different urgent care clinic and was tested for Flu, RSV, and COVID-19, all were negative. They stated that the sinus infection was still present and was prescribed augmentin, sudafed , and nasal rinse with saline. After completing augmentin I continued with sudafed and nasal rinse due to residual congestion. Congestion cleared up around the end of January.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cough
Hospital-Tage: -
Labordaten: Flu Negative, RSV Negative, COVID-19 Negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin; Calcium; Iron; ZYRTEC
Allergien: None
Vorherige Impfungen: 3/10/2021 Johnson and Johnson COVID-19 vaccine. Pain at injection site, abdomen, and down leg.

VAERS 2602657

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: VA
Alter: 62,0
Geschlecht: F
Eingang: 23.03.2023
Impfdatum: 21.09.2022
Beginn: 27.01.2023
Tage bis Beginn: 128,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cough Laboratory test Nasopharyngitis Productive cough

Symptomtext

I thought it was a very bad cold but after taking OTC medication it didn't get any better. I had a bad cough and lots of phlegm, I saw my doctor and tested for COVID but it was negative and I went home. After a few days I called again because it was getting worse and I was prescribed an antibiotic Cefuroxime Acetyl 250MG tablets I had to take twice a day for 10 days. I had an appointment with my pulmonologist and let him know the antibiotic wasn't working so he upped the dosage of the same medication as well as added steroids'. Afterwards I felt fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cough
Hospital-Tage: -
Labordaten: Yes; Not listed
Aktuelle Erkrankungen: None
Vorgeschichte: Stage 2 Kidney Disease
Andere Medikamente: Yes; Not listed
Allergien: None
Vorherige Impfungen: -

VAERS 2591893

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: HI
Alter: 76,0
Geschlecht: M
Eingang: 06.03.2023
Impfdatum: 30.09.2022
Beginn: 01.11.2022
Tage bis Beginn: 32,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac monitoring abnormal Peripheral swelling Sinus arrest

Symptomtext

In November 2022, my cardiologist had his physician's assistant call me to schedule a time to have me come in to have a heart monitor put on for two weeks. I was able to get in January 2023 and wear the monitor and go back in for the results. I had a telehealth conference for the results, I was notified that my heart had paused over one thousand times. I was asked if I had passed out or fainted during the two-week period. We scheduled to have a pacemaker put in the second Thursday of March. I am feeling better although I really did not feel bad before, I was trying to find out why my leg was swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac monitoring abnormal
Hospital-Tage: -
Labordaten: Heart monitor
Aktuelle Erkrankungen: No
Vorgeschichte: A-Fib; Emphysema
Andere Medikamente: ELIQUIS; amlodipine; potassium; colon health 4 in 1; furosemide; losartan; carvedilol; oxybutynin; pravastatin; vitamin D3; coQ10; vitamin E; zinc; vitamin B-6; VICTOZA; TRESIBA
Allergien: No
Vorherige Impfungen: -

VAERS 2554843

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 06.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough

Symptomtext

Mild COVID infection with cough. Treated with paxlovid. Improvement in 24 hours. Symptom free in 48 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2551450

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 02.10.2022
Beginn: 03.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac monitoring normal Heart rate increased Laboratory test normal

Symptomtext

Rapid heartbeat lasted through evening, elevated during simply daily activities. Prescribed heart monitor. Awaiting test results.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac monitoring normal
Hospital-Tage: -
Labordaten: Lab work and test indicate normal readings
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure; high cholesterol
Andere Medikamente: Multivitamin; flaxseed oil; simvastatin; baby aspirin; omeprazole; glucosamine hydrochloride
Allergien: Sulfa; PERCOCET; VICODIN
Vorherige Impfungen: -

VAERS 2545894

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 23.09.2022
Beginn: 26.12.2022
Tage bis Beginn: 94,0
Dosis: 5
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Rhinorrhoea SARS-CoV-2 test Sneezing

Symptomtext

I have a runny nose with sneezing. Horrible cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cough
Hospital-Tage: -
Labordaten: COVID-19 antigen test, PCR test 12/26/2022
Aktuelle Erkrankungen: No
Vorgeschichte: Thyroid; High Cholesterol
Andere Medikamente: Black seed oil; FLONASE mist; levothyroxine; loratadine; omeprazole; simvastatin; sodium chloride; vitamin D; CENTRUM woman's multivitamin
Allergien: Side affect to KEFLEX; Tetanus vaccine; colchicine
Vorherige Impfungen: Tetanus

VAERS 2544665

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: IL
Alter: 60,0
Geschlecht: M
Eingang: 28.12.2022
Impfdatum: 27.09.2022
Beginn: 06.12.2022
Tage bis Beginn: 70,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Exposure to SARS-CoV-2 Rhinorrhoea SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

I had a runny nose and a cough but this is not unusual for me this time of year, my wife however, did test positive for COVID-19, this prompted me to test as well. I began testing on 12/06/2022 and tested daily until 12/10/2022 at 2AM I tested positive for the COVID-19 virus. I took PAXLOVID and I have recovered from the COVID-19 virus and back to my normal self.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID-19 tests negative started on 12/06/2022 negative until 12/10/2022 which resulted in positive. Negative result on 12/16/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; Heart disease
Andere Medikamente: Vitamin C; vitamin E; vitamin D; nifedipine; levocetirizine; meloxicam; aspirin; atorvastatin; metoprolol
Allergien: Penicillin; sulfa
Vorherige Impfungen: -

VAERS 2537772

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: NY
Alter: 70,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 17.09.2022
Beginn: 15.11.2022
Tage bis Beginn: 59,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

11/15/2022 late in the evening I developed a runny nose. 11/16 tickle in the throat, and increased volume of nasal drainage. 11/17 Tele-visit with doctor as at home COVID-19 test was positive. Doctor recommended treating symptomatically and resting. Symptoms lasted until at least 11/30 with head congestion. Symptoms tapered off into nothing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 11/17 at home COVID-19 test was positive.
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure; Coronary Artery Disease
Andere Medikamente: Clopidogrel; ethyl eicosapentaenoic acid; TOPROL; lisinopril; atorvastatin; low dose aspirin; SYNTHROID; ZETIA; VALTREX; amlodipine; coQ10; vitamin D3
Allergien: Mango; papaya; codfish; dust; mold; cats
Vorherige Impfungen: -

VAERS 2528874

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: AR
Alter: 92,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 19.10.2022
Beginn: 09.12.2022
Tage bis Beginn: 51,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test positive

Symptomtext

hospitalized with covid; fully vaccinated with 2 boosters

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: positive covid pcr 12/7/22
Aktuelle Erkrankungen: unknown
Vorgeschichte: Coronary Artery Disease, Hyperlipidemia, Hypertension, Peptic Ulcer Disease, Reflux, Thyroid and Other (Chronic neck and back pain; A-fib; Fibromyalgia; Osteoporosis)
Andere Medikamente: unknown
Allergien: aspirin, morphine, IV dye
Vorherige Impfungen: -

VAERS 2528381

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

gering

Staat: MA
Alter: 36,0
Geschlecht: M
Eingang: 10.12.2022
Impfdatum: 11.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 16,0
Dosis: 4
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Tinnitus

Symptomtext

Tinnitus that lasted approximately 1.5 months. Treatment is to monitor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid, end of July 2022
Vorgeschichte: None
Andere Medikamente: Claritin 10mg Famotidine 20mg
Allergien: Ceclor, Supprax, Cipro
Vorherige Impfungen: -

VAERS 2516898

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

gering

Staat: IL
Alter: 82,0
Geschlecht: M
Eingang: 25.11.2022
Impfdatum: 14.10.2022
Beginn: 15.11.2022
Tage bis Beginn: 32,0
Dosis: 5
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test COVID-19 Chest X-ray Chest discomfort Cough Electrocardiogram Rhinorrhoea SARS-CoV-2 test positive Sneezing Symptom recurrence

Symptomtext

One month after latest booster protecting from Omicron I had Covid (a different variant, possible BQ 1 or BQ1.11. After 5 days on an antiviral medication I no longer had symptoms: hacki.ng dry cough, sneezing, runny nose, tightness in chest. Three days later the symptoms returned . treated in ER and was told I now have rebound Covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: PCR EKG, chest x-ray, blood work,
Aktuelle Erkrankungen: None
Vorgeschichte: Afib, PE, HT,MVP, OAB, Lumbar fusion, bilateral hip replacements, dry eyes chronic back pain
Andere Medikamente: Eliquis, Losartan, Metoprolol, Amlodipine, Duloxetine, Tizanidine, Bethanechol, Myrbetriq, Prolia, Calcium citrate, Vitamin D3, Atorvastatin, Restasis
Allergien: Levaquin, Ceftin
Vorherige Impfungen: -

VAERS 2483892

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

gering

Staat: OH
Alter: 74,0
Geschlecht: M
Eingang: 22.11.2022
Impfdatum: 06.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anticoagulant therapy Atrial fibrillation Cardiac flutter Electrocardiogram abnormal Muscular weakness

Symptomtext

A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster; A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster; This spontaneous case was reported by a patient and describes the occurrence of the first episode of ATRIAL FIBRILLATION (A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster) and the second episode of ATRIAL FIBRILLATION (A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster) in a 74-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. Co-suspect product included non-company product INFLUENZA VACCINE (FLU VACCINE VII) for an unknown indication. Concurrent medical conditions included Blood pressure high. Concomitant products included CARVEDILOL, LOSARTAN and AMLODIPINE for Blood pressure high. On 06-Oct-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form and dose of INFLUENZA VACCINE (FLU VACCINE VII) (unknown route) 1 dosage form. On 06-Oct-2022 at 6:00 PM, the patient experienced the first episode of ATRIAL FIBRILLATION (A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster) (seriousness criterion medically significant). On an unknown date, the patient experienced the second episode of ATRIAL FIBRILLATION (A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster) (seriousness criterion medically significant). The patient was treated with APIXABAN (ELIQUIS) at an unspecified dose and frequency. At the time of the report, last episode of ATRIAL FIBRILLATION (A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster) had not resolved. It was reported that patient received 5 shots of Moderna COVID-19 vaccine. Shot 1: First Primary monovalent dose on 04-FEB-2021 (Lot number- 026L20A & Exp. Date: unknown). Shot 2: 2nd Primary monovalent dose on 04-MAR-2021 (Lot number- 013A21A & Exp. Date: unknown). Shot 3: First Monovalent Booster dose on 27-OCT-2021 (Lot number- 003F21A & Exp. Date unknown). Shot 4: 2nd Monovalent Booster dose on 20-APR-2022 (Lot number- 005M21A & Exp. Date: unknown). Patient had bivalent and Flu shot at the same time (12 noon) in different arms. It was reported that on 6-oct-2022 at 6 PM his apple watch notified him that he had atrial fibrillation. He called his Cardiologist who told him to go to the emergency room. He visited the ER and they started him on Eliquis. He was fine after that. He had second atrial fibrillation on Nov-2022 since then the doctor had some procedures that will be done in Dec-2022. He stated that he saw on the internet and some friends also had Atrial fibrillation after receiving the Bivalent booster. He is not sure if there was any mention of Myocarditis or Pericarditis. He is not sure if those other people had a Flu vaccine and the Bivalent Booster at the same time. His doctor did not mention anything about Myocarditis. They only spoke about Atrial fibrillation. Company Comment :This spontaneous case concerns a 74 year old male with hypertension who experienced the unexpected, serious (medically significant) adverse event of special interest Atrial fibrillation a few hours after receiving a dose of mRNA1273 bivalent BA .4/5 as fifth dose in the COVID-19 vaccine series. The patient experienced sudden onset atrial fibrillation post vaccination notified to him by a device. He was advised by his cardiologist to visit the emergency department for evaluation. The patient was started on eliquis and was eventually discharged. The patient had another episode of atrial fibrillation approximately a month after the initial incident and was scheduled for ancillary procedures the next month. Further details on the clinical course and additional treatment were not provided. The patient's advanced age and concurrent hypertension may be considered as risk factors for atrial fibrillation. The benefit-risk relationship of mRNA-1273 is not affected by this report. Event seriousness assessed as per medical judgment. This case was linked to US-MODERNATX, INC.-MOD-2022-673920, US-MODERNATX, INC.-MOD-2022-673920 (Linked Report).; Sender's Comments: This spontaneous case concerns a 74 year old male with hypertension who experienced the unexpected, serious (medically significant) adverse event of special interest Atrial fibrillation a few hours after receiving a dose of mRNA1273 bivalent BA .4/5 as fifth dose in the COVID-19 vaccine series. The patient experienced sudden onset atrial fibrillation post vaccination notified to him by a device. He was advised by his cardiologist to visit the emergency department for evaluation. The patient was started on eliquis and was eventually discharged. The patient had another episode of atrial fibrillation approximately a month after the initial incident and was scheduled for ancillary procedures the next month. Further details on the clinical course and additional treatment were not provided. The patient's advanced age and concurrent hypertension may be considered as risk factors for atrial fibrillation. The benefit-risk relationship of mRNA-1273 is not affected by this report. Event seriousness assessed as per medical judgment. US-MODERNATX, INC.-MOD-2022-673920:Same reporter US-MODERNATX, INC.-MOD-2022-673920:Same reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anticoagulant therapy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure high
Vorgeschichte: -
Andere Medikamente: CARVEDILOL; LOSARTAN; AMLODIPINE
Allergien: -
Vorherige Impfungen: -

VAERS 2483892

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: OH
Alter: 74,0
Geschlecht: M
Eingang: 22.11.2022
Impfdatum: 06.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anticoagulant therapy Atrial fibrillation Cardiac flutter Electrocardiogram abnormal Muscular weakness

Symptomtext

A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster; A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster; This spontaneous case was reported by a patient and describes the occurrence of the first episode of ATRIAL FIBRILLATION (A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster) and the second episode of ATRIAL FIBRILLATION (A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster) in a 74-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. Co-suspect product included non-company product INFLUENZA VACCINE (FLU VACCINE VII) for an unknown indication. Concurrent medical conditions included Blood pressure high. Concomitant products included CARVEDILOL, LOSARTAN and AMLODIPINE for Blood pressure high. On 06-Oct-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form and dose of INFLUENZA VACCINE (FLU VACCINE VII) (unknown route) 1 dosage form. On 06-Oct-2022 at 6:00 PM, the patient experienced the first episode of ATRIAL FIBRILLATION (A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster) (seriousness criterion medically significant). On an unknown date, the patient experienced the second episode of ATRIAL FIBRILLATION (A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster) (seriousness criterion medically significant). The patient was treated with APIXABAN (ELIQUIS) at an unspecified dose and frequency. At the time of the report, last episode of ATRIAL FIBRILLATION (A-Fib after Bivalent Booster/2nd A-fib since received a combination of Bivalent Booster) had not resolved. It was reported that patient received 5 shots of Moderna COVID-19 vaccine. Shot 1: First Primary monovalent dose on 04-FEB-2021 (Lot number- 026L20A & Exp. Date: unknown). Shot 2: 2nd Primary monovalent dose on 04-MAR-2021 (Lot number- 013A21A & Exp. Date: unknown). Shot 3: First Monovalent Booster dose on 27-OCT-2021 (Lot number- 003F21A & Exp. Date unknown). Shot 4: 2nd Monovalent Booster dose on 20-APR-2022 (Lot number- 005M21A & Exp. Date: unknown). Patient had bivalent and Flu shot at the same time (12 noon) in different arms. It was reported that on 6-oct-2022 at 6 PM his apple watch notified him that he had atrial fibrillation. He called his Cardiologist who told him to go to the emergency room. He visited the ER and they started him on Eliquis. He was fine after that. He had second atrial fibrillation on Nov-2022 since then the doctor had some procedures that will be done in Dec-2022. He stated that he saw on the internet and some friends also had Atrial fibrillation after receiving the Bivalent booster. He is not sure if there was any mention of Myocarditis or Pericarditis. He is not sure if those other people had a Flu vaccine and the Bivalent Booster at the same time. His doctor did not mention anything about Myocarditis. They only spoke about Atrial fibrillation. Company Comment :This spontaneous case concerns a 74 year old male with hypertension who experienced the unexpected, serious (medically significant) adverse event of special interest Atrial fibrillation a few hours after receiving a dose of mRNA1273 bivalent BA .4/5 as fifth dose in the COVID-19 vaccine series. The patient experienced sudden onset atrial fibrillation post vaccination notified to him by a device. He was advised by his cardiologist to visit the emergency department for evaluation. The patient was started on eliquis and was eventually discharged. The patient had another episode of atrial fibrillation approximately a month after the initial incident and was scheduled for ancillary procedures the next month. Further details on the clinical course and additional treatment were not provided. The patient's advanced age and concurrent hypertension may be considered as risk factors for atrial fibrillation. The benefit-risk relationship of mRNA-1273 is not affected by this report. Event seriousness assessed as per medical judgment. This case was linked to US-MODERNATX, INC.-MOD-2022-673920, US-MODERNATX, INC.-MOD-2022-673920 (Linked Report).; Sender's Comments: This spontaneous case concerns a 74 year old male with hypertension who experienced the unexpected, serious (medically significant) adverse event of special interest Atrial fibrillation a few hours after receiving a dose of mRNA1273 bivalent BA .4/5 as fifth dose in the COVID-19 vaccine series. The patient experienced sudden onset atrial fibrillation post vaccination notified to him by a device. He was advised by his cardiologist to visit the emergency department for evaluation. The patient was started on eliquis and was eventually discharged. The patient had another episode of atrial fibrillation approximately a month after the initial incident and was scheduled for ancillary procedures the next month. Further details on the clinical course and additional treatment were not provided. The patient's advanced age and concurrent hypertension may be considered as risk factors for atrial fibrillation. The benefit-risk relationship of mRNA-1273 is not affected by this report. Event seriousness assessed as per medical judgment. US-MODERNATX, INC.-MOD-2022-673920:Same reporter US-MODERNATX, INC.-MOD-2022-673920:Same reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anticoagulant therapy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure high
Vorgeschichte: -
Andere Medikamente: CARVEDILOL; LOSARTAN; AMLODIPINE
Allergien: -
Vorherige Impfungen: -

VAERS 2509666

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: MI
Alter: 36,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 29.09.2022
Beginn: 02.10.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Hypertensive crisis

Symptomtext

Hypertensive Crisis OCT 2nd 2022 - 195/138 BP OCT 27th 2022- 209/143 BP OCT 29th 2022 - 167/101 Normal BP for me 110/70

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertensive crisis
Hospital-Tage: -
Labordaten: PCM follow up once back in town. Was working in remote area and only in town briefly. Retired nurse with photo documentation of pressures. Unable to access emergency care due to extremely remote location with 2hr+ ambulance drive. BP came down with prolonged hot shower, hydration, and use of robaxin.
Aktuelle Erkrankungen: -
Vorgeschichte: Ehler Danlos Syndrome
Andere Medikamente: Meloxicam 15mg, nurtec 75m
Allergien: None
Vorherige Impfungen: -

VAERS 2497113

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

gering

Staat: WA
Alter: 62,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 29.10.2022
Beginn: 29.10.2022
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 Wrong product administered

Symptomtext

No adverse event; Patient received updated booster before primary series/Patient received the Moderna bivalent vaccine instead of the first dose of her Moderna primary series vaccine.; This spontaneous case was reported by a pharmacist and describes the occurrence of WRONG PRODUCT ADMINISTERED (Patient received updated booster before primary series/Patient received the Moderna bivalent vaccine instead of the first dose of her Moderna primary series vaccine.) and NO ADVERSE EVENT (No adverse event) in a 62-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. No Medical History information was reported. On 29-Oct-2022, the patient received first dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 29-Oct-2022, the patient experienced WRONG PRODUCT ADMINISTERED (Patient received updated booster before primary series/Patient received the Moderna bivalent vaccine instead of the first dose of her Moderna primary series vaccine.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, WRONG PRODUCT ADMINISTERED (Patient received updated booster before primary series/Patient received the Moderna bivalent vaccine instead of the first dose of her Moderna primary series vaccine.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for WRONG PRODUCT ADMINISTERED (Patient received updated booster before primary series/Patient received the Moderna bivalent vaccine instead of the first dose of her Moderna primary series vaccine.). Concomitant medications were not reported. The patient signed up to receive the Moderna Covid-19 vaccine bivalent dose on 31OCT2022. Patient was accidentally vaccinated on 29-Oct-2022 with Moderna COVID-19 Vaccine Bivalent before getting the primary series. No treatment information was provided by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 31-Oct-2022: Live Follow-up received include :Suspect (Moderna Bivalent) Date of administration updated On 31-Oct-2022: Live Follow-up received include : Patient details updated, Suspect (Moderna Vaccine ) lot number added.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2484354

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 15.10.2022
Beginn: 15.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Product leakage

Symptomtext

While administering the vaccine a portion "leaked out" either from the injection site or barrel of syringe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product leakage
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2484273

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

gering

Staat: NJ
Alter: 60,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 20.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Device leakage Product administration error Underdose

Symptomtext

administration error: upon pushing out the liquid inside the syringe, it leaked out of the junction between the needle and syringe

Weitere VAERSDATA-Felder

Praegender Schweregrund: Device leakage
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2483651

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: OR
Alter: 80,0
Geschlecht: M
Eingang: 20.10.2022
Impfdatum: 17.10.2022
Beginn: 17.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Incorrect route of product administration No adverse event

Symptomtext

No adverse event; The dose was administered using a 5/8ths inch needle and was suspected to have been given not by intramuscular injection; This spontaneous case was reported by a pharmacist and describes the occurrence of INCORRECT ROUTE OF PRODUCT ADMINISTRATION (The dose was administered using a 5/8ths inch needle and was suspected to have been given not by intramuscular injection) and NO ADVERSE EVENT (No adverse event) in an 80-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer COVID-19 vaccine (Dose 1), Pfizer COVID-19 vaccine (Dose 3) and Pfizer COVID-19 vaccine (Dose 2). Past adverse reactions to the above products included No adverse event with Pfizer COVID-19 vaccine, Pfizer COVID-19 vaccine and Pfizer COVID-19 vaccine. On 17-Oct-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 17-Oct-2022, the patient experienced INCORRECT ROUTE OF PRODUCT ADMINISTRATION (The dose was administered using a 5/8ths inch needle and was suspected to have been given not by intramuscular injection). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, INCORRECT ROUTE OF PRODUCT ADMINISTRATION (The dose was administered using a 5/8ths inch needle and was suspected to have been given not by intramuscular injection) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for INCORRECT ROUTE OF PRODUCT ADMINISTRATION (The dose was administered using a 5/8ths inch needle and was suspected to have been given not by intramuscular injection). No concomitant medications were provided. The patient received 4th dose of the Moderna COVID-19 vaccine on 16-Apr-2022. No symptoms were reported. No additional doses, medications, or treatments taken at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect route of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2483546

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 25.09.2022
Beginn: 10.10.2022
Tage bis Beginn: 15,0
Dosis: 5
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 SARS-CoV-2 antibody test positive

Symptomtext

Tested positive for Covid

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: SARS CoV-2 Rapid ag, with POSITIVE result.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, Low platelets
Andere Medikamente: Atacand 32 , Atorvastatin, Amlodopine, Synthroid.
Allergien: Gluten
Vorherige Impfungen: -

VAERS 2483487

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

gering

Staat: CO
Alter: 6,0
Geschlecht: M
Eingang: 19.10.2022
Impfdatum: 19.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injury associated with device

Symptomtext

vaccinating technician has a puncture wound from needle after vaccination given ("needle-stick")

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injury associated with device
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none known
Vorgeschichte: none known
Andere Medikamente: none known
Allergien: none known
Vorherige Impfungen: -

VAERS 2475129

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

gering

Staat: NJ
Alter: 63,0
Geschlecht: F
Eingang: 12.10.2022
Impfdatum: 01.10.2022
Beginn: 10.10.2022
Tage bis Beginn: 9,0
Dosis: 4
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Extra dose administered Inappropriate schedule of product administration No adverse event SARS-CoV-2 test

Symptomtext

No adverse event; Patient had the Moderna bivalent booster on 01Oct22 and 10Oct2022; Patient had the Moderna bivalent booster on 01Oct22 and 10Oct2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXTRA DOSE ADMINISTERED (Patient had the Moderna bivalent booster on 01Oct22 and 10Oct2022), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient had the Moderna bivalent booster on 01Oct22 and 10Oct2022) and NO ADVERSE EVENT (No adverse event) in a 63-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch nos. 060F22A and AS7164B) for COVID-19 prophylaxis. The patient's past medical history included COVID-19 (April or May 2022 (Treatment received: Paxlovid)) in 2022. Concomitant products included INFLUENZA VACCINE for Flu vaccination, MONTELUKAST SODIUM (SINGULAIR), LEVOCETIRIZINE DIHYDROCHLORIDE (ALLEGRA [LEVOCETIRIZINE DIHYDROCHLORIDE]) and ALENDRONATE SODIUM (FOSAMAX) for an unknown indication. On 01-Oct-2022, the patient received fourth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) .5 milliliter. On 10-Oct-2022, received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) dosage was changed to .5 milliliter. On 10-Oct-2022, the patient experienced EXTRA DOSE ADMINISTERED (Patient had the Moderna bivalent booster on 01Oct22 and 10Oct2022) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient had the Moderna bivalent booster on 01Oct22 and 10Oct2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXTRA DOSE ADMINISTERED (Patient had the Moderna bivalent booster on 01Oct22 and 10Oct2022), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient had the Moderna bivalent booster on 01Oct22 and 10Oct2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2022, SARS-CoV-2 test: (Positive) Positive. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXTRA DOSE ADMINISTERED (Patient had the Moderna bivalent booster on 01Oct22 and 10Oct2022) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient had the Moderna bivalent booster on 01Oct22 and 10Oct2022). No Other vaccines given within 1 month prior to Moderna COVID-19 vaccine. On 17-MAR-2021 patient has received First Moderna dose of 0.5 mL with lot no. 047A21A. On 14-APR-2021 patient has received Second Moderna dose of 0.5 mL with lot no. 040B21A. On 16-NOV-2021 patient has received First Moderna Booster dose with lot no. 051F21a. No treatment information was reported with respect to 4th and 5th Bivalent Booster dose. This case was linked to MOD-2022-656967 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: Test Date: 2022; Test Name: COVID Test; Test Result: Positive ; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (April or May 2022 (Treatment received: Paxlovid))
Andere Medikamente: INFLUENZA VACCINE; SINGULAIR; ALLEGRA [LEVOCETIRIZINE DIHYDROCHLORIDE]; FOSAMAX
Allergien: -
Vorherige Impfungen: -

VAERS 2475124

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

gering

Staat: AR
Alter: 22,0
Geschlecht: F
Eingang: 12.10.2022
Impfdatum: 06.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Maternal exposure during pregnancy No adverse event Wrong product administered

Symptomtext

No adverse event; Pregnant patient received a bivalent booster dose as a first dose of the Moderna COVID19 vaccine; Maternal exposure during pregnancy; This spontaneous prospective pregnancy case was reported by a pharmacist and describes the occurrence of WRONG PRODUCT ADMINISTERED (Pregnant patient received a bivalent booster dose as a first dose of the Moderna COVID19 vaccine), MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy) and NO ADVERSE EVENT (No adverse event) in a 22-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. No Medical History information was reported. On 06-Oct-2022, the patient received first dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 06-Oct-2022, the patient experienced WRONG PRODUCT ADMINISTERED (Pregnant patient received a bivalent booster dose as a first dose of the Moderna COVID19 vaccine) and MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). On 06-Oct-2022, MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy) had resolved. At the time of the report, WRONG PRODUCT ADMINISTERED (Pregnant patient received a bivalent booster dose as a first dose of the Moderna COVID19 vaccine) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for WRONG PRODUCT ADMINISTERED (Pregnant patient received a bivalent booster dose as a first dose of the Moderna COVID19 vaccine) and MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy). No concomitant and treatment medications were reported. Pregnant patient received a bivalent booster dose as a first dose of the Moderna COVID19 vaccine. Company comment: This spontaneous case concerns a 22-year-old female patient, with no medical history reported, who experienced maternal exposure during pregnancy with no adverse events associated, after a booster dose of mRNA-1273.222 vaccine (no information about previous vaccination schedule was provided). Gestational age, last menstrual period and estimated date of delivery were not reported. Pregnancy outcome not available. No further clinical information was provided for medical reviewing. Additionally, wrong product administrated was considered in the case since patient received a bivalent booster dose as a first dose. The benefit-risk relationship of the mRNA-1273.222 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 22-year-old female patient, with no medical history reported, who experienced maternal exposure during pregnancy with no adverse events associated, after a booster dose of mRNA-1273.222 vaccine (no information about previous vaccination schedule was provided). Gestational age, last menstrual period and estimated date of delivery were not reported. Pregnancy outcome not available. No further clinical information was provided for medical reviewing. Additionally, wrong product administrated was considered in the case since patient received a bivalent booster dose as a first dose. The benefit-risk relationship of the mRNA-1273.222 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Maternal exposure during pregnancy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2475019

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

gering

Staat: VT
Alter: 70,0
Geschlecht: M
Eingang: 12.10.2022
Impfdatum: 10.10.2022
Beginn: 10.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered No adverse event Product storage error

Symptomtext

vial was initially stored in the refrigerator on 08Oct2022, vial was first punctured on 08Oct2022 around 9 AM, administration of vaccine on 10Oct2022 at 12 PM; no adverse event; received a dose 12 hours after puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received a dose 12 hours after puncture), PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 08Oct2022, vial was first punctured on 08Oct2022 around 9 AM, administration of vaccine on 10Oct2022 at 12 PM) and NO ADVERSE EVENT (no adverse event) in a 70-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer (Dose 2) and Pfizer (Dose 1). Past adverse reactions to the above products included No adverse event with Pfizer and Pfizer. On 10-Oct-2022 at 12:00 PM, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 10-Oct-2022 at 12:00 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (received a dose 12 hours after puncture). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 08Oct2022, vial was first punctured on 08Oct2022 around 9 AM, administration of vaccine on 10Oct2022 at 12 PM) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (received a dose 12 hours after puncture), PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 08Oct2022, vial was first punctured on 08Oct2022 around 9 AM, administration of vaccine on 10Oct2022 at 12 PM) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (received a dose 12 hours after puncture) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 08Oct2022, vial was first punctured on 08Oct2022 around 9 AM, administration of vaccine on 10Oct2022 at 12 PM). Concomitant medications were not reported. Vial size was 2.5 ml. The vial stored at room temperature post puncture and did not undergo any temperature excursions. Total amount of time the vial was exposed to room temperature range for 48 hours. Treatment medications were not reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2473120

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: AR
Alter: 22,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 06.10.2022
Beginn: 06.10.2022
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 Wrong product administered

Symptomtext

No Adverse event; received bivalent booster instead of primary dose one; This spontaneous case was reported by a pharmacist and describes the occurrence of WRONG PRODUCT ADMINISTERED (received bivalent booster instead of primary dose one) and NO ADVERSE EVENT (No Adverse event) in a 22-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 vaccination. No Medical History information was reported. On 06-Oct-2022, the patient received first dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 06-Oct-2022, the patient experienced WRONG PRODUCT ADMINISTERED (received bivalent booster instead of primary dose one). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse event). At the time of the report, WRONG PRODUCT ADMINISTERED (received bivalent booster instead of primary dose one) and NO ADVERSE EVENT (No Adverse event) outcome was unknown. The action taken with mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown) was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No Adverse event) to be not related. No further causality assessment was provided for WRONG PRODUCT ADMINISTERED (received bivalent booster instead of primary dose one). No concomitant medications were reported. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 06-Oct-2022: Live Significant information received- Narrative updated, Reporter Additional mail id added.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2472699

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

gering

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 08.10.2022
Impfdatum: 08.10.1922
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Incorrect product formulation administered

Symptomtext

Pt was given the Moderna bivalent booster instead of the flu shot, no symptoms were seen at time of incident, pt previously recieved two doses of pfizer with last dose adminstered more than 2 months ago.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: none
Vorherige Impfungen: -

VAERS 2472282

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

gering

Staat: IL
Alter: 57,0
Geschlecht: M
Eingang: 07.10.2022
Impfdatum: 06.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Inappropriate schedule of product administration No adverse event

Symptomtext

No adverse event; Patient received the bivalent booster as their first dose; This spontaneous case was reported by a pharmacist and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received the bivalent booster as their first dose) and NO ADVERSE EVENT (No adverse event) in a 57-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 vaccination. No Medical History information was reported. On 06-Oct-2022, the patient received first dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) .5 milliliter. On 06-Oct-2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received the bivalent booster as their first dose). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received the bivalent booster as their first dose) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received the bivalent booster as their first dose). No concomitant medication information was provided. It was reported that patient received bivalent product for first dose instead of monovalent dose. No treatment medication were provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2471313

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

gering

Staat: NY
Alter: 76,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 03.10.2022
Beginn: 03.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Oral discomfort Tongue discomfort

Symptomtext

lips burning; tongue burning; This spontaneous case was reported by a patient and describes the occurrence of ORAL DISCOMFORT (lips burning) and TONGUE DISCOMFORT (tongue burning) in a 76-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 vaccination. The patient never had COVID positive test or diagnosis. Previously administered products included for Flu: Flu vaccine (Last year). Past adverse reactions to the above products included No adverse event with Flu vaccine. Concurrent medical conditions included Penicillin allergy, Drug allergy (Sulfa allergy), Allergy to nuts (hazel nuts) and Blood pressure high (diagnosed prior to getting the vaccine). Concomitant products included LABETALOL for Blood pressure high. On 03-Oct-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 03-Oct-2022, the patient experienced ORAL DISCOMFORT (lips burning) and TONGUE DISCOMFORT (tongue burning). At the time of the report, ORAL DISCOMFORT (lips burning) and TONGUE DISCOMFORT (tongue burning) had not resolved. On 30-Jan-2021 patient received the first dose of vaccine lot number 012M20A. On 27-Feb-2021 patient received the second dose of vaccine lot number 014M20A. On 01-Nov-2021 patient received the first booster dose of vaccine. On 13-Apr-2022 patient received the second booster dose of vaccine lot number 046L21A. It was reported that patient did not experienced similar event in the past. No death was not occurred and autopsy was not done. No treatment information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oral discomfort
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy to nuts (hazel nuts); Blood pressure high (diagnosed prior to getting the vaccine); Drug allergy (Sulfa allergy); Penicillin allergy
Vorgeschichte: Comments: The patient never had COVID positive test or diagnosis.
Andere Medikamente: LABETALOL
Allergien: -
Vorherige Impfungen: -

VAERS 2469741

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7164B

gering

Staat: WV
Alter: 68,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 01.10.2022
Beginn: 01.10.2022
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Extra dose administered Wrong product administered

Symptomtext

Patient received the wrong vaccination resulting in her having 2 Moderna bivalent vaccinations 10 days apart. Patient said she is feeling fine and actually felt better than when she had the first dose. I have been checking in with the patient every couple days, and she is doing fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Heredity Spherocytosis
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2465216

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7164B

gering

Staat: MA
Alter: 67,0
Geschlecht: M
Eingang: 30.09.2022
Impfdatum: 27.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

No adverse event Wrong product administered

Symptomtext

No adverse event; Received 0.5 ml Bivalent booster dose instead of first primary Monovalent dose; This spontaneous case was reported by a pharmacist and describes the occurrence of WRONG PRODUCT ADMINISTERED (Received 0.5 ml Bivalent booster dose instead of first primary Monovalent dose) and NO ADVERSE EVENT (No adverse event) in a 67-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7164B) for COVID-19 prophylaxis. No Medical History information was reported. On 27-Sep-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) .5 milliliter. On 27-Sep-2022, the patient experienced WRONG PRODUCT ADMINISTERED (Received 0.5 ml Bivalent booster dose instead of first primary Monovalent dose). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, WRONG PRODUCT ADMINISTERED (Received 0.5 ml Bivalent booster dose instead of first primary Monovalent dose) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for WRONG PRODUCT ADMINISTERED (Received 0.5 ml Bivalent booster dose instead of first primary Monovalent dose). Concomitant medication was not provided. Treatment information was not provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2462061

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7164b

gering

Staat: WI
Alter: 42,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 23.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Incorrect dose administered Syringe issue Underdose

Symptomtext

Technician administered vaccine intramuscular into right deltoid. Vaccine dripped a large clear droplett down patients arm upon administration. It is likely vaccine leaked out of syringe. We were using pre drawn syringe so likely leur lock syringe was loose or faulty. According to CDC Website dose could be repeated immediately or can wait 8 weeks for re administration due to risk of pericarditis. pt wanted to wait 8 weeks to re administer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: None. No known reactions/ patient was fine.
Aktuelle Erkrankungen: none reported
Vorgeschichte: none reported on consent form
Andere Medikamente: Unknown
Allergien: unknown
Vorherige Impfungen: -